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Biomechanics and Medicine in Swimming XI

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<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong><br />

Per-Ludvik Kjendlie, Robert Keig Stallman, Jan Cabri (eds)<br />

<strong>XI</strong><br />

OSLO 2010<br />

NORWAY


<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> <strong>XI</strong><br />

Per-Ludvik Kjendlie, Robert Robert Keig Keig Stallman, Jan Jan Cabri Cabri (eds) (eds)


Bibliographic <strong>in</strong>formation:<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong>.<br />

Proceed<strong>in</strong>gs of the <strong>XI</strong>th International Symposium for <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, Oslo, 16th -19th June 2010<br />

Per-Ludvik Kjendlie, Robert Keig Stallman <strong>and</strong> Jan Cabri (Eds)<br />

Published by the Norwegian School of Sport Science, Oslo, 2010<br />

ISBN 978-82-502-0438-6 (pr<strong>in</strong>ted)<br />

ISBN 978-82-502-0439-3 (electronic / pdf version)<br />

Pr<strong>in</strong>ted by Nordbergtrykk as<br />

Front cover photos © by Per Eide / Innovation Norway <strong>and</strong><br />

Per-Ludvik Kjendlie<br />

Front Cover Graphics by Beta Grafisk AS


Scientific Committee<br />

Kjendlie, Per-Ludvik, NOR, (Chair)<br />

Stallman, Robert, NOR, (Chair)<br />

Cabri, Jan, NOR, (Chair)<br />

Alves, Fransisco (POR)<br />

Arellano, Raul (ESP)<br />

Aspenes, Stian (NOR)<br />

Barbosa, Tiago (POR)<br />

Castro, Flavio (BRA)<br />

Chatard, Jean Claude (FRA)<br />

Chollet, Didier (FRA)<br />

Clarys, Jan Pieter (BEL)<br />

Costill, David (USA)<br />

da Silva, Antonio (POR)<br />

Daly, Dan (BEL)<br />

Dekerle, Jeanne (FRA)<br />

Dopsaj, Milivoj (SRB)<br />

Esser-Noethlics, Marc (NOR)<br />

Fern<strong>and</strong>es, Ricardo (POR)<br />

Holl<strong>and</strong>er, Peter (HOL)<br />

Issur<strong>in</strong>, Vladimir (ISR)<br />

Jürimäe, Toivo (EST)<br />

Kesk<strong>in</strong>en, Kari (FIN)<br />

Langendorfer, Steven (USA)<br />

Lemyre, Nicolas (NOR)<br />

Mason, Bruce (AUS)<br />

Millet, Gregoire (SUI)<br />

Moran, Kev<strong>in</strong> (NZL)<br />

Nomura , Teruo( JPN)<br />

Ogita, Futoshi ( JPN)<br />

Onodera, Sho ( JPN)<br />

Payton, Carl (GBR)<br />

Pendergast, David (USA)<br />

Pr<strong>in</strong>s, Jan (USA)<br />

Psychariakis, Stelios (GBR)<br />

Pyne, David (AUS)<br />

Rejman, Marek (POL)<br />

Rodrigues, Ferran (ESP)<br />

S<strong>and</strong>ers, Ross (GBR)<br />

Seifert, Ludovic (FRA)<br />

Stager, Joel (USA)<br />

Swa<strong>in</strong>e, Ian (GBR)<br />

Toussa<strong>in</strong>t, Huub (HOL)<br />

Ungerechts, Bodo (GER)<br />

Vik<strong>and</strong>er, Nils (NOR)<br />

Vilas-Boas, João Paulo (POR)<br />

Wakayoshi, Kohji ( JPN)<br />

Zamparo, Paola (ITA)<br />

BMS International Steer<strong>in</strong>g Group<br />

Kari Kesk<strong>in</strong>en, F<strong>in</strong>l<strong>and</strong> (Chair)<br />

Jan Pieter Clarys, Belgium<br />

Bodo Ungerechts, Germany<br />

João Paulo Vilas-Boas, Portugal<br />

Local Organiz<strong>in</strong>g Committee<br />

Robert Stallman (Chair)<br />

Per-Ludvik Kjendlie (Chair)<br />

Cabri, Jan (Chair)<br />

Bakke, Tom Atle<br />

Caspersen, Cecilie<br />

Dahl, Dagmar<br />

Kesk<strong>in</strong>en, Kari (<strong>in</strong>tn. advisor)<br />

Midtun, Ingvild Riise<br />

Olstad, Bjørn Harald<br />

Ste<strong>in</strong>bekken, Karol<strong>in</strong>e<br />

Vilas-Boas, João Paulo (<strong>in</strong>tn. advisor)<br />

Sponsors<br />

The publish<strong>in</strong>g of this book was supported by:<br />

World Commission for Sport Sciences<br />

The Norwegian School of Sport Sciences<br />

Department of Physical Performance<br />

Norwegian Research Centre for Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Performance<br />

Norwegian Swimm<strong>in</strong>g Federation<br />

Norwegian Life Sav<strong>in</strong>g Society<br />

Norwegian Rheumatism Association<br />

AP Lab<br />

Coaches Infoservices<br />

Cortex Biophysik GmbH<br />

Hector Eng<strong>in</strong>eer<strong>in</strong>g Inc.<br />

Ide AS<br />

Klubben AS<br />

Nespresso<br />

Pahlen Norge<br />

Sensorize Srl<br />

Sport-Thieme GmbH<br />

T<strong>in</strong>e AS<br />

Vita<br />

Voss Water<br />




<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

4<br />

Preface<br />

Biomechancis <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g.<br />

40 Years of Swimm<strong>in</strong>g Science.<br />

The local organiz<strong>in</strong>g committee for BMS2010 is proud to welcome the delegates of the <strong>XI</strong><br />

International Symposium for <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g. It is an honor for<br />

us, for the Norwegian School of Sport Sciences, <strong>and</strong> for Norway, to host this unique conference<br />

<strong>and</strong> to present this Book of Proceed<strong>in</strong>gs. We feel that BMS <strong>XI</strong> is a reference work<br />

which covers the central advances <strong>in</strong> aquatic science s<strong>in</strong>ce BMS 2006 <strong>in</strong> Porto <strong>and</strong> of which<br />

you will have considerable pleasure.<br />

The International Symposium for <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g rema<strong>in</strong>s<br />

the most prestigious of all aquatic oriented scientific congresses <strong>in</strong> the world. It has also<br />

reta<strong>in</strong>ed its’ high ideal of the classic peer review process, so essential to scientific progress.<br />

Every submission has had the benefit of expert creative critique. Eleven times now, we have<br />

presented cutt<strong>in</strong>g edge research <strong>in</strong> a variety of aquatic activities <strong>and</strong> sports. Each time the<br />

challenge has been to present the best possible overview of the most important developments<br />

<strong>in</strong> the four year period s<strong>in</strong>ce the previous BMS symposium.<br />

The first symposium was held <strong>in</strong> Brussels <strong>in</strong> 1970 <strong>and</strong> it has now been held <strong>in</strong> ten different<br />

countries <strong>and</strong> on both sides of the Atlantic. Today, BMS has a unique place <strong>and</strong> a proud<br />

tradition. The series of eleven published BMS Proceed<strong>in</strong>gs has formed the backbone of literature<br />

<strong>in</strong> aquatic research for four decades. They are a collection of peer reviewed scientific<br />

papers comm<strong>and</strong><strong>in</strong>g considerable respect <strong>and</strong> serv<strong>in</strong>g as a valuable resource for all who are<br />

<strong>in</strong>terested <strong>in</strong> keep<strong>in</strong>g up to date with aquatic research. Perhaps we should more properly<br />

be called a gather<strong>in</strong>g of experts <strong>in</strong> aquatic human movement. S<strong>in</strong>ce the laws of nature are<br />

completely democratic, advances applied to one activity can also be applied to others. While<br />

the majority of papers lie with<strong>in</strong> biomechanics, physiology <strong>and</strong> tra<strong>in</strong><strong>in</strong>g, others are grow<strong>in</strong>g<br />

<strong>in</strong> popularity; sociology, education, psychology, anthropometry, epidemiology, drown<strong>in</strong>g<br />

prevention, special needs swimm<strong>in</strong>g, learn to swim, life sav<strong>in</strong>g, etc. - all are represented.<br />

Its’ said that life beg<strong>in</strong>s at forty. We can thus expect the next forty years to be as brilliant<br />

as the last forty. The first edition of the proceed<strong>in</strong>gs (1971) gathered an <strong>in</strong>tellectually rich<br />

mixture of the early pioneers, the established researchers <strong>and</strong> young, aspir<strong>in</strong>g <strong>in</strong>vestigators.<br />

It read like the Who’s Who of aquatic research, <strong>in</strong>clud<strong>in</strong>g the pioneers T.K. Cureton Jr. who<br />

already <strong>in</strong> 1930 had published a biomechanical analysis of the crawl kick <strong>and</strong> Dr. Ernst<br />

Jokl. It also <strong>in</strong>cluded established researchers of the day such as Dr. James “Doc” Counsilman<br />

who <strong>in</strong>troduced us to Bernoulli’s pr<strong>in</strong>ciple as a possible explanation for propulsion <strong>in</strong><br />

swimm<strong>in</strong>g <strong>and</strong> Dr. Per-Olof Åstr<strong>and</strong> who <strong>in</strong>troduced the first swimm<strong>in</strong>g mill or flume. Dr.<br />

Leon Lewillie <strong>and</strong> Dr. Barthels <strong>and</strong> Dr. Adrian <strong>in</strong>troduced underwater electromyography.<br />

Dr. Mitsumasa Miyashita <strong>and</strong> Dr. Richard Nelson presented, at that time, sophisticated<br />

analyses of the crawl.<br />

A systematic attempt to broaden the base of BMS characterized the Oslo meet<strong>in</strong>g. Areas<br />

previously less well represented are present <strong>in</strong> larger numbers than ever before. This<br />

was extremely satisfy<strong>in</strong>g to us <strong>and</strong> we hope that the BMS family will cont<strong>in</strong>ue this tradition.<br />

There are really three pr<strong>in</strong>ciples here which are important. Firstly, the quality of the<br />

research is what counts, not the activity to which it is applied. Secondly, by <strong>in</strong>clud<strong>in</strong>g more<br />

academic discipl<strong>in</strong>es <strong>and</strong> aquatic activities, a far greater degree of cross-fertilization of ideas<br />

is possible. To give an obvious example, the biomechanical techniques applied to analyze<br />

competitive swimm<strong>in</strong>g can also be used to analyze recreational swimm<strong>in</strong>g, learn to swim,<br />

water polo <strong>and</strong> life sav<strong>in</strong>g. And thirdly, multi-discipl<strong>in</strong>ary research will grow. We know that<br />

this is where reality is best mirrored.<br />

The BMS Symposium 2010 <strong>in</strong>cludes 127 poster presentations, 125 oral presentations,<br />

three workshops <strong>and</strong> four poolside demonstrations. Also, n<strong>in</strong>e keynote speakers presented<br />

outst<strong>and</strong><strong>in</strong>g lectures to the audience. The keynote speakers Dr. Stephen Langendorfer, Dr.


Nicolas Lemyre, Dr. Bruce Mason, Dr. Katszuo Matsuuchi, Dr. Jan Pr<strong>in</strong>s, Dr. Ferran Rodriguez,<br />

Dr. Annie Rouard, Dr. Ludovic Seifert <strong>and</strong> Dr. João Paulo Vilas-Boas are honored<br />

especially for their contribution. These contributions ensure that the essence of our conference<br />

series is passed on, <strong>and</strong> these backbone presentations present the current research <strong>in</strong><br />

their respective fields. In honor of the BMS community’s 40th anniversary, the first paper<br />

<strong>in</strong> this book is from the h<strong>and</strong> of Dr. Vilas-Boas <strong>and</strong> is entitled “Past, Present <strong>and</strong> Future of<br />

Swimm<strong>in</strong>g Science”.<br />

The 147 papers <strong>in</strong> this book are organized <strong>in</strong>to 6 different chapters, reflect<strong>in</strong>g each paper’s<br />

scientific discipl<strong>in</strong>e. We take also this opportunity to thank all of the authors who<br />

contributed to these papers. Their contribution often represents months of work, sometimes<br />

years. It builds on a lifetime of experience <strong>and</strong> collegial exchange of ideas, often these days,<br />

across <strong>in</strong>ternational borders.<br />

The BMS Symposium 2010 would not have been possible without our partners, exhibitors<br />

<strong>and</strong> sponsors. We thank The Norwegian School of Sport Sciences, The Norwegian<br />

Swimm<strong>in</strong>g Federation, The Norwegian Lifesav<strong>in</strong>g Association <strong>and</strong> the Norwegian<br />

Rheumatism Association. This k<strong>in</strong>d of contact between BMS <strong>and</strong> practitioners ensures that<br />

aquatic science adapts to, <strong>and</strong> studies real life, applied situations. We would also like to<br />

thank our sponsors <strong>and</strong> exhibitors for their contribution to mak<strong>in</strong>g BMS 2010 happen;<br />

All of the volunteers are thanked for mak<strong>in</strong>g BMS a memorable conference. We hope<br />

you, <strong>in</strong> the midst of your hard work, ga<strong>in</strong>ed valuable experience as well as enjoyable moments.<br />

The Scientific <strong>and</strong> Organiz<strong>in</strong>g committees provided laudable effort <strong>in</strong> prepar<strong>in</strong>g for<br />

this conference. We thank you deeply for your contribution. We thank also the International<br />

Steer<strong>in</strong>g Group of BMS for provid<strong>in</strong>g expert advice <strong>and</strong> for provid<strong>in</strong>g the cont<strong>in</strong>uity which<br />

has made 40 years of BMS possible. F<strong>in</strong>ally we wish to honor The Norwegian School of<br />

Sport Science <strong>and</strong> its Rector, Prof. Sigmund Lol<strong>and</strong>, for mak<strong>in</strong>g BMS <strong>in</strong> Oslo possible. In<br />

difficult f<strong>in</strong>ancial times all over the world, the support of The Norwegian School of Sport<br />

Sciences ensured the conference by provid<strong>in</strong>g the venue, pool, personnel <strong>and</strong> specifically<br />

sponsor<strong>in</strong>g the banquet. F<strong>in</strong>ally this book would not have been a reality without the editorial<br />

assistance of Bjørn Harald Olstad <strong>and</strong> Ingvild Riise Midtun.<br />

We hope you will enjoy read<strong>in</strong>g the contributions of this f<strong>in</strong>e congress!<br />

Per-Ludvik Kjendlie Robert Keig Stallman Jan Cabri<br />

Oslo, June 16 th 2010<br />

Preface<br />

5


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table of Contents<br />

Preface 4<br />

Biomechancis <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g.; 40 Years of Swimm<strong>in</strong>g<br />

Science. 4<br />

Chapter 1. Invited Lectures 11<br />

The Leon Lewillie Memorial Lecture: <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g, Past, Present <strong>and</strong> Future - Vilas-Boas, J.P. 12<br />

Apply<strong>in</strong>g a Developmental Perspective to Aquatics <strong>and</strong> Swimm<strong>in</strong>g -<br />

Langendorfer, S.J. 20<br />

The Psycho-Physiology of Overtra<strong>in</strong><strong>in</strong>g <strong>and</strong> Athlete Burnout <strong>in</strong><br />

Swimm<strong>in</strong>g - Lemyre, P.-N. 22<br />

Biomechanical Services <strong>and</strong> Research for Top Level Swimm<strong>in</strong>g: the<br />

Australian Institute of Sport Model - Mason, B.R. 25<br />

Aquatic Tra<strong>in</strong><strong>in</strong>g <strong>in</strong> Rehabilitation <strong>and</strong> Preventive <strong>Medic<strong>in</strong>e</strong> - Pr<strong>in</strong>s, J.<br />

28<br />

Tra<strong>in</strong><strong>in</strong>g at Real <strong>and</strong> Simulated Altitude <strong>in</strong> Swimm<strong>in</strong>g: Too High<br />

Expectations? - Rodríguez, F.A. 30<br />

Muscle Fatigue <strong>in</strong> Swimm<strong>in</strong>g - Rouard, A.H. 33<br />

Inter-Limb Coord<strong>in</strong>ation <strong>in</strong> Swimm<strong>in</strong>g - Seifert, L. 35<br />

Chapter 2. <strong>Biomechanics</strong> 41<br />

Comparison of Manik<strong>in</strong> Carry Performance by Lifeguards <strong>and</strong> Lifesavers<br />

When Us<strong>in</strong>g Barefoot, Flexible <strong>and</strong> Fiber F<strong>in</strong>s - Abraldes,<br />

J.A., Soares, S.2, Lima, A.B., Fern<strong>and</strong>es, R.J. Vilas-Boas, J.P. 42<br />

Effect of Stroke Drills on Intra-cycle Hip Velocity <strong>in</strong> Front Crawl -<br />

Arellano R., Domínguez-Castells R., Perez-Infantes E., Sánchez E.45<br />

The Usefulness of the Fully Tethered Swimm<strong>in</strong>g for 50-m Breaststroke<br />

Performance Prediction - Barbosa A.C. Milivoj Dopsaj M.2, Okicic T.<br />

Andries Júnior O. 47<br />

Jo<strong>in</strong>t Torque Request for Different F<strong>in</strong> Uses - Gouvernet, G., Rao, G.,<br />

Barla, C. 1, Baly, L., Grélot, L., Berton, E. 50<br />

3D Computational Fluid-structure Interaction Model for the Estimation<br />

of Propulsive Forces of a Flexible Monof<strong>in</strong><br />

Bideau, N. , Razafimahery, F. , Monier, L. , Mahiou, B. ,<br />

Nicolas, G. , Bideau, B. , Rakotomanana, L. 52<br />

Do Fastsk<strong>in</strong> Swimsuits Influence Coord<strong>in</strong>ation <strong>in</strong> Front Crawl Swimm<strong>in</strong>g<br />

<strong>and</strong> Glide? - Chollet, D., Chavallard, F., Seifert, L., Lemaître, F.<br />

55<br />

The Effect of Wear<strong>in</strong>g a Synthetic Rubber Suit on Hydrostatic Lift<br />

<strong>and</strong> Lung Volume - Cortesi, M. , Zamparo, P. , Tam, E., Da Boit, M.,<br />

Gatta, G. 57<br />

The Development of a Component Based Approach for Swim Start<br />

Analysis - Cossor, J.M., Slawson, S.E.², Justham, L.M., Conway, P.P.²,<br />

West, A.A. 59<br />

Hydrodynamic Characterization of the First <strong>and</strong> Second Glide Positions<br />

of the Underwater Stroke Technique <strong>in</strong> Breaststroke - Costa,<br />

L.; Ribeiro, J.; Figueiredo, P.; Fern<strong>and</strong>es, R.J.; Mar<strong>in</strong>ho, D.; Silva,<br />

A.J.,4; Rouboa, A.,4; Vilas-Boas, J.P.1; Machado, L. 62<br />

6<br />

Biomechanical Characterization of the Backstroke Start <strong>in</strong> Immerged<br />

<strong>and</strong> Emerged Feet Conditions - De Jesus, K., De Jesus, K., Figueiredo,<br />

P., Gonçalves, P., Pereira, S.M., Vilas-Boas, J.P. Fern<strong>and</strong>es, R.J. 64<br />

Tethered Force Production <strong>in</strong> St<strong>and</strong>ard <strong>and</strong> Contra-st<strong>and</strong>ard Scull<strong>in</strong>g<br />

<strong>in</strong> Synchronized Swimm<strong>in</strong>g - Diogo, V., Soares, S., Tour<strong>in</strong>o, C.,<br />

Abraldes, J.A., Ferragut, C., Morouço, P., Figueiredo, P., Vilas-Boas, J.P.,<br />

Fern<strong>and</strong>es, R.J. 67<br />

Pull<strong>in</strong>g Force Characteristics of 10 s Maximal Tethered Eggbeater<br />

Kick <strong>in</strong> Elite Water Polo Players: A Pilot Study - Dopsaj, M. 69<br />

Motor Coord<strong>in</strong>ation Dur<strong>in</strong>g the Underwater Undulatory Swimm<strong>in</strong>g<br />

Phase of the Start for High Level Swimmers - Elipot, M. , 2, Houel,<br />

N. 2, Hellard, P. 2, Dietrich, G. 72<br />

Relationship between Arm Coord<strong>in</strong>ation <strong>and</strong> Energy Cost <strong>in</strong> Front<br />

Crawl Swimm<strong>in</strong>g - Fern<strong>and</strong>es, R.J., Morais, P., Kesk<strong>in</strong>en, K.L., Seifert,<br />

L., Chollet, D., Vilas-Boas, J.P. 74<br />

Evaluation of the Validity of Radar for Measur<strong>in</strong>g Throw<strong>in</strong>g Velocities<br />

<strong>in</strong> Water Polo - Ferragut, C., Alcaraz, P.E.1, Vila, H., Abraldes, J.A.,<br />

Rodriguez, N. 77<br />

Biophysical Analysis of the 200m Front Crawl Swimm<strong>in</strong>g: a Case<br />

Study - Figueiredo, P., Sousa, A.1; Gonçalves, P., Pereira, S.M., Soares,<br />

S., Vilas-Boas, J.P., Fern<strong>and</strong>es, R.J. 79<br />

Measur<strong>in</strong>g Active Drag with<strong>in</strong> the Different Phases of Front Crawl<br />

Swimm<strong>in</strong>g - Formosa, D. P., Mason, B.R. & Burkett, B. J. 82<br />

The Mechanical Power Output <strong>in</strong> Water Polo Game: a Case Report -<br />

Gatta, G., Fantozzi, S., Cortesi, M., Patti, F., Bonifazi, M. 84<br />

Comparison of Comb<strong>in</strong>ations of Vectors to def<strong>in</strong>e the Plane of the<br />

H<strong>and</strong> <strong>in</strong> order to calculate the Attack Angle dur<strong>in</strong>g the Scull<strong>in</strong>g Motion<br />

- Gomes, L.E.1, Melo, M.O.1, La Torre, M. 1, Loss, J.F. 86<br />

The Acute Effect of Front Crawl Spr<strong>in</strong>t-resisted Swimm<strong>in</strong>g on the<br />

Direction of the Resultant Force of the H<strong>and</strong> - Gourgoulis, V., Aggeloussis,<br />

N., Mavridis, G., Boli, A., Toubekis, A.G., Kasimatis, P., Vezos,<br />

N., Mavrommatis, G. 89<br />

Relationship between Eggbeater Kick <strong>and</strong> Support Scull Skills, <strong>and</strong><br />

Isok<strong>in</strong>etic Peak Torque - Homma, M. 91<br />

A Biomechanical Comparison of Elite Swimmers Start Performance<br />

Us<strong>in</strong>g the Traditional Track Start <strong>and</strong> the New Kick Start - Honda,<br />

K.E., S<strong>in</strong>clair, P.J., Mason, B.R. & Pease, D.L. 94<br />

K<strong>in</strong>ematic Analysis of Undulatory Underwater Swimm<strong>in</strong>g dur<strong>in</strong>g<br />

a Grab Start of National Level Swimmers - Houel N., Elipot M.,<br />

Andrée F., Hellard H. 97<br />

Comparison of Front Crawl Swimm<strong>in</strong>g Drag between Elite <strong>and</strong> Non-<br />

Elite Swimmers Us<strong>in</strong>g Pressure Measurement <strong>and</strong> Motion Analysis<br />

- Ichikawa, H., Miwa, T., Takeda, T., Takagi, H., Tsubakimoto, S.<br />

100<br />

Whole Body Observation <strong>and</strong> Visualized Motion Analysis of Swimm<strong>in</strong>g<br />

- Ito, S., Okuno, K. 102<br />

A Full Body Computational Fluid Dynamic Analysis of the Freestyle<br />

Stroke of a Previous Spr<strong>in</strong>t Freestyle World Record Holder - Keys,<br />

M.1; Lyttle, A.2; Blanksby, B.A.1 & Cheng, L. 105<br />

An Analysis of an Underwater Turn for Butterfly <strong>and</strong> Breaststroke -<br />

Kishimoto, T.,Takeda, T.,Sugimoto, S., Tsubakimoto, S.2 <strong>and</strong> Takagi, H.<br />

108<br />

Mechanical <strong>and</strong> Propulsive Efficiency of Swimmers <strong>in</strong> Different Zones<br />

of Energy Supply - Kolmogorov, S.V., Vorontsov, A.R., Rumyantseva,<br />

O.A., Kocherg<strong>in</strong>, A.B. 110


Prediction of Propulsive Force Exerted by the H<strong>and</strong> <strong>in</strong> Swimm<strong>in</strong>g -<br />

Kudo, S. <strong>and</strong> Lee, M.K. 112<br />

Arm Coord<strong>in</strong>ation, Active Drag <strong>and</strong> Propell<strong>in</strong>g Efficiency <strong>in</strong> Front<br />

Crawl - Seifert, L., Schnitzler, C., Alberty, M., Chollet, D. 1, Toussa<strong>in</strong>t,<br />

H.M. 115<br />

Modell<strong>in</strong>g Arm Coord<strong>in</strong>ation <strong>in</strong> Front Crawl - Seifert, L., Chollet, D.<br />

117<br />

Different Frequential Acceleration Spectrums <strong>in</strong> Front Crawl - Madera,<br />

J., González, L.M., García Massó, X., Benavent, J., Colado, J.C.,<br />

Tella, V. 119<br />

The Glid<strong>in</strong>g Phase <strong>in</strong> Swimm<strong>in</strong>g: The Effect of Water Depth - Mar<strong>in</strong>ho,<br />

D.A., Barbosa, T.M., Mantripragada, N., Vilas-Boas, J.P., Rouard,<br />

A.H., Mantha, V.R., Rouboa, A.I., Silva, A.J. 122<br />

A Method to Estimate Active Drag over a Range of Swimm<strong>in</strong>g Velocities<br />

which may be used to Evaluate the Stroke Mechanics of the<br />

Swimmer - Mason, B.R., Formosa, D.P., Toussa<strong>in</strong>t, H.M. 124<br />

50m Race Components Times Analysis Based on a Regression Analysis<br />

Model Applied to Age-Group Swimmers - Morales, E. , Arellano,<br />

R. , Femia, P. , Mercade, J. , Halj<strong>and</strong> R. 127<br />

Regression Analysis Model Applied to Age-Group Swimmers: Study<br />

of Stroke Rate, Stroke Length <strong>and</strong> Stroke Index - Morales, E., Arellano,<br />

R., Femia, P., Mercade, J. 130<br />

Advanced Biomechanical Simulations <strong>in</strong> Swimm<strong>in</strong>g Enabled by Extensions<br />

of Swimm<strong>in</strong>g Human Simulation Model “SWUM” -<br />

Nakashima, M., Kiuchi, H., Maeda, S., Kamiya, S., Nakajima, K.,<br />

Takagi, H. 132<br />

Influences of the Back Plate on Competitive Swimm<strong>in</strong>g Start<strong>in</strong>g Motion<br />

<strong>in</strong> Particular Projection Skill; K<strong>in</strong>ematical Characterisation of<br />

a Basic Head-out Aquatic Exercise dur<strong>in</strong>g an Incremental Protocol<br />

- Oliveira, C., Teixeira, G., Costa, M.J., Mar<strong>in</strong>ho, D.A., Silva, A.J.,<br />

Barbosa, T.M. , 137<br />

Influence of Swimm<strong>in</strong>g Speed on the Affected- <strong>and</strong> Unaffected-Arm<br />

Stroke Phases of Competitive Unilateral Arm Amputee Front<br />

Crawl Swimmers - Osborough, C.D., Payton, C.J., Daly, D.J. 140<br />

Co-ord<strong>in</strong>ation Changes dur<strong>in</strong>g a Maximal Effort 100 m Short Course<br />

Breaststroke Swim - Oxford, S., James, R., Price, M., Payton, C.<br />

142<br />

The Effect of Angle of Attack <strong>and</strong> Depth on Passive Drag - Pease, D.L.<br />

1, Vennell, R. 145<br />

Graphic Removal of Water Wave Impact <strong>in</strong> the Pool Wall dur<strong>in</strong>g the<br />

Flip Turn - Pereira, S.M., Gonçalves, P., Fern<strong>and</strong>es, R.J., Machado, L.,<br />

Roesler, H., Vilas-Boas, J.P. 148<br />

Extend<strong>in</strong>g the Critical Force Model to Approach Critical Power <strong>in</strong><br />

Tethered Swimm<strong>in</strong>g, <strong>and</strong> its Relationship to the Indices at Maximal<br />

Lactate Steady-State - Pessôa Filho, D.M., Denadai, B.S. 151<br />

Prelim<strong>in</strong>ary Results of a “Multi-2D” K<strong>in</strong>ematic Analysis of “Straight-<br />

vs. Bent-arm” Freestyle Swimm<strong>in</strong>g, Us<strong>in</strong>g High-Speed Videography.<br />

- Pr<strong>in</strong>s, J.H., Murata, N.M., & Allen, J. S. III. 154<br />

Biomechanical Factors Influenc<strong>in</strong>g Tumble Turn Performance of Elite<br />

Female Swimmers - Puel, F., Morlier, J., Cid, M., Chollet, D., Hellard,<br />

P. 155<br />

Front Crawl <strong>and</strong> Backstroke Arm Coord<strong>in</strong>ation <strong>in</strong> Swimmers with<br />

Down Syndrome - Querido, A., Marques-Aleixo, I., Figueiredo, P.,<br />

Seifert, L., Chollet, D., Vilas-Boas, J.P., Daly, D.J., Corredeira, R.,<br />

Fern<strong>and</strong>es, R.J. 157<br />

Preface<br />

Identify<strong>in</strong>g Determ<strong>in</strong>ant Movement Sequences <strong>in</strong> Monof<strong>in</strong> Swimm<strong>in</strong>g<br />

Technique - Rejman, M. & Staszkiewicz, A. 160<br />

Evaluation of the Glid<strong>in</strong>g Capacity of a Swimmer - Roig, A. 163<br />

Effects of a BlueseventyTM Bodysuit on Spatial-temporal <strong>and</strong><br />

Coord<strong>in</strong>ative Parameters Dur<strong>in</strong>g an All-out 50-m Front<br />

Crawl - Silveira, R.P., Kanefuku, J.Y., Moré, F.C., Castro, F.A.S.<br />

165<br />

Fatigue Analysis of 100 Meters All-Out Front Crawl Us<strong>in</strong>g Surface<br />

EMG - Stirn, I. Jarm, T., Kapus, V., Strojnik, V. 168<br />

Comparison Among Three Types of Relay Starts <strong>in</strong> Competitive<br />

Swimm<strong>in</strong>g - Takeda, T., Takagi, H., Tsubakimoto, S. 170<br />

A Study About the 3D Acceleration <strong>in</strong> Front Crawl <strong>and</strong> its Relation<br />

With Performance - Tella, V., Madera, J., Colado, J.C., Mateu, J.,<br />

García Massó, X., González, L.M. 173<br />

Aquatic Space Activities – Practice Needs Theory - Ungerechts, B.,<br />

Klauck, J². 175<br />

Analysis of Swim Turn<strong>in</strong>g, Underwater Glid<strong>in</strong>g <strong>and</strong> Stroke Resumption<br />

Phases <strong>in</strong> Top Division Swimmers us<strong>in</strong>g a Wearable Inertial<br />

Sensor Device - Vannozzi, G., Donati, M., Gatta G. & Cappozzo, A.<br />

178<br />

Influence of Swimm<strong>in</strong>g Start Styles on <strong>Biomechanics</strong> <strong>and</strong> Angular<br />

Momentum - Vantorre, J., Seifert, L., Bideau, B., Nicolas, G., Fern<strong>and</strong>es,<br />

R.J., Vilas-Boas, J.P., Chollet, D. 180<br />

The Validity <strong>and</strong> Reliability of a Procedure for Competition Analysis<br />

<strong>in</strong> Swimm<strong>in</strong>g Based on Individual Distance Measurements - Veiga,<br />

S., Cala, A., González Frutos, P., Navarro, E. 182<br />

An Analysis of the Underwater Glid<strong>in</strong>g Motion <strong>in</strong> Collegiate Competitive<br />

Swimmers - Wada, T., Sato, T., Ohishi, K., Tago, T., Izumi, T.,<br />

Matsumoto, T., Yamamoto, N., Isaka, T., Shimoyama, Y. 185<br />

Head Out Swimm<strong>in</strong>g <strong>in</strong> Water Polo: a Comparison with Front Crawl<br />

<strong>in</strong> Young Female Players - Zamparo, P., Falco, S. 187<br />

Chapter 3. Physiology <strong>and</strong> Bioenergetics 191<br />

Models of Vertical Swimm<strong>in</strong>g Abilities <strong>in</strong> Elite Female Senior Water<br />

Polo Players - Dopsaj, M. 192<br />

Critical Velocity <strong>and</strong> the Velocity at Maximal Lactate Steady State <strong>in</strong><br />

Swimm<strong>in</strong>g - Espada, M.A., Alves, F.B. 194<br />

Modell<strong>in</strong>g the VO 2 Slow Component <strong>in</strong> Elite Long Distance Swimmers<br />

at the Velocity Associated with Lactate Threshold - Hellard, P. ,<br />

Dekerle, J., Nesi, X., Toussa<strong>in</strong>t, J.F., Houel, N., Hausswirth, C. 196<br />

The Impact of Tension <strong>in</strong> Abdom<strong>in</strong>al <strong>and</strong> Lumbar Musculature <strong>in</strong><br />

Swimmers on Ventilatory <strong>and</strong> Cardiovascular Functions - Henrich,<br />

T.W., Pankey, R.B. Soukup, G.J. 199<br />

Relationship between Propell<strong>in</strong>g Efficiency <strong>and</strong> Swimm<strong>in</strong>g Performance<br />

<strong>in</strong> Elite Swimmers. - Huang, Z., Kurobe, K., Nishiwaki, M.,<br />

Ozawa, G., Tanaka, T., Taguchi, N., Ogita, F. 201<br />

Effect of Increas<strong>in</strong>g Energy Cost on Arm Coord<strong>in</strong>ation at Different<br />

Exercise Intensities <strong>in</strong> Elite Spr<strong>in</strong>t Swimmers - Komar, J.1, Leprêtre,<br />

P.M.2, Alberty, M.3, Vantorre, J.1, Fern<strong>and</strong>es, R.J.4, Hellard, P.,6,<br />

Chollet, D.1, Seifert, L. 204<br />

Swimm<strong>in</strong>g <strong>and</strong> Respiratory Muscle Endurance Tra<strong>in</strong><strong>in</strong>g: A Case<br />

Study - Lemaître, F., Chavallard, F., Chollet, D. 206<br />

7


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Heart Rate Responses Dur<strong>in</strong>g Gradually Increas<strong>in</strong>g <strong>and</strong> Decreas<strong>in</strong>g<br />

Exercise <strong>in</strong> Water - Nishimura, K., Nose, Y., Yoshioka, A., Kawano, H.,<br />

Onodera, S., Takamoto, N. 208<br />

Effects of Recently Developed Swimwear on Drag Dur<strong>in</strong>g Front<br />

Crawl Swimm<strong>in</strong>g; - Ogita, F., Huang, Z., Kurobe, K., Ozawa, G.,<br />

Taguchi,T., Tanaka, T. 211<br />

Relationship between Heart Rate <strong>and</strong> Water Depth <strong>in</strong> the St<strong>and</strong><strong>in</strong>g<br />

Position - Onodera, S., Yoshioka, A., Matsumoto, N., Takahara,<br />

T., Nose, Y. 1, Hirao, M., Seki, K., Nishimura, K., Baik, W., Hara, H.,<br />

Murakawa, T. 213<br />

Oxygen Uptake K<strong>in</strong>etics Around the Respiratory Compensation Po<strong>in</strong>t<br />

<strong>in</strong> Swimm<strong>in</strong>g - Pessôa Filho, D.M., Reis, J.F., Alves, F.B., Denadai,<br />

B.S. 215<br />

Hormonal, Immune, Autonomic <strong>and</strong> Mood State Variation <strong>in</strong> the<br />

Initial Preparation Phase of a W<strong>in</strong>ter Season, <strong>in</strong> Portuguese Male<br />

Swimmers - Rama, L., Alves, F., Teixeira, A. 217<br />

Oxygen Uptake K<strong>in</strong>etics <strong>and</strong> Performance <strong>in</strong> Swimm<strong>in</strong>g - Reis, J.F.,<br />

Alves, F.B. 220<br />

Maximum Blood Lactate Concentration after two Different Specific<br />

Tests <strong>in</strong> Freestyle Swimm<strong>in</strong>g - Rozi, G., Thanopoulos, V., Dopsaj, M.<br />

222<br />

Can Blood Glucose Threshold be Determ<strong>in</strong>ed <strong>in</strong> Swimmers Early<br />

<strong>in</strong> the Swimm<strong>in</strong>g Season? - Sengoku, Y., Nakamura, K., Takeda, T. ,<br />

Nabekura, Y., Tsubakimoto, S. 224<br />

The Effects of Rubber Swimsuits on Swimmers Us<strong>in</strong>g a Lactic Acid<br />

Curve Test - Shiraki, T., Wakayoshi, K., Hata, H., Yamamoto, T., Tomikawa,<br />

M. 226<br />

Some Factors Limit<strong>in</strong>g Energy Supply <strong>in</strong> 200m Front Crawl Swimm<strong>in</strong>g<br />

- Strumbelj, B., Usaj, A., Kapus, J., Bednarik, J. 228<br />

Lactate Comparison Between 100m Freestyle <strong>and</strong> Tethered Swimm<strong>in</strong>g<br />

of Equal Duration - Thanopoulos, V., Rozi, G., Platanou, T.<br />

230<br />

Blood Lactate Concentration <strong>and</strong> Clearance <strong>in</strong> Elite Swimmers Dur<strong>in</strong>g<br />

Competition - Vescovi, J.D., Falenchuk, O., Wells G.D. 233<br />

Determ<strong>in</strong>ation <strong>and</strong> Validity of Critical Velocity <strong>in</strong> Front Crawl, Arm<br />

Stroke <strong>and</strong> Leg Kick as an Index of Endurance Performance <strong>in</strong><br />

Competitive Swimmers - Wakayoshi, K., Shiraki, T., Ogita, F., Kitajima,<br />

M. 236<br />

Differences In Methods Determ<strong>in</strong><strong>in</strong>g The Anaerobic Threshold Of<br />

Triathletes In The Water - Zoretić, D., Wertheimer, V., Leko, G. 238<br />

Chapter 4. Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Performance 241<br />

Physiological Responses <strong>and</strong> Performance Characteristics of 200m<br />

Cont<strong>in</strong>uous Swimm<strong>in</strong>g <strong>and</strong> 4x50m ‘’Broken Swimm<strong>in</strong>g’’ with Different<br />

Rest Intervals - Beidaris, N., Botonis, P. <strong>and</strong> Platanou, T.242<br />

General Indexes of Crawl Swimm<strong>in</strong>g Velocity of Junior Water Polo<br />

Players <strong>in</strong> a Match - Bratusa, F.Z., Perisic, S.M., Dopsaj, J.M. 245<br />

Bench Press <strong>and</strong> Leg Press Strength <strong>and</strong> its Relationship with In-<br />

Water Force <strong>and</strong> Swimm<strong>in</strong>g Performance when Measured <strong>in</strong>-season<br />

<strong>in</strong> Male <strong>and</strong> Female Age-group Swimmers - Carl, D.L., Leslie, N.,<br />

Dickerson, T., Griff<strong>in</strong>, B., Markste<strong>in</strong>er, A. 247<br />

Effect of Start Time Feedback on Swimm<strong>in</strong>g Start Performance. - de<br />

la Fuente, B. <strong>and</strong> Arellano, R. 249<br />

8<br />

Predictors of Performance <strong>in</strong> Pre-Pubertal <strong>and</strong> Pubertal Male <strong>and</strong><br />

Female Swimmers - Douda, H.T., Toubekis, A.G., Georgiou, Ch.,<br />

Gourgoulis, V. <strong>and</strong> Tokmakidis, S.P. 252<br />

Changes of Competitive Performance, Tra<strong>in</strong><strong>in</strong>g Load <strong>and</strong> Tethered<br />

Force Dur<strong>in</strong>g Taper<strong>in</strong>g <strong>in</strong> Young Swimmers - Drosou, E., Toubekis,<br />

A.G., Gourgoulis, V., Thomaidis, S., Douda, H., Tokmakidis, S.P. 254<br />

Perceived Exertion at Different Percents of The Critical Velocity <strong>in</strong><br />

Front Crawl - Franken, M., Diefenthaeler, F., de Souza Castro, F.A.<br />

257<br />

Ventilatory <strong>and</strong> Biomechanical Responses <strong>in</strong> Short vs. Long Interval<br />

Tra<strong>in</strong><strong>in</strong>g <strong>in</strong> Elite Long Distance Swimmers. - Hellard, P., Dekerle, J.,<br />

Nesi, X., Toussa<strong>in</strong>t, J.F., Houel, N.1, Hausswirth, C. 259<br />

Talent Prognosis <strong>in</strong> Young Swimmers - Hohmann, A.1, Seidel, I. 262<br />

Determ<strong>in</strong>ation of Lactate Threshold with Four Different Analysis<br />

Techniques for Pool Test<strong>in</strong>g <strong>in</strong> Swimmers; Competitive Systematization<br />

<strong>in</strong> Age-group Swimm<strong>in</strong>g: An Evaluation of Performances,<br />

Maturational Considerations, <strong>and</strong> International Paradigms - Kojima,<br />

K. <strong>and</strong> Stager, J.M. 267<br />

Effects of Reduced Knee-bend on 100 Butterfly Performance: A Case<br />

Study Us<strong>in</strong>g the Men’s Asian <strong>and</strong> Japanese Record Holder - Ide, T.,<br />

Yoshimura, Y., Kawamoto, K., Takise, S., Kawakami, T. 270<br />

Stability <strong>and</strong> Prediction of 100-m Breaststroke Performance Dur<strong>in</strong>g<br />

The Careers of Elite Swimmers - Costa, M.J.; Mar<strong>in</strong>ho, D.A., Reis,<br />

V.M., Silva, A.J., Bragada, J.A., Barbosa, T.M.,4 272<br />

Effect of Subjective Effort on Stroke Tim<strong>in</strong>g <strong>in</strong> Breaststroke Swimm<strong>in</strong>g<br />

- Ohba, M., Sato, S., Shimoyama, Y., Sato, D. 274<br />

Models for Assess<strong>in</strong>g General Horizontal Swimm<strong>in</strong>g Abilities of<br />

Junior Water Polo Players Accord<strong>in</strong>g to Play<strong>in</strong>g Position - Özkol,<br />

Z., Dopsaj, M., Thanopoulos, V., Bratusa, Z. 276<br />

A Markov Cha<strong>in</strong> Model of Elite Water Polo Competition - Pfeiffer,<br />

M., Hohmann, A., Siegel, A., Böhnle<strong>in</strong>, S. 278<br />

Throw<strong>in</strong>g Accuracy of Water Polo Players of Different Tra<strong>in</strong><strong>in</strong>g Age<br />

<strong>and</strong> Fitness Levels <strong>in</strong> a Static Position <strong>and</strong> after Previous Swimm<strong>in</strong>g<br />

- Platanou, T. <strong>and</strong> Botonis, P. 281<br />

The Effect of Cognition-Based Technique Tra<strong>in</strong><strong>in</strong>g on Stroke Length<br />

<strong>in</strong> Age-Group Swimmers - Schmidt, A.C., Ungerechts, B.E., Buss, W.1<br />

& Schack, T. 283<br />

Assess<strong>in</strong>g Mental Workload at Maximal Intensity <strong>in</strong> Swimm<strong>in</strong>g Us<strong>in</strong>g<br />

the NASA-TLX Questionnaire - Schnitzler, C., Seifert, L., Chollet,<br />

D. 286<br />

Does the Y-Intercept of a Regression L<strong>in</strong>e <strong>in</strong> the Critical Velocity<br />

Concept Represent the Index for Evaluat<strong>in</strong>g Anaerobic Capacity? -<br />

Shimoyama, Y., Okita, K., Baba,Y., Sato, D. 288<br />

Evaluation of Force Production <strong>and</strong> Fatigue us<strong>in</strong>g an Anaerobic Test<br />

Performed by Differently Matured Swimmers - Soares, S., Silva, R.,<br />

Aleixo, I., Machado, L., Fern<strong>and</strong>es, R.J., Maia, J., Vilas-Boas, J.P.291<br />

Identification of a Bias <strong>in</strong> the Natural Progression of Swim Performance<br />

- Stager, J.M., Brammer, C.L., Tanner, D.A. 294<br />

Tethered Swimm<strong>in</strong>g as an Evaluation Tool of S<strong>in</strong>gle Arm-Stroke<br />

Force - Toubekis, A.G., Gourgoulis, V., Tokmakidis, S.P. 296<br />

Blood Lactate Responses Dur<strong>in</strong>g Interval Tra<strong>in</strong><strong>in</strong>g Correspond<strong>in</strong>g<br />

to Critical Velocity <strong>in</strong> Age-Group Female Swimmers - Tsalis, G.,<br />

Toubekis, A.G., Michailidou, D., Gourgoulis, V., Douda, H., Tokmakidis,<br />

S.P. 299


Monitor<strong>in</strong>g Swim Tra<strong>in</strong><strong>in</strong>g Based on Mean Intensity Stra<strong>in</strong> <strong>and</strong><br />

Individual Stress Reaction of an Elite Swimmer - Ungerechts, B.E.,<br />

Steffen, R., <strong>and</strong> Vogel, K. 302<br />

Accelerometry as a Means of Quantify<strong>in</strong>g Tra<strong>in</strong><strong>in</strong>g Distance <strong>and</strong><br />

Speed <strong>in</strong> Competitive Swimmers. - Wright, B.V. , H<strong>in</strong>man, M.G. ,<br />

Stager, J.M. 305<br />

Critical Swimm<strong>in</strong>g Speed Obta<strong>in</strong>ed by the 200-400 Meters Model <strong>in</strong><br />

Young Swimmers - Zacca, R., Castro, F.A.S. 307<br />

Chapter 5. Education, Advice <strong>and</strong> Biofeedback 311<br />

The Evolution of Swimm<strong>in</strong>g Science Research: Content analysis of<br />

the “<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g” Proceed<strong>in</strong>gs Books<br />

from 1971 to 2006 - Barbosa, T.M., P<strong>in</strong>to, E., Cruz, A.M., Mar<strong>in</strong>ho,<br />

D.A.,, Silva, A.J., Reis, V.M., Costa, M.J., Queirós ,T.M. 312<br />

Quantitative Data Supplements Qualitative Evaluations of Butterfly<br />

Swimm<strong>in</strong>g - Becker, T.J., Havriluk, R. 314<br />

The Effect of Restrict<strong>in</strong>g the Visual Perceptual Task <strong>in</strong> the Temporal<br />

Organization of Crawl Swimm<strong>in</strong>g: Surface Characteristics - Brito,<br />

C.A.F., Belvis, W.C., Oliveira, M. 2 317<br />

Analyses of Instruction for Breath Control While Swimm<strong>in</strong>g the<br />

Breaststroke - Hara, H., Yoshioka, A., Matsumoto, N., Nose, Y., Watanabe,<br />

R., Shibata, Y., Onodera, S. 319<br />

Performance Level Differences <strong>in</strong> Swimm<strong>in</strong>g: Relative Contributions<br />

of Strength <strong>and</strong> Technique - Havriluk, R. 321<br />

Evaluation of K<strong>in</strong>aesthetic Differentiation Abilities <strong>in</strong> Male <strong>and</strong> Female<br />

Swimmers - Invernizzi, P.L., Longo, S., Scurati, R., Michielon,<br />

G. 324<br />

Swimm<strong>in</strong>g <strong>in</strong> Eyesight Deprivation: Relationships with Sensory-<br />

Perception, Coord<strong>in</strong>ation <strong>and</strong> laterality - Invernizzi, P.L., Longo, S.,<br />

Tad<strong>in</strong>i, F., Scurati, R. 326<br />

Progression <strong>in</strong> Teach<strong>in</strong>g Beg<strong>in</strong>n<strong>in</strong>g Swimm<strong>in</strong>g: Rank Order by Degree<br />

of Difficulty - Junge, M., Blixt, T., Stallman, R.K, , 329<br />

The Construct Validity of a Traditional 25m Test of Swimm<strong>in</strong>g Competence<br />

- Junge, M., Blixt, T., Stallman, R.K., 331<br />

Us<strong>in</strong>g a Scalogram to Identify an Appropriate Instructional Order for<br />

Swimm<strong>in</strong>g Items - Langendorfer, S.J., Chaya, J.A. 333<br />

Imagery Tra<strong>in</strong><strong>in</strong>g <strong>in</strong> Young Swimmers: Effects on the Flow State <strong>and</strong><br />

on Performance - Scurati, R., Michielon, G., Longo, S., Invernizzi,<br />

P.L. 336<br />

Shallow or Deep Water for Adjustment? A Study <strong>in</strong> Children Aged 3<br />

to 6 Years - Scurati, R., Michielon, G., Longo, S., Invernizzi, P.L.<br />

339<br />

The Effect of a Target Sound Made by a Model Swimmer’s Dolph<strong>in</strong><br />

Kick Movement on Another Swimmer’s Dolph<strong>in</strong> Kick Performance<br />

- Shimojo, H., Ichikawa, H., Tsubakimoto, S., Takagi, H. 341<br />

Tendencies <strong>in</strong> Natural Selection of High Level Young Swimmers -<br />

TimakovaT.S., Klyuchnikova M.V. 343<br />

The Cognitive Interplay Between Sensory <strong>and</strong> Biomechanical Features<br />

While Execut<strong>in</strong>g Flip Turns Wear<strong>in</strong>g Different Swim Suits - Vieluf,<br />

S., Ungerechts, B.E., Toussa<strong>in</strong>t, H.M., Lex, H. 1, Schack, T. 346<br />

The Role of Verbal Information about Sensory Experience from<br />

Movement Apparatus <strong>in</strong> the Process of Swimm<strong>in</strong>g Economization<br />

- Zatoń, K. 349<br />

Preface<br />

Chapter 6. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Water Safety 353<br />

Crucial F<strong>in</strong>d<strong>in</strong>gs from the 4W Model of Drown<strong>in</strong>g for Practical <strong>and</strong><br />

Teach<strong>in</strong>g Applications - Avramidis, S., McKenna, J., Long, J., Butterly,<br />

R., Llewellyn, J.D. 354<br />

Swimm<strong>in</strong>g, Cycl<strong>in</strong>g, Runn<strong>in</strong>g <strong>and</strong> Cardiovascular Health - Bagheri,<br />

A.B., Mohebbi, H.D., Azizi, M.H., Saiiari, A.R. 357<br />

Analysis of Aerobic/Anaerobic Performance <strong>in</strong> Functionally Disabled<br />

Swimmers: Low Classes vs High Classes - De Aymerich, J., Benavent,<br />

J., Tella, V., Colado, J.C., González, L.M., García-Massó, X. 2,<br />

Madera, J. 359<br />

Athletic Rehabilitation of a Platform Diver for Return to Competition<br />

after a Shoulder Dislocation - Fuj<strong>in</strong>awa, O., Kondo, Y., Tachikawa,<br />

K., Jigami, H., Hirose, K., Matsunaga, H. 362<br />

Comparisons of Water- <strong>and</strong> L<strong>and</strong>-based Physical Activity Interventions<br />

<strong>in</strong> Japanese Subjects with Metabolic Syndrome - Hanai, A. <strong>and</strong><br />

Yamatsu, K. 364<br />

Estimation Method for Energy Expenditure by Acceleration of Human<br />

Head dur<strong>in</strong>g Water Walk<strong>in</strong>g - Kaneda, K., Ohgi, Y., Tanaka, C.<br />

366<br />

Real <strong>and</strong> Perceived Swimm<strong>in</strong>g Competency, Risk Estimation, <strong>and</strong><br />

Prevent<strong>in</strong>g Drown<strong>in</strong>g among New Zeal<strong>and</strong> Youth - Moran, K.<br />

368<br />

Keep<strong>in</strong>g the Safety Messages Simple: The International Task Force on<br />

Open-Water Recreational Drown<strong>in</strong>g Prevention - Quan, L., Bennett,<br />

E., Moran, K. (co-chairs) 371<br />

Immune Status Changes <strong>and</strong> URTI Incidence <strong>in</strong> the Initial 7 Weeks<br />

of a W<strong>in</strong>ter Tra<strong>in</strong><strong>in</strong>g Season <strong>in</strong> Portuguese Swimmers - Rama, L.,<br />

Alves, F.B., Rosado, F., Azevedo, S., Matos, A., Henriques, A., Paiva, A.<br />

3, Teixeira, AM. 374<br />

Swimm<strong>in</strong>g Ability, Perceived Competence <strong>and</strong> Perceived Risk among<br />

Young Adults - Stallman, R.K., Dahl D.1, Moran, K., Kjendlie, P.L.,<br />

377<br />

Movement Economy <strong>in</strong> Breaststroke Swimm<strong>in</strong>g: A Survival Perspective<br />

- Stallman R.K., Major J., Hemmer S., Haavaag G. 379<br />

Post-exercise Hypotension <strong>and</strong> Blood Lipoprote<strong>in</strong> Changes follow<strong>in</strong>g<br />

Swimm<strong>in</strong>g Exercise - Tanaka, H., Sommerlad, S.M., Renzi, C.P.,<br />

Barnes, J.N., <strong>and</strong> Nualnim, N. 381<br />

A Conceptual Paper on the Benefits of a Non-Governmental Search<br />

<strong>and</strong> Rescue Organization - Wengel<strong>in</strong>, M., de Wet, T. 384<br />

Author Index 0<br />

9


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

10


Chapter 1. Invited Lectures


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The Leon Lewillie Memorial Lecture: <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, Past, Present <strong>and</strong><br />

Future<br />

Vilas-Boas, J.P.<br />

University of Porto, Faculty of Sport, CIFI2D, Portugal<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g (BMS) is a series of <strong>in</strong>ternational<br />

symposia organized every four years. The organizers are an International<br />

Steer<strong>in</strong>g Group, under the auspices of the World Commission<br />

of Science <strong>and</strong> Sport (WCSS), together with a competent Conference<br />

host. The WCSS is a work<strong>in</strong>g group under the umbrella of the International<br />

Council of Sports Science <strong>and</strong> Physical Education (ICSSPE),<br />

<strong>and</strong> its purpose is to promote the application of science to sport. The<br />

BMS series started <strong>in</strong> 1970, <strong>in</strong> Brussels, by the h<strong>and</strong>s of Leon Lewillie<br />

<strong>and</strong> J.P. Clarys, with the first proceed<strong>in</strong>gs book published one year later.<br />

This paper aims to present an overview of, <strong>and</strong> synthesize the ma<strong>in</strong> axes<br />

of the contributions of the ten books published from 1971 to 2006, <strong>and</strong><br />

to speculate about the future tendencies of the research <strong>and</strong> knowledge<br />

evolution <strong>in</strong> this specific doma<strong>in</strong>.<br />

Key words: biomechanics, medic<strong>in</strong>e, swimm<strong>in</strong>g, research, review<br />

IntroductIon<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g (BMS) is, <strong>in</strong> our days, a<br />

br<strong>and</strong> name that means “aquatic swimm<strong>in</strong>g science”, despite that, <strong>in</strong><br />

stricto senso, it refers to two very specific fields of <strong>in</strong>terest, practice, <strong>and</strong><br />

research (<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong>). The power <strong>and</strong> strength of the<br />

BMS br<strong>and</strong> name is mostly related to the popularity <strong>and</strong> scientific relevance<br />

of the “International Symposium of <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g” series (firstly entitled “<strong>Biomechanics</strong> <strong>in</strong> Swimm<strong>in</strong>g”),<br />

whose 40th anniversary we celebrate <strong>in</strong> Oslo. Thanks to Leon Lewillie<br />

<strong>and</strong> J. P. Clarys, s<strong>in</strong>ce 1970, <strong>and</strong> each four years, BMS is the meet<strong>in</strong>g<br />

po<strong>in</strong>t of those that, worldwide, are struggl<strong>in</strong>g daily for the progress of<br />

knowledge <strong>in</strong> swimm<strong>in</strong>g science, <strong>and</strong> so progressively enlarg<strong>in</strong>g frontiers<br />

to new fields <strong>and</strong> topics. Dur<strong>in</strong>g this 40 year period, eleven scientific<br />

books related to swimm<strong>in</strong>g were published (the 11 th be<strong>in</strong>g the present<br />

volume), all of them - <strong>and</strong> hopefully also this one - be<strong>in</strong>g determ<strong>in</strong>ant<br />

for the spread<strong>in</strong>g <strong>and</strong> consolidation of swimm<strong>in</strong>g knowledge, <strong>and</strong> for<br />

the progress of aquatic swimm<strong>in</strong>g sports <strong>and</strong> activities. Despite this, it<br />

is not necessarily <strong>in</strong>dexed scientific literature, though it is peer reviewed<br />

literature, very attractive for authors, <strong>and</strong> much appreciated by the community.<br />

In the BMS book series, several authors were asked to, or decided<br />

to produce literature overviews to def<strong>in</strong>e the state of the art <strong>in</strong> general<br />

swimm<strong>in</strong>g science, or strictly <strong>in</strong> the <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> fields.<br />

We have the honor of be<strong>in</strong>g <strong>in</strong>vited to follow the steps of scientists like<br />

Leon Lewillie (BMS IV, 1983) himself, James Hay (BMS V, 1988), Jan-<br />

Pieter Clarys (BMS VII, 1996), <strong>and</strong> Mitsumasa Miyashita (BMS VIII,<br />

1999), which provided literature overviews on similar topics. Try<strong>in</strong>g not<br />

to be redundant with their contributions, despite the time lag between<br />

those <strong>and</strong> the present text, it was decided to follow a slightly different<br />

approach, <strong>in</strong> this case specifically centered on the ten BMS books available<br />

until now.<br />

The aim of this paper was to analyze the ten BMS books available <strong>in</strong><br />

order to characterize the past <strong>and</strong> the actual state of the art of <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g research <strong>and</strong> knowledge, try<strong>in</strong>g to<br />

obta<strong>in</strong> foundations to speculate about the future trends of development.<br />

Methods<br />

To address the purpose of this contribution, we analyzed the first ten<br />

books of the series <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g (Lewillie<br />

<strong>and</strong> Clarys, 1971; Clarys <strong>and</strong> Lewillie, 1975; Teraud <strong>and</strong> Bed<strong>in</strong>gfield,<br />

12<br />

1979; Holl<strong>and</strong>er, Huj<strong>in</strong>g <strong>and</strong> de Groot, 1983; Ungerechts, Wilke <strong>and</strong><br />

Reischle, 1988; MacLaren, Reilly <strong>and</strong> Lees, 1992; Troup, Holl<strong>and</strong>er,<br />

Strasse, Trappe, Cappaert, Trappe, 1996; Kesk<strong>in</strong>en, Komi <strong>and</strong> Holl<strong>and</strong>er,<br />

1999; Chatard, 2003; Vilas-Boas, Alves <strong>and</strong> Marques, 2006) -<br />

despite their titles not always be<strong>in</strong>g exactly the same - characteriz<strong>in</strong>g<br />

their contents <strong>and</strong> authorship, <strong>and</strong> relat<strong>in</strong>g the output with the general<br />

body of knowledge <strong>in</strong> swimm<strong>in</strong>g science.<br />

This approach was conducted <strong>in</strong> four steps: (i) number of papers<br />

published; (ii) affiliation of the first author (consider<strong>in</strong>g todays’ political<br />

geography); (iii) number of papers per category of analysis, <strong>and</strong> (iv) scientific<br />

content. The categories of analysis were def<strong>in</strong>ed based on Clarys<br />

(1996, Foreword to BMS VII). However, some were merged <strong>and</strong> others<br />

subdivided. The categories were as follows:<br />

(i) <strong>Biomechanics</strong>, <strong>in</strong>clud<strong>in</strong>g hydrodynamics, k<strong>in</strong>ematics, k<strong>in</strong>etics,<br />

stroke parameters analysis, <strong>and</strong> coord<strong>in</strong>ation;<br />

(ii) Physiology, <strong>in</strong>clud<strong>in</strong>g biochemistry, nutrition, ergogenic aids<br />

<strong>and</strong> supplements, <strong>and</strong> thermoregulation;<br />

(iii) Biophysics, <strong>in</strong>clud<strong>in</strong>g efficiency <strong>and</strong> energy cost studies, as well<br />

as those that explicitly tried to relate biomechanical <strong>and</strong> physiological<br />

approaches;<br />

(iv) Psychology;<br />

(v) <strong>Medic<strong>in</strong>e</strong>, <strong>in</strong>clud<strong>in</strong>g <strong>in</strong>juries <strong>and</strong> therapeutics;<br />

(vi) Electromyography;<br />

(vii) (K<strong>in</strong>)anthropometry;<br />

(viii) Instrumentation;<br />

(ix) Evaluation;<br />

(x) Pedagogy <strong>and</strong> educational water activities;<br />

(xi) Tra<strong>in</strong><strong>in</strong>g;<br />

(xii) Miscellaneous, <strong>and</strong><br />

(xiii) Reviews.<br />

The analysis was performed consider<strong>in</strong>g the researcher’s personal classification<br />

of each paper, consider<strong>in</strong>g, by order: (i) title; (ii) key-words;<br />

(iii) editorial classification, <strong>and</strong> (iv) content of the article. Some of the<br />

papers were the object of double or triple classification s<strong>in</strong>ce they clearly<br />

affiliate to two or three categories. Consequently, the summation of the<br />

entries per category doesn’t match with the total number of papers. The<br />

percentage analysis, however, was referred to the total number of papers<br />

analyzed (622), <strong>and</strong> not to the total number of entries (781), <strong>in</strong> order to<br />

more realistically express the importance of each topic. Thus, 159 entries<br />

were second or third entries of one paper, which means that 25.6 % of<br />

the papers required second or third entries.<br />

To allow further analysis of the f<strong>in</strong>d<strong>in</strong>gs, <strong>and</strong> try<strong>in</strong>g to characterize<br />

more globally the swimm<strong>in</strong>g science peer reviewed <strong>and</strong> <strong>in</strong>dexed research<br />

tendencies, a PubMed TM search was conducted on the 15 th January 2010.<br />

The same percent distribution analysis <strong>and</strong> the same categories (with the<br />

exception of “Reviews”) were considered for the search; dates were not<br />

restricted, <strong>and</strong> “Human” was imposed as a limit. “Miscellaneous” was<br />

assumed to be extractable from the subtraction of the sum of the output<br />

for the other selected categories to the total output of the search (9835<br />

references).<br />

results<br />

The distribution of the 622 analyzed papers for the 10 books published<br />

between 1971 <strong>and</strong> 2006 is presented <strong>in</strong> Fig. 1.


180<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

40<br />

20<br />

0<br />

1971<br />

1975<br />

1979<br />

1983<br />

1988<br />

Figure 1. Distribution of the 622 papers analyzed by the 10 BMS books<br />

studied (values are number of papers per book).<br />

A tendency can be perceived for a progressive <strong>in</strong>crease <strong>in</strong> the number of<br />

papers published per book, particularly relevant <strong>in</strong> the last three editions,<br />

with a maximum value of 143 <strong>in</strong> 2006.<br />

Fig. 2 presents the number of different countries that contributed<br />

to the publication of each volume, consider<strong>in</strong>g only the affiliation of the<br />

first author. The covers of the different books allow the reader to keep <strong>in</strong><br />

m<strong>in</strong>d the variation rate of the number of published papers per volume.<br />

It can be observed that a greater number of countries contributed to<br />

the three last volumes, but this is <strong>in</strong> absolute values, not consider<strong>in</strong>g the<br />

<strong>in</strong>creased number of papers. A relatively stabilised number of participat<strong>in</strong>g<br />

countries, at least <strong>in</strong> the three last events (about 20 to 25), can be<br />

perceived.<br />

30<br />

28<br />

26<br />

24<br />

22<br />

20<br />

18<br />

16<br />

14<br />

12<br />

10<br />

8<br />

6<br />

4<br />

2<br />

0<br />

1971<br />

1975<br />

1979<br />

1983<br />

1988<br />

Figure 2. Number of different countries that contributed to the publication<br />

of each volume, consider<strong>in</strong>g only the affiliation of the first author<br />

(values are number of countries per volume). The covers of the BMS<br />

volumes were reta<strong>in</strong>ed from Fig. 1 to allow weight<strong>in</strong>g the k<strong>in</strong>etics of the<br />

number of countries by the relative amount of published papers.<br />

In Fig. 3, the number of papers published per country is presented. A<br />

total of 41 countries were considered (Curaçao at the Netherl<strong>and</strong>s Antilles,<br />

was considered a country). It is possible to verify that Japan, <strong>and</strong><br />

the United States of America (USA), are the highest contributors to the<br />

total amount of published material. A second cluster seems to be composed<br />

of Belgium, France, <strong>and</strong> Germany, <strong>and</strong> a third one by Portugal,<br />

Spa<strong>in</strong>, <strong>and</strong> the United K<strong>in</strong>gdom (UK). These eight countries (20% of<br />

the total 40 represented countries) are the greatest contributors, total<strong>in</strong>g<br />

70% of the first author’s affiliation. The rema<strong>in</strong><strong>in</strong>g 30% are spread<br />

among a total of 32 countries (80%).<br />

1992<br />

1992<br />

1996<br />

1996<br />

1999<br />

1999<br />

2003<br />

2003<br />

2006<br />

2006<br />

100<br />

90<br />

80<br />

70<br />

60<br />

50<br />

40<br />

30<br />

20<br />

10<br />

0<br />

chaPter1.<strong>in</strong>vitedLectures<br />

Algeria<br />

Argent<strong>in</strong>a<br />

Australia<br />

Austria<br />

Belgium<br />

Brazil<br />

Bulgaria<br />

Canada<br />

Ch<strong>in</strong>a<br />

Congo<br />

Curaçao NED<br />

Czech Republic<br />

Denmark<br />

Estonia<br />

F<strong>in</strong>l<strong>and</strong><br />

France<br />

Germany<br />

Greece<br />

Hungary<br />

Irel<strong>and</strong><br />

Israel<br />

Italy<br />

Japan<br />

Lithuania<br />

Netherl<strong>and</strong>s<br />

New Zeal<strong>and</strong><br />

Norway<br />

Pol<strong>and</strong><br />

Portugal<br />

Romania<br />

Russia<br />

Senegal<br />

Serbia & Montenegro<br />

Slovakia<br />

Slovenia<br />

South Africa<br />

Spa<strong>in</strong><br />

Sweden<br />

Switzerl<strong>and</strong><br />

UK<br />

USA<br />

Figure 3. Number of contributions per country for the ten books studied,<br />

consider<strong>in</strong>g the affiliation of the first author (numbers are papers<br />

per country out of 622).<br />

Figs. 4 <strong>and</strong> 5 present the distribution of the 622 papers analyzed by the<br />

13 different categories of the scientific doma<strong>in</strong>’s classification, consider<strong>in</strong>g<br />

the totality of the 10 books, <strong>and</strong> consider<strong>in</strong>g the particular distribution<br />

per book (Figure 5).<br />

From Figs. 4 <strong>and</strong> 5 a tendency can be observed <strong>in</strong> the follow<strong>in</strong>g hierarchy<br />

of the research doma<strong>in</strong>s on the global BMS scene: (i) <strong>Biomechanics</strong>;<br />

(ii) Physiology, <strong>and</strong> (iii) Evaluation. It is also possible to perceive a<br />

tendency for the preservation of this hierarchy along the BMS series<br />

(book to book analysis). One of the noticeable exceptions is the reverse<br />

importance of <strong>Biomechanics</strong> <strong>and</strong> Physiology <strong>in</strong> BMS VI. A deeper<br />

analysis <strong>in</strong> this particular tendency shows a much stronger relevance of<br />

<strong>Biomechanics</strong> <strong>in</strong> BMS I to III. BMS IV is characterized by an <strong>in</strong>creased<br />

importance of Physiology <strong>and</strong> Biophysics, which reaches a balanced status<br />

<strong>in</strong> BMS V, <strong>and</strong> overtakes <strong>Biomechanics</strong> <strong>in</strong> BMS VI. From BMS VII<br />

to X, <strong>Biomechanics</strong> rega<strong>in</strong>s the leadership to Physiology <strong>and</strong> Biophysics.<br />

Evaluation <strong>and</strong> Tra<strong>in</strong><strong>in</strong>g seem to ga<strong>in</strong> relevance only <strong>in</strong> the second part<br />

of the series.<br />

300<br />

250<br />

200<br />

150<br />

100<br />

50<br />

0<br />

<strong>Biomechanics</strong><br />

Physiology<br />

Biophysics<br />

EMG<br />

Anthropometry<br />

Psychology<br />

Figure 4. Absolute distribution of the 622 papers analyzed by the 13<br />

different categories of classification of the scientific doma<strong>in</strong>s (values are<br />

number of papers per category).<br />

<strong>Medic<strong>in</strong>e</strong><br />

Instruments<br />

Evaluation<br />

Education<br />

Tra<strong>in</strong><strong>in</strong>g<br />

Miscellaneous<br />

Reviews<br />

13


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

14<br />

60<br />

50<br />

40<br />

30<br />

20<br />

10<br />

0<br />

<strong>Biomechanics</strong><br />

Physiology<br />

Biophysics<br />

EMG<br />

Anthropometry<br />

Psychology<br />

<strong>Medic<strong>in</strong>e</strong><br />

Instruments<br />

Evaluation<br />

Education<br />

Tra<strong>in</strong><strong>in</strong>g<br />

Miscellaneous<br />

Reviews<br />

I (1971)<br />

IV (1983)<br />

I (1971)<br />

II (1975)<br />

III (1979)<br />

IV (1983)<br />

V (1988)<br />

VI (1992)<br />

X (2006)<br />

VII (1996)<br />

VII (1996)<br />

VIII (1999)<br />

IX (2003)<br />

X (2006)<br />

Figure 5. Distribution of the 622 papers analyzed by the 13 different<br />

categories of classification of the scientific doma<strong>in</strong>s <strong>in</strong> each of the ten<br />

books studied (values are number of papers per category <strong>and</strong> per book).<br />

The PubMed TM search output, <strong>in</strong> absolute terms, is presented <strong>in</strong> Fig. 6.<br />

The same categories were used, with the exception of “Reviews”. From<br />

PubMed TM , a slightly different hierarchy of research doma<strong>in</strong>s was extracted,<br />

if compared with the BMS profile. Particularly, a tendency was<br />

noted for a higher importance of Physiology <strong>and</strong> <strong>Medic<strong>in</strong>e</strong>, <strong>and</strong> reduced<br />

expression of <strong>Biomechanics</strong>, <strong>in</strong>clusively compared with Tra<strong>in</strong><strong>in</strong>g, for<br />

<strong>in</strong>stance.<br />

5000<br />

4500<br />

4000<br />

3500<br />

3000<br />

2500<br />

2000<br />

1500<br />

1000<br />

500<br />

0<br />

<strong>Biomechanics</strong><br />

Physiology<br />

Biophysics<br />

EMG<br />

Anthropometry<br />

Psychology<br />

Figure 6. PubMed TM search conducted on the 15 th January 2010 us<strong>in</strong>g<br />

the categories selected, <strong>and</strong> limited to “Humans” (values are absolute<br />

number of references).<br />

dIscussIon<br />

The analysis of the number of papers published by volume of the BMS<br />

series shows a trend to a progressive <strong>and</strong> steady growth. However, this is<br />

most noticeable after BMS VIII, when the editors decided not to select<br />

commercial editorial companies to publish the books. So, most probably,<br />

the restrictions imposed by commercial editors regard<strong>in</strong>g the f<strong>in</strong>ancial<br />

weight of the book are the ma<strong>in</strong> reason for the above referred effect.<br />

However, the option for non-commercial editions may also have some<br />

detrimental effects, namely: (i) constra<strong>in</strong><strong>in</strong>g the social perfusion of the<br />

edition, <strong>and</strong> (ii) reduc<strong>in</strong>g the overall quality of the published material<br />

due to a reduced need for selection of publishable papers.<br />

The analysis of the country of affiliation of the first author provided<br />

also very <strong>in</strong>terest<strong>in</strong>g results. Over forty represented countries <strong>in</strong> the<br />

BMS series is an extremely impressive number, <strong>and</strong> the overall tendency<br />

for growth naturally reveals a healthy trend for the worldwide spread<strong>in</strong>g<br />

of the aquatic swimm<strong>in</strong>g science community. However, there is also a<br />

<strong>Medic<strong>in</strong>e</strong><br />

Instruments<br />

Evaluation<br />

Education<br />

Tra<strong>in</strong><strong>in</strong>g<br />

Miscellaneous<br />

perceived tendency for stabilization dur<strong>in</strong>g the last three volumes. In<br />

the mean time, analysis may also reflect the attraction of the conference<br />

(program, host <strong>in</strong>stitution <strong>and</strong> geographical location), <strong>and</strong> not necessarily<br />

the distribution of swimm<strong>in</strong>g scientists over the planet. In this<br />

regard, a detailed analysis reveals also some <strong>in</strong>terest<strong>in</strong>g f<strong>in</strong>d<strong>in</strong>gs. For<br />

<strong>in</strong>stance, despite Japan always be<strong>in</strong>g represented, its representation was<br />

elevated <strong>in</strong> BMS VIII <strong>and</strong> rema<strong>in</strong>s so until today. The participation of<br />

the USA can be analyzed <strong>in</strong> the opposite direction. American scientists<br />

assumed a serious predom<strong>in</strong>ance dur<strong>in</strong>g BMS I to III, <strong>and</strong> VI <strong>and</strong> VII,<br />

but seem to retract afterwards. Another perceived effect, particularly <strong>in</strong><br />

the last editions, was a “house effect”, mean<strong>in</strong>g an <strong>in</strong>crease of the participation<br />

of scientists from the organiz<strong>in</strong>g country, or from countries<br />

<strong>in</strong> the neighborhood. This was clearly perceptible <strong>in</strong> BMS I to V, VII,<br />

IX <strong>and</strong> X, <strong>and</strong> partially <strong>in</strong> BMS VIII, with an <strong>in</strong>creased participation<br />

of Russian scientists. F<strong>in</strong>ally, the affiliation analysis revealed that eight<br />

countries (20%), divided <strong>in</strong>to three groups, are responsible for 70% of<br />

the published material, which evidences an excessive centralization that<br />

must be reduced <strong>in</strong> the future through <strong>in</strong>ternational partnerships with<br />

less represented countries.<br />

Analyz<strong>in</strong>g the distribution of the published papers by the research<br />

doma<strong>in</strong> categories selected for this study, a tendency can be<br />

found, as stated before, for a prevalence of <strong>Biomechanics</strong> over Physiology<br />

(<strong>in</strong>clud<strong>in</strong>g Biochemistry, Nutrition, <strong>and</strong> Thermoregulation) <strong>and</strong> the<br />

other doma<strong>in</strong>s. This is not <strong>in</strong> accordance with previous results reported<br />

by Clarys (1996, Foreword to BMS VII) about swimm<strong>in</strong>g research, nor<br />

with the results extracted now from PubMed TM (Figure 7).<br />

%<br />

50<br />

45<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

<strong>Biomechanics</strong><br />

Physiology<br />

Not <strong>in</strong>cluded <strong>in</strong> Clarys (1996) search<br />

Biophysics<br />

EMG<br />

Anthropometry<br />

Clarys (1996, Foreword to BMS VII)<br />

Total BMS<br />

Total PubMed<br />

Psychology<br />

Figure 7. Comparison of the BMS series results (Total BMS) regard<strong>in</strong>g<br />

the percent distribution of published papers by the swimm<strong>in</strong>g science<br />

studied categories, with the PubMed TM results, <strong>and</strong> the ones previously<br />

published by Clarys (1996, Foreword to BMS VII).<br />

It is perceivable from Fig. 7 that the BMS series seems to over represent<br />

the relative importance of <strong>Biomechanics</strong> <strong>in</strong> the scene of global<br />

swimm<strong>in</strong>g science production. The orig<strong>in</strong> of the series (“<strong>Biomechanics</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g”) might be considered the first determ<strong>in</strong>ant factor of this<br />

situation, afterward preserved <strong>in</strong> time (with the exception of BMS VI),<br />

but other reasons should be exam<strong>in</strong>ed, such as the relevance of swimm<strong>in</strong>g<br />

technique <strong>and</strong> biomechanics <strong>in</strong> the context of the determ<strong>in</strong>ant<br />

factors of swimm<strong>in</strong>g competitive performance. The nature <strong>and</strong> ma<strong>in</strong><br />

focus of the data base searched might also have contributed to this perceived<br />

effect. In the case of the PubMed TM search, the predom<strong>in</strong>ant role<br />

of the medical areas might determ<strong>in</strong>e a higher presence of papers from<br />

the Physiology <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> doma<strong>in</strong>s. This hypothesis is consistent<br />

with the f<strong>in</strong>d<strong>in</strong>g of an <strong>in</strong>creased importance of these scientific fields<br />

(Physiology, <strong>Medic<strong>in</strong>e</strong>, Biophysics) <strong>in</strong> the BMS IV, which <strong>in</strong>cludes the<br />

proceed<strong>in</strong>g of both the 4 th International Symposium of <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, <strong>and</strong> the 5 th FINA International Congress<br />

<strong>Medic<strong>in</strong>e</strong><br />

Instruments<br />

Evaluation<br />

Education<br />

Not <strong>in</strong>cluded <strong>in</strong> Clarys (1996) search<br />

Tra<strong>in</strong><strong>in</strong>g<br />

Miscellaneous


on Swimm<strong>in</strong>g <strong>Medic<strong>in</strong>e</strong>, <strong>and</strong> marked the first impulse for the <strong>in</strong>crease<br />

of these areas <strong>in</strong> the BMS series. From the compared evidence, however,<br />

it should be supposed that the BMS series still supports the relevance of<br />

<strong>Biomechanics</strong> compared to other swimm<strong>in</strong>g science doma<strong>in</strong>s, an importance<br />

which, consider<strong>in</strong>g the global scientific scene, should be re<strong>in</strong>forced<br />

<strong>in</strong> the future.<br />

A DEEPER ANALYSIS OF BMS SERIES CONTENTS<br />

Despite previous data suggest<strong>in</strong>g that the BMS series is not cop<strong>in</strong>g<br />

with the general progression of scientific research regard<strong>in</strong>g the balance<br />

between different scientific doma<strong>in</strong>s, its deeper content analysis seems<br />

to clearly demonstrate that BMS books played, <strong>and</strong> cont<strong>in</strong>ue to play,<br />

a decisive role <strong>in</strong> the promotion <strong>and</strong> spread<strong>in</strong>g of swimm<strong>in</strong>g scientific<br />

knowledge, always keep<strong>in</strong>g pace with peer reviewed <strong>in</strong>dexed literature,<br />

but particularly assum<strong>in</strong>g a very relevant catalytic role <strong>in</strong> encourag<strong>in</strong>g<br />

future steps forward <strong>in</strong> the progress of swimm<strong>in</strong>g science. It is obvious<br />

that the BMS series does not conta<strong>in</strong> all the relevant swimm<strong>in</strong>g research,<br />

not even <strong>in</strong> the biomechanics doma<strong>in</strong>, but it can be hypothesized<br />

that the knowledge <strong>in</strong>cluded satisfactorily covers all, or almost all, of the<br />

relevant progresses that swimm<strong>in</strong>g science has achieved over the years.<br />

We will now survey the ten BMS books (I to X, disregard<strong>in</strong>g their orig<strong>in</strong>al<br />

titles), highlight<strong>in</strong>g those contributions that, <strong>in</strong> our view, strongly<br />

contributed to the above named effects. We will focus our attention<br />

ma<strong>in</strong>ly on both experimental <strong>and</strong> theoretical orig<strong>in</strong>al contributions.<br />

BMS I (1971)<br />

In this volume, Counsilman <strong>in</strong>troduced the revolutionary concept of<br />

quasi-static lift (L) theory on human swimm<strong>in</strong>g propulsion (P), <strong>and</strong><br />

Kent <strong>and</strong> Atha analysed different transient body position effects on<br />

breaststroke drag (D) us<strong>in</strong>g passive drag tow<strong>in</strong>g methodology, but<br />

suggest<strong>in</strong>g the need of future active drag (Da) assessments. P <strong>and</strong> D<br />

periodical changes dur<strong>in</strong>g a swimm<strong>in</strong>g cycle are expected consider<strong>in</strong>g<br />

coord<strong>in</strong>ative analysis (Nemessuri <strong>and</strong> Vaday; Vaday <strong>and</strong> Namessuri), as<br />

well as, consequently, the existence of an acceleration profile, represented<br />

by <strong>in</strong>tra-cycle velocity variations - IVV (Miyashita). The Astr<strong>and</strong> <strong>and</strong><br />

Englesson “Aquatic Swim-mill” - the first swimm<strong>in</strong>g flume -, was probably<br />

the “must” <strong>in</strong> <strong>in</strong>strumentation progress presented <strong>in</strong> BMS I. The<br />

first results on VO 2 measurements at different velocities us<strong>in</strong>g this ergometer<br />

were produced by Holmér. Goldfuss <strong>and</strong> Nelson related swimm<strong>in</strong>g<br />

actions to the measured tethered force exerted by the swimmer,<br />

<strong>in</strong> what seem to be the first comb<strong>in</strong>ation of both image <strong>and</strong> force data.<br />

Electromyography - EMG - (Barthels <strong>and</strong> Adrian) was also used as it<br />

was assumed to be the “unique” solution to monitor muscular activity<br />

dur<strong>in</strong>g swimm<strong>in</strong>g despite serious normalization difficulties (Lewillie).<br />

In parallel to the presented experimental approaches, Seireg <strong>and</strong> Baz<br />

presented the first complete mathematical analysis of the human biomechanics<br />

of swimm<strong>in</strong>g <strong>in</strong> the sagittal plane (x <strong>and</strong> y equations of l<strong>in</strong>ear<br />

motion <strong>and</strong> z jo<strong>in</strong>t torques).<br />

BMS II (1975)<br />

This volume fulfilled some of the higher expectations that emerged from<br />

the previous book. Serious improvements occur <strong>in</strong> the development of<br />

new <strong>in</strong>strumentation, namely for image acquisition, particularly to allow<br />

dual-media observation of the swimmer (under <strong>and</strong> overwater views)<br />

(McIntyre <strong>and</strong> Hay). Van Manen <strong>and</strong> Rijken resume the experiments<br />

conducted <strong>in</strong> The Netherl<strong>and</strong>s Ship Model Bas<strong>in</strong>, underl<strong>in</strong><strong>in</strong>g the “tow<strong>in</strong>g<br />

carriage” that allowed new <strong>in</strong>cursions <strong>in</strong> the measurement of P <strong>and</strong><br />

D. In this regard, a very contemporary question was discussed <strong>in</strong> those<br />

days: the effect of swimsuits on D, show<strong>in</strong>g that wear<strong>in</strong>g a suit, compared<br />

to a naked situation, reduces D <strong>in</strong> females by about 9%. Us<strong>in</strong>g the<br />

“tow<strong>in</strong>g carriage”, Rennie et al. calculated Da comb<strong>in</strong><strong>in</strong>g load (positive<br />

<strong>and</strong> negative extra loads), the energy cost of swimm<strong>in</strong>g <strong>and</strong> efficiency<br />

(e), follow<strong>in</strong>g one of the most well-known swimm<strong>in</strong>g biophysical relationships:<br />

VO 2 net/d = Da/e, where VO 2 net is the aerobic exercise<br />

Oxygen consumption subtracted of the basal VO 2 <strong>and</strong> d is swimm<strong>in</strong>g<br />

chaPter1.<strong>in</strong>vitedLectures<br />

distance. The authors concluded that men have a higher Da <strong>and</strong> energy<br />

cost (VO 2 net/d) than their female counterparts <strong>and</strong> a similar e,<br />

<strong>and</strong> that VO 2 net/d rises with hydrostatic torque. Holmér used the same<br />

approach, <strong>and</strong> concluded that Da values are 1.5 to 2 times higher than<br />

passive D.<br />

The importance of IVV analysis was once more stressed. Bober<br />

<strong>and</strong> Czabanski used the IVV comb<strong>in</strong>ed with film images to <strong>in</strong>vestigate<br />

breaststroke coord<strong>in</strong>ation changes with mean velocity <strong>and</strong> Barthels <strong>and</strong><br />

Adrian related h<strong>and</strong> k<strong>in</strong>ematics with hip acceleration us<strong>in</strong>g film analysis.<br />

Sixteen millimeter film was also used, synchronized with EMG telemetric<br />

signals, to evaluate h<strong>and</strong>icapped swimmers perform<strong>in</strong>g breaststroke,<br />

front crawl <strong>and</strong> backstroke (Maes et al.).<br />

As <strong>in</strong> BMS I, also <strong>in</strong> BMS II some essays on mathematical model<strong>in</strong>g<br />

were published (Francis <strong>and</strong> Dean; Jensen <strong>and</strong> Blanksby).<br />

BMS III (1979)<br />

The third volume was biomechanically marked by two contributions<br />

extensively referred to <strong>in</strong> swimm<strong>in</strong>g literature, one related to D, <strong>and</strong><br />

the other to P. Clarys extensively reviewed the state of the art <strong>in</strong> D<br />

hydrodynamics <strong>and</strong> its relationship to morphology, <strong>and</strong> used the already<br />

described “Tow<strong>in</strong>g Carriage” to assess Da. On the other h<strong>and</strong>, Schleihauf<br />

developed <strong>and</strong> experimentally supported the L <strong>and</strong> propulsive drag<br />

(Dp) theory of swimm<strong>in</strong>g propulsion. Once aga<strong>in</strong> the global dynamical<br />

effect of P <strong>and</strong> D changes dur<strong>in</strong>g the stroke cycle motivated researchers<br />

to analyse IVV: Holmér used l<strong>in</strong>ear accelerometry <strong>and</strong> <strong>in</strong>tegration<br />

to assess swimm<strong>in</strong>g velocity, <strong>and</strong> Vervaecke <strong>and</strong> Persyn analysed coord<strong>in</strong>ation<br />

of the breaststroke kick related to anthropometric, flexibility<br />

<strong>and</strong> force data. Piette <strong>and</strong> Clarys used an EMG telemetric system to<br />

compare competitive <strong>and</strong> non-competitive front crawl swimmers us<strong>in</strong>g<br />

different normalization procedures <strong>and</strong> Okamoto <strong>and</strong> Wolf reported,<br />

for the first time <strong>in</strong> the BMS series, the use of f<strong>in</strong>e-wire electrodes <strong>in</strong><br />

the aquatic environment.<br />

In BMS III only one mathematical model<strong>in</strong>g approach to swimm<strong>in</strong>g<br />

biomechanics was <strong>in</strong>cluded ( Jensen <strong>and</strong> McIlwa<strong>in</strong>), aim<strong>in</strong>g to<br />

estimate segmental forces <strong>and</strong> jo<strong>in</strong>t torques <strong>in</strong> the dolph<strong>in</strong> kick. Swimm<strong>in</strong>g<br />

starts, however, were extensively studied (Disch et al.; Stevenson<br />

<strong>and</strong> Morehouse; Zatsiorsky et al.), <strong>and</strong> the first paper on swimm<strong>in</strong>g<br />

turns of the series appears (Nicol <strong>and</strong> Krüger), study<strong>in</strong>g the forces exerted<br />

on the wall us<strong>in</strong>g force plates.<br />

BMS III also <strong>in</strong>cluded several relevant contributions on “Tra<strong>in</strong><strong>in</strong>g<br />

Methods”, start<strong>in</strong>g the tendency for a progressive enlargement of the<br />

<strong>in</strong>terest doma<strong>in</strong>s of the series.<br />

BMS IV (1983)<br />

This volume was a comb<strong>in</strong>ed proceed<strong>in</strong>gs book of the <strong>Biomechanics</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g <strong>and</strong> the FINA Swimm<strong>in</strong>g <strong>Medic<strong>in</strong>e</strong> congresses, promot<strong>in</strong>g<br />

an <strong>in</strong>crease of the <strong>in</strong>cluded scientific doma<strong>in</strong>s. P <strong>and</strong> D were, once more,<br />

central topics. Schleihauf et al. extended previous contributions to the<br />

study of the propulsive potential of the forearm <strong>and</strong> to arm jo<strong>in</strong>t torques.<br />

Still <strong>in</strong> the P doma<strong>in</strong>, one of the first papers on the propulsive effect<br />

generated by undulatory swimm<strong>in</strong>g movements was <strong>in</strong>cluded, compar<strong>in</strong>g<br />

dolph<strong>in</strong>s <strong>and</strong> butterflyers (Ungerechts), underly<strong>in</strong>g the importance<br />

of the quantification of the added mass effect to underst<strong>and</strong> P <strong>and</strong> D.<br />

In another paper Ungerechts showed that the Re number does not represent<br />

satisfactorily the flow regimen around bodies that change form<br />

periodically, provid<strong>in</strong>g a historical contribution to the hydrodynamics of<br />

swimm<strong>in</strong>g. Da was once aga<strong>in</strong> revisited (Kemper et al.). It was shown<br />

that for much higher velocities (1.73 vs. 1.15 m/s), skilled swimmers are<br />

submitted to a much lower Da value (32.2 vs. 57.0 N), though passive<br />

drag values are similar at 0.75 m/s (22.5 vs. 21.2 N), relatively to their<br />

non elite counterparts. Ohmichi et al. (1983) measured the waves caused<br />

by swimmers us<strong>in</strong>g a “Wave High Meter”, <strong>and</strong> compar<strong>in</strong>g different velocities<br />

<strong>and</strong> strokes.<br />

Nigg proposed a model to estimate the added work associated with<br />

IVV <strong>in</strong> swimm<strong>in</strong>g (3% extra work performed for velocity variations of<br />

15


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

about 10%), underl<strong>in</strong><strong>in</strong>g the importance of simultaneously consider<strong>in</strong>g<br />

both energy cost <strong>and</strong> its biomechanical determ<strong>in</strong>ant factors. Holmér<br />

elaborated on the swimm<strong>in</strong>g economy of the four competitive strokes,<br />

relat<strong>in</strong>g it to P, D, IVV <strong>and</strong> buoyancy.<br />

Tra<strong>in</strong><strong>in</strong>g contributions were scarce (Miyashita <strong>and</strong> Kanehisa), or<br />

partially hidden by their common physiological (Cazorla et al.; Nomura;<br />

Treffene), biomechanical (Schleihauf ) or EMG (Olbrecht <strong>and</strong> Clarys)<br />

content. However, physiology <strong>and</strong> thermoregulation presented relevant<br />

<strong>and</strong> <strong>in</strong>novative contributions (Chatard et al.; Craig; Nielsen; Novák et<br />

al.; Zeman et al.). Decisive, also for its rarity as a longitud<strong>in</strong>al design,<br />

<strong>and</strong> for the preservation of the Swedish tradition <strong>in</strong> this regard, was<br />

the five year follow-up physiological study of Gullstr<strong>and</strong> <strong>and</strong> Holmér.<br />

Lavoie et al. presented the backward extrapolation method for the assessment<br />

of VO 2 <strong>in</strong> swimm<strong>in</strong>g reduc<strong>in</strong>g the mechanical constra<strong>in</strong>s imposed<br />

by masks <strong>and</strong> tubes.<br />

BMS V (1988)<br />

One of the ma<strong>in</strong> topics was, once more, the P production mechanism.<br />

Although De Groot <strong>and</strong> Van Ingen Schenau theoretically demonstrate<br />

why L dom<strong>in</strong>ated propulsion is more efficient than Dp dom<strong>in</strong>ated P<br />

forces, Ungerechts showed that peak acceleration of the breaststroker<br />

dur<strong>in</strong>g the kick happens near the turn<strong>in</strong>g phase of the feet, suggest<strong>in</strong>g<br />

that a quasi-static approach to the hydrodynamics of P <strong>in</strong> swimm<strong>in</strong>g<br />

seems to be <strong>in</strong>sufficient. In parallel, Shleihauf et al. went even deeper <strong>in</strong><br />

the quasi-static propulsive theory, <strong>and</strong> provided evidence of four propulsive<br />

phases <strong>in</strong> backstroke arm action. Concern<strong>in</strong>g D, the “MAD-<br />

System” was referred to <strong>in</strong> the series for the first time. A very creative use<br />

of the device allowed Holl<strong>and</strong>er et al. to show that the leg contribution<br />

to total power output <strong>in</strong> front crawl is only slightly higher than 10%.<br />

Toussa<strong>in</strong>t et al. used the same system to show that propell<strong>in</strong>g efficiency<br />

decreases with swimm<strong>in</strong>g v (r = -0.84) between 1.05 <strong>and</strong> 1.3 m/s. The<br />

EMG validations of the “MAD-System” (Clarys et al.) <strong>and</strong> tethered<br />

swimm<strong>in</strong>g front crawl (Bollens et al.) were also provided. Consequently,<br />

the relationships between stroke frequency, tethered force <strong>and</strong> EMG,<br />

found by Cabri et al., ga<strong>in</strong>ed <strong>in</strong>creased relevance for front crawl performance<br />

analysis.<br />

Us<strong>in</strong>g <strong>in</strong>verse dynamics from the IVV curve, Van Tilborgh et al. calculated<br />

the resultant impulses per phase of the breaststroke technique,<br />

emphasiz<strong>in</strong>g the importance of body undulation <strong>in</strong> this technique. This<br />

was one of the few studies of this volume centered on IVV assessment.<br />

However, this parameter was the basis of a historical paper on swimm<strong>in</strong>g<br />

evaluation <strong>and</strong> advice (Persyn et al.), <strong>in</strong>tegrated with force <strong>and</strong><br />

flexibility measurements, hydrodynamics, hydrostatics <strong>and</strong> other biomechanical<br />

data, as well as with markers of aerobic <strong>and</strong> anaerobic capacities,<br />

anthropometry, <strong>and</strong> performance parameters.<br />

Medical contributions were ma<strong>in</strong>ly restricted to the analysis of<br />

chronic <strong>in</strong>juries related to swimm<strong>in</strong>g sports (Mutoh et al.), while physiological<br />

contributions were vast <strong>and</strong> mostly referred to evaluation (Olbrecht<br />

et al.), tra<strong>in</strong><strong>in</strong>g (Van H<strong>and</strong>el et al.; Yamamoto), <strong>and</strong> performance<br />

(Chatard et al.; Telford et al.), mostly consider<strong>in</strong>g [La-] responses, <strong>and</strong><br />

<strong>in</strong> some cases comb<strong>in</strong>ed with VO 2 <strong>and</strong> strok<strong>in</strong>g parameters (Kesk<strong>in</strong>en<br />

<strong>and</strong> Komi). The tra<strong>in</strong><strong>in</strong>g content was explicitly related to physiology,<br />

ma<strong>in</strong>ly because the latter essentially referred to energy metabolism <strong>and</strong><br />

to swimm<strong>in</strong>g economy, <strong>and</strong> associated factors (Cazorla et al.; Montepetit<br />

et al.; Van H<strong>and</strong>el et al.).<br />

BMS VI (1992)<br />

The theoretical <strong>in</strong>crease of SL with efficiency <strong>and</strong> power output, <strong>and</strong><br />

decrease of drag <strong>and</strong> stroke frequency (Toussa<strong>in</strong>t), allows reta<strong>in</strong><strong>in</strong>g this<br />

parameter as a measure of swimm<strong>in</strong>g proficiency. This is, perhaps, one<br />

of the reasons why several papers were devoted to stroke parameters<br />

<strong>and</strong> competition analysis (Kesk<strong>in</strong>en <strong>and</strong> Komi; McArdle <strong>and</strong> Reilly;<br />

Wakayoshi et al.; Wirtz et al.). Propell<strong>in</strong>g <strong>and</strong> mechanical efficiencies<br />

were also specifically addressed (Cappaert et al. a, b), although a swimm<strong>in</strong>g<br />

economy profile was criticized as a swimm<strong>in</strong>g skill measurement<br />

16<br />

(Chatard et al.). One of the factors already theoretically associated with<br />

efficiency is the IVV, a topic that rega<strong>in</strong>s its traditional importance <strong>in</strong><br />

this volume (Chollet et al.; Hahn <strong>and</strong> Krug; Manley <strong>and</strong> Atha; Mason<br />

et al.; Persyn et al.; Tourny et al.; Ungerechts). Ungerechts, Persyn et<br />

al. <strong>and</strong> Mason et al. used videogrametry, but both Manley <strong>and</strong> Atha,<br />

<strong>and</strong> Hahn <strong>and</strong> Krug used the swim-speed-recorder technology, based<br />

on an impeller attached to the swimmer’s body to monitor swimm<strong>in</strong>g<br />

velocity, <strong>and</strong> Chollet et al. used a more conventional cable speedometer.<br />

Two most relevant conclusions emerged from these studies: (i) most of<br />

the breaststroke studies revealed a two peak IVV profile, <strong>and</strong> (ii) IVV<br />

tends to reduce with mean velocity, <strong>in</strong>clud<strong>in</strong>g the number of velocity<br />

peaks per stroke.<br />

EMG was also a very relevant topic <strong>in</strong> this volume cover<strong>in</strong>g issues<br />

like effects of front crawl speed (Rouard et al.), paddle swimm<strong>in</strong>g (Monteille<br />

<strong>and</strong> Rouard), swimm<strong>in</strong>g f<strong>in</strong>s (Cabri et al.), water polo (Clarys et<br />

al.) <strong>and</strong> Synchronized swimm<strong>in</strong>g (Z<strong>in</strong>zen et al.).<br />

Physiological contributions were many; they were focused on pure<br />

swimm<strong>in</strong>g but also on water polo (Hohmann <strong>and</strong> Frase) <strong>and</strong> life sav<strong>in</strong>g<br />

(Daniel <strong>and</strong> Klauck). Particular emphasis was given to lactate metabolism<br />

<strong>and</strong> test<strong>in</strong>g (Kelly et al.; Kesk<strong>in</strong>en <strong>and</strong> Komi; Olbrecht et al.; Peyreburn<br />

<strong>and</strong> Hardy; Roi <strong>and</strong> Cerizza). However, it should be underl<strong>in</strong>ed<br />

that also much attention was dedicated to the study of the aerobic <strong>and</strong><br />

anaerobic contributions to different tra<strong>in</strong><strong>in</strong>g sets <strong>and</strong> performances, <strong>and</strong><br />

its variation with work / rest ratios (Troup et al.), age <strong>and</strong> performance<br />

level (Takahashi et al.).<br />

Of particular <strong>in</strong>terest was the attempt to match anthropometrical<br />

<strong>and</strong> technical profiles (Colman et al.) relat<strong>in</strong>g physical characteristics<br />

<strong>and</strong> undulation <strong>in</strong> breaststroke, as well as to establish a psychological<br />

profile that predisposes for swimm<strong>in</strong>g performance (Stallman et al.),<br />

consider<strong>in</strong>g self-control <strong>and</strong> motivation, both for tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competition.<br />

BMS VII (1996)<br />

Energy related biomechanical factors were at the centre of this BMS<br />

volume. S<strong>and</strong>ers (a, b) provided evidence support<strong>in</strong>g the idea that body<br />

undulation may contribute to <strong>in</strong>creased propulsion <strong>and</strong>/or reduced drag,<br />

while Vilas-Boas <strong>and</strong> Alves et al. provided evidence of the relationship<br />

between energy cost <strong>and</strong> IVV <strong>in</strong> swimm<strong>in</strong>g, respectively for breaststroke<br />

<strong>and</strong> backstroke. Moreover, Vilas-Boas found that flat breaststroke was<br />

more economical than undulat<strong>in</strong>g variations, contradict<strong>in</strong>g the tendency,<br />

at the time, to emphasize body undulation. Convergently, Cappaert<br />

et al. stated that top breaststrokers are characterized by lower IVV<br />

than their lower performance counterparts, <strong>and</strong> emphasized that higher<br />

level Olympic butterfly swimmers show lower trunk angulation to the<br />

horizontal. Cappaert, however, wasn’t able to f<strong>in</strong>d any correlation of<br />

the segmental <strong>and</strong> full body angular momentum around the CM with<br />

swimm<strong>in</strong>g performance <strong>in</strong> a sample of 8 breaststrokers. Energy was also<br />

the focus of other contributions, namely consider<strong>in</strong>g spr<strong>in</strong>t swimm<strong>in</strong>g<br />

metabolism (R<strong>in</strong>g et al.), aerobic/anaerobic energy partition dur<strong>in</strong>g a<br />

400m freestyle event (Nomura et al.) <strong>and</strong> energy expenditure dur<strong>in</strong>g<br />

heavy tra<strong>in</strong><strong>in</strong>g <strong>and</strong> taper (Trappe et al., Van Heest).<br />

Wakayoshi et al. provided another contribution explicitly relat<strong>in</strong>g<br />

physiologic <strong>and</strong> biomechanical parameters dur<strong>in</strong>g swimm<strong>in</strong>g. They<br />

found an <strong>in</strong>terest<strong>in</strong>g co<strong>in</strong>cidence between the OBLA <strong>in</strong>tensity <strong>and</strong> a<br />

“biomechanical turn<strong>in</strong>g po<strong>in</strong>t”, where SL decreases <strong>and</strong> SR <strong>in</strong>creases are<br />

observed dur<strong>in</strong>g an <strong>in</strong>cremental front crawl test (SL drop).<br />

Swimm<strong>in</strong>g propulsion cont<strong>in</strong>ued to be addressed. Berger et al.<br />

compared propulsive forces measured through the MAD-System <strong>and</strong><br />

a Shleihauf-like quasi-static approach. The MAD-System underestimated<br />

the quasi-static effective propulsive force by about 15%. Rouard<br />

et al. studied the time duration <strong>and</strong> the impulse of the different P force<br />

components <strong>in</strong> each phase of the freestyle arm-stroke cycle, conclud<strong>in</strong>g<br />

the non-existence of significant correlation between these variables <strong>and</strong><br />

performance. The authors also found higher propulsive drag than lift<br />

impulses throughout the stroke.


Critical tethered force (Ikuta et al.) <strong>and</strong> critical swim-bench power<br />

(Swa<strong>in</strong>e), as well as EMG (Monteil et al.) <strong>and</strong> electrical stimulation<br />

(Pichon et al.) were also the object of analysis. Moreover, analysis of<br />

tra<strong>in</strong><strong>in</strong>g contents <strong>and</strong> consequences (Mujika et al. a, b), as well as an<br />

analysis of the effect of sea-level altitude exposure to altitude acclimatized<br />

swimmers (D’Acquisto et al.), were also <strong>in</strong>cluded.<br />

BMS VIII (1999)<br />

Volume eight is characterized by an <strong>in</strong>creased number of papers that<br />

allow diversification of topics <strong>and</strong> approaches, <strong>in</strong>clud<strong>in</strong>g a full section<br />

devoted to pedagogy, where new questions were considered, like the development<br />

of <strong>in</strong>teractive software to teach diagnosis <strong>and</strong> advice of swimmers<br />

(Persyn <strong>and</strong> Colman). New topics also <strong>in</strong>cluded: mechanical accelerometry<br />

to characterize arm-stroke k<strong>in</strong>ematics (Ichikawa et al.; Ohgi<br />

et al.); the effect of breath<strong>in</strong>g actions on swimm<strong>in</strong>g k<strong>in</strong>ematics (Alves et<br />

al.; Barbosa et al.); the effect of body position (prone <strong>and</strong> sup<strong>in</strong>e) on the<br />

underwater undulatory swimm<strong>in</strong>g technique (Arellano et al.); the comparison<br />

of pool <strong>and</strong> flume swimm<strong>in</strong>g (Wilson et al.); the analysis of the<br />

effect of swimm<strong>in</strong>g-lane separation ropes on the wave dissipation effect<br />

(Togashi et al., Fujishima et al.); measurements of nasal pressure (Hara<br />

et al.), <strong>and</strong> mono-f<strong>in</strong> force production analysis (Rejman).<br />

The coord<strong>in</strong>ation of swimm<strong>in</strong>g actions (Chollet et al.; Hohmann<br />

et al.; Soares et al.,) as well as the IVV (Fujishima <strong>and</strong> Miyashita; Kolmogorov<br />

<strong>and</strong> Lyap<strong>in</strong>; Mart<strong>in</strong>s-Silva et al.; Reischle) cont<strong>in</strong>ue to be relevant<br />

issues. In this latter doma<strong>in</strong>, the mathematical model of Fujishima<br />

<strong>and</strong> Miyashita allowed further underst<strong>and</strong><strong>in</strong>g of the <strong>in</strong>ertial effect of<br />

IVV over the power dissipation <strong>and</strong> the mean velocity atta<strong>in</strong>ed by the<br />

swimmer. They didn’t consider, however, the added mass effect of the<br />

water, a topic that Klauck, Kolmogorov <strong>and</strong> Lyap<strong>in</strong>, <strong>and</strong> Colman et al.<br />

addressed. Klauck arrived at a value of 300 to 700 N for towed subjects<br />

<strong>in</strong> an extended prone position (1 to 1.6 m/s), while Kolmogorov <strong>and</strong> Lyap<strong>in</strong><br />

reported values of 85 to 100 N for front crawl swimmers at 2 m/s.<br />

Both outcomes suggest the need for further development <strong>in</strong> this field.<br />

Cappaert <strong>and</strong> Van Heest showed that the maximal values of angular<br />

momentum obta<strong>in</strong>ed dur<strong>in</strong>g a front crawl stroke cycle around the<br />

longitud<strong>in</strong>al axis (body-roll) <strong>and</strong> the saggital axis (body lateral sway)<br />

correlates with energy cost. The effect of body-roll on the <strong>in</strong>sweep h<strong>and</strong><br />

velocity was revisited by Payton et al., this time us<strong>in</strong>g an empirical approach.<br />

Results were <strong>in</strong> opposition to those obta<strong>in</strong>ed with the model<br />

published <strong>in</strong> BMSVII: body-roll didn’t contribute to the h<strong>and</strong> velocity<br />

dur<strong>in</strong>g the <strong>in</strong>sweep.<br />

Hydrodynamics (both propulsion <strong>and</strong> drag) was also a central topic<br />

of BMSVIII. Vortex propulsive effects were analysed (Colman et al.;<br />

Ungerechts et al.), despite not provid<strong>in</strong>g yet a consistent empirical basis<br />

for measur<strong>in</strong>g their contribution. On the contrary, the estimation of<br />

propulsion based on h<strong>and</strong> pressure differences (Takagi <strong>and</strong> Wilson) allowed<br />

results underestimat<strong>in</strong>g, but highly consistent with external loads<br />

supported dur<strong>in</strong>g scull<strong>in</strong>g motions. Drag was analyzed <strong>and</strong> compared<br />

both <strong>in</strong> passive <strong>and</strong> active conditions (Shimonagata et al.; Strojnik et<br />

al.). Active drag was measured us<strong>in</strong>g a similar approach to the classical<br />

“velocity perturbation method”. Once this method is based on the<br />

assumption of constant maximal power output, Strojnik et al. tried to<br />

correct the data for the measured power changes, arriv<strong>in</strong>g at variations<br />

of more than 200% <strong>in</strong> the f<strong>in</strong>al result. They concluded that the method is<br />

<strong>in</strong>appropriate. Lyttle at al. analysed the effect of the glide depth (surface,<br />

0.2, 0.4, <strong>and</strong> 0.6m) on passive drag at velocities rang<strong>in</strong>g from 1.6 to<br />

3.1 m/s. Their f<strong>in</strong>d<strong>in</strong>gs showed that glid<strong>in</strong>g at the surface (the dorsum<br />

of the swimmer break<strong>in</strong>g the water surface) caused significantly higher<br />

drag values at all velocities, <strong>and</strong> that 0.4 m seems to be optimal depth<br />

required to m<strong>in</strong>imize D.<br />

Coach<strong>in</strong>g <strong>and</strong> tra<strong>in</strong><strong>in</strong>g effects were analyzed. Attention was paid<br />

once aga<strong>in</strong> to the effect of different comb<strong>in</strong>ations of work to rest ratios<br />

(Shimoyama <strong>and</strong> Nomura; Wakayoshi et al.). Interval hypoxia (Bulgakova<br />

et al.; Ogita <strong>and</strong> Tabata; Volkov <strong>and</strong> Smirnov), <strong>and</strong> altitude tra<strong>in</strong><strong>in</strong>g<br />

(Nomura et al.) were shown to enhance anaerobic tra<strong>in</strong><strong>in</strong>g load <strong>and</strong><br />

chaPter1.<strong>in</strong>vitedLectures<br />

effects, but not produc<strong>in</strong>g significant differences <strong>in</strong> aerobic performance<br />

related parameters (OBLA <strong>and</strong> VO 2 max).<br />

In the “Exercise Test<strong>in</strong>g” section emphasis was given to the “critical<br />

speed” concept (Fern<strong>and</strong>es <strong>and</strong> Vilas-Boas; MacLaren <strong>and</strong> Coulson;<br />

Matsunami et al.) show<strong>in</strong>g that it can be used to monitor changes <strong>in</strong> the<br />

tra<strong>in</strong><strong>in</strong>g status, <strong>in</strong>clusively of juvenile swimmers, be<strong>in</strong>g strongly related<br />

to 4mM velocity (r=0.82) <strong>and</strong> OBLA <strong>in</strong>tensities (r=0.81). Kesk<strong>in</strong>en <strong>and</strong><br />

Kesk<strong>in</strong>en revisited the study of the k<strong>in</strong>etics of SL with swimm<strong>in</strong>g <strong>in</strong>tensity,<br />

re<strong>in</strong>forc<strong>in</strong>g the idea of Wakayoshi et al. (BMS VII) that the SL<br />

drop po<strong>in</strong>t may be a good predictor of the ability to swim long distances<br />

at sub-maximal <strong>in</strong>tensities.<br />

BMS IX (2003)<br />

Contrary to BMS VIII, this volume <strong>in</strong>cludes a considerable number<br />

of papers on start (6) <strong>and</strong> turn (3) analysis. Emphasis was given to the<br />

k<strong>in</strong>ematical, but particularly to the dynamics of swimm<strong>in</strong>g turns (Daniel<br />

et al.; Roeseler). Goya et al. didn’t analyze the turn<strong>in</strong>g action, but simply<br />

the push-off from the wall, <strong>and</strong> the subsequent glid<strong>in</strong>g phase. They<br />

found similar curves to those observed by Daniel et al., but significant<br />

differences between top <strong>and</strong> tra<strong>in</strong>ed swimmers both <strong>in</strong> <strong>in</strong>tensity <strong>and</strong> duration.<br />

Where starts are concerned, the ma<strong>in</strong> topic was the comparison<br />

of different techniques, particularly the grab start (GS) <strong>and</strong> the track<br />

start (TS) (Issur<strong>in</strong> <strong>and</strong> Verbitsky; Krüger et al.; Vilas-Boas et al.). Issur<strong>in</strong><br />

<strong>and</strong> Verbitsky analysed the reaction time <strong>and</strong> the time to 15m dur<strong>in</strong>g<br />

the Sydney Olympic f<strong>in</strong>als, <strong>and</strong> found evidence <strong>in</strong> favor of the TS<br />

although the GS was more used. Vilas-Boas et al. <strong>in</strong>volved both k<strong>in</strong>emetry<br />

<strong>and</strong> dynamometry to compare the same techniques, but divid<strong>in</strong>g<br />

the TS <strong>in</strong>to its two variants (forward - TRF - <strong>and</strong> rearward projection<br />

- TSR - of the CM). They found the GS faster <strong>in</strong> the reaction time. The<br />

GS also allowed a higher impulse than the TSF, but lower than the TSR.<br />

All the observed aerial differences vanished when the glide phase to 6m<br />

was considered. De la Fuente et al. also exam<strong>in</strong>ed the importance of the<br />

water phase of the start<strong>in</strong>g action. EMG analysis of the start was added<br />

by Krüger et al.. They found that the faster technique to the 7.5 m mark<br />

was the GS, characterized also by higher impulse, <strong>and</strong> a significantly<br />

different muscular recruitment pattern compared to TS.<br />

Coord<strong>in</strong>ation of technical movements was approached by different<br />

authors (Alberty et al.; Boulesteix et al.; Chollet et al.; Mauro et al.;<br />

Potdev<strong>in</strong> et al.; Schnitzeler et al.; Seifert et al.; Takagi et al.) <strong>in</strong> the four<br />

swimm<strong>in</strong>g techniques, <strong>and</strong> related both with fatigue, IVV, race-pace <strong>in</strong><br />

competition events, breath<strong>in</strong>g <strong>and</strong> non-breath<strong>in</strong>g crawl technique, SR,<br />

gender, level of performance, use of wet suits, <strong>and</strong> conventional <strong>and</strong> unconventional<br />

techniques.The evidence provided by Alberty et al is <strong>in</strong>terest<strong>in</strong>g<br />

to note, that the coord<strong>in</strong>ation of front crawl changes with fatigue,<br />

but not IVV. This latter parameter was used for different purposes: (i) to<br />

analyze hydrodynamic concepts of swimm<strong>in</strong>g propulsion (Persyn et al.);<br />

(ii) to provide evidence on non-stationary swimm<strong>in</strong>g mechanics based<br />

on hip k<strong>in</strong>ematics (Ungerechts et al.); (iii) to compare the k<strong>in</strong>ematics of<br />

the hip <strong>and</strong> the CM <strong>in</strong> butterfly (Barbosa et al.); (iv) to analyze timespace<br />

factors determ<strong>in</strong>ant of the CM k<strong>in</strong>ematics <strong>in</strong> breaststroke (Silva<br />

et al.; Soons et al.); (v) to directly monitor hip velocity examples of the<br />

four strokes <strong>in</strong> a flume (Buckwitz et al.); (vi) to compare the swimm<strong>in</strong>g<br />

technique of children <strong>and</strong> adult swimmers (Kjendlie et al., a), <strong>and</strong> (vii)<br />

to analyse the effect of wear<strong>in</strong>g a breath<strong>in</strong>g snorkel (Kjendlie et al., b).<br />

Bideu et al. proposed a device that can monitor IVV, but also can resist<br />

swimm<strong>in</strong>g progression with a controlled <strong>and</strong> constant load. With this<br />

device, authors were able to revisit the “velocity perturbation” active drag<br />

measurement method without the limitations associated with the variability<br />

of the drag opposed to the towed device.<br />

Arellano et al. characterized the underwater butterfly kick<strong>in</strong>g of elite<br />

<strong>and</strong> age-group swimmers us<strong>in</strong>g several k<strong>in</strong>ematical variables, <strong>in</strong>clud<strong>in</strong>g<br />

the Strouhal number (Sh). Ito <strong>and</strong> Okuno returned to Schleihauf ’s<br />

model of swimm<strong>in</strong>g propulsion, conclud<strong>in</strong>g that swimmers should drive<br />

the h<strong>and</strong> backwards along the longitud<strong>in</strong>al axis of the body to maximize<br />

propulsion, <strong>and</strong> that they need to favor scull<strong>in</strong>g actions when maximum<br />

17


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

swimm<strong>in</strong>g economy is required. More fundamental research was provided<br />

by Klauck, who developed a forward dynamics model to predict<br />

swimmer’s velocity on an “if/what” basis.<br />

In this volume, the concept of Critical Velocity, <strong>and</strong> associated parameters,<br />

were revisited (Clipet et al.; Dopsaj et at.; Ogita <strong>and</strong> Miyashita;<br />

Rodriguez et al.; Soares et al.; Takahashi et al.; Wakayoshi <strong>and</strong><br />

Ogita;), but with particular emphasis on their possible contribution to<br />

the assessment of anaerobic components of swimm<strong>in</strong>g performance. The<br />

SL drop <strong>in</strong>tensity was, once aga<strong>in</strong>, susta<strong>in</strong>ed as a valuable <strong>in</strong>dicator of<br />

relevant aerobic tra<strong>in</strong><strong>in</strong>g <strong>in</strong>tensities (Dekerle et al.; Nomura <strong>and</strong> Shimoyama).<br />

More direct approaches to this doma<strong>in</strong> <strong>in</strong>cluded VO 2 k<strong>in</strong>etics<br />

(Baron et al.; Fern<strong>and</strong>es et al., Ogita et al.; Rodriguez <strong>and</strong> Mader;<br />

Rodriguez et al.), <strong>and</strong> assessment methods (Cardoso et al.), among other<br />

relevant metabolic parameters, open<strong>in</strong>g new perspectives on the importance<br />

of O 2 metabolism for swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g <strong>and</strong> performance. In the<br />

mean time, Strumbelj et al. provided evidence that maximal [La] <strong>and</strong><br />

m<strong>in</strong>imal pH values do not differ between maximal efforts from 100 to<br />

400 m performed by 200 to 400 m specialists, underp<strong>in</strong>n<strong>in</strong>g the importance<br />

of both aerobic <strong>and</strong> anaerobic metabolism <strong>in</strong> swimm<strong>in</strong>g.<br />

Psychological aspects of swimm<strong>in</strong>g were also considered (Sugano et<br />

al.; Vik<strong>and</strong>er <strong>and</strong> Stallman; Zientek), as well as talent selection (Bügner<br />

<strong>and</strong> Hohmann; Saavedra et al.) <strong>and</strong> the <strong>in</strong>fluence of maturation, tra<strong>in</strong><strong>in</strong>g<br />

<strong>and</strong> competition on the evolution of swimm<strong>in</strong>g performance (Hellard<br />

et al.).<br />

BMS X (2006)<br />

In the last volume of the BMS series, some new research <strong>in</strong>terests <strong>and</strong><br />

methods were <strong>in</strong>cluded, particularly relevant <strong>in</strong> the hydrodynamics doma<strong>in</strong>.<br />

“Particle Image Velocimetry” (PIV) was <strong>in</strong>troduced (Kamata et<br />

al.; Matsuuchi et al.; Miwa et al.; Yamada et al.) as a technique of flow<br />

visualisation <strong>and</strong> quantification (applied to mono-f<strong>in</strong>, scull<strong>in</strong>g, butterfly<br />

kick <strong>and</strong> h<strong>and</strong> movement dur<strong>in</strong>g front crawl). Results support previous<br />

assumptions about the importance of unsteady flow to swimm<strong>in</strong>g<br />

propulsion, <strong>and</strong> practical consequences were extracted (Ungerechts <strong>and</strong><br />

Klauck). The <strong>in</strong>troduction of “Computational Fluid Dynamics” (CFD)<br />

approaches <strong>in</strong>to the series also dist<strong>in</strong>guishes this volume (Lyttle <strong>and</strong><br />

Keys). These authors studied the underwater kick<strong>in</strong>g action, show<strong>in</strong>g<br />

that large <strong>and</strong> low frequency kicks seem to be better than small <strong>and</strong><br />

high frequency ones. Experimentally, Gavilán et al. further concluded<br />

that the wav<strong>in</strong>g energy transfer along the body starts from the hips,<br />

<strong>and</strong> that the upper body is ma<strong>in</strong>ly a stabilizer. The same problem was<br />

addressed by Sugimoto et al., who used the computer model proposed<br />

by Nakajima to estimate the propulsive action of each body part dur<strong>in</strong>g<br />

underwater dolph<strong>in</strong> kick. Toussa<strong>in</strong>t et al. reported very high front<br />

crawl propulsive efficiency values at also high swimm<strong>in</strong>g velocities. They<br />

considered that the arm rotation <strong>and</strong> the associated axial flow possibly<br />

established at very high velocities allow br<strong>in</strong>g<strong>in</strong>g added water mass to<br />

the propell<strong>in</strong>g segments, enhanc<strong>in</strong>g efficiency.<br />

Another area of great <strong>in</strong>terest <strong>in</strong> this volume was the movement coord<strong>in</strong>ation,<br />

re<strong>in</strong>forced by efforts on pattern recognition (Oghi; Oliveira<br />

et al.), that allow fast video-based evaluation solutions <strong>and</strong> feedback<br />

(Soons et al.). Chollet et al. analysed the effect of technical mistakes <strong>in</strong><br />

backstroke coord<strong>in</strong>ation, <strong>and</strong> Schnitzeler et al. (a) studied the stability<br />

of coord<strong>in</strong>ation dur<strong>in</strong>g maximal <strong>and</strong> sub-maximal swims. Seifert et al.<br />

(a) compared objective (k<strong>in</strong>ematical parameters obta<strong>in</strong>ed from digitalization)<br />

<strong>and</strong> subjective approaches (based on expertise), to assess stroke<br />

phases <strong>in</strong> coord<strong>in</strong>ation studies. A similar <strong>in</strong>terest was shown by Schnitzler<br />

et al. (b, c) who used mechanical velocimetry to <strong>in</strong>crease the capacity<br />

to discrim<strong>in</strong>ate the propulsive phases dur<strong>in</strong>g one stroke cycle <strong>in</strong> order<br />

to empower traditional coord<strong>in</strong>ation analysis. Tella et al. also comb<strong>in</strong>ed<br />

IVV, coord<strong>in</strong>ation <strong>and</strong> fatigue studies, <strong>and</strong> found that IVV empowers<br />

the underst<strong>and</strong><strong>in</strong>g of the coord<strong>in</strong>ative changes that occur with fatigue.<br />

IVV <strong>and</strong> acceleration were aga<strong>in</strong> a central topic of research. Mechanical<br />

velocimetry was used by Craig et al. <strong>and</strong> other authors. Us<strong>in</strong>g<br />

this method, Pedersen <strong>and</strong> Kjendlie reported significant reductions <strong>in</strong><br />

18<br />

the mean maximal velocity when breath<strong>in</strong>g every cycle, compared with<br />

controlled breath<strong>in</strong>g. Soares et al. used the IVV frequency spectrum to<br />

analyze changes <strong>in</strong> the mechanical output profile dur<strong>in</strong>g a maximal 50<br />

m test, presumably allow<strong>in</strong>g the evaluation of “energetic dom<strong>in</strong>ancy<br />

transitions” relevant for speed tra<strong>in</strong><strong>in</strong>g. CM <strong>and</strong> hip IVV were compared<br />

(Capitão et al.; Morouço et al.), be<strong>in</strong>g considered to provide similar patterns,<br />

<strong>and</strong> Barbosa et al. analyzed the relationship of IVV of the CM to<br />

energy cost of swimm<strong>in</strong>g consider<strong>in</strong>g the four competitive strokes, <strong>and</strong><br />

controll<strong>in</strong>g the velocity effect.<br />

Fatigue was explored through an EMG frequency spectrum decrease<br />

dur<strong>in</strong>g an exhaustive 4 x 50 m front crawl test (Caty et al.).<br />

Further use of EMG was proposed by Hohmann et al. to analyse the<br />

backstroke start technique to which Krüger et al. added k<strong>in</strong>ematic <strong>and</strong><br />

k<strong>in</strong>etic parameters. Takeda <strong>and</strong> Nomura compared the GS <strong>and</strong> the TS<br />

analyz<strong>in</strong>g the take-off velocity <strong>and</strong> its extensional <strong>and</strong> rotational components,<br />

underl<strong>in</strong><strong>in</strong>g the importance of the rear leg action dur<strong>in</strong>g the<br />

TS. Seifert et al. (b) also analyzed starts, but for breaststroke events,<br />

consider<strong>in</strong>g the coord<strong>in</strong>ation of the actions dur<strong>in</strong>g the underwater cycle.<br />

This was the ma<strong>in</strong> discrim<strong>in</strong>at<strong>in</strong>g parameter of an Olympic breaststroke<br />

medalist after the admittance of the butterfly kick. Turns were studied<br />

by Pereira et al. us<strong>in</strong>g k<strong>in</strong>ematical <strong>and</strong> k<strong>in</strong>etic variables. As expected,<br />

peak normalized horizontal force exerted on the wall was determ<strong>in</strong>ant<br />

for performance. Pr<strong>in</strong>z <strong>and</strong> Patz also studied the flip turn, analyz<strong>in</strong>g the<br />

effects of the tuck <strong>in</strong>dex, the depth of the wall contact, <strong>and</strong> the contact<br />

time on the velocity of push-off.<br />

Pedagogical <strong>and</strong> didactical aspects of swimm<strong>in</strong>g also received a<br />

deeper analysis <strong>in</strong> this volume. Havriluk measured the effects of an <strong>in</strong>structional<br />

<strong>in</strong>tervention of one week duration on swimm<strong>in</strong>g technique<br />

us<strong>in</strong>g biomechanical parameters such as h<strong>and</strong> force to time curves <strong>and</strong><br />

active drag. The ma<strong>in</strong> effects were observed on drag. Different <strong>in</strong>structional<br />

programs were also compared (Invernizzi et al., a, b), <strong>in</strong>clud<strong>in</strong>g<br />

heuristic <strong>and</strong> analytical approaches. Heuristic approaches were shown<br />

to be preferable.<br />

Critical velocity <strong>and</strong> critical power concepts were once more <strong>in</strong>vestigated<br />

(Dekerle et al. a, b; Filipatou et al.; Greco et al.), <strong>in</strong>clusively based<br />

on reduced distances (Thanapoulos et al.), <strong>and</strong> applied to def<strong>in</strong>e tra<strong>in</strong><strong>in</strong>g<br />

sets for velocities above the anaerobic threshold (Wakayoshi et al.). Reis<br />

<strong>and</strong> Alves showed that critical velocity <strong>and</strong> v4 changes similarly with<br />

tra<strong>in</strong><strong>in</strong>g for age group swimmers. To further analyze metabolic transition<br />

zones, the anaerobic ventilatory threshold (Morais et al., a) <strong>and</strong> the<br />

VO 2 at the lactate threshold (Morais et al., b) were studied. In the same<br />

perspective, Machado et al. proposed a mathematical based method to<br />

assess the <strong>in</strong>dividual anaerobic threshold, <strong>and</strong> Kjendlie <strong>and</strong> Stallman<br />

verified the validity of non-paced tests for the same use. Complementarily,<br />

Shimoyama et al. observed that OBLA changes are ma<strong>in</strong>ly determ<strong>in</strong>ed<br />

by physiologic rather than biomechanical factors. VO 2 <strong>and</strong><br />

other respiratory, ventilatory <strong>and</strong> cardiologicaly relevant parameters<br />

were analysed (Fern<strong>and</strong>es et al., Machado et al., Madeira et al., a, b,<br />

Querido et al., Strumbelj et al.). The effects of us<strong>in</strong>g a respiratory snorkel<br />

on the breath<strong>in</strong>g frequency <strong>in</strong> front crawl were also studied (Kapus et<br />

al.). Physiological (VO 2 max., v@OBLA, [La]max) <strong>and</strong> biomechanical<br />

(active drag, maximal propulsive power) characteristics of an Olympic<br />

female gold medalist were provided by Ogita et al. <strong>and</strong> compared with<br />

elite college swimmers. The results showed that it was not the physiologic<br />

parameters that dist<strong>in</strong>guished the Olympic champion, but a slight<br />

drag reduction observed at high swimm<strong>in</strong>g velocities, emphasiz<strong>in</strong>g the<br />

relevance of the biomechanical factors to excel <strong>in</strong> swimm<strong>in</strong>g.<br />

Specific tra<strong>in</strong><strong>in</strong>g modes also attracted attention. Peak<strong>in</strong>g <strong>and</strong> taper<strong>in</strong>g<br />

(Issour<strong>in</strong> et al.), altitude tra<strong>in</strong><strong>in</strong>g (Marcadé et al.), assisted (Pretto<br />

et al.) <strong>and</strong> resisted (Llop et al., Mavridis et al.) tra<strong>in</strong><strong>in</strong>g were addressed.<br />

Water-polo was extensively studied (Bratusa <strong>and</strong> Dopsaj; Bratusa et<br />

al.; Dopsaj et al.; Klauck et al.; Platanou <strong>and</strong> Geladas; Stirn <strong>and</strong> Strojnik;),<br />

but also life-sav<strong>in</strong>g ( Juntunen et al.), triathlon (Bernavent et al.),<br />

water runn<strong>in</strong>g wear<strong>in</strong>g wet vest (Stallman et al., a, b), <strong>and</strong> synchronised<br />

swimm<strong>in</strong>g (Homma <strong>and</strong> Homma, a, b; Ito) were considered. Ito anal-


ysed, <strong>in</strong> a w<strong>in</strong>d tunnel, five different configurations of the h<strong>and</strong> consider<strong>in</strong>g<br />

their hydrodynamic behaviour. It was found that a cupped h<strong>and</strong> is<br />

better than a flat one, but with straight <strong>and</strong> closed f<strong>in</strong>gers.<br />

Medical <strong>and</strong> rehabilitation topics were not so abundant <strong>in</strong> BMS X,<br />

but did <strong>in</strong>clude very relevant issues like muscular imbalance (Becker<br />

et al.), <strong>in</strong>jury <strong>in</strong>cidence (Haupenthal et al.) <strong>and</strong> the <strong>in</strong>cidence, consequences<br />

<strong>and</strong> strategies fac<strong>in</strong>g the detection of Auxiliary Arch of Langer<br />

(Clarys et al.). Susceptibility to peroxidation of red blood cells <strong>in</strong> swimmers<br />

(Monteiro et al.), effects of exercise on the cross-sectional area of<br />

the vena cava (Onodera et al.), <strong>and</strong> immunological responses to swim<br />

tra<strong>in</strong><strong>in</strong>g (Teixeira et al.) were also <strong>in</strong>cluded, as well as nutrition (Soultanakis<br />

et al.; Toubekis et al.) <strong>and</strong> supplementation (Shiraki <strong>and</strong> Nomura)<br />

analysis.<br />

conclusIons And Future PersPectIVes<br />

Follow<strong>in</strong>g recent trends, future developments <strong>in</strong> <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g probably will lie upon the development of numerical<br />

methods <strong>and</strong> simulations, both for <strong>in</strong>ternal (muscular <strong>and</strong> <strong>in</strong>tersegmental)<br />

<strong>and</strong> external (hydrodynamic) biomechanics, as CFD already<br />

allows. 3D mov<strong>in</strong>g models will be <strong>in</strong>cluded <strong>in</strong> the simulation studies<br />

with capabilities to respect biomechanical redundancy. Detailed <strong>and</strong> sophisticated<br />

experimental approaches will also progress, like the PIV approaches<br />

already <strong>in</strong>cluded <strong>in</strong> the series <strong>in</strong> the last issue. These approaches<br />

(comb<strong>in</strong><strong>in</strong>g model<strong>in</strong>g <strong>and</strong> experimentation) will allow a deeper underst<strong>and</strong><strong>in</strong>g<br />

of P <strong>and</strong> D mechanisms, <strong>in</strong>clud<strong>in</strong>g consistent analysis of added<br />

mass <strong>in</strong>ertial effects, <strong>and</strong> possible propulsive repercussions of eventual<br />

axial flow over the propulsive segments. Optical fibre <strong>and</strong> other <strong>in</strong>-bedded<br />

m<strong>in</strong>iaturized sensors, together with nanotechnology contributions<br />

will prevail <strong>and</strong> provide revolutionary contributions for future scientists.<br />

It is possible that ambulatory k<strong>in</strong>ematics will prevail over image/external<br />

light based k<strong>in</strong>ematical process<strong>in</strong>g systems. Special garments, made of<br />

<strong>in</strong>telligent textile fabrics will allow both biomechanical <strong>and</strong> physiologic<br />

evaluation <strong>and</strong> feedback, <strong>in</strong>clud<strong>in</strong>g <strong>in</strong> real-time. It is possible that this<br />

type of material will allow new developments <strong>in</strong> the swimwear <strong>in</strong>dustry,<br />

allow<strong>in</strong>g “exoskeletons” to be circumstantially created dur<strong>in</strong>g immersion,<br />

based on textiles with memory of shape. Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> test<strong>in</strong>g <strong>in</strong> anaerobic<br />

bio-energetic zones will concentrate more research efforts, probably<br />

of <strong>in</strong>ter-discipl<strong>in</strong>ary nature. In fact, it is possible to preview that those<br />

<strong>in</strong>ter-discipl<strong>in</strong>ary studies, comb<strong>in</strong><strong>in</strong>g the physiological, biomechanical,<br />

<strong>and</strong> psycho-cognitive doma<strong>in</strong>s, will provide paramount <strong>in</strong>formation for<br />

the progress of knowledge <strong>in</strong> aquatic sports <strong>and</strong> activities.<br />

Also an <strong>in</strong>crease will be seen <strong>in</strong> the exchange of methodology <strong>and</strong><br />

<strong>in</strong>strumentation between various activity areas <strong>and</strong> more activity areas<br />

will be represented. There may be a shift <strong>in</strong> emphasis between scientific<br />

doma<strong>in</strong>s <strong>and</strong> activities with cont<strong>in</strong>ued growth of areas previously less<br />

well represented. This is <strong>in</strong> fact, recommended.<br />

reFerences:<br />

Chatard J. C. (ed.) (2003). Swimm<strong>in</strong>g Science IX. <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX. Publications de l’Université de Sa<strong>in</strong>t-<br />

Étienne, Sa<strong>in</strong>t-Étienne.<br />

Clarys J.P., Lewillie L. (eds.) (1975). Swimm<strong>in</strong>g II. University Park<br />

Press, Baltimore.<br />

Holl<strong>and</strong>er A. P., Huij<strong>in</strong>g P. A., de Groot, G. (eds.) (1983). <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g. Human K<strong>in</strong>etics Publishers, Champaign,<br />

Ill<strong>in</strong>ois.<br />

Kesk<strong>in</strong>en K., Komi P., Holl<strong>and</strong>er (eds A. P.) (1999). <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII. Dep. of Biology of Physical Activity,<br />

University of Jyväskylä, Jyväskylä.<br />

Lewillie L., Clarys J.P. (eds.) (1971). Proceed<strong>in</strong>gs of the First International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Swimm<strong>in</strong>g, Waterpolo <strong>and</strong> Div<strong>in</strong>g. Université<br />

Libre de Bruxelles, Bruxelles.<br />

MacLaren D., Reilly T., Lees A. (eds.) (1992). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g, Swimm<strong>in</strong>g Science VI. E & FN Spon, London.<br />

Terauds J., Bed<strong>in</strong>gfield E. W. (eds.) (1979). Swimm<strong>in</strong>g III. University<br />

chaPter1.<strong>in</strong>vitedLectures<br />

Park Press, Baltimore.<br />

Troup J. P., Holl<strong>and</strong>er A. P., Strasse D., Trappe S. W., Cappaert J. M.,<br />

Trappe T. A. (eds.) (1996). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g<br />

VII. E & FN Spon, London.<br />

Ungerechts B. E., Wilke K., Reischle K. (eds.) (1988). Swimm<strong>in</strong>g Science<br />

V. Human K<strong>in</strong>etics Publishers, Champaign, Ill<strong>in</strong>ois.<br />

Vilas-Boas J. P., Alves F., Marques A. (eds.) (2006). <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X. Portuguese Journal of Sport Sciences,<br />

Suppl 2.<br />

AcKnoWledGeMents<br />

Part of this study was supported by grant: PTDC/DES/101224/2008<br />

19


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Apply<strong>in</strong>g a Developmental Perspective to Aquatics<br />

<strong>and</strong> Swimm<strong>in</strong>g<br />

langendorfer, s.J.<br />

Bowl<strong>in</strong>g Green State University, Bowl<strong>in</strong>g Green, Ohio, USA<br />

Most typically <strong>in</strong> the aquatic field <strong>in</strong>structors <strong>and</strong> coaches employ an<br />

“error correction model” to view all swimm<strong>in</strong>g behaviours. Us<strong>in</strong>g a<br />

“straw person” approach, cl<strong>in</strong>icians expect all learners regardless of age or<br />

skill to swim like an elite adult swimmer. In this approach errors are corrected<br />

ma<strong>in</strong>ly when external experts such as teachers or coaches expunge<br />

those errors us<strong>in</strong>g comm<strong>and</strong> style direct teach<strong>in</strong>g. In comm<strong>and</strong> teach<strong>in</strong>g,<br />

a coach verbally describes <strong>and</strong> then demonstrates the expected “expert”<br />

way of swimm<strong>in</strong>g followed by identify<strong>in</strong>g the “errors” the learner<br />

makes that deviate from the expert model. In contrast, a “developmental<br />

perspective” is def<strong>in</strong>ed as a view <strong>in</strong> which one expects <strong>and</strong> anticipates<br />

regular, ordered changes to occur <strong>in</strong> swimm<strong>in</strong>g behaviours across the<br />

entire lifespan. From a developmental perspective, changes <strong>in</strong> swimm<strong>in</strong>g<br />

behaviour occur as a result of systemic <strong>in</strong>teractions among <strong>in</strong>dividual,<br />

task, <strong>and</strong> environmental characteristics as proposed by Newell (1986).<br />

For example, this view expects that someone learn<strong>in</strong>g to swim on the<br />

front gradually <strong>and</strong> systematically will change the arm, leg, <strong>and</strong> breath<strong>in</strong>g<br />

patterns they use to move through the water because their body size<br />

or density changes, or the way they <strong>in</strong>teract with the task is altered. In<br />

this paper I provide a conceptual overview that compares <strong>and</strong> contrasts<br />

the developmental <strong>and</strong> error correction approaches <strong>in</strong> swimm<strong>in</strong>g by<br />

draw<strong>in</strong>g upon contemporary th<strong>in</strong>k<strong>in</strong>g <strong>in</strong> dynamical systems <strong>and</strong> motor<br />

development theory. In particular, I highlight the three essential cl<strong>in</strong>ical<br />

skills that aquatic cl<strong>in</strong>icians need to possess when us<strong>in</strong>g “developmentally<br />

appropriate practices” (DAP) (i.e., developmental assessment, <strong>in</strong>dividualization<br />

of <strong>in</strong>struction, <strong>and</strong> developmental task analysis). For each<br />

DAP cl<strong>in</strong>ical skill, I provide practical illustrations for how these DAP<br />

skills apply to learn<strong>in</strong>g <strong>in</strong> aquatics <strong>and</strong> swimm<strong>in</strong>g. I argue that the predom<strong>in</strong>ance<br />

of the error correction model with<strong>in</strong> swimm<strong>in</strong>g <strong>and</strong> aquatics<br />

has severely limited the field’s acceptance <strong>and</strong> use of best <strong>in</strong>structional,<br />

learn<strong>in</strong>g, <strong>and</strong> assessment practices as well as unnecessarily constra<strong>in</strong>ed<br />

th<strong>in</strong>k<strong>in</strong>g about swimm<strong>in</strong>g skill acquisition <strong>in</strong> ways that acceptance of a<br />

developmental perspective would remedy.<br />

Keywords: swimm<strong>in</strong>g skill acquisition, developmental perspective,<br />

developmentally appropriate practices, developmental task analysis<br />

IntroductIon<br />

Virtually all authors <strong>and</strong> practitioners <strong>in</strong> the aquatics field approach the<br />

acquisition of skill from what is known as an “error correction model.”<br />

From this ubiquitous “error model,” practitioners view swimm<strong>in</strong>g skills<br />

from an “all or noth<strong>in</strong>g” perspective <strong>in</strong> which they expect a s<strong>in</strong>gle “correct”<br />

way of perform<strong>in</strong>g each aquatic skill. Regardless of a swimmer’s<br />

age, skill level, or ability, or the task goal <strong>and</strong> environment, <strong>in</strong>structors<br />

presume the “right way” to perform any aquatic skill is to match the way<br />

a hypothetical elite adult swimmer would perform it.<br />

Because of the presumption under the error model that there is a<br />

s<strong>in</strong>gle right way to perform a skill, the aquatic skill acquisition process<br />

becomes one of expung<strong>in</strong>g errors. Expung<strong>in</strong>g errors ma<strong>in</strong>ly creates a<br />

negative, or “glass-half-full,” approach especially for young, <strong>in</strong>experienced,<br />

or differently-abled learners. The primary view is that these <strong>in</strong>dividuals<br />

are wrong <strong>in</strong> how they are try<strong>in</strong>g to swim. Even if they make<br />

a s<strong>in</strong>gle change, they are still not swimm<strong>in</strong>g the “correct” way which<br />

can be quite frustrat<strong>in</strong>g for a young or <strong>in</strong>experienced learner. The error<br />

model also tends to engender a s<strong>in</strong>gle direct pedagogical approach, often<br />

called “comm<strong>and</strong> style,” or “tell-show-do,” teach<strong>in</strong>g (Mossten, 1966).<br />

This paper proposes that an alternative way of view<strong>in</strong>g skill acquisition<br />

known as the developmental perspective provides a number of advantages<br />

20<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> /Chapter 1 Invited Lectures Page 22<br />

presume the “right way” to perform any aquatic skill is to match the way a<br />

hypothetical elite adult swimmer would perform it.<br />

Because of the presumption under the error model that there is a s<strong>in</strong>gle right way<br />

to perform a skill, the aquatic skill acquisition process becomes one of expung<strong>in</strong>g<br />

errors. Expung<strong>in</strong>g errors ma<strong>in</strong>ly creates a negative, or “glass-half-full,” approach<br />

especially for young, <strong>in</strong>experienced, or differently-abled learners. The primary view is<br />

to that both these practitioners <strong>in</strong>dividuals are wrong <strong>and</strong> learners. <strong>in</strong> how they Under are try<strong>in</strong>g the to swim. developmental Even if they make perspective a<br />

practitioners s<strong>in</strong>gle change, presume they are still that not all swimm<strong>in</strong>g voluntary the “correct” motor skills way which <strong>in</strong>clud<strong>in</strong>g can be swimm<strong>in</strong>g<br />

quite<br />

frustrat<strong>in</strong>g for a young or <strong>in</strong>experienced learner. The error model also tends to<br />

skills engender change a s<strong>in</strong>gle gradually direct pedagogical over time approach, as a result often called of a “comm<strong>and</strong> number style,” of complex or “tell<strong>in</strong>teractionsshow-do,” among teach<strong>in</strong>g <strong>in</strong>dividual (Mossten, 1966). learners, tasks be<strong>in</strong>g learned, <strong>and</strong> the environ-<br />

This paper proposes that an alternative way of view<strong>in</strong>g skill acquisition known as<br />

mental the developmental context. As perspective a more provides positive a number <strong>and</strong> hopeful of advantages means to both of practitioners promot<strong>in</strong>g skill<br />

acquisition, <strong>and</strong> learners. the Under developmental the developmental perspective underst<strong>and</strong>s practitioners presume that motor that all skills<br />

voluntary motor skills <strong>in</strong>clud<strong>in</strong>g swimm<strong>in</strong>g skills change gradually over time as a<br />

may result take of a on number a variety of complex of coord<strong>in</strong>ation <strong>in</strong>teractions among patterns. <strong>in</strong>dividual These learners, different tasks be<strong>in</strong>g patterns<br />

learned, <strong>and</strong> the environmental context. As a more positive <strong>and</strong> hopeful means of<br />

are acquired <strong>in</strong> a regular, but gradual, sequence of changes. Developmen-<br />

promot<strong>in</strong>g skill acquisition, the developmental perspective underst<strong>and</strong>s that motor<br />

tally, skills the may different take on a patterns variety of coord<strong>in</strong>ation are not viewed patterns. as These right different or wrong, patterns or are correct<br />

acquired <strong>in</strong> a regular, but gradual, sequence of changes. Developmentally, the different<br />

vs. patterns <strong>in</strong>correct, are not but viewed only as right as less or wrong, or more or correct developmentally vs. <strong>in</strong>correct, but advanced only as less or along a<br />

developmental more developmentally cont<strong>in</strong>uum advanced as along illustrated a developmental <strong>in</strong> Figure cont<strong>in</strong>uum 1. as illustrated <strong>in</strong><br />

Figure 1.<br />

Less developmentally advanced More developmentally advanced<br />

Figure 1. Figure 1.<br />

In facilitat<strong>in</strong>g learn<strong>in</strong>g, the developmental perspective encourages practitioners to use a<br />

much more diverse set of learner-centered teach<strong>in</strong>g <strong>and</strong> learn<strong>in</strong>g approaches <strong>in</strong>stead of<br />

just the direct comm<strong>and</strong> style implied by the error model. For example, <strong>in</strong>structors<br />

may use <strong>in</strong>direct teach<strong>in</strong>g-learn<strong>in</strong>g approaches such as movement exploration, guided<br />

discovery, or task sett<strong>in</strong>g (Mossten, 1966). The developmental perspective also<br />

provides the opportunity for more diagnostic <strong>and</strong> prescriptive formative assessment to<br />

<strong>in</strong>dividualize their teach<strong>in</strong>g (Langendorfer & Bruya, 1995).<br />

In facilitat<strong>in</strong>g learn<strong>in</strong>g, the developmental perspective encourages practitioners<br />

to use a much more diverse set of learner-centered teach<strong>in</strong>g <strong>and</strong><br />

learn<strong>in</strong>g approaches <strong>in</strong>stead of just the direct comm<strong>and</strong> style implied<br />

by the error model. For example, <strong>in</strong>structors may use <strong>in</strong>direct teach<strong>in</strong>glearn<strong>in</strong>g<br />

approaches such as movement exploration, guided discovery, or<br />

task sett<strong>in</strong>g (Mossten, 1966). The developmental perspective also provides<br />

the opportunity for more diagnostic <strong>and</strong> prescriptive formative assessment<br />

to <strong>in</strong>dividualize their teach<strong>in</strong>g (Langendorfer & Bruya, 1995).<br />

METHOD<br />

I argue <strong>in</strong> this paper for the wider adoption of the developmental perspective over the<br />

error correction model <strong>in</strong> the teach<strong>in</strong>g <strong>and</strong> coach<strong>in</strong>g of swimm<strong>in</strong>g, water safety, <strong>and</strong><br />

aquatic skills. My argument is not based upon a s<strong>in</strong>gle empirical study, but draws upon<br />

a variety of exist<strong>in</strong>g developmental studies <strong>and</strong> expository articles, both terrestrial <strong>and</strong><br />

aquatic, that contrast with the observed weaknesses of the error model. I also propose<br />

apply<strong>in</strong>g several unique developmental approaches to the aquatic field as a means for<br />

exp<strong>and</strong><strong>in</strong>g the repertoire or tool box skills of aquatic practitioners.<br />

The first unique element that has not previously been applied to aquatics is<br />

Newell’s (1986) constra<strong>in</strong>ts model. The constra<strong>in</strong>ts model draws upon contemporary<br />

Method<br />

I argue <strong>in</strong> this paper for the wider adoption of the developmental perspective<br />

over the error correction model <strong>in</strong> the teach<strong>in</strong>g <strong>and</strong> coach<strong>in</strong>g<br />

of swimm<strong>in</strong>g, water safety, <strong>and</strong> aquatic skills. My argument is not<br />

based upon a s<strong>in</strong>gle empirical study, but draws upon a variety of exist<strong>in</strong>g<br />

developmental studies <strong>and</strong> expository articles, both terrestrial <strong>and</strong><br />

aquatic, that contrast with the observed weaknesses of the error model.<br />

I also propose apply<strong>in</strong>g several unique developmental approaches to the<br />

aquatic field as a means for exp<strong>and</strong><strong>in</strong>g the repertoire or tool box skills of<br />

aquatic practitioners.<br />

The first unique element that has not previously been applied to<br />

aquatics is Newell’s (1986) constra<strong>in</strong>ts model. The constra<strong>in</strong>ts model<br />

draws upon contemporary dynamical systems theory. Newell (1986)<br />

uses a triangle as a simple metaphor to portray how swimm<strong>in</strong>g coor-<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> /Chapter 1 Invited Lectures Page 23<br />

d<strong>in</strong>ation patterns may vary accord<strong>in</strong>g to relationships, called constra<strong>in</strong>ts,<br />

among an <strong>in</strong>dividual, the task goal, <strong>and</strong> environmental context (see Figure<br />

dynamical 2). For example, systems theory. as an <strong>in</strong>dividual Newell (1986) swimmer uses a grows triangle or gets as a stronger, simple metaphor the to<br />

way portray she how swims swimm<strong>in</strong>g a front crawl coord<strong>in</strong>ation (or freestyle) patterns stroke may vary gradually accord<strong>in</strong>g changes to relationships, the<br />

arm called pull, constra<strong>in</strong>ts, leg kick, among or body an position <strong>in</strong>dividual, because the task her goal, size <strong>and</strong> <strong>and</strong> environmental fitness enable context (see<br />

Figure 2). For example, as an <strong>in</strong>dividual swimmer grows or gets stronger, the way she<br />

her to <strong>in</strong>teract with<strong>in</strong> the water environment differently than when she<br />

swims a front crawl (or freestyle) stroke gradually changes the arm pull, leg kick, or<br />

was body smaller position <strong>and</strong> because less fit. her Similarly, size <strong>and</strong> the fitness constra<strong>in</strong>ts enable her model to <strong>in</strong>teract proposes with<strong>in</strong> that the if water<br />

an environment <strong>in</strong>structor alters differently characteristics than when of she the was front smaller crawl stroke <strong>and</strong> less (e.g., fit. how Similarly, far, the<br />

how constra<strong>in</strong>ts fast; added model buoyancy), proposes that the if crawl an <strong>in</strong>structor pattern alters also characteristics may change. Teach<strong>in</strong>g of the front crawl<br />

stroke (e.g., how far, how fast; added buoyancy), the crawl pattern also may change.<br />

can Teach<strong>in</strong>g <strong>in</strong>fluence can the <strong>in</strong>fluence swimm<strong>in</strong>g the swimm<strong>in</strong>g skill not skill because not because the swimmer the swimmer does what does what a<br />

a teacher demonstrates or <strong>in</strong>structs, or <strong>in</strong>structs, but because but because the <strong>in</strong>structor the <strong>in</strong>structor manipulates manipu- the task goal<br />

lates (e.g., the speed, task stroke goal (e.g., length) speed, or stroke characteristics length) of or the characteristics environment of (e.g., the water<br />

temperature, depth).<br />

environment (e.g., water temperature, depth).<br />

Individual<br />

Developmental level of<br />

movement<br />

Task<br />

Environment<br />

Figure 2.<br />

A second unique element to apply to aquatics is a concept called developmentally<br />

A appropriate second unique practices, element also known to apply as to DAP aquatics (Bredekamp, is a concept 1987). called I propose de- for our<br />

velopmentally purposes that appropriate we modify practices, this concept also <strong>and</strong> known call as it DAAP, DAP (Bredekamp,<br />

or developmentally<br />

appropriate aquatic practices, to emphasize how we can apply this early childhood<br />

educational concept to the teach<strong>in</strong>g-learn<strong>in</strong>g of aquatics across the lifespan.<br />

Roberton (1993) proposed that we should def<strong>in</strong>e DAP as the process of identify<strong>in</strong>g<br />

where an <strong>in</strong>dividual falls along a lifespan developmental cont<strong>in</strong>uum <strong>and</strong> match<strong>in</strong>g<br />

tasks to the needs <strong>and</strong> read<strong>in</strong>ess of each <strong>in</strong>dividual. In order to accomplish Roberton’s<br />

def<strong>in</strong>ition of DAP, she suggests that practitioners need to acquire three dist<strong>in</strong>ct<br />

developmental skills. Practitioners need 1) to possess developmental assessment skills<br />

by us<strong>in</strong>g developmental sequences, 2) to appreciate how to <strong>in</strong>dividualize <strong>in</strong>struction,


1987). I propose for our purposes that we modify this concept <strong>and</strong> call<br />

it DAAP, or developmentally appropriate aquatic practices, to emphasize<br />

how we can apply this early childhood educational concept to the<br />

teach<strong>in</strong>g-learn<strong>in</strong>g of aquatics across the lifespan.<br />

Roberton (1993) proposed that we should def<strong>in</strong>e DAP as the process<br />

of identify<strong>in</strong>g where an <strong>in</strong>dividual falls along a lifespan developmental<br />

cont<strong>in</strong>uum <strong>and</strong> match<strong>in</strong>g tasks to the needs <strong>and</strong> read<strong>in</strong>ess of<br />

each <strong>in</strong>dividual. In order to accomplish Roberton’s def<strong>in</strong>ition of DAP,<br />

she suggests that practitioners need to acquire three dist<strong>in</strong>ct developmental<br />

skills. Practitioners need 1) to possess developmental assessment<br />

skills by us<strong>in</strong>g developmental sequences, 2) to appreciate how to <strong>in</strong>dividualize<br />

<strong>in</strong>struction, <strong>and</strong> 3) to know how to make tasks easier or harder,<br />

depend<strong>in</strong>g upon the needs of the <strong>in</strong>dividual.<br />

Developmental assessment. Employ<strong>in</strong>g developmental aquatic assessment<br />

skills requires practitioners to reject the error correction model<br />

assumption that there is one correct way to perform a skill <strong>and</strong> appreciate<br />

that all swimm<strong>in</strong>g skills change <strong>in</strong> regular, ordered sequences. Several<br />

developmental aquatic assessment <strong>in</strong>struments have been published<br />

(Erbaugh, 1978; Langendorfer & Bruya, 1995). They represent us<strong>in</strong>g<br />

aquatic developmental sequences to identify where along a developmental<br />

cont<strong>in</strong>uum a swimmer’s skill or stroke falls.<br />

Individualiz<strong>in</strong>g <strong>in</strong>struction. Individualiz<strong>in</strong>g how one provides <strong>in</strong>struction<br />

requires a shift away from the traditional “one-size-fits-all”<br />

teacher-centered techniques to focus<strong>in</strong>g on the needs of each learner.<br />

Learner-centered teach<strong>in</strong>g focuses on help<strong>in</strong>g each swimmer to move<br />

from where she is to be<strong>in</strong>g more advanced. Generally this means that<br />

a practitioner needs to employ more <strong>in</strong>direct teach<strong>in</strong>g techniques such<br />

as exploration, guided discovery, or task sett<strong>in</strong>g (Mossten, 1966). It also<br />

requires the use of developmental assessment to determ<strong>in</strong>e each swimmer’s<br />

developmental level.<br />

Mak<strong>in</strong>g tasks easier or harder. The third developmental skill for structur<strong>in</strong>g<br />

an appropriate aquatic environment is the recognition that, <strong>in</strong><br />

l<strong>in</strong>e with Newell’s (1986) constra<strong>in</strong>ts model, task performances change<br />

accord<strong>in</strong>g to their relationship to the complexity of the task. One very<br />

simple means for systematically vary<strong>in</strong>g task complexity uses developmental<br />

task analysis, or DTA (Herkowitz, 1978; Morris, 1976; Roberton,<br />

1989). One variation on DTA <strong>in</strong>cludes constra<strong>in</strong>ts-based task analysis<br />

(Haywood & Getchell, 2009). Each of these techniques create a structure<br />

by which task factors can be systematically altered as the primary<br />

means for chang<strong>in</strong>g the coord<strong>in</strong>ation patterns of aquatic skills (see Table<br />

1).<br />

results<br />

In this section, I provide several explicit examples of how to employ Roberton’s<br />

proposed skills for DAAP with<strong>in</strong> an aquatic <strong>in</strong>structional program<br />

to facilitate optimal learn<strong>in</strong>g under a developmental perspective.<br />

In do<strong>in</strong>g so, I reference Newell’s constra<strong>in</strong>ts model <strong>and</strong> one version of<br />

an aquatic DTA. Where appropriate, I contrast how the developmental<br />

perspective differs from the error correction approach.<br />

I propose to use a hypothetical example of a mixed age (from 7 to<br />

20 years old) class of 15 swimmers who all desire to learn how to swim<br />

the front crawl stroke. I purposefully have chosen a class with somewhat<br />

extreme age differences to illustrate how DAAP should work regardless<br />

of diversity. I also want to illustrate the common fallacies associated with<br />

homogeneous group<strong>in</strong>g of swimmers that so often is mistakenly applied<br />

to swimm<strong>in</strong>g <strong>in</strong>struction.<br />

Developmental assessment. The first step that needs to be taken with<br />

our hypothetical class is to identify the swimm<strong>in</strong>g skill levels of each<br />

class member on a variety of swimm<strong>in</strong>g skills prerequisite to front crawl<br />

swimm<strong>in</strong>g. For this purpose, I use the Aquatic Read<strong>in</strong>ess Assessment<br />

(ARA) (Langendorfer & Bruya, 1995) because the ARA is comprised<br />

of n<strong>in</strong>e components, each represent<strong>in</strong>g developmental sequences relat<strong>in</strong>g<br />

to front (or prone) swimm<strong>in</strong>g. The components allow me to developmentally<br />

assess the comfort level of each class member <strong>in</strong> the water,<br />

their skills <strong>in</strong> enter<strong>in</strong>g the water, float<strong>in</strong>g, submerg<strong>in</strong>g, controll<strong>in</strong>g their<br />

chaPter1.<strong>in</strong>vitedLectures<br />

breath<strong>in</strong>g, <strong>and</strong> mov<strong>in</strong>g on their front <strong>in</strong> the water us<strong>in</strong>g arms, legs, <strong>and</strong><br />

an appropriate body position.<br />

I complete a separate ARA assessment form for each class member<br />

dur<strong>in</strong>g the first session of the class. S<strong>in</strong>ce each ARA component represents<br />

a developmental sequence, I am able to diagnose each swimmer’s<br />

levels along a developmental cont<strong>in</strong>uum (see Figure 1) <strong>and</strong> prescribe<br />

what levels they needed to work toward next.<br />

Individualiz<strong>in</strong>g <strong>in</strong>struction. Between the first <strong>and</strong> second class sessions,<br />

I create an <strong>in</strong>dividualized aquatic education plan (I.A.E.P) for each<br />

class member, identify<strong>in</strong>g their current developmental levels, any contra<strong>in</strong>dications,<br />

short term goals, <strong>and</strong> longer term goals based on feedback<br />

from each person. At the second class session, each member receives a<br />

copy of their own I.A.E.P. with notes about suggested skills to work on.<br />

Dur<strong>in</strong>g subsequent class sessions, the pool is set up with learn<strong>in</strong>g<br />

stations complete with lam<strong>in</strong>ated task cards conta<strong>in</strong><strong>in</strong>g both verbal <strong>and</strong><br />

pictorial <strong>in</strong>structions. Each swimmer’s I.A.E.P. <strong>in</strong>dicates the next levels<br />

on which s/he needs to work <strong>and</strong> l<strong>in</strong>ks those to selected learn<strong>in</strong>g stations.<br />

Swimmers work <strong>in</strong> pairs <strong>and</strong> small groups at stations to assist each<br />

other <strong>and</strong> do peer review. As <strong>in</strong>structor, I provide the general focus of<br />

stations <strong>Biomechanics</strong> for that <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> session, <strong>in</strong> rotate Swimm<strong>in</strong>g among <strong>XI</strong> /Chapter stations 1 Invited to clarify Lectures tasks, provide Page 25<br />

assistance <strong>and</strong> feedback, <strong>and</strong> direct <strong>in</strong>struction as needed by <strong>in</strong>dividuals.<br />

I also do spot assessments to update I.A.E.P.s as needed.<br />

Mak<strong>in</strong>g Dur<strong>in</strong>g tasks subsequent easier class or harder. sessions, One the of pool the is primary set up with mechanisms learn<strong>in</strong>g stations I use<br />

complete with lam<strong>in</strong>ated task cards conta<strong>in</strong><strong>in</strong>g both verbal <strong>and</strong> pictorial <strong>in</strong>structions.<br />

to Each structure swimmer’s DAAP I.A.E.P. tasks <strong>in</strong>dicates at each the next learn<strong>in</strong>g levels on station which is s/he an needs aquatic to work devel- <strong>and</strong><br />

opmental l<strong>in</strong>ks those task to selected analysis learn<strong>in</strong>g (DTA). stations. I create Swimmers separate work <strong>in</strong> DTAs pairs <strong>and</strong> with small factors groups ap- at<br />

stations to assist each other <strong>and</strong> do peer review. As <strong>in</strong>structor, I provide the general<br />

propriate to each skill. Note <strong>in</strong> the DTA <strong>in</strong> Table 1 that complexity<br />

focus of stations for that session, rotate among stations to clarify tasks, provide<br />

is assistance related <strong>and</strong> directly feedback, to <strong>and</strong> characteristics direct <strong>in</strong>struction of as the needed <strong>in</strong>dividual, by <strong>in</strong>dividuals. or body-scaled.<br />

I also do spot<br />

assessments to update I.A.E.P.s as needed.<br />

This normalization negates the need to try to achieve a homogenous<br />

Mak<strong>in</strong>g tasks easier or harder. One of the primary mechanisms I use to structure<br />

group<strong>in</strong>g DAAP tasks because at each each learn<strong>in</strong>g task station is scaled is an aquatic to the developmental <strong>in</strong>dividual’s task capabilities. analysis (DTA). For<br />

example, I create separate water DTAs depth with <strong>and</strong> factors distance appropriate swum to each are skill. described Note <strong>in</strong> <strong>in</strong> the terms DTA <strong>in</strong> of Table the<br />

1 that complexity is related directly to characteristics of the <strong>in</strong>dividual, or body-scaled.<br />

height of each <strong>in</strong>dividual, not <strong>in</strong> absolute distance units such as centi-<br />

This normalization negates the need to try to achieve a homogenous group<strong>in</strong>g because<br />

each task is scaled to the <strong>in</strong>dividual’s capabilities. For example, water depth <strong>and</strong><br />

distance swum are described <strong>in</strong> terms of the height of each <strong>in</strong>dividual, not <strong>in</strong> absolute<br />

distance units such as centimeters or meters.<br />

meters or meters.<br />

Table 1. A proposed aquatic developmental task analysis.<br />

Table 1. A proposed aquatic developmental task analysis.<br />

Swim Water Distance to Support Assistance Equipment<br />

Factors<br />

Complexity<br />

depth be swum<br />

Easy Waist deep 1-2 body One or Full assist by Propulsive<br />

(simple)<br />

lengths more<br />

flotation<br />

aids<br />

practitioner equipment<br />

Chest deep 2-5 body Natural Partial assist No<br />

lengths body by<br />

equipment<br />

buoyancy practitioner used<br />

Deeper 10 body Attached<br />

Resistive<br />

Hard than lengths or weight No equipment<br />

(difficult) st<strong>and</strong><strong>in</strong>g<br />

height<br />

more<br />

assistance<br />

DISCUSSION<br />

I propose that my hypothetical class <strong>in</strong> which learn<strong>in</strong>g to swim front crawl stroke is<br />

approached from a developmental perspective <strong>and</strong> employ<strong>in</strong>g the three D.A.A.P. skills<br />

proposed by Roberton (1993) appears to be rather different <strong>in</strong> a number of ways than a<br />

similar class organized accord<strong>in</strong>g to an error correction model. Those ways <strong>in</strong>clude the<br />

use of formative assessment, I.A.E.P.s, need-based lesson plann<strong>in</strong>g, <strong>in</strong>dividualized<br />

learn<strong>in</strong>g stations, <strong>and</strong> structur<strong>in</strong>g learn<strong>in</strong>g tasks us<strong>in</strong>g aquatic developmental task<br />

analysis.<br />

Under the typical error correction model, assessment is primarily summative <strong>in</strong><br />

nature. It typically occurs dur<strong>in</strong>g the f<strong>in</strong>al session, not the first session. When it does<br />

occur formatively, feedback is <strong>in</strong> the form of the “errors” that the swimmer is<br />

committ<strong>in</strong>g, not diagnostic corrective feedback about what the swimmer already can<br />

do <strong>and</strong> what s/he needs to do next. The I.A.E.P. allows the formative assessment us<strong>in</strong>g<br />

dIscussIon<br />

I propose that my hypothetical class <strong>in</strong> which learn<strong>in</strong>g to swim front<br />

crawl stroke is approached from a developmental perspective <strong>and</strong> employ<strong>in</strong>g<br />

the three D.A.A.P. skills proposed by Roberton (1993) appears<br />

to be rather different <strong>in</strong> a number of ways than a similar class organized<br />

accord<strong>in</strong>g to an error correction model. Those ways <strong>in</strong>clude the use of<br />

formative assessment, I.A.E.P.s, need-based lesson plann<strong>in</strong>g, <strong>in</strong>dividualized<br />

learn<strong>in</strong>g stations, <strong>and</strong> structur<strong>in</strong>g learn<strong>in</strong>g tasks us<strong>in</strong>g aquatic developmental<br />

task analysis.<br />

Under the typical error correction model, assessment is primarily<br />

summative <strong>in</strong> nature. It typically occurs dur<strong>in</strong>g the f<strong>in</strong>al session, not the<br />

first session. When it does occur formatively, feedback is <strong>in</strong> the form of<br />

the “errors” that the swimmer is committ<strong>in</strong>g, not diagnostic corrective<br />

feedback about what the swimmer already can do <strong>and</strong> what s/he needs<br />

to do next. The I.A.E.P. allows the formative assessment us<strong>in</strong>g the ARA<br />

to be translated <strong>in</strong>dividually for each class member <strong>and</strong> allows them to<br />

work on the specific developmentally appropriate next levels.<br />

The learn<strong>in</strong>g station approach employed <strong>in</strong> my hypothetical class is<br />

learner-centered <strong>and</strong> allows each member to take responsibility for her<br />

21


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

or his own learn<strong>in</strong>g while the <strong>in</strong>structor serves as a facilitator, not the<br />

primary <strong>in</strong>strument for demonstrat<strong>in</strong>g the right way to perform each<br />

skill. Each <strong>in</strong>dividual can work on those skills that they should master<br />

next. In contrast, a typical error model class would all be work<strong>in</strong>g on the<br />

same skills regardless of their <strong>in</strong>dividual needs.<br />

The presence of aquatic DTAs allows both swimmers <strong>and</strong> <strong>in</strong>structors<br />

to create a multitude of learn<strong>in</strong>g activities that they might otherwise not<br />

create without a DTA. It is noteworthy that the relatively simple DTA<br />

<strong>in</strong> Table 1 with only 5 factors each with 3 levels of complexity allow 243<br />

different <strong>and</strong> unique learn<strong>in</strong>g situations that few if any <strong>in</strong>structors might<br />

create under an error correction model.<br />

conclusIons<br />

This paper compares <strong>and</strong> contrasts the developmental perspective with<br />

a more typical error correction model, identify<strong>in</strong>g significant ways that<br />

developmentally appropriate practices can <strong>in</strong>dividualize acquisition of<br />

swimm<strong>in</strong>g, water safety, <strong>and</strong> aquatic skills. It <strong>in</strong>troduces Newell’s (1986)<br />

constra<strong>in</strong>ts model <strong>and</strong> Roberton’s three DAP <strong>in</strong>structional skills required<br />

of swimm<strong>in</strong>g practitioners for employ<strong>in</strong>g a developmental perspective.<br />

reFerences<br />

Bredekamp, S. (1987). Developmentally appropriate practices <strong>in</strong> early childhood<br />

education. Wash<strong>in</strong>gton, DC: National Association for the Education<br />

of Young Children.<br />

Erbaugh, S.J. (1978). Assessment of swimm<strong>in</strong>g performance of preschool<br />

children. Perceptual <strong>and</strong> Motor Skills, 47, 1179-1182.<br />

Haywood, K.M., & Getchell, N. (2009). Life Span Motor Development.<br />

Champaign, IL: Human K<strong>in</strong>etics.<br />

Herkowitz, J. (1978). Developmental task analysis: The design of movement<br />

experiences <strong>and</strong> evaluation of motor development status. In M.<br />

Ridenour (Ed.), Motor development: Issues <strong>and</strong> applications (pp. 139-<br />

164). Pr<strong>in</strong>ceton, NJ: Pr<strong>in</strong>ceton Book Co.<br />

Langendorfer, S.J., & Bruya, L.D. (1995). Aquatic read<strong>in</strong>ess: Develop<strong>in</strong>g<br />

water competence <strong>in</strong> young children. Champaign, IL: Human K<strong>in</strong>etics.<br />

Morris, G.S.D. (1976). How to change the games children play M<strong>in</strong>neapolis:<br />

Burgess.<br />

Mossten, M. (1966). Teach<strong>in</strong>g from comm<strong>and</strong> to discovery. Columbus,<br />

OH: Merrill.<br />

Newell, K.M. (1986). Constra<strong>in</strong>ts on the development of coord<strong>in</strong>ation.<br />

In M.G. Wade & H.T.A. Whit<strong>in</strong>g (Eds.), Motor development <strong>in</strong><br />

children: Aspects of coord<strong>in</strong>ation <strong>and</strong> control (pp. 341-360). Dordrecht,<br />

Netherl<strong>and</strong>s: Mat<strong>in</strong>us Nijhoff Publishers.<br />

Roberton, M.A. (1989). Developmental sequence <strong>and</strong> developmental<br />

task analysis. In J. Sk<strong>in</strong>ner et al. (Eds.), Future directions <strong>in</strong> exercise <strong>and</strong><br />

sport science research (pp. 369-381). Champaign, IL: Human K<strong>in</strong>etics.<br />

Roberton, M.A. (1993). Developmentally appropriate practices. Presentation<br />

to the Midwest Association for Health, Physical Education,<br />

Recreation, <strong>and</strong> Dance. Toledo, Ohio.<br />

Roberton, M.A., & Halverson, L.E. (1984). Develop<strong>in</strong>g children – their<br />

chang<strong>in</strong>g movement. Philadelphia: Lea & Febiger.<br />

22<br />

The Psycho-Physiology of Overtra<strong>in</strong><strong>in</strong>g <strong>and</strong> Athlete<br />

Burnout <strong>in</strong> Swimm<strong>in</strong>g<br />

lemyre, P.-n.<br />

Norwegian School of Sport Sciences, Oslo, Norway<br />

Underst<strong>and</strong><strong>in</strong>g swimmers’ response to tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competition cont<strong>in</strong>ues<br />

to be a significant challenge. Although a great deal of research has<br />

previously attempted to better underst<strong>and</strong> the psychological <strong>and</strong> physiological<br />

factors lead<strong>in</strong>g to maladaptive tra<strong>in</strong><strong>in</strong>g responses <strong>in</strong> an elite<br />

swimmer population, very few attempted to <strong>in</strong>tegrate these two fundamental<br />

perspectives. Therefore, the aim of this study was to <strong>in</strong>vestigate<br />

the relationship between personal dispositions, contextual motivation<br />

factors, subjective performance satisfaction, hormonal variation <strong>and</strong> burnout<br />

<strong>in</strong> elite swimmers. 53 elite swimmers (F=21, M=32) participated <strong>in</strong> a<br />

protocol of 6x200m progressive <strong>in</strong>tervals dur<strong>in</strong>g morn<strong>in</strong>g (07.00-08.30)<br />

<strong>and</strong> afternoon (14.00-15.30) tra<strong>in</strong><strong>in</strong>g sessions. Venous blood was drawn<br />

before <strong>and</strong> after each sets of <strong>in</strong>tervals <strong>and</strong> was analyzed for adrenocorticotropic<br />

hormone (ACTH) <strong>and</strong> cortisol by radio immune assays. This<br />

protocol was used at three time po<strong>in</strong>ts dur<strong>in</strong>g the season, correspond<strong>in</strong>g<br />

to the easy, very hard <strong>and</strong> peak<strong>in</strong>g time periods of the swimm<strong>in</strong>g season.<br />

Questionnaires assess<strong>in</strong>g psychological variables were used together with<br />

the two-bout exercise test at three time po<strong>in</strong>ts dur<strong>in</strong>g the season. Us<strong>in</strong>g<br />

hierarchical regression analysis, results <strong>in</strong>dicated that variation <strong>in</strong> basal<br />

cortisol (15%), maladaptive perfectionism disposition (20%), perceived<br />

mastery motivational climate (12%) <strong>and</strong> subjective performance satisfaction<br />

expla<strong>in</strong>ed together a total of 67% of the variance <strong>in</strong> athlete burnout<br />

at season’s end. Hormonal monitor<strong>in</strong>g is costly <strong>and</strong> <strong>in</strong>vasive, current f<strong>in</strong>d<strong>in</strong>gs<br />

support the <strong>in</strong>itial use of psychological monitor<strong>in</strong>g, while hormonal<br />

monitor<strong>in</strong>g may be used as a second step to help athletes steer away from<br />

maladaptive tra<strong>in</strong><strong>in</strong>g outcomes such as athlete burnout.<br />

Key words: overtra<strong>in</strong><strong>in</strong>g, burnout, prevention, hormones, motivation<br />

IntroductIon<br />

Elite swimmers are exceptionally gifted <strong>in</strong>dividuals born with the physiology<br />

to excel <strong>in</strong> their respective discipl<strong>in</strong>e. Typically, they are highly<br />

motivated <strong>and</strong> dedicated to tra<strong>in</strong><strong>in</strong>g <strong>and</strong> reach<strong>in</strong>g very high goals.<br />

This determ<strong>in</strong>ation helps them persevere through the most dem<strong>and</strong><strong>in</strong>g<br />

workouts <strong>and</strong> survive harsh tra<strong>in</strong><strong>in</strong>g conditions. These qualities <strong>and</strong><br />

the high commitment <strong>in</strong>volved <strong>in</strong> be<strong>in</strong>g a high perform<strong>in</strong>g swimmer<br />

have raised these swimmers to the level of elite performances. However,<br />

when fac<strong>in</strong>g frustrat<strong>in</strong>g setbacks, the same exact qualities that have<br />

elevated them elite performance may become their worst enemies <strong>and</strong><br />

lead to overtra<strong>in</strong><strong>in</strong>g (Hall, Cawthraw, & Kerr, 1997). Result<strong>in</strong>g <strong>in</strong> long<br />

term decrement of performance capacity, an overtra<strong>in</strong><strong>in</strong>g state orig<strong>in</strong>ates<br />

from a long last<strong>in</strong>g imbalance between tra<strong>in</strong><strong>in</strong>g <strong>and</strong> recovery. Restoration<br />

may take several weeks or months (Kreider, Fry, & O’Toole, 1998).<br />

After some time, swimmers may get used to the new state of tiredness<br />

<strong>and</strong> adjust to feel<strong>in</strong>g tired all the time. Elite swimmers experienc<strong>in</strong>g<br />

endur<strong>in</strong>g physiological <strong>and</strong>/or psychological exertion, without significant<br />

recovery or achiev<strong>in</strong>g the desired goal, may develop athlete burnout.<br />

Burnout has been def<strong>in</strong>ed as a state of mental, emotional, <strong>and</strong> physical<br />

exhaustion (Freudenberger, 1980) brought on by persistent devotion to a<br />

goal, without recogniz<strong>in</strong>g the need to recuperate, <strong>in</strong> the quest for a goal<br />

that may be opposed to reality.<br />

Recently, as <strong>in</strong>ter-discipl<strong>in</strong>ary research has taken a closer look at athlete<br />

burnout, some researchers (Gould, 1996; Hall & al., 1997; Lemyre,<br />

Hall, & Roberts, 2007) have suggested that “motivation gone awry” may<br />

play an important role <strong>in</strong> the onset of burnout. The focus of the present<br />

research is to <strong>in</strong>vestigate this hypothesis. We adopted contemporary social-cognitive<br />

motivational theory as our conceptual base for this study.<br />

From a motivational viewpo<strong>in</strong>t, it is clear that swimmers have many


different achievement goals; two ma<strong>in</strong> goals have been identified <strong>and</strong><br />

found to operate <strong>in</strong> the social context of sport, namely a task goal orientation<br />

<strong>and</strong> an ego goal orientation (Roberts, 2001). When the swimmer<br />

adopts a task oriented goal, success <strong>and</strong> failure are judged by whether<br />

one has mastered the activity, improved at the task or met self-imposed<br />

st<strong>and</strong>ards. When the swimmer adopts an ego oriented goal, success <strong>and</strong><br />

failure are judged by whether one demonstrates normative ability <strong>and</strong><br />

avoids demonstrat<strong>in</strong>g comparative <strong>in</strong>ability. The way a swimmer def<strong>in</strong>es<br />

success <strong>in</strong>fluences the level of self-determ<strong>in</strong>ation they experience <strong>in</strong> the<br />

sport. When success is task oriented it is argued that the swimmer is<br />

<strong>in</strong>tr<strong>in</strong>sically motivated. The activity is freely experienced, self-endorsed,<br />

<strong>and</strong> the locus of causality is perceived as <strong>in</strong>ternal (Deci & Ryan, 2000).<br />

However, some actions can be motivated by external sources of control<br />

that are not endorsed by the self. Both personal dispositions <strong>and</strong><br />

situational factors (e.g., motivational climate) are presumed to affect the<br />

motivational state. Behaviors are extr<strong>in</strong>sically motivated when external<br />

sources of control are perceived. With<strong>in</strong> Self-determ<strong>in</strong>ation theory,<br />

extr<strong>in</strong>sic motivation is multidimensional <strong>and</strong> consists of three different<br />

types of motivation presented on a cont<strong>in</strong>uum go<strong>in</strong>g from lower to<br />

higher levels of perceived locus of causality or self-determ<strong>in</strong>ation: external<br />

regulation, <strong>in</strong>trojected regulation <strong>and</strong> identified regulation. F<strong>in</strong>ally,<br />

swimmers may be amotivated when they do not perceive cont<strong>in</strong>gencies<br />

between their behavior <strong>and</strong> outcome, the action is perceived to be out of<br />

their control even though they may cont<strong>in</strong>ue to participate.<br />

It has been suggested (e.g., Silva, 1990) that though psychological<br />

processes underp<strong>in</strong>n<strong>in</strong>g athlete burnout are important, the phenomenon<br />

occurs only when these psychological processes are comb<strong>in</strong>ed with<br />

negative tra<strong>in</strong><strong>in</strong>g adaptation. Susta<strong>in</strong>ed failure to adapt to tra<strong>in</strong><strong>in</strong>g generates<br />

excessive fatigue. Tra<strong>in</strong><strong>in</strong>g when the body’s adaptivity is lost, leads<br />

to overtra<strong>in</strong><strong>in</strong>g (Silva, 1990; Urhausen, Gabriel & K<strong>in</strong>dermann, 1998)<br />

<strong>and</strong> <strong>in</strong>creases vulnerability to athlete burnout (e.g., Lemyre, Roberts, &<br />

Stray-Gundersen, 2007). Athletes, then, suffer from a neuroendocr<strong>in</strong>e<br />

imbalance <strong>and</strong> typically experience a noticeable drop <strong>in</strong> performance.<br />

Research f<strong>in</strong>d<strong>in</strong>gs (e.g., Urhausen et al., 1998; Meeusen, Piacent<strong>in</strong>i,<br />

Busschaert, Buyse, DeSchutter & Stray-Gundersen, 2004) support that<br />

athletes experienc<strong>in</strong>g the overtra<strong>in</strong><strong>in</strong>g syndrome seem to suffer from a<br />

dysfunctional hypothalamic-pituitary-adrenal (HPA) axis response to<br />

exercise. This results <strong>in</strong> an altered hormonal response to <strong>in</strong>tense tra<strong>in</strong><strong>in</strong>g<br />

<strong>and</strong> competition. Recent f<strong>in</strong>d<strong>in</strong>gs (Meeusen et al., 2004) from research<br />

monitor<strong>in</strong>g hormonal reaction <strong>in</strong> athletes us<strong>in</strong>g a two-bout exercise protocol,<br />

to detect differences <strong>in</strong> tra<strong>in</strong><strong>in</strong>g adaptation status, suggest that<br />

hormonal variation witnessed <strong>in</strong> cortisol <strong>and</strong> adrenocorticotropic hormone<br />

(ACTH) levels, comb<strong>in</strong>ed with responses to exercise are <strong>in</strong>dicative<br />

of adaptive resources <strong>in</strong> an elite athlete. Lower ACTH <strong>and</strong> cortisol<br />

responses have been recorded <strong>in</strong> overtra<strong>in</strong>ed athletes.<br />

Cortisol variation represents an important marker of work<strong>in</strong>g capacity<br />

<strong>and</strong> performance level (Meeusen et al., 2004) <strong>and</strong> has been l<strong>in</strong>ked to<br />

changes <strong>in</strong> mood, sleep quality, sensory stimuli recognition, <strong>and</strong> to the<br />

ext<strong>in</strong>ction of previously acquired habits (i.e., active recovery). Cortisol<br />

is also related to many important physiological changes. The hormone<br />

is known to suppress the immune system. Because basal cortisol levels<br />

represent the endpo<strong>in</strong>t of the HPA axis, it has been suggested that basal<br />

cortisol levels may be used for tra<strong>in</strong><strong>in</strong>g monitor<strong>in</strong>g (e.g., Urhausen et al.,<br />

1998). Higher levels of basal cortisol have been l<strong>in</strong>ked to normal stress<br />

response to high-<strong>in</strong>tensity tra<strong>in</strong><strong>in</strong>g, while a drop <strong>in</strong> basal cortisol has<br />

been used as a marker of overtra<strong>in</strong><strong>in</strong>g (Lehmann et al., 1993). Us<strong>in</strong>g a<br />

two-bout exercise test to <strong>in</strong>vestigate ACTH as a marker of overtra<strong>in</strong><strong>in</strong>g<br />

<strong>and</strong> burnout, Meeusen <strong>and</strong> colleagues (2004) found hyperactivity<br />

<strong>in</strong> the HPA axis dur<strong>in</strong>g the morn<strong>in</strong>g bout followed by a depletion <strong>in</strong><br />

the ACTH pool (Urhausen et al., 1998) for the afternoon test. These<br />

f<strong>in</strong>d<strong>in</strong>gs suggest that a hypersensitivity of the pituitary followed by an<br />

exhaustion of resources is to be found <strong>in</strong> athletes suffer<strong>in</strong>g from severe<br />

overtra<strong>in</strong><strong>in</strong>g <strong>and</strong> burnout. Unfortunately, research efforts <strong>in</strong>vestigat<strong>in</strong>g<br />

tra<strong>in</strong><strong>in</strong>g adaptation us<strong>in</strong>g cortisol <strong>and</strong> ACTH as markers have failed<br />

to offer a consistent account of the processes <strong>in</strong>volved (for a review, see<br />

chaPter1.<strong>in</strong>vitedLectures<br />

Viru & Viru, 2001). When <strong>in</strong>vestigat<strong>in</strong>g pathological tra<strong>in</strong><strong>in</strong>g responses<br />

found <strong>in</strong> overtra<strong>in</strong>ed athletes, Urhausen <strong>and</strong> colleagues (1995) identified<br />

the <strong>in</strong>ability to susta<strong>in</strong> <strong>in</strong>tense exercise as an important symptom. Overtra<strong>in</strong>ed<br />

athletes are believed to be able to perform well at the beg<strong>in</strong>n<strong>in</strong>g<br />

of a race, or a hard tra<strong>in</strong><strong>in</strong>g session, but they experience problems susta<strong>in</strong><strong>in</strong>g<br />

their normal level of performance or even complet<strong>in</strong>g the actual<br />

exercise session. From this perspective, recent studies (e.g., Ronsen,<br />

Haug, Pederson & Bahr, 2001; Meeusen, 2004) have used two consecutive<br />

maximal exercise test protocols to <strong>in</strong>vestigate tra<strong>in</strong><strong>in</strong>g adaptation<br />

<strong>and</strong> maladaptation. They found that beyond the <strong>in</strong>formation provided<br />

by hormonal responses recorded dur<strong>in</strong>g the first bout of exercise, the<br />

<strong>in</strong>formation gathered from hormonal variation dur<strong>in</strong>g the second bout<br />

offered valuable <strong>in</strong>dication of an athlete’s recovery capacity <strong>and</strong> ability to<br />

complete a second bout normally.<br />

When elite swimmers are tired, fatigue may become a trigger for<br />

a shift <strong>in</strong> self-regulation from <strong>in</strong>tr<strong>in</strong>sic to more extr<strong>in</strong>sic criteria. For<br />

example, Davis, Botterill, <strong>and</strong> MacNeill (2002) have found that an<br />

<strong>in</strong>crease <strong>in</strong> fatigue levels leads to a neurochemical response produc<strong>in</strong>g<br />

a series of mood disturbances. It is hypothesized <strong>in</strong> this study that a<br />

recorded shift from <strong>in</strong>tr<strong>in</strong>sic motivation to <strong>in</strong>trojected regulation may<br />

<strong>in</strong>dicate a sign that the swimmer is experienc<strong>in</strong>g significant fatigue.<br />

When this happens, it is reasonable to surmise that the tired swimmer<br />

functions on automatic pilot, becomes emotionally <strong>and</strong> mentally more<br />

detached from the purpose of quality action <strong>and</strong> experiences a shift <strong>in</strong><br />

self-regulation. At this po<strong>in</strong>t the swimmer may be more likely to follow<br />

a coach’s plan without any question<strong>in</strong>g or adaptation. In an attempt to<br />

better underst<strong>and</strong> the determ<strong>in</strong>ants of healthy tra<strong>in</strong><strong>in</strong>g response <strong>in</strong> elite<br />

swimmers, the aim of this study was to look at how motivation can go<br />

awry <strong>and</strong> lead to overtra<strong>in</strong><strong>in</strong>g <strong>and</strong> burnout. Overtra<strong>in</strong><strong>in</strong>g <strong>and</strong> burnout<br />

share diagnosis characteristics such as performance loss, fatigue, exhaustion,<br />

<strong>and</strong> mood disturbance (Kenttä & Hassmén, 2002). However, when<br />

a swimmer is overtra<strong>in</strong>ed, motivation rema<strong>in</strong>s, whereas the burned out<br />

swimmer experienc<strong>in</strong>g a shift <strong>in</strong> quality of motivation may devalue sport<br />

<strong>and</strong> express cynicism. Most cl<strong>in</strong>ical problems of overreach<strong>in</strong>g <strong>and</strong> overtra<strong>in</strong><strong>in</strong>g<br />

are observed <strong>in</strong> swimmers tra<strong>in</strong><strong>in</strong>g with a high metabolic load<br />

of more than 4,000 kilocalories per day (Ste<strong>in</strong>acker & Lehmann, 2002).<br />

Chronic stress <strong>and</strong> overtra<strong>in</strong><strong>in</strong>g are expected to cause <strong>in</strong>creases <strong>in</strong> basal<br />

cortisol, which can be <strong>in</strong>terpreted as an <strong>in</strong>dication of metabolic problems.<br />

Therefore it is hypothesized that maladaptive motivation shifts,<br />

together with variation <strong>in</strong> basal cortisol <strong>in</strong> elite swimmers, can better<br />

predict overtra<strong>in</strong><strong>in</strong>g <strong>and</strong> burnout at season’s end.<br />

Methods<br />

An elite American collegiate swim team (female=21; male=32) was recruited<br />

to participate <strong>in</strong> this study. Questionnaires assess<strong>in</strong>g motivation<br />

were used together with a two-bout exercise test at three time po<strong>in</strong>ts<br />

dur<strong>in</strong>g the year, correspond<strong>in</strong>g to the easy (September), very hard (November)<br />

<strong>and</strong> peak<strong>in</strong>g time (March) periods of the collegiate swimm<strong>in</strong>g<br />

season. A protocol of 6x200m <strong>in</strong>tervals dur<strong>in</strong>g morn<strong>in</strong>g (07.00-08.30)<br />

<strong>and</strong> afternoon (14.00-15.30) tra<strong>in</strong><strong>in</strong>g practices was used at each of the<br />

time po<strong>in</strong>ts. Venous blood was drawn before <strong>and</strong> after each sets of <strong>in</strong>tervals,<br />

as well as the follow<strong>in</strong>g morn<strong>in</strong>g, <strong>and</strong> was assayed for cortisol by<br />

radio immune assays. A sum score for basal cortisol was put together by<br />

us<strong>in</strong>g cortisol levels for the early morn<strong>in</strong>g blood draw, the after noon<br />

blood draw before the second exercise bout <strong>and</strong> the day after morn<strong>in</strong>g<br />

blood draw. Basal cortisol <strong>in</strong> November <strong>and</strong> March were thereafter<br />

subtracted from the September score to look at how variation can<br />

predict maladaptive tra<strong>in</strong><strong>in</strong>g response. In September, achievement goals<br />

(POSQ; Roberts & al., 1998) <strong>and</strong> quality of motivation (SMS; Pelletier<br />

& al., 1997) were measured. Perception of the motivational climate<br />

(PMCSQ; Seifriz, Chi, & Duda, 1992) <strong>and</strong> athlete burnout (ABQ;<br />

Raedeke & Smith, 2002) were recorded <strong>in</strong> November. Athlete burnout<br />

<strong>and</strong> quality of motivation (SIMS; St<strong>and</strong>age & al., 2003) were aga<strong>in</strong> recorded<br />

at season’s end. Performance markers (improvement <strong>in</strong> personal<br />

bests) <strong>and</strong> total tra<strong>in</strong><strong>in</strong>g loads <strong>and</strong> <strong>in</strong>tensity were also recorded.<br />

23


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

One of the primary purposes of this study was to <strong>in</strong>vestigate whether<br />

motivation was related to the development of overtra<strong>in</strong><strong>in</strong>g <strong>and</strong> burnout<br />

<strong>in</strong> elite swimmers. No significant correlation was found between<br />

achievement goal orientations <strong>in</strong> September <strong>and</strong> burnout levels at midseason<br />

or season’s end. In contrast, strong correlations were found between<br />

perceptions of performance climate on the team <strong>and</strong> feel<strong>in</strong>gs of<br />

burnout <strong>in</strong> November (.570, p


Biomechanical Services <strong>and</strong> Research for Top Level<br />

Swimm<strong>in</strong>g: the Australian Institute of Sport Model<br />

Mason, B.r.<br />

Australian Institute of Sport, Australia<br />

This keynote address paper reviews the Australian Institute of Sport’s<br />

<strong>in</strong>fluence on competitive swimm<strong>in</strong>g with<strong>in</strong> Australia. This <strong>in</strong>volves the<br />

effective utilis<strong>in</strong>g of biomechanical servic<strong>in</strong>g <strong>and</strong> research tools. The<br />

A.I.S. was established <strong>in</strong> 1981 as a consequence of the nation’s poor<br />

performance at the 1976 Olympic Games. After its establishment, up<br />

to eleven years passed before Australian swimm<strong>in</strong>g performances were<br />

positively <strong>in</strong>fluenced by the efforts of the national sports <strong>in</strong>stitute. The<br />

early days of the <strong>in</strong>stitute <strong>in</strong>volved primarily applied servic<strong>in</strong>g. This later<br />

evolved <strong>in</strong>to a greater role for research projects. Most of the early research<br />

<strong>in</strong>volved the development of specialised analysis systems which<br />

<strong>in</strong> turn resulted <strong>in</strong> the capability to carry out more fundamental research.<br />

Some of the research projects are discussed with<strong>in</strong> the paper. The ma<strong>in</strong><br />

swimm<strong>in</strong>g biomechanics research projects <strong>in</strong>itiatives at the A.I.S. are<br />

<strong>in</strong>: drag analysis, start <strong>and</strong> turn <strong>in</strong>vestigations <strong>and</strong> computation fluid<br />

dynamics.<br />

Keywords: <strong>Biomechanics</strong>, swimm<strong>in</strong>g, servic<strong>in</strong>g, research, Australian<br />

Institute of sport<br />

At the 1956 Melbourne Olympic Games, Australia won 35 medals, the<br />

third highest number of medals of all nations compet<strong>in</strong>g. Dur<strong>in</strong>g the<br />

1960 Rome Olympics, Australia was fifth <strong>in</strong> the medal tally with 22<br />

medals <strong>and</strong> <strong>in</strong> the 1964 Tokyo Olympics, Australia was eighth with 18<br />

medals. By the 1976 Montreal Olympics, Australia had slipped to 32 nd<br />

<strong>in</strong> the <strong>in</strong>ternational medal tally with only 5 medals <strong>in</strong>clud<strong>in</strong>g no gold.<br />

The Australian Institute of Sport (A.I.S.) was established <strong>in</strong> Canberra<br />

dur<strong>in</strong>g 1981 by the Australian Government as a consequence of several<br />

consultancy reports that were completed after the 1976 Montreal<br />

Olympics <strong>and</strong> <strong>in</strong>itiated as a result of Australia’s poor performance <strong>in</strong><br />

those Olympic Games. These reports <strong>in</strong>dicated that if Australia wanted<br />

to rega<strong>in</strong> its sport<strong>in</strong>g em<strong>in</strong>ence, a government funded <strong>in</strong>stitute of sport<br />

needed to be established to assist <strong>in</strong> the development of Australia’s elite<br />

sportsmen <strong>and</strong> sports women. By the end of 1982, the A.I.S. had eight<br />

residential sports <strong>and</strong> a sport science medic<strong>in</strong>e centre with all the traditional<br />

sport science discipl<strong>in</strong>es represented. However, over these first<br />

few years, the services that were able to be provided were split over all<br />

sports with only a s<strong>in</strong>gle scientist <strong>in</strong> each discipl<strong>in</strong>e to provide m<strong>in</strong>imal<br />

service for each <strong>in</strong>stitute sport.<br />

Competitive swimm<strong>in</strong>g is probably Australia’s premier Olympic<br />

sport, as this is traditionally where Australia w<strong>in</strong>s most of its Olympic<br />

medals. Table 1 provides <strong>in</strong>sight as to Australia’s performances <strong>in</strong> competitive<br />

swimm<strong>in</strong>g, before <strong>and</strong> follow<strong>in</strong>g the development of the A.I.S.<br />

The table also provides a reason for variations to trends over the period<br />

<strong>in</strong> the Olympic medal tally for each Olympic Games.<br />

On observation of the trend <strong>in</strong> the Olympic swimm<strong>in</strong>g medal tally over<br />

the period; it can readily be identified that a longitud<strong>in</strong>al relationship<br />

existed between Australia’s Olympic swimm<strong>in</strong>g medal tallies at successive<br />

Olympic Games <strong>and</strong> the establishment of the A.I.S. It was also<br />

quite obvious that follow<strong>in</strong>g the establishment of the national sports<br />

<strong>in</strong>stitute there was a period of 11 years before Australia was able to reap<br />

the rewards that resulted from the A.I.S. <strong>in</strong>volvement <strong>in</strong> the development<br />

of Australia’s elite swimm<strong>in</strong>g talent.<br />

chaPter1.<strong>in</strong>vitedLectures<br />

Table 1. Australia’s Swimm<strong>in</strong>g medal tally from the 1956 Olympics to<br />

the 2008 Beij<strong>in</strong>g Olympics<br />

Olympics Australian Medal tally Explanation for Variance<br />

1956 14<br />

1960 13<br />

1964 9<br />

1968 8<br />

1972 10 Shane Gould = 5 medals<br />

1976 1<br />

1980 7 Moscow boycott<br />

1981 A.I.s. established<br />

1984 12 Los Angeles boycott<br />

1988 3<br />

1992 9<br />

1996 12<br />

2000 18<br />

2004 15<br />

2008 20<br />

My orig<strong>in</strong>al appo<strong>in</strong>tment <strong>in</strong> 1982 was as the head of the A.I.S. <strong>Biomechanics</strong><br />

department. Throughout this early period of about five years, I<br />

was responsible for the biomechanical servic<strong>in</strong>g of all the <strong>in</strong>stitute sports<br />

with only a support officer to assist me. General commercial biomechanics<br />

equipment was used <strong>in</strong> servic<strong>in</strong>g, rather than specialized sport analysis<br />

equipment. For swimm<strong>in</strong>g servic<strong>in</strong>g, underwater high speed c<strong>in</strong>e film<br />

<strong>and</strong> video was used to capture athlete performance dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g <strong>and</strong><br />

this was used with subjective analysis to assist the coach <strong>and</strong> swimmer.<br />

Dur<strong>in</strong>g the next five years another biomechanist, a support officer <strong>and</strong><br />

a technician were appo<strong>in</strong>ted to the department. This enabled greater specialization<br />

for the servic<strong>in</strong>g of each sport. Each biomechanist now only<br />

serviced half the number of <strong>in</strong>stitute sports <strong>and</strong> this resulted <strong>in</strong> more specialized<br />

servic<strong>in</strong>g for each sport. However dur<strong>in</strong>g this period other sports<br />

were also added to the A.I.S. portfolio. Although research projects were<br />

<strong>in</strong>frequently completed to identify solutions to particular problems posed<br />

by the coaches, the vast majority of the biomechanics department’s role<br />

was directed toward applied servic<strong>in</strong>g. One swimm<strong>in</strong>g related research<br />

project completed dur<strong>in</strong>g this period <strong>in</strong>volved the identification of acceleration<br />

profiles with<strong>in</strong> breaststroke <strong>and</strong> butterfly swimm<strong>in</strong>g. This research<br />

identified a catch the wave phase <strong>in</strong> these strokes, with the better swimmers<br />

more able to utilize propulsion from catch<strong>in</strong>g the wave.<br />

More staff were added to the biomechanics department <strong>in</strong> the early<br />

1990’s, <strong>in</strong>clud<strong>in</strong>g another biomechanist, several post graduate scholarship<br />

holders <strong>and</strong> another technical officer. This resulted <strong>in</strong> the formation of<br />

biomechanics teams that specialized <strong>in</strong> the servic<strong>in</strong>g of particular sports.<br />

It was dur<strong>in</strong>g this period that research to develop specialized analysis<br />

systems for particular sports, began to occur. In swimm<strong>in</strong>g, a large competition<br />

analysis system was developed that could analyze many competitors<br />

<strong>in</strong> the one race. The system was <strong>in</strong>itially designed to assist A.I.S. swimmers<br />

but toward the mid 1990’s was commissioned by the national swimm<strong>in</strong>g<br />

body to analyze all swimmers compet<strong>in</strong>g <strong>in</strong> the national championships<br />

held each year. This large analysis system was used for analyses<br />

dur<strong>in</strong>g national swimm<strong>in</strong>g championships through 2004. Throughout<br />

this period the “big analysis system” was cont<strong>in</strong>ually undergo<strong>in</strong>g ref<strong>in</strong>ement<br />

<strong>and</strong> was commissioned by the competition management of swim<br />

meets to be used for the analyses of all swimmers <strong>in</strong> the 1998 FINA<br />

World championships <strong>in</strong> Perth, the 1999 Pan Pacific Championships<br />

25


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

<strong>in</strong> Sydney, the 2000 Sydney Olympic Games <strong>and</strong> the 2002 Commonwealth<br />

Games <strong>in</strong> Manchester.<br />

Follow<strong>in</strong>g the successful analyses of swimmers with the “Big System”<br />

dur<strong>in</strong>g the mid 1990’s <strong>and</strong> the need for coaches to have similar<br />

analysis <strong>in</strong>formation available to them between sessions dur<strong>in</strong>g <strong>in</strong>ternational<br />

competition meets abroad, a portable competition analysis system<br />

called SWAN was developed. Each SWAN system could analyze only<br />

a s<strong>in</strong>gle swimmer with<strong>in</strong> each race, but it was portable enough to take<br />

overseas with the team. Dur<strong>in</strong>g the late 1990’s <strong>and</strong> early 2000’s the<br />

SWAN analysis system accompanied the Australian Swim team to most<br />

<strong>in</strong>ternational competition meets. Also dur<strong>in</strong>g this period, the <strong>in</strong>itial<br />

development of a start <strong>and</strong> turn SWAN analysis system was developed<br />

to be used <strong>in</strong> a tra<strong>in</strong><strong>in</strong>g environment. The output from this system <strong>in</strong>cluded<br />

underwater visual video images <strong>and</strong> both tim<strong>in</strong>g <strong>and</strong> force analyses.<br />

However, the output for the coach was not <strong>in</strong> a concise form <strong>and</strong><br />

was presented <strong>in</strong> a number of formats <strong>in</strong>clud<strong>in</strong>g video, hard copy paper<br />

pr<strong>in</strong>t outs of data <strong>and</strong> hard copy graphs. Probably the greatest barrier<br />

to development of advanced analysis systems dur<strong>in</strong>g this period was the<br />

level of technology that was available for <strong>in</strong>clusion <strong>in</strong>to such systems.<br />

Prior to the Sydney Olympic Games, the A.I.S. sport science <strong>and</strong> medic<strong>in</strong>e<br />

departments provided most of the support to the Australian national<br />

swim team. It was also dur<strong>in</strong>g this period that each of the state governments<br />

established state <strong>in</strong>stitutes of sport. With the approach of the 2000<br />

Olympic Games there was <strong>in</strong>creased Australian Government fund<strong>in</strong>g to<br />

prepare Australian elite athletes for the Sydney games. Dur<strong>in</strong>g this period,<br />

the state <strong>in</strong>stitutes were able to obta<strong>in</strong> federal fund<strong>in</strong>g for elite sports performance<br />

enhancement, such that they were now perform<strong>in</strong>g many of the<br />

functions previously provided only by the national sports <strong>in</strong>stitute.<br />

In 2006, the A.I.S. embarked on a new concept of direct<strong>in</strong>g resources<br />

<strong>in</strong>to particular sports, such that the A.I.S. would lead the way <strong>in</strong> Australia<br />

<strong>in</strong> these sports by concentrat<strong>in</strong>g its efforts <strong>in</strong> set directions. The<br />

Aquatics, Test<strong>in</strong>g Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Research Unit (A.T.T.R.U.) was established<br />

<strong>in</strong> January, 2006 <strong>and</strong> it operated out of a new 10 lane, three metre<br />

consistent depth, 50 metre long technology pool. The A.T.T.R.U. was to<br />

work with just aquatic sports <strong>and</strong> had as it fundamental role the servic<strong>in</strong>g<br />

<strong>and</strong> research for both A.I.S. swim teams <strong>and</strong> the Australian National<br />

swim team. Along with this development was a concentration of biomechanical<br />

<strong>and</strong> technology resources <strong>in</strong>to elite Australian Swimm<strong>in</strong>g.<br />

Initially the research objective of the A.T.T.R.U. was to develop state<br />

of the art analysis systems. These systems would operate <strong>in</strong> a tra<strong>in</strong><strong>in</strong>g<br />

environment <strong>and</strong> would provide almost immediate feedback to coaches<br />

<strong>and</strong> swimmers. A system called Wetplate (Figure 1) was developed that<br />

provided the coach with immediate feedback analysis of starts, turns<br />

<strong>and</strong> relay changeovers <strong>in</strong> a concise computer generated visual format.<br />

Additional to the Wetplate analysis equipment, was another system designed<br />

to look particularly at the free swimm<strong>in</strong>g element of the sport.<br />

This was the active drag analysis system <strong>and</strong> provided as feedback to the<br />

coach <strong>and</strong> swimmer, a video image of the swimmer’s actions along with<br />

a mov<strong>in</strong>g graph of the propulsive force profile generated by the swimmer’s<br />

technique.<br />

Figure 1. The Wetplate system.<br />

26<br />

It became clear for the A.T.T.R.U. at this po<strong>in</strong>t <strong>in</strong> time that the major<br />

research focus of the unit was on equipment <strong>and</strong> system development.<br />

This <strong>in</strong> itself is a legitimate research area as it <strong>in</strong>volves the br<strong>in</strong>g<strong>in</strong>g together<br />

of different technologies to produce a system that is able to provide<br />

<strong>in</strong>sight <strong>in</strong>to performance enhancement. Such systems are generally<br />

not available commercially, so to provide the <strong>in</strong>formation to the swimmer<br />

<strong>and</strong> coach there needed to be commercially available equipment,<br />

such as Gig E cameras, computers <strong>and</strong> transducers that when assembled<br />

together to form a system were able to provide what was required. The<br />

analysis of skills needed pert<strong>in</strong>ent <strong>and</strong> accurate <strong>in</strong>formation concern<strong>in</strong>g<br />

the execution of the skill <strong>in</strong> an immediate time frame. The analysis<br />

results had also to be presented <strong>in</strong> a concise format that could easily be<br />

<strong>in</strong>terpreted by the coach <strong>and</strong> swimmer. The evolution of these systems<br />

would result <strong>in</strong> questions by the coach that would result <strong>in</strong> more tradition<br />

fact f<strong>in</strong>d<strong>in</strong>g research projects.<br />

By 2008, the Wetplate <strong>and</strong> Active Drag Analysis systems were well<br />

entrenched <strong>in</strong>to the tra<strong>in</strong><strong>in</strong>g program of the A.I.S. swimm<strong>in</strong>g squad<br />

<strong>and</strong> were regularly called upon at event camps <strong>and</strong> national swim team<br />

camps. At these camps, Swimm<strong>in</strong>g Australia held <strong>in</strong>tensive preparation<br />

sessions for elite Australian <strong>in</strong>ternational swimmers. Because of the vast<br />

amount of <strong>in</strong>formation provided by the Wetplate system, it took quite<br />

some time to identify those parameters <strong>and</strong> underst<strong>and</strong> the <strong>in</strong>teraction<br />

of these parameters, to make a significant difference to improve a swimmer’s<br />

performance. Small research projects were at first carried out by<br />

the post graduate scholarship holders to do just that. Some such projects<br />

<strong>in</strong>volved research<strong>in</strong>g the optimal angle of the knee to be utilized <strong>in</strong><br />

maximiz<strong>in</strong>g propulsion off the wall <strong>in</strong> turns. Another project <strong>in</strong>volved<br />

<strong>in</strong>vestigat<strong>in</strong>g the propulsive ga<strong>in</strong>s to be made by us<strong>in</strong>g the new FINA<br />

approved start<strong>in</strong>g blocks with the kick plate. It soon became apparent<br />

that to optimize the learn<strong>in</strong>g <strong>and</strong> performance enhancement potential<br />

of the new swim analysis systems, that the swimmer’s coach needed to<br />

play a particularly active role with the swimmer dur<strong>in</strong>g feedback at the<br />

Wetplate analysis session. Feedback by the coach was more readily accepted<br />

than by the biomechanist, but this model required that the coach<br />

underst<strong>and</strong> what was meant by each parameter assessed, underst<strong>and</strong><br />

how each parameter related to performance <strong>and</strong> be able to provide appropriate<br />

<strong>in</strong>formation to the swimmer that could readily be adopted <strong>and</strong><br />

<strong>in</strong>corporated <strong>in</strong>to the swimmer’s actions dur<strong>in</strong>g skill performance.<br />

The A.T.T.R.U. also f<strong>in</strong>ancially supported <strong>and</strong> accommodated several<br />

Ph.D. scholarship programmes <strong>in</strong> conjunction with an Australian<br />

University. In these Ph.D. programmes, part fund<strong>in</strong>g came from the<br />

A.I.S. while other fund<strong>in</strong>g came from the university. These Ph.D. programmes<br />

<strong>in</strong>vestigated research topics of <strong>in</strong>terest to elite swimm<strong>in</strong>g performance.<br />

One such Ph.D. project researched methods by which the<br />

active drag analysis could be utilized to present the propulsive force profiles<br />

of swimmers, <strong>in</strong> conjunction with video footage of their technique,<br />

to identify <strong>and</strong> elim<strong>in</strong>ate technique <strong>in</strong>efficiencies for the elite swimmers<br />

that were analyzed. The procedures developed were able to be used <strong>in</strong> all<br />

the swimm<strong>in</strong>g strokes <strong>and</strong> resulted <strong>in</strong> identify<strong>in</strong>g problems associated<br />

with such actions as breath<strong>in</strong>g <strong>and</strong> asymmetry <strong>in</strong> the swimmer’s technique.<br />

In freestyle swimm<strong>in</strong>g the active drag analysis procedures were<br />

able to identify that most of the propulsive action of the arm dur<strong>in</strong>g the<br />

first half of the underwater stroke was utilized to compensate for the<br />

forward movement of the recovery arm above the water. It was the last<br />

half the stroke that produced the forward acceleration of the swimmer’s<br />

body. The <strong>in</strong>formation from the active drag analysis focused upon the<br />

total force produced by the entire body as a whole, rather than solely<br />

by the arms or legs. Another Ph.D. research project focused upon how<br />

best to utilize the new kick plate start<strong>in</strong>g blocks. The Wetplate system<br />

enabled the data for this project to be analyzed. Recently, a post doctoral<br />

researcher from Irel<strong>and</strong> was funded by the A.I.S. to work with<strong>in</strong> the<br />

A.T.T.R.U. with the objective to analyze the most effective placement<br />

of the dolph<strong>in</strong> kick <strong>in</strong> breaststroke starts <strong>and</strong> turns. This research project<br />

arose as a consequence of the new FINA rules for Breaststroke.<br />

The A.T.T.R.U. has recently focused upon active drag analysis as


it provides valuable <strong>in</strong>formation about the free swimm<strong>in</strong>g component<br />

of the sport. The mean active drag of a swimmer mov<strong>in</strong>g at a constant<br />

velocity is equal <strong>in</strong> magnitude, but opposite <strong>in</strong> direction to the mean<br />

propulsive force produced by the swimmer. The method of active drag<br />

assessment, used at the A.I.S., may only be performed at the swimmer’s<br />

maximum swimm<strong>in</strong>g velocity. The assumption made to calculate a value<br />

for active drag is that there is an equal power output by the swimmer <strong>in</strong><br />

both free swimm<strong>in</strong>g at the maximum swim velocity <strong>and</strong> <strong>in</strong> the assisted<br />

condition where the swimmer applies maximum effort to stay with the<br />

tow. The method used is similar to the velocity perturbation method<br />

(VPM) developed <strong>in</strong> Russia (Kolmogorov & Duplishcheva, 1992) but<br />

<strong>in</strong>stead of resist<strong>in</strong>g the swimmer, the A.I.S. method assists the swimmer<br />

by pull<strong>in</strong>g the swimmer through the water at a slightly higher velocity<br />

than the swimmer’s maximum swim velocity. However, the value of<br />

the mean active drag for the swimmer is only pert<strong>in</strong>ent at the swimmer’s<br />

maximum swim velocity. Therefore, the active drag value for a<br />

swimmer can only be compared with that of another swimmer if both<br />

swimmers had identical maximum swim velocities. If swimmers had<br />

different maximum swim velocities their active drag values could not be<br />

compared, as velocity plays a major role <strong>in</strong> the magnitude of the active<br />

drag. The question arose, could a swimmer’s active drag be estimated for<br />

any given speed if the active drag for the swimmer’s maximum speed was<br />

known. . Recent research <strong>in</strong> the A.T.T.R.U. (Mason et al., 2009) that<br />

looked at the relationship between active drag <strong>and</strong> passive drag at the<br />

swimmer’s maximum velocity found a very high relationship between<br />

the two. The measurement of passive drag can be readily measured at<br />

different velocities with little error. The problem that exists is that active<br />

drag cannot be measured directly but may be calculated us<strong>in</strong>g other<br />

<strong>in</strong>direct measurements which may produce a wide range of values. A<br />

research project to <strong>in</strong>vestigate whether active drag could be estimated<br />

from a force measurement obta<strong>in</strong>ed <strong>in</strong> fully tethered swimm<strong>in</strong>g <strong>in</strong>dicated<br />

this was not the case (Mason et al., 2009). Therefore, could an<br />

equation that represented the magnitude of a swimmer’s passive drag<br />

through a range of swim velocities be useful <strong>in</strong> obta<strong>in</strong><strong>in</strong>g an estimation<br />

for active drag over a range of swim velocities. The equation for passive<br />

( b⋅V<br />

)<br />

drag was established as an exponential equation F = a ⋅ e , where<br />

a <strong>and</strong> b are constants for a particular swimmer. A similar exponential<br />

equation with a higher value for a could also be used to represent the<br />

active drag of the swimmer over a similar range of velocities. The constant<br />

p a (passive) reflects the more <strong>in</strong>nate characteristics of the <strong>in</strong>dividual<br />

swimmer <strong>and</strong> their suitability to aquatics motion. The constant<br />

aa− p (active- passive) reflects the efficiency of the swimmer’s technique.<br />

In both cases, the lower the constant’s value, the better suited the swimmer<br />

to aquatics motion or to technical efficiency. The aa− p <strong>and</strong> the p a<br />

therefore provide an <strong>in</strong>dex which may be used to evaluate a swimmer’s<br />

capabilities. Huub Toussa<strong>in</strong>t spent three weeks as a visit<strong>in</strong>g researcher<br />

with the A.T.T.R.U. <strong>in</strong> early 2009. This was followed later on that year<br />

with a visit by A.T.T.R.U. staff to Innosport <strong>in</strong> E<strong>in</strong>dhoven. Dur<strong>in</strong>g<br />

this visit, an active drag research project was conducted to <strong>in</strong>vestigate<br />

differences between the A.I.S. method by which active drag is estimated<br />

<strong>and</strong> the measurement of active drag (MAD) method of active drag assessment.<br />

The A.T.T.R.U. has a three year relationship with the mathematical<br />

division of the Commonwealth Science <strong>and</strong> Industrial Research Organisation<br />

(C.S.I.R.O.) to develop a system by which computational<br />

fluid dynamics (CFD) may be utilized to evaluate proposed changes<br />

to a swimmer’s technique <strong>in</strong> a computer environment, prior to mak<strong>in</strong>g<br />

a physical change <strong>in</strong> the swimmer’s technique. Physically chang<strong>in</strong>g the<br />

technique of a swimmer is a difficult <strong>and</strong> a time consum<strong>in</strong>g process.<br />

Even when changes are made, the result may possibly cause a deterioration<br />

rather than an improvement <strong>in</strong> the swimmer’s performance <strong>and</strong><br />

such a change may not be easily reversed. It makes sense to evaluate<br />

the benefits of proposed changes of technique <strong>in</strong> a computer environment<br />

rather than attempt<strong>in</strong>g to make physical changes to the swimmer’s<br />

technique without such evaluation. The CSIRO are us<strong>in</strong>g a CFD pro-<br />

chaPter1.<strong>in</strong>vitedLectures<br />

gramme which utilizes smooth particle hydrodynamics (SPH) to model<br />

the swimmers actions <strong>in</strong> water. The A.T.T.R.U. have obta<strong>in</strong>ed a body<br />

scanner to be able to accurately represent the physical characteristics of<br />

each swimmer <strong>in</strong> the CFD computer <strong>and</strong> are presently attempt<strong>in</strong>g to<br />

f<strong>in</strong>d a reliable method by which the 3D k<strong>in</strong>ematic model of each swimmer’s<br />

actions are able to be recorded for the CFD computer programme.<br />

Australian Swimm<strong>in</strong>g itself has been organiz<strong>in</strong>g competition<br />

analysis to be performed at national Championships s<strong>in</strong>ce 2004. The<br />

A.T.T.R.U. is at present build<strong>in</strong>g a new portable competition analysis<br />

system utilis<strong>in</strong>g GigE cameras. It is proposed that the new Platypus<br />

system will cut down post analysis process<strong>in</strong>g by a factor of ten <strong>and</strong> will<br />

be able to provide much more accurate data to the coach than the competition<br />

analysis systems that are used at the present time.<br />

This paper has attempted to provide an overview of where the A.I.S.<br />

is head<strong>in</strong>g <strong>in</strong> the pursuit of biomechanical systems that will enhance<br />

performance <strong>and</strong> enable quality research to f<strong>in</strong>d solutions to questions<br />

that are be<strong>in</strong>g asked <strong>in</strong> elite competitive swimm<strong>in</strong>g. The paper commenced<br />

with a brief history as to why the A.I.S. was established <strong>and</strong><br />

followed this with where the A.I.S. is mov<strong>in</strong>g <strong>in</strong> an attempt to provide<br />

Australian elite swimmers with systems, unique <strong>in</strong> the world, that will<br />

enhance performance <strong>in</strong> swimm<strong>in</strong>g.<br />

reFerences<br />

Kolmogorov S.V., & Duplishcheva O.A. (1992). Active Drag, Useful<br />

Mechanical Power Output <strong>and</strong> Hydrodynamic Force Coefficient <strong>in</strong><br />

Different Swimm<strong>in</strong>g Strokes at Maximum Velocity. Journal of <strong>Biomechanics</strong>,<br />

25, 3, 311-318.<br />

Mason BR, Formosa DP, Raleigh V. (2009). The use of passive drag<br />

to <strong>in</strong>terpret variations <strong>in</strong> active drag measurements. Harrison AJ,<br />

Anderson R, Kenny I, editors. Proceed<strong>in</strong>gs of the XXVII International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports, Limerick, Irel<strong>and</strong>, 452-455.<br />

Mason B.R., Formosa D.P., & Rollason S. (2009). A comparison between<br />

the values obta<strong>in</strong>ed from active drag analysis compared to<br />

forces produced <strong>in</strong> tethered swimm<strong>in</strong>g. Harrison AJ, Anderson R,<br />

Kenny I, editors. Proceed<strong>in</strong>gs of the XXVII International Symposium on<br />

<strong>Biomechanics</strong> <strong>in</strong> Sports, Limerick, Irel<strong>and</strong>, 86-89.<br />

27


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Aquatic Tra<strong>in</strong><strong>in</strong>g <strong>in</strong> Rehabilitation <strong>and</strong> Preventive<br />

<strong>Medic<strong>in</strong>e</strong><br />

Pr<strong>in</strong>s, J.<br />

Department of K<strong>in</strong>esiology <strong>and</strong> Rehabilitation Science, University of Hawaii,<br />

Honolulu, Hawaii. U.S.A.<br />

IntroductIon<br />

Aquatic physical rehabilitation is now recognized <strong>and</strong> utilized as a “procedure,”<br />

rather than a modality. The <strong>in</strong>creased focus can be attributed <strong>in</strong><br />

part to its evolution from the limited conf<strong>in</strong>es of “Hubbard Tanks,” to<br />

the larger venues of swimm<strong>in</strong>g pools. The larger exercis<strong>in</strong>g areas serve<br />

as a venue for perform<strong>in</strong>g a greater variety of exercises, <strong>in</strong>clud<strong>in</strong>g those<br />

that require susta<strong>in</strong>ed propulsive movements.<br />

The physical properties of water provide a unique environment for<br />

improv<strong>in</strong>g strength, flexibility, <strong>and</strong> cardiovascular condition<strong>in</strong>g. Although<br />

exercise <strong>in</strong> the water, <strong>in</strong>clud<strong>in</strong>g formal swimm<strong>in</strong>g strokes have<br />

historically been used for the recovery from <strong>in</strong>jury, there is now an <strong>in</strong>creased<br />

focus on <strong>in</strong>corporat<strong>in</strong>g specific aquatic exercise protocols for<br />

treat<strong>in</strong>g persons with acute or chronic cl<strong>in</strong>ical conditions, <strong>in</strong>clud<strong>in</strong>g persons<br />

with permanent physical disabilities (Becker & Cole 1994; Cole<br />

et al. 2004; Genuario & Vegso 1990; LeFort 1994; Pr<strong>in</strong>s & Cutner<br />

1999); The<strong>in</strong> & Brody 1998).<br />

oVerVIeW And PrecAutIons<br />

As a rule, voluntary movements <strong>in</strong> the water are viewed as “learned<br />

skills” requir<strong>in</strong>g <strong>in</strong>struction <strong>and</strong> tak<strong>in</strong>g time to develop. Furthermore,<br />

k<strong>in</strong>esthetic feedback provided by the water is subtle, <strong>and</strong> therefore, effective<br />

movement patterns need to be practiced <strong>and</strong> closely monitored.<br />

A person who has previous aquatic experience may be expected to beg<strong>in</strong><br />

aquatic physical therapy with less apprehension than someone unfamiliar<br />

with the water. However, past experience can be an impediment to recovery<br />

because there rema<strong>in</strong>s the risk of “overuse” or <strong>in</strong> the case of recovery<br />

from <strong>in</strong>jury, the person may revert back to familiar swimm<strong>in</strong>g stroke patterns<br />

that may exacerbate symptoms <strong>and</strong> prolong the recovery period.<br />

The recommendation, therefore, is that when <strong>in</strong>itiat<strong>in</strong>g aquatic exercise<br />

follow<strong>in</strong>g <strong>in</strong>jury, participants rema<strong>in</strong> under the supervision of a<br />

tra<strong>in</strong>ed cl<strong>in</strong>ician or aquatic specialist until such time as they are pa<strong>in</strong><br />

free <strong>and</strong> able to cont<strong>in</strong>ue <strong>in</strong>dependently with their rout<strong>in</strong>es, <strong>and</strong> when<br />

warranted, transition to l<strong>and</strong>-based physical therapy (Pr<strong>in</strong>s & Cutner<br />

1999; The<strong>in</strong> & Brody 1998).<br />

the AdVAntAGes oF eXercIsInG In the WAter<br />

Two important physical properties of water; buoyancy <strong>and</strong> viscosity, are<br />

key elements <strong>in</strong> design<strong>in</strong>g effective aquatic exercises.<br />

The Force of Buoyancy <strong>and</strong> its Effect on Weight Bear<strong>in</strong>g Dur<strong>in</strong>g Immersion:<br />

The advantage derived from buoyancy is direct; when a person enters<br />

the water there is an immediate reduction <strong>in</strong> the effects of gravity on the<br />

body. The buoyant force of water decreases the effective weight of an <strong>in</strong>dividual<br />

<strong>in</strong> proportion to the degree of immersion. The ability to control<br />

jo<strong>in</strong>t compression forces by vary<strong>in</strong>g degrees of immersion is of particular<br />

benefit <strong>in</strong> the treatment of persons who demonstrate <strong>in</strong>tolerance to axial<br />

load<strong>in</strong>g, particularly <strong>in</strong> the sp<strong>in</strong>e, hips, <strong>and</strong> lower extremities. By monitor<strong>in</strong>g<br />

the depths at which functional movements such as walk<strong>in</strong>g <strong>and</strong><br />

stepp<strong>in</strong>g are performed, the effect of gravity can be re-<strong>in</strong>troduced which<br />

<strong>in</strong> turn promotes effective recovery through gradual strengthen<strong>in</strong>g (Cole<br />

et al. 2004; Pr<strong>in</strong>s & Cutner 1999).<br />

Viscosity of Water <strong>and</strong> Muscle Strengthen<strong>in</strong>g: The viscosity of the water<br />

offers tangible resistance. Because of the “drag” forces created by the<br />

water, the degree of effort is determ<strong>in</strong>ed by the cross-sectional area of<br />

the mov<strong>in</strong>g body or limb, coupled with the velocity of the movement.<br />

28<br />

Water can be seen as provid<strong>in</strong>g a “variable accommodat<strong>in</strong>g” resistance.<br />

The advantage of an accommodat<strong>in</strong>g resistance is that it matches<br />

the applied force or effort. In cl<strong>in</strong>ical terms, because the resistance of<br />

the water approximates the applied muscular forces, the probability of<br />

exceed<strong>in</strong>g tissue tolerances is reduced <strong>and</strong> consequently, the likelihood<br />

of exacerbation of the <strong>in</strong>jury is dramatically reduced. The term “variable”<br />

refers to be<strong>in</strong>g able to change the speed or velocity of the movement.<br />

Because most human motion is variable <strong>in</strong> nature, functional ga<strong>in</strong>s are<br />

more likely to occur when exercis<strong>in</strong>g <strong>in</strong> this manner (LeFort 1994; Pr<strong>in</strong>set<br />

al. 2006; Rahmann et al. 2009).<br />

Cardio-respiratory Fitness <strong>and</strong> Muscular Endurance <strong>in</strong> the Water: The loss<br />

of cardio-respiratory fitness can be significant dur<strong>in</strong>g recovery from <strong>in</strong>jury.<br />

Therefore, early resumption of exercise is now considered essential<br />

to the successful return to pre-<strong>in</strong>jury activity. Aquatic therapy allows<br />

the <strong>in</strong>jured person to beg<strong>in</strong> exercis<strong>in</strong>g earlier. Aquatic runn<strong>in</strong>g or jogg<strong>in</strong>g,<br />

when supported by a floatation device, offers additional benefits,<br />

most notably, the ma<strong>in</strong>tenance of rapid stride frequencies without the<br />

impact of l<strong>and</strong><strong>in</strong>g, <strong>and</strong> coord<strong>in</strong>ated movements between the arms <strong>and</strong><br />

legs (Becker & Cole 1994; Pr<strong>in</strong>s et al. 2006).<br />

Insufficient muscular endurance, rather than <strong>in</strong>sufficient strength, is<br />

now seen as the primary factor present <strong>in</strong> an <strong>in</strong>dividual’s <strong>in</strong>ability to<br />

ma<strong>in</strong>ta<strong>in</strong> the marg<strong>in</strong>s of safety of the sp<strong>in</strong>e, particularly when perform<strong>in</strong>g<br />

the “activities of daily liv<strong>in</strong>g”. Recent research shows that the ability<br />

to improve <strong>and</strong> ma<strong>in</strong>ta<strong>in</strong> sp<strong>in</strong>al stability follow<strong>in</strong>g <strong>in</strong>jury requires low<br />

<strong>in</strong>tensity, cont<strong>in</strong>uous muscle activation (Cole, et al. 2004; McGill 2001).<br />

As noted above, aquatic exercise allows for susta<strong>in</strong>ed movements with<br />

less risk of overuse.<br />

Social, Emotional, <strong>and</strong> Psychological Benefits of Aquatic Physical Therapy:<br />

Patient motivation <strong>and</strong> compliance with treatment are positive determ<strong>in</strong>ants<br />

for the success of any rehabilitation program. Because of the<br />

unique properties of water, aquatic physical therapy is an excellent rehabilitation<br />

choice, ensur<strong>in</strong>g a high degree of compliance (Becker, Cole<br />

1994).<br />

clInIcAl dIAGnoses And condItIons treAted<br />

WIth AQuAtIc eXercIses.<br />

Injuries to the Sp<strong>in</strong>e <strong>and</strong> Extremities: The therapeutic advantages of exercis<strong>in</strong>g<br />

<strong>in</strong> the water for early restoration of jo<strong>in</strong>t mobility <strong>in</strong> the sp<strong>in</strong>e,<br />

comb<strong>in</strong>ed with progressive strengthen<strong>in</strong>g are well documented (Fappiano<br />

& Gangaway 2008; Lund et al. 2008; Rahmann et al. 2009).<br />

Exercises <strong>in</strong> water are used for strengthen<strong>in</strong>g the cervical <strong>and</strong> thoracic<br />

regions <strong>and</strong> are coupled with strengthen<strong>in</strong>g of the scapula stabilizers<br />

<strong>and</strong> glenohumeral musculature (Becker & Cole 1994; Cole et al. 2004;<br />

Pr<strong>in</strong>s & Cutner 1999).<br />

For treatment of cervical <strong>in</strong>juries, an added advantage of the water<br />

is the ability to perform neck-strengthen<strong>in</strong>g exercises while float<strong>in</strong>g <strong>in</strong><br />

the prone position. When a mask <strong>and</strong> snorkel are used for breath<strong>in</strong>g <strong>in</strong><br />

the prone position, the buoyant force of the water can be relied on to<br />

support the weight of the head. This relieves <strong>in</strong>jured muscles <strong>and</strong> associated<br />

soft tissue from the responsibility of counteract<strong>in</strong>g anticipated<br />

gravitational forces.<br />

Although the treatment of lower back <strong>in</strong>juries can take various<br />

forms, a common goal is to <strong>in</strong>crease strength <strong>and</strong> mobility of the weakened<br />

area. Be<strong>in</strong>g supported by the water while st<strong>and</strong><strong>in</strong>g or walk<strong>in</strong>g<br />

at vary<strong>in</strong>g depths, alters the axial load<strong>in</strong>g on the sp<strong>in</strong>e. Gravitational<br />

forces are also m<strong>in</strong>imized when the patient assumes a prone or sup<strong>in</strong>e<br />

float<strong>in</strong>g position. Swimm<strong>in</strong>g <strong>and</strong> kick<strong>in</strong>g <strong>in</strong> the prone <strong>and</strong>/or sup<strong>in</strong>e<br />

body positions, utiliz<strong>in</strong>g the neutral sp<strong>in</strong>e concept <strong>and</strong> modify<strong>in</strong>g stroke<br />

mechanics for <strong>in</strong>dividual patients (Cole et al. 2004; Lund et al. 2008) .<br />

When recover<strong>in</strong>g from hip, knee <strong>and</strong> ankle <strong>in</strong>jury, especially after<br />

surgery, the force of buoyancy can be used to decrease the weight of the<br />

body while promot<strong>in</strong>g early ambulation. Because jo<strong>in</strong>t reaction forces<br />

on the knee can reach several times body weight (Fappiano & Ganga-


way 2008; Lund et al. 2008); Rahmann et al. 2009), aquatic rehabilitation<br />

reduces the negative consequences of gravitational <strong>and</strong> compressive<br />

forces, allow<strong>in</strong>g safe <strong>and</strong> effective therapy.<br />

Treatment of Arthritis, Diabetes, Neurological Deficits <strong>and</strong> Permanent<br />

Physical Disabilities: Aquatic physical therapy is now also prescribed for<br />

persons diagnosed with arthritis <strong>and</strong> diabetes. The water reduces the<br />

pressure-<strong>in</strong>duced loads on the jo<strong>in</strong>ts <strong>and</strong> consequently allows cont<strong>in</strong>ued<br />

exercis<strong>in</strong>g with less risk of <strong>in</strong>ternal <strong>in</strong>jury. This is of particular importance<br />

because <strong>in</strong>discrim<strong>in</strong>ate participation <strong>in</strong> physical activities may<br />

compromise the health of both Type 1 <strong>and</strong> Type 2 diabetics because<br />

these conditions are vulnerable to the stresses imposed by many types of<br />

activities (Becker & Cole 1994; Cole et al. 2004).<br />

Exercis<strong>in</strong>g <strong>in</strong> the water is recommended for persons with neurological<br />

deficits which may have developed as a result of a Stroke (CVA), tumors<br />

of the C.N.S., <strong>and</strong> conditions associated with progressive skeletal<br />

muscle dysfunction such as Multiple Sclerosis. Because the density of<br />

water necessitates slower <strong>and</strong> more controlled movements, re-learn<strong>in</strong>g<br />

functional neuro-motor patterns is facilitated by the hydrostatic pressure<br />

which <strong>in</strong>creases proprioceptive <strong>and</strong> k<strong>in</strong>esthetic awareness. Individuals<br />

are also less apprehensive about practic<strong>in</strong>g these skills <strong>in</strong> the water because<br />

the risk of <strong>in</strong>jury from loss of balance is elim<strong>in</strong>ated (Becker &<br />

Cole 1994; Degano & Geigle 2009).<br />

Aquatic exercise has been used extensively as a rehabilitative <strong>and</strong><br />

therapeutic modality for <strong>in</strong>dividuals with permanent physical disabilities.<br />

The freedom of movement <strong>and</strong> the ability to exercise muscles which<br />

cannot overcome gravitational constra<strong>in</strong>ts make swimm<strong>in</strong>g <strong>and</strong> related<br />

aquatic activities <strong>in</strong>valuable for persons with a wide range of physically<br />

disabl<strong>in</strong>g conditions such as Amputation, Cerebral Palsy <strong>and</strong> Paraplegia<br />

(Becker & Cole 1994).<br />

reseArch In AQuAtIc rehABIlItAtIon<br />

By comb<strong>in</strong><strong>in</strong>g active physical therapy <strong>in</strong> the water with ongo<strong>in</strong>g research<br />

<strong>in</strong> the biomechanics of aquatic motion, a multi-discipl<strong>in</strong>ary approach<br />

to rehabilitation can promote the design of new equipment <strong>and</strong><br />

the efficacy of treatment protocols. Examples of research that focuses<br />

on aquatic physical therapy <strong>in</strong>clude monitor<strong>in</strong>g k<strong>in</strong>ematic <strong>and</strong> k<strong>in</strong>etic<br />

changes as they relate to <strong>in</strong>creas<strong>in</strong>g mobility <strong>and</strong> relative strength dur<strong>in</strong>g<br />

aquatic physical therapy (Becker & Cole 1994; Pr<strong>in</strong>s et al. 2006; Pr<strong>in</strong>s<br />

& Cutner 1999).<br />

reFerences<br />

Becker, B.E. & Colem Andrew J. (1994). The future of aquatic rehabilitation.<br />

J Back & Musculoskeletal Rehab vol 4, 319-320.<br />

Cole, A. J., Fredericson, M., Hohnson, J., Moschetti, M., Eagleston,<br />

R. A. & Stratton S.A. (2004). Sp<strong>in</strong>e Pa<strong>in</strong>. In: Aquatic Rehabilitation<br />

Strategies. Butterworth He<strong>in</strong>emann (New York, NY).<br />

Dundar, U., Solak, O., Yigit, I., Evcik, D. & Kavuncu V. (2009). Cl<strong>in</strong>ical<br />

effectiveness of aquatic exercise to treat chronic low back pa<strong>in</strong>: a<br />

r<strong>and</strong>omized controlled trial. Sp<strong>in</strong>e. 15 (14), 1436-40.<br />

Degano, A. C. & Geigle, P. R. (2009). Use of aquatic physical therapy<br />

<strong>in</strong> the treatment of balance <strong>and</strong> gait impairments follow<strong>in</strong>g traumatic<br />

bra<strong>in</strong> <strong>in</strong>jury: a case report. J Aquatic Phys Therapy. 17(1), 16-21<br />

Fappiano, M & Gangaway J.M.K. (2008). Aquatic physical therapy improves<br />

jo<strong>in</strong>t mobility, strength, <strong>and</strong> edema <strong>in</strong> lower extremity orthopedic<br />

<strong>in</strong>juries. J Aquatic Phys Therapy. 16(1), 10-14.<br />

Genuario, S.E. & Vegso J.J. (1990). The use of a swimm<strong>in</strong>g pool <strong>in</strong> the<br />

rehabilitation <strong>and</strong> recondition<strong>in</strong>g of athletic <strong>in</strong>juries. Contemp Orthopedics<br />

20, 381.<br />

LeFort, S. & T.E. Hannah (1994). Return to work follow<strong>in</strong>g an aquafitness<br />

<strong>and</strong> muscle strengthen<strong>in</strong>g program for the low back <strong>in</strong>jured. Arch<br />

Phys Med Rehabil. (75) 1247.<br />

chaPter1.<strong>in</strong>vitedLectures<br />

Lund H., Weile U., Christensen R., Rostock B., Downey A., Bartels<br />

E.M., Danneskiold, Samsøe B., Bliddal H. (2008). A r<strong>and</strong>omized<br />

controlled trial of aquatic <strong>and</strong> l<strong>and</strong>-based exercise <strong>in</strong> patients with<br />

knee osteoarthritis J Rehabil. Med. 40(2):137-44.<br />

McGill, S.M. (2001). Low Back Stability: From formal description to<br />

issues for performance <strong>and</strong> rehabilitation Ex & Sports Sci Rev. 29,<br />

26-31.<br />

Pr<strong>in</strong>s, J.H. I., Kimura, M. Turner, M. Weisbach, L. & Lehoullier (2006).<br />

The application of k<strong>in</strong>ematic motion analysis <strong>in</strong> the evaluation of<br />

therapeutic exercises used <strong>in</strong> aquatic rehabilitation. Arch Phys Med<br />

Rehabil, 87 (11), e33.<br />

Pr<strong>in</strong>s, J.H. & Cutner D (1999). Aquatic therapy <strong>in</strong> the rehabilitation<br />

of athletic <strong>in</strong>juries. In: Cl<strong>in</strong>ics <strong>in</strong> Sports <strong>Medic<strong>in</strong>e</strong> ,18, 447-462. W.B.<br />

Saunders, Philadelphia.<br />

Rahmann, A.E., Brauer, S.G. & Nitz J.C. (2009). A specific <strong>in</strong>patient<br />

aquatic physiotherapy program improves strength after total hip or<br />

knee replacement surgery: a r<strong>and</strong>omized controlled trial. Arch Phys<br />

Med Rehabil. 90(5), 745-55<br />

The<strong>in</strong>, J.M. & Brody LT(1998). Aquatic-based rehabilitation <strong>and</strong> tra<strong>in</strong><strong>in</strong>g<br />

for the elite athlete. J Orthpedic & Sports Physl Therapy. 27(1),<br />

32-41.<br />

29


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Tra<strong>in</strong><strong>in</strong>g at Real <strong>and</strong> Simulated Altitude <strong>in</strong><br />

Swimm<strong>in</strong>g: Too High Expectations?<br />

rodríguez, F.A.<br />

Institut Nacional d’Educació Física de Catalunya, Universitat de Barcelona,<br />

Spa<strong>in</strong><br />

Altitude/hypoxic tra<strong>in</strong><strong>in</strong>g is a common practice among swimmers although<br />

scientific evidence is scarce <strong>and</strong> its benefits rema<strong>in</strong> controversial.<br />

While acute hypoxia deteriorates swimm<strong>in</strong>g performance, chronic hypoxia<br />

may <strong>in</strong>duce acclimatization effects which could improve aerobic<br />

capacity <strong>and</strong> therewith performance upon return to sea level. Other potential<br />

benefits such as improved exercise economy, enhanced muscle<br />

buffer capacity <strong>and</strong> pH regulation, <strong>and</strong> improved mitochondrial function<br />

have also been postulated. This paper aims to review current methods<br />

of altitude/hypoxic tra<strong>in</strong><strong>in</strong>g <strong>and</strong> to discuss the available scientific<br />

evidence on the effects <strong>and</strong> potential benefits on sea-level swimm<strong>in</strong>g<br />

performance.<br />

Table 1. A summary of studies of altitude/hypoxic tra<strong>in</strong><strong>in</strong>g with<br />

swimmers<br />

Table 1. A summary of studies of altitude/hypoxic tra<strong>in</strong><strong>in</strong>g with swimmers<br />

30<br />

of controlled studies on AT <strong>in</strong> swimm<strong>in</strong>g <strong>and</strong> the evidence support<strong>in</strong>g<br />

most approaches <strong>in</strong> athletes (Wilber, 2004), particularly <strong>in</strong> swimmers<br />

(Truijens & Rodríguez, 2010), rema<strong>in</strong>s <strong>in</strong>conclusive. Moreover, field observations<br />

<strong>and</strong> also research studies (Chapman et al., 1998) show that<br />

AT may work for some athletes <strong>and</strong> not for others.<br />

It has been estimated that an Olympic swimmer should improve<br />

his or her performance by about 1% with<strong>in</strong> the year lead<strong>in</strong>g up to the<br />

Olympics to stay <strong>in</strong> contention for a medal (Pyne et al., 2004). A recent<br />

meta-analysis concluded that the expectable performance benefit from<br />

AT for elite athletes can be as high as 1.6% (Bonetti & Hopk<strong>in</strong>s, 2009).<br />

Perhaps a worthy strategy if a medal is just some tenths of a second away.<br />

This paper aims to provide a brief, critical overview of peer-reviewed<br />

scientific literature on AT for the improvement of swimm<strong>in</strong>g performance<br />

at sea-level.<br />

Is AltItude/hYPo<strong>XI</strong>c trAInInG Better thAn<br />

trAInInG At seA leVel?<br />

Table 1 presents a summary of AT studies from the <strong>in</strong>ternational scientific<br />

literature, with swimmers. In view of this table, the answer to the question<br />

should likely be negative. However, the heterogeneity of research<br />

designs, test<strong>in</strong>g methods, performance level of subjects <strong>and</strong> performance<br />

Key words: Altitude tra<strong>in</strong><strong>in</strong>g, hypoxia, hypoxic tra<strong>in</strong><strong>in</strong>g, <strong>in</strong>termittent<br />

<strong>in</strong>dicators make it difficult to derive sound conclusions based on the<br />

hypoxia<br />

limited evidence available. Most of our knowledge derives from studies<br />

conducted <strong>in</strong> other sports such as long distance runn<strong>in</strong>g, cycl<strong>in</strong>g, Nordic<br />

IntroductIon<br />

ski<strong>in</strong>g <strong>and</strong> orienteer<strong>in</strong>g.<br />

Altitude/hypoxic tra<strong>in</strong><strong>in</strong>g (AT) plays an important role <strong>in</strong> prepar<strong>in</strong>g<br />

swimmers <strong>Biomechanics</strong> all over <strong>and</strong> the <strong>Medic<strong>in</strong>e</strong> world. Unfortunately, <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> there /Chapter is a 1 remarkable Invited Lectures lack<br />

Page 46<br />

Mode of hypoxia /<br />

Strategy<br />

Natural altitude<br />

LH-TH<br />

Natural altitude<br />

LH-TH<br />

Natural altitude<br />

LH-TH<br />

IHE hypobaric<br />

Hi-Lo<br />

IHE normobaric<br />

Hi-Lo<br />

IHE hypobaric<br />

Hi-Lo<br />

IHT normobaric<br />

Lo-Hi<br />

IHT hypobaric<br />

Lo-Hi<br />

Level /<br />

Gender<br />

College<br />

M<br />

Elite junior<br />

M+F<br />

Elite<br />

M<br />

Elite <strong>and</strong><br />

subelite<br />

M+F<br />

Elite<br />

M+F<br />

Tra<strong>in</strong>ed<br />

M+F<br />

Tra<strong>in</strong>ed<br />

M+F<br />

Tra<strong>in</strong>ed<br />

M<br />

Control /<br />

Design<br />

No<br />

Pre-post<br />

No<br />

Pre-post<br />

No<br />

Pre-post, same<br />

group at two<br />

altitudes<br />

Yes<br />

Pre-post,<br />

matchedpaired<br />

Yes<br />

Pre-post, two<br />

groups liv<strong>in</strong>g<br />

at 1200 m<br />

Yes<br />

Matchedpaired,<br />

r<strong>and</strong>omized,<br />

double bl<strong>in</strong>d<br />

Yes<br />

Matchedpaired,<br />

r<strong>and</strong>omized,<br />

double bl<strong>in</strong>d<br />

Yes<br />

Matchedpaired,<br />

r<strong>and</strong>omized<br />

n<br />

VO2max Altitude Duration Effect on<br />

performance §<br />

15 4.2 L/m<strong>in</strong> 2300 m 2 wks ↔<br />

at 200 <strong>and</strong> 500 yd TT<br />

16 ? 2100-2300 m 3 wks ↑<br />

Vmax <strong>and</strong> V4 (+2-3%*)<br />

at <strong>in</strong>cremental 5x100<br />

or 5x400 m test<br />

9 59 1850 vs 1200 m 13 d ↔<br />

Vmax at 4x200 & 2000<br />

m TT <strong>in</strong> 1850-m group<br />

8/8 59 Rest at<br />

≈4000-5500 m<br />

9/9 58<br />

at 1200 m<br />

Sleep/rest 5 d at<br />

≈2500 m <strong>and</strong> 8 d<br />

at ≈3000 m vs<br />

controls at 1200 m<br />

6/7 55 Rest at<br />

≈4000-5500 m<br />

8/8 48-50 Tra<strong>in</strong><strong>in</strong>g at<br />

≈2500 m<br />

6/6 56 Tra<strong>in</strong><strong>in</strong>g at<br />

≈1600-2400 m<br />

3 h/d over 2<br />

wks<br />

13 d,<br />

16 h/d<br />

3 h/d,<br />

5 d/wk over 4<br />

wks<br />

12.5 m<strong>in</strong> of<br />

high <strong>in</strong>tensity<br />

bouts added,<br />

3x/wk over 5<br />

wks<br />

2 daily HT<br />

sessions,<br />

5 d/wk over 3<br />

wks<br />

↑<br />

Vmax at 200 m TT<br />

(0.9%*)<br />

↔<br />

Vmax at 5x200 m<br />

<strong>and</strong> 2000 m TT<br />

conducted at 1200 m<br />

Only controls improved<br />

↔<br />

Vmax at 100 & 400 m<br />

<strong>and</strong> <strong>in</strong>cremental<br />

swimm<strong>in</strong>g flume test <strong>in</strong><br />

both groups<br />

↔<br />

at 100 <strong>and</strong> 400 m TT<br />

Both groups equally<br />

improved<br />

↔<br />

at 100 <strong>and</strong> 200 m TT<br />

Both groups equally<br />

improved<br />

Effect on VO2max § Other outcomes § References<br />

↔ Faulkner et al.<br />

(1967)<br />

?<br />

Not measured<br />

↔<br />

No changes <strong>in</strong> either<br />

group<br />

↑<br />

VO2peak at 200-m TT<br />

(+9.3%*) <strong>and</strong> at 400-m<br />

TT (+5.4%*)<br />

after 1-wk taper<br />

↔<br />

n.s.<br />

(+4.5% <strong>in</strong> H group)<br />

Both groups equally<br />

improved<br />

↑<br />

at <strong>in</strong>cremental<br />

swimm<strong>in</strong>g flume test<br />

(+7.5%*) after 2-wks<br />

taper<br />

↔<br />

Both groups equally<br />

improved<br />

↔<br />

Both groups equally<br />

improved<br />

↑ tHb-mass (+6.3%*) Friedmann et al.<br />

(2005)<br />

↑ Vmax at 2000 m TT<br />

at 1200-m group only<br />

↑ MCV <strong>and</strong> retics <strong>in</strong><br />

1850-m group only<br />

↑ <strong>in</strong> [Hb], Htc, retics*<br />

tHb-mass not measured<br />

↑ tHb mass (+8.5%*)<br />

↑ Vmax <strong>and</strong> TT 2000 m<br />

<strong>in</strong> controls only* after<br />

1-2 d, not after 15 d<br />

↑ Ventilatory threshold<br />

(+12.1%*)<br />

↔ tHB-mass<br />

↔ MAOD <strong>in</strong> both<br />

groups<br />

↑ MAOD <strong>in</strong> IHT group<br />

(+29%) vs control<br />

group (+14%)*<br />

Roels et al.<br />

(2006)<br />

Rodríguez et al.<br />

(2003)<br />

Robach et al.<br />

(2006)<br />

Rodríguez et al.<br />

(2007)<br />

Truijens et al.<br />

(2003)<br />

Ogita & Tabata<br />

(2003)<br />

LH-TH: Liv<strong>in</strong>g high-tra<strong>in</strong><strong>in</strong>g high; LH-TL: Liv<strong>in</strong>g high-tra<strong>in</strong><strong>in</strong>g low; IHE: Intermittent hypoxic exposure at rest <strong>and</strong>/or sleep; IHT: Intermittent hypoxic tra<strong>in</strong><strong>in</strong>g; M/F: male/female; TT: Time trial; MAOD: Maximal<br />

accumulated oxygen deficit; H: hypoxia/altitude group; N: normoxia group; Vmax: maximal speed; V4: speed at 4 mmol/L lactate. § Added effect <strong>in</strong> the experimental group (controlled studies); ↑: Increase; ↔: No change;<br />

*Significantly different from values measured before altitude/hypoxic tra<strong>in</strong><strong>in</strong>g or compared to control group (p≤0.05); n.s.: non-significant difference (p>0.05).


clAssIcAl AltItude trAInInG<br />

Classically, AT has consisted of liv<strong>in</strong>g <strong>and</strong> tra<strong>in</strong><strong>in</strong>g at natural (terrestrial)<br />

altitude, i.e. “liv<strong>in</strong>g high-tra<strong>in</strong><strong>in</strong>g high” (LH-TH). The prevail<strong>in</strong>g paradigm<br />

which supports this practice is that LH-TH (about 2,000-3,000<br />

m) is l<strong>in</strong>ked to an accelerated production of erythrocytes, which leads to<br />

an <strong>in</strong>crease <strong>in</strong> VO2max, ultimately improv<strong>in</strong>g endurance performance.<br />

Surpris<strong>in</strong>gly though, there are no reports <strong>in</strong> the available scientific<br />

literature of controlled studies with swimmers. Even if designs without<br />

a sea level control group are very questionable <strong>and</strong> are considered not<br />

suitable for tra<strong>in</strong><strong>in</strong>g research, it is of note that three uncontrolled studies<br />

have tested LH-TH <strong>in</strong> swimmers. Two of them failed to prove positive<br />

effects neither on 100- <strong>and</strong> 500 yd swimm<strong>in</strong>g performance nor on VO-<br />

2max<br />

(Faulkner et al., 1967; Roels et al., 2006). In fact, the latter showed<br />

a small improvement when subjects lived <strong>and</strong> tra<strong>in</strong>ed dur<strong>in</strong>g 13 days<br />

at 1200 m but not at 1850 m. The third study with junior swimmers is<br />

rather puzzl<strong>in</strong>g, s<strong>in</strong>ce it showed an improvement on maximal speed <strong>and</strong><br />

4 mmol/L lactate speed <strong>in</strong> an <strong>in</strong>cremental 5x100 or 5x400-m test, but<br />

not on VO 2max , despite an <strong>in</strong>crease of total haemoglob<strong>in</strong> mass.<br />

A more recent approach, first developed by Lev<strong>in</strong>e <strong>and</strong> Stray-<br />

Gundersen <strong>and</strong> known as “liv<strong>in</strong>g high-tra<strong>in</strong><strong>in</strong>g low” (LH-TL), has been<br />

shown to improve sea level performance <strong>in</strong> runners of various levels. In<br />

essence, LH-TL allows robust altitude acclimatization, while simultaneously<br />

allow<strong>in</strong>g athletes to ‘‘tra<strong>in</strong> low’’ for the purpose of replicat<strong>in</strong>g<br />

sea-level tra<strong>in</strong><strong>in</strong>g <strong>in</strong>tensity <strong>and</strong> oxygen flux (Lev<strong>in</strong>e & Stray-Gundersen,<br />

1997; Stray-Gundersen et al., 1999). However, LH-TL, proven useful<br />

with long distance runners <strong>and</strong> orienteerers (Wehrl<strong>in</strong> et al., 2006) <strong>in</strong><br />

events last<strong>in</strong>g 8-20 m<strong>in</strong>utes, has never been tested <strong>in</strong> swimm<strong>in</strong>g, <strong>in</strong><br />

which most events are below 5 m<strong>in</strong>.<br />

Hence, based on available scientific literature, tra<strong>in</strong><strong>in</strong>g at natural<br />

altitude has failed so far to prove useful for the enhancement of sea<br />

level performance <strong>in</strong> swimmers (Wilber, 2004; Truijens & Rodríguez,<br />

2010). This fact is particularly remarkable bear<strong>in</strong>g <strong>in</strong> m<strong>in</strong>d that swimm<strong>in</strong>g<br />

coaches from many countries <strong>in</strong>clude AT <strong>in</strong> their plann<strong>in</strong>g <strong>and</strong><br />

swimmers are among the most frequent users of high altitude tra<strong>in</strong><strong>in</strong>g<br />

facilities.<br />

InterMIttent hYPo<strong>XI</strong>c trAInInG (Iht)<br />

S<strong>in</strong>ce most events <strong>in</strong> swimm<strong>in</strong>g require large activation of the anaerobic<br />

metabolism (Rodríguez & Mader, 2010), the enhanc<strong>in</strong>g effects of IHT<br />

on anaerobic metabolism or buffer capacity have lead swimm<strong>in</strong>g scientists<br />

to test the hypothesis that this method could improve swimm<strong>in</strong>g<br />

performance more than equivalent tra<strong>in</strong><strong>in</strong>g at sea level.<br />

Two studies have been conducted with swimmers (table 1). In a first<br />

study (Truijens et al., 2003), sixteen well-tra<strong>in</strong>ed collegiate <strong>and</strong> master<br />

swimmers were matched for gender, performance level <strong>and</strong> tra<strong>in</strong><strong>in</strong>g history<br />

<strong>and</strong> assigned to either IHT or control groups <strong>in</strong> a r<strong>and</strong>omized,<br />

double bl<strong>in</strong>d, placebo controlled design. All subjects completed a five<br />

week tra<strong>in</strong><strong>in</strong>g program, consist<strong>in</strong>g of three high <strong>in</strong>tensity tra<strong>in</strong><strong>in</strong>g sessions<br />

weekly <strong>in</strong> a swimm<strong>in</strong>g flume breath<strong>in</strong>g hypoxic (≈2,500 m) or<br />

normoxic air, <strong>and</strong> supplemental low to moderate <strong>in</strong>tensity sessions <strong>in</strong> a<br />

pool. Although both groups improved performance <strong>in</strong> 100- <strong>and</strong> 400-m<br />

time trials <strong>and</strong> VO 2max , no differences between groups could be demonstrated.<br />

Moreover, neither swimm<strong>in</strong>g economy nor anaerobic capacity<br />

improved with this tra<strong>in</strong><strong>in</strong>g. In a second matched-paired, controlled<br />

study us<strong>in</strong>g a similar tra<strong>in</strong><strong>in</strong>g regimen, Ogita <strong>and</strong> Tabata (2003) found<br />

a 10% <strong>in</strong>crease <strong>in</strong> anaerobic capacity as measured by the maximal accumulated<br />

oxygen deficit (MAOD) after two weeks of hypoxic tra<strong>in</strong><strong>in</strong>g<br />

<strong>in</strong> n<strong>in</strong>e competitive male swimmers. However, both groups equally<br />

improved VO 2max <strong>and</strong> swimm<strong>in</strong>g performance <strong>in</strong> 100 <strong>and</strong> 200-m time<br />

trials, thus it was not possible to establish an additional benefit.<br />

InterMIttent hYPo<strong>XI</strong>A eXPosure (Ihe)<br />

Another strategy is IHE at rest or dur<strong>in</strong>g sleep <strong>in</strong> hypobaric or normobaric<br />

environments (nitrogen houses, hypoxic tents/rooms) or us<strong>in</strong>g<br />

hypoxic breath<strong>in</strong>g apparatuses comb<strong>in</strong>ed with sea-level tra<strong>in</strong><strong>in</strong>g. This<br />

chaPter1.<strong>in</strong>vitedLectures<br />

should theoretically <strong>in</strong>duce physiological adaptations without hamper<strong>in</strong>g<br />

tra<strong>in</strong><strong>in</strong>g workload, thus allow<strong>in</strong>g a comparison with LH-TL.<br />

Two IHE studies have been conducted with swimmers us<strong>in</strong>g hypobaric<br />

chambers (table 1). In a first study (Rodríguez et al., 2003), sixteen<br />

elite <strong>and</strong> sub-elite swimmers were assigned to one of two groups <strong>in</strong> a<br />

matched-paired, r<strong>and</strong>omized design, <strong>and</strong> half of them comb<strong>in</strong>ed sealevel<br />

tra<strong>in</strong><strong>in</strong>g with IHE over 2 weeks (3 h/d) at a simulated altitude of<br />

4,000-5,500 m <strong>and</strong> were compared to the control group. Although all<br />

swimmers followed identical tra<strong>in</strong><strong>in</strong>g plans, the IHE group significantly<br />

improved swimm<strong>in</strong>g performance <strong>in</strong> a 200-m time trial (-1.3 s, 0.9%),<br />

associated with an <strong>in</strong>crease <strong>in</strong> peak VO 2 both at 200-m (+9.3%) <strong>and</strong><br />

400-m (+5.4%) time trials.<br />

In a second, match-paired, r<strong>and</strong>omized, double bl<strong>in</strong>d, placebo controlled<br />

study (Rodríguez et al., 2007), 4 weeks of 4,000-5,500 m IHE<br />

was adm<strong>in</strong>istered to 13 swimmers <strong>and</strong> 10 runners distributed <strong>in</strong> two<br />

groups (IHE <strong>and</strong> controls). Swimmers performed duplicated 100 <strong>and</strong><br />

400 m time trials, <strong>and</strong> VO 2max tests <strong>in</strong> a swimm<strong>in</strong>g flume with<strong>in</strong> three<br />

weeks before, <strong>and</strong> dur<strong>in</strong>g the first <strong>and</strong> third week after the <strong>in</strong>tervention.<br />

When swimmers were considered separately, the IHE group, but not<br />

controls, showed a significant <strong>in</strong>crease <strong>in</strong> VO 2 at the ventilatory threshold<br />

(VT, +8.9) <strong>and</strong> <strong>in</strong> maximal m<strong>in</strong>ute ventilation (+10.6%) immediately<br />

after the <strong>in</strong>tervention, as well as a significant <strong>in</strong>crease <strong>in</strong> VO 2max relative<br />

to body mass (+7.5%) <strong>and</strong> VO 2 at VT (+12.1%) two weeks after, follow<strong>in</strong>g<br />

a pre-competition taper. Intrigu<strong>in</strong>gly, these changes could not<br />

be attributed to <strong>in</strong>creased red blood cell or haemoglob<strong>in</strong> mass (Gore et<br />

al., 2006), sub-maximal swimm<strong>in</strong>g economy (Truijens et al., 2008), nor<br />

to hypoxic <strong>and</strong> hypercapnic ventilatory control changes (Townsend et<br />

al., 2004). The hypothesis was raised that these changes could have been<br />

the comb<strong>in</strong>ed effect of IHE <strong>and</strong> taper<strong>in</strong>g, thus suggest<strong>in</strong>g that this approach<br />

might be useful immediately before competition.<br />

In another controlled study us<strong>in</strong>g normobaric hypoxia, a group of<br />

swimmers spent 13 days liv<strong>in</strong>g <strong>and</strong> tra<strong>in</strong><strong>in</strong>g at 1200 m, while another<br />

group (IHE) was exposed to 16 h per day to simulated altitude at 2,500<br />

(5 days) <strong>and</strong> 3,000 m (8 more days) <strong>in</strong> hypoxic rooms. Despite an <strong>in</strong>crease<br />

<strong>in</strong> total haemoglob<strong>in</strong> <strong>in</strong> the IHE group (+8.5%), no improvement<br />

was observed <strong>in</strong> VO 2max or maximal speed at 4x200-m <strong>and</strong> 2,000-m<br />

maximal tests (Robach et al., 2006). Interest<strong>in</strong>gly, swimmers <strong>in</strong> the control<br />

group (LH-TH at 1,200 m) did improve performance <strong>in</strong> both tests<br />

immediately after, but not 15 days after the <strong>in</strong>tervention, aga<strong>in</strong> without<br />

any significant change <strong>in</strong> haemoglob<strong>in</strong> mass.<br />

In terms of haematological response, it is of note that a<br />

recent analysis of 15 LH-TL studies conducted at real <strong>and</strong> simulated<br />

altitude has <strong>in</strong>dicated that moderate altitude/hypoxic exposure of more<br />

than 12 h per day is likely to <strong>in</strong>crease total haemoglob<strong>in</strong> mass by about<br />

1% per 100 hours of exposure (Gore et al., 2008). This would imply a<br />

m<strong>in</strong>imal duration of 21 days to atta<strong>in</strong> about a 5% <strong>in</strong>crease <strong>in</strong> haemoglob<strong>in</strong>.<br />

Hence, despite the large amount of research performed <strong>in</strong> the last<br />

decade <strong>and</strong> some promis<strong>in</strong>g results, swimm<strong>in</strong>g performance enhancement<br />

by means of IHE is still controversial, both <strong>in</strong> terms of performance<br />

benefits <strong>and</strong> mechanisms <strong>in</strong>volved, which do not seem to be<br />

related to haematological acclimatization effects.<br />

conclusIons<br />

Based on available scientific literature, there is no evidence that tra<strong>in</strong><strong>in</strong>g<br />

at natural altitude enhances swimm<strong>in</strong>g performance more than tra<strong>in</strong><strong>in</strong>g<br />

at sea level. Based on research conducted <strong>in</strong> other sports, AT would<br />

require at least 3 to 4 weeks at 2,100 to 2,500 m of altitude to elicit a<br />

robust acclimatization response (primarily red cell mass <strong>in</strong>crease) <strong>in</strong> the<br />

majority of athletes. The optimal approach is likely to be LH-TL, <strong>in</strong><br />

which one “lives high” (i.e. 2,100-2,500 m) to get the benefits of altitude<br />

acclimatization <strong>and</strong> “tra<strong>in</strong>s low” (1,250 m or less) to avoid the detrimental<br />

effects of hypoxic exercise. In fact, tra<strong>in</strong><strong>in</strong>g at hypoxia (as <strong>in</strong> LH-<br />

TH or IHT) does not appear to provide any physiologic advantage over<br />

normoxic exercise <strong>and</strong> might even impair performance. Whether the<br />

31


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

performance benefits would be similar for swimmers compared to other<br />

endurance tra<strong>in</strong>ed athletes is not known <strong>and</strong> requires further research.<br />

Swimm<strong>in</strong>g performance enhancement by means of IHE is still controversial.<br />

However, it is likely that at least 12 h/day at 2,100–3,000 m<br />

for 3 to 4 weeks may suffice to achieve a significant <strong>in</strong>crease of red cell<br />

mass. Shorter exposure to more severe hypoxia (e.g. 4,000 to 5,500 m, 3<br />

h/day for 2 to 4 weeks) comb<strong>in</strong>ed with sea-level tra<strong>in</strong><strong>in</strong>g may enhance<br />

VO 2max , ventilatory threshold <strong>and</strong> middle-distance swimm<strong>in</strong>g performance<br />

after pre-competition taper<strong>in</strong>g, although the mechanisms are<br />

unclear.<br />

In any case, there is substantial <strong>in</strong>dividual variability <strong>in</strong> the outcome<br />

of every AT strategy. S<strong>in</strong>ce none of these approaches has conclusively<br />

proven to enhance swimm<strong>in</strong>g performance, more research is warranted<br />

to clarify their effects <strong>and</strong> mechanisms.<br />

the AltItude ProJect<br />

To clarify these effects <strong>and</strong> mechanisms <strong>in</strong> swimmers, a group of researchers<br />

from universities <strong>and</strong> sports organizations of different nations<br />

have developed a major collaborative <strong>in</strong>ternational swimm<strong>in</strong>g study<br />

called The Altitude Project start<strong>in</strong>g <strong>in</strong> October 2010 (Rodríguez &<br />

Lev<strong>in</strong>e, 2010). The project is open to sports <strong>and</strong> scientific organizations<br />

from all countries will<strong>in</strong>g to contribute with recruit<strong>in</strong>g <strong>and</strong> fund<strong>in</strong>g<br />

athletes, coaches <strong>and</strong> scientists. Information is available from: thealtitudeproject@gmail.com.<br />

reFerences<br />

Bonetti, D. L. & Hopk<strong>in</strong>s, W. G. (2009). Sea-level exercise performance<br />

follow<strong>in</strong>g adaptation to hypoxia: a meta-analysis. Sports Med, 39(2),<br />

107-27.<br />

Chapman, R. F., Stray-Gundersen, J. & Lev<strong>in</strong>e, B. D. (1998). Individual<br />

variation <strong>in</strong> response to altitude tra<strong>in</strong><strong>in</strong>g. J Appl Physiol, 85(4), 1448-<br />

56.<br />

Faulkner, J. A., Daniels, J. T. & Balke, B. (1967). Effects of tra<strong>in</strong><strong>in</strong>g at<br />

moderate altitude on physical performance capacity. J Appl Physiol,<br />

23(1), 85-9.<br />

Friedmann, B., Frese, F., Menold, E. & Bartsch, P. (2005). Individual<br />

variation <strong>in</strong> the reduction of heart rate <strong>and</strong> performance at lactate<br />

thresholds <strong>in</strong> acute normobaric hypoxia. Int J Sports Med, 26(7), 531-<br />

6.<br />

Gore, C. J., Rodriguez, F. A., Truijens, M. J., Townsend, N. E., Stray-<br />

Gundersen, J. & Lev<strong>in</strong>e, B. D. (2006). Increased serum erythropoiet<strong>in</strong><br />

but not red cell production after 4 wk of <strong>in</strong>termittent hypobaric hypoxia<br />

(4,000-5,500 m). J Appl Physiol, 101(5), 1386-93.<br />

Gore C. J., Clark, S. A. & Saunders, P. U. (2008). Erythropoietic <strong>and</strong><br />

non-erythropoietic aspects of athlete performance after hypoxic exposure.<br />

Proceed<strong>in</strong>gs of the I International Symposium of Altitude Tra<strong>in</strong><strong>in</strong>g<br />

(Granada): 4-7.<br />

Lev<strong>in</strong>e, B. D. & Stray-Gundersen, J. (1992). A practical approach to<br />

altitude tra<strong>in</strong><strong>in</strong>g: where to live <strong>and</strong> tra<strong>in</strong> for optimal performance enhancement.<br />

Int J Sports Med, 13 Suppl 1, S209-12.<br />

Lev<strong>in</strong>e, B. D. & Stray-Gundersen, J. (1997). “Liv<strong>in</strong>g high-tra<strong>in</strong><strong>in</strong>g low”:<br />

effect of moderate-altitude acclimatization with low-altitude tra<strong>in</strong><strong>in</strong>g<br />

on performance. J Appl Physiol, 83(1), 102-12.<br />

Pyne, D., Trew<strong>in</strong>, C. & Hopk<strong>in</strong>s, W. (2004). Progression <strong>and</strong> variability<br />

of competitive performance of Olympic swimmers. J Sports Sci, 22(7),<br />

613-20.<br />

Robach P., Schmitt L., Brugniaux J. V., Nicolet G., Roels B., Millet G.,<br />

Hellard P., Duvallet A., Fouillot J-P., Moutereau S., Lasne F., Pialoux<br />

V., Olsen N. V. & Richalet J-P. (2006). Liv<strong>in</strong>g high-tra<strong>in</strong><strong>in</strong>g low:<br />

effect on erythropoiesis <strong>and</strong> aerobic performance <strong>in</strong> highly-tra<strong>in</strong>ed<br />

swimmers. Eur J Appl Physiol, 96(4), 423-33.<br />

Roberts, D. & Smith, D. J. (1992). Tra<strong>in</strong><strong>in</strong>g at moderate altitude: iron status<br />

of elite male swimmers. J Lab Cl<strong>in</strong> Med, 120(3), 387-91.<br />

Rodríguez, F. A., Murio, J. & Ventura, J. L. (2003). Effects of <strong>in</strong>termittent<br />

hypobaric hypoxia <strong>and</strong> altitude tra<strong>in</strong><strong>in</strong>g on physiological <strong>and</strong><br />

32<br />

performance parameters <strong>in</strong> swimmers. Med Sci Sports Exerc, 35 (5),<br />

S115.<br />

Rodríguez, F. A., Truijens, M. J., Townsend, N. E., Stray-Gundersen,<br />

J., Gore, C. J. & Lev<strong>in</strong>e, B. D. (2007). Performance of runners <strong>and</strong><br />

swimmers after four weeks of <strong>in</strong>termittent hypobaric hypoxic exposure<br />

plus sea level tra<strong>in</strong><strong>in</strong>g. J Appl Physiol, 103(5), 1523-35.<br />

Rodríguez, F. A. & Mader, A. (2010, <strong>in</strong> press). Energy systems <strong>in</strong> swimm<strong>in</strong>g.<br />

In: Seifert, L., Chollet, D. & Mujika, I., Swimm<strong>in</strong>g: Science <strong>and</strong><br />

Performance. Hauppauge, New York: Nova Science Publishers.<br />

Rodríguez, F. A. & Lev<strong>in</strong>e, B. D. (2010). The Altitude Project: an <strong>in</strong>ternational<br />

collaborative research project on altitude tra<strong>in</strong><strong>in</strong>g <strong>in</strong> elite<br />

swimmers. In, Abstracts Book, <strong>XI</strong> International Symposium for <strong>Biomechanics</strong><br />

& <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, Oslo.<br />

Roels, B., Hellard, P., Schmitt, L., Robach, P., Richalet, J. P. & Millet,<br />

G.P. (2006). Is it more effective for highly tra<strong>in</strong>ed swimmers to live<br />

<strong>and</strong> tra<strong>in</strong> at 1200m than at 1850m <strong>in</strong> terms of performance <strong>and</strong> haematological<br />

benefits? Br J Sports Med, 40(2), e4.<br />

Stray-Gundersen J., Chapman R. F., Lev<strong>in</strong>e B. D. (2001). “Liv<strong>in</strong>g hightra<strong>in</strong><strong>in</strong>g<br />

low” altitude tra<strong>in</strong><strong>in</strong>g improves sea level performance <strong>in</strong> male<br />

<strong>and</strong> female elite runners. J Appl Physiol, 91(3), 1113-20.<br />

Townsend N. E., Gore C. J., Stray-Gundersen J., Rodríguez F. A., Truijens<br />

M. J. & Lev<strong>in</strong>e B. D. (2004). Ventilatory acclimatization to <strong>in</strong>termittent<br />

hypoxia <strong>in</strong> well-tra<strong>in</strong>ed runners <strong>and</strong> swimmers. J Appl Physiol,<br />

36(5), S337.<br />

Truijens, M. J., Rodriguez, F. A., Townsend, N. E., Stray-Gundersen, J.,<br />

Gore, C. J. & Lev<strong>in</strong>e, B. D. (2008). The effect of <strong>in</strong>termittent hypobaric<br />

hypoxic exposure <strong>and</strong> sea level tra<strong>in</strong><strong>in</strong>g on submaximal economy<br />

<strong>in</strong> well-tra<strong>in</strong>ed swimmers <strong>and</strong> runners. J Appl Physiol, 104(2), 328-37.<br />

Truijens, M. J., Toussa<strong>in</strong>t, H. M., Dow, J. & Lev<strong>in</strong>e, B. D. (2003). Effect<br />

of high-<strong>in</strong>tensity hypoxic tra<strong>in</strong><strong>in</strong>g on sea-level swimm<strong>in</strong>g performances.<br />

J Appl Physiol, 94(2), 733-43.<br />

Truijens, M. J. & Rodríguez, F. A. (2010, <strong>in</strong> press). Altitude <strong>and</strong> hypoxic<br />

tra<strong>in</strong><strong>in</strong>g <strong>in</strong> swimm<strong>in</strong>g. In: Seifert, L., Chollet, D., Mujika, I., Swimm<strong>in</strong>g:<br />

Science <strong>and</strong> Performance. Hauppauge, New York: Nova Science<br />

Publishers.<br />

Wehrl<strong>in</strong>, J. P., Zuest, P., Hallen, J. & Marti, B. (2006). Live high-tra<strong>in</strong><br />

low for 24 days <strong>in</strong>creases haemoglob<strong>in</strong> mass <strong>and</strong> red cell volume <strong>in</strong><br />

elite endurance athletes. J Appl Physiol, 100(6), 1938-1945.<br />

Wilber, R. L. (2004). Altitude tra<strong>in</strong><strong>in</strong>g <strong>and</strong> athletic performance. Champaign,<br />

Ill<strong>in</strong>ois: Human K<strong>in</strong>etics.


Muscle Fatigue <strong>in</strong> Swimm<strong>in</strong>g<br />

rouard, A.h.<br />

Laboratoire de Physiologie de l’Exercice, Université de Savoie, France<br />

Fatigue is a complex process which could be related to different alterations<br />

either of the central nervous system <strong>and</strong>/or of the muscles.<br />

Few studies have focused on the biomechanical evaluation of fatigue<br />

<strong>in</strong> swimm<strong>in</strong>g. EMG results <strong>in</strong>dicated either an <strong>in</strong>crease of <strong>in</strong>tegrated<br />

EMG (IEMG) for muscles with sub-maximal activation or a decrease<br />

of IEMG for muscles strongly <strong>in</strong>volved. Moreover, the frequency contents<br />

shift toward lower frequencies either for Maximal Voluntary Contraction<br />

(MVC) realised before <strong>and</strong> after an exhaustive test or dur<strong>in</strong>g a<br />

maximal swimm<strong>in</strong>g test. Changes <strong>in</strong> muscular activation were associated<br />

with a decrease of force production (dry l<strong>and</strong> strength or tethered or<br />

semi-tethered or swimm<strong>in</strong>g h<strong>and</strong> forces) <strong>and</strong> to changes <strong>in</strong> the path of<br />

the h<strong>and</strong>. Fatigue appears to be related to the task, the subject <strong>and</strong> the<br />

muscle.<br />

Key words: front crawl, fatigue, electromyography, forces, k<strong>in</strong>ematics.<br />

IntroductIon<br />

The swimmers performance is determ<strong>in</strong>ed by the ability to generate<br />

propulsive forces while reduc<strong>in</strong>g the resistance to forward motion. Propulsive<br />

forces are ma<strong>in</strong>ly generated by 3D limb movements <strong>in</strong> response<br />

to unstable loads created by the water. As <strong>in</strong> all human activities, fatigue<br />

could be def<strong>in</strong>ed as an acute impairment of performance. In regard to<br />

the movement generation process, fatigue could be related to central<br />

<strong>and</strong>/or peripheral alterations. The central component of fatigue could be<br />

due to the decrease of the CNS activation (nervous order <strong>and</strong>/ or motor<br />

neuron activation). The peripheral fatigue is related to an alteration<br />

of the neuromuscular junction <strong>and</strong>/or the deficit of substrates, blood<br />

flow, <strong>and</strong>/or dysfunction of the sarcomer. Consequently, fatigue is a very<br />

complex phenomenon, which could be evaluated through different approaches<br />

(physiology, Electromyography (EMG) <strong>and</strong> Mechanics).<br />

Because of the complexity of the movement <strong>in</strong> an aquatic environment,<br />

few biomechanical studies have focused on fatigue <strong>in</strong> swimm<strong>in</strong>g.<br />

EMG has largely been used <strong>in</strong> the evaluation of fatigue dur<strong>in</strong>g susta<strong>in</strong>ed<br />

isometric contractions. Many authors have observed a shift to<br />

lower frequencies of the EMG signal spectrum. In the 90’s, a novel approach<br />

(time-frequency treatment) was proposed for calculat<strong>in</strong>g spectral<br />

parameters from the surface myo-electric signal dur<strong>in</strong>g cyclic dynamic<br />

contractions for which changes <strong>in</strong> muscle length, force <strong>and</strong> electrode<br />

position contributed to the non-stationary status of the signal (Knaflitz<br />

<strong>and</strong> Bonato, 1999). Recently this approach was applied to swimm<strong>in</strong>g<br />

movement (Caty et al, 2007).<br />

The present review concerns the effect of fatigue on muscular activation<br />

<strong>and</strong> the associated changes <strong>in</strong> forces <strong>and</strong> h<strong>and</strong> trajectories<br />

Methods<br />

Most of the studies on fatigue <strong>in</strong> swimm<strong>in</strong>g have been conducted on<br />

male <strong>in</strong>ternational swimmers. Different maximal tests were performed<br />

by the subjects depend<strong>in</strong>g on the authors (i.e. maximal 400m swim <strong>in</strong> a<br />

flume for Monteil et al, 1996, or maximal 4*50m for Caty et al, 2007).<br />

Dur<strong>in</strong>g the test, EMG was synchronised with video acquisition. For<br />

EMG, the authors used either surface electrodes (Wakayoshi et al, 1994,<br />

Rouard et al, 1997, Caty et al, 2007) or f<strong>in</strong>e wire electrodes (Monteil et al,<br />

1996). Shoulder <strong>and</strong> upper limb muscles were those most <strong>in</strong>vestigated.<br />

All the authors applied the same guidel<strong>in</strong>es for the location of the electrodes<br />

(belly of the muscle) <strong>and</strong> the sk<strong>in</strong> preparation (Clarys <strong>and</strong> Cabri,<br />

1993). Signals were stored on a memory card or on the soundtrack of the<br />

video camera. For the amplitude treatment, the raw EMG signals were<br />

rectified, smoothed <strong>and</strong> then <strong>in</strong>tegrated (IEMG). For each subject, <strong>and</strong><br />

each muscle, the IEMG were normalised accord<strong>in</strong>g to the maximal dy-<br />

chaPter1.<strong>in</strong>vitedLectures<br />

namic value observed dur<strong>in</strong>g the test<strong>in</strong>g procedures. For the frequency<br />

treatment, Aujouannet et al (2006) applied a Fourier transformation to<br />

evaluate the frequency contents of static Maximal Voluntary Contractions<br />

(MVC) performed just before <strong>and</strong> after the exhaustive swimm<strong>in</strong>g<br />

test (4*50m). For the swimm<strong>in</strong>g signals, Caty et al (2007) extracted, with<br />

a statistical detector, the activation <strong>in</strong>terval correspond<strong>in</strong>g to each stroke<br />

<strong>and</strong> each muscle. For each detected muscle burst, the Choi-Williams<br />

transformation was then computed. These particular transformations<br />

had already proven effective <strong>in</strong> the analysis of strongly non-stationary<br />

EMG signals recorded dur<strong>in</strong>g dynamic exercise (Knaflitz <strong>and</strong> Bonato,<br />

1999). The <strong>in</strong>stantaneous mean frequency of the signal burst (MNF, Hz)<br />

was calculated for each stroke cycle.<br />

For the k<strong>in</strong>ematic evaluation of fatigue, at least 2 underwater cameras<br />

were used to analyse the 3D movements of the upper limbs. The<br />

video was digitised frame by frame to get the h<strong>and</strong> trajectories <strong>and</strong>/or<br />

the h<strong>and</strong> velocity <strong>and</strong>/or different angles (sweep back <strong>and</strong> attack h<strong>and</strong><br />

angles, limbs angles).<br />

Dur<strong>in</strong>g the MVC, the forces were recorded us<strong>in</strong>g a stra<strong>in</strong> gauge, while<br />

dur<strong>in</strong>g swimm<strong>in</strong>g the authors used either direct force measurements<br />

such as a tethered or semi- tethered apparatus (Aujouannet et al, 2006,<br />

Rouard et al, 2006) or an <strong>in</strong>direct approach calculat<strong>in</strong>g the lift, drag<br />

<strong>and</strong> resultant h<strong>and</strong> forces accord<strong>in</strong>g to Schleihauf ’s method (Monteil<br />

et al, 1996)<br />

results<br />

Results <strong>in</strong>dicated a decrease of IEMG for the most activated muscles<br />

(M. Deltoideus or M. Flexor carpi) (Wakayoshi et al, 1994; Caty et al,<br />

2007) (Figure 1) or an <strong>in</strong>crease of IEMG for muscles with sub-maximal<br />

contractions depend<strong>in</strong>g on the phase of the stroke (M <strong>in</strong>ternal or external<br />

rotators) (Monteil, 1996) (Figure 2).<br />

Figure 1: Mean (SD) of the normalised IEMG of the muscles Flexor<br />

(FCU) <strong>and</strong> Extensor (ECU) carpi ulnaris for the 1 st <strong>and</strong> the 4 th of the<br />

maximal 4* 50m test (adapted from Caty et al, 2007)<br />

Figure 2: Normalised IEMG of the shoulder muscles at the beg<strong>in</strong>n<strong>in</strong>g<br />

(fresh) <strong>and</strong> end (fatigue) of a maximal 400m test swam <strong>in</strong> a flume<br />

(adapted from Monteil et al, 1996).<br />

A shift of spectral parameters of the EMG’s of the M. biceps <strong>and</strong> triceps<br />

brachii toward lower frequency was observed dur<strong>in</strong>g maximal voluntary<br />

contractions (MVC) realised before <strong>and</strong> after a maximal 4*50m swimm<strong>in</strong>g<br />

test (Aujouannet et al, 2006). Dur<strong>in</strong>g the 4*50maximal test a de-<br />

33


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

rivative of the <strong>in</strong>stantaneous mean frequency (MNF) was noted for the<br />

M. antagonist Flexor <strong>and</strong> Extensor carpi (Caty et al, 2007) (Figure 3)<br />

Figure 3: Mean (SD) of the percentage of decrease (PD%) of the Instantaneous<br />

Mean Frequency (MNF) between the 1 st 25m <strong>and</strong> the last<br />

25m of the maximal 4*50m test (adapted from Caty et al, 2007).<br />

These changes were associated with a decrease <strong>in</strong> force production either<br />

for the maximal dry l<strong>and</strong> strength or for maximal tethered force or for<br />

maximal power (Rouard et al, 2006) (Figure 4).<br />

Figure 4: Means (SD) of Isometric (Fiso), full tethered (Fpmax), ½<br />

tethered (Fp) forces <strong>and</strong> power (P) before <strong>and</strong> after a maximal 4*50m<br />

test (Rouard et al, 2006).<br />

Concern<strong>in</strong>g the h<strong>and</strong> forces, both the Resultant <strong>and</strong> Efficient components<br />

decreased dur<strong>in</strong>g the <strong>in</strong>sweep phase <strong>and</strong> <strong>in</strong>creased dur<strong>in</strong>g the outsweep<br />

<strong>in</strong> a state of fatigue <strong>in</strong>dicat<strong>in</strong>g a shift of the force production from<br />

the <strong>in</strong>-sweep to the out-sweep at the end of the maximal 400m front<br />

crawl test, swum <strong>in</strong> a flume (Monteil et al, 1996) (figure 5).<br />

Figure 5: Resultant <strong>and</strong> Efficient component forces at the beg<strong>in</strong>n<strong>in</strong>g<br />

<strong>and</strong> at the end of a 400m test swam <strong>in</strong> a flume (N=9) (adapted from<br />

Monteil, 1996).<br />

K<strong>in</strong>ematic data corroborated the EMG <strong>and</strong> k<strong>in</strong>etics results. In a fatigue<br />

state, the spatial h<strong>and</strong> path rema<strong>in</strong>ed unchanged with a greater duration<br />

of the catch, <strong>in</strong>sweep <strong>and</strong> outsweep phases (Aujouannet et al, 2006)<br />

(figure 6).<br />

34<br />

Figure 6: Spatial (A) <strong>and</strong> temporal (B) values of the h<strong>and</strong> path for the<br />

1 st 50 (white bar) <strong>and</strong> the 4 th 50 m (grey bar) of the maximal 4*50m test:<br />

F (maximal forward coord<strong>in</strong>ate), B (maximal backward), Ex (exit from<br />

the water), D (maximal depth), O (maximal outward) <strong>and</strong> I (maximal<br />

<strong>in</strong>ward) * significant difference between the 1 st <strong>and</strong> 4 th 50 m at p


of the EMG to lower frequency <strong>in</strong> the fatigue condition either for the<br />

MVC or dur<strong>in</strong>g the swim test <strong>in</strong>dicated a preferential recruitment of<br />

slow motor units <strong>and</strong>/or a decrease of velocity conduction. Large <strong>in</strong>dividual<br />

differences were observed reflect<strong>in</strong>g the variability <strong>in</strong> muscle<br />

fibre <strong>and</strong>/or motor unit recruitment <strong>and</strong>/or subject capacity restoration.<br />

The muscular fatigue contributed to the decrease of force production<br />

either for the dry l<strong>and</strong> or swimm<strong>in</strong>g forces, especially dur<strong>in</strong>g the<br />

<strong>in</strong>-sweep phase.<br />

The k<strong>in</strong>ematic <strong>and</strong> k<strong>in</strong>etic results suggested that <strong>in</strong> fatigue conditions<br />

swimmers <strong>in</strong>creased the first glid<strong>in</strong>g phase <strong>and</strong> limited the force<br />

production dur<strong>in</strong>g the <strong>in</strong>-sweep (i.e. the most mechanically constra<strong>in</strong>ed<br />

phase) to favor the f<strong>in</strong>al up-sweep phase.<br />

conclusIon<br />

Muscular fatigability is specific to the muscle, the exercise <strong>and</strong> the subject.<br />

The muscular changes contributed to the loss of force <strong>and</strong> to a decrease<br />

of h<strong>and</strong> velocity. Biomechanical methods allowed the resolv<strong>in</strong>g of<br />

<strong>in</strong>dividual strategies of swimm<strong>in</strong>g <strong>and</strong> adjustments caused by fatigue. In<br />

this way, biomechanical evaluation could be a useful tool to <strong>in</strong>dividualize<br />

the tra<strong>in</strong><strong>in</strong>g process of top level swimmers, especially regard<strong>in</strong>g cop<strong>in</strong>g<br />

with fatigue.<br />

Future <strong>in</strong>vestigations will be required to evaluate the load-shar<strong>in</strong>g<br />

across muscles <strong>and</strong>/or to determ<strong>in</strong>e the central <strong>and</strong> peripheral components<br />

of fatigue <strong>in</strong> swimm<strong>in</strong>g.<br />

reFerences<br />

Aujouannet YA, Bonifazi M, H<strong>in</strong>tzy F, Vuillerme N, Rouard AH<br />

(2006). Effects of a high-<strong>in</strong>tensity swim test on k<strong>in</strong>ematic parameters<br />

<strong>in</strong> high-level athletes. Applied Physiology, Nutrition <strong>and</strong> Metabolism,<br />

31, 150–158.<br />

Caty, V., Aujouannet, Y., H<strong>in</strong>tzy, F., Bonifazi, M., Clarys, J.P.,Rouard,<br />

A.H. (2007). Wrist stabilisation <strong>and</strong> forearm muscle coactivation<br />

dur<strong>in</strong>g freestyle swimm<strong>in</strong>g. J Electromyogr K<strong>in</strong>esiol., 17(3), 285-91.<br />

Clarys, J.P. & Cabri, J. (1993). Electromyography <strong>and</strong> the study of sports<br />

movements: A review. Journal of Sports Sciences, 11, 379-448.<br />

Knaflitz M. Bonato P (1999). Time-frequency methods applied to muscle<br />

fatigue assessment dur<strong>in</strong>g dynamic contractions. J Electromyogr<br />

K<strong>in</strong>esiol, 9, 337-350.<br />

Monteil,K.M., Rouard, A.H., Dufour, A.B., Cappaert, J.M., Troup,J.P<br />

(1996) Swimmers’shoulder: EMG of the rotators dur<strong>in</strong>g a flume test.<br />

In: <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VII., 83-89.<br />

Rouard, A. H., Billat, R. P., Deschodt, V., Clarys, J. P. (1997) Muscular<br />

activations dur<strong>in</strong>g repetitions of scull<strong>in</strong>g movements up to exhaustion<br />

<strong>in</strong> swimm<strong>in</strong>g. Arch Physiol Biochem., 105(7), 655-62.<br />

Rouard, A.H. et al (2006). Isometric force, tethered force <strong>and</strong> power<br />

ratios as tools for the evaluation of technical ability <strong>in</strong> freestyle swimm<strong>in</strong>g.<br />

In <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X, 249-250.<br />

Wakayoshi K, et al (1994) Electromyographyc evidence of selective<br />

muscle fatigue dur<strong>in</strong>g competitive swimm<strong>in</strong>g. In: <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science<br />

<strong>in</strong> Aquatic Sports, 39, 16-23.<br />

Inter-Limb Coord<strong>in</strong>ation <strong>in</strong> Swimm<strong>in</strong>g<br />

seifert, l.<br />

chaPter1.<strong>in</strong>vitedLectures<br />

Centre d’Etude des Transformations des Activités Physiques et Sportives<br />

(CETAPS), University of Rouen, Faculty of Sports Sciences, France<br />

Expert <strong>and</strong> non-expert swimmers show both similarities <strong>and</strong> differences<br />

<strong>in</strong> their <strong>in</strong>ter-limb coord<strong>in</strong>ation, which should be of <strong>in</strong>terest to scientists<br />

<strong>and</strong> coaches. The effects of speed, active drag, energy cost <strong>and</strong> breath<strong>in</strong>g<br />

have been analysed dur<strong>in</strong>g <strong>in</strong>cremental tests <strong>and</strong> rac<strong>in</strong>g, particularly <strong>in</strong><br />

front crawl. In the past, it was reported that <strong>in</strong>ter-limb coord<strong>in</strong>ation<br />

should show an opposition mode, i.e. cont<strong>in</strong>uity between the propulsions<br />

of the two limbs, <strong>in</strong> order to m<strong>in</strong>imize the <strong>in</strong>tra-cyclic speed variations.<br />

However, the <strong>in</strong>ter-limb coord<strong>in</strong>ation mode adopted by swimmers<br />

emerges from the three types of constra<strong>in</strong>ts def<strong>in</strong>ed by Newell (1986):<br />

organismic, task <strong>and</strong> environmental. The swimmer’s skill level, specialty,<br />

gender, anthropometry, h<strong>and</strong>edness <strong>and</strong> breath<strong>in</strong>g laterality act as organismic<br />

constra<strong>in</strong>ts; the imposed race pace, stroke frequency, breath<strong>in</strong>g<br />

frequency <strong>and</strong> pattern can be considered as task constra<strong>in</strong>ts; <strong>and</strong> active<br />

drag <strong>and</strong> its correspondent speed are the environmental constra<strong>in</strong>ts.<br />

Inter-limb coord<strong>in</strong>ation was found to vary from catch-up or glide mode<br />

to superposition mode, <strong>in</strong>dicat<strong>in</strong>g that the opposition mode is only the<br />

best ‘theoretically’ <strong>and</strong> that the glide mode is not a technical mistake.<br />

Therefore, rather than focus<strong>in</strong>g on develop<strong>in</strong>g an ideal coord<strong>in</strong>ation<br />

mode, coaches would do better to vary the learn<strong>in</strong>g situations for swimmers<br />

as they seek to develop optimal coord<strong>in</strong>ation. This paper presents<br />

new <strong>in</strong>formation about <strong>in</strong>ter-limb coord<strong>in</strong>ation based on the relative<br />

duration of arm stroke phases <strong>and</strong> the time gap between propulsive actions<br />

assessed by the <strong>in</strong>dex of coord<strong>in</strong>ation (IdC) <strong>in</strong> front crawl. Interest<strong>in</strong>g<br />

f<strong>in</strong>d<strong>in</strong>gs have emerged with implications for how both expert <strong>and</strong><br />

non-expert swimmers should be coached.<br />

Key words: motor control, biomechanics, coord<strong>in</strong>ation mode, constra<strong>in</strong>t.<br />

IntroductIon<br />

Why is it important to talk about <strong>in</strong>ter-limb coord<strong>in</strong>ation <strong>in</strong> swimm<strong>in</strong>g?<br />

The forward displacement dur<strong>in</strong>g swimm<strong>in</strong>g results from the ratio between<br />

propulsive <strong>and</strong> resistive forces, <strong>and</strong> many studies have thus quite<br />

rightly focused on active drag m<strong>in</strong>imization, propulsion generation <strong>and</strong>/<br />

or propulsive efficiency (Toussa<strong>in</strong>t & Truijens, 2005). However, two<br />

swimmers can apply the same force <strong>and</strong>/or deliver the same power output<br />

without exhibit<strong>in</strong>g the same <strong>in</strong>ter-limb coord<strong>in</strong>ation. In fact, the<br />

swimmer has to organize the transition between the underwater <strong>and</strong><br />

above-water phases of the cycle (except <strong>in</strong> breaststroke), <strong>and</strong> the time<br />

devoted to propulsion <strong>and</strong> glide dur<strong>in</strong>g the underwater part of the cycle.<br />

Thus, <strong>in</strong>ter-limb coord<strong>in</strong>ation may not automatically serve only to propel<br />

the body forward, as part of the motor organization may be dedicated<br />

to float<strong>in</strong>g <strong>and</strong> breath<strong>in</strong>g. Inter-limb coord<strong>in</strong>ation is related to motor<br />

control <strong>and</strong> motor learn<strong>in</strong>g, which raises the question: Is there a direct<br />

l<strong>in</strong>k between coord<strong>in</strong>ation <strong>and</strong> propulsion? The key po<strong>in</strong>t def<strong>in</strong><strong>in</strong>g the beg<strong>in</strong>n<strong>in</strong>g<br />

of propulsion is subject to debate, as Newton’s third law dictates<br />

a backward h<strong>and</strong> movement, while the Bernoulli hydrodynamics law favours<br />

a h<strong>and</strong> scull<strong>in</strong>g movement. Our studies of <strong>in</strong>ter-limb coord<strong>in</strong>ation<br />

thus deliberately used key po<strong>in</strong>ts that were qualitatively easy to observe.<br />

These may have overestimated the boundaries of propulsion (beg<strong>in</strong>n<strong>in</strong>g<br />

<strong>and</strong> end) but nevertheless provided a useful tool for analys<strong>in</strong>g propulsive<br />

behaviour. For example, <strong>in</strong> front crawl, Chollet et al. (2000) assumed<br />

that arm propulsion starts when the h<strong>and</strong> moves backward. This means<br />

that relative h<strong>and</strong> speed calculated by subtract<strong>in</strong>g absolute hip speed<br />

from the absolute h<strong>and</strong> speed observed on 2D is used to determ<strong>in</strong>e the<br />

backward h<strong>and</strong> speed (i.e. <strong>in</strong> the swimmer’s reference <strong>and</strong> not <strong>in</strong> the<br />

pool reference). Then, from the key po<strong>in</strong>ts determ<strong>in</strong><strong>in</strong>g the beg<strong>in</strong>n<strong>in</strong>g<br />

35


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

<strong>and</strong> the end of the arm stroke phases <strong>in</strong> front crawl (entry+catch, pull,<br />

push, recovery), Chollet et al. (2000) established an <strong>in</strong>dex of coord<strong>in</strong>ation<br />

(IdC) that quantifies the time lag between the propulsion of one<br />

arm <strong>and</strong> that of the second arm. The IdC has been adapted for the four<br />

strokes (backstroke, Chollet et al., 2008; butterfly, Chollet et al., 2006;<br />

breaststroke, Chollet et al., 2004; for a review, Chollet & Seifert, 2010,<br />

Seifert & Chollet, 2008) <strong>in</strong> order to assess the time gaps quantify<strong>in</strong>g the<br />

upper limb coord<strong>in</strong>ation <strong>in</strong> the alternat<strong>in</strong>g strokes <strong>and</strong> the upper-lower<br />

limb coord<strong>in</strong>ation <strong>in</strong> the simultaneous strokes. Therefore, when IdC =<br />

0%, the mode is opposition; when IdC < 0%, the mode is catch-up; <strong>and</strong><br />

when IdC > 0%, the mode is superposition. From a functional po<strong>in</strong>t of<br />

view, it is nevertheless reasonable to consider the opposition mode as<br />

-1% < IdC < 1%. It should also be noted that these <strong>in</strong>dicators rema<strong>in</strong><br />

<strong>in</strong>dices of coord<strong>in</strong>ation <strong>and</strong> not propulsion. Coord<strong>in</strong>ation can be studied<br />

from an ‘egocentric’ po<strong>in</strong>t of view (degrees of freedom, i.e. limb movement<br />

possibilities like flexion <strong>and</strong> extension, pronation <strong>and</strong> sup<strong>in</strong>ation,<br />

rotation, etc.) rather than from an ‘allocentric’ po<strong>in</strong>t of view (propulsion<br />

phases <strong>and</strong> concepts). Seifert et al. (2010a) therefore recently assessed<br />

upper-lower coord<strong>in</strong>ation <strong>in</strong> breaststroke from the angle <strong>and</strong> angular<br />

velocity of the elbow <strong>and</strong> knee to determ<strong>in</strong>e their coupl<strong>in</strong>g by the calculation<br />

of the cont<strong>in</strong>uous relative phase.<br />

Two swimmers can achieve the same performance (swimm<strong>in</strong>g<br />

speed) us<strong>in</strong>g different modes of <strong>in</strong>ter-limb coord<strong>in</strong>ation. Thus, a second<br />

question arises: Is there a relationship between coord<strong>in</strong>ation <strong>and</strong><br />

performance? In other words, is there an ideal <strong>in</strong>ter-limb coord<strong>in</strong>ation<br />

mode? Should the coach advise the swimmer to favour superposition<br />

coord<strong>in</strong>ation rather than opposition? Is the catch-up or glide mode a<br />

technical mistake? Should the beg<strong>in</strong>ner imitate the expert swimmer?<br />

Or is it reasonable to allow a temporary ‘non-expert’ coord<strong>in</strong>ation mode<br />

at the beg<strong>in</strong>n<strong>in</strong>g of the learn<strong>in</strong>g <strong>and</strong> tra<strong>in</strong><strong>in</strong>g process? The aim of this<br />

paper is to show that coord<strong>in</strong>ation emerges pr<strong>in</strong>cipally from <strong>in</strong>teract<strong>in</strong>g<br />

constra<strong>in</strong>ts (Newell, 1986): environmental (aquatic resistances <strong>and</strong><br />

speed as resistance equal to speed squared), task (imposed by the operator,<br />

e.g. swimm<strong>in</strong>g at maximal <strong>in</strong>tensity, swimm<strong>in</strong>g <strong>in</strong> fatigue condition)<br />

<strong>and</strong> organismic (correspond<strong>in</strong>g to the swimmer’s characteristics,<br />

i.e. anthropometry, morphology, strength, etc.). From this perspective,<br />

the swimmer’s <strong>in</strong>ter-limb coord<strong>in</strong>ation is a consequence of <strong>in</strong>teract<strong>in</strong>g<br />

constra<strong>in</strong>ts <strong>and</strong> not a cause (for a review, see Davids et al., 2008). Thus,<br />

coaches should (i) take the organismic constra<strong>in</strong>ts <strong>in</strong>to account, (ii) f<strong>in</strong>d<br />

means to m<strong>in</strong>imize the environmental constra<strong>in</strong>ts, <strong>and</strong> (iii) manipulate<br />

the task constra<strong>in</strong>ts to destabilize <strong>in</strong>adequate coord<strong>in</strong>ation <strong>in</strong> order to<br />

br<strong>in</strong>g about a coord<strong>in</strong>ation mode not expected from the beg<strong>in</strong>ner’s <strong>in</strong>itial<br />

behaviour. Direct manipulation of coord<strong>in</strong>ation to improve performance<br />

requires great care, however, <strong>and</strong> the swimmer should <strong>in</strong>itially work<br />

at adopt<strong>in</strong>g the imposed behaviour without try<strong>in</strong>g to improve performance.<br />

For example, if superposition coord<strong>in</strong>ation is the target coord<strong>in</strong>ation,<br />

the swimmer may <strong>in</strong>crease his stroke frequency, thereby slipp<strong>in</strong>g<br />

through the water without achiev<strong>in</strong>g the expected performance. When<br />

coaches directly manipulate coord<strong>in</strong>ation, they therefore need to keep <strong>in</strong><br />

m<strong>in</strong>d the importance of ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the same performance level.<br />

The follow<strong>in</strong>g sections present the similar behaviours <strong>and</strong> ma<strong>in</strong> differences<br />

between expert <strong>and</strong> non-expert front crawl swimmers regard<strong>in</strong>g<br />

(i) the effects of swim speed, active drag <strong>and</strong> energy cost; (ii) the<br />

relationships between coord<strong>in</strong>ation, propulsion <strong>and</strong> efficiency; (iii) the<br />

relationships between coord<strong>in</strong>ation <strong>and</strong> performance, bear<strong>in</strong>g <strong>in</strong> m<strong>in</strong>d<br />

that coord<strong>in</strong>ation may be either flexible or stable; <strong>and</strong> (iv) the effect of<br />

breath<strong>in</strong>g, which suggests that swimmers organise their limb coupl<strong>in</strong>g<br />

not only to propel but also to breathe <strong>and</strong> float.<br />

coordInAtIon, sWIM sPeed, ActIVe drAG And enerGY<br />

cost<br />

Accord<strong>in</strong>g to Newton’s second law ( ∑ F = m. a , where F is the force, m<br />

the mass <strong>and</strong> a the acceleration), forward body displacement is related<br />

to the differences between the propulsive forces generated by the swimmer<br />

<strong>and</strong> the aquatic resistive forces (i.e. the environmental constra<strong>in</strong>ts).<br />

36<br />

In fact, forward body displacement seems to be a more complex process<br />

<strong>and</strong> the swimmer may cross several solutions, probably the production of<br />

propulsive forces, the m<strong>in</strong>imization of active drag, the maximization of<br />

propulsive efficiency (i.e. m<strong>in</strong>imization of k<strong>in</strong>etic energy) <strong>and</strong> the monitor<strong>in</strong>g<br />

of <strong>in</strong>ter-limb coord<strong>in</strong>ation.<br />

Thus, when active drag <strong>and</strong> speed (active drag changes with speed<br />

squared) <strong>in</strong>crease, <strong>in</strong>ter-limb coord<strong>in</strong>ation is affected, particularly by a<br />

decrease <strong>in</strong> the time lag between two propulsions, which means that<br />

the relative duration of the glide <strong>and</strong> catch phases decreases. In front<br />

crawl, Chollet et al. (2000) <strong>and</strong> Seifert et al. (2004, 2007b) showed that<br />

speed <strong>in</strong>creases lead to similar motor behaviour <strong>in</strong> expert male, expert<br />

female, <strong>and</strong> non-expert male swimmers: they <strong>in</strong>crease the IdC <strong>and</strong> simultaneously<br />

<strong>in</strong>crease stroke rate <strong>and</strong> decrease stroke length. Seifert et<br />

al. (2010b) used an arms-only protocol both on the Measur<strong>in</strong>g Active<br />

Drag (MAD) system to assess active drag dur<strong>in</strong>g an <strong>in</strong>cremental test<br />

<strong>and</strong> while swimm<strong>in</strong>g <strong>in</strong> free condition to assess <strong>in</strong>ter-arm coord<strong>in</strong>ation<br />

<strong>in</strong> front crawl. They showed a l<strong>in</strong>ear regression between active drag <strong>and</strong><br />

IdC (0.64 < R² < 0.98), confirm<strong>in</strong>g that swimmers have to modify their<br />

motor organization when the task (speed) <strong>and</strong> environmental (drag)<br />

constra<strong>in</strong>ts <strong>in</strong>crease.<br />

Similar results were found when energy cost <strong>in</strong>creased: reach<strong>in</strong>g<br />

higher speed leads to higher energy expenditure <strong>and</strong> <strong>in</strong>creases IdC <strong>and</strong><br />

stroke rate (Morais et al., 2008; Seifert et al., 2009).<br />

coordInAtIon, ProPulsIon And eFFIcIencY<br />

Only expert swimmers atta<strong>in</strong> high speeds, as they are able to generate<br />

high power output <strong>and</strong> reach high IdC. Indeed, when expert swimmers<br />

<strong>in</strong>crease their speed <strong>and</strong>/or their stroke rate above a critical value (respectively<br />

~1.8 m.s -1 <strong>and</strong> 50 stroke.m<strong>in</strong> -1 ), only the superposition mode<br />

is observed (Potdev<strong>in</strong> et al., 2006; Seifert et al., 2007b), which may be<br />

attributed to the dom<strong>in</strong>ance of wave drag. When mov<strong>in</strong>g at high speed<br />

<strong>in</strong> whole stroke (> 1.5-1.7 m.s -1 ), wave drag becomes even greater, account<strong>in</strong>g<br />

for up to 50-60% of total drag (Toussa<strong>in</strong>t & Truijens, 2005;<br />

Vennell et al., 2006). Us<strong>in</strong>g a process similar to the calculation of “hull<br />

speed” for a ship, the authors mentioned above found that the hull speed<br />

for a swimmer with an arbitrary height of 2 m was 1.77 m.s -1 (Toussa<strong>in</strong>t<br />

& Truijens, 2005). This f<strong>in</strong>d<strong>in</strong>g co<strong>in</strong>cides with the large <strong>in</strong>crease <strong>in</strong> active<br />

drag found above this critical speed (> 1.7-1.8 m.s -1 ), as determ<strong>in</strong>ed<br />

by the wave drag, the environmental constra<strong>in</strong>ts elicit<strong>in</strong>g a superposition<br />

coord<strong>in</strong>ation of the arms. Indeed, it was recently shown that an<br />

<strong>in</strong>crease <strong>in</strong> speed leads to simultaneous changes <strong>in</strong> drag force, power<br />

output <strong>and</strong> <strong>in</strong>ter-arm coord<strong>in</strong>ation. While swimm<strong>in</strong>g only with arms<br />

<strong>in</strong> the free swimm<strong>in</strong>g condition, expert front crawl swimmers switch<br />

the <strong>in</strong>ter-arm coord<strong>in</strong>ation from catch-up mode (IdC < 0%) to superposition<br />

mode (IdC > 0%) above a speed of 1.5-1.6 m.s -1 at maximal<br />

<strong>in</strong>tensity (Seifert et al., 2010c). Us<strong>in</strong>g arms-only on the MAD system,<br />

the same swimmers exhibited a drag force of 100-110 N at maximal<br />

<strong>in</strong>tensity, develop<strong>in</strong>g a mechanical power output of ~200 W (Seifert et<br />

al., 2010c). Conversely, less-expert swimmers also swimm<strong>in</strong>g at maximal<br />

speed exhibited a drag force < 100 N, power output < 180 W <strong>and</strong> <strong>in</strong>terarm<br />

coord<strong>in</strong>ation <strong>in</strong> catch-up mode (IdC < -6%), which did not enable<br />

them to reach the same speeds as the expert swimmers. On the other<br />

h<strong>and</strong>, a high IdC does not guarantee high speed, as the swimmer can<br />

slip through the water <strong>and</strong>/or spend a long time <strong>in</strong> the propulsive phase<br />

because of slowed h<strong>and</strong> speed, mean<strong>in</strong>g low propulsive efficiency. Notably,<br />

Seifert et al. (2010b) showed that IdC <strong>in</strong>creases with active drag<br />

<strong>in</strong> experts, but that at maximal <strong>in</strong>tensity (swimm<strong>in</strong>g 25m all out) IdC<br />

is not correlated with propulsive efficiency for this sample of swimmers.<br />

Moreover, when speed <strong>in</strong>creased, expert swimmers <strong>in</strong>creased IdC while<br />

their hip <strong>in</strong>tra-cyclic speed variation rema<strong>in</strong>ed stable with a coefficient<br />

of variation close to 0.15 (Schnitzler et al., 2008; Seifert et al., 2010c).<br />

Conversely, non-expert swimmers did not significantly change their<br />

arm coord<strong>in</strong>ation (which rema<strong>in</strong>ed <strong>in</strong> catch-up mode) while their hip<br />

<strong>in</strong>tra-cyclic speed variation <strong>in</strong>creased (from 0.16 to 0.21). These results<br />

suggest that, unlike non-experts, expert swimmers make effective motor


adaptations to <strong>in</strong>creased aquatic resistance. They also <strong>in</strong>dicate that IdC<br />

is an <strong>in</strong>terest<strong>in</strong>g tool to assess motor control <strong>and</strong> motor learn<strong>in</strong>g, even<br />

though the l<strong>in</strong>ks between coord<strong>in</strong>ation <strong>and</strong> propulsion <strong>and</strong> efficiency are<br />

not automatic. Therefore, if the coach’s goal is to relate coord<strong>in</strong>ation to<br />

performance, the effectiveness of <strong>in</strong>ter-arm coord<strong>in</strong>ation (i.e. IdC value)<br />

should be analyzed with regard to some of the <strong>in</strong>dicators of propulsive<br />

efficiency (power output, <strong>in</strong>tra-cyclic speed variations, swim speed/h<strong>and</strong><br />

speed ratio, stroke <strong>in</strong>dex, power output/ total power ratio).<br />

coordInAtIon And PerForMAnce: Fle<strong>XI</strong>BIlItY–<br />

stABIlItY?<br />

As noted, the IdC value does not rema<strong>in</strong> the same whatever the speed.<br />

Indeed, swimm<strong>in</strong>g speed is not uniform as the application of propulsive<br />

forces <strong>in</strong> water leads to acceleration <strong>and</strong> deceleration with<strong>in</strong> the cycle,<br />

i.e. to <strong>in</strong>tra-cyclic speed variations of the centre of gravity (Miller, 1975;<br />

Miyashita, 1971). The opposition mode of coord<strong>in</strong>ation thus appears as<br />

‘theoretically’ ideal because it should allow propulsive cont<strong>in</strong>uity (assumed<br />

by the alternat<strong>in</strong>g actions of the two arms) <strong>and</strong> limit the <strong>in</strong>tracyclic<br />

speed variations of the centre of gravity. In practice, there is not<br />

an ideal mode of coord<strong>in</strong>ation as <strong>in</strong>ter-arm coord<strong>in</strong>ation changes with<br />

the task <strong>and</strong> environmental constra<strong>in</strong>ts. Moreover, an analysis of expert<br />

front crawl spr<strong>in</strong>ters swimm<strong>in</strong>g from their slowest to their fastest speeds<br />

showed <strong>in</strong>ter-<strong>in</strong>dividual variations <strong>in</strong> the range of <strong>in</strong>ter-arm coord<strong>in</strong>ation<br />

modes <strong>and</strong> <strong>in</strong> speeds (Fig. 1). This raises the question: Is the expert<br />

swimmer an ultra-specialist <strong>in</strong> one stroke <strong>and</strong> one race distance or a<br />

swimmer with flexible behavior, able to w<strong>in</strong> <strong>in</strong> several strokes <strong>and</strong> events<br />

(like L. Manaudou <strong>and</strong> M. Phelps)?<br />

Speed (m . a<br />

Figure 1. Quadratic regression between <strong>in</strong>ter-arm coord<strong>in</strong>ation <strong>and</strong><br />

speed for expert front crawl spr<strong>in</strong>ters (adapted from Seifert & Chollet,<br />

2009).<br />

-1 )<br />

The results suggested four theoretical profiles (Fig. 2): 1) small scales<br />

of speed <strong>and</strong> coord<strong>in</strong>ation, 2) a small scale of speed <strong>and</strong> a large scale of<br />

coord<strong>in</strong>ation, 3) a large scale of speed <strong>and</strong> a small scale of coord<strong>in</strong>ation,<br />

<strong>and</strong> 4) large scales of speed <strong>and</strong> coord<strong>in</strong>ation.<br />

Speed<br />

Figure 2. Four profiles of relationship between coord<strong>in</strong>ation <strong>and</strong> speed<br />

(adapted from Seifert et al., 2009)<br />

chaPter1.<strong>in</strong>vitedLectures<br />

The first profile corresponds to swimmers with little ‘motor flexibility’<br />

<strong>in</strong> coord<strong>in</strong>ation <strong>and</strong> speed. These could be ‘ultra-specialists’, tra<strong>in</strong><strong>in</strong>g<br />

mostly <strong>in</strong> one way. For example, because they tra<strong>in</strong> mostly for endurance,<br />

triathletes ma<strong>in</strong>ta<strong>in</strong> their <strong>in</strong>ter-arm coord<strong>in</strong>ation <strong>in</strong> catch-up mode with<br />

extremely negative values for IdC (Hue et al., 2003). The second profile<br />

corresponds to an <strong>in</strong>effective high value for coord<strong>in</strong>ation, because high<br />

speed cannot be atta<strong>in</strong>ed. As po<strong>in</strong>ted out by Seifert et al. (2007a), some<br />

non-expert swimmers switch to superposition coord<strong>in</strong>ation mode because<br />

they spend more time with their h<strong>and</strong> <strong>in</strong> the propulsive phase,<br />

due to slow h<strong>and</strong> speed, but therefore do not generate high force. The<br />

third profile corresponds to swimmers with stable <strong>in</strong>ter-arm coord<strong>in</strong>ation<br />

while reach<strong>in</strong>g high speeds. These swimmers may be focused on<br />

the change <strong>in</strong> the ratio between stroke rate <strong>and</strong> stroke length. For example,<br />

Figure 3 shows one swimmer of the French team (participated<br />

<strong>in</strong> the 4 x 100m at the Atlanta Olympic Games <strong>in</strong> 1996) who kept his<br />

coord<strong>in</strong>ation stable with IdC close to the ‘theoretically’ more efficient<br />

coord<strong>in</strong>ation mode (i.e. opposition), mostly chang<strong>in</strong>g his stroke rate/<br />

stroke length ratio.<br />

Figure 3. Changes <strong>in</strong> stroke rate (SR) <strong>and</strong> stroke length (SL) while <strong>in</strong>dex<br />

of coord<strong>in</strong>ation (IdC) rema<strong>in</strong>s stable dur<strong>in</strong>g 7 x 25 m <strong>in</strong>creased <strong>in</strong><br />

speed.<br />

The fourth profile demonstrates that, the longer the coord<strong>in</strong>ation curve,<br />

the greater the swimmer’s range of coord<strong>in</strong>ation, <strong>in</strong>dicat<strong>in</strong>g motor flexibility<br />

<strong>in</strong> coord<strong>in</strong>ation. Indeed, the higher the maximal coord<strong>in</strong>ation <strong>and</strong><br />

the lower the m<strong>in</strong>imal coord<strong>in</strong>ation of the curve, the more the swimmer<br />

is explor<strong>in</strong>g human potential. To the coach, this <strong>in</strong>dicates that the swimmer<br />

atta<strong>in</strong>s a range of speeds depend<strong>in</strong>g on the type of coord<strong>in</strong>ation<br />

mode: catch-up mode by us<strong>in</strong>g glide time, or superposition mode by<br />

overlapp<strong>in</strong>g the propulsive phases. From this perspective, the IdC value<br />

itself does not <strong>in</strong>dicate the swimmer’s performance, but only the behavioral<br />

flexibility with respect to the <strong>in</strong>teract<strong>in</strong>g constra<strong>in</strong>ts (Newell, 1986;<br />

Seifert et al., 2007b). As suggested above, coord<strong>in</strong>ation should be related<br />

to other parameters of propulsive efficiency <strong>in</strong> order to draw conclusions<br />

about performance.<br />

On the other h<strong>and</strong>, race analyses have mostly po<strong>in</strong>ted out that high<br />

performance is related to stability or m<strong>in</strong>imal change <strong>in</strong> the strok<strong>in</strong>g<br />

parameters, i.e. speed, stroke length <strong>and</strong> stroke rate (Sidney et al., 2010).<br />

Concern<strong>in</strong>g arm coord<strong>in</strong>ation, expert swimmers showed relatively stable<br />

IdC values over the course of a race, whereas lower expertise <strong>and</strong>/or<br />

fatigue was <strong>in</strong>dicated by an <strong>in</strong>crease <strong>in</strong> IdC (Seifert et al., 2007a). For<br />

example, dur<strong>in</strong>g a 100m race, Seifert et al. (2007a) observed that the<br />

non-expert swimmers (who seemed more tired as they took 8.5 s more<br />

than the experts to complete the 100m) <strong>in</strong>creased IdC from opposition<br />

to superposition coord<strong>in</strong>ation <strong>in</strong> the last part of the 100m. Accord<strong>in</strong>g<br />

to Suito et al. (2008) <strong>and</strong> Toussa<strong>in</strong>t et al. (2006), these changes <strong>in</strong> arm<br />

coord<strong>in</strong>ation may be related to lower h<strong>and</strong> speed, power output <strong>and</strong><br />

propell<strong>in</strong>g efficiency <strong>in</strong> the last part of the 100m (for the analyses of<br />

37


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

the 200m event, see Alberty et al. (2005); for the 400m, see Schnitzler<br />

et al. (2010)).<br />

Last, as regards the task <strong>and</strong> environmental constra<strong>in</strong>ts, coord<strong>in</strong>ation<br />

flexibility or/<strong>and</strong> stability are useful <strong>in</strong>dicators of motor skill <strong>in</strong> swimm<strong>in</strong>g.<br />

WhY coordInAtIon? to Go ForWArd? or Also<br />

For FloAtInG And BreAthInG?<br />

As suggested <strong>in</strong> the <strong>in</strong>troduction, the limbs are coord<strong>in</strong>ated not only to<br />

propel the body forward, but also to facilitate or improve float<strong>in</strong>g <strong>and</strong><br />

breath<strong>in</strong>g. For example, expert <strong>and</strong> non-expert swimmers hav<strong>in</strong>g unilateral<br />

breath<strong>in</strong>g patterns (every 2 or 4 strokes) showed an asymmetric<br />

coord<strong>in</strong>ation, which was most often related to breath<strong>in</strong>g laterality (i.e. a<br />

preferential breath<strong>in</strong>g side) <strong>and</strong> motor laterality (arm dom<strong>in</strong>ance) (Seifert<br />

et al., 2005). This means that catch-up coord<strong>in</strong>ation mostly occurred<br />

to the same side as breath<strong>in</strong>g <strong>and</strong> arm dom<strong>in</strong>ance, while the swimmer<br />

showed superposition coord<strong>in</strong>ation to the other side. This coord<strong>in</strong>ation<br />

asymmetry was found to be greater <strong>in</strong> non-expert swimmers because<br />

the time spent <strong>in</strong>hal<strong>in</strong>g led them to a lag time <strong>in</strong> propulsion (Lerda<br />

et al., 2001). Notably, non-experts prolonged the catch with the arms<br />

extended forward to facilitate head rotation dur<strong>in</strong>g breath<strong>in</strong>g <strong>and</strong> thus<br />

by catch-up to the breath<strong>in</strong>g side. Conversely, swimmers with bilateral<br />

breath<strong>in</strong>g patterns (every 3 or 5 strokes) tended to balance the arm coord<strong>in</strong>ation<br />

by distribut<strong>in</strong>g the asymmetries (Seifert et al., 2005). Thus, it<br />

may be advisable to vary the learn<strong>in</strong>g situations to encourage symmetric<br />

coord<strong>in</strong>ation, i.e. alternat<strong>in</strong>g tasks with unilateral, bilateral <strong>and</strong> frontal<br />

snorkel breath<strong>in</strong>g. To confirm this hypothesis, breath<strong>in</strong>g laterality was<br />

manipulated <strong>in</strong> non-expert swimmers by impos<strong>in</strong>g seven breath<strong>in</strong>g patterns,<br />

divided <strong>in</strong>to unilateral patterns <strong>and</strong> bilateral patterns (Seifert et<br />

al., 2008). The authors showed that breath<strong>in</strong>g to the preferential side<br />

led to an asymmetry, <strong>in</strong> contrast to the other breath<strong>in</strong>g patterns, <strong>and</strong> the<br />

asymmetry was even greater when the swimmer breathed to his nonpreferential<br />

side (Seifert et al., 2008). Moreover, coord<strong>in</strong>ation was symmetric<br />

<strong>in</strong> patterns with breath<strong>in</strong>g that was bilateral, axed (as <strong>in</strong> breath<strong>in</strong>g<br />

with a frontal snorkel) or removed (as <strong>in</strong> apnoea). From this viewpo<strong>in</strong>t,<br />

arm coord<strong>in</strong>ation was not only determ<strong>in</strong>ed by propulsion but also by<br />

breath<strong>in</strong>g <strong>and</strong> motor laterality, suggest<strong>in</strong>g that <strong>in</strong>structors should help<br />

swimmers (i) to determ<strong>in</strong>e their preferred side for unilateral breath<strong>in</strong>g<br />

<strong>and</strong> (ii) to adapt the breath<strong>in</strong>g pattern (e.g. by us<strong>in</strong>g bilateral patterns,<br />

apnoea <strong>in</strong> spr<strong>in</strong>t, frontal snorkel) dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g sessions when coord<strong>in</strong>ation<br />

asymmetry is disturb<strong>in</strong>g the stroke too much.<br />

conclusIon<br />

The ma<strong>in</strong> contribution of <strong>in</strong>ter-limb coord<strong>in</strong>ation analysis over the past<br />

decade has been the development of a useful tool for underst<strong>and</strong><strong>in</strong>g<br />

motor skills <strong>in</strong> swimm<strong>in</strong>g. The ma<strong>in</strong> f<strong>in</strong>d<strong>in</strong>gs can be summarized as follows:<br />

(i) there is no “correct” coord<strong>in</strong>ation but only coord<strong>in</strong>ation <strong>in</strong> relationship<br />

to <strong>in</strong>teract<strong>in</strong>g constra<strong>in</strong>ts, (ii) appropriate coord<strong>in</strong>ation is not<br />

synonymous with good propulsion because a certa<strong>in</strong> coord<strong>in</strong>ation mode<br />

is also adopted to facilitate breath<strong>in</strong>g or float<strong>in</strong>g, <strong>and</strong> (iii) coord<strong>in</strong>ation is<br />

not the cause but mostly the consequence of these constra<strong>in</strong>ts, thus impos<strong>in</strong>g<br />

a certa<strong>in</strong> coord<strong>in</strong>ation mode does not guarantee high performance<br />

or efficiency. It is therefore advisable to analyse the organismic, task<br />

<strong>and</strong> environmental constra<strong>in</strong>ts lead<strong>in</strong>g to the current behaviour rather<br />

than consider<strong>in</strong>g an ‘ideal’ behaviour based on a ‘theoretical’ background.<br />

AcKnoWledGMent<br />

I thank Didier Chollet, my pr<strong>in</strong>cipal colleague, who <strong>in</strong>itiated the research<br />

about <strong>in</strong>ter-limb coord<strong>in</strong>ation <strong>and</strong> supported me <strong>and</strong> many PhD<br />

students to work on this topic.<br />

38<br />

reFerences<br />

Alberty, M., Sidney, M., Huot-March<strong>and</strong>, F., Hespel, J.M., &<br />

Pelayo. P. (2005). Intracyclic velocity variations <strong>and</strong> arm coord<strong>in</strong>ation<br />

dur<strong>in</strong>g exhaustive exercise <strong>in</strong> front crawl stroke. International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 26, 471-475.<br />

Chollet, D., Chalies, S. & Chatard, J.C. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: description <strong>and</strong> usefulness. International Journal<br />

of Sports <strong>Medic<strong>in</strong>e</strong>, 21, 54-59.<br />

Chollet, D., & Seifert, L. (2010). Inter-limb coord<strong>in</strong>ation <strong>in</strong> the four<br />

competitive strokes. In L., Seifert, D., Chollet, & I., Mujika (Eds)<br />

The world book of swimm<strong>in</strong>g: from science to performance, Nova Science<br />

Publishers, Hauppauge, New York, <strong>in</strong> press.<br />

Chollet, D., Seifert, L., Boulesteix, L., & Carter, M. (2006). Arm to<br />

leg coord<strong>in</strong>ation <strong>in</strong> elite butterfly swimmers. International Journal of<br />

Sports <strong>Medic<strong>in</strong>e</strong>, 27, 322-329.<br />

Chollet, D., Seifert, L. & Carter, M. (2008). Arm coord<strong>in</strong>ation <strong>in</strong> elite<br />

backstroke swimmers. Journal of Sport Sciences, 26, 675-682.<br />

Chollet, D., Seifert, L., Leblanc, H., Boulesteix, L., & Carter, M. (2004).<br />

Evaluation of arm-leg coord<strong>in</strong>ation <strong>in</strong> flat breaststroke. International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 25, 486-495.<br />

Davids, K., Button, C., & Bennett, S. (2008) Dynamics of skill acquisition<br />

– A constra<strong>in</strong>ts-led approach, Champaign, Ill<strong>in</strong>ois, Human K<strong>in</strong>etics<br />

Publishers.<br />

Hue, O., Benavente, H., & Chollet, D. (2003). Swimm<strong>in</strong>g skill <strong>in</strong> triathletes<br />

<strong>and</strong> swimmers us<strong>in</strong>g the <strong>in</strong>dex of coord<strong>in</strong>ation. Journal of Human<br />

Movement Studies, 44, 107-120.<br />

Lerda, R., Cardelli, C., & Chollet D. (2001). Analysis of the <strong>in</strong>teractions<br />

between breath<strong>in</strong>g <strong>and</strong> arm actions <strong>in</strong> the front crawl. Journal of Human<br />

Movement Studies, 40, 129-144.<br />

Miller D. (1975). <strong>Biomechanics</strong> of swimm<strong>in</strong>g. Exercise <strong>and</strong> Sports Science<br />

Reviews, 3, 219-248.<br />

Miyashita M. (1971). An analysis of fluctuations of swimm<strong>in</strong>g speed. In<br />

J.P. Clarys & L. Lewillie (Eds) Swimm<strong>in</strong>g Science I, Brussels, University<br />

of Brussels, 53-57.<br />

Morais, P., Vilas-Boas, J.P., Seifert, L., Chollet, D., Kesk<strong>in</strong>en, K.L., &<br />

Fern<strong>and</strong>es R. (2008). Relationship between energy cost <strong>and</strong> the <strong>in</strong>dex<br />

of coord<strong>in</strong>ation <strong>in</strong> front crawl – a pilot study, 16th FINA World<br />

Sports <strong>Medic<strong>in</strong>e</strong> Congress, Journal of Sports Sciences, 26, (Suppl. 1), 11<br />

Newell, K.M. (1986). Constra<strong>in</strong>ts on the development of coord<strong>in</strong>ation.<br />

In M.G. Wade & H.T.A. Whit<strong>in</strong>g (Eds) Motor development <strong>in</strong><br />

children: aspect of coord<strong>in</strong>ation <strong>and</strong> control, (pp. 341-360). Dordrecht,<br />

Nijhoff.<br />

Potdev<strong>in</strong>, F., Bril, B., Sidney, M., & Pelayo, P. (2006). Stroke frequency<br />

<strong>and</strong> arm coord<strong>in</strong>ation <strong>in</strong> front crawl swimm<strong>in</strong>g. International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 27, 193-198.<br />

Schnitzler, C., Seifert, L., & Chollet, D. (2010) Arm coord<strong>in</strong>ation <strong>and</strong><br />

performance level <strong>in</strong> 400-m front crawl, Research Quarterly for Exercise<br />

<strong>and</strong> Sport, <strong>in</strong> press.<br />

Schnitzler, C., Seifert, L., Ernwe<strong>in</strong>, V., & Chollet, D. (2008). Intra-cyclic<br />

velocity variations as a tool to assess arm coord<strong>in</strong>ation adaptations <strong>in</strong><br />

elite swimmers. International Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 29, 480-486.<br />

Seifert, L. Boulesteix, L., & Chollet, D. (2004). Effect of gender on the<br />

adaptation of arm coord<strong>in</strong>ation <strong>in</strong> front crawl. International Journal of<br />

Sports <strong>Medic<strong>in</strong>e</strong>, 25, 217-223.<br />

Seifert, L., Chehensse, A., Tourny-Chollet, C., Lemaitre, F., &<br />

Chollet, D. (2008). Effect of breath<strong>in</strong>g pattern on arm coord<strong>in</strong>ation<br />

symmetry <strong>in</strong> front crawl. Journal of Strength <strong>and</strong> Condition<strong>in</strong>g<br />

Research, 22, 1670-1676.<br />

Seifert, L., & Chollet, D. (2008). Inter-limbs coord<strong>in</strong>ation <strong>and</strong> constra<strong>in</strong>ts<br />

<strong>in</strong> swimm<strong>in</strong>g: a review. In N.P. Beaulieu (Ed) Physical activity<br />

<strong>and</strong> children: new research, Nova Science Publishers, Hauppauge, New<br />

York, 65-93.<br />

Seifert, L., & Chollet, D. (2009). Modell<strong>in</strong>g spatial-temporal <strong>and</strong> coord<strong>in</strong>ative<br />

parameters <strong>in</strong> swimm<strong>in</strong>g, Journal of Science <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Sport, 12, 495-499.


Seifert, L., Chollet, D., & Allard, P. (2005). Arm coord<strong>in</strong>ation symmetry<br />

<strong>and</strong> breath<strong>in</strong>g effect <strong>in</strong> front crawl. Human Movement Science,<br />

24, 234-256.<br />

Seifert, L., Chollet, D., & Chatard, J.C. (2007a). Changes <strong>in</strong> coord<strong>in</strong>ation<br />

<strong>and</strong> k<strong>in</strong>ematics dur<strong>in</strong>g a 100-m front crawl. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science<br />

<strong>in</strong> Sports <strong>and</strong> Exercise, 39, 1784-1793.<br />

Seifert, L., Chollet, D., & Rouard, A. (2007b). Swimm<strong>in</strong>g constra<strong>in</strong>ts<br />

<strong>and</strong> arm coord<strong>in</strong>ation. Human Movement Science, 26, 68-86.<br />

Seifert, L., Daly, D., Burkett, B., & Chollet, D. (2009). The profile of<br />

aquatic motor skills for able-bodied <strong>and</strong> swimmers with an impairment.<br />

In L.T. Pelligr<strong>in</strong>o (Ed) H<strong>and</strong>book of Motor Skills: Development,<br />

Impairment <strong>and</strong> Therapy, Nova Science Publishers, Hauppauge, New<br />

York, 65-94<br />

Seifert, L., Leblanc, H., Chollet, D., & Delignières D. (2010a). Interlimb<br />

coord<strong>in</strong>ation <strong>in</strong> swimm<strong>in</strong>g: effect of speed <strong>and</strong> skill level, Human<br />

Movement Science, 29, 103-113.<br />

Seifert, L., Schnitzler, C., Alberty, M., Chollet, D., & Toussa<strong>in</strong>t, H.M.<br />

(2010b). Arm coord<strong>in</strong>ation, active drag <strong>and</strong> propell<strong>in</strong>g efficiency <strong>in</strong><br />

front crawl. In Kjendlie, P.L., Stallman, R., & Cabri, J. (Eds) <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong>, School of Physical Education,<br />

Oslo, Norway, <strong>in</strong> press.<br />

Seifert L., Toussa<strong>in</strong>t H.M., Alberty M., Schnitzler C. Chollet D.<br />

(2010c). Arm coord<strong>in</strong>ation, power <strong>and</strong> efficiency <strong>in</strong> national <strong>and</strong> regional<br />

front crawl swimmers, Human Movement Science, <strong>in</strong> press.<br />

Sidney, M., Alberty, M., Leblanc, H., & Chollet, D. (2010). Strok<strong>in</strong>g parameters<br />

dur<strong>in</strong>g competition. In L., Seifert, D., Chollet, & I., Mujika<br />

(Eds) The world book of swimm<strong>in</strong>g: from science to performance, Nova<br />

Science Publishers, Hauppauge, New York, <strong>in</strong> press.<br />

Suito, H., Ikegami,Y., Nunome, H., Sano, S., Sh<strong>in</strong>kai, H., & Tsujimoto,<br />

N. (2008). The effect of fatigue on the underwater arm stroke motion<br />

<strong>in</strong> the 100-m front crawl. Journal of Applied <strong>Biomechanics</strong>, 24,<br />

316-324.<br />

Toussa<strong>in</strong>t, H.M., Carol, A., Kranenborg, H., & Truijens, M. (2006).<br />

Effect of fatigue on strok<strong>in</strong>g characteristics <strong>in</strong> an arms-only 100-m<br />

front-crawl race. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports <strong>and</strong> Exercise, 38, 1635-<br />

1642.<br />

Toussa<strong>in</strong>t, H.M., & Truijens, M. (2005). Biomechanical aspects of peak<br />

performance <strong>in</strong> human swimm<strong>in</strong>g. Animal Biology, 55, 17-40.<br />

Vennell, R., Pease, D., & Wilson, B. (2006). Wave drag on humans<br />

swimmers. Journal of <strong>Biomechanics</strong>, 39, 664-671.<br />

chaPter1.<strong>in</strong>vitedLectures<br />

39


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi


Chapter 2. <strong>Biomechanics</strong>


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Comparison of Manik<strong>in</strong> Carry Performance by<br />

Lifeguards <strong>and</strong> Lifesavers When Us<strong>in</strong>g Barefoot,<br />

Flexible <strong>and</strong> Fiber F<strong>in</strong>s<br />

Abraldes, J.A. 1 , soares, s. 2 , lima, A.B. 2, 3 , Fern<strong>and</strong>es, r.J. 2 ,<br />

Vilas-Boas, J.P. 2<br />

1 University of Murcia, Faculty of Sports Sciences, Murcia, Spa<strong>in</strong><br />

2 University of Porto, Faculty of Sport, Cifi2d, Porto, Portugal<br />

3 Federal University of Ceará, Institute of Physical Education <strong>and</strong> Sports,<br />

Brazil<br />

The use of f<strong>in</strong>s is fundamental <strong>in</strong> aquatic sport <strong>and</strong> sav<strong>in</strong>g rescue activities,<br />

large variety of models exist<strong>in</strong>g <strong>in</strong> the market. The ma<strong>in</strong> purpose of<br />

this study was to compare two groups (lifeguards <strong>and</strong> lifesavers) perform<strong>in</strong>g<br />

a manik<strong>in</strong> carry effort us<strong>in</strong>g barefoot, flexible <strong>and</strong> fibre f<strong>in</strong>s. Ten<br />

licensed lifeguards <strong>and</strong> ten lifesavers performed 3 x 25 m with barefoot,<br />

flexible <strong>and</strong> fibre f<strong>in</strong>s <strong>in</strong> manik<strong>in</strong> carry connected to a cable speedometer<br />

that measured <strong>in</strong>stantaneous velocity (v). For lifesavers, fibre f<strong>in</strong>s<br />

allowed higher v values compared with flexible f<strong>in</strong>s. No differences between<br />

f<strong>in</strong>s models were observed regard<strong>in</strong>g v of lifeguards. Additionally,<br />

the use of flexible or fibre f<strong>in</strong>s do not show differences <strong>in</strong> fatigue <strong>in</strong>dex<br />

for both groups.<br />

Key words: <strong>Biomechanics</strong>, lifesav<strong>in</strong>g, rescue, fatigue<br />

IntroductIon<br />

The use of f<strong>in</strong>s is fundamental <strong>in</strong> some professional <strong>and</strong> sport aquatic<br />

activities (e.g. div<strong>in</strong>g, underwater fish<strong>in</strong>g, sea rescu<strong>in</strong>g, f<strong>in</strong> swimm<strong>in</strong>g,<br />

underwater hockey <strong>and</strong> sportive div<strong>in</strong>g). Aquatic rescue considers both<br />

professional <strong>and</strong> sportive events, <strong>in</strong> which lifeguards <strong>and</strong> lifesavers are<br />

be<strong>in</strong>g <strong>in</strong>volved, respectively. The purpose of each group is different: lifeguards<br />

are required to rescue a person for sav<strong>in</strong>g his/her life <strong>and</strong> don’t<br />

compete; lifesavers are asked to achieve a best performance aga<strong>in</strong>st the<br />

stopwatch <strong>and</strong> don’t save real persons. F<strong>in</strong>s are a fundamental element<br />

for both lifesavers <strong>and</strong> lifeguards, besides lifesavers don’t use f<strong>in</strong> <strong>in</strong> every<br />

events. Besides the difference <strong>in</strong> purposes, to choose the best f<strong>in</strong> model<br />

is a common concern of lifesavers <strong>and</strong> lifeguards.<br />

F<strong>in</strong>s can be classified <strong>in</strong> two major types: mono <strong>and</strong> s<strong>in</strong>gle f<strong>in</strong>s. Each<br />

type presents a large variety of models, be<strong>in</strong>g dist<strong>in</strong>guished by their stiffness,<br />

surface (width <strong>and</strong> length), flexibility <strong>and</strong> composition. Although<br />

monof<strong>in</strong>s allow higher velocities when compared to s<strong>in</strong>gle f<strong>in</strong>s (Zamparo<br />

et al., 2006), they could not be used for lifesav<strong>in</strong>g purposes, s<strong>in</strong>ce<br />

they do not allow walk<strong>in</strong>g <strong>in</strong> a real rescue situation.<br />

There are a limited number of studies on s<strong>in</strong>gle f<strong>in</strong>s efficacy. Nevertheless,<br />

some physiological parameters were studied by Daniel <strong>and</strong><br />

Klauck (1992). Authors found that lactate accumulation <strong>and</strong> heart rate<br />

trends <strong>in</strong> life-sav<strong>in</strong>g are comparable to those produced by competitive<br />

swimmers. Economy <strong>and</strong> efficiency were assessed by Zamparo et al.<br />

(2006), that found that large <strong>and</strong> heavy f<strong>in</strong>s were characterized by approximately<br />

the same economy <strong>and</strong> efficiency of f<strong>in</strong>s with smaller surface<br />

but better buoyancy. Carry<strong>in</strong>g by chest or head techniques were<br />

characterized by Juntunen et al. (2006), <strong>and</strong> the velocity <strong>in</strong> aquatic<br />

rescues was assessed by Abraldes et al. (2007). Last ones showed that<br />

velocity was higher when f<strong>in</strong>s were used, <strong>in</strong>dependently of the f<strong>in</strong> type.<br />

Consider<strong>in</strong>g the large variety of f<strong>in</strong> models available, it is important<br />

to underst<strong>and</strong> which is the best f<strong>in</strong> model fitt<strong>in</strong>g the needs of both lifesavers<br />

<strong>and</strong> lifeguards. Some studies were conducted <strong>in</strong> this topic, but <strong>in</strong><br />

different populations, analys<strong>in</strong>g swimm<strong>in</strong>g or mannequ<strong>in</strong>-carry events<br />

us<strong>in</strong>g different effort distances (Abraldes et al., 2007), but lifeguards <strong>and</strong><br />

lifesavers were never compared. Specialized literature leads to th<strong>in</strong>k that<br />

the best f<strong>in</strong> model is not necessarily the same for different populations<br />

but studies results are not homogeneous. In carry efforts related stud-<br />

42<br />

ies, results were different from those above. In fact, although differences<br />

were not found between different f<strong>in</strong> models <strong>in</strong> 25 m mannequ<strong>in</strong> carry<br />

effort (Abraldes, 2004), <strong>in</strong> another study with a similar sample, Abraldes<br />

(2005) found best carry performances when stiff f<strong>in</strong>s were used, comparatively<br />

with flexible, short <strong>and</strong> fibre f<strong>in</strong>s. Additionally, for 50 m carry<br />

performed by university students, Abraldes (2006) found that the use of<br />

stiff f<strong>in</strong>s allows higher performances comparatively with flexible f<strong>in</strong>s, but<br />

only <strong>in</strong> the first 25 m of the effort. Contradictory f<strong>in</strong>d<strong>in</strong>gs could probably<br />

be related with differences <strong>in</strong> subjects’ number <strong>and</strong> characteristics.<br />

Lastly, Abraldes et al. (2007) analyzed carry velocity with barefoot, flexible<br />

<strong>and</strong> fibre f<strong>in</strong>s obta<strong>in</strong>ed by lifeguards. Authors observed that fibre<br />

f<strong>in</strong>s can provide a steadier velocity dur<strong>in</strong>g a short spr<strong>in</strong>t, comparatively<br />

with flexible f<strong>in</strong>s.<br />

S<strong>in</strong>ce it was never tried to compare lifesavers <strong>and</strong> lifeguards concern<strong>in</strong>g<br />

f<strong>in</strong> models, the ma<strong>in</strong> purpose of this study was to compare these<br />

two groups perform<strong>in</strong>g a manik<strong>in</strong> carry effort us<strong>in</strong>g barefoot, flexible<br />

<strong>and</strong> fibre f<strong>in</strong>s. Complementarily, it was aimed to study fatigue <strong>in</strong> carry,<br />

s<strong>in</strong>ce literature is scarce about this subject.<br />

Methods<br />

Twenty subjects, 10 licensed lifeguards <strong>and</strong> 10 lifesavers, were tested.<br />

The ma<strong>in</strong> physical characteristics of the subjects are described <strong>in</strong> Table 1.<br />

Table 1. Mean ± SD values of the subjects ma<strong>in</strong> physical characteristics.<br />

Subjects<br />

Age<br />

(years)<br />

Weight<br />

(kg)<br />

High<br />

(cm)<br />

BMI<br />

(kg.m -2 )<br />

Lifesavers (n=10) 17.08±2.24 72.90±11.71 176.43±3.96 23.37±3.33<br />

Lifeguards (n=10) 27.44±10.79 76.22±11.92 179.33±7.45 23.56±2.14<br />

All tests were performed <strong>in</strong> a short course (25 m) <strong>in</strong>door swimm<strong>in</strong>g pool<br />

with a mean depth of 2 m. The protocol consisted of a 3 x 25 m maximal<br />

swim trials carry<strong>in</strong>g a manik<strong>in</strong> (Swedish model), with a m<strong>in</strong>imum<br />

recovery time of 30 m<strong>in</strong>. The manik<strong>in</strong> was constructed with a closed<br />

PITET plastic type, had a total height of 1 m <strong>and</strong> was totally filled<br />

of water <strong>in</strong> order to have a total l<strong>and</strong> weight of 80 kg. The trials’ order<br />

was r<strong>and</strong>omized, perform<strong>in</strong>g with barefoot, with flexible f<strong>in</strong>s (Gabbiano<br />

Francis, 45 cm length <strong>and</strong> 20 cm width, with a closed shoe part <strong>and</strong> a<br />

small open<strong>in</strong>g for the toes f<strong>in</strong>gers), <strong>and</strong> with fibre f<strong>in</strong>s (Special Films,<br />

model Sebak Saber 140 Hard M, 65 cm length <strong>and</strong> 22 cm width, be<strong>in</strong>g<br />

rectangular on is tail, with a open shoe part on the heel <strong>and</strong> fixed to the<br />

lifeguard foot by a brace).<br />

Each 25 m bout started with<strong>in</strong> the water, with the subjects <strong>in</strong> contact<br />

with the wall or the start<strong>in</strong>g block, head <strong>in</strong> emersion <strong>and</strong> carry<strong>in</strong>g the<br />

mannequ<strong>in</strong> (lateral-dorsal position). Subjects could kick<strong>in</strong>g <strong>and</strong> use one<br />

arm for propulsion. A cable speedometer (Lima et al., 2006), was connected<br />

to the mannequ<strong>in</strong> <strong>in</strong> order to obta<strong>in</strong> <strong>in</strong>stantaneous velocity (v)<br />

dur<strong>in</strong>g total event. The cable speedometer uses an <strong>in</strong>cremental sensor<br />

with 500 po<strong>in</strong>ts resolution per revolution. A brake eng<strong>in</strong>e allows the full<br />

system <strong>in</strong>ertia to be <strong>in</strong>significant, keep<strong>in</strong>g the l<strong>in</strong>e always stretched. Accuracy<br />

<strong>and</strong> reliability of the speedometer was confirmed by Lima (2006).<br />

Dur<strong>in</strong>g the data analysis, the first two s the v curves of each swimmer<br />

were removed, m<strong>in</strong>imiz<strong>in</strong>g the effect of the <strong>in</strong>itial impulse, <strong>and</strong> focused<br />

the analysis on leg kick<strong>in</strong>g only (there were no propulsive actions with<br />

the arms). The v were assessed over 2 s periods (Fig. 1), on three moments<br />

of the total v curve: (i) mean v correspondent to the <strong>in</strong>itial 2-4 s<br />

of the total effort time; (ii) mean v correspondent to the middle part of<br />

total effort time <strong>and</strong> (iii) mean v correspondent to the last 2 s of total<br />

effort time. Total effort time was def<strong>in</strong>ed as the time duration between<br />

the first <strong>and</strong> the last v peak of the v(t) curve, after <strong>in</strong>itial impulse has<br />

been removed.


Figure 1. Instantaneous velocity curve obta<strong>in</strong>ed us<strong>in</strong>g the velocymetric<br />

system <strong>and</strong> time <strong>in</strong>tervals (segments) used to calculate mean <strong>in</strong>itial (1),<br />

middle (2) <strong>and</strong> f<strong>in</strong>al (3) velocities.<br />

The mean slopes correspond<strong>in</strong>g to the <strong>in</strong>dividual regression l<strong>in</strong>es plotted<br />

between <strong>in</strong>itial <strong>and</strong> middle v, between middle <strong>and</strong> f<strong>in</strong>al v <strong>and</strong> between<br />

<strong>in</strong>itial <strong>and</strong> f<strong>in</strong>al v were calculated for both groups. The mean fatigue<br />

<strong>in</strong>dexes (FI) correspond<strong>in</strong>g to the first <strong>and</strong> second middle <strong>and</strong> to the<br />

total effort time were also assessed accord<strong>in</strong>g to the follow<strong>in</strong>g formula:<br />

−1<br />

FI = ( Xiv<br />

− Xfv<br />

). Xiv<br />

, (1)<br />

where X iv is the mean v computed dur<strong>in</strong>g 2 s <strong>in</strong> the beg<strong>in</strong>n<strong>in</strong>g of each<br />

part of the test (the total test distance or each middle part considered)<br />

<strong>and</strong> X fv is the mean v computed dur<strong>in</strong>g 2 s <strong>in</strong> the end of the respective<br />

distance. Formula 1 has already been used by Soares (2006). Mean v,<br />

slope of the v(t) decl<strong>in</strong>e (v decay) <strong>and</strong> FI <strong>in</strong> the first <strong>and</strong> second middle<br />

parts of each 25 m, <strong>and</strong> <strong>in</strong> the total test, were used as fatigue criterions<br />

to study the fatigue <strong>in</strong>duced dur<strong>in</strong>g the total effort time, <strong>and</strong> dur<strong>in</strong>g each<br />

middle parts, consider<strong>in</strong>g the three conditions tested.<br />

The normality (Shapiro-Wilk test), sphericity (Mauchly Test) <strong>and</strong><br />

homocedasticity of all distributions were confirmed. A paired simple Ttest<br />

was used to compare vmean, slopes <strong>and</strong> FI correspond<strong>in</strong>g to the first<br />

<strong>and</strong> second middle of the total effort time. T-Test was used for comparisons<br />

between lifesavers <strong>and</strong> lifeguards too. Tests were performed for each<br />

group. Repeated measures ANOVA have been applied to test differences<br />

between the three tested conditions. Significance was accepted at 0.05.<br />

results<br />

The v atta<strong>in</strong>ed <strong>in</strong> the <strong>in</strong>itial, middle <strong>and</strong> f<strong>in</strong>al moments of the 25 m carry<br />

effort can be observed <strong>in</strong> Table 2. Lifesavers performed faster than lifeguards<br />

<strong>in</strong> all three segments when us<strong>in</strong>g fibre f<strong>in</strong>s. Carry velocity with<br />

flexible or fibre f<strong>in</strong>s seemed to be <strong>in</strong>different for lifeguards. Lifesavers<br />

<strong>and</strong> lifeguards performed slower <strong>in</strong> the barefoot condition <strong>in</strong> any segment<br />

of the 25 m effort.<br />

Table 2. Mean ± SD values of the velocity (m·s-1 ) correspond<strong>in</strong>g to <strong>in</strong>itial,<br />

middle <strong>and</strong> f<strong>in</strong>al segments of the total carry effort performed with<br />

barefoot, flexible <strong>and</strong> fibre f<strong>in</strong>s by lifesavers <strong>and</strong> lifeguards.<br />

Initial Middle F<strong>in</strong>al<br />

Lifesavers Lifeguards Lifesavers Lifeguards Lifesavers Lifeguards<br />

Barefoot 0.77±0.08 * 0.67±0.06 0.71±0.09 0.66±0.07 0.61±0.11 ¤ 0.57±0.10 ¤<br />

Flexible 1.12±0.12a 1.03±0.10ª 1.09±0.11ª 0.98±0.20ª 0.99±0.10ª 0.93±0.12ª<br />

Fibre 1.31±0.11 *ab 1.09±0.12 a 1.33±0.09 *ab 1.07±0.19a 1.21±0.11 *ab 1.01±0.12a Differences (p≤0.05) between groups: *different from lifeguards;<br />

Differences (p≤0.05) between conditions: adifferent from barefoot; bdifferent<br />

from flexible f<strong>in</strong>s;<br />

Differences (p≤0.05) with<strong>in</strong> conditions: ¤different from <strong>in</strong>itial velocity<br />

of the same group.<br />

Figure 2 presents analysis related to each half effort part. As can be<br />

observed (panel A), there were no differences <strong>in</strong> the total carry time of<br />

lifesavers <strong>and</strong> lifeguards <strong>in</strong> any condition. In Figure 2 (panel B), it may<br />

be observed that the use of fibre f<strong>in</strong>s allowed for lifesavers to perform<br />

faster (<strong>in</strong> each middle part <strong>and</strong> for the total effort) comparatively with<br />

flexible f<strong>in</strong>s. On the contrary, lifeguards atta<strong>in</strong>ed similar v mean with<br />

both f<strong>in</strong> models. In barefoot condition, only <strong>in</strong> the first middle effort<br />

part, the lifesavers atta<strong>in</strong>ed higher v than lifeguards.<br />

A<br />

B<br />

C<br />

total carry time (s)<br />

vmean (m.s -1 )<br />

slope (m.s -2 )<br />

D<br />

FI (%)<br />

45<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

Lifesavers Lifeguards<br />

a<br />

Barefoot Flexible f<strong>in</strong>s<br />

condition<br />

Fiber f<strong>in</strong>s<br />

a<br />

Lifesavers Lifeguards<br />

a,b<br />

chaPter2.<strong>Biomechanics</strong><br />

1,6<br />

1,4<br />

1,2<br />

1<br />

a,¤<br />

a,¤<br />

*,a,b,¤<br />

a<br />

a<br />

a<br />

*,a,b<br />

a<br />

a<br />

a<br />

*,a,b<br />

a<br />

0,8<br />

0,6<br />

0,4<br />

0,2<br />

0<br />

*,¤<br />

¤<br />

Barefoot Flexible Fiber Barefoot Flexible Fiber Barefoot Flexible Fiber<br />

First half Second half Total<br />

0,025<br />

-0,025<br />

-0,075<br />

-0,125<br />

-0,175<br />

-0,225<br />

-0,275<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

-5<br />

First half second half Total<br />

Barefoot Flexible Fiber Barefoot Flexible Fiber Barefoot Flexible Fiber<br />

¤<br />

¤ ¤<br />

Lifesavers Lifeguards<br />

¤<br />

¤<br />

¤<br />

Lifesavers Lifeguards<br />

Barefoot Flexible Fiber Barefoot Flexible Fiber Barefoot Flexible Fiber<br />

First half Second half Total<br />

Figure 2. Mean ± SD values of lifesavers <strong>and</strong> lifeguards when carry with<br />

barefoot, flexible, <strong>and</strong> fibre f<strong>in</strong>s. A: total duration of the mannequ<strong>in</strong> carry<br />

effort (t); B: velocities (v mean , m·s -1 ) of the first <strong>and</strong> second halves of the<br />

effort, <strong>and</strong> for the total effort; C: slopes of v(t) decl<strong>in</strong>e (m·s -2 ); D: fatigue<br />

<strong>in</strong>dexes (FI, %).<br />

Differences (p≤0.05) between groups: *different from lifeguards;<br />

Differences (p≤0.05) between conditions: adifferent from barefoot; bdifferent<br />

from flexible f<strong>in</strong>s;<br />

Differences (p≤0.05) between half parts: ¤different from second middle<br />

part.<br />

Figure 2 (C) shows that the use of fibre f<strong>in</strong>s by the lifesavers implies the<br />

rise of the v <strong>and</strong> fatigue <strong>in</strong>hibition dur<strong>in</strong>g the first middle effort part.<br />

The decl<strong>in</strong>e of lifesavers v does not appeared to be, <strong>in</strong> general, different<br />

from the results observed for lifeguards. Figure 2 (D) reveals that fatigue<br />

<strong>in</strong>duced by carry<strong>in</strong>g is similar for both studied groups <strong>and</strong> conditions,<br />

<strong>and</strong> that the use of fibre f<strong>in</strong>s help lifesavers to delay fatigue <strong>in</strong> the first<br />

middle part of the effort. The differences <strong>in</strong> results are very similar to<br />

the slop results, with the same punctual differences be<strong>in</strong>g observed. Ad-<br />

a<br />

a<br />

43


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

ditionally, high SD values for FI are evident, show<strong>in</strong>g a large <strong>in</strong>dividual<br />

variability among subjects.<br />

dIscussIon<br />

Due to the high variability <strong>in</strong> f<strong>in</strong> models, a careful selection is required<br />

<strong>in</strong> order to <strong>in</strong>crease performance or to facilitate rescue situations. As no<br />

study compared the performance obta<strong>in</strong>ed by lifesavers <strong>and</strong> lifeguards<br />

when us<strong>in</strong>g different f<strong>in</strong> models, the purpose of the study was to compare<br />

lifeguards <strong>and</strong> lifesavers when us<strong>in</strong>g flexible <strong>and</strong> fibre f<strong>in</strong>s, which<br />

were compared also with the barefoot condition.<br />

The observed higher v at the end of the 25m effort (f<strong>in</strong>al v) atta<strong>in</strong>ed<br />

by lifesavers when us<strong>in</strong>g fibre f<strong>in</strong>s could be due to the fact that they are<br />

commonly used <strong>in</strong> tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competition situations. Contrarily, fibre<br />

f<strong>in</strong>s do not seem to be so often used <strong>in</strong> rescue situations, requir<strong>in</strong>g lifeguards<br />

a more specific adaptation. This statement is only based on observation<br />

of the lifeguards’ behaviour <strong>in</strong> rescue scenes. The <strong>in</strong>itial, mean <strong>and</strong><br />

f<strong>in</strong>al segments vmean of lifesavers <strong>and</strong> lifeguards <strong>in</strong> the 25 m mannequ<strong>in</strong><br />

carry test were similar when flexible f<strong>in</strong>s were used. The <strong>in</strong>existence of<br />

differences <strong>in</strong> v atta<strong>in</strong>ed by lifeguards us<strong>in</strong>g four different f<strong>in</strong> models<br />

was already po<strong>in</strong>ted out by Abraldes et al. (2007). It is possible that the<br />

eventual lower tra<strong>in</strong><strong>in</strong>g level of lifeguards compared to lifesavers did not<br />

allow for a specialized use of any of the tested f<strong>in</strong> models. Other possible<br />

explanation is that lifesavers usually carry dummies <strong>in</strong> st<strong>and</strong>ard events,<br />

<strong>and</strong> lifeguards carry real persons <strong>in</strong> real <strong>and</strong> unexpected circumstances.<br />

Additionally, it is speculated that lifesavers revealed a higher level of<br />

technical carry<strong>in</strong>g competence at the beg<strong>in</strong>n<strong>in</strong>g of the barefoot effort,<br />

once they got a higher <strong>in</strong>itial vmean. This difference <strong>in</strong> vmean between<br />

lifesavers <strong>and</strong> lifeguards observed <strong>in</strong> barefoot condition was not evident<br />

<strong>in</strong> the middle <strong>and</strong> f<strong>in</strong>al moments of the test. Regard<strong>in</strong>g fatigue related<br />

parameters, v decay <strong>and</strong> FI seem to be similar between lifesavers <strong>and</strong><br />

lifeguards <strong>in</strong> the three conditions tested. This absence of differences<br />

could be a consequence of the short effort duration of the particular test<br />

used. Moreover, it can be expla<strong>in</strong>ed by the <strong>in</strong>exact location of the po<strong>in</strong>t<br />

of exponential rise of fatigue. In the present study, the effort was divided<br />

<strong>in</strong> two parts, without the exact po<strong>in</strong>t of evident fatigue occurrence be<strong>in</strong>g<br />

determ<strong>in</strong>ed. Future studies should focus on a more precise assessment of<br />

the po<strong>in</strong>t of fatigue appearance. Soares et al. (2006) have studied fatigue<br />

analys<strong>in</strong>g velocity <strong>in</strong> 30 s maximal swimm<strong>in</strong>g efforts. The authors could<br />

determ<strong>in</strong>e one or two fatigue thresholds over the 30 s v(t) curves, none<br />

of which be<strong>in</strong>g co<strong>in</strong>cident with the middle of the effort. Fatigue thresholds<br />

were above the 15 s.<br />

Lastly, a noticeable result was the <strong>in</strong>crease of vmean dur<strong>in</strong>g the first<br />

middle carries performed by the lifesavers with the fibre f<strong>in</strong>s, which<br />

favour its use by this population. Another highlight is the significant<br />

variability of FI data. The abnormally higher SD values could expla<strong>in</strong>, <strong>in</strong><br />

part, the absence of significant differences observed for FI, which suggests<br />

the need of further research.<br />

conclusIons<br />

Fibre f<strong>in</strong>s allow a higher v of lifesavers when compared with flexible<br />

f<strong>in</strong>s, but for lifeguards it is <strong>in</strong>different the type of f<strong>in</strong>s used. The effect<br />

of the use of flexible or fibre f<strong>in</strong>s is not evident <strong>in</strong> fatigue <strong>in</strong>dex both for<br />

lifesavers <strong>and</strong> lifeguards.<br />

reFerences<br />

Abraldes, J. A. (2004). Efecto de la utilización de dist<strong>in</strong>tos tipos de aleta<br />

sobre pruebas de nado y remolque en salvamento acuático. X<strong>XI</strong>I Congreso<br />

Nacional de Educación Física. 1-8. A Coruña: Universidad de La<br />

Coruña y Universidad de Santiago de Compostela.<br />

Abraldes, J. A. (2005). Estudio de la efectividad de la aleta en función<br />

del tipo de prueba en distancia de 25 metros: buceo, nado y remolque.<br />

In J. Palacios et al. 4º Congreso de Salvamento y Socorrismo de Galicia.<br />

44<br />

Lugo: Fundación Idissa, 341-349.<br />

Abraldes, J. A. (2006). Evaluation of swim f<strong>in</strong>s accord<strong>in</strong>g to the time<br />

taken <strong>in</strong> swim tests <strong>and</strong> manik<strong>in</strong> tow tests. Cultura, Ciencia y Deporte,<br />

5(2), 67-72.<br />

Abraldes, J. A., Soares, S., Lima, A. B., Fern<strong>and</strong>es, R. & Vilas-Boas, J.<br />

P. (2007). The Effect of F<strong>in</strong> Use on the Speed of Lifesav<strong>in</strong>g Rescues.<br />

International Journal of Aquatic Research & Education, 1(4), 329-340.<br />

Daniel, K. & Klauck, J. (1992). Physiological <strong>and</strong> biomechanical load<br />

parameters <strong>in</strong> life sav<strong>in</strong>g. In Reilly T <strong>and</strong> MacLaren D (Eds.). Abstracts<br />

of the 6th <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g. Liverpool.<br />

Juntunen, P., Lesk<strong>in</strong>en, T., Louhevaara, V. & Kesk<strong>in</strong>en, K. (2006). <strong>Biomechanics</strong><br />

of tow<strong>in</strong>g <strong>in</strong> skilled <strong>and</strong> less-skilled lifesavers. Port J Sport<br />

Sci, 6(Supp. 2), 48-50.<br />

Lewis, E.R. & Lorch, D. (1979). Swim f<strong>in</strong> design utiliz<strong>in</strong>g pr<strong>in</strong>ciples of<br />

mar<strong>in</strong>e animal locomotion. In Terauds J <strong>and</strong> Bed<strong>in</strong>gfield E (Eds.).<br />

Swimm<strong>in</strong>g III. Baltimore: University Park Press, 289-297.<br />

Lima, A. B. (2006). Concepção, desenvolvimento de resultados e eficiência<br />

no tre<strong>in</strong>o da técnica em Natação. Tese de doutoramento. FCDEF-<br />

UP, Porto.<br />

Lima, A. B., Semblano, P., Fern<strong>and</strong>es, D., Gonçalves, P., Morouço, P.,<br />

Sousa, F. et al. (2006). A k<strong>in</strong>ematical, imagiological <strong>and</strong> acoustical<br />

biofeedback system for the technical tra<strong>in</strong><strong>in</strong>g <strong>in</strong> breaststroke swimm<strong>in</strong>g.<br />

Port J Sport Sci, 6(Suppl. 1), 22.<br />

Soares, S., Lima, A. B., Santos, I., Machado, L., Fern<strong>and</strong>es, R., Correia,<br />

M.V. et al. (2006). Velocimetric characterization of a 30 sec maximal<br />

test <strong>in</strong> swimm<strong>in</strong>g: consequences for bioenergetical evaluation. Port J<br />

Sport Sci, 6(Suppl. 2), 265-268.<br />

Zamparo, P., Pendergast, D. R., Term<strong>in</strong>, A., M<strong>in</strong>etti, A. E. (2006). Economy<br />

<strong>and</strong> efficiency of swimm<strong>in</strong>g at the surface with f<strong>in</strong>s of different<br />

size <strong>and</strong> stiffness. Eur J Appl Physiol, 96(4), 459-470.


Effect of Stroke Drills on Intra-cycle Hip Velocity <strong>in</strong><br />

Front Crawl<br />

Arellano r., domínguez-castells r., Perez-Infantes e., sánchez<br />

e.<br />

University of Granada, Granada, Spa<strong>in</strong><br />

Competitive strokes have been widely analysed, while k<strong>in</strong>ematics of coord<strong>in</strong>ative<br />

drills, used to tra<strong>in</strong> or teach swimm<strong>in</strong>g techniques, have been<br />

scarcely studied. The aim of this work is to evaluate the differences <strong>in</strong> the<br />

<strong>in</strong>tra-cycle hip velocity among freestyle swimm<strong>in</strong>g drills. Thirteen national<br />

<strong>and</strong> regional level swimmers performed five 25-m freestyle trials,<br />

us<strong>in</strong>g different stroke drills <strong>in</strong> a r<strong>and</strong>om order. The propulsive phase of<br />

each stroke was analysed. Mean <strong>and</strong> peak (one or two) velocity were obta<strong>in</strong>ed,<br />

<strong>and</strong> their correspond<strong>in</strong>g phase percentage. The first peak recorded<br />

corresponded to the <strong>in</strong>ward movement, which co<strong>in</strong>cided with the f<strong>in</strong>al<br />

propulsion or downward movement of the opposite arm. The second<br />

one corresponded to the f<strong>in</strong>al backward-upward movement, which, is <strong>in</strong><br />

most cases, the highest value of velocity while the non-propulsive arm<br />

is extended horizontally <strong>in</strong> front of the shoulder. The freestyle stroke<br />

drills applied to teach or tra<strong>in</strong> different types of <strong>in</strong>ter-limb coord<strong>in</strong>ation<br />

reduce the mean <strong>and</strong> peak values of <strong>in</strong>tra-cycle hip velocity while the<br />

percentage location of peak hip-velocity value dur<strong>in</strong>g the underwater<br />

stroke phase is similar without significant statistical differences.<br />

Key words: swimm<strong>in</strong>g k<strong>in</strong>ematics, swimm<strong>in</strong>g technique.<br />

IntroductIon<br />

Current teach<strong>in</strong>g <strong>and</strong> competitive swimm<strong>in</strong>g programs are composed<br />

of the correct comb<strong>in</strong>ation of skill acquisition <strong>and</strong> condition<strong>in</strong>g exercises.<br />

Many swimm<strong>in</strong>g books or papers describe or classify these swimm<strong>in</strong>g<br />

exercises propos<strong>in</strong>g guidel<strong>in</strong>es to use them properly or <strong>in</strong> a skill<br />

assessment context (Goldsmith et a. 2007; Guzman, 1998; Laughl<strong>in</strong> &<br />

Delves, 1996; Maglischo, 2003; Sweetenham & Atk<strong>in</strong>son, 2003). The<br />

classifications used to <strong>in</strong>clude coord<strong>in</strong>ative drills: arm-arm coord<strong>in</strong>ation,<br />

arm-breath<strong>in</strong>g coord<strong>in</strong>ation <strong>and</strong> arm-leg coord<strong>in</strong>ation. Lately, armarm<br />

coord<strong>in</strong>ation drills have become very popular applied to develop<br />

the crawl-stroke swimm<strong>in</strong>g technique <strong>in</strong> master swimm<strong>in</strong>g, triathlon<br />

<strong>and</strong> competitive swimm<strong>in</strong>g while they were <strong>and</strong> are broadly used <strong>in</strong> the<br />

advanced learn<strong>in</strong>g stages of technique development <strong>in</strong> ‘learn to swim’<br />

programs (Figueiredo et al., 2009; Seifert & Chollet, 2009).<br />

While hip or centre of mass <strong>in</strong>tra-cycle velocity has been studied<br />

<strong>in</strong> the current competitive strokes us<strong>in</strong>g observational or biomechanical<br />

methods (Barbosa, et al., 2005; Figueiredo, et al., 2009; Psycharakis et al.<br />

2009), this has not been the case with the stroke drills applied to teach or<br />

tra<strong>in</strong> swimm<strong>in</strong>g technique. Stroke coord<strong>in</strong>ation, bi-dimensional or tridimensional<br />

k<strong>in</strong>ematics, <strong>in</strong>tra-cycle velocity, body-trunk rotation, stroke<br />

frequency <strong>and</strong> stroke length have been some subjects of study frequently<br />

applied to formal strokes but missed out <strong>in</strong> these drills. A first attempt<br />

was performed to analyse the differences <strong>in</strong> body rotation <strong>and</strong> 3D h<strong>and</strong><br />

swimm<strong>in</strong>g path between freestyle swimm<strong>in</strong>g <strong>and</strong> one arm crawl stroke<br />

drills (López et al. 2002). Less body rotation <strong>and</strong> h<strong>and</strong> depth were found<br />

dur<strong>in</strong>g the practice of formal one-arm <strong>and</strong> catch-up crawl stroke, while<br />

a modified one-arm stroke drill obta<strong>in</strong>ed similar values to that recorded<br />

dur<strong>in</strong>g no breath<strong>in</strong>g freestyle swimm<strong>in</strong>g.<br />

The purpose of this study is to reveal the differences <strong>in</strong> <strong>in</strong>tra-cycle<br />

hip velocity between formal front crawl <strong>and</strong> four other front crawl<br />

swimm<strong>in</strong>g coord<strong>in</strong>ation drills.<br />

Methods<br />

Thirteen national <strong>and</strong> regional level swimmers (five males <strong>and</strong> eight<br />

females, aged 19.58±2.23) participated <strong>in</strong> this study as volunteers. All<br />

of them had tra<strong>in</strong>ed <strong>in</strong> swimm<strong>in</strong>g for 6-8 years. Every participant had<br />

chaPter2.<strong>Biomechanics</strong><br />

previous experience of the exercises. The protocol was fully expla<strong>in</strong>ed<br />

to them <strong>and</strong> they provided written consent to participate <strong>in</strong> the study,<br />

which was approved by the university ethics committee. This <strong>in</strong>vestigation<br />

was performed <strong>in</strong> September, at the beg<strong>in</strong>n<strong>in</strong>g of the competitive<br />

season. The characteristics of the participants are presented <strong>in</strong> Table 1.<br />

Table 1. Anthropometric characteristics of participants <strong>in</strong> the study<br />

(n=13).<br />

Body mass<br />

(kg)<br />

Height<br />

(cm)<br />

Max. body length<br />

(cm)<br />

Arm span<br />

(cm)<br />

Mean (SD) 67.4 (10.5) 171 (7) 228 (11) 181 (11)<br />

After a st<strong>and</strong>ard warm-up, swimmers r<strong>and</strong>omly performed five 25-m freestyle<br />

trials, us<strong>in</strong>g a different stroke drill <strong>and</strong> no-breath<strong>in</strong>g freestyle. They<br />

always started <strong>in</strong> the water <strong>and</strong> were <strong>in</strong>structed to swim as fast as possible,<br />

keep<strong>in</strong>g to the stroke drill technique. All trials were performed dur<strong>in</strong>g a<br />

specific test<strong>in</strong>g session. Each participant performed every trial with a rest<br />

<strong>in</strong>terval of more than 5 m<strong>in</strong>utes (see Table 2 for stroke drill def<strong>in</strong>itions).<br />

Table 2. Stroke drills applied <strong>in</strong> the study.<br />

A No-breath<strong>in</strong>g formal freestyle swimm<strong>in</strong>g (reference technique)<br />

B Crawl catch-up stroke, kick<strong>in</strong>g some seconds after each stroke<br />

C One arm front crawl with the rest<strong>in</strong>g arm extended <strong>in</strong> front,<br />

breath<strong>in</strong>g on the arm-mov<strong>in</strong>g side<br />

D One arm front crawl with the rest<strong>in</strong>g arm close to the body,<br />

breath<strong>in</strong>g on the no-mov<strong>in</strong>g side<br />

E Controlled two-arm freestyle, swimmer perform arm-pull <strong>and</strong><br />

arm-recovery simultaneously f<strong>in</strong>ish<strong>in</strong>g each half cycle with<br />

one arm rest<strong>in</strong>g close to the body <strong>and</strong> the second one rest<strong>in</strong>g<br />

extended <strong>in</strong> front, kick<strong>in</strong>g some seconds after each stroke.<br />

Dur<strong>in</strong>g each trial the swimmers` time <strong>and</strong> <strong>in</strong>tra-cycle velocity were recorded<br />

synchronized with underwater video record<strong>in</strong>g. With this <strong>in</strong>formation,<br />

peak <strong>and</strong> mean velocity for each stroke (<strong>and</strong> its phases) were<br />

obta<strong>in</strong>ed.<br />

The behaviour of the swimmers dur<strong>in</strong>g the experiment was recorded<br />

with two underwater cameras, which were attached by a metal device to<br />

the lateral edge of the pool. Both cameras were placed 50cm below the<br />

water surface <strong>and</strong> were positioned 10 <strong>and</strong> 15m from the start<strong>in</strong>g wall of<br />

the pool, respectively. The swimmers swam <strong>in</strong> lane 3, so that the cameras<br />

were able to record at least 15m of their performance from a lateral view.<br />

An electronic timer connected to a touch pad was used to measure<br />

the swimmer’s times. Velocity was measured by a l<strong>in</strong>ear encoder,<br />

attached to the swimmers` waist us<strong>in</strong>g a belt. The associated software<br />

enabled us to receive the data <strong>and</strong> videos <strong>in</strong> the computer <strong>in</strong> real time,<br />

ready to be processed through two USB 2.0 ports.<br />

Velocity data were sampled at 200Hz <strong>and</strong> the video signal synchronized<br />

at 50 Hz. After select<strong>in</strong>g the stroke-phase sections of the videos,<br />

<strong>and</strong> before further process<strong>in</strong>g, data were filtered us<strong>in</strong>g a Butterworth<br />

filter, with a cut-off frequency of 6 Hz.<br />

For every participant, three strokes were selected <strong>and</strong> represented, <strong>in</strong><br />

order to compare the velocity variations among them. A complete underwater<br />

stroke phase was considered from the beg<strong>in</strong>n<strong>in</strong>g of the entry of<br />

the h<strong>and</strong> <strong>in</strong>to the water until it was completely out. All the underwater<br />

stroke durations (100%) were normalized to a percentage scale, mak<strong>in</strong>g<br />

it easier to compare strokes of different duration.<br />

A statistical analysis was performed us<strong>in</strong>g Microsoft Excel 2007 <strong>and</strong><br />

Statistica/Mac Plus 5.1. Then, the raw data was checked for normal distribution<br />

characteristics (p=0.96 for velocity). And f<strong>in</strong>ally, an analysis of<br />

variance with repeated measures was applied to determ<strong>in</strong>e variability between<br />

exercises us<strong>in</strong>g Scheffé post-hoc tests for <strong>in</strong>tra-group comparisons.<br />

45


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

Mean values of 25m-velocity <strong>and</strong> 25m-performance for every swimm<strong>in</strong>g<br />

drill were obta<strong>in</strong>ed (see Table 3). The recorded times <strong>and</strong> mean<br />

velocities were slower <strong>in</strong> all the swimm<strong>in</strong>g drills compared with the nobreath<strong>in</strong>g<br />

freestyle (p


Goldsmith, W., Richards, R., & Sweetenham, B. (2007). Coach<strong>in</strong>g<br />

Drills & Performance Enhancement Skills <strong>in</strong> Swimm<strong>in</strong>g. Swimm<strong>in</strong>g<br />

Retrieved 10/11/2009, 2009, from http://www.coaches<strong>in</strong>fo.com/<br />

<strong>in</strong>dex.php<br />

Guzman, R. J. (1998). Swimm<strong>in</strong>g drills for every stroke. Champaign, IL:<br />

Human K<strong>in</strong>etics.<br />

Laughl<strong>in</strong>, T., & Delves, J. (1996). Total Immersion. The revolutionary way<br />

to swim better, faster <strong>and</strong> easier. (1 ed. Vol. 1). New York, USA: FIRE-<br />

SIDE.<br />

López, G., Gutiérrez, M., & Arellano, R. (2002). Upper extremity k<strong>in</strong>ematics<br />

dur<strong>in</strong>g different breath<strong>in</strong>g patterns <strong>and</strong> selected stroke drills <strong>in</strong><br />

front crawl swimm<strong>in</strong>g. Paper presented at the XXth International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports, Cáceres (Spa<strong>in</strong>).<br />

Maglischo, E. W. (2003). Swimm<strong>in</strong>g Fastest (1 ed. Vol. 1). Champa<strong>in</strong>, IL,<br />

USA: Human K<strong>in</strong>etics.<br />

Psycharakis, S. G., Naemi, R., Connaboy, C., McCabe, C., & S<strong>and</strong>ers, R.<br />

H. (2009). Three-dimensional analysis of <strong>in</strong>tracycle velocity fluctuations<br />

<strong>in</strong> frontcrawl swimm<strong>in</strong>g. Sc<strong>and</strong> J Med Sci Sports.<br />

Seifert, L., & Chollet, D. (2009). Modell<strong>in</strong>g spatial-temporal <strong>and</strong> coord<strong>in</strong>ative<br />

parameters <strong>in</strong> swimm<strong>in</strong>g. J Sci Med Sport, 12(4), 495-499.<br />

Sweetenham, B., & Atk<strong>in</strong>son, J. (2003). Championship Swim Tran<strong>in</strong>g (1<br />

ed. Vol. 1). Campa<strong>in</strong>gn (Ill<strong>in</strong>ois): Human K<strong>in</strong>etics.<br />

AcKnoWledGMents<br />

This study <strong>and</strong> its presentation were partially f<strong>in</strong>anced by: A) Secretary<br />

of State for Research, M<strong>in</strong>istry of Science <strong>and</strong> Innovation. Call<br />

for Basic/Fundamental Research Projects, December, 31, 2008. Ref.<br />

DEP2009-08411. “Study of Swimm<strong>in</strong>g Propulsive Movements [scull<strong>in</strong>g]<br />

us<strong>in</strong>g 3D Analysis, Fluid Visualization, CFD <strong>and</strong> PIV”. B) The<br />

support program of subject practices of the University of Granada, coord<strong>in</strong>ated<br />

by Physical Education <strong>and</strong> Sports Department <strong>and</strong> the Research<br />

Group of Physical Activity <strong>and</strong> Sports on Aquatic Environment<br />

[CTS.527]. Special thanks to the swimmers for their cooperation.<br />

chaPter2.<strong>Biomechanics</strong><br />

The Usefulness of the Fully Tethered Swimm<strong>in</strong>g for<br />

50-m Breaststroke Performance Prediction<br />

Barbosa A.c. 1 , Milivoj dopsaj M. 2 , okicic t. 3 , Andries Júnior<br />

o. 1<br />

1 Faculty of Physical Education, Camp<strong>in</strong>as State University, Sao Paulo, Brazil<br />

2 Faculty of Sport <strong>and</strong> Physical Education, Belgrade University, Belgrade,<br />

Serbia<br />

3 Faculty of Sport <strong>and</strong> Physical Education, Nis University, Nis, Serbia<br />

The present study aimed to identify the relationship between 50-m<br />

breaststroke performance <strong>and</strong> force-time variables obta<strong>in</strong>ed from a<br />

30-s maximal tethered swimm<strong>in</strong>g test. Fourteen high-competitive male<br />

breaststrokers from Brazil <strong>and</strong> Serbia accomplished a 30-s maximal<br />

breaststroke effort <strong>in</strong> tethered swimm<strong>in</strong>g. The mean value of peak force,<br />

average force (F avg ), impulse force (I mp F), rate of force development <strong>and</strong><br />

full stroke duration (DUR) was reta<strong>in</strong>ed for analysis as <strong>in</strong>dependent<br />

variables. Time <strong>in</strong> 50m breaststroke, obta<strong>in</strong>ed <strong>in</strong> long course competitions,<br />

was converted <strong>in</strong> average swimm<strong>in</strong>g velocity (VEL 50m ) to be used<br />

as dependent variable. Multiple regression analysis with the backward<br />

method was employed to construct the model, which was statistically<br />

significant (F=29.933, p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

(Dopsaj et al., 2000; Dopsaj et al., 2003). The 2000 N load cell had 4<br />

attached stra<strong>in</strong> gauges <strong>and</strong> an accuracy of 30 g. One of its extremities<br />

was fixed to a special designed support, attached to the start<strong>in</strong>g platform<br />

or to the pool border, while the other was connected to an <strong>in</strong>extensible<br />

cable, <strong>in</strong> which swimmer was tethered. Mechanical deformations <strong>in</strong> the<br />

load cell, generated by swimmer’s efforts, were recognized by an A/D<br />

<strong>in</strong>terface, which converted the analogue voltage <strong>in</strong> a digital signal. In<br />

sequence, the force values were obta<strong>in</strong>ed through the calibration straight<br />

l<strong>in</strong>e. The m<strong>in</strong>or acquisition frequency used was 200 Hz. Raw data was<br />

low-pass filtered with a cut-off frequency of 8 Hz. The system was calibrated<br />

us<strong>in</strong>g <strong>in</strong>crements of 5 Kg until the maximum weight of 50 Kg.<br />

It was checked before every test<strong>in</strong>g session us<strong>in</strong>g a weight of 10 Kg.<br />

As warm-up, swimmers performed a 10-m<strong>in</strong>ute active stretch <strong>and</strong> 15<br />

m<strong>in</strong>utes of free swimm<strong>in</strong>g. After, a specific procedure described earlier<br />

(Dopsaj et al., 2000) was conducted <strong>in</strong> order to get swimmers familiarized<br />

with the equipment.<br />

Figure 1. Example of a typical force-time curve dur<strong>in</strong>g the 30-s tethered<br />

test<br />

As test protocol, the swimmers accomplished a 30-s self-chosen cycle<br />

frequency maximal breaststroke effort <strong>in</strong> tethered swimm<strong>in</strong>g, whereas<br />

the beg<strong>in</strong>n<strong>in</strong>g <strong>and</strong> the end were signalized by a whistle. In order to<br />

m<strong>in</strong>imize the effects of swimm<strong>in</strong>g <strong>in</strong>tensities transition, the first second<br />

swam maximally was discarded. A typical f-t curve obta<strong>in</strong>ed <strong>in</strong> the test<br />

protocol is shown <strong>in</strong> Figure 1. Ma<strong>in</strong> po<strong>in</strong>ts of force-time curve <strong>in</strong> a<br />

complete were marked, as shown <strong>in</strong> Figure 2.<br />

Figure 2. Visualization of the determ<strong>in</strong>ant po<strong>in</strong>ts used <strong>in</strong> the force-time<br />

curve’s analysis. F peak = Peak force; I mp F = impulse of force represented<br />

by the curve’s area; F m<strong>in</strong> 1 = beg<strong>in</strong>n<strong>in</strong>g of the stroke; F m<strong>in</strong> 2 = end of the<br />

stroke; ∆t = time variation; ∆F = force variation.<br />

Through these po<strong>in</strong>ts, five <strong>in</strong>dependent variables were extracted, as follows:<br />

1) Peak force (F peak ), represented by the maximum force value<br />

found <strong>in</strong> a complete stroke, expressed <strong>in</strong> N. 2) Average Force (F avg ),<br />

represented by the average of all force values found <strong>in</strong> a complete stroke,<br />

i.e., between m<strong>in</strong>imum force 1 (F m<strong>in</strong> 1) <strong>and</strong> 2 (F m<strong>in</strong> 2), expressed <strong>in</strong> N.<br />

3) Impulse Force (I mp F), represented by force-time curve’s area found<br />

48<br />

<strong>in</strong> a complete stroke, i.e., between F m<strong>in</strong> 1 <strong>and</strong> F m<strong>in</strong> 2, expressed <strong>in</strong> Ns.<br />

Integration was made us<strong>in</strong>g the trapeze method. 4 ) Stroke Explosiveness<br />

(RFD), represented by the rate of force development (RFD) <strong>in</strong> a<br />

complete stroke, expressed <strong>in</strong> N/s. RFD was calculated us<strong>in</strong>g the equation:<br />

RFD = (∆F / ∆t) x 1000, where ∆F = F pea k - F m<strong>in</strong> 1, expressed <strong>in</strong> N<br />

<strong>and</strong> ∆t = Time value when F peak was reached - time value found <strong>in</strong> F m<strong>in</strong> 1,<br />

expressed <strong>in</strong> ms. 5) Full Stroke Duration (DUR), represented by the difference<br />

between time values found <strong>in</strong> F m<strong>in</strong> 2 <strong>and</strong> F m<strong>in</strong> 1, expressed <strong>in</strong> ms.<br />

The variables’ value reta<strong>in</strong>ed for analysis was the average of all movement<br />

cycles executed dur<strong>in</strong>g the test protocol. Time <strong>in</strong> 50m breaststroke,<br />

<strong>in</strong> different moments of the periodisation, obta<strong>in</strong>ed <strong>in</strong> competitive conditions,<br />

two weeks before or after the tethered test, was converted <strong>in</strong><br />

average swimm<strong>in</strong>g velocity (VEL 50m ) to be used as dependent variable.<br />

Mean ( Χ ), st<strong>and</strong>ard deviation (SD), m<strong>in</strong>imum (M<strong>in</strong>), maximum<br />

(Max) <strong>and</strong> coefficient of variation (CV) were used as basic descriptive<br />

statistics. The relationship model was established through Multiple Regression<br />

Analysis (MRA) with the Backward Elim<strong>in</strong>ation Method. An<br />

equation of the regression model was generated us<strong>in</strong>g the variables be<strong>in</strong>g<br />

statistically significant <strong>and</strong> most accurately described the criterion.<br />

All statistical analysis was conducted us<strong>in</strong>g SPSS for W<strong>in</strong>dows (Version<br />

16.0; SPSS, Inc., Chicago, IL). The significance level was set at 95%<br />

(p


dIscussIon<br />

The present results showed a high significant relationship between 50-m<br />

breaststroke performance <strong>and</strong> tethered swimm<strong>in</strong>g test, corroborat<strong>in</strong>g to<br />

previous study, which observed the same for high competitive crawlstrokers<br />

(Dopsaj et al., 2000), <strong>and</strong> confirm<strong>in</strong>g the <strong>in</strong>itial hypothesis that<br />

breaststroke swim velocity is related to tethered swim variables.<br />

The current equation for performance prediction was composed by<br />

three variables. The stronger partial relation with 50-m breaststroke performance<br />

was f<strong>in</strong>d at impulse of force (I mp F, t value = 6.257), than at<br />

full stroke duration (DUR, t value = -5.849, <strong>and</strong> f<strong>in</strong>ally at average force<br />

(F avg , t value = -5.643). Basically, a lower DUR <strong>and</strong> F avg correspond to<br />

a greater performance <strong>in</strong> 50-m breaststroke, while a greater I mp F would<br />

lead to a higher swimm<strong>in</strong>g velocity.<br />

The negative relationship of F avg is possibly related to a greater<br />

glid<strong>in</strong>g time adopted by the most qualified breaststrokers (Takagi et<br />

al., 2004), which would cause a dim<strong>in</strong>ishment <strong>in</strong> the effective time of<br />

force production. Indeed, it highlights the importance of the streaml<strong>in</strong>e<br />

position dur<strong>in</strong>g the glid<strong>in</strong>g phase, which is said to be determ<strong>in</strong>ant for<br />

breaststroke performance (Takagi et al., 2004).<br />

Theoretically, a greater glid<strong>in</strong>g time would also lead to a lower stroke<br />

rate, but it does not seem to be that significant. Takagi et al. (2004) compared<br />

the qualified <strong>and</strong> the elim<strong>in</strong>ated breaststrokers of the 9th FINA<br />

World Swimm<strong>in</strong>g Championships <strong>and</strong> did not f<strong>in</strong>d significant differences<br />

between their stroke rates. Besides, the present equation po<strong>in</strong>ted<br />

out an <strong>in</strong>verse relationship between DUR <strong>and</strong> swimm<strong>in</strong>g performance<br />

<strong>in</strong> 50m breaststroke specifically, signaliz<strong>in</strong>g that the decrease of full<br />

stroke duration (i.e., the <strong>in</strong>crease of the stroke rate) would cause a stronger<br />

swimm<strong>in</strong>g rhythm <strong>and</strong> consequently a greater swimm<strong>in</strong>g velocity.<br />

The participation of DUR <strong>in</strong> the model can still be stronger due to<br />

its effect on I mp F calculation. The I mp F, already considered <strong>in</strong> a previous<br />

crawl-stroke model (Dopsaj et al., 2000), represents the work<strong>in</strong>g<br />

potential to be realized <strong>in</strong> conventional non-tethered swimm<strong>in</strong>g. Consequently,<br />

its positive relationship is reasonable <strong>and</strong> highlights the necessity<br />

of f<strong>in</strong>d<strong>in</strong>g the proper tra<strong>in</strong><strong>in</strong>g loads <strong>and</strong> methods which could<br />

improve this variable significantly. Besides, as a result of the curve’s area,<br />

it is basically affected by five ma<strong>in</strong> factors: (1) F peak : establish the maximum<br />

height reached <strong>in</strong> the curve; (2) RFD: determ<strong>in</strong>e the <strong>in</strong>cl<strong>in</strong>ation of<br />

the curve before the F peak ; (3) “relax<strong>in</strong>g” phase: determ<strong>in</strong>e the <strong>in</strong>cl<strong>in</strong>ation<br />

of the curve after the F peak ; (4) DUR: represent the base of the curve;<br />

(5) glid<strong>in</strong>g time: determ<strong>in</strong>e the time of the curve which will be with<br />

no height, i.e., without force production <strong>and</strong> consequently null impulse.<br />

Thus, the decrease of DUR should be associated to an <strong>in</strong>crease of I mp F,<br />

even though this relation is apparently concurrent.<br />

Thus, despite of the critics about technique modifications, essentially<br />

due to the hydrodynamics limitations caused by the null velocity, the<br />

tethered swimm<strong>in</strong>g usefulness was confirmed by the current model, allow<strong>in</strong>g<br />

breaststroke performance prediction with 82.1% of confidence<br />

<strong>and</strong> an error of ±0.74s, even though high competitive breaststrokers<br />

were used.<br />

Besides, differently from a simple time measurement, the tethered<br />

swimm<strong>in</strong>g method allows the assessment of the propulsive force variables<br />

<strong>and</strong>, consequently, to underst<strong>and</strong> how much different each one<br />

is <strong>in</strong>volved with swimm<strong>in</strong>g performance, what variables are needed to<br />

be improved for gett<strong>in</strong>g better results <strong>and</strong>, after test<strong>in</strong>g swimmers at<br />

different moments of the periodisation, identify deeper how the different<br />

tra<strong>in</strong><strong>in</strong>g loads adm<strong>in</strong>istrated are <strong>in</strong>fluenc<strong>in</strong>g performance <strong>in</strong> 50m<br />

breaststroke.<br />

conclusIon<br />

It can be concluded that elite breaststrokers’ 50-m performance is highly<br />

related to an associated behaviour of some force-time curve’s variables,<br />

i.e., the impulse of force, average force <strong>and</strong> stroke duration. Therefore,<br />

tethered swimm<strong>in</strong>g can be used as an important tool not only for crawlstrokers,<br />

as previously reported (Dopsaj et al., 2000), but also <strong>in</strong> spr<strong>in</strong>t<br />

breaststrokers.<br />

chaPter2.<strong>Biomechanics</strong><br />

reFerences<br />

Adams T. A., Mart<strong>in</strong>, R. B., Yeater, R. A. & Gilson, K. A. (1983). Tethered<br />

force <strong>and</strong> velocity relationships. Swimm<strong>in</strong>g Technique, 20, 21-6.<br />

Bollens, E., Annemans, L., Vaes, W. & Clarys, J. P. (1988). Peripheral<br />

EMG comparison between fully tethered <strong>and</strong> free front crawl swimm<strong>in</strong>g.<br />

In: Ungerechts BE, Wilke K, Reischle K (Ed.). International<br />

series on sports science – Swimm<strong>in</strong>g Science V vol. 18. Champaign:<br />

Human K<strong>in</strong>etics, 173-181.<br />

Bonen, B., Wilson, A., Yarkony, M. & Belcastro, A. N. (1980).<br />

Maximal oxygen uptake dur<strong>in</strong>g free, tethered, <strong>and</strong> flume swimm<strong>in</strong>g.<br />

J Appl Physiol, 48, 232-35.<br />

Cabri, J., Annemans, L., Clarys, J. P., Bollens, E. & Publie, J. (1988). The<br />

relation of stroke frequency, force, <strong>and</strong> EMG <strong>in</strong> front crawl tethered<br />

swimm<strong>in</strong>g. In: Ungerechts BE, Wilke K, Reischle K (ed.). International<br />

series on sports science – Swimm<strong>in</strong>g Science V vol. 18. Champaign:<br />

Human K<strong>in</strong>etics, 183-189.<br />

Dopsaj, M., Matković, I. & Zdravković, I. (2000). The relationship between<br />

50m-freestyle results <strong>and</strong> characteristics of tethered forces <strong>in</strong><br />

male spr<strong>in</strong>t swimmers: a new approach to tethered swimm<strong>in</strong>g test.<br />

Facta Universitatis – Series: Physical Education <strong>and</strong> Sport, 1(7), 15-22.<br />

Dopsaj, M., Matković, I., Thanopoulos, V. & Okičić, T. (2003). Reliability<br />

<strong>and</strong> validity of basic k<strong>in</strong>ematics <strong>and</strong> mechanical characteristics<br />

of pull<strong>in</strong>g force <strong>in</strong> swimmers measured by method of tethered swimm<strong>in</strong>g<br />

with maximum <strong>in</strong>tensity of 60 seconds. Facta Universitatis –<br />

Series: Physical Education <strong>and</strong> Sport, 1(10), 11-22.<br />

Lutomsky, P., Stankowsky, T., Konarsky, J., Pietrusik, K., Cierezko, A.<br />

& Strzelczyk, R. (2008). From studies on the thrust <strong>in</strong> swimm<strong>in</strong>g. J<br />

Hum Sports Exerc, 3(2), 25-32.<br />

Maglischo, C. W., Maglischo, E. W., Sharp, R. L., Zier, D. J. & Katz,<br />

A. (1984). Tethered <strong>and</strong> non-tethered crawl swimm<strong>in</strong>g. In: Terauds<br />

J, Barthels K, Kreighbaum E, Mann R, Crakes J, DelMar CA (Ed.).<br />

Proceed<strong>in</strong>gs of ISBS: Sports <strong>Biomechanics</strong>, 163-176.<br />

Morouço, P., Alves, S., Villas-Boas, J. P. & Fern<strong>and</strong>es, R. (2008). Association<br />

between 30sec maximal tethered swimm<strong>in</strong>g <strong>and</strong> swimm<strong>in</strong>g<br />

performance <strong>in</strong> front crawl. Proceed<strong>in</strong>g of the <strong>XI</strong>II North American<br />

Congress on <strong>Biomechanics</strong>, abstract 380.<br />

Papoti, M., Vitório, R., Velosa, A. B., Cunha, S. A., Silva, A. S. R., Mart<strong>in</strong>s,<br />

L. E. B. & Gobatto, C. (2007a). Use of load cells to measurements<br />

of underwater dolph<strong>in</strong> kick force <strong>in</strong> swimm<strong>in</strong>g tethered. Port<br />

J Sports Sci, 7(3), 313-18.<br />

Papoti, M., Mart<strong>in</strong>s, L. E., Cunha, S. A., Zagatto, A. M. & Gobatto, C.<br />

A. (2007b). Effects of taper on swimm<strong>in</strong>g force <strong>and</strong> swimmer performance<br />

after an experimental ten-week tra<strong>in</strong><strong>in</strong>g program. J Strength<br />

Cond Res, 21(2), 538-42.<br />

Papoti, M., Mart<strong>in</strong>s, L., Cunha, S., Zagatto, A. & Gobatto, C. (2003).<br />

St<strong>and</strong>ardization of a specific protocol to determ<strong>in</strong>e anaerobic condition<strong>in</strong>g<br />

<strong>in</strong> swimmers dur<strong>in</strong>g a 30sec effort us<strong>in</strong>g load cells. Port J<br />

Sports Sci, 3(3), 36-42.<br />

Takagi, H., Sugimoto, S., Nishijima, N. & Wilson, B. Differences <strong>in</strong><br />

stroke phases, arm-leg coord<strong>in</strong>ation <strong>and</strong> velocity fluctuation due to<br />

event, gender <strong>and</strong> performance level <strong>in</strong> breaststroke. Sports <strong>Biomechanics</strong>,<br />

3(1), 15-27.<br />

Yeater, R. A., Mart<strong>in</strong>, R. B., White, M. K. & Gilson, K. H. (1981). Tethered<br />

swimm<strong>in</strong>g forces <strong>in</strong> the crawl, breast <strong>and</strong> back strokes <strong>and</strong> their<br />

relationship to competitive performance. J <strong>Biomechanics</strong>, 14(8), 527-<br />

37.<br />

AcKnoWledGeMents<br />

Authors would like to thank CAPES for the f<strong>in</strong>ancial support, CEFISE<br />

for the tethered swimm<strong>in</strong>g system used <strong>in</strong> Brazil <strong>and</strong> coaches Flávio<br />

Lopes <strong>and</strong> Carlos Matheus for the scientific cooperation.<br />

49


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Jo<strong>in</strong>t Torque Request for Different F<strong>in</strong> Uses<br />

Gouvernet, G. 1,2 , rao, G. 2 , Barla, c. 1 , Baly, l. 1 , Grélot, l. 2 ,<br />

Berton, e. 2<br />

1 Oxylane Research, Lille, France<br />

2 Institut des Sciences du Mouvement “E.J. Marey”, Marseille, France<br />

The purpose of the present study was to exam<strong>in</strong>e the jo<strong>in</strong>t torques of<br />

different f<strong>in</strong> swimm<strong>in</strong>g activities us<strong>in</strong>g different f<strong>in</strong>s. Three different f<strong>in</strong><br />

uses were <strong>in</strong> focus: body-board, swimm<strong>in</strong>g, <strong>and</strong> snorkell<strong>in</strong>g. Inverse dynamics<br />

was used to estimate the jo<strong>in</strong>t torque of the lowers body jo<strong>in</strong>ts<br />

(knee <strong>and</strong> hip). For each practice we recorded the three-dimensional<br />

k<strong>in</strong>ematics with underwater camcorders. Apart from the k<strong>in</strong>ematics <strong>in</strong>puts,<br />

the forces <strong>and</strong> torques were measured by a robot which reproduced<br />

mean k<strong>in</strong>ematics of each practice <strong>and</strong> measured the forces <strong>and</strong> torques<br />

components at the ankle. Thus, jo<strong>in</strong>t torques was measured at the ankle<br />

<strong>and</strong> computed at the knee <strong>and</strong> hip jo<strong>in</strong>ts. Jo<strong>in</strong>t torque pattern <strong>and</strong> peak<br />

values differed for the ankle <strong>and</strong> knee jo<strong>in</strong>ts but were not statistically<br />

different at the hip whatever the practice. This method allows to measure<br />

torques <strong>and</strong> forces on ankle <strong>and</strong> <strong>in</strong> this way precisely quantify the effect<br />

of f<strong>in</strong> blade on human jo<strong>in</strong>ts.<br />

Key word: swimm<strong>in</strong>g-f<strong>in</strong>, F<strong>in</strong>, Muscular request, snorkell<strong>in</strong>g, Bodyboard<br />

IntroductIon<br />

Depend<strong>in</strong>g on the f<strong>in</strong> sport, swimmers expectations are not the same<br />

(acceleration, endurance, or muscular ga<strong>in</strong>). Therefore, f<strong>in</strong> design with<br />

a specific shape <strong>and</strong> material has been designed for each specific sport.<br />

For the last few years, sophisticated numerical model have enabled<br />

for modell<strong>in</strong>g propulsive <strong>and</strong> drag forces for a swimmer without f<strong>in</strong>s.<br />

The numerical model (SWUM) of Nakashima (2007) considers a fullbody<br />

musculoskeletal model guided by different k<strong>in</strong>ematics of swimm<strong>in</strong>g<br />

styles (crawl, breast) <strong>and</strong> compute global swimm<strong>in</strong>g forces. But<br />

this last model regards segments as rigid bodies, <strong>and</strong> the f<strong>in</strong> blade cannot<br />

be simplified as rigid part. Thus, this previous model can not be used to<br />

quantify the effect of a deformable f<strong>in</strong> blade.<br />

Moreover, at the same speed, swimm<strong>in</strong>g with a large <strong>and</strong> stiff f<strong>in</strong><br />

blade requires less energy than with a short <strong>and</strong> flexible f<strong>in</strong> (Zamparo<br />

2006). So, f<strong>in</strong> structure (shape <strong>and</strong> stiffness) entails a modification of f<strong>in</strong><br />

forces on foot <strong>and</strong> consequently of the energetic expenditure. The aim of<br />

this study was thus to <strong>in</strong>vestigate the <strong>in</strong>fluence of different f<strong>in</strong> types on<br />

jo<strong>in</strong>t torques dur<strong>in</strong>g f<strong>in</strong> swimm<strong>in</strong>g activities.<br />

Methods<br />

In order to assess jo<strong>in</strong>t torque, an <strong>in</strong>verse dynamic model is used where<br />

jo<strong>in</strong>t k<strong>in</strong>ematics <strong>and</strong> hydrodynamics f<strong>in</strong> forces have to be described for<br />

each activity.<br />

Mean k<strong>in</strong>ematics of each f<strong>in</strong> swimm<strong>in</strong>g activities were determ<strong>in</strong>ed<br />

from experimentation. Six male <strong>and</strong> 2 female skilled participants of all<br />

activities were asked to practice the three activities <strong>in</strong> usual conditions.<br />

Subject’s average (±SD) body mass, stature, <strong>and</strong> age were respectively<br />

71±7.2 kg, 1.73±0.13 m, <strong>and</strong> 27±3.2 years. For swimm<strong>in</strong>g, subjects swim<br />

hold<strong>in</strong>g out their arms on a board, <strong>and</strong> their heads <strong>in</strong> water. Bodyboarders<br />

were told to adopt the same velocity as when they go to the<br />

reach, with their chests lifted-up <strong>and</strong> their elbows on the body-board<br />

flexed at 90°. And for snorkell<strong>in</strong>g, they practise with masks <strong>and</strong> snorkel,<br />

arms along the body, swimm<strong>in</strong>g only with legs. Each subject swims 2<br />

pool lengths for each of the 3 practices. For each practice, st<strong>and</strong>ard DE-<br />

CATHLON f<strong>in</strong>s were used (Figure 1).<br />

50<br />

Figure 1. F<strong>in</strong>s for body-board (a), swimm<strong>in</strong>g (b), <strong>and</strong> snorkell<strong>in</strong>g (c).<br />

Eleven markers were positioned on the left lower limb. The tri-dimensional<br />

motion of lower limbs was simultaneously recorded by four<br />

cameras, on full frame with 800x650 pixels at 50 Hz (DALSA Falcom<br />

1.4M100). A sufficient calibration space (4m long) was placed on<br />

the swimm<strong>in</strong>g pool. The picture def<strong>in</strong>ition allowed a good precision<br />

of track<strong>in</strong>g. The three-dimensional positions were computed by the<br />

DLT method (SIMI Motion Systems GmBh, Germany ). Data were<br />

smoothed us<strong>in</strong>g a Butterworth lower pass filter at 6Hz. Dur<strong>in</strong>g each<br />

swim, three cycles were selected. The cycles were cut at the higher position<br />

of the subject’s foot. Then, the cycles were averaged to obta<strong>in</strong> a<br />

representative k<strong>in</strong>ematical cycle per subject per <strong>and</strong> swimm<strong>in</strong>g activities<br />

(body-board, swimm<strong>in</strong>g, or snorkell<strong>in</strong>g).<br />

For each activity recorded, the foot motions averaged over the subjects<br />

were reproduced us<strong>in</strong>g a custom-made robot. This twice-f<strong>in</strong> robot<br />

reproduces the k<strong>in</strong>ematics of the two feet by velocity control. Ankle<br />

angle <strong>and</strong> vertical kick<strong>in</strong>g were controlled (Figure 2). Also, the distance<br />

of the robot from the water surface could be adjusted, <strong>in</strong> order to reproduce<br />

the good kick<strong>in</strong>g depth too. The foot motion on sagittal plane was<br />

used as an <strong>in</strong>put parameter of the robot. A waterproof six-component<br />

sensor is located on the foot form of the robot, at the same position as<br />

the ankle jo<strong>in</strong>t; <strong>in</strong> this way forces <strong>and</strong> torques produced by f<strong>in</strong> on foot are<br />

measured. Moreover, the robot moved forward at the velocity measured<br />

<strong>in</strong> each f<strong>in</strong> swimm<strong>in</strong>g activities. Thus, sagittal ankle motions reproduced<br />

the foot motion of each activity with a match<strong>in</strong>g velocity. This simulation<br />

of f<strong>in</strong> swimm<strong>in</strong>g activities allowed us to consider measured forced<br />

as close to real forces encountered dur<strong>in</strong>g swimm<strong>in</strong>g as possible.<br />

Three-dimensional force <strong>and</strong> torque measurements were made on<br />

the foot robot which reproduced mean motion of each activity. Inverse<br />

dynamics computations were carried out to estimate the threedimensional<br />

net forces <strong>and</strong> torques at the knee <strong>and</strong> hip jo<strong>in</strong>ts. Net jo<strong>in</strong>t<br />

moments were estimated tak<strong>in</strong>g <strong>in</strong>to account gravity, <strong>in</strong>ertial body parameters,<br />

as well as Archimedes thrust (FA=ρ water .V.g), the volume (V)<br />

be<strong>in</strong>g assessed as a function of body mass <strong>and</strong> segment density (Zatiorsky<br />

1990). This force was applied at the segment centre of mass.<br />

Both swimm<strong>in</strong>g (frequency, amplitude <strong>and</strong> depth of the kick), <strong>and</strong><br />

muscle torque variables were analyzed.


Ankle<br />

Figure 2. Diagram 0.5 of the robot’s k<strong>in</strong>ematics<br />

chaPter2.<strong>Biomechanics</strong><br />

-0.5<br />

0 20 40 60 80 100<br />

results<br />

Kick amplitudes did 0.3not<br />

appeared as a significant parameter (p>0.05). 0.3 0.6<br />

0<br />

However, snorkell<strong>in</strong>g kicks substantially differed <strong>in</strong> frequency <strong>and</strong><br />

depth. Snorkell<strong>in</strong>g frequency was lower than the two others practices<br />

(Table1). This last 0.1 result agrees with measurement made with different<br />

0.1 0.2<br />

0<br />

0<br />

snorkel f<strong>in</strong>s by Zamparo 0 et al. (2006). The kick depth, def<strong>in</strong>ed as the<br />

higher position of ankle dur<strong>in</strong>g a cycle, showed snorkell<strong>in</strong>g depths closer<br />

to the water surface -0.1 than swimm<strong>in</strong>g <strong>and</strong> body-board values.<br />

0<br />

-0.1 -0.2<br />

-0<br />

-0<br />

Table 1. Ma<strong>in</strong> ankle k<strong>in</strong>ematic parameters for the three practices: frequency,<br />

amplitude,<br />

-0.3<br />

<strong>and</strong> depth of swimm<strong>in</strong>g kicks.<br />

-0.3 -0.6<br />

-0<br />

Frequency Amplitude Depth<br />

Swimm<strong>in</strong>g<br />

-0.5 (Hz)<br />

1.01 0 ± 0.1720 (m)<br />

0.42 40± 0.02<br />

(m)<br />

60 -0.16 80 ± 0.08 100<br />

-0.5-1<br />

0 20 40 60 80 100<br />

-1<br />

Snorkell<strong>in</strong>g<br />

Body-board<br />

0.85 ± 0.19<br />

0.98 ± 0.18<br />

0.36 ± 0.02<br />

0.42 ± Knee 0.02<br />

0.02 ± 0.26<br />

data1<br />

-0.08 ± 0.08<br />

Body-board<br />

Ankle<br />

Swimm<strong>in</strong>g data1<br />

Hip<br />

Snork Bod<br />

1<br />

Concern<strong>in</strong>g the <strong>in</strong>verse dynamics results, torques values gradually <strong>in</strong>-<br />

0.5 1.5<br />

creased from the ankle to the hip jo<strong>in</strong>t. For all jo<strong>in</strong>ts, the highest amplitude<br />

was found around 0.6 the flexion/extension axis.<br />

0.3<br />

1<br />

0<br />

The robot reproduces seven stock swimm<strong>in</strong>g cycles with a st<strong>and</strong>ard<br />

deviation lower than 4%. On the ankle jo<strong>in</strong>t, amplitude patterns are<br />

lower for body-board. 0.2In<br />

knee <strong>and</strong> hip torque amplitudes, no difference<br />

0.5<br />

0.1<br />

0<br />

were found between the three activities. Forces <strong>and</strong> torques patterns<br />

measured on the ankle sensor of the robot showed only one oscillation.<br />

The torque pattern -0.2 computed by the model described a double oscillation<br />

dur<strong>in</strong>g stroke cycle, both <strong>in</strong> the knee <strong>and</strong> the hip (Figure 3). In the<br />

0<br />

-0.1<br />

-0.5<br />

-0<br />

knee jo<strong>in</strong>t, dur<strong>in</strong>g the snorkell<strong>in</strong>g activity, the second upper peak disap-<br />

-0.6<br />

peared, because value of this peak staid negative while the two others<br />

were positive, as well as <strong>in</strong> the second lower peak for body-board activity<br />

-0.3<br />

-1<br />

-0<br />

80<br />

on knee. In the hip jo<strong>in</strong>t, the oscillations were synchronous but snorkel-<br />

-1<br />

l<strong>in</strong>g 100amplitudes were lower 0 than 20 others. 40 60 80 100<br />

-0.5 -1.5<br />

0 20 40 60 80 100<br />

data1 Body-board Swimm<strong>in</strong>g<br />

Figure 3. Evolution of tri-dimensional jo<strong>in</strong>t torques for body-board,<br />

snorkell<strong>in</strong>g Snorkel<strong>in</strong>g <strong>and</strong> swimm<strong>in</strong>g activities.<br />

data1 Bod<br />

Flexion / Extension<br />

Flexion / Extension<br />

Flexion / Extension<br />

Flexion / Extension<br />

0.5<br />

0.3<br />

0.1<br />

0<br />

-0.1<br />

-0.3<br />

0.51<br />

Ankle<br />

Ankle Knee<br />

51<br />

0<br />

0<br />

-0<br />

-0<br />

data1 Bod<br />

1


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

dIscussIon<br />

These results must be carefully considered because variability <strong>in</strong>creases at<br />

each proximal jo<strong>in</strong>t. This <strong>in</strong>crease <strong>in</strong> variability may expla<strong>in</strong> the absence<br />

of significant difference <strong>in</strong> amplitude between activities at the hip jo<strong>in</strong>t,<br />

despite graphical proof. The <strong>in</strong>verse dynamic model allows us to compute<br />

knee <strong>and</strong> hip torques. But modell<strong>in</strong>g torques show a double oscillation<br />

whereas measured torque on ankle shows a s<strong>in</strong>gle oscillation. The first half<br />

cycle of swimm<strong>in</strong>g activities is the down kick of foot <strong>and</strong> first a positive,<br />

then a negative torque on the knee can be observed. Probably the drag<br />

forces of each segment were underestimated, which needs further research.<br />

F<strong>in</strong> swimmer k<strong>in</strong>ematics is <strong>in</strong>fluenced by the body position dur<strong>in</strong>g<br />

f<strong>in</strong> swimm<strong>in</strong>g activities. For each f<strong>in</strong> swimm<strong>in</strong>g activity, kick frequency<br />

<strong>and</strong> amplitude are different but also depth of the kick foot. Thanks to<br />

this new method, we can assess to three-dimensional forces <strong>and</strong> torques<br />

on the ankle for the three f<strong>in</strong> swimm<strong>in</strong>g activities. These three practices<br />

show ma<strong>in</strong> differences <strong>in</strong> amplitude but not <strong>in</strong> the tim<strong>in</strong>g pattern.<br />

conclusIon<br />

This method has the ma<strong>in</strong> advantage of allow<strong>in</strong>g us to measure the effect<br />

of f<strong>in</strong> blade on ankle jo<strong>in</strong>t, <strong>and</strong> also to compute the amount of torque<br />

on the knee <strong>and</strong> hip. However, the muscular capacity of the subjects as<br />

a function of both the swimmer level <strong>and</strong> f<strong>in</strong> swimm<strong>in</strong>g activities needs<br />

to be clarified.<br />

reFerences<br />

Nakashima, M., Zatou, K. & Mioura, Y. (2007). Development of swimm<strong>in</strong>g<br />

human simulation model consider<strong>in</strong>g rigid body dynamics <strong>and</strong><br />

unsteady fluid forces for whole body, Journal of Fluid Science <strong>and</strong> Technology,<br />

2(1), 56-67.<br />

Zamparo, P., Pendergast, D. R., Mollendorf, J., Term<strong>in</strong>, B., & M<strong>in</strong>etti, A.<br />

M. (2006). Economy <strong>and</strong> efficiency of swimm<strong>in</strong>g at the surface with<br />

f<strong>in</strong>s of different size <strong>and</strong> stiffness. Eur J Appl Physiol, 96, 459–470.<br />

52<br />

3D Computational Fluid-structure Interaction Model<br />

for the Estimation of Propulsive Forces of a Flexible<br />

Monof<strong>in</strong><br />

Bideau, n. 1 , razafimahery, F. 1 , Monier, l. 1 , Mahiou, B. 1 ,<br />

nicolas, G. 2 , Bideau, B. 2 , rakotomanana, l. 1<br />

1Institut de Recherche Mathématique, University of Rennes 1, Rennes,<br />

France<br />

2M2S, University of Rennes 2, Rennes, France<br />

The goal of this study was to analyse the dynamic performance of a<br />

monof<strong>in</strong> for a given k<strong>in</strong>ematics. The problem is formulated with<strong>in</strong> the<br />

framework of a 3D fluid-structure <strong>in</strong>teraction model. The numerical solution<br />

is computed us<strong>in</strong>g the f<strong>in</strong>ite element method. Namely, the role of<br />

the added mass is highlighted by the modal analysis of the coupled problem.<br />

Moreover, <strong>in</strong>stantaneous propulsive forces <strong>and</strong> torques are calculated.<br />

Both qualitative <strong>and</strong> quantitative results were obta<strong>in</strong>ed. In particular, the<br />

effect of its deformability <strong>and</strong> the <strong>in</strong>fluence of added mass are po<strong>in</strong>ted out.<br />

Key words: Monof<strong>in</strong>, Propulsion, F<strong>in</strong>ite elements, Fluid-structure<br />

Interaction<br />

IntroductIon<br />

The current paper contributes to the <strong>in</strong>vestigations of biomechanical<br />

aspects of propulsion <strong>in</strong> monof<strong>in</strong> swimm<strong>in</strong>g. The estimation of the dynamical<br />

response of the f<strong>in</strong> is one of the key po<strong>in</strong>ts of the performance <strong>in</strong><br />

monof<strong>in</strong> swimmers. This can be achieved through dynamic measurement<br />

or modell<strong>in</strong>g. Throughout the history of swimm<strong>in</strong>g research, different attempts<br />

have been made to measure accurately the propulsive forces, us<strong>in</strong>g<br />

experimental or modell<strong>in</strong>g approaches. The dynamic underst<strong>and</strong><strong>in</strong>g<br />

<strong>in</strong> monof<strong>in</strong>-swimm<strong>in</strong>g motion was <strong>in</strong>troduced by Rejman (1999) from an<br />

experimental po<strong>in</strong>t of view. Us<strong>in</strong>g stra<strong>in</strong> gauges glued on each side of the<br />

f<strong>in</strong>s surface, the author put <strong>in</strong> relation the local forces dur<strong>in</strong>g up <strong>and</strong> down<br />

motions with swimm<strong>in</strong>g speed. However this approach is not sufficient<br />

to describe the flow over the f<strong>in</strong>. More recently, (Zamparo et al., 2005)<br />

used a methodology previously applied to fish locomotion to calculate efficiency<br />

for f<strong>in</strong> swimm<strong>in</strong>g at low speeds. While energy flows were precisely<br />

quantified, it rema<strong>in</strong>s very difficult to evaluate the <strong>in</strong>fluence of the f<strong>in</strong> on<br />

global performance. To compensate for this drawback, recent approaches<br />

based on computational modell<strong>in</strong>g can be used. In that sense, two major<br />

approaches have been proposed <strong>in</strong> the literature. The F<strong>in</strong>ite Element<br />

Method (FEM) has been <strong>in</strong>tensively used to model the foil <strong>and</strong> swimmer<br />

dynamics (Von Loebbecke, 2009). Most of them, based on Computational<br />

Fluid Dynamics (CFD) neglected the elasticity of the foil. Indeed, no constitutive<br />

law is considered for the structure. Some authors have studied<br />

the mechanical properties of f<strong>in</strong> without fluid (Bideau et al., 2003). To our<br />

knowledge, there is no study consider<strong>in</strong>g de dynamical behaviour of the<br />

whole cont<strong>in</strong>uum model (solid <strong>and</strong> fluid features at the same time). In this<br />

paper, a new method that is devoted to computation of propulsive forces<br />

generated by a flexible monof<strong>in</strong> is described. From this method, the added<br />

mass is calculated, <strong>and</strong> shows the great impact of this parameter.<br />

Figure 1. Example of the mesh of the solid doma<strong>in</strong> (monof<strong>in</strong>) <strong>and</strong> the<br />

fluid doma<strong>in</strong> (pool) used <strong>in</strong> the FEM simulation


¾<br />

¾<br />

¾<br />

Methods<br />

A three-dimensional model of the f<strong>in</strong>-water system is proposed which<br />

is built on the follow<strong>in</strong>g assumptions. Based on cont<strong>in</strong>uum theory, a<br />

fluid-structure <strong>in</strong>teraction is developed with <strong>in</strong>ertial coupl<strong>in</strong>g. The system<br />

is depicted <strong>in</strong> Figure 1 <strong>and</strong> is composed of a solid doma<strong>in</strong> (ΩS )<br />

coupled with a surround<strong>in</strong>g fluid doma<strong>in</strong> (ΩF ). The boundary (Γ) ¾<br />

corresponds to the deformable fluid-structure <strong>in</strong>terface. The external<br />

excitation for the stroke motion (i.e. the rate of undulation) ¾ is assumed<br />

to be lower than the wave speed ¾ <strong>in</strong> the f<strong>in</strong>, so that the fluid can be ¾ de-<br />

¾<br />

scribed with the acoustic pressure (Mor<strong>and</strong> <strong>and</strong> Ohayon, 1995). It corresponds<br />

to an undulatory type of low frequency swimm<strong>in</strong>g. The f<strong>in</strong> is<br />

assumed to be a deformable elastic structure. Namely, the monof<strong>in</strong> is<br />

modelled us<strong>in</strong>g a multilayer structure, whose constitutive law is written<br />

by means of the Cauchy stress tensorσ<br />

. The imposed k<strong>in</strong>ematics at the<br />

lead<strong>in</strong>g edge of the monof<strong>in</strong> (that corresponds to the swimmer’s ankle)<br />

results <strong>in</strong> a volume force γ ie. If we denote by u the displacement field of<br />

the monof<strong>in</strong> <strong>and</strong> p pressure field with<strong>in</strong> the fluid doma<strong>in</strong>, the problem<br />

consists <strong>in</strong> f<strong>in</strong>d<strong>in</strong>g (u,p) solutions of the follow<strong>in</strong>g three-dimensional<br />

¾<br />

boundary value problem:<br />

¾<br />

r ∂ 2 u<br />

∂t 2 u<br />

=<br />

=<br />

divσ + γ ie<br />

0<br />

(ΩS )<br />

(Γ0 )<br />

(1)<br />

(2)<br />

σ.n = −pn (Γ) (3)<br />

∆p − 1<br />

2<br />

c0 ∂ 2 p<br />

∂t 2 = div(−r 0γ ie) (Ω F ) (4)<br />

∂p<br />

∂<br />

= −r0 ∂n<br />

2 u<br />

∂t 2 .n − r0γ ie.n (Γ1) (5)<br />

∂p<br />

= −r0γ ie.n (Γ) (6)<br />

∂n<br />

¾<br />

p = 0 (Γg ∪ Γs ∪ Γe) (7)<br />

xω(t) + zω<br />

γ ie =<br />

2 (t)<br />

0<br />

zω(t) − xω 2 ⎡<br />

⎤<br />

⎢<br />

⎥<br />

⎢<br />

⎥<br />

⎣<br />

⎢ (t) ⎦<br />

⎥<br />

Where c is the wave velocity <strong>in</strong> the fluid, r is the density of the mono-<br />

0 ¾<br />

f<strong>in</strong>, r is the fluid density <strong>and</strong> n is the unit outward normal to the f<strong>in</strong><br />

0<br />

doma<strong>in</strong>. The coupl<strong>in</strong>g results <strong>in</strong> a new term <strong>in</strong> the <strong>in</strong>ertial contribution of<br />

the system. Indeed, this added mass characterizes the energy transmission<br />

¾<br />

between the f<strong>in</strong> <strong>and</strong> the water. The specificity of the present method is that<br />

¾<br />

the temporal evolution ¾ of dynamical features is available. Namely, transient<br />

added mass, three-dimensional forces <strong>and</strong> torques at the po<strong>in</strong>t correspond<strong>in</strong>g<br />

to the swimmer’s ankle as well as energy balance are obta<strong>in</strong>ed.<br />

S<strong>in</strong>ce this result<strong>in</strong>g fluid-structure <strong>in</strong>teraction problem is too complex to<br />

be solved analytically, we analyzed us<strong>in</strong>g the means of numerical approximation.<br />

We will briefly outl<strong>in</strong>e the solution methodology used to solve<br />

the govern<strong>in</strong>g equations. The latter are solved with the F<strong>in</strong>ite Element<br />

Method us<strong>in</strong>g the commercial software COMSOL Multiphysics (Comsol<br />

Inc., Burl<strong>in</strong>gton, USA) . Numerical simulations are carried out for the<br />

fluid flow <strong>in</strong> a pool with the follow<strong>in</strong>g dimensions: In the pool, a f<strong>in</strong> with<br />

realistic dimensions (0.80 m chord <strong>and</strong> 0.50 wide) is located at the distance<br />

of 5 m from left wall. In this study a monolithic approach is used.<br />

Indeed, the equations govern<strong>in</strong>g the fluid flow <strong>and</strong> the displacement of the<br />

structure are solved simultaneously with s<strong>in</strong>gle solver. The ma<strong>in</strong> steps of<br />

the methodology are the follow<strong>in</strong>g: first, based on realistic pictures, the<br />

geometry of the monof<strong>in</strong> is created. The result<strong>in</strong>g volume, which is the<br />

form of an Initial Graphics Exchange Specification (IGES) file format,<br />

is then <strong>in</strong>put <strong>in</strong>to the commercial software COMSOL Multiphysics <strong>and</strong><br />

transformed to an unstructured volume mesh with triangular elements.<br />

The second step consists <strong>in</strong> the mesh<strong>in</strong>g. The f<strong>in</strong>al volume mesh (Figure<br />

1) consists of 6256 triangular elements for the f<strong>in</strong> <strong>and</strong> 128676 triangular<br />

elements for the water. The third step consists <strong>in</strong> a modal analysis of the<br />

three-dimensional coupled problem. γ ie is set to zero <strong>and</strong> a time harmonic<br />

solution of the problem is computed. This allows obta<strong>in</strong><strong>in</strong>g the fundamental<br />

vibration characteristics of the immersed monof<strong>in</strong> <strong>and</strong> therefore<br />

the quantitative <strong>and</strong> qualitative effect of the added mass can be po<strong>in</strong>ted<br />

out. The f<strong>in</strong>al step of the ¾ methodology consists <strong>in</strong> a transient analysis of<br />

propulsive forces. Thus, <strong>in</strong> the numerical experiments that are presented,<br />

the monof<strong>in</strong> is undergo<strong>in</strong>g time-dependent motion that comb<strong>in</strong>es translat<strong>in</strong>g<br />

<strong>and</strong> rotat<strong>in</strong>g motions as follows<br />

chaPter2.<strong>Biomechanics</strong><br />

ω(t) = θ0 s<strong>in</strong>(ω 0t +ψ) h(t) = h0 s<strong>in</strong>(ω 0t)<br />

with<br />

ω0 =1.7rad.s −1<br />

θ0 = π<br />

rad<br />

4<br />

π<br />

ψ =<br />

2 rad h0 = 3<br />

4 c<br />

<strong>in</strong> which c is the chord of the monof<strong>in</strong>. In the numerical experiments, c<br />

is set to 0.7m. The material properties used <strong>in</strong> the FEM simulation are<br />

given <strong>in</strong> Table 1.<br />

Table 1. Material characteristics used <strong>in</strong> the FEM simulation. E is the<br />

Young’s modulus, ν is the Poisson’s coefficient <strong>and</strong> r is the density of<br />

the monof<strong>in</strong>. (Data provided by Breier SAS company)<br />

¾<br />

E [Pa] ν<br />

r [kg.m<br />

¾<br />

¾<br />

¾ ¾<br />

¾ ¾<br />

¾<br />

−3 ]<br />

Carbon 12K<br />

146.10<br />

¾<br />

9<br />

0.32 1565<br />

Low density Polyethylene 146.10<br />

¾ ¾<br />

¾<br />

9<br />

0.38 920<br />

Rubber<br />

0,05.10<br />

¾ ¾<br />

¾<br />

9 0.49 1250<br />

Some of the key parameters associated with the performance of the<br />

monof<strong>in</strong> are the lift force L, the thrust ¾ force ¾ T (equal to negative drag<br />

force D) <strong>and</strong> the result<strong>in</strong>g torque at the swimmer’s. Thanks to the present<br />

FEM method, the accurate efforts (result<strong>in</strong>g force <strong>and</strong> result<strong>in</strong>g<br />

torque) at the po<strong>in</strong>t O, which corresponds to the swimmer ankle, are<br />

computed. The <strong>in</strong>stantaneous resultant force components are calculated<br />

by directly <strong>in</strong>tegrat<strong>in</strong>g the traction vector on the f<strong>in</strong> surface. In particular,<br />

if σ is the stress tensor <strong>and</strong> n is the outward normal unit to the f<strong>in</strong><br />

surface A, the resultant force is given by<br />

R(t) = ∫ σ.ndΓ<br />

= L(t).x + L(t).z<br />

A<br />

where T(t) <strong>and</strong> L(t) are the <strong>in</strong>stantaneous thrust force <strong>and</strong> <strong>in</strong>stantaneous<br />

lift force respectively. It known that the performance of flexible<br />

f<strong>in</strong>s depends largely on the effective dynamic properties of the structure.<br />

Therefore, ¾ modal analysis was performed <strong>in</strong> this work. This allowed for<br />

¾<br />

the quantification of the added mass effect on the f<strong>in</strong> by compar<strong>in</strong>g the<br />

natural frequencies <strong>and</strong> modal shapes <strong>in</strong> the case where the f<strong>in</strong> is submerged<br />

or not. The first natural frequencies fi = λi /2π are reported <strong>in</strong><br />

Table 2. In this study transient force <strong>and</strong> torque at the swimmer’s ankle<br />

is computed. Figure 3 shows the variation of the thrust.<br />

Table 2. Comparison of first natural frequencies fi = λi /2π [Hz] obta<strong>in</strong>ed<br />

with the Coupled FEM. ¾<br />

f1 f2 f3<br />

2D <strong>in</strong> water 6.08 41.12 70.03<br />

3D <strong>in</strong> vacuum 13.01 ¾ 113.51 256.34<br />

3D <strong>in</strong> water 4.395 23.87 41.87<br />

53


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 2. Plot of the third modal shape for the monof<strong>in</strong> blade with the<br />

von Mises stress (top) <strong>and</strong> plot of the fluid pressure at time 1.5s of the<br />

transient analysis (bottom).<br />

There is a significant difference between the modal shapes of rigid f<strong>in</strong><br />

model <strong>and</strong> that of flexible f<strong>in</strong> model. This highlights the necessity of account<strong>in</strong>g<br />

as accurately as possible not only the fluid-structure <strong>in</strong>teraction<br />

but also the deformability of the elements dur<strong>in</strong>g a propulsion analysis of<br />

a f<strong>in</strong>. Modal shapes of the immersed f<strong>in</strong> are not the same as those of the<br />

dry f<strong>in</strong> case. This is due to the non-symmetry of the added mass matrix.<br />

Therefore, <strong>in</strong>clud<strong>in</strong>g the effect of coupl<strong>in</strong>g between the f<strong>in</strong> <strong>and</strong> the surround<strong>in</strong>g<br />

water is essential for an accurate description of the dynamic behaviour<br />

of flexible f<strong>in</strong>s. Moreover, this feature is an important parameter<br />

<strong>in</strong> the design of optimal swim f<strong>in</strong> especially for competitive swimmers.<br />

If we compare the eigenfrequencies obta<strong>in</strong>ed with the present model with<br />

those obta<strong>in</strong>ed with the correspond<strong>in</strong>g two-dimensional model (Bideau<br />

et al., 2009), it can be observed that tak<strong>in</strong>g <strong>in</strong>to account for three-dimensional<br />

effects leads to a decrease of the deformation of the f<strong>in</strong>. This can be<br />

expla<strong>in</strong>ed by the fact that the three-dimensional model is less constra<strong>in</strong>ed<br />

that the two-dimensional one, which allows more flexibility <strong>in</strong> the third<br />

direction. Indeed, two-dimensional shapes can only take <strong>in</strong>to account for<br />

the <strong>in</strong>-plane flexion. As an example, the third modal shape of the monof<strong>in</strong><br />

blade is depicted on figure 2. On the same figure, the pressure field of<br />

the fluid is plotted at time t=1.5s. In fact, the pressure is be<strong>in</strong>g exam<strong>in</strong>ed<br />

to better underst<strong>and</strong> the generation of thrust. The temporal evolution of<br />

those variables tends to an oscillat<strong>in</strong>g behaviour when <strong>in</strong>creas<strong>in</strong>g the rigidity<br />

of the f<strong>in</strong> plate. It can be noticed that there is a significant variation<br />

of the frequency of the thrust evolution <strong>in</strong> regards to the applied stroke<br />

k<strong>in</strong>ematics that are harmonically vary<strong>in</strong>g. This can be expla<strong>in</strong>ed by the<br />

elasticity of the flexible f<strong>in</strong>. The elastic energy is stored <strong>in</strong> a first time <strong>and</strong><br />

distributed <strong>in</strong> a second part. Therefore, the stra<strong>in</strong> energy of the structure is<br />

seen to greatly affect the propulsive characteristics (propulsive force <strong>and</strong><br />

result<strong>in</strong>g moment) of the monof<strong>in</strong> (Figure 3).<br />

Figure 3. Temporal evolution of thrust <strong>and</strong> lift for different material<br />

characteristics.<br />

54<br />

conclusIon<br />

A 3D fluid-<strong>in</strong>teraction model has been presented. It is based monolithic<br />

resolution of the whole system fluid <strong>and</strong> solid. The present work <strong>in</strong>vestigated<br />

the properties of propulsive force of a three-dimensional deformable<br />

monof<strong>in</strong>. In particular, the added mass effect of the coupled<br />

dynamics has been po<strong>in</strong>ted out. The transient propulsive force end<br />

torque computation has been <strong>in</strong>vestigated by means of FEM method.<br />

The <strong>in</strong>fluence of the elasticity (i.e. stra<strong>in</strong> energy) has been <strong>in</strong>vestigated<br />

<strong>and</strong> shows that he flexibility of the f<strong>in</strong> blade <strong>in</strong>crease the thrust. To our<br />

knowledge it is the first fluid-structure <strong>in</strong>teraction model for the whole<br />

monof<strong>in</strong>-water system solved by 3D FEM approach.<br />

reFerences<br />

Bideau B. , Colobert B, Nicolas G, Fusco N, Cretual A, Multon F, Delamarche<br />

P (2003). How to compute the mechanical properties of<br />

monof<strong>in</strong>s? In Chatard J.C. (Ed), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g<br />

IX, p.505-511, St Etienne.<br />

Bideau N, Mahiou B, Monier L, Razafimahery F, Bideau B, Nicolas G,<br />

Razafimahery F, Rakotomanana L (2009). 2D dynamical efficiency<br />

of a swimf<strong>in</strong> : a fluid-structure approach. Computer Methods <strong>in</strong> <strong>Biomechanics</strong><br />

<strong>and</strong> Biomedical Eng<strong>in</strong>eer<strong>in</strong>g, 11, 53-54.<br />

Mor<strong>and</strong> H <strong>and</strong> Ohayon R (1995). Fluid-Structure Interaction. John<br />

Wiley & Sons.<br />

Rejman M (1999). Dynamic criteria for description of s<strong>in</strong>gle f<strong>in</strong> technique.<br />

In K.L. Kesk<strong>in</strong>en, P.V. Komi <strong>and</strong> P. Holl<strong>and</strong>er (Eds) <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII, p.171-176, Jyväskylä.<br />

Von Loebbecke A, Mittal R, Mark R, Hahn J (2009). A computational<br />

method for analysis of underwater dolph<strong>in</strong> kick hydrodymamics <strong>in</strong><br />

human swimm<strong>in</strong>g. Sports <strong>Biomechanics</strong>, 8, 60-77.<br />

Zamparo P, Pendergast DR, Term<strong>in</strong> B, M<strong>in</strong>etti AE (2005) Economy<br />

<strong>and</strong> efficiency of swimm<strong>in</strong>g at the surface with f<strong>in</strong>s of different size<br />

<strong>and</strong> stiffness. European Journal of Applied Physiology, 96, 459-470.


Do Fastsk<strong>in</strong> Swimsuits Influence Coord<strong>in</strong>ation <strong>in</strong><br />

Front Crawl Swimm<strong>in</strong>g <strong>and</strong> Glide?<br />

chollet, d. 1 , chavallard, F. 1 , seifert, l. 1 , lemaître, F. 1<br />

1 C.E.T.A.P.S. EA 3832, Faculté des Sciences du Sport, Université de Rouen,<br />

France<br />

The aim of this study was to compare the effect of Fastsk<strong>in</strong> swimsuits<br />

(FS) on spatio-temporal parameters, IdC <strong>and</strong> propulsive phases (PP) <strong>in</strong><br />

front crawl swimm<strong>in</strong>g at four velocities. The results showed a lower IdC<br />

with FS (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

with a st<strong>and</strong>ard suit (SS). The statistical analysis was performed us<strong>in</strong>g<br />

Student t tests.<br />

The second part was a cl<strong>in</strong>ical case study. The subject was an <strong>in</strong>ternational<br />

swimmer, a member of the French national swim team for many<br />

years (31 years old, 190cm, 89kg), <strong>and</strong> was a specialist of short distances<br />

<strong>in</strong> front crawl swimm<strong>in</strong>g (93.93% WR on the 50-m event, <strong>and</strong> 93.98%<br />

WR on the 100-m event). This swimmer performed the whole experiment<br />

four times: <strong>in</strong> a st<strong>and</strong>ard suit, <strong>in</strong> an Arena Extrem® suit, <strong>in</strong> an<br />

Arena Powersk<strong>in</strong>-Revolution® suit <strong>and</strong> <strong>in</strong> a Speedo LZR® suit.<br />

results<br />

The results of the first part of this study showed no significant differences<br />

<strong>in</strong> buoyancy, glide or passive torque. A significant decrease <strong>in</strong> IdC<br />

(Fig. 1a) <strong>and</strong> the percentage of propulsive phase of the stroke (Fig. 1b)<br />

was detected by look<strong>in</strong>g at the average values (without tak<strong>in</strong>g <strong>in</strong>to account<br />

the velocities).<br />

Figure 1. Modifications <strong>in</strong> mean IdC (a, left) <strong>and</strong> mean percentage of<br />

propulsive phase (b, right) without (SS) <strong>and</strong> with Fastsk<strong>in</strong> suits (FS)<br />

(**: p


Fastsk<strong>in</strong> suit, a real spr<strong>in</strong>ter does not have to stack his action to reach<br />

his highest speed. Similar to the f<strong>in</strong>d<strong>in</strong>gs <strong>in</strong> the global population, the<br />

propulsive phases were significantly reduced when wear<strong>in</strong>g a Fastsk<strong>in</strong><br />

suit (46.40±4.03 vs. 51.26±3.88 %). Moreover, the SLZR had a specific<br />

<strong>in</strong>fluence on the stroke length/stroke rate ratio <strong>and</strong> also on coord<strong>in</strong>ation<br />

<strong>and</strong> the propulsive phases. In fact, it appeared that the effect of wear<strong>in</strong>g<br />

this suit was the opposite of the effects of the two other Fastsk<strong>in</strong>s. It<br />

thus seems that the morphologic characteristics of the swimmer <strong>and</strong> the<br />

technical characteristics of the swimsuit have comb<strong>in</strong>ed <strong>and</strong> specific effects.<br />

Passive torque measurement also <strong>in</strong>dicated these differences. Each<br />

swimmer be<strong>in</strong>g unique, the same swimsuit could have a different effect<br />

for another swimmer. This case study also showed that the same swimmer<br />

wear<strong>in</strong>g different swimsuits was affected differently.<br />

conclusIon<br />

The new generation Fastsk<strong>in</strong> suit, which does not improve buoyancy,<br />

had the effect of improv<strong>in</strong>g glide <strong>and</strong> reduc<strong>in</strong>g drag. Because of these<br />

effects, swimmers have fewer constra<strong>in</strong>ts, can therefore swim higher <strong>in</strong><br />

the water, <strong>and</strong> do not need to stack their actions. Coord<strong>in</strong>ation when<br />

wear<strong>in</strong>g a Fastsk<strong>in</strong> suit corresponds at a given speed to coord<strong>in</strong>ation at a<br />

slower speed without a Fastsk<strong>in</strong> suit.<br />

reFerences<br />

Benjanuvatra, N., Dawson, G., Blanksby, B. A. & Elliott, B. C. (2002).<br />

Comparison of buoyancy, passive <strong>and</strong> net active drag forces between<br />

Fastsk<strong>in</strong> <strong>and</strong> st<strong>and</strong>ard swimsuits. Journal of Science <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Sport, 5(2), 115-123.<br />

Chatard, J. C., Senegas, X., Selles, M., Dreanot, P. & Geyssant, A.<br />

(1995). Wet suit effect: a comparison between competitive swimmers<br />

<strong>and</strong> triathletes. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports <strong>and</strong> Exercise, 27(4), 580-<br />

586.<br />

Chatard, J. C. & Wilson, B. (2008). Effect of Fastsk<strong>in</strong> Suits on performance,<br />

drag <strong>and</strong> energy cost of performance. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong><br />

Sports <strong>and</strong> Exercise, 40(6),1149-1154.<br />

Chollet, D., Chalies, S. & Chatard, J. C. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: description <strong>and</strong> usefulness. International Journal<br />

of Sports <strong>Medic<strong>in</strong>e</strong>, 21(1), 54-59.<br />

Hue, O., Benavente, H. & Chollet, D. (2003). The effect of wet suit use<br />

by triathletes: an analysis of the different phases of arm movement.<br />

Journal of Sport Sciences, 21, 1025-1030.<br />

Naemi, R. & S<strong>and</strong>ers, R. H. (2008). A “hydrok<strong>in</strong>ematic method of measur<strong>in</strong>g<br />

the glide efficiency of a human swimmer. Journal of Biomechanical<br />

Eng<strong>in</strong>eer<strong>in</strong>g, 130(6), 061016.<br />

McLean, S. P. & H<strong>in</strong>richs, R. N. (1998). Sex differences <strong>in</strong> the center of<br />

buoyancy location of competitive swimmers. Journal of Sports Sciences,<br />

16(4), 373-383.<br />

Millet, G. P., Chollet, D., Chalies, S. & Chatard, J. C. (2002). Coord<strong>in</strong>ation<br />

<strong>in</strong> front crawl <strong>in</strong> elite triathletes <strong>and</strong> elite swimmers. International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 23, 99-104.<br />

Mollendorf, J. C., Term<strong>in</strong>, A. C. 2nd., Oppenheim, E. & Pendergaast,<br />

D. R. (2004). Effect of swim suit design on passive drag. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong><br />

Science <strong>in</strong> Sports <strong>and</strong> Exercise, 36(6), 1029-1035.<br />

Roberts, B. S., Kamel, K. S., Hedrick, C. E., McLean, S. P., Sharp, R. L.<br />

(2003). Effect of a FastSk<strong>in</strong> suit on submaximal freestyle swimm<strong>in</strong>g.<br />

<strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports <strong>and</strong> Exercise, 35(3), 519-524.<br />

Seifert, L., Chollet, D. & Rouard, A. (2007). Swimm<strong>in</strong>g constra<strong>in</strong>ts <strong>and</strong><br />

arm coord<strong>in</strong>ation. Human Movement Science, 26, 68-86.<br />

Toussa<strong>in</strong>t, H. M., Truijens, M., Elz<strong>in</strong>ga, M. J., Van den Ven, A., De Best,<br />

H., Snabel, B., et al. (2002). Effects of a Fast-sk<strong>in</strong> “body” suit on drag<br />

dur<strong>in</strong>g front crawl swimm<strong>in</strong>g. Sports <strong>Biomechanics</strong>, 1(1), 1-10.<br />

chaPter2.<strong>Biomechanics</strong><br />

The Effect of Wear<strong>in</strong>g a Synthetic Rubber Suit on<br />

Hydrostatic Lift <strong>and</strong> Lung Volume<br />

Cortesi, M. 1 , Zamparo, P. 2 , Tam, E. 1, Da Boit, M. 1 , Gatta, G. 1<br />

1 Faculty of Exercise <strong>and</strong> Sport Science, University of Bologna, Italy<br />

2 Faculty of Exercise <strong>and</strong> Sport Science, University of Verona, Italy<br />

Buoyancy improvement is the result of the use of a technical suit to<br />

<strong>in</strong>crease swimm<strong>in</strong>g speed. Hydrostatic lift <strong>and</strong> lung volumes were measured<br />

<strong>in</strong> 9 competitive swimmers while wear<strong>in</strong>g a “st<strong>and</strong>ard” swimsuit<br />

(S) or a full body synthetic rubber suit (Xg). The average values of the<br />

hydrostatic lift were 14.51 ± 4.53 N with S <strong>and</strong> 14.33 ± 3.99 N with<br />

Xg. The average values of lung volumes when wear<strong>in</strong>g S <strong>and</strong> XG were<br />

VC 6.31/6.14 L, ERV 2.12/1.79 L, VT 0.94/0.88 L, IRV 3.26/3.47 L,<br />

respectively. A strong thoracic <strong>and</strong>/or abdom<strong>in</strong>al compression caused<br />

by the technical suits may be related to the observed reduction <strong>in</strong> the<br />

chest <strong>and</strong> abdom<strong>in</strong>al circumferences dur<strong>in</strong>g maximal <strong>in</strong>spiration <strong>and</strong><br />

expiration, as well as to the reduction <strong>in</strong> the lung volumes <strong>and</strong> <strong>in</strong> the<br />

hydrostatic lift. The improvement <strong>in</strong> performance obta<strong>in</strong>ed by wear<strong>in</strong>g<br />

Xg is not related to better static buoyancy.<br />

KeYWords: hydrostatic lift, buoyancy, bodysuit, swimm<strong>in</strong>g, lung<br />

volume<br />

IntroductIon<br />

In the last World Championships, held <strong>in</strong> Rome <strong>in</strong> 2009, swimmers utilized<br />

suits produced partially or entirely with <strong>in</strong>dustrial polymers <strong>and</strong> 43<br />

world records were broken. Even if the effect of these technical suits <strong>in</strong><br />

determ<strong>in</strong><strong>in</strong>g the <strong>in</strong>crease <strong>in</strong> swimm<strong>in</strong>g speed is still not fully understood,<br />

their advantage may be related to the <strong>in</strong>crease of buoyancy. Benjanuvatra<br />

et al. (2002) did not f<strong>in</strong>d any improvement <strong>in</strong> buoyancy when wear<strong>in</strong>g<br />

technical (cloth) suits. However, accord<strong>in</strong>g to Technical Commission of<br />

F.I.N.A., the possible air-trapp<strong>in</strong>g effect, i.e. “air sacks” between the suit<br />

<strong>and</strong> the swimmers body, has to be taken <strong>in</strong>to account for suits entirely<br />

made <strong>in</strong> polyurethane/neoprene. Indeed, the hydrostatic weight of these<br />

suits should be less than 1 N accord<strong>in</strong>g to F.I.N.A. rules (Dubai Charter<br />

on F.I.N.A. requirements for swimwear approval 2009).<br />

The aim of this work was to evaluate the differences <strong>in</strong> hydrostatic<br />

lift <strong>in</strong> swimmers wear<strong>in</strong>g (or not wear<strong>in</strong>g) a suit made of polyurethane/<br />

neoprene <strong>and</strong> to relate these f<strong>in</strong>d<strong>in</strong>gs with possible variations <strong>in</strong> lung<br />

volume.<br />

Methods<br />

N<strong>in</strong>e male swimmers (23.25 ± 3.01 years of age; 1.80 ± 0.03 m of stature;<br />

75.45 ± 6.96 kg of body mass) were asked to perform two different<br />

tests. In the first test their hydrostatic lift was measured <strong>in</strong> a swimm<strong>in</strong>g<br />

pool (water temperature: 27.5°C) while wear<strong>in</strong>g a “st<strong>and</strong>ard” textile<br />

brief swimm<strong>in</strong>g-suit (S) or a full body shoulder-to-ankle technical suit<br />

(X-glide Power-sk<strong>in</strong> Arena Italy, not modified: Xg). Before the measurements<br />

the subjects were asked to warm-up for about 10 m<strong>in</strong>utes. After the<br />

warm-up, the subject wore the swimm<strong>in</strong>g suit required for the test. Particular<br />

attention was paid to reproduce the pre-race situation ask<strong>in</strong>g the<br />

subjects not to perform any “not conventional” manoeuvre of “adaptation”<br />

of the swimsuit. After the warm up phase, the subjects were kept for 10<br />

s under the water surface. They were held <strong>in</strong> position throughout a cable,<br />

connected to a pulley system positioned on the swimm<strong>in</strong>g pool floor <strong>and</strong><br />

fastened to the subject waist (Figure 1). The cable was also connected to a<br />

load cell (Tesys 400, Globus, Italy) positioned on the pool's edge that allowed<br />

to measure the subject’s hydrostatic lift (the force with which their<br />

body tended to rise towards the water surface). Ten measurements were<br />

collected <strong>in</strong> both conditions (with S <strong>and</strong> Xg swimm<strong>in</strong>g suits). Dur<strong>in</strong>g<br />

these tests the subjects were required to hold their breath after a forced<br />

maximum <strong>in</strong>spiration <strong>and</strong> not to exhale for the entire duration of the test.<br />

57


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 1. The set up utilized for measur<strong>in</strong>g the subject’s hydrostatic<br />

weight. In this case the subject is wear<strong>in</strong>g a “st<strong>and</strong>ard” swimm<strong>in</strong>g suit.<br />

The second test was carried out <strong>in</strong> the laboratory: chest circumferences<br />

were measured at maximal <strong>in</strong>spiration <strong>and</strong> maximal expiration when<br />

the subjects were wear<strong>in</strong>g the S or Xg suits. Lung volumes (VC: Vital<br />

Capacity, ERV: Expiratory Reserve Volume, VT: Tidal Volume, IRV:<br />

Inspiratory Reserve Volume) <strong>in</strong> the two conditions were measured<br />

(St<strong>and</strong>ard Lung Function Test) by means of a portable spirometer (K4<br />

Cosmed, Italy). These tests were carried out accord<strong>in</strong>g to st<strong>and</strong>ard technical<br />

procedures (Guidel<strong>in</strong>es for lung function test 1994). The subjects<br />

were first familiarized with the procedures; they were asked to repeat<br />

these measurements four times, the average value of these measures was<br />

utilized for further analysis.<br />

With regard to the statistical analysis, mean <strong>and</strong> st<strong>and</strong>ard deviation<br />

(SD) were calculated for all the variables. Test-retest <strong>in</strong>tra-class correlation<br />

coefficient (ICC) was calculated to assess the reliability of the<br />

hydrostatic lift. Non/parametric Wilcoxon test was used to compare differences<br />

of hydrostatic lift values <strong>in</strong> the two conditions of suit. The 95%<br />

level of significance was accepted for all comparisons (p


eFerences<br />

Benjanuvatra, N., Dawson, G., Blanksby, B. A. & Elliott, B. C. (2002).<br />

Comparison of buoyancy, passive <strong>and</strong> net active drag forces between<br />

Fastsk<strong>in</strong> <strong>and</strong> st<strong>and</strong>ard swimsuits. Journal of Science <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Sport, 5(2), 115-23.<br />

Bixler, B., Pease, D. & Fairhurst, F. (2007). The accuracy of computational<br />

fluid dynamics analysis of the passive drag of a male swimmer.<br />

Sports <strong>Biomechanics</strong>, 6(1), 81-98.<br />

Chatard, J. C. & Wilson, B. (2008). Effect of fast-sk<strong>in</strong> suits on performance,<br />

drag, <strong>and</strong> energy cost of swimm<strong>in</strong>g. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong><br />

Sport Exercises, 40(6), 1149-54.<br />

Corda<strong>in</strong>, L. & Kopriva, R. (1991). Wetsuits, body density, <strong>and</strong> swimm<strong>in</strong>g<br />

performance. British Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 25, 31-33.<br />

Guidel<strong>in</strong>es for the measurement of respiratory function. Recommendations<br />

of the British Thoracic Society <strong>and</strong> the Association of Respiratory<br />

Technicians <strong>and</strong> Physiologists (1994). Respiratory <strong>Medic<strong>in</strong>e</strong>, 88,<br />

165–194.<br />

McLean, S. P. & H<strong>in</strong>richs, R. N. (2000). Buoyancy, Gender, <strong>and</strong> Swimm<strong>in</strong>g<br />

Performance. Journal of Applied <strong>Biomechanics</strong>, 16, 248-63.<br />

Mollendorf, J. C., Term<strong>in</strong>, A. C., Oppenheim, E. & Pendergast, D. R.<br />

(2004). Effect of swim suit design on passive drag. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science<br />

<strong>in</strong> Sports <strong>and</strong> Exercise, 36(6), 1029-35.<br />

Pendergast, D. R., Mollendorf, J. C., Cuviello, R. & Term<strong>in</strong>, I. I. (2006).<br />

Application of teoretical pr<strong>in</strong>ciples to swimsuit drag reduction. Sports<br />

Eng<strong>in</strong>eer<strong>in</strong>g, 9, 65-76.<br />

Perrier, D. & Monteil, K. (2004). Triathlon wet suit <strong>and</strong> technical parameters<br />

at the start <strong>and</strong> end of a 1500-m swim. Journal of Applied<br />

<strong>Biomechanics</strong>, 20, 3-13.<br />

Perrier, D. & Monteil, M. (2002). Vitesse de nage en triathlon: étude<br />

comparative du cycle de bras en comb<strong>in</strong>aison <strong>in</strong>tégrale et sans manche.<br />

Science & Sports, 17(3), 117-21.<br />

Roberts, B. S., Kamel, K. S., Hedrick, C., Mclean, S. P. & Sharp, R. L.<br />

(2003), Effect of a fastsk<strong>in</strong> suit on submaximal freestyle swimm<strong>in</strong>g.<br />

<strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports <strong>and</strong> Exercise, 35(3), 519-24.<br />

Tomikawa, M. & Nomura, T. (2009). Relationships between swim<br />

performance, maximal oxygen uptake <strong>and</strong> peak power output when<br />

wear<strong>in</strong>g a wetsuit. Journal of Science <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Sport 12(2), 317-22.<br />

Tomikawa, M., Shimoyama, Y., Ichikawa, H. & Nomura, T. (2003). The<br />

effects of triathlon wet suit on stroke parameters, physiological parameters<br />

<strong>and</strong> performance dur<strong>in</strong>g swimm<strong>in</strong>g. <strong>in</strong> Chatard J.C., (eds)<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX, 517-22, Université de<br />

St.Etienne.<br />

Toussa<strong>in</strong>t, H. M., Truijens, M., Elz<strong>in</strong>ga, M. J., Van de Ven, A., de Best,<br />

H. & De Groot, G. (2002). Effect of a Fast-sk<strong>in</strong> “body” suit on drag<br />

dur<strong>in</strong>g front crawl swimm<strong>in</strong>g. Sports <strong>Biomechanics</strong>, 1(1), 1-10.<br />

Yamamoto, K., Miyachi, M., Hara, S., Yamaguchi, H. & Onodera, S.<br />

(1999). Effect of a float<strong>in</strong>g swimsuit on oxygen uptake <strong>and</strong> heart rate<br />

dur<strong>in</strong>g swimm<strong>in</strong>g. <strong>in</strong> Kesk<strong>in</strong>en K., Komi P.V., Holl<strong>and</strong>er A.P., (eds)<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII, 375-79, University of<br />

Jyvaskyla.<br />

chaPter2.<strong>Biomechanics</strong><br />

The Development of a Component Based Approach<br />

for Swim Start Analysis<br />

cossor, J.M.¹, slawson, s.e.², Justham, l.M.², conway, P.P.²,<br />

West, A.A.²<br />

¹British Swimm<strong>in</strong>g, Loughborough, Engl<strong>and</strong><br />

²Wolfson School of Mechanical <strong>and</strong> Manufactur<strong>in</strong>g Eng<strong>in</strong>eer<strong>in</strong>g, Loughborough<br />

University, Loughborough, Engl<strong>and</strong><br />

A component-based system was developed to provide greater quantitative<br />

feedback of starts based on <strong>in</strong>put from British Swim coaches.<br />

Currently the <strong>in</strong>formation provided by the system comprises <strong>in</strong>tegrated<br />

vision, force data from an <strong>in</strong>strumented start<strong>in</strong>g platform <strong>and</strong> wireless<br />

three-axis acceleration data. Initial test<strong>in</strong>g has demonstrated the reliability<br />

of the system <strong>and</strong> the direct impact of <strong>in</strong>tervention with an elite<br />

athlete.<br />

Key words: swimm<strong>in</strong>g, starts, vision system, force platform, wireless<br />

acceleration<br />

IntroductIon<br />

Swimm<strong>in</strong>g races are divided <strong>in</strong>to the start, turn, <strong>and</strong> free swimm<strong>in</strong>g<br />

sections. The contribution of each phase to overall performance is dependant<br />

on race length. The start has a greater contribution to success<br />

<strong>in</strong> the spr<strong>in</strong>t events compared with longer distances. Analysis of female<br />

freestyle spr<strong>in</strong>t events at the Beij<strong>in</strong>g Olympics, illustrates that a 1% reduction<br />

<strong>in</strong> start time would be larger than the time difference between<br />

the first <strong>and</strong> second places (Slawson, 2010).<br />

Research on swimm<strong>in</strong>g starts has <strong>in</strong>cluded <strong>in</strong>formation on the block,<br />

flight, underwater <strong>and</strong> free swimm<strong>in</strong>g phases. Block time has been the<br />

most measured parameter although forces <strong>and</strong> velocities leav<strong>in</strong>g the<br />

block are generally discussed <strong>in</strong> relation to the block phase. Arellano et<br />

al. (2005) <strong>and</strong> Mason et al. (2007) suggested that <strong>in</strong>creased horizontal<br />

force results <strong>in</strong> better starts. Flight time <strong>and</strong> distance are the ma<strong>in</strong> reported<br />

parameters associated with the flight phase although the angle<br />

of entry has been noted as be<strong>in</strong>g important to overall start performance<br />

(Ruschel et al., 2007). While it is noted that the underwater phase can<br />

be the longest <strong>in</strong> terms of time, the block <strong>and</strong> flight phases significantly<br />

<strong>in</strong>fluence the drag forces experienced by the swimmer <strong>in</strong> the glide phase<br />

(Mason et al., 2007). Transition <strong>in</strong>to the break out <strong>and</strong> the free swimm<strong>in</strong>g<br />

sections also contribute to the overall start time <strong>and</strong> variations<br />

between swimmers are usually attributed to differences <strong>in</strong> underwater<br />

kick<strong>in</strong>g skill.<br />

The use of vision systems is still the most common analysis technique<br />

but it can be user <strong>in</strong>tensive <strong>and</strong> costly. Force plate analysis has<br />

been successful utilised due to the reliability of the system along with<br />

the capability to provide real time measures. To date, the limitation of<br />

utilis<strong>in</strong>g force data has been <strong>in</strong> the <strong>in</strong>terpretation of these data <strong>and</strong> the<br />

subsequent development of <strong>in</strong>terventions for improved performance.<br />

Accelerometers have been used <strong>in</strong> the underst<strong>and</strong><strong>in</strong>g of human movement<br />

<strong>and</strong> performance <strong>in</strong> areas such as gait, sleep <strong>and</strong> healthcare. Research<br />

us<strong>in</strong>g accelerometers <strong>in</strong> swimm<strong>in</strong>g has <strong>in</strong>cluded the derivation of<br />

<strong>in</strong>formation on stroke count, lap count <strong>and</strong> stroke type (James et al., 2004,<br />

Ohji, 2006, <strong>and</strong> Davey et al., 2008). Acceleration systems can be characterised<br />

<strong>in</strong>to either real-time data transmission or logg<strong>in</strong>g <strong>and</strong> download<br />

units. Only the latter system has been used <strong>in</strong> swimm<strong>in</strong>g research <strong>and</strong><br />

only on a one to one basis. Although useful <strong>in</strong>formation on free swimm<strong>in</strong>g<br />

performance has been dissem<strong>in</strong>ated from these studies, a wireless networked<br />

solution would enable data to be collected real time from a pool of<br />

athletes. A system has been designed, implemented <strong>and</strong> evaluated <strong>in</strong> the<br />

current research that allows many wireless nodes to transmit <strong>in</strong> real-time<br />

to a co-ord<strong>in</strong>at<strong>in</strong>g receiv<strong>in</strong>g unit that acts as the <strong>in</strong>terface to visualisation,<br />

analysis <strong>and</strong> storage on conventional personal computers.<br />

59


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

This study was used to determ<strong>in</strong>e <strong>and</strong> evaluate the efficacy of performance<br />

variables that significantly contribute to the overall start<strong>in</strong>g performance.<br />

In addition, <strong>in</strong> pool test<strong>in</strong>g has demonstrated the reliability of<br />

the system <strong>and</strong> the impact of <strong>in</strong>tervention strategies on the performance<br />

of elite athletes.<br />

Methods<br />

A force platform <strong>in</strong>corporat<strong>in</strong>g four Kistler (9317B) transducers <strong>in</strong>to<br />

a start<strong>in</strong>g block with similar dimensions to the Omega OSB9 block<br />

has been designed at the Sports Technology Institute at Loughborough<br />

University. Three orthogonal axes of force data were synchronised with<br />

video output from a Photron SA1 high-speed camera set at 50fps with<br />

a resolution of 1024 x 1024 pixels. A wireless accelerometer node was<br />

placed at the small of the back of the swimmer <strong>in</strong> order to ga<strong>in</strong> <strong>in</strong>formation<br />

on the accelerations generated dur<strong>in</strong>g the start. A schematic of the<br />

test<strong>in</strong>g set up is illustrated <strong>in</strong> Figure 1.<br />

Figure 1. Set up <strong>in</strong>corporat<strong>in</strong>g a video, force platform <strong>and</strong> wireless accelerometer<br />

node.<br />

A variety of tests were conducted us<strong>in</strong>g the <strong>in</strong>strumented block to<br />

capture force data on twenty male <strong>and</strong> female swimmers rang<strong>in</strong>g from<br />

National to International level over a period of twelve months. Tests<br />

<strong>in</strong>cluded swimmers perform<strong>in</strong>g a number of trials on one day, the same<br />

swimmers repeat<strong>in</strong>g trials one month later, as well as some swimmers<br />

test<strong>in</strong>g the difference between grab <strong>and</strong> track start<strong>in</strong>g techniques. An<br />

external analogue trigger synchronised the capture of data from the<br />

force platform <strong>and</strong> video camera whilst simultaneously generat<strong>in</strong>g an<br />

audio signal for the swimmer to start. Various parameters of the block<br />

<strong>and</strong> flight phases of the start were determ<strong>in</strong>ed from the analysis of the<br />

force data <strong>and</strong> correlated with the images recorded via the vision system.<br />

Dur<strong>in</strong>g the block phase the time to first movement, horizontal <strong>and</strong> vertical<br />

forces, <strong>and</strong> overall block time were determ<strong>in</strong>ed. Us<strong>in</strong>g the moments<br />

generated on the force platform, centre of pressure was exam<strong>in</strong>ed. Flight<br />

distance <strong>and</strong> time to 15m were determ<strong>in</strong>ed via the vision data whilst flight<br />

times, time to the first stroke <strong>and</strong> number of strokes prior to 15m were<br />

determ<strong>in</strong>ed from accelerometer data generated by the wireless node.<br />

results<br />

The <strong>in</strong>itial focus of the research was on the validation of the data from<br />

the force platform. A number of University swimmers were tested us<strong>in</strong>g<br />

both grab <strong>and</strong> track starts. Unfortunately it was noted that this level<br />

of swimmer was unable to demonstrate a consistent enough dive force<br />

profile to enable performance improvements to be evident between different<br />

dives.<br />

Further test<strong>in</strong>g was undertaken with an International level swimmer<br />

where a significantly high degree of repeatability was evident <strong>in</strong> the<br />

force profiles (see Figure 2). Very little difference between the tim<strong>in</strong>g,<br />

60<br />

amplitude <strong>and</strong> profile of the <strong>in</strong>dividual trials for the elite swimmer were<br />

observed compared with the significant variability <strong>in</strong> these parameters<br />

shown for the trials provided by an amateur swimmer as seen <strong>in</strong> Table<br />

1. There was 0.7% difference <strong>in</strong> the impulse for the elite swimmer compared<br />

to 9.8% for the University swimmer. Likewise there were only<br />

1.2% differences <strong>in</strong> tim<strong>in</strong>g <strong>and</strong> maximum forces <strong>in</strong> the horizontal <strong>and</strong><br />

vertical planes for the elite athlete but 16.3% <strong>and</strong> 14% differences respectively<br />

for the University swimmer. Hence via the detailed exam<strong>in</strong>ation<br />

of the characteristics of start<strong>in</strong>g force profiles over repeated trials<br />

it is possible to determ<strong>in</strong>e relevant measures of athlete skill level (i.e.<br />

variance <strong>in</strong> tim<strong>in</strong>g, impulse, <strong>and</strong> number of peaks) without the aid of<br />

vision systems.<br />

Table 1. Horizontal <strong>and</strong> vertical force data for different levels of swimmers.<br />

Elite<br />

Uni<br />

Dive Max y Time Max Z Time Unload time Impulse y Impulse z<br />

1 414.72 0.75 725.17 0.73 0.92 151.67 444.28<br />

2 415.27 0.76 741.22 0.73 0.94 149.59 444.34<br />

1 554.17 0.51 929.48 0.64 0.87 181.67 530.17<br />

2 454.62 0.70 857.96 0.70 0.94 159.31 565.67<br />

An <strong>in</strong>tervention was designed for the International level swimmer <strong>in</strong><br />

order to improve their start<strong>in</strong>g performance. The force profiles for the<br />

new dive technique <strong>in</strong> both the horizontal <strong>and</strong> vertical components are<br />

illustrated <strong>in</strong> Figure 2. The st<strong>and</strong>ard dive technique profiles are provided<br />

for comparison. With the new dive technique, the tim<strong>in</strong>g of the first<br />

movement was observed to be earlier (0.1s) with the same peak force <strong>in</strong><br />

the horizontal direction while there was a 6% reduction <strong>in</strong> peak vertical<br />

force compared to the traditional start. This type of quantitative feedback<br />

on measures of performance highlight the benefits of a system that<br />

is not labour or time <strong>in</strong>tensive <strong>and</strong> allows for immediate feedback so that<br />

changes <strong>in</strong> technique can be observed.<br />

Figure 2. Comparison of force data an elite swimmer us<strong>in</strong>g different<br />

techniques.


In Figure 3 an example of the <strong>in</strong>formation provided to the coach <strong>and</strong><br />

swimmer is illustrated. From the force data it is possible to determ<strong>in</strong>e<br />

the block time, the time of first movement, peak horizontal <strong>and</strong> vertical forces<br />

as well as centre of pressure <strong>in</strong>formation. The vision system <strong>in</strong>formation is<br />

used to provide <strong>in</strong>formation relevant to the flight phase of the start i.e.<br />

the flight distance <strong>and</strong> flight time. The tim<strong>in</strong>g of the first stroke as well as the<br />

number of strokes through to the 15 m mark can be determ<strong>in</strong>ed us<strong>in</strong>g the<br />

acceleration data. The <strong>in</strong>clusion of the vision data <strong>in</strong> the report provides<br />

a detailed <strong>in</strong>itial underst<strong>and</strong><strong>in</strong>g of the force data collected dur<strong>in</strong>g the<br />

block <strong>and</strong> flight phases.<br />

Figure 3. Track start analysis comb<strong>in</strong><strong>in</strong>g vision systems, force profiles<br />

<strong>and</strong> acceleration data.<br />

dIscussIon<br />

Individual monitor<strong>in</strong>g components have been developed that enable<br />

parameters relevant to the performance of various components of the<br />

start phase of swimm<strong>in</strong>g to be quantified. The three ma<strong>in</strong> monitor<strong>in</strong>g<br />

components <strong>in</strong>clude vision <strong>in</strong>formation, force profiles <strong>and</strong> acceleration<br />

data through a network of distributed wireless nodes. Each of these<br />

components is able to provide feedback to the coaches <strong>and</strong> the athletes<br />

but it is the synchronisation <strong>and</strong> <strong>in</strong>tegration that allows a greater level of<br />

underst<strong>and</strong><strong>in</strong>g to be obta<strong>in</strong>ed.<br />

From the video images it is possible to provide qualitative feedback<br />

immediately after each start. By synchronis<strong>in</strong>g this with the force platform<br />

<strong>in</strong>formation, quantitative values dur<strong>in</strong>g the block phase can be<br />

calculated <strong>and</strong> fed back to the coaches <strong>and</strong> swimmers. An example of<br />

this <strong>in</strong>tegrated analysis approach was shown with the elite level athlete<br />

whilst undergo<strong>in</strong>g an <strong>in</strong>tervention <strong>in</strong> their start<strong>in</strong>g technique resulted <strong>in</strong><br />

quantifiable visible differences <strong>in</strong> both the horizontal <strong>and</strong> vertical force<br />

components. The addition of wireless acceleration <strong>in</strong>formation is unique<br />

to this analysis of swimm<strong>in</strong>g starts where <strong>in</strong>formation on strok<strong>in</strong>g <strong>and</strong><br />

tim<strong>in</strong>g is <strong>in</strong>cluded <strong>in</strong> the data analysis.<br />

Results from a number of trials of the <strong>in</strong>tegrated system have highlighted<br />

the reliability of the data <strong>and</strong> the impact of <strong>in</strong>terventions. The<br />

synchronisation of data from a number of monitor<strong>in</strong>g modalities provides<br />

accurate, timely <strong>and</strong> relevant feedback to both the coaches <strong>and</strong><br />

chaPter2.<strong>Biomechanics</strong><br />

athletes support<strong>in</strong>g enhanced impact from test<strong>in</strong>g. Future work will be<br />

focussed on the development of a more complete underst<strong>and</strong><strong>in</strong>g of force<br />

<strong>and</strong> acceleration data <strong>and</strong> the implications for skill <strong>and</strong> performance<br />

improvement throughout the various phases of the start.<br />

conclusIon<br />

An <strong>in</strong>tegrated component-based system has been developed that allows<br />

swimm<strong>in</strong>g starts to be analysed <strong>in</strong> greater detail than possible with previous<br />

systems via <strong>in</strong>tegrated video, force <strong>and</strong> acceleration data. Feedback<br />

was provided to the coach <strong>and</strong> athlete for <strong>in</strong>terventions <strong>in</strong> tra<strong>in</strong><strong>in</strong>g to<br />

be made <strong>and</strong> the impacts to be quantified <strong>in</strong> detail. Future work will<br />

exam<strong>in</strong>e the impact on start<strong>in</strong>g performance of the wedge <strong>in</strong>cluded on<br />

the next generation Omega OSB11 start<strong>in</strong>g blocks, which are likely to<br />

be used <strong>in</strong> the London 2012 Olympic Games.<br />

reFerences<br />

Arellano, R., Llana, S., Tella, V., Morales, E. & Mercade, J. (2005). A<br />

Comparison CMJ, Simulated <strong>and</strong> Swimm<strong>in</strong>g Grab Start Force record<strong>in</strong>gs<br />

<strong>and</strong> their Relationships with the Start Performance. Proceed<strong>in</strong>gs<br />

of X<strong>XI</strong>II International Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports,<br />

Ch<strong>in</strong>a, 923-926.<br />

Davey, N., Anderson, M. & James, D. (2008). Validation Trial of an<br />

Accelerometer-Based Sensor Platform for Swimm<strong>in</strong>g. Sports Technology,<br />

1,(4-5), 202-207.<br />

James, D., Davey, N. & Rice, T. (2004). An Accelerometer Based Sensor<br />

Platform for Insitu Elite Athlete Performance Analysis. Proceed<strong>in</strong>gs<br />

of IEEE Sensors, Austria, 3, 1373-1376.<br />

Mason, B., Alcock, A. &Fowlie, J. (2007). A K<strong>in</strong>etic Analysis <strong>and</strong> Recommendations<br />

for Elite Swimmers Perform<strong>in</strong>g the Spr<strong>in</strong>t Start.<br />

Proceed<strong>in</strong>gs of XXV International Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports,<br />

Brazil, 192-195.<br />

Ohji, Y. (2006). MEMS Sensor Application for the Motion Analysis <strong>in</strong><br />

Sports Science. ABCM Symposium Series <strong>in</strong> Mechantronics, 2, 501-508.<br />

Ruschel, C., Araujo, L., Pereira, S. & Roesler, H. (2007). K<strong>in</strong>ematical<br />

Analysis of the Swimm<strong>in</strong>g start: Block, Flight <strong>and</strong> Underwater<br />

Phases. Proceed<strong>in</strong>gs of XXV International Symposium on <strong>Biomechanics</strong><br />

<strong>in</strong> Sport, Brazil, 385-388.<br />

Slawson, S. (2010). Intelligent User Centric Components for Harsh<br />

Distributed Environments. Thesis Loughborough University.<br />

61


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Hydrodynamic Characterization of the First <strong>and</strong><br />

Second Glide Positions of the Underwater Stroke<br />

Technique <strong>in</strong> Breaststroke<br />

costa, l. 1 ; ribeiro, J. 1 ; Figueiredo, P. 1 ; Fern<strong>and</strong>es, r.J. 1 ; Mar<strong>in</strong>ho,<br />

d. 2,3 ; silva, A.J. 3,4 ; rouboa, A. 3,4 ; Vilas-Boas, J.P. 1 ; Machado,<br />

l. 1<br />

1 University of Porto, Faculty of Sport, Cifi2d, Porto, Portugal<br />

2 University of Beira Interior, Covilhã, Portugal<br />

3 Research Center In Sports, Health <strong>and</strong> Human Development, Vila Real,<br />

Portugal<br />

4 University of Trás-os-Montes <strong>and</strong> Alto Douro, Vila Real, Portugal<br />

The aim of the present study was to characterize two different ventral<br />

glide positions, both used after start <strong>and</strong> turns: the arms extended at the<br />

front, <strong>and</strong> the arms extended along the trunk, respectively the first <strong>and</strong><br />

the second glide positions of the breaststroke underwater stroke. Inverse<br />

Dynamics was used for obta<strong>in</strong><strong>in</strong>g the passive drag <strong>and</strong> the drag coefficient,<br />

based upon the velocity to time curve of each glide, monitored<br />

through a swim-meter. The first glide position presented lower values<br />

of drag <strong>and</strong> drag coefficient, manag<strong>in</strong>g to reach higher velocities. The<br />

cross sectional area (planimetry) values were lower for first glide position<br />

<strong>in</strong> comparison with the second one (759.95 ±124.12 cm2 vs. 814.46 ±<br />

111.23 cm2). These results po<strong>in</strong>t out the need of technical evaluation<br />

<strong>and</strong> control <strong>in</strong> order to reduce drag dur<strong>in</strong>g swimm<strong>in</strong>g performance.<br />

KeY Words: swimm<strong>in</strong>g, breaststroke, passive drag, drag coefficient,<br />

glid<strong>in</strong>g position<br />

IntroductIon<br />

In swimm<strong>in</strong>g the total event time is determ<strong>in</strong>ed by the start, swim, turn<br />

<strong>and</strong> f<strong>in</strong>ish partial times (Halj<strong>and</strong> <strong>and</strong> Saagpakk, 1994). Starts <strong>and</strong> turns<br />

appear to be a significant part of the total swimm<strong>in</strong>g event time (Vilas-<br />

Boas <strong>and</strong> Fern<strong>and</strong>es, 2003). Chatard et al. (1990) stated that the glid<strong>in</strong>g<br />

phase after starts <strong>and</strong> turns corresponds to 10 to 25% of the total<br />

event time (depend<strong>in</strong>g on events <strong>and</strong> the length of the swimm<strong>in</strong>g pool).<br />

D’Acquisto et al. (1988) showed that, dur<strong>in</strong>g the breaststroke events, the<br />

glid<strong>in</strong>g phases represent 44% of the total swimm<strong>in</strong>g time. These authors<br />

showed that the glid<strong>in</strong>g phase dist<strong>in</strong>guishes elite from good level breaststroke<br />

swimmers, with higher glid<strong>in</strong>g time for the elite swimmers. Race<br />

analysis suggested that rather than the start technique used by swimmers;<br />

it is the position under the water that mostly determ<strong>in</strong>es the success of the<br />

start (Cossor <strong>and</strong> Mason, 2001). Therefore, it is essential to analyse <strong>and</strong><br />

underst<strong>and</strong> this phase. The passive drag of swimmers mov<strong>in</strong>g underwater<br />

<strong>in</strong> a streaml<strong>in</strong>ed position has been measured experimentally (Clarys, 1979;<br />

Kolmogorov et al., 1997; Lyttle et al., 2000; Toussa<strong>in</strong>t et al., 2004; Vilas-<br />

Boas et al., <strong>in</strong> press). However, there are other glid<strong>in</strong>g phases <strong>in</strong> which the<br />

swimmers assume a prone position but with the arms extended at the side<br />

of the trunk, as <strong>in</strong> the second glide position after the breaststroke underwater<br />

arm stroke. To our knowledge, these two glide positions were compared<br />

experimentally only by Vilas-Boas et al. (<strong>in</strong> press), <strong>and</strong> numerically<br />

by Mar<strong>in</strong>ho et al. (2009). In both cases, the glides were compared <strong>in</strong> common<br />

velocities, not consider<strong>in</strong>g the total range of velocities at which they<br />

are usually performed. The aim of the present study was to experimentally<br />

characterize the first <strong>and</strong> second glid<strong>in</strong>g positions of the breaststroke underwater<br />

stroke used after starts <strong>and</strong> turns at the total range of velocities<br />

commonly performed, consider<strong>in</strong>g: (i) glid<strong>in</strong>g velocity (v); (ii) body cross<br />

sectional area (S); (iii) drag coefficient (C D ), <strong>and</strong> (iv) passive drag (D).<br />

Methods<br />

Six Portuguese national level male swimmers (18.2 ± 4.0 years old, 178.2<br />

± 9.0 cm of height <strong>and</strong> 64.4 ± 11.4 kg of body mass) participated <strong>in</strong> this<br />

62<br />

study. Test<strong>in</strong>g sessions were conducted <strong>in</strong> a 25 m pool, 2 m deep, with water<br />

temperature at 27.5 ºC. It was used a similar methodology to the described <strong>in</strong><br />

Vilas-Boas et al. (<strong>in</strong> press), namely the S determ<strong>in</strong>ation us<strong>in</strong>g planimetry, <strong>and</strong><br />

the passive drag assessed through <strong>in</strong>verse dynamics based upon the velocity to<br />

time (v (t) ) curve of each glide, monitored through a swim-meter (Lima et al.<br />

2006). Acceleration (a) was obta<strong>in</strong>ed through the numerical derivative of the<br />

velocity curve. The drag force was computed us<strong>in</strong>g the expression:<br />

D = m . a . (1)<br />

To quantify the drag coefficient, the follow<strong>in</strong>g equation was used, assum<strong>in</strong>g<br />

water density (ρ) as 1000 kg/m3 :<br />

C D = 2 D / ρ S v 2 (2)<br />

Each swimmer performed 3 repetitions of the breaststroke underwater stroke,<br />

at maximal <strong>in</strong>tensity (2 m<strong>in</strong> of <strong>in</strong>terval). Dur<strong>in</strong>g the rest <strong>in</strong>terval, swimmers<br />

received proper feedback <strong>in</strong> order to improve their performance. The video<br />

images <strong>and</strong> data process<strong>in</strong>g (v (t) curves <strong>and</strong> acceleration to time curves representations)<br />

of the first <strong>and</strong> second glide of the underwater breaststroke were<br />

obta<strong>in</strong>ed accord<strong>in</strong>g to Vilas-Boas et al. (<strong>in</strong> press). Not all swimmers atta<strong>in</strong>ed<br />

all velocity values, be<strong>in</strong>g reta<strong>in</strong>ed the v values (<strong>in</strong>dependently <strong>in</strong> each glide)<br />

for which there were values from at least three swimmers. The processes of D<br />

<strong>and</strong> C D calculations were described also <strong>in</strong> Vilas-Boas et al. (<strong>in</strong> press).<br />

results<br />

The ma<strong>in</strong> results of this study are presented <strong>in</strong> Table 1 <strong>and</strong> <strong>in</strong> Figures<br />

1 <strong>and</strong> 2. Table 1 shows the S values for each swimmer <strong>in</strong> the first <strong>and</strong><br />

second glides while Fig. 1 <strong>and</strong> 2 show D <strong>and</strong> C D , respectively, for each<br />

glide <strong>and</strong> for all v values atta<strong>in</strong>ed.<br />

Table 1. Individual <strong>and</strong> mean ± SD values of the cross-sectional area of<br />

the body (S) assessed for the two studied breaststroke glid<strong>in</strong>g positions.<br />

Swimmer<br />

S (cm2)<br />

for first glide position<br />

S (cm2)<br />

for second glide position<br />

1 971.13 942.1<br />

2 719.73 886.91<br />

3 641.7 668.47<br />

4 689.17 769.24<br />

5 692.6 718.05<br />

6 845.34 901.99<br />

Mean ± SD 759.95 ±124.12 814.46 ± 111.23<br />

The mean ± SD v values for the first <strong>and</strong> second glide positions were<br />

1.50 ± 0.22m/s <strong>and</strong> 1.15 ± 0.24m/s, respectively. The first glide presented<br />

higher values of mean v, while the second glid<strong>in</strong>g was characterized<br />

by higher values of acceleration (0.61 ± 0.24m/s 2 to 0.66 ± 0.06m/<br />

s 2 versus 0.40 ± 0.06 m/s 2 to 0.63 ± 0.16m/s 2 for common values of v,<br />

second <strong>and</strong> first glide respectively). The common velocities for the two<br />

glid<strong>in</strong>g phases were 1.20, 1.30, 1.40 <strong>and</strong> 1.50m/s (Fig. 1 <strong>and</strong> 2)<br />

Drag (N) first glide<br />

80<br />

second glide<br />

70<br />

60<br />

50<br />

40<br />

30<br />

20<br />

10<br />

0<br />

0.8 0.9 1 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8<br />

Velocity (m/s)<br />

Figure 1. Drag versus velocity curve <strong>in</strong> two dist<strong>in</strong>ct glid<strong>in</strong>g positions:<br />

first glide <strong>and</strong> second glide of the breaststroke underwater stroke


Drag Coefficient first glide<br />

1.6<br />

1.4<br />

1.2<br />

1<br />

0.8<br />

0.6<br />

0.4<br />

0.2<br />

0<br />

second glide<br />

0.8 0.9 1 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8<br />

Velocity (m/s)<br />

Figure 2. Drag Coefficient versus velocity curve <strong>in</strong> two dist<strong>in</strong>ct glid<strong>in</strong>g positions:<br />

first glide <strong>and</strong> second glide of the breaststroke underwater stroke.<br />

dIscussIon<br />

The relatively low v values found <strong>in</strong> this study may be expla<strong>in</strong>ed by the<br />

level <strong>and</strong> age of the swimmers tested, all of national level, not <strong>in</strong>ternational<br />

elite, <strong>and</strong> mix<strong>in</strong>g junior <strong>and</strong> senior swimmers. However, the<br />

higher v values were obta<strong>in</strong>ed dur<strong>in</strong>g the first glide, probably due to its<br />

time proximity to the wall impulse, as well as to the higher hydrodynamics<br />

that characterised it.<br />

As expected, <strong>in</strong> accordance with our previous results (Vilas-Boas, <strong>in</strong><br />

press), <strong>and</strong> with the literature us<strong>in</strong>g similar methodology (Clarys, 1979),<br />

swimmers showed a smaller S area <strong>in</strong> the first glide position than <strong>in</strong> the<br />

second position. This fact could be expla<strong>in</strong>ed by the “compressive” effect<br />

over the shoulders <strong>and</strong> chest width produced by the flexed shoulders,<br />

which could be one of the ma<strong>in</strong> determ<strong>in</strong>ant factors associated with a reduced<br />

drag <strong>in</strong> the first glide. It is important to note that the obta<strong>in</strong>ed S<br />

values may slightly differ from the actual glid<strong>in</strong>g S values, once it is possible<br />

that the glid<strong>in</strong>g alignment of the body may differ from the st<strong>and</strong><strong>in</strong>g<br />

position. In fact, we must assume that it is possible that some swimmers<br />

may adopt, at least <strong>in</strong> some <strong>in</strong>stants dur<strong>in</strong>g the glide, an <strong>in</strong>cl<strong>in</strong>ed body position<br />

with respect to the glid<strong>in</strong>g direction. Our observation of the recorded<br />

video images revealed some <strong>in</strong>cl<strong>in</strong>ed glid<strong>in</strong>g directions, with a coaxial <strong>and</strong><br />

convenient body alignment, but not any <strong>in</strong>cl<strong>in</strong>ed body position regard<strong>in</strong>g<br />

the direction of motion that would change S values. We are conv<strong>in</strong>ced that<br />

this approach is also more accurate for S <strong>and</strong> C D assessment than calculat<strong>in</strong>g<br />

active drag C D values us<strong>in</strong>g a constant estimation of S based upon body<br />

volume powered 2/3 (Kolmogorov & Duplischeva, 1982).<br />

The D values calculated <strong>in</strong> this study (Fig. 1) are consistent with previously<br />

passive drag values published for competitive swimmers. Clarys<br />

(1979) reported D values of about 52 N at 1.3m/s for male national-level<br />

swimmers. Vilas-Boas et al. (<strong>in</strong> press) found values of 34.66 ± 7.869 N <strong>and</strong><br />

42.92 ± 5.658 N, respectively for the first <strong>and</strong> second studied glide positions,<br />

but at lower velocities than the studied <strong>in</strong> this paper for the first one, <strong>and</strong><br />

higher for the second one. In the present study, D ranged between 23.35<br />

N <strong>and</strong> 58.25 N. For both glides the drag <strong>in</strong>crease with velocity (Fig. 1).<br />

However the first glide is characterised by drag values lower for all velocities<br />

(Fig. 1), probably due to a parallel <strong>and</strong> concurrent effect of S <strong>and</strong> C D . The<br />

<strong>in</strong>creased body length <strong>and</strong> slenderness associated with the flexed shoulders<br />

<strong>and</strong> extended position of the arms along the longitud<strong>in</strong>al axis of the body<br />

may reduce C D , as well as may have an effect upon the reduction of S.<br />

For the first glide, the C D changed from 0.52 at 1.3 m/s to 0.44 at 1.6<br />

m/s. After analysis of Table 2, it is possible to state that C D decreases with<br />

v. For the second glide the drag coefficient changed from 0.95 at 0.8 m/s<br />

to 0.47 at 1.5 m/s. The <strong>in</strong>verse relationship between the C D <strong>and</strong> v found<br />

<strong>in</strong> the current study seems to correspond to what was observed <strong>in</strong> other<br />

experimental situations (e.g. Lyttle et al., 2000). Moreover, the glid<strong>in</strong>g position<br />

with arms extended at the front (first glide) presented lower drag<br />

coefficient values (Fig. 2). This body position is accepted by the swimm<strong>in</strong>g<br />

technical <strong>and</strong> scientific communities as the most hydrodynamic position,<br />

be<strong>in</strong>g called streaml<strong>in</strong>e position, because it seems to be the one that al-<br />

chaPter2.<strong>Biomechanics</strong><br />

lows a higher reduction of the negative hydrodynamic effects of the human<br />

body morphology: a body with various pressure po<strong>in</strong>ts due to large<br />

changes <strong>in</strong> its shape. This position seems to smooth the anatomical shape,<br />

especially at the head <strong>and</strong> shoulders, allow<strong>in</strong>g better penetration of the<br />

body <strong>in</strong> the water dur<strong>in</strong>g the underwater phases <strong>in</strong> swimm<strong>in</strong>g.<br />

In Fig. 2. the C D for the first glide position presents lower values for<br />

the different velocities <strong>in</strong> study, while the second glide position provides<br />

a greater range of values, caus<strong>in</strong>g more variability. This f<strong>in</strong>d<strong>in</strong>g po<strong>in</strong>ts out<br />

the presumably higher <strong>in</strong>stability of the second glid<strong>in</strong>g position. Be<strong>in</strong>g<br />

so, attention needs to be paid to its tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competitive execution.<br />

conclusIon<br />

The first glide position with arms extended at the front is characterised by<br />

lower values of D <strong>and</strong> C D , despite it is performed at higher velocities. The<br />

C D decreases with velocity, particularly dur<strong>in</strong>g the second glide. As a practical<br />

consequence, swimmers <strong>and</strong> coaches should stress the need for body<br />

position control dur<strong>in</strong>g its execution, particularly dur<strong>in</strong>g the more resistive<br />

glide (the second one). These results also po<strong>in</strong>ted out the need of technical<br />

evaluation, control <strong>and</strong> advice to allow drag reductions dur<strong>in</strong>g swimm<strong>in</strong>g<br />

performance, <strong>and</strong> not only emphasis<strong>in</strong>g propulsion <strong>in</strong>crease possibilities.<br />

reFerences<br />

Clarys, J. (1979). Human Morphology <strong>and</strong> Hydrodynamics. In J. Terauds<br />

(Ed.), Swimm<strong>in</strong>g Science III (p. 3-41). Baltimore: University Park Press.<br />

Chatard, J., Lavoie, J., Bourgo<strong>in</strong>, B. & e Lacour, J. (1990). The Contribution<br />

of Passive Drag as a Determ<strong>in</strong>ant of Swimm<strong>in</strong>g Performance. Int.<br />

J. Sports <strong>Medic<strong>in</strong>e</strong>. 11(2), 367-372.<br />

Cossor, J. & Masson, B. (2001). Swim start performance at the Sydney<br />

2000 Olympic Games. Proceed<strong>in</strong>gs of swim sessions of the <strong>XI</strong>X Symposium<br />

on <strong>Biomechanics</strong> <strong>in</strong> Sports (edit by J. Blackwell e R. S<strong>and</strong>ers), (p.<br />

70-74) San Francisco: University of San Francisco.<br />

D’Acquisto L. J., Costill D. L., Gehtsen, G. M., Wong-Tai, Y. & Lee, G.<br />

(1988). Breaststroke economy skill <strong>and</strong> performance: study of breaststroke<br />

mechanics us<strong>in</strong>g a computer based “velocity video”. Journal of<br />

Swimm<strong>in</strong>g Research, 4, 9-14.<br />

Halj<strong>and</strong>, R. & Saagpakk, R. (1984). Swimm<strong>in</strong>g Competition analysis of the<br />

European spr<strong>in</strong>t swimm<strong>in</strong>g championship, LEN, Stavanger.<br />

Kolmogorov, S. & Duplischeva, O. (1992). Active drag, useful mechanical<br />

power output <strong>and</strong> hydrodynamic force coefficient <strong>in</strong> different swimm<strong>in</strong>g<br />

strokes at maximal velocity. Journal of <strong>Biomechanics</strong>, 25, 311-318.<br />

Kolmogorov, S., Rumyantseva, O., Gordon, B. & Cappaert, J. (1997). Hydrod<strong>in</strong>amics<br />

characteristics of competitive swimmers of different genders<br />

<strong>and</strong> performance levels. Journal of Applied <strong>Biomechanics</strong>, 13, 88-97.<br />

Lima, A. B., Semblano, P., Fern<strong>and</strong>es, D., Gonçalves, P., Morouço, P.,<br />

Sousa, F. et al. (2006). A k<strong>in</strong>ematical, imagiological <strong>and</strong> acoustical biofeedback<br />

system for the technical tra<strong>in</strong><strong>in</strong>g <strong>in</strong> breaststroke swimm<strong>in</strong>g<br />

Portuguese Journal of Sport Sciences, 6(Suppl. 1), 22.<br />

Lyttle, A., Blanksby, B., Elliot, B. & Lloyd, D. (2000). Net forces dur<strong>in</strong>g<br />

tethered simulation of underwater streaml<strong>in</strong>ed glid<strong>in</strong>g <strong>and</strong> kick<strong>in</strong>g<br />

technique of the freestyle turn. Journal of Sports Sciences, 18, 801-807.<br />

Mar<strong>in</strong>ho, D. A., Reis, V. M., Alves, F. B., Vilas-Boas, J. P., Machado, L.,<br />

Silva, A. et al. (2009). Hydrodynamic drag dur<strong>in</strong>g glid<strong>in</strong>g <strong>in</strong> swimm<strong>in</strong>g.<br />

Journal of Applied <strong>Biomechanics</strong>, 25, 253-257.<br />

Toussa<strong>in</strong>t, H. M., Roos, P. E. & Kolmogorov, S. (2004). The determ<strong>in</strong>ation<br />

of drag <strong>in</strong> front crawl swimm<strong>in</strong>g. Journal of <strong>Biomechanics</strong>, 37, 1655-<br />

1663.<br />

Vilas-Boas, J. P. & Fern<strong>and</strong>es, R. (2003). Swimm<strong>in</strong>g starts <strong>and</strong> turns: determ<strong>in</strong>ant<br />

factors of swimm<strong>in</strong>g performance. In P. Pelayo & M. Sydney<br />

(Eds.), Proceed<strong>in</strong>gs des “3èmes Journées Spécialisées en Natation” (pp.<br />

84-95). Lille, France: Faculté des Sciences du Sport et de l’Education<br />

Physique de l’Université de Lille.<br />

Vilas-Boas, J.P., Costa, L., Fern<strong>and</strong>es, R., Ribeiro, J., Figueiredo, P.,<br />

Mar<strong>in</strong>ho, D., et al. (<strong>in</strong> press). Determ<strong>in</strong>ation of the drag coefficient<br />

dur<strong>in</strong>g the first <strong>and</strong> second glid<strong>in</strong>g positions of the breaststroke underwater.<br />

Journal Applied of <strong>Biomechanics</strong>.<br />

63


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Biomechanical Characterization of the Backstroke<br />

Start <strong>in</strong> Immerged <strong>and</strong> Emerged Feet Conditions<br />

de Jesus, K. 1 , de Jesus, K. 1 , Figueiredo, P. 1 , Gonçalves, P. 1 ,<br />

Pereira, s.M. 1,2 , Vilas-Boas, J.P. 1 , Fern<strong>and</strong>es, r.J. 1<br />

1University of Porto, Faculty of Sport, Cifi2d, Porto, Portugal<br />

2University of the State of Santa Catar<strong>in</strong>a, Florianópolis, Brazil<br />

The aim of this study was to describe <strong>and</strong> compare two variations of the<br />

backstroke start technique, one with the feet parallel completely submerged<br />

(BSFI) <strong>and</strong> the other with the feet parallel, completely above<br />

the surface (BSFE). Dual-media video images were recorded us<strong>in</strong>g two<br />

cameras positioned <strong>in</strong> the sagittal plane of the movement. K<strong>in</strong>etic data<br />

were obta<strong>in</strong>ed us<strong>in</strong>g an underwater force plate. H<strong>and</strong>grips were used<br />

allow<strong>in</strong>g the same body elevation relative to the water surface. F<strong>in</strong>d<strong>in</strong>gs<br />

registered greater flight time <strong>and</strong> water reach of the centre of mass at<br />

BSFI. BSFE seems to produce a greater impulse, <strong>and</strong> time of h<strong>and</strong>s-off,<br />

foot take-off <strong>and</strong> total start. Through segmental coord<strong>in</strong>ation analysis it<br />

is possible to speculate that the jo<strong>in</strong>t extension time duration might be<br />

the variable that best characterizes impulsive synergies.<br />

Key words: swimm<strong>in</strong>g, backstroke, starts, k<strong>in</strong>ematics<br />

IntroductIon<br />

The start is unanimously accepted as an important element for success<br />

<strong>in</strong> competitive swimm<strong>in</strong>g, especially <strong>in</strong> the short events, represent<strong>in</strong>g<br />

~25% of the competition time. Specifically <strong>in</strong> the backstroke swimm<strong>in</strong>g<br />

events, the start has been estimated to represent up to 30% of the competition<br />

time <strong>in</strong> the 50 m event (Lyttle <strong>and</strong> Benjanuvatra, 2004).<br />

Traditionally, comparisons between different start<strong>in</strong>g techniques<br />

used for sup<strong>in</strong>e swimm<strong>in</strong>g events were conducted to f<strong>in</strong>d out which one<br />

is the best (Vilas-Boas et al., 2003; Welcher et al., 2008), rather than<br />

study<strong>in</strong>g how swimm<strong>in</strong>g starts should be performed to obta<strong>in</strong> the optimal<br />

mechanical output. Concern<strong>in</strong>g the backstroke swimm<strong>in</strong>g start, the<br />

number of studies is rather scarce (cf. Hohmann et al., 2006 <strong>and</strong> Kruger<br />

et al., 2006), none of which has yet dealt with the technical adjustments<br />

allowed by the new rules endorsed by FINA that authorize the swimmers<br />

to position their feet above water level.<br />

Differences <strong>in</strong> foot position when on the wall - high (above water<br />

level) or low (submerged) - may determ<strong>in</strong>e the direction of the resultant<br />

vector <strong>and</strong>, therefore, significantly <strong>in</strong>fluence start<strong>in</strong>g performance.<br />

A higher foot position may produce a more horizontal component of<br />

the wall reaction force, while a lower foot position may produce a vector<br />

angle with a more pronounced vertical component, <strong>in</strong>creas<strong>in</strong>g the flight<br />

time (Van Ingen Schenau, 1989). The present study aimed to describe<br />

<strong>and</strong> compare two backstroke swimm<strong>in</strong>g start variations under different<br />

constra<strong>in</strong>ts determ<strong>in</strong>ed by the high <strong>and</strong> low foot position relative to the<br />

water surface.<br />

Methods<br />

Six male high-level swimmers (22.5 ± 2.94 years old, 1.80 ± 0.07 m<br />

height, <strong>and</strong> 76.6 ± 8.94 kg body weight) performed two sets of 4 maximal<br />

<strong>in</strong>tensity backstroke starts us<strong>in</strong>g the two variations: feet parallel <strong>and</strong><br />

submerged (BSFI) <strong>and</strong> feet parallel <strong>and</strong> above the surface (BSFE). Rest<br />

periods of 2 m<strong>in</strong> were respected between each repetition <strong>and</strong> a 1 h <strong>in</strong>terval<br />

was ma<strong>in</strong>ta<strong>in</strong>ed between sets (BSFI <strong>and</strong> BSFE).<br />

Two-dimensional k<strong>in</strong>ematics <strong>in</strong> the sagittal plane was implemented<br />

us<strong>in</strong>g a dual-media camera set-up (Vilas-Boas et al., 1997). Both cameras<br />

(DCR-HC42E PAL System <strong>and</strong> SVHS-JVCGR-SX1) operated<br />

at a frequency of 50 Hz, with 1/250 digital shutter, <strong>and</strong> were fixed on a<br />

special support placed at the lateral wall of the pool (at 2.50 m from the<br />

edge of the pool deck). One camera was placed 30 cm above the water<br />

surface, <strong>and</strong> the other one was placed at a depth of 30 cm below the<br />

64<br />

surface camera (<strong>in</strong> an IKELITE waterproof box). Cameras were placed<br />

at 6.78 m from the plane of movement, synchronized <strong>in</strong> real time, calibrated<br />

with a 2.1 m x 3 m structure, <strong>and</strong> edited <strong>and</strong> mixed on a mix<strong>in</strong>g<br />

table (Panasonic digital mixer WJ-AVE55 VHS) that exported the f<strong>in</strong>al<br />

image to a VTR. Images were digitized for k<strong>in</strong>ematic analysis us<strong>in</strong>g the<br />

Arial Performance Analysis System (APAS). The anthropometric biomechanical<br />

model used was the one proposed by de Leva (1996) us<strong>in</strong>g<br />

13 anatomical po<strong>in</strong>ts.<br />

K<strong>in</strong>etic assessment was conducted through an underwater extensometric<br />

platform (Roesler, 1997) mounted on a support fixed to the pool<br />

wall, measur<strong>in</strong>g at 1000 Hz sampl<strong>in</strong>g rate. The h<strong>and</strong>grip system was<br />

adapted to comply with the swimm<strong>in</strong>g rules <strong>and</strong> to allow the same elevation<br />

of the body relative to the water surface. Start<strong>in</strong>g signals conformed<br />

to the FIN swimm<strong>in</strong>g rules us<strong>in</strong>g a starter device (ProStart, Colorado,<br />

USA). This device was programmed <strong>and</strong> <strong>in</strong>strumented to simultaneously<br />

produce the start sound, export a LED signal to the video system,<br />

<strong>and</strong> a trigger signal to the Analogical/Digital converter (Biopac, 16 bit).<br />

The backstroke start was divided <strong>in</strong>to three phases (adapted from<br />

Hohmann et al., 2006): (i) h<strong>and</strong>s-off (HO), from the start signal to the<br />

<strong>in</strong>stant the h<strong>and</strong>s lose contact with the h<strong>and</strong>grip; (ii) take-off (TO),<br />

from the h<strong>and</strong>s-off to the <strong>in</strong>stant the feet leave the force plate <strong>and</strong> (iii)<br />

flight (FL), between the <strong>in</strong>stant the feet leave the force plate until the<br />

first water touch. These time reference po<strong>in</strong>ts were selected accord<strong>in</strong>g to<br />

the characteristic of each velocity-time curve <strong>in</strong> each movement phase.<br />

Several l<strong>in</strong>ear k<strong>in</strong>ematic, temporal <strong>and</strong> k<strong>in</strong>etic parameters were determ<strong>in</strong>ed.<br />

Temporal variables were: start time (ST) - from the start signal<br />

to the first water touch; h<strong>and</strong>s-off time (HOT); take-off time (TOT),<br />

<strong>and</strong> flight time (FLT). K<strong>in</strong>ematical variables were: CM horizontal <strong>and</strong><br />

vertical position at the start<strong>in</strong>g signal (X0 <strong>and</strong> Y0, respectively) <strong>and</strong> at<br />

water touch (X1 <strong>and</strong> Y1), <strong>and</strong> CM horizontal <strong>and</strong> vertical displacement<br />

(Dx <strong>and</strong> Dy, respectively) dur<strong>in</strong>g HO, TO <strong>and</strong> FL phases. The k<strong>in</strong>etic<br />

variable selected was the horizontal impulse (HI, the product of the<br />

horizontal component of the wall reaction force times the impulse time<br />

duration). Angular k<strong>in</strong>ematical variables were the variation with time of<br />

the angular position of the hip, knee <strong>and</strong> ankle (jo<strong>in</strong>t angles), <strong>and</strong> their<br />

first derivative (angular velocity of each referred jo<strong>in</strong>t) were also studied.<br />

The phase’s duration were normalized for the ST.<br />

Descriptive statistics <strong>and</strong> paired samples Student’s tests were used<br />

(normality verified by the Kolmogorov-Smirnov test). Significance level<br />

was established at 95% (p


Table 1. Mean ± SD values of the 15 l<strong>in</strong>ear biomechanical parameters<br />

studied for backstroke start variants with feet immersed <strong>and</strong> emerged<br />

(BSFI <strong>and</strong> BSFE, respectively).<br />

BSFI BSFE p<br />

ST (s) * 0.93 ± 0.08 0.98 ± 0.11 0.01<br />

HOT (s) * 0.55 ± 0.04 0.59 ± 0.08 0.03<br />

TOT (s) * 0.23 ± 0.05 0.27 ± 0.04


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

dIscussIon<br />

The results showed that a higher foot position of BSFE produces a<br />

higher horizontal wall approximation of the CM <strong>in</strong> the start<strong>in</strong>g position.<br />

In the same way, BSFE presented a higher HOT. Differences may<br />

certa<strong>in</strong>ly be attributed to the foot segment constra<strong>in</strong>t <strong>in</strong> the start<strong>in</strong>g<br />

position, which seems to imply a more complex lower <strong>and</strong> upper limb<br />

movement sequence to release h<strong>and</strong>grip contact at BSFE. Previous values<br />

published without these constra<strong>in</strong>ts presented values between 0.42<br />

<strong>and</strong> 0.52 s (Kruger et al., 2006). Differences may be attributed to the<br />

higher competitive level of the swimmers of the referred study. In accordance<br />

with the analys<strong>in</strong>g movements reported <strong>in</strong> previous studies<br />

such as vertical, horizontal, drop or rebound jumps (Bobbert <strong>and</strong> Van<br />

IngenSchenau, 1988; Rodacki <strong>and</strong> Fowler, 2001), dur<strong>in</strong>g the backstroke<br />

start (both variants), the CM is <strong>in</strong>itially accelerated by the extension of<br />

the hip jo<strong>in</strong>t, although BSFE registered lower time to reach jo<strong>in</strong>t peak<br />

angular velocity. We can speculate that the more tucked position of the<br />

BSFE may imply a higher pre-stretch<strong>in</strong>g of the subsequent propulsive<br />

muscles. In this situation, the force production capacity of these muscles<br />

can be maximized if the time between the stretch <strong>and</strong> shorten<strong>in</strong>g actions,<br />

<strong>and</strong> their load<strong>in</strong>g characteristics respect particular limits. This has<br />

yet, however, to be verified.<br />

At BSFI condition a higher knee jo<strong>in</strong>t angular displacement was<br />

observed, which seems to contribute to a higher DxCM-HO.<br />

The present results confirmed the hypothesis that the BSFI start<br />

condition might result <strong>in</strong> a different resultant vector angle with a more<br />

pronounced vertical component as noted by the higher DyCM-TO.<br />

As Counsilman (1971) previously stated, few swimmers can perform<br />

successfully the BSFE due to the longer tra<strong>in</strong><strong>in</strong>g required to <strong>in</strong>crease<br />

the vertical component at the <strong>in</strong>stant of take-off. Temporal analysis also<br />

revealed that BSFE obta<strong>in</strong>ed higher TOT. It may be due to the specific<br />

placement of the feet above water level, which seems to imply that the<br />

body mass was accelerated through a greater distance after the start signal<br />

until the take-off, which expla<strong>in</strong>s the higher impulse.<br />

The analysis of segmental co-ord<strong>in</strong>ation <strong>in</strong>dicated that BSFI showed<br />

greater angular velocity of the knee jo<strong>in</strong>t at the beg<strong>in</strong>n<strong>in</strong>g of the take-off<br />

phase; while, the BSFE condition presented a greater time of the knee<br />

jo<strong>in</strong>t maximal extension. Additionally, BSFI imposed a lower time to<br />

reach ankle jo<strong>in</strong>t maximal extension, at the end of TO phase.<br />

The paired sample T-test revealed higher FLT <strong>and</strong> X1 for the BSFI.<br />

In a previous study, Miller et al. (1984) found values of 0.11 ± 0.06 s<br />

(100 m events) <strong>and</strong> 0.11 ± 0.05 s (200 m events) for FLT dur<strong>in</strong>g the<br />

backstroke start without foot position specified (but assumed to be<br />

BSFI), values that suggested be<strong>in</strong>g lower than those found <strong>in</strong> our study<br />

for both variants. Additionally, these authors found similar values to<br />

ours for X1, 2.77 ± 0.12 m (100 m) <strong>and</strong> 2.78 ± 0.12 m (200 m). Nevertheless,<br />

differences may be attributed to the end po<strong>in</strong>t measurement<br />

of the flight analysis, which was established by Miller et al. (1984) as<br />

distance to the h<strong>and</strong> contact with the water <strong>in</strong>stead of the distance to<br />

the CM at the h<strong>and</strong> touch.<br />

conclusIons<br />

As a performance parameter, the total time spent dur<strong>in</strong>g the start was<br />

lower for BSFI than BSFE, allow<strong>in</strong>g the conclusion that the first, be<strong>in</strong>g<br />

faster than the second should be preferred for competitive use. This<br />

observed superiority of the BSFI may be at least partially justified by<br />

the higher flight time (FLT) <strong>and</strong> reach of the centre of mass (X1). These<br />

f<strong>in</strong>d<strong>in</strong>gs seem to confirm the hypothesis that a lower foot position can<br />

determ<strong>in</strong>e the CM water reach by constra<strong>in</strong><strong>in</strong>g the orientation of the resultant<br />

wall reaction vector. Inter-segmental coord<strong>in</strong>ative analysis of the<br />

lower limbs showed that the relative time at which the knee <strong>and</strong> ankle<br />

peak jo<strong>in</strong>t angular velocity occurs might be an important variable to<br />

characterize the co-ord<strong>in</strong>ation pattern, <strong>and</strong> to expla<strong>in</strong> the performance<br />

capacity of the BSFI. It is recommended that coaches beg<strong>in</strong> monitor<strong>in</strong>g<br />

the backstroke start variation strategies to improve <strong>in</strong>ter-segmental<br />

coord<strong>in</strong>ation, which can be the determ<strong>in</strong><strong>in</strong>g factor of success of the start.<br />

66<br />

reFerences<br />

Bobbert, M. & Van Ingen Schnenau, G. (1988). Co-ord<strong>in</strong>ation <strong>in</strong> vertical<br />

jump<strong>in</strong>g. J Biomech, 21, 249-62.<br />

Counsilman, J. E. (1971). La natación: ciencia y técnica para la preparación<br />

de campeones. Englewood Cliffs, New Jersey: Prentice-Hall, Inc.<br />

De Leva, P. (1996). Adjustments to Zatsiorsky-Seluyanov’s segment <strong>in</strong>ertia<br />

parameters. J Biomech, 29(9), 1223-30.<br />

Hohmann, A., Fehr, U., Kirsten, R. & Krüger, T. (2006). Emg-model of<br />

backstroke start technique. Port J Sport Sci, 6(1), 37-40.<br />

Krüger, T., Hohmann, A., Kirsten, R. & Wick, D. (2006). K<strong>in</strong>ematics<br />

<strong>and</strong> dynamics of backstroke start. Port J Sport Sci, 6(1), 58-60.<br />

Lyttle, A. & Benjanuvatra, N. (2004). Start right: biomechanical review<br />

of dive start performance [electronic version]. Available at Coaches<br />

Information Website: http://www.coaches<strong>in</strong>fo.com/category/swimm<strong>in</strong>g/321/<br />

Miller, D., Hay, J. & Wilson, B. (1984). Start<strong>in</strong>g technique of elite swimmers.<br />

J Sports Sci, 2, 21-27.<br />

Rodacki, A. & Fowler, N. (2001). Intermuscular coord<strong>in</strong>ation dur<strong>in</strong>g<br />

pendulum rebound exercises. J Sports Sci, 19, 411-425.<br />

Roesler, H. (1997). Development of underwater platform for force <strong>and</strong><br />

force moment measurement <strong>in</strong> all coord<strong>in</strong>ate axes for biomechanical<br />

applications. PhD thesis, Federal University of Rio Gr<strong>and</strong>e do Sul,<br />

Porto Alegre.<br />

Van Ingen Schenau, G. (1989). From rotation to translation: constra<strong>in</strong>ts<br />

on multi-jo<strong>in</strong>t movements <strong>and</strong> the unique action of bi-articular muscles.<br />

H Mov Sci, 8, 301-377.<br />

Vilas-Boas, J. P., Cunha, P., Figueiras, T., Ferreira, M. & Duarte, J.<br />

(1997). Movement analysis <strong>in</strong> simultaneously swimm<strong>in</strong>g techniques.<br />

Kolner Swimmsporttage–Symposiums. Bericht, Germany: Sport Fahnemann<br />

Verlag.<br />

Vilas-Boas, J. P., Cruz, J., Sousa, F., Conceição, F., Fern<strong>and</strong>es, R. & Carvalho,<br />

J. (2003). Biomechanical analysis of ventral swimm<strong>in</strong>g starts:<br />

Comparison of the Grab Start with Two Track-Start Techniques.<br />

<strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g IXth. Sa<strong>in</strong>t-Étienne, France:<br />

Université de Sa<strong>in</strong>t-Etienne.<br />

Welcher, R., H<strong>in</strong>richs, R. & George, T. (2008). Front-or-rear weighted<br />

track start or grab start: which is the best for female swimmers? Sports<br />

Biomech, 7(1), 100-13.


Tethered Force Production <strong>in</strong> St<strong>and</strong>ard <strong>and</strong> Contrast<strong>and</strong>ard<br />

Scull<strong>in</strong>g <strong>in</strong> Synchronized Swimm<strong>in</strong>g<br />

diogo, V. 1 , soares, s. 1 , tour<strong>in</strong>o, c. 2 , Abraldes, J.A. 3 , Ferragut,<br />

c. 4 , Morouço, P. 5 , Figueiredo, P. 1 , Vilas-Boas, J.P. 1 , Fern<strong>and</strong>es,<br />

r.J. 1<br />

1 University of Porto, Faculty of Sport, Cifi2d, Porto, Portugal<br />

2 University of Vigo, Faculty of Education <strong>and</strong> Sport Sciences, Spa<strong>in</strong><br />

3 University of Murcia, Faculty of Sports Sciences, Murcia, Spa<strong>in</strong><br />

4 Catholic University of Murcia, Faculty of Sports Sciences, Murcia, Spa<strong>in</strong><br />

5 Polytechnic Institute of Leiria, CIMH, Portugal<br />

Studies carried out <strong>in</strong> synchronized swimm<strong>in</strong>g are scarce, <strong>in</strong>clusively<br />

with respect to the biomechanical analysis of scull<strong>in</strong>g. The purpose of<br />

this study was to measure the force produced <strong>in</strong> st<strong>and</strong>ard <strong>and</strong> contrast<strong>and</strong>ard<br />

scull<strong>in</strong>g, us<strong>in</strong>g a 30 s maximal tethered synchronized swimm<strong>in</strong>g<br />

test. 13 synchronized swimmers performed a 2x30 s maximum<br />

<strong>in</strong>tensity tethered synchronized swimm<strong>in</strong>g test, <strong>in</strong> st<strong>and</strong>ard <strong>and</strong> contrast<strong>and</strong>ard<br />

scull<strong>in</strong>g conditions, respectively. The variables were: absolute<br />

<strong>and</strong> relative maximal force, the time when maximal force occurred, the<br />

mean force, the mean values of maximal <strong>and</strong> m<strong>in</strong>imal force, <strong>and</strong> the<br />

fatigue <strong>in</strong>dex. Results showed that higher values of maximal force were<br />

found <strong>in</strong> the st<strong>and</strong>ard scull<strong>in</strong>g. The Fatigue Index evidenced that the<br />

maximal force decl<strong>in</strong>ed with time <strong>in</strong> all participants <strong>and</strong> <strong>in</strong> both scull<strong>in</strong>g<br />

conditions.<br />

Key words: biomechanics, scull<strong>in</strong>g, synchronized swimm<strong>in</strong>g, tethered<br />

swimm<strong>in</strong>g<br />

IntroductIon<br />

Synchronized swimm<strong>in</strong>g is a technical <strong>and</strong> physically dem<strong>and</strong><strong>in</strong>g sport,<br />

<strong>in</strong> which the strength <strong>and</strong> the velocity of movements are comb<strong>in</strong>ed with<br />

high flexibility requirements (Chu, 1999). In this sport, scull<strong>in</strong>g is an often-used<br />

technique, consist<strong>in</strong>g <strong>in</strong> underwater arm stroke patterns whose<br />

purpose is the production of hydrodynamic force. This force will allow<br />

support, balance <strong>and</strong> propulsion of the swimmer’s body (Chu, 1999).<br />

Although the importance of scull<strong>in</strong>g <strong>in</strong> synchronized swimm<strong>in</strong>g<br />

is undeniable, very few studies were conducted, <strong>and</strong> none seem<br />

to have quantified the force produced by the swimmer. The appearance<br />

of fatigue dur<strong>in</strong>g scull<strong>in</strong>g was also not yet studied. Know<strong>in</strong>g that there<br />

is a high relationship between strength <strong>and</strong> performance <strong>in</strong> swimm<strong>in</strong>g<br />

(Risch <strong>and</strong> Castro, 2007), <strong>and</strong> that strength tra<strong>in</strong><strong>in</strong>g (with emphasis on<br />

neural adaptations) expla<strong>in</strong>s, <strong>in</strong> part, the specific positive changes <strong>in</strong> velocity<br />

<strong>and</strong> aerobic performance due to a better economy of movement<br />

(Hoff et al., 2002), the purpose of this study was to measure the force<br />

<strong>and</strong> the fatigue produced <strong>in</strong> st<strong>and</strong>ard <strong>and</strong> contra-st<strong>and</strong>ard scull<strong>in</strong>g <strong>in</strong><br />

synchronized swimm<strong>in</strong>g, us<strong>in</strong>g a 30s maximal tethered test.<br />

Methods<br />

Thirteen synchronized swimmers with the same performance level v<br />

vvolunteered to participate <strong>in</strong> this study. Mean (± SD) physical characteristics<br />

of the sample were: age 15.8 (2.1) years; body weight 50.5 (8.2)<br />

Kg; height 160.9 (7.4) cm; arm span 161.2 (9.7) cm.<br />

A 30 s tethered swimm<strong>in</strong>g protocol was used <strong>in</strong> order to determ<strong>in</strong>e<br />

<strong>in</strong>dividual force to time - F (t) - curves <strong>in</strong> two conditions: (i) st<strong>and</strong>ard<br />

scull<strong>in</strong>g (movement towards the head, with the body placed <strong>in</strong> sup<strong>in</strong>e<br />

position, the arms <strong>in</strong> the lateral of the trunk, the wrist <strong>in</strong> dorsal flexion<br />

<strong>and</strong> the h<strong>and</strong> palm oriented toward the feet) <strong>and</strong> (ii) contra-st<strong>and</strong>ard<br />

scull<strong>in</strong>g (movement towards the feet with the body <strong>in</strong> sup<strong>in</strong>e position,<br />

the arms <strong>in</strong> the lateral of the trunk, the wrist <strong>in</strong> palmar flexion <strong>and</strong> the<br />

h<strong>and</strong> palm oriented towards the head). After familiarization with the<br />

equipment <strong>and</strong> a st<strong>and</strong>ardized warm-up, each subject performed a 30<br />

s maximum <strong>in</strong>tensity tethered synchronized swimm<strong>in</strong>g test. Individual<br />

chaPter2.<strong>Biomechanics</strong><br />

F (t) curves were obta<strong>in</strong>ed with the subjects attached by a non-elastic<br />

cable to a stra<strong>in</strong>-gauge system (Globus, Italy). The beg<strong>in</strong>n<strong>in</strong>g <strong>and</strong> the<br />

end of the test were established through an acoustical signal produced<br />

by a researcher. Tests were conducted <strong>in</strong> an <strong>in</strong>door, heated (27.5ºC), <strong>and</strong><br />

2 m deep swimm<strong>in</strong>g-pool.<br />

The absolute <strong>and</strong> relative maximal forces (Fmax <strong>and</strong> RFmax, be<strong>in</strong>g<br />

RFmax = Force.body weight -1 ), the time at which Fmax occurred<br />

(FmaxTime), the mean force (Fmean), the average of Fmax (FmaxAvg<br />

= average of all force values <strong>in</strong> the first 5 s of the test), the average of<br />

m<strong>in</strong>imal force (Fm<strong>in</strong>Avg = average of all force values <strong>in</strong> the last 5 s of<br />

the test) <strong>and</strong> the fatigue <strong>in</strong>dex (FI (%) = ([FmaxAvg-Fm<strong>in</strong>Avg)/Fmax-<br />

Avg]x100) were computed. The force values of the first 2 s test were<br />

elim<strong>in</strong>ated <strong>in</strong> order to remove the high <strong>in</strong>ertial values associated with<br />

the first pull (Fig. 1).<br />

After the normality of the distributions was confirmed (Kolmogorov-Smirnov<br />

test), T- Test for repeated measures was used to compare<br />

mean values of each variable obta<strong>in</strong>ed for st<strong>and</strong>ard <strong>and</strong> contra st<strong>and</strong>ard<br />

scull<strong>in</strong>g techniques. Pearson product-moment correlation coefficient<br />

was also computed for the study of relevant association of variables. Significance<br />

level was established at 95% (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

(r=-0.58) <strong>and</strong> Fmean (r=-0.81) for st<strong>and</strong>ard action, <strong>and</strong> with Fm<strong>in</strong>Avg<br />

(r=-0.91 <strong>and</strong> r=-0.54) for both scull<strong>in</strong>g variants.<br />

Table 2. Individual <strong>and</strong> Mean ± SD values of absolute maximal (Fmax)<br />

<strong>and</strong> relative (relative Fmax) force, the time when the Fmax occurred<br />

(Fmax Time), mean force (Fmean), the average of maximal <strong>and</strong> m<strong>in</strong>imum<br />

forces (FmaxAvg <strong>and</strong> Fm<strong>in</strong>Avg, respectively) <strong>and</strong> the fatigue <strong>in</strong>dex<br />

(FI) <strong>in</strong> contra-st<strong>and</strong>ard scull<strong>in</strong>g (n=13).<br />

Swimmer Fmax (N)<br />

68<br />

Relative<br />

Fmax<br />

(N/Kg)<br />

FmaxTime<br />

(s)<br />

Fmean<br />

(N)<br />

Fm<strong>in</strong>Avg<br />

(N)<br />

FmaxAvg<br />

(N)<br />

FI (%)<br />

#1 32.2 0.63 2.3 15.5 8.3 24.4 66.2<br />

#2 37.2 0.71 4.1 21.4 17.0 25.9 34.3<br />

#3 30.4 0.53 4.8 15.5 11.3 19.5 41.9<br />

#4 31.1 0.70 9.6 16.6 12.2 20.6 40.6<br />

#5 32.9 0.73 4.9 13.5 11.5 18.5 37.7<br />

#6 35.4 0.80 3.4 16.2 13.9 20.0 30.4<br />

#7 41.9 0.67 3.1 15.8 11.9 20.8 42.8<br />

#8 24.0 0.72 2.9 12.5 10.5 14.7 29.0<br />

#9 30.0 0.67 6.9 16.3 14.7 19.3 23.7<br />

#10 34.0 0.64 6.2 18.9 13.7 25.4 47.2<br />

#11 43.6 0.69 2.5 24.3 18.6 32.7 43.2<br />

#12 35.8 0.66 8.1 19.1 16.8 23.8 29.2<br />

#13 40.8 0.82 3.9 23.4 19.6 26.5 26.2<br />

X ± SD 34.6±5.4* 0.69±0.07* 4.8±2.3 17.6±3.6 13.8±3.4 22.5±4.6 37.9±11.3<br />

*Different (p


<strong>and</strong> non-st<strong>and</strong>ard scull<strong>in</strong>g <strong>in</strong> synchronized swimm<strong>in</strong>g. A pilot study.<br />

Open Sports Sci J<br />

Hoff, J., Gran, A. & Helgerud, J. (2002). Maximal strength tra<strong>in</strong><strong>in</strong>g<br />

improves aerobic endurance performance. Sc<strong>and</strong> J Med Sci Sports, 12,<br />

288-95.<br />

Ito, S. (2006). Fundamental fluid dynamic research on Configuration of<br />

the h<strong>and</strong> palm <strong>in</strong> Synchronized Swimm<strong>in</strong>g. Port J Sport Sci, 6(Suppl.<br />

2), 265-268.<br />

Kjendlie, P. L. & Thorsvald, K. (2006). A tethered swimm<strong>in</strong>g power test<br />

is highly reliable. In: Vilas-Boas J. P., Alves F., Marques A. (Eds.).<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X (pp. 231-233). Revista<br />

Portuguesa de Ciências do Desporto, Porto.<br />

Lauder, M. A. & Dabnichki, P. (2005). Estimat<strong>in</strong>g propulsive forces –<br />

s<strong>in</strong>k or swim? J Biomech, 38, 1984-1990.<br />

Morouço, P., Soares, S., Vilas-Boas, J. P. & Fern<strong>and</strong>es, R. (2008). Force<br />

characteristics of elite swimmers <strong>in</strong> a 30-s tethered swimm<strong>in</strong>g effort<br />

test. J Sport Sci, 26(Suppl. 1), 11.<br />

Rackham, G. W. (1974). An analysis of arm propulsion <strong>in</strong> swimm<strong>in</strong>g.<br />

In: Lewillie L., Clarys J. P. (Eds). 2d International Symposium on <strong>Biomechanics</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g (pp. 174-179). Brussels, Belgium: University<br />

Park Press.<br />

Risch, O. & Castro, F. (2007). Desempenho em natação e pico de força<br />

em tethered swimm<strong>in</strong>g. In: <strong>XI</strong>I Congresso Brasileiro de Biomecânica<br />

(pp. 441-446). São Paulo.<br />

Sidney, M., Pelayo, P. & Robert, A. (1996). Tethered forces <strong>in</strong> crawl<br />

stroke <strong>and</strong> their relationship to anthropometrics characteristics <strong>and</strong><br />

spr<strong>in</strong>t swimm<strong>in</strong>g performance. J Hum Mov Stud, 31, 1-12.<br />

Strojnik, V., Bednarik, J. & Strumbelj, B. (1999). Active <strong>and</strong> passive drag<br />

<strong>in</strong> swimm<strong>in</strong>g. In: Kesk<strong>in</strong>en K. L., Komi P. V., Holl<strong>and</strong>er A. P. (Eds.).<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII (pp. 113-117). University<br />

of Jyvaskyla, Jyvaskyla, F<strong>in</strong>l<strong>and</strong>.<br />

Toussa<strong>in</strong>t, H. & Beek, P. (1992). <strong>Biomechanics</strong> of competitive front<br />

crawl swimm<strong>in</strong>g. Sports Med, 13(1), 8-24.<br />

Vorontsov, A., Dyrco, V., B<strong>in</strong>evsky, D., Solomat<strong>in</strong>, V. & Sidorov, N.<br />

(1999). Patterns of growth for some characteristics of physical development,<br />

functional <strong>and</strong> motor abilities <strong>in</strong> boy-swimmers 11-18 years.<br />

In: Kesk<strong>in</strong>en K., Komi P., Holl<strong>and</strong>er A. P. (Eds). <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII. Jyväskulä, F<strong>in</strong>l<strong>and</strong>: Gummerus Pr<strong>in</strong>t<strong>in</strong>g,<br />

327-335.<br />

Wirtz, W., Bieder, A., Wilke, K. & Klauck, J. (1999). Semi-tethered<br />

swimm<strong>in</strong>g as a diagnostic tool for swimm<strong>in</strong>g technique <strong>and</strong> physical<br />

performance. In: Kesk<strong>in</strong>en K. L., Komi, P. V., Holl<strong>and</strong>er, A. P. (Eds.).<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII (pp. 265-268). University<br />

of Jyvaskyla, Jyvaskyla, F<strong>in</strong>l<strong>and</strong>.<br />

chaPter2.<strong>Biomechanics</strong><br />

Pull<strong>in</strong>g Force Characteristics of 10 s Maximal<br />

Tethered Eggbeater Kick <strong>in</strong> Elite Water Polo Players:<br />

A Pilot Study<br />

dopsaj, M.<br />

University of Belgrade, Faculty of Sport <strong>and</strong> Physical Education, Serbia<br />

This paper aimed to def<strong>in</strong>e the basic k<strong>in</strong>etic <strong>and</strong> mechanical characteristics<br />

of 10 s maximal tethered eggbeater kicks <strong>in</strong> elite water polo players<br />

<strong>in</strong> the chest-forward position with h<strong>and</strong>s above the water. The study<br />

<strong>in</strong>volved 14 male elite water polo players. The follow<strong>in</strong>g measurements<br />

of the k<strong>in</strong>etic characteristics of pull<strong>in</strong>g force were taken: the duration of<br />

a s<strong>in</strong>gle leg eggbeater kick, the maximal (peak) force values, the average<br />

force values, the impulse of force, the s<strong>in</strong>gle leg eggbeater kick rate of force<br />

development <strong>and</strong> the s<strong>in</strong>gle leg eggbeater kick frequency. Reliability analysis<br />

showed high statistical significance of the measurement results of the<br />

test at ICC=0.9681. Besides, the pull<strong>in</strong>g force realized at FmaxEBK <strong>and</strong><br />

FavgEBK was determ<strong>in</strong>ed to have changed significantly at the time <strong>in</strong>terval<br />

of 10s. The result<strong>in</strong>g models could help towards the development of<br />

the water polo tra<strong>in</strong><strong>in</strong>g technology, as well as the establishment of a new<br />

method to test the specific leg fitness <strong>in</strong> elite senior water polo players.<br />

Key words: eggbeater kick, tethered pull<strong>in</strong>g force, water polo<br />

IntroductIon<br />

Water polo players realize all of their technical <strong>and</strong> tactical (TE-TA)<br />

tasks from two basic positions <strong>in</strong> the water: the horizontal <strong>and</strong> the vertical<br />

position (Dopsaj & Thanopoulos, 2006). Although the general physiological<br />

load <strong>in</strong>dicators categorize water polo as a sport that requires a<br />

high level of aerobic endurance, a great number of TE-TA activities are<br />

realized through the maximal <strong>in</strong>terval <strong>in</strong>tensity <strong>in</strong> shorter <strong>in</strong>tervals <strong>in</strong><br />

which the energy is dom<strong>in</strong>antly supplied by an anaerobic-alactic system<br />

– the ATP/CP system (Smith, 1998).<br />

Calculations, based on time <strong>and</strong> motion analysis, have <strong>in</strong>dicated that<br />

field players spend only 45% to 55% of game time <strong>in</strong> the horizontal<br />

body position. The rema<strong>in</strong>der of the time is spent perform<strong>in</strong>g activities<br />

<strong>in</strong> predom<strong>in</strong>antly vertical body positions, with or without contact with<br />

the opponent, <strong>and</strong> with a moderate to high <strong>in</strong>tensity, as <strong>in</strong>dicated by<br />

heart rate record<strong>in</strong>gs <strong>in</strong> some studies (Platanou, 2009).<br />

In water polo, duel play is the players’ basic position <strong>in</strong> both the offense<br />

<strong>and</strong> the defense. The position essentially enables players to block<br />

the opponent by hold<strong>in</strong>g their arms so as to perform the TE-TA elements,<br />

us<strong>in</strong>g the eggbeater kick technique simultaneously (S<strong>and</strong>ers,<br />

1999; Dopsaj & Thanopoulos, 2006). Essentially, the eggbeater kick is<br />

also used to raise the upper body for the purpose of receiv<strong>in</strong>g a pass,<br />

pass<strong>in</strong>g, shoot<strong>in</strong>g for goal, or block<strong>in</strong>g the opponent’s shoot<strong>in</strong>g, pass<strong>in</strong>g<br />

or receiv<strong>in</strong>g actions. The eggbeater kick is a cyclic action of the lower<br />

limbs with the actions of the right <strong>and</strong> left sides be<strong>in</strong>g similar but opposite<br />

<strong>in</strong> phase, meant to susta<strong>in</strong> the body <strong>in</strong> the elevated position or to<br />

push the opponent’s body strongly (S<strong>and</strong>ers, 1999).<br />

Previous studies have established that most water polo realizations<br />

from the vertical position, with or without contact with the opponent,<br />

are done at the maximal <strong>and</strong>/or submaximal effort <strong>in</strong>tensity <strong>in</strong> the anaerobic<br />

alactate energy system (Smith, 1998; Platanou, 2004; Takagi et<br />

al., 2005; Platanou, 2009), which po<strong>in</strong>ts towards the conclusion that<br />

the specific tra<strong>in</strong><strong>in</strong>g of the lower extremities <strong>in</strong>directly affects game effectiveness.<br />

However, so far no research has published studies of the<br />

pull<strong>in</strong>g force characteristics realized <strong>in</strong> water <strong>and</strong> by eggbeater kick<br />

techniques with<strong>in</strong> the effort system which is dom<strong>in</strong>ant <strong>in</strong> competitions.<br />

This paper aimed to def<strong>in</strong>e the basic k<strong>in</strong>etic <strong>and</strong> mechanical characteristics<br />

of 10 s maximal tethered eggbeater kicks <strong>in</strong> elite water polo<br />

players <strong>in</strong> order to def<strong>in</strong>e a descriptive model of the characteristics measured<br />

<strong>in</strong> the population of highly tra<strong>in</strong>ed water polo players.<br />

69


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Methods<br />

The study <strong>in</strong>volved 14 male top senior national level water polo players<br />

(Age=21.5±5.1 yrs, Height=187.2±6.1 cm, Mass=84.5±11.9 kg, tra<strong>in</strong><strong>in</strong>g<br />

experience=11.7±3.6 yrs). The tests were conducted <strong>in</strong> the middle of the<br />

national premier league preparation period for the 2006/07 competition<br />

season. Egg beater kick pull<strong>in</strong>g force was tested by the method of<br />

tethered swimm<strong>in</strong>g (Sidney et al., 1996; Dopsaj et al., 2003). Before the<br />

test the players warmed up swimm<strong>in</strong>g <strong>in</strong>dependently up to 400m, <strong>and</strong><br />

did 10 m<strong>in</strong> of specific water polo warm-up <strong>in</strong> the vertical position with<br />

the emphasis on eggbeater kick exercises. After a 10 m<strong>in</strong> rest the test<strong>in</strong>g<br />

procedure started. On his turn, each player put on a belted harness<br />

adjust<strong>in</strong>g it to his body size. Then he hooked a 1cm-thick PVC rope to<br />

the belt at back hip region. The other end of the 5m rope was attached to<br />

a water-resistant high-resolution (100 kHz) tensiometric dynamometer<br />

placed on a metal support fixed on the side of the pool (Dopsaj et al.,<br />

2003). The dynamometer was connected to a PC. After they entered the<br />

pool, the players did a 15s pre-test trial of eggbeater kick tethered swim<br />

at self chosen <strong>in</strong>tensity <strong>in</strong> order to get familiar with the equipment <strong>and</strong><br />

the test<strong>in</strong>g procedure. After the 1 m<strong>in</strong> rest, test<strong>in</strong>g procedure started,<br />

where the players had to realize the one test trial of maximal pull force of<br />

10 seconds us<strong>in</strong>g eggbeater kicks only while <strong>in</strong> the chest-forward position,<br />

with h<strong>and</strong>s above the water wrist-high, <strong>in</strong> semi-flexed position <strong>and</strong><br />

<strong>in</strong> front of the shoulders, i.e. the chest. The follow<strong>in</strong>g measurements of<br />

the k<strong>in</strong>etic characteristics of pull<strong>in</strong>g force at a s<strong>in</strong>gle leg eggbeater kick<br />

were taken: the duration (Time EBK ), expressed <strong>in</strong> ms; the realized maximal<br />

(peak) force value (F maxEBK ), expressed <strong>in</strong> N; the average realized<br />

force value (F avgEBK ), expressed <strong>in</strong> N; the impulse of force (I mp F EBK ),<br />

expressed <strong>in</strong> N⋅s; the explosive rate of force production (RFD EBK ), expressed<br />

<strong>in</strong> N⋅s -1 ; <strong>and</strong> the frequency (Hz EBK) , expressed <strong>in</strong> the numbers of<br />

s<strong>in</strong>gle leg kicks per m<strong>in</strong>ute (Slk⋅m<strong>in</strong> -1 ). All data were treated <strong>in</strong> absolute<br />

<strong>and</strong> relative values with the descriptive statistical method. L<strong>in</strong>ear regression<br />

analysis was used to def<strong>in</strong>e a model of variable change dur<strong>in</strong>g the<br />

test<strong>in</strong>g time. S<strong>in</strong>ce the test<strong>in</strong>g method had not been previously used for<br />

eggbeater kick techniques, the reliability was determ<strong>in</strong>ed by apply<strong>in</strong>g<br />

reliability analysis with Split-half model criteria.<br />

results<br />

All descriptive data are shown <strong>in</strong> Table 1 (Mean, St<strong>and</strong>ard Deviation<br />

<strong>and</strong> Coefficient of Variation). The reliability analysis showed that the<br />

result<strong>in</strong>g measurements of pull<strong>in</strong>g force characteristics of 10s maximal<br />

tethered egg beater kick were highly statistically significant at 96.81%<br />

(Spearman-Brown rtt coefficient – 0.9681), with Interclass Correlation<br />

Coefficient at s<strong>in</strong>gle measurements IC= 0.918, F=157.63, p=0.000, <strong>and</strong><br />

at average measurements IC= 0.994, F=157.63, p=0.000.<br />

Table 2 gives the results of the def<strong>in</strong>ed regression models show<strong>in</strong>g<br />

the dependence <strong>in</strong> the change of tethered pull<strong>in</strong>g force characteristics<br />

<strong>in</strong> 10s (where: y values are variable units; x values are observed time<br />

<strong>in</strong>tervals <strong>in</strong> ms). Statistical significance was determ<strong>in</strong>ed <strong>in</strong> only two variables,<br />

F maxEBK <strong>and</strong> F avgEBK at the level of F=26.21, p=0.000 <strong>and</strong> F=43.95,<br />

p=0.000, respectively.<br />

Figure 1 gives the F-t curve tethered eggbeater pull<strong>in</strong>g force of two<br />

players play<strong>in</strong>g <strong>in</strong> different positions (central defender <strong>and</strong> peripheral<br />

player), while Figure 2 is a graphic representation of the observed tethered<br />

force pull<strong>in</strong>g characteristics with the regression l<strong>in</strong>es show<strong>in</strong>g the<br />

trend of change.<br />

70<br />

Table 1. The descriptive statistics of 10 s maximum chest-forward tethered<br />

s<strong>in</strong>gle leg eggbeater kick<br />

Time EBK (ms) F maxEBK (N)<br />

I mp F EBK<br />

(N-s)<br />

F avgEBK (N)<br />

RFD EBK<br />

(N-s -1 )<br />

Hz EBK<br />

(Slk-m<strong>in</strong> -1 )<br />

Mean 497.78 190.52 72.95 140.44 336.73 122.08<br />

Sd 56.95 36.04 14.32 21.12 98.89 14.70<br />

Cv% 11.44 18.92 19.64 15.04 29.37 12.04<br />

Relative 10 s tethered eggbeater kick descriptive statistics<br />

FrelEBK (N-kg-1 ImpFrelEBK ) (N-s-kg-1 FavgrelEBK ) (N-kg-1 RFDrelEBK ) (N-s-1-kg-1 )<br />

Mean 2.295 0.880 1.689 4.105<br />

Sd 0.534 0.214 0.327 1.610<br />

Cv% 23.26 24.30 19.34 39.21<br />

Egg beater kick tethered pull<strong>in</strong>g force (N)<br />

280<br />

260<br />

240<br />

220<br />

200<br />

180<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

0 1000 2000 3000 4000 5000 6000 7000 8000 9000 10000 11000<br />

Time (ms)<br />

V. U.<br />

N. J.<br />

Figure 1. Tethered eggbeater 10 s maximal pull<strong>in</strong>g force <strong>in</strong> the chestforward<br />

position <strong>in</strong> the two players (central guard – red l<strong>in</strong>e; peripheral<br />

– black l<strong>in</strong>e).<br />

Egg Beater Kick Pull<strong>in</strong>g Force Characteristics<br />

700<br />

600<br />

500<br />

400<br />

300<br />

200<br />

100<br />

0<br />

0 1000 2000 3000 4000 5000 6000 7000 8000 9000 10000 11000<br />

Time (ms)<br />

Fmax (N)<br />

ImpF (N·s)<br />

Favg (N)<br />

RFD (N·s-1)<br />

t (ms)<br />

HZ (kicks·m<strong>in</strong>-1)<br />

Figure 2. L<strong>in</strong>ear regression trend l<strong>in</strong>e models of tethered eggbeater 10<br />

s maximal pull<strong>in</strong>g force characteristics <strong>in</strong> the chest-forward position <strong>in</strong><br />

the peripheral player.<br />

Table 2. The l<strong>in</strong>ear regression model equation of 10 s maximum chestforward<br />

tethered leg eggbeater kick for all observed pull<strong>in</strong>g force variables<br />

Model Adj. R2 F <strong>and</strong> p value<br />

TimeEBK (ms) y = 0.0036x + 467.8573 R2 = 0.063 F=0.796, p=0.382<br />

FmaxEBK (N) Y = -0.0037x + 205.9223 R2 = 0.512 F=26.21, p=0.000<br />

ImpFEBK (N⋅s) y = -0.0010x + 75.7146 R2 = 0.086 F=2.71, p=0.113<br />

FavgEBK (N) y = -0.0037x + 159.2081 R2 = 0.641 F=43.95, p=0.000<br />

RFDEBK (N⋅s-1 ) y = 0.0035x + 328.7769 R2 = 0.018 F=0.573, p=0.457<br />

HzEBK (Slk⋅m<strong>in</strong>-1 ) y = -0.0006x + 140.1895 R2 = 0.0061 F=0.071, p=0.793<br />

dIscussIon<br />

In comparison with the absolute values, the variation coefficient showed<br />

high homogeneity <strong>in</strong> all tested variables, with the value of all variables<br />

below 30 % (from 11% with Time EBK to 29% with RFD EBK ). The rela-


tive <strong>in</strong>dicators showed a similar trend (F relEBK, I mp F relEBK <strong>and</strong> Favg relEBK<br />

– 23.26, 24.30 <strong>and</strong> 19.34 %, respectively), while the only variation of the<br />

results with respect to the homogeneous group was shown <strong>in</strong> RFD relEBK<br />

(39.21 %). The descriptive <strong>and</strong> variation <strong>in</strong>dicators can be used as scientifically<br />

valid for further comparative analysis.<br />

The ma<strong>in</strong> force that keeps the water polo players suspended <strong>in</strong> the<br />

water while perform<strong>in</strong>g other skills is hydrodynamic lift force, which is<br />

caused by the flow of water over the foot <strong>and</strong> leg of the athlete. With<br />

respect to the obta<strong>in</strong>ed descriptive <strong>in</strong>dicators, it can be ma<strong>in</strong>ta<strong>in</strong>ed that<br />

the <strong>in</strong>terval at 95% likelihood <strong>in</strong> assess<strong>in</strong>g the tra<strong>in</strong><strong>in</strong>g level of the analyzed<br />

tethered pull<strong>in</strong>g force characteristics realized with 10s maximal<br />

<strong>in</strong>tensity <strong>in</strong> male top senior national level water polo players was as follows:<br />

Time EBK = 441 – 555 ms; F maxEBK = 155 – 227 N; F avgEBK = 119 –<br />

162 N; I mp F EBK = 59 – 87 N⋅s; RFD EBK = 238 – 436 N⋅s -1 ; Hz EBK = 107<br />

– 137 Slk⋅m<strong>in</strong> -1 for absolute values of the s<strong>in</strong>gle leg eggbeater kick. At<br />

the reliability rate of 95%, the descriptive variable results yielded the follow<strong>in</strong>g<br />

relative values: F relEBK =1.76–2.83 N⋅kg -1 ; Favg relEBK =1.36–2.02<br />

N⋅kg -1 ; I mp F relEBK =0.67–1.09 N⋅s⋅kg -1 ; RFD relEBK =2.49–5.72 N⋅s -1 ⋅kg -1<br />

for relative values of the s<strong>in</strong>gle leg eggbeater kick.<br />

With respect to the basic k<strong>in</strong>etic <strong>in</strong>dicator, i.e., the duration of a<br />

s<strong>in</strong>gle eggbeater kick, it was established that it ranged from 441 to 555<br />

ms at the likelihood level of 95% (average Time EBK value ± SD value).<br />

As compared to the results published by Marion & Taylor (2008), the<br />

time for one complete eggbeater kick cycle was between 0.5 sec <strong>and</strong> 0.65<br />

s. However, here the authors studied the eggbeater kick technique with<br />

the athletes <strong>in</strong> vertical position, while <strong>in</strong> the present study the water<br />

polo players realized the maximal pull force with<strong>in</strong> 10 s <strong>in</strong> the semivertical<br />

chest-forward position. It is possible that the ensu<strong>in</strong>g difference<br />

<strong>in</strong> the duration of a s<strong>in</strong>gle leg cycle was due to the different measurement<br />

methods as well as to the nature of the task <strong>and</strong> the <strong>in</strong>tensity of<br />

legwork under load.<br />

A study of the vertical force exerted dur<strong>in</strong>g the eggbeater kick <strong>in</strong><br />

water polo concluded that the vertical force of the kick ranged from<br />

60 to 112 N (Yanagi, Amano et al. 1995, as cited <strong>in</strong> Marion & Taylor,<br />

2008). Accord<strong>in</strong>g to Marion & Taylor (2008) for an athlete with a<br />

weight of 600 N, the eggbeater contributes <strong>in</strong> 10-20% of the upward<br />

force required to balance the body weight. The current study established<br />

that senior top water polo players’ average values of maximal s<strong>in</strong>gle leg<br />

eggbeater kick pull force (peak force) can be achieved with maximal<br />

effort <strong>in</strong> 10 s at the average level of 190±36 N, i.e. rang<strong>in</strong>g between 155<br />

<strong>and</strong> 227 N with 95% reliability. Moreover, the rate of force development<br />

of the eggbeater kick was shown to be at the level rang<strong>in</strong>g between 238<br />

– 436 N⋅s -1 with 95% likelihood level. In our results, the average BM<br />

was 84.5 kg <strong>and</strong> the pull<strong>in</strong>g force realized by the given method was at<br />

the level of 23.40±5.44 % of the subjects’ BM, i.e. with<strong>in</strong> the reliability<br />

range of 18.0 to 28.8%.<br />

Presumably, all the measured k<strong>in</strong>etic characteristics of legwork <strong>in</strong> the<br />

given water polo technique are due to the years of the players’ adaptation<br />

to the exertions of tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competition so that the experimental<br />

results can represent an actual model of the players’ abilities to cope with<br />

the task given <strong>in</strong> the test. New water polo rules <strong>in</strong>troduced <strong>in</strong> 2006 resulted<br />

<strong>in</strong> more <strong>in</strong>tensive competitor efforts, especially for technical <strong>and</strong><br />

tactical elements where legwork is the dom<strong>in</strong>ant movement (eggbeater,<br />

jumps, shots, duel play <strong>and</strong> defender actions) for which players must be<br />

prepared through an adequate system of tra<strong>in</strong><strong>in</strong>g (Platanou, 2009). Such<br />

data <strong>in</strong>dicate that more <strong>in</strong>tensified tra<strong>in</strong><strong>in</strong>g <strong>and</strong> the <strong>in</strong>troduction of specific<br />

changes <strong>in</strong> the tra<strong>in</strong><strong>in</strong>g work are necessary to achieve best results <strong>in</strong><br />

water polo, especially <strong>in</strong> vertical <strong>and</strong> semi-vertical water polo positions.<br />

Besides, the approach given here highlights the dem<strong>and</strong> for def<strong>in</strong><strong>in</strong>g<br />

specific methods to test the abilities of water polo players.<br />

conclusIon<br />

The results <strong>in</strong>dicated the descriptive values of the k<strong>in</strong>etic characteristics<br />

of the 10s maximal tethered eggbeater kick <strong>in</strong> elite water polo players<br />

chaPter2.<strong>Biomechanics</strong><br />

with regard to the absolute <strong>and</strong> relative values. The reliability analysis<br />

showed that the reliability of measur<strong>in</strong>g the pull<strong>in</strong>g force characteristics<br />

of 10s maximal tethered egg beater kick was highly statistically significant<br />

at 96.81%, with ICC at s<strong>in</strong>gle measures = 0.918, <strong>and</strong> at ICC average<br />

measures = 0.994. It was also established that only two variables of<br />

the measured value showed statistically significant change <strong>in</strong> the time<br />

<strong>in</strong>terval of 10s, namely FmaxEBK <strong>and</strong> FavgEBK. In our results, the average<br />

tethered pull force peaked at 23.40±5.44 % of the subjects’ body<br />

mass.<br />

Moreover, the result<strong>in</strong>g data could also help towards the development<br />

of water polo tra<strong>in</strong><strong>in</strong>g technology, <strong>and</strong> the establishment of a new<br />

method to test the specific leg fitness <strong>in</strong> elite senior water polo players.<br />

reFerences<br />

Dopsaj, M., Matkovic, I., Thanopoulos, V., & Okicic, T. (2003). Reliability<br />

<strong>and</strong> validity of basic k<strong>in</strong>ematics <strong>and</strong> mechanical characteristics<br />

of pull<strong>in</strong>g force <strong>in</strong> swimmers measured by the method of tethered<br />

swimm<strong>in</strong>g with maximum <strong>in</strong>tensity of 60 seconds. FACTA UNI-<br />

VERSITATIS: Series Physical Education <strong>and</strong> Sport, 1(10):11-22.<br />

Dopsaj, M., & Thanopoulos, V. (2006). The structure of evaluation <strong>in</strong>dicators<br />

of vertical swimm<strong>in</strong>g work ability of top water polo players.<br />

Revista Portuguesa de Ciencias do Desporto (Portugese Journal of Sport<br />

Sciences), 6(2), 124-126.<br />

Gast<strong>in</strong>, P. B. (2001). Energy system <strong>in</strong>teraction <strong>and</strong> relative contribution<br />

dur<strong>in</strong>g maximal exercise. Sports <strong>Medic<strong>in</strong>e</strong>, 31(10), 725-741.<br />

Marion, A., & Taylor, C. (2008). The technique of the eggbeater kick.<br />

http://www.coaches<strong>in</strong>fo.com/ (09.01.2010).<br />

Platanou T. (2004). Time motion analysis of <strong>in</strong>ternational level water<br />

polo players. J Hum Mov Stud, 46, 319-331.<br />

Platanou, T. (2009). Cardiovascular <strong>and</strong> metabolic requirements of water<br />

polo. Serb J Sports Sci, 3(3), 85-97<br />

S<strong>and</strong>ers, R. (1999). Analysis of the eggbeater kick used to ma<strong>in</strong>ta<strong>in</strong><br />

height <strong>in</strong> water polo, J Appl <strong>Biomechanics</strong>, 15, 284-291.<br />

Smith, H. K. (1998). Applied physiology of water polo. Sports Med, 26,<br />

317–334.<br />

Sidney, M., Pelayo, P., & Robert, A. (1996). Tethered forces <strong>in</strong> crawl<br />

stroke <strong>and</strong> their relationship to anthropometrics characteristics <strong>and</strong><br />

spr<strong>in</strong>t swimm<strong>in</strong>g performances. J Hum Mov Studies, 31, 1-12.<br />

Takagi, H., Nishigima, T., Enomoto, I., & Stewart, A. M. (2005). Determ<strong>in</strong><strong>in</strong>g<br />

factors of game performance <strong>in</strong> the 2001 World Water Polo<br />

Championships. J Hum Mov Stud, 49 (5), 333-352.<br />

71


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Motor Coord<strong>in</strong>ation Dur<strong>in</strong>g the Underwater<br />

Undulatory Swimm<strong>in</strong>g Phase of the Start for High<br />

Level Swimmers<br />

elipot, M. 1, 2 , houel, n. 2 , hellard, P. 2 , dietrich, G. 1<br />

1 Université Paris Descartes, Paris, France<br />

2 Fédération française de natation, Paris, France<br />

The aim of the present study was to identify the ma<strong>in</strong> motor coord<strong>in</strong>ation<br />

<strong>in</strong>volved dur<strong>in</strong>g the underwater undulatory swimm<strong>in</strong>g phase of<br />

the start. Twelve French high-level swimmers took part <strong>in</strong> this study.<br />

Swimmers were filmed dur<strong>in</strong>g the entire underwater phase of the start<br />

(i.e. fifteen meters from the start platform). Specific anatomical l<strong>and</strong>marks<br />

were identified on the body of the swimmers <strong>and</strong> 2D space coord<strong>in</strong>ates<br />

of these l<strong>and</strong>marks were calculated. Cross correlation functions<br />

were used to <strong>in</strong>vestigate the motor coord<strong>in</strong>ation between the actions of<br />

the hip, the knee <strong>and</strong> the ankle. Results show that high-level swimmers<br />

regulate the leg amplitude thanks to a strong synergy between the hip<br />

<strong>and</strong> the ankle <strong>and</strong> an <strong>in</strong>dependent action of the knee.<br />

Key words: Motor control, start, underwater undulatory swimm<strong>in</strong>g<br />

INTRODUCTION<br />

High-level athletes are characterised by superior tactical, physical <strong>and</strong><br />

technical levels. Improv<strong>in</strong>g one of these factors will lead to a performance<br />

improvement. As <strong>in</strong> many other sports, swimm<strong>in</strong>g performance<br />

is strongly l<strong>in</strong>ked to the technical level of the swimmers. Swimm<strong>in</strong>g<br />

performance optimisation requires an accurate analysis of the swimmers’<br />

movement. <strong>Biomechanics</strong> <strong>and</strong> motor control sciences give useful tools<br />

to realise such analysis. Motor control theories, <strong>and</strong> more especially the<br />

jo<strong>in</strong>t synergies theories, will <strong>in</strong>deed help to underst<strong>and</strong> how high level<br />

swimmers are able to produce specific, appropriate <strong>and</strong> efficient motor<br />

pattern.<br />

Many previous researches have already shown that start performance<br />

is determ<strong>in</strong>ant to achieve a good race performance. Depend<strong>in</strong>g on the<br />

studies, start performance is def<strong>in</strong>ed as the time to complete the 10 or<br />

15 first meters from the start wall (Alves, 1993; Arellano et al., 1996;<br />

Mason <strong>and</strong> Cossor, 2000). The start consists of 3 phases: the impulsion<br />

phase, the aerial phase <strong>and</strong> the underwater phase (Maglischo, 2003).<br />

This underwater phase of the start could be divided <strong>in</strong> 2 phases, i.e. the<br />

glide phase <strong>and</strong> the underwater undulatory swimm<strong>in</strong>g phase (Maglischo,<br />

2003).<br />

Dur<strong>in</strong>g the glide, swimmers aim to keep the supra-maximal velocity<br />

created dur<strong>in</strong>g the impulsion <strong>and</strong> aerial phases as high as possible <strong>and</strong><br />

as long as possible. A previous study has already shown that dur<strong>in</strong>g the<br />

glide phase high level swimmers presented a strong jo<strong>in</strong>t synergy between<br />

the shoulders, the hip <strong>and</strong> the knee (Elipot et al, 2009). It seems<br />

that with this synergic action of those three jo<strong>in</strong>ts high level swimmers<br />

are able to hold a streaml<strong>in</strong>ed position dur<strong>in</strong>g the whole glide phase.<br />

Hydrodynamic resistance are decreased <strong>and</strong> supra-maximal velocity is<br />

kept longer. Dur<strong>in</strong>g the underwater undulatory swimm<strong>in</strong>g, the swimmers’<br />

aim is to produce velocities with leg action. Swimmers have then<br />

to f<strong>in</strong>d the optimal compromise between the amplitude <strong>and</strong> the frequency<br />

of the leg undulatory movements (Arellano, 2008). Swimmers<br />

have to f<strong>in</strong>d the optimal compromise between propulsion force creation<br />

<strong>and</strong> hydrodynamic resistance decrease. Identify<strong>in</strong>g the motor coord<strong>in</strong>ation<br />

dur<strong>in</strong>g this underwater undulatory swimm<strong>in</strong>g phase of the start is a<br />

major step to underst<strong>and</strong> <strong>and</strong> optimise this phase.<br />

The aim of this study was to determ<strong>in</strong>e the motor coord<strong>in</strong>ation that<br />

high-level swimmers are able to produce dur<strong>in</strong>g the underwater undulatory<br />

swimm<strong>in</strong>g phase of the start.<br />

72<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong><br />

Swimmers have then to f<strong>in</strong>d the optimal compromise between the amplitude <strong>and</strong> the<br />

frequency of the leg undulatory movements (Arellano, 2008). Swimmers have to f<strong>in</strong>d<br />

the optimal compromise between propulsion force creation <strong>and</strong> hydrodynamic<br />

resistance decrease. Identify<strong>in</strong>g the motor coord<strong>in</strong>ation dur<strong>in</strong>g this underwater<br />

undulatory swimm<strong>in</strong>g phase of the start is a major step to underst<strong>and</strong> <strong>and</strong> optimise this<br />

phase.<br />

Methods The aim of this study was to determ<strong>in</strong>e the motor coord<strong>in</strong>ation that high-level<br />

swimmers are able to produce dur<strong>in</strong>g the underwater undulatory swimm<strong>in</strong>g phase of the<br />

Subjects start. <strong>and</strong> <strong>in</strong>structions:<br />

Twelve male swimmers participated <strong>in</strong> this study. All were <strong>in</strong>formed of<br />

METHODS<br />

the Subjects aim of <strong>and</strong> the <strong>in</strong>structions: study <strong>and</strong> signed a consent form. All participants were<br />

high-level Twelve male swimmers participated <strong>and</strong> were <strong>in</strong> members this study. of All the were French <strong>in</strong>formed National of the aim of Swim- the<br />

study <strong>and</strong> signed a consent form. All participants were high-level swimmers <strong>and</strong> were<br />

m<strong>in</strong>g Team. Swimmers’ characteristics are summarized <strong>in</strong> Table 1.<br />

members of the French National Swimm<strong>in</strong>g Team. Swimmers’ characteristics are<br />

summarized <strong>in</strong> Table 1.<br />

Table 1. Swimmers’ general characteristics (n = 12).<br />

Table 1. Swimmers’ general characteristics (n = 12).<br />

Height (m) Weight ( kg)<br />

Best performance (freestyle)<br />

50-m (s) 50-m (%) 100-m (s) 100-m (%)<br />

Mean 1.83 76.1 24.39 116.47 52.26 111.4<br />

SD 4.89 5.18 1.26 6.02 1.68 3.57<br />

Swimmers were asked to perform 3 grab starts as fast as possible. Only the best<br />

start was analysed (i.e. the best time to complete 15 meters from the start wall). All<br />

swimmers were regularly tra<strong>in</strong>ed to perform this k<strong>in</strong>d of start <strong>and</strong> use it dur<strong>in</strong>g<br />

competition.<br />

Experimental set up <strong>and</strong> data analysis:<br />

Swimmers were filmed by 4 m<strong>in</strong>i-DV camcorders (576x720 pixels) dur<strong>in</strong>g the<br />

whole underwater phase of the start (i.e. fifteen meters from the start platform) (Fig. 1).<br />

The camcorder 1, 2 <strong>and</strong> 3 were placed the swimm<strong>in</strong>g pool portholes <strong>and</strong> the camcorder<br />

4 was placed <strong>in</strong> the water <strong>in</strong> a waterproof hous<strong>in</strong>g. The camcorders position has been<br />

chosen so as to m<strong>in</strong>imise to reconstruction error due to optical distortions (Snell low).<br />

All camcorders were synchronised us<strong>in</strong>g a light signal <strong>and</strong> sampl<strong>in</strong>g frequency was<br />

25Hz. Images were de<strong>in</strong>terlaced <strong>and</strong> odd <strong>and</strong> even fields were both used.<br />

N<strong>in</strong>e anatomical l<strong>and</strong>marks were identified on swimmer’s body: the toe, the<br />

lateral malleolus, the knee, the iliac sp<strong>in</strong>e, the acromion, a f<strong>in</strong>ger hip, the wrist, the<br />

elbow <strong>and</strong> the centre of the head. To m<strong>in</strong>imise the error dur<strong>in</strong>g the digitis<strong>in</strong>g process,<br />

only the right side of the swimmers has been identified. Both sides were supposed to be<br />

symmetric. Us<strong>in</strong>g a modified DLT 2D technique (<strong>in</strong>spired from Drenk et al., 1999) <strong>and</strong><br />

the Dempster anthropometric data (Dempster, 1959), jo<strong>in</strong>ts’ positions <strong>and</strong> swimmers’<br />

centre of mass position have been calculated. Reconstruction error was calculated as<br />

<strong>in</strong>dicated by Kwon <strong>and</strong> Casebolt (2006). Mean reconstruction error was 6.2 mm <strong>and</strong><br />

maximal reconstruction error was 12.2 mm. Data were filtered us<strong>in</strong>g a Butterworth II<br />

filter (W<strong>in</strong>ter, 1990). Cut-off frequencies were <strong>in</strong>cluded between 5 Hz <strong>and</strong> 7 Hz.<br />

Swimmers were asked to perform 3 grab starts as fast as possible. Only<br />

the best start was analysed (i.e. the best time to complete 15 meters from<br />

the start wall). All swimmers were regularly tra<strong>in</strong>ed to perform this k<strong>in</strong>d<br />

of start <strong>and</strong> use it dur<strong>in</strong>g competition.<br />

Experimental set up <strong>and</strong> data analysis:<br />

Swimmers were filmed by 4 m<strong>in</strong>i-DV camcorders (576x720 pixels)<br />

dur<strong>in</strong>g the whole underwater phase of the start (i.e. fifteen meters from<br />

the start platform) (Fig. 1). The camcorder 1, 2 <strong>and</strong> 3 were placed the<br />

swimm<strong>in</strong>g pool portholes <strong>and</strong> the camcorder 4 was placed <strong>in</strong> the water<br />

<strong>in</strong> a waterproof hous<strong>in</strong>g. The camcorders position has been chosen so<br />

as to m<strong>in</strong>imise to reconstruction error due to optical distortions (Snell<br />

low). All camcorders were synchronised us<strong>in</strong>g a light signal <strong>and</strong> sampl<strong>in</strong>g<br />

frequency was 25Hz. Images were de<strong>in</strong>terlaced <strong>and</strong> odd <strong>and</strong> even<br />

fields were both used.<br />

N<strong>in</strong>e anatomical l<strong>and</strong>marks were identified on swimmer’s body: the<br />

toe, the lateral malleolus, the knee, the iliac sp<strong>in</strong>e, the acromion, a f<strong>in</strong>ger<br />

hip, the wrist, the elbow <strong>and</strong> the centre of the head. To m<strong>in</strong>imise the<br />

error dur<strong>in</strong>g the digitis<strong>in</strong>g process, only the right side of the swimmers<br />

has been identified. Both sides were supposed to be symmetric. Us<strong>in</strong>g a<br />

modified DLT 2D technique (<strong>in</strong>spired from Drenk et al., 1999) <strong>and</strong> the<br />

Dempster anthropometric data (Dempster, 1959), jo<strong>in</strong>ts’ positions <strong>and</strong><br />

swimmers’ centre of mass position have been calculated. Reconstruction<br />

error was calculated as <strong>in</strong>dicated by Kwon <strong>and</strong> Casebolt (2006). Mean<br />

reconstruction error was 6.2 mm <strong>and</strong> maximal reconstruction error<br />

was 12.2 mm. Data were filtered us<strong>in</strong>g a Butterworth II filter (W<strong>in</strong>ter,<br />

1990). <strong>Biomechanics</strong> Cut-off <strong>and</strong> frequencies <strong>Medic<strong>in</strong>e</strong> <strong>XI</strong> were <strong>in</strong>cluded Chapter 2 <strong>Biomechanics</strong> between 5 Hz <strong>and</strong> 7 Hz.<br />

Camcorder 1<br />

Camcorder<br />

2<br />

Camcorder<br />

3<br />

Figure 1. Experimental set up<br />

Figure 1. Experimental set up<br />

To avoid between-subjects variations due to the slope of the trajectory to reach the<br />

To water avoid surface, between-subjects data were expressed variations <strong>in</strong> a (O’, due n, t to ,b) the local slope reference of the frame trajectory attached to the<br />

swimmers’ centre of mass <strong>and</strong> with n coll<strong>in</strong>ear to the velocity vector <strong>and</strong> t perpendicular<br />

to reach the water surface, data were expressed <strong>in</strong> a (O’, n, t ,b) local<br />

to n (Fresney frame of reference). Dur<strong>in</strong>g the whole underwater phase, the velocity of<br />

reference the centre of frame mass, attached the jo<strong>in</strong>t positions, to the swimmers’ velocities <strong>and</strong> centre angles of for mass the hip, <strong>and</strong> the with knee n <strong>and</strong> the<br />

coll<strong>in</strong>ear ankle, the to angles the velocity between vector the x-axis <strong>and</strong> <strong>and</strong> t perpendicular the limbs (angle to of n (Fresney attack) were frame calculated.<br />

of Only reference). the jo<strong>in</strong>ts longitud<strong>in</strong>al Dur<strong>in</strong>g the <strong>and</strong> whole vertical underwater positions were phase, expressed the velocity <strong>in</strong> the orig<strong>in</strong>al of the global<br />

frame (O, x, y, z).<br />

centre Motor of mass, coord<strong>in</strong>ation the jo<strong>in</strong>t was positions, <strong>in</strong>vestigated velocities by comput<strong>in</strong>g <strong>and</strong> angles the cross for correlation the hip, the functions<br />

knee between <strong>and</strong> all the ankle, calculated the k<strong>in</strong>ematics angles between variables. the These x-axis k<strong>in</strong>ematic <strong>and</strong> the data limbs were (angle represented<br />

of <strong>in</strong> form attack) of were time-dependent calculated. signals. Only the Results jo<strong>in</strong>ts were longitud<strong>in</strong>al obta<strong>in</strong>ed us<strong>in</strong>g <strong>and</strong> Matlab vertical software posi- (The<br />

Matworks Inc., USA). Level of confidence was set at 95% (p


elation functions between all the calculated k<strong>in</strong>ematics variables. These<br />

k<strong>in</strong>ematic data were represented <strong>in</strong> form of time-dependent signals. Results<br />

were obta<strong>in</strong>ed us<strong>in</strong>g Matlab software (The Matworks Inc., USA).<br />

Level of confidence was set at 95% (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Kwon, Y. H. & Casebolt, J. B. (2006). Effects of light refraction on the<br />

accuracy of camera calibration <strong>and</strong> reconstruction <strong>in</strong> underwater motion<br />

analysis. Sports <strong>Biomechanics</strong>, 5, 95-120.<br />

Maglischo, E. W. (2003). Swimm<strong>in</strong>g fastest. Champaign: Human K<strong>in</strong>etics.<br />

Mason, B. & Cossor, J. (2000). What can we learn from competition<br />

analysis at the 1999 Pan Pacific Swimm<strong>in</strong>g Championships? In R.<br />

S<strong>and</strong>ers & Y. Hong (Eds.), Proceed<strong>in</strong>gs of XVIII Symposium on <strong>Biomechanics</strong><br />

<strong>in</strong> Sports (pp. 75-82). Hong Kong, Ch<strong>in</strong>a: The Ch<strong>in</strong>ese University<br />

of Hong Kong.<br />

Rejman, M. & Ochmann, B. (2005). Application of artificial neural<br />

networks <strong>in</strong> monof<strong>in</strong> swimm<strong>in</strong>g technique assessment. The Human<br />

Movements, 6, 24-33.<br />

W<strong>in</strong>ter, D. A. (1990). <strong>Biomechanics</strong> <strong>and</strong> motor control of human movement.<br />

New York: A. Wiley-Interscience Publication.<br />

AcKnoWledGeMents<br />

The authors wish to thank the “M<strong>in</strong>istère de la Jeunesse, des Sports et<br />

de la Vie Associative” <strong>and</strong> the “Fédération Française de Natation” for<br />

f<strong>in</strong>anc<strong>in</strong>g this study. The authors also wish to thank Frédéric Frontier,<br />

Frédéric Clerc, Isabelle Amaudry <strong>and</strong> the “INSEP” for logistic support,<br />

<strong>and</strong> Jean-Lyonel Rey, Stéphane Lecat, Eric Boissière <strong>and</strong> Yves Thomass<strong>in</strong><br />

for their contributions.<br />

74<br />

Relationship between Arm Coord<strong>in</strong>ation <strong>and</strong> Energy<br />

Cost <strong>in</strong> Front Crawl Swimm<strong>in</strong>g<br />

Fern<strong>and</strong>es, r.J. 1 , Morais, P. 1 , Kesk<strong>in</strong>en, K.l. 2 , seifert, l. 3 ,<br />

chollet, d. 3 , Vilas-Boas, J.P. 1<br />

1 University of Porto, Faculty of Sport, Cifi2d, Portugal<br />

2 F<strong>in</strong>nish Society of Sport Sciences, F<strong>in</strong>l<strong>and</strong><br />

3 University of Rouen, Faculty of Sport Sciences, France<br />

The aim of the study was to assess the relationship between the Index of<br />

Coord<strong>in</strong>ation (IdC) <strong>and</strong> the Energy Cost of exercise (C) <strong>in</strong> front crawl<br />

swimm<strong>in</strong>g. Seven high level swimmers performed a paced <strong>in</strong>termittent<br />

<strong>in</strong>cremental protocol of 7 × 200 m (0.05 m.s -1 <strong>in</strong>crements, 30 s <strong>in</strong>tervals),<br />

until maximal oxygen consumption <strong>in</strong>tensities. IdC was assessed as the<br />

time gap between the propulsion of the two arms. Oxygen consumption<br />

was measured through direct breath×breath oximetry <strong>and</strong> lactate analyses<br />

were conducted at rest, <strong>in</strong> the <strong>in</strong>tervals <strong>and</strong> at the end of exercise.<br />

Along the protocol, concomitant with the velocity raise, both C <strong>and</strong> IdC<br />

<strong>in</strong>creased (r=0.98 <strong>and</strong> r=0.99, p


for displac<strong>in</strong>g the body over a given unit of distance (Zamparo et al, 2005).<br />

Furthermore, it is accepted as an important bioenergetical determ<strong>in</strong>ant<br />

of swimm<strong>in</strong>g performance (Wakayoshi et al, 1995; Kjendlie et al., 2004;<br />

Fern<strong>and</strong>es et al., 2006). However, the body of scientific literature needs<br />

approaches on the relationships between the IdC <strong>and</strong> the C <strong>in</strong> try<strong>in</strong>g to<br />

underst<strong>and</strong> how these two variables may be connected. The present study<br />

aimed at assess<strong>in</strong>g relationships between the IdC <strong>and</strong> the C <strong>in</strong> front crawl,<br />

especially at <strong>in</strong>tensities rang<strong>in</strong>g between ~70 % <strong>and</strong> 100% of the maximal<br />

oxygen consumption ( V � O 2 max). We hypothesised that if velocity is<br />

controlled, IdC <strong>and</strong> C are <strong>in</strong>versely related.<br />

Methods<br />

Seven high-level swimmers (17.0 ± 1.8 years; 168.0 ± 8.8 cm; 58.4 ± 8.2<br />

kg) participant <strong>in</strong> national swimm<strong>in</strong>g championships were tested. Mean<br />

(± SD) ma<strong>in</strong> physiological characteristics were: 18.0 (6.9) % of fat mass,<br />

54.9 (10.1) ml.kg -1 .m<strong>in</strong> -1 of V � O 2 max <strong>and</strong> 7.5 (2.4) of blood lactate<br />

concentrations ([La - ]) at <strong>in</strong>tensities correspond<strong>in</strong>g to V � O 2 max. In an<br />

<strong>in</strong>door 25 m swimm<strong>in</strong>g pool, the participants performed an <strong>in</strong>termittent<br />

<strong>in</strong>cremental protocol, with <strong>in</strong>crements of 0.05 m·s -1 each 200 m stage (<strong>and</strong><br />

30 s <strong>in</strong>tervals), until exhaustion (Fern<strong>and</strong>es et al., 2003). Initial velocity<br />

was established accord<strong>in</strong>g to the <strong>in</strong>dividual level of fitness <strong>and</strong> was set<br />

at the swimmer’s <strong>in</strong>dividual performance on the 400 m freestyle m<strong>in</strong>us<br />

seven <strong>in</strong>crements of velocity. Swimm<strong>in</strong>g velocity was controlled us<strong>in</strong>g a<br />

visual pacer (TAR 1.1, GBK-electronics, Aveiro, Portugal) with successive<br />

flash<strong>in</strong>g lights, 2.5 m apart, on the bottom of the pool.<br />

V � O 2 was measured through direct breath-by-breath oximetry (K4<br />

b 2 , Cosmed, Rome, Italy) connected to the swimmer by a respiratory snorkel<br />

<strong>and</strong> valve system (Kesk<strong>in</strong>en et al., 2003). Capillary blood samples (25<br />

µl) for [La - ] analysis were collected from the earlobe at rest, <strong>in</strong> the 30 s rest<br />

<strong>in</strong>terval, at the end of exercise <strong>and</strong> dur<strong>in</strong>g the recovery period (YSI1500L-<br />

Sport auto-analyser, Yellow Spr<strong>in</strong>gs Incorporated, Ohio, USA). The C was<br />

calculated by divid<strong>in</strong>g total energy expenditure (Ė) by velocity (v) <strong>and</strong><br />

converted to SI units, were 1 mlO 2 is equivalent to 20.1 J (Zamparo et al.,<br />

2005; Fern<strong>and</strong>es et al., 2006):<br />

C = Ė /v (1)<br />

The Ė corrected for body mass was calculated us<strong>in</strong>g the V � O 2 net (difference<br />

between the value measured <strong>in</strong> the end of the stage <strong>and</strong> the rest<br />

value), <strong>and</strong> the blood lactate net (difference between the value measured<br />

<strong>in</strong> two consecutive stages) transformed <strong>in</strong>to V � O 2 equivalents us<strong>in</strong>g a<br />

2.7mlO 2 kg -1 mmol -1 proportionality constant <strong>and</strong> by Equation (2) (cf.<br />

Fern<strong>and</strong>es et al., 2006)<br />

Ė = V� O2net + [La-]net (2)<br />

Two video cameras (JVC GR-SX1 SVHS <strong>and</strong> JVC GR-SXM 25 SVHS)<br />

were fixed on the lateral wall of the pool at a 10 m distance perpendicular<br />

to the swimmers’ plane of movement. The cameras were connected to<br />

a double entry <strong>and</strong> edited on a mix<strong>in</strong>g table (Panasonic Digital Mixer<br />

WJ-AVE55 VHS), provid<strong>in</strong>g a dual-media image (Panasonic AG 7355),<br />

below <strong>and</strong> above the water surface (Vilas-Boas et al., 2006), at a frequency<br />

of 50 Hz (1:250/s shutter speed).<br />

For each step of the <strong>in</strong>cremental protocol, two arm strokes were analysed<br />

<strong>in</strong> every 50 m of the 200 m. Arm strok<strong>in</strong>g coord<strong>in</strong>ation was obta<strong>in</strong>ed<br />

through IdC (Chollet et al., 2000), be<strong>in</strong>g each arm stroke broken down<br />

<strong>in</strong>to four phases: (i) entry <strong>and</strong> catch (correspond<strong>in</strong>g to the time between<br />

the entry of the h<strong>and</strong> <strong>in</strong>to the water <strong>and</strong> the beg<strong>in</strong>n<strong>in</strong>g of its backward<br />

movement); (ii) pull (correspond<strong>in</strong>g to the time between the beg<strong>in</strong>n<strong>in</strong>g<br />

of the h<strong>and</strong>’s backward movement <strong>and</strong> its arrival <strong>in</strong> a vertical plane to the<br />

shoulder); (iii) push (correspond<strong>in</strong>g to the time from the position of the<br />

h<strong>and</strong> below the shoulder to its release from the water) <strong>and</strong> (iv) recovery<br />

(correspond<strong>in</strong>g to the po<strong>in</strong>t of water release to water re-entry of the arm,<br />

i.e., the above water phase). The duration of each phase was measured<br />

for each arm-stroke cycle with a precision of 0.02 s. The duration of the<br />

propulsive phases was the addition of the pull <strong>and</strong> the push phases, <strong>and</strong><br />

the duration of the non-propulsive phases was obta<strong>in</strong>ed by the sum of<br />

chaPter2.<strong>Biomechanics</strong><br />

the catch <strong>and</strong> the recovery phases (the duration of a complete arm-stroke<br />

was the sum of the propulsive <strong>and</strong> non-propulsive phases). The IdC was<br />

calculated as the time gap between the propulsion of the two arms as a<br />

percentage of the duration of the complete arm stroke cycle. Higher negative<br />

percentage values expressed an evident discont<strong>in</strong>uity <strong>in</strong> the <strong>in</strong>ter-arm<br />

propulsion, tend<strong>in</strong>g to IdC=0% as the time gap was dim<strong>in</strong>ish<strong>in</strong>g.<br />

Mean ± SD computations for descriptive analysis were obta<strong>in</strong>ed <strong>in</strong><br />

each stage for all variables (all data were checked for distribution normality<br />

with the Shapiro-Wilk test). Pearson correlation coefficient <strong>and</strong> partial<br />

correlation were applied. Level of significance was established at 5%.<br />

results<br />

The mean ± SD values of velocity, % V � O 2 max, C, <strong>and</strong> IdC, obta<strong>in</strong>ed <strong>in</strong><br />

each step dur<strong>in</strong>g the <strong>in</strong>termittent <strong>in</strong>cremental test, are presented <strong>in</strong> Table<br />

1. An <strong>in</strong>crease of swimm<strong>in</strong>g <strong>in</strong>tensity implies an <strong>in</strong>crease of both C <strong>and</strong><br />

IdC (Table 1).<br />

Table 1. Mean values of velocity, % V� O2max, IdC <strong>and</strong> C obta<strong>in</strong>ed <strong>in</strong><br />

each 200 m step of the <strong>in</strong>cremental protocol (n=7).<br />

Step velocity (m·s-1 ) % V� O2max C ( J·kg-1 ·m-1 1 1.15 ± 0.1 72.1 ± 8.7<br />

)<br />

9.4 ± 2.5<br />

IdC (%)<br />

-12.5 ± 2.5<br />

2 1.20 ± 0.1 76.5 ± 9.1 10.3 ± 2.8 -12.1 ± 2.7<br />

3 1.25 ± 0.1 77.8 ± 5.3 10.1 ± 3.0 -11.8 ± 2.6<br />

4 1.30 ± 0.1 85.5 ± 3.3 11.5 ± 3.2 -10.9 ± 2.6<br />

5 1.35 ± 0.1 90.9 ± 3.2 12.7 ± 2.8 -9.7 ± 2.7<br />

6 1.40 ± 0.1 97.3 ± 3.2 13.7 ± 2.4 -8.2 ± 2.7<br />

7 1.45 ± 0.1 100.0 ± 0.0 14.0 ± 4.2 -6.8 ± 2.5<br />

The relationships between velocity <strong>and</strong> C, <strong>and</strong> velocity <strong>and</strong> IdC are<br />

shown <strong>in</strong> Fig. 1 (left panel), be<strong>in</strong>g possible to observe a high correlation<br />

value between these variables (r=0.98 <strong>and</strong> r=0.99, respectively, both for<br />

p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

dIscussIon<br />

Despite a previous case study by Morais et al. (2008), <strong>and</strong> a study that was<br />

conducted with spr<strong>in</strong>t swimmers perform<strong>in</strong>g at <strong>in</strong>cremental sub-maximal<br />

<strong>in</strong>tensities (Komar et al., 2010), the present study is the first that aimed to<br />

relate IdC <strong>and</strong> C <strong>in</strong> front crawl. The present results agree with both the<br />

referred studies, f<strong>in</strong>d<strong>in</strong>g positive <strong>and</strong> significant r values between both variables.<br />

In this study, however, it was confirmed that this is true for velocity<br />

values rang<strong>in</strong>g from very low to heavy exercise <strong>in</strong>tensities (~ V � O2max).<br />

All swimmers reached their maximal aerobic power dur<strong>in</strong>g the <strong>in</strong>cremental<br />

protocol, which was assured by traditional physiological criteria (cf.<br />

Fern<strong>and</strong>es et al., 2003). Subjects presented V � O2max mean values similar<br />

to those described <strong>in</strong> the literature for experienced competitive swimmers<br />

(Wakayoshi et al, 1995; Rodriguez <strong>and</strong> Mader, 2003; Fern<strong>and</strong>es et al., 2006).<br />

The obta<strong>in</strong>ed mean values of [La - ]max are <strong>in</strong> accordance with the literature<br />

for <strong>in</strong>tensities of exercise correspond<strong>in</strong>g to V � O2max (Fern<strong>and</strong>es et al.,<br />

2003; Rodriguez <strong>and</strong> Mader, 2003; Fern<strong>and</strong>es et al., 2006).<br />

Along the <strong>in</strong>cremental protocol it was observed that an <strong>in</strong>crease <strong>in</strong> the<br />

swimm<strong>in</strong>g <strong>in</strong>tensity led to an <strong>in</strong>crease of the IdC. This is consistent with<br />

previous studies that showed a raise of IdC values with <strong>in</strong>creas<strong>in</strong>g race paces,<br />

namely from 1500/800 to 50 m freestyle (Chollet et al., 2000; Seifert et al.,<br />

2004; Seifert et al., 2007). This <strong>in</strong>crease seems to be a strategy that swimmers<br />

use to overcome higher active drag that is related with higher swimm<strong>in</strong>g<br />

velocity (Seifert et al., 2004). These data also reveals that swimmers changed<br />

their arm stroke coord<strong>in</strong>ation, from moderate to heavy exercise <strong>in</strong>tensities, <strong>in</strong><br />

order to be able to reach higher swimm<strong>in</strong>g velocity. In fact, this shift <strong>in</strong> IdC<br />

from a catch-up pattern to a pattern closer to the opposition coord<strong>in</strong>ation<br />

mode, aim<strong>in</strong>g to achieve higher propulsive cont<strong>in</strong>uity at V � O 2 max swimm<strong>in</strong>g<br />

<strong>in</strong>tensity, was also described before (Chollet et al., 2000; Seifert et al.,<br />

2004; Seifert et al., 2007). The values of IdC obta<strong>in</strong>ed <strong>in</strong> the present study<br />

were similar to those obta<strong>in</strong>ed <strong>in</strong> the previously mentioned studies <strong>and</strong> it did<br />

not reach positive values s<strong>in</strong>ce IdC>0% only occurs after 93% of the swimmers<br />

maximal velocity, which corresponds to the 100 m maximal velocity<br />

(Seifert et al., 2004).<br />

Such as the IdC, the C values also <strong>in</strong>creased with velocity. This fact has<br />

been described before for front crawl stroke with similar C values (Zamparo<br />

et al., 2005; Morais et al., 2008; Komar et al, 2010), <strong>and</strong> seems to be justified<br />

by the <strong>in</strong>creas<strong>in</strong>g power output (P = Dv) necessary to overcome drag (D),<br />

<strong>and</strong> presumably by the <strong>in</strong>crease <strong>in</strong> <strong>in</strong>ternal work associated with a higher<br />

stroke rate.<br />

The ma<strong>in</strong> f<strong>in</strong>d<strong>in</strong>g of this study was the very high direct relationship between<br />

IdC <strong>and</strong> C, which is, as stated, <strong>in</strong> accordance with previous studies <strong>in</strong><br />

swimm<strong>in</strong>g, but also <strong>in</strong> human terrestrial locomotion, namely <strong>in</strong> the walk-run<br />

transition (cf. Seifert et al., 2007). Studies have been carried out <strong>in</strong> order<br />

to relate the C with other biomechanical parameters. Barbosa et al. (2008)<br />

showed that the C is highly related to stroke parameters, namely with stroke<br />

rate <strong>and</strong> stroke length, while Chatard et al. (1990) showed that C is dependent<br />

on swimm<strong>in</strong>g technique. In this sense, after observ<strong>in</strong>g that the IdC, a<br />

coord<strong>in</strong>ative parameter, is strongly related with C, our results seems to be<br />

consistent with literature (Alberty et al., 2005), <strong>in</strong>dicat<strong>in</strong>g that the mode of<br />

coord<strong>in</strong>ation might be an <strong>in</strong>dividual response to physiological constra<strong>in</strong>ts<br />

associated to the task. However, despite the agreement of the results of other<br />

approaches, the simple analysis of the r value obta<strong>in</strong>ed between IdC <strong>and</strong> C<br />

shows that the C <strong>in</strong>crease with the <strong>in</strong>creased cont<strong>in</strong>uity of technique (higher<br />

IdC), which seems to be paradoxal, be<strong>in</strong>g probably expla<strong>in</strong>able by the fact<br />

that both parameters are strongly <strong>in</strong>fluenced by velocity (as shown <strong>in</strong> fig.<br />

1). In accordance, we decided to analyse the partial correlation of the two<br />

variables remov<strong>in</strong>g the effect of velocity. Surpris<strong>in</strong>gly, IdC <strong>and</strong> C did not<br />

correlate significantly (r=0.42, p=0.40). Furthermore, the obta<strong>in</strong>ed r value<br />

rema<strong>in</strong>s positive, while it was theoretically expected a negative relationship.<br />

Indeed, we hypothesised that, controll<strong>in</strong>g the velocity effect, the reduction of<br />

propulsive discont<strong>in</strong>uities should allow the front crawl technique to become<br />

more economical, <strong>in</strong>stead of imply<strong>in</strong>g higher energy costs. Samples with<br />

higher number of subjects as well as other factors (e.g. <strong>in</strong>tracyclic velocity<br />

variation) should be searched to expla<strong>in</strong> these apparently conflict<strong>in</strong>g f<strong>in</strong>d<strong>in</strong>gs.<br />

Particularly, we recommend to study IdC <strong>and</strong> C at the same swimm<strong>in</strong>g<br />

76<br />

velocity performed <strong>in</strong> different subjects, <strong>and</strong> <strong>in</strong> the same subjects manipulat<strong>in</strong>g<br />

coord<strong>in</strong>ation.<br />

reFerences<br />

Alberty, M., Sidney, M., Huot-March<strong>and</strong>, F., Hespel, J. M. & Pelayo, P.<br />

(2005) Intracyclic velocity variations <strong>and</strong> arm coord<strong>in</strong>ation dur<strong>in</strong>g exhaustive<br />

exercise <strong>in</strong> front crawl stroke. Int J Sports Med, 26(6), 471-5.<br />

Barbosa, T. M., Fern<strong>and</strong>es, R. J., Kesk<strong>in</strong>en, K. L. & Vilas-Boas, J. P. (2008).<br />

The <strong>in</strong>fluence of stroke mechanics <strong>in</strong>to energy cost of elite swimmers. Eur<br />

J Appl Physiol, 103(2), 139-49.<br />

Chatard, J. C., Collomp, C., Maglischo, E. & Maglischo, C. (1990). Swimm<strong>in</strong>g<br />

skill <strong>and</strong> strok<strong>in</strong>g characteristics of front crawl swimmers. Int J<br />

Sports Med, 11(2), 156-61.<br />

Chollet, D., Chalies, S. & Chatard, J. C. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: description <strong>and</strong> usefulness. Int J Sports Med, 21(1), 54-9.<br />

Fern<strong>and</strong>es, R. J., Cardoso, C. S., Soares, S. M., Ascensão, A., Colaco, P. J. &<br />

Vilas-Boas, J. P. (2003). Time limit <strong>and</strong> VO2 slow component at <strong>in</strong>tensities<br />

correspond<strong>in</strong>g to VO2max <strong>in</strong> swimmers. Int J Sports Med, 24(8),<br />

576-81.<br />

Fern<strong>and</strong>es, R. J., Billat, V. L., Cruz, A. C., Colaço, P. J., Cardoso, C. S. &<br />

Vilas-Boas, J. P. (2006). Does net energy cost of swimm<strong>in</strong>g affect time<br />

to exhaustion at the <strong>in</strong>dividual’s maximal oxygen consumption velocity? J<br />

Sports Med Phys Fitness, 46(3), 373-80.<br />

Kjendlie, P. L., Ingjer, F., Stallman, R. & Stray-Gundersen, J. (2004). Factors<br />

affect<strong>in</strong>g swimm<strong>in</strong>g economy <strong>in</strong> children <strong>and</strong> adults. Eur J Appl Physiol,<br />

93, 1164-8.<br />

Komar, J., Leprêtre, P. M., Alberty, M., Vantorre, J., Fern<strong>and</strong>es, R.J., Hellard,<br />

et al. (2010). Effect of Increas<strong>in</strong>g Energy Cost on Arm Coord<strong>in</strong>ation<br />

at Different Exercise Intensities <strong>in</strong> Elite Spr<strong>in</strong>t Swimmers. In: Kjendlie,<br />

P.L., Stallman, R.K. & Cabri, J. (eds.). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g <strong>XI</strong>. Oslo. In Press.<br />

Kesk<strong>in</strong>en, K. L. & Komi, P. V. (1993). Strok<strong>in</strong>g characteristics of front crawl<br />

swimm<strong>in</strong>g dur<strong>in</strong>g exercise. J Appl Biomech, 9, 219-26.<br />

Kesk<strong>in</strong>en, K. L., Rodríguez, F. A. & Kesk<strong>in</strong>en, O. P. (2003). Respiratory<br />

snorkel <strong>and</strong> valve system for breath-by-breath gas analysis <strong>in</strong> swimm<strong>in</strong>g.<br />

Sc<strong>and</strong> J Med Sci Sports, 13, 322-29.<br />

Morais, P., Vilas-Boas, J. P., Seifert, L., Chollet, D., Kesk<strong>in</strong>en, K.L. & Fern<strong>and</strong>es,<br />

R. (2008). Relationship between energy cost <strong>and</strong> the <strong>in</strong>dex of<br />

coord<strong>in</strong>ation <strong>in</strong> crawl - a pilot study. J Sport Sci, 26(Suppl. 1), 11.<br />

Rodriguez, F. A. & Mader, A. (2003). Energy metabolism dur<strong>in</strong>g 400<br />

<strong>and</strong> 100m crawl swimm<strong>in</strong>g: Computer simulation based on free swimm<strong>in</strong>g<br />

measurements. In: Chatard, J. C. (ed.). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g IX. Sa<strong>in</strong>t-Étienne: Publications de l’Université de Sa<strong>in</strong>t-<br />

Étienne, 373-378.<br />

Seifert, L., Chollet, D. & Bardy, B. G. (2004). Effect of swimm<strong>in</strong>g velocity<br />

on arm coord<strong>in</strong>ation <strong>in</strong> the front crawl: a dynamic analysis. J Sports Sci,<br />

22(7), 651-60.<br />

Seifert, L., Chollet, D. & Rouard, A. (2007). Swimm<strong>in</strong>g constra<strong>in</strong>ts <strong>and</strong> arm<br />

coord<strong>in</strong>ation. Hum Mov Sci, 26(1), 68-86.<br />

Vilas-Boas, J. P. (1996). Speed fluctuations <strong>and</strong> energy cost with different<br />

breaststroke techniques, In: Troup J, Holl<strong>and</strong>er AP, Strass D (eds.). <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VII. London: E&FN SPON, 167-<br />

171.<br />

Vilas-Boas, J. P., Cunha, P., Figueiras, T., Ferreira, M. & Duarte, J. A. (1996).<br />

Movement analysis <strong>in</strong> simultaneous swimm<strong>in</strong>g techniques. In: Wilke<br />

K, Daniel K, Hoffmann U, Klauck, J (eds.). Symposiumsbericht Kolner<br />

Schwimmsportage. Bockenem: Sport Fahnemann Verlag, 95-103.<br />

Wakayoshi, K., D’Acquisto, L., Cappaert, J. & Troup, J. (1995). Relationship<br />

between oxygen uptake, stroke rate <strong>and</strong> swimm<strong>in</strong>g velocity <strong>in</strong> competitive<br />

swimm<strong>in</strong>g. Int J Sports Med, 16(1), 19-23.<br />

Zamparo, P., Pendargast, D., Mollendorf, J., Term<strong>in</strong>, A. & M<strong>in</strong>etti, A. (2005).<br />

An Energy Balance of Front Crawl. Eur J Appl Physiol, 94, 134-44.<br />

AcKnoWledGeMents<br />

This study was supported by grant: PTDC/DES/101224/2008


Evaluation of the Validity of Radar for Measur<strong>in</strong>g<br />

Throw<strong>in</strong>g Velocities <strong>in</strong> Water Polo<br />

Ferragut, c. 1 , Alcaraz, P.e. 1 , Vila, h. 1 , Abraldes, J.A. 2 , rodriguez,<br />

n. 1<br />

1Department of Sport Sciences, San Antonio Catholic University, Murcia,<br />

Spa<strong>in</strong><br />

2Department of Sport Sciences, University of Murcia, San Javier (Murcia),<br />

Spa<strong>in</strong><br />

Many studies have been published report<strong>in</strong>g measurements of<br />

velocity of balls, implements <strong>and</strong> corporal segments <strong>in</strong> sports<br />

where those skills are basic for performance. Skill <strong>in</strong> pass<strong>in</strong>g <strong>and</strong><br />

throw<strong>in</strong>g is vital <strong>in</strong> Water Polo because accuracy <strong>and</strong> the ability<br />

to produce high velocities are also valuable dur<strong>in</strong>g the game for<br />

shots at goal. The aim of the present study was twofold; firstly to<br />

evaluate the validity of the radar gun measurements versus high<br />

velocity 2D photogrammetric analysis, <strong>in</strong> two different situation,<br />

<strong>and</strong> secondly, to establish a valid methodology to asses throw<strong>in</strong>g<br />

velocity <strong>in</strong> Water Polo. The participants carried out 48 throws at<br />

maximum <strong>in</strong>tensity from the penalty position (24 throws), <strong>and</strong><br />

from an oblique position to the goal (θ ~ 20º) <strong>in</strong> the same penalty<br />

l<strong>in</strong>e (24 throws) with <strong>and</strong> without goalkeeper. They executed<br />

throws by alternat<strong>in</strong>g manner with a 3-m<strong>in</strong> rest between each.<br />

The ball maximum velocity was measured with radar gun placed<br />

ten meters beh<strong>in</strong>d the goal, <strong>and</strong> aligned with the penalty l<strong>in</strong>e.<br />

Simultaneously; a 2D photogrammetric study was accomplished.<br />

The camera was mounted on a rigid tripod at a height of 1.0 m<br />

<strong>and</strong> placed at a distance of 10 m from the middle of the athlete’s<br />

lane. The optical axis of the camera was perpendicular to the direction<br />

of throw<strong>in</strong>g for each different situation. One trial by each<br />

participant for each throw condition was analyzed. Pearson correlation<br />

coefficients were used to determ<strong>in</strong>e the <strong>in</strong>terrelationship<br />

among the maximum velocity obta<strong>in</strong>ed by the radar gun <strong>and</strong> the<br />

2D analysis. For frontal throws without goalkeeper the ICC was<br />

0.96, <strong>and</strong> with goalkeeper was 0.84. Analyz<strong>in</strong>g throws <strong>in</strong> oblique<br />

situation (θ ~ 20º), the ICC was 0.94 without goalkeeper <strong>and</strong><br />

0.96 with goalkeeper. All throws <strong>in</strong> the frontal situation showed a<br />

correlation coefficient of r = 0.91 <strong>and</strong> <strong>in</strong> the oblique position the<br />

correlation coefficient was r = 0.94 (p ≤ 0.001). In conclusion, the<br />

radar gun is a valid method to measure throw<strong>in</strong>g velocity <strong>in</strong> water<br />

polo, both for frontal as well as for oblique throws.<br />

Key words: Validity, Photogrammetric, 2d, radar gun, water polo<br />

throw<strong>in</strong>g, water polo<br />

IntroductIon<br />

In the last decades, many studies have been published be<strong>in</strong>g <strong>in</strong>terested<br />

<strong>in</strong> the measurement of velocity of balls, implements <strong>and</strong> corporal segments<br />

<strong>in</strong> sports where those skills are basic for performance. (DeRenne,<br />

Ho, & Blitzblau, 1990; Gorostiaga, Granados et al, 2005; Granados,<br />

Izquierdo et al. 2007; Lachowetz, Evon et al., 1998; McCluskey et al.;<br />

Skoufas, Stefanidis et al, 2003; Van den Tillaar & Ettema, 2004, Van<br />

den Tillaar & Ettema, 2007).<br />

Skill <strong>in</strong> pass<strong>in</strong>g <strong>and</strong> throw<strong>in</strong>g is vital <strong>in</strong> water polo because accuracy<br />

<strong>and</strong> the ability to produce high velocities are also valuable dur<strong>in</strong>g the<br />

game for shots at the goal. Two basic factors are of importance with<br />

regard to the efficiency of shots: accuracy <strong>and</strong> throw<strong>in</strong>g velocity. Naturally,<br />

the faster the ball is thrown at the goal, the less time defenders <strong>and</strong><br />

goalkeeper have to save the shot (Muijtjens, Joris et al, 1991). For these<br />

reasons, evaluat<strong>in</strong>g throw<strong>in</strong>g velocity is an important issue for coaches<br />

<strong>in</strong> order to assess the tra<strong>in</strong><strong>in</strong>g rout<strong>in</strong>es.<br />

In order to measure throw<strong>in</strong>g velocity different methodologies like<br />

chaPter2.<strong>Biomechanics</strong><br />

high velocity c<strong>in</strong>ematography have been used (Elliott & Armour, 1988;<br />

McCluskey et al.; Van den Tillaar & Ettema, 2004, Van den Tillaar &<br />

Ettema, 2007). This technique is knowns to have high sensitivity, validity<br />

<strong>and</strong> reliability (Bartlett, 1997). However, this method is time consum<strong>in</strong>g<br />

<strong>and</strong> is not suitable for use <strong>in</strong> the playfield. For these reasons, it<br />

is an unpractical method <strong>in</strong> order to provide fast feedback for coaches<br />

<strong>and</strong> athletes. Electronic tim<strong>in</strong>g gates is another way to assess throw<strong>in</strong>g<br />

velocity (Gorostiaga, Granados et al, 2005; Granados, Izquierdo et al,<br />

2007), but it is unpractical <strong>in</strong> water polo because of the play<strong>in</strong>g medium<br />

(water).<br />

In the last years, several studies have used radar guns as an alternative<br />

way to assess throw<strong>in</strong>g velocity <strong>in</strong> team sports. This equipment has<br />

a lot of advantages, because we can assess throw<strong>in</strong>g velocity without<br />

<strong>in</strong>terfer<strong>in</strong>g <strong>in</strong> the playfield. Furthermore, velocities are measured <strong>in</strong>stantaneously<br />

<strong>and</strong> <strong>in</strong> real competitive conditions. However, consider<strong>in</strong>g that<br />

radar gun calculates the objects velocities through the emission <strong>and</strong> reception<br />

of electromagnetic waves <strong>and</strong> its operation is based on Doppler’s<br />

pr<strong>in</strong>ciple, it is necessary validate the st<strong>and</strong>ardization protocols <strong>in</strong> order<br />

to avoid or at least to control the error range of the data obta<strong>in</strong>ed. For<br />

this reason, the protocol used <strong>in</strong> each study must be rigorous, especially<br />

<strong>in</strong> the radar gun position<strong>in</strong>g <strong>and</strong> it must be carefully applied <strong>in</strong> order<br />

to avoid obstacles between the object <strong>and</strong> the radar gun. The quality<br />

of the data is based on the rectil<strong>in</strong>ear trajectories of the object. If the<br />

object does not achieve a rectil<strong>in</strong>ear trajectory, it is uncerta<strong>in</strong> to obta<strong>in</strong><br />

valid data. Therefore, the aim of the present study was twofold; firstly to<br />

<strong>in</strong>vestigate the validity of the radar versus high velocity 2D photogrammetric<br />

analysis, <strong>in</strong> two different situation: throw<strong>in</strong>g from the penalty<br />

position <strong>and</strong> throw<strong>in</strong>g <strong>in</strong> oblique position to the goal (θ ~ 20º) <strong>in</strong> the<br />

same penalty l<strong>in</strong>e <strong>and</strong> secondly, to establish a valid methodology to asses<br />

throw<strong>in</strong>g velocity <strong>in</strong> water polo.<br />

Methods<br />

Two male water polo players were recruited for the study (35 ± 2 years<br />

old). The participants carried out 48 throws at maximum <strong>in</strong>tensity from<br />

the penalty position (24 throws), <strong>and</strong> from an oblique position to the<br />

goal (θ ~ 20º) <strong>in</strong> the same penalty l<strong>in</strong>e (24 throws) with <strong>and</strong> without<br />

goalkeeper. Before beg<strong>in</strong>n<strong>in</strong>g the measurements, the players performed<br />

a st<strong>and</strong>ardized warm up. They executed throws by alternat<strong>in</strong>g manner<br />

with a 3-m<strong>in</strong> rest between each. An official water polo ball was used.<br />

The study was approved by the Human Subjects Ethics Committee of<br />

the San Antonio Catholic University of Murcia, the participants were<br />

<strong>in</strong>formed of the protocol <strong>and</strong> procedures prior to their <strong>in</strong>volvement <strong>and</strong><br />

written consent to participate was obta<strong>in</strong>ed.<br />

The ball maximum velocity was measured through the use of a radar<br />

gun (StalkerPro Inc., Plano, USA) with a frequency of 100 Hz <strong>and</strong> a<br />

sensibility of 0.045 m·s -1 , placed ten meters beh<strong>in</strong>d the goal, <strong>and</strong> aligned<br />

with the penalty l<strong>in</strong>e.<br />

Simultaneously, <strong>and</strong> with the aim of study<strong>in</strong>g the reliability of the<br />

radar gun, a 2D photogrammetric study was accomplished. The shots<br />

were recorded us<strong>in</strong>g a digital m<strong>in</strong>i DV video camera (Sony, HDR,<br />

HC9E, Japan) operat<strong>in</strong>g at 100 Hz. The camera was mounted on a rigid<br />

tripod at a height of 1.0 m <strong>and</strong> placed at a distance of 10 m from the<br />

middle of the athlete’s lane. The optical axis of the camera was perpendicular<br />

to the direction of throw<strong>in</strong>g for each different situation, <strong>and</strong> the<br />

field of view of the camera was zoomed so that the ball was visible <strong>in</strong> a<br />

10–m wide region. This field of view ensured that the maximum velocity<br />

of the ball would be recorded. The movement space was calibrated with<br />

two 2–m high poles that were placed along the midl<strong>in</strong>e of the athlete’s<br />

lane <strong>and</strong> 5 m apart. For 2D Analysis, The recommendations exposed by<br />

Bartlett were followed (Bartlett, 1997).<br />

Kwon3D biomechanical analysis software (Visol, Cheolsan-dong,<br />

Korea) was used to analyze the video images of the trials. Two l<strong>and</strong>marks<br />

that def<strong>in</strong>ed a model of the ball were digitized <strong>in</strong> each image.<br />

Coord<strong>in</strong>ate data were smoothed us<strong>in</strong>g a second-order Butterworth digital<br />

filter with a cut-off frequency of 6 Hz, <strong>and</strong> the velocity of the ball’s<br />

77


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

centre of mass were calculated from the coord<strong>in</strong>ate data us<strong>in</strong>g the f<strong>in</strong>ite<br />

differences method (W<strong>in</strong>ter, 1990).<br />

All digitiz<strong>in</strong>g was performed by the same operator <strong>in</strong> order to maximize<br />

the consistency of the dependent variables. The reliability of <strong>in</strong>traparticipant<br />

digitiz<strong>in</strong>g <strong>and</strong> <strong>in</strong>ter-participant digitiz<strong>in</strong>g was very high.<br />

An <strong>in</strong>traclass correlation coefficient (ICC) value of 0.999 was obta<strong>in</strong>ed<br />

when three <strong>in</strong>stants of the same video sequence were digitized five<br />

times, <strong>and</strong> an ICC value of 0.998 was obta<strong>in</strong>ed when two researchers<br />

digitized three <strong>in</strong>stants of the same sequence.<br />

One trial by each participant for each throw condition was analyzed.<br />

After the throws were analyzed, Pearson correlation coefficients (SPSS<br />

15.0, SPSS Inc, Chicago, USA) were used to determ<strong>in</strong>e the <strong>in</strong>terrelationship<br />

among the maximum velocity obta<strong>in</strong>ed by the radar gun <strong>and</strong><br />

the 2D analysis. The alpha level was set to p ≤ 0.05.<br />

results<br />

The results obta<strong>in</strong>ed are presented <strong>in</strong> Table 1. Scientific community<br />

established that, when a high <strong>and</strong> statistic significant correlation coefficient<br />

between the <strong>in</strong>struments analyzed exists, we can say that they<br />

are valid enough. In the present study we found <strong>in</strong>traclass correlation<br />

coefficients higher (ICC) than 0.80 for all throw<strong>in</strong>g situations <strong>and</strong> all of<br />

them reach statistical significance.<br />

For frontal throws without goalkeeper the ICC was 0.96, <strong>and</strong> with<br />

goalkeeper was 0.84. If we analyze throws <strong>in</strong> oblique situation (α ~ 20º),<br />

the ICC was 0.94 without goalkeeper <strong>and</strong> 0.96 with goalkeeper.<br />

When we analyzed all throws <strong>in</strong> frontal situation the Pearson correlation<br />

coefficient obta<strong>in</strong>ed was 0.91 <strong>and</strong> <strong>in</strong> oblique position was 0.94.<br />

Table 1. Pearson correlation coefficient between radar gun <strong>and</strong> photogrammetry<br />

<strong>in</strong>struments <strong>in</strong> different situations<br />

Variable<br />

78<br />

V Radar (km·h -1 )<br />

Mean ± SD<br />

V Video (km·h -1 )<br />

Mean ± SD<br />

Frontal without goalkeeper (n = 12) 51.3 ± 6.8 51.8 ± 6.7 0.958 0.000<br />

Frontal with goalkeeper (n = 12) 51.3 ± 3.2 50.2 ± 4.2 0.840 0.001<br />

Oblique without goalkeeper (n= 12) 50.8 ± 3.7 49.9 ± 4.7 0.939 0.000<br />

Oblique with goalkeeper (n = 12) 49.3 ± 5.6 49.4 ± 5.7 0.965 0.000<br />

Frontal (n = 24) 51.3 ± 5.1 51.0 ± 5.5 0.911 0.000<br />

Oblique (n = 24) 50.0 ± 4.7 49.7 ± 5.1 0.941 0.000<br />

Total (n=48) 50.6 ± 4.9 50.3 ± 5.2 0.927 0.000<br />

dIscussIon<br />

The ma<strong>in</strong> goal of this study is to validate the radar gun as valid <strong>in</strong>strument<br />

to measure throw<strong>in</strong>g velocities <strong>in</strong> water polo.<br />

This is a very important issue, because skills <strong>in</strong> pass<strong>in</strong>g <strong>and</strong> throw<strong>in</strong>g<br />

the ball are vital <strong>in</strong> water polo for reasons of accuracy <strong>and</strong> ability to<br />

produce high velocities, which are valuable dur<strong>in</strong>g the game. In water<br />

polo, the overhead throw is the most effective <strong>and</strong> frequently used to<br />

propel the ball <strong>and</strong> to score goals (Bloomfield, Blanksby et al, 1990).<br />

The overhead throw accounts for up to 90% of all passes <strong>and</strong> shots dur<strong>in</strong>g<br />

a game. In this pattern, the ball comes from beh<strong>in</strong>d the body <strong>and</strong><br />

is brought up over the head <strong>and</strong> released <strong>in</strong> front of the body. The goal<br />

of the overhead throw is to achieve high endpo<strong>in</strong>t velocity (Bloomfield,<br />

Blanksby et al, 1990). Naturally, the faster the ball is thrown at the goal,<br />

the less time defenders <strong>and</strong> goalkeeper have to save the shot (Muijtjens,<br />

Joris et al, 1991).<br />

For this reason measur<strong>in</strong>g throw<strong>in</strong>g velocity dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g sessions<br />

<strong>and</strong> dur<strong>in</strong>g real competition match is an important issue for coaches<br />

<strong>and</strong> athletes. But unfortunately, these measures are really complicated<br />

because of the water. The radar gun solves the problems mentioned, because<br />

we can obta<strong>in</strong> the results of the measures immediately, we can<br />

assess throw<strong>in</strong>g velocity without gett<strong>in</strong>g <strong>in</strong>side the playfield <strong>and</strong> we can<br />

measure throw<strong>in</strong>g velocity <strong>in</strong> a real match. Now it is possible to use<br />

the radar gun as a valid method for measure throw<strong>in</strong>g velocity even <strong>in</strong><br />

oblique throw situations <strong>in</strong> water polo.<br />

ICC<br />

(r)<br />

p<br />

conclusIon<br />

The results suggest that the measurements obta<strong>in</strong>ed with radar are valid,<br />

both for frontal throws (r=0.911, p=0.000) as well as for oblique throws<br />

(r=0.941, p=0.000) (θ ~ 20º), with <strong>and</strong> without goalkeeper.<br />

The radar gun is a valid method to measure throw<strong>in</strong>g velocity dur<strong>in</strong>g a<br />

water polo tra<strong>in</strong><strong>in</strong>g session <strong>and</strong> dur<strong>in</strong>g a water polo match, so for frontal<br />

throws as well for oblique throws (r=0.91, p=0.000).<br />

reFerences<br />

Bartlett, R. (1997). Introduction to Sports <strong>Biomechanics</strong>. London: E & FN<br />

Spon.<br />

Bloomfield, J., Blanksby, B. A., Ackl<strong>and</strong>, T. R., & Allison, G. T. (1990).<br />

The <strong>in</strong>fluence of strength tra<strong>in</strong><strong>in</strong>g on overhead throw<strong>in</strong>g velocity of<br />

elite water polo players. Australian Journal of Science <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Sport, 22(3), 63-69.<br />

DeRenne, C., Ho, K., & Blitzblau, A. (1990). Effects of weighted implement<br />

tra<strong>in</strong><strong>in</strong>g on throw<strong>in</strong>g velocity. J. Appl. Sport Sci. Res., 4(1), 16-19.<br />

Elliott, B. C. & Armour, J. (1988). The penalty throw <strong>in</strong> water polo: a<br />

c<strong>in</strong>ematographic analysis. J Sports Sci, 6(2), 103-114.<br />

Gorostiaga, E. M., Granados, C., Ibanez, J. & Izquierdo, M. (2005).<br />

Differences <strong>in</strong> physical fitness <strong>and</strong> throw<strong>in</strong>g velocity among elite <strong>and</strong><br />

amateur male h<strong>and</strong>ball players. Int J Sports Med, 26(3), 225-232.<br />

Granados, C., Izquierdo, M., Ibanez, J., Bonnabau, H. & Gorostiaga,<br />

E. M. (2007). Differences <strong>in</strong> physical fitness <strong>and</strong> throw<strong>in</strong>g velocity<br />

among elite <strong>and</strong> amateur female h<strong>and</strong>ball players. Int J Sports Med,<br />

28(10), 860-867.<br />

Lachowetz, T., Evon, J. & Pastiglione, J. (1998). The Effects of an Upper<br />

Body Strength Program on Intercollegiate Baseball Throw<strong>in</strong>g Velocity.<br />

Journal of Strength <strong>and</strong> Cond. Res., 12 (2), 116-119.<br />

McCluskey, L., Lynskey, S., Leung, C. K., Woodhouse, D., Briffa, K.<br />

& Hopper, D. Throw<strong>in</strong>g velocity <strong>and</strong> jump height <strong>in</strong> female water<br />

polo players: Performance predictors. Journal of Science <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Sport, In Press, Corrected Proof.<br />

Muijtjens, A., Joris, H. J., Kemper, H. C. & Ingen Schenau Van, G.<br />

J. (1991). Throw<strong>in</strong>g practice with different ball weights: effects on<br />

throw<strong>in</strong>g velocity <strong>and</strong> muscle strength <strong>in</strong> female h<strong>and</strong>ball players.<br />

Research <strong>in</strong> Sports <strong>Medic<strong>in</strong>e</strong>: An International journal, 2(2), 103-113.<br />

Skoufas, D., Stefanidis, P., Michailidis, C. & Kotzamanidou, M. (2003).<br />

The effect of h<strong>and</strong>ball tra<strong>in</strong><strong>in</strong>g with underweighted balls on the<br />

throw<strong>in</strong>g velocity of novice h<strong>and</strong>ball players. Journal of Human Movement<br />

Studies, 44(4), 157-171.<br />

Van den Tillaar, R. & Ettema, G. (2004). Effect of body size <strong>and</strong> gender<br />

<strong>in</strong> overarm throw<strong>in</strong>g performance. Eur J Appl Physiol, 91(4), 413-418.<br />

Van den Tillaar, R. & Ettema, G. (2007). A three-dimensional analysis<br />

of overarm throw<strong>in</strong>g <strong>in</strong> experienced h<strong>and</strong>ball players. J Appl Biomech,<br />

23(1), 12-19.<br />

W<strong>in</strong>ter, D. A. (1990). <strong>Biomechanics</strong> <strong>and</strong> motor control of human movement<br />

(2nd ed.). New York, N.Y.: Wiley-Interscience.<br />

AcKnoWledGeMents<br />

The authors would like to acknowledge fund<strong>in</strong>g support from Spanish<br />

Government grant DEP 2008-06114. I+D (BOE 20 Nov 2007), <strong>and</strong> to<br />

Francisco Argudo Iturriaga for his support dur<strong>in</strong>g the measurements.


Biophysical Analysis of the 200m Front Crawl<br />

Swimm<strong>in</strong>g: a Case Study<br />

Figueiredo, P. 1 , sousa, A. 1 ; Gonçalves, P. 1 , Pereira, s.M. 1,2 ,<br />

soares, s. 1 , Vilas-Boas, J.P. 1 , Fern<strong>and</strong>es, r.J. 1<br />

1 University of Porto, Faculty of Sport, CIFI2D<br />

2 Federal University of Santa Catar<strong>in</strong>a, Santa Catar<strong>in</strong>a, Brazil<br />

The performance of a swimmer dur<strong>in</strong>g 200 m front crawl swim was<br />

analysed, <strong>in</strong>tegrat<strong>in</strong>g coord<strong>in</strong>ative, biomechanical, electrophysiological<br />

<strong>and</strong> bioenergetical data. One male swimmer (participant at the 2008<br />

Olympic Games <strong>and</strong> national record holder) swam 200m for the assessment<br />

of the <strong>in</strong>tracyclic velocity variation (IVV) <strong>in</strong> x, y <strong>and</strong> z axes, arm<br />

coord<strong>in</strong>ation, oxygen uptake <strong>and</strong> neuromuscular activity. Afterwards, the<br />

swimmer performed 50, 100 <strong>and</strong> 150 m at the 200 m pace for blood<br />

lactate k<strong>in</strong>etics analysis. This study highlighted the stability of the IVVx,<br />

cont<strong>in</strong>uity of arm coord<strong>in</strong>ation <strong>in</strong> the last 100 m. The electromyography<br />

data evidenced a significant fatigue <strong>in</strong>volvement. Moreover, oxygen consumption<br />

rate values decreased as blood lactate concentrations rate<br />

<strong>and</strong> absolute values <strong>in</strong>creased along the effort.<br />

Key words: eMG, Intracyclic velocity variation, Arm coord<strong>in</strong>ation,<br />

energy expenditure, Biophysics.<br />

IntroductIon<br />

Propulsive <strong>and</strong> drag forces act<strong>in</strong>g on the swimmer’s body are major performance<br />

determ<strong>in</strong>ants, be<strong>in</strong>g affected by technique, motor organisation<br />

<strong>and</strong> control. However, muscular activity, as well as energy expenditure<br />

of exercise, is considered as swimm<strong>in</strong>g <strong>in</strong>fluenc<strong>in</strong>g parameters (Clarys<br />

<strong>and</strong> Cabri, 1993; Fern<strong>and</strong>es et al., 2006). In this sense, to underst<strong>and</strong> the<br />

real <strong>in</strong>volvement of the above parameters <strong>in</strong> swimm<strong>in</strong>g, a biophysical<br />

approach is needed (Pendergast et al., 2006), comb<strong>in</strong><strong>in</strong>g data from different<br />

areas. The 200 m front crawl is dependent on both anaerobic <strong>and</strong><br />

aerobic energy systems, imply<strong>in</strong>g higher levels of fatigue (Costill et al.,<br />

1992). However, the <strong>in</strong>teractions between the performance <strong>in</strong>fluenc<strong>in</strong>g<br />

factors <strong>in</strong> this specific event were not yet discussed.<br />

The aim of the present study was to analyse the 200 m front crawl maximal<br />

effort, performed by an elite Olympic swimmer, assess<strong>in</strong>g the <strong>in</strong>tracyclic<br />

velocity variation of the centre of mass, arm coord<strong>in</strong>ation, energy<br />

expenditure <strong>and</strong> neuromuscular activity.<br />

Methods<br />

A male swimmer, 2008 Olympic Games participant <strong>and</strong> 200m front<br />

crawl national record holder (21 years old, 71kg of body mass, 180cm<br />

of height, 182cm of arm span <strong>and</strong> 8.8% of body fat mass) volunteered<br />

to participate <strong>in</strong> the present study. The test session took place <strong>in</strong> a 25 m<br />

<strong>in</strong>door swimm<strong>in</strong>g pool.<br />

Briefly, the subject, after a moderate <strong>in</strong>tensity <strong>in</strong>dividual warm-up,<br />

performed a 200 m front crawl test at maximal <strong>in</strong>tensity (as <strong>in</strong> competition),<br />

with push <strong>in</strong>-water start. The swimmer was monitored when pass<strong>in</strong>g<br />

through a specific pre-calibrated space with dimensions of 3x1.5x3m<br />

for the horizontal (x), vertical (y) <strong>and</strong> lateral (z) directions. Thirty po<strong>in</strong>ts<br />

of calibration were used, <strong>and</strong> the synchronisation of the images was obta<strong>in</strong>ed<br />

us<strong>in</strong>g a pair of lights observable <strong>in</strong> the field of view of each one of<br />

the six video cameras (Sony® DCR-HC42E, Japan). The angle between<br />

the optical axes of the two surface cameras was approximately 120º,<br />

while the angles between the optical axes of adjacent underwater cameras<br />

varied from 75º to 110º. Two complete arm stroke cycles, without<br />

breath<strong>in</strong>g, for each 50m of the 200m front crawl were digitised us<strong>in</strong>g the<br />

APASystem (Ariel Dynamics, USA) at a frequency of 50 Hz, manually<br />

<strong>and</strong> frame by frame. Zatsiorsky <strong>and</strong> Seluyanov’s model, adapted by de<br />

Leva (1996) was used to analyse the k<strong>in</strong>ematic data. Twenty-one body<br />

l<strong>and</strong>marks were digitised <strong>in</strong> each frame to represent the endpo<strong>in</strong>ts of the<br />

chaPter2.<strong>Biomechanics</strong><br />

head, torso, upper arms, forearms, h<strong>and</strong>s, thighs, shanks <strong>and</strong> feet. Direct<br />

L<strong>in</strong>ear Transformation algorithm was used for three-dimensional reconstruction,<br />

as well as a 6 Hz low pass digital filter for the smooth<strong>in</strong>g<br />

of the data. The velocity (v) was calculated by divid<strong>in</strong>g the displacement<br />

of centre of mass (CM) <strong>in</strong> one stroke cycle for its total duration. Additionally,<br />

stroke rate (SR) was assessed through the <strong>in</strong>verse of its time<br />

duration, <strong>and</strong> stroke length (SL) was determ<strong>in</strong>ed through the horizontal<br />

displacement of the CM dur<strong>in</strong>g a stroke cycle.<br />

To analyse the <strong>in</strong>tracyclic velocity variation (IVV) for the x, y <strong>and</strong><br />

z axes of the CM, was calculated through the coefficient of variation of<br />

the v (t) distribution.<br />

Arm movement was broken <strong>in</strong>to four phases (entry/catch, pull, push<br />

<strong>and</strong> recovery) (Chollet et al., 2000), us<strong>in</strong>g the above-referred digitised<br />

model. The duration of the propulsive phase was considered to be the<br />

sum of the pull <strong>and</strong> push phases, <strong>and</strong> the duration of the non-propulsive<br />

phase the sum of the entry/catch <strong>and</strong> recovery phases. Arm coord<strong>in</strong>ation<br />

was quantified us<strong>in</strong>g the Index of Coord<strong>in</strong>ation (IdC) proposed<br />

by Chollet et al. (2000), measur<strong>in</strong>g the lag time between the propulsive<br />

phases. The IdC was calculated for two complete arm strokes per 50m,<br />

<strong>and</strong> expressed as a percentage of complete arm stroke duration.<br />

For the total energy expenditure (Ė) assessment, oxygen uptake<br />

(VO 2 ) was recorded breath-by-breath by the K4b² telemetric gas exchange<br />

system (Cosmed, Roma, Italy), dur<strong>in</strong>g the 200m front crawl exercise.<br />

Artefacts were manually elim<strong>in</strong>ated <strong>and</strong> data were averaged every<br />

5 s (cf. Sousa et al., <strong>in</strong> press). After 90 m<strong>in</strong> of rest <strong>in</strong>terval, the swimmer<br />

performed a 50m front crawl test to assess blood lactate concentration<br />

[La - ], at the same swimm<strong>in</strong>g v as the previous 200m (controlled by a<br />

visual light pacer - TAR 1.1, GBK-EIectronics, Aveiro, Portugal - with a<br />

flash every 5m). Twenty-four hours later, the swimmer performed 150m<br />

<strong>and</strong> 100m, with 90 m<strong>in</strong> <strong>in</strong>terval between tests, <strong>in</strong> order to simulate as<br />

much as possible the 200m test conditions, also us<strong>in</strong>g a respiratory snorkel<br />

<strong>and</strong> valve system. Capillary blood samples (5µl) were collected from<br />

the ear lobe, at rest, as well as at 1, 3, 5, <strong>and</strong> 7 m<strong>in</strong> of recovery, to assess<br />

rest <strong>and</strong> post exercise [La - ] (Lactate Pro, Arkray, Inc.). It was ensured,<br />

by measur<strong>in</strong>g, that swimmer had similar blood lactate concentration rest<br />

values prior to each test.<br />

The Ė corrected for body mass was calculated us<strong>in</strong>g the VO 2 net<br />

(difference between the average value of each 50m length <strong>and</strong> the rest<br />

value), <strong>and</strong> the blood lactate net (difference between the value measured<br />

<strong>in</strong> two consecutive lengths), transformed <strong>in</strong>to VO 2 equivalents us<strong>in</strong>g a<br />

2.7 mlO 2 .kg -1 .mmol -1 constant (di Prampero et al., 1978). Anaerobic<br />

alactic energy sources were assumed to be negligible <strong>in</strong> this type of effort<br />

(Rodriguez <strong>and</strong> Mader 2003).<br />

For the muscular analysis active differential surface electromyography<br />

(EMG) record<strong>in</strong>gs were used of the flexor carpi radialis, biceps<br />

brachii, triceps brachii, pectoralis major, upper trapezius, rectus femoris,<br />

biceps femoris <strong>and</strong> tibialis anterior muscles dur<strong>in</strong>g the 200m front<br />

crawl. These muscles were selected accord<strong>in</strong>g to their ma<strong>in</strong> function <strong>and</strong><br />

anatomic localisation, be<strong>in</strong>g considered important <strong>in</strong> front crawl swimm<strong>in</strong>g<br />

(Figueiredo et al., 2009). The sk<strong>in</strong> of the swimmer was shaved <strong>and</strong><br />

rubbed with an alcohol solution. Silver/silver chloride circular surface<br />

electrodes, with preamplifiers (An AD621 BN), were placed <strong>in</strong> a bipolar<br />

configuration with 2.0 cm <strong>in</strong>ter-electrodes distance, <strong>in</strong> l<strong>in</strong>e with the<br />

muscle’s fibre orientation. Electrodes were placed <strong>in</strong> the midpo<strong>in</strong>t of<br />

the contracted muscle belly as suggested by Clarys <strong>and</strong> Cabri (1993),<br />

<strong>and</strong> covered with an adhesive b<strong>and</strong>age (Opsite Flexifix) to avoid contact<br />

with water (Figueiredo et al., 2009). A reference electrode was attached<br />

to the patella. The total ga<strong>in</strong> of the amplifier was set at 1100, with a common<br />

mode rejection ratio of 110 dB. Additionally, the swimmer used a<br />

complete swimsuit, <strong>in</strong> order to reduce the mobility of the electrodes <strong>and</strong><br />

to <strong>in</strong>crease the comfort of the swimmer, allow<strong>in</strong>g normal motion.<br />

The EMG signals were recorded at a sampl<strong>in</strong>g frequency of 1000<br />

Hz with a 16-bit resolution <strong>and</strong> then converted by an analogical/digital<br />

converter (BIOPAC System, Inc). To synchronise EMG <strong>and</strong> video, an<br />

electronic flashlight signal / electronic trigger was marked simultane-<br />

79


Figure 1. General biomechanical parameters (v, SL<br />

front crawl effort.<br />

2.3<br />

Figure 1. General biomechanical parameters (v, SL <strong>and</strong> SR) values dur<strong>in</strong>g the 200m<br />

v<br />

1.6<br />

0.9<br />

front crawl effort.<br />

SR<br />

43<br />

<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

ously on 0.9the<br />

video <strong>and</strong> EMG record<strong>in</strong>gs. The EMG data analysis was<br />

1.5<br />

performed us<strong>in</strong>g the MATLAB 2008a software environment (Math-<br />

41<br />

Works Inc., 0.8 Natick, Massachusetts, USA). A new highly sensitive spectral<br />

<strong>in</strong>dex (FInsmk), proposed by Dimitrov et al. (2006), was calculated<br />

1.4<br />

for one 0.7 stroke cycle for 40 each 25m. The FInsmk has been proposed to<br />

overcome the relatively low sensitivity of the median frequency <strong>and</strong> the<br />

IVVx<br />

mean frequency. 0.6 The FInsmk <strong>in</strong>dices were calculated as the ratio between<br />

the 0.3 1.3 39<br />

IVVy<br />

spectral moments of order (-1) <strong>and</strong> order, k:<br />

results<br />

0.2<br />

In Figure 1 it is possible to observe the decay of v, SL <strong>and</strong> SR through<br />

the 200 m front crawl with a slightly <strong>in</strong>creas<strong>in</strong>g of the SR <strong>in</strong> the last<br />

0.1<br />

length.<br />

Values for IVV (x, y <strong>and</strong> z) <strong>and</strong> coord<strong>in</strong>ative organisation param-<br />

0.0<br />

eters (IdC <strong>and</strong> stroke phases) 1st are 50mpresented 2nd 50m <strong>in</strong> fig. 3rd 2 (left 50mpanel 4th <strong>and</strong> 50mright<br />

panel, respectively) 43 for the four laps of the 200m Lapsfront<br />

crawl test. 2.3<br />

Velocity (m.s -1 )<br />

(1)<br />

where k was 5, PS(f ) was the spectral power for the currency frequency f<br />

<strong>and</strong> f1 = 8 Hz <strong>and</strong> f2 = 500 Hz were the high <strong>and</strong> low-pass frequencies<br />

of the amplifier filter. The relative changes <strong>in</strong> values of the spectral <strong>in</strong>dex,<br />

Figure for different 2. repetitions Values were calculated for <strong>in</strong>tracyclic aga<strong>in</strong>st the first velocity repetition of the variation (IVV) <strong>in</strong> x, y <strong>and</strong> z axes (left panel)<br />

correspond<strong>in</strong>g set: for <strong>in</strong>stance, FInnsmk/FI1nsmk x 100, % (n = 1, 2,<br />

<strong>and</strong> values of velocity (v), stroke rate (SR), stroke length (SL), <strong>in</strong>dex of coord<strong>in</strong>ation<br />

..., 8 lap number).<br />

(IdC), L<strong>in</strong>ear regression entry/catch, analysis method pull, was push, performed recovery, on muscle EMG propulsive phase <strong>and</strong> non-propulsive phase <strong>in</strong><br />

parameters (laps 1–8). The regression l<strong>in</strong>e gradients were analysed to<br />

the four laps of the 200m front crawl.<br />

compare rate of change <strong>and</strong>, hence, rate of fatigue development. The<br />

97<br />

level of significance for all statistical tests was set at p < 0.05.<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong><br />

The k<strong>in</strong>etics of bioenergetical parameters (Ė, VO2 <strong>and</strong> [La - 0.0<br />

-20<br />

1st 50m 2nd 50m 3rd 50m 4th 50m<br />

1st 50m 2nd 50m 3rd 50m 4th 50m<br />

Laps<br />

Laps<br />

Figure 2. Values for <strong>in</strong>tracyclic velocity variation (IVV) <strong>in</strong> x, y <strong>and</strong> z<br />

axes (left panel) <strong>and</strong> values of velocity (v), stroke rate (SR), stroke length<br />

(SL), <strong>in</strong>dex of coord<strong>in</strong>ation (IdC), entry/catch, pull, push, recovery, propulsive<br />

phase <strong>and</strong> non-propulsive phase <strong>in</strong> the four laps of the 200m<br />

front crawl.<br />

The k<strong>in</strong>etics of bioenergetical parameters (Ė, VO2 <strong>and</strong> [La<br />

]) <strong>and</strong> the spectral<br />

<strong>in</strong>dices, reveal<strong>in</strong>g the muscular function dur<strong>in</strong>g the 200m front crawl are shown <strong>in</strong> fig. 3<br />

(left <strong>and</strong> right panel, respectively). For the spectral <strong>in</strong>dices high relationships were<br />

observed (r>0.74, p0.74, p0.74, anterior (r=-0.18, p0.74, p


dIscussIon<br />

The k<strong>in</strong>etics of the strok<strong>in</strong>g parameters (SL <strong>and</strong> SR) along the 200m<br />

is <strong>in</strong> agreement with the literature (Alberty et al., 2005). Moreover, the<br />

decrease of v along the test can be expla<strong>in</strong>ed by different SR <strong>and</strong> SL<br />

comb<strong>in</strong>ations, as previously reported (Huot-March<strong>and</strong>, et al., 2005).<br />

The decrease of the SL values could be l<strong>in</strong>ked to the development of<br />

local muscular fatigue, reflect<strong>in</strong>g a decl<strong>in</strong><strong>in</strong>g capacity to deliver power<br />

output. In addition, the swimmer tried to <strong>in</strong>crease SR <strong>in</strong> order to compensate<br />

the SL decrease.<br />

The observed stability of IVVx <strong>and</strong> the larger magnitudes of IVV<br />

found for y <strong>and</strong> z than <strong>in</strong> x axis, are <strong>in</strong> agreement with the literature<br />

(Psycharakis et al., 2010). This IVVx stability suggests a coord<strong>in</strong>ative<br />

adaptation of the upper limbs, as Figueiredo et al., (2009) reported no<br />

relationship between IVV <strong>and</strong> IdC <strong>in</strong> x, y <strong>and</strong> x axes dur<strong>in</strong>g the 200<br />

m front crawl effort. The coord<strong>in</strong>ative adaptation pattern might be expla<strong>in</strong>ed<br />

by the swimmer’s <strong>in</strong>ability to m<strong>in</strong>imise the resistive force as the<br />

arm coord<strong>in</strong>ation change (<strong>in</strong>creas<strong>in</strong>g the values of IdC) manly <strong>in</strong> the<br />

last 50m of the 200m front crawl (Alberty et al., 2005; Figueiredo et al,<br />

<strong>in</strong> press), however IdC ma<strong>in</strong>ta<strong>in</strong>ed <strong>in</strong> catch-up mode (


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Measur<strong>in</strong>g Active Drag with<strong>in</strong> the Different Phases<br />

of Front Crawl Swimm<strong>in</strong>g<br />

Formosa, d. P. 1, 2 Mason, B.r. 1 & Burkett, B. J. 2<br />

1 Australian Institute of Sport, Australia<br />

2 University of the Sunsh<strong>in</strong>e Coast, Australia<br />

The aim of this study was to quantify the passive <strong>and</strong> active drag forces<br />

<strong>in</strong> front crawl swimm<strong>in</strong>g at the swimmer’s maximum swimm<strong>in</strong>g velocity<br />

<strong>and</strong> to present this data as a force-time profile. This method enabled<br />

the m<strong>in</strong>imum <strong>and</strong> maximum force with respect to the phase with<strong>in</strong> the<br />

stroke to be identified. Elite freestylers (n=18) completed three maximum<br />

swim velocity time trials to determ<strong>in</strong>e their maximum velocity.<br />

This was followed by three passive drag trials <strong>and</strong> three active drag trials<br />

us<strong>in</strong>g a tow<strong>in</strong>g device mounted upon a force platform. The computed<br />

active drag <strong>and</strong> the propulsive force profiles were represented as a forcetime<br />

graph, allow<strong>in</strong>g identification of <strong>in</strong>tra-cyclic force fluctuations. The<br />

force-time profiles were synchronised to video footage which provided<br />

unique quantitative stroke mechanic feedback to the elite coaches <strong>and</strong><br />

athletes.<br />

KeYWords: biomechanics, swimm<strong>in</strong>g, front crawl, active drag, technique<br />

IntroductIon<br />

An elite swimmer’s success dur<strong>in</strong>g the free swimm<strong>in</strong>g phase is primarily<br />

dependent upon their ability to m<strong>in</strong>imise active drag, whilst optimis<strong>in</strong>g<br />

propulsive force. Active drag is def<strong>in</strong>ed as the water resistance associated<br />

with the swimm<strong>in</strong>g motion (Kolmogorov et al, 1997). Before 1974<br />

passive drag, def<strong>in</strong>ed as the amount of water resistance that a human<br />

body experiences <strong>in</strong> an unchang<strong>in</strong>g body position, was considered the<br />

best method of predict<strong>in</strong>g active drag (Chatard et al, 1990). In the late<br />

1980’s, a research team <strong>in</strong> the Netherl<strong>and</strong>s developed the first system<br />

to measure active drag, known as the MAD system. The MAD system<br />

required the participant to swim at a constant velocity, whilst press<strong>in</strong>g<br />

upon fixed pads with the h<strong>and</strong>s. The swimmer’s legs were elevated <strong>and</strong><br />

restricted with pull buoy. This system was limited to front crawl only.<br />

Kolmogorov & Duplischeva (1992) developed the Velocity Perturbation<br />

Method (VPM) which measured active drag irrespective of swimm<strong>in</strong>g<br />

stroke. Us<strong>in</strong>g the VPM method participants were <strong>in</strong>structed to swim<br />

maximally dur<strong>in</strong>g two conditions; without <strong>and</strong> with a hydrodynamic<br />

body. The hydrodynamic body was of a known resistance, therefore allow<strong>in</strong>g<br />

active drag to be determ<strong>in</strong>ed by the velocity differences between<br />

the two conditions. The common assumption made <strong>in</strong> calculat<strong>in</strong>g active<br />

drag was that at a constant velocity the propulsive force was equal to the<br />

oppos<strong>in</strong>g active drag (Kolmogorov & Duplishcheva, 1992; Toussa<strong>in</strong>t et<br />

al, 2004). Regardless of the method adopted, active drag was calculated<br />

as a mean value, therefore ignor<strong>in</strong>g the fluctuations <strong>in</strong> the propulsive<br />

force dur<strong>in</strong>g the stroke phases. The swimm<strong>in</strong>g stroke is typically segmented<br />

<strong>in</strong>to dist<strong>in</strong>ct phases consist<strong>in</strong>g of the entry <strong>and</strong> catch, pull, push<br />

<strong>and</strong> recovery (Chollet et al., 2000). The primary aim of this study was<br />

to quantify the passive <strong>and</strong> active drag values as a force-time profile by<br />

us<strong>in</strong>g a motorised tow<strong>in</strong>g device. The secondary aim of this study was<br />

to exam<strong>in</strong>e the force-time profile to determ<strong>in</strong>e <strong>in</strong> which segment of the<br />

stroke phase a swimmer produced m<strong>in</strong>imum <strong>and</strong> maximum force, <strong>and</strong><br />

therefore provid<strong>in</strong>g unique biomechanical feedback to elite coaches <strong>and</strong><br />

athletes.<br />

Methods<br />

Follow<strong>in</strong>g human ethics approval by the University of the Sunsh<strong>in</strong>e<br />

Coast <strong>and</strong> the Australian Institute of Sport, eighteen Australian na-<br />

82<br />

tional front crawl swimmers (10 male aged 21 ± 2.2 years, 8 female aged<br />

20 ± 3.0 years) were tested to determ<strong>in</strong>e the participant’s passive <strong>and</strong><br />

active drag profile.<br />

Firstly, the swimmers completed a typical 20 m<strong>in</strong> <strong>in</strong>dividual race<br />

preparation warm up, followed by three <strong>in</strong>dividual maximum swimm<strong>in</strong>g<br />

velocity trials. The maximum velocity trials were measured over a 10 m<br />

<strong>in</strong>terval us<strong>in</strong>g two 50 Hz cameras (Samsung model: SCC-C4301P). The<br />

cameras were time coded. Us<strong>in</strong>g a custom computer program, the mean<br />

velocity was calculated for each trial. The trial with the highest mean velocity<br />

was selected for the passive <strong>and</strong> active drag trials. The passive <strong>and</strong><br />

active drag test<strong>in</strong>g was conducted us<strong>in</strong>g a motorised tow<strong>in</strong>g device, which<br />

enabled a constant tow<strong>in</strong>g velocity to be accurately set. The tow<strong>in</strong>g device<br />

was positioned directly upon a calibrated Kistler force platform (Kistler<br />

Instruments <strong>in</strong> W<strong>in</strong>terthur Switzerl<strong>and</strong> Dimensions: 900 x 600 m Type<br />

Z12697). The tow<strong>in</strong>g device <strong>and</strong> the force plate enabled the force required<br />

to tow the swimmer through the water to be measured. The validity <strong>and</strong><br />

reliability of the system was determ<strong>in</strong>ed prior to data collection. Dur<strong>in</strong>g<br />

the three passive drag trials the swimmers were towed at their maximum<br />

swimm<strong>in</strong>g velocity. The swimmers were <strong>in</strong>structed to hold the end of the<br />

tow l<strong>in</strong>e around the middle f<strong>in</strong>ger of their dom<strong>in</strong>ant h<strong>and</strong>, with the nondom<strong>in</strong>ant<br />

h<strong>and</strong> <strong>in</strong>terlock<strong>in</strong>g to m<strong>in</strong>imise any additional movement. The<br />

criteria for a successful passive trial was that the swimmer ma<strong>in</strong>ta<strong>in</strong>ed a<br />

streaml<strong>in</strong>e position just below the water surface, with no arm strokes nor<br />

kick<strong>in</strong>g nor breath<strong>in</strong>g, <strong>and</strong> there was visible water flow pass<strong>in</strong>g over the<br />

head, back <strong>and</strong> feet. Three active drag trials were completed at a velocity<br />

five percent greater than the swimmer’s maximum swimm<strong>in</strong>g velocity. The<br />

active drag trials consisted of the participants actively swimm<strong>in</strong>g whilst<br />

us<strong>in</strong>g their typical stroke characteristics with an Eyel<strong>in</strong>e ® tow belt attached<br />

to the lumbar region <strong>and</strong> the dynamometer. Through pilot test<strong>in</strong>g<br />

the five percent <strong>in</strong>crease <strong>in</strong> tow<strong>in</strong>g velocity was considered to not have any<br />

major effect on the swimmer’s stroke pattern while still allow<strong>in</strong>g cont<strong>in</strong>uous<br />

force measurement.<br />

Data capture was collected for a total of seven seconds, one second<br />

prior to <strong>and</strong> six seconds after the synchronisation trigger was depressed.<br />

The sensitivity of the amplifier was set at 5000 pC for both conditions.<br />

Data was processed us<strong>in</strong>g a 12 bit A to D card, sampled at 500 Hz, <strong>and</strong><br />

a 5 Hz Butterworth low pass digital filter was applied to the force data<br />

collected (Formosa et al, 2009). Each trial was video-recorded at 50 Hz<br />

us<strong>in</strong>g three genlocked cameras; a side-on underwater, side-on above <strong>and</strong><br />

head-on camera. The side-on underwater <strong>and</strong> side-on above water cameras<br />

were synchronised with an Edirol video mixer (EDI-V8).<br />

The follow<strong>in</strong>g formulas were used to determ<strong>in</strong>e active drag:<br />

1<br />

2<br />

1<br />

F = 0. 5C<br />

⋅ r ⋅ A⋅V<br />

(1)<br />

2<br />

0. 5C<br />

⋅ r ⋅ A⋅V<br />

2 Fb<br />

(2)<br />

F =<br />

−<br />

2<br />

Where C a constant, ρ is a water density, A is the frontal surface area<br />

of the swimmer & Fb is the force needed to pull the swimmer at the<br />

103<br />

<strong>in</strong>creased <strong>Biomechanics</strong> velocity, <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> which <strong>XI</strong> was Chapter measured 2 <strong>Biomechanics</strong> by the force platform. F 1 = force<br />

applied by the swimmer dur<strong>in</strong>g free swimm<strong>in</strong>g (unaided) <strong>and</strong> is assumed<br />

Where Cto a constant, be equal ρ is a to water the density, total A drag is the force frontal surface dur<strong>in</strong>g area free of the swimm<strong>in</strong>g. swimmer & F 2 =<br />

Fb is the force needed to pull the swimmer at the <strong>in</strong>creased velocity, which was<br />

the force applied by the swimmer dur<strong>in</strong>g free swimm<strong>in</strong>g <strong>in</strong> the assisted<br />

measured by the force platform. F 1 = force applied by the swimmer dur<strong>in</strong>g free<br />

condition. swimm<strong>in</strong>g (unaided) <strong>and</strong> is assumed to be equal to the total drag force dur<strong>in</strong>g free<br />

Here swimm<strong>in</strong>g. it was F 2assumed<br />

= the force applied an equal by the power swimmer output dur<strong>in</strong>g free <strong>in</strong> swimm<strong>in</strong>g both the <strong>in</strong> free the assisted swimm<strong>in</strong>g<br />

condition.<br />

<strong>and</strong> the active drag swimm<strong>in</strong>g conditions existed:<br />

Here it was assumed an equal power output <strong>in</strong> both the free swimm<strong>in</strong>g <strong>and</strong> the active<br />

drag swimm<strong>in</strong>g conditions existed:<br />

1 2 P P =<br />

(3)<br />

If 1 2 P P = <strong>and</strong> therefore F1 ⋅V1<br />

= F2<br />

⋅V2<br />

(4)<br />

substitution of 1 F <strong>and</strong> F 2 gives:<br />

3<br />

3<br />

0. 5C<br />

A V 0.<br />

5C<br />

A V Fb<br />

V ⋅ − ⋅ ⋅ ⋅ = ⋅ ⋅ ⋅ ρ ρ<br />

(5)<br />

1<br />

2<br />

2<br />

Rearrang<strong>in</strong>g the formula to f<strong>in</strong>d C:<br />

Fb<br />

⋅V2<br />

C =<br />

3 3<br />

0.<br />

5ρ<br />

⋅ A⋅<br />

( V2<br />

−V1<br />

)<br />

(6)<br />

substitution of C gives the follow<strong>in</strong>g formula for active drag:<br />

2<br />

Fb<br />

⋅V2<br />

⋅V1<br />

F1<br />

= 3 3<br />

V2<br />

−V1<br />

(7)<br />

V 1=<br />

the swimmer’s free swim maximum velocity <strong>and</strong> V 2 = 5% greater than the<br />

swimmer’s free swim maximum velocity (Kolmogorov & Duplishcheva, 1992) (Note:<br />

equation was modified for assisted, rather than resisted). To identify the force<br />

distribution with<strong>in</strong> the stroke cycle, phases were considered as entry <strong>and</strong> catch, pull,<br />

push <strong>and</strong> recovery (Chollet et al, 2000).<br />

RESULTS<br />

The coefficient of variation between the tow<strong>in</strong>g device velocity <strong>and</strong> the side-on cameras<br />

was 0.6 % (90% Confidence Intervals (CI) 0.5 to 0.7). The Pearson product moment


V = the swimmer’s free swim maximum velocity <strong>and</strong><br />

1<br />

V = 5% greater<br />

2<br />

than the swimmer’s free swim maximum velocity (Kolmogorov & Duplishcheva,<br />

1992) (Note: equation was modified for assisted, rather than<br />

resisted). To identify the force distribution with<strong>in</strong> the stroke cycle, phases<br />

were considered as entry <strong>and</strong> catch, pull, push <strong>and</strong> recovery (Chollet<br />

et al, 2000).<br />

chaPter2.<strong>Biomechanics</strong><br />

± 7.2 N at 1.76 m·s-1 for female participants (Maglischo et al, 1988).<br />

Similarly, Kolmogorov & Duplishcheva (1992) observed male <strong>and</strong> female<br />

passive values rang<strong>in</strong>g from 69.7 – 103.0 N <strong>and</strong> 44.2 - 56.9 N, respectively<br />

at velocities 1.73 - 1.91 m·s-1<strong>and</strong> 1.52 - 1.67 m·s-1 , respectively.<br />

The active drag obta<strong>in</strong>ed <strong>in</strong> this study does not concur with the<br />

literature. Toussa<strong>in</strong>t et al. (2004) compared active drag values collected<br />

with both the MAD <strong>and</strong> VPM systems. Active drag measured at a velocity<br />

of 1.64 m·s -1 was 66.9 N (MAD) <strong>and</strong> 53.2 N (VPM). Similar<br />

f<strong>in</strong>d<strong>in</strong>gs were reported by Toussa<strong>in</strong>t et al. (1988) when compar<strong>in</strong>g active<br />

results<br />

The coefficient of variation between the tow<strong>in</strong>g device velocity <strong>and</strong> the<br />

side-on cameras was 0.6 % (90% Confidence Intervals (CI) 0.5 to 0.7).<br />

The Pearson product moment coefficient between the tow<strong>in</strong>g device<br />

pull<strong>in</strong>g velocity <strong>and</strong> the calculated side-on camera velocity was r =1.0.<br />

With<strong>in</strong> a test<strong>in</strong>g day the typical error of measurement from the force<br />

platform set up was 4.0 N (90% CI 3.4 to 4.8) or 5.2% (4.4 to 6.3) for<br />

passive drag; <strong>and</strong> 2.5 N (2.1 to 3.0) or 4.9% (4.1 to 5.9) for the active<br />

drag. Test<strong>in</strong>g sessions with<strong>in</strong> <strong>and</strong> between days of test<strong>in</strong>g, reported <strong>in</strong>traclass<br />

correlation coefficients (ICCs) of between 0.97 (0.93 to 0.99)<br />

<strong>and</strong> 0.99 (0.96 to 1.00) for passive <strong>and</strong> active drag respectively.<br />

The mean passive drag value for the male participants was 78.9 ±<br />

1.6 N at a mean velocity of 1.89 m·s<br />

83<br />

-1 , whilst the mean passive drag value<br />

for the female participants was 49.7 ± 1.8 N at a mean velocity of 1.72<br />

m·s-1 . The mean active drag value for the male participants was 228.4<br />

± 10.8 N at a maximum velocity of 1.89 m·s-1 , compared to the female<br />

mean value of 164.4 ± 11.7 N, at a maximum velocity of 1.72 m·s-1 104<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong><br />

.<br />

Figure 1: Male participant n<strong>in</strong>e propulsive force profile at 1.84 m·s -1 .<br />

1. L entry R push 2, R recovery, L pull 3, L push R entry 4. L recovery, R pull (Chollet<br />

et al., 2000).<br />

Figure 2: Male participant ten propulsive force profile at 1.81 m·s -1 .<br />

1. R entry L push 2. L recovery, R pull 3. R push L entry 4. R recovery, L pull (Chollet<br />

et al., 2000).<br />

DISCUSSION<br />

The aim of this study was to quantify active drag dur<strong>in</strong>g freestyle swimm<strong>in</strong>g, whilst<br />

provid<strong>in</strong>g a valuable biomechanical feedback tool for elite coaches <strong>and</strong> athletes. The<br />

mean passive drag values measured were comparable to those previously reported, such<br />

as the force values of 53.3 ± 7.2 N at 1.76 m·s -1 for female participants (Maglischo et al,<br />

1988). Similarly, Kolmogorov & Duplishcheva (1992) observed male <strong>and</strong> female<br />

passive values rang<strong>in</strong>g from 69.7 – 103.0 N <strong>and</strong> 44.2 - 56.9 N, respectively at velocities<br />

1.73 - 1.91 m·s -1 <strong>and</strong> 1.52 - 1.67 m·s -1 1 2 3 4<br />

Figure 1: Male participant n<strong>in</strong>e propulsive force profile at 1.84 m·s<br />

1 2 3 4<br />

, respectively.<br />

The active drag obta<strong>in</strong>ed <strong>in</strong> this study does not concur with the literature. Toussa<strong>in</strong>t<br />

et al. (2004) compared active drag values collected with both the MAD <strong>and</strong> VPM<br />

-1 104<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong><br />

.<br />

1. Figure L entry 1: R Male push participant 2, R recovery, n<strong>in</strong>e L propulsive pull 3, L push force R profile entry 4. at L 1.84 recovery, m·s<br />

R pull (Chollet et al., 2000).<br />

-1 .<br />

1. L entry R push 2, R recovery, L pull 3, L push R entry 4. L recovery, R pull (Chollet<br />

et al., 2000).<br />

Figure 2: Male participant ten propulsive force profile at 1.81 m·s -1 .<br />

1. R entry L push 2. L recovery, R pull 3. R push L entry 4. R recovery, L pull (Chollet<br />

et al., 2000).<br />

DISCUSSION<br />

The aim of this study was to quantify active drag dur<strong>in</strong>g freestyle swimm<strong>in</strong>g, whilst<br />

provid<strong>in</strong>g a valuable biomechanical feedback tool for elite coaches <strong>and</strong> athletes. The<br />

mean passive drag values measured were comparable to those previously reported, such<br />

as the force values of 53.3 ± 7.2 N at 1.76 m·s -1 for female participants (Maglischo et al,<br />

1988). Similarly, Kolmogorov & Duplishcheva (1992) observed male <strong>and</strong> female<br />

passive values rang<strong>in</strong>g from 69.7 – 103.0 N <strong>and</strong> 44.2 - 56.9 N, respectively at velocities<br />

1.73 - 1.91 m·s -1 <strong>and</strong> 1.52 - 1.67 m·s -1 1 2 3 4<br />

1 2 3 4<br />

Figure 2: Male participant ten propulsive force profile at 1.81 m·s<br />

, respectively.<br />

The active drag obta<strong>in</strong>ed <strong>in</strong> this study does not concur with the literature. Toussa<strong>in</strong>t<br />

et al. (2004) compared active drag values collected with both the MAD <strong>and</strong> VPM<br />

-1 drag of females <strong>and</strong> males. Us<strong>in</strong>g the function D=Aυ<br />

.<br />

1. R entry L push 2. L recovery, R pull 3. R push L entry 4. R recovery,<br />

L pull (Chollet et al., 2000).<br />

dIscussIon<br />

The aim of this study was to quantify active drag dur<strong>in</strong>g freestyle swimm<strong>in</strong>g,<br />

whilst provid<strong>in</strong>g a valuable biomechanical feedback tool for elite<br />

coaches <strong>and</strong> athletes. The mean passive drag values measured were comparable<br />

to those previously reported, such as the force values of 53.3<br />

n to obta<strong>in</strong> a range<br />

of values from the MAD system, the researchers were able to make a<br />

comparison with the mean results from the present study. The values<br />

measured us<strong>in</strong>g the MAD system were 70.2 N at a maximum velocity<br />

of 1.72 m·s-1 (females), whilst for males, the maximum velocity was<br />

1.89 m.s-1 with an active drag of 111.4 N. This variation between the<br />

results may be due to the different methods used to assess active drag.<br />

The MAD system was limited to arm propulsion only, whilst the VPM<br />

system measured the whole body whilst <strong>in</strong> a resisted state.<br />

Represent<strong>in</strong>g active drag <strong>in</strong> a force-time graph synchronised to video<br />

footage allowed researchers <strong>and</strong> coaches to identify the propulsive force<br />

fluctuations with<strong>in</strong> the stroke phases. As illustrated <strong>in</strong> figures 1 <strong>and</strong> 2<br />

each <strong>in</strong>dividual presented a unique force profile, therefore strengthen<strong>in</strong>g<br />

the importance of represent<strong>in</strong>g propulsive force as a force–time graph,<br />

rather than a mean value. The project provided coaches <strong>and</strong> athletes with<br />

a quantitative biomechanical analysis associated with video footage. This<br />

allowed identification of the weaker phases of the stroke cycle. This project<br />

provided quantifiable <strong>in</strong>formation to identify modification aspects<br />

required to optimise the swimmer’s technique based upon scientific<br />

feedback. An example of a practical application was: follow<strong>in</strong>g the data<br />

analysis <strong>and</strong> feedback to the coach <strong>and</strong> athlete, an <strong>in</strong>tervention strategy<br />

was derived to modify the weaknesses <strong>in</strong> the stroke mechanics. Future<br />

test<strong>in</strong>g quantified that after <strong>in</strong>tervention, participant ten reduced the<br />

active drag by a mean of 27.8 N, whilst swimm<strong>in</strong>g at the same velocity.<br />

Participant n<strong>in</strong>e <strong>in</strong>creased the swimm<strong>in</strong>g velocity, however ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g<br />

a similar mean active drag value.<br />

There are a limited number of researchers that have explored the<br />

propulsive force production throughout different stroke phases of front<br />

crawl, however most researchers have exam<strong>in</strong>ed this through digitis<strong>in</strong>g.<br />

There was significant variation between m<strong>in</strong>imum <strong>and</strong> maximum propulsive<br />

force range for left <strong>and</strong> right stroke phases between <strong>and</strong> with<strong>in</strong><br />

participants. By exam<strong>in</strong><strong>in</strong>g the force-time graph synchronised to video<br />

footage this allowed researchers to identify dur<strong>in</strong>g which exact phase,<br />

m<strong>in</strong>imum <strong>and</strong> maximum force production occurred. It was evident that<br />

mean m<strong>in</strong>imum propulsive force was generated dur<strong>in</strong>g the first pull<br />

phase of the stroke cycle. The tow<strong>in</strong>g device used to calculate active<br />

drag, measured the whole body propulsive action. This considered the<br />

effect the recover arm had on the total body propulsive force. This did<br />

not <strong>in</strong>dicate the pull phase was not generat<strong>in</strong>g propulsive force, however<br />

the arm produc<strong>in</strong>g the pull<strong>in</strong>g motion was counteract<strong>in</strong>g the equal <strong>and</strong><br />

oppos<strong>in</strong>g forces of the recover<strong>in</strong>g arm. The force-time graph <strong>in</strong>dicated<br />

that the maximum propulsive force production occurred dur<strong>in</strong>g the f<strong>in</strong>al<br />

push phases of the stroke cycle. Previous researchers have adopted an<br />

<strong>in</strong>direct method to determ<strong>in</strong>e the forces associated with the h<strong>and</strong>s/arms<br />

(Maglischo et al, 1988; Schleihauf, 1979). These researchers digitised<br />

the h<strong>and</strong>/arm motion to determ<strong>in</strong>e the lift <strong>and</strong> drag components. The<br />

researchers reported maximum propulsive force dur<strong>in</strong>g the f<strong>in</strong>al push<br />

phase. In the present study, exam<strong>in</strong><strong>in</strong>g the force-time graph synchronised<br />

to video footage, it was evident that maximum propulsive force<br />

was unable to be produced until the recover<strong>in</strong>g arm was <strong>in</strong> the water<br />

follow<strong>in</strong>g the catch.<br />

conclusIon<br />

The present study demonstrated the importance of represent<strong>in</strong>g active<br />

drag as <strong>in</strong>stantaneous force, rather than a mean value. This provided<br />

unique <strong>and</strong> valuable <strong>in</strong>sight <strong>in</strong>to the <strong>in</strong>tra-cyclic force fluctuations with-


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

<strong>in</strong> a stroke cycle. The graphical demonstration allowed comparison for<br />

future <strong>in</strong>tervention studies. The values measured from the tow<strong>in</strong>g device<br />

were comparable to previous research dur<strong>in</strong>g the passive drag condition.<br />

However the active drag values were much greater than previously<br />

<strong>in</strong>vestigated. Through exam<strong>in</strong><strong>in</strong>g the force-time graph synchronised to<br />

video footage, it was evident that m<strong>in</strong>imum force was produced dur<strong>in</strong>g<br />

the pull phase <strong>and</strong> maximum force dur<strong>in</strong>g the push phase. The tow<strong>in</strong>g<br />

device used to calculate active drag, measured the whole body propulsive<br />

action, therefore tak<strong>in</strong>g <strong>in</strong>to consideration the effect the recover arm had<br />

on the total body propulsive force.<br />

reFerences<br />

Chatard, J. C., Collomp, C., Maglischo, E. & Maglischo C. (1990).<br />

Swimm<strong>in</strong>g Skill <strong>and</strong> Strok<strong>in</strong>g Characteristics of Front Crawl Swimmers.<br />

International Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 11, 156-161.<br />

Chollet, D., Chalies, S. & Chatard, J. C. (2000). A New Index of Coord<strong>in</strong>ation<br />

for the Crawl: Description <strong>and</strong> Usefulness. International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 21(1), 54-59.<br />

Formosa, D. P., Mason B. R. & Burkett, B. (2009). Measur<strong>in</strong>g propulsive<br />

force with<strong>in</strong> the different phases of backstroke swimm<strong>in</strong>g. In A. J.<br />

Harrison, R. Anderson & I. Kenny (Eds.), Proceed<strong>in</strong>gs of the XXVII<br />

International Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports (pp. 98-101), Irel<strong>and</strong>.<br />

Kolmogorov, S. V. & Duplishcheva, O. A. (1992). Active Drag, Useful<br />

Mechanical Power Output <strong>and</strong> Hydrodynamic Force Coefficient <strong>in</strong><br />

Different Swimm<strong>in</strong>g Strokes at Maximum Velocity. Journal of <strong>Biomechanics</strong>,<br />

25(3), 311-318.<br />

Kolmogorov, S. V., Rumyantseva, O. A., Gordon, B. J. & Cappaert, J. M.<br />

(1997). Hydrodynamic Characteristics of Competitive Swimmers of<br />

Different Genders <strong>and</strong> Performance Levels. Journal of Applied <strong>Biomechanics</strong>,<br />

13(1), 88-97.<br />

Maglischo, C. W., Maglischo, E. W., Higg<strong>in</strong>s, J., H<strong>in</strong>richs, R., Luedtke,<br />

D., Schleihauf, R. E., et al. (1988). A Biomechanical Analysis of the<br />

1984 U.S. Olympic Freestyle Distance Swimmers. In B. E Ungerechts,<br />

K Wilke & K Reischle (Eds.), In Proceed<strong>in</strong>gs of the International<br />

Symposium of <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g (pp. 351-360).<br />

Bielefeld, Germany: Human K<strong>in</strong>etics Books, Champaign.<br />

Schleihauf, R. E. (1979). Swimm<strong>in</strong>g propulsion: a hydrodynamic analysis.<br />

Swimm<strong>in</strong>g III, 8, 70-110.<br />

Toussa<strong>in</strong>t, H. M., de Groot, G., Savelberg, H. H., Vervoorn, K., Holl<strong>and</strong>er,<br />

A. P. & van Ingen Schenau, G. J. (1988). Active drag related to<br />

velocity <strong>in</strong> male <strong>and</strong> female swimmers. Journal of <strong>Biomechanics</strong>, 21(5),<br />

435-438.<br />

Toussa<strong>in</strong>t, H. M., Roos, P. E. & Kolmogorov, S. (2004). The determ<strong>in</strong>ation<br />

of drag <strong>in</strong> front crawl swimm<strong>in</strong>g. Journal of <strong>Biomechanics</strong>, 37(11),<br />

1655-1663.<br />

AcKnoWledGMents<br />

The researchers would like to thank the Australian Institute of Sport,<br />

Aquatics Test<strong>in</strong>g, Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> research, Australian <strong>and</strong> National swimm<strong>in</strong>g<br />

team for their contribution to the research.<br />

84<br />

The Mechanical Power Output <strong>in</strong> Water Polo Game: a<br />

Case Report<br />

Gatta, G. 1 , Fantozzi, s. 2 , cortesi, M. 1 , Patti, F. 1 , Bonifazi, M. 3<br />

1Faculty of Exercise <strong>and</strong> Sport Science, University of Bologna,<br />

Italy<br />

2Computer Sciences <strong>and</strong> Systems, Bologna, Italy<br />

3Faculty of <strong>Medic<strong>in</strong>e</strong>, University of Siena, Italy<br />

3Italian Swimm<strong>in</strong>g Federation, Roma, Italy<br />

In water polo some authors have assessed the physical requirements of<br />

the game by analys<strong>in</strong>g physiological <strong>in</strong>dices or consider<strong>in</strong>g the distances<br />

covered at various swimm<strong>in</strong>g speeds <strong>in</strong> the match. In this work, the<br />

passive drag was measured <strong>in</strong> “best glide” (Swim) <strong>and</strong> “head-up” (Wp)<br />

position <strong>in</strong> a water polo player. The active drag was estimated <strong>in</strong>directly<br />

from the passive drag. The mechanical power required to play a match is<br />

calculated on the data of a match model obta<strong>in</strong>ed from a video analysis<br />

<strong>in</strong> a series of <strong>in</strong>ternational water polo matches. The average mechanical<br />

power of a water polo match <strong>in</strong> the Swim model was 150489 J/2400 s=<br />

62.70 W, while <strong>in</strong> WP model it was 481375 J/2400 s= 200.57 W. The<br />

mechanical power required <strong>in</strong> water polo players could be more than<br />

three-fold higher than that required for freestyle swimm<strong>in</strong>g at the same<br />

velocities.<br />

KeYWords: water polo, mechanical power, drag, acceleration,<br />

trudgeon<br />

IntroductIon<br />

A precise def<strong>in</strong>ition of the performance model <strong>in</strong> sports games is far<br />

from be<strong>in</strong>g simple. In water polo some authors have assessed the physical<br />

requirements of the match by analys<strong>in</strong>g physiological <strong>in</strong>dices as heart<br />

rate or consider<strong>in</strong>g the distances covered at various swimm<strong>in</strong>g speeds <strong>in</strong><br />

a series of matches (P<strong>in</strong>n<strong>in</strong>gton et al. 1987, Hohmann & Frase 1992,<br />

Rudic et al. 1999, Platanou & Geladas 2006). Coaches still develop<br />

tra<strong>in</strong><strong>in</strong>g programs consider<strong>in</strong>g swimm<strong>in</strong>g speeds but this does not take<br />

<strong>in</strong>to account that, dur<strong>in</strong>g the match, the water polo player does not move<br />

as a swimmer <strong>in</strong> the best hydrodynamic position, but: 1) swims with the<br />

head raised <strong>and</strong> often <strong>in</strong> contact with opponents, therefore not totally<br />

<strong>in</strong> a hydrodynamic position that is subjected to a higher drag; 2) starts<br />

statically <strong>in</strong> maximum acceleration, without any push from a fixed support.<br />

For this reason we believe that motion patterns of swimm<strong>in</strong>g used<br />

so far underestimate the real amount of mechanical power developed by<br />

the player dur<strong>in</strong>g the match.<br />

The purpose of this work was to compare, <strong>in</strong> a water polo player, the<br />

mechanical power required to play a match as computed with two different<br />

methods: the method used so far <strong>in</strong> swimm<strong>in</strong>g, <strong>and</strong> a new model<br />

based on the specific analysis of the technique of water polo.<br />

Methods<br />

To obta<strong>in</strong> the power required to swim at different speeds, the resistive<br />

force of the water must be computed, def<strong>in</strong>ed by the value of the drag.<br />

The estimation of active drag is still quite complex <strong>and</strong> the methods used<br />

do not f<strong>in</strong>d an agreement among scientists, while the measurement of<br />

passive drag is easier, <strong>and</strong> more reliable. In a water polo player (27 years,<br />

1.77 m, 79 kg), two <strong>in</strong>dices of passive drag (pd) were measured with the<br />

method of tow<strong>in</strong>g at different speeds. The first <strong>in</strong>dex was obta<strong>in</strong>ed <strong>in</strong><br />

the position of “best glide” (Swim), i.e. a ly<strong>in</strong>g down position with head<br />

between the arms, while the second <strong>in</strong>dex was obta<strong>in</strong>ed <strong>in</strong> a “head-up”<br />

position, similar to the previous one, but with head above water, common<br />

<strong>in</strong> water polo play<strong>in</strong>g (Wp).<br />

For the test we used a tow electromechanical motor (Ben-Hur,<br />

ApLab, Roma) dragg<strong>in</strong>g the swimmer through a cable at a programmed<br />

speed, while assess<strong>in</strong>g the resistance of the fluid (see figure 1).


Figure 1. Tow<strong>in</strong>g system (Ben Hur) used for passive drag evaluation.<br />

Trials were carried out at <strong>in</strong>creas<strong>in</strong>g speeds (1.2-1.4-1.6-1.8-2 m/sec)<br />

<strong>and</strong> the curves of the equation:<br />

D = k * V n (1)<br />

(where D = drag, k = drag coefficient, V = swimm<strong>in</strong>g velocity, n = exponent<br />

velocity) were graphically assessed (Bonifazi et al. 2005). From the<br />

formulas obta<strong>in</strong>ed, the active drag <strong>in</strong> the two conditions was estimated<br />

(Kjendlie & Stallmann 2008), as 1.5 times (a) the value of passive drag.<br />

This estimate was performed to compute the work, but it does not affect<br />

the comparison between the two models under exam<strong>in</strong>ation. Furthermore,<br />

the power required dur<strong>in</strong>g acceleration was estimated. In these<br />

cases the resistance is even greater than normally due to the effect of the<br />

“added mass” of water next to the swimmer. First of all, the maximum<br />

acceleration reached by the typical water polo start<strong>in</strong>g <strong>in</strong> “trudgeon” was<br />

computed deriv<strong>in</strong>g the speed signal (expressed <strong>in</strong> m/s) given as output<br />

from the speed encoder. Then, the drag <strong>in</strong> acceleration from static start<strong>in</strong>g<br />

(Wp acceleration = WpA) was obta<strong>in</strong>ed by the tow Ben Hur, while<br />

it provided an acceleration at the swimmer equal to the maximum acceleration<br />

computed by the speed encoder.<br />

From the previously obta<strong>in</strong>ed drag force formulas, the value of the<br />

mechanical power required to the water polo player was computed multiply<strong>in</strong>g<br />

the drag by speed:<br />

Power-drag (Pd) = D * v (2)<br />

It is also possible to write:<br />

Pd = k * v n * v (b) (3)<br />

These values were applied to the model of an <strong>in</strong>ternational match<br />

(Rudic et al. 1999). The match model is obta<strong>in</strong>ed from the <strong>in</strong>dividual<br />

analysis of distances <strong>and</strong> velocities <strong>in</strong> the Rome 1994 World Championship<br />

by record<strong>in</strong>g 14 players <strong>in</strong> 7 matches with a video analysis system<br />

(Play-controller Prhomos Perugia, Italy). The average values of distances<br />

travelled <strong>in</strong> swimm<strong>in</strong>g was 1651 ± 450 m dur<strong>in</strong>g the match, consider<strong>in</strong>g<br />

a play<strong>in</strong>g time of 7 m<strong>in</strong>utes per set (1680 s) but the actual duration of<br />

the match is 40 m<strong>in</strong>utes (2400 s).<br />

results<br />

It was possible to derive the trend of passive drags from the tow<strong>in</strong>g tests<br />

at speeds of 1.2-1.4-1.6-1.8-2 m/sec.<br />

Figure 1. Passive drag with tow<strong>in</strong>g test<br />

chaPter2.<strong>Biomechanics</strong><br />

A visual <strong>in</strong>spection of Figure 1 allows appreciat<strong>in</strong>g the larger values of<br />

passive drag <strong>in</strong> Wp compared to the Swim. The drag value relative to the<br />

acceleration phase was calculated <strong>in</strong> starts from st<strong>and</strong>still at velocities<br />

≥ 1.9 m/sec. After the graphical analysis, the equations of passive drag<br />

obta<strong>in</strong>ed were converted <strong>in</strong>to equations of power-drag (Table 1) accord<strong>in</strong>g<br />

to the aforementioned steps (a <strong>and</strong> b):<br />

Table 1. Equations of power drag.<br />

Power drag(Swim) = (36.22*v1.70 * v)*1.5<br />

Power drag(Wp) = (71.22*v1.85 * v)*1.5<br />

Power drag(WpA) = (112.68*v1.40 * v)*1.5<br />

The total swimm<strong>in</strong>g time was def<strong>in</strong>ed for four ranges of velocity <strong>and</strong> the<br />

values of mechanical power were calculated for all steps from the work<br />

of Rudic (1999). The sum of mechanical power of each step represents<br />

the total mechanical power for both the models (Table 2).<br />

Table 2. Mechanical power results on <strong>in</strong>ternational game’s model (Rudic<br />

1999)<br />

*calculated with WpA<br />

Velocity Time played Power drag Power drag Mechanical<br />

work<br />

Mechanical<br />

work<br />

(m/sec) (sec) (Swim) W (Wp) W (Swim) J (Wp) J<br />

0 468 - - - -<br />

0,5 1097 8,36 14,82 9172 16254<br />

1,35 360 122,16 251,27 43979 90458<br />

1,9 475 204,92 788,76* 97338 374663*<br />

total 2400 150489 481375<br />

Consider<strong>in</strong>g normal freestyle swimm<strong>in</strong>g (Swim), the average mechanical<br />

power <strong>in</strong> a water polo match was 150489 J / 2400 s = 62.70 W, while<br />

<strong>in</strong> the WP model it was 481375 J / 2400 s = 200.57 W. Then, the second<br />

value was 3.2 times higher (Wm/Sm = 200,57/62,70 = 3,20).<br />

dIscussIon<br />

Dur<strong>in</strong>g a water polo match, players perform a series of swimm<strong>in</strong>g spr<strong>in</strong>ts<br />

alternated to stationary phases, with mixed aerobic-anaerobic metabolic<br />

requirements. Several authors have <strong>in</strong>vestigated the functional model of<br />

water polo play<strong>in</strong>g. Functional tests <strong>and</strong> metabolic <strong>in</strong>vestigations were<br />

carried out <strong>and</strong> the data obta<strong>in</strong>ed were related to the distance travelled<br />

at different speeds <strong>in</strong> a match (P<strong>in</strong>n<strong>in</strong>gton et al. 1987, Hohmann &<br />

Frase 1992, Rudic et al. 1999, Platanou & Geladas 2006). Given the<br />

difficulty of quantify<strong>in</strong>g the energy consumption of water polo players<br />

dur<strong>in</strong>g the match, coaches plan tra<strong>in</strong><strong>in</strong>g activities us<strong>in</strong>g normal swimm<strong>in</strong>g<br />

parameters as reference. However, water polo <strong>in</strong>volves a different<br />

swimm<strong>in</strong>g technique that is much more expensive than normal freestyle,<br />

due to the need to keep the head out of the water, to control the ball <strong>and</strong><br />

85


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

other players. This position <strong>in</strong>creases the resistance, which <strong>in</strong> water has a<br />

very significant impact due to the density of the medium. Furthermore,<br />

start<strong>in</strong>g statically, the water polo player cannot push from the edge of<br />

the pool <strong>and</strong> thus uses the technical act of “trudgeon”. The acceleration<br />

phase requires additional energy expenditure, as it is overloaded by the<br />

higher drag due to the additional water mass <strong>in</strong> front of the swimmer.<br />

These considerations lead to revise the power values that are required<br />

<strong>in</strong> water polo players to move to a given swimm<strong>in</strong>g speed. Rodriguez<br />

(1994) found higher energy expenditure <strong>in</strong> tests performed by water<br />

polo compared to swimmers. Perform<strong>in</strong>g on a reference athlete a series<br />

of tow<strong>in</strong>g tests, we compared the values of drag, def<strong>in</strong><strong>in</strong>g the power<br />

required to move, compar<strong>in</strong>g the technique of water polo with normal<br />

freestyle. Estimat<strong>in</strong>g these values at different speeds dur<strong>in</strong>g a model<br />

game, we suggest that the mechanical power required to the water polo<br />

players could be more than three-fold higher than that required for freestyle<br />

swimm<strong>in</strong>g at the same velocities.<br />

This study highlights the importance of develop<strong>in</strong>g specific tra<strong>in</strong><strong>in</strong>g<br />

programs for water polo, address<strong>in</strong>g the higher requirements of<br />

mechanical power, tak<strong>in</strong>g <strong>in</strong>to account the specific movement techniques<br />

<strong>and</strong> compar<strong>in</strong>g the distances travelled us<strong>in</strong>g different swimm<strong>in</strong>g<br />

techniques. However, further acquisitions will be performed with more<br />

athletes <strong>and</strong> matches, with the aim of identify<strong>in</strong>g the specific differences<br />

between the models.<br />

reFerences<br />

Bonifazi, M., Adami, A., Veronesi, A., Castioni, M. & Cevese, A.,<br />

(2005). Comparison between passive drag <strong>and</strong> drag dur<strong>in</strong>g leg kick<strong>in</strong>g<br />

of the crawl stroke <strong>in</strong> top level swimmers. Medic<strong>in</strong>a dello Sport,<br />

58, 81-87.<br />

Hohmann, A. & Frase, R. (1992). Analysis of swimm<strong>in</strong>g speed <strong>and</strong> energy<br />

metabolism <strong>in</strong> competitive water polo games. <strong>in</strong> MacLaren J.<br />

E., Reilly T., Lees A., (eds) <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g,<br />

313-19, N Spon, London.<br />

Kjendlie P. L. & Stallmann R. K. (2008). Drag characteristics of competitive<br />

swimm<strong>in</strong>g children <strong>and</strong> adults. Journal of Applied <strong>Biomechanics</strong>,<br />

24(1), 35-42.<br />

P<strong>in</strong>n<strong>in</strong>gton, H. C., Dawson, B. & Blanksby, B. A. (1987). Cardiorespiratory<br />

responses of water polo players perform<strong>in</strong>g the head-<strong>in</strong>-thewater<br />

<strong>and</strong> the head-out-the-water front crawl swimm<strong>in</strong>g technique.<br />

The Australian Journal of Science <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Sport, 19(1), 15-19.<br />

Platanou, T. & Geladas, N. (2006). The <strong>in</strong>fluence of game duration <strong>and</strong><br />

play<strong>in</strong>g position on <strong>in</strong>tensity of exercise dur<strong>in</strong>g match-play <strong>in</strong> elite<br />

water polo players. Journal of Sports Science, 24(11), 1173-81.<br />

Rodriguez, F. A. (1994). Physiological test<strong>in</strong>g of swimmers <strong>and</strong> water<br />

polo players <strong>in</strong> Spa<strong>in</strong>. <strong>in</strong> Miyashita M., Mutoh Y., Richardson A.B.,<br />

(eds) <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Aquatic Sports, 172-77, Karger, Basel.<br />

Rudic, R., D’Ottavio, S., Bonifazi, M., Alippi, B., Gatta, G. & Sardella,<br />

F. (1999). Il modello funzionale nella pallanuoto. La Tecnica del Nuoto<br />

26, 21-24.<br />

86<br />

Comparison of Comb<strong>in</strong>ations of Vectors to def<strong>in</strong>e the<br />

Plane of the H<strong>and</strong> <strong>in</strong> order to calculate the Attack<br />

Angle dur<strong>in</strong>g the Scull<strong>in</strong>g Motion<br />

Gomes, l.e. 1 , Melo, M.o. 1 , la torre, M. 1 , loss, J.F. 1<br />

1 Federal University of Rio Gr<strong>and</strong>e do Sul, Porto Alegre, Brazil<br />

Studies <strong>in</strong>to swimm<strong>in</strong>g propulsion describe different comb<strong>in</strong>ations of<br />

vectors to def<strong>in</strong>e the h<strong>and</strong> plane, which may alter the attack angle. The<br />

study aims (i) to verify the agreement between the attack angles calculated<br />

us<strong>in</strong>g different comb<strong>in</strong>ations of vectors, described <strong>in</strong> the literature<br />

<strong>and</strong> proposed by this study, to def<strong>in</strong>e the plane of the h<strong>and</strong> <strong>and</strong> (ii) to<br />

verify the variation <strong>in</strong> vector length of the methods found to be agreement<br />

<strong>in</strong> order to establish which method is most recommended when<br />

estimat<strong>in</strong>g the attack angle dur<strong>in</strong>g scull<strong>in</strong>g motion. The methods of calculat<strong>in</strong>g<br />

attack angles used from the literature <strong>and</strong> the one proposed<br />

by this study are <strong>in</strong> agreement. The variation <strong>in</strong> vector lengths of the<br />

proposed method was smaller than <strong>in</strong> the other vectors. We recommend<br />

us<strong>in</strong>g the proposed method to calculate the attack angle when analyz<strong>in</strong>g<br />

this movement.<br />

Key words: swimm<strong>in</strong>g, synchronized swimm<strong>in</strong>g, propulsion<br />

IntroductIon<br />

Propulsion is one of the key factors determ<strong>in</strong><strong>in</strong>g performance <strong>in</strong> human<br />

competitive swimm<strong>in</strong>g. However, as yet, this phenomenon is not<br />

fully understood <strong>and</strong> research to determ<strong>in</strong>e propulsive forces exerted<br />

by swimmers’ h<strong>and</strong>s <strong>and</strong> arms has been strictly experimental. In this<br />

experimental research, studies <strong>in</strong>to propulsion have been based on quasisteady<br />

analyses, which depend on the assumption that the flow under<br />

steady conditions (constant velocity, constant attack <strong>and</strong> sweepback<br />

angles) is comparable to the flow dur<strong>in</strong>g the actual swimm<strong>in</strong>g stroke.<br />

Quasi-steady analysis <strong>in</strong>volves the follow<strong>in</strong>g steps: (1) measur<strong>in</strong>g<br />

the lift <strong>and</strong> drag forces act<strong>in</strong>g on model h<strong>and</strong>s <strong>in</strong> an open-water channel<br />

or <strong>in</strong> a w<strong>in</strong>d tunnel for a wide range of h<strong>and</strong> orientations <strong>and</strong>, then<br />

calculat<strong>in</strong>g the lift <strong>and</strong> drag coefficients for each condition; (2) record<strong>in</strong>g<br />

an underwater action of a swimmer us<strong>in</strong>g three-dimensional film<strong>in</strong>g to<br />

determ<strong>in</strong>e the path, velocity <strong>and</strong> orientation of the h<strong>and</strong> relative to the<br />

water (attack <strong>and</strong> sweepback angles); (3) comb<strong>in</strong><strong>in</strong>g the results from<br />

steps 1 <strong>and</strong> 2 to determ<strong>in</strong>e the lift <strong>and</strong> drag forces us<strong>in</strong>g hydrodynamic<br />

equations.<br />

Thus, <strong>in</strong> order to estimate h<strong>and</strong> forces <strong>in</strong> actual swimm<strong>in</strong>g, it is<br />

necessary to def<strong>in</strong>e the plane of the h<strong>and</strong> us<strong>in</strong>g l<strong>and</strong>marks to calculate<br />

attack angle dur<strong>in</strong>g underwater action of a swimmer, s<strong>in</strong>ce the attack<br />

angle is def<strong>in</strong>ed as the angle between the plane of the h<strong>and</strong> <strong>and</strong> the<br />

velocity vector of the h<strong>and</strong> (Payton <strong>and</strong> Bartlett, 1995). Unfortunately,<br />

problems may arise dur<strong>in</strong>g this procedure, such as errors derived from<br />

the digitiz<strong>in</strong>g procedure, s<strong>in</strong>ce the h<strong>and</strong> is hard to accurately digitize,<br />

because it is small <strong>and</strong> l<strong>and</strong>marks are placed close together (Payton <strong>and</strong><br />

Bartlett, 1995).<br />

From these arguments, Lauder at al. (2001) established the accuracy<br />

<strong>and</strong> reliability of current <strong>and</strong> newly proposed procedures for the reconstruction<br />

of h<strong>and</strong> velocity, sweepback <strong>and</strong> attack angles from underwater<br />

three-dimensional video analysis. They suggested that a greater distance<br />

between the l<strong>and</strong>marks would be beneficial <strong>in</strong> reduc<strong>in</strong>g errors aris<strong>in</strong>g from<br />

the digitiz<strong>in</strong>g procedure. Thus, five additional comb<strong>in</strong>ations of vectors<br />

were identified <strong>in</strong> order to def<strong>in</strong>e the plane of the h<strong>and</strong>. They have suggested<br />

that their proposed method, ‘Lauder 1’, improves accuracy when<br />

measur<strong>in</strong>g the sweepback angle <strong>and</strong>, more importantly, the attack angle.<br />

However, there are a number of untested possible comb<strong>in</strong>ations that may<br />

be used to def<strong>in</strong>e the plane of the h<strong>and</strong>. Moreover, <strong>in</strong> order to achieve their<br />

purposes, Lauder et al. (2001) used a full-scale mechanical arm capable<br />

of simulat<strong>in</strong>g a controlled <strong>and</strong> highly repeatable underwater phase of the


front-crawl stroke. This mechanical arm has a restrict movement, s<strong>in</strong>ce the<br />

medio-lateral direction was not considered as there was little or no h<strong>and</strong><br />

motion <strong>in</strong> this direction due to the mechanical constra<strong>in</strong>ts.<br />

Therefore, the purposes of this study, which <strong>in</strong>volved synchronized<br />

swimmers <strong>and</strong> swimmers <strong>in</strong> a real situations, were (i) to verify the agreement<br />

between the attack angles calculated us<strong>in</strong>g different comb<strong>in</strong>ations<br />

of vectors, described <strong>in</strong> the literature <strong>and</strong> proposed by this study, to<br />

def<strong>in</strong>e the plane of the h<strong>and</strong> <strong>and</strong> (ii) to verify the variation <strong>in</strong> vector<br />

length of the methods found to be agreement <strong>in</strong> order to establish which<br />

method is most recommended when estimat<strong>in</strong>g the attack angle dur<strong>in</strong>g<br />

scull<strong>in</strong>g motion performed <strong>in</strong> a stationary vertical position (head above<br />

the water’s surface).<br />

Methods<br />

The sample consisted of 16 participants (10 female synchronized swimmers<br />

<strong>and</strong> 6 female swimmers; age 13.7±2.3 years; height 1.56±0.11 m;<br />

weight 51.7±4.2 kg). In order to participate <strong>in</strong> the study, swimmers were<br />

required to have at least 6 months of exercise <strong>in</strong>clud<strong>in</strong>g scull<strong>in</strong>g actions<br />

dur<strong>in</strong>g their tra<strong>in</strong><strong>in</strong>g program. All the participants or their guardians,<br />

<strong>in</strong> those cases where the participants were not legally capable, signed<br />

<strong>in</strong>formed consent forms. The Ethics Committee of the university where<br />

the study was undertaken approved this study.<br />

Record<strong>in</strong>g took place <strong>in</strong> an <strong>in</strong>door 25 m swimm<strong>in</strong>g pool. Two digital<br />

video cameras ( JVC GR-DVL 9800) were positioned beh<strong>in</strong>d two glass<br />

w<strong>in</strong>dows <strong>in</strong> the side of the pool beneath the water level. The distance<br />

between these w<strong>in</strong>dows was 11.2 m. The sampl<strong>in</strong>g frequency of the video<br />

cameras was 50 fields-per-second. The Digital Video for W<strong>in</strong>dows<br />

(Dvideow) software was used to track the markers. Each camera was<br />

connected to a computer, which was l<strong>in</strong>ked to an <strong>in</strong>tranet <strong>in</strong> order to<br />

start the record<strong>in</strong>g at same time for both cameras. The spatial resolution<br />

of the video system used was 1024 x 768 pixels.<br />

A cube (0.80 m x 0.80 m x 0.80 m) was used as a control object with<br />

12 control object po<strong>in</strong>ts. The distance between the control object <strong>and</strong> a<br />

po<strong>in</strong>t equidistant between the w<strong>in</strong>dows was 6.7 m.<br />

L<strong>and</strong>marks were placed on the distal end of the third f<strong>in</strong>ger (1),<br />

metacarpophalangeal jo<strong>in</strong>ts of the second (2) <strong>and</strong> fifth f<strong>in</strong>gers (3), on<br />

the centre of the wrist jo<strong>in</strong>t (4) <strong>and</strong> the elbow (5) of the right limb, thus,<br />

the movement was considered symmetrical. After this, each participant<br />

performed a warm-up with scull<strong>in</strong>g actions <strong>and</strong> familiarization with the<br />

experimental conditions with the right side of the body directed toward<br />

the equidistant po<strong>in</strong>t between the w<strong>in</strong>dows, <strong>in</strong> the position to be used<br />

dur<strong>in</strong>g record<strong>in</strong>g. All tasks were performed at the calibrated volume.<br />

Each participant was asked to perform 20 seconds of scull<strong>in</strong>g actions,<br />

ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g a stationary vertical position with the head above the<br />

water surface <strong>and</strong> with the water at ch<strong>in</strong> level <strong>in</strong> order to ma<strong>in</strong>ta<strong>in</strong> all<br />

l<strong>and</strong>marks submerged dur<strong>in</strong>g record<strong>in</strong>g. This length of time was chosen<br />

<strong>in</strong> order to allow the participants sufficient time to stabilize the movement,<br />

while ma<strong>in</strong>tenance of the chosen position was the only criterion<br />

for st<strong>and</strong>ardization of scull<strong>in</strong>g movement performance. Based on a qualitative<br />

criterion of stability, three cycles of scull<strong>in</strong>g motion were chosen<br />

for digitalization.<br />

Most of the studies found <strong>in</strong> the literature analyzed only one cycle<br />

of scull<strong>in</strong>g motion. By contrast, <strong>in</strong> the present study, it was decided to<br />

analyze three consecutive cycles of scull<strong>in</strong>g, chosen when the movement<br />

seemed to be stable. An experienced digitizer, us<strong>in</strong>g Dvideow software,<br />

manually digitized these. By analyz<strong>in</strong>g three cycles, the <strong>in</strong>fluence of<br />

any r<strong>and</strong>om error that may occur dur<strong>in</strong>g the digitaliz<strong>in</strong>g procedure was<br />

m<strong>in</strong>imized.<br />

Three-dimensional coord<strong>in</strong>ates were obta<strong>in</strong>ed us<strong>in</strong>g a direct l<strong>in</strong>ear<br />

transformation method. The accuracy of the measurements was calculated<br />

<strong>and</strong> was equal to 0.004 m. The coefficient of variation was 0.5% when<br />

the distance between two rigidly l<strong>in</strong>ked markers at the known distance<br />

was reconstructed. All three-dimensional coord<strong>in</strong>ates were smoothed<br />

us<strong>in</strong>g a seventh order low-pass Butterworth digital filter with cut-offs<br />

around 4 <strong>and</strong> 5 Hz, accord<strong>in</strong>g to Residual Analysis (W<strong>in</strong>ter, 2005).<br />

chaPter2.<strong>Biomechanics</strong><br />

The calculations of the attack angle were made us<strong>in</strong>g the Matlab<br />

software (version 7.1). Figures 1 <strong>and</strong> 2 show the vectors that were used<br />

to reconstruct the h<strong>and</strong> orientation <strong>and</strong> Table 1 shows the different<br />

comb<strong>in</strong>ations of these vectors described by Schleihauf (1979), Berger et<br />

al. (1995), Lauder et al. (2001) (Lauder 1 – 5) <strong>and</strong> the new comb<strong>in</strong>ation<br />

(NC) proposed by this study.<br />

Figure 1. Vectors on h<strong>and</strong> that can be used to reconstruct the h<strong>and</strong> orientation.<br />

Figure 2. Vectors on h<strong>and</strong> <strong>and</strong> forearm that may be used to reconstruct<br />

the h<strong>and</strong> orientation.<br />

The angle of attack was def<strong>in</strong>ed as the angle between the plane of the<br />

h<strong>and</strong> <strong>and</strong> the velocity vector of the h<strong>and</strong> (Payton <strong>and</strong> Bartlett, 1995).<br />

The plane of the h<strong>and</strong> was def<strong>in</strong>ed by the cross-product of vectors 1 <strong>and</strong><br />

2, which def<strong>in</strong>e a vector perpendicular (VP) to the plane of the h<strong>and</strong>. The<br />

velocity vector (v) was calculated us<strong>in</strong>g the raw coord<strong>in</strong>ate data from<br />

the midpo<strong>in</strong>t between the distal end of the second <strong>and</strong> fifth f<strong>in</strong>ger. The<br />

attack angle was calculated as 90° m<strong>in</strong>us the angle between v <strong>and</strong> VP.<br />

Once the angles were calculated, (1) the time of each cycle of scull<strong>in</strong>g<br />

motion was normalized (from 1 to 100%), (2) each participant was<br />

represented by the average of the three cycles <strong>and</strong> (3) the average cycle<br />

of all participants was calculated <strong>and</strong> used to verify the agreement between<br />

the attack angles calculated us<strong>in</strong>g different comb<strong>in</strong>ations of vectors<br />

described <strong>in</strong> the literature <strong>and</strong> proposed by this study. The degree<br />

of agreement between the attack angles calculated us<strong>in</strong>g the different<br />

comb<strong>in</strong>ations of vectors used to def<strong>in</strong>e the plane of h<strong>and</strong> was established<br />

based on graphical techniques from Bl<strong>and</strong> <strong>and</strong> Altman (1986),<br />

<strong>in</strong> which the data were presented graphically by plott<strong>in</strong>g the difference<br />

between each method versus their average obta<strong>in</strong>ed by step 3. Thus one<br />

hundred po<strong>in</strong>ts were plotted for each normalized time. The mean differences<br />

(bias) <strong>and</strong> st<strong>and</strong>ard deviation (SD) of the differences between the<br />

values obta<strong>in</strong>ed with the methods, expressed <strong>in</strong> degree, were calculated.<br />

The limits of agreement were set at bias ± 2SD. All statistical procedures<br />

were performed us<strong>in</strong>g Matlab software. Thus, the analysis of the results<br />

comprised of two steps: (1) the agreement between the attack angles<br />

calculated was verified us<strong>in</strong>g different comb<strong>in</strong>ations of vectors, which<br />

were used to def<strong>in</strong>e the plane of the h<strong>and</strong>; (2) the means <strong>and</strong> st<strong>and</strong>ard<br />

deviations were calculated of these vector lengths <strong>in</strong> the methods that<br />

were found to agree. Therefore, from these values, the variation <strong>in</strong> vector<br />

length of the methods that were found to agree was estimated.<br />

Table 1. Different comb<strong>in</strong>ations of vectors for the reconstruction of the<br />

plane of the h<strong>and</strong> (see Figures 1 <strong>and</strong> 2 for location).<br />

Comb<strong>in</strong>ations Vector 1 Vector 2<br />

Schleihauf VE VC<br />

Berger et al. VB VE<br />

Lauder 1 VD VC<br />

Lauder 2 VD VI<br />

Lauder 3 VH VD<br />

Lauder 4 VD VG<br />

Lauder 5 VF VD<br />

NC VH VI<br />

87


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

Accord<strong>in</strong>g to figures 3 to 5, the comb<strong>in</strong>ation of vectors for the reconstruction<br />

of the plane of the h<strong>and</strong> of Schleihauf is <strong>in</strong> agreement with the<br />

comb<strong>in</strong>ation proposed <strong>in</strong> Lauder 1. The two methods are <strong>in</strong> agreement<br />

with the new comb<strong>in</strong>ation (NC) proposed <strong>in</strong> this study. The variation<br />

<strong>in</strong> vector length of the methods found to be <strong>in</strong> agreement is presented<br />

<strong>in</strong> Table 2.<br />

Table 2. Variation (%) <strong>in</strong> vector length of the methods that were <strong>in</strong><br />

agreement.<br />

Comb<strong>in</strong>ations Vector 1 Vector 2<br />

Schleihauf 12 17.9<br />

Lauder 1 7.2 17.9<br />

NC 7.8 8.4<br />

dIscussIon<br />

The results of this study show that the attack angles calculated from<br />

Schleihauf, Lauder 1 <strong>and</strong> NC methods are <strong>in</strong> agreement, that is, the<br />

three methods may be used <strong>in</strong>terchangeably <strong>in</strong> order to calculate the attack<br />

angle. However, when the variation <strong>in</strong> vector length of these methods<br />

is observed there are greater variations between the Schleihauf <strong>and</strong><br />

Lauder 1 methods.<br />

Lauder at al. (2001) also found the Schleihauf <strong>and</strong> Lauder 1 methods<br />

to be very similar <strong>and</strong> the mean percentage error <strong>in</strong> vector length<br />

reconstruction was smaller <strong>in</strong> Lauder 1 than Schleihauf. Furthermore,<br />

they concluded that the method proposed by Berger at al. (1995) differed<br />

from both Schleihauf <strong>and</strong> Lauder 1. This f<strong>in</strong>d<strong>in</strong>g is <strong>in</strong> accordance<br />

with the f<strong>in</strong>d<strong>in</strong>gs of this study, s<strong>in</strong>ce the method from Berger et<br />

al. (1995) was found not to be <strong>in</strong> agreement with the Schleihauf <strong>and</strong><br />

Lauder 1 methods.<br />

The plane of the h<strong>and</strong> is found by calculat<strong>in</strong>g the cross product between<br />

two vectors, which represent the plane of the h<strong>and</strong>. These two<br />

vectors are calculated from three po<strong>in</strong>ts, as <strong>in</strong> the Berger et al. (1995) <strong>and</strong><br />

NC methods. Nevertheless, Schleihauf <strong>and</strong> Lauder 1 use four po<strong>in</strong>ts to<br />

def<strong>in</strong>e the plane of the h<strong>and</strong>, although the po<strong>in</strong>ts do not necessary lie<br />

<strong>in</strong> a s<strong>in</strong>gle plane.<br />

Although Lauder at al. (2001) suggested that, s<strong>in</strong>ce the method<br />

from Berger et al. (1995) requires fewer po<strong>in</strong>ts for reconstruction, it<br />

could offer a clear advantage <strong>in</strong> real life, when some of the po<strong>in</strong>ts may<br />

be obscured by water turbulence. Our results suggest it is better to use<br />

Schleihauf, Lauder 1 or NC when analyz<strong>in</strong>g the scull<strong>in</strong>g motion. Moreover,<br />

the vectors used <strong>in</strong> the method from Berger et al. (1995) appear to<br />

be more sensitive to slight changes <strong>in</strong> the h<strong>and</strong> shape than those used <strong>in</strong><br />

Schleihauf, Lauder 1 <strong>and</strong> NC.<br />

Figure 3. Agreement between Schleihauf <strong>and</strong> Lauder 1 methods for reconstruct<strong>in</strong>g<br />

the attack angle.<br />

88<br />

Figure 4. Agreement between Schleihauf <strong>and</strong> NC methods for reconstruct<strong>in</strong>g<br />

the attack angle.<br />

Figure 5. Agreement between Lauder 1 <strong>and</strong> NC methods for reconstruct<strong>in</strong>g<br />

the attack angle.<br />

Us<strong>in</strong>g three po<strong>in</strong>ts may present an advantage, <strong>and</strong> the NC method is<br />

better than the Schleihauf <strong>and</strong> Lauder 1 methods. Furthermore, Lauder<br />

1 <strong>and</strong> NC presented a smaller variation <strong>in</strong> their vector lengths than the<br />

methods from Schleihauf (1979) <strong>and</strong> Berger et al. (1995) because there<br />

is a greater distance between the po<strong>in</strong>ts, which might be beneficial <strong>in</strong> reduc<strong>in</strong>g<br />

error. In addition, the vectors used <strong>in</strong> the NC method presented<br />

a smaller variation <strong>in</strong> their lengths than other two. Thus, it is suggested<br />

that the NC method should be used <strong>in</strong> order to calculate the attack<br />

angle dur<strong>in</strong>g analysis of scull<strong>in</strong>g motion.<br />

conclusIon<br />

The attack angles calculated from Schleihauf, Lauder 1 <strong>and</strong> NC (the<br />

new method proposed by this study) methods were found to be <strong>in</strong> agreement.<br />

However, there was less variation <strong>in</strong> the length of the vectors used<br />

<strong>in</strong> the NC method than <strong>in</strong> those of the other two methods. Therefore,<br />

given that the results of the present study were obta<strong>in</strong>ed <strong>in</strong> a real situation<br />

as opposed to a model, we suggest us<strong>in</strong>g the NC method to calculate<br />

the attack angle <strong>in</strong> the analysis of the scull<strong>in</strong>g motion.<br />

reFerences<br />

Berger, M., Groot, G. & Holl<strong>and</strong>er, P. (1995). Hydrodynamic drag <strong>and</strong><br />

lift forces on human h<strong>and</strong>/arm models. J Biomech, 28, 125-33.<br />

Bl<strong>and</strong>, J. M. & Altman, D. G. (1986). Statistical methods for assess<strong>in</strong>g<br />

agreement between two methods of cl<strong>in</strong>ical measurement. Lancet,<br />

327, 307-10.<br />

Lauder, M. A., Dabnichki, P. & Bartlett, R. M. (2001). Improved accuracy<br />

<strong>and</strong> reliability of sweepback angle, pitch angle <strong>and</strong> h<strong>and</strong> velocity<br />

calculations <strong>in</strong> swimm<strong>in</strong>g. J Biomech, 34, 31-9.<br />

Payton, C. J. & Bartlett, R. M. (1995). Estimat<strong>in</strong>g propulsive forces <strong>in</strong><br />

swimm<strong>in</strong>g from three-dimensional k<strong>in</strong>ematic data. J Sports Sci, 13,<br />

447-54.<br />

Schleihauf, R. (1979). A Hydrodynamic Analysis of Swimm<strong>in</strong>g Propulsion.<br />

Swimm<strong>in</strong>g III (pp. 70-109). Edmonton, Canada: University of<br />

Alberta.<br />

W<strong>in</strong>ter, D. (2005). <strong>Biomechanics</strong> <strong>and</strong> Motor Control of Human Movement.<br />

New Jersey: John Wiley & Sons, Inc.


The Acute Effect of Front Crawl Spr<strong>in</strong>t-resisted<br />

Swimm<strong>in</strong>g on the Direction of the Resultant Force of<br />

the H<strong>and</strong><br />

Gourgoulis, V. 1 , Aggeloussis, n. 1 , Mavridis, G. 1 , Boli, A. 1 ,<br />

toubekis, A.G. 2 , Kasimatis, P. 1 , Vezos, n. 1 , Mavrommatis, G. 1<br />

1 Democritus University of Thrace, Komot<strong>in</strong>i, Greece<br />

2 Kapodistrian University of Athens, Athens, Greece<br />

The aim of the study was to <strong>in</strong>vestigate the acute effect of front crawl<br />

spr<strong>in</strong>t-resisted swimm<strong>in</strong>g on the direction of the resultant force of the<br />

h<strong>and</strong>. Five female swimmers swam 25 m with maximal <strong>in</strong>tensity with<br />

<strong>and</strong> without added resistance. The underwater motion of the h<strong>and</strong> was recorded<br />

us<strong>in</strong>g 4 cameras (60 Hz) <strong>and</strong> the Ariel Performance Analysis System<br />

was used for the digitization. The results showed that the magnitude<br />

of the drag <strong>and</strong> lift forces, as well as the magnitude of the resultant force<br />

was not modified significantly dur<strong>in</strong>g resisted swimm<strong>in</strong>g. However, the<br />

angle formed between the resultant force <strong>and</strong> the axis of the swimm<strong>in</strong>g<br />

propulsion was decreased significantly <strong>in</strong> the pull phase. Thus, it could be<br />

speculated that spr<strong>in</strong>t-resisted swimm<strong>in</strong>g could contribute to the learn<strong>in</strong>g<br />

of a more effective application of the propulsive forces.<br />

Key words: front crawl, resisted swimm<strong>in</strong>g, resultant force.<br />

IntroductIon<br />

In front crawl swimm<strong>in</strong>g, the propulsive forces generated ma<strong>in</strong>ly from<br />

the arms. The way swimmers use their arms to apply these forces is decisive<br />

for effective swimm<strong>in</strong>g propulsion (Arellano, 1999). The resultant<br />

propulsive force produced by a swimmer’s h<strong>and</strong> is a comb<strong>in</strong>ation of two<br />

types of propulsive forces: the drag force <strong>and</strong> the lift force. For effective<br />

swimm<strong>in</strong>g propulsion the resultant of these two forces should be aimed,<br />

as much as possible, <strong>in</strong> the swimm<strong>in</strong>g direction (Rushall et al., 1994;<br />

Schleihauf, 2004; Toussa<strong>in</strong>t et al., 2000). In addition, <strong>in</strong> front crawl<br />

swimm<strong>in</strong>g, which is a stroke with alternate arm movement, it is necessary<br />

to avoid significant deviations of the resultant force vector from<br />

the swimm<strong>in</strong>g direction, s<strong>in</strong>ce this may cause undesirable sideways <strong>and</strong><br />

vertical deviations of the body, <strong>in</strong>creas<strong>in</strong>g the resistive forces (Vorontsov<br />

& Rumyantsev, 2000).<br />

Moreover, it is considered that tra<strong>in</strong><strong>in</strong>g methods such as spr<strong>in</strong>tresisted<br />

swimm<strong>in</strong>g where the swimmers swim aga<strong>in</strong>st a resistance <strong>in</strong><br />

addition to the natural water resistance are more effective for the improvement<br />

of the swimm<strong>in</strong>g performance than dry l<strong>and</strong> tra<strong>in</strong><strong>in</strong>g methods<br />

(Girold et al., 2007; Llop et al., 2006; Williams et al., 2001). In the<br />

past, the acute effect of spr<strong>in</strong>t-resisted swimm<strong>in</strong>g has been <strong>in</strong>vestigated<br />

<strong>in</strong> various k<strong>in</strong>ematic characteristics of the stroke, such as the time of the<br />

underwater motion of the h<strong>and</strong>, the velocity of the h<strong>and</strong>, its medial –<br />

lateral displacements, the stroke rate, the stroke length, the stroke depth<br />

<strong>and</strong> the swimm<strong>in</strong>g velocity (Maglischo et al., 1984; Maglischo et al.,<br />

1985; Williams et al., 2001).<br />

However, there is a lack of data regard<strong>in</strong>g the effect of the spr<strong>in</strong>t-resisted<br />

swimm<strong>in</strong>g on the direction of the resultant force. It could be speculated<br />

that, if dur<strong>in</strong>g spr<strong>in</strong>t resisted swimm<strong>in</strong>g the angle between the<br />

resultant force vector <strong>and</strong> the axis of swimm<strong>in</strong>g propulsion is decreased,<br />

then this tra<strong>in</strong><strong>in</strong>g method could probably contribute to the learn<strong>in</strong>g of a<br />

more effective application of the propulsive forces. Therefore, the aim of<br />

the present study was to exam<strong>in</strong>e the acute effect of front crawl spr<strong>in</strong>tresisted<br />

swimm<strong>in</strong>g on the direction of the resultant force of the h<strong>and</strong>.<br />

Methods<br />

Five female competitive swimmers participated <strong>in</strong> the study (age: 20.4<br />

± 6.1 years, height: 1.73 ± 0.03 m, body mass: 59.1 ± 6.67 kg, best performance<br />

<strong>in</strong> the 100 m front crawl swimm<strong>in</strong>g: 62.59 ± 2.88 s). Each<br />

swimmer swam <strong>in</strong> r<strong>and</strong>omized order two trials of 25 m front crawl with<br />

chaPter2.<strong>Biomechanics</strong><br />

maximal <strong>in</strong>tensity. One of the trials was performed without added resistance<br />

<strong>and</strong> the other one was performed with an added resistance. A<br />

bowl with a diameter of 32 cm <strong>and</strong> a capacity of 6 l was used as added<br />

resistance. The bowl was pulled by its convex side <strong>and</strong> it was tethered on<br />

a belt, which was around the waist of each swimmer, with a 1.5 m long<br />

elastic tube (Mavridis et al., 2006). All trials were executed us<strong>in</strong>g a sixbeat<br />

kick <strong>and</strong> without breath<strong>in</strong>g <strong>in</strong> the middle of the distance, where the<br />

underwater stroke was recorded.<br />

The underwater motion of the right h<strong>and</strong> was recorded us<strong>in</strong>g four<br />

camcorders (60 Hz), which were positioned beh<strong>in</strong>d four stationary periscope<br />

systems. The synchronisation of the cameras was achieved us<strong>in</strong>g<br />

a LED system visible <strong>in</strong> the field of view of each camera. A calibration<br />

frame with dimensions of 1m x 3m x 1m for the transverse (X), the<br />

longitud<strong>in</strong>al (Y) <strong>and</strong> the vertical (Z) directions, respectively, conta<strong>in</strong><strong>in</strong>g<br />

24 control po<strong>in</strong>ts, was used for the calibration of the recorded space <strong>in</strong><br />

the middle of the 25 m swimm<strong>in</strong>g pool (Gourgoulis et al., 2008a). Before<br />

film<strong>in</strong>g, selected po<strong>in</strong>ts were marked on each swimmer’s sk<strong>in</strong> correspond<strong>in</strong>g<br />

to the acromion of the right shoulder, the greater trochanter<br />

of the right <strong>and</strong> left hip, <strong>and</strong> four po<strong>in</strong>ts on the right h<strong>and</strong>: the center<br />

of the wrist, the tip of the middle f<strong>in</strong>ger, the <strong>in</strong>dex <strong>and</strong> the little f<strong>in</strong>ger<br />

metacarpophalangeal jo<strong>in</strong>ts. These po<strong>in</strong>ts were digitized us<strong>in</strong>g the Ariel<br />

Performance Analysis System (Ariel Dynamics Inc., San Diego CA,<br />

USA) <strong>and</strong> their three dimensional coord<strong>in</strong>ates were calculated us<strong>in</strong>g the<br />

direct l<strong>in</strong>ear transformation procedure.<br />

For a detailed description <strong>and</strong> quantification, the underwater stroke<br />

of the right h<strong>and</strong> was divided <strong>in</strong>to three dist<strong>in</strong>ct phases: (a) entry <strong>and</strong><br />

catch, (c) pull <strong>and</strong> (c) push (Chollet et al., 2000). The hydrodynamic<br />

coefficients <strong>and</strong> the methodology presented by S<strong>and</strong>ers (1999) were<br />

used for the estimation of the drag force, the lift force <strong>and</strong> the resultant<br />

force of the swimmer’s h<strong>and</strong>. Moreover, the component of the resultant<br />

force <strong>in</strong> the swimm<strong>in</strong>g direction, def<strong>in</strong>ed as the effective propulsive<br />

force generated from the swimmer’s h<strong>and</strong>, <strong>and</strong> the angle between the<br />

resultant force <strong>and</strong> the axis of propulsion were calculated (Gourgoulis et<br />

al., 2008c). The stroke length, the stroke rate <strong>and</strong> the mean swimm<strong>in</strong>g<br />

velocity were also calculated (Gourgoulis et al., 2008b).<br />

For the statistical treatment of the data, the t-test for dependent<br />

samples was used. The normal distribution <strong>and</strong> the homogeneity of variance<br />

were verified us<strong>in</strong>g the Kolmogorov – Smirnov test <strong>and</strong> the Levene<br />

test, respectively. The significance level was set as p < 0.05.<br />

results<br />

Dur<strong>in</strong>g resisted swimm<strong>in</strong>g the stroke length, the stroke rate <strong>and</strong> the<br />

mean swimm<strong>in</strong>g velocity were decreased significantly (Table 1).<br />

Table 1. Stroke length (m), stroke rate (cycles⋅s -1 ) <strong>and</strong> mean swimm<strong>in</strong>g<br />

velocity (m⋅ s -1 ) dur<strong>in</strong>g front crawl swimm<strong>in</strong>g with <strong>and</strong> without added<br />

resistance.<br />

Without<br />

added resistance<br />

With<br />

added resistance<br />

t- value<br />

Stroke length 1.88 ± 0.07 1.28 ± 0.08 13.155*<br />

Stroke rate 0.84 ± 0.04 0.74 ± 0.06 5.188*<br />

Mean swimm<strong>in</strong>g<br />

velocity<br />

* p < 0.05<br />

1.57 ± 0.09 0.95 ± 0.13 26.750*<br />

Dur<strong>in</strong>g the pull <strong>and</strong> the push phase, the magnitude of the mean drag<br />

force, the mean lift force, the mean resultant force <strong>and</strong> the mean effective<br />

propulsive force, were not altered significantly, <strong>in</strong> comparison with<br />

free swimm<strong>in</strong>g. On the other h<strong>and</strong>, the angle between the vector of<br />

the resultant force <strong>and</strong> the axis of swimm<strong>in</strong>g propulsion was decreased<br />

significantly dur<strong>in</strong>g the pull phase <strong>in</strong> the resisted swimm<strong>in</strong>g condition.<br />

This modification was not observed dur<strong>in</strong>g the push phase (Table 2).<br />

89


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 2. Mean drag force (N), mean lift force (N), mean resultant force<br />

(N), mean effective force (N), <strong>and</strong> angle between the vector of the resultant<br />

force <strong>and</strong> the axis of swimm<strong>in</strong>g propulsion (deg) dur<strong>in</strong>g front crawl<br />

swimm<strong>in</strong>g with <strong>and</strong> without added resistance.<br />

90<br />

Without<br />

added<br />

resistance<br />

With<br />

added<br />

resistance<br />

t- value<br />

Pull phase Drag force 9.20 ± 2.57 9.16 ± 2.46 0.028<br />

Lift force 7.50 ± 2.45 5.76 ± 1.59 2.679<br />

Resultant force 12.34 ± 2.59 11.21 ± 2.38 1.061<br />

Effective force<br />

Angle between the vector of the<br />

resultant force <strong>and</strong> the axis of<br />

9.47 ± 1.71 10.04 ± 2.12 0.532<br />

swimm<strong>in</strong>g propulsion 36.31 ± 14.73 13.26 ± 15.37 2.877*<br />

Push phase Drag force 7.27 ± 2.40 8.76 ± 4.62 0.562<br />

Lift force 12.59 ± 2.32 11.70 ± 4.52 0.630<br />

Resultant force 14.93 ± 2.50 14.85 ± 6.28 0.033<br />

Effective force<br />

Angle between the vector of the<br />

resultant force <strong>and</strong> the axis of<br />

12.89 ± 2.06 13.19 ± 6.44 0.121<br />

* p < 0.05<br />

swimm<strong>in</strong>g propulsion -5.18 ± 16.76 -16.09 ± 9.56 1.462<br />

dIscussIon<br />

The results showed that dur<strong>in</strong>g resisted swimm<strong>in</strong>g the mean swimm<strong>in</strong>g<br />

velocity decreased significantly. This was expected, because both the<br />

stroke length, as well as the stroke rate decreased due to the <strong>in</strong>creased<br />

resistance that should be overcame by the swimmers (Llop et al., 2006;<br />

Maglischo et al., 1985; Williams et al., 2001).<br />

Dur<strong>in</strong>g spr<strong>in</strong>t-resisted swimm<strong>in</strong>g no significant modifications were<br />

observed <strong>in</strong> the magnitude of the drag <strong>and</strong> lift forces, <strong>in</strong> any of the propulsive<br />

phases of the underwater stroke. Consequently, it was not observed<br />

any significant modification <strong>in</strong> the magnitude of the resultant<br />

force <strong>and</strong> the effective force. However, the drag force seems to predom<strong>in</strong>ate<br />

more aga<strong>in</strong>st lift force <strong>in</strong> the pull phase dur<strong>in</strong>g resisted swimm<strong>in</strong>g,<br />

<strong>in</strong> comparison with free swimm<strong>in</strong>g. Although this fact was not statistically<br />

significant, it could be seen as a positive modification, as accord<strong>in</strong>g<br />

to Rushall et al. (1994), S<strong>and</strong>ers (1998) <strong>and</strong> Maglischo (2003), it is<br />

more effective when swimmers rely more on drag, rather than on lift<br />

forces. Such comb<strong>in</strong>ation of the drag <strong>and</strong> lift forces has as consequence<br />

to maximize their contribution to the forward direction <strong>and</strong> as much as<br />

possible of the resultant force to be aimed <strong>in</strong> the swimm<strong>in</strong>g direction.<br />

Optimally, the angle between the resultant force <strong>and</strong> the axis of swimm<strong>in</strong>g<br />

propulsion should be as close as possible to zero (Schleihauf, 2004;<br />

Vorontsov & Rumyantsev, 2000). In the present study, although the<br />

magnitude of the drag <strong>and</strong> the lift forces were not altered significantly,<br />

the angle formed between the resultant force <strong>and</strong> the axis of swimm<strong>in</strong>g<br />

propulsion was decreased significantly <strong>in</strong> the pull phase dur<strong>in</strong>g resisted<br />

swimm<strong>in</strong>g, <strong>in</strong> comparison with free swimm<strong>in</strong>g. The mean value of the<br />

above mentioned angle was decreased from approximately 36 degrees<br />

dur<strong>in</strong>g free swimm<strong>in</strong>g to 13 degrees dur<strong>in</strong>g resisted swimm<strong>in</strong>g <strong>and</strong> thus<br />

the resultant force was steered more <strong>in</strong> the forward swimm<strong>in</strong>g direction.<br />

conclusIon<br />

The ma<strong>in</strong> f<strong>in</strong>d<strong>in</strong>gs of the present study <strong>in</strong>dicate that although the magnitude<br />

of the drag <strong>and</strong> lift forces, as well as the magnitude of the resultant<br />

force <strong>and</strong> the effective propulsive force were not modified significantly<br />

dur<strong>in</strong>g resisted swimm<strong>in</strong>g, <strong>in</strong> comparison with free swimm<strong>in</strong>g,<br />

the angle formed between the resultant force <strong>and</strong> the axis of the swimm<strong>in</strong>g<br />

propulsion was decreased significantly <strong>in</strong> the pull phase. Thus, it<br />

could be speculated that front crawl spr<strong>in</strong>t-resisted swimm<strong>in</strong>g with the<br />

concrete added resistance could be considered a specific tra<strong>in</strong><strong>in</strong>gs form,<br />

which probably could contribute to the learn<strong>in</strong>g of a more effective application<br />

of the propulsive forces dur<strong>in</strong>g the pull phase.<br />

reFerences<br />

Arellano R. (1999). Vortices <strong>and</strong> propulsion. In: S<strong>and</strong>ers R. & L<strong>in</strong>sten J.<br />

(eds.), Swimm<strong>in</strong>g: Applied Proceed<strong>in</strong>gs of the XVII International Symposium<br />

on <strong>Biomechanics</strong> <strong>in</strong> Sports (pp 53 – 66). Perth, Western Australia:<br />

School of Biomedical <strong>and</strong> Sports Science.<br />

Chollet D., Chalies S., Chatard J. C. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: description <strong>and</strong> usefulness. Int J Sports Med, 21,<br />

54 – 59.<br />

Girold S., Maur<strong>in</strong> D., Dugué B., Chatard J. C., Millet G. (2007). Effects<br />

of dry-l<strong>and</strong> vs. resisted <strong>and</strong> assisted - spr<strong>in</strong>t exercises on swimm<strong>in</strong>g<br />

spr<strong>in</strong>t performances. J Strength Cond Res, 21 (2), 599 – 605.<br />

Gourgoulis V., Aggeloussis N., Kasimatis P., Vezos N., Boli A., Mavromatis<br />

G. (2008a). Reconstruction accuracy <strong>in</strong> underwater three<br />

dimensional k<strong>in</strong>ematic analysis. J Sci Med Sport, 11, 90-95.<br />

Gourgoulis V., Aggeloussis N., Vezos N., Antoniou P., Mavromatis G.<br />

(2008b). H<strong>and</strong> orientation <strong>in</strong> h<strong>and</strong> paddle swimm<strong>in</strong>g. Int J Sports<br />

Med, 29, 429 – 434.<br />

Gourgoulis V., Aggeloussis N., Vezos N., Kasimatis P., Antoniou P.,<br />

Mavromatis G. (2008c). Estimation of h<strong>and</strong> forces <strong>and</strong> propell<strong>in</strong>g<br />

efficiency dur<strong>in</strong>g front crawl swimm<strong>in</strong>g with h<strong>and</strong> paddles. J Biomech,<br />

41, 208 – 215.<br />

Llop F., Tella V., Colado J.C., Diaz G., Navarro F. (2006). Evolution of<br />

butterfly technique when resisted swimm<strong>in</strong>g with parachute, us<strong>in</strong>g<br />

different resistances. In: Vilas-Boas J. P., Alves F., Marques A. (eds.).<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> swimm<strong>in</strong>g. Xth International Symposium<br />

(pp 302 – 304). Porto, Portugal.<br />

Maglischo C. W., Maglischo E. W., Sharp R. L., Zier D. J., Katz A.<br />

(1984). Tethered <strong>and</strong> nontethered crawl swimm<strong>in</strong>g. In: Terauds J.,<br />

Barthels K., Kreighbaum E., Mann R., Crakes J. (eds.). Proceed<strong>in</strong>gs<br />

of ISBS: Sports <strong>Biomechanics</strong> (pp 163-176). Del Mar, C. A.: Academic<br />

Publication.<br />

Maglischo E. W., Maglischo C. W., Zier D. J., Santos T. R. (1985). The<br />

effect of spr<strong>in</strong>t – assisted <strong>and</strong> spr<strong>in</strong>t resisted swimm<strong>in</strong>g on stroke mechanics.<br />

J Swim Res, 1, 27-33.<br />

Maglischo E. W. (2003). Swimm<strong>in</strong>g fastest. Champaign, IL: Human<br />

K<strong>in</strong>etics.<br />

Mavridis G., Kabitsis Ch., Gourgoulis V., Toubekis A. (2006). Swimm<strong>in</strong>g<br />

velocity improved by specific resistance tra<strong>in</strong><strong>in</strong>g <strong>in</strong> age-group<br />

swimmers. In: Vilas-Boas J. P., Alves F., Marques A. (eds.). <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> swimm<strong>in</strong>g. Xth International Symposium (pp<br />

304 – 306). Porto, Portugal.<br />

Rushall B. S., Sprig<strong>in</strong>gs E. J., Holt L. E., Cappaert J. M. (1994). A Reevaluation<br />

of forces <strong>in</strong> swimm<strong>in</strong>g. J Swim Res, 10, 6 – 30.<br />

S<strong>and</strong>ers R. H. (1998). Lift performance <strong>in</strong> aquatic sports. In: Riehle H.<br />

J. & Vieten M. M. (eds). Proceed<strong>in</strong>gs XVI International Symposium of<br />

<strong>Biomechanics</strong> <strong>in</strong> Sports (pp 25 – 39). Germany: University of Konstanz.<br />

S<strong>and</strong>ers R. (1999). Hydrodynamic characteristics of a swimmer’s h<strong>and</strong>.<br />

J Appl Biomech, 15, 3 – 26.<br />

Schleihauf R. E. (2004). <strong>Biomechanics</strong> of Human Movement. Bloom<strong>in</strong>gton,<br />

Indiana: Authorhouse.<br />

Toussa<strong>in</strong>t H. M., Holl<strong>and</strong>er A. P., Berg Cvd., Vorontsov A. R. (2000).<br />

<strong>Biomechanics</strong> of swimm<strong>in</strong>g. In: Garrett W. E., Kirkendall D. T.<br />

(eds.). Exercise <strong>and</strong> Sport Science (pp 639-660). Philadelphia, Lipp<strong>in</strong>cott:<br />

Williams & Wilk<strong>in</strong>s.<br />

Vorontsov A. R., Rumyantsev V. A. (2000). Propulsive forces <strong>in</strong> swimm<strong>in</strong>g.<br />

In: Zatsiorsky V. M. (ed.). <strong>Biomechanics</strong> <strong>in</strong> Sport – Performance,<br />

enhancement <strong>and</strong> <strong>in</strong>jury prevention (pp 205-231). International Olympic<br />

Committee: Blackwell Science Ltd.<br />

Williams B. K., S<strong>in</strong>clair P., Galloway M. (2001). The effect of resisted<br />

<strong>and</strong> assisted freestyle swimm<strong>in</strong>g on stroke mechanics. In: Blackwell<br />

J. R., S<strong>and</strong>ers R. H. (eds.). Proceed<strong>in</strong>gs of Swim Sessions. <strong>XI</strong>X International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports (pp 131 – 134). San<br />

Francisco, USA.


Relationship between Eggbeater Kick <strong>and</strong> Support<br />

Scull Skills, <strong>and</strong> Isok<strong>in</strong>etic Peak Torque<br />

homma, M. 1<br />

1 University of Tsukuba, Tsukuba, Japan<br />

Eggbeater kick <strong>and</strong> support scull are essential basic propulsive techniques<br />

<strong>in</strong> synchronized swimm<strong>in</strong>g. The aim of the present study was to<br />

ascerta<strong>in</strong> the relationship between muscle strength, <strong>and</strong> eggbeater kick<br />

skills <strong>and</strong> vertical position support skills <strong>in</strong> elite synchronized swimmers.<br />

The isok<strong>in</strong>etic peak torque of legs, trunk <strong>and</strong> shoulders were measured<br />

us<strong>in</strong>g the BIODEX System 3. From the f<strong>in</strong>d<strong>in</strong>gs <strong>in</strong> this study, to improve<br />

eggbeater kick skills, the importance of strengthen<strong>in</strong>g the muscles<br />

associated with hip flexion such as the hamstr<strong>in</strong>gs, rectus abdom<strong>in</strong>is,<br />

<strong>and</strong> psoas major was suggested. To improve the support scull skills, upper<br />

arm abductors such as the <strong>in</strong>frasp<strong>in</strong>atus <strong>and</strong> teres m<strong>in</strong>or should be<br />

tra<strong>in</strong>ed <strong>and</strong> the muscles around the scapula should be strengthened <strong>in</strong><br />

proper balance.<br />

Key words: propulsive techniques, muscle strength, synchronized<br />

swimm<strong>in</strong>g<br />

IntroductIon<br />

The eggbeater kick (Figure 1) is a rotational movement of the lower legs<br />

<strong>in</strong> which a swimmer opens the legs sideways with the hip jo<strong>in</strong>t flexed<br />

<strong>and</strong> bends the knees while swivell<strong>in</strong>g both feet <strong>in</strong> oppos<strong>in</strong>g circles. The<br />

load above the water surface is at least 13 kg when both arms are raised<br />

us<strong>in</strong>g this kick (Homma, 2000). Thus, strength to control the body,<br />

hip <strong>and</strong> leg muscles is needed to elevate the body dur<strong>in</strong>g synchronized<br />

swimm<strong>in</strong>g rout<strong>in</strong>es. Support scull is a rotational movement of the forearms<br />

<strong>in</strong> which a swimmer bends the elbows <strong>and</strong> sculls the water us<strong>in</strong>g<br />

the forearms via <strong>in</strong>ternal <strong>and</strong> external shoulder rotations (Homma <strong>and</strong><br />

Homma, 2006). About 14 - 15 kg of load is applied at the maximum<br />

height above the water surface to support a vertical posture (Figure 2),<br />

which is the basic position <strong>in</strong> synchronized swimm<strong>in</strong>g (Homma, 2000).<br />

Thus, the body can only be kept elevated by scull<strong>in</strong>g. Support scull is an<br />

unusual movement <strong>in</strong> which the forearms are sup<strong>in</strong>ated while the shoulders<br />

are externally rotated, <strong>and</strong> the muscles <strong>in</strong>volved with <strong>in</strong>ternal <strong>and</strong><br />

external shoulder rotation are thought to be <strong>in</strong>volved. Stress fractures of<br />

the ulna mostly, due to scull<strong>in</strong>g, have been reported <strong>in</strong> junior synchronized<br />

swimmers (Nagano <strong>and</strong> Ohata, 1982).<br />

A previous study of the relationship between eggbeater kick skills<br />

<strong>and</strong> leg muscle strength <strong>and</strong> between the cross-sectional area of the<br />

thigh <strong>and</strong> abdom<strong>in</strong>al muscles for elite synchronized swimmers found a<br />

correlation with the isok<strong>in</strong>etic peak torque, but not the cross-sectional<br />

area of the legs (Homma <strong>and</strong> Kuno, 2001). The isok<strong>in</strong>etic peak torque<br />

for knee flexion/extension, <strong>in</strong>ternal/external shoulder rotation <strong>and</strong> hip<br />

abduction/adduction was measured <strong>in</strong> the study, <strong>and</strong> a significant correlation<br />

was seen between moderate-speed hip abduction <strong>and</strong> knee flexion.<br />

This f<strong>in</strong>d<strong>in</strong>g suggested that the eggbeater kick can be re<strong>in</strong>forced<br />

by strengthen<strong>in</strong>g the hamstr<strong>in</strong>gs, sartorius, gluteus medius <strong>and</strong> gluteus<br />

m<strong>in</strong>imus by tra<strong>in</strong><strong>in</strong>g at moderate speed.<br />

The aim of the present study was to ascerta<strong>in</strong> the relationship between<br />

eggbeater kick skills (technical ability of eggbeater kick) <strong>and</strong> the<br />

leg <strong>and</strong> trunk muscle strength, <strong>and</strong> the relationship between vertical position<br />

support skills (technical ability for support<strong>in</strong>g vertical position)<br />

<strong>and</strong> muscle strength of <strong>in</strong>ternal <strong>and</strong> external shoulder rotation.<br />

Methods<br />

Ten female synchronized swimmers (average height, body mass <strong>and</strong> age,<br />

1.64 ± 0.04 m, 54.5 ± 2.8 kg, 23.8 ± 1.9 yrs, respectively), silver-medallists<br />

at the 2007 World Championships, who were all c<strong>and</strong>idates for the<br />

2008 Beij<strong>in</strong>g Olympic Games, participated <strong>in</strong> the study.<br />

chaPter2.<strong>Biomechanics</strong><br />

Figure 1. Rais<strong>in</strong>g the arms out of the water us<strong>in</strong>g the eggbeater kick.<br />

Figure 2. Vertical position us<strong>in</strong>g support scull.<br />

Eggbeater kick skills <strong>and</strong> vertical position support skills were assessed<br />

based on their respective test scores obta<strong>in</strong>ed dur<strong>in</strong>g the first qualify<strong>in</strong>g<br />

trial for the 2008 Beij<strong>in</strong>g Olympics <strong>in</strong> September 2007 (Qualify<strong>in</strong>g<br />

Trial) <strong>and</strong> the skill evaluation test for Beij<strong>in</strong>g Olympic c<strong>and</strong>idates <strong>in</strong><br />

June 2007 (Skill Evaluation Test).<br />

Eggbeater kick skills were assessed based on the two scores: 1) eggbeater<br />

kick (EB) score <strong>and</strong> 2) height score. International judges <strong>and</strong><br />

national coaches determ<strong>in</strong>ed scores of up to 5 po<strong>in</strong>ts <strong>in</strong> half-po<strong>in</strong>t <strong>in</strong>crements.<br />

EB score obta<strong>in</strong>ed as one of the rout<strong>in</strong>e set of tests conducted<br />

dur<strong>in</strong>g the Qualify<strong>in</strong>g Trial. The rout<strong>in</strong>e set comprised five features<br />

that are essential for perform<strong>in</strong>g a rout<strong>in</strong>e <strong>and</strong> <strong>in</strong>cluded propulsive<br />

techniques <strong>and</strong> figures. Dur<strong>in</strong>g the assessment of eggbeater kick skills,<br />

swimmers were required to raise both arms <strong>and</strong> move forward while<br />

count<strong>in</strong>g to 12. Swimmers were assessed based on height, stability <strong>and</strong><br />

smoothness. Height score obta<strong>in</strong>ed as part of the Skill Evaluation Test.<br />

Swimmers moved forward 5 m while scull<strong>in</strong>g <strong>in</strong> the water without rais-<br />

91


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

<strong>in</strong>g the arms. Swimmers were subjectively assessed based on height.<br />

Vertical position support skills were assessed based on the two<br />

scores: 1) vertical position score <strong>and</strong> 2) design score. The vertical position<br />

support skills were assessed by <strong>in</strong>struct<strong>in</strong>g each swimmer to support<br />

the highest possible vertical position for 15 seconds <strong>and</strong> enter the water<br />

while support<strong>in</strong>g this position. This test most closely reflects support<br />

scull skills. Vertical position score obta<strong>in</strong>ed as part of a rout<strong>in</strong>e set of<br />

tests conducted dur<strong>in</strong>g the Qualify<strong>in</strong>g Trial. International judges determ<strong>in</strong>ed<br />

vertical position scores which swimmers were assessed based<br />

on height, presence, stability, <strong>and</strong> correct position. Design scores (vertical<br />

position correctness <strong>and</strong> extension) were determ<strong>in</strong>ed by the national<br />

coach <strong>and</strong> six <strong>in</strong>ternational judges with a maximum score of 5 po<strong>in</strong>ts <strong>in</strong><br />

half-po<strong>in</strong>t <strong>in</strong>crements dur<strong>in</strong>g the Skill Evaluation Test.<br />

The isok<strong>in</strong>etic peak torque for knee flexion <strong>and</strong> extension (angle rate:<br />

60 or 180˚/s), trunk flexion <strong>and</strong> extension (angle rate: 60 or 120˚/s) <strong>and</strong><br />

shoulder <strong>in</strong>ternal <strong>and</strong> external rotations (angle rate: 60 or 120˚/s) were<br />

measured us<strong>in</strong>g the BIODEX System 3 (Biodex Medical Systems Inc.).<br />

Isok<strong>in</strong>etic peak torque per body weight was also calculated.<br />

The relationship between EB <strong>and</strong> height score to the isok<strong>in</strong>etic peak<br />

torque for knee extension <strong>and</strong> flexion or trunk extension <strong>and</strong> flexion<br />

<strong>and</strong> the relationship between vertical position <strong>and</strong> design scores to the<br />

isok<strong>in</strong>etic peak torque for shoulder <strong>in</strong>ternal <strong>and</strong> external rotations were<br />

analyzed us<strong>in</strong>g Spearman’s rank correlation coefficients with the level of<br />

significance set at p


dIscussIon<br />

The results of the present study confirmed a relationship between eggbeater<br />

kick skills <strong>and</strong> the isok<strong>in</strong>etic peak torque for 60 or 180˚/s (left)<br />

knee flexion or 60˚/s trunk flexion. Homma <strong>and</strong> Homma (2005) suggested<br />

that when teach<strong>in</strong>g the eggbeater kick, it is important to elevate<br />

the knees above the greater trochanter <strong>and</strong> elevate the heels near the<br />

gluteal region. Execut<strong>in</strong>g the kick is thought to <strong>in</strong>volve low- <strong>and</strong> moderate-speed<br />

<strong>and</strong> low-speed hip <strong>and</strong> knee flexion, respectively, suggest<strong>in</strong>g<br />

the importance of strengthen<strong>in</strong>g the muscles associated with hip<br />

flexion such as the hamstr<strong>in</strong>gs, rectus abdom<strong>in</strong>is, <strong>and</strong> psoas major. This<br />

f<strong>in</strong>d<strong>in</strong>g supported the previous study for elite synchronized swimmers<br />

(Homma <strong>and</strong> Kuno, 2001) that strengthen<strong>in</strong>g the hamstr<strong>in</strong>gs, sartorius,<br />

gluteus medius <strong>and</strong> gluteus m<strong>in</strong>imus by tra<strong>in</strong><strong>in</strong>g at moderate speed can<br />

re<strong>in</strong>force the eggbeater kick. On the other h<strong>and</strong>, hip abduction was not<br />

measured <strong>in</strong> the present study due to technical limitation of analyzer.<br />

Therefore, hip abduction could not be compared with previous f<strong>in</strong>d<strong>in</strong>gs<br />

(Homma <strong>and</strong> Kuno, 2001), but knee flexion was comparable, suggest<strong>in</strong>g<br />

a close correlation between eggbeater kick skills <strong>and</strong> left knee flexion.<br />

Furthermore, the present study identified a correlation with low-speed<br />

trunk flexion, suggest<strong>in</strong>g the importance of strengthen<strong>in</strong>g the rectus abdom<strong>in</strong>is,<br />

obliquus <strong>in</strong>ternus abdom<strong>in</strong>is, psoas major <strong>and</strong> rectus femoris<br />

that bend the trunk, by tra<strong>in</strong><strong>in</strong>g at low speed.<br />

The significant relationship between external shoulder rotation <strong>and</strong><br />

vertical position support skills might have been due to the specificity of<br />

support scull movements. The support scull is a rotational movement of<br />

the forearms with bent elbows, <strong>and</strong> it is an unusual movement where<br />

a swimmer bends the elbows <strong>and</strong> externally rotates the shoulder while<br />

sup<strong>in</strong>at<strong>in</strong>g the forearms with the palms fac<strong>in</strong>g the face (Homma <strong>and</strong><br />

Homma, 2006). Internal shoulder rotation is occasionally used dur<strong>in</strong>g<br />

rout<strong>in</strong>e activities, whereas external shoulder rotation is rare. Therefore,<br />

rather than <strong>in</strong>dividual differences <strong>in</strong> <strong>in</strong>ternal rotation, those <strong>in</strong> external<br />

rotation are closely related to support scull skills. Therefore, upper arm<br />

abductors such as the <strong>in</strong>frasp<strong>in</strong>atus <strong>and</strong> teres m<strong>in</strong>or should be tra<strong>in</strong>ed.<br />

These muscles are called <strong>in</strong>ner muscles, <strong>and</strong> s<strong>in</strong>ce they are <strong>in</strong> the deep<br />

layers of the shoulder, athletes are not often aware of them. Unlike<br />

outer muscles, tra<strong>in</strong><strong>in</strong>g <strong>in</strong>ner muscles is more difficult <strong>and</strong> should be<br />

performed us<strong>in</strong>g rubber b<strong>and</strong>s <strong>and</strong> light-weight dumbbells, with careful<br />

monitor<strong>in</strong>g of muscle movement. Also, large muscles that connect<br />

the trunk <strong>and</strong> upper arms such as the pectoralis major <strong>and</strong> latissimus<br />

dorsi are important when scull<strong>in</strong>g with fixed shoulders. Therefore, to<br />

improve support scull skills, the muscles around the scapula should be<br />

strengthened <strong>in</strong> proper balance. Although we reached these implications<br />

<strong>in</strong> the present study, how the muscles contribute to the eggbeater kick<br />

or scull<strong>in</strong>g movements should be analyzed with EMG <strong>in</strong> future studies.<br />

S<strong>in</strong>ce eggbeater kick <strong>and</strong> scull<strong>in</strong>g movements are symmetry, there were<br />

no significant differences between right <strong>and</strong> left peak torques. However,<br />

for only one side, some significant correlations between peak torques<br />

<strong>and</strong> scores were obta<strong>in</strong>ed, therefore, dom<strong>in</strong>ance assessment is needed<br />

<strong>in</strong> a future.<br />

The BIODEX was used <strong>in</strong> the present study to measure the isok<strong>in</strong>etic<br />

peak torque of s<strong>in</strong>gle jo<strong>in</strong>t movements. As they differ from the<br />

natural output characteristics for synchronized swimm<strong>in</strong>g, a method<br />

of quantify<strong>in</strong>g the muscle strength <strong>and</strong> power required for float<strong>in</strong>g us<strong>in</strong>g<br />

the support scull <strong>and</strong> eggbeater kick is required. However, periodic<br />

check<strong>in</strong>g of the muscle strength of synchronized swimmers us<strong>in</strong>g a<br />

muscle function analyzer is useful for tra<strong>in</strong><strong>in</strong>g purposes, <strong>and</strong> cont<strong>in</strong>ued<br />

use of the system as a control test is warranted.<br />

reFerences<br />

Homma, M. (2000). Load above the water surface dur<strong>in</strong>g the movements<br />

<strong>in</strong> synchronized swimm<strong>in</strong>g. Bullet<strong>in</strong> of sports methodology, University<br />

of Tsukuba, 16, 13-22.<br />

Homma, M. & Homma, M. (2005). Coach<strong>in</strong>g po<strong>in</strong>ts for the technique<br />

of the eggbeater kick <strong>in</strong> synchronized swimm<strong>in</strong>g based on three-<br />

chaPter2.<strong>Biomechanics</strong><br />

dimensional motion analysis. Sports <strong>Biomechanics</strong>, 4(1), 73-88.<br />

Homma, M. & Homma, M. (2006). Support scull techniques of elite<br />

synchronised swimmers. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X,<br />

220-223.<br />

Homma, M. & Kuno, S. (2001). Relationship between eggbeater kick<br />

skills <strong>and</strong> isok<strong>in</strong>etic peak torque <strong>and</strong> muscle cross-sectional area <strong>in</strong><br />

elite synchronized swimmers. Japanese Journal of Physical Fitness <strong>and</strong><br />

Sports <strong>Medic<strong>in</strong>e</strong>, 50(6), 929.<br />

Nagano, T. & Ohata, N. (1982). Stress fracture of the ulna <strong>in</strong> a synchronized<br />

swimmer. East-Japanese Journal of Sports <strong>Medic<strong>in</strong>e</strong>.<br />

AcKnoWledGeMents<br />

I would like to thank the project research, Institute of Sport <strong>and</strong> Health<br />

Sciences <strong>in</strong> University of Tsukuba for a grant that made it possible to<br />

complete this study.<br />

93


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

A Biomechanical Comparison of Elite Swimmers<br />

Start Performance Us<strong>in</strong>g the Traditional Track Start<br />

<strong>and</strong> the New Kick Start<br />

honda, K.e. 1, 2 , s<strong>in</strong>clair, P.J. 1 , Mason, B.r. 2 & Pease, d.l. 2<br />

1 The University of Sydney, Australia<br />

2 Australian Institute of Sport, Australia<br />

The <strong>in</strong>ternational govern<strong>in</strong>g body for swimm<strong>in</strong>g ‘FINA’ has approved<br />

the development of a new start<strong>in</strong>g block (Omega, OSB11) with an <strong>in</strong>cl<strong>in</strong>ed<br />

kick plate at the rear of the block. The purpose of this study was to<br />

determ<strong>in</strong>e the effects of the new start platform on performance relative<br />

to that of the traditional track start. Fourteen elite swimmers completed<br />

three ‘dive <strong>and</strong> glide’ starts us<strong>in</strong>g the kick plate <strong>and</strong> three traditional<br />

track starts. Results <strong>in</strong>dicated the kick start to be a significantly faster<br />

start than the track start. The kick start was significantly faster off the<br />

block with a higher horizontal velocity at take off <strong>and</strong> an <strong>in</strong>creased on<br />

block horizontal force. This advantage was ma<strong>in</strong>ta<strong>in</strong>ed through the time<br />

to 5 m <strong>and</strong> 7.5 m. It is recommended coaches <strong>and</strong> athletes should spend<br />

time adapt<strong>in</strong>g to the new block <strong>and</strong> this new start<strong>in</strong>g technique.<br />

Keywords: biomechanics, swimm<strong>in</strong>g start, track start, kick start,<br />

osB11.<br />

IntroductIon<br />

The goal of a swimm<strong>in</strong>g race is to complete the required distance <strong>in</strong> the<br />

least amount of time, with races be<strong>in</strong>g won or lost by a hundredth of a<br />

second. A race is made up of a number of key components, the free swim<br />

(where the athlete is strok<strong>in</strong>g), starts, turns <strong>and</strong> f<strong>in</strong>ishes. The velocity<br />

achieved by a swimmer is greatest dur<strong>in</strong>g the start<strong>in</strong>g phase, therefore<br />

it is important for a swimmer to ma<strong>in</strong>ta<strong>in</strong> the velocity achieved off the<br />

start block for as long as possible before slow<strong>in</strong>g to race pace (Welcher,<br />

H<strong>in</strong>richs, & George, 2008). Although the time a swimmer spends start<strong>in</strong>g<br />

is less than <strong>in</strong> the free swim <strong>and</strong> turn<strong>in</strong>g phases, an effective start is<br />

important for success (Miller, Hay, & Wilson, 1984).<br />

Researchers have broken down the swimm<strong>in</strong>g start <strong>in</strong>to three phases<br />

(Guimaraes & Hay 1985; Schnabel & Kuchler 1998). Block time (start<br />

signal until toes off block) flight time (time spent <strong>in</strong> the air), <strong>and</strong> underwater<br />

or glide time (from water entry until first kick). Swimmers<br />

can only atta<strong>in</strong> maximum performances dur<strong>in</strong>g the start phase if they<br />

are able to skilfully execute all three phases (Schnabel & Kuchler 1998).<br />

The performance measure of a start is usually set to time to 15 m<br />

(Cossor & Mason 2001), <strong>in</strong>corporated <strong>in</strong> this is the block time, flight<br />

time <strong>and</strong> the water time (Guimaraes & Hay 1985). Ruschel et al, (2007)<br />

suggest that water phase is <strong>in</strong>timately connected to the <strong>in</strong>dividual characteristics<br />

of each subject, like the streaml<strong>in</strong>e position <strong>and</strong> the underwater<br />

stroke technique used, be<strong>in</strong>g <strong>in</strong>fluenced by several factors <strong>and</strong> actions<br />

that happen from the <strong>in</strong>stant of entry <strong>in</strong> the water to the beg<strong>in</strong>n<strong>in</strong>g of<br />

the first kick<strong>in</strong>g <strong>and</strong> the first stroke movements. A study by Guimaraes<br />

<strong>and</strong> Hay (1985) observed 94% of the variance <strong>in</strong> start time was attributed<br />

to the water time.<br />

The requirements for a superior start <strong>in</strong>clude a fast reaction time,<br />

significant jump<strong>in</strong>g power, a high take-off velocity <strong>and</strong> a decrease <strong>in</strong><br />

drag force dur<strong>in</strong>g entry. A low resistance streaml<strong>in</strong>e position dur<strong>in</strong>g underwater<br />

glid<strong>in</strong>g to m<strong>in</strong>imize the loss of horizontal velocity as well as<br />

an <strong>in</strong>crease <strong>in</strong> propulsive efficiency dur<strong>in</strong>g the transition stage can assist<br />

<strong>in</strong> a superior start (Schnabel & Kuchler 1998; Breed & Young 2003).<br />

Over the last 40 years, the swim start technique has cont<strong>in</strong>ued to<br />

evolve, from the conventional or arm sw<strong>in</strong>g start to the grab start <strong>and</strong><br />

the track start. In the late 1970’s the track start debuted <strong>and</strong> has ga<strong>in</strong>ed<br />

<strong>in</strong> popularity <strong>and</strong> proven successful <strong>in</strong> <strong>in</strong>ternational competition. The<br />

track start has one foot at the front edge of the block, the other placed<br />

94<br />

towards the back on the start<strong>in</strong>g platform with h<strong>and</strong>s grabb<strong>in</strong>g the front<br />

edge of the block. Due to these changes <strong>in</strong> the swimmers foot placement,<br />

the track start employs a wider base of support than the grab start<br />

result<strong>in</strong>g <strong>in</strong> greater stability for the swimmer (Sh<strong>in</strong> & Groppel, 1986;<br />

Breed & McElroy, 2000).<br />

In 2009 a new start<strong>in</strong>g technique has developed with the <strong>in</strong>troduction<br />

of an <strong>in</strong>cl<strong>in</strong>e or ‘kick’ plate mounted to the start platform. This newly<br />

designed start block by Omega (OSB11, Corgémont, Switzerl<strong>and</strong>, Figure<br />

1), has the <strong>in</strong>ternational govern<strong>in</strong>g body for swimm<strong>in</strong>g ‘FINA’ approval<br />

<strong>and</strong> has allowed the development of the kick start. The kick start<br />

is essentially a modified track start that allows the rear foot to be raised<br />

off the platform <strong>and</strong> placed upon a kick plate. The kick plate is angled<br />

at 30 deg to the surface of the block <strong>and</strong> can be moved through five<br />

different locations on the start<strong>in</strong>g platform. Omega claims that “tests<br />

undertaken by top level swimmers showed faster races versus a st<strong>and</strong>ard<br />

block” however no data was provided to support this statement. To date,<br />

no study has exam<strong>in</strong>ed the biomechanical factors associated with a successful<br />

start us<strong>in</strong>g the OSB11. Hence the purpose of this study was to<br />

determ<strong>in</strong>e the effects of the new angled start platform on performance<br />

relative to that of the traditional track start. This study hypothesized<br />

that the kick start would <strong>in</strong>crease the amount of horizontal force be<strong>in</strong>g<br />

applied, enabl<strong>in</strong>g faster start times <strong>and</strong> greater horizontal velocity when<br />

compared to the track start.<br />

Methods<br />

The subject cohort for this study consisted of fourteen elite swimm<strong>in</strong>g<br />

subjects (9 male aged 20.8 ± 3.0 years, 5 female aged 21.4 ± 2.8 years)<br />

all of which were members of the Australian Institute of Sport (AIS)<br />

Swim Team. All participants had personal best times which atta<strong>in</strong>ed a<br />

m<strong>in</strong>imum of 850 FINA po<strong>in</strong>ts (http://www.f<strong>in</strong>a.org/swimm<strong>in</strong>g/FINA<br />

po<strong>in</strong>ts/<strong>in</strong>dex.php). The experimental procedure was approved by the<br />

AIS ethics committee.<br />

The participants completed a warm up, based around their pre-race<br />

rout<strong>in</strong>e which consisted of some spr<strong>in</strong>t <strong>and</strong> dive drills to ensure the athlete<br />

was ready to perform at their maximal capacity. Before the commencement<br />

of the test<strong>in</strong>g session their weight was obta<strong>in</strong>ed us<strong>in</strong>g the<br />

force platform built <strong>in</strong>to the start block. This was used to normalise the<br />

force data.<br />

Normal competitive start<strong>in</strong>g procedures were used for each trail. The<br />

participants were <strong>in</strong>structed to perform a maximal effort dive <strong>and</strong> glide<br />

until their forward momentum ceased, while not kick<strong>in</strong>g or swimm<strong>in</strong>g.<br />

The participants completed three ‘dive <strong>and</strong> glide’ starts us<strong>in</strong>g the kick<br />

plate <strong>in</strong> their preferred position <strong>and</strong> three traditional track starts, <strong>in</strong> a<br />

r<strong>and</strong>omised sequence.<br />

‘Wetplate’ is the proprietary system used to analyse the starts. It is


comprised of an <strong>in</strong>strumented start block constructed us<strong>in</strong>g a Kistler<br />

force platform (Z20314, W<strong>in</strong>terthur, Switzerl<strong>and</strong>, figure 2). Wetplate<br />

not only allows for the determ<strong>in</strong>ation of the overall force profile of<br />

the start itself but also allows measurement of the grab force through<br />

two Kistler tri-axial transducers (9601A) placed <strong>in</strong> a bar at the front<br />

of the start block. The contribution of the rear foot is also measured on<br />

a second <strong>in</strong>strumented <strong>in</strong>cl<strong>in</strong>e plate by 4 Kistler tri-axial transducers<br />

(9251A) developed to the specifications of the OSB11 start platform.<br />

The system <strong>in</strong>cludes a series of calibrated high speed digital cameras<br />

(Pulnix, TMC-6740GE), one above water to capture the start <strong>and</strong><br />

entry with 3 underwater to obta<strong>in</strong> vision from 0m to 15m. The tim<strong>in</strong>g<br />

to 5m <strong>and</strong> 7.5m was assessed us<strong>in</strong>g ‘SwimTrak’ an analogue video<br />

camera tim<strong>in</strong>g system <strong>in</strong> which the cameras (Samsung, SCC-C4301P)<br />

were located perpendicular to the plane of motion at 0m, 5m <strong>and</strong> 7.5m.<br />

De<strong>in</strong>terlac<strong>in</strong>g the video signal allowed for the respective split times to<br />

be determ<strong>in</strong>ed to a resolution of 1/50 th of a second. All calculations were<br />

timed from when the participants head passed the specified po<strong>in</strong>ts.<br />

Figure 2: The AIS Wetplate Instrumented Start<strong>in</strong>g Platform with Grab<br />

bar <strong>and</strong> Kick Plate<br />

Data was collected for a total of 12 seconds, 1 second prior to <strong>and</strong> 11<br />

seconds after the start signal. The start signal is <strong>in</strong>tegrated <strong>in</strong>to the analysis<br />

system <strong>and</strong> triggers the data collection from the force plates <strong>and</strong> the<br />

cameras. A 10Hz Butterworth low pass digital filter was applied to the<br />

force data collected through Wetplate.<br />

A two way repeated measures analysis of variance (ANOVA) was<br />

performed to assess the ma<strong>in</strong> effects of style (Kick Start vs. Track Start)<br />

<strong>and</strong> gender (male vs. female). When the assumption of equal variances<br />

was violated, significance was adjusted us<strong>in</strong>g the Greenhouse-Geisser<br />

procedure (V<strong>in</strong>cent, 1995). All presented values are expressed as mean<br />

± SD, <strong>and</strong> P values less than or equal to 0.05 were considered as statistically<br />

significant.<br />

results<br />

The performance differences between the kick start <strong>and</strong> traditional track<br />

start are presented <strong>in</strong> Table 1. Males recorded faster times <strong>and</strong> higher<br />

velocities than females for both the track start <strong>and</strong> the kick start. However<br />

there were no significant <strong>in</strong>teractions between gender <strong>and</strong> the style<br />

of the start for any of the variables <strong>and</strong> so results were pooled <strong>in</strong> Table 1.<br />

All force data presented has been normalised to the participant’s weight<br />

<strong>and</strong> expressed <strong>in</strong> Body Weights (BW).<br />

chaPter2.<strong>Biomechanics</strong><br />

Table 1: Comparison between Kick Start <strong>and</strong> Traditional Track Start.<br />

Mean <strong>and</strong> SD<br />

Variables Kick Start Track Start<br />

Significance<br />

Level<br />

Time to 5m (s) 1.62 ± 0.01 1.66 ± 0.01 0.002**<br />

Time to 7.5m (s) 2.69 ± 0.02 2.73 ± 0.02 0.032*<br />

Time on Block (s) 0.77 ± 0.01 0.80 ± 0.01 0.001**<br />

Take-off Horizontal Velocity (m/sˉ¹) 4.48± 0.04 4.41 ± 0.03 0.009**<br />

Average Velocity between 5m & 7.5m<br />

(m/sˉ¹)<br />

2.39± 0.04 2.37± 0.04 0.644<br />

Average Horizontal Force (BW) 0.60± 0.01 0.57 ± 0.01 0.003**<br />

Peak Horizontal Force on the Block<br />

(BW)<br />

1.13± 0.04 1.09 ± 0.04 0.151<br />

* Significant difference between Kick Start <strong>and</strong> Track Start p < 0.05<br />

** Significant difference between Kick Start <strong>and</strong> Track Start p < 0.01<br />

dIscussIon<br />

This study hypothesized that the kick start would <strong>in</strong>crease the amount of<br />

horizontal force be<strong>in</strong>g applied when compared to the track start, enabl<strong>in</strong>g<br />

shorter start times <strong>and</strong> greater horizontal velocity off the block. Results<br />

showed the kick start was the significantly superior method when look<strong>in</strong>g<br />

at performance <strong>in</strong>dicators of time to 5 m <strong>and</strong> time to 7.5 m.<br />

This study <strong>in</strong>cluded n<strong>in</strong>e male subjects, but only five females. It is<br />

possible the different subject numbers may have masked differences between<br />

genders ow<strong>in</strong>g to a reduced statistical power. The ma<strong>in</strong> <strong>in</strong>tent<br />

of this study, however, was to <strong>in</strong>vestigate differences between the start<br />

techniques, not to determ<strong>in</strong>e whether strategies would be different for<br />

males <strong>and</strong> females.<br />

The new block allows the kick start to achieve an average on block<br />

time of 0.77s compared to the track starts of 0.80s. This was significant<br />

(p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

force application to drive the body forward with an <strong>in</strong>creased horizontal<br />

velocity. The atta<strong>in</strong>ment of greater horizontal velocity has been seen as a<br />

benefit to overall dive performance (Galbraith et al, 2008)<br />

There was a significantly greater horizontal velocity when leav<strong>in</strong>g<br />

blocks, however this was not the case for the average velocity between<br />

5 m <strong>and</strong> 7.5 m. This suggests that swimmers’ decelerate more from the<br />

kick start; however this should not be surpris<strong>in</strong>g because this was only<br />

a dive <strong>and</strong> glide study. Higher velocity leads to a larger drag force, as<br />

the drag force act<strong>in</strong>g on a body mov<strong>in</strong>g through a fluid is proportional<br />

to the square of its velocity (Guimaraes & Hay 1985). In a start which<br />

enabled the use of kick<strong>in</strong>g, the athlete may be better able to ma<strong>in</strong>ta<strong>in</strong> a<br />

higher velocity.<br />

The use of the dive <strong>and</strong> glide allowed for the comparison of the<br />

starts without the <strong>in</strong>fluence of other underwater variables such as kick<strong>in</strong>g<br />

technique <strong>and</strong> the transition to strok<strong>in</strong>g, however this does limit the<br />

research. Further test<strong>in</strong>g of the kick start with the full dive parameters<br />

to 15m, <strong>in</strong>clud<strong>in</strong>g analysis of flight, entry <strong>and</strong> underwater movements, is<br />

needed to encompass the start as a whole.<br />

conclusIon<br />

The results of this study <strong>in</strong>dicated that the kick start on the new OSB11<br />

start platform to be significantly faster start than the traditional track<br />

start. Prior research <strong>in</strong>to swimm<strong>in</strong>g starts has tended to suggest that<br />

“what one does most, one does best” (Pearson et. al 1998). Despite the<br />

participants own bias towards their preferred <strong>and</strong> experienced technique,<br />

the track start, the kick start was significantly faster off the block<br />

with a higher horizontal velocity <strong>and</strong> an <strong>in</strong>creased on block horizontal<br />

force. This advantage was ma<strong>in</strong>ta<strong>in</strong>ed through the time to 5 m <strong>and</strong> 7.5<br />

m. Even though further research is needed <strong>in</strong>to the kick start to look<br />

at the full start to 15 m, <strong>in</strong>clud<strong>in</strong>g the effect of the underwater kick<br />

<strong>and</strong> transition to strok<strong>in</strong>g, it is recommended that coaches <strong>and</strong> athletes<br />

should spend time <strong>in</strong> adapt<strong>in</strong>g to these new blocks <strong>and</strong> this new start<strong>in</strong>g<br />

technique.<br />

reFerences<br />

Allen, D. M., Miller, M. K., Pe<strong>in</strong>, R. & Oyster, C. (1999). A k<strong>in</strong>etic<br />

<strong>and</strong> k<strong>in</strong>ematic comparison of the grab start <strong>and</strong> track start <strong>in</strong> swimm<strong>in</strong>g.<br />

Research Quarterly for Exercise Science, March (Suppl.). A-15,<br />

(abstract).<br />

Breed, R. V. P. & McElroy, G. K. (2000). A biomechnical comparison<br />

of the grab, sw<strong>in</strong>g <strong>and</strong> track starts <strong>in</strong> swimm<strong>in</strong>g. Journal of Human<br />

Movement Studies, 39, 277-293.<br />

Breed, R. V.P. & Young, W. B. (2003). The effect of a resistance tra<strong>in</strong><strong>in</strong>g<br />

programme on the grab, track <strong>and</strong> sw<strong>in</strong>g starts <strong>in</strong> swimm<strong>in</strong>g. Journal<br />

of Sports Sciences, 21(3), 213-220.<br />

Cossor, J. & Mason, B. (2001). Swim start performances at the Sydney<br />

2000 Olympic Games. In: Proceed<strong>in</strong>gs of <strong>XI</strong>X Symposium on <strong>Biomechanics</strong><br />

<strong>in</strong> Sports. San Francisco: University of California at San Francisco,<br />

25-30.<br />

Counsilman, J. E., Counsilman, B. E., Nomura, T. & Endo, M. (1988).<br />

Three Types of Grab Starts for Competitive Swimm<strong>in</strong>g. In Swimm<strong>in</strong>g<br />

Science V. Human K<strong>in</strong>etics. BE Ungerechts, K Wilke, K Reischle.<br />

(Eds) Champaign, IL., 81-91.<br />

Galbraith, H., Scurr, J., Hencken, L., Wood, L. & Graham-Smith, P.<br />

(2008). Biomechanical comparison of the track start <strong>and</strong> the modified<br />

one-h<strong>and</strong>ed track start <strong>in</strong> competitive swimm<strong>in</strong>g: An <strong>in</strong>tervention<br />

study. Journal of Applied <strong>Biomechanics</strong>, 24, 307-315.<br />

Guimaraes, A. C. S. & Hay, J. G. (1985). A Mechanical Analysis of the<br />

Grab Start<strong>in</strong>g Technique <strong>in</strong> Swimm<strong>in</strong>g. International Journal of Sport<br />

<strong>Biomechanics</strong>, (1), 25-35.<br />

Miller, J. A., Hay, J. G. & Wilson, B. D. (1984). Start<strong>in</strong>g technique of<br />

elite swimmers. Journal of Sports Sciences, 2, 213–223.<br />

96<br />

Pearson, C. T., McElroy, G. K., Blitvich, J. D., Subic, A. & Blanksby, B.<br />

A. (1998). A comparison of the swimm<strong>in</strong>g start us<strong>in</strong>g traditional <strong>and</strong><br />

modified start<strong>in</strong>g blocks. Journal of Human Movement Studies, 34(2),<br />

49–66.<br />

Ruschel, C., Araujo, L. G., Pereira, S. M. & Roesler, H. (2007). K<strong>in</strong>ematic<br />

Analysis of the swimm<strong>in</strong>g start: block flight <strong>and</strong> underwater<br />

phases. In: HJ Menzel, MH Chagas (Eds). Proceed<strong>in</strong>gs of XXV International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports. 385-388.<br />

Schnabel, U. & Kuchler, J. (1998). Analysis of the Start<strong>in</strong>g Phase <strong>in</strong><br />

Competitive Swimm<strong>in</strong>g. In: H. J. Ruehle, M. M. Vieten MM (Eds.).<br />

Proceed<strong>in</strong>gs of XVI International Symposium of <strong>Biomechanics</strong> <strong>in</strong> Sports.<br />

247-250.<br />

Sh<strong>in</strong>, I. & Groppel, J. L. (1986). A Comparison of the Grab Start <strong>and</strong><br />

Track Start as Utilized by Competitive Swimmers. In DM L<strong>and</strong>ers<br />

(Eds). Sport <strong>and</strong> Elite Performers. Human K<strong>in</strong>etics, Champaign, IL.<br />

171-175.<br />

V<strong>in</strong>cent, W. J. (1995). Statistics <strong>in</strong> K<strong>in</strong>esiology. Human K<strong>in</strong>etics, Champagne<br />

IL.<br />

Welcher, R. L., H<strong>in</strong>richs, R. N. & George, T. R. (2008). Front- or Rear-<br />

Weighted Track Start or Grab start: Which is the Best for Female<br />

Swimmers? Sports <strong>Biomechanics</strong> 7(1), 100-113.<br />

AcKnoWledGMents<br />

The authors would like to gratefully acknowledge the support <strong>and</strong> assistance<br />

of the AIS, Aquatics Test<strong>in</strong>g, Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Research Unit for<br />

their contribution to the test<strong>in</strong>g procedure, the AIS, Technical Research<br />

Laboratory for their cont<strong>in</strong>ued effort to produce world class equipment<br />

<strong>and</strong> the AIS, Swim team for their participation.


K<strong>in</strong>ematics Analysis of Undulatory Underwater<br />

Swimm<strong>in</strong>g dur<strong>in</strong>g a Grab Start of National Level<br />

Swimmers<br />

houel n., elipot M., Andrée F., hellard h.<br />

Département Recherche Fédération Française de Natation Pôle Natation<br />

INSEP France<br />

The aim of this study was to determ<strong>in</strong>e the k<strong>in</strong>ematic parameters that<br />

improve performance dur<strong>in</strong>g the underwater phase of grab starts. A<br />

three dimensional analysis of the underwater phase of twelve swimmers<br />

of national level was conducted. Stepwise regression identified the ma<strong>in</strong><br />

k<strong>in</strong>ematic parameters that <strong>in</strong>fluence the horizontal velocity of the swimmer<br />

each 0.5 m <strong>in</strong> the range of 5 to 7.5 m. For this population of swimmers,<br />

the results enable proposition of four pr<strong>in</strong>ciples to improve the<br />

underwater phase: to be streaml<strong>in</strong>ed at the beg<strong>in</strong>n<strong>in</strong>g of the underwater<br />

glid<strong>in</strong>g phase, to start the dolph<strong>in</strong> kick<strong>in</strong>g after 5.5 m, to have a high<br />

undulation frequency, to move like a dolph<strong>in</strong> us<strong>in</strong>g only feet <strong>and</strong> leg<br />

segments <strong>in</strong> underwater undulatory swimm<strong>in</strong>g.<br />

Key words: swimm<strong>in</strong>g starts, k<strong>in</strong>ematics, undulations, underwater<br />

phase.<br />

IntroductIon<br />

In 50 <strong>and</strong> 100 m swimm<strong>in</strong>g races, performance has been strongly l<strong>in</strong>ked<br />

to start performance (Arellano et al., 1996; Mason <strong>and</strong> Cossor, 2000).<br />

Start performance is def<strong>in</strong>ed as the time observed between the start signal<br />

<strong>and</strong> the moment when the swimmer’s head reaches 10 m (Arellano<br />

et al., 1996) or 15 m (Issur<strong>in</strong> <strong>and</strong> Verbitsky, 2002; Mason <strong>and</strong> Cossor,<br />

2000).<br />

The start is divided <strong>in</strong> three phases: the impulse phase on the start<strong>in</strong>g<br />

block (<strong>in</strong>clud<strong>in</strong>g reaction time), the flight phase, <strong>and</strong> the underwater<br />

phase. Swimmers currently use the grab start or the track start <strong>in</strong> national<br />

<strong>and</strong> <strong>in</strong>ternational events. The results of studies conducted s<strong>in</strong>ce<br />

the 70’s def<strong>in</strong><strong>in</strong>g the most effective start rema<strong>in</strong> contradictory (Issur<strong>in</strong> et<br />

Verbitsky, 2002; Vilas-Boas et al., 2003). However, there is some agreement<br />

that horizontal <strong>and</strong> vertical velocity, as well as m<strong>in</strong>imized hydrodynamic<br />

resistance when enter<strong>in</strong>g <strong>in</strong> the water have direct impact on<br />

the underwater phase (Holthe <strong>and</strong> McLean, 2001; Miller et al., 2002;<br />

Elipot et al., 2009).<br />

The underwater phase is described as glid<strong>in</strong>g <strong>and</strong> underwater leg<br />

propulsion (Elipot et al., 2009). When enter<strong>in</strong>g the water, swimmer’s<br />

velocity (around 3.61 m.s -1 ) is greater than can be produced by underwater<br />

propulsion (Elipot et al., 2009). Dur<strong>in</strong>g the glid<strong>in</strong>g phase, the<br />

streaml<strong>in</strong>e position (Mar<strong>in</strong>ho et al., 2009) <strong>in</strong>fluences directly the hydrodynamic<br />

resistance. Swimmer propulsive movements should ideally<br />

be <strong>in</strong>itiated when the underwater velocity reaches between 2.2 <strong>and</strong> 1.9<br />

m.s -1 (Lyttle et al., 2000). Based on this result, Elipot et al. (2009) showed<br />

that the optimal beg<strong>in</strong>n<strong>in</strong>g of the propulsive movement appeared when<br />

the swimmer centre of mass reached 5.61 to 6.01 m from the wall start.<br />

At this distance, underwater propulsion becomes more critical.<br />

The underwater leg propulsion phase is currently termed “undulatory<br />

underwater swimm<strong>in</strong>g” (Arellano et al., 2006; Loebbecke et al.,<br />

2008). The undulatory underwater swimm<strong>in</strong>g of fish <strong>and</strong> human locomotion<br />

has been studied us<strong>in</strong>g an oscillat<strong>in</strong>g foil (Anderson et al., 1998;<br />

Read et al., 2003). These studies showed that the oscillation of the foils<br />

created a vortex wake associated with drag or thrust (Anderson et al.,<br />

1998; Read et al., 2003). Under specific conditions, an oscillat<strong>in</strong>g foil<br />

can modify the von Karman street of the wake <strong>and</strong> generate propulsive<br />

force or lift for manoeuvr<strong>in</strong>g (Anderson et al., 1998; Read et al., 2003).<br />

These specific conditions are def<strong>in</strong>ed by Reynolds number, the angle<br />

of attack, the Strouhal number <strong>and</strong> the optimal phase angle between<br />

heave <strong>and</strong> pitch of the oscillat<strong>in</strong>g foil (Anderson et al., 1998; Read et<br />

chaPter2.<strong>Biomechanics</strong><br />

al., 2003). The Reynolds number is def<strong>in</strong>ed as Re=U.l/v, where U is the<br />

mean swimm<strong>in</strong>g velocity; l is the characteristic length of the body <strong>and</strong> v<br />

is the k<strong>in</strong>ematic viscosity. Re represents the nature (lam<strong>in</strong>ar to turbulent)<br />

of the flow circulation around the body. The angle of attack α is the angle<br />

between the flow velocity <strong>and</strong> the chord of the body. The angle of attack<br />

<strong>in</strong>fluences directly the drag <strong>and</strong> lift coefficient (Rouboa et al., 2006). The<br />

Strouhal number is a dimensionless number which represent the ratio of<br />

unsteady <strong>and</strong> steady motion def<strong>in</strong>ed as St=A.f/U, where A is the maximal<br />

amplitude of the body (or heave translation); <strong>and</strong> f is the motion frequency<br />

of the oscillat<strong>in</strong>g body. St is an important factor <strong>in</strong> determ<strong>in</strong><strong>in</strong>g<br />

propulsion forces <strong>and</strong> swimm<strong>in</strong>g efficiency (Anderson et al., 1998; Read<br />

et al., 2003). The phase angle ψ represents the relation between pitch<br />

<strong>and</strong> heave of the oscillat<strong>in</strong>g body. An optimal ψ associated to a fixed St<br />

changes the α <strong>and</strong> <strong>in</strong>fluence directly the propulsion forces (Read et al.,<br />

2003). All these specific conditions can’t be easily estimated dur<strong>in</strong>g the<br />

start underwater phase because of the decrease of the swimmers’ velocity,<br />

the modification the swimmers’ segment orientation <strong>and</strong> coord<strong>in</strong>ation.<br />

But some of these (U, α, A, f, ψ) can be described <strong>and</strong> studied dur<strong>in</strong>g<br />

each part of the underwater phase. As per our knowledge, each of the<br />

<strong>in</strong>dependent phases of glid<strong>in</strong>g <strong>and</strong> underwater leg propulsion have been<br />

clearly <strong>in</strong>vestigated, but few papers clearly present the important factor<br />

that the swimmer should achieve to limit the loss of velocity dur<strong>in</strong>g the<br />

underwater phase of a start.<br />

The aim of this study was to determ<strong>in</strong>e the most important factors<br />

related to performance <strong>in</strong> the underwater phase of grab starts.<br />

Methods<br />

The experiment takes place <strong>in</strong> the swimm<strong>in</strong>g pool of the National Institute<br />

of Sport <strong>and</strong> Physical Education (INSEP, France). Twelve swimmers<br />

of national level (mean ± st<strong>and</strong>ard deviation SD: age= 21.41 ± 4.54<br />

years; high= 183.33 ± 4.88 cm; mass= 75.8 ± 5.09 kg) volunteered to<br />

participate <strong>in</strong> the study. All were <strong>in</strong>formed of the objectives <strong>and</strong> signed<br />

a consent form. All swimmers practiced grab start <strong>and</strong> undulatory underwater<br />

swimm<strong>in</strong>g on a regular basis <strong>and</strong> used them for competitive<br />

rac<strong>in</strong>g. The swimmers were asked to perform a competitive grab start as<br />

efficiently as possible.<br />

The underwater area between the wall (0 m) to 10 m was recorded<br />

us<strong>in</strong>g three cameras (Panasonic NV-GS17 <strong>and</strong> Sony DCR-HC20E).<br />

Two cameras (camera 1, 2) were fixed beh<strong>in</strong>d portholes. These cameras<br />

recorded a sagittal view of the swimmers’ trajectories. The third camera<br />

was placed <strong>in</strong> a waterproof hous<strong>in</strong>g. This camera recorded a slant<strong>in</strong>g<br />

view of the swimmer motion. The angles between the pr<strong>in</strong>cipal axis of<br />

camera 3 <strong>and</strong> the other cameras were between 60° <strong>and</strong> 70°. The underwater<br />

area was divided <strong>in</strong>to two zones measur<strong>in</strong>g 5�2�2 m (length,<br />

width, weight): The first zone covered the volume from the start wall to<br />

the 5 m, the second zone from the 5 m to the 10 m. Each zone was recorded<br />

by two cameras. To limits the effect of the image distortions (due<br />

to camera lens deformation) on reconstruction accuracy, only the po<strong>in</strong>ts<br />

conta<strong>in</strong>ed <strong>in</strong> the 2/3 centre of the camera field have been reconstructed.<br />

The cameras were positioned to m<strong>in</strong>imize optical refraction effects<br />

(Snells’law). A large distance divided the cameras <strong>and</strong> the centre of each<br />

zone (Kwon, 1999). The cameras’ optical axes were perpendicular to the<br />

air–water <strong>in</strong>terface plane. Cameras were synchronised with a light flash.<br />

The video was <strong>in</strong>terlaced scan <strong>and</strong> both odd <strong>and</strong> even fields were used<br />

thereby yield<strong>in</strong>g an effective sampl<strong>in</strong>g rate of 50Hz. The glid<strong>in</strong>g <strong>and</strong><br />

undulatory underwater swimm<strong>in</strong>g phase was recorded from the <strong>in</strong>stant<br />

when the swimmers were completely under water until the <strong>in</strong>stant they<br />

began arm propulsion. To m<strong>in</strong>imise errors dur<strong>in</strong>g the digitiz<strong>in</strong>g process,<br />

the two sides of the swimmer’s body were assumed to be symmetric.<br />

Only the right side was digitized. N<strong>in</strong>e anatomic l<strong>and</strong>marks were identified<br />

on the swimmers with software SimiMotion (Simi Reality Motion<br />

Systems GmbH, Germany): the toe, the lateral malleolus, the knee, the<br />

iliac sp<strong>in</strong>e, the acromion, a f<strong>in</strong>ger tip, the wrist, the elbow, <strong>and</strong> the centre<br />

of the head. A modified double plane direct l<strong>in</strong>ear transformation method<br />

(<strong>in</strong>spired by Drenk et al., 1999) was used to calculate the l<strong>and</strong>mark<br />

97


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

coord<strong>in</strong>ates <strong>in</strong> space. Space mean reconstruction accuracy, calculated as<br />

described by Kwon & Casebolt (2006), was 6.2 mm. Data were filtered<br />

with a Butterworth II filter (W<strong>in</strong>ter, 1990). Cut-off frequencies were<br />

between 5 <strong>and</strong> 7 Hz. The l<strong>and</strong>mark’s positions associated with Dempster’s<br />

anthropometric data (1959) were used to determ<strong>in</strong>e the trajectory<br />

of the centre of mass. Us<strong>in</strong>g the coord<strong>in</strong>ates of the l<strong>and</strong>marks <strong>and</strong> the<br />

centre of mass, the follow<strong>in</strong>g variables were def<strong>in</strong>ed:<br />

- time (t) of the centre of mass position,<br />

- the horizontal velocity of the centre of mass (Vx g ) <strong>and</strong> hip (Vx h );<br />

- the angle of attack of segments trunk (α tr ), thigh (α th ), leg (α le ),<br />

foot (α fo ) which were def<strong>in</strong>ed as the angle between each segment<br />

<strong>and</strong> the velocity vector of this proximal l<strong>and</strong>marks;<br />

- the mean kick frequency (f ) of the underwater undulatory swimm<strong>in</strong>g<br />

or the reverse period of the ankle motion;<br />

- the mean kick amplitude (A) or the mean peak to peak amplitude<br />

of the ankle dur<strong>in</strong>g the underwater undulatory swimm<strong>in</strong>g;<br />

- the phase time of the knee (P k ) <strong>and</strong> the ankle (P a ), that is, the<br />

time between the beg<strong>in</strong>n<strong>in</strong>g of the hip undulatory motion <strong>and</strong><br />

the respective distal jo<strong>in</strong>t (knee or ankle) undulatory motion.<br />

These variables were calculated for each swimmer every 0.5 m between<br />

5 m to 7.5 m. After 7.5 m, more than 40% (five swimmers) of the total<br />

number of swimmers began arm propulsion. For the range of distance,<br />

the normality of the variables was tested us<strong>in</strong>g Jarque-Bera Test. The<br />

effect of the <strong>in</strong>dependent variables (α tr , α th , α le , α fo, f, A, P k, P a ) on the<br />

dependent variables Vx g <strong>and</strong> Vx h at each normalized distance was analysed<br />

us<strong>in</strong>g stepwise l<strong>in</strong>ear regression. The limit of significance was set as<br />

p≤0.05. Time (t) at each distance was compared with Vx g <strong>and</strong> Vx h us<strong>in</strong>g<br />

correlation coefficients.<br />

results<br />

Statistical results showed that there was a reverse correlation between<br />

Vx g, Vx h <strong>and</strong> t at each distance. The regression equation of the parameters<br />

that <strong>in</strong>fluence Vx g, Vx h at each distance are given <strong>in</strong> Table 1 <strong>and</strong><br />

Table 2 with correspond<strong>in</strong>g R 2 <strong>and</strong> p values. These results showed that<br />

different parameters <strong>in</strong>fluence Vx g <strong>and</strong> Vx h at different phases of the<br />

underwater undulatory swimm<strong>in</strong>g except at 5 m. At 5.5 m, the stepwise<br />

regression analysis showed that decrease of mean kick amplitude (A)<br />

<strong>and</strong> attack of trunk (α tr ) are the selected variables to improve respectively<br />

Vx g <strong>and</strong> Vx h At 5.5, 6 <strong>and</strong> 7.5 m, the parameters that <strong>in</strong>fluence the<br />

horizontal velocity (Vx g <strong>and</strong> Vx h ) are different for the centre of mass <strong>and</strong><br />

the hip. Between 5.5 to 6.5 m, the stepwise regression analysis showed<br />

that the decrease of angles of attack of different segments (α tr at 5.5 m,<br />

α fo at 6 m, α th at 6.5 m) are selected variables to improve the horizontal<br />

velocity Vx g <strong>and</strong> Vx h . Between 6 to 7.5 m <strong>in</strong>crease of the phase time (P k<br />

<strong>and</strong> P a ) was related to <strong>in</strong>creas<strong>in</strong>g horizontal velocity Vx g <strong>and</strong> Vx h . At<br />

6.5 m the decrease of the angles of attack of thigh (α th ) <strong>and</strong> the <strong>in</strong>crease<br />

of the phase time of the knee (P k ) were related to improve horizontal<br />

velocity Vx g <strong>and</strong> Vx h (R 2 =0.79 for Vx g <strong>and</strong> R 2 =0.79 for Vx h ). At 7.5 m<br />

the <strong>in</strong>crease of phase time of the knee (P k ) <strong>and</strong> mean kick frequency (f )<br />

improved respectively Vx g <strong>and</strong> Vx h<br />

Table 1: Regression equation with statistical coefficient <strong>and</strong> p values of<br />

<strong>in</strong>dependent variables which present Vxg. Distance (m) Equation R2 5<br />

P values<br />

5.5 Vxg = -0.03 A 0.43 P=0.03<br />

6 Vxg = -0.02 αfo 0.7 P=0.01<br />

6.5 Vxg = -0.009 αth + 1.12 Pa 0.79 P=0.004<br />

7 Vxg = 2.29 Pa 0.52 P=0.017<br />

7.5 Vxg = 1.89 Pk 0.68 P=0.01<br />

98<br />

Table 2: Regression equation with statistical coefficient <strong>and</strong> p values of<br />

<strong>in</strong>dependent variables which present Vxh. Distance (m) Equation R2 5<br />

P values<br />

5.5<br />

6<br />

Vxh = -0.02 αtr 0.56 P=0.01<br />

6.5 Vxh = -0.019 αth + 1.12 Pa 0.89 P=0.0004<br />

7 Vxh = 2.25 Pa 0.52 P=0.017<br />

7.5 Vxh = 0.62 f 0.68 P=0.01<br />

dIscussIon<br />

The <strong>in</strong>verse correlation between time of the centre of mass position <strong>and</strong><br />

the horizontal velocity Vx g <strong>and</strong> Vx h confirm that horizontal velocity <strong>in</strong>fluences<br />

directly the swimmer performance (Elipot et al., 2009). The most<br />

important limitation of the result us<strong>in</strong>g stepwise l<strong>in</strong>ear regression analysis<br />

is the low number (n) of subjects to predict <strong>in</strong>dependent variables (k) us<strong>in</strong>g<br />

stepwise regression (Fonton et al., 1998). In the present study: n0.8, the<br />

stepwise regression presents the <strong>in</strong>dependent variables as best predictors<br />

<strong>and</strong> expla<strong>in</strong>s more that 50% of the event variability (Fonton et al., 1998).<br />

The results of the present study <strong>in</strong>dicated that the swimmer should stay<br />

<strong>in</strong> a streaml<strong>in</strong>ed position <strong>and</strong> limit the underwater undulatory swimm<strong>in</strong>g<br />

before he reaches 5.5 m. At this distance, mean velocities are Vx g = 2.18<br />

± 0.21 m.s -1 <strong>and</strong> Vx h = 2.15 ± 0.27 m.s -1 . This is <strong>in</strong> agreement with the<br />

previous works (Lyttle et al, 2000; Elipot et al., 2009). If the swimmer<br />

would have begun its underwater undulatory swimm<strong>in</strong>g too early, hydrodynamic<br />

resistances would have <strong>in</strong>creased <strong>and</strong> limited the performance of<br />

the underwater phase of the start (Elipot et al., 2009). Decreas<strong>in</strong>g of the<br />

angle of attack the trunk (α tr ) as selected variable of Vx h , confirmed that<br />

the angles of attack directly <strong>in</strong>fluence drag <strong>and</strong> also lift coefficients of the<br />

body. So it has an impact on the swimm<strong>in</strong>g propulsion efficiency (Rouboa<br />

et al., 2006). Decreas<strong>in</strong>g the angle of attack of the thigh (α th ) at 6.5 m <strong>and</strong><br />

<strong>in</strong>creas<strong>in</strong>g the phase time of the ankle (P a ) improves the horizontal velocity<br />

Vx g <strong>and</strong> Vx h. This result is <strong>in</strong> agreement with studies realised on fish<br />

(Loebbecke et al., 2008). For the dolph<strong>in</strong>s, the propulsion m<strong>in</strong>imizes the<br />

displacement of the drag produc<strong>in</strong>g forward parts of the body, <strong>and</strong> maximizes<br />

the displacement of the thrust produc<strong>in</strong>g fluke. The displacement<br />

wave that travels the length of the body also has a small magnitude along<br />

the torso, <strong>and</strong> reaches a maximum at the toes. After 7 m, the <strong>in</strong>crease of the<br />

phase time of the knee (P k ) <strong>and</strong> the ankle (P a ) improves horizontal velocity.<br />

At 7.5 m, the mean velocities of the swimmers were Vx g = 1.76 ± 0.15 m.s -1<br />

<strong>and</strong> Vx h = 1.81 ± 0.15 m.s -1 , mean kick frequency (f= 2.32 ± 0.21 Hz) <strong>and</strong><br />

mean amplitude (70.8 ± 6.04 cm) were higher than the velocity, frequency<br />

<strong>and</strong> amplitude observed <strong>in</strong> the study of Gavilan et al. (2006). The result of<br />

the stepwise regression <strong>and</strong> the comparison with the results of Gavillan<br />

et al. (2006) confirmed that the swimmer can improve his velocity with<br />

<strong>in</strong>creas<strong>in</strong>g frequency if he ma<strong>in</strong>ta<strong>in</strong>s large mean kick amplitude.<br />

conclusIon<br />

The stepwise regression enabled four pr<strong>in</strong>ciples to be proposed to improve<br />

the underwater phase of the swimmer: i) to be streaml<strong>in</strong>e with<br />

l<strong>in</strong>ear adjustment of the trunk <strong>and</strong> the lower body segments at the beg<strong>in</strong>n<strong>in</strong>g<br />

of the underwater glid<strong>in</strong>g phase, ii) to start the dolph<strong>in</strong> kick<strong>in</strong>g<br />

after 5.5 m, with a high undulation’s frequency iii) to move like dolph<strong>in</strong>s<br />

us<strong>in</strong>g only foot <strong>and</strong> leg for propulsive segment <strong>in</strong> underwater undulatory<br />

swimm<strong>in</strong>g, iv) to use an optimal phase time coord<strong>in</strong>ation of the lower<br />

body segments to improve propulsive forces.


eFerences<br />

Anderson, J. M., Streitlien, K., Barret, D. S. & Triantafyllou, M. S.<br />

(1998). Oscillat<strong>in</strong>g foils of high propulsive efficiency. J Fluid Mech,<br />

360, 41-72.<br />

Arellano, R., Moreno, F. J., Mart<strong>in</strong>ez, M. & Ona, A. (1996). A device<br />

for quantitative measurement of start<strong>in</strong>g time <strong>in</strong> swimm<strong>in</strong>g. <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> swimm<strong>in</strong>g VII. E & FN Spon, London,<br />

195-200.<br />

Drenk, V., Hildebr<strong>and</strong>, F., K<strong>in</strong>dler, M. & Kliche, D. (1999). A 3D video<br />

technique for analysis of swimm<strong>in</strong>g <strong>in</strong> a flume. Scientific Proceed<strong>in</strong>g<br />

of the XVII International Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sport, Perth,<br />

Australia, 361-364.<br />

Elipot, M., Hellard, P., Taiar, R., Boissière, E., Rey, J. L., Lecat, S. &<br />

Houel, N. (2009). Analysis of swimmers velocity dur<strong>in</strong>g the underwater<br />

glid<strong>in</strong>g motion follow<strong>in</strong>g grab start. J Biomech, 42, 1367-1370.<br />

Fonton, N. H. & Palm, R. (1998). Comparaison empirique de methods<br />

de prediction en regression l<strong>in</strong>eaire multiple. Rev Stat Appliqué,<br />

XLVI(3), 53-64.<br />

Holthe, M. J. & Mc Lean, S. P. (2001). K<strong>in</strong>ematic comparison of grab<br />

<strong>and</strong> track starts <strong>in</strong> swimm<strong>in</strong>g. <strong>Biomechanics</strong> Symposia, 31-34.<br />

Issur<strong>in</strong>, V. B. & Verbitsky, O. (2002). Track start versus Grab Start: Evidence<br />

of the Sydney Olympic Games. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g IX, University of Sa<strong>in</strong>t Etienne, France, 213-218.<br />

Gavilan, A., Arellano, R. & S<strong>and</strong>ers, R. (2006). Underwater undulatory<br />

swimm<strong>in</strong>g: study of frequency, amplitude <strong>and</strong> phase characteristics<br />

of the ‘body wave’. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X, Portuguese<br />

Journal of Sport Sciences, 35-37.<br />

Kwon, Y. H. & Casebolt, J. B. (2006). Effects of light refraction on accuracy<br />

of camera calibration <strong>and</strong> reconstruction <strong>in</strong> underwater motion<br />

analysis. Sports <strong>Biomechanics</strong>, 5(1), 95-120.<br />

Loebbecke, A. V., Mittal, R., Fish, F. & Mark, R. (2009). A comparaison<br />

of k<strong>in</strong>ematics of dolph<strong>in</strong> kick <strong>in</strong> human <strong>and</strong> cetacean. Hum Mov<br />

Sci, 99-112.<br />

Lyttle, A. D., Blanksby, B. A., Elliot, B. C. & Lloyd, D. G. (2000). Bet<br />

forces dur<strong>in</strong>g tethered simulation of underwater streaml<strong>in</strong>ed glid<strong>in</strong>g<br />

<strong>and</strong> kick<strong>in</strong>g techniques of freestyle turn. Journal of Sports Sciences,<br />

18, 801-807.<br />

Mason, B. & Cossor, J. (2000). What we can learn from competition<br />

analysis at 1999 pan Pacific Swimm<strong>in</strong>g Championships. In proceed<strong>in</strong>gs<br />

of XVIII Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports, HongKong, 75-82.<br />

Mar<strong>in</strong>ho, D. A., Reis, V. M., Alves, F. B., Vilas-Boas, J. P., Machado, L.,<br />

Silva, J., et al. (2009). Hydrodynamic drag dur<strong>in</strong>g glid<strong>in</strong>g <strong>in</strong> swimm<strong>in</strong>g.<br />

Journal of applied <strong>Biomechanics</strong>, 25, 253-257.<br />

Miller, M. K., Allen, D. & Pe<strong>in</strong>, R. (2002). A k<strong>in</strong>ematic <strong>and</strong> k<strong>in</strong>etic<br />

comparison of the grab <strong>and</strong> the track starts <strong>in</strong> swimm<strong>in</strong>g. <strong>Biomechanics</strong><br />

<strong>and</strong> medic<strong>in</strong>e <strong>in</strong> Swimm<strong>in</strong>g IX, University of de Sa<strong>in</strong>t-Etienne,<br />

France, 231-234.<br />

Read, D. A., Hover, F. S. & Triantafyllou, M. S. (2003). Forces on ocsillat<strong>in</strong>g<br />

foils for propulsion <strong>and</strong> maneuver<strong>in</strong>g. Journal of Fluids <strong>and</strong><br />

Structures, 17, 163-183.<br />

Rouboa, A., Silva, A., Leal, L., Rocha, J. & Alves, F. (2006). The effect<br />

of swimmer’s h<strong>and</strong>/forearm acceleration on propulsive forces<br />

us<strong>in</strong>g computational fluid dynamics. Journal of <strong>Biomechanics</strong>, 39,<br />

1239-1248.<br />

Vilas-Boas, J. P., Cruz, M. J., Sousa, F., Conceiçao, F., Fern<strong>and</strong>es, R.<br />

& Carvalho, J. (2003). Biomechanical analysis of ventral swimm<strong>in</strong>g<br />

starts: comparison of the grab start with two track start techniques.<br />

<strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> Swimm<strong>in</strong>g IX. University of de Sa<strong>in</strong>t-<br />

Etienne, France, 249-252.<br />

W<strong>in</strong>ter, D. A. (2000). <strong>Biomechanics</strong> <strong>and</strong> motor control of human<br />

movement. Human K<strong>in</strong>etics, New York: A. Wiley-Interscience Publication,<br />

Second Edition.<br />

chaPter2.<strong>Biomechanics</strong><br />

AcKnoWledGeMents<br />

The authors wish to thank the “M<strong>in</strong>istère de la Jeunesse, des Sports et<br />

de la Vie Associative” <strong>and</strong> the “Fédération Française de Natation” for<br />

f<strong>in</strong>anc<strong>in</strong>g this study. The authors also wish to thank Frédéric Frontier,<br />

Frédéric Clerc, Isabelle Amaudry <strong>and</strong> the “INSEP” for logistic support,<br />

<strong>and</strong> Jean-Lyonel Rey, Stéphane Lecat, Eric Boissière <strong>and</strong> Yves Thomass<strong>in</strong><br />

for their contributions.<br />

99


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Comparison of Front Crawl Swimm<strong>in</strong>g Drag between<br />

Elite <strong>and</strong> Non-Elite Swimmers Us<strong>in</strong>g Pressure<br />

Measurement <strong>and</strong> Motion Analysis<br />

Ichikawa, h. 1 , Miwa, t. 1 , takeda, t. 2 , takagi, h. 2 , tsubakimoto,<br />

s. 2<br />

1 Japan Institute of Sports Sciences, Tokyo, Japan<br />

2 University of Tsukuba, Ibaraki, Japan<br />

The purpose of the study was to suggest a methodology to quantify the<br />

drag force dur<strong>in</strong>g front crawl swimm<strong>in</strong>g <strong>and</strong> to compare the drag force<br />

between elite <strong>and</strong> non-elite swimmers. Subjects were asked to swim<br />

front crawl us<strong>in</strong>g arms only <strong>in</strong> swimm<strong>in</strong>g flume, which set the velocity<br />

to 1.3 m/s. The pressure distribution on the swimmer’s h<strong>and</strong>s <strong>and</strong><br />

the orientation of the swimmer’s h<strong>and</strong>s were measured to calculate the<br />

propulsive force. The position of the umbilicus was recorded us<strong>in</strong>g high<br />

speed camera with 250 fps to calculate the swimm<strong>in</strong>g acceleration. The<br />

drag force was estimated accord<strong>in</strong>g to the equation of motion “ma = Fp +<br />

Fd” along with swimm<strong>in</strong>g direction. The elite swimmer swam efficiently<br />

with lower drag force (averag<strong>in</strong>g at 21N) compared to the non-elite<br />

swimmer (average 50N). Our methodology would be useful to compare<br />

the dynamics <strong>and</strong> to discuss the performance of swimm<strong>in</strong>g.<br />

Key words: drag force, propulsive force, <strong>in</strong>ertial term, dynamics, front<br />

crawl swimm<strong>in</strong>g<br />

IntroductIon<br />

The dynamics of swimm<strong>in</strong>g is expressed as a mass model,<br />

ma + F<br />

100<br />

= Fgra<br />

+ Fsta<br />

dyn<br />

(1)<br />

where m <strong>and</strong> a are a swimmer’s mass <strong>and</strong> acceleration vector of the<br />

swimmer’s whole body. F gra is downward force vector due to gravity, F sta<br />

is upward hydrostatic force vector that is called buoyancy, <strong>and</strong> F dyn is<br />

unsteady hydrodynamic force that Namashima (2006) was modell<strong>in</strong>g as<br />

tangential <strong>and</strong> normal resistive fluid force, which are proportional to the<br />

local flow velocity, <strong>and</strong> <strong>in</strong>ertial force due to added mass, which is proportional<br />

to the local flow acceleration. The component on the swimm<strong>in</strong>g<br />

direction of Equation 1 was expressed as,<br />

ma +<br />

= Fdyn−<br />

swim = Fp<br />

Fd<br />

(2)<br />

where a <strong>and</strong> F dyn-swim are the component along with swimm<strong>in</strong>g direction<br />

of a <strong>and</strong> F dyn , respectively. The F dyn-swim is separated <strong>in</strong>to forward force<br />

F p , which is propulsive force, <strong>and</strong> backward force F d , which is drag force.<br />

Many researchers have suggested some methodologies to quantify the<br />

drag force <strong>in</strong> swimm<strong>in</strong>g as “active drag”, although it is difficult to quantify<br />

the drag force <strong>in</strong> swimm<strong>in</strong>g (Di Prampero et al. 1974, Clarys et al.<br />

1974, Holl<strong>and</strong>er et al. 1986, Kolmogorov et al.1992). The methodologies<br />

have some assumptions, such as “swimm<strong>in</strong>g velocity is constant” (Di<br />

Prampero et al. 1974, Holl<strong>and</strong>er et al. 1986), “propulsive <strong>and</strong> drag force<br />

are <strong>in</strong> balance” (Clarys et al. 1974, Kolmogorov et al. 1992). Almost all<br />

previous researches expressed the drag force as a s<strong>in</strong>gle value, which was<br />

a mean value dur<strong>in</strong>g some strokes. The drag force is, however, chang<strong>in</strong>g<br />

from moment to moment dur<strong>in</strong>g swimm<strong>in</strong>g, so the assumptions <strong>and</strong><br />

the expression of drag force would make us overlook some <strong>in</strong>formation<br />

of swimm<strong>in</strong>g dynamics. It is important to observe the dynamics<br />

of the propulsive <strong>and</strong> drag forces dur<strong>in</strong>g swimm<strong>in</strong>g quantitatively <strong>and</strong><br />

cont<strong>in</strong>uously, because it would lead to better discussion of the swimm<strong>in</strong>g<br />

technique <strong>and</strong> performance.<br />

In the present study, the drag force, which is chang<strong>in</strong>g dur<strong>in</strong>g front<br />

crawl swimm<strong>in</strong>g, was quantified with a methodology that is accord<strong>in</strong>g<br />

to the equation of motion (Eq.2) to discuss the dynamics of front crawl<br />

dur<strong>in</strong>g swimm<strong>in</strong>g quantitatively <strong>and</strong> cont<strong>in</strong>uously, because it wo<br />

discussion of the swimm<strong>in</strong>g technique <strong>and</strong> performance.<br />

In the present study, the drag force, which is chang<strong>in</strong>g d<br />

swimm<strong>in</strong>g, was quantified with a methodology that is accord<strong>in</strong>g<br />

motion (Eq.2) to discuss the dynamics of front crawl swimm<strong>in</strong>g. T<br />

study were to suggest a methodology to quantify the drag force d<br />

swimm<strong>in</strong>g. The purposes of the study were to suggest a methodology to<br />

swimm<strong>in</strong>g, <strong>and</strong> to compare the drag force between an elite (a com<br />

quantify the drag force dur<strong>in</strong>g front crawl swimm<strong>in</strong>g, <strong>and</strong> to compare<br />

<strong>and</strong> a non-elite (a triathlete) swimmer.<br />

the drag force between an elite (a competitive swimmer) <strong>and</strong> a non-elite<br />

(a triathlete) swimmer.<br />

METHODS<br />

METHODS The subjects were a well-tra<strong>in</strong>ed male competitive swimmer <strong>and</strong> a m<br />

The profile subjects of were the a well-tra<strong>in</strong>ed subjects is male shown competitive <strong>in</strong> Table swimmer 1. The <strong>and</strong> subjects a male were asked<br />

triathlete. crawl The us<strong>in</strong>g profile arms of the only subjects <strong>in</strong> a swimm<strong>in</strong>g is shown <strong>in</strong> Table flume, 1. The which subjects was set the flow<br />

were m/s. asked In to the swim experiment, the front crawl the pressure us<strong>in</strong>g arms distribution only <strong>in</strong> a swimm<strong>in</strong>g on swimmer's h<strong>and</strong>s<br />

flume, the which h<strong>and</strong>s was <strong>and</strong> set the position flow<strong>in</strong>g velocity of the at umbilicus 1.3 m/s. In the were experiment, measured dur<strong>in</strong>g the<br />

the pressure distribution on swimmer’s h<strong>and</strong>s, the orientation of the<br />

h<strong>and</strong>s Table <strong>and</strong> 1. the Characteristics position of the umbilicus of the were subjects. measured dur<strong>in</strong>g the trial.<br />

Bes<br />

Table Subject 1. Characteristics of the Height subjects. [m] Weight [kg] Age [yrs]<br />

100<br />

Best record for<br />

Subject Competitive Height [m] Weight [kg] Age [yrs]<br />

1.79 74.0 100m-Fr. 22.4 [sec] 49.6<br />

swimmer<br />

Competitive swimmer 1.79 74.0 22.4 49.6<br />

Triathlete 1.70 1.70 68.0 68.0 22.7 82.022.7<br />

82.0<br />

Twelve small pressure sensors, 6 mm diameter <strong>and</strong> 0.7 mm thick, (PS-<br />

05KC, Kyowa, Twelve Japan) small were pressure attached on sensors, the swimmer’s 6 mm both diameter h<strong>and</strong>s. The <strong>and</strong> 0.7 mm<br />

attach<strong>in</strong>g Kyowa, positions Japan) were were the palmar attached <strong>and</strong> dorsal on the sides swimmer's at the metacarpo- both h<strong>and</strong>s. The a<br />

phalangeal were the (MP) palmar II jo<strong>in</strong>t, <strong>and</strong> the middle dorsal po<strong>in</strong>t sides of at MP the III metacarpophalangeal <strong>and</strong> IV jo<strong>in</strong>ts, <strong>and</strong> (MP) I<br />

MP po<strong>in</strong>t V jo<strong>in</strong>t of (Fig. MP 1). III The <strong>and</strong> pressure IV jo<strong>in</strong>ts, values were <strong>and</strong> recorded MP V at jo<strong>in</strong>t 500Hz (Fig. to 1). The pre<br />

calculate recorded the hydrodynamic at 500Hz to force calculate Fh<strong>and</strong> exerted the hydrodynamic on the swimmer’s h<strong>and</strong>s force Fh<strong>and</strong> exerted<br />

us<strong>in</strong>g h<strong>and</strong>s the follow<strong>in</strong>g us<strong>in</strong>g the equation, follow<strong>in</strong>g equation,<br />

3<br />

h<strong>and</strong> ∑<br />

i=<br />

1<br />

( p − p )<br />

F = A w<br />

Eq.3 , ,<br />

h<strong>and</strong><br />

i<br />

palm i<br />

dorsum i<br />

where where A Ah<strong>and</strong> was the plane area of the h<strong>and</strong>. The <strong>in</strong>dex i <strong>in</strong>dicates a po<br />

h<strong>and</strong> was the plane area of the h<strong>and</strong>. The <strong>in</strong>dex i <strong>in</strong>dicates a position<br />

pressure to attach sensor, the pressure that sensor, is i = that 1 is is MP i = 1 II is jo<strong>in</strong>t, MP II 2 jo<strong>in</strong>t, is the 2 is midpo<strong>in</strong>t the of MP II<br />

midpo<strong>in</strong>t 3 is MP of MP V jo<strong>in</strong>t. III <strong>and</strong> The IV jo<strong>in</strong>ts ppalm <strong>and</strong> <strong>and</strong> 3 is pdorsum MP V jo<strong>in</strong>t. were The the ppalm measured <strong>and</strong> pressure<br />

pdorsum dorsal were sides the measured of the h<strong>and</strong>, pressure respectively. on the palmar The <strong>and</strong> dorsal wi is the sides weight of of divide<br />

the sensor’s h<strong>and</strong>, respectively. position, The <strong>and</strong> wi is it the was weight def<strong>in</strong>ed of divided as w1<br />

area = w3<br />

on = the 0.25 each <strong>and</strong> w2 = 0.5 <strong>in</strong><br />

sensor’s And position, it was <strong>and</strong> assumed it was def<strong>in</strong>ed that as the w1 direction = w3 = 0.25 of <strong>and</strong> the w2 = hydrodynamic 0.5 <strong>in</strong> forc<br />

the<br />

perpendicular<br />

present study. And<br />

to<br />

it<br />

plane<br />

was assumed<br />

of the<br />

that<br />

h<strong>and</strong>.<br />

the direction of the hydrodynamic<br />

force on a h<strong>and</strong> was perpendicular to plane of the h<strong>and</strong>.<br />

Figure 1. A photograph of a pressure sensor (top) <strong>and</strong> the positions to<br />

be attached the pressure sensors on the palmar <strong>and</strong> dorsal sides of a left<br />

h<strong>and</strong> (bottom). The sensors were also attached on the right h<strong>and</strong> of the<br />

swimmer <strong>in</strong> a similar position as the illustration.


To calculate the orientation of the both h<strong>and</strong>s dur<strong>in</strong>g underwater phase,<br />

the visual markers were attached on the tip of the 1st , 3rd <strong>and</strong> 5th f<strong>in</strong>gers<br />

<strong>and</strong> the wrist of the swimmer. The swimm<strong>in</strong>g flume used <strong>in</strong> the experiment<br />

has w<strong>in</strong>dows at the bottom <strong>and</strong> the left side of a swimmer. Four<br />

synchronized cameras (TK-C1461, Victor, Japan) were set on to register<br />

motion of the swimmer’s h<strong>and</strong>s through the w<strong>in</strong>dows. Each visual<br />

marker on the video was digitized manually at a frequency of 60 field/<br />

second us<strong>in</strong>g a digitiz<strong>in</strong>g software (Video Annotator for Excel, JISS,<br />

Japan) <strong>and</strong> the three dimensional coord<strong>in</strong>ates were calculated us<strong>in</strong>g 3D-<br />

DLT method us<strong>in</strong>g a computational software (Mathematica 7, Wolfram<br />

Research, USA). The orientation of the h<strong>and</strong>s was expressed as the normal<br />

vector of the h<strong>and</strong> plane, which was calculated by the method of<br />

least squares with the 3-D coord<strong>in</strong>ates of the four markers on the h<strong>and</strong>.<br />

One other visual marker, fixed on the umbilicus, was used as an alternative<br />

po<strong>in</strong>t to the centre of gravity. The movement of the marker was<br />

recorded by a high speed camera (Fastcam-pci, Photron, Japan) with<br />

250 fps from the bottom view. The positions were digitized manually<br />

<strong>and</strong> calibrated it along with swimm<strong>in</strong>g direction only us<strong>in</strong>g the referred<br />

software (Video Annotator for Excel <strong>and</strong> Mathematica).<br />

The component on the swimm<strong>in</strong>g direction of the hydrodynamic<br />

force Fh<strong>and</strong> on each h<strong>and</strong> was calculated us<strong>in</strong>g the normal vector of the<br />

h<strong>and</strong>. It was def<strong>in</strong>ed that the propulsive force Fp was the summation of<br />

the components of the left <strong>and</strong> right h<strong>and</strong>s. The swimm<strong>in</strong>g acceleration<br />

a was calculated as the second-order derivative of the position of<br />

the umbilicus with respect to time. The <strong>in</strong>ertial term ma was def<strong>in</strong>ed as<br />

the product of the swimm<strong>in</strong>g acceleration <strong>and</strong> the swimmer’s mass. The<br />

estimation of the drag force Fd was based on the equation of motion<br />

Eq.2, <strong>Biomechanics</strong> so the drag force <strong>and</strong> was <strong>Medic<strong>in</strong>e</strong> obta<strong>in</strong>ed as <strong>XI</strong> the difference Chapter of the 2 <strong>in</strong>ertial <strong>Biomechanics</strong><br />

term ma <strong>and</strong> the propulsive force Fp (Fig. 2). Note that the obta<strong>in</strong>ed<br />

Fd <strong>in</strong> the present study was backward force <strong>and</strong> would be expressed as<br />

negative value.<br />

The coefficient of drag Cd was calculated <strong>in</strong> each trial us<strong>in</strong>g the follow<strong>in</strong>g<br />

equation,<br />

as the difference of the <strong>in</strong>ertial term ma <strong>and</strong> the propulsive force Fp (Fig. 2). Note that<br />

the obta<strong>in</strong>ed Fd <strong>in</strong> the present study was backward force <strong>and</strong> would be expressed as<br />

negative value.<br />

The 2Fcoefficient<br />

of drag Cd was calculated <strong>in</strong> each trial us<strong>in</strong>g the follow<strong>in</strong>g equation,<br />

RESULTS<br />

The <strong>in</strong>ertial term, propulsive <strong>and</strong> drag force dur<strong>in</strong>g 5 seconds were obta<strong>in</strong>ed <strong>in</strong> each<br />

subject (Fig. 3). The mean drag forces were 21.3 N <strong>in</strong> the competitive swimmer <strong>and</strong><br />

50.3 N <strong>in</strong> the triathlete, respectively. It was observed that the competitive swimmer had<br />

phases of no propulsive force. On the other h<strong>and</strong>, the triathlete kept produc<strong>in</strong>g<br />

146<br />

chaPter2.<strong>Biomechanics</strong><br />

with high stroke frequency. To compare the drag estimated <strong>in</strong> the present<br />

study with that of previous studies, the mean <strong>and</strong> absolute values of<br />

Reynolds numbers <strong>and</strong> coefficient of drag were calculated <strong>and</strong> plotted<br />

<strong>in</strong> same plane with the reported values (Takagi et al. 1998) <strong>in</strong> Fig. 4.<br />

Figure 3. The <strong>in</strong>ertial term, propulsive force <strong>and</strong> drag force dur<strong>in</strong>g front<br />

crawl swimm<strong>in</strong>g of the competitive swimmer (Left graphic) <strong>and</strong> the<br />

triathlete (Right graphic).<br />

Figure 4. The relationship between Reynolds number <strong>and</strong> coefficient<br />

of active swimm<strong>in</strong>g drag reported by previous researches (Takagi et al.<br />

d Cd<br />

= Eq.4,<br />

1998) <strong>and</strong> the mean <strong>and</strong> absolute values obta<strong>in</strong>ed by this study, which<br />

2<br />

rA<br />

2Fd<br />

wholev<br />

is <strong>in</strong>dicated by the plus “+” (the competitive swimmer) <strong>and</strong> the cross “x”<br />

Cd<br />

= Eq.4, 2<br />

ρAwholev<br />

(the triathlete) markers.<br />

where where r was ρ density was of density water, <strong>and</strong> of v water, was the mean <strong>and</strong> v swimm<strong>in</strong>g was the velocity, mean swimm<strong>in</strong>g velocity, which was 1.3<br />

which was 1.3 m/s. The Awhole was the swimmer’s surface area, which was dIscussIon<br />

calculated m/s. The Awhole by the Shitara’s was formula the for swimmer’s Japanese male, surface area, which It was seemed calculated that it would by be difficult the Shitara’s for the triathlete to ma<strong>in</strong>ta<strong>in</strong> the <strong>in</strong>-<br />

formula for Japanese male,<br />

structed swimm<strong>in</strong>g velocity, which was 1.3 m/s. The Fig. 3 demonstrated<br />

0.<br />

619 0.<br />

460 4<br />

Awhole = 105. 29 × ( H × 100)<br />

× W / 10 Eq.5, the reason was the larger drag force. The drag force of the triathlete<br />

reached 150 N. It must be noted that the drag force was expressed as<br />

where H <strong>and</strong> W were the swimmer’s height <strong>and</strong> weight, respectively (Shitara et al.<br />

where H <strong>and</strong> W were the swimmer’s height <strong>and</strong> weight, respectively negative value <strong>in</strong> the Fig. 3, although it was less than 100 N <strong>in</strong> the com-<br />

(Shitara 2009). et al. 2009). To discuss To discuss validity of of the the drag drag force Fforce Fd obta<strong>in</strong>ed by our methodology, the<br />

d obta<strong>in</strong>ed petitive swimmer. To overcome the larger drag force <strong>and</strong> to ma<strong>in</strong>ta<strong>in</strong> the<br />

by our coefficient methodology, of the drag coefficient Cd was of compared drag C with the reported values (Takagi et al. 1998).<br />

d was compared with the velocity, the triathlete had to keep produc<strong>in</strong>g the propulsive force with<br />

reported values (Takagi et al. 1998).<br />

high stroke frequency without a break. As a result, the triathlete’s effectiveness<br />

of swimm<strong>in</strong>g could be lower. It was not so large de-acceleration<br />

of the competitive swimmer, although he had phases of no propulsive<br />

force (Fig. 3). It was because the drag force was not so large <strong>in</strong> the phases.<br />

The lower drag force would provide him effective swimm<strong>in</strong>g.<br />

The validity of the obta<strong>in</strong>ed drag force <strong>in</strong> the methodology deserves<br />

more discussion. The comparison of the coefficient of drag with the previous<br />

researches <strong>in</strong> the Fig. 4 showed that the obta<strong>in</strong>ed values would be<br />

Figure 2. A schematic view to quantify the drag force Fd dur<strong>in</strong>g front lower <strong>in</strong> some degree. It was observed that the drag force was positive<br />

crawl swimm<strong>in</strong>g. The drag force was obta<strong>in</strong>ed as the difference of the value <strong>in</strong> every <strong>in</strong>-sweep phases of the both subjects (Fig. 3), although the<br />

<strong>in</strong>ertial term ma <strong>and</strong> the propulsive force Fp along with swimm<strong>in</strong>g di- drag force should be negative value, which meant backward force, <strong>in</strong> the<br />

rection.<br />

def<strong>in</strong>ition of the Equation 2. In this study, the drag force was calculated<br />

as the difference between the measured <strong>in</strong>ertial term <strong>and</strong> propulsive<br />

results Figure 2. A schematic view to quantify the drag force Fd force. dur<strong>in</strong>g The positive front drag crawl force swimm<strong>in</strong>g.<br />

resulted from the smaller propulsive force<br />

The The <strong>in</strong>ertial drag term, force propulsive was <strong>and</strong> obta<strong>in</strong>ed drag force as dur<strong>in</strong>g the difference 5 seconds were of obthe<br />

<strong>in</strong>ertial than the term <strong>in</strong>ertial ma term. <strong>and</strong> It was the assumed propulsive that the propulsive force was exta<strong>in</strong>ed<br />

<strong>in</strong> each subject (Fig. 3). The mean drag forces were 21.3 N <strong>in</strong> erted by the h<strong>and</strong>s only <strong>and</strong> that the direction of the hydrodynamic force<br />

force Fp along with swimm<strong>in</strong>g direction.<br />

the competitive swimmer <strong>and</strong> 50.3 N <strong>in</strong> the triathlete, respectively. It on the h<strong>and</strong> was perpendicular to plane of the h<strong>and</strong>s. However, there are<br />

was observed that the competitive swimmer had phases of no propulsive possibilities that any segments additional to the h<strong>and</strong>s, especially the<br />

force. On the other h<strong>and</strong>, the triathlete kept produc<strong>in</strong>g propulsive force forearms, contribute to produce forward force. It seemed that the hy-<br />

101


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

drodynamic forward force, which was not measured as propulsive force,<br />

would not be so small <strong>and</strong> was added as the positive drag force <strong>in</strong> our<br />

methodology. It is needed to take <strong>in</strong>to consideration any hydrodynamic<br />

forward force, which is exerted not only by the h<strong>and</strong>s but also by any<br />

other segments <strong>and</strong> measure the force as positive propulsive force, such<br />

as attach<strong>in</strong>g pressure sensors on swimmer’s forearm, <strong>in</strong> order to obta<strong>in</strong><br />

exact drag force dur<strong>in</strong>g swimm<strong>in</strong>g.<br />

conclusIon<br />

In the comparison of the dynamics dur<strong>in</strong>g front crawl swimm<strong>in</strong>g between<br />

the elite swimmer (competitive swimmer) <strong>and</strong> the non-elite<br />

swimmer (triathlete), it was suggested that the drag force would affect<br />

the performance of swimm<strong>in</strong>g strongly. The methodology <strong>in</strong> the present<br />

study provides us <strong>in</strong>formation on the dynamics, such as the <strong>in</strong>ertial term<br />

(swimm<strong>in</strong>g acceleration), the propulsive force <strong>and</strong> the drag force, dur<strong>in</strong>g<br />

front crawl swimm<strong>in</strong>g, although the accuracy of the measurement needs<br />

to be improved. In conclusion, it can be stated that the observation of<br />

the parameters chang<strong>in</strong>g from moment to moment would be useful to<br />

compare the dynamics between the elite swimmer <strong>and</strong> the non-elite<br />

swimmer <strong>and</strong> discuss the technique of swimm<strong>in</strong>g.<br />

reFerences<br />

Clarys, J. P. (1978). Relationship of human form to passive <strong>and</strong> active<br />

hydrodynamic drag. <strong>Biomechanics</strong> VI-B (ed.) Asmmussen E. <strong>and</strong> Jorgensen<br />

K., Baltimore, University Park Press, 120-125.<br />

Di Prampero, P. E., Pendergast, D. R., Wilson, D. W. & Rennie, D. W.<br />

(1974). Energetics of swimm<strong>in</strong>g <strong>in</strong> man. Journal of Applied Physiology,<br />

37(1), 1-5.<br />

Holl<strong>and</strong>er, A. P., de Groot, G., van Ingen Schenau, G. J., Toussa<strong>in</strong>t, H.<br />

M., de Best, H., Peeters, W., et al. (1986). Measurement of active drag<br />

dur<strong>in</strong>g crawl arm stroke swimm<strong>in</strong>g. Journal of Sports Sciences, 4(1),<br />

21-30.<br />

Kolmogorov, S. V. & Duplisheva, A. (1992). Active drag, useful mechanical<br />

power output <strong>and</strong> hydrodynamic force coefficient <strong>in</strong> different<br />

swimm<strong>in</strong>g strokes at maximal velocity. Journal of <strong>Biomechanics</strong>,<br />

25(3), 311-318.<br />

Nakashima, M. (2006). “SWUM” <strong>and</strong> “Swumsuit” - A model<strong>in</strong>g technique<br />

of a self-propelled swimmer. Proceed<strong>in</strong>g of the Xth International<br />

Symposium <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g (ed.) Vilas-Boas<br />

J. P., Alves F. <strong>and</strong> Marques A., 66-68.<br />

Shitara, K., Takai, Y., Ohta, M., Wakahara, T., Kanehisa, H., Fukunaga,<br />

T., et al. (2009). Development of an equation for predict<strong>in</strong>g body surface<br />

area based on three-dimensional photonic image scann<strong>in</strong>g. Japanese<br />

Journal of Physical Fitness <strong>and</strong> Sports <strong>Medic<strong>in</strong>e</strong>, 58(4), 463-474.<br />

Takagi, H., Shimizu, Y. & Kodan, N. (1998). A hydrodynamic study of<br />

active drag <strong>in</strong> swimm<strong>in</strong>g. Transactions of the Japan Society of Mechanical<br />

Eng<strong>in</strong>eers. B, 64(618), 405-411.<br />

102<br />

Whole Body Observation <strong>and</strong> Visualized Motion<br />

Analysis of Swimm<strong>in</strong>g<br />

Ito, s. 1 , okuno, K. 2<br />

1 Kogaku<strong>in</strong> University, Tokyo,. 2 Waseda University, Tokyo<br />

It is an advantage to film a swimmer’s whole body <strong>in</strong> order to underst<strong>and</strong><br />

the swimmer’s technique. However, it is difficult to underst<strong>and</strong> details,<br />

such as twist<strong>in</strong>g arms or stroke paths. Equipment was constructed<br />

which provides a cont<strong>in</strong>uous image of swimm<strong>in</strong>g motions by blend<strong>in</strong>g<br />

underwater <strong>and</strong> overwater images with a video mixer. Underwater <strong>and</strong><br />

overwater images were taken by cameras loaded onto a cart placed on<br />

a poolside track. The view from above the swimmer was observed by<br />

an overhang<strong>in</strong>g camera to observe wave resistance.. In order to grasp<br />

detailed swimm<strong>in</strong>g motions, logger data were synchronized with the actual<br />

motion images. Wavelet transformation, a chronological frequency<br />

analysis, was also performed on these logger data <strong>and</strong> the dom<strong>in</strong>ant<br />

frequency was viewed chronologically with different swimm<strong>in</strong>g styles.<br />

Key words: observation, visualization, motion analysis, wavelet<br />

transform<br />

IntroductIon<br />

Swimm<strong>in</strong>g is the successive motion of propulsive <strong>and</strong> recovery movements<br />

<strong>in</strong> the water. Analysis of the swimm<strong>in</strong>g motion can be provided to<br />

swimmers <strong>and</strong> coaches for improvement of performance. It is important<br />

to underst<strong>and</strong> the underwater motion <strong>in</strong> order to improve swimm<strong>in</strong>g<br />

technique. Track<strong>in</strong>g underwater cameras are often used <strong>in</strong> competition<br />

but are not generally used <strong>in</strong> tra<strong>in</strong><strong>in</strong>g because of their <strong>in</strong>stallation <strong>and</strong><br />

cost. Barbosa et al. (2006) were able to produce a cont<strong>in</strong>uous image of<br />

the swimm<strong>in</strong>g movements by blend<strong>in</strong>g underwater <strong>and</strong> overwater images<br />

with a video mixer. Ito, (2003) has also developed the same equipment<br />

<strong>and</strong> can capture the swimmer’s whole body motion <strong>in</strong>clud<strong>in</strong>g recovery<br />

overwater. Both underwater <strong>and</strong> overwater images were recorded by the<br />

cameras loaded onto a cart placed on a poolside rail track. The view from<br />

above the swimmer <strong>in</strong>clud<strong>in</strong>g the waves generated around the swimmer<br />

could not be seen <strong>in</strong> this record<strong>in</strong>g. In order to compensate for this<br />

defect, a view from above the swimmer was recorded, to consider wave<br />

resistance.<br />

It is still difficult to observe detailed movement, such as twist<strong>in</strong>g<br />

arms underwater. In order to observe these detailed motions of the<br />

forearm <strong>in</strong> swimm<strong>in</strong>g, Ohgi (2006) captured 3D accelerations <strong>and</strong> 3D<br />

angular velocities by a data logger <strong>and</strong> analyzed change <strong>in</strong> movement<br />

caused by fatigue. However, no actual motion images were used <strong>in</strong> analyz<strong>in</strong>g<br />

their data.<br />

In this study, a whole body swimm<strong>in</strong>g image <strong>in</strong>clud<strong>in</strong>g a view from<br />

above, was taken <strong>and</strong> also synchroniz<strong>in</strong>g the three-dimensional acceleration<br />

<strong>and</strong> the angular velocity data on the forearm <strong>and</strong> analyzed them<br />

to underst<strong>and</strong> subtle differences <strong>in</strong> S-shaped <strong>and</strong> I-shaped movements<br />

<strong>in</strong> free style. A chronological dom<strong>in</strong>ant frequency was obta<strong>in</strong>ed by us<strong>in</strong>g<br />

wavelet transformation <strong>in</strong> these obta<strong>in</strong>ed data.<br />

Methods<br />

The experiments were performed <strong>in</strong> a 50m x 25m <strong>in</strong>door swimm<strong>in</strong>g<br />

pool. The subject of the experiments was an elite breast stroke swimmer<br />

who had won a gold medal <strong>in</strong> 4 x 100m medley relay <strong>in</strong> Universiade<br />

Belgrade 2009. The observation equipment consisted of underwater <strong>and</strong><br />

overwater cameras <strong>in</strong> a frame <strong>in</strong>stalled on a cart placed on a metal pipe<br />

track. A crane tripod with a camera above the swimmer was <strong>in</strong>stalled on<br />

the same cart. The underwater <strong>and</strong> over water images were synthesized<br />

<strong>in</strong>to a whole body image by a video mixer. The image taken from above<br />

the swimmer was <strong>in</strong>serted <strong>in</strong>to the video mixer image us<strong>in</strong>g 4 image<br />

dividers.


y a video mixer. The image taken from above the swimmer was <strong>in</strong>serted<br />

mixer image us<strong>in</strong>g 4 image dividers.<br />

RESULTS <strong>and</strong> DISCUSSION<br />

Figure 3 shows the composite underwater <strong>and</strong> overwater image of the swimm<strong>in</strong>g<br />

motion obta<strong>in</strong>ed by the observation equipment. The picture appears as if the swimmer<br />

chaPter2.<strong>Biomechanics</strong><br />

had been observed <strong>in</strong> a water tank through a w<strong>in</strong>dow. Figure 3 also shows the threedimensional<br />

accelerations <strong>and</strong> the angular velocity obta<strong>in</strong>ed by the data logger attached<br />

on the forearm synchronized with the motion image. In the case of the breaststroke<br />

Fig. 1 Data logger of motion sensors<br />

Fig.1 Data logger of motion sensors<br />

Figure 1 shows a data logger of motion sensors which has 3<br />

accelerometer components, 3 gyroscopic components, a depth<br />

ws a data sensor logger <strong>and</strong> a of propeller motion system sensors speedometer which built-<strong>in</strong> has (PD3G3Gy 3 accelerometer components,<br />

components, made by a Leonard depth Little sensor company). <strong>and</strong> It has a a propeller cyl<strong>in</strong>drical shape system of speedometer built-<strong>in</strong><br />

diameter φ 23mm <strong>and</strong> length of 235mm <strong>and</strong> is composed of<br />

ade by Leonard a CPU, 256MB Little memory, company). <strong>and</strong> 8 A/D converter It has a components. cyl<strong>in</strong>drical shape of diameter φ<br />

ngth of 235mm The data logger <strong>and</strong> can is measure composed 8 hours cont<strong>in</strong>uously of a CPU, <strong>in</strong> 128Hz. 256MB memory, <strong>and</strong> 8 A/D<br />

The data logger was set on the backside of the left forearm on a<br />

mponents. three-dimensional The data coord<strong>in</strong>ate logger axis can as shown measure <strong>in</strong> Fig.2. 8 Data hours were cont<strong>in</strong>uously Fig.3-5,6,7 respectively. <strong>in</strong> 128Hz.<br />

sampled at 128Hzd, that is, almost 500000 datum <strong>in</strong> one hour.<br />

ger was set on the backside of the left forearm on a three-dimensional<br />

The three-dimensional acceleration <strong>and</strong> the angular velocity data<br />

is as shown taken <strong>in</strong> from Fig.2. the data Data logger were <strong>and</strong> correspond<strong>in</strong>g sampled to at swimm<strong>in</strong>g 128Hzd, that is, almost 500000<br />

movements, were extracted with Igor ProVer.6 of the Wavemet-<br />

e hour. The three-dimensional acceleration <strong>and</strong> the angular velocity data<br />

ric Co. Ltd. These wave data were synchronized with the swim-<br />

151<br />

e data logger <strong>Biomechanics</strong> m<strong>in</strong>g motion <strong>and</strong> images correspond<strong>in</strong>g <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> by Pixel Runner <strong>XI</strong> to of Tellus Chapter swimm<strong>in</strong>g Image 2 <strong>Biomechanics</strong><br />

Co. Ltd. movements, were extracted<br />

by match<strong>in</strong>g the motion image with the arm enter<strong>in</strong>g the water<br />

oVer.6 of <strong>and</strong> the the peak Wavemetric po<strong>in</strong>t of the data Co. waves. Ltd. These wave data style. were synchronized<br />

imm<strong>in</strong>g motion images by Pixel Runner of Tellus Image Co. Ltd. by<br />

Time A<br />

motion image with the arm enter<strong>in</strong>g the water <strong>and</strong> the peak po<strong>in</strong>t of the<br />

y direction<br />

[m/s 2 ]] 1. Arm Side Slide<br />

[m/s 2 ]] 2. Arm Extension<br />

[m/s 2 ]] 3. Arm Pull<br />

[m]] 4. Depth<br />

[deg/s] 5. Arm Pitch<br />

[deg/s] 6. Arm Roll<br />

[deg/s] 7. Arm Yaw<br />

152<br />

Fig.3 <strong>Biomechanics</strong> Chronological <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> 3D <strong>XI</strong> acceleration, Chapter 2 <strong>Biomechanics</strong> 3D gyro <strong>and</strong> depth data of arm<br />

stroke synchronized with whole body image of under <strong>and</strong> over water<br />

shown <strong>in</strong> Fig. 3, a sequence of open<strong>in</strong>g <strong>and</strong> clos<strong>in</strong>g motion of the arms appeared <strong>in</strong> Arm<br />

Slide <strong>in</strong> Fig. 3-1. Concern<strong>in</strong>g the acceleration of Arm Extension <strong>in</strong> Fig.3-2, two peaks<br />

were seen <strong>in</strong> each stroke, although the motion of the arm itself was carried out<br />

smoothly. S<strong>in</strong>ce the accelerometer has also gathered gravitational acceleration, the<br />

Extension negative peak <strong>in</strong> was Fig.3-2, obta<strong>in</strong>ed two when peaks the arm were was seen mov<strong>in</strong>g <strong>in</strong> each downward. stroke, The although effect of the<br />

motion gravitational of the acceleration arm itself was was seen as carried well <strong>in</strong> out the acceleration smoothly. of S<strong>in</strong>ce Arm Pull the <strong>in</strong> accelerom-<br />

Fig.3-3.<br />

The complex 3 component angular velocity of arm Pitch, Roll, <strong>and</strong> Yaw is shown <strong>in</strong><br />

eter has also gathered gravitational acceleration, the negative peak was<br />

In order to underst<strong>and</strong> these data better, synchroniz<strong>in</strong>g this motion image <strong>and</strong> the<br />

obta<strong>in</strong>ed when the arm was mov<strong>in</strong>g downward. The effect of gravita-<br />

data waves was a very effective mean to grasp the differences <strong>in</strong> details of an <strong>in</strong>dividual<br />

tional swimmer's acceleration strokes even was <strong>in</strong> the seen same swimm<strong>in</strong>g as well <strong>in</strong> style. the acceleration of Arm Pull <strong>in</strong><br />

The graph at the top of Fig. 4 shows the transition of flexion/extension motion of<br />

Fig.3-3. the forearm The described complex with 3 angular component velocity. angular The graph velocity <strong>in</strong> the middle of arm <strong>in</strong>dicates Pitch, the Roll,<br />

<strong>and</strong> wavelet Yaw transformation is shown <strong>in</strong> for Fig.3-5,6,7 the same data respectively.<br />

<strong>and</strong> the graph at the bottom shows the<br />

transition of depth. Each of them was acquired with the sensor attached on the forearm<br />

In <strong>in</strong> order the freestyle to underst<strong>and</strong> stroke. Compar<strong>in</strong>g these the data graphs better, at the synchroniz<strong>in</strong>g top <strong>and</strong> the bottom, this the motion angular image<br />

velocity <strong>and</strong> the <strong>in</strong> the data stroke waves phase was is a almost very constant, effective while mean that to <strong>in</strong> grasp the recovery the differences phase<br />

decreased rapidly. The Fourier transformation converts a spectrum space of a certa<strong>in</strong><br />

<strong>in</strong> period details <strong>in</strong>to of a frequency an <strong>in</strong>dividual space. On swimmer’s the other h<strong>and</strong>, strokes the wavelet even transformation <strong>in</strong> the same is swimm<strong>in</strong>g<br />

the time<br />

series data of the momentary frequency conversion <strong>in</strong> the same time space. In other<br />

recovery phase<br />

acceleration:<br />

Arm extention<br />

i i ll x direction<br />

acceleration:<br />

SliceSectionC\<br />

Arm side slide<br />

stroke/pull phase<br />

i i<br />

z direction<br />

Fig. 4. Gyro sensor data of x-direction, wavelet transform for the<br />

acceleration:<br />

Arm pull<br />

i i<br />

Fig. 2 Def<strong>in</strong>ition of 3-coomponents on data logger<br />

Fig.2 Def<strong>in</strong>ition of 3-components on data logger<br />

Regard<strong>in</strong>g the logger signal process<strong>in</strong>g, the wavelet transformation was<br />

analyzed by us<strong>in</strong>g free macro software of Ethographer (Sakamoto et al.,<br />

same wave <strong>and</strong> transition of depth acquired with the sensor attached<br />

on the forearm <strong>in</strong> the freestyle stroke.<br />

2009) on Igor Pro. Wavelet transformation is one of the techniques of<br />

Regard<strong>in</strong>g the chronological the frequency logger signal analysis. The process<strong>in</strong>g, Morlet function the of wavelet 15 cycles<br />

<strong>Biomechanics</strong> Fig. 5(a) <strong>and</strong> Section <strong>Medic<strong>in</strong>e</strong> of TimeA <strong>XI</strong> Fig. 5(b) Chapter Section of 2 Time <strong>Biomechanics</strong><br />

B<br />

transformation Figs. 5. was Time sliced analyzed section data by of wavelet transform output, Fig.4 at<br />

us<strong>in</strong>g was employed free macro as the software mother wavelet of Ethographer <strong>in</strong> this study. A (Sakamoto key advantage<br />

time A <strong>and</strong> B shown <strong>in</strong> Fig.4. The sliced section shows momentary<br />

et al., 2009) cycle on (=1/frequency) Igor Pro. analysis. Wavelet<br />

over Fourier transformation is temporal resolution. In addition, wavelet<br />

transformation is one of the techniques of the chronological frequency analysis. The<br />

transformation captures both frequency <strong>and</strong> location <strong>in</strong>formation.<br />

Morlet function of 15 cycles was employed as the mother wavelet <strong>in</strong> this study. A key<br />

advantage results <strong>and</strong> over dIscussIon Fourier transformation is temporal resolution. In addition, wavelet<br />

transformation Figure 3 shows the captures composite both underwater frequency <strong>and</strong> overwater <strong>and</strong> location image of the <strong>in</strong>formation.<br />

swimm<strong>in</strong>g motion obta<strong>in</strong>ed by the observation equipment. The picture<br />

RESULTS appears as if the <strong>and</strong> swimmer DISCUSSION had been observed <strong>in</strong> a water tank through<br />

a w<strong>in</strong>dow. Figure 3 also shows the three-dimensional accelerations <strong>and</strong><br />

Figure 3 shows the composite underwater <strong>and</strong> overwater image of the swimm<strong>in</strong>g<br />

the angular velocity obta<strong>in</strong>ed by the data logger attached on the forearm<br />

motion synchronized obta<strong>in</strong>ed with the by motion the observation image. In the case equipment. of the breaststroke The picture appears as if the swimmer<br />

had shown been <strong>in</strong> Fig. observed 3, a sequence <strong>in</strong> of a open<strong>in</strong>g water <strong>and</strong> tank clos<strong>in</strong>g through motion a of w<strong>in</strong>dow. the arms Figure 3 also shows the threedimensional<br />

appeared <strong>in</strong> Arm accelerations Slide <strong>in</strong> Fig. 3-1. <strong>and</strong> Concern<strong>in</strong>g the angular the acceleration velocity of Arm obta<strong>in</strong>ed by the data logger attached<br />

on the forearm synchronized with the motion image. In the Fig. case 6. Cycle of the sliced breaststroke section data of wavelet transform output, Fig.4<br />

at sliced section, Cycle 2.2 sec. This is a stroke cycle of freestroke<br />

<strong>in</strong> this case. The bottom peak shows the turn phase.<br />

103<br />

Time B


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The graph at the top of Fig. 4 shows the transition of flexion/<br />

extension motion of the forearm described with angular velocity.<br />

The graph <strong>in</strong> the middle <strong>in</strong>dicates the wavelet transformation<br />

for the same data <strong>and</strong> the graph at the bottom shows the transition<br />

of depth. Each of them was acquired with the sensor attached on the<br />

forearm <strong>in</strong> the freestyle stroke. Compar<strong>in</strong>g the graphs at the top <strong>and</strong><br />

the bottom, the angular velocity <strong>in</strong> the stroke phase is almost constant,<br />

while that <strong>in</strong> the recovery phase decreased rapidly. The Fourier transformation<br />

converts a spectrum space of a certa<strong>in</strong> period <strong>in</strong>to a frequency<br />

space. On the other h<strong>and</strong>, the wavelet transformation is the time series<br />

data <strong>Biomechanics</strong> of the momentary <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> frequency <strong>XI</strong> Chapter conversion 2 <strong>Biomechanics</strong> <strong>in</strong> the same time space. In<br />

other words the Fourier transformation is less useful <strong>in</strong> analyz<strong>in</strong>g nonstationary<br />

data, where there is no repetition with<strong>in</strong> the region sampled.<br />

The wavelet transformation allows the components of a non-stationary<br />

signal to be analyzed better. In the middle of Fig. 4, the thick striped<br />

pattern appears <strong>in</strong> the dom<strong>in</strong>ant cycle for about 2 seconds of the respective<br />

movements. The output of wavelet transformation can be sliced <strong>in</strong><br />

x <strong>and</strong> y directions. Figure 5(a) <strong>and</strong> 5(b) are the sections of Fig. 4 at<br />

Time A <strong>and</strong> B respectively. These sliced sections show momentary cycle<br />

(=1/frequency) analyses. In these figures, the primary peak <strong>in</strong>dicates the<br />

stroke Fig. cycle. 6. Cycle The sliced secondary section data peak of wavelet appears transform <strong>in</strong> the cycle output, of Fig.4 S-shaped stroke.<br />

Figure at sliced 6 shows section, cycle Cycle sliced 2.2 sec. section This is data a stroke of cycle wavelet of freestroke transformation out-<br />

<strong>in</strong> this case. The bottom peak shows the turn phase.<br />

put at Slice Section C <strong>in</strong> Fig. 4 <strong>in</strong> Cycle 2.2 sec. This is a stroke cycle of<br />

freestyle <strong>in</strong> this case. The bottom peak shows the turn phase.<br />

words the Fourier transformation is less useful <strong>in</strong> analyz<strong>in</strong>g non-stationary data, where<br />

there Thus, is no the repetition wavelet with<strong>in</strong> transformation the region sampled. converts The wavelet motion transformation waves allows to pat- the<br />

tern components designs. of Three a non-stationary acceleration signal waves to be analyzed <strong>and</strong> three better. angular In the middle velocity of Fig. waves 4, the<br />

thick striped pattern appears <strong>in</strong> the dom<strong>in</strong>ant cycle for about 2 seconds of the respective<br />

acquired with a motion logger <strong>in</strong>dicate six motion patterns. The four<br />

movements. The output of wavelet transformation can be sliced <strong>in</strong> x <strong>and</strong> y directions.<br />

swimm<strong>in</strong>g Figure 5(a) styles <strong>and</strong> 5(b) freestyle, are the sections breaststroke, of Fig. 4 backstroke at Time A <strong>and</strong> <strong>and</strong> B respectively. butterfly stroke, These<br />

consist sliced sections of 24 pattern show momentary pictures. cycle The (=1/frequency) difference of analyses. picture In patterns these figures, should the<br />

primary peak <strong>in</strong>dicates the stroke cycle. The secondary peak appears <strong>in</strong> the cycle of S-<br />

lead shaped to another stroke. Figure motion 6 shows analysis cycle with sliced wavelet section transform. data of wavelet Figure transformation 7 shows<br />

output the at transition Slice Section of C flexion/extention <strong>in</strong> Fig. 4 <strong>in</strong> Cycle 2.2 motion sec. This of is a the stroke forearm cycle of described freestyle <strong>in</strong><br />

this case. The bottom peak shows the turn phase.<br />

with angular Thus, the wavelet velocity, transformation the wavelet converts transform motion for waves the to same pattern data designs. <strong>and</strong> Three the<br />

transition acceleration of waves depth <strong>and</strong> <strong>in</strong> three the butterfly angular velocity stroke. waves Two acquired stripe patterns with a motion appear logger <strong>in</strong><br />

<strong>in</strong>dicate six motion patterns. The four swimm<strong>in</strong>g styles freestyle, breaststroke,<br />

the backstroke wavelet <strong>and</strong> transform butterfly stroke, picture. consist Each of 24 stripe pattern shows pictures. the The basic difference stroke of picture cycle<br />

<strong>and</strong> patterns the cycle should of lead a keyhole to another shaped motion analysis stroke with <strong>in</strong> the wavelet butterfly transform. stroke. Figure 7 shows<br />

104<br />

Fig. 7 Gyro sensor data of x-direction, wavelet transform for the same wave <strong>and</strong><br />

transition of depth acquired <strong>in</strong> the butterfly stroke.<br />

conclusIons<br />

The motion film<strong>in</strong>g equipment was developed to show the whole<br />

body, <strong>in</strong> a synthesized swimm<strong>in</strong>g image of the underwater <strong>and</strong><br />

overwater motion. Furthermore, this synthesized swimm<strong>in</strong>g image<br />

was synchronized with the data obta<strong>in</strong>ed with the data logger<br />

which samples the 3D acceleration <strong>and</strong> 3D angular velocity<br />

of the forearm movement.<br />

Wavelet transformation was performed on the motion data <strong>and</strong> the<br />

various motions were visualized as a new motion analysis method. As<br />

implied by the wavelet transformation, it should be possible to express<br />

the difference <strong>in</strong> the strokes even <strong>in</strong> the same event or to express a collapse<br />

of technique by fatigue by show<strong>in</strong>g the motion as picture patterns.<br />

153<br />

reFerences<br />

Barbosa, T.M., Lima, F., Portela, A., Novais, D., Machado, L., Colaço,<br />

P., Gonçalves, P., Fern<strong>and</strong>es, R.J., Kesk<strong>in</strong>en, K.L. & Vilas-Boas. J.P.<br />

(2006) Relationships between energy cost, swimm<strong>in</strong>g velocity <strong>and</strong><br />

speed fluctuation <strong>in</strong> competitive swimm<strong>in</strong>g strokes. In: <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X. Eds: Vilas-Boas, J.P., Alves, F. <strong>and</strong><br />

Marques, A. Portuguese Journal of Sport Sciences 6 (Supl 2), 192-194.<br />

Ito, S. (2003), Swimm<strong>in</strong>g form analysis of competitive free style,Proc.<br />

Annual Meet<strong>in</strong>g, Japan Society of Mechanical Eng<strong>in</strong>eers, 03-1, 65-<br />

66.<br />

Ohgi, Y. (2006), Pattern match<strong>in</strong>g application for the swimm<strong>in</strong>g stroke<br />

recognition, <strong>Biomechanics</strong> of <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X, J.P.Vilas-<br />

Boas, F. Alves, A. Marques, eds., Proc. of Xth International Symposium<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, 69-70.<br />

Sakamoto, K.Q., Sato, K., Ishizuka, M., Watanuki, Y., Takahashi, A.,<br />

Daunt, F. & Wanless, S. (2009). Can Ethograms Be Automatically<br />

Generated Us<strong>in</strong>g Body Acceleration Data from Free-Rang<strong>in</strong>g Birds?<br />

PLoS ONE 4(4), e5379.


A Full Body Computational Fluid Dynamic Analysis of<br />

the Freestyle Stroke of a Previous Spr<strong>in</strong>t Freestyle<br />

World Record Holder<br />

Keys, M. 1 ; lyttle, A. 2 ; Blanksby, B.A. 1 & cheng, l. 1<br />

1 The University of Western Australia, Australia<br />

2 Western Australian Institute of Sport, Australia<br />

Computational Fluid Dynamics (CFD) allows simulation of complex<br />

fluid flow regimes <strong>and</strong> geometry. A case-study exam<strong>in</strong>ed propulsive <strong>and</strong><br />

drag forces experienced across the body dur<strong>in</strong>g full-body freestyle swimm<strong>in</strong>g<br />

us<strong>in</strong>g CFD. An elite male swimmer was scanned us<strong>in</strong>g a whole<br />

body 3D scanner <strong>and</strong> manual digitis<strong>in</strong>g provided the 3D freestyle k<strong>in</strong>ematics<br />

to animate the model. A F<strong>in</strong>ite Volume Method of CFD modell<strong>in</strong>g<br />

was used which <strong>in</strong>corporated a realisable K-ε turbulence model. The<br />

CFD analysis enabled an exam<strong>in</strong>ation of the forces distributed across<br />

the body throughout the full freestyle stroke. This project <strong>in</strong>creases the<br />

level of foundational knowledge <strong>and</strong> presents practical po<strong>in</strong>ts that may<br />

improve swimm<strong>in</strong>g performance.<br />

Key words: computational Fluid dynamics; Freestyle; drag; Propulsion<br />

IntroductIon<br />

Typically, current techniques of elite swimmers are derived from a mix<br />

of natural genetics, feel for the water, knowledge of experienced coaches,<br />

<strong>and</strong> trial <strong>and</strong> error methods. Although this is considered to be effective,<br />

little is known of the hydrodynamic factors mak<strong>in</strong>g one technique faster<br />

than another.<br />

It is widely accepted that an <strong>in</strong>creased underst<strong>and</strong><strong>in</strong>g of fluid flow<br />

patterns <strong>in</strong> swimm<strong>in</strong>g should enhance performance. However, it is very<br />

difficult to quantify the relative effects of these flow patterns experimentally<br />

when swimm<strong>in</strong>g with, at best, only approximations of total body<br />

effects were be<strong>in</strong>g provided. To date, research has <strong>in</strong>corporated one or<br />

more of the follow<strong>in</strong>g methods to estimate the drag/propulsion effects<br />

<strong>and</strong> flow patterns:<br />

• Physical test<strong>in</strong>g us<strong>in</strong>g either force plates, drag l<strong>in</strong>es or tow<strong>in</strong>g<br />

devices.<br />

• Analysis <strong>and</strong> numerical modell<strong>in</strong>g of recorded flow l<strong>in</strong>es <strong>and</strong><br />

vortex patterns measured by <strong>in</strong>ject<strong>in</strong>g dye or Particle Image Velocimetry<br />

(PIV) methods, based on swimmers <strong>in</strong> a test pool or<br />

swimm<strong>in</strong>g flume.<br />

• Entirely numerical modell<strong>in</strong>g which use estimations of drag <strong>and</strong><br />

<strong>in</strong>ertia effects on shapes similar to those of human limbs.<br />

Each method provided valuable <strong>in</strong>formation <strong>and</strong> some empirical data<br />

concern<strong>in</strong>g a few of the questions raised. However, <strong>in</strong>herent limitations<br />

exist <strong>and</strong> fluid flows around an irregularly shaped human form that is<br />

always chang<strong>in</strong>g <strong>in</strong> shape <strong>and</strong> position, are highly complex. Hence, none<br />

of these techniques can provide a full underst<strong>and</strong><strong>in</strong>g of what is actually<br />

occurr<strong>in</strong>g throughout a full swimm<strong>in</strong>g stroke cycle.<br />

Computational Fluid Dynamics (CFD) can be used to model <strong>and</strong><br />

solve complex problems of fluid flow <strong>and</strong> is ideally suited to analys<strong>in</strong>g<br />

drag <strong>and</strong> propulsion across the body when swimm<strong>in</strong>g. Based on fundamental<br />

fluid mechanics pr<strong>in</strong>ciples, CFD allows complex fluid flow<br />

regimes <strong>and</strong> geometry to be simulated, provid<strong>in</strong>g visualization of the<br />

result<strong>in</strong>g variables across the entire solution doma<strong>in</strong>. This can provide<br />

<strong>in</strong>sights <strong>in</strong>to problems thus far unobta<strong>in</strong>able via known physical test<strong>in</strong>g<br />

techniques. To date, CFD predictions of forces act<strong>in</strong>g on a swimmer<br />

have been limited to passive drag studies (Bixler et al., 2007), h<strong>and</strong> motion<br />

through the water (Bixler & Riewald, 2001; Sato & H<strong>in</strong>o, 2002)<br />

<strong>and</strong> underwater kick<strong>in</strong>g (Lyttle et al., 2006; Von Loebbecke et al., 2009).<br />

The current study was the culm<strong>in</strong>ation of several years spent devel-<br />

chaPter2.<strong>Biomechanics</strong><br />

op<strong>in</strong>g a full body strok<strong>in</strong>g CFD model. The objective was to exam<strong>in</strong>e the<br />

distribution of forces across the human body for an elite spr<strong>in</strong>t freestyler.<br />

A better underst<strong>and</strong><strong>in</strong>g of the <strong>in</strong>teraction of propulsive <strong>and</strong> drag forces<br />

across the body will <strong>in</strong>crease the foundational knowledge of swimm<strong>in</strong>g<br />

hydrodynamics.<br />

Methods<br />

A CFD case-study exam<strong>in</strong>ed the propulsion <strong>and</strong> drag forces across the<br />

body dur<strong>in</strong>g a full freestyle swimm<strong>in</strong>g stroke. At the time of the k<strong>in</strong>ematic<br />

record<strong>in</strong>gs, the swimmer used held both the 50m <strong>and</strong> 100m<br />

freestyle World Records. Therefore the technique exam<strong>in</strong>ed was highly<br />

evolved.<br />

The 3D k<strong>in</strong>ematics recorded one full stroke cycle with a separate<br />

above- <strong>and</strong> below-water camera used on each side of the swimmer.<br />

Each camera was po<strong>in</strong>ted at 45-60° to the horizontal plane. The swimmer<br />

performed regular freestyle at race pace <strong>and</strong> a full 3D k<strong>in</strong>ematic<br />

analysis was performed us<strong>in</strong>g manual video digitiz<strong>in</strong>g. Medial <strong>and</strong> lateral<br />

body l<strong>and</strong>marks, rather than jo<strong>in</strong>t centres, were digitized for each<br />

body segment to allow for calculat<strong>in</strong>g full segment rotations. Cartesian<br />

coord<strong>in</strong>ates for the derived jo<strong>in</strong>t centres were then converted to a polar<br />

coord<strong>in</strong>ate system.<br />

A full 3D surface scan of the swimmer provided accurate 3D geometry<br />

for the CFD simulations. The laser scann<strong>in</strong>g of the swimmer was<br />

performed us<strong>in</strong>g a Cyberware WBX whole body laser scanner, with a<br />

density of one po<strong>in</strong>t every 4mm. Higher resolution scans were also conducted<br />

of the h<strong>and</strong>s, head <strong>and</strong> feet (density of one po<strong>in</strong>t every 0.67mm).<br />

The higher resolutions acknowledged the importance of these areas <strong>in</strong><br />

sett<strong>in</strong>g the <strong>in</strong>itial flow conditions <strong>and</strong> <strong>in</strong> develop<strong>in</strong>g thrust. The higher<br />

resolution scans were then aligned <strong>and</strong> merged seamlessly <strong>in</strong>to the full<br />

body scan to provide more accuracy at these locations (see Figure 1).<br />

The 3D model was then processed to extract 288 non-uniform rational<br />

b-spl<strong>in</strong>es (NURBS), curved surfaces form<strong>in</strong>g a 3D solid model of the<br />

swimmers.<br />

The computer simulation was performed us<strong>in</strong>g the CFD software<br />

package “FLUENT” (version 6.3.26; Fluent Inc., Lebanon, NH) which<br />

utilizes the F<strong>in</strong>ite Volume Method of CFD modell<strong>in</strong>g. A realizable K-ε<br />

turbulence model, together with a multi-phase fluid doma<strong>in</strong>, was used<br />

with st<strong>and</strong>ard wall functions to simulate the boundary layer. This was<br />

comb<strong>in</strong>ed with the use of prism cells near the wall boundaries <strong>and</strong> tetrahedral<br />

cells <strong>in</strong> the ma<strong>in</strong> fluid doma<strong>in</strong>. The doma<strong>in</strong> surfaces conta<strong>in</strong>ed<br />

vary<strong>in</strong>g mesh densities to def<strong>in</strong>e the detail around highly curved areas<br />

while still ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g a workable mesh size. The surface mesh on the<br />

swimmer comprised approximately 100000 triangular surface elements<br />

with the total simulation consist<strong>in</strong>g of close to 5 million cells (see Figure<br />

1 for sample triangulated mesh<strong>in</strong>g surround<strong>in</strong>g the h<strong>and</strong>).<br />

Figure 1. 3D laser scanned image of the subject (top) <strong>and</strong> sample triangulated<br />

mesh surround<strong>in</strong>g the h<strong>and</strong> (bottom).<br />

105


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

Results below detail the forces on <strong>in</strong>dividual body segments throughout<br />

the full freestyle stroke. For a summary of momentum changes of the<br />

rigid (body segments) <strong>and</strong> flexible (jo<strong>in</strong>ts) body parts, see Table 1. The<br />

full freestyle stroke was analysed over a cycle time of 1.04s. Momentum<br />

values were reported as a means of compar<strong>in</strong>g between different<br />

cycle times <strong>and</strong> relative body weights. These momentum changes were<br />

then averaged to a per-second value to enable comparison with previous<br />

studies. Figure 2 displays the resultant forces over the entire body<br />

throughout the stroke cycle, <strong>and</strong> Table 2 outl<strong>in</strong>es the temporal po<strong>in</strong>ts<br />

associated with critical events <strong>in</strong> the stroke cycle. The swimmer’s velocity<br />

was between 1.9m.s -1 <strong>and</strong> 2.3m.s -1 , with the average over this cycle<br />

be<strong>in</strong>g 2.08m.s -1 .<br />

Table 1. The momentum (Ns) changes per second <strong>in</strong> the swimmer from<br />

the full freestyle stroke simulation over one full stroke cycle.<br />

Left Side Right Side Total<br />

Total per cycle 31.23<br />

Total * 30.03<br />

H<strong>and</strong> * 12.21 11.59 23.80<br />

Wrist * 4.65 6.47 11.12<br />

Forearm * 3.89 6.03 9.92<br />

Elbow * 2.35 4.21 6.56<br />

Upper Arm * -0.50 0.27 -0.23<br />

Shoulder * -9.17 -8.02 -17.20<br />

Head * -10.18<br />

Neck * -0.37<br />

Upper Trunk * -37.94<br />

Mid Trunk * -24.74<br />

Pelvis * 3.18<br />

Hips * -4.55 -2.85 -7.41<br />

Thighs * 9.46 8.82 18.28<br />

Knees * 4.18 5.23 9.41<br />

Lower Leg * 14.81 12.57 27.39<br />

Ankles * 0.38 -2.29 -1.91<br />

Feet * 10.67 9.67 20.34<br />

Comb<strong>in</strong>ed Arms * 13.44 20.54 33.98<br />

Comb<strong>in</strong>ed Legs * 34.95 31.16 66.10<br />

Trunk <strong>and</strong> Head * -70.05<br />

* per second<br />

Force (N)<br />

106<br />

500<br />

400<br />

300<br />

200<br />

100<br />

-100<br />

-200<br />

Overall Propulsion/Drag on Freestlye Swimmer<br />

0<br />

0.13 0.33 0.53 0.73 0.93 1.13<br />

Time (sec)<br />

Figure 2. Overall propulsion/drag throughout a full stroke cycle (negative<br />

values <strong>in</strong>dicate net drag force)<br />

Table 2. Critical temporal po<strong>in</strong>ts through the total measured freestyle<br />

stroke cycle.<br />

Time (s) Description<br />

0.19<br />

Left foot reaches top as right foot reaches bottom of<br />

sweep<br />

0.20 Right h<strong>and</strong> exits the water<br />

0.37<br />

Left foot reaches bottom as right foot reaches top of<br />

sweep<br />

0.44 Left h<strong>and</strong> reaches the deepest po<strong>in</strong>t<br />

0.56<br />

Left foot reaches top as right foot reaches bottom of<br />

sweep<br />

0.58 Right h<strong>and</strong> enters the water<br />

0.64 Left forearm at closest po<strong>in</strong>t to vertical<br />

0.70 Left h<strong>and</strong> exits the water<br />

0.73<br />

Left foot reaches bottom as right foot reaches top of<br />

sweep<br />

0.90<br />

Left foot reaches top as right foot reaches bottom of<br />

sweep<br />

0.98 Right h<strong>and</strong> at deepest po<strong>in</strong>t<br />

1.04 Right forearm at closest po<strong>in</strong>t to vertical<br />

1.06<br />

Left foot reaches bottom as right foot reaches top of<br />

sweep<br />

1.08 Left h<strong>and</strong> enters the water<br />

dIscussIon<br />

The race analysis of the swimmer used <strong>in</strong> this study from his 50m Freestyle<br />

f<strong>in</strong>al at the 2008 Australian Olympic Trials (f<strong>in</strong>al time - 21.28sec)<br />

revealed that the free swimm<strong>in</strong>g component made up over 87% of total<br />

race time. Thus, major benefits will accrue if this swimmer can improve<br />

technique dur<strong>in</strong>g the strok<strong>in</strong>g phases. To date, no studies have successfully<br />

exam<strong>in</strong>ed propulsive <strong>and</strong> drag forces across the total body while<br />

swimm<strong>in</strong>g. This <strong>in</strong>formation is crucial <strong>in</strong> order to optimise swimm<strong>in</strong>g<br />

technique.<br />

Exam<strong>in</strong><strong>in</strong>g the breakdown of force distributions revealed that the<br />

arms <strong>and</strong> legs create significant amounts of propulsion, with the trunk<br />

contribut<strong>in</strong>g the majority of the drag. The h<strong>and</strong>s provided a total propulsive<br />

momentum of 23.8Ns; while the comb<strong>in</strong>ed contributions of the<br />

wrist, forearm <strong>and</strong> elbow were 27.6Ns. This highlights that the forearm<br />

position dur<strong>in</strong>g the underwater arm stroke was as critical as that of the<br />

h<strong>and</strong>s. The head contributed less drag than the upper <strong>and</strong> lower trunk<br />

components. That could be because it is occasionally positioned <strong>in</strong> only<br />

a semi-submerged state, <strong>and</strong> that the lesser volume <strong>in</strong>fluences the potential<br />

amount of wave drag experienced. The thighs, knees <strong>and</strong> lower legs<br />

also contributed greater percentages of propulsion than the feet. This<br />

also re<strong>in</strong>forces the importance of entire leg movements <strong>and</strong> position<strong>in</strong>g,<br />

rather than just focus<strong>in</strong>g on the feet position<strong>in</strong>g. However, this may be<br />

due to the feet com<strong>in</strong>g out of the water regularly, <strong>and</strong> the possibility of<br />

wave assistance.<br />

The overall changes <strong>in</strong> forces throughout the stroke were characterized<br />

by six clear cycles, conta<strong>in</strong><strong>in</strong>g four small peaks <strong>and</strong> two large peaks.<br />

These peaks represent the six beat kick pattern that was adopted. The<br />

two large peaks correlated with the peak propulsion of the left <strong>and</strong> right<br />

arm strokes; <strong>and</strong> occurred simultaneously with two of the kick cycles.<br />

These peaks, particularly those associated with the arm stroke propulsion,<br />

were reflected by <strong>in</strong>creases <strong>in</strong> the swimmer’s <strong>in</strong>stantaneous velocity.<br />

The two highest velocity peaks occurred just after the peak propulsive<br />

forces, namely at 0.64s <strong>and</strong> 1.14s, when the swimmer’s velocity surged<br />

to 2.3m.s -1 .<br />

The <strong>in</strong>itial review of the <strong>in</strong>dividual arm force profiles confirmed the<br />

observations detailed <strong>in</strong> the overall drag <strong>and</strong> propulsion review. There


was a def<strong>in</strong>ite peak associated with the left <strong>and</strong> right arms as they moved<br />

through the cycle. The left arm peak occurred at 0.55s <strong>and</strong> the right at<br />

1.07s. There was a secondary, lower peak that occurred prior to these, at<br />

0.33s for the left, <strong>and</strong> 0.89s for the right arms.<br />

The first phase was with the arm out <strong>in</strong> front of the head <strong>and</strong> appeared<br />

to create an equal amount of drag for both arms of around -34N<br />

to -38N; <strong>and</strong> lasted for between 0.09 <strong>and</strong> 0.11s. This is due to the drag<br />

result<strong>in</strong>g from plac<strong>in</strong>g the arm <strong>in</strong>to a zone of high mov<strong>in</strong>g water. The<br />

h<strong>and</strong> was seen as the first po<strong>in</strong>t to start accelerat<strong>in</strong>g out of this extended<br />

position when it beg<strong>in</strong>s to move at around 0.18s. This is followed by the<br />

<strong>in</strong>itial acceleration phase where the swimmer pushes out laterally from<br />

the body <strong>and</strong> rapidly accelerates the h<strong>and</strong>s <strong>and</strong> forearms; with a peak<br />

force <strong>in</strong> this phase of between 50N <strong>and</strong> 100N. The force is governed <strong>in</strong>itially<br />

by accelerat<strong>in</strong>g the forearm <strong>and</strong> h<strong>and</strong>, <strong>and</strong> then slowly transitions<br />

towards be<strong>in</strong>g more velocity based. The right h<strong>and</strong> had a 15% greater acceleration<br />

<strong>and</strong> velocity <strong>in</strong> this phase, which partially expla<strong>in</strong>s the slightly<br />

greater forces generated at this time.<br />

The third phase appears to be a transition from the swimmer push<strong>in</strong>g<br />

outwards by us<strong>in</strong>g mostly lateral muscles, <strong>and</strong> then beg<strong>in</strong>s to pull<br />

<strong>in</strong>wards towards the midl<strong>in</strong>e of the body. The simulation showed considerable<br />

deceleration by the forearm <strong>and</strong> h<strong>and</strong>s at this po<strong>in</strong>t, <strong>and</strong> was<br />

probably the reason for the decreased propulsion. Results <strong>in</strong>dicated that<br />

keep<strong>in</strong>g this section of the pull-through at high acceleration <strong>and</strong> high<br />

velocity would help improve the overall stroke technique.<br />

The fourth phase was the ma<strong>in</strong> power pull<strong>in</strong>g section of the stroke,<br />

<strong>and</strong> achieved peak propulsive forces between 260N <strong>and</strong> 340N. It should<br />

be noted that this peak force does not occur at either the peak acceleration<br />

or velocity, of the h<strong>and</strong> or forearm. It also appears to occur just after<br />

the swimmer exposes the best angle of the h<strong>and</strong> <strong>and</strong> forearm at 90º to<br />

the direction of travel (see Figure 3). The swimmer’s peak <strong>in</strong>stantaneous<br />

velocity occurr<strong>in</strong>g just after this po<strong>in</strong>t substantiates that this force is a<br />

true peak.<br />

The fifth phase is the section where the arm exits the water <strong>and</strong><br />

is almost a po<strong>in</strong>t where drag is suddenly created. This could result from<br />

the arm decelerat<strong>in</strong>g as it approaches the end of the stroke, or, also may<br />

be due to some of the wave formation effects. The sixth phase is the<br />

recovery where each arm, <strong>in</strong> turn, is out of the water.<br />

Figure 3. Pressure graph depict<strong>in</strong>g position of the peak net force dur<strong>in</strong>g<br />

the stroke.<br />

conclusIon<br />

The current study provided <strong>in</strong>sight <strong>in</strong>to how propulsion <strong>and</strong> drag forces<br />

are generated throughout a full freestyle swimm<strong>in</strong>g stroke through the<br />

use of CFD analysis. The resultant outcome of the analysis is both an<br />

<strong>in</strong>creased level of foundational knowledge related to the production of<br />

propulsion <strong>and</strong> drag forces, as well as the provision of practical po<strong>in</strong>ts<br />

that may be used to improve freestyle performance.<br />

reFerences<br />

Bixler, B. & Riewald, S. (2001). Analysis of a swimmer’s h<strong>and</strong> <strong>and</strong> arm<br />

<strong>in</strong> steady flow conditions us<strong>in</strong>g computational fluid dynamics. Journal<br />

of <strong>Biomechanics</strong>, 35,713-717.<br />

Bixler, B., Pearse, D. & Fairhurst, F. (2007). The accuracy of computational<br />

fluid dynamics analysis of the passive drag of a male swimmer.<br />

Sports <strong>Biomechanics</strong>, 6(1), 81-98.<br />

chaPter2.<strong>Biomechanics</strong><br />

Loebbecke, A., Von Mittal, R., Mark, R. & Hahn, J. (2009). A computational<br />

method for analysis of underwater dolph<strong>in</strong> kick hydrodynamics<br />

<strong>in</strong> human swimm<strong>in</strong>g. Sports <strong>Biomechanics</strong>, 8(1),60-77.<br />

Lyttle, A., & Keys, M. (2006) The application of computational fluid dynamics<br />

for technique prescription <strong>in</strong> underwater kick<strong>in</strong>g. Portuguese<br />

Journal of Sport Sciences, 6(Suppl. 2), 233-35.<br />

Sato, Y. & H<strong>in</strong>o, T. (2002). Estimation of Thrust of Swimmer’s H<strong>and</strong><br />

Us<strong>in</strong>g CFD. Presented at 8th Symposium of Nonl<strong>in</strong>ear <strong>and</strong> Free-Surface<br />

Flows, Hiroshima, pp. 71-75.<br />

107


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

An Analysis of an Underwater Turn for Butterfly <strong>and</strong><br />

Breaststroke<br />

Kishimoto, t. 1 ,takeda, t. 2 ,sugimoto, s. 3 , tsubakimoto, s. 2 <strong>and</strong><br />

takagi, h. 2<br />

1 Edogawa School for the Disabled, Tokyo, Japan<br />

2 University of Tsukuba, Ibaraki, Japan<br />

3 National Agency for the Advancement Sports <strong>and</strong> Health, Tokyo, Japan<br />

The purpose of this study was to analyze selected characteristics of the<br />

“Apnea Turn”, a new underwater turn <strong>and</strong> to compare this turn with<br />

the conventional “Open Turn”. The subjects were ten elite competitive<br />

butterflyers <strong>and</strong> breast strokers. The 5 m Round Trip Time (5 m-RTT)<br />

of the Apnea turn was faster than the Open turn (5.55±0.27 s <strong>and</strong><br />

5.62±0.33 s). While the times of the <strong>in</strong>to turn phase <strong>and</strong> out of turn<br />

phase of 5 m-RTT for the Apnea turn were faster than the Open turn,<br />

the time of the pivot phase was significantly slower than the Open turn.<br />

The push off velocity of the Apnea turn was significantly higher than the<br />

Open turn (3.02±0.11 m·s -1 vs 2.92±0.06 m·s -1 ). These results suggest<br />

that the Apnea turn may improve swimm<strong>in</strong>g performance <strong>and</strong> may be a<br />

prospective new turn<strong>in</strong>g method.<br />

Key words: underwater turn, elite swimmers, round trip time, swimm<strong>in</strong>g<br />

performance<br />

IntroductIon<br />

The “Open Turn” (Maglischo 2003) is commonly used <strong>in</strong> competitive<br />

swimm<strong>in</strong>g with most swimmers turn<strong>in</strong>g near the surface to breathe after<br />

touch<strong>in</strong>g the wall with their h<strong>and</strong>s, especially <strong>in</strong> the butterfly <strong>and</strong><br />

breast stroke (Colw<strong>in</strong> 2002). However, it actually causes an <strong>in</strong>crease <strong>in</strong><br />

the wave resistance <strong>in</strong> the vic<strong>in</strong>ity of the water surface before <strong>and</strong> after<br />

push<strong>in</strong>g from the wall, <strong>and</strong> may decrease speed. Therefore, turn<strong>in</strong>g under<br />

water may enhance performance by reduc<strong>in</strong>g resistance.<br />

The present study exam<strong>in</strong>ed an “Apnea Turn” that is carried out with<br />

the whole body under water dur<strong>in</strong>g the pivot operation <strong>and</strong> push from<br />

the wall. This method may decrease the wave drag by pivot<strong>in</strong>g underwater.<br />

A verification of performance improvement was carried out to clarify<br />

the characteristics of the Apnea turn <strong>and</strong> to consider its possibility as a<br />

new turn<strong>in</strong>g method for competitive swimmers.<br />

Method<br />

The subjects were ten elite competitive swimmers whose specialties were<br />

butterfly <strong>and</strong> breast stroke. Their age, height <strong>and</strong> weight were 21.1±1.2<br />

years, 176.3±6.2 cm <strong>and</strong> 68.7±6.5 kg, respectively. Two trials were performed<br />

for both the Open turn <strong>and</strong> Apnea turn. The best attempts were<br />

analyzed. The subjects swam from 10 m <strong>in</strong>to the turn <strong>and</strong> 10 m after<br />

turn<strong>in</strong>g. The subjects were asked to exert the maximum performance.<br />

This study conformed to the competitive regulations, ie 1) touch<strong>in</strong>g both<br />

h<strong>and</strong>s to the wall, 2) rema<strong>in</strong><strong>in</strong>g always on the front. All participants<br />

provided an <strong>in</strong>formed consent <strong>and</strong> all procedures were approved by the<br />

<strong>in</strong>stitutional review board.<br />

Figure 1 shows the placement of the cameras. This study used two<br />

sets of underwater <strong>and</strong> over water simultaneous record<strong>in</strong>g video camera<br />

systems, <strong>and</strong> another underwater camera to record the subjects for analysis<br />

(60Hz). To obta<strong>in</strong> the 2D position coord<strong>in</strong>ates, we used the “Fram-<br />

DIAS version” <strong>and</strong> “AviUtil99” for two dimensional motion analysis.<br />

108<br />

y axis<br />

z axis<br />

Underwater camera put <strong>in</strong> 5m to<br />

the wall, <strong>and</strong> 10m to the side<br />

wall, 1.4m to the water surface.<br />

x axis<br />

2 on the water <strong>and</strong> underwater cameras put <strong>in</strong> the<br />

side wall, set position were 1.5m <strong>and</strong> 3.5m to the<br />

wall, 0.20m <strong>and</strong> -0.20m to the water surface.<br />

Figure 1 Camera placement for three dimensional analysis<br />

Figure 2 also shows the camera placement from above. The 5 m RTT<br />

was considered as the 1) total time from the 5 m po<strong>in</strong>t to touch<strong>in</strong>g the<br />

wall), 2) time of pivot phase (from touch<strong>in</strong>g the wall to push<strong>in</strong>g off the<br />

wall, 3) time from push<strong>in</strong>g off the wall to the 5 m po<strong>in</strong>t <strong>and</strong> also the<br />

calculated values of 4) the velocity of the turn-<strong>in</strong> phase (swimm<strong>in</strong>g velocity<br />

from the 5 m po<strong>in</strong>t to the 2.5 m po<strong>in</strong>t), 5) the velocity of approach<br />

phase (swimm<strong>in</strong>g velocity from the 2.5 m po<strong>in</strong>t to touch<strong>in</strong>g the wall), 6)<br />

the velocity of the glide phase (swimm<strong>in</strong>g velocity from the wall to the<br />

2.5 m po<strong>in</strong>t), <strong>and</strong> 7) the velocity of turn- out phase (swimm<strong>in</strong>g velocity<br />

from the 2.5 m po<strong>in</strong>t to the 5 m po<strong>in</strong>t).<br />

Figure 2 The design of turn<strong>in</strong>g phase <strong>in</strong> this study<br />

The def<strong>in</strong>ition of <strong>in</strong>dexes dur<strong>in</strong>g the push off phase <strong>in</strong> this study is<br />

shown <strong>in</strong> figure 3. We calculated 1) the “push off velocity”, the velocity<br />

of the swimmer’s center of gravity (CG) when the swimmer’s feet leave<br />

the wall.), 2) the vertical component of the “push off velocity”, 3) the<br />

horizontal component of the “push off velocity”, 4) the distance between<br />

the wall <strong>and</strong> the CG when the swimmer’s feet touch the wall <strong>and</strong> 5) the<br />

distance between the water surface <strong>and</strong> the CG when the swimmer’s<br />

feet touch the wall.<br />

Figure 3 Def<strong>in</strong>ition of push off the wall <strong>in</strong> this study<br />

The SPSS statistics process<strong>in</strong>g software (11.5J) were used for statistical<br />

analysis. The t-test was used to determ<strong>in</strong>e significant differences between<br />

the two trials, the pearson’s correlation analysis was performed to<br />

discuss relationships between <strong>in</strong>dexes. p


esults<br />

Table 1 shows a comparison between swimm<strong>in</strong>g velocities <strong>and</strong> the times<br />

of each phase. The average 5 m RTT was 5.62±0.33s for the Open turn,<br />

<strong>and</strong> 5.55±0.27s for the Apnea turn. There was no significant difference<br />

between the two turns but the 5 m RTT for the Apnea was shorter than<br />

for the Open turn for six of the 10 subjects. The mean times of the turn<strong>in</strong><br />

phase <strong>and</strong> turn-out for the Apnea turn was significantly shorter than<br />

the Open turn but the pivot phase for the Apnea turn was significantly<br />

longer than the Open turn (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Mechanical <strong>and</strong> Propulsive Efficiency of Swimmers<br />

<strong>in</strong> Different Zones of Energy Supply<br />

Kolmogorov, s.V. 1,2 , Vorontsov, A.r. 2 , rumyantseva, o.A. 1 ,<br />

Kocherg<strong>in</strong>, A.B. 2<br />

1 Pomor State University, Arkhangelsk, Russia<br />

2 All-Russian Swimm<strong>in</strong>g Federation, Moscow, Russia<br />

Dimensionless coefficients for mechanical <strong>and</strong> propulsive efficiency (e g ,<br />

e p ) have been studied us<strong>in</strong>g physiological <strong>and</strong> biomechanical methods <strong>in</strong><br />

swimm<strong>in</strong>g various strokes. The research has been conducted <strong>in</strong> the three<br />

zones of energy supply: below the threshold of anaerobic metabolism<br />

(AT), above the zone of maximal oxygen consumption (VO 2 max ) <strong>and</strong><br />

<strong>in</strong> the zone between AT <strong>and</strong> VO 2 max . The highest values of e g <strong>and</strong> e p for<br />

male <strong>and</strong> female swimmers have been revealed <strong>in</strong> the zone between AT<br />

<strong>and</strong> VO 2 max . In all the three zones of energy supply the values of e g are<br />

higher for male swimmers. At the same time the values of e p are equal<br />

for male <strong>and</strong> female swimmers.<br />

Key words: Metabolic <strong>and</strong> mechanical power, efficiency, velocity<br />

IntroductIon<br />

Development of efficient technologies to tra<strong>in</strong> swimmers assumes<br />

solv<strong>in</strong>g of an important theoretical <strong>and</strong> practical problem of <strong>in</strong>terdependence<br />

between energy supply, on the one h<strong>and</strong>, <strong>and</strong> swimm<strong>in</strong>g<br />

biomechanics, on the other one. In case of biological objects’ steady<br />

non-stationary motion <strong>in</strong> water, at the first stage metabolic energy is<br />

transformed with losses <strong>in</strong>to mechanical one, which at the second stage<br />

is transformed with additional losses <strong>in</strong>to useful activity result, i.e. <strong>in</strong>to<br />

swimm<strong>in</strong>g velocity. To describe precisely basic mechanisms of the phenomenon<br />

under study, this process of human swimm<strong>in</strong>g was formalised<br />

<strong>in</strong> form of mathematic model (Kolmogorov, 1997):<br />

v 0 =P ai × e g × e p /Fr �<br />

110<br />

f .d .�<br />

, (1)<br />

<strong>in</strong> which v 0 is mean swimm<strong>in</strong>g velocity at the competition or tra<strong>in</strong><strong>in</strong>g<br />

distance (m·s -1 ); P ai is power of active energetic metabolism (W);<br />

e g is dimensionless coefficient of mechanical efficiency, i.e. ratio of total<br />

external mechanical power (P to ) to P ai ; e p is dimensionless coefficient of<br />

propulsive efficiency, i.e. ratio of useful external mechanical power (P uo )<br />

to P to ; F r(f.d.) is frontal component of active drag force (N).<br />

Hence, the goal of this research has been to <strong>in</strong>vestigate experimentally<br />

regularities of metabolic energy transformation <strong>in</strong>to swimm<strong>in</strong>g<br />

velocity at different zones of energy supply on the basis of equation 1.<br />

Methods<br />

The research was conducted at the period of spr<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g mesocycle<br />

last<strong>in</strong>g from January to April. Twenty-n<strong>in</strong>e university swimmers (15<br />

female subjects aged from 17 to 22 <strong>and</strong> 14 male subjects aged from<br />

18 to 23) took part <strong>in</strong> the research. Correct study<strong>in</strong>g of regularities of<br />

metabolic energy transformation <strong>in</strong>to useful activity result is possible<br />

only <strong>in</strong> conditions when character <strong>and</strong> direction of tra<strong>in</strong><strong>in</strong>g load carried<br />

out by the subjects dur<strong>in</strong>g the tra<strong>in</strong><strong>in</strong>g mesocycle, are taken <strong>in</strong>to<br />

consideration. Therefore, the time of experimental <strong>in</strong>vestigation of this<br />

process <strong>in</strong> the three different zones of energy supply was coord<strong>in</strong>ated<br />

with certa<strong>in</strong> periods of purposeful technical <strong>and</strong> functional tra<strong>in</strong><strong>in</strong>g. It is<br />

this circumstance that expla<strong>in</strong>s the order of tests.<br />

In February the first test was conducted <strong>in</strong> the zone of energy supply<br />

below the threshold of anaerobic metabolism (AT). Test 1 was carried<br />

out <strong>in</strong> a swimm<strong>in</strong>g pool on the basis of tra<strong>in</strong><strong>in</strong>g series of 8×200 m by the<br />

basic stroke with 45 s breaks.<br />

In March the second test was conducted <strong>in</strong> the zone of energy supply<br />

above the maximal oxygen consumption (VO 2 max ). Test 2 was carried<br />

out <strong>in</strong> the flume, with peri-limit<strong>in</strong>g metabolic power be<strong>in</strong>g applied <strong>in</strong><br />

swimm<strong>in</strong>g by the basic stroke. The work lasted one m<strong>in</strong>ute for spr<strong>in</strong>ters<br />

<strong>and</strong> two m<strong>in</strong>utes for medium distance swimmers.<br />

In April the third test was conducted <strong>in</strong> the zone of energy supply<br />

between AT <strong>and</strong> VO2 max . Test 3 was carried out <strong>in</strong> the flume <strong>in</strong> the<br />

course of tra<strong>in</strong><strong>in</strong>g series of 3×1 m<strong>in</strong>utes (for spr<strong>in</strong>ters) <strong>and</strong> 3×2 m<strong>in</strong>utes<br />

(for medium distance swimmers) by basic stroke, <strong>in</strong>tervals of work <strong>and</strong><br />

rest be<strong>in</strong>g altered as 1:1.<br />

Prelim<strong>in</strong>ary, <strong>in</strong>dividual swimm<strong>in</strong>g velocities <strong>in</strong> all the three zones<br />

of energy supply were calculated for each subject on the basis of special<br />

tests <strong>in</strong> the swimm<strong>in</strong>g pool.<br />

To def<strong>in</strong>e experimentally variables <strong>in</strong> equation 1, a complex of physiological<br />

<strong>and</strong> biomechanical research methods was applied.<br />

The power of active energetic metabolism (Pai , W) <strong>in</strong> all the three<br />

tests was calculated as a ratio of energetic expenditures at the test distance<br />

(E, J) to work time at this distance (t, s). Energetic expenditures<br />

were def<strong>in</strong>ed experimentally by the method of <strong>in</strong>direct calorimetry. For<br />

this purpose, all necessary gaseous parameters of the ventilation air were<br />

measured with the help of the mobile system “MetaMax” <strong>and</strong> lactate<br />

concentration was determ<strong>in</strong>ed <strong>in</strong> capillary blood before <strong>and</strong> after the<br />

test. When the research was conducted <strong>in</strong> the swimm<strong>in</strong>g pool (test<br />

№ 1), gas analytical measurements were taken dur<strong>in</strong>g rest breaks between<br />

tra<strong>in</strong><strong>in</strong>g distances. When the research was conducted <strong>in</strong> the flume<br />

(tests № 2 <strong>and</strong> № 3), gas analytical measurements were taken before,<br />

dur<strong>in</strong>g <strong>and</strong> after the test. All experimental results were reduced to conditions<br />

of STPD. Quantitative values of E were calculated on the basis<br />

of special equations (Capelli et al., 1998; Zamparo et al., 1999), which<br />

correspond entirely to the three studied zones of energetic supply <strong>and</strong><br />

are described <strong>in</strong> detail <strong>in</strong> the specified papers.<br />

Total external mechanical power (Pto ), frontal component of active<br />

drag force (Fr(f.d.) ) <strong>and</strong> useful external mechanical power (Puo ) were<br />

def<strong>in</strong>ed us<strong>in</strong>g a biohydrodynamic method (Kolmogorov, 2008), which<br />

consists of a complex of <strong>in</strong>dependent biomechanical <strong>and</strong> hydrodynamic<br />

methods to measure necessary physical values. At first, total external<br />

mechanical power (Pto max ) was def<strong>in</strong>ed by the method of small perturbations<br />

at the maximal swimm<strong>in</strong>g velocity (v0 max ) (Kolmogorov et.<br />

al., 1997). Afterwards, the correspond<strong>in</strong>g value of Pto exp was calculated<br />

for every experimental swimm<strong>in</strong>g velocity <strong>in</strong> the studied zones of energetic<br />

metabolism (v0 exp ) on the basis of the well-known (Touissant <strong>and</strong><br />

Truijens, 2005) <strong>and</strong> verified experimentally dependence between these<br />

parameters (Kolmogorov <strong>and</strong> Koukovyak<strong>in</strong>, 2001):<br />

3 3<br />

Pto exp =Pto max /v0max× v0exp . (2)<br />

The frontal component of active drag force under conditions of swimmer’s<br />

steady non-stationary forward motion (Fr(f.d.) ) was def<strong>in</strong>ed experimentally<br />

for every experimental swimm<strong>in</strong>g velocity (v0 exp ) us<strong>in</strong>g the<br />

correspond<strong>in</strong>g hydrodynamic method (oriented specially to measure<br />

this physical value) (Kolmogorov, 2008). This paper describes <strong>in</strong> detail<br />

the theory, necessary mathematic models <strong>and</strong> practical technology to<br />

def<strong>in</strong>e Fr(f.d.) with<strong>in</strong> the whole range of v0 exp relevant for the research.<br />

Useful external mechanical power (Puo ) was def<strong>in</strong>ed from the follow<strong>in</strong>g<br />

equation:<br />

P uo = Fr (f.d.) × v0exp.<br />

(3)<br />

When the parameters, <strong>in</strong>dicated above, were def<strong>in</strong>ed for every experimental<br />

swimm<strong>in</strong>g velocity <strong>in</strong> the studied zones of energetic metabolism<br />

(v 0 exp ), dimensionless coefficients of mechanical (e g =P to exp /P ai ) <strong>and</strong> propulsive<br />

(e p = P uo / P to exp ) efficiency were calculated.<br />

results<br />

Tables 1 <strong>and</strong> 2 represent experimental results of the studied process <strong>in</strong><br />

dolph<strong>in</strong> swimm<strong>in</strong>g by a female subject <strong>and</strong> <strong>in</strong> brass by a male subject,<br />

correspond<strong>in</strong>gly. These tables give only key parameters of P ai , e g , e p , F r(f.d.)<br />

<strong>and</strong> v 0 exp which are necessary to solve quantitatively equation (1) <strong>and</strong>


which express entirely the transformation process of metabolic energy<br />

<strong>in</strong>to useful activity result <strong>in</strong> human swimm<strong>in</strong>g. All <strong>in</strong>termediate values<br />

are omitted to concentrate attention on the studied process. The values<br />

of subjects’ body length (L) <strong>and</strong> body mass (m 0 ) functionally connected<br />

with P ai <strong>and</strong> F r(f.d.) are given for the moment of experimental period<br />

end<strong>in</strong>g, s<strong>in</strong>ce the range of their variations was <strong>in</strong>significant.<br />

Table 1. Experimental values of active energetic metabolism power <strong>and</strong><br />

efficiency of its transformation <strong>in</strong>to swimm<strong>in</strong>g velocity <strong>in</strong> the studied<br />

zones of energy supply <strong>in</strong> dolph<strong>in</strong> swimm<strong>in</strong>g by a spr<strong>in</strong>ter female subject<br />

(L = 1.73 m, m 0 = 60.1 kg).<br />

Values<br />

Test 1<br />

below AT<br />

Test 2<br />

above VO 2 max<br />

Test 3<br />

between AT <strong>and</strong> VO 2 max<br />

P ai , W 838.41 1781.25 1173.95<br />

e g 0.062 0.061 0.068<br />

e p 0.655 0.649 0.714<br />

F r(f.d.), N 25.20 46.90 39.50<br />

v 0 exp , m·s�1 1.30 1.50 1.44<br />

Table 2. Experimental values of active energetic metabolism power <strong>and</strong><br />

efficiency of its transformation <strong>in</strong>to swimm<strong>in</strong>g velocity <strong>in</strong> the studied<br />

zones of energy supply <strong>in</strong> brass swimm<strong>in</strong>g by a medium distances male<br />

subject (L = 1.90 m, m 0 = 76.0 kg).<br />

Values<br />

Test 1<br />

below AT<br />

Test 2<br />

above VO 2 max<br />

Test 3<br />

between AT <strong>and</strong> VO 2 max<br />

P ai , W 993.32 2100.49 1440.71<br />

e g 0.073 0.066 0.076<br />

e p 0.714 0.693 0.752<br />

F r(f.d.), N 42.57 65.79 58.05<br />

v 0 exp , m·s�1 1.22 1.46 1.42<br />

Table 3 represents mean group values of mechanical <strong>and</strong> propulsive efficiency<br />

for female <strong>and</strong> male subjects, who took part <strong>in</strong> this research, <strong>in</strong><br />

the studied zones of energy supply. The matter is that the frontal component<br />

of active drag force depends essentially on a swimm<strong>in</strong>g stroke,<br />

whereas power of active energetic metabolism <strong>in</strong> all the studied zones of<br />

energy supply depends on human body mass. Therefore, the summaris<strong>in</strong>g<br />

Table 3 <strong>in</strong>cludes only the values of e g <strong>and</strong> e p which reflect <strong>in</strong>tegrally<br />

efficiency of metabolic energy transformation process <strong>in</strong>to useful activity<br />

result <strong>in</strong> human swimm<strong>in</strong>g.<br />

Table 3. Dimensionless coefficients of mechanical (e g ) <strong>and</strong> propulsive<br />

(e p ) efficiency <strong>in</strong> the studied zones of energy supply for female <strong>and</strong> male<br />

subjects (P is the level of differences significance).<br />

Test 1<br />

below AT<br />

e g<br />

e p<br />

between 1 <strong>and</strong> 2 P<br />

Test 2<br />

above VO 2 max<br />

e g<br />

e p<br />

Women P Men<br />

0.0604±0.0018<br />

0.647±0.009<br />

0.0592±0.0022<br />

0.656±0.008<br />


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

conclusIon<br />

Effective <strong>and</strong> safe ways to improve swimmers’ sports results <strong>in</strong> the process<br />

of tra<strong>in</strong><strong>in</strong>g mesocycle are, first of all, connected with decreas<strong>in</strong>g of<br />

unavoidable losses at both stages of metabolic energy transformation<br />

<strong>in</strong>to useful activity result, which is quantitatively reflected <strong>in</strong> dynamics<br />

of values of mechanical <strong>and</strong> propulsive efficiency.<br />

reFerences<br />

Capelli, C., Pendergast, D. R. & Term<strong>in</strong>, B. (1998). Energetic of swimm<strong>in</strong>g<br />

at maximal speeds <strong>in</strong> humans. Europ J Appl Physiol, 78, 385–393.<br />

Craig, A. & Pendergast, D. (1979). Relationship of stroke rate, distance<br />

per stroke, <strong>and</strong> velocity <strong>in</strong> competitive swimm<strong>in</strong>g. Med <strong>and</strong> Sci Sports<br />

Exerc, 11(3), 278-283.<br />

Kolmogorov, S. V. (1997). Transformation effectiveness of elite swimmers<br />

metabolic <strong>and</strong> mechanic energy. In: Eriksson, B. & Gullstr<strong>and</strong>,<br />

L. (ed.). Proceed<strong>in</strong>gs <strong>XI</strong>I FINA Wold congress on sports medic<strong>in</strong>e. Goteborg:<br />

Chalmers Reproservice, 453–462.<br />

Kolmogorov, S., Rumyantseva, 0., Gordon, B. & Cappaert, J. (1997).<br />

Hydrodynamic characterristics of competitive swimmers of different<br />

genders <strong>and</strong> performance levels. J Appl <strong>Biomechanics</strong>, 13, 88-97.<br />

Kolmogorov, S. & Koukovyak<strong>in</strong>, A. (2001). Dependence between swimm<strong>in</strong>g<br />

velocity <strong>and</strong> hydrodynamic characteristics. In: Mester, J., K<strong>in</strong>g,<br />

G., Struder, H., Tsolakidis, E., Osterburg, A. (ed.). Perspectives <strong>and</strong><br />

Profiles, 6 th annual congress of the European college of sport science. Cologne:<br />

Sport und Bush Strauss GmbH, 537.<br />

Kolmogorov, S. V. (2008). K<strong>in</strong>ematic <strong>and</strong> dynamic characteristics of<br />

steady-state non-stationary motion of elite swimmers. Russian Journal<br />

of <strong>Biomechanics</strong>, 12(4), 56-70.<br />

Toussa<strong>in</strong>t, H. M. (1988). Mechanics <strong>and</strong> energetics of swimm<strong>in</strong>g: Doctoral<br />

dissertation. Amsterdam: Vrije Universiteit.<br />

Touissant, H. & Truijens, M. (2005). Biomechanical aspects of peak<br />

performance <strong>in</strong> human swimm<strong>in</strong>g. J Animal Biology, 55 (1), 17-40.<br />

Utk<strong>in</strong>, V. L. (1993). Optimization of sports locomotions on the basis<br />

of model<strong>in</strong>g energetics of muscular contraction. In: Zatsiorsky, V.M.<br />

(ed.). Contemporary problems of biomechanics vol. 7. Nizhniy Novgorod:<br />

Publish<strong>in</strong>g house of the Russian academy of sciences, 5–22 (<strong>in</strong> Russian).<br />

Zamparo, P., Capelli, C. & Guerr<strong>in</strong>i, G. (1999). Energetic of kayak<strong>in</strong>g<br />

at submaximal maximal speeds. Europ J Appl Physiol, 80, 542–548.<br />

Zamparo, P. (2006). Effects of age <strong>and</strong> gender on the propell<strong>in</strong>g efficiency<br />

of the arm stroke. Europ J Appl Physiol, 97, 52-58.<br />

112<br />

Prediction of Propulsive Force Exerted by the H<strong>and</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g<br />

Kudo, s. 1 <strong>and</strong> lee, M.K. 1<br />

1 Republic Polytechnic, S<strong>in</strong>gapore<br />

The aim of this study was to develop a method to predict propulsive<br />

forces exerted by the h<strong>and</strong> <strong>in</strong> swimm<strong>in</strong>g based on the pressure distribution<br />

on the h<strong>and</strong>. Hydrodynamic forces act<strong>in</strong>g on the h<strong>and</strong> were predicted<br />

us<strong>in</strong>g 12 pressure sensors, <strong>and</strong> the h<strong>and</strong> direction was determ<strong>in</strong>ed<br />

by a motion capture system. We comb<strong>in</strong>ed <strong>in</strong>formation to predict the<br />

propulsive forces exerted by the h<strong>and</strong> dur<strong>in</strong>g the front crawl stroke. The<br />

proportion of drag <strong>and</strong> lift forces relative to the propulsive forces was<br />

55% <strong>and</strong> 45%, respectively. The best-fit equations used to predict hydrodynamic<br />

forces <strong>in</strong> a previous study may cause errors <strong>in</strong> the prediction of<br />

hydrodynamic forces act<strong>in</strong>g on the h<strong>and</strong> due to multicoll<strong>in</strong>earity. Such<br />

errors can be m<strong>in</strong>imized with a lesser order of best-fit equations. In<br />

addition, feedback on the propulsive forces exerted by the h<strong>and</strong> can be<br />

generated with<strong>in</strong> a few hours.<br />

Key words: pressure, h<strong>and</strong> k<strong>in</strong>ematics, drag, lift.<br />

IntroductIon<br />

Propulsive force exerted by the h<strong>and</strong> <strong>and</strong> hydrodynamic forces act<strong>in</strong>g<br />

on the h<strong>and</strong> <strong>in</strong> swimm<strong>in</strong>g have been quantified <strong>and</strong> used to analyze the<br />

technique of swimm<strong>in</strong>g strokes (Cappaert et al., 1995; Schleihaulf et al.,<br />

1983; Shleihauf et al., 1988). However, the method to predict hydrodynamic<br />

forces act<strong>in</strong>g on the h<strong>and</strong> could <strong>in</strong>volve considerable errors as the<br />

effect of h<strong>and</strong> acceleration <strong>and</strong> wave drag act<strong>in</strong>g on the model have not<br />

been taken <strong>in</strong>to consideration <strong>in</strong> previous studies on the prediction of<br />

hydrodynamic forces act<strong>in</strong>g on the h<strong>and</strong> (Pai <strong>and</strong> Hay, 1988; Kudo et al.,<br />

2008). Acceleration us<strong>in</strong>g a h<strong>and</strong> model has been taken <strong>in</strong>to account <strong>in</strong><br />

l<strong>in</strong>ear motion (S<strong>and</strong>ers, 1999). Errors <strong>in</strong> the prediction of hydrodynamic<br />

forces on the h<strong>and</strong> could also result from the time consum<strong>in</strong>g method of<br />

manual digitization of l<strong>and</strong>marks on the swimmer’s h<strong>and</strong> from recorded<br />

image taken from multiple po<strong>in</strong>ts of view (Payton <strong>and</strong> Bartlett, 1995;<br />

Lauder et al., 2001).<br />

A pressure method was developed to predict hydrodynamic forces<br />

act<strong>in</strong>g on the h<strong>and</strong> <strong>in</strong> swimm<strong>in</strong>g based on the pressure at 12 po<strong>in</strong>ts of<br />

the h<strong>and</strong> surface (Kudo et al., 2008). The study measured hydrodynamic<br />

forces act<strong>in</strong>g on a h<strong>and</strong> model <strong>and</strong> pressures on the model surface so as<br />

to develop a best-fit equation to predict hydrodynamic forces act<strong>in</strong>g on<br />

the model. However, a method to predict propulsive forces exerted by<br />

the swimmer’s h<strong>and</strong> us<strong>in</strong>g the pressure method dur<strong>in</strong>g swimm<strong>in</strong>g has<br />

not been developed. Propulsive forces by the h<strong>and</strong> are useful <strong>in</strong>formation<br />

for both swimmer <strong>and</strong> coach <strong>in</strong> the analysis of technique <strong>in</strong> swimm<strong>in</strong>g.<br />

Thus, the aim of this study was to develop a method to predict<br />

propulsive forces exerted by the h<strong>and</strong> us<strong>in</strong>g the pressure method dur<strong>in</strong>g<br />

swimm<strong>in</strong>g. This study also considered the h<strong>and</strong> size of a swimmer <strong>in</strong> a<br />

best-fit equation because the h<strong>and</strong> size of a swimmer can be different<br />

from the size of a h<strong>and</strong> model used <strong>in</strong> the previous study.<br />

Methods<br />

A swimmer whose h<strong>and</strong> size was 0.0136 m 2 was asked to swim the front<br />

crawl stroke at sub-maximal effort for 18 m <strong>in</strong> the swimm<strong>in</strong>g pool at<br />

Republic Polytechnic follow<strong>in</strong>g some light warm up. A right-h<strong>and</strong>ed<br />

Cartesian coord<strong>in</strong>ate system was embedded at the bottom of the pool;<br />

the x-direction def<strong>in</strong>ed the direction of swimm<strong>in</strong>g, the y-direction def<strong>in</strong>ed<br />

the side-to-side direction, <strong>and</strong> the z-direction def<strong>in</strong>ed the vertical<br />

direction.<br />

A portable data logger with 12 pressure sensors (MMT, Japan) was


developed to measure pressure on the h<strong>and</strong> <strong>and</strong> to predict hydrodynamic<br />

forces act<strong>in</strong>g on the h<strong>and</strong> dur<strong>in</strong>g swimm<strong>in</strong>g. The data logger was attached<br />

on the back of the swimmer, <strong>and</strong> twelve pressure sensors were<br />

attached on the swimmer’s h<strong>and</strong> accord<strong>in</strong>g to Kudo et al. (2008). An<br />

underwater motion capture system us<strong>in</strong>g eight cameras (Qualisys, Sweden)<br />

was used to acquire k<strong>in</strong>ematic data of the h<strong>and</strong> dur<strong>in</strong>g swimm<strong>in</strong>g.<br />

Three reflective markers were attached on the right h<strong>and</strong>, the third f<strong>in</strong>gertip,<br />

trapezium <strong>and</strong> pisiform bone. The data logger <strong>and</strong> the motion<br />

capture system were synchronized, <strong>and</strong> the signals were recorded at 100<br />

Hz. The signals of data logger <strong>and</strong> motion capture system for a right<br />

h<strong>and</strong> stoke were smoothed us<strong>in</strong>g a fourth order, zero lag, low-pass Butterworth<br />

filter (W<strong>in</strong>ter, 1990). Static pressures due to the h<strong>and</strong> depth<br />

dur<strong>in</strong>g swimm<strong>in</strong>g were taken <strong>in</strong>to account based on the marker data so<br />

as to predict hydrodynamic forces (drag <strong>and</strong> lift forces) act<strong>in</strong>g on the<br />

h<strong>and</strong> by the pressure method (Kudo et al., 2008)<br />

The present study constructed a new best-fit equation us<strong>in</strong>g a dependent<br />

value which hydrodynamic forces act<strong>in</strong>g on the h<strong>and</strong> model<br />

divided by the size of the h<strong>and</strong> model used <strong>in</strong> the previous study (Kudo<br />

et al., 2008), tak<strong>in</strong>g <strong>in</strong>to consideration the h<strong>and</strong> size of a swimmer. Thus,<br />

the magnitude of hydrodynamic forces act<strong>in</strong>g on the swimmer’s h<strong>and</strong><br />

was predicted by multiply<strong>in</strong>g the predicted values from the best-fit<br />

equations by the h<strong>and</strong> size of a swimmer (Loetz et al., 1988; Takagi <strong>and</strong><br />

Wilson, 1999). For construct<strong>in</strong>g the best-fit equations <strong>in</strong> the present<br />

study, hydrodynamic forces were decomposed <strong>in</strong>to the three directions<br />

<strong>in</strong> the local reference h<strong>and</strong>-centric system; a direction parallel to the<br />

longitud<strong>in</strong>al axis of the h<strong>and</strong> (z-axis), a direction perpendicular to the<br />

plane of h<strong>and</strong> motion <strong>in</strong> the two consecutive frames (x-axis), a direction<br />

perpendicular to the z- <strong>and</strong> x-axes (y-axis). Us<strong>in</strong>g k<strong>in</strong>ematic data from<br />

the motion capture system the directions of drag <strong>and</strong> lift forces, the<br />

angle of attack (AP) <strong>and</strong> sweepback angle (SB) were computed. Propulsive<br />

forces exerted by the h<strong>and</strong> dur<strong>in</strong>g swimm<strong>in</strong>g were computed us<strong>in</strong>g<br />

the h<strong>and</strong> k<strong>in</strong>ematics <strong>and</strong> hydrodynamic forces on the swimmer’s h<strong>and</strong>.<br />

The best-fit equations used to predict hydrodynamic forces act<strong>in</strong>g on<br />

the h<strong>and</strong> model by the pressure method <strong>in</strong> the previous study consisted<br />

of 12 regression coefficients <strong>and</strong> higher order polynomials. The number<br />

of regression coefficients was up to 36. Therefore, there might be a<br />

considerable effect of multicoll<strong>in</strong>earity on the prediction (Kutner et al.,<br />

2004). Different order of best-fit equations, <strong>in</strong>clud<strong>in</strong>g the order of bestfit<br />

equation from the pressure method <strong>in</strong> the previous study (B-Eq1)<br />

<strong>and</strong> the first order of best-fit equations (B-Eq2), were used to predict<br />

hydrodynamic forces act<strong>in</strong>g on the swimmer’s h<strong>and</strong> to check the effect<br />

of multicoll<strong>in</strong>earity on the prediction. In addition, the variance <strong>in</strong>flation<br />

factor (VIF) was computed to quantify the effect of multicoll<strong>in</strong>earity.<br />

results<br />

Mean propulsive forces exerted by the h<strong>and</strong> predicted by B-Eq1 over a<br />

stroke was 15 ± 11 N. Mean propulsive forces exerted by the h<strong>and</strong> predicted<br />

by B-Eq2 over a stroke was 33 ± 24 N, <strong>and</strong> the maximum value<br />

of propulsive force was 77 N (Figure 1). The contribution of drag <strong>and</strong> lift<br />

forces to propulsive force predicted by B-Eq2 was 55% <strong>and</strong> 45%, respectively.<br />

Mean h<strong>and</strong> speed over a stroke was 2.3 ± 0.3 ms -1 <strong>and</strong> maximum<br />

h<strong>and</strong> speed was 2.7 ms -1 . The angle of attack (AP) changed from 24˚ to<br />

85˚, <strong>and</strong> the sweepback angle (SB) changed from 73˚ to 254˚ over a stroke.<br />

Mean values of VIF were 12.86 ± 7.05 for the first-order polynomial<br />

equations with the 12 sets of pressure, 39.28 ± 32.50 for the secondorder<br />

polynomial equations with the pressure sets, <strong>and</strong> 196.10 ± 298.10<br />

for the third-order polynomial equations with the pressure sets.<br />

contribution of drag <strong>and</strong> lift forces to propulsive force predicted by B-Eq2 was 55% <strong>and</strong><br />

45%, respectively. Mean h<strong>and</strong> speed over a stroke was 2.3 ± 0.3 ms<br />

chaPter2.<strong>Biomechanics</strong><br />

-1 <strong>and</strong> maximum<br />

h<strong>and</strong> speed was 2.7 ms -1 . The angle of attack (AP) changed from 24� to 85�, <strong>and</strong> the<br />

sweepback angle (SB) changed from 73� to 254� over a stroke.<br />

Mean values of VIF were 12.86 ± 7.05 for the first-order polynomial equations with<br />

the 12 sets of pressure, 39.28 ± 32.50 for the second-order polynomial equations with<br />

the pressure sets, <strong>and</strong> 196.10 ± 298.10 for the third-order polynomial equations with the<br />

pressure sets.<br />

Force (N)<br />

Propulsion<br />

Propulsion from drag force<br />

Propulsion from lift force<br />

Frame<br />

Figure 1 Propulsive force exerted by the swimmer’s h<strong>and</strong><br />

Figure 1 Propulsive force exerted by the swimmer’s h<strong>and</strong><br />

DISCUSSION<br />

This study developed a method to predict propulsive forces exerted by the h<strong>and</strong> <strong>in</strong><br />

swimm<strong>in</strong>g. Feedback on propulsive forces exerted by the h<strong>and</strong> predicted can be<br />

provided to the swimmer <strong>and</strong> coach with<strong>in</strong> a few hours by comb<strong>in</strong><strong>in</strong>g the pressure<br />

method with k<strong>in</strong>ematic data from the motion capture system. Additionally, the<br />

contribution of drag <strong>and</strong> lift forces to propulsion by the h<strong>and</strong> can be provided to help<br />

swimmers <strong>and</strong> coaches <strong>in</strong> the analysis of stroke technique to improve swimm<strong>in</strong>g<br />

performance.<br />

The mean of hydrodynamic forces act<strong>in</strong>g on the h<strong>and</strong> predicted by the best-fit<br />

equation <strong>in</strong> the previous study (B-Eq1) was different from that by B-Eq2. The mean of<br />

VIF changed considerably among the three different orders of best-fit question. The<br />

results mean that multicoll<strong>in</strong>earity might affect the predicted values. A maximum VIF<br />

value <strong>in</strong> excess of 10 <strong>in</strong>dicates that multicoll<strong>in</strong>earity may <strong>in</strong>fluence the least square<br />

dIscussIon<br />

This study developed a method to predict propulsive forces exerted by<br />

the h<strong>and</strong> <strong>in</strong> swimm<strong>in</strong>g. Feedback on propulsive forces exerted by the<br />

h<strong>and</strong> predicted can be provided to the swimmer <strong>and</strong> coach with<strong>in</strong> a<br />

few hours by comb<strong>in</strong><strong>in</strong>g the pressure method with k<strong>in</strong>ematic data from<br />

the motion capture system. Additionally, the contribution of drag <strong>and</strong><br />

lift forces to propulsion by the h<strong>and</strong> can be provided to help swimmers<br />

<strong>and</strong> coaches <strong>in</strong> the analysis of stroke technique to improve swimm<strong>in</strong>g<br />

performance.<br />

The mean of hydrodynamic forces act<strong>in</strong>g on the h<strong>and</strong> predicted by<br />

the best-fit equation <strong>in</strong> the previous study (B-Eq1) was different from<br />

that by B-Eq2. The mean of VIF changed considerably among the three<br />

different orders of best-fit question. The results mean that multicoll<strong>in</strong>earity<br />

might affect the predicted values. A maximum VIF value <strong>in</strong> excess<br />

of 10 <strong>in</strong>dicates that multicoll<strong>in</strong>earity may <strong>in</strong>fluence the least square<br />

estimates of regression coefficients (Kutner et al., 2004). The values of<br />

correlation coefficient were 0.69 <strong>in</strong> propulsions predicted by B-Eq1 <strong>and</strong><br />

B-Eq2, 0.79 <strong>in</strong> propulsions from drag forces predicted by the two bestfit<br />

equations, <strong>and</strong> 0.88 <strong>in</strong> propulsions from lift forces predicted by the<br />

two best-fit equations. The results <strong>in</strong>dicate that the trend of the prediction<br />

is similar <strong>in</strong> the two equations. Based on the VIF values B-Eq2<br />

may be better to predict hydrodynamic forces act<strong>in</strong>g on the h<strong>and</strong> dur<strong>in</strong>g<br />

swimm<strong>in</strong>g. The erroneous effect on the prediction of hydrodynamic<br />

forces act<strong>in</strong>g on the h<strong>and</strong> dur<strong>in</strong>g swimm<strong>in</strong>g can be detected us<strong>in</strong>g the<br />

<strong>in</strong>formation on the magnitude of hydrodynamic forces act<strong>in</strong>g on the<br />

h<strong>and</strong>, k<strong>in</strong>ematics of h<strong>and</strong>, as well as AP <strong>and</strong> SB. Further study is necessary<br />

to validate the pressure method to predict propulsive forces exerted<br />

by the h<strong>and</strong> dur<strong>in</strong>g swimm<strong>in</strong>g especially for the magnitude of hydrodynamic<br />

force predicted.<br />

The present study showed that a swimmer is able to generate propulsive<br />

forces by the h<strong>and</strong> <strong>in</strong> the down-sweep phase between 20 <strong>and</strong> 40<br />

frames (Figures 1 <strong>and</strong> 2). The majority of propulsion resulted from lift<br />

forces. Dur<strong>in</strong>g the down-sweep phase, drag force by the h<strong>and</strong> did not<br />

have substantial contribution to propulsive force because the h<strong>and</strong> was<br />

still mov<strong>in</strong>g forward. The swimmer <strong>in</strong> this study did not <strong>in</strong>corporate<br />

sideway sweep of the h<strong>and</strong> <strong>in</strong> the <strong>in</strong>ward sweep phase between 40 <strong>and</strong><br />

60 frames (Figure 2). Thus, the contribution of lift forces to propulsive<br />

forces was small (Figure 1). Propulsive forces from lift forces exerted by<br />

the swimmer’s h<strong>and</strong> can be <strong>in</strong>creased if the swimmer performed further<br />

<strong>in</strong>ward sweep. The gaps of the h<strong>and</strong> trajectories <strong>in</strong> the xy-plane between<br />

40 <strong>and</strong> 60 frames were large <strong>and</strong> the trajectories moved backwards, <strong>in</strong>dicat<strong>in</strong>g<br />

that the h<strong>and</strong> moved backwards with large velocities (Figure<br />

2). Therefore, propulsive forces from drag forces reached the maximum<br />

value (69 N) between 40 <strong>and</strong> 60 frames that is 90% of propulsive forces<br />

by the h<strong>and</strong> (Figure 1). Berger et al. (1999) reported mean propulsive<br />

forces exerted by the h<strong>and</strong> <strong>in</strong> the front crawl stroke of 21 N among n<strong>in</strong>e<br />

swimmers at a mean swimm<strong>in</strong>g velocity of 1.15 ms-1 . Berger et al. (1999)<br />

<strong>and</strong> Schleihauf et al. (1983) showed that a swimmer atta<strong>in</strong>ed maximum<br />

propulsion of approximately 100 N by the h<strong>and</strong>. The propulsive forces <strong>in</strong><br />

this study were not considerably different from the two previous studies.<br />

113


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The difference can be due to a skill level of a swimmer. The subject <strong>in</strong> this<br />

study was a recreational swimmer while the subjects <strong>in</strong> the two previous<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b 8<br />

studies were competitive swimmers of <strong>in</strong>ternational or national st<strong>and</strong>ard.<br />

Also, the different values of propulsive forces among three studies<br />

can be due to the different method to predict hydrodynamic forces act<strong>in</strong>g<br />

on the h<strong>and</strong> dur<strong>in</strong>g swimm<strong>in</strong>g.<br />

z coord<strong>in</strong>ate<br />

(mm)<br />

II<br />

x coord<strong>in</strong>ate<br />

y<br />

(mm)<br />

coord<strong>in</strong>ate<br />

Figure 2. H<strong>and</strong> trajectories <strong>in</strong> the fixed pool-centric reference system. (mm) The threedimensional<br />

coord<strong>in</strong>ates of h<strong>and</strong> was obta<strong>in</strong>ed by tak<strong>in</strong>g the midpo<strong>in</strong>t of the f<strong>in</strong>ger<br />

tip <strong>and</strong> the po<strong>in</strong>t between trapezium <strong>and</strong> pisiform. I = frame 20; II = frame 40; III =<br />

frame 60.<br />

REFERENCES<br />

Berger, M. A. M., Holl<strong>and</strong>er, A. P., de Groot, G. (1999). Determ<strong>in</strong><strong>in</strong>g propulsive force<br />

<strong>in</strong> front crawl swimm<strong>in</strong>g: A comparison of two methods. Journal of Sports<br />

Sciences, 17, 97-105.<br />

Cappaert, J. M., Pease, D. L., Troup, J. P. (1995). Three-dimensional analysis of the<br />

men's 100-m freestyle dur<strong>in</strong>g the 1992 Olympic games. Journal of Applied<br />

<strong>Biomechanics</strong>, 11, 103-112.<br />

<strong>in</strong>g Kudo, propulsive S., Yanai, T., force Wilson, <strong>in</strong> front B., Takagi, crawl H., swimm<strong>in</strong>g: Vennell, R. (2008). A comparison Prediction of of fluid two<br />

methods. forces Journal act<strong>in</strong>g on of a Sports h<strong>and</strong> Sciences, model <strong>in</strong> 17, unsteady 97-105. flow conditions. Journal of<br />

Biomechancis, 41, 1131-1136.<br />

Kudo, S., Vennell, R., Wilson, B., Waddell, N., Sato, Y. (2008). Influence of surface<br />

penetration of measured fluid force on a h<strong>and</strong> model. Journal of Biomechancis, 41,<br />

114<br />

y coord<strong>in</strong>ate<br />

(mm)<br />

III<br />

xy-plane<br />

III<br />

x coord<strong>in</strong>ate<br />

(mm)<br />

xz-plane<br />

I<br />

II<br />

z<br />

x<br />

Swim<br />

direction<br />

y<br />

III<br />

I<br />

I<br />

II<br />

yz-plane<br />

III<br />

II<br />

I<br />

z coord<strong>in</strong>ate<br />

(mm)<br />

reFerences<br />

Berger, M. A. M., Holl<strong>and</strong>er, A. P., de Groot, G. (1999). Determ<strong>in</strong>-<br />

Cappaert, J. M., Pease, D. L., Troup, J. P. (1995). Three-dimensional<br />

analysis of the men’s 100-m freestyle dur<strong>in</strong>g the 1992 Olympic<br />

3502-3505.<br />

games. Journal of Applied <strong>Biomechanics</strong>, 11, 103-112.<br />

Kudo, S., Yanai, T., Wilson, B., Takagi, H., Vennell, R. (2008). Prediction<br />

of fluid forces act<strong>in</strong>g on a h<strong>and</strong> model <strong>in</strong> unsteady flow conditions.<br />

Journal of Biomechancis, 41, 1131-1136.<br />

Kudo, S., Vennell, R., Wilson, B., Waddell, N., Sato, Y. (2008). Influence<br />

of surface penetration of measured fluid force on a h<strong>and</strong> model.<br />

Journal of Biomechancis, 41, 3502-3505.<br />

Kutner, M. H., Nachtsheim, C. J., Neter, J. (2004). Applied l<strong>in</strong>ear regression<br />

models. New York: McGraw-Hill/Irw<strong>in</strong>.<br />

Lauder, M. A., Dabnichki, P., Bartlett, R. M. (2001). Improved accuracy<br />

<strong>and</strong> reliability of sweepback angle, pitch angle <strong>and</strong> h<strong>and</strong> velocity calculations<br />

<strong>in</strong> swimm<strong>in</strong>g. Journal of <strong>Biomechanics</strong>, 34, 31-39.<br />

Loetz, C., Reischle, K., Schmitt, G. (1988). The evaluation of highly<br />

skilled swimmers via quantitative <strong>and</strong> qualitative analysis. In B.<br />

E. Ungerechts, Wilke, K., Reischle, K. (Eds.), Swimm<strong>in</strong>g science V.<br />

Champaign, IL: Human K<strong>in</strong>etics Books, 361-367.<br />

Pai, YC., Hay, J. G. (1988). A hydrodynamic study of the oscillation<br />

motion <strong>in</strong> swimm<strong>in</strong>g. International Journal of Sport <strong>Biomechanics</strong>, 4,<br />

21-37.<br />

Payton, C. J., Bartlett, R. M. (1995). Estimat<strong>in</strong>g propulsive forces <strong>in</strong><br />

swimm<strong>in</strong>g from three-dimensional k<strong>in</strong>ematic data. Journal of Sports<br />

Sciences, 13, 447-454.<br />

S<strong>and</strong>ers, R. H. (1999). Hydrodynamic characteristics of a swimmer’s<br />

h<strong>and</strong>. Journal of Applied <strong>Biomechanics</strong>, 15, 3-26.<br />

Schleihauf, R., Gray, L., DeRose, J. (1983). Three-dimensional analysis<br />

of h<strong>and</strong> propulsion <strong>in</strong> the spr<strong>in</strong>t front crawl stroke. In P. A. Holl<strong>and</strong>er,<br />

Huij<strong>in</strong>g, P. A., <strong>and</strong> de Groot, G. (Ed.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g. Champaign, IL.: Human K<strong>in</strong>etics, 173-184.<br />

Schleihauf, R. E., Higg<strong>in</strong>s, J. R., H<strong>in</strong>richs, R., Luedtke, D., Maglischo,<br />

C., Maglischo, E. W. (1988). Propulsive techniques: Front crawl<br />

stoke, butterfly, backstroke, <strong>and</strong> breaststroke. In B. E. Ungerechts,<br />

Wilke, K., Reischle, K. (Eds.), Swimm<strong>in</strong>g science V. Champaign, IL:<br />

Human K<strong>in</strong>etics Books, 53-59.<br />

Takagi, H., Wilson, B. (1999). Calculation hydrodynamic forces by us<strong>in</strong>g<br />

pressure differences <strong>in</strong> swimm<strong>in</strong>g. In K. L. Kesk<strong>in</strong>en, P. V. Komi,<br />

A. P. Holl<strong>and</strong>er. (Eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII.<br />

Jyväskylä: Gummerus Pr<strong>in</strong>t<strong>in</strong>g, 101-106.<br />

W<strong>in</strong>ter, D. A. (1990). <strong>Biomechanics</strong> <strong>and</strong> motor control of human movement.<br />

New York: John Wiley & Sons, Inc.


Arm Coord<strong>in</strong>ation, Active Drag <strong>and</strong> Propell<strong>in</strong>g<br />

Efficiency <strong>in</strong> Front Crawl<br />

seifert, l. 1 , schnitzler, c. 1,2 , Alberty, M. 3 , chollet, d. 1 , toussa<strong>in</strong>t,<br />

h.M. 4<br />

1 CETAPS EA 3832, Faculty of Sports Sciences, University of Rouen, France<br />

2 Faculty of Sports Sciences, Strasbourg Marc Bloch University, France<br />

3 LEMH EA 3608, Faculty of Sports Sciences, University of Lille, France<br />

4 Move Institute, Vrije University, Amsterdam, The Netherl<strong>and</strong>s<br />

Active drag, regularity <strong>and</strong> Index of Coord<strong>in</strong>ation (IdC) all <strong>in</strong>crease<br />

with speed <strong>in</strong> front crawl swimm<strong>in</strong>g, but the l<strong>in</strong>k between those parameters<br />

rema<strong>in</strong>s unclear. The aim of this study was thus to exam<strong>in</strong>e<br />

the relationships between the <strong>in</strong>dex of coord<strong>in</strong>ation (IdC) <strong>and</strong> propell<strong>in</strong>g<br />

efficiency (e p ) <strong>and</strong> the active drag (D). Thirteen national level male<br />

swimmers completed two <strong>in</strong>cremental speed tests swimm<strong>in</strong>g front crawl<br />

with arms only <strong>in</strong> free condition <strong>and</strong> us<strong>in</strong>g a Measurement of Active<br />

Drag (MAD) system. The results showed that <strong>in</strong>ter-arm coord<strong>in</strong>ation<br />

was l<strong>in</strong>ked to active drag <strong>and</strong> not propell<strong>in</strong>g efficiency.<br />

Key words: <strong>Biomechanics</strong>, motor control, efficiency<br />

IntroductIon<br />

Swimm<strong>in</strong>g speed results from the <strong>in</strong>teraction of propulsive <strong>and</strong> resistive<br />

forces. However, as the swimmer’s h<strong>and</strong> lacks a fixed push of po<strong>in</strong>t to<br />

propel the body forward, mechanical power applied by the h<strong>and</strong> <strong>in</strong> the<br />

water is wasted <strong>in</strong> k<strong>in</strong>etic energy imparted to the water (P k ). Thus the<br />

total mechanical power out-put (P o ) is the sum of the k<strong>in</strong>etic power (P k )<br />

<strong>and</strong> power delivered to overcome drag force (P d ). Toussa<strong>in</strong>t et al. (2006)<br />

def<strong>in</strong>ed the propell<strong>in</strong>g efficiency (e p ) as the ratio between P d <strong>and</strong> P o . The<br />

question rema<strong>in</strong>s how the <strong>in</strong>ter-arm coord<strong>in</strong>ation <strong>in</strong> front crawl can be<br />

organised to have the highest e p ? For example, does superposition mode<br />

of coord<strong>in</strong>ation, <strong>in</strong> comparison to catch-up mode, relates to a higher<br />

e p ? Indeed, <strong>in</strong> superposition mode the total propell<strong>in</strong>g force is shared<br />

by the two h<strong>and</strong>s (for a brief moment <strong>in</strong> time) <strong>and</strong> it looks like force is<br />

generated with a double h<strong>and</strong>-surface. Previously, Toussa<strong>in</strong>t et al. (1991)<br />

demonstrated that us<strong>in</strong>g paddles e p <strong>in</strong>creases by 7.8%.<br />

Chollet et al. (2000) proposed the Index of Coord<strong>in</strong>ation (IdC) to<br />

quantify the lag time, cont<strong>in</strong>uity or superposition between the propulsive<br />

actions of the two arms. These authors observed that IdC changed<br />

from catch-up (IdC0%) mode when the<br />

swimmers <strong>in</strong>creased their speed from the 800-m race pace to 100-m<br />

race pace. Exam<strong>in</strong><strong>in</strong>g eight race paces (from 1500-m to maximal speed),<br />

Seifert et al. (2007b) noted that above a critical value of speed (1.8 m·s -1 )<br />

<strong>and</strong> stroke rate (50 stroke·m<strong>in</strong>ute -1 ), only the superposition coord<strong>in</strong>ation<br />

mode occurred <strong>in</strong> elite spr<strong>in</strong>ters. Thus, it seemed that swimm<strong>in</strong>g at<br />

higher speeds requires an <strong>in</strong>crease <strong>in</strong> IdC. In fact, Alberty et al. (2009),<br />

Seifert et al. (2007a) respectively showed that through a 400-m <strong>and</strong> a<br />

100-m, some swimmers <strong>in</strong>creased their IdC from the first to the last lap<br />

but at the same time, decreased their swimm<strong>in</strong>g speed <strong>and</strong> their stroke<br />

length due to fatigue. In this case, the <strong>in</strong>crease <strong>in</strong> propulsive cont<strong>in</strong>uity<br />

between the two arms (i.e. higher IdC) seemed an effective way to deal<br />

with fatigue, i.e. a reduction <strong>in</strong> ability to deliver work per stroke. Because<br />

of the above, the first aim of this study was to explore whether <strong>in</strong>terarm<br />

coord<strong>in</strong>ation was l<strong>in</strong>ked to propell<strong>in</strong>g efficiency when swimm<strong>in</strong>g at<br />

maximal speed on 25-m.<br />

Secondly, consider<strong>in</strong>g that active drag (D) <strong>in</strong>creases with speed<br />

square, <strong>and</strong> that IdC also <strong>in</strong>creases with speed follow<strong>in</strong>g a quadratic regression<br />

(Seifert & Chollet, 2009), the relationship between active drag<br />

<strong>and</strong> <strong>in</strong>ter-arm coord<strong>in</strong>ation was <strong>in</strong>vestigated, also. This was carried out<br />

to exam<strong>in</strong>e to what extent overcom<strong>in</strong>g the aquatic resistances is related<br />

to the <strong>in</strong>crease of the propulsive forces <strong>and</strong> to the m<strong>in</strong>imization of the<br />

chaPter2.<strong>Biomechanics</strong><br />

k<strong>in</strong>etic power or to the <strong>in</strong>crease of the propulsive cont<strong>in</strong>uity between the<br />

two arms. In other words, there exists a challenge to explore <strong>in</strong>ter-arm<br />

coord<strong>in</strong>ation changes as a function of active drag, <strong>and</strong> to the question<br />

wether these changes relate to propell<strong>in</strong>g efficiency.<br />

Methods<br />

Thirteen national male front crawl swimmers (mean age: 21.5±3.9yr,<br />

mean height: 185.5±5.2cm, mean weight: 80.5±7.8kg, time on 100-m<br />

front crawl: 53.4±3.2, years of practice: 11.8±3.5) performed two <strong>in</strong>termittent<br />

graded speed tests <strong>in</strong> r<strong>and</strong>omised order, us<strong>in</strong>g an arms-only<br />

front crawl stroke (us<strong>in</strong>g a pull-buoy): one on the MAD-system (10<br />

bouts of 25-m) <strong>and</strong> one <strong>in</strong> the free swimm<strong>in</strong>g condition (8 bouts of<br />

25-m), from slow (~60%) to 100% of maximal speed (with an absolute<br />

<strong>in</strong>crement of 0.05 m·s-1 , which corresponded to a relative <strong>in</strong>crement of<br />

5% of maximal speed). The bout was self-paced to avoid the speed variations<br />

that can arise when the swimmer follows a target. To be sure that<br />

the normalized v (expressed <strong>in</strong> % of maximal speed) on the MADsystem<br />

<strong>and</strong> <strong>in</strong> free swimm<strong>in</strong>g condition were close for each bout, two<br />

more bouts were allowed on the MAD-system as this condition was<br />

uncommon for the swimmers. Four m<strong>in</strong>utes of rest were given before<br />

the next bout was swum.<br />

For the MAD-system condition, the swimmers swum by push<strong>in</strong>g<br />

off from fixed pads with each stroke. These push-off pads were attached<br />

to a 22-m rod <strong>and</strong> the distance between them was 1.35 m. The rod was<br />

mounted 0.8 m below the water surface <strong>and</strong> was connected to a force<br />

transducer, enabl<strong>in</strong>g direct measurement of push-off forces for each<br />

stroke. Assum<strong>in</strong>g a constant mean swimm<strong>in</strong>g speed, the mean propell<strong>in</strong>g<br />

force equals the mean drag force (D <strong>in</strong> N). Hence, swimm<strong>in</strong>g one<br />

bout on the system yields one data-po<strong>in</strong>t for the speed-drag curve. Follow<strong>in</strong>g<br />

the equation D = K • vn , the relationship between drag force <strong>and</strong><br />

speed was established for each swimmer <strong>and</strong> thus the <strong>in</strong>dividual K factor<br />

<strong>and</strong> n coefficient were determ<strong>in</strong>ed. Accord<strong>in</strong>g to Toussa<strong>in</strong>t et al. (2006),<br />

while swimmers swim on the MAD-system, propulsion is generated<br />

without wast<strong>in</strong>g k<strong>in</strong>etic energy (Pk =0) <strong>and</strong> consequently all Po of can be<br />

used to overcome drag. Thus, Po equals Pd . Know<strong>in</strong>g that, Pd = D • v2 ,<br />

Pd = K • v3 . If assumed that dur<strong>in</strong>g all-out 25-m spr<strong>in</strong>ts, Po was maximal<br />

<strong>and</strong>, equal on the MAD-system <strong>and</strong> <strong>in</strong> the free condition, propell<strong>in</strong>g<br />

efficiency (ep ) could be calculated as: ep = Pd / Po = K • v3 free / K • v3 MAD<br />

For the free swimm<strong>in</strong>g condition, two underwater video cameras<br />

filmed from frontal <strong>and</strong> side views at 50Hz. They were connected to<br />

a double-entry audio-visual mixer, a video timer, a video recorder <strong>and</strong><br />

a monitor<strong>in</strong>g screen to mix <strong>and</strong> genlock the frontal <strong>and</strong> lateral views<br />

on the same screen, from which the mean stroke rate was calculated. A<br />

third camera, mixed with the side view for time synchronisation, filmed<br />

all trials with a profile view from above the pool. This camera measured<br />

the time over the 12.5-m distance (from 10-m to 22.5-m) to obta<strong>in</strong> the<br />

velocity. Stroke length was calculated from the mean speed <strong>and</strong> stroke<br />

rate values. From the video device, three operators analysed the key<br />

po<strong>in</strong>ts of each arm phase with a bl<strong>in</strong>d technique, i.e. without know<strong>in</strong>g<br />

the analyses of the other two operators. Each arm stroke was broken<br />

<strong>in</strong>to four phases: entry <strong>and</strong> catch of the h<strong>and</strong> <strong>in</strong> the water, pull, push<br />

<strong>and</strong> recovery. The duration of the propulsive phases was the sum of pull<br />

<strong>and</strong> push phases <strong>and</strong> that of the non-propulsive phases was the sum of<br />

entry <strong>and</strong> recovery phases. Arm coord<strong>in</strong>ation was quantified us<strong>in</strong>g the<br />

<strong>in</strong>dex of coord<strong>in</strong>ation (IdC) as def<strong>in</strong>ed by Chollet et al. (2000). The IdC<br />

represented the lag time between the propulsive phases of each arm.<br />

The mean IdC, which was calculated from three complete strokes, was<br />

expressed as a percentage of the mean stroke duration. When there was<br />

a lag time between the propulsive phases of each arm, the stroke coord<strong>in</strong>ation<br />

was <strong>in</strong> “catch-up” (IdC0% corresponded to the “superposition”<br />

of the propulsive phases of both arms. Accord<strong>in</strong>g to Seifert <strong>and</strong> Chollet<br />

(2009) quadratic regression was calculated to model the relationships<br />

between IdC <strong>and</strong> speed.<br />

115


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Assum<strong>in</strong>g that dur<strong>in</strong>g all-out 25-m spr<strong>in</strong>ts, P o was maximal <strong>and</strong><br />

equal <strong>in</strong> the MAD- system <strong>and</strong> <strong>in</strong> the free condition, e p for each swimmer<br />

was calculated. Pearson correlation was assessed between e p <strong>and</strong> IdC<br />

for the maximal swimm<strong>in</strong>g condition. An ANOVA analysed the effect<br />

of bouts of 25-m on IdC <strong>and</strong> D. Quadratic regression between IdC <strong>and</strong><br />

v <strong>in</strong> the free condition <strong>and</strong> a power regression between D <strong>and</strong> v <strong>in</strong> the<br />

MAD-system condition were established for each swimmer; then, the<br />

average equation for the whole sample of swimmers were calculated. If<br />

assumed that dur<strong>in</strong>g all-out 25-m spr<strong>in</strong>ts, P o was maximal <strong>and</strong> equal<br />

both on the MAD-system <strong>and</strong> <strong>in</strong> the free condition, it was also assumed<br />

that the effort was equal when swimm<strong>in</strong>g bout 1 at 60% of maximal<br />

speed on the MAD-system <strong>and</strong> bout 1 at 60% of maximal speed <strong>in</strong><br />

the free condition (<strong>and</strong> so on for bout 2 at 65% of maximal speed, then<br />

bout 3 at 70% of maximal speed). Regressions between IdC <strong>and</strong> D were<br />

established for each swimmer, after which the average equation for the<br />

whole sample of swimmers was calculated. For all tests, the level of significance<br />

was set at 95% (p


On the other h<strong>and</strong>, the results showed that the whole sample of the<br />

13 swimmers <strong>in</strong>creased their IdC <strong>and</strong> active drag when speed <strong>in</strong>creased.<br />

The <strong>in</strong>ter-arm coord<strong>in</strong>ation switched from catch-up to superposition<br />

mode at a lower speed value than observed by Seifert et al. (2007b) because<br />

<strong>in</strong> the study, the swimmers swam arms only. The positive l<strong>in</strong>ear<br />

regression between IdC <strong>and</strong> active drag confirmed that the environmental<br />

constra<strong>in</strong>ts (aquatic resistances) led the swimmers to modify their<br />

arm coord<strong>in</strong>ation <strong>in</strong> order to overcome these aquatic resistances <strong>and</strong> to<br />

swim faster.<br />

conclusIon<br />

In national front crawl swimmers, <strong>in</strong>ter-arm coord<strong>in</strong>ation was not l<strong>in</strong>ked<br />

to e p <strong>in</strong> the conditions of the experiment. However, even if <strong>in</strong>ter-<strong>in</strong>dividual<br />

differences of IdC existed at maximal speed, the whole sample of<br />

the 13 swimmers changed their <strong>in</strong>ter-arm coord<strong>in</strong>ation the same way<br />

to adapt to the environmental constra<strong>in</strong>ts; notably, a significant positive<br />

relationship was found between IdC <strong>and</strong> active drag. Consequently, if a<br />

great IdC does not guarantee e p <strong>and</strong> high speed, high IdC, together with<br />

high power out-put <strong>and</strong> e p , was required to reach high swimm<strong>in</strong>g speed<br />

<strong>and</strong> thus overcome the associated active drag. These results suggest that<br />

power out-put <strong>and</strong> e p have to be taken <strong>in</strong> consideration to <strong>in</strong>terpret arm<br />

coord<strong>in</strong>ation’s appropriateness for tra<strong>in</strong><strong>in</strong>g purposes.<br />

reFerences<br />

Alberty M, Sidney M, Huot-March<strong>and</strong> F, Hespel JM, Pelayo P. (2005).<br />

Intracyclic velocity variations <strong>and</strong> arm coord<strong>in</strong>ation dur<strong>in</strong>g exhaustive<br />

exercise <strong>in</strong> front crawl stroke. Int J Sports Med, 26, 471-475.<br />

Alberty M, Sidney M, Pelayo P, Toussa<strong>in</strong>t HM. (2009). Strok<strong>in</strong>g characteristics<br />

dur<strong>in</strong>g time to exhaustion tests. Med Sci Sports Exerc, 41,<br />

637-644.<br />

Chollet D, Chalies S, Chatard JC. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: description <strong>and</strong> usefulness. Int J Sports Med, 21, 54-59.<br />

Seifert L, Chollet D. (2009). Modell<strong>in</strong>g spatial-temporal <strong>and</strong> coord<strong>in</strong>ative<br />

parameters <strong>in</strong> swimm<strong>in</strong>g. J Sci Med Sport, 12, 495-499.<br />

Seifert L, Chollet D, Chatard JC. (2007a). K<strong>in</strong>ematic Changes dur<strong>in</strong>g a<br />

100-m front crawl: effects of performance level <strong>and</strong> gender. Med Sci<br />

Sports Exerc, 39, 1784-1793.<br />

Seifert L, Chollet D, Rouard A. (2007b). Swimm<strong>in</strong>g constra<strong>in</strong>ts <strong>and</strong><br />

arm coord<strong>in</strong>ation. Hum Mov Sci, 26, 68-86.<br />

Toussa<strong>in</strong>t HM. (1990). Differences <strong>in</strong> propell<strong>in</strong>g efficiency between<br />

competitive <strong>and</strong> triathlon swimmers. Med Sci Sports Exerc, 22, 409-<br />

415.<br />

Toussa<strong>in</strong>t HM, Carol A, Kranenborg H, Truijens M. (2006). Effect of<br />

fatigue on strok<strong>in</strong>g characteristics <strong>in</strong> an arms-only 100-m front-crawl<br />

race. Med Sci Sports Exerc, 38, 1635-1642.<br />

Toussa<strong>in</strong>t HM, Janssen T, Kluft M. (1991). Effect of propell<strong>in</strong>g surface<br />

size on the mechanics <strong>and</strong> energetics of front crawl swimm<strong>in</strong>g. J<br />

Biomech, 24, 205-211.<br />

Modell<strong>in</strong>g Arm Coord<strong>in</strong>ation <strong>in</strong> Front Crawl<br />

seifert, l., chollet, d.<br />

chaPter2.<strong>Biomechanics</strong><br />

CETAPS EA 3832, Faculty of Sport Sciences, University of Rouen, France<br />

Arm coord<strong>in</strong>ation changes consistently from catch-up to superposition<br />

mode when speed is <strong>in</strong>creased. We modelled the relationships between<br />

the <strong>in</strong>dex of coord<strong>in</strong>ation (IdC) <strong>and</strong> speed (V). The subjects performed<br />

an <strong>in</strong>cremental speed test of 8 × 25-m steps. After check<strong>in</strong>g the change<br />

of arm coord<strong>in</strong>ation with speed, five models of regression were tested:<br />

power, logarithmic, exponential, l<strong>in</strong>ear <strong>and</strong> quadratic. The model was<br />

made by averag<strong>in</strong>g the <strong>in</strong>dividual coefficients; then the percent of error<br />

with the model was determ<strong>in</strong>ed for each swimmer. The quadratic<br />

modell<strong>in</strong>g (IdC =aV²+bV+c) showed the highest coefficient of determ<strong>in</strong>ation<br />

(0.81


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

to 22.5-m) to obta<strong>in</strong> the velocity. Stroke length was calculated from the<br />

mean speed <strong>and</strong> stroke rate values. From the video device, three operators<br />

analysed the key po<strong>in</strong>ts of each arm phase with a bl<strong>in</strong>d technique,<br />

i.e. without know<strong>in</strong>g the analyses of the other two operators. Each arm<br />

stroke was broken <strong>in</strong>to four phases: entry <strong>and</strong> catch of the h<strong>and</strong> <strong>in</strong> the<br />

water, pull, push <strong>and</strong> recovery. The duration of the propulsive phases<br />

was the sum of pull <strong>and</strong> push phases <strong>and</strong> that of the non-propulsive<br />

phases was the sum of the entry <strong>and</strong> recovery phases. Arm coord<strong>in</strong>ation<br />

was quantified us<strong>in</strong>g the <strong>in</strong>dex of coord<strong>in</strong>ation (IdC) def<strong>in</strong>ed by Chollet<br />

et al. (2000). The IdC represents the lag time between the propulsive<br />

phases of each arm. The mean IdC, which was calculated from three<br />

complete strokes, was expressed as a percentage of the mean stroke duration.<br />

When there was a lag time between the propulsive phases of each<br />

arm, the stroke coord<strong>in</strong>ation was <strong>in</strong> “catch-up” (IdC0% corresponded<br />

to the “superposition” of the propulsive phases of both arms.<br />

After check<strong>in</strong>g the change of arm coord<strong>in</strong>ation with speed by oneway<br />

ANOVA with repeated measures, five models of regression were<br />

tested: power, logarithmic, exponential, l<strong>in</strong>ear <strong>and</strong> quadratic. Know<strong>in</strong>g<br />

that -30%


Seifert L, Chollet D. (2009). Modell<strong>in</strong>g spatial-temporal <strong>and</strong> coord<strong>in</strong>ative<br />

parameters <strong>in</strong> swimm<strong>in</strong>g. J Sci Med Sport, 12: 495-499.<br />

Seifert L, Chollet D, Rouard A (2007). Swimm<strong>in</strong>g constra<strong>in</strong>ts <strong>and</strong> arm<br />

coord<strong>in</strong>ation. Hum Mov Sci, 26: 68-86.<br />

Toussa<strong>in</strong>t HM, Truijens M. (2005). Biomechanical aspects of peak performance<br />

<strong>in</strong> human swimm<strong>in</strong>g. Animal Biol, 55: 17-40.<br />

chaPter2.<strong>Biomechanics</strong><br />

Different Frequential Acceleration Spectrums <strong>in</strong><br />

Front Crawl<br />

Madera, J., González, l.M., García Massó, X., Benavent, J.,<br />

colado, J.c., tella, V.<br />

Universidad de Valencia, Valencia, España<br />

This study analyzed the three different frequency spectrums of acceleration<br />

that def<strong>in</strong>e the hip acceleration produced by front crawl swimmers<br />

dur<strong>in</strong>g a high-speed test. The swimmers (n=79) performed 25 meters<br />

at maximum speed. The acceleration (m·s -2 ) was obta<strong>in</strong>ed by the derivative<br />

analysis of the variation of the swimmer’s hip position<br />

with time. The amplitude <strong>in</strong> the time doma<strong>in</strong> was calculated with<br />

the root mean square; while the peak power, the peak power frequency<br />

<strong>and</strong> the spectrum area were calculated <strong>in</strong> the frequency<br />

doma<strong>in</strong> with Fourier analysis. Results showed that 27.85% of<br />

the swimmers have a front crawl frequential spectrum of type 1,<br />

30.38% of type 2 <strong>and</strong> 41.77% of type 3. Type 1 frequential spectrum<br />

showed more concentration as opposed to produc<strong>in</strong>g accelerations<br />

<strong>in</strong> front crawl <strong>and</strong> may be the cause of a better efficiency.<br />

Key words: Front crawl swimm<strong>in</strong>g, acceleration, spectrum types.<br />

IntroductIon<br />

From the biomechanical po<strong>in</strong>t of view, swimm<strong>in</strong>g performance depends<br />

on the mechanical <strong>in</strong>teraction between water <strong>and</strong> the dynamical actions<br />

of the swimmer’s body. From this <strong>in</strong>teraction arises a force opposition<br />

(i.e. propulsion vs drag) that is the source of the swimm<strong>in</strong>g velocity. All<br />

this orig<strong>in</strong>ates a succession of velocity fluctuations dur<strong>in</strong>g every swimm<strong>in</strong>g<br />

cycle (Miller, 1975). These <strong>in</strong>tra-cycle velocity variations have been<br />

studied to improve the swimm<strong>in</strong>g performance, consider<strong>in</strong>g spatialtemporal<br />

parameters (Alves et al., 1994; Holmer, 1979; Miyashita, 1971;<br />

Vilas-Boas, 1992 <strong>and</strong> 1996; Alberty et al., 2005; Tella et al. 2006).<br />

Most of the available literature is ma<strong>in</strong>ly concentrated on velocity<br />

analysis. However, the acceleration is the direct result of the force application<br />

that is <strong>in</strong>ferred <strong>in</strong> swimm<strong>in</strong>g. So, there will be major or m<strong>in</strong>or<br />

displacements of the swimmer depend<strong>in</strong>g on the forces magnitude<br />

(Reiwald & Bixler, 2001), be<strong>in</strong>g the most effective the forces that produce<br />

accelerations <strong>in</strong> the swimm<strong>in</strong>g direction (Bixler, 2005).<br />

With the aim of characteriz<strong>in</strong>g the forces applied <strong>in</strong> the front crawl<br />

stroke, Tella et al. (2008) analyzed the acceleration produced <strong>in</strong> the<br />

swimm<strong>in</strong>g direction, focus<strong>in</strong>g their analysis on both the time <strong>and</strong> frequency<br />

doma<strong>in</strong>s (i.e., the power spectrum analysis) of the swimmers’ hip<br />

acceleration. Accord<strong>in</strong>g to these results, the extent of the acceleration<br />

generated at specific frequencies may directly <strong>in</strong>fluence swimm<strong>in</strong>g efficiency.<br />

Also, this study presented three spectrum profiles <strong>in</strong> the frequeny<br />

doma<strong>in</strong> for front crawl swimm<strong>in</strong>g; one, two or more power peak (PP)<br />

spectrums.<br />

The ma<strong>in</strong> objective of this work was to identify the proportion of<br />

the aforementioned type of spectrums <strong>in</strong> a larger number of front crawl<br />

swimmers, <strong>and</strong> to analyze the differences of both temporal <strong>and</strong> frequency<br />

parameters. As a secondary objective, we related these parameters<br />

with performance.<br />

Methods<br />

After hav<strong>in</strong>g signed an <strong>in</strong>formed consent, all the procedures described<br />

<strong>in</strong> this study fulfilled the requirements listed <strong>in</strong> the Hels<strong>in</strong>ki Declaration<br />

of 1975 <strong>and</strong> its later amendment <strong>in</strong> October 2000, seventy-n<strong>in</strong>e<br />

regional <strong>and</strong> national front crawl swimmers (mean ± st<strong>and</strong>ard error of<br />

the mean (SEM) age 16.89±0.367 years; weight 63.172±1.3373; height<br />

172.54±1.142 cm) took part <strong>in</strong> the experiments. The swimmers neither<br />

suffered musculoskeletal pathologies nor restrictions, which may have<br />

h<strong>in</strong>dered their performance dur<strong>in</strong>g events.<br />

119


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

After a st<strong>and</strong>ard warm up (25-30 m<strong>in</strong>), swimmers performed a 25<br />

m front crawl at maximum speed with water start. A reproducibility test<br />

was performed for this protocol by tak<strong>in</strong>g two <strong>in</strong>dividual measurements<br />

with a 48-h <strong>in</strong>terval between them.<br />

<strong>Biomechanics</strong> Swimm<strong>in</strong>g acceleration <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> was <strong>in</strong> Swimm<strong>in</strong>g obta<strong>in</strong>ed <strong>XI</strong> from the Chapter position–time 2 <strong>Biomechanics</strong> data b<br />

recorded us<strong>in</strong>g a position transducer (SignalFrame, SportMetrics, Valencia,<br />

Spa<strong>in</strong>), record<strong>in</strong>g at 1 kHz. The position signal of the velocity<br />

was derived twice to obta<strong>in</strong> the correspond<strong>in</strong>g acceleration signal (m·s- 21<br />

2 ). METHODS The apparatus consisted <strong>in</strong> a resistive sensor (i.e. which produced a<br />

resistance After hav<strong>in</strong>g of 250 signed g) with an <strong>in</strong>formed a coiled cable consent, that all was the fastened procedures to the described swim- <strong>in</strong> this study<br />

fulfilled the requirements listed <strong>in</strong> the Hels<strong>in</strong>ki Declaration of 1975 <strong>and</strong> its later<br />

mers’ amendment waists at <strong>in</strong> the October height 2000, of second seventy-n<strong>in</strong>e <strong>and</strong> third regional lumbar <strong>and</strong> vertebrae national by front means crawl swimmers<br />

of (mean a belt. All ± st<strong>and</strong>ard the pre- <strong>and</strong> error post-test of the data mean were (SEM) registered age 16.89±0.367 <strong>and</strong> converted years; weight<br />

from 63.172±1.3373; analogical to height digital 172.54±1.142 (12-bit; DAQCard–700; cm) took part National <strong>in</strong> the experiments. Instrument, The swimmers<br />

Aust<strong>in</strong>, neither USA). suffered The musculoskeletal data were stored pathologies on a hard nor disk restrictions, for subsequent which analy- may have h<strong>in</strong>dered<br />

their performance dur<strong>in</strong>g events.<br />

ses. Synchronized After a st<strong>and</strong>ard to the warm position up (25-30 signal, m<strong>in</strong>), several swimmers full stroke performed cycles a 25 were m front crawl at<br />

recorded maximum us<strong>in</strong>g speed an with underwater water start. video A reproducibility camera, perpendicular test was performed to the swimfor<br />

this protocol<br />

mer’s by tak<strong>in</strong>g plane two of displacement <strong>in</strong>dividual measurements (the signal with was registered a 48-h <strong>in</strong>terval at 50 between Hz). them.<br />

To Swimm<strong>in</strong>g analyze the acceleration was signals, obta<strong>in</strong>ed a from specific the program position–time was data written recorded us<strong>in</strong>g a<br />

position transducer (SignalFrame, SportMetrics, Valencia, Spa<strong>in</strong>), record<strong>in</strong>g at 1 kHz.<br />

<strong>and</strong> run <strong>in</strong> Matlab 7.1 (R14) (Mathworks Inc., Natick, USA). The accel-<br />

The position signal of the velocity was derived twice to obta<strong>in</strong> the correspond<strong>in</strong>g<br />

eration acceleration signal was signal filtered (m·s to preserve only those frequencies of <strong>in</strong>terest<br />

for the study. A Butterworth fourth-order digital filter was used for this<br />

purpose with a b<strong>and</strong>-pass of 1–20 Hz. This signal was then analyzed <strong>in</strong><br />

both the time <strong>and</strong> frequency doma<strong>in</strong>s. Given the fact that the size of the<br />

acceleration is unstable <strong>in</strong> the first <strong>and</strong> f<strong>in</strong>al seconds for each swimm<strong>in</strong>g<br />

set, the eight central seconds were selected <strong>in</strong> each trial to analyze the<br />

acceleration signal (Caty et al., 2007). The signal amplitude was exam<strong>in</strong>ed<br />

<strong>in</strong> the time doma<strong>in</strong> with a root mean square (RMS), <strong>and</strong> processed<br />

<strong>in</strong> 100 ms-sized blocks. In the case of a set of n values {x1 ,x2 ,…,xn }, the<br />

RMS value is given by the follow<strong>in</strong>g formula:<br />

(1)<br />

The frequency spectrum amplitude was analyzed with the periodogram<br />

method (Pollock, 1999), which permits to discover the hidden frequencies<br />

<strong>in</strong> a signal. The periodogram considers all the frequencies <strong>and</strong> correlates<br />

each frequency with the data of the series <strong>in</strong> order to estimate<br />

the importance of a particular frequency <strong>in</strong> the series. It assigns to each<br />

frequency a value called <strong>in</strong>tensity of frequency denoted by:<br />

-2 ). The apparatus consisted <strong>in</strong> a resistive sensor (i.e. which<br />

produced a resistance of 250 g) with a coiled cable that was fastened to the swimmers’<br />

waists at the height of second <strong>and</strong> third lumbar vertebrae by means of a belt. All the pre<strong>and</strong><br />

post-test data were registered <strong>and</strong> converted from analogical to digital (12-bit;<br />

DAQCard–700; National Instrument, Aust<strong>in</strong>, USA). The data were stored on a hard<br />

disk for subsequent analyses. Synchronized to the position signal, several full stroke<br />

cycles were recorded us<strong>in</strong>g an underwater video camera, perpendicular to the<br />

swimmer’s plane of displacement (the signal was registered at 50 Hz).<br />

To analyze the acceleration signals, a specific program was written <strong>and</strong> run <strong>in</strong><br />

Matlab 7.1 (R14) (Mathworks Inc., Natick, USA). The acceleration signal was filtered<br />

to preserve only those frequencies of <strong>in</strong>terest for the study. A Butterworth fourth-order<br />

digital filter was used for this purpose with a b<strong>and</strong>-pass of 1–20 Hz. This signal was<br />

then analyzed <strong>in</strong> both the time <strong>and</strong> frequency doma<strong>in</strong>s. Given the fact that the size of<br />

the acceleration is unstable <strong>in</strong> the first <strong>and</strong> f<strong>in</strong>al seconds for each swimm<strong>in</strong>g set, the<br />

eight central seconds were selected <strong>in</strong> each trial to analyze the acceleration signal (Caty<br />

et al., 2007). The signal amplitude was exam<strong>in</strong>ed <strong>in</strong> the time doma<strong>in</strong> with a root mean<br />

square (RMS), <strong>and</strong> processed <strong>in</strong> 100 ms-sized blocks. In the case of a set of n values<br />

{x1,x2,…,xn}, the RMS value is given by the follow<strong>in</strong>g formula:<br />

(1)<br />

The frequency spectrum amplitude was analyzed with the periodogram method<br />

(Pollock, 1999), which permits to discover the hidden frequencies <strong>in</strong> a signal. The<br />

periodogram considers all the frequencies <strong>and</strong> correlates each frequency with the data of<br />

the series <strong>in</strong> order to estimate the importance of a particular frequency <strong>in</strong> the series. It<br />

assigns to each frequency a value called <strong>in</strong>tensity of frequency denoted by:<br />

I(w)=[a(w)] 2 + [b(w)] 2 performed through Bonferroni post- hoc tests, because of its control<br />

over the Type I error (error rate) <strong>and</strong> its strength when the number of<br />

comparisons is small. All differences with p


Table 2. Temporal values.<br />

Spectrum Type N Mean SEM p<br />

SF (cycles·m<strong>in</strong>-1 ) 1 22 53.24 0.99<br />

2 24 53.21 0.94<br />

3 33 53.21 0.74<br />

Total 79 53.22 0.50<br />

SL (m·cycle-1 ) 1 22 1.82 0.03<br />

2 24 1.69 0.04<br />

3 33 1.76 0.04<br />

Total 79 1.75 0.02<br />

V (m·s-1 1 22 1.61 0.03<br />

)<br />

2<br />

3<br />

24<br />

33<br />

1.49<br />

1.55<br />

0.03<br />

0.02<br />

Total 79 1.55 0.02<br />

*<br />

RMS (m·s-2 ) 1 22 6.44 0.41<br />

2 24 4.84 0.29<br />

3 33 5.56 0.30<br />

Total 79 5.59 0.20 **<br />

SF, stroke frequency; SL, stroke length, V, mean velocity;<br />

RMS, root square mean<br />

* p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

rate, distance per stroke, <strong>and</strong> velocity relationships dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g<br />

for competitive swimm<strong>in</strong>g. In Swimm<strong>in</strong>g Science III (edited by J.<br />

Terauds <strong>and</strong> E.W. Bed<strong>in</strong>gfield), pp. 265–274. University Park Press:<br />

Baltimore, MD: University Park Press.<br />

Counsilman, J.E. <strong>and</strong> Wasilak, J. (1982). The importance of h<strong>and</strong> speed<br />

<strong>and</strong> h<strong>and</strong> acceleration. In ASCA World Cl<strong>in</strong>ic Yearbook. American<br />

Swimm<strong>in</strong>g Coaches Association: Fort Lauderle.<br />

Holmer, I. (1979). Analysis of acceleration as a measure of swimm<strong>in</strong>g<br />

proficiency. In Swimm<strong>in</strong>g Science III. (edited by J. Terauds & E.W.<br />

Bed<strong>in</strong>gfield), pp 119-125. Baltimore, Maryl<strong>and</strong>: University Park<br />

Press.<br />

Miller, D. (1975). <strong>Biomechanics</strong> of swimm<strong>in</strong>g. Exercise of Sport Science<br />

Review, 3, 219-248.<br />

Miyashita M. (1971). An analysis of fluctuations of swimm<strong>in</strong>g speed.<br />

In Proceed<strong>in</strong>g of the First International Symposium on <strong>Biomechanics</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g, Waterpolo <strong>and</strong> Div<strong>in</strong>g. (edited by L. Lewillie & J.P. Clarys<br />

JP), pp 53-58. Bruxelles: Université Libre de Bruxelles.<br />

Pelayo, P., Sidney, M., Kherif, T., Chollet, D. <strong>and</strong> Tourny, C. (1996).<br />

Strok<strong>in</strong>g characteristics <strong>in</strong> freestyle swimm<strong>in</strong>g <strong>and</strong> relationships with<br />

anthropometric characteristics. Journal of Applied <strong>Biomechanics</strong>, 12,<br />

197–206.<br />

Pollock, D.G.S., 1999. A H<strong>and</strong>book of time-series Analysis Signal Process<strong>in</strong>g<br />

<strong>and</strong> Dynamics. Academic Press, London, pp. 399–425.<br />

Tella, V., Toca-Herrera, J.L., Gallach, J.E., Benavent, J., González, L.M.<br />

& Arellano R. (2008). Effect of fatigue on the <strong>in</strong>tra-cycle acceleration<br />

<strong>in</strong> front crawl swimm<strong>in</strong>g: A time-frequency analysis. Journal of<br />

<strong>Biomechanics</strong>, 41, 86-92.<br />

Vilas-Boas JP. (1992). A photo-optical method for acquisition of biomechanical<br />

data <strong>in</strong> swimmers. In X Symposium of the International<br />

Society of <strong>Biomechanics</strong> <strong>in</strong> Sports (edited by R. Ronado, G. Ferr<strong>in</strong>go &<br />

G. Santambrogio), pp 142-146. Milan: Ermes.<br />

Vilas-Boas JP. (1996). Speed fluctuations <strong>and</strong> energy cost of different<br />

breaststroke techniques. In <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g:<br />

Swimm<strong>in</strong>g Science VII. (edited by J.P. Troup, A.P. Holl<strong>and</strong>er, D. Strass,<br />

S.W. Trappe, J.M. Cappaert & T.A. Trappe), pp 167-171. London:<br />

E. & F. N. Spon.<br />

122<br />

The Glid<strong>in</strong>g Phase <strong>in</strong> Swimm<strong>in</strong>g: The Effect of Water<br />

Depth<br />

Mar<strong>in</strong>ho, d.A. 1,2 , Barbosa, t.M. 2,3 , Mantripragada, n. 2,4 , Vilas-<br />

Boas, J.P. 5,6 , rouard, A.h. 7 , Mantha, V.r. 2 , rouboa, A.I. 8 ,<br />

silva, A.J. 2,8<br />

1 University of Beira Interior, Covilhã, Portugal<br />

2 Research Centre <strong>in</strong> Sports, Health <strong>and</strong> Human Development, Vila Real,<br />

Portugal<br />

3 Polytechnic Institute of Bragança, Bragança, Portugal<br />

4 IIT Kharagpur, Mumbai, India<br />

5 University of Porto, Faculty of Sport, Porto, Portugal<br />

6 Research Centre of Education, Innovation <strong>and</strong> Intervention <strong>in</strong> Sports,<br />

Porto, Portugal<br />

7 University of Savoie, Chambery, France<br />

8 University of Trás-os-Montes <strong>and</strong> Alto Douro, Vila Real, Portugal<br />

The aim of this study was to analyse the effect of depth on drag dur<strong>in</strong>g<br />

the underwater glid<strong>in</strong>g. CFD simulations were applied to the flow<br />

around a 3D model of a male adult swimmer <strong>in</strong> a prone glid<strong>in</strong>g position<br />

with the arms extended at the front. The doma<strong>in</strong> to perform the simulations<br />

was created with 3.0 m depth, 3.0 m width <strong>and</strong> 11.0 m length.<br />

The drag coefficient <strong>and</strong> the hydrodynamic drag force were computed,<br />

us<strong>in</strong>g a steady flow velocity of 2.50 m/s for depths of 0.20, 0.50, 1.0,<br />

1.50, 2.0, 2.50 <strong>and</strong> 2.80 m. As the depth <strong>in</strong>creased, the drag coefficient<br />

<strong>and</strong> drag force decreased. The water depth seems to have a positive effect<br />

on reduc<strong>in</strong>g hydrodynamic drag dur<strong>in</strong>g the glid<strong>in</strong>g after starts <strong>and</strong><br />

turns, although a compromise between decreas<strong>in</strong>g drag (by <strong>in</strong>creas<strong>in</strong>g<br />

water depth) <strong>and</strong> glid<strong>in</strong>g travel distance should be a ma<strong>in</strong> concern of<br />

swimmers.<br />

Key words: cFd, hydrodynamics, simulations, human model<br />

IntroductIon<br />

Aim<strong>in</strong>g to achieve higher performances, swimmers should take full advantage<br />

of each component of swimm<strong>in</strong>g race to st<strong>and</strong> out <strong>in</strong> swimm<strong>in</strong>g<br />

competitions. Dur<strong>in</strong>g starts <strong>and</strong> turns, the glid<strong>in</strong>g phase represents a<br />

determ<strong>in</strong>ant race component. Dur<strong>in</strong>g the crucial glid<strong>in</strong>g phase, swimmers<br />

must m<strong>in</strong>imize the hydrodynamic drag force resist<strong>in</strong>g forward motion.<br />

The position adopted by the swimmers under the water represents<br />

an important concern <strong>and</strong> seems to determ<strong>in</strong>e the success of the start<br />

(Vilas-Boas et al., 2000). Another <strong>in</strong>terest<strong>in</strong>g <strong>and</strong> less studied issue is<br />

related to the ideal depth to perform this underwater glid<strong>in</strong>g. Vennel et<br />

al. (2006) showed that to avoid significant wave drag, a swimmer must<br />

be deeper than 1.8 chest depths <strong>and</strong> 2.8 chest depths below the surface<br />

for glid<strong>in</strong>g velocities of 0.90 m/s <strong>and</strong> 2.0 m/s, respectively, which<br />

corresponds to water depths of 0.45 m <strong>and</strong> 0.70 m, respectively, for a<br />

swimmer with 0.25 m of chest depth. Lyttle et al. (1999) also showed<br />

that there is no significant wave drag when a typical adult swimmer is<br />

at least 0.60 m under the water surface. In both studies, at water depths<br />

higher than these values, hydrodynamic drag was almost constant, depend<strong>in</strong>g<br />

only on viscous <strong>and</strong> form drag. However, one can notice that<br />

new swimm<strong>in</strong>g pools attempted to <strong>in</strong>corporate some key elements that<br />

characterize a “fast swimm<strong>in</strong>g pool”, as the Beij<strong>in</strong>g 2008 swimm<strong>in</strong>g pool<br />

(The Beij<strong>in</strong>g Bubble Build<strong>in</strong>g, “The Ice Cube”), with its 3.0 m depth, is<br />

a good example. Additionally, one can also observe some elite swimmers<br />

perform<strong>in</strong>g this underwater glid<strong>in</strong>g at higher depths. Thus, us<strong>in</strong>g computational<br />

fluid dynamics methodology one can compute the hydrodynamic<br />

drag when glid<strong>in</strong>g at different water depths (Bixler et al., 2007).<br />

Hence, the aim of this study was to analyse the effect of depth on drag<br />

dur<strong>in</strong>g the underwater glid<strong>in</strong>g <strong>in</strong> a swimm<strong>in</strong>g pool of 3.0 m depth, us<strong>in</strong>g<br />

computational fluid dynamics.


Methods<br />

To obta<strong>in</strong> the geometry of a male human body, a model was created<br />

through computer tomography scans techniques (Mar<strong>in</strong>ho et al., 2010).<br />

The surfaces of the swimmer were then developed us<strong>in</strong>g ANSYS-FLU-<br />

ENT 6.3 pre-processor GAMBIT, (Ansys Inc ® . Canonsburg, USA). The<br />

entire computational doma<strong>in</strong> was volume meshed <strong>and</strong> solved through<br />

FLUENT solver.<br />

The three-dimensional computational doma<strong>in</strong> represent<strong>in</strong>g a part<br />

of swimm<strong>in</strong>g pool was about 3.0 m <strong>in</strong> depth, 3.0 m wide <strong>and</strong> 11.0 m <strong>in</strong><br />

length. The entire computational doma<strong>in</strong> consisted of 900 millions cells<br />

of hybrid mesh composed of prisms <strong>and</strong> pyramids.<br />

Computational fluid dynamics simulations were carried out to simulate<br />

the flow around a three-dimensional model of a male adult swimmer<br />

<strong>in</strong> a prone glid<strong>in</strong>g position with the arms extended at the front<br />

(Mar<strong>in</strong>ho et al., 2009). General Mov<strong>in</strong>g Object (GMO) model was<br />

used to model the body as the mov<strong>in</strong>g object. Dur<strong>in</strong>g the glid<strong>in</strong>g, the<br />

swimmer model’s horizontal axis l<strong>in</strong>e runn<strong>in</strong>g lengthwise was placed at<br />

different water depths viz., (i) 0.20 m (just under the surface), (ii) 0.50<br />

m, (iii) 1.0 m, (iv) 1.50 m (middle of the pool), (v) 2.0 m, (vi) 2.50 m <strong>and</strong>,<br />

(vii) 2.80 m (bottom of the pool), respectively. The drag coefficient <strong>and</strong><br />

the hydrodynamic drag force were computed us<strong>in</strong>g a steady flow velocity<br />

of 2.5 m/s for the different depths <strong>in</strong> each case.<br />

results<br />

Table 1 presents the drag coefficient <strong>and</strong> the drag force values when<br />

glid<strong>in</strong>g at a water depth of 0.20 m, 0.50 m, 1.0 m, 1.50 m, 2.0 m, 2.50<br />

m <strong>and</strong> 2.80 m. These values were computed at the time of 2 seconds<br />

when the swimmer was approximately at the middle of the computational<br />

pool.<br />

It was observed that, both drag coefficient <strong>and</strong> drag force values fall with<br />

<strong>in</strong>crease <strong>in</strong> depth of swimm<strong>in</strong>g tank, which swimmer model is chosen<br />

for simulation of glid<strong>in</strong>g.<br />

Table 1. Drag coefficient <strong>and</strong> drag force values for different water depths<br />

dur<strong>in</strong>g glid<strong>in</strong>g at the time of 2 seconds.<br />

Water depths (m) Drag coefficient Drag force (N)<br />

0.20 0.67 100.20<br />

0.50 0.62 92.30<br />

1.00 0.53 80.50<br />

1.50 0.44 65.40<br />

2.00 0.36 53.40<br />

2.50 0.30 44.70<br />

2.80 0.28 42.00<br />

dIscussIon<br />

The aim of this study was to analyse the effect of depth on drag dur<strong>in</strong>g<br />

the underwater glid<strong>in</strong>g, us<strong>in</strong>g computational fluid dynamics. It was noticed<br />

that hydrodynamic drag decreased with depth <strong>in</strong>crease, present<strong>in</strong>g<br />

the lowest hydrodynamic drag values near the bottom of the computational<br />

swimm<strong>in</strong>g pool (water depth of 2.80 m).<br />

Computational fluid dynamics methodology has been shown to be a<br />

reliable tool to exam<strong>in</strong>e the water flow around a submerged human body<br />

model (Bixler et al., 2007). Thus, an attempt was performed to analyse<br />

the hydrodynamic drag dur<strong>in</strong>g the underwater glid<strong>in</strong>g, simulat<strong>in</strong>g a<br />

swimm<strong>in</strong>g pool with 3.0 m depth <strong>and</strong> to verify if drag values rema<strong>in</strong>ed<br />

constant at depths higher than a critical po<strong>in</strong>t, beyond which wave drag<br />

seems to be almost null (Lyttle et al., 1999; Vennel et al., 2006).<br />

The water depth seems to have a positive effect on reduc<strong>in</strong>g hydrodynamic<br />

drag dur<strong>in</strong>g the glid<strong>in</strong>g. Moreover, glid<strong>in</strong>g near the bottom of<br />

the pool also presented lower drag values compared to glid<strong>in</strong>g at a water<br />

chaPter2.<strong>Biomechanics</strong><br />

depth, for <strong>in</strong>stance, <strong>in</strong> the middle of the swimm<strong>in</strong>g pool. This f<strong>in</strong>d<strong>in</strong>g<br />

could suggest that the positive effects of water depth are more powerful<br />

than the possible negative hydrodynamic effects of turbulence near the<br />

bottom of the pool, expected when the simulations are not carried-out<br />

with a mov<strong>in</strong>g model. In fact, one of the <strong>in</strong>novations of this study was<br />

the possibility to carry-out the simulations <strong>and</strong> the drag analysis with<br />

a mov<strong>in</strong>g human body, as performed by Lecriva<strong>in</strong> et al. (2008) <strong>in</strong> the<br />

analysis of the upper arm propulsion.<br />

The values found <strong>in</strong> this study, concern<strong>in</strong>g hydrodynamic drag, were<br />

very similar to others presented <strong>in</strong> CFD studies (e.g., Bixler et al., 2007;<br />

Mar<strong>in</strong>ho et al., 2009), us<strong>in</strong>g similar velocities <strong>and</strong> similar water depths.<br />

Nevertheless, <strong>in</strong> opposition to what occurred <strong>in</strong> the studies of Lyttle et<br />

al. (1999) <strong>and</strong> Vennel et al. (2006), hydrodynamic drag decreased with<br />

depth, <strong>in</strong> the entire range of depths computed <strong>in</strong> FLUENT 6.3 (0.20<br />

m to 2.80 m). These differences signify an <strong>in</strong>terest<strong>in</strong>g aspect for future<br />

<strong>in</strong>vestigation <strong>and</strong> to further analysis with computational fluid dynamics<br />

simulations. However, one can attribute these differences between the<br />

experimental analysis <strong>and</strong> computational fluid dynamics could be one of<br />

the reasons not to f<strong>in</strong>d good match of data. Indeed, although significant<br />

improvements on computational fluid dynamics simulations, it raises the<br />

question, whereas this methodology truly represents the real swimm<strong>in</strong>g<br />

conditions. In this paper, a significant effort was performed to dim<strong>in</strong>ish<br />

this difference, us<strong>in</strong>g a mov<strong>in</strong>g human body. We believe this approach<br />

could lead to obta<strong>in</strong> more accurate results. In the future, it should be<br />

also attempted to perform the same analysis with the swimmer kick<strong>in</strong>g<br />

(underwater dolph<strong>in</strong> kick<strong>in</strong>g), s<strong>in</strong>ce the time when the swimmer is<br />

passively glid<strong>in</strong>g is very short compar<strong>in</strong>g with the total underwater distance.<br />

Moreover, active drag can be significantly different from passive<br />

drag values (Kjendlie & Stallman, 2008), thus generaliz<strong>in</strong>g these data to<br />

the underwater dolph<strong>in</strong> kick<strong>in</strong>g should be made with careful.<br />

conclusIons<br />

Reduc<strong>in</strong>g the drag experienced by swimmers dur<strong>in</strong>g the glide of the<br />

wall can enhance start <strong>and</strong> turn performances. Therefore, a compromise<br />

between decreas<strong>in</strong>g drag (by <strong>in</strong>creas<strong>in</strong>g swimmer’s deepness from<br />

water surface) <strong>and</strong> glid<strong>in</strong>g travel distance should be a ma<strong>in</strong> concern of<br />

swimmers <strong>and</strong> an important goal to be studied <strong>in</strong> future <strong>in</strong>vestigations.<br />

Although <strong>in</strong>creas<strong>in</strong>g depth position could contribute to decrease drag<br />

force, this reduction seems to be lower with depth, especially after 2.0 m<br />

depth, thus suggest<strong>in</strong>g that possibly perform<strong>in</strong>g the underwater glid<strong>in</strong>g<br />

(<strong>and</strong> the underwater dolph<strong>in</strong> kick<strong>in</strong>g) more than 2.0 m depth could not<br />

be ga<strong>in</strong>ful for the swimmer.<br />

reFerences<br />

Bixler, B., Pease, D., & Fairhurst, F. (2007). The accuracy of computational<br />

fluid dynamics analysis of the passive drag of a male swimmer.<br />

Sports <strong>Biomechanics</strong>, 6, 81-98.<br />

Kjendlie, P.L., & Stallman, R. (2008). Drag characteristics of competitive<br />

swimm<strong>in</strong>g children <strong>and</strong> Adults. Journal of Applied <strong>Biomechanics</strong>,<br />

24, 35-42.<br />

Lecriva<strong>in</strong>, G., Slaouti, A., Payton, C., & Kennedy, I. (2008). Us<strong>in</strong>g reverse<br />

eng<strong>in</strong>eer<strong>in</strong>g <strong>and</strong> computational fluid dynamics to <strong>in</strong>vestigate a<br />

lower arm amputee swimmer’s performance. Journal of <strong>Biomechanics</strong>,<br />

41, 2855-2859.<br />

Lyttle, A.D., Blanksby, B.A., Elliott, B.C., & Lloyd, D.G. (1999). Optimal<br />

depth for streaml<strong>in</strong>ed glid<strong>in</strong>g. In K.L. Kesk<strong>in</strong>en, P.V. Komi, &<br />

A.P. Holl<strong>and</strong>er (Eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII<br />

(pp. 165-170). Jyvaskyla: Gummerus Pr<strong>in</strong>t<strong>in</strong>g.<br />

Mar<strong>in</strong>ho, D.A., Reis, V.M., Alves, F.B., Vilas-Boas, J.P., Machado, L.,<br />

Silva, AJ, et al. (2009). The hydrodynamic drag dur<strong>in</strong>g glid<strong>in</strong>g <strong>in</strong><br />

swimm<strong>in</strong>g. Journal of Applied <strong>Biomechanics</strong>, 25, 253-257.<br />

Mar<strong>in</strong>ho, D.A., Reis, V.M., Vilas-Boas, J.P., Alves, F.B., Machado, L.,<br />

Rouboa, A.I., et al. (2010). Design of a three-dimensional h<strong>and</strong>/<br />

forearm model to apply Computational Fluid Dynamics. Brazilian<br />

Archives of Biology <strong>and</strong> Technology (<strong>in</strong> press).<br />

123


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Vennel, R., Pease, D., & Wilson, B. (2006). Wave drag on human swimmers.<br />

Journal of <strong>Biomechanics</strong>, 39, 664-671.<br />

Vilas-Boas, J.P., Cruz, M.J., Sousa, F., Conceição, F., & Carvalho, J.M.<br />

(2000). Integrated k<strong>in</strong>ematic <strong>and</strong> dynamic analysis of two track-start<br />

techniques. In R. S<strong>and</strong>ers, & Y. Hong (Eds.), Proceed<strong>in</strong>gs of the XVIII<br />

International Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports, Applied Program –<br />

Application of Biomechanical Study <strong>in</strong> Swimm<strong>in</strong>g (pp.113-117). Hong<br />

Kong: The Ch<strong>in</strong>ese University Press.<br />

AcKnoWledGeMents<br />

This work was supported by the Portuguese Government by Grants of<br />

FCT (PTDC/DES/098532/2008).<br />

124<br />

A Method to Estimate Active Drag over a Range of<br />

Swimm<strong>in</strong>g Velocities which may be used to Evaluate<br />

the Stroke Mechanics of the Swimmer<br />

Mason, B.r. 1 , Formosa, d.P. 1 , toussa<strong>in</strong>t, h.M. 2<br />

1 Australian Institute of Sport, Australia<br />

2 Innosport, The Netherl<strong>and</strong>s<br />

This research project aimed to estimate values of active drag over a range<br />

of swimm<strong>in</strong>g velocities. The data required to do this was the passive drag<br />

values for the swimmer at various swim velocities, together with the active<br />

drag force value for the <strong>in</strong>dividual at their maximum swim velocity. The<br />

( b⋅V<br />

)<br />

drag force is represented by an exponential equation F = a ⋅ e , where<br />

a <strong>and</strong> b are constants for a particular swimmer. The constant a p (passive)<br />

reflects the more <strong>in</strong>nate characteristics of the <strong>in</strong>dividual swimmer<br />

<strong>and</strong> their suitability to aquatics motion. The constant aa− p (active- passive)<br />

reflects the efficiency of the swimmer’s technique. In both cases, the<br />

lower the constant’s value, the better suited the swimmer is to aquatics<br />

motion or to technical efficiency. The aa− p <strong>and</strong> the a p provide an<br />

<strong>in</strong>dex to evaluate a swimmer’s capabilities.<br />

Keywords: <strong>Biomechanics</strong>, swimm<strong>in</strong>g, active drag, passive drag, stroke<br />

mechanics<br />

IntroductIon<br />

A swimmer’s ability to swim faster is depended upon an <strong>in</strong>crease of propulsive<br />

force, which exceeds the drag force presently act<strong>in</strong>g on the swimmer’s<br />

motion. However, active drag <strong>in</strong>creases exponentially with a progressive<br />

<strong>in</strong>crease <strong>in</strong> the swimmer’s mean velocity. When the active drag<br />

<strong>and</strong> mean maximal propulsive force generated by the swimmer reach<br />

equilibrium, the swimmer atta<strong>in</strong>s their mean maximum swim velocity.<br />

However, at any constant swim velocity, mean active drag is equal <strong>in</strong><br />

magnitude to the mean propulsive force exerted by the swimmer. Know<strong>in</strong>g<br />

the magnitude of the mean active drag oppos<strong>in</strong>g the forward motion<br />

provides <strong>in</strong>formation that may be used to evaluate the swimmer’s mean<br />

propulsive force.<br />

Initially it was thought that tethered swimm<strong>in</strong>g would provide a<br />

reasonable measure of the swimmer’s propulsion. Researchers have discounted<br />

this theory (Mason et al, 2009a). The MAD system developed <strong>in</strong><br />

the Netherl<strong>and</strong>s provided a measure of active drag at different velocities<br />

(Toussa<strong>in</strong>t et al, 2004). However, researchers have questioned whether the<br />

swimm<strong>in</strong>g actions us<strong>in</strong>g the MAD system represent swimm<strong>in</strong>g propulsive<br />

technique. The major challenge researchers faced was the ability to<br />

measure total propulsive force generated by the swimmer dur<strong>in</strong>g the free<br />

swim phase. Therefore, methods were developed to estimate the swimmers’<br />

mean propulsive force. The Velocity Perturbation Method provided<br />

a value for active drag, however only at the swimmer’s maximum velocity<br />

(Kolmogorov & Duplishcheva, 1992). Similarly, a method developed at<br />

the Australian Institute of Sport also identified the magnitude of active<br />

drag at maximum swim velocity (Formosa et al., 2009). Both these methods<br />

used to evaluate active drag were dependent upon the assumption that<br />

the swimmer applied equal power while swimm<strong>in</strong>g at their maximum velocity<br />

dur<strong>in</strong>g the free swim <strong>and</strong> assisted/resisted conditions. Passive drag is<br />

measured at various velocities by tow<strong>in</strong>g the swimmer <strong>in</strong> a streaml<strong>in</strong>e position.<br />

Researchers have identified that the measurement of passive drag<br />

was highly correlated to that of active drag at the swimmer’s maximum<br />

velocity (Mason et al, 2009b). This high relationship between active <strong>and</strong><br />

passive drag justified the procedures used <strong>in</strong> this present research project.<br />

The aim of this study was to develop a method to estimate the active drag<br />

of the swimmer over a full range of swimm<strong>in</strong>g velocities. The method<br />

developed relied upon hav<strong>in</strong>g mean passive drag measures of the swimmer<br />

over a range of velocities, as well as the mean active drag of the swimmer<br />

at the swimmer’s maximum swim velocity.


Methods<br />

Eleven Australian (2 male; 9 female) national freestyle swimmers participated<br />

<strong>in</strong> the study. Seven were members of the Australian swimm<strong>in</strong>g team<br />

at the Beij<strong>in</strong>g Olympics.<br />

Each of the subjects completed all the tests required <strong>in</strong> a s<strong>in</strong>gle <strong>in</strong>dividual<br />

test<strong>in</strong>g session. The subjects were given sufficient rest between test<br />

trials so that fatigue would not be an issue. Firstly, subjects completed three<br />

maximum velocity trials over a 10 m <strong>in</strong>terval, start<strong>in</strong>g from 25 m out <strong>and</strong><br />

the velocity was measured from 15 m to 5 m out from the wall. The velocity<br />

was determ<strong>in</strong>ed us<strong>in</strong>g video cameras with a resolution of 0.02 s. The fastest<br />

trial was utilised to determ<strong>in</strong>e the subject’s maximum swim velocity.<br />

The equipment used <strong>in</strong> the active <strong>and</strong> passive drag test<strong>in</strong>g consisted<br />

of a motorised tow<strong>in</strong>g device that could tow a swimmer over a range of<br />

constant velocities. The tow<strong>in</strong>g device was mounted on a Kistler force TM<br />

platform which enabled the force required to tow the subject to be monitored.<br />

The eight component force signals from the force platform were<br />

captured by computer at a 500 Hz sampl<strong>in</strong>g rate. Only the Y component<br />

was utilized <strong>and</strong> was smoothed with a 5 Hz low pass digital filter. Four<br />

complete stroke cycles were captured for analysis <strong>and</strong> extra data on either<br />

side of these strokes was also collected to allow for smooth<strong>in</strong>g. The velocity<br />

of the tow<strong>in</strong>g device was also monitored for accuracy with the video<br />

camera system.<br />

In the passive drag test<strong>in</strong>g the tow rope was attached to the swimmer<br />

by way of a loop through which the subject’s f<strong>in</strong>gers could grasp. Follow<strong>in</strong>g<br />

passive drag familiarization, three passive drag trials were completed<br />

at the subject’s constant maximum swim velocity <strong>and</strong> the mean tow force<br />

value from the three trials used. The subject was towed through the water<br />

ensur<strong>in</strong>g a shallow lam<strong>in</strong>ar flow over the body. A series of passive drag trials<br />

was next completed over a range of 10 different tow velocities from 2.2<br />

to 1.0 m·s -1. Only a s<strong>in</strong>gle trial was completed for each velocity.<br />

F<strong>in</strong>ally, <strong>in</strong> the active drag test<strong>in</strong>g the rope was attached to a belt<br />

around the swimmer’s waist. The five active drag trials were completed at a<br />

five percent greater velocity than the swimmer’s maximum swim velocity<br />

to ensure a force was always applied by the tow<strong>in</strong>g device. The swimmers<br />

were <strong>in</strong>structed to swim at maximum effort for each of the trials. The<br />

detailed equations used to determ<strong>in</strong>e active drag from the recorded tow<strong>in</strong>g<br />

force that represented active drag at the swimmer’s maximum velocity<br />

are described <strong>in</strong> previous articles by the researchers (Formosa et al, 2009).<br />

The mean of the middle three values was used as the value for active drag.<br />

results<br />

The exponential function used to determ<strong>in</strong>e the passive drag equations<br />

( b⋅V<br />

)<br />

was <strong>Biomechanics</strong> as <strong>in</strong>dicated. <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> F = <strong>in</strong> aSwimm<strong>in</strong>g<br />

⋅ e where <strong>XI</strong> Chapter a <strong>and</strong> 2 <strong>Biomechanics</strong> b are constants b for 33 a<br />

particular swimmer.<br />

The first step to create the equation was to plot the curve for passive<br />

The exponential function used to determ<strong>in</strong>e the passive drag equations was as <strong>in</strong>dicated.<br />

drag <strong>and</strong> ( b⋅Vobta<strong>in</strong><br />

) LN (logarithmic value to the base e) values for pas-<br />

F = a ⋅ e where a<strong>and</strong> b are constants for a particular swimmer.<br />

sive The drag. first step The to create processes the equation for was subject to plot 7 the are curve displayed for passive <strong>and</strong> drag <strong>and</strong> illustrate obta<strong>in</strong> LN the<br />

(logarithmic value to the base e) values for passive drag. The processes for subject 7<br />

procedures used.<br />

are displayed <strong>and</strong> illustrate the procedures used.<br />

Tow<br />

Velocity<br />

(m·s -1 )<br />

Raw<br />

Passive<br />

drag<br />

(N)<br />

Raw<br />

LN<br />

(Passive<br />

Drag)<br />

2.2 128.43 4.855<br />

2.1 108.79 4.689<br />

2 95.88 4.563<br />

1.9 80.64 4.390<br />

1.81 69 4.234<br />

1.8 69.95 4.248<br />

1.7 60.22 4.098<br />

1.6 50.1 3.914<br />

1.5 40.5 3.701<br />

1.3 34.29 3.535<br />

1.1 23.88 3.173<br />

P a s s iv e D r a g ( N )<br />

140<br />

120<br />

100<br />

80<br />

60<br />

40<br />

20<br />

1 1.2 1.4 1.6 1.8 2 2.2 2.4<br />

Velocity (m.s -1 )<br />

The next stage <strong>in</strong> the process was to f<strong>in</strong>d a l<strong>in</strong>ear trend l<strong>in</strong>e for the graph of LN(drag)<br />

aga<strong>in</strong>st time <strong>and</strong> the equation that represented that trend l<strong>in</strong>e. The smoothed passive<br />

drag values could then be computed as EXP ( 1.<br />

524 ⋅Velocity + 1.<br />

4936)<br />

Tow<br />

Velocity<br />

(m·s -1 Smoothed Smoothed<br />

LN(Pass Pass Drag<br />

Establish trend l<strong>in</strong>e for LN (Drag)<br />

) drag) (N)<br />

2.2 4.85 127.28<br />

2.1 4.69 109.29<br />

2 4.54 93.84<br />

y = 1.524x + 1.4936<br />

1.9 4.39 80.58<br />

R<br />

1.8 4.25 70.25<br />

1.8 4.24 69.19<br />

1.7 4.08 59.41<br />

2 5<br />

4.8<br />

EXP(<br />

1.<br />

524 ⋅Velocity + 1.<br />

4936 4.6 )<br />

4.4<br />

4.2<br />

4<br />

3.8<br />

= 0.9957<br />

3.6<br />

3.4<br />

3.2<br />

3<br />

The next stage <strong>in</strong> the process was to f<strong>in</strong>d a l<strong>in</strong>ear trend l<strong>in</strong>e for the<br />

graph of LN(drag) aga<strong>in</strong>st time <strong>and</strong> the equation that represented that<br />

trend l<strong>in</strong>e. The smoothed passive drag values could then be computed as<br />

L N (D r a g )<br />

1.6 50.1 3.914<br />

1.5 40.5 3.701<br />

1.3 34.29 3.535<br />

1.1 23.88 3.173<br />

40<br />

20<br />

1 1.2 1.4 1.6 1.8 2 2.2 2.4<br />

chaPter2.<strong>Biomechanics</strong><br />

Velocity (m.s -1 )<br />

The next stage <strong>in</strong> the process was to f<strong>in</strong>d a l<strong>in</strong>ear trend l<strong>in</strong>e for the graph of LN(drag)<br />

aga<strong>in</strong>st time <strong>and</strong> the equation that represented that trend l<strong>in</strong>e. The smoothed passive<br />

drag values could then be computed as EXP ( 1.<br />

524 ⋅Velocity + 1.<br />

4936)<br />

Tow<br />

Velocity<br />

(m·s -1 Smoothed Smoothed<br />

LN(Pass Pass Drag<br />

) drag) (N)<br />

Establish trend l<strong>in</strong>e for LN (Drag)<br />

2.2 4.85 127.28<br />

2.1<br />

2<br />

1.9<br />

1.8<br />

1.8<br />

1.7<br />

1.6<br />

1.5<br />

1.3<br />

4.69<br />

4.54<br />

4.39<br />

4.25<br />

4.24<br />

4.08<br />

3.93<br />

3.78<br />

3.47<br />

109.29<br />

93.84<br />

80.58<br />

70.25<br />

69.19<br />

59.41<br />

51.01<br />

43.80<br />

32.29<br />

y = 1.524x + 1.4936<br />

R<br />

1.1 3.17 23.81<br />

The smoothed curve of passive drag aga<strong>in</strong>st velocity was then able to be plotted <strong>and</strong> the<br />

exponential equation for passive drag determ<strong>in</strong>ed.<br />

( b⋅V<br />

)<br />

F = a ⋅ e<br />

a = EXP(<br />

1.<br />

4936)<br />

= 4.<br />

454<br />

b = 1.<br />

524<br />

2 5<br />

4.8<br />

4.6<br />

4.4<br />

4.2<br />

4<br />

3.8<br />

3.6<br />

3.4<br />

3.2<br />

3<br />

1 1.2<br />

= 0.9957<br />

1.4 1.6 1.8 2 2.2<br />

Velocity (m.s<br />

2.4<br />

-1 )<br />

The smoothed curve of passive drag aga<strong>in</strong>st velocity was then able to be<br />

plotted <strong>and</strong> the exponential equation for passive drag determ<strong>in</strong>ed.<br />

( b⋅V<br />

)<br />

F = a ⋅ e<br />

a = EXP(<br />

1.<br />

4936)<br />

=<br />

b = 1.<br />

524<br />

Tow Velocity<br />

(m·s -1 )<br />

4.<br />

454<br />

L N (D r a g )<br />

Smoothed LN(Pass<br />

drag)<br />

Smoothed<br />

Pass Drag<br />

(N)<br />

2.2 4.85 127.28<br />

2.1 4.69 109.29<br />

2 4.54 93.84<br />

1.9 4.39 80.58<br />

1.8 4.25 70.25<br />

1.8 4.24 69.19<br />

1.7 4.08 59.41<br />

1.6 3.93 51.01<br />

1.5 3.78 43.80<br />

1.3 3.47 32.29<br />

1.1 3.17 23.81<br />

Tow Vel<br />

(m·s -1 )<br />

Smoothed Passive Drag<br />

(N)<br />

2.2 127.31<br />

2.1 109.31<br />

2 93.86<br />

1.9 80.59<br />

1.8 69.20<br />

1.7 59.42<br />

1.6 51.02<br />

1.5 43.81<br />

1.4 37.61<br />

1.2 27.73<br />

1.1 23.81<br />

0.8 15.07<br />

125


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The variable for the active drag equation could then be computed<br />

through substitution know<strong>in</strong>g the one value for active drag at the swimmer’s<br />

maximum swim velocity.<br />

126<br />

where 210 N = active drag at 1.81 m·s -1<br />

Drag (N)<br />

Velocity (m·s -1 ) Passive (N) Active (N)<br />

250<br />

200<br />

150<br />

100<br />

50<br />

0<br />

2.2 127.31 380.49<br />

2.1 109.31 326.71<br />

2 93.86 280.53<br />

1.9 80.59 240.87<br />

1.8 69.20 206.82<br />

1.7 59.42 177.59<br />

1.6 51.02 152.49<br />

1.5 43.81 130.93<br />

1.4 37.61 112.42<br />

1.2 27.73 82.89<br />

1.1 23.81 71.17<br />

0.8 15.07 45.05<br />

Drag vs Velocity<br />

Passive Active Difference<br />

0.6 0.8 1 1.2 1.4 1.6 1.8 2<br />

Velocity (m.s -1 )<br />

where b used for active <strong>and</strong> passive drag<br />

F = a ⋅e<br />

bv<br />

a = F / e<br />

bv<br />

b = 1.<br />

524<br />

= 210/<br />

e<br />

( 1.<br />

524×<br />

1.<br />

81 )<br />

= 13<br />

. 31204<br />

Table 1: Characteristics of each swimmer, together with the constants<br />

used to derive the active <strong>and</strong> passive drag equations. a a is the constant<br />

for active drag, p a is the constant for passive drag <strong>and</strong> aa− p is the<br />

constant for the difference between active <strong>and</strong> passive drag. b is a constant<br />

represent<strong>in</strong>g a swimmer’s overall drag.<br />

Subject Gender Event (m) R2 Trend<br />

p aa aa− p<br />

1 M 200 0.9921 8.01 1.21 19.97 11.96<br />

2 F 200 0.9702 3.91 1.59 18.68 14.78<br />

3 F 200 0.9944 3.81 1.48 18.92 15.11<br />

4 F 100 0.9831 5.21 1.29 22.97 17.77<br />

5 F 100 0.9779 5.60 1.28 22.12 16.52<br />

6 F 400 0.9718 5.99 1.29 14.63 8.64<br />

7 M 200 0.9957 4.45 1.52 13.31 8.86<br />

8 F 200 0.9859 4.84 1.45 11.42 6.59<br />

9 F 100 0.9768 6.43 1.21 19.85 13.41<br />

10 F 200 0.9819 4.91 1.36 24.57 19.67<br />

11 F 200 0.9879 6.07 1.31 15.83 9.76<br />

a b<br />

dIscussIon<br />

In both active <strong>and</strong> passive drag equations, the value of the drag force is<br />

represented as an exponential function of swimm<strong>in</strong>g velocity. The active<br />

drag values will however rise or <strong>in</strong>crease more rapidly than that of passive<br />

drag. There will still be a similar exponential relationship between the two<br />

curves <strong>and</strong> only the <strong>in</strong>creased rate of rise will differentiate between the<br />

active <strong>and</strong> passive drag equations. Given that the rate of rise between the<br />

active <strong>and</strong> passive drag equations is represented by a s<strong>in</strong>gle constant, these<br />

two constants may be used as an <strong>in</strong>dex to describe the <strong>in</strong>dividual swimmer’s<br />

capabilities. The constant <strong>in</strong> the equation for passive drag would<br />

represent an <strong>in</strong>dex of the swimmer’s <strong>in</strong>nate physical characteristics such<br />

as size, shape <strong>and</strong> cross sectional frontal surface area. A lower <strong>in</strong>dex <strong>in</strong>dicates<br />

a more efficient body shape for aquatics movement. The difference<br />

between the constant used <strong>in</strong> the active drag equation <strong>and</strong> the constant<br />

<strong>in</strong> the passive drag equation could be used as an <strong>in</strong>dex to represent the<br />

efficiency of the swimmer technique. This <strong>in</strong>dex may provide <strong>in</strong>sight as to<br />

the capability of the swimmer to compete <strong>in</strong> particular events.<br />

Exponential functions for both active <strong>and</strong> passive drag were ex-<br />

( b⋅V<br />

)<br />

pressed by the equation F = a ⋅ e , where b was constant for a<br />

particular swimmer <strong>and</strong> a def<strong>in</strong>ed the active or passive drag constant.<br />

The a a represented the constant used <strong>in</strong> the active drag equation, p a<br />

represented the constant used <strong>in</strong> the passive drag equation <strong>and</strong> aa− p<br />

represented the constant used for the difference between active <strong>and</strong> passive<br />

drag. The constant a was useful, <strong>in</strong> that a p def<strong>in</strong>ed the unique<br />

aquatic characteristics of the <strong>in</strong>dividual. This research suggested that the<br />

lower the number, the more effective the <strong>in</strong>dividual characteristic was<br />

with respect to movement through water. The constant aa− p provided<br />

valuable <strong>in</strong>sight <strong>in</strong>to the efficiency of the swimmer’s technique. Once<br />

aga<strong>in</strong>, the lower the value of a the more efficient was the technique.<br />

a−<br />

p<br />

For example, subject six was the Australian 400 m freestyle champion<br />

over a number of consecutive years. The data identified that subject six<br />

had a lower a value than all but one other subject. This highlighted<br />

a−<br />

p<br />

that subject six had an efficient technique. Similarly, subject eight presented<br />

the lowest aa− p value <strong>and</strong> she demonstrated excellent technical<br />

skills. Subject one had the highest a p value <strong>and</strong> this <strong>in</strong>dicated his anthropometric<br />

characteristics were not ideal for swimm<strong>in</strong>g. However, the<br />

a value demonstrated good technical efficiency <strong>in</strong> the swimmer. The<br />

a−<br />

p<br />

exam<strong>in</strong>ation of the aa− p of swimmers at various times <strong>in</strong> the season<br />

may identify changes <strong>in</strong> technical efficiency.


conclusIon<br />

The present study demonstrated the importance of be<strong>in</strong>g able to generate<br />

an equation to represent a swimmer’s active drag over a range of<br />

velocities. This novel concept may provide <strong>in</strong>sight as to the suitability<br />

of the <strong>in</strong>dividual to swim specific swimm<strong>in</strong>g events, as well as, <strong>in</strong>dicate<br />

the efficiency of the swimmer’s technique. This will provide valuable <strong>in</strong>formation<br />

to coaches <strong>and</strong> swimmers regard<strong>in</strong>g the athlete’s suitability to<br />

the sport, as well as provide an evaluation of improvement <strong>in</strong> technical<br />

efficiency.<br />

reFerences<br />

Formosa, D.P., Mason B.R., Burkett B. (2009). Measur<strong>in</strong>g propulsive<br />

force with<strong>in</strong> the different phases of backstroke swimm<strong>in</strong>g. In A. J.<br />

Harrison, R. Anderson & I. Kenny (Eds.), Proceed<strong>in</strong>gs of the XXVII<br />

International Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports (pp. 98-101).Irel<strong>and</strong><br />

Kolmogorov S.V., & Duplishcheva O.A. (1992). Active Drag, Useful<br />

Mechanical Power Output <strong>and</strong> Hydrodynamic Force Coefficient <strong>in</strong><br />

Different Swimm<strong>in</strong>g Strokes at Maximum Velocity. Journal of <strong>Biomechanics</strong>,<br />

25 (3), 311-318.<br />

Mason B.R., Formosa D.P., & Rollason S. (2009a). A comparison between<br />

the values obta<strong>in</strong>ed from active drag analysis compared to forces<br />

produced <strong>in</strong> tethered swimm<strong>in</strong>g. In A. J. Harrison, R. Anderson &<br />

I. Kenny (Eds.), Proceed<strong>in</strong>gs of the XXVII International Symposium on<br />

<strong>Biomechanics</strong> <strong>in</strong> Sports (pp. 86-89).Irel<strong>and</strong><br />

Mason, B.R., Formosa, D.P., & Raleigh, V. (2009b). The use of passive<br />

drag to <strong>in</strong>terpret variations <strong>in</strong> active drag measurements. In A. J. Harrison,<br />

R. Anderson & I. Kenny (Eds.), Proceed<strong>in</strong>gs of the XXVII International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports (pp. 452-455).Irel<strong>and</strong>.<br />

Toussa<strong>in</strong>t H.M., Roos P.E., & Kolmogorov S. (2004). The determ<strong>in</strong>ation<br />

of drag <strong>in</strong> front crawl swimm<strong>in</strong>g. Journal of <strong>Biomechanics</strong>, 37<br />

(11), 1655-1663.<br />

AcKnoWleGMents<br />

The researchers would like to thank the Australian Institute of Sport<br />

Swimm<strong>in</strong>g programme <strong>and</strong> Australian National Swim team for their<br />

participation <strong>in</strong> the study.<br />

chaPter2.<strong>Biomechanics</strong><br />

50m Race Components Times Analysis Based on a<br />

Regression Analysis Model Applied to Age-Group<br />

Swimmers<br />

Morales, e. 1 , Arellano, r. 1 , Femia, P. 1 , Mercade, J. 1 ,<br />

halj<strong>and</strong> r. 2<br />

1 University of Granada, Spa<strong>in</strong><br />

2 University of Tall<strong>in</strong>n, Tall<strong>in</strong>n, Estonia<br />

This <strong>in</strong>vestigation aimed to develop a regression model of the Race<br />

Component evolution <strong>in</strong> a large sample of regional age-group Spanish<br />

swimmers. Subjects were 280 regional swimmers selected of different<br />

clubs. The time spent start<strong>in</strong>g (ST), the time spent strok<strong>in</strong>g (STT1 -<br />

STT2), the time spent turn<strong>in</strong>g (TT) <strong>and</strong> the time spent f<strong>in</strong>ish<strong>in</strong>g (FT),<br />

were used for analysis. Inverse function approximation of the partials<br />

times by ag<strong>in</strong>g <strong>and</strong> was carried out. Furthermore, regression analysis<br />

of partials times <strong>and</strong> event time for age <strong>and</strong> genders were calculated,<br />

respectively. It seems that the times of the swimmers studied have a<br />

tendency to resemble <strong>in</strong>ternationals swimmer´s times. The estimation<br />

formula applied was different time accord<strong>in</strong>g to gender. The cross<strong>in</strong>g age<br />

<strong>in</strong> the swimm<strong>in</strong>g partials times were about 12-14 years old.<br />

Key words: performance development, competition analysis, technique<br />

test<strong>in</strong>g<br />

IntroductIon<br />

The dynamic process of tra<strong>in</strong><strong>in</strong>g needs as much <strong>in</strong>formation as possible<br />

from competitive performance, which, together with <strong>in</strong>formation from<br />

tra<strong>in</strong><strong>in</strong>g <strong>and</strong> test<strong>in</strong>g, will help to the coach to monitor the tra<strong>in</strong><strong>in</strong>g program.<br />

Race components (RC) data must be considered when analys<strong>in</strong>g<br />

swimm<strong>in</strong>g performances dur<strong>in</strong>g <strong>in</strong>ternational swimm<strong>in</strong>g competitions<br />

(see www.swim.ee). To improve the swimmer test<strong>in</strong>g efficiency, this<br />

analysis has also to <strong>in</strong>clude the results of swimm<strong>in</strong>g tests made dur<strong>in</strong>g a<br />

tra<strong>in</strong><strong>in</strong>g season or several tra<strong>in</strong><strong>in</strong>g seasons.<br />

The RC is composed of the start<strong>in</strong>g time (ST), strok<strong>in</strong>g (STT),<br />

turn<strong>in</strong>g (TT) <strong>and</strong> f<strong>in</strong>ish<strong>in</strong>g (FT) (Pai, Hay, & Wilson, 1984). Swimm<strong>in</strong>g<br />

tra<strong>in</strong><strong>in</strong>g has to be oriented to improve all rac<strong>in</strong>g components, but<br />

the lack of a specific model makes it difficult to know which are the<br />

strongest <strong>and</strong> weakest race components of any <strong>in</strong>dividual. The coach<br />

must tra<strong>in</strong> the swimmer accord<strong>in</strong>g to swimm<strong>in</strong>g time <strong>and</strong> age. The<br />

50m freestyle performances should improve with age <strong>in</strong> each period of<br />

growth, <strong>in</strong> parallel with the RC.<br />

Some studies have been published where regression equations were<br />

applied <strong>in</strong> the analysis of RC obta<strong>in</strong>ed from different competitions (Absaliamov<br />

& Timakovoy, 1990; Arellano et al., 1996; Nomura, 2006). The<br />

study aim was to develop a regression model of the RC evolution <strong>in</strong> a<br />

large sample of regional age-group Spanish swimmers.<br />

Methods<br />

The sample was composed of 180 regional swimmers (162 males <strong>and</strong><br />

118 females). The age of these subjects ranged from 9 to 22 years.<br />

The procedures that have been used to record the times obta<strong>in</strong>ed<br />

by swimmers dur<strong>in</strong>g the performance test of 50 m freestyle were: a)<br />

references were put on the swimm<strong>in</strong>g pool at the distances selected (5,<br />

10, 15 <strong>and</strong> 20 m) to know when the head crossed this l<strong>in</strong>e; b) the 50m<br />

trials were recorded by five video cameras connected to a m<strong>in</strong>i DV video<br />

recorder through a video-timer <strong>and</strong> video selector; c) the images from<br />

the first two video cameras were mixed to see the over- <strong>and</strong> under- water<br />

phases of the start <strong>in</strong> the same frame (until 5m); d) third <strong>and</strong> fourth<br />

cameras were used to measure the 10 <strong>and</strong> 15 m time; the fifth camera<br />

was placed at the end of the swimm<strong>in</strong>g pool for video record<strong>in</strong>g the<br />

turn<strong>in</strong>g phase (20 <strong>and</strong> 25 m) <strong>and</strong>; e) all the images from the cameras<br />

127


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

were recorded at a distance of 8 m from the perpendicular plane of the<br />

swimmer’s displacement (see figure 1).<br />

Figure 1. Picture with the references <strong>and</strong> video cameras set-up on the<br />

swimm<strong>in</strong>g pool.<br />

The regression analysis was developed us<strong>in</strong>g the SPSS 17.0 statistical<br />

software (SPPS Inc., Chicago, Ill., USA). Kolmogorov-Smirnov test<br />

showed the normal distribution of the sample. The regression analysis<br />

was used to discover the tendency <strong>and</strong> model of the RC. Inverse function<br />

approximation of the RC times (ST, STT, TT, FT) by age (AGE)<br />

<strong>and</strong> gender (GEN) was carried out. The type of generic equation obta<strong>in</strong>ed<br />

was:<br />

b<br />

y = a + a′ ⋅ GEN + (1 − b′ ⋅GEN<br />

)<br />

(1)<br />

AGE<br />

The estimation formula of time from age <strong>and</strong> gender was as follows:<br />

⎧<br />

b1<br />

yMen = a1<br />

+<br />

⎪ AGE<br />

⎨<br />

⎪ b2<br />

(2)<br />

yWoman = a2<br />

+<br />

⎪⎩<br />

AGE<br />

Furthermore, the regression analysis <strong>and</strong> <strong>in</strong>verse function for every partial<br />

time was calculated respectively.<br />

results<br />

Each RC time with related to the f<strong>in</strong>al time <strong>and</strong> expressed as a percentage.<br />

Student T-tests for <strong>in</strong>dependent samples demonstrated significant<br />

differences between genders for each partial time (Table 1).<br />

Table 1. T-test for <strong>in</strong>dependent samples accord<strong>in</strong>g to gender <strong>in</strong> each<br />

percentage of partial times.<br />

Var. Means Difference E.T T (gl) P<br />

% ST Male.<br />

Female.<br />

% STT1 Male.<br />

Female.<br />

% TT Male.<br />

Female.<br />

% STT2 Male.<br />

Female.<br />

% FT Male.<br />

Female.<br />

128<br />

26.280<br />

26.832<br />

10.291<br />

10.346<br />

30.575<br />

30.339<br />

22.340<br />

22.153<br />

10.561<br />

10.304<br />

*P


The graphs of male <strong>and</strong> female models were put on top of each other.<br />

The cross<strong>in</strong>g age po<strong>in</strong>t for each partial time was calculated. The equation<br />

obta<strong>in</strong>ed was:<br />

b1<br />

⎫<br />

yMale = a1<br />

+<br />

age ⎪ b1 b2<br />

(3)<br />

⎬ ⇒ a1 + = a2<br />

+<br />

b2 age age<br />

yFemale = a ⎪<br />

2 +<br />

age⎪⎭<br />

age<br />

of cut<br />

b − b<br />

=<br />

a − a<br />

2 1<br />

1 2<br />

Accord<strong>in</strong>g to this equation <strong>and</strong> for each model of partial time the cross<strong>in</strong>g<br />

age po<strong>in</strong>t was obta<strong>in</strong>ed (see Table 4). This shows differences <strong>in</strong> the<br />

development <strong>and</strong> when the boys beg<strong>in</strong> to perform better than girls (see<br />

Figure 2).<br />

Table 4. Cross<strong>in</strong>g age po<strong>in</strong>t for each partial time<br />

Cross<strong>in</strong>g age<br />

ST = 10.61<br />

STT1 =12.02<br />

TT = 12.66<br />

STT2 = 13.20<br />

T50 = 12.08<br />

dIscussIon<br />

As was expected, the temporal analysis <strong>in</strong> a 50m freestyle test improves<br />

with age <strong>in</strong> the period of growth (see figure 3). The results obta<strong>in</strong>ed <strong>in</strong><br />

percentages of RC times were different between genders <strong>and</strong> males had<br />

lower results than females. Our results showed significant differences<br />

between the percentages of younger swimmers from our study compared<br />

with <strong>in</strong>ternationals swimmers <strong>in</strong> all variables except <strong>in</strong> STT2. However,<br />

no differences were found from the data obta<strong>in</strong>ed <strong>in</strong> the percentage of<br />

TT (about 30%) by Thompson & Halj<strong>and</strong> (1997).<br />

Figure 3. Evolution of percentages of RC times due to age.<br />

The evolution of RC times follows <strong>in</strong>verse models <strong>in</strong> both genders that<br />

are parallel but cross over. The times of girls are better than the times<br />

of boys until cross<strong>in</strong>g age, which is about 12-14 years old. At this age<br />

Taylor et al. (2003) <strong>and</strong> Hellard et al. (2003) found significant <strong>in</strong>crease<br />

<strong>in</strong> swimm<strong>in</strong>g speed at 50m <strong>and</strong> a significant <strong>in</strong>crease <strong>in</strong> strength. These<br />

results confirm the relationship between growth, anthropometric <strong>and</strong><br />

strength development <strong>and</strong> swimm<strong>in</strong>g efficiency.<br />

chaPter2.<strong>Biomechanics</strong><br />

conclusIons<br />

Race components change with the development of many physical fitness<br />

factors. With growth, the times of the swimmers studied have a tendency<br />

to come closer to the times of <strong>in</strong>ternational swimmers. Temporal<br />

analysis has the same generic equation for boys <strong>and</strong> girls but there are<br />

two different models accord<strong>in</strong>g to gender. The <strong>in</strong>verse function of the<br />

partial time by age <strong>and</strong> gender was the better approximation carried out<br />

<strong>in</strong> this tra<strong>in</strong><strong>in</strong>g test of 50m freestyle. The times of girls are better than<br />

those of boys until the cross<strong>in</strong>g age of about 12-14 years old.<br />

reFerences<br />

Absaliamov <strong>and</strong> Timakovoy (1990). Aseguramiento Científico de<br />

la Competición. (A.I. Zvonarev, Trans.).(1 ed.). (Vol.1). Moscow:<br />

Vneshtorgizdat.<br />

Arellano, R., Brown, P., Cappaert, J., Nelson, R.C. (1996). Application<br />

of regression equations <strong>in</strong> the analysis of 50 <strong>and</strong> 100 m swimm<strong>in</strong>g<br />

races of 1992 Olympic Games. Joao Abrantes (Ed.).<strong>XI</strong>V International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports. (pp. 274-276). Lisbon,<br />

Portugal.<br />

Hay, J.G., Guimaraes, A.C. S., Grimston, S.K. (1983). A Quantitative<br />

Look at Swimm<strong>in</strong>g <strong>Biomechanics</strong>. In J.G. Hay (Ed), Start<strong>in</strong>g, Strok<strong>in</strong>g<br />

& Turn<strong>in</strong>g (A Compilation of Research on the <strong>Biomechanics</strong> of<br />

swimm<strong>in</strong>g, The University of Iowa, 1983-86) (pp.76-82). Iowa: <strong>Biomechanics</strong><br />

Laboratory, Department of Exercise Science.<br />

Hellard, P. Caudal, N., et al. (2003). Tra<strong>in</strong><strong>in</strong>g, anthropometrics <strong>and</strong> performance<br />

relationships <strong>in</strong> French male swimmers of three age categories<br />

for 200m events. <strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g IX.<br />

J.C. Chatard. Sa<strong>in</strong>t-Etienne, Université de Sa<strong>in</strong>t-Etienne: 457-562.<br />

Nomura, T. (2006). Estimation of the lap-time of 200m freestyle from<br />

age <strong>and</strong> the event time. Revista portuguesa de ciências do desporto.<br />

Vol. 6, Supl. 2. (pp. 239-241).<br />

Pai, Y.-C., Hay, J.G., Wilson, B.D. (1984). Strok<strong>in</strong>g Techniques of Elite<br />

Swimmers. Journal of Sports Sciences (2), 225-239.<br />

Taylor, S., Maclaren, D. et al. (2003). The effects of age, maturation<br />

<strong>and</strong> growth on tethered swimm<strong>in</strong>g performance. <strong>Biomechanics</strong><br />

<strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g IX. J.C. Chatard. Sa<strong>in</strong>t-Etienne,<br />

Université de Sa<strong>in</strong>t-Etienne: 185-190.<br />

Thompsom, K. G., Halj<strong>and</strong>, R. (1997). “The secrets of competitive<br />

breastroke swimm<strong>in</strong>g” Swimm<strong>in</strong>g Time. Nov.:26-28.<br />

AcKnoWledGeMents<br />

Esther Morales would like to thank the University of Granada for the<br />

grant that enabled her to carry out this research. She would also like to<br />

thank the Physical Education <strong>and</strong> Sports Department <strong>and</strong> the Research<br />

Group “CTS-527: Physical Activity <strong>and</strong> Sports <strong>in</strong> Aquatic Environment”<br />

of the University of Granada for the use of equipment <strong>and</strong> help<br />

<strong>in</strong> prepar<strong>in</strong>g this paper <strong>and</strong> the research on which it is based.<br />

129


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Regression Analysis Model Applied to Age-Group<br />

Swimmers: Study of Stroke Rate, Stroke Length <strong>and</strong><br />

Stroke Index<br />

Morales, e., Arellano, r., Femia, P., Mercade, J.<br />

University of Granada, Spa<strong>in</strong><br />

This <strong>in</strong>vestigation aimed to develop a regression model of the K<strong>in</strong>ematics<br />

Characteristics (KC) evolution <strong>in</strong> a large sample of regional<br />

age-group Spanish swimmers. Subjects were 280 regional swimmers<br />

selected from different clubs. The 50 m time, Stroke rate (SR), Stroke<br />

length (SL) <strong>and</strong> Stroke Index (SI) were used for analysis. Inverse function<br />

approximation of the race times by age (AGE) <strong>and</strong> gender (GEN)<br />

was carried out. Quadratic function approximation of the SL <strong>and</strong> SI<br />

by ag<strong>in</strong>g was carried out. L<strong>in</strong>eal function by ag<strong>in</strong>g was def<strong>in</strong>ed for ST.<br />

Furthermore, the analysis regression of KC for age <strong>and</strong> genders were calculated<br />

respectively. 50 m times were different between genders. There<br />

is a tendency to improve the parameters SL <strong>and</strong> SI with age <strong>in</strong> both<br />

genders. SR does not show a clear trend <strong>and</strong> has an irregular behaviour.<br />

Key words: stroke rate, stroke length, stroke <strong>in</strong>dex, regression analysis,<br />

age-group.<br />

IntroductIon<br />

The swimmer´s time obta<strong>in</strong>ed after perform<strong>in</strong>g a competitive event can<br />

be considered as important <strong>in</strong>formation to help the coach<strong>in</strong>g process<br />

that follows the competitive performance. The dynamic process of tra<strong>in</strong><strong>in</strong>g<br />

needs as much <strong>in</strong>formation as possible from that performance. This<br />

<strong>in</strong>formation will help the coach to monitor the tra<strong>in</strong><strong>in</strong>g program.<br />

The Race Component (RC) Time to be <strong>in</strong>clude <strong>in</strong> the analysis of<br />

swimm<strong>in</strong>g performance dur<strong>in</strong>g <strong>in</strong>ternational swimm<strong>in</strong>g competition<br />

(Hay,Guimaraes, & Grimston, 1983) <strong>and</strong> it is very important to now<br />

the follow of race. In order to improve the swimmer´s efficiency stroke<br />

rate, stroke length <strong>and</strong> stroke <strong>in</strong>dex to be <strong>in</strong>clude <strong>in</strong> the analysis of competition.<br />

Technical performance <strong>in</strong> cyclic activities <strong>and</strong>, more specifically,<br />

swimm<strong>in</strong>g performance (Hay, 2002) has traditionally been assessed<br />

by analysis the changes <strong>in</strong> <strong>and</strong> management of velocity, stroke rate <strong>and</strong><br />

stroke length (Graig, & Perdergast, 1979; Pai, Hay & Wilson, 1984;<br />

Kenndy, Brown, Chegarlur & Nelson, 1990; Chegarlur & Brown, 1992;<br />

Chollet, Pelayo, Tourny, & Sidney, 1996). Several groups of researchers<br />

have analysed the technical <strong>and</strong> k<strong>in</strong>ematics characteristics (KC), stroke<br />

rate (SR), stroke lengh (SL) <strong>and</strong> stroke <strong>in</strong>dex (SI), dur<strong>in</strong>g <strong>in</strong>ternational<br />

competitions to determ<strong>in</strong>e their relationship with performance.<br />

Some studies have been published where regression equations were<br />

applied <strong>in</strong> the analysis of RC obta<strong>in</strong>ed <strong>in</strong> different competitions (Absaliamov<br />

& Timakovoy, 1090; Arellano, Brown, Cappaert & Nelson,<br />

1996; Nomura, 2006). The study aim was to develop a regression model<br />

of the KC evolution <strong>in</strong> a large sample of regional age-group Spanish<br />

swimmers.<br />

Method<br />

The subjects were 280 swimmers (162 males <strong>and</strong> 118 females) regional<br />

swimmers. The age of these subjects ranged from 9 to 22 years.<br />

The procedures that have been used to record the 50 m time <strong>and</strong> k<strong>in</strong>ematics<br />

characteristics obta<strong>in</strong>ed by swimmers dur<strong>in</strong>g the performance<br />

test of 50 m freestyle were: a) references were put on the swimm<strong>in</strong>g pool<br />

at the distances selected (5, 10, 15 <strong>and</strong> 20 m) to know when the head<br />

crossed this l<strong>in</strong>e; b) the 50m trials were recorded by five video cameras<br />

connected to a m<strong>in</strong>i DV video recorder through a video-timer <strong>and</strong> video<br />

selector; c) the images from the first two video cameras were mixed to<br />

130<br />

see the over- <strong>and</strong> under- water phases of the start <strong>in</strong> the same frame<br />

(until 5m); d) third <strong>and</strong> fourth cameras were used to measure the 10<br />

<strong>and</strong> 15 m time; the fifth camera was placed at the end of the swimm<strong>in</strong>g<br />

pool for video record<strong>in</strong>g the turn<strong>in</strong>g phase (20 <strong>and</strong> 25 m) <strong>and</strong>; e) all the<br />

images from the cameras were recorded at a distance of 8 m from the<br />

perpendicular plane of the swimmer’s displacement (see figure 1).<br />

Figure 1. Picture with the references <strong>and</strong> video cameras set-up on the<br />

swimm<strong>in</strong>g pool.<br />

KC obta<strong>in</strong>ed by swimmers dur<strong>in</strong>g the performance test of 50 m freestyle<br />

was calculated <strong>in</strong> all lap. The results showed the average of laps. The<br />

number of cycles utilized for to do the calculation was three. The equations<br />

def<strong>in</strong><strong>in</strong>g SR, SL <strong>and</strong> SI were as follows:<br />

nº cycles ( c)<br />

SR<br />

cycles time ( s)<br />

SL<br />

= (1)<br />

espace ( m)<br />

nº cicles<br />

= (2)<br />

SI = speed • SL (3)<br />

The regression analysis was developed us<strong>in</strong>g the SPSS 17.0 statistical<br />

software (SPSS Inc., Chicago, Ill., USA). The Kolmogorov-Smirnov test<br />

showed the normal distribution of the sample. The regression analysis<br />

was used to discover the tendency <strong>and</strong> model of the 50 m time <strong>and</strong> KC.<br />

Inverse function approximation of the race times by age (AGE) <strong>and</strong><br />

gender (GEN) was carried out. Also, quadratic function approximation<br />

of the SL, <strong>and</strong> SI by age <strong>and</strong> GEN, <strong>and</strong> l<strong>in</strong>eal function of the SR by<br />

AGE <strong>and</strong> GEN was carried out.<br />

results<br />

The T-test for <strong>in</strong>dependent samples expla<strong>in</strong>s the difference between<br />

genders for each KC (Table 1).<br />

Table 1. T-test for <strong>in</strong>dependent samples accord<strong>in</strong>g to gender <strong>in</strong> SR, SL<br />

<strong>and</strong> SI.<br />

Var. Means Difference E.T T (gl) P<br />

Fc Mas.<br />

Fem.<br />

Lc Mas.<br />

Fem.<br />

Ic Mas.<br />

Fem<br />

53.018<br />

51.259<br />

1.427<br />

1.530<br />

1.846<br />

2.026<br />

*P


The regression analysis was used to discover the tendency <strong>and</strong> model<br />

of evolution of 50 m time, SR, SL <strong>and</strong> SI accord<strong>in</strong>g to age <strong>and</strong> gender.<br />

The type of equations obta<strong>in</strong>ed for gender <strong>in</strong> each partial time <strong>and</strong> event<br />

time can be observed <strong>in</strong> Table 2.<br />

Table 2. Model of regression analysis of SR, SL <strong>and</strong> SI by age (AGE)<br />

<strong>and</strong> gender (GEN)<br />

Male Models R2 SR = 44.378+0.734*AGE *** 0.106<br />

SL= -0.128+0.188*AGE+0.004*AGE 2 *** 0.480<br />

SI= -1.782+0.405*AGE+0.007*AGE 2 *** 0.646<br />

T50= 1.443+431.231*AGE -1 *** 0.647<br />

Female models R 2<br />

SR = 47.981+0.263*AGE *** 0.014<br />

SL= -0.529+0.269*AGE+0.007*AGE 2 *** 0.542<br />

SI= -2.978+0.643*AGE+0.018*AGE 2 *** 0.684<br />

T50= 7.323+360.161*AGE -1 *** 0.703<br />

***P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

J.-C. Chatard. Sa<strong>in</strong>t-Etienne, Université de Sa<strong>in</strong>t-Etienne: 457-462.<br />

Jahnig, W. (1987). Grundlegende strukturelle Betrachtungen. Sport<br />

Schwimmen. E. Schramm. Berl<strong>in</strong>, Sportverlag Berl<strong>in</strong>: 74-86.<br />

Kenndy, P., Brown, P., Chegarlur, S. N., & Nelson, R. C. (1990).<br />

Analysis of male <strong>and</strong> female Olympic swimmers <strong>in</strong> the 100 m<br />

events. International Journal of sport <strong>Biomechanics</strong>, 6, 187-<br />

197.<br />

Maglischo, E. W. (1993). Swimm<strong>in</strong>g Even Faster. Mounta<strong>in</strong><br />

View, CA, Mayfield Publish<strong>in</strong>g Company.<br />

Nomura, T. (2006). Estimation of the lap-time of 200m freestyle<br />

from age <strong>and</strong> the event time. Revista portuguesa de ciências do<br />

desporto. Vol. 6, Supl. 2. (pp. 239-241).<br />

Pai, Y. C., Hay, J. G., & Wilson, B. D. (1984). Strok<strong>in</strong>g techniques<br />

of elite swimmers. Journal of Sports Science, 2, 225-<br />

239.<br />

Sánchez, J. A. (1999). Análisis de la actividad competitiva en<br />

natación: diferencias en función de la longitud del vaso, el<br />

nivel de ejecución, el sexo, el estilo y la distancia de prueba.<br />

Deparatamento de personalidad, evaluación y tratamiento<br />

psicológico. Tesis doctoral. Granada, Universidad de Granada.<br />

Taylor, S., Maclaren, D., et al. (2003). The effects of age, maturation<br />

<strong>and</strong> growth on tethered swimm<strong>in</strong>g performance. <strong>Biomechanics</strong><br />

<strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g IX. J.-C. Chatard. Sa<strong>in</strong>t-<br />

Etiene, Université de Sa<strong>in</strong>t-Etiene: 185-190.<br />

Tella, V. (1998). Modificaciones de Variables C<strong>in</strong>emáticas y<br />

Antropométricas en Nadadores Infantiles y Juniors. Tesis doctoral,<br />

Valencia.<br />

Vorontsov, A. <strong>and</strong> B<strong>in</strong>evsky, D. (2003). Swimm<strong>in</strong>g speed, stroke<br />

rate <strong>and</strong> stroke length dur<strong>in</strong>g marimal 100 m freestyle of boys<br />

11-16 years of age. <strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g<br />

IX. J.-C. Chatard. Sa<strong>in</strong>t- Etienne, Université de Sa<strong>in</strong>t-Etienne:<br />

195-200.<br />

AcKnoWledGeMents<br />

Esther Morales would like to thank the University of Granada for the<br />

grant that enabled her to carry out this research. She would also like to<br />

thank the Physical Education <strong>and</strong> Sports Department <strong>and</strong> the Research<br />

Group “CTS-527: Physical Activity <strong>and</strong> Sports <strong>in</strong> Aquatic Environment”<br />

of the University of Granada for the use of equipment <strong>and</strong> help<br />

<strong>in</strong> prepar<strong>in</strong>g this paper <strong>and</strong> the research on which it is based.<br />

132<br />

Advanced Biomechanical Simulations <strong>in</strong> Swimm<strong>in</strong>g<br />

Enabled by Extensions of Swimm<strong>in</strong>g Human<br />

Simulation Model “SWUM”<br />

nakashima, M. 1 , Kiuchi, h. 1 , Maeda, s. 1 , Kamiya, s. 1 , nakajima,<br />

K. 1 , takagi, h. 2<br />

1 Tokyo Institute of Technology, Tokyo, Japan<br />

2 University of Tsukuba, Tsukuba, Japan<br />

S<strong>in</strong>ce the authors presented the simulation model “SWUM” <strong>and</strong> its<br />

implementation software “Swumsuit” <strong>in</strong> BMS-2006, major extensions<br />

have been successively made on SWUM, such as optimiz<strong>in</strong>g calculation,<br />

musculoskeletal simulation, <strong>and</strong> multi agent/object simulation, <strong>in</strong> order<br />

to extend its capability of analysis. In this paper, these three extensions<br />

are expla<strong>in</strong>ed <strong>and</strong> the various recent results from their implementation<br />

presented. The usefulness of the extensions was confirmed s<strong>in</strong>ce many<br />

reasonable results were obta<strong>in</strong>ed.<br />

Key words: Biomechanical Simulation, Optimization, Musculoskeletal<br />

model, SWUM<br />

IntroductIon<br />

There are many biomechanical problems to be solved <strong>in</strong> human swimm<strong>in</strong>g.<br />

In order to discuss such problems quantitatively, numerical<br />

simulation is becom<strong>in</strong>g a powerful <strong>and</strong> useful tool. The authors have<br />

developed a simulation model, “SWUM,” (SWimm<strong>in</strong>g hUman Model)<br />

(Nakashima et al., 2007b) <strong>and</strong> a free software, “Swumsuit,” as the implementation<br />

of SWUM (Nakashima, 2005, 2006). By SWUM, it is possible<br />

to analyze the dynamics of the whole swimmer’s body with a short<br />

computation time due to model<strong>in</strong>g the fluid force act<strong>in</strong>g on the swimmer.<br />

S<strong>in</strong>ce it was reported <strong>in</strong> the last symposium (Nakashima 2006),<br />

major extensions have been successively made on SWUM, such as optimiz<strong>in</strong>g<br />

calculation, musculoskeletal simulation, <strong>and</strong> multi agent/object<br />

simulation, <strong>in</strong> order to extend the capability of analysis. In this paper,<br />

these extensions are expla<strong>in</strong>ed <strong>and</strong> the various recent results by them are<br />

presented <strong>in</strong> order to exam<strong>in</strong>e their usefulness.<br />

Methods<br />

All analyses <strong>in</strong> this paper were carried out us<strong>in</strong>g SWUM. It was designed<br />

to solve the six degrees-of-freedom absolute movement of the whole<br />

swimmer’s body as a s<strong>in</strong>gle rigid body by the time <strong>in</strong>tegration method, us<strong>in</strong>g<br />

the <strong>in</strong>puts of the swimmer’s body geometry <strong>and</strong> relative jo<strong>in</strong>t motion.<br />

The swimm<strong>in</strong>g speed, roll, pitch <strong>and</strong> yaw motions, propulsive efficiency,<br />

jo<strong>in</strong>t torques <strong>and</strong> so on, are computed as the output data. The swimmer’s<br />

body is represented by a series of 21 rigid body segments. Each body segment<br />

is represented by a truncated elliptic cone. The unsteady fluid force<br />

<strong>and</strong> gravitational force are taken <strong>in</strong>to account as the external forces act<strong>in</strong>g<br />

on the whole body. The unsteady fluid force is assumed to be the sum<br />

of the <strong>in</strong>ertial force due to the added mass of the fluid, normal <strong>and</strong> tangential<br />

drag forces <strong>and</strong> buoyancy. These components are also assumed to<br />

be computable, without solv<strong>in</strong>g the flow, from the local position, velocity,<br />

acceleration, direction, angular velocity <strong>and</strong> angular acceleration for each<br />

part of the swimmer’s body at each time step. The coefficients <strong>in</strong> this fluid<br />

force model were identified us<strong>in</strong>g the results of an experiment with a limb<br />

model <strong>and</strong> measurements of the drag act<strong>in</strong>g on swimmers tak<strong>in</strong>g a glide<br />

position <strong>in</strong> the previous studies (Nakashima et al., 2007b). For the simulation<br />

example of six beat crawl stroke <strong>in</strong> the previous study, the swimm<strong>in</strong>g<br />

speed of the simulation became a reasonable value, <strong>in</strong>dicat<strong>in</strong>g the validity<br />

of the simulation model. With respect to the six beat crawl stroke, the authors<br />

have already analyzed contributions of each fluid force component<br />

<strong>and</strong> of each body part to the thrust, effect of the flutter kick, estimation of<br />

the active drag, roll motion, <strong>and</strong> propulsive efficiency (Nakashima, 2007a).<br />

Analyses of the other three strokes <strong>and</strong> comparison among four strokes


(<strong>in</strong>clud<strong>in</strong>g crawl stroke) have also been carried out (Nakashima 2007b).<br />

The details are described <strong>in</strong> the references respectively. Some of the analysis<br />

data <strong>and</strong> animation movies are open to the public at the SWUM website<br />

(http://www.swum.org/).<br />

The first extension made on SWUM was for the optimiz<strong>in</strong>g calculation.<br />

In the optimiz<strong>in</strong>g calculation, a s<strong>in</strong>gle simulation of the time<br />

<strong>in</strong>tegration is repeated chang<strong>in</strong>g the design variables until a given objective<br />

function is maximized. For the design variables, all the <strong>in</strong>put data,<br />

such as the body geometry of the swimmer <strong>and</strong> jo<strong>in</strong>t motion, can be<br />

employed. With respect to the objective function, the user can describe<br />

it freely us<strong>in</strong>g the output data, such as maximiz<strong>in</strong>g the swimm<strong>in</strong>g speed<br />

<strong>and</strong> maximiz<strong>in</strong>g the propulsive efficiency. As the optimiz<strong>in</strong>g algorithm,<br />

the Downhill Simplex method was employed. This extension has been<br />

implemented <strong>in</strong> Swumsuit version 2.0.0.<br />

The second extension was the musculoskeletal simulation. In the<br />

musculoskeletal simulation, the human body is modeled as a series of<br />

body segments accompany<strong>in</strong>g muscles modeled as wires. For the musculoskeletal<br />

calculation of the present study, commercial software, Any-<br />

Body Model<strong>in</strong>g System (AnyBody) (AnyBody Technology, Denmark)<br />

was employed. The whole body musculoskeletal model with 458 muscles<br />

shown <strong>in</strong> Fig.1 was employed for the present study. With respect to the<br />

data connection between SWUM <strong>and</strong> AnyBody, the jo<strong>in</strong>t motion (relative<br />

body motion) is given as <strong>in</strong>put data <strong>and</strong> the absolute movement of<br />

the whole body is calculated as output data <strong>in</strong> SWUM. These motion<br />

data are <strong>in</strong>put <strong>in</strong>to AnyBody. The fluid forces act<strong>in</strong>g on swimmer are<br />

also <strong>in</strong>put <strong>in</strong>to AnyBody as external forces distributed on the swimmer’s<br />

body. This extension has been implemented <strong>in</strong> Swumsuit 3.0.0.<br />

Figure 1. Whole body musculoskeletal model with 458 muscles employed<br />

for the musculoskeletal simulation.<br />

The third extension was “multi agent/object simulation.” “Multi agents”<br />

means multiple swimmers <strong>and</strong> “multi objects” means implements for<br />

swimm<strong>in</strong>g such as f<strong>in</strong>s, a start<strong>in</strong>g block, the pool wall, <strong>and</strong> so on. Before<br />

this extension, SWUM had been capable of analyz<strong>in</strong>g one swimmer<br />

only by one simulation program. In the multi agent/object simulation,<br />

multiple simulation programs for multiple agents/objects run simultaneously<br />

to analyze. In addition to this, mechanical <strong>in</strong>teraction among<br />

the agents/objects can be described freely by the user. For example, if the<br />

user would like to attach a f<strong>in</strong> to the swimmer, it can be simulated by<br />

locat<strong>in</strong>g a sufficiently strong “virtual” spr<strong>in</strong>g between the swimmer <strong>and</strong><br />

f<strong>in</strong>. This extension has been implemented <strong>in</strong> Swumsuit 4.0.0.<br />

With respect to the accuracy of simulation, it is difficult to estimate<br />

the general value for all cases. The validation study for each case will be<br />

necessary for the future task.<br />

results And dIscussIon<br />

The optimiz<strong>in</strong>g calculation for the trunk motion of the underwater dolph<strong>in</strong><br />

kick has already been carried out by the authors (Nakashima, 2009).<br />

From this optimization, it was found that the obta<strong>in</strong>ed optimal motion<br />

which maximizes the propulsive efficiency is considerably similar to that<br />

of an elite athlete swimmer, <strong>in</strong> which the amplitude of the upper limbs’<br />

displacement is small, the trunk moves as a ‘pitch<strong>in</strong>g seesaw’ with a node,<br />

<strong>and</strong> the lower limbs form a travel<strong>in</strong>g wave. As the next application of<br />

the optimiz<strong>in</strong>g calculation, the optimization of arm stroke <strong>in</strong> the freestyle<br />

swimm<strong>in</strong>g has recently been tackled by the authors (Nakashima et<br />

al., 2009). In this optimization, the maximum jo<strong>in</strong>t torque characteristics<br />

were imposed, <strong>and</strong> the design variables were jo<strong>in</strong>t angles dur<strong>in</strong>g the<br />

underwater stroke. As the next step, the optimization for more detailed<br />

maximum jo<strong>in</strong>t torque characteristics, which depend on jo<strong>in</strong>t angles <strong>and</strong><br />

angular velocities, is now <strong>in</strong> progress. An example of its results is shown <strong>in</strong><br />

chaPter2.<strong>Biomechanics</strong><br />

Figure 2. In this optimization, the swimm<strong>in</strong>g speed was maximized under<br />

the constra<strong>in</strong>ts of the jo<strong>in</strong>t torque characteristics <strong>and</strong> the range of motion<br />

of the jo<strong>in</strong>ts. Note that the time t was nondimensionalized by the stroke<br />

cycle. In order to reduce the calculation time, PSO (Particle Swarm Optimization)<br />

was employed as the optimiz<strong>in</strong>g method <strong>in</strong>stead of the Downhill<br />

Simplex method. The dark l<strong>in</strong>es emitt<strong>in</strong>g from the swimmer’s body<br />

represent the po<strong>in</strong>t of application, direction, <strong>and</strong> magnitude of the fluid<br />

force act<strong>in</strong>g on the swimmer. It was found that the thrust by the h<strong>and</strong> had<br />

two clear peaks when pull<strong>in</strong>g (t = 0.29) <strong>and</strong> push<strong>in</strong>g (t = 0.54) the water.<br />

Figure 2. Simulation results of optimiz<strong>in</strong>g calculation (maximiz<strong>in</strong>g<br />

swimm<strong>in</strong>g speed under constra<strong>in</strong>ts with respect to jo<strong>in</strong>t torque characteristics).<br />

Top: side view, bottom: bottom view.<br />

Next, the musculoskeletal simulation of the crawl stroke was carried out<br />

by Nakashima et al. (2007a). The simulation results of muscle activities<br />

were compared to those of an experiment <strong>in</strong> a previous study. It was<br />

found that most of the tim<strong>in</strong>gs of the muscle activations <strong>in</strong> the simulation<br />

agreed with those <strong>in</strong> the experiment. The analyses of the other<br />

three strokes have also been conducted (Nakashima et al., 2008). Many<br />

reasonable tendencies were obta<strong>in</strong>ed <strong>in</strong> the simulation results. As a next<br />

step, the exam<strong>in</strong>ation of quantitative accuracy of the simulation is now<br />

<strong>in</strong> progress. For this exam<strong>in</strong>ation, the simulation results based on motion<br />

analysis data were compared with experimental EMG data, which<br />

were measured simultaneously with the swimm<strong>in</strong>g motion. An example<br />

of the simulated <strong>and</strong> experimental results is shown <strong>in</strong> Fig.3. It was found<br />

that the swimm<strong>in</strong>g motion obta<strong>in</strong>ed <strong>in</strong> the experiment was represented<br />

well by the simulation. Note that the time t is nondimensional. It was<br />

also found that the upper limb muscles were activated dur<strong>in</strong>g the h<strong>and</strong><br />

stroke (Fig.3 (d)), <strong>and</strong> that the lower limb muscles were activated dur<strong>in</strong>g<br />

the kick (Fig.3 (f )). If the accuracy of such musculoskeletal simulation<br />

becomes satisfactory, it will be greatly useful for the tra<strong>in</strong><strong>in</strong>g <strong>and</strong> coach<strong>in</strong>g<br />

of swimmers.<br />

Figure 3. Results of musculoskeletal simulation <strong>and</strong> images <strong>in</strong> the experiment<br />

for the breaststroke.<br />

Figure 4. Simulation results of synchronized swimm<strong>in</strong>g by three swimmers.<br />

133


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

As an example of multi agents (multiple swimmers) simulation, simple<br />

synchronized swimm<strong>in</strong>g by three swimmers was simulated. In this simulation,<br />

three swimmers performed the flutter kick <strong>in</strong> order to obta<strong>in</strong><br />

thrust <strong>and</strong> fluid force, which lifts the lower limbs. In order to represent<br />

h<strong>and</strong>s grasp<strong>in</strong>g each other, virtual spr<strong>in</strong>gs <strong>and</strong> dampers were employed.<br />

Animation images as the simulation results are shown <strong>in</strong> Fig.4. Note<br />

that the time t is nondimensional. At the <strong>in</strong>itial stage (Fig.4(a)), all the<br />

swimmers swam <strong>in</strong> the same direction. Due to the virtual spr<strong>in</strong>gs <strong>and</strong><br />

dampers attached to their h<strong>and</strong>s, they gradually gathered (Fig.4(b)(c)).<br />

F<strong>in</strong>ally, the swimmers’ upper limbs stably formed a hexagon (Fig.4(d)).<br />

This simulation was very simple s<strong>in</strong>ce it was conducted for the demonstration.<br />

By carefully configur<strong>in</strong>g the <strong>in</strong>teractions among a larger<br />

number of swimmers, an entire simulation of a complicated team performance<br />

<strong>in</strong> synchronized swimm<strong>in</strong>g will become possible <strong>in</strong> the near<br />

future.<br />

As an example of multi objects (a swimmer <strong>and</strong> multiple objects),<br />

monof<strong>in</strong> swimm<strong>in</strong>g was simulated. The monof<strong>in</strong> was divided <strong>in</strong>to five<br />

rigid plates <strong>in</strong> this simulation <strong>in</strong> order to represent its elastic deformation<br />

<strong>in</strong> the sagittal plane. The truncated elliptic cones were employed<br />

<strong>in</strong> order to model the five rigid plates, <strong>and</strong> the plates were represented<br />

by flatten<strong>in</strong>g the cones. Virtual spr<strong>in</strong>gs <strong>and</strong> dampers were employed <strong>in</strong><br />

order to represent connections among the plates. In addition to these,<br />

rotational spr<strong>in</strong>gs <strong>and</strong> dampers were also employed <strong>in</strong> order to represent<br />

the elasticity of the monof<strong>in</strong> itself. The animation images of the simulation<br />

results are shown <strong>in</strong> Fig.5. It was found that large fluid forces were<br />

act<strong>in</strong>g on the monof<strong>in</strong>. In the near future, detailed simulation of the<br />

monof<strong>in</strong> swimm<strong>in</strong>g will be carried out.<br />

Figure 5. Simulation results of monof<strong>in</strong> swimm<strong>in</strong>g.<br />

As the third example of the multi agent/object simulation, the shoot<strong>in</strong>g<br />

motion <strong>in</strong> water polo was simulated. Animation images of the simulation<br />

results are shown <strong>in</strong> Fig.6. In this simulation, the swimmer’s h<strong>and</strong><br />

<strong>and</strong> the ball were connected by a virtual spr<strong>in</strong>g <strong>and</strong> damper before the<br />

release of the ball. From the moment of release (t = 0.68), the spr<strong>in</strong>g <strong>and</strong><br />

damper coefficients were set as zero. The ball was modeled as a series of<br />

four segments of truncated cones. From Fig.6, it can be found that the<br />

ball was smoothly released <strong>and</strong> flew <strong>in</strong> an appropriate direction. It was<br />

also found that a large fluid force was act<strong>in</strong>g on the swimmer’s feet due<br />

to the breaststroke kick at the moment of release. The velocity of the<br />

shot ball was 13.5m/s.<br />

conclusIon<br />

In this paper, three extensions of the swimm<strong>in</strong>g human simulation model<br />

SWUM to the optimiz<strong>in</strong>g calculation, musculoskeletal simulation,<br />

<strong>and</strong> multi agent/object simulation were expla<strong>in</strong>ed <strong>and</strong> various recent<br />

results were presented. The usefulness of the extensions was confirmed<br />

s<strong>in</strong>ce many reasonable results were obta<strong>in</strong>ed. More detailed quantitative<br />

validation will be the future task. In future studies, various mechanical<br />

problems <strong>in</strong> swimm<strong>in</strong>g <strong>and</strong> aquatic activities will be analyzed by the<br />

present extensions.<br />

134<br />

Figure 6. Simulation results of shoot<strong>in</strong>g motion <strong>in</strong> water polo.<br />

reFerences<br />

Nakashima, M. (2005). Development of computer simulation software<br />

“Swumsuit” to analyze mechanics of human swimm<strong>in</strong>g, Proc 10th Int<br />

Symp on Comp Sim <strong>in</strong> Biomech (ISCSB2005): 65-66.<br />

Nakashima, M. (2006). “SWUM” <strong>and</strong> “Swumsuit” -a model<strong>in</strong>g technique<br />

of a self-propelled swimmer. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g X: 66-68.<br />

Nakashima, M. (2007a). Mechanical study of st<strong>and</strong>ard six beat front<br />

crawl swimm<strong>in</strong>g by us<strong>in</strong>g swimm<strong>in</strong>g human simulation model. J<br />

Fluid Sci & Tech, 2(1): 290-301.<br />

Nakashima, M. (2007b). Analysis of breast, back <strong>and</strong> butterfly strokes<br />

by the swimm<strong>in</strong>g human simulation model SWUM, In: Bio-mechanisms<br />

of Swimm<strong>in</strong>g <strong>and</strong> Fly<strong>in</strong>g -Fluid Dynamics, Biomimetic Robots,<br />

<strong>and</strong> Sports Science-: Spr<strong>in</strong>ger, 361-372.<br />

Nakashima, M. (2009). Simulation analysis of the effect of trunk undulation<br />

on swimm<strong>in</strong>g performance <strong>in</strong> underwater dolph<strong>in</strong> kick of<br />

human. J Biomech Sci & Eng, 4(1): 94-104.<br />

Nakashima, M, Motegi, Y. (2007a). Proc 11th Int Symp on Comp Sim<br />

<strong>in</strong> Biomech (ISCSB2007): 59-60.<br />

Nakashima, M., Satou, K., Miura, Y. (2007b). Development of swimm<strong>in</strong>g<br />

human simulation model consider<strong>in</strong>g rigid body dynamics <strong>and</strong><br />

unsteady fluid force for whole body. J Fluid Sci & Tech, 2(1): 56-67.<br />

Nakashima, M., Motegi, Y. (2008). Musculoskeletal simulation to estimate<br />

muscle activity <strong>in</strong> swimm<strong>in</strong>g. Proc 1st Int Sci Conf Aquatic<br />

Space Activities: 327-332.<br />

Nakashima, M., Sato, Y. (2009). Optimization of arm stroke <strong>in</strong><br />

freestyle swimm<strong>in</strong>g by simulation, The Impact of Technology<br />

on Sport III (APCST2009): 207-211.


Influences of the Back Plate on Competitive<br />

Swimm<strong>in</strong>g Start<strong>in</strong>g Motion <strong>in</strong> Particular Projection<br />

Skill<br />

nomura, t. 1 , takeda, t. 2 , takagi, h. 2<br />

1 Kyoto Institute of Technology, Kyoto, Japan<br />

2 University of Tsukuba, Tsukuba, Japan<br />

The purpose of this study was to identify the <strong>in</strong>fluences of the back<br />

plate to competitive swimm<strong>in</strong>g start<strong>in</strong>g motion <strong>in</strong> particular projection<br />

skill. Ten male college elite competitive swimmers performed the track<br />

start from the conventional platform <strong>and</strong> from the platform with the<br />

back plate. The <strong>in</strong>fluences of the back plate to competitive swimm<strong>in</strong>g<br />

start<strong>in</strong>g motion <strong>in</strong> particular projection skill were identified as follows:<br />

(1) At the set position, the centre of mass displaced to a anterior position<br />

(-0.205±0.054 m); (2) The rear leg knee jo<strong>in</strong>t angle of the set<br />

position was about 90 degree (84.3±11.3 degree); (3) Just before take<br />

off, the body was accelerated <strong>in</strong>to the horizontal direction (horizontal<br />

8.76±0.87 m/s 2 , vertical 0.16±1.13 m/s 2 ); (4) At take off, the projection<br />

angle could be kept near horizontal (-8.2±5.2 degree); (5) There were no<br />

significant differences <strong>in</strong> flight phase.<br />

Key words: Back plate block, competitive swimm<strong>in</strong>g start, Projection<br />

skill<br />

IntroductIon<br />

A faster start has characteristics that move the centre of mass fast <strong>in</strong> the<br />

forward direction while the feet are <strong>in</strong> contact with the start<strong>in</strong>g block,<br />

maximize the force exerted through the feet <strong>in</strong> the backward direction,<br />

<strong>and</strong> maximize the force exerted through the h<strong>and</strong>s aga<strong>in</strong>st the start<strong>in</strong>g<br />

block <strong>in</strong> the forward <strong>and</strong> upward direction (Guimarães & Hay, 1985).<br />

Various <strong>in</strong>vestigations have been conducted on styles of set position as<br />

grab, track, h<strong>and</strong>le, <strong>and</strong> so on (Bkanksby et al., 2002; Issur<strong>in</strong> & Verbitsky,<br />

2003; Takeda & Nomura, 2006; Galbraith et al., 2008; Welcher<br />

et al., 2008). They found that there was no significant difference of start<br />

time among the grab start, the track start, <strong>and</strong> the h<strong>and</strong>le start. Furthermore,<br />

the 94% of variance <strong>in</strong> the start time was expla<strong>in</strong>ed by the<br />

water time that was the duration of the period between from first water<br />

contact to 9 m (Guimarães & Hay, 1985). It was considered that the<br />

swimm<strong>in</strong>g start consisted of plural skills, as projection, immersion <strong>and</strong><br />

underwater actions. The underwater speed depends on the horizontal<br />

velocity at the entry. Furthermore, the horizontal velocity at entry results<br />

from the horizontal velocity at takeoff. Therefore, an important<br />

factor is the start<strong>in</strong>g motion on the block to start fast. On the other<br />

h<strong>and</strong>, few studies have been consider<strong>in</strong>g the conditions of the start<strong>in</strong>g<br />

block (Pereira et al., 2003). The start<strong>in</strong>g platform with an adjustable back<br />

plate (posterior foot support) sett<strong>in</strong>g is approved by the <strong>in</strong>ternational<br />

swimm<strong>in</strong>g govern<strong>in</strong>g body (FINA) <strong>in</strong> the facility rule 2.7. But there is<br />

no scientific evidence of the <strong>in</strong>fluences of the platform with the back<br />

plate on the performance of competitive swimm<strong>in</strong>g start. Therefore, the<br />

purpose of this study was to identify the <strong>in</strong>fluences of the back plate<br />

on competitive swimm<strong>in</strong>g start<strong>in</strong>g motion <strong>in</strong> particular projection skill.<br />

Methods<br />

Ten male college elite competitive swimmers were used as subjects <strong>in</strong><br />

this study (Height = 177.5 ± 5.3 cm, Weight = 74.6 ± 8.4 kg, Age = 21.1<br />

± 1.3 yrs). The characteristics of subjects are showed <strong>in</strong> Table 1. Subjects<br />

performed the track start <strong>in</strong> two conditions. One trial started from the<br />

conventional platform (CON). The other trial started from the platform<br />

with the back plate (BKP).<br />

Table 1. Characteristics of subjects.<br />

No. Height Mass Age Specialty Distance<br />

chaPter2.<strong>Biomechanics</strong><br />

Personal<br />

Best<br />

(cm) (kg) (yrs) (m) (m<strong>in</strong>’sec)<br />

0 188.0 86 23 Free style 50 23.33<br />

1 176.5 69 21 Butterfly 100 52.40<br />

2 175.0 73 22 Breast stroke 100 1’01.51<br />

3 175.8 81 21 Individual Medley 400 4’22.30<br />

4 179.0 81 21 Free style 100 50.09<br />

5 174.0 67 22 Free style 100 50.78<br />

6 171.0 65 21 Butterfly 100 53.77<br />

7 181.0 81 19 Breast stroke 100 1’01.78<br />

8 172.0 62 19 Free style 200 3’59.38<br />

9 183.0 81 22 Breaststroke 100 1’01.71<br />

The start<strong>in</strong>g block specifications were as follows; Height from water<br />

surface was 0.75m. The conventional platform was 0.5m width × 0.7m<br />

length, with a 10º slope. As a back plate a pedal for a track <strong>and</strong> field’s<br />

start<strong>in</strong>g equipment was used. It was set 0.44m from the front edge of the<br />

platform, <strong>and</strong> with a 35º slope from the platform.<br />

A digital video camera equipment (Fps = 60Hz, Shutter speed = 250Hz)<br />

was connected to a start<strong>in</strong>g <strong>and</strong> tim<strong>in</strong>g system <strong>and</strong> used to record the<br />

performance of each trial from a sagittal view. Seventeen calibration<br />

po<strong>in</strong>ts were set over a 2.1m width × 2.5m height frame placed at the<br />

start area on the swimmer’s plane of movement. The digital video was<br />

analyzed by digitiz<strong>in</strong>g 13 po<strong>in</strong>ts of the body: left f<strong>in</strong>ger tip, left wrist,<br />

left elbow, left shoulder, left hip, left ear, vertex, left knee, left ankle, left<br />

toe, right knee, right ankle, right toe. It was assumed that arm <strong>and</strong> torso<br />

were symmetrical. K<strong>in</strong>ematic variables were calculated us<strong>in</strong>g 2D-DLT<br />

method with a self-made motion analysis software (Note Player). The<br />

accuracy of coord<strong>in</strong>ates was evaluated by the difference of the actual<br />

value <strong>and</strong> the estimated value (horizontal = 0.034m, vertical = 0.013m).<br />

Butterworth low-pass filter with a cut-off frequency of 6 Hz was used to<br />

remove noise from all raw data.<br />

The objective <strong>in</strong> perform<strong>in</strong>g a swimm<strong>in</strong>g start while the feet are <strong>in</strong><br />

contact with the start<strong>in</strong>g block is to move the centre of mass (CM) as<br />

fast as possible <strong>in</strong> the forward direction. For the purpose of this study,<br />

the projection motion was divided <strong>in</strong>to set position, acceleration phase,<br />

take-off <strong>and</strong> flight phase. The set position was a still position previous to<br />

the start<strong>in</strong>g signal. The acceleration phase was from the start<strong>in</strong>g signal<br />

until take-off. The take-off is the <strong>in</strong>stant on time when the forward leg<br />

leaved from the block. The flight phase was def<strong>in</strong>ed from the take-off<br />

until the first contact with the water surface. K<strong>in</strong>ematic variables for the<br />

projection motion consisted of 15 items, as shown <strong>in</strong> Table 2 <strong>and</strong> Figure<br />

1. The x-axis was def<strong>in</strong>ed to be the horizontal axis <strong>in</strong> the ma<strong>in</strong> plane of<br />

movement. The y-axis was def<strong>in</strong>ed to be the vertical one.<br />

results<br />

At the start<strong>in</strong>g position, the coord<strong>in</strong>ate of CM <strong>in</strong> BKP was<br />

(-0.205±0.054 m, 1.367±0.029 m). It was significantly forwarded <strong>and</strong><br />

at a higher position than <strong>in</strong> CON (-0.253±0.054 m, 1.355±0.031 m).<br />

The knee jo<strong>in</strong>t angles of front <strong>and</strong> rear leg <strong>in</strong> BKP were respectively<br />

140.1±5.7º, <strong>and</strong> 84.3±11.3º. The knees were extended significantly<br />

narrower than <strong>in</strong> CON (145.5±8.0º <strong>and</strong> 97.1±11.4º). The ankle jo<strong>in</strong>t<br />

angles of front <strong>and</strong> rear leg <strong>in</strong> BKP were, respectively, 140.6±8.4º, <strong>and</strong><br />

104.1±8.4º. The front ankle was dorsal-flexed significantly narrower<br />

than that <strong>in</strong> CON (147.1±10.5º). On the other h<strong>and</strong>, the rear ankle <strong>in</strong><br />

135


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 2. K<strong>in</strong>ematic variables for projective motion.<br />

Phase Symbol Unit Explanation<br />

Set position<br />

Acceleration<br />

Take-off<br />

Flight<br />

136<br />

Px m<br />

Py m<br />

Horizontal position of CM from the front<br />

edge of the platform<br />

Vertical position of CM from the water<br />

surface<br />

θ_knee deg Angle of knee jo<strong>in</strong>t at the set position<br />

θ_ankle deg Angle of ankle jo<strong>in</strong>t at the set position<br />

θ_before deg<br />

Mean pre-projection angle on velocity<br />

vector of CM dur<strong>in</strong>g 0.3 second just before<br />

to the take-off<br />

Ax_before m/s 2 Mean horizontal acceleration of CM dur<strong>in</strong>g<br />

0.3 second just before the take-off<br />

Ay_before m/s 2 Mean vertical acceleration of CM dur<strong>in</strong>g<br />

0.3 second just before the take-off<br />

T_take-off sec<br />

θ_take-off deg<br />

θ_body deg<br />

Time duration from start<strong>in</strong>g signal to<br />

take-off<br />

Angle of the velocity vector of CM at the<br />

take-off<br />

Angle of CM connected with the front<br />

edge of platform <strong>and</strong> the horizontal l<strong>in</strong>e at<br />

the take-off<br />

V_take-off m/s Velocity of CM at the take-off<br />

Vx_take-off m/s Horizontal velocity of CM at the take-off<br />

Vy_take-off m/s Vertical velocity of CM the take-off<br />

D_flight m<br />

Distance of flight (horizontal distance from<br />

the wall to f<strong>in</strong>gertip contact with water<br />

surface)<br />

Vx_flight m/s Mean horizontal velocity dur<strong>in</strong>g flight<br />

CM<br />

Ax_before<br />

ƒ Æ_before CM Vx_take-off<br />

Ay_before<br />

ƒ Æ_take-off<br />

Vy_take-off<br />

V_take-off<br />

ƒ Æ_body<br />

CM<br />

Vx_flight<br />

dVx/dt<br />

CM<br />

dVy/dt<br />

Ax_before<br />

(Vx_before)<br />

ƒ Æ_before CM Vx_take-off<br />

Ay_before<br />

(Vy_before)<br />

Px, Py<br />

ƒ Æ_knee<br />

(V_before)<br />

ƒ Æ_take-off<br />

Vy_take-off<br />

V_take-off<br />

ƒ Æ_ankle<br />

ƒ Æ_body<br />

CM<br />

Vx_flight<br />

dVx/dt<br />

CM<br />

dVy/dt<br />

Ax_before<br />

(Vx_before)<br />

ƒ Æ_before<br />

Ay_before<br />

(Vy_before)<br />

(V_before)<br />

dVx/dt<br />

dVy/dt<br />

(Vx_before)<br />

(Vy_before)<br />

Px, Py<br />

ƒ Æ_knee<br />

(V_before)<br />

ƒ Æ_ankle<br />

Back plate 35 deg<br />

Platform 10 deg Height 0.75m<br />

(0,0)<br />

D_flight<br />

T_take-off<br />

Acceleration Flight<br />

Set position Take-off Entry<br />

Figure 1. Diagrammatic representation of k<strong>in</strong>ematic variables.<br />

BKP was plantar-flexed <strong>and</strong> positioned significantly wider than one <strong>in</strong><br />

CON (76.4±7.2º). Dur<strong>in</strong>g the last 0.3 second before to the take-off <strong>in</strong><br />

the acceleration phase, the mean pre-projection angle of CM <strong>in</strong> BKP<br />

was -6.7±4.4º. It was significantly nearer to the horizontal than that <strong>in</strong><br />

CON (-8.2±4.3º). Mean horizontal acceleration <strong>in</strong> BKP was 8.76±0.87<br />

m/s 2 . It was significantly larger than that <strong>in</strong> CON (7.96±0.79 m/s 2 ). On<br />

the other h<strong>and</strong>, mean vertical acceleration <strong>in</strong> BKP was 0.16±1.13 m/s 2 .<br />

It was near to the zero than that <strong>in</strong> CON (-0.58±0.79 m/s 2 ). At take-off,<br />

projection angle of CM <strong>in</strong> BKP was -8.2±5.2º. It was significantly more<br />

close to the horizontal <strong>and</strong> larger than that <strong>in</strong> CON (-10.5±4.9º). Verti-<br />

cal velocity of CM at the take-off <strong>in</strong> BKP was -0.65±0.45 m/s. It was<br />

near to the zero than that <strong>in</strong> CON (-0.81±0.45 m/s). In other items for<br />

the take-off (T_take-off, θ_body, V_take-off <strong>and</strong> Vx_take-off ), significant<br />

differences were not observed between start<strong>in</strong>g conditions. Dur<strong>in</strong>g<br />

flight phase, non-significant differences were also perceived. The ma<strong>in</strong><br />

results of this study are shown <strong>in</strong> Table 3.<br />

Table 3. K<strong>in</strong>ematic variables compared between conventional <strong>and</strong> <strong>in</strong><br />

back plate start<strong>in</strong>g conditions.<br />

Phase Symbol Unit<br />

Set<br />

position<br />

Accele-<br />

ration<br />

Take-<br />

off<br />

Flight<br />

CON BKP<br />

Significant<br />

Mean S.D Mean S.D Difference<br />

Px m -0.253 ± 0.054 -0.205 ± 0.054 ***<br />

Py m 1.355 ± 0.031 1.367 ± 0.029 **<br />

θ_knee (front) deg 145.5 ± 8.0 140.1 ± 5.7 **<br />

θ_knee (rear) deg 97.1 ± 11.4 84.3 ± 11.3 ***<br />

θ_ankle (front) deg 147.1 ± 10.5 140.6 ± 8.4 **<br />

θ_ankle (rear) deg 76.4 ± 7.2 104.1 ± 8.4 ***<br />

θ_before deg -8.2 ± 4.3 -6.7 ± 4.4 *<br />

Ax_before m/s 2 7.96 ± 0.79 8.76 ± 0.87 *<br />

Ay_before m/s 2 -0.58 ± 0.79 0.16 ± 1.13 **<br />

T_take-off sec 0.784 ± 0.033 0.764 ± 0.046 N.S.<br />

θ_take-off deg -10.5 ± 4.9 -8.2 ± 5.2 *<br />

θ_body deg 20.5 ± 5.4 20.9 ± 5.9 N.S.<br />

V_take-off m/s 4.47 ± 0.30 4.41 ± 0.32 N.S.<br />

Vx_take-off m/s 4.38 ± 0.22 4.34 ± 0.26 N.S.<br />

Vy_take-off m/s -0.81 ± 0.45 -0.65 ± 0.45 *<br />

D_flight m 3.00 ± 0.19 2.99 ± 0.18 N.S.<br />

Vx_flight m/s 4.48 ± 0.16 4.46 ± 0.17 N.S.<br />

* p < 0.05, ** p < 0.01, *** p < 0.001<br />

dIscussIon<br />

At the set position, the CM at the back plate condition is displaced to<br />

comparatively anterior position regard<strong>in</strong>g the CON. It was <strong>in</strong> agreement<br />

with study of squatt<strong>in</strong>g-to-st<strong>and</strong><strong>in</strong>g movement that heel elevation<br />

primarily <strong>in</strong>fluenced postural adjustment as anterior displacement<br />

of the hip (Sriwarno et al., 2008). In the back plate condition, the rear<br />

knee jo<strong>in</strong>t angle obta<strong>in</strong>ed a value close to the 90º. The knee angle of the<br />

posterior leg was recommended 90º by a manufacturer of start<strong>in</strong>g blocks<br />

with back plate that approved by FINA. However, isometric force-angle<br />

relationship of knee extension reported that higher force is produced at<br />

105º to 120º than <strong>in</strong> other jo<strong>in</strong>t angle conditions (L<strong>in</strong>dahl et al., 1969).<br />

Moreover, the relationship isometric knee-hip extension force <strong>and</strong> the<br />

percentage of leg length that was criterion of the knee flexion had <strong>in</strong>vestigated.<br />

The force exhibited a peak when the foot position was at<br />

80-90% of leg length (Yamauchi et al., 2007). If this ratio was angle<br />

converted, it became about 106º to 128º. Therefore, at the set position <strong>in</strong><br />

the back plate condition, the rear knee jo<strong>in</strong>t should be extended a little<br />

more. As a result, CM moved ahead slightly.<br />

It seemed that the θ_before <strong>in</strong> BKP approached horizontally was a<br />

preferable effect with back plate, because mov<strong>in</strong>g CM fast to the forward<br />

direction was one important factor for a faster start (Guimarães<br />

& Hay, 1985). It was supported by Ax_before <strong>in</strong> BKP which was grater<br />

than one <strong>in</strong> CON <strong>and</strong> Ay_before <strong>in</strong> BKP was approximat<strong>in</strong>g to become<br />

zero. The force distribution on the start<strong>in</strong>g block had reported that a<br />

higher force at last stage of the start movement, <strong>and</strong> force gradually<br />

became lower until take-off (Krüger et al., 2003). It was considered


that the cause that the body weight could not be supported by the leg<br />

because θ_take-off was about 2º lower than θ_before.<br />

There were a few <strong>in</strong>fluences of the back plate at take-off <strong>and</strong> dur<strong>in</strong>g<br />

flight phase. The important aspect was that swimmers could improve<br />

with any technique with some <strong>in</strong>tensive practice (S<strong>and</strong>ers & Bonnar,<br />

2008). As subjects did not have an enough skill for us<strong>in</strong>g a back plate yet,<br />

they could not keep the dom<strong>in</strong>ation on the start<strong>in</strong>g block.<br />

conclusIon<br />

In conclusion, the <strong>in</strong>fluences of the back plate to competitive swimm<strong>in</strong>g<br />

start<strong>in</strong>g motion <strong>in</strong> particular projection skill were identified as follows:<br />

(1) At the set position, the centre of mass displaced to a comparatively<br />

anterior position; (2) The rear leg knee jo<strong>in</strong>t angle at the set position<br />

was set at about 90º; (3) Just before take-off, the body was accelerated<br />

<strong>in</strong>to the horizontal direction; (4) At take-off, the projection angle could<br />

be kept nearer the horizontal. For a fast start, it is suggested that some<br />

<strong>in</strong>tensive practice make best us<strong>in</strong>g of these advantages on the start<strong>in</strong>g<br />

block.<br />

reFerences<br />

Blanksby B., Nicholson L., & Elliott B. (2002). Biomechanical analysis<br />

of the grab, track <strong>and</strong> h<strong>and</strong>le swimm<strong>in</strong>g starts: an <strong>in</strong>tervention study.<br />

Sports Biomech, 1, 11-24.<br />

Galbraith H., Scurr J., Hencken C., Wood L., & Graham-Smith P.<br />

(2008). Biomechanical comparison of the track start <strong>and</strong> the modified<br />

one-h<strong>and</strong>ed track start <strong>in</strong> competitive swimm<strong>in</strong>g: an <strong>in</strong>tervention<br />

study. J Appl Biomech, 24, 307-15.<br />

Guimarães A.C.S., & Hay J.G. (1985). A mechanical analysis of the<br />

grab start<strong>in</strong>g technique <strong>in</strong> swimm<strong>in</strong>g. Int J Sport Biomech, 1, 25-35.<br />

Issur<strong>in</strong> V., & Verbitsky O. (2003). Track start vs. grab start: Evidence<br />

from the Sydney Olympic Games. In: <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g IX, (pp. 213-218). Sa<strong>in</strong>t-Etienne: University of Sa<strong>in</strong>t-<br />

Etienne.<br />

Krüger T., Wick D., Hohmann A., El-Bahrawi M., & Koth A. (2003).<br />

<strong>Biomechanics</strong> of the grab <strong>and</strong> track start technique. In: <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX (pp. 219-223). Sa<strong>in</strong>t-Etienne: University<br />

of Sa<strong>in</strong>t-Etienne.<br />

L<strong>in</strong>dahl O., Mov<strong>in</strong> A., & R<strong>in</strong>gqvist I. (1969). Knee extension: Measurement<br />

of the isometric force <strong>in</strong> different positions of the knee jo<strong>in</strong>t.<br />

Acta Orthop. Sc<strong>and</strong><strong>in</strong>av., 40, 79-85.<br />

Pereira S., Araujo L., & Roesler H. (2003). The <strong>in</strong>fluence of variation <strong>in</strong><br />

height <strong>and</strong> slope of start<strong>in</strong>g platforms on the start<strong>in</strong>g time of speed<br />

swimmers. In: <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX (pp. 237-<br />

241). Sa<strong>in</strong>t-Etienne: University of Sa<strong>in</strong>t-Etienne.<br />

S<strong>and</strong>ers R., & Bonnar S. (2008). Start technique; recent f<strong>in</strong>d<strong>in</strong>gs.<br />

Coaches<strong>in</strong>fo.com. Retrieved February 25, 2010, from http://<br />

www.coaches<strong>in</strong>fo.com/<strong>in</strong>dex.php?option= com_content&id=134<br />

&Itemid=138.<br />

Sriwarno A.B., Shimomura Y., Iwanaga K., & Katsuura T. (2008). The<br />

effect of heel elevation on postural adjustment <strong>and</strong> activity of lowerextremity<br />

muscles dur<strong>in</strong>g deep squatt<strong>in</strong>g-to-st<strong>and</strong><strong>in</strong>g movement <strong>in</strong><br />

normal subjects. J.Phys.Ther.Sci., 20, 31-38.<br />

Takeda T., & Nomura T. (2006). What are differences between grab <strong>and</strong><br />

track start? Portuguese Journal of Sport Sciences, 6(Supl. 2), 102-105.<br />

Welcher R.L., H<strong>in</strong>richs R.N., & George T.R. (2008). Front- or rearweighted<br />

track start or grab start: which is the best for female swimmers?<br />

Sports Biomech, 7, 100-13.<br />

Yamauchi J., Mishima C., Fujiwara M., Nakayama S., & Ishii N. (2007).<br />

Steady-state force-velocity relation <strong>in</strong> human multi-jo<strong>in</strong>t movement<br />

determ<strong>in</strong>ed with force clamp analysis. J Biomech., 40, 1433-1442.<br />

AcKnoWledGeMents<br />

This study was supported by The Grant <strong>in</strong> Aid for Scientific Research<br />

(C) 20500543 of Japan Society for the Promotion Science.<br />

chaPter2.<strong>Biomechanics</strong><br />

K<strong>in</strong>ematical Characterisation of a Basic Head-out<br />

Aquatic Exercise dur<strong>in</strong>g an Incremental Protocol<br />

oliveira, c. 1,4 , teixeira, G. 1,4 , costa, M.J. 2,4 , Mar<strong>in</strong>ho, d.A. 3,4 ,<br />

silva, A.J. 1,4 , Barbosa, t.M. 2,4<br />

1University of Trás-os-Montes <strong>and</strong> Alto Douro, Vila Real, Portugal<br />

2Polytechnic Institute of Bragança, Bragança, Portugal<br />

3University of Beira Interior, Covilhã, Portugal<br />

4Research Centre <strong>in</strong> Sports, Health <strong>and</strong> Human Development, Vila Real,<br />

Portugal<br />

The aim of this study was to analyze the relationships between musical<br />

cadence <strong>and</strong> k<strong>in</strong>ematical characteristics of a basic head-out aquatic exercise,<br />

when immersed to the breast. Six young women with at least one year<br />

of experience conduct<strong>in</strong>g head-out aquatic classes were videotaped <strong>in</strong> the<br />

sagital plane with a pair of cameras provid<strong>in</strong>g a dual projection from both<br />

above <strong>and</strong> underwater perform<strong>in</strong>g 5 <strong>in</strong>cremental bouts (120 b.m<strong>in</strong> -1 , 135<br />

b.m<strong>in</strong> -1 , 150 b.m<strong>in</strong> -1 , 165 b.m<strong>in</strong> -1 <strong>and</strong> 180 b.m<strong>in</strong> -1 ) of the basic head-out<br />

aquatic exercise “rock<strong>in</strong>g horse”. There was a decrease of the cycle period<br />

throughout the <strong>in</strong>cremental protocol. Relationships between horizontal<br />

or vertical displacements with music cadence were not significant. On the<br />

other h<strong>and</strong>, <strong>in</strong>creased cadence imposed <strong>in</strong>creased segmental <strong>and</strong> centre of<br />

mass’ velocities. As a conclusion expert <strong>and</strong> fit subjects seem to <strong>in</strong>crease<br />

segmental velocity with <strong>in</strong>creas<strong>in</strong>g musical cadence to avoid the decrease of<br />

the segmental range of motion.<br />

Key words: head-out aquatic exercises, rock<strong>in</strong>g horse, musical cadence,<br />

k<strong>in</strong>ematics<br />

IntroductIon<br />

Massive research has been produced throughout the last decades <strong>in</strong> order<br />

to better underst<strong>and</strong> the role of head-out aquatic exercises <strong>in</strong> populations’<br />

health (Barbosa et al, 2009a). Indeed, such studies aimed to characterize the<br />

physiological acute <strong>and</strong>/or chronic response of subjects perform<strong>in</strong>g headout<br />

aquatic exercises. Moreover, the comprehensive knowledge about the<br />

biomechanical (i.e. k<strong>in</strong>ematical) behavior perform<strong>in</strong>g this aquatic activity<br />

is quite reduced.<br />

Conduct<strong>in</strong>g head-out aquatic exercise sessions, <strong>in</strong>structors often use<br />

the music cadence to achieve a pre-imposed <strong>in</strong>tensity of exertion. Music<br />

cadences between 130 <strong>and</strong> 150 b.m<strong>in</strong> -1 are suggested by technical literature<br />

for head-out aquatic exercises (K<strong>in</strong>der <strong>and</strong> See, 1992). At least one empirical<br />

study reported that for healthy <strong>and</strong> physically active subjects <strong>in</strong>structors<br />

should choose music cadences between 136 <strong>and</strong> 158 b.m<strong>in</strong> -1 (Barbosa et<br />

al., 2009b).<br />

Increases <strong>in</strong> the music cadence imposes significant <strong>in</strong>creases <strong>in</strong> the acute<br />

physiological adaptation (e.g., rate of perceived effort, heart rate or blood<br />

lactate) of the subjects (Hoshijima et al., 1999; Barbosa et al., 2009b). It<br />

is hypothesized that <strong>in</strong>creased physiological response may be expla<strong>in</strong>ed by<br />

the fact that <strong>in</strong>creas<strong>in</strong>g music cadence will also <strong>in</strong>crease movement velocity<br />

<strong>and</strong> frequency, decreas<strong>in</strong>g the segmental range of motion. However, to<br />

our knowledge there is no study <strong>in</strong> the literature report<strong>in</strong>g the k<strong>in</strong>ematical<br />

changes imposed by an <strong>in</strong>cremental cadence protocol at head-out aquatic<br />

exercises.<br />

The aim of this study was to analyze the relationships between musical<br />

cadence <strong>and</strong> k<strong>in</strong>ematical characteristics of a basic head-out aquatic exercise,<br />

when immersed to the xiphoid process (i.e., breast).<br />

Methods<br />

Six non-pregnant, cl<strong>in</strong>ically healthy <strong>and</strong> physically active young women<br />

hold<strong>in</strong>g a graduation degree <strong>in</strong> Sports Sciences <strong>and</strong> at least one year of<br />

experience conduct<strong>in</strong>g head-out aquatic classes volunteered to participate<br />

<strong>in</strong> this study (23.67 ± 0.52 y-old; 57.42 ± 4.78 kg of body mass; 1.64 ± 0.07<br />

m of height; 22.17 ± 2.56 kg.m -2 of body mass <strong>in</strong>dex).<br />

137


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The protocol consisted of five bouts of 16 repetitions perform<strong>in</strong>g the basic<br />

head-out aquatic exercise “rock<strong>in</strong>g horse” at the “water tempo” immersed<br />

to the xiphoid process (i.e., breast). Bouts <strong>in</strong>tensity were 80 %, 90 %, 100<br />

%, 110 % <strong>and</strong> 120 % of the cadence reported by Barbosa et al. (2009b) to<br />

achieve a 4 mmol.l -1 of blood lactate, represent<strong>in</strong>g respectively 120 b.m<strong>in</strong> -1 ,<br />

135 b.m<strong>in</strong> -1 , 150 b.m<strong>in</strong> -1 , 165 b.m<strong>in</strong> -1 <strong>and</strong> 180 b.m<strong>in</strong> -1 cadences. Musical cadence<br />

was controlled electronically by a metronome (Korg, MA-30, Tokyo,<br />

Japan) connected to a sound system.<br />

The protocol was videotaped <strong>in</strong> sagital plane with a pair of cameras provid<strong>in</strong>g<br />

a dual projection from both underwater (GR-SXM25 SVHS, JVC,<br />

Yokoama, Japan) <strong>and</strong> above (GR-SX1 SVHS, JVC, Yokoama, Japan) the<br />

water surface. The images of both cameras were recorded <strong>in</strong>dependently.<br />

The study comprised the k<strong>in</strong>ematical analysis of the full cycles (Ariel Performance<br />

Analysis System, Ariel Dynamics Inc., USA) through a VCR<br />

(Panasonic, AG 7355, Japan) at a frequency of 50 Hz. Zatsiorsky’s model<br />

with an adaptation by de Leva (1996) was used with the division of the<br />

trunk <strong>in</strong> two articulated parts. To create a s<strong>in</strong>gle image of dual projection as<br />

described previously (Vilas-Boas et al., 1997; Barbosa et al., 2005), the <strong>in</strong>dependent<br />

digitalization from both cameras was reconstructed with the help<br />

of a calibration object (0.675 x 0.855 m; 6 control po<strong>in</strong>ts) <strong>and</strong> a 2D-DLT<br />

algorithm (Abdel-Aziz <strong>and</strong> Karara, 1971). For the analysis of the curve of<br />

the centre of mass’s k<strong>in</strong>ematics a filter with a cut-off frequency of 5 Hz was<br />

used, as suggested by W<strong>in</strong>ter (1990). For the segmental k<strong>in</strong>ematics a cut-off<br />

frequency of 9 Hz was used, near to the value proposed by W<strong>in</strong>ter (1990). A<br />

double-passage filter<strong>in</strong>g for the signal process<strong>in</strong>g was used.<br />

The follow<strong>in</strong>g variables were analysed: (i) cycle period; (ii) 2D l<strong>in</strong>ear<br />

position ranges (foot, h<strong>and</strong> <strong>and</strong> centre of mass), <strong>and</strong> (iii) 2D l<strong>in</strong>ear velocity<br />

ranges (foot, h<strong>and</strong> <strong>and</strong> centre of mass).<br />

The normality of the distributions was assessed with the Shapiro-Wilk<br />

test. L<strong>in</strong>ear regression equations models <strong>and</strong> its coefficients of determ<strong>in</strong>ation<br />

were used to describe the relationships between musical cadence <strong>and</strong> biomechanical<br />

variables. The level of statistical significance was set at p ≤ 0.05.<br />

results<br />

Figure 1 presents a qualitative analysis from the centre of mass k<strong>in</strong>ematics<br />

from a s<strong>in</strong>gle subject dur<strong>in</strong>g the second bout at 135 b.m<strong>in</strong>-1 . Figure 2 displays<br />

the simple scatter gram from the cycle period accord<strong>in</strong>g to the musical<br />

cadence imposed. There was a decrease of the cycle period throughout the<br />

experimental protocol (R2 = 0.83; P < 0.01). Figure 3 <strong>and</strong> 4 presents respectively<br />

the overlay scatter gram for 2D displacement <strong>and</strong> 2D velocity accord<strong>in</strong>g<br />

to the musical cadence imposed. There were non-significant relationship<br />

between horizontal (0.01 < R2 < 0.31) or vertical (0.01 < R2 < 0.03) displacements<br />

with the cadence imposed. On the other h<strong>and</strong>, for the horizontal <strong>and</strong><br />

vertical velocities there were several significant relationships with the musical<br />

cadence. Increased cadence imposed <strong>in</strong>creased centre of mass’ velocities<br />

for its horizontal (R2 = 0.26; P < 0.01) <strong>and</strong> vertical components (R2 = 0.41; P<br />

< 0.01), h<strong>and</strong>’s horizontal velocity (R2 = 0.26; P < 0.01), foot’s horizontal (R2 = 0.23; P = 0.02) <strong>and</strong> vertical (R2 <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b 65<br />

<strong>and</strong> 4 presents respectively the overlay scatter gram for 2D displacement <strong>and</strong> 2D<br />

velocity accord<strong>in</strong>g to the musical cadence imposed. There were non-significant<br />

relationship between horizontal (0.01 < R<br />

= 0.23; P = 0.01) velocities.<br />

2 < 0.31) or vertical (0.01 < R 2 < 0.03)<br />

displacements with the cadence imposed. On the other h<strong>and</strong>, for the horizontal <strong>and</strong><br />

vertical velocities there were several significant relationships with the musical cadence.<br />

Increased cadence imposed <strong>in</strong>creased centre of mass’ velocities for its horizontal (R 2 =<br />

0.26; P < 0.01) <strong>and</strong> vertical components (R 2 = 0.41; P < 0.01), h<strong>and</strong>’s horizontal<br />

velocity (R 2 = 0.26; P < 0.01), foot’s horizontal (R 2 = 0.23; P = 0.02) <strong>and</strong> vertical (R 2 =<br />

0.23; P = 0.01) velocities.<br />

A B<br />

C D<br />

Figure 1. Qualitative analysis from the centre of mass’ horizontal displacement (panel<br />

A), vertical displacement (panel B), horizontal velocity (panel C) <strong>and</strong> vertical velocity<br />

(panel D) from a s<strong>in</strong>gle subject perform<strong>in</strong>g the second bout at 135 b.m<strong>in</strong> -1 Figure 1. Qualitative analysis from the centre of mass’ horizontal displacement<br />

(panel A), vertical displacement (panel B), horizontal velocity . (panel<br />

C) <strong>and</strong> vertical velocity (panel D) from a s<strong>in</strong>gle subject perform<strong>in</strong>g the second<br />

bout at 135 b.m<strong>in</strong>-1 .<br />

138<br />

Figure 2. Simple scatter gram from the cycle period accord<strong>in</strong>g to the<br />

cadence imposed.<br />

Figure 3. Overlay scatter gram from horizontal displacement <strong>and</strong> vertical<br />

displacement accord<strong>in</strong>g to the cadence imposed.


Figure 4. Overlay scatter gram from horizontal velocity <strong>and</strong> vertical velocity<br />

accord<strong>in</strong>g to the cadence imposed.<br />

dIscussIon<br />

The aim of this study was to analyze the relationships between musical<br />

cadence <strong>and</strong> k<strong>in</strong>ematical characteristics of a basic head-out aquatic exercise,<br />

when immersed to the breast. Ma<strong>in</strong> data suggests that expert <strong>and</strong><br />

fit subjects <strong>in</strong>crease segmental velocity with <strong>in</strong>creas<strong>in</strong>g musical cadence<br />

to avoid the decrease of the segmental range of motion.<br />

There was a very high relationship between cycle period <strong>and</strong> the<br />

cadence, with a decrease of the time variable throughout the <strong>in</strong>cremental<br />

protocol. On one h<strong>and</strong>, there were no significant relationships between<br />

any of the displacement variables <strong>and</strong> the musical cadence. On the other<br />

habd, most of the velocity variables were moderate, positive <strong>and</strong> significantly<br />

related to the musical cadence.<br />

Cycle period is considered as be<strong>in</strong>g:<br />

P =<br />

n<br />

∑ ti<br />

i=<br />

1<br />

(1)<br />

Where P is the cycle period (<strong>in</strong> s) <strong>and</strong> t is the duration (<strong>in</strong> s) of each<br />

phase, be<strong>in</strong>g the exercise composed by i partial phases. The duration of<br />

each phase can be computed as:<br />

d<br />

i t i = (2)<br />

vi<br />

Where t i is the duration of each partial phase of the exercise (<strong>in</strong> s), d i is<br />

the segment displacement (<strong>in</strong> m) dur<strong>in</strong>g the partial phase <strong>and</strong> v i is the<br />

segment velocity (<strong>in</strong> m·s -1 ) dur<strong>in</strong>g the partial phase.<br />

Although it was hypothesized <strong>in</strong> the <strong>in</strong>troduction section that <strong>in</strong>creas<strong>in</strong>g<br />

cadence would impose a decrease of the segments range of mo-<br />

chaPter2.<strong>Biomechanics</strong><br />

tion; the subjects decreased the t i through an <strong>in</strong>crease of the v i . It can<br />

be speculated that this specific motor control, as well as, biomechanical<br />

strategy, can be related to the subjects’ profile. They were: (i) expert subjects,<br />

i.e., head-out aquatic exercise <strong>in</strong>structors that are aware from the<br />

need to ma<strong>in</strong>ta<strong>in</strong> at all time a large range of motion perform<strong>in</strong>g basic<br />

exercises, <strong>in</strong>dependently from the cadence imposed <strong>and</strong>; (ii) very active<br />

subjects that not only are aware from this technical tips, but are also<br />

physically fit, allow<strong>in</strong>g them to ma<strong>in</strong>ta<strong>in</strong> such range of motion at different<br />

musical cadences.<br />

As a conclusion, expert <strong>and</strong> fit subjects seem to <strong>in</strong>crease segmental<br />

velocity with <strong>in</strong>creas<strong>in</strong>g cadences to avoid the decrease of the segmental<br />

range of motion.<br />

reFerences<br />

Abdel-Aziz Y, Karara, H. (1971). Direct l<strong>in</strong>ear transformation: from<br />

comparator coord<strong>in</strong>ates <strong>in</strong>to object coord<strong>in</strong>ates <strong>in</strong> close range photogrammetry.<br />

Proceed<strong>in</strong>gs of the Symposium on close-range photogrammetry,<br />

p. 1-18, Church Falls.<br />

Barbosa TM, Kesk<strong>in</strong>en KL, Fern<strong>and</strong>es RJ, Colaço P, Lima AB, Vilas-<br />

Boas JP. (2005). Energy cost <strong>and</strong> <strong>in</strong>tracyclic variation of the velocity<br />

of the centre of mass <strong>in</strong> butterfly stroke. Eur J Appl Phys 93:519-523.<br />

Barbosa TM, Mar<strong>in</strong>ho DA, Bragada JA, Reis VM, Silva AJ. (2009a).<br />

Physiological assessment of head-out aquatic exercises <strong>in</strong> healthy<br />

subjects: a qualitative review. J Sports Sci Med. 8: 179-189<br />

Barbosa TM, Sousa V, Silva AJ, Reis V, Mar<strong>in</strong>ho DA, Bragada JA.<br />

(2009b). Effects of music cadence <strong>in</strong> the acute physiological adaptations<br />

to head-out aquatic exercises. J Strength Cond Res. Epub ahead<br />

of pr<strong>in</strong>t<br />

de Leva P. (1996). Adjustments to Zatsiorsky-Seluyanov’s segment <strong>in</strong>ertia<br />

parameters. Journal of <strong>Biomechanics</strong> 29:1223-1230.<br />

Hoshijima Y, Torigoe K, Yamamoto M, Nishimura S, Abo N, Imoto M,<br />

Miyachi M, Onodera S. (1999). Effects of music rhythm on heart<br />

rate <strong>and</strong> oxygen uptake dur<strong>in</strong>g squat exercises <strong>in</strong> water <strong>and</strong> on l<strong>and</strong>.<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII, p. 337-339. Gummerus<br />

Pr<strong>in</strong>t<strong>in</strong>g.<br />

K<strong>in</strong>der T, See J. (1992). Aqua Aerobics - A Scientific Approach.<br />

Dubuque: Eddie Bowers Publish<strong>in</strong>g<br />

Vilas-Boas JP, Cunha P, Figueiras T, Ferreira M, Duarte J. (1997).<br />

Movement analysis <strong>in</strong> simultaneous swimm<strong>in</strong>g techniques. Cologne<br />

Swimm<strong>in</strong>g Symposium. Verlag. p.95-103. Sport Fahnemann<br />

W<strong>in</strong>ter D (1990). Biomechanic <strong>and</strong> Motor Control of Human Movement.<br />

Chichester: John Wiley & Sons.<br />

139


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Influence of Swimm<strong>in</strong>g Speed on the Affected- <strong>and</strong><br />

Unaffected-Arm Stroke Phases of Competitive<br />

Unilateral Arm Amputee Front Crawl Swimmers<br />

osborough, c.d. 1 , Payton, c.J. 1 , daly, d.J. 2<br />

1 Manchester Metropolitan University, Alsager, United K<strong>in</strong>gdom<br />

2 Katholieke Universiteit Leuven, Leuven, Belgium<br />

The purpose of this study was to determ<strong>in</strong>e whether the arm stroke<br />

phases used by competitive unilateral arm amputee crawl swimmers<br />

differed between their affected <strong>and</strong> unaffected sides <strong>and</strong> whether these<br />

phases changed with an <strong>in</strong>crease <strong>in</strong> speed. Thirteen highly-tra<strong>in</strong>ed<br />

swimmers were video-taped underwater from two side-views dur<strong>in</strong>g five<br />

<strong>in</strong>creas<strong>in</strong>gly faster 25 m front crawl trials. At all swimm<strong>in</strong>g speeds, the<br />

stroke phases of the affected <strong>and</strong> unaffected arms differed significantly.<br />

As speed <strong>in</strong>creased, the duration of the affected-arm’s Entry <strong>and</strong> Glide<br />

phase <strong>and</strong> the unaffected-arm’s Pull phase decreased significantly; the<br />

duration of both arms’ Push phase <strong>in</strong>creased significantly. The amputees<br />

used a coord<strong>in</strong>ation strategy that asymmetrically adjusted<br />

their arm movements to ma<strong>in</strong>ta<strong>in</strong> the stable repetition of their<br />

overall stroke cycle at different speeds.<br />

Key words: swimm<strong>in</strong>g; disability sport; Motor control; <strong>Biomechanics</strong><br />

IntroductIon<br />

Stroke phases have been frequently used to describe the propulsive <strong>and</strong><br />

non-propulsive arm actions of able-bodied front crawl swimmers. Maglischo<br />

et al. (1988) reported that while there were four propulsive phases<br />

<strong>in</strong> the front crawl underwater arm stroke action: (1) Downsweep; (2)<br />

Insweep; (3) Outsweep; <strong>and</strong> (4) Upsweep, able-bodied swimmers were<br />

unable to generate large propulsive forces <strong>in</strong> more than two of these phases.<br />

Later, Chollet et al. (2000), when formulat<strong>in</strong>g the Index of Coord<strong>in</strong>ation<br />

for front crawl, separated the complete action of the arm stroke cycle<br />

<strong>in</strong>to four dist<strong>in</strong>ct phases: (A) Entry <strong>and</strong> Catch; (B) Pull; (C) Push; (D)<br />

Recovery, of which they assumed, B <strong>and</strong> C were propulsive <strong>and</strong> A <strong>and</strong> D<br />

were non-propulsive.<br />

For competitive swimmers with a s<strong>in</strong>gle elbow-level amputation, the<br />

roles that the affected- <strong>and</strong> unaffected-arm have with<strong>in</strong> the front crawl<br />

arm stroke cycle may differ from each other. It would be expected that the<br />

primary function of the unaffected-arm is to generate propulsion. However,<br />

uncerta<strong>in</strong>ty rema<strong>in</strong>s as to whether the affected-arm of a unilateral<br />

arm amputee can contribute effectively to propulsion at swimm<strong>in</strong>g speeds<br />

higher than 1 m∙s -1 . Rather, the affected-arm might simply function to<br />

control <strong>in</strong>ter-arm asymmetry so that stable repetition of the overall arm<br />

stroke cycle is ma<strong>in</strong>ta<strong>in</strong>ed. Underst<strong>and</strong><strong>in</strong>g the roles of both the affected-<br />

<strong>and</strong> unaffected-arm dur<strong>in</strong>g the stroke phases would be of great practical<br />

importance to swimmers, teachers <strong>and</strong> coaches. No exam<strong>in</strong>ation of the<br />

arm stroke phases has been undertaken with a s<strong>in</strong>gle homogenous group<br />

of highly-tra<strong>in</strong>ed swimmers with a s<strong>in</strong>gle-arm amputation.<br />

For unilateral arm amputee front crawl swimmers, <strong>in</strong>creases <strong>in</strong> swimm<strong>in</strong>g<br />

speed are achieved by <strong>in</strong>creas<strong>in</strong>g stroke frequency (Osborough et al.,<br />

2009). However, it is unclear how these swimmers vary the duration of<br />

their arm stroke phases <strong>in</strong> order to accommodate an <strong>in</strong>crease <strong>in</strong> stroke frequency<br />

<strong>and</strong> swimm<strong>in</strong>g speed. The purpose of this study was to determ<strong>in</strong>e<br />

if the arm stroke phases used by competitive unilateral arm amputee front<br />

crawl swimmers differed between their affected <strong>and</strong> unaffected sides <strong>and</strong><br />

whether these phases altered with an <strong>in</strong>crease <strong>in</strong> swimm<strong>in</strong>g speed.<br />

Methods<br />

Thirteen (3 male <strong>and</strong> 10 female) competitive swimmers (age 16.9 ± 3.1<br />

yrs) participated <strong>in</strong> this study. All participants were s<strong>in</strong>gle-arm amputees,<br />

at the level of the elbow. The mean 50 m front crawl personal best<br />

time was 32.7 ± 3.1 s. Twelve of the swimmers competed <strong>in</strong> the Inter-<br />

140<br />

national Paralympic Committee S9 classification for front crawl; one<br />

male swimmer competed <strong>in</strong> the S8 classification. The procedure for the<br />

data collection was approved by the Institutional Ethics Committee. All<br />

participants provided written <strong>in</strong>formed consent before tak<strong>in</strong>g part <strong>in</strong><br />

the study.<br />

Participants completed five 25 m front crawl trials. Seven of the<br />

swimmers performed the trials from slow to maximum swimm<strong>in</strong>g speed<br />

(SS max ); the rema<strong>in</strong>der performed the trials from maximum to slow<br />

swimm<strong>in</strong>g speed. To control for the effects of the breath<strong>in</strong>g action on<br />

the swimm<strong>in</strong>g stroke, participants were <strong>in</strong>structed not to take a breath<br />

through a 10 m test section of the pool.<br />

Two digital video camcorders (Panasonic NVDS33), sampl<strong>in</strong>g at<br />

50 Hz with a shutter speed of 1/350 s were used to film the participants.<br />

Each of the camcorders was enclosed <strong>in</strong> a waterproof hous<strong>in</strong>g<br />

suspended underwater from one of two trolleys that ran along the side<br />

of the pool, parallel to the participants’ swimm<strong>in</strong>g direction. This set-up<br />

enabled the participants to be video-taped under the water, from opposite<br />

sides, over the 10 m test section.<br />

The digital video footage was transferred to a laptop computer <strong>and</strong><br />

analysed us<strong>in</strong>g SIMI Motion 7.2 software. Three consecutive, nonbreath<strong>in</strong>g<br />

stroke cycles for each participant, were then selected for<br />

analysis. The estimated locations of the gleno-humeral jo<strong>in</strong>t centre <strong>and</strong><br />

the elbow jo<strong>in</strong>t centre of both the affected <strong>and</strong> unaffected arms were<br />

digitised at 50 Hz to obta<strong>in</strong> the angular position of the upper-arms, as<br />

a function of time. Before film<strong>in</strong>g, the sk<strong>in</strong> overlay<strong>in</strong>g the jo<strong>in</strong>t centres<br />

was marked with black pen to help estimate their location.<br />

At 80%, 85%, 90%, 95% <strong>and</strong> 100% of each participant’s SS max <strong>in</strong>dividual<br />

arm stroke phases, expressed as a percentage of the duration of<br />

the complete arm stroke cycle, were determ<strong>in</strong>ed from the angle made by<br />

the shoulder-to-elbow position vector relative to the horizontal. Each<br />

upper-arm movement was divided <strong>in</strong>to four phases (Fig. 1): Entry <strong>and</strong><br />

Glide (A); Pull (B); Push (C); <strong>and</strong> Recovery (D):<br />

(A) Entry <strong>and</strong> Glide: from where the elbow jo<strong>in</strong>t centre entered<br />

the water (0°) to where the shoulder-to-elbow position vector made an<br />

angle of 25° with the horizontal. This latter position corresponded to a<br />

po<strong>in</strong>t where typically the swimmers actively <strong>in</strong>itiated extension of their<br />

affected-arm.<br />

(B) Pull: from the end of the Entry <strong>and</strong> Glide (25°) to where the<br />

shoulder-to-elbow position vector made an angle of 90° with the horizontal.<br />

(C) Push: from the end of the Pull (90°) to where the shoulder-toelbow<br />

position vector made an angle of 155° with the horizontal. This<br />

latter position corresponded to a po<strong>in</strong>t where, as a result of the roll<strong>in</strong>g<br />

action of the swimmers’ trunk <strong>and</strong> the bow-wave created by the swimmers’<br />

movement through the water, the most-distal part of the swimmers’<br />

affected-arm typically exited the water.<br />

(D) Recovery: from the end of the Push (155°) to where the elbow<br />

jo<strong>in</strong>t centre entered the water (360°).<br />

Figure 1. Divisions of the arm stroke phases: (A) Entry <strong>and</strong> Glide; (B)<br />

Pull; (C) Push; <strong>and</strong> (D) Recovery for a unilateral arm amputee front<br />

crawl swimmer.


Repeated measures general l<strong>in</strong>ear modell<strong>in</strong>g tests were used to compare<br />

the changes <strong>in</strong> the relative durations of the Entry <strong>and</strong> Glide, Pull, Push<br />

<strong>and</strong> Recovery phases between the affected <strong>and</strong> unaffected arms <strong>and</strong> between<br />

the percentage swimm<strong>in</strong>g speeds. In all comparisons, the level of<br />

statistical significance was set at p < .05.<br />

results<br />

There were significant differences (p < .05) between the affected- <strong>and</strong><br />

unaffected-arm for the relative durations of each arm stroke phase across<br />

the five percentage speed <strong>in</strong>crements (Fig. 2). The affected-arm on average<br />

spent relatively longer <strong>in</strong> all arm stroke phases, with the exception of<br />

the Pull phase, when compared to the unaffected-arm.<br />

The mean relative duration of the Entry <strong>and</strong> Glide phase (A) for the<br />

affected <strong>and</strong> unaffected arms did not significantly change as the participants<br />

<strong>in</strong>creased their swimm<strong>in</strong>g speed. While the unaffected-arm’s relative<br />

Entry <strong>and</strong> Glide phase duration rema<strong>in</strong>ed relatively constant (23.2<br />

± 8.0% vs. 23.1 ± 6.8%, for 80% <strong>and</strong> 100% of SS max respectively) with an<br />

<strong>in</strong>crease <strong>in</strong> swimm<strong>in</strong>g speed, there was a slight reduction <strong>in</strong> the affectedarm’s<br />

relative Entry <strong>and</strong> Glide phase duration between 80% <strong>and</strong> 100% of<br />

SS max (38.3 ± 9.5% vs. 36.2 ± 11.6%).<br />

The mean relative duration of the Pull phase (B) for the unaffectedarm,<br />

but not for the affected-arm, changed significantly (p < .05) as the<br />

participants <strong>in</strong>creased their swimm<strong>in</strong>g speed. While the affected-arm’s<br />

relative Pull phase duration rema<strong>in</strong>ed relatively unchanged (10.9 ± 2.8%<br />

vs. 11.0 ± 2.3%, for 80% <strong>and</strong> 100% of SS max respectively) with an <strong>in</strong>crease<br />

<strong>in</strong> swimm<strong>in</strong>g speed, there was a significant reduction (p < .05)<br />

<strong>in</strong> the unaffected-arm’s relative Pull phase duration between 80% <strong>and</strong><br />

100% of SS max (23.1 ± 5.9% vs. 20.5 ± 4.9%).<br />

The mean relative duration of the Push phase (C) for both the affected<br />

<strong>and</strong> unaffected arms changed significantly (p < .05) as the participants<br />

<strong>in</strong>creased their swimm<strong>in</strong>g speed. At 80% of SS max , the mean Push<br />

phase durations were 18.4 ± 6.4% <strong>and</strong> 13.8 ± 2.7% for the affected- <strong>and</strong><br />

unaffected-arm respectively. At 100% of SS max , the mean Push phase<br />

durations were 19.4 ± 5.3% <strong>and</strong> 15.4 ± 3.9% for the affected- <strong>and</strong> unaffected-arm<br />

respectively.<br />

The mean relative duration of the Recovery phase (D) for the affected<br />

<strong>and</strong> unaffected arms did not significantly change as the participants<br />

<strong>in</strong>creased their swimm<strong>in</strong>g speed.<br />

Figure 2. Means <strong>and</strong> st<strong>and</strong>ard deviations of relative arm stroke phase<br />

durations for both the affected- <strong>and</strong> unaffected-arms (* Differences<br />

between arms are statistically significant p < .01). Bold bars <strong>in</strong>dicate<br />

affected-arm.<br />

dIscussIon<br />

The purpose of this study was to determ<strong>in</strong>e whether the arm stroke<br />

phases used by competitive unilateral arm amputee front crawl swim-<br />

chaPter2.<strong>Biomechanics</strong><br />

mers differed between their affected <strong>and</strong> unaffected sides <strong>and</strong> whether<br />

these phases changed with an <strong>in</strong>crease <strong>in</strong> swimm<strong>in</strong>g speed.<br />

At all swimm<strong>in</strong>g speeds, the stroke phases of the affected <strong>and</strong> unaffected<br />

arms differed significantly. Whilst all swimmers pulled their affected-arm<br />

through the water fastest, the affected-arm on average spent<br />

relatively longer <strong>in</strong> all arm stroke phases, with the exception of the Pull<br />

phase, when compared to the unaffected-arm. Unfortunately, it is not<br />

possible to directly compare these f<strong>in</strong>d<strong>in</strong>gs with those for able-bodied<br />

swimmers or other swimmers with various loco-motor disabilities, s<strong>in</strong>ce<br />

arm stroke phases are only reported <strong>in</strong> the literature as mean values of<br />

both arms (e.g., Chollet et al., 2000; Potdev<strong>in</strong> et al., 2006; Satkunskiene<br />

et al., 2005).<br />

As a consequence of their physical impairment, at all swimm<strong>in</strong>g<br />

speeds the arm amputees used an asymmetrical strategy for coord<strong>in</strong>at<strong>in</strong>g<br />

their affected-arm movement with their unaffected-arm. It was apparent<br />

that the amputees held their affected-arm stationary <strong>in</strong> the Entry<br />

<strong>and</strong> Glide phase before pull<strong>in</strong>g it rapidly under the shoulder. As the<br />

affected-arm was then pushed towards the hip, its motion slowed before<br />

the Recovery phase commenced. Conversely, the amputees’ unaffectedarm<br />

moved steadily though the Entry <strong>and</strong> Glide phase <strong>and</strong> the Pull<br />

phase before be<strong>in</strong>g rapidly pushed <strong>in</strong>to the Recovery phase. Such different<br />

bi-lateral motor control strategies might be l<strong>in</strong>ked to how these<br />

swimmers learnt to organise the motor skills necessary to swim front<br />

crawl.<br />

As swimm<strong>in</strong>g speed <strong>in</strong>creased the relative durations of certa<strong>in</strong> arm<br />

stroke phases changed. With <strong>in</strong>creas<strong>in</strong>g speed: 1) the affected-arm’s Entry<br />

<strong>and</strong> Glide phase decreased, while the unaffected-arm’s Entry <strong>and</strong><br />

Glide phase rema<strong>in</strong>ed unchanged; 2) the unaffected-arm’s Pull phase<br />

decreased, while the affected-arm’s Pull phase rema<strong>in</strong>ed unchanged; <strong>and</strong><br />

3) both arms’ Push phase <strong>in</strong>creased. Both Chollet et al. (2000) <strong>and</strong> Potdev<strong>in</strong><br />

et al. (2006) showed that for able-bodied swimmers, the relative<br />

duration of the Entry <strong>and</strong> Catch phase (mean of both arms) decreased,<br />

while the relative durations of the Pull <strong>and</strong> Push <strong>in</strong>creased with <strong>in</strong>creas<strong>in</strong>g<br />

swimm<strong>in</strong>g speed. The authors suggested that <strong>in</strong> mak<strong>in</strong>g these adaptations,<br />

able-bodied swimmers were able to take advantage of longer<br />

periods of propulsive force application. In the current study propulsion<br />

was not measured. However, as a consequence of task (e.g., swimm<strong>in</strong>g<br />

faster), physical (e.g., s<strong>in</strong>gle-arm amputation) <strong>and</strong> environmental (e.g.,<br />

larger resistive forces at higher speeds) constra<strong>in</strong>ts, the unilateral arm<br />

amputee front crawl swimmers asymmetrically adjusted their arm movements<br />

to ma<strong>in</strong>ta<strong>in</strong> the stable repetition of the overall arm stroke cycle.<br />

conclusIon<br />

The results from this study show that at all swimm<strong>in</strong>g speeds the stroke<br />

phases of the affected <strong>and</strong> unaffected arms differed significantly. The<br />

affected-arm on average spent relatively longer <strong>in</strong> all arm stroke phases,<br />

with the exception of the Pull phase, when compared to the unaffected<br />

arm. Such differences might be l<strong>in</strong>ked to how these swimmers learnt<br />

to organise the motor skills necessary to swim front crawl. As swimm<strong>in</strong>g<br />

speed <strong>in</strong>creased, the duration of the affected-arm’s Entry <strong>and</strong><br />

Glide phase <strong>and</strong> the unaffected-arm’s Pull phase significantly decreased,<br />

while the duration of both arms’ Push phase significantly <strong>in</strong>creased. The<br />

arm amputees used a coord<strong>in</strong>ation strategy that asymmetrically adjusted<br />

their arm movements <strong>in</strong> order to ma<strong>in</strong>ta<strong>in</strong> the stable repetition of their<br />

overall arm stroke cycle when swimm<strong>in</strong>g at different speeds.<br />

reFerences<br />

Chollet, D., Chalies, S., & Chatard, J.C. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: Description <strong>and</strong> usefulness. International Journal<br />

of Sports <strong>Medic<strong>in</strong>e</strong>, 21(1), 54-59.<br />

Maglischo, C.W., Maglischo, E.W., Higg<strong>in</strong>s, J., H<strong>in</strong>richs, R., Luedtke,<br />

D., Schleihauf, R.E., & Thayer, A. (1988). A biomechanical analysis<br />

of the 1984 U.S. Olympic freestyle distance swimmers. In B.E. Ungerechts,<br />

K. Wilke, K. Reischle (Eds.), Swimm<strong>in</strong>g Science V, Champaign,<br />

IL: Human K<strong>in</strong>etics, 351-360.<br />

141


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Osborough, C.D., Payton, C.J., & Daly, D. (2009). Relationships between<br />

the front crawl stroke parameters of competitive unilateral arm<br />

amputee swimmers, with selected anthropometric characteristics.<br />

Journal of Applied <strong>Biomechanics</strong>, 25(4), 304-312.<br />

Potdev<strong>in</strong>, F., Bril, B., Sidney, M., & Pelayo, P. (2006). Stroke frequency<br />

<strong>and</strong> arm coord<strong>in</strong>ation <strong>in</strong> front crawl swimm<strong>in</strong>g. International Journal<br />

of Sports <strong>Medic<strong>in</strong>e</strong>, 27(3), 193-198.<br />

Satkunskiene, D., Schega, L., Kunze, K., Birz<strong>in</strong>yte, K., & Daly, D.<br />

(2005). Coord<strong>in</strong>ation <strong>in</strong> arm movements dur<strong>in</strong>g crawl stroke <strong>in</strong> elite<br />

swimmers with a loco-motor disability. Human Movement Science,<br />

24(1), 54-65.<br />

AcKnoWledGeMents<br />

The authors would like to acknowledge the follow<strong>in</strong>g: British Disability<br />

Swimm<strong>in</strong>g for their support <strong>in</strong> this project; Professor Ross S<strong>and</strong>ers for<br />

the use of his facilities at the Centre for Aquatics Research <strong>and</strong> Education,<br />

The University of Ed<strong>in</strong>burgh; <strong>and</strong> Miss Casey Lee for her assistance<br />

dur<strong>in</strong>g data collection.<br />

142<br />

Co-ord<strong>in</strong>ation Changes dur<strong>in</strong>g a Maximal Effort 100<br />

m Short Course Breaststroke Swim<br />

oxford, s. 1 , James, r. 1 , Price, M. 1 , Payton, c. 2<br />

1 Coventry University, UK<br />

2 Manchester Metropolitan University, UK<br />

The aim of the study was to establish the changes <strong>in</strong> co-ord<strong>in</strong>ation that<br />

occur dur<strong>in</strong>g a 100 m breaststroke swim from a water start by: 1) measur<strong>in</strong>g<br />

the k<strong>in</strong>ematic changes that occur as the swimmer progressed<br />

through the four laps <strong>and</strong>, 2) analys<strong>in</strong>g the co-ord<strong>in</strong>ation of the arms<br />

<strong>and</strong> legs (transition phase) correspond<strong>in</strong>g to the time between the end<br />

of the leg propulsion <strong>and</strong> the start of the arm propulsion phases. Breaststroke<br />

participants (n=8, females <strong>and</strong> n=18, males) performed a 100 m<br />

maximal swim <strong>in</strong> a 25 m pool. They were recorded underwater us<strong>in</strong>g<br />

three 50 Hz cameras (one at each end of the pool <strong>and</strong> one mounted on<br />

a trolley). The last three strokes prior to turns were analysed. Significant<br />

changes <strong>in</strong> clean swim speed (p


The aims of this study were to: (1) <strong>in</strong>vestigate co-ord<strong>in</strong>ation changes<br />

dur<strong>in</strong>g a 100 m short course breaststroke swim <strong>and</strong> (2) compare k<strong>in</strong>ematic<br />

variables between each of the four laps of the100 m swim.<br />

Method<br />

Twenty six specialist breaststroke participants (8 females: mean age, 19.1<br />

+ 2.3 yrs; mean body mass, 70.0 + 8.0 kg; mean height, 1.70 + 0.05 m;<br />

18 males: mean age 18.9 + 2.2 yrs.; mean body mass 69.3 + 7.3 kg;<br />

height 1.78 + 0.06 m; short course 100 m breaststroke mean best times<br />

females 88.7 + 5.4 s <strong>and</strong> males 77.0 + 5.5 s) volunteered to participate <strong>in</strong><br />

this study. The selection criterion for the study was that participants had<br />

to be competitive <strong>in</strong> the 100 m breaststroke event at County st<strong>and</strong>ard<br />

or above with<strong>in</strong> that season. The study was approved by the Coventry<br />

University Ethics Committee. The requirements of the study were expla<strong>in</strong>ed<br />

to participants <strong>and</strong> each participant provided written <strong>in</strong>formed<br />

consent. Twelve body l<strong>and</strong>marks (lateral malleolus, lateral femoral condyle,<br />

greater femoral trochanter, styloid process, epicondyle of humerus<br />

<strong>and</strong> acromion process) were marked us<strong>in</strong>g black v<strong>in</strong>yl tape.<br />

Each swimmer performed a self-selected 800 m warm-up <strong>in</strong> a 25 m<br />

pool. They were then <strong>in</strong>structed to perform a maximal effort 100 m swim<br />

from a water start without the use of race strategy. Three cameras operat<strong>in</strong>g<br />

at 50 Hz were used to record the 100 m swim. Two cameras (Sony<br />

video DCR-TRV460E) were submerged <strong>in</strong> waterproof hous<strong>in</strong>gs, one<br />

at each end of the swimmer’s lane, to record frontal <strong>and</strong> rear views. The<br />

third camera, a waterproof bullet camera, was connected to a visual display<br />

unit (Sony digital video cassette recorder GV-D800E), which was<br />

attached to a trolley. The trolley was moved manually to ma<strong>in</strong>ta<strong>in</strong> the<br />

swimmer’s hip marker <strong>in</strong> the centre of the visual display unit throughout<br />

the entire 100 m swim.<br />

Time to complete 100 m was recorded via a video analysis package<br />

(Dartfish Tra<strong>in</strong>er 2.5.2.19, Fribourg, Switzerl<strong>and</strong>) as the time from<br />

when the feet left the wall at the start until the double h<strong>and</strong> touch on<br />

the wall at the end. Clean swim speed, stroke rate <strong>and</strong> stroke length<br />

were determ<strong>in</strong>ed over a 10 m section of the pool that was not affected<br />

by start<strong>in</strong>g, turn<strong>in</strong>g or f<strong>in</strong>ish<strong>in</strong>g technique. The time taken for the hip<br />

marker to travel this 10 m distance from the 15 m marker to the 5 m<br />

marker from the end of the pool was determ<strong>in</strong>ed from the video. Stroke<br />

length was calculated from the mean clean swim speed <strong>and</strong> stroke rates<br />

for each of the four laps, over the 10 m section of pool.<br />

Stroke cycle time was calculated as the mean of the last three full<br />

strokes completed <strong>in</strong> the 10 m section of each lap from the frontal <strong>and</strong><br />

sagittal camera views. To quantify co-ord<strong>in</strong>ation, five stroke phases were<br />

identified: 1) Arm Propulsion - from the <strong>in</strong>itial separation of the arms<br />

from the extended position <strong>in</strong> front of the body until the first forward<br />

movement of the elbows when the h<strong>and</strong>s were under the head; 2) Arm<br />

Recovery - from the end of the arm propulsion phase until the start of<br />

the separation of the h<strong>and</strong>s from the extended position; 3) Leg Propulsion<br />

- from the start of the first backwards movement of the feet relative<br />

to the body (the po<strong>in</strong>t where the knees were maximally flexed at the<br />

start) until the <strong>in</strong>stant when the knees were fully extended ; 4) Leg recovery<br />

– from the end of the leg propulsion phase until the frame prior<br />

to the first backwards movement of the feet <strong>in</strong> relation to the body; 5)<br />

Transition phase - from the end of the leg propulsion phase until the<br />

start of the arm propulsion phase. Each of the arm <strong>and</strong> leg phases were<br />

expressed as a percentage of a complete arm or leg stroke respectfully.<br />

Transition phase was expressed as a percentage of a complete leg stroke.<br />

The complete arm <strong>and</strong> leg strokes were calculated as the mean of three<br />

complete strokes. Means <strong>and</strong> st<strong>and</strong>ard deviations were calculated for<br />

all the data. Analysis of variance with Bonferroni post-hoc tests were<br />

used to compare laps (1, 2, 3 <strong>and</strong> 4) us<strong>in</strong>g selected variables at the same<br />

po<strong>in</strong>t of each lap (clean swim speed, stroke rate, stroke length, stroke<br />

cycle time, arm recovery, arm propulsion, leg propulsion, leg recovery<br />

<strong>and</strong> transition time). Correlation coefficients were determ<strong>in</strong>ed among<br />

selected variables. The level of significance was set at p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

utilised the glide co-ord<strong>in</strong>ation throughout the swim. The glide coord<strong>in</strong>ation<br />

is characterised by a positive transition time mean<strong>in</strong>g that<br />

there is a delay from the end of the kick propulsion phase to the start of<br />

the arm propulsion phase. This corresponds to a period of no propulsion<br />

<strong>in</strong> the swimm<strong>in</strong>g stroke. The glide co-ord<strong>in</strong>ation is normally associated<br />

with swimm<strong>in</strong>g the 200 m breaststroke (Leblanc et al., 2009; Soares<br />

et al., 1999). N<strong>in</strong>e of the participants used the overlap co-ord<strong>in</strong>ation<br />

throughout the swim, which is characterised by a negative transition<br />

phase mean<strong>in</strong>g that the arm propulsion phase starts before the end of<br />

the leg propulsion phase. Swimmers adopt this co-ord<strong>in</strong>ation pattern as<br />

it has been shown to reduce velocity fluctuations <strong>and</strong> helps ma<strong>in</strong>ta<strong>in</strong> a<br />

higher mean velocity (Seifert & Chollet, 2005).<br />

The transition phase changed <strong>in</strong> the majority of participants from<br />

the 1 st to the 4 th lap. Eighteen of the participants either <strong>in</strong>creased the<br />

amount of overlap with<strong>in</strong> their stroke (n=5), changed from glide to<br />

overlap co-ord<strong>in</strong>ation (n=5), or decreased the time spent <strong>in</strong> the glide<br />

phase of the stroke (n=8). The rema<strong>in</strong><strong>in</strong>g participants altered their coord<strong>in</strong>ation<br />

<strong>in</strong> the other direction by <strong>in</strong>creas<strong>in</strong>g the amount of glide (n=8)<br />

thus show<strong>in</strong>g an <strong>in</strong>crease <strong>in</strong> transition time.<br />

These changes <strong>in</strong> the participant’s co-ord<strong>in</strong>ation are likely to be a<br />

result of fatigue. Fatigue has been shown to hamper the sensorimotor<br />

system, affect<strong>in</strong>g such functions as awareness, feedback <strong>and</strong> coord<strong>in</strong>ation,<br />

which ma<strong>in</strong>ta<strong>in</strong> form <strong>and</strong> stability, result<strong>in</strong>g <strong>in</strong> the <strong>in</strong>ability<br />

to ma<strong>in</strong>ta<strong>in</strong> ideal mechanics (Toussa<strong>in</strong>t et al., 2006). This means that<br />

as the participants become fatigued, as the race distance progresses,<br />

they change their co-ord<strong>in</strong>ation pattern therefore caus<strong>in</strong>g the participants<br />

to move towards or <strong>in</strong>crease the overlap co-ord<strong>in</strong>ation <strong>in</strong> their<br />

stroke. These alterations <strong>in</strong> co-ord<strong>in</strong>ation could be a direct result of the<br />

participants try<strong>in</strong>g to ma<strong>in</strong>ta<strong>in</strong> homeostasis through compensatory<br />

mechanisms of the neuromuscular system to ma<strong>in</strong>ta<strong>in</strong> effective mechanical<br />

power output. It is hypothesised that the results of the study<br />

suggest that the participants are becom<strong>in</strong>g less mechanically efficient<br />

as the swim progresses as there is a significant decrease <strong>in</strong> clean swim<br />

speed from the 1 st to the 4 th lap <strong>and</strong> subsequent decreases <strong>in</strong> stroke<br />

length <strong>and</strong> stroke rate (table 1).<br />

conclusIon<br />

The f<strong>in</strong>d<strong>in</strong>gs of this study give us a better underst<strong>and</strong><strong>in</strong>g of the effects<br />

of fatigue <strong>and</strong> the subsequent changes that occur <strong>in</strong> the co-ord<strong>in</strong>ation of<br />

the arms <strong>and</strong> legs <strong>in</strong> 100 m breaststroke swim.<br />

As the participants fatigued they decreased the transition phase of<br />

the stroke by either <strong>in</strong>creas<strong>in</strong>g the amount of overlap or reduc<strong>in</strong>g the<br />

glide phase of the stroke <strong>in</strong> an attempt to ma<strong>in</strong>ta<strong>in</strong> clean swim speed.<br />

reFerences<br />

Alberty M, Sidney M, Huot-March<strong>and</strong> F, Hespel JM, Pelayo P. (2005).<br />

Intracyclic velocity variations <strong>and</strong> arm coord<strong>in</strong>ation dur<strong>in</strong>g exhaustive<br />

exercise <strong>in</strong> front crawl stroke. Int J Sports Med, 26: 471-475.<br />

Beelen, A., <strong>and</strong> Sargeant, A.J (1991). Effects of fatigue on maximal<br />

power output at different contraction velocities <strong>in</strong> humans. J Appl<br />

Phys, 71: 2332-2337.<br />

Chollet D, Seifert L, Leblanc H, Boulesteix L, Carter M (2004). Evaluation<br />

of arm <strong>and</strong> leg coord<strong>in</strong>ation <strong>in</strong> flat breaststroke. Int J Sports<br />

Med. 25 (7): 486-95.<br />

Leblanc H, Seifert L, Baudry L, Chollet D. (2009). Arm-leg coord<strong>in</strong>ation<br />

<strong>in</strong> recreational <strong>and</strong> competitive breaststroke swimmers. Sci Med<br />

Sport. 12 (3): 352-6.<br />

Maglischo, E.W (2003). Swimm<strong>in</strong>g Fastest. Champaign, IL: Human<br />

K<strong>in</strong>etics.<br />

Pelayo P, Alberty M, Sidney M, Potdev<strong>in</strong> F, Dekerle J. (2007) Aerobic<br />

Potential, stroke parameters, <strong>and</strong> co-ord<strong>in</strong>ation <strong>in</strong> swimm<strong>in</strong>g frontcrawl<br />

performance. Int J Sports Phys Perf, 2, 347-359.<br />

144<br />

Schnitzler, C., Seifert, L., Ernwe<strong>in</strong>, V., Chollet, D. (2008). Arm coord<strong>in</strong>ation<br />

adaptations assessment <strong>in</strong> swimm<strong>in</strong>g. Int J Sports Med, 29,<br />

480-486.<br />

Seifert, L., Chollet, D <strong>and</strong> Bardy, B.G. (2004). Effect of swimm<strong>in</strong>g velocity<br />

on arm co-ord<strong>in</strong>ation <strong>in</strong> the front crawl: a dynamic analysis. J<br />

Sport Sci, 22, 651-660.<br />

Seifert, L., <strong>and</strong> Chollet, D. (2005). A new <strong>in</strong>dex of flat breaststroke propulsion:<br />

A comparison of elite men <strong>and</strong> women. J Sport Sci, 23 (3),<br />

309-320.<br />

Seifert, L., Chollet, D <strong>and</strong> Chatard, JC. (2007). K<strong>in</strong>ematic changes dur<strong>in</strong>g<br />

a 100 m front crawl: Effects of performance level <strong>and</strong> gender.<br />

Med Sci Sports Exerc, 39, 1784-1793<br />

Soares, P.M., Sousa, F, Paulo Vilas-Bous, J. (1999). Differences <strong>in</strong><br />

breaststroke synchronisation <strong>in</strong>duced by different race velocities. In:<br />

Kesk<strong>in</strong>en, K.L., Komi, P.V., <strong>and</strong> Holl<strong>and</strong>, A.P. eds. <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII, Gummerus Pr<strong>in</strong>t<strong>in</strong>g House, Jyväskyla,<br />

F<strong>in</strong>l<strong>and</strong>, 53-57.<br />

Toussa<strong>in</strong>t, H.M., Beelen, A., Rodenburg, A., Sarnt, A.J., Groot, G.,<br />

Holl<strong>and</strong>er, P., van Ingen-Schenau, G.J. (1988). Propell<strong>in</strong>g efficiency<br />

of front crawl swimm<strong>in</strong>g. J Appl Phys, 65, 2506-2512.13.<br />

Toussa<strong>in</strong>t, H.M., Caral, A., Kranenborg, H., Truijens, M.J<br />

(2006). Effects of fatigue on strok<strong>in</strong>g characteristics <strong>in</strong> armsonly<br />

100 m front-crawl race. Med Sci Sports Exerc, 38 (9),<br />

1635-1642


The Effect of Angle of Attack <strong>and</strong> Depth on Passive<br />

Drag<br />

Pease, d.l. 1 , Vennell, r. 2<br />

1 Australian Institute of Sport, Canberra, Australia<br />

2 University of Otago, Duned<strong>in</strong>, New Zeal<strong>and</strong><br />

In order to quantify the effect of angle of attack <strong>and</strong> depth on drag force<br />

dur<strong>in</strong>g underwater glid<strong>in</strong>g the current study was undertaken. This aim<br />

was achieved by utilis<strong>in</strong>g a flume <strong>and</strong> an anatomically accurate mannequ<strong>in</strong><br />

whose orientation could be precisely controlled. Measurements<br />

were obta<strong>in</strong>ed with the mannequ<strong>in</strong> oriented with the longitud<strong>in</strong>al axis<br />

at angles of attack of -4, -2, 0, +2 <strong>and</strong> +4 degrees relative to water flow.<br />

Measurements were taken at depths rang<strong>in</strong>g from 0.2 – 0.8m <strong>and</strong> at<br />

velocities rang<strong>in</strong>g from 0-2.55ms -1 . There was generally little effect<br />

from the angle of attack other than near the surface (0.2m) where<br />

there was a tendency for the wave drag to be lower for the negative<br />

angles. This f<strong>in</strong>d<strong>in</strong>g <strong>in</strong>dicates that as swimmers approach<br />

the surface it may be beneficial to adopt a slight negative angle of<br />

attack <strong>in</strong> order to m<strong>in</strong>imise the drag force.<br />

Key words: swimm<strong>in</strong>g, passive drag, wave drag, angle of attack, flume<br />

IntroductIon<br />

Previous research <strong>in</strong>to the drag forces (both active <strong>and</strong> passive) act<strong>in</strong>g<br />

dur<strong>in</strong>g human swimm<strong>in</strong>g has shown differences due to body size, shape,<br />

velocity <strong>and</strong> depth. However, one factor, which has not previously been<br />

<strong>in</strong>vestigated, is that of the angle of attack or pitch angle of the athlete’s<br />

body relative to the water flow. Angle of attack is a factor, which has<br />

been highlighted as an issue <strong>in</strong> previous study but due to the <strong>in</strong>ability<br />

to systematically control this factor it has been generally described as a<br />

limitation.<br />

Therefore, the present study was undertaken to try <strong>and</strong> quantify the effect<br />

of angle of attack on the drag forces act<strong>in</strong>g upon a streaml<strong>in</strong>ed human<br />

swimmer by utilis<strong>in</strong>g an anatomically accurate mannequ<strong>in</strong> whose orientation<br />

relative to the water flow direction could be precisely controlled.<br />

It was hypothesized that, as angle of attack changed, there would<br />

be significant changes <strong>in</strong> the magnitude of the total drag force as well<br />

as changes <strong>in</strong> the relative contribution of the component forces, viscous,<br />

form, <strong>and</strong> wave drag. These changes would be primarily due to the<br />

changes <strong>in</strong> exposed frontal area with <strong>in</strong>creas<strong>in</strong>g (positive <strong>and</strong> negative)<br />

angles of attack away from the zero angle.<br />

Based on the f<strong>in</strong>d<strong>in</strong>gs from previous research (Vennell, Pease, &<br />

Wilson, 2006) there are <strong>in</strong>creases <strong>in</strong> the total drag force, <strong>and</strong> more specifically<br />

the wave drag contribution to that total force, as depth of the<br />

swimmer decreases. Therefore, another aspect of the current study was<br />

to exam<strong>in</strong>e the <strong>in</strong>teraction between angle of attack <strong>and</strong> submergence<br />

depth <strong>and</strong> the measured drag force.<br />

Previous studies have quantified body angles similar to angle of attack<br />

dur<strong>in</strong>g free surface swimm<strong>in</strong>g (Zamparo, 2006; Zamparo et al.,<br />

2008) with the aim of us<strong>in</strong>g that angle as an <strong>in</strong>dicator of body position.<br />

In general the angle of the trunk to the horizontal is used to represent<br />

angle of attack. In those studies body angles of approximately 15 degrees<br />

were found. However, dur<strong>in</strong>g the streaml<strong>in</strong>ed portion of a swimm<strong>in</strong>g<br />

race when the athlete is fully submerged, <strong>and</strong> not mov<strong>in</strong>g on a<br />

fluid boundary, it was theorised that the angle of attack would be much<br />

less due to the freedom of the athlete’s body to move <strong>in</strong> the vertical as<br />

well as the horizontal plane. This is unlike surface swimm<strong>in</strong>g where the<br />

movement trajectory is fixed <strong>and</strong> essentially limited to the horizontal<br />

plane. By allow<strong>in</strong>g for movement <strong>in</strong> the vertical plane as well as the<br />

horizontal, the trajectory of the centre of mass is more <strong>in</strong> l<strong>in</strong>e with the<br />

angle of the body thereby reduc<strong>in</strong>g the angle of attack relative to the<br />

surround<strong>in</strong>g water flow.<br />

chaPter2.<strong>Biomechanics</strong><br />

Therefore, the current study exam<strong>in</strong>ed smaller angles of attack which<br />

may be achieved by fully submerged swimmers <strong>in</strong> a streaml<strong>in</strong>e position<br />

such as that experienced follow<strong>in</strong>g starts <strong>and</strong> turns.<br />

Methods<br />

All test<strong>in</strong>g was conducted <strong>in</strong> the aquatic treadmill or ’flume’ at the University<br />

of Otago, as described by Britton, Rogers, <strong>and</strong> Reimann (1998).<br />

In order to achieve the desired control over position of the body<br />

relative to water flow it was necessary to utilise an anatomically accurate<br />

mannequ<strong>in</strong> rather than live subjects. The mannequ<strong>in</strong> used was the<br />

same as that described <strong>in</strong> previous research (Bixler & Pease, 2006; Bixler,<br />

Pease, & Fairhurst, 2007; Vennell et al., 2006) <strong>and</strong> had a total surface<br />

area of 1.859m 2 which allowed for the determ<strong>in</strong>ation of an estimate for<br />

viscous frictional force.<br />

The mount<strong>in</strong>g structure used to support the mannequ<strong>in</strong> was similar<br />

to that used <strong>in</strong> the previous studies. However, <strong>in</strong> the previous work the<br />

mannequ<strong>in</strong> was mounted via a tow<strong>in</strong>g arrangement through the f<strong>in</strong>gertips,<br />

which allowed for free movement of the rest of the mannequ<strong>in</strong>’s<br />

body. Therefore a new mount<strong>in</strong>g was necessary which allowed for the<br />

ma<strong>in</strong>tenance of orientation at all times. In the modified structure the<br />

mannequ<strong>in</strong> is fixed directly to a vertical aerofoil spar, which is attached<br />

at the back of the mannequ<strong>in</strong>. This aerofoil spar is then bolted to the<br />

same vertical pole <strong>and</strong> mount<strong>in</strong>g structure described by Vennell et al.<br />

(2006). The vertical spar is <strong>in</strong>f<strong>in</strong>itely adjustable <strong>in</strong> terms of mannequ<strong>in</strong><br />

depth between 0 <strong>and</strong> 0.9m. However, for the purposes of the current<br />

study the depths utilised were 0.2 – 0.8m at 0.1m <strong>in</strong>crements. Depth<br />

was measured as the distance between the water free surface <strong>and</strong> the<br />

central longitud<strong>in</strong>al axis of the mannequ<strong>in</strong>.<br />

The vertical pole then was clamped to a horizontally oriented triaxial<br />

load cell, AMTI model MC3-6-1000, with the Z axis parallel to<br />

the water flow direction. The load cell was <strong>in</strong> turn <strong>in</strong>terfaced with an<br />

AMTI MCA6 amplifier <strong>and</strong> f<strong>in</strong>ally to a PowerLab unit which allowed<br />

for cont<strong>in</strong>uous data collection. Vertical position of the mannequ<strong>in</strong>s was<br />

controlled by rais<strong>in</strong>g or lower<strong>in</strong>g the vertical spar <strong>and</strong> pole. The position<br />

was then fixed by a set screw at the gimbal, <strong>and</strong> a scaffold<strong>in</strong>g clamp attached<br />

<strong>in</strong> series with the tri-axial load cell.<br />

In order to obta<strong>in</strong> the optimal drag-velocity curves for the mannequ<strong>in</strong>,<br />

data was collected for 13 velocities: 0, 0.34, 0.55, 0.75, 0.95, 1.16,<br />

1.36, 1.57, 1.77, 1.94, 2.15, 2.36, <strong>and</strong> 2.55 ms -1 respectively at each of<br />

the tow depths described previously. These conditions were repeated for<br />

each of the angles of attack; -4, -2, 0, +2, <strong>and</strong> +4° respectively. Angles of<br />

attack were based on a 0° orientation def<strong>in</strong>ed as that position with the<br />

m<strong>in</strong>imum projected frontal cross sectional area. Six tests of five seconds<br />

<strong>in</strong> duration were undertaken for each test condition.<br />

The projected frontal areas for these tested angles of attack were:<br />

0.1282, 0.1156, 0.1079, 0.1124, <strong>and</strong> 0.1280m 2 respectively. While attack<br />

angles greater than those tested may be exhibited <strong>in</strong> real situations,<br />

due to the uncerta<strong>in</strong>ty of the magnitude of load changes beyond the<br />

angles measured, limits were set <strong>in</strong> order to m<strong>in</strong>imise the possibility of<br />

damag<strong>in</strong>g either the mannequ<strong>in</strong> or the test<strong>in</strong>g support structure. Secondly,<br />

if angles greater than those tested had been utilised there would<br />

have been protrusion of the mannequ<strong>in</strong> through the water surface at<br />

the m<strong>in</strong>imum depth, which would have changed the wetted area <strong>and</strong><br />

thereby affected the results.<br />

In order to detect any effects of angle of attack on the drag forces,<br />

correlation coefficients were determ<strong>in</strong>ed between the angles of attack<br />

<strong>and</strong> the respective drag force components. In order to utilise correlational<br />

analyses a l<strong>in</strong>ear relationship between angle of attack <strong>and</strong> drag was<br />

hypothesized due to the l<strong>in</strong>early decreas<strong>in</strong>g depth of the lead<strong>in</strong>g edge<br />

of the mannequ<strong>in</strong>. Dur<strong>in</strong>g the pilot test<strong>in</strong>g the data were analysed for<br />

normality of distribution <strong>and</strong> were deemed to be suitable for parametric<br />

analysis. Due to the limitation of only utilis<strong>in</strong>g the s<strong>in</strong>gle mannequ<strong>in</strong><br />

the magnitude of the correlation coefficient needed to be very high <strong>in</strong><br />

order to achieve statistical significance (r≥.858 for significance at the 0.1<br />

level <strong>and</strong> r≥.959 for significance at the .05 level)<br />

145


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

The measured total drag force across all velocities at all depths for angles<br />

of attack of -4, 0, <strong>and</strong> +4 degrees respectively are presented <strong>in</strong> contour<br />

form <strong>in</strong> FFigure 1 Contour plots of total drag force for all angles of<br />

attack with depth on the Y axis, velocity on the X axis <strong>and</strong> contours<br />

<strong>in</strong>dicat<strong>in</strong>g drag force <strong>in</strong> Newtons. A) -4 deg B) 0 deg C) +4 Degigure<br />

1. The contour plots demonstrate more clearly the changes that are occurr<strong>in</strong>g<br />

with chang<strong>in</strong>g depth as seen by the <strong>in</strong>creased contour density at<br />

the shallower depths at the higher velocities.<br />

146<br />

Figure 1 Contour plots of total drag force for all angles of attack with<br />

depth on the Y axis, velocity on the X axis <strong>and</strong> contours <strong>in</strong>dicat<strong>in</strong>g drag<br />

force <strong>in</strong> Newtons. A) -4 deg B) 0 deg C) +4 Deg


In order to assess the significance of the effect of angle of attack on the<br />

various drag forces experienced by the mannequ<strong>in</strong>, Pearson correlation<br />

coefficients were determ<strong>in</strong>ed between angle of attack <strong>and</strong> the respective<br />

drag force components at all tested depths <strong>and</strong> velocities. These correlation<br />

matrices are presented <strong>in</strong> Table 1.<br />

Table 1 Correlation Matrices of angle of attack to; total drag (A) <strong>and</strong><br />

wave drag (B) force at all depths <strong>and</strong> velocities. Correlations with significance<br />

of P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Graphic Removal of Water Wave Impact <strong>in</strong> the Pool<br />

Wall dur<strong>in</strong>g the Flip Turn<br />

Pereira, s.M. 1,2 , Gonçalves, P. 2 , Fern<strong>and</strong>es, r.J. 2 , Machado, l. 2 ,<br />

roesler, h. 1 , Vilas-Boas, J.P. 2<br />

1 University of the State of Santa Catar<strong>in</strong>a, Florianópolis, Brazil<br />

2 University of Porto, Faculty of Sport, Cifi2d, Porto, Portugal<br />

The aim of this study was to develop a graphical removal technique of<br />

the water wave that precedes the contact of the swimmer with the wall<br />

dur<strong>in</strong>g the front-crawl flip turn, as well as to characterize <strong>and</strong> quantify<br />

it. To do this the researchers used an underwater force platform <strong>and</strong> two<br />

digital video cameras. In a pilot approach, a swimmer performed 8 turns<br />

without touch<strong>in</strong>g the wall. Follow<strong>in</strong>g the pilot study, 17 swimmers of<br />

both genders, <strong>in</strong>cluded the swimmer who participated <strong>in</strong> pilot approach,<br />

performed 154 complete flip turns. The water wave was removed graphically<br />

through a rout<strong>in</strong>e programmed <strong>in</strong> MatLab that was based on the<br />

symmetry of the wave, <strong>and</strong> the <strong>in</strong>stant <strong>in</strong> time that the wave made<br />

contact with the wall. The average values for the maximum force of the<br />

wave were similar <strong>in</strong> both trials as well as to those previously published.<br />

Furthermore, the removal technique provided satisfactory results.<br />

Key words: dynamometry, swimm<strong>in</strong>g, flip turn, wave measurement<br />

IntroductIon<br />

To move a body through the aquatic environment, swimmers transmit a<br />

volume of water that is expla<strong>in</strong>ed by hydrodynamic drag. The volume of<br />

water depends, amongst other factors upon the swimmer’s body volume<br />

<strong>and</strong> the speed of travel (Barbosa & Vilas-Boas, 2005).<br />

When the swimmer approaches the wall <strong>in</strong> the turn, some of the<br />

water volume displaced, hits the wall before the swimmer’s feet make<br />

contact. This anticipated force record makes it difficult to assess the real<br />

contact force of the swimmer. It is difficult to calculate the force generated<br />

by the wave <strong>and</strong> to remove it from the total force curve (Blanksby<br />

et al., 1998; Lyttle, 2000; Roesler, 2002).<br />

Blanksby et al. (1998) were the first authors to recognize the presence<br />

of the bow water wave <strong>in</strong> the k<strong>in</strong>etic analysis of the turn <strong>in</strong> breaststroke<br />

swimmers of different ages. These researchers tried to elim<strong>in</strong>ate<br />

the wave’s effects through signal process<strong>in</strong>g. However, as the frequency<br />

of the wave was similar to the frequency of the swimmer’s force signal,<br />

this was not possible to totally elim<strong>in</strong>ate the bow wave without los<strong>in</strong>g a<br />

considerable amount of useful data.<br />

Lyttle <strong>and</strong> Mason (1997) attempted to expla<strong>in</strong> the slope of the wave<br />

shape dur<strong>in</strong>g the k<strong>in</strong>etic analysis of turns <strong>in</strong> front crawl <strong>and</strong> butterfly<br />

swimmers. The data at the <strong>in</strong>stant <strong>in</strong> time that the swimmer touched the<br />

wall (<strong>in</strong>strumented with a 3D force platform) was recorded manually. The<br />

force records from the wave reached a maximum value of 500 N, <strong>and</strong> the<br />

duration of the wave was not mentioned. The authors concluded that the<br />

magnitude of this force was proportional to the size of the force platform<br />

s<strong>in</strong>ce the force recorded by the wave should have been equal to the pressure<br />

generated, multiplied by the surface area of the force platform.<br />

Roesler (2002) conducted a study us<strong>in</strong>g two force platforms, placed<br />

side by side on the wall of the pool, where the swimmer’s contact zone<br />

was only on one of the platforms. Recorded force peak values were<br />

around 371 N with a wave duration of around 0.14 s. The second platform,<br />

even without the swimmer’s contact, detected a load seven times<br />

smaller than the force produced by the wave on the first platform. This<br />

decrease was attributed to the distance that the wave travelled to reach<br />

the second platform.<br />

The aim of the present study was to develop a graphical removal<br />

technique of the bow wave that precedes the contact of the swimmer<br />

with the wall dur<strong>in</strong>g the front-crawl flip turn, as well as characteriz<strong>in</strong>g<br />

<strong>and</strong> quantify<strong>in</strong>g it.<br />

148<br />

Methods<br />

In order to characterize <strong>and</strong> quantify the force time curve produced by<br />

the wave before the turn, an extensometric underwater force platform<br />

was used, developed <strong>in</strong> accordance with Roesler (1997). Dimensions<br />

<strong>and</strong> characteristics were: 500 x 500 x 70 mm, load <strong>and</strong> sensitivity of<br />

4000 <strong>and</strong> 2 N (respectively), natural frequency of 400 Hz, ga<strong>in</strong> = 600.<br />

The force platform allowed data acquisition of force only <strong>in</strong> the perpendicular<br />

component to the surface of the platform. The platform mean<br />

measurement error was calculated after calibration <strong>and</strong> was given from<br />

the weight<strong>in</strong>g values obta<strong>in</strong>ed from the platform <strong>and</strong> the real weight of<br />

dead-weights previously measure <strong>in</strong> a precision scale. The mean difference<br />

between the values acquired on the platform <strong>and</strong> the dead weights<br />

was less than 1%. The acquired signals were converted by an analog to<br />

digital (A / D) converter, with a 16 bit resolution (BIOPAC Systems,<br />

Inc.) <strong>and</strong> with <strong>in</strong>put voltage of ± 10 volts. The acquisition rate was of<br />

1000 Hz, powered by a 12 volts source, which allowed the subsequent<br />

import of the signal to a PC.<br />

The platform was set <strong>in</strong> an upright position on the opposite wall of<br />

the start<strong>in</strong>g blocks, <strong>in</strong> a metallic support that also <strong>in</strong>cluded a sta<strong>in</strong>less<br />

steel frame for improved comfort <strong>and</strong> safety of the swimmer. As the<br />

platform was 0.7 m apart from the turn<strong>in</strong>g wall, the black l<strong>in</strong>es at the<br />

bottom of the pool were modified to fit the new sett<strong>in</strong>g, rema<strong>in</strong><strong>in</strong>g at the<br />

official distance to allow normal turn<strong>in</strong>g performances.<br />

Data from the force platform were acquired through the program<br />

Acqknowledge ® (BIOPAC System Inc.). Signal process<strong>in</strong>g was programmed<br />

<strong>in</strong>to a MatLab base <strong>and</strong> consisted of: calibration, filter<strong>in</strong>g<br />

(Butterworth 4th order, with a cutoff frequency of 100 Hz) <strong>and</strong> DC<br />

offset removal. Normalization was done digitally by the program shar<strong>in</strong>g<br />

files <strong>and</strong> turned over by the force of the weight of the swimmer.<br />

Two video cameras were used to monitor the water <strong>and</strong> the swimmer<br />

movements, particularly the time of the <strong>in</strong>itial contact of the swimmer<br />

at the force platform. A digital type HC42E Sony camera was <strong>in</strong>stalled<br />

<strong>in</strong> a waterproof case (Sony SPK-HCB) <strong>and</strong> attached to the bottom of<br />

the pool perpendicular to the swimmers direction of movement (frontal<br />

to sagittal <strong>in</strong>termediate plan). A surveillance video camera (type B7W<br />

submergible camera - AC 230V) was fixed at the bottom of the pool,<br />

fac<strong>in</strong>g upward perpendicular to the swimm<strong>in</strong>g direction (frontal plan),<br />

<strong>in</strong> order to monitor the movement of the wave dur<strong>in</strong>g the turn.<br />

When the swimmer started swimm<strong>in</strong>g towards to the turn<strong>in</strong>g wall,<br />

a trigger was activated to the A/D convert<strong>in</strong>g system, which connected<br />

a underwater light visible by the video cameras. This process allowed<br />

synchroniz<strong>in</strong>g the video setup <strong>and</strong> the force records.<br />

A male swimmer of 22 years old, 1.82 m <strong>in</strong> height <strong>and</strong> 84.9 kg body<br />

weight, f<strong>in</strong>alist of spr<strong>in</strong>t races at the Portuguese National Championships,<br />

performed 8 flip turns. He started from the center of the pool,<br />

12.5 m apart from the turn<strong>in</strong>g wall, with maximum speed, but without<br />

touch<strong>in</strong>g the platform, as shown <strong>in</strong> Figure 1.<br />

Figure 1. Sequence of images of the wave generated by the movement of<br />

the swimmer perform<strong>in</strong>g the turn without touch<strong>in</strong>g the force platform.


These trials allowed verify<strong>in</strong>g that the force signal produced by the wave<br />

was reasonably symmetric (Fig. 3). In normal turn<strong>in</strong>g situations, swimmers<br />

touch the platform, allow<strong>in</strong>g it to record the swimmer’s push<strong>in</strong>g<br />

action aga<strong>in</strong>st the wall. However, as already stated, before the swimmer<br />

touches the wall, a water wave hits the platform be<strong>in</strong>g also recorded. To<br />

remove this extraneous force, two assumptions were made: (i) the wave<br />

force to time curve be<strong>in</strong>g symmetrical, <strong>and</strong> (ii) that the peak value of the<br />

water wave force occurs at the time <strong>in</strong>stant of swimmer’s wall contact.<br />

From the force platform data was extracted the time of water wave force<br />

start, <strong>and</strong> from the image-based k<strong>in</strong>ematics the time of swimmer’s first<br />

contact was obta<strong>in</strong>ed. We assume this to be co<strong>in</strong>cident with half water<br />

wave curve. This half force to time curve of the water wave was then mirrored<br />

<strong>and</strong> its values were subtracted from the total force values registered<br />

by the platform (Fig. 2) to allow obta<strong>in</strong><strong>in</strong>g: (i) the swimmer’s contact<br />

force to time curve, <strong>and</strong> (ii) the water wave force to time curve.<br />

Solid l<strong>in</strong>e: force registered; dotted<br />

l<strong>in</strong>e: wave mirror<strong>in</strong>g; vertical<br />

l<strong>in</strong>e: time of contact<br />

Solid l<strong>in</strong>e: force registered; dotted<br />

l<strong>in</strong>e: force after wave removal;<br />

vertical l<strong>in</strong>e: time of contact<br />

Figure 2. Graphical representation of the removal of the water wave of<br />

the total force to time curve obta<strong>in</strong>ed dur<strong>in</strong>g a crawl flip turn.<br />

With a sample of 17 swimmers, 9 males <strong>and</strong> 8 females, aged 17.88 ±<br />

3.19 years, height 1.73 ± 0.09, body mass 64.48 ± 11.90 kg, all participants<br />

at the Absolute Portuguese National Championships, 154 valid<br />

turns were analysed. The force to time curve produced by the water wave<br />

was elim<strong>in</strong>ated graphically from the force to time curve produced by<br />

the swimmer’s contact. Moreover, the wave force to time curve was also<br />

treated to characterize their ma<strong>in</strong> characteristics. Descriptive statistics<br />

were used for data analysis.<br />

RESULTS<br />

The force curves generated by the water wave obta<strong>in</strong>ed without the<br />

swimmer touch<strong>in</strong>g the wall resulted <strong>in</strong> a mean curve (Fig. 3).<br />

Figure 3. Mean force curve of the water wave generated by the displacement<br />

of the swimmer dur<strong>in</strong>g the turn without touch<strong>in</strong>g the force<br />

platform.<br />

chaPter2.<strong>Biomechanics</strong><br />

It is possible to observe that the behavior of the curve is not l<strong>in</strong>ear but<br />

follows a pattern tend<strong>in</strong>g to a symmetrical condition, as observed before<br />

by Fujishima (1999). Mean results obta<strong>in</strong>ed for the quantitative parameters<br />

of the water wave obta<strong>in</strong>ed with the turns performed without<br />

touch<strong>in</strong>g the wall are presented <strong>in</strong> Table 1, as well as the data regard<strong>in</strong>g<br />

eight turns from the same swimmer touch<strong>in</strong>g the wall <strong>and</strong> the 154 turns<br />

performed by the total sample of 17 swimmers.<br />

Table 1. Mean values (Mean) ± st<strong>and</strong>ard deviations (SD) obta<strong>in</strong>ed for<br />

the variables: maximum <strong>and</strong> mean force value produced by the water<br />

wave, <strong>and</strong> wave impulse, grouped <strong>in</strong> normalized <strong>and</strong> absolute values <strong>in</strong> 3<br />

situations of wave measurement dur<strong>in</strong>g the flip turn.<br />

WAVE DATA<br />

Turn<strong>in</strong>g trials<br />

8 turns without<br />

touch<strong>in</strong>g the wall<br />

8 turns touch<strong>in</strong>g<br />

the wall<br />

154 turns touch<strong>in</strong>g<br />

the wall<br />

NORMALIZADED VALUES ABSOLUT VALUES<br />

Maximal<br />

(N/bw)<br />

Mean ±<br />

SD<br />

Mean (N/<br />

bw)<br />

Mean ±<br />

SD<br />

Impulse<br />

(N.s/bw)<br />

Mean ±<br />

SD<br />

0.38 ± 0.77 0.16 ± 0.33 0.01 ± 0.002<br />

0.52 ± 0.12 0.24 ± 0.06 0.01 ± 0.008<br />

0.49 ± 0.24 0.19 ± 0.12 0.04 ± 0.02<br />

Maximal<br />

(N)<br />

Mean ±<br />

SD<br />

320.17 ±<br />

65.59<br />

448.88 ±<br />

106.32<br />

323.17 ±<br />

191.94<br />

Mean<br />

(N)<br />

Mean ±<br />

SD<br />

140.62 ±<br />

28.05<br />

206.97 ±<br />

65.76<br />

128.68 ±<br />

90.44<br />

Impulse<br />

(N.s)<br />

Mean ±<br />

SD<br />

10.5 ± 0.17<br />

15.44 ± 4.07<br />

27.16 ± 19.29<br />

Figures 4 <strong>and</strong> 5 represent an example of the swimmer’s contact/impulse<br />

force to time curve, before (Fig. 4) <strong>and</strong> after removal (Fig. 5) of the water<br />

wave specific curve. In this case, the wave was almost fully <strong>in</strong>corporated<br />

<strong>in</strong>to the swimmers’ contact curve, <strong>and</strong> the <strong>in</strong>terference of the wave phenomenon<br />

<strong>in</strong>to the swimmers’ k<strong>in</strong>etics is presumably important, mak<strong>in</strong>g<br />

it more difficult to assess the effect of the wave over the impulse curve.<br />

Figure 4. Example of a force to time curve produced dur<strong>in</strong>g a flip turn<br />

with the effect of the water wave impact.<br />

Figure 5. Example of a force to time curve produced dur<strong>in</strong>g a flip turn<br />

without the effect of the water wave impact.<br />

149


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The comparison of the impulse (time <strong>in</strong>tegral of the force curve) with<br />

<strong>and</strong> without the water wave k<strong>in</strong>etic effect showed values of 314.48 ±<br />

62.75, <strong>and</strong> 288.57 ± 51.79 N.s, respectively. This difference stresses out<br />

a reduction of 10.87 % of the orig<strong>in</strong>al force to time curve area when the<br />

water wave effect is removed.<br />

dIscussIon<br />

The behavior of the force to time curve recorded at the turn<strong>in</strong>g wall due<br />

to the water wave produced by a swimmer is variable, <strong>and</strong> the factors<br />

that determ<strong>in</strong>e its behavior are not yet fully understood. Supposedly,<br />

they are likely related to the aided mass of water displaced with the<br />

swimmer, to its cross-sectional area, <strong>and</strong> to the speed <strong>and</strong> direction of<br />

its displacement.<br />

The data collected dur<strong>in</strong>g the turn<strong>in</strong>g experiments where the swimmer<br />

did not touch the wall are <strong>in</strong> agreement with Roesler (2002), but<br />

only partially with Lyttle <strong>and</strong> Mason (1997). In fact these authors found<br />

higher maximum values, but us<strong>in</strong>g a method <strong>in</strong> which the wave k<strong>in</strong>etics<br />

may <strong>in</strong>clude a not negligible contribution of the swimmers’ contact<br />

force (once the <strong>in</strong>strumentation that allowed the assessment of the <strong>in</strong>itial<br />

contact <strong>in</strong>stant was triggered manually). The possibly larger force<br />

plate used by these researchers might also <strong>in</strong>fluence the appropriateness<br />

of this comparison.<br />

The k<strong>in</strong>etic characteristics of the water wave at the wall (mean data<br />

of 154 turns performed by 17 swimmers) were similar to those provided<br />

by the mean results of eight trials performed without contact at the wall<br />

by one swimmer, despite the diversity of <strong>in</strong>dividual responses. However,<br />

when compar<strong>in</strong>g the results of the same swimmer touch<strong>in</strong>g or not the<br />

wall, it was observed that the water wave force values without touch<strong>in</strong>g<br />

the wall tended to be smaller, probably because the swimmer refra<strong>in</strong>ed<br />

himself <strong>in</strong> order to avoid touch<strong>in</strong>g the wall. S<strong>in</strong>ce he is one of the best<br />

<strong>and</strong> stronger swimmers of the sample, his results tended to be higher<br />

than those obta<strong>in</strong>ed for the global sample.<br />

conclusIon<br />

The comparison of the force to time curve characteristics of the water<br />

wave produced by a swimmer dur<strong>in</strong>g a flip turn, with <strong>and</strong> without<br />

touch<strong>in</strong>g the wall, support satisfactorily the solution proposed to remove<br />

the water wave effect upon the swimmers’ k<strong>in</strong>etics. It can be accepted<br />

that the error associated with the wave data elim<strong>in</strong>ation through this<br />

procedure is not significant, ensur<strong>in</strong>g data <strong>in</strong>tegrity of the swimmer’s<br />

k<strong>in</strong>etics at the wall, <strong>and</strong> allow<strong>in</strong>g greater accuracy for its assessment.<br />

reFerences<br />

Barbosa, T. M., & Vilas-Boas, J. P. (2005). Study of different concepts of<br />

efficiency of human locomotion <strong>in</strong> water. Portuguese Journal of Sport<br />

Sciences, 3(5), 337–347.<br />

Blanksby, B., Simpson, J. R., Elliot, B., & McElroy, K. (1998). Biomechanical<br />

factors <strong>in</strong>fluenc<strong>in</strong>g breaststroke turns by age-group swimmers.<br />

Journal of Applied <strong>Biomechanics</strong>, 14(2), 181–189.<br />

Blanksby, B., Skender, S., Elliott, B., McElroy, K., & L<strong>and</strong>ers, G. (2004).<br />

An analysis of rollover backstroke turns by age-group swimmers.<br />

Sports <strong>Biomechanics</strong>, 3(3), 1-14.<br />

Fujishima, M., Sato, Y., & Miyashita, M. (1999). Improvement of wave<br />

absorption by a new lane-marker covered with mesh. Paper presented<br />

at the International Symposium on <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g, Jyväskylä, F<strong>in</strong>l<strong>and</strong>.<br />

Lyttle, A. (2000). Hydrodynamics of the human body dur<strong>in</strong>g the freestyle<br />

tumble turn. The University of Western Australia.<br />

Lyttle, A., & Mason, B. (1997). A k<strong>in</strong>ematic <strong>and</strong> k<strong>in</strong>etic analysis of<br />

freestyle <strong>and</strong> butterfly turns. Journal of Swimm<strong>in</strong>g Research, 12, 7–11.<br />

Roesler, H. (1997). Development of underwater platform for measur<strong>in</strong>g<br />

forces <strong>and</strong> moments <strong>in</strong> the three coord<strong>in</strong>ate axes for use <strong>in</strong> biomechanics.<br />

Universidade do Rio Gr<strong>and</strong>e do Sul, Porto Alegre.<br />

150<br />

Roesler, H. (2002, June, 2003). Turn<strong>in</strong>g force measurement <strong>in</strong> swimm<strong>in</strong>g<br />

us<strong>in</strong>g underwater force platform. Paper presented at the International<br />

Symposium on <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g,<br />

Sa<strong>in</strong>t-Etienne, France.<br />

AcKnoWledGeMents<br />

This work was supported <strong>in</strong> part by a grant of the FCT - Science <strong>and</strong><br />

Technology Foundation, Portugal.


Extend<strong>in</strong>g the Critical Force Model to Approach<br />

Critical Power <strong>in</strong> Tethered Swimm<strong>in</strong>g, <strong>and</strong> its<br />

Relationship to the Indices at Maximal Lactate<br />

Steady-State<br />

Pessôa Filho, d.M., denadai, B.s.<br />

Paulista State University, Brazil<br />

This study aimed at compar<strong>in</strong>g tethered-power (CP Teth ), assessed us<strong>in</strong>g<br />

the critical force model, to the power at maximal lactate steady state<br />

(P TethMLSS ), <strong>and</strong> critical velocity (CV) to the velocity at maximal lactate<br />

steady state (v MLSS ). Ten swimmers were submitted to measurements of<br />

the CP Teth (l<strong>in</strong>ear <strong>and</strong> non-l<strong>in</strong>ear adjustments of impulse aga<strong>in</strong>st time),<br />

CV (l<strong>in</strong>ear plott<strong>in</strong>g of time <strong>and</strong> velocity <strong>in</strong> the 200, 400 <strong>and</strong> 800-m),<br />

P TethMLSS (3-4 trials rang<strong>in</strong>g from 95 to 105% of non-l<strong>in</strong>ear Fcrit),<br />

<strong>and</strong> v MLSS (3-4 trials rang<strong>in</strong>g from 85 to 95% of the 400-m free-crawl<br />

performance). Estimated CP Teth <strong>and</strong> P TethMLSS were obta<strong>in</strong>ed from the<br />

tethered-force equation times hydrofoil velocity. The results showed that<br />

neither CV (1.19 ± 0.11m·s -1 ) nor CP Teth (98±22W) matches the statements<br />

for maximal lactate steady state, once differences (p ≤ 0.05) were<br />

noted <strong>in</strong> relation to v MLSS (1.17 ± 0.10m·s -1 ) <strong>and</strong> P TethMLSS (89±15W),<br />

respectively.<br />

Keywords: critical tethered-force; tethered swimm<strong>in</strong>g; maximal lactate<br />

steady state; swimm<strong>in</strong>g hydrodynamics<br />

IntroductIon<br />

Time to exhaustion is l<strong>in</strong>early related to the steady-load applied while<br />

swimm<strong>in</strong>g at full-tethered conditions (Ikuta et al., 1996). These authors<br />

def<strong>in</strong>ed critical force (Fcrit), the slope of the l<strong>in</strong>ear plot between impulse<br />

<strong>and</strong> maximal susta<strong>in</strong>able time, as the tethered force that could<br />

be ma<strong>in</strong>ta<strong>in</strong>ed without fatigue. Despite the fact, that the measurements<br />

of endurance pull<strong>in</strong>g force provide good relationships to long-distance<br />

performance (Swa<strong>in</strong>e, 1996) <strong>and</strong> to blood lactate accumulation <strong>in</strong>dex<br />

(Ikuta et al., 1996), the relationship between pull<strong>in</strong>g force <strong>and</strong> swimm<strong>in</strong>g<br />

<strong>in</strong>tensity at maximal lactate steady-state (MLSS) rema<strong>in</strong>s to be<br />

established.<br />

The MLSS corresponds to the highest constant workload that can<br />

be ma<strong>in</strong>ta<strong>in</strong>ed over time without cont<strong>in</strong>uous blood lactate accumulation<br />

(Beneke et al., 2001). The time to exhaustion-based model is a simple,<br />

rapid <strong>and</strong> non-<strong>in</strong>vasive test to evaluate endurance capacity, but the accuracy<br />

of <strong>in</strong>direct tests to estimate MLSS has been questioned. Dekerle<br />

et al. (2005) suggested that the determ<strong>in</strong>ation of critical velocity (CV)<br />

leads to an overestimation of the metabolic rate associated with MLSS,<br />

<strong>and</strong> that the differences between these variables tend to be greater with<br />

the improvement of aerobic performance. Although Ikuta et al. (1996)<br />

did not measure the force or velocity at MLSS, they assumed its correspondence<br />

to the Fcrit based on the correlations between this parameter<br />

<strong>and</strong> endurance <strong>in</strong>dices obta<strong>in</strong>ed under free crawl condition.<br />

It should be noted that the <strong>in</strong>terchangeable use of MLSS <strong>and</strong> CV<br />

(or critical power, CP) to represent the upper limit of heavy exercise<br />

doma<strong>in</strong> has been refuted either <strong>in</strong> cycl<strong>in</strong>g (Pr<strong>in</strong>gle & Jones, 2002) or <strong>in</strong><br />

swimm<strong>in</strong>g (Dekerle et al., 2009). Despite the slight differences between<br />

these variables, CP leads to an overestimation of physiological rate associated<br />

to MLSS (Pr<strong>in</strong>gle & Jones, 2002; Dekerle et al., 2003). Thus,<br />

it was postulated that exercis<strong>in</strong>g just above MLSS is hardly tolerable<br />

once it <strong>in</strong>duces to a cont<strong>in</strong>uous <strong>in</strong>creas<strong>in</strong>g <strong>in</strong> blood lactate concentration<br />

<strong>and</strong> VO 2 (Pr<strong>in</strong>gle & Jones, 2002; Dekerle et al., 2009). Nevertheless,<br />

this slight difference between MLSS <strong>and</strong> CV (or PC) should be <strong>in</strong>terpreted<br />

with caution, due to methodological limitations of model<strong>in</strong>g CV<br />

(or PC) (Dekerle et al., 2003) <strong>and</strong> of the precise control of load under<br />

MLSS test<strong>in</strong>g procedures (Pr<strong>in</strong>gle & Jones, 2002).<br />

The assessment of stroke force by means of tethered swimm<strong>in</strong>g is<br />

chaPter2.<strong>Biomechanics</strong><br />

simple <strong>and</strong> versatile, besides it has provided a great deal of specificity for<br />

swimmer evaluation, tra<strong>in</strong><strong>in</strong>g <strong>and</strong> free swimm<strong>in</strong>g performance ( Johnson<br />

et al., 1993; Rouard et al., 2006). Furthermore, accord<strong>in</strong>g to Kjendlie<br />

& Thorsvald (2006), force measurement with tethered swimm<strong>in</strong>g is<br />

highly reliable <strong>and</strong> shows low values of variation for test-retest protocol.<br />

Thus, assum<strong>in</strong>g tethered swimm<strong>in</strong>g as a steady-force environment, one<br />

of the purposes of this study was to compare <strong>and</strong> to relate the values of<br />

power output at MLSS (PTethMLSS ) <strong>in</strong> relation to the critical force (PF crit<br />

) model. Another purpose was to proceed with the same analysis for<br />

reciprocal tests under free crawl swimm<strong>in</strong>g, allow for further comparisons<br />

through the two swimm<strong>in</strong>g conditions (non- <strong>and</strong> full-tethered),<br />

as for blood lactate concentration at MLSS, <strong>and</strong> for amplitude of the<br />

differences between P Fcrit vs. P TethMLSS <strong>and</strong> velocity at MLSS (v MLSS )<br />

vs. CV.<br />

Methods<br />

Ten well-tra<strong>in</strong>ed male swimmers (16.6 ± 1.4 years, 69.8 ± 9.5kg, 175.8<br />

± 4.6cm) were submitted to four <strong>in</strong>dependent tests <strong>in</strong> order to measure<br />

the P TethC , CV, P TethMLSS <strong>and</strong> v MLSS . They were <strong>in</strong>formed of all test protocols<br />

<strong>and</strong> we obta<strong>in</strong>ed their <strong>in</strong>formed consent. The study was approved<br />

by the local Ethics Committee.<br />

The active drag force (Fr) <strong>in</strong> maximal free crawl swimm<strong>in</strong>g was estimated<br />

based on subjects body mass, us<strong>in</strong>g drag proportionality coefficient<br />

(A = ((0.35 x mass)) + 2), accord<strong>in</strong>g to Toussa<strong>in</strong>t et al. (1998). This<br />

procedure is not a direct measurement of active body drag, <strong>and</strong> it takes<br />

<strong>in</strong>to account an early assumption that the resistance is related to the<br />

square of the swimm<strong>in</strong>g velocity (Fr = Av 2 ) (Toussa<strong>in</strong>t et al., 1998). On<br />

a practical note, this approach provides a good deal of applications for<br />

hydrodynamics assessment on poolside throughout the tra<strong>in</strong><strong>in</strong>g season.<br />

To estimate Fcrit, loads rang<strong>in</strong>g from 75 to 100% of the Fr <strong>in</strong> the<br />

pulley-rope system were attached to the swimmer. Three trials last<strong>in</strong>g 3<br />

to 15 m<strong>in</strong>utes were performed until exhaustion, i.e. the <strong>in</strong>stant that the<br />

swimmer was not able to generate force enough to prevent him from<br />

be<strong>in</strong>g pulled back by the load. The impulse (load times trials duration, N<br />

x s) was plotted aga<strong>in</strong>st trials duration by means of a l<strong>in</strong>ear curve fitt<strong>in</strong>g<br />

(i = a + b(t)), <strong>and</strong> a non-l<strong>in</strong>ear two-parameter equation (t = a/(i – b)),<br />

where the slope gives Fcrit <strong>in</strong> both adjustments (Ikuta et al., 1996). The<br />

load related to MLSS <strong>in</strong>tensity was obta<strong>in</strong>ed <strong>in</strong> three to four trials rang<strong>in</strong>g<br />

from 95 to 105% of non-l<strong>in</strong>ear Fcrit. The greatest fraction that did<br />

not elicit a lactate accumulation above 1mmol.L -1 between 10 th <strong>and</strong> 30 th<br />

m<strong>in</strong>utes was considered the tethered-force at MLSS (F MLSS ). Blood<br />

samples (~25µl) from ear lobe were analyzed for lactate concentration<br />

([La]) us<strong>in</strong>g an automated analyzer (YSI 2300, Yellow Spr<strong>in</strong>gs, Ohio,<br />

USA). The test was <strong>in</strong>terrupted by 30s break for blood sampl<strong>in</strong>g at the<br />

10 th <strong>and</strong> 30 th m<strong>in</strong>utes, as suggested by Beneke et al. (2001).<br />

To approach mechanical tethered-power (P Teth ) from Fcrit <strong>and</strong><br />

F MLSS , we considered two assumptions. First, the hydrofoil moves backward<br />

with uniform velocity dur<strong>in</strong>g the entire stroke. Second, an external<br />

<strong>and</strong> constant load<strong>in</strong>g generates an oppos<strong>in</strong>g load force (F Load ) equal to<br />

the tethered-force of hydrofoil (F Teth ). Thus, added weight must prevent<br />

the swimmer from mov<strong>in</strong>g forward (v = 0) accord<strong>in</strong>g to F Load + Fr –<br />

F Teth = 0, where Fr approaches zero <strong>in</strong> this condition. This statement<br />

for hydrofoil motion <strong>in</strong> tethered swimm<strong>in</strong>g is an unequivocal rewrite of<br />

the mechanical assumption for hydrofoil described by de Groot & van<br />

Ingen Schenau (1988). Therefore, the relationship between forward <strong>and</strong><br />

backward forces <strong>in</strong> steady state condition equals:<br />

F Load = F Teth = 0,5Cx Hydr × ρ × S Hydr × u 2 (1)<br />

where F Load <strong>and</strong> F Teth are noted <strong>in</strong> Newtons; Cx Hydr is the drag coefficient<br />

for hydrofoil (~2.2), p is the water density (~1000kg/m 3 ), S Hydr<br />

is the hydrofoil plane area (estimated from h<strong>and</strong> <strong>and</strong> forearm volume<br />

powered by two thirds, i.e. V Hydr 2/3 ), <strong>and</strong> u 2 is the squared hydrofoil velocity<br />

(v Hydr, m·s -1 ). The volume of h<strong>and</strong> <strong>and</strong> forearm was determ<strong>in</strong>ed<br />

151


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

accord<strong>in</strong>g to anthropometric measurements, follow<strong>in</strong>g Hatze’s model<br />

of human body.<br />

Rearrang<strong>in</strong>g equation 1 to “u”, an approximation of hydrofoil velocity<br />

is obta<strong>in</strong>ed:<br />

v Hydro = (F Load /(0,5Cx Hydr × ρ × S Hydr )) 1/2 (2)<br />

The amount of mechanical power used beneficially to the stroke task of<br />

overcome steady-load resistance was:<br />

P Teth (W) = F Teth (N) × v Hydro (m·s -1 ) (3)<br />

Further, the P TethC <strong>and</strong> P TethMLSS were obta<strong>in</strong>ed by <strong>in</strong>sert<strong>in</strong>g Fcrit <strong>and</strong><br />

F MLSS <strong>in</strong>to Equation 2 <strong>and</strong> thereafter to Equation 3.<br />

Test protocols <strong>in</strong> free style swimm<strong>in</strong>g:<br />

Swimm<strong>in</strong>g crawl velocity correspondent to MLSS was determ<strong>in</strong>ed from<br />

three to four trials <strong>in</strong> the range of 85 to 95% of the 400 meters velocity.<br />

The CV was obta<strong>in</strong>ed from l<strong>in</strong>ear adjustment of the free-crawl time<br />

performance <strong>in</strong> the 200, 400 <strong>and</strong> 800 meters, follow<strong>in</strong>g the model vt<br />

Lim -1 (Dekerle et al., 2005).<br />

Statistical analysis:<br />

The Pearson’s coefficient provided the correlation among variables, <strong>and</strong><br />

the difference between them was designed by test-T for paired data.<br />

Bl<strong>and</strong> <strong>and</strong> Altman analysis was applied to compare the endurance <strong>in</strong>dex<br />

obta<strong>in</strong>ed from the models. The level of significance was p ≤ 0.05.<br />

results<br />

Active drag value corresponded to 26.41 ± 3.34v2 at 1.63 ± 0.07m·s-1 freestyle velocity. For comparison between time-based protocols <strong>in</strong> free<br />

<strong>and</strong> tethered swim conditions (Figure 1), a range of ~85 a 100%Frmax was closely related to exhaustion range ~3 a 12 m<strong>in</strong> (r2 = 0.973). It was<br />

<strong>in</strong> the same order to the association observed between velocity performance<br />

<strong>and</strong> 200, 400 e 800-m distances (r2 = 0.975). However, dissimi-<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b 98<br />

larities were observed between higher <strong>and</strong> middle <strong>in</strong>tensity efforts of<br />

the protocols (ρ = 0.000 <strong>and</strong> ρ = 0.045, respectively), but not between<br />

observed between higher <strong>and</strong> middle <strong>in</strong>tensity efforts of the protocols (ρ = 0.000 <strong>and</strong> ρ<br />

long-last<strong>in</strong>g <strong>and</strong> low <strong>in</strong>tensity ones (ρ = 0.449).<br />

Im puls e (N x s )<br />

= 0.045, respectively), but not between long-last<strong>in</strong>g <strong>and</strong> low <strong>in</strong>tensity ones (ρ = 0.449).<br />

40000<br />

Velocity Impulse (m/s) (N x s)<br />

Table 1: Values of endurance variables <strong>in</strong> tethered <strong>and</strong> free swimm<strong>in</strong>g conditions.<br />

Fcrit (N) – Fcrit (N) – PFcrit (W) - FMLSS (N)<br />

l<strong>in</strong>ear* non-l<strong>in</strong>ear l<strong>in</strong>ear<br />

PTethMLSS<br />

(W)<br />

CV<br />

(m·s -1 )*<br />

vMLSS<br />

(m·s -1 )<br />

55.14<br />

(±7.82) †<br />

54.06 98.49<br />

(±7.24) (±21.63) ‡<br />

51.74<br />

(±5.63) †<br />

89.21<br />

(±15.11) ‡<br />

1.19<br />

(±0.11) §<br />

1.17<br />

(±0.10) §<br />

4.4<br />

152<br />

ctate (mmol/L)<br />

Lactate (mmol/L)<br />

y = 54.3x + 3721.9<br />

R 2 = 0.991<br />

3.6<br />

2.8<br />

2.0<br />

Velocity (m/s)<br />

1.6<br />

1.56<br />

y = 23.536x + 1.3584<br />

R 2 = 0.983<br />

has no similarity to velocity at MLSS either. Difference of blood lactate concentration<br />

between paired trials of each test condition (tethered <strong>and</strong> free swimm<strong>in</strong>g) was noted as<br />

significant for the first (ρ = 0.0002) <strong>and</strong> second (ρ = 0.038) ones (Figure 2). However,<br />

lactate concentration at MLSS did not differ <strong>in</strong> all test protocols (ρ = 0.448 for blood<br />

concentration of 3.84 ± 0.60mmol.L -1 <strong>and</strong> 3.61 ± 0.97mmol.L -1 <strong>in</strong> the tethered <strong>and</strong> free<br />

swim, respectively). Also, a strong positive relationship was analyzed <strong>in</strong> all endurance<br />

variables (Table 2).<br />

Figure 2: Lactate profile <strong>in</strong> the bouts of either protocol to determ<strong>in</strong>e MLSS <strong>in</strong>tensity:<br />

swimm<strong>in</strong>g velocity (dotted l<strong>in</strong>es <strong>and</strong> filled symbols) <strong>and</strong> tethered-force (cont<strong>in</strong>uous<br />

l<strong>in</strong>es <strong>and</strong> open symbols). Marked differences were significant at the end of trials (p ≤<br />

0.05) between each of the low ( † ) <strong>and</strong> middle ( ‡ ) <strong>in</strong>tensities across protocols.<br />

Table 1: Values of endurance variables <strong>in</strong> tethered <strong>and</strong> free swimm<strong>in</strong>g conditions.<br />

Fcrit (N) – Fcrit (N) – PFcrit (W) - FMLSS (N) PTethMLSS CV<br />

l<strong>in</strong>ear* non-l<strong>in</strong>ear l<strong>in</strong>ear<br />

(W) (m·s -1 vMLSS<br />

)* (m·s -1 )<br />

55.14<br />

(±7.82) †<br />

54.06 98.49<br />

(±7.24) (±21.63) ‡<br />

51.74<br />

(±5.63) †<br />

89.21<br />

(±15.11) ‡<br />

1.19<br />

(±0.11) §<br />

1.17<br />

(±0.10) §<br />

6.0<br />

5.2<br />

4.4<br />

104.0%Fcrit<br />

92.8%v400<br />

100.8%Fcrit<br />

‡<br />

3.6<br />

2.8<br />

97.5%Fcrit<br />

†<br />

90.3%v400<br />

‡<br />

2.0<br />

1.2<br />

0.4<br />

86.9%v400 †<br />

0 10<br />

M<strong>in</strong>utes<br />

30<br />

Figure 2: Lactate profile <strong>in</strong> the bouts of either protocol to determ<strong>in</strong>e<br />

MLSS <strong>in</strong>tensity: swimm<strong>in</strong>g velocity (dotted l<strong>in</strong>es <strong>and</strong> filled symbols)<br />

<strong>and</strong> tethered-force (cont<strong>in</strong>uous l<strong>in</strong>es <strong>and</strong> open symbols). Marked differences<br />

were significant at the end of trials (p ≤ 0.05) between each of the<br />

low ( † ) <strong>and</strong> middle ( ‡ ) <strong>in</strong>tensities across protocols.<br />

Table 1: Values of endurance variables <strong>in</strong> tethered <strong>and</strong> free swimm<strong>in</strong>g<br />

conditions.<br />

Lactate (mmol/L)<br />

Fcrit (N) –<br />

l<strong>in</strong>ear*<br />

55.14<br />

(±7.82) †<br />

Fcrit (N) – PFcrit (W) -<br />

F<br />

non-l<strong>in</strong>ear l<strong>in</strong>ear MLSS (N) PTethMLSS (W)<br />

54.06<br />

(±7.24)<br />

98.49<br />

(±21.63) ‡<br />

97.5%Fcrit<br />

90.3%v400<br />

51.74<br />

(±5.63) †<br />

89.21<br />

(±15.11) ‡<br />

CV<br />

(m·s -1 )*<br />

1.19<br />

(±0.11) §<br />

v MLSS<br />

(m·s -1 )<br />

1.17<br />

(±0.10) §<br />

*PS: The model i-t Lim -1 gives a mean adjustment of R 2 = 0.998 ± 0.003,<br />

<strong>and</strong> for the model v-t Lim -1 of R 2 = 0.975 ± 0.033. Differences between<br />

Fcrit <strong>and</strong> F MLSS ( † ρ = 0.009), P TethC <strong>and</strong> P TethMLSS ( ‡ ρ = 0.011), <strong>and</strong> CV<br />

<strong>and</strong> v MLSS ( § ρ = 0.035) were analysed.<br />

Table 2: Pearson’s Coefficient of the velocity <strong>and</strong> mechanical endurance<br />

variable.<br />

CV (m·s -1 ) P TethC (W·kg -1 ) v MLSS (m·s -1 )<br />

P TethMLSS (W.kg -1 ) 0.862** 0.763 ** 0.756**<br />

v MLSS (m·s -1 ) 0.974 ** 0.615*<br />

P TethC (W.kg -1 ) 0.724**<br />

*Significance at 0.05. **Significance at 0.01.<br />

Figure 1: L<strong>in</strong>ear adjustments for determ<strong>in</strong>ation of Fcrit (A) <strong>and</strong> CV (B) for subject 4.<br />

The critical force, <strong>and</strong> associated mechanical power have shown to be different<br />

from both tethered-force <strong>and</strong> mechanical power at MLSS (Table 1). Critical velocity<br />

has no similarity to velocity at MLSS either. Difference of blood lactate concentration<br />

between paired trials of each test condition (tethered <strong>and</strong> free swimm<strong>in</strong>g) was noted as<br />

significant for the first (ρ = 0.0002) <strong>and</strong> second (ρ = 0.038) ones (Figure 2). However,<br />

lactate concentration at MLSS did not differ <strong>in</strong> all test protocols (ρ = 0.448 for blood<br />

concentration of 3.84 ± 0.60mmol.L -1 <strong>and</strong> 3.61 ± 0.97mmol.L -1 <strong>in</strong> the tethered <strong>and</strong> free<br />

swim, respectively). Also, a strong positive relationship was analyzed <strong>in</strong> all endurance<br />

variables (Table 2).<br />

Figure 2: Lactate profile <strong>in</strong> the bouts of either protocol to determ<strong>in</strong>e MLSS <strong>in</strong>tensity:<br />

swimm<strong>in</strong>g velocity (dotted l<strong>in</strong>es <strong>and</strong> filled symbols) <strong>and</strong> tethered-force (cont<strong>in</strong>uous<br />

l<strong>in</strong>es <strong>and</strong> open symbols). Marked differences were significant at the end of trials (p ≤<br />

0.05) between each of the low ( † ) <strong>and</strong> middle ( ‡ 30000<br />

1.52<br />

20000<br />

A<br />

1.48<br />

1.44<br />

1.4<br />

B<br />

10000<br />

1.36<br />

100 300 500 700 0 0.002 0.004 0.006 0.008 0.01<br />

Time (s)<br />

Time (s-1)<br />

y = 54.3x + 3721.9<br />

R<br />

6.0<br />

104.0%Fcrit<br />

5.2<br />

92.8%v400<br />

100.8%Fcrit<br />

‡<br />

4.4<br />

3.6<br />

97.5%Fcrit<br />

†<br />

2.8<br />

90.3%v400<br />

‡<br />

2.0<br />

86.9%v400 †<br />

1.2<br />

0.4<br />

0 10 30<br />

M<strong>in</strong>utes<br />

) <strong>in</strong>tensities across protocols.<br />

2 40000<br />

y = 23.536x + 1.3584<br />

30000<br />

= R0.991 20000<br />

10000<br />

100 300 500<br />

Time (s)<br />

700<br />

2 Figure 1: L<strong>in</strong>ear adjustments for determ<strong>in</strong>ation of Fcrit (A) <strong>and</strong> CV<br />

(B) for subject 4.<br />

1.6<br />

The critical force, <strong>and</strong> associated mechanical power have shown to be<br />

different from 1.56both<br />

tethered-force <strong>and</strong> mechanical power at MLSS<br />

(Table 1). Critical velocity has no similarity = 0.983 to velocity at MLSS either.<br />

Difference 1.52 of blood lactate concentration between paired trials of each<br />

test condition (tethered <strong>and</strong> free swimm<strong>in</strong>g) was noted as significant<br />

for the first 1.48 (ρ = 0.0002) <strong>and</strong> second (ρ = 0.038) ones (Figure 2). However,<br />

lactate concentration at MLSS did not differ <strong>in</strong> all test protocols<br />

1.44<br />

(ρ = 0.448 for blood concentration of 3.84 ± 0.60mmol.L<br />

1.4<br />

1.36<br />

0 0.002 0.004 0.006 0.008<br />

Time (s-1)<br />

0.01<br />

-1 <strong>and</strong> 3.61 ±<br />

0.97mmol.L-1 dIscussIon<br />

Blood lactate concentration, <strong>in</strong> both tethered <strong>and</strong> non-tethered test conditions,<br />

are <strong>in</strong> agreement with the value of 3mmol.L<br />

<strong>in</strong> the tethered <strong>and</strong> free swim, respectively). Also, a strong<br />

positive relationship was analyzed <strong>in</strong> all endurance variables (Table 2).<br />

6.0<br />

5.2<br />

104.0%Fcrit<br />

92.8%v400<br />

100.8%Fcrit<br />

-1 , which has been<br />

suggested by Takahashi et al. (2009) as a suitable value for MLSS <strong>in</strong><br />

swimm<strong>in</strong>g. Velocity (1.24 ± 0.11m·s-1 ) <strong>and</strong> lactate concentration (2.8 ±<br />

1.2mmol.L-1 ) reported by Dekerle et al. (2005) for MLSS <strong>in</strong> freestyle<br />

conditions, are also not dissimilar from those showed <strong>in</strong> the present<br />

study.<br />

Despite the fact that subjects could swim at different levels of lactate<br />

steady-state the first two trials, when both protocols are compared, the<br />

physiological <strong>in</strong>tensity at MLSS did not differ <strong>in</strong> tethered <strong>and</strong> free swimm<strong>in</strong>g<br />

conditions, which is <strong>in</strong> agreement with the concept that MLSS depends<br />

on the motor pattern of the exercise (BENEKE et al., 2001). Therefore,<br />

the lack of statistical difference between blood lactate concentration<br />

at MLSS <strong>in</strong>to tethered <strong>and</strong> non-tethered swimm<strong>in</strong>g conditions suggest<br />

that the mode of exercise <strong>and</strong> metabolic profiles are similar.<br />

Results from tethered-force vs. time adjustments given a slope value<br />

(5.63 ± 0.80kg) were close to that (6.87 ± 1.02kg) orig<strong>in</strong>ally reported to<br />

Ikuta et al. (1996). Submaximal reference of mechanical tethered-power<br />

is not available. Swa<strong>in</strong>e (1994) evaluated endurance power <strong>in</strong> swimbench<br />

report<strong>in</strong>g 115.4 ± 18.4W. From another study, Swa<strong>in</strong>e (1996)<br />

reported values of 120.7 ± 9.4W for the slope of the relationship between<br />

total work done <strong>and</strong> time-limited <strong>in</strong> swim-bench. Toussa<strong>in</strong>t et<br />

al. (1998) did estimate critical power dur<strong>in</strong>g freestyle by plott<strong>in</strong>g energy


cost aga<strong>in</strong>st time performance <strong>in</strong> six distances, yield<strong>in</strong>g 114.5W. These<br />

references are out of range for tethered-power at MLSS, but are approached<br />

to the range of tethered-power at Fcrit (P Fcrit ).<br />

The estimated powers (P Fcrit <strong>and</strong> P TethMLSS ) are related, but statistically<br />

different, as the relationship observed to CV <strong>and</strong> v MLSS <strong>in</strong> nontethered<br />

crawl. Dekerle et al. (2005) also found significance for difference<br />

between v MLSS <strong>and</strong> CV <strong>in</strong> swimmers, despite the good relationship (r =<br />

0.87) between these variables. Also, the physiological responses when<br />

swimm<strong>in</strong>g 5% below <strong>and</strong> 5% above CV are those characteriz<strong>in</strong>g the<br />

heavy (susta<strong>in</strong>able steady-state) <strong>and</strong> severe (non-susta<strong>in</strong>able) <strong>in</strong>tensity<br />

doma<strong>in</strong>, whil<strong>in</strong>g responses at CV lies with<strong>in</strong> severe doma<strong>in</strong>s (Dekerle<br />

et al. 2009). These results support the conclusion that CP <strong>and</strong> MLSS do<br />

not represent the same physiological parameter, whilst associated workrate<br />

seemed to be correlated among group of tra<strong>in</strong>ed athletes (Pr<strong>in</strong>gle &<br />

Jones, 2002; Dekerle et al., 2005). It should be po<strong>in</strong>ted out that power<br />

parameters obta<strong>in</strong>ed from tethered swimm<strong>in</strong>g protocols further <strong>in</strong>crease<br />

the dissociation between the MLSS <strong>and</strong> CP, <strong>and</strong> the <strong>in</strong>ter<strong>in</strong>dividual<br />

differences for these variables. Otherwise, tethered swimm<strong>in</strong>g may be<br />

considered a reasonable ergometer to access aerobic endurance capacity<br />

based on both <strong>in</strong>vasive (lactate concentration profile) <strong>and</strong> non-<strong>in</strong>vasive<br />

(time to exhaustion model) methods, s<strong>in</strong>ce it ensures a force controll<strong>in</strong>g<br />

environment that is a requirement for MLSS <strong>and</strong> CP protocols<br />

Moreover, the differences <strong>in</strong> power output at tethered <strong>and</strong> non-tethered<br />

swimm<strong>in</strong>g seems to corroborate the conclusion of Dekerle et al.<br />

(2003) that the accuracy <strong>and</strong> reliability for evaluation of aerobic endurance<br />

relies on MLSS determ<strong>in</strong>ation, despite PC practicality. Nevertheless,<br />

the optimization of tra<strong>in</strong><strong>in</strong>g adaptation requires the def<strong>in</strong>ition of<br />

work-rate clusters of common profile of physiological response among<br />

subjects. Whether physiological response at VC (or PC) <strong>and</strong> at MLSS<br />

provides or not a common reference of exercise <strong>in</strong>tensity, it rema<strong>in</strong>s to<br />

be elucidated.<br />

Neither CV nor the mechanical power at Fcrit matches the assumption<br />

for MLSS, the highest constant <strong>in</strong>tensity that can be ma<strong>in</strong>ta<strong>in</strong>ed<br />

without progressive <strong>in</strong>creases <strong>in</strong> blood lactate concentration over time.<br />

Thus, the <strong>in</strong>terchangeable use of these parameters seems to be unreliable.<br />

However, further research about physiological contextualization of the<br />

mechanical power output at Fcrit <strong>and</strong> at MLSS must take <strong>in</strong>to account<br />

the technical ability of mov<strong>in</strong>g forward. This would improve the usefulness<br />

of data when assess<strong>in</strong>g exercise tolerance, assist<strong>in</strong>g <strong>in</strong> plann<strong>in</strong>g<br />

programme <strong>and</strong> predict<strong>in</strong>g performance <strong>in</strong> swimm<strong>in</strong>g.<br />

reFerences<br />

Beneke R., Leithäuser R.M., & Hütler M. (2001). Dependence of the<br />

maximal lactate steady-state on the motor pattern of exercise. Brit J<br />

Sports Med, 35, 192-196.<br />

Dekerle J., Baron B., Dupont L., Vanvelcenaher J., & Pelayo P. (2003).<br />

Maximal lactate steady state, respiratory compensation threshold <strong>and</strong><br />

critical power. Eur J Appl Physiol, 89, 281–288.<br />

Dekerle J., Pelayo P., Clipet B., Depretz G., Lefevre T., & Sidney M.<br />

(2005). Critical swimm<strong>in</strong>g speed does not represent the speed at<br />

maximal lactate steady-state. Int J Sport Med, 26, 524–530.<br />

Dekerle J., Brickley G., Alberty M., & Pelayo P. (2009). Character<strong>in</strong>z<strong>in</strong>g<br />

the slope of the distance-time relationship <strong>in</strong> swimm<strong>in</strong>g. J Sci Med<br />

Sport, doi: 10.1016/j.jsams.2009.05.007.<br />

deGroot G., & Ingen Schenau G.V. (1988). Fundamentals mechanics<br />

applied to swimm<strong>in</strong>g: technique <strong>and</strong> propell<strong>in</strong>g efficiency. In: Ungerechts<br />

B.E., Wilke K., & Reischle K. (ed) Swimm<strong>in</strong>g Science V, vol.<br />

18 (pp: 17-30).<br />

Ikuta Y., Wakayoshi K., & Nomura T. (1996). Determ<strong>in</strong>ations <strong>and</strong> validity<br />

of critical swimm<strong>in</strong>g force as performance <strong>in</strong>dex <strong>in</strong> tethered<br />

swimm<strong>in</strong>g. In: Troup J.P., Holl<strong>and</strong>er A.P., Strasse D., Trappe S.W.,<br />

Cappaert J.M., & Trappe T.A. (ed) <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g VII, (pp: 146-151), E & FN SPON, London.<br />

Johnson R.E., Sharp R.L., & Hedrick C.E. (1993). Relationship of<br />

chaPter2.<strong>Biomechanics</strong><br />

swimm<strong>in</strong>g power <strong>and</strong> dryl<strong>and</strong> power to spr<strong>in</strong>t freestyle performance:<br />

a multiple regression approach. J Swim Res, 09, 10-14.<br />

Kjendlie P-L., & Thorsvald K. (2006). A tethered swimm<strong>in</strong>g power test<br />

is high reliable. In: Vilas-Boas J.P., Alves F., & Marques A. (ed). <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X. Rev Port Ciên Desp, 6(2),<br />

231-235.<br />

Pr<strong>in</strong>gle J.S. & Jones A.M. (2002). Maximal lactate steady state, critical<br />

power <strong>and</strong> EMG dur<strong>in</strong>g cycl<strong>in</strong>g. EurJ Appl Physiol, 88, 214–226.<br />

Rouard A.H., Aujouannet Y.A., H<strong>in</strong>tz F., & Bonifazi M. (2006). Isometric<br />

force, tethered force <strong>and</strong> power ratios as tools for the evaluation<br />

of technical ability <strong>in</strong> freestyle swimm<strong>in</strong>g. In: Vilas-Boas J.P.,<br />

Alves F., & Marques A. (ed) <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g<br />

X. Rev Port Ciên Desp, 6(2), 249-250.<br />

Swa<strong>in</strong>e I.L. (1994). The relationship between physiological variables<br />

from a swim bench ramp test <strong>and</strong> midlle-distance swimm<strong>in</strong>g performance.<br />

J Swim Res, 10, 41-48.<br />

Swa<strong>in</strong>e I.L. (1996). The relationship between 1500 m swimm<strong>in</strong>g performance<br />

<strong>and</strong> critical Power us<strong>in</strong>g an isok<strong>in</strong>etic swim bench. In:<br />

Troup J.P., Holl<strong>and</strong>er A.P., Strasse D., Trappe S.W., Cappaert J.M.,<br />

& Trappe T.A. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VII, (pp: 229-<br />

233), E & FN SPON, London.<br />

Takahashi S., Wakayoshi K., Hayashi A., Sakaguchi Y., & Kitagawa K.<br />

(2009). A method for determ<strong>in</strong><strong>in</strong>g critical swimm<strong>in</strong>g velocity. International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 30, 119–123.<br />

Toussa<strong>in</strong>t H.M., Wakayoshi K., Holl<strong>and</strong>er A.P., & Ogita F. (1998).<br />

Simulated front crawl swimm<strong>in</strong>g performance related to critical<br />

speed <strong>and</strong> critical power. Med Sci Sports Exerc, 30(1), 144-151.<br />

AcKnoWledGeMents<br />

The authors wish to tank the subjects who agreed to participate <strong>in</strong> the<br />

study, <strong>and</strong> FUNDUNESP (00155-09/DFP) for the fund<strong>in</strong>g support.<br />

153


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Prelim<strong>in</strong>ary Results of a “Multi-2D” K<strong>in</strong>ematic<br />

Analysis of “Straight- vs. Bent-arm” Freestyle<br />

Swimm<strong>in</strong>g, Us<strong>in</strong>g High-Speed Videography.<br />

Pr<strong>in</strong>s, J.h., Murata, n.M., & Allen, J. s. III.<br />

University of Hawaii. U.S.A.<br />

Synchronized, high-speed digital cameras were used for underwater<br />

videotap<strong>in</strong>g of swimmers, each of whom were required to perform a<br />

series of trials with both bent-arm <strong>and</strong> straight-arm pull patterns. The<br />

result<strong>in</strong>g video footage was digitized <strong>and</strong> processed us<strong>in</strong>g “Multi 2-D”<br />

motion capture software. Results demonstrated (1.) The advantages of<br />

us<strong>in</strong>g high-speed videography for quantify<strong>in</strong>g swimm<strong>in</strong>g stroke mechanics.<br />

(2) The result<strong>in</strong>g data provided <strong>in</strong>sight <strong>in</strong>to the relationship<br />

between the vary<strong>in</strong>g degrees of elbow-bend dur<strong>in</strong>g the pull cycle, <strong>and</strong><br />

fluctuations <strong>in</strong> l<strong>in</strong>ear hip <strong>and</strong> wrist velocities.<br />

Key words: Freestyle stroke mechanics; high-speed videography;<br />

motion analysis;.<br />

IntroductIon<br />

The accessibility of high-speed digital cameras, coupled with the ability<br />

to synchronize the video output from multiple cameras, has made it<br />

possible to analyze swimmers <strong>in</strong> more detail. Motion analysis software<br />

makes possible the k<strong>in</strong>ematic analysis of the result<strong>in</strong>g video footage.<br />

One area of <strong>in</strong>terest is the perceived outcomes between a “bent-arm” vs.<br />

“straight-arm” underwater pull <strong>in</strong> Freestyle (Front-Crawl) swimm<strong>in</strong>g.<br />

Follow<strong>in</strong>g the success of a select number of Olympic f<strong>in</strong>alists who have<br />

used a straight-arm Freestyle arm recovery, there is now a question of<br />

whether a straight-arm recovery, coupled with a similarly straight-arm<br />

underwater pull leads to the generation of <strong>in</strong>creased propulsive forces.<br />

The purpose of this paper is to describe the prelim<strong>in</strong>ary results of a k<strong>in</strong>ematic<br />

analysis of the straight-arm vs. bent-arm underwater pull, us<strong>in</strong>g<br />

selected variables of these two types of pull patterns.<br />

Methods<br />

Four members (age= 19.4 +/- 0.8 yr; height 183 cms +/- 6.2 cms) of the<br />

Men’s University of Hawaii “Division I” Intercollegiate swimm<strong>in</strong>g team<br />

participated <strong>in</strong> this pilot study. Each swimmer was filmed for a total of<br />

6 trials, dur<strong>in</strong>g 3 of which they were <strong>in</strong>structed to ma<strong>in</strong>ta<strong>in</strong> their natural<br />

bent elbow position (B.A.), followed by 3 trials us<strong>in</strong>g a straight-arm<br />

(S.A.) underwater pull. Subjects were asked to swim at a pace as close<br />

as possible to their best 200 meter swimm<strong>in</strong>g time.<br />

Two high-speed digital cameras (Basler Model A602f ), <strong>in</strong>stalled <strong>in</strong><br />

custom hous<strong>in</strong>gs, were mounted to rigid frames which themselves were<br />

anchored to the pool deck. The cameras were placed at a depth of 0.3<br />

meters, each at right angles to each other for frontal <strong>and</strong> lateral view<strong>in</strong>g.<br />

The cameras were controlled via dual cabl<strong>in</strong>g from a desktop<br />

computer located on the pool deck. One cable was assigned for<br />

camera control via Firewire (IEEE 1394), the second cable was<br />

used for camera frame synchronization. Frame rate was set at 100<br />

frames/second.<br />

Rotational jo<strong>in</strong>t segments were identified us<strong>in</strong>g a series of light<br />

emitt<strong>in</strong>g diodes (LED’s) housed <strong>in</strong> waterproof hous<strong>in</strong>gs. The LED’s<br />

were taped to the body <strong>and</strong> were powered by a battery pack attached to a<br />

belt worn by the swimmer at the waist. Calibration was conducted us<strong>in</strong>g<br />

a 4-po<strong>in</strong>t frame (1m x 1m), located <strong>in</strong> the plane of motion.<br />

Motion analysis software (Vicon Motus, Denver, CO), was used for<br />

video capture, data analysis, <strong>and</strong> generat<strong>in</strong>g reports. The software <strong>in</strong>cludes<br />

a “Multi 2-D” (M2-D) feature, which enables multiple cameras<br />

to be synchronized. Each sequence was digitized us<strong>in</strong>g a comb<strong>in</strong>ation<br />

of auto-track<strong>in</strong>g <strong>and</strong> manual modes.<br />

154<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b<br />

Rotational jo<strong>in</strong>t segments were identified us<strong>in</strong>g a series of light emitt<strong>in</strong>g diodes<br />

(LED’s) housed <strong>in</strong> waterproof hous<strong>in</strong>gs. The LED’s were taped to the body <strong>and</strong> were<br />

powered by a battery pack attached to a belt worn by the swimmer at the waist.<br />

Calibration was conducted us<strong>in</strong>g a 4-po<strong>in</strong>t frame (1m x 1m), located <strong>in</strong> the plane of<br />

results<br />

motion.<br />

Motion analysis software (Vicon Motus, Denver, CO), was used for video capture,<br />

Follow<strong>in</strong>g data analysis, video <strong>and</strong> generat<strong>in</strong>g capture reports. <strong>and</strong> digitiz<strong>in</strong>g, The software the <strong>in</strong>cludes follow<strong>in</strong>g a “Multi variables 2-D” (M2-D) were<br />

measured feature, which us<strong>in</strong>g enables the Motus multiple cameras software: to be (1) synchronized. Degree of Each elbow-bend; sequence was (2)<br />

digitized us<strong>in</strong>g a comb<strong>in</strong>ation of auto-track<strong>in</strong>g <strong>and</strong> manual modes.<br />

L<strong>in</strong>ear velocities of the hip <strong>in</strong> the saggital plane (X –axis); (3) L<strong>in</strong>ear<br />

velocities RESULTS: of the wrist <strong>in</strong> the saggital (X), Vertical (Y), & the Resultant<br />

Follow<strong>in</strong>g video capture <strong>and</strong> digitiz<strong>in</strong>g, the follow<strong>in</strong>g variables were measured us<strong>in</strong>g<br />

(R), the directions; Motus software: (4) (1) Angular Degree of velocities elbow-bend; of the (2) L<strong>in</strong>ear wrist velocities as measured of the hip from <strong>in</strong> the the<br />

shoulder. saggital plane A composite (X –axis); (3) of L<strong>in</strong>ear the data velocities is presented of the wrist <strong>in</strong> Table the saggital 1. (X), Vertical<br />

(Y), & the Resultant (R), directions; (4) Angular velocities of the wrist as measured<br />

from the shoulder. A composite of the data is presented <strong>in</strong> Table 1.<br />

Table 1. Data shows Degree of Elbow Bend, L<strong>in</strong>ear Hip <strong>and</strong> Wrist Ve-<br />

Table 1. Data shows Degree of Elbow Bend, L<strong>in</strong>ear Hip <strong>and</strong> Wrist Velocities &<br />

locities & Angular Wrist Velocities as a function of Elbow Positions.<br />

Angular Wrist Velocities as a function of Elbow Position.<br />

Degree of<br />

Elbow Bend<br />

Hip – L<strong>in</strong>ear<br />

Velocity (LHV)<br />

Wrist - L<strong>in</strong>ear<br />

Velocities<br />

103<br />

Wrist - Angular<br />

Velocities<br />

(degrees/sec)<br />

301.9 to 398.3<br />

(degrees) - X-axis (m/sec) (LWV) - (m/sec)<br />

Natural Bent- Range 121 to 1.41 to 1.92 X – 1.41 to 2.31<br />

Arm Pull 134<br />

Y – 1.36 to 2.72<br />

R - 1.70 to 2.73<br />

Straight-Arm Range 160 to 1.52 to 2.02 X – 1.78 to 2.52 123.7 to 186.4<br />

Pull<br />

178<br />

Y – 1.36 to 2.52<br />

R - 1.70 to 2.53<br />

DISCUSSION:<br />

The study focused on two areas of <strong>in</strong>terest: First, was the adoption of high-speed video<br />

technology coupled with motion analysis software to capture <strong>and</strong> analyze the<br />

underwater pull patterns of swimmers. The second area of <strong>in</strong>terest was the possible<br />

<strong>in</strong>teraction between the degree of elbow bend dur<strong>in</strong>g the underwater pull, <strong>and</strong> l<strong>in</strong>ear<br />

changes <strong>in</strong> wrist <strong>and</strong> hip velocities <strong>in</strong> the primary plane of motion.<br />

The decision to use the “Multi 2-D” (M2-D) feature <strong>in</strong>corporated <strong>in</strong>to the software<br />

was made because it provided a means of monitor<strong>in</strong>g selected k<strong>in</strong>ematic parameters,<br />

specifically the potential changes <strong>in</strong> hip velocity as a function of underwater elbow<br />

flexion. In spite of the <strong>in</strong>herent limitations of 2D vs. 3D analyses, the M2-D feature<br />

was designed with gait analysis <strong>in</strong> m<strong>in</strong>d, i.e. plac<strong>in</strong>g the cameras at right angles to each<br />

other, mak<strong>in</strong>g it ideally suited for observ<strong>in</strong>g swimm<strong>in</strong>g stroke mechanics. The second<br />

<strong>in</strong>novation, i.e. design<strong>in</strong>g <strong>and</strong> implement<strong>in</strong>g a system of waterproof LED’s that were<br />

taped to the swimmer’s jo<strong>in</strong>t segments, proved <strong>in</strong>valuable for digitiz<strong>in</strong>g the result<strong>in</strong>g<br />

footage.<br />

With respect to the ability to film at higher frame rates, the results were<br />

immediately apparent. Past experience us<strong>in</strong>g cameras that were limited to st<strong>and</strong>ard<br />

frame rates (30 fps or 60 fields/sec) consistently produced blurr<strong>in</strong>g of the h<strong>and</strong>s,<br />

particularly at the end of the pull, the phase referred to as the “follow-through”. As<br />

dIscussIon<br />

The study focused on two areas of <strong>in</strong>terest: First, was the adoption of<br />

high-speed video technology coupled with motion analysis software to<br />

capture <strong>and</strong> analyze the underwater pull patterns of swimmers. The<br />

second area of <strong>in</strong>terest was the possible <strong>in</strong>teraction between the degree<br />

of elbow bend dur<strong>in</strong>g the underwater pull, <strong>and</strong> l<strong>in</strong>ear changes <strong>in</strong> wrist<br />

<strong>and</strong> hip velocities <strong>in</strong> the primary plane of motion.<br />

The decision to use the “Multi 2-D” (M2-D) feature <strong>in</strong>corporated<br />

<strong>in</strong>to the software was made because it provided a means of monitor<strong>in</strong>g<br />

selected k<strong>in</strong>ematic parameters, specifically the potential changes <strong>in</strong> hip<br />

velocity as a function of underwater elbow flexion. In spite of the <strong>in</strong>herent<br />

limitations of 2D vs. 3D analyses, the M2-D feature was designed<br />

with gait analysis <strong>in</strong> m<strong>in</strong>d, i.e. plac<strong>in</strong>g the cameras at right angles to each<br />

other, mak<strong>in</strong>g it ideally suited for observ<strong>in</strong>g swimm<strong>in</strong>g stroke mechanics.<br />

The second <strong>in</strong>novation, i.e. design<strong>in</strong>g <strong>and</strong> implement<strong>in</strong>g a system<br />

of waterproof LED’s that were taped to the swimmer’s jo<strong>in</strong>t segments,<br />

proved <strong>in</strong>valuable for digitiz<strong>in</strong>g the result<strong>in</strong>g footage.<br />

With respect to the ability to film at higher frame rates, the results<br />

were immediately apparent. Past experience us<strong>in</strong>g cameras that were<br />

limited to st<strong>and</strong>ard frame rates (30 fps or 60 fields/sec) consistently produced<br />

blurr<strong>in</strong>g of the h<strong>and</strong>s, particularly at the end of the pull, the phase<br />

referred to as the “follow-through”. As anticipated, these distortions are<br />

amplified with the caliber of swimmer be<strong>in</strong>g filmed. By <strong>in</strong>creas<strong>in</strong>g the<br />

frame-rate to 100 fps, there was a significant change <strong>in</strong> the image quality,<br />

which allowed the automatic digitiz<strong>in</strong>g feature <strong>in</strong>corporated <strong>in</strong> the<br />

software to work function effectively.<br />

After the result<strong>in</strong>g data was filtered <strong>and</strong> processed, two primary observations<br />

emerged. The major observation was the manner <strong>in</strong> which the<br />

l<strong>in</strong>ear hip velocity (LHV) changed over the duration of the underwater<br />

pull cycle. Figure 1 is a sample report that comb<strong>in</strong>es the lateral synchronized<br />

video frame with two graphs that plot LHV <strong>and</strong> LWV <strong>in</strong> the plane<br />

of motion as a function of “time. “ The vertical l<strong>in</strong>e <strong>in</strong> the two graphs is<br />

a feature of the software, which allows the synchronization of each video<br />

frame with the respective time <strong>in</strong>tervals on the selected graphs.<br />

Figure 1. Synchronized video frame comb<strong>in</strong>ed with l<strong>in</strong>ear variations <strong>in</strong><br />

“hip & wrist velocity”, each plotted as a function of “time”.


Independent of whether they were swimm<strong>in</strong>g with “bent” or “straight”<br />

arms, “peak“ LHV for all 4 swimmers, occurred approximately midway<br />

through the stroke, i.e. when the h<strong>and</strong>s were pass<strong>in</strong>g underneath the<br />

vertical l<strong>in</strong>e of the shoulder. When the l<strong>in</strong>ear wrist velocity (LWV) was<br />

comb<strong>in</strong>ed with this data it was evident that peak LWV slightly preceded<br />

“peak” LHV.<br />

The second observation was the relatively smaller difference between<br />

the degrees of elbow-bend when the subjects were asked to swim with<br />

“normal strokes”, as compared to consciously pull<strong>in</strong>g with “straightarms”.<br />

Tradition has dictated that we recommend maximum elbowbend<br />

close to 90 degrees, when the h<strong>and</strong>s pass vertically below the l<strong>in</strong>e<br />

of the shoulders. However, the subjects <strong>in</strong> the study held their arms<br />

at a more obtuse angle, the measured range for these 4 subjects be<strong>in</strong>g<br />

between 121 <strong>and</strong> 134 degrees. Determ<strong>in</strong><strong>in</strong>g whether these elbow positions<br />

are co<strong>in</strong>cidental, or a trend, will have to wait for an <strong>in</strong>crease <strong>in</strong><br />

subject number as the study is cont<strong>in</strong>ued.<br />

conclusIon<br />

Given the chronological constra<strong>in</strong>ts for manuscript submittal, <strong>and</strong> the<br />

time needed for familiarization of the equipment described <strong>in</strong> the study,<br />

this manuscript should be treated as an <strong>in</strong>troduction <strong>in</strong>to the utilization<br />

of improved technology for study<strong>in</strong>g swimm<strong>in</strong>g stroke mechanics.<br />

Although the small subject number produced no measurable differences,<br />

either with<strong>in</strong> or between subjects, when swimm<strong>in</strong>g with either BA <strong>and</strong><br />

SA positions, what was <strong>in</strong>trigu<strong>in</strong>g was the consistent positions of the<br />

h<strong>and</strong>, dur<strong>in</strong>g the underwater pull cycle, where maximum hip velocity<br />

was produced. In time, by <strong>in</strong>creas<strong>in</strong>g the number of subjects <strong>and</strong> ref<strong>in</strong><strong>in</strong>g<br />

the test<strong>in</strong>g protocols, the expectation is that we will cont<strong>in</strong>ue to open<br />

new avenues of research <strong>in</strong> swimm<strong>in</strong>g biomechanics.<br />

reFerences<br />

Cappaert JM, Pease DL, Troup JP (1995). Three-dimensional<br />

analysis of the men’s 100m freestyle dur<strong>in</strong>g the 1992 Olympic<br />

games. J Appl Biomech. 11(1): 103-112.<br />

Kikodelis, T., Kolllia I., <strong>and</strong> Hatzitaki, V (2005). Bilateral <strong>in</strong>terarm<br />

coord<strong>in</strong>ation <strong>in</strong> freestyle swimm<strong>in</strong>g: effect of skill level<br />

<strong>and</strong> swimm<strong>in</strong>g speed. J. Sports Sci. 23(7):737-45.<br />

Maglischo EW (2003). Swimm<strong>in</strong>g fastest. Champaign, ILL:<br />

Human K<strong>in</strong>etics<br />

Psycharakis, SG <strong>and</strong> RH S<strong>and</strong>ers (2008). Shoulder <strong>and</strong> hip roll<br />

changes dur<strong>in</strong>g 200-m front crawl swimm<strong>in</strong>g. Me.Sci.Sports<br />

Exerc. 40(12):2129-2136.<br />

Seifert, L, Chollet, D., Bardy, B.G. (2004). Effect of swimm<strong>in</strong>g<br />

velocity on arm coord<strong>in</strong>ation <strong>in</strong> the front crawl: a dynamic<br />

analysis. Journal of Sports Sciences, 22, 651–660.<br />

chaPter2.<strong>Biomechanics</strong><br />

Biomechanical Factors Influenc<strong>in</strong>g Tumble Turn<br />

Performance of Elite Female Swimmers<br />

Puel, F. 1 , Morlier, J. 1 , cid, M. 1 , chollet, d. 2 , hellard, P. 3<br />

1Laboratoire de Mécanique Physique, CNRS UMR 5469, Université Bordeaux<br />

1, France<br />

2Centre d’Étude des Transformations des Activités Physiques et Sportives,<br />

EA 3832, Faculté des Sciences du Sport et de l’Éducation Physique, Université<br />

de Rouen, France<br />

3Département d’Études et Recherches, Fédération Française de Natation,<br />

Paris, France<br />

The aim of this study was to exam<strong>in</strong>e the effects of k<strong>in</strong>ematic <strong>and</strong> dynamic<br />

parameters on the turn performance (3mRTT). Eight elite female<br />

swimmers were analysed dur<strong>in</strong>g a crawl tumble turn at maximum<br />

speed. The movements were filmed us<strong>in</strong>g 5 underwater cameras <strong>and</strong> a<br />

3D force platform recorded wall forces. Results showed that the time of<br />

maximum horizontal force <strong>and</strong> the glide duration were related to the<br />

performance criterion. The best female swimmers were able to develop<br />

maximal horizontal force earlier dur<strong>in</strong>g the push-off phase. Further<br />

studies with an extended population (elite male <strong>and</strong> less-skilled female<br />

swimmers) would analyse the effects of more parameters, especially<br />

from the contact phase.<br />

Key words: swimm<strong>in</strong>g, K<strong>in</strong>ematics, dynamics, turn, Performance<br />

IntroductIon<br />

In elite swimmers, only few opportunities are available to improve performance.<br />

Swimm<strong>in</strong>g performance can be def<strong>in</strong>ed as the time taken to<br />

complete a race. It can be subdivided <strong>in</strong>to start<strong>in</strong>g, strok<strong>in</strong>g <strong>and</strong> turn<strong>in</strong>g.<br />

Turns represent a paramount factor for determ<strong>in</strong><strong>in</strong>g the f<strong>in</strong>al performance<br />

of a swimm<strong>in</strong>g race. Blanksby et al. (1996) <strong>and</strong> Cossor et al.<br />

(1999) reported significant correlations with 50 m freestyle times <strong>and</strong><br />

both 2.5 m (r = 0.72 to 0.85) <strong>and</strong> 5 m (r = 0.90 to 0.97) round trip<br />

times (RTT). In addition, Blanksby et al. (1996) found that the fastest<br />

<strong>and</strong> slowest young freestyle swimmers differed significantly between the<br />

50 m time <strong>and</strong> these two measures of turn<strong>in</strong>g performance (2.5m <strong>and</strong><br />

5m RTT). Chow et al. (1984) found that the correlation between the<br />

total turn time <strong>and</strong> the event time <strong>in</strong>creased with the distance of the<br />

event. It is noticeable too that turn<strong>in</strong>g is faster than strok<strong>in</strong>g (Blanksby<br />

et al., 1996 <strong>and</strong> 2004).<br />

A successful swim turn results from a multitude of factors <strong>and</strong> requires<br />

a complex series of moves to optimise the total turn<strong>in</strong>g performance.<br />

The freestyle tumble turn can be divided <strong>in</strong> the approach, rotation,<br />

wall contact, glide, underwater propulsion, <strong>and</strong> stroke resumption<br />

phases. For the contact phase, Pr<strong>in</strong>s <strong>and</strong> Patz (2006) dist<strong>in</strong>guished passive<br />

(“brak<strong>in</strong>g”) <strong>and</strong> active (“push-off ”) sub-phases. Lyttle et al. (2000)<br />

studied glid<strong>in</strong>g position <strong>and</strong> kick<strong>in</strong>g technique <strong>and</strong> established an optimal<br />

range of speeds (1.9 to 2.2 m/s) at which to beg<strong>in</strong> underwater<br />

propulsion <strong>in</strong> order to prevent energy loss from excessive active drag.<br />

The first aim of this study was to analyse relations with both k<strong>in</strong>ematic<br />

<strong>and</strong> dynamic factors from each phase <strong>and</strong> the 3 m round trip time<br />

(3mRTT) as measure of turn<strong>in</strong>g performance. The second aim was to<br />

develop a model for performance us<strong>in</strong>g a stepwise multiple regression.<br />

Methods<br />

Eight elite female swimmers participated <strong>in</strong> this study (Table 1).<br />

155


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 1. Swimmer’s general characteristics (n = 8, SD: st<strong>and</strong>ard deviation,<br />

WR: world record, PB: personal best).<br />

Age (years)<br />

200 m freestyle<br />

Body mass (kg) Height (cm)<br />

WR / PB (%)<br />

Mean 22.3 62.2 174.7 96.73<br />

SD 4.1 6.2 5.8 2.25<br />

The swimmers were analysed dur<strong>in</strong>g a crawl tumble turn at maximum<br />

speed, when pass<strong>in</strong>g through a specific pre-calibrated space with mean<br />

dimensions of 4.2 x 1.1 x 1.9 m for the horizontal (ma<strong>in</strong> movement<br />

direction), vertical (pool depth) <strong>and</strong> lateral (lane width) directions, respectively<br />

placed <strong>in</strong> contact with the turn<strong>in</strong>g wall <strong>and</strong> the water surface.<br />

Five stationary m<strong>in</strong>i-DV video cameras (Sony DCR-HC62E <strong>and</strong><br />

DCR-HC96E) were located underwater at different depths <strong>in</strong> waterproof<br />

cases. The angle between axes of adjacent cameras was approximately<br />

45° <strong>and</strong> the five cameras were located on a semi-ellipse centred<br />

on the turn<strong>in</strong>g wall. Twelve to 14 calibration po<strong>in</strong>ts were used, <strong>and</strong> the<br />

synchronization of the images was obta<strong>in</strong>ed us<strong>in</strong>g an underwater strobe<br />

flash (Epoque ES-150 DS α) visible <strong>in</strong> the field of each video camera.<br />

An underwater piezoelectric 3D force platform (Kistler 9253B12) was<br />

also mounted on the turn<strong>in</strong>g wall record<strong>in</strong>g at a frequency of 2000 Hz.<br />

One complete turn was analysed for each swimmer. The test<strong>in</strong>g session<br />

took place <strong>in</strong> a 50 m <strong>in</strong>door pool.<br />

The anatomical reference po<strong>in</strong>ts of <strong>in</strong>terest were digitized manually,<br />

frame by frame (at a frequency of 50 Hz). The po<strong>in</strong>ts digitized for each<br />

camera were: centre of the skull (head), shoulders, elbows, wrists, f<strong>in</strong>gertips,<br />

hips, knees, ankles <strong>and</strong> tiptoes. Image coord<strong>in</strong>ates were transformed<br />

to 3D object-space coord<strong>in</strong>ates us<strong>in</strong>g the Direct L<strong>in</strong>ear Transformation<br />

algorithm (Abdel-Aziz & Karara, 1971). Reconstruction precision of<br />

calibration po<strong>in</strong>ts was 14.1 ± 9.1 mm with a maximal error of 42.8 mm.<br />

Miss<strong>in</strong>g coord<strong>in</strong>ates were <strong>in</strong>terpolated by a cubic spl<strong>in</strong>e function <strong>and</strong><br />

then smoothed by the Savitzky-Golay filter<strong>in</strong>g method (<strong>in</strong>terpolation<br />

order: 2, w<strong>in</strong>dow size: 13).<br />

The k<strong>in</strong>ematic data were the horizontal velocity of the head at the<br />

beg<strong>in</strong>n<strong>in</strong>g of the turn (when the head was 3 m before the wall, VIn <strong>in</strong><br />

m/s), 1 m before the rotation phase (V1mR <strong>in</strong> m/s), at the beg<strong>in</strong>n<strong>in</strong>g<br />

of the rotation phase (VR <strong>in</strong> m/s), at the maximum horizontal force<br />

peak (VPe <strong>in</strong> m/s), at the end of the push-off (VG <strong>in</strong> m/s), at the end<br />

of the glide (VU <strong>in</strong> m/s) <strong>and</strong> at the end of the turn (when the head<br />

was 3 m after the wall, VOut <strong>in</strong> m/s). The delimitation between the<br />

approach <strong>and</strong> the rotation phase was determ<strong>in</strong>ed when the swimmer<br />

<strong>in</strong>creased her head depth (vertical displacement). The horizontal position<br />

of the head when rotation began was also computed (RD <strong>in</strong> m).<br />

The end of the push-off (synchronisation po<strong>in</strong>t with dynamic data) <strong>and</strong><br />

the delimitation between the glide <strong>and</strong> the underwater propulsive phase<br />

was obta<strong>in</strong>ed by observ<strong>in</strong>g video data. This time ended the glide duration<br />

(GT <strong>in</strong> s).<br />

The dynamic data recorded were: maximum horizontal force peak<br />

(Pe <strong>in</strong> N) <strong>and</strong> f<strong>in</strong>al contact time (synchronisation po<strong>in</strong>t with k<strong>in</strong>ematic<br />

data). Vertical <strong>and</strong> lateral forces helped to discern the first contact time<br />

<strong>and</strong> the delimitation between the brak<strong>in</strong>g <strong>and</strong> the push-off phases. PeT<br />

(<strong>in</strong> s) was the time between the beg<strong>in</strong>n<strong>in</strong>g of the push-off <strong>and</strong> the maximum<br />

horizontal force peak. %PeT (<strong>in</strong> %) was the ratio between PeT <strong>and</strong><br />

the push-off duration (PoT <strong>in</strong> s).<br />

Pearson correlation <strong>and</strong> l<strong>in</strong>ear regression tests were used to identify<br />

the relationships among the tumble turn performance criterion<br />

(3mRTT as the time taken to swim from 3 m <strong>in</strong> to 3 m out the turn<strong>in</strong>g<br />

wall, <strong>in</strong> s) <strong>and</strong> both k<strong>in</strong>ematic <strong>and</strong> dynamic factors. The level of significance<br />

was set at 95 % (p


conclusIon<br />

The purpose of this study was to exam<strong>in</strong>e the effects of k<strong>in</strong>ematic <strong>and</strong><br />

dynamic parameters on the crawl tumble turn performance. Results<br />

showed that the time of maximum horizontal force is preponderant.<br />

The glide phase is also critical. In the future, it would be <strong>in</strong>terest<strong>in</strong>g<br />

to analyse the effects of more computed parameters, especially dur<strong>in</strong>g<br />

the contact phase (e.g. impulses <strong>and</strong> push-off angles) <strong>and</strong> to extend the<br />

population (recreational female swimmers <strong>and</strong> elite male swimmers).<br />

More subjects with the same protocol may help to provide a deeper<br />

underst<strong>and</strong><strong>in</strong>g of turn<strong>in</strong>g performance <strong>and</strong> develop a new hypothesis<br />

about the swimm<strong>in</strong>g level (which could affect the ability) or the gender<br />

(which could have an effect upon physical factors).<br />

reFerences<br />

Abdel-Aziz Y., & Karara H. (1971). Direct l<strong>in</strong>ear transformation from<br />

comparator coord<strong>in</strong>ates <strong>in</strong>to object space coord<strong>in</strong>ates <strong>in</strong> close-range<br />

photogrammetry. Proceed<strong>in</strong>gs of the Symposium on Close-Range photogrammetry,<br />

1-18.<br />

Blanksby B., Gathercole D., & Marshall R. (1996). Force plate <strong>and</strong><br />

video analysis of the tumble turn by age-group swimmers. Journal of<br />

Swimm<strong>in</strong>g Research, 11, 40-45.<br />

Blanksby B., Skender S., Elliott B., McElroy K., & L<strong>and</strong>ers G. (2004).<br />

An analysis of the rollover backstroke turn by age-group swimmers.<br />

Sports Biomech, 3(1), 1-14.<br />

Chow J., Hay J., Wilson B., & Imel C. (1984). Turn<strong>in</strong>g techniques of<br />

elite swimmers. Journal of Sports Sciences, 2(3), 241-255.<br />

Cossor J. M., Blanksby B. A., & Elliott B. C. (1999). The <strong>in</strong>fluence of<br />

plyometric tra<strong>in</strong><strong>in</strong>g on the freestyle tumble turn. J Sci Med Sport, 2(2),<br />

106-116.<br />

Klauck J. (2005). Push-off forces vs. k<strong>in</strong>ematics <strong>in</strong> swimm<strong>in</strong>g turns:<br />

model based estimates of time-dependent variables. Human Movement,<br />

6, 112-115.<br />

Lyttle A. D., Blanksby B. A., Elliott B. C., & Lloyd D. G. (2000). Net<br />

forces dur<strong>in</strong>g tethered simulation of underwater streaml<strong>in</strong>ed glid<strong>in</strong>g<br />

<strong>and</strong> kick<strong>in</strong>g techniques of the freestyle turn. J Sports Sci, 18(10), 801-<br />

807.<br />

Pr<strong>in</strong>s J. H., & Patz A. (2006). The <strong>in</strong>fluence of tuck <strong>in</strong>dex, depth of<br />

foot-plant, <strong>and</strong> wall contact time on the velocity of push-off <strong>in</strong> the<br />

freestyle flip turn. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X, 82-85.<br />

Takahashi G., Yoshida A., Tsubakimoto S., & Miyashita M. (1983).<br />

Propulsive force generated by swimmers dur<strong>in</strong>g a turn<strong>in</strong>g motion.<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, 192-198.<br />

AcKnoWledGMents<br />

The authors wish to thank Michel Knopp <strong>and</strong> Nicolas Houel from the<br />

French Swimm<strong>in</strong>g Federation (F.F.N.) for their contribution dur<strong>in</strong>g the<br />

data acquisition process.<br />

chaPter2.<strong>Biomechanics</strong><br />

Front Crawl <strong>and</strong> Backstroke Arm Coord<strong>in</strong>ation <strong>in</strong><br />

Swimmers with Down Syndrome<br />

Querido, A. 1 , Marques-Aleixo, I. 1 , Figueiredo, P. 1 , seifert, l.<br />

2 1 , chollet, d. 2, Vilas-Boas, J.P. 1, daly, d.J. 3, corredeira, r. ,<br />

Fern<strong>and</strong>es, r.J. 1<br />

1University of Porto, Faculty of Sport, Cifi2d, Portugal<br />

2University of Rouen, Faculty of Sport Sciences, France<br />

3Katholieke Universiteit Leuven, Faculty of K<strong>in</strong>esiology <strong>and</strong> Rehabilitation<br />

Sciences, Belgium<br />

The aim of this study was to characterize the Index of Arm Coord<strong>in</strong>ation<br />

(IdC) <strong>in</strong> swimmers with Down syndrome (DS). The IdC for the<br />

front crawl (N=6) was -11.3% ± 5.2% <strong>and</strong> for the backstroke -13.5 ±<br />

4.8%. This <strong>in</strong>dicates that all swimmers demonstrated a catch-up mode<br />

coord<strong>in</strong>ation <strong>in</strong> both strokes. Swimmers with DS did not adapt their<br />

arm coord<strong>in</strong>ation as usually occurs <strong>in</strong> swimmers with higher level of<br />

proficiency. In front crawl significant positive correlations were found<br />

between IdC <strong>and</strong> the push phase as well as the propulsive phase. An<br />

<strong>in</strong>verse correlation was found between IdC <strong>and</strong> the non-propulsive<br />

phase. In backstroke, the catch-up coord<strong>in</strong>ation mode was used by all<br />

swimmers. In this study h<strong>and</strong> lag time values far above those of elite<br />

swimmers were observed. There was an <strong>in</strong>verse relationship between<br />

IdC <strong>and</strong> velocity.<br />

Key words: down syndrome, arm coord<strong>in</strong>ation, front crawl, backstroke<br />

IntroductIon<br />

Although cyclic activities, such as swimm<strong>in</strong>g, have traditionally been<br />

assessed by velocity, stroke rate <strong>and</strong> stroke length, recent studies have<br />

shown that the evaluation of arm coord<strong>in</strong>ation provides new <strong>in</strong>formation<br />

to the classic analysis (Chollet et al., 2008). For assess<strong>in</strong>g arm coord<strong>in</strong>ation,<br />

Chollet et al. (2000) proposed the Index of Coord<strong>in</strong>ation<br />

(IdC), which seems to give relevant <strong>in</strong>formation on a swimmer’s skill. In<br />

the alternat<strong>in</strong>g strokes, i.e. front crawl <strong>and</strong> backstroke, arm coord<strong>in</strong>ation<br />

is quantified as the time between propulsive phases of the right <strong>and</strong> left<br />

arms, i.e., by the time lag between the propulsion moments of consecutive<br />

strokes. Accord<strong>in</strong>g to Chollet et al. (2000), three possible modes of<br />

coord<strong>in</strong>ation can be found: (i) catch-up, with significant discont<strong>in</strong>uity<br />

between propulsion moments of both arms (IdC < 0%); (ii) opposition,<br />

show<strong>in</strong>g cont<strong>in</strong>uity between propulsive phases of both arms (IdC = 0%)<br />

<strong>and</strong> (iii) superposition, <strong>in</strong> which overlapp<strong>in</strong>g of propulsive phases is seen<br />

(IdC > 0%).<br />

Studies focus<strong>in</strong>g specifically on swimmers with Down syndrome<br />

(DS) are very scarce. S<strong>in</strong>ce <strong>in</strong>dividuals with DS typically have a comb<strong>in</strong>ation<br />

of physical <strong>and</strong> cognitive limitations that significantly affect their<br />

motor performance <strong>and</strong> contribute to a high variability of their motor<br />

behavior (Epste<strong>in</strong>, 1989; Laht<strong>in</strong>en, 2007), it is important to underst<strong>and</strong><br />

if these typical characteristics, such as lower muscular strength, higher<br />

percentage of body fat <strong>and</strong> anthropometric traits are reflected <strong>in</strong> their<br />

<strong>in</strong>ter arm coord<strong>in</strong>ation. The purpose of this study was therefore to characterize<br />

the IdC <strong>in</strong> alternat<strong>in</strong>g strokes performed by swimmers with<br />

DS, as well as to establish the relative duration of the propulsive <strong>and</strong><br />

non-propulsive phases.<br />

Methods<br />

Six <strong>in</strong>ternational level swimmers with DS volunteered to participate <strong>in</strong><br />

this study (age: 20.2 ± 4.8 years, height: 154.3 ± 12.1 cm, weight: 58.4<br />

± 14.1 kg <strong>and</strong> fat mass: 16.4 ± 11.6 %). The participant’s guardians provided<br />

<strong>in</strong>formed written consent to take part <strong>in</strong> the study, which was<br />

approved by the local ethics committee.<br />

All swimmers performed 2 x 20 m swims at maximal <strong>in</strong>tensity, the<br />

157


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

first <strong>in</strong> front crawl (non breath<strong>in</strong>g cycles) <strong>and</strong> the second <strong>in</strong> backstroke.<br />

Two digital cameras (Sony ® DCR-HC42E), placed <strong>in</strong>side a sealed<br />

hous<strong>in</strong>g (SPK - HCB), recorded two complete underwater arm stroke<br />

cycles <strong>in</strong> the lateral <strong>and</strong> frontal views. The lateral camera was placed at a<br />

depth of 2 m <strong>and</strong> 11.5 m from the lane <strong>in</strong> which the participant swum.<br />

The frontal camera was placed at 0.5 m depth. A rigid calibration frame<br />

(2.10x0.70-m) was recorded at the beg<strong>in</strong>n<strong>in</strong>g of the trials for calibration<br />

purposes. Subsequently, each frame (50Hz) was digitized manually<br />

us<strong>in</strong>g the APASystem (Ariel Dynamics Inc., USA). N<strong>in</strong>e anatomical<br />

po<strong>in</strong>ts were used: the hip (femoral condyle), <strong>and</strong> on both sides of the<br />

body, the longest f<strong>in</strong>ger tips, wrist, elbow <strong>and</strong> shoulder of each swimmer.<br />

After bi-dimensional reconstruction us<strong>in</strong>g a DLT procedure (Abel-Aziz<br />

<strong>and</strong> Karara, 1978), a low pass filter of 5 Hz was used.<br />

The front crawl arm stroke was divided <strong>in</strong>to four phases (Chollet et<br />

al., 2000): (i) entry <strong>and</strong> catch (time between the entry of the h<strong>and</strong> <strong>in</strong>to<br />

the water <strong>and</strong> the beg<strong>in</strong>n<strong>in</strong>g of its backward movement); (ii) pull (time<br />

between the beg<strong>in</strong>n<strong>in</strong>g of the h<strong>and</strong>’s backward movement <strong>and</strong> when it<br />

reaches a vertical plane with the shoulder); (iii) push (time from the position<br />

of the h<strong>and</strong> below the shoulder to its release from the water) <strong>and</strong><br />

(iv) recovery (time from the po<strong>in</strong>t of water release to water re-entry of<br />

the arm, i.e., the above water phase). In backstroke, each arm stroke was<br />

divided <strong>in</strong>to 6 phases (Chollet et al, 2006): (i) entry <strong>and</strong> catch (time between<br />

the entry of the h<strong>and</strong> <strong>in</strong>to the water <strong>and</strong> the start of its backward<br />

movement that is followed by a diagonal h<strong>and</strong> sweep); (ii) pull (time<br />

between the beg<strong>in</strong>n<strong>in</strong>g of the h<strong>and</strong>’s backward movement <strong>and</strong> when the<br />

l<strong>in</strong>e shoulder-h<strong>and</strong> is at 90° to the truck); (iii) push (time from the po<strong>in</strong>t<br />

h<strong>and</strong> at shoulder level <strong>and</strong> the end of the h<strong>and</strong>’s backward movement);<br />

(iv) h<strong>and</strong> lag time (time dur<strong>in</strong>g which the h<strong>and</strong> stops at the thigh after<br />

the push phase <strong>and</strong> before start<strong>in</strong>g to move upward to clear the water);<br />

(v) clear<strong>in</strong>g (time from the beg<strong>in</strong>n<strong>in</strong>g of the h<strong>and</strong> release upward to the<br />

beg<strong>in</strong>n<strong>in</strong>g of its exit from the water) <strong>and</strong> (vi) recovery (time correspond<strong>in</strong>g<br />

to the po<strong>in</strong>t of water release to water re-entry of the arm).<br />

The duration of the propulsive phases of front crawl <strong>and</strong> backstroke<br />

was the sum of the pull <strong>and</strong> the push phases. The duration of the nonpropulsive<br />

phases was obta<strong>in</strong>ed by the sum of the catch <strong>and</strong> the recovery<br />

phases (for front crawl) <strong>and</strong> the addition of the catch, h<strong>and</strong> lag<br />

time, clear<strong>in</strong>g <strong>and</strong> recovery phases (for backstroke). The duration of a<br />

complete arm-stroke was the sum of the propulsive <strong>and</strong> non-propulsive<br />

phases. The IdC was considered as the time gap between the propulsion<br />

of the two arms <strong>and</strong> expressed as a percentage of the duration of the<br />

complete arm stroke cycle.<br />

Mean ± SD were calculated for all variables (all data were checked<br />

for distribution normality with the Shapiro-Wilk test). Pearson correlation<br />

coefficient was applied <strong>and</strong> the level of significance was established<br />

at 95% (p


arm coord<strong>in</strong>ation was observed exclusively. For the front crawl, the use<br />

of a catch-up coord<strong>in</strong>ation mode is usually considered by coaches <strong>and</strong><br />

<strong>in</strong>structors as a technical fault (Seifert <strong>and</strong> Chollet, 2008) <strong>and</strong> is observed<br />

<strong>in</strong> less skilled swimmers (Seifert et al., 2008). This coord<strong>in</strong>ation<br />

mode does seem to be efficient at slow paces, as it favors a glide phase<br />

follow<strong>in</strong>g propulsive actions (Seifert et al., 2004b). These authors found<br />

that when the velocity <strong>in</strong>creases above a critical value, a transition from<br />

catch-up to superposition mode is seen. In the present study swimmers<br />

performed a maximal <strong>in</strong>tensity protocol <strong>and</strong> the use of catch-up coord<strong>in</strong>ation<br />

appears to be <strong>in</strong>dicative of a less proficient technique. Interest<strong>in</strong>gly,<br />

Seifert et al. (2004a) showed that women have more negative IdC<br />

values than men due to their higher fat mass values, different fat mass<br />

distribution, lower arm strength, <strong>and</strong> as a result greater difficulty <strong>in</strong> overcom<strong>in</strong>g<br />

forward resistance. These are also characteristics of <strong>in</strong>dividuals<br />

with DS (Aleixo et al., 2009). Other physical characteristics, such as a<br />

smaller propulsive surface, also found <strong>in</strong> swimmers with loco-motor disabilities,<br />

can also <strong>in</strong>fluence their <strong>in</strong>ter-arm coord<strong>in</strong>ation (Satkunskiene<br />

et al., 2005). The direct relationship found between the IdC <strong>and</strong> the<br />

push phase <strong>and</strong> propulsive phases, also described <strong>in</strong> the literature on<br />

able bodied swimmers (Figueiredo et al., <strong>in</strong> press) emphasizes the importance<br />

of the propulsive phase duration <strong>in</strong> an arm stroke.<br />

In backstroke, the catch-up coord<strong>in</strong>ation mode is the only pattern<br />

of arm coord<strong>in</strong>ation used, with IdC values vary<strong>in</strong>g between -25% <strong>and</strong><br />

-5% (Seifert <strong>and</strong> Chollet, 2008). This fact seems to be due to the limited<br />

shoulder range of movement <strong>and</strong> to the alternat<strong>in</strong>g body-roll (Chollet<br />

et al., 2008), which impose a particular arm coord<strong>in</strong>ation <strong>and</strong> an additional<br />

stroke phase - clear<strong>in</strong>g phase (Lerda <strong>and</strong> Cardelli, 2003). This<br />

clear<strong>in</strong>g phase prevents cont<strong>in</strong>uity between the propulsive phases of the<br />

two arms. This is only found when a three-peak stroke pattern is used,<br />

creat<strong>in</strong>g some propulsion <strong>in</strong> the beg<strong>in</strong>n<strong>in</strong>g of the upsweep (Maglisho,<br />

2003). This three-peak stroke pattern was not seen <strong>in</strong> the present study.<br />

On the contrary, a h<strong>and</strong> lag time phase was found <strong>in</strong> all swimmers <strong>in</strong><br />

accordance with Chollet et al. (2006) <strong>and</strong> Chollet et al. (2008). These<br />

authors po<strong>in</strong>ted out that this arm phase can affect the arm coord<strong>in</strong>ation<br />

<strong>in</strong> backstroke, s<strong>in</strong>ce it leads to propulsive discont<strong>in</strong>uity, expla<strong>in</strong><strong>in</strong>g why<br />

elite swimmers limit their h<strong>and</strong> lag time to approximately 2% of the<br />

stroke cycle duration (a much lower value than found <strong>in</strong> the present<br />

study). The very existence of this phase is, however, controversial because<br />

some studies (e.g. Lerda <strong>and</strong> Cardelli, 2003; Lerda et al., 2005) did not<br />

report this.<br />

Although the participants <strong>in</strong> this study are <strong>in</strong>ternational level Down<br />

Syndrome swimmers, their arm coord<strong>in</strong>ation does not correspond to the<br />

values of typical elite swimmers without DS, suggest<strong>in</strong>g the presence<br />

of technical faults or physical shortcom<strong>in</strong>gs (e.g. higher h<strong>and</strong> lag time).<br />

The IdC values of the present swimmers are closer to those found by<br />

Cardelli (2003) for less expert swimmers (-11.3%) compared to more<br />

expert backstrokers (-9.7%). The <strong>in</strong>verse correlation between IdC <strong>and</strong><br />

velocity was also found by Chollet et al. (2008), corroborat<strong>in</strong>g the f<strong>in</strong>d<strong>in</strong>gs<br />

elsewhere of higher (less negative) IdC values at higher swimm<strong>in</strong>g<br />

velocities.<br />

conclusIon<br />

International level swimmers with DS presented a catch-up arm coord<strong>in</strong>ation<br />

mode <strong>in</strong> front crawl, which may be associated with less proficient<br />

arm coord<strong>in</strong>ation. Tra<strong>in</strong>ed swimmers usually change from catch-up to<br />

superposition with <strong>in</strong>creas<strong>in</strong>g velocities. The catch-up coord<strong>in</strong>ation mode<br />

was also found <strong>in</strong> all swimmers for the backstroke. This is <strong>in</strong> concordance<br />

with the literature on less skilled swimmers <strong>and</strong> for skilled swimmers at<br />

low velocities. The high values of h<strong>and</strong> lag time contributed to this.<br />

It can also be po<strong>in</strong>ted out that this <strong>in</strong>strument can be very helpful<br />

to coaches <strong>in</strong> better underst<strong>and</strong><strong>in</strong>g underwater stroke phases. These<br />

f<strong>in</strong>d<strong>in</strong>gs also emphasize the importance of augment<strong>in</strong>g the propulsive<br />

phases of the arms <strong>and</strong>, with this, dim<strong>in</strong>ish<strong>in</strong>g the lag time of the swimmers.<br />

Technical mistakes can also be detected through the study of the<br />

arm coord<strong>in</strong>ation.<br />

chaPter2.<strong>Biomechanics</strong><br />

reFerences<br />

Abdel-Aziz Y. I., & Karara H. M. (1971). Direct l<strong>in</strong>ear transformation<br />

from comparator coord<strong>in</strong>ates <strong>in</strong>to object space coord<strong>in</strong>ates <strong>in</strong> close<br />

range photogrammetry. American Society of Photogrammetry Symposium<br />

on Close Range Photogrammetry, 1-18. Falls Church: American<br />

Society of Photogrammetry.<br />

Aleixo I., Vale S., Figueiredo P., Silva A., Corredeira R., & Fern<strong>and</strong>es<br />

R. J. (2009). Comparison of body mass <strong>in</strong>dex between swimmers <strong>and</strong><br />

non tra<strong>in</strong>ed <strong>in</strong>dividuals with Down’s syndrome. J Sports Sci Med, 8<br />

(supp 11), 194-5.<br />

Chollet D., Carter M., & Seifert L. (2006). Effect of technical mistakes<br />

on arm coord<strong>in</strong>ation <strong>in</strong> backstroke. Port J Sport Sci, 6, 30-2.<br />

Chollet D., Chalies S., & Chatard J. C. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: description <strong>and</strong> usefulness. Int J Sports Med,<br />

21(1), 54-9.<br />

Chollet D., Seifert L., & Carter M. (2008). Arm coord<strong>in</strong>ation <strong>in</strong> elite<br />

backstroke swimmers. J Sports Sci, 26 (7), 675-82.<br />

Epste<strong>in</strong> C. J. (1989). Down syndrome (trisomy 21). In: CR Scriver, AL<br />

Beaudet, WS Sly, D Valle (eds.), The metabolic bases of <strong>in</strong>herited disease,<br />

6 th Edition. New-York, McGraw-Hill, Inc, 291-326.<br />

Figueiredo P., Vilas-Boas J. P., Seifert L., Chollet D., & Fern<strong>and</strong>es R.<br />

J. (<strong>in</strong> press). Inter-lim coord<strong>in</strong>ative structure <strong>in</strong> a 200 m front crawl<br />

event. Open Sports Sci J.<br />

Laht<strong>in</strong>en U. (2007). Physical performance of <strong>in</strong>dividuals with <strong>in</strong>tellectual<br />

disability: a 30-year follow-up. Adapt Phys Act Quart, 24 (2),<br />

125-43.<br />

Lerda R., & Cardelli C. (2003). Analysis of stroke organization <strong>in</strong> the<br />

backstroke as a function of skill. Res Quart Exerc Sport, 74, 215-19.<br />

Lerda R., Cardelli C., & Coudereau J. P. (2005). Backstroke organization<br />

<strong>in</strong> physical education students as a function of skill <strong>and</strong> sex.<br />

Percep Motor Skills, 100, 779-90.<br />

Maglischo E. W. (2003). Swimm<strong>in</strong>g fastest. Champaign, IL. Human<br />

K<strong>in</strong>etics.<br />

Satkunskiene D., Schega L., Kunze K., Birz<strong>in</strong>yte K., & Daly D. (2005).<br />

Coord<strong>in</strong>ation <strong>in</strong> arm movements dur<strong>in</strong>g crawl stroke <strong>in</strong> elite swimmers<br />

with a locomotor disability. Human Mov Sci, 24, 54-65.<br />

Seifert L., Boulesteix L., & Chollet D. (2004a). Effect of gender on<br />

the adaptation of arm coord<strong>in</strong>ation <strong>in</strong> front crawl. Int J sports Med,<br />

25, 217-23.<br />

Seifert L., Chollet D., & Bardy B. G. (2004b). Effect of swimm<strong>in</strong>g velocity<br />

on arm coord<strong>in</strong>ation <strong>in</strong> the front crawl: a dynamic analysis. J<br />

Sports Sci, 22 (7), 651-60.<br />

Seifert L., Chollet D., & Chatard J. C. (2008). K<strong>in</strong>ematic changes dur<strong>in</strong>g<br />

a 100-m front crawl: effects of performance level <strong>and</strong> gender. Med<br />

Sci Sports Exerc, 39(10), 1784-93. Erratum <strong>in</strong>: Med Sci Sports Exerc,<br />

40 (3), 591.<br />

Seifert L., Chollet D., & Rouard A. (2007). Swimm<strong>in</strong>g constra<strong>in</strong>ts <strong>and</strong><br />

arm coord<strong>in</strong>ation. Hum Mov Sci, 26 (1), 68-86.<br />

W<strong>in</strong>ter D. (1990) <strong>Biomechanics</strong> <strong>and</strong> motor control of human movement.<br />

John Wiley, Chichester.<br />

159


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Identify<strong>in</strong>g Determ<strong>in</strong>ant Movement Sequences <strong>in</strong><br />

Monof<strong>in</strong> Swimm<strong>in</strong>g Technique<br />

rejman, M. & staszkiewicz, A.<br />

University School of Physical Education, Wroclaw, Pol<strong>and</strong><br />

The aim of this study is to identify errors <strong>in</strong> leg <strong>and</strong> monof<strong>in</strong> movement<br />

structure, which lower the effectiveness of swimm<strong>in</strong>g. The movement<br />

cycles of six swimmers were filmed underwater <strong>in</strong> a progressive trial<br />

(900 m at <strong>in</strong>creas<strong>in</strong>g speeds). Results due to k<strong>in</strong>ematical analysis were<br />

obta<strong>in</strong>ed as temporal data for: angle of foot bend<strong>in</strong>g <strong>in</strong> relation to the<br />

shank, proximal end of the monof<strong>in</strong> <strong>in</strong> relation to the foot <strong>and</strong> for angle<br />

of attack of the distal part <strong>and</strong> entire f<strong>in</strong> surface. The parameters were<br />

selected accord<strong>in</strong>g to an exist<strong>in</strong>g functional model of monof<strong>in</strong> swimm<strong>in</strong>g.<br />

Hence, the identification of determ<strong>in</strong>ant movement sequences<br />

<strong>and</strong> technical key elements <strong>in</strong> monof<strong>in</strong> swimm<strong>in</strong>g <strong>and</strong> their quantification,<br />

make sense <strong>in</strong> order to anticipate <strong>and</strong> elim<strong>in</strong>ate errors.<br />

Key words: swimm<strong>in</strong>g, monof<strong>in</strong>, determ<strong>in</strong>ant movement sequence,<br />

technique errors<br />

IntroductIon<br />

The surface area of a monof<strong>in</strong> is about 20 times larger than human feet,<br />

<strong>and</strong> it is a more relevant source of propulsion. Monof<strong>in</strong> swimm<strong>in</strong>g for<br />

learn<strong>in</strong>g, leisure or water rescue requires basic technical ability. At elite<br />

sport<strong>in</strong>g level, a perfect technique is required, as the monof<strong>in</strong> does not<br />

“forgive errors”. An error may objectively be def<strong>in</strong>ed as a performance of<br />

movement not <strong>in</strong> accordance with a given pattern. From motor po<strong>in</strong>t of<br />

view, it may be a movement not <strong>in</strong> accordance with the orig<strong>in</strong>al <strong>in</strong>tention<br />

(Brehmer <strong>and</strong> Sperle, 1984). A determ<strong>in</strong>ant movement sequence is<br />

literally the general execution of movement activity which is determ<strong>in</strong>ed<br />

to be “correct” by objective parameters. The ability to verbally name a<br />

movement precisely allows the comb<strong>in</strong><strong>in</strong>g of cognizant execution of action,<br />

with the perception of what this action should be, support<strong>in</strong>g the<br />

<strong>in</strong>tellectual process of teach<strong>in</strong>g <strong>and</strong> perfect<strong>in</strong>g technique (Richard et al.,<br />

2005).<br />

Explicit conditions generat<strong>in</strong>g monof<strong>in</strong> propulsion form the basis of<br />

several biomechanical analyses of technique, which develop a description<br />

of the exist<strong>in</strong>g processes generat<strong>in</strong>g propulsion (e.g. Colman et al.,<br />

(1999), formulate quality criteria for swimm<strong>in</strong>g technique (e.g. Shup<strong>in</strong>g<br />

et al., 2002; Rejman, 2006) <strong>and</strong> create a search through model<strong>in</strong>g<br />

(e.g. Wu 1971). The rema<strong>in</strong><strong>in</strong>g analysis is set aside for the aspects of<br />

biomechanical application - useful <strong>in</strong> tra<strong>in</strong><strong>in</strong>g procedures (e.g. Rejman<br />

<strong>and</strong> Ochmann, 2009; Persyn <strong>and</strong> Colman, 1997). Therefore, the aim of<br />

this study was to identify errors <strong>in</strong> leg <strong>and</strong> monof<strong>in</strong> movement structure,<br />

which lower the effectiveness of swimm<strong>in</strong>g. The research assignments<br />

formulated with<strong>in</strong> the context of the use a monof<strong>in</strong> for maximum swimm<strong>in</strong>g<br />

speed are: (1) the identification of errors <strong>in</strong> the leg <strong>and</strong> monof<strong>in</strong><br />

movement <strong>in</strong> order to describe their structure <strong>and</strong> scale; (2) the identification<br />

of determ<strong>in</strong>ant movement sequences <strong>and</strong> key technical elements<br />

of leg <strong>and</strong> monof<strong>in</strong> movement <strong>in</strong> terms of potential errors, with an aim<br />

towards their anticipation <strong>and</strong> elim<strong>in</strong>ation; (3) the identification of the<br />

relation between monof<strong>in</strong> swimm<strong>in</strong>g speed <strong>and</strong> the structure <strong>and</strong> scale<br />

of errors, with an aim towards the isolation of determ<strong>in</strong>ant movement<br />

sequences with<strong>in</strong> the measure of quality of monof<strong>in</strong> swimm<strong>in</strong>g technique.<br />

Methods<br />

Six representatives of the Polish Monof<strong>in</strong> Swimm<strong>in</strong>g Team (homogenous<br />

<strong>in</strong> terms of age, somatic parameters <strong>and</strong> championship level of<br />

technique) took part <strong>in</strong> the research. They conducted a progressive test<br />

(swimm<strong>in</strong>g 900 m at <strong>in</strong>creas<strong>in</strong>g speeds). To register parameters describ<strong>in</strong>g<br />

the leg <strong>and</strong> f<strong>in</strong> movements, the swimmers were filmed underwater.<br />

160<br />

Identification marks were place on the axes of the hip, knee <strong>and</strong> ankle<br />

jo<strong>in</strong>ts. The monof<strong>in</strong> was also marked (at the tail - where the plate is<br />

jo<strong>in</strong>ed to the feet, at the middle <strong>and</strong> at the edge of the f<strong>in</strong>). The marks<br />

served to divided the f<strong>in</strong> <strong>in</strong>to proximal (between tail <strong>and</strong> middle) <strong>and</strong><br />

distal (between middle <strong>and</strong> edge) parts, as well as to monitor the entire<br />

surface of the f<strong>in</strong>. A r<strong>and</strong>om cycle (each 100m) from each swimmer<br />

was chosen. SIMI System (SIMI Reality Motion Systems GmbH, Germany)<br />

was used for k<strong>in</strong>ematic analysis. The results were obta<strong>in</strong>ed <strong>in</strong> the<br />

form of temporal data for the angles of bend at the foot <strong>in</strong> relation to<br />

the shank (KAT), the proximal part <strong>in</strong> relation to the foot (ATM), the<br />

angle of attack of the distal part (HME) <strong>and</strong> the entire surface of the<br />

f<strong>in</strong> (HME). The exist<strong>in</strong>g model exactly these parameters were found to<br />

create maximum swimm<strong>in</strong>g speed when they are optimized (Rejman<br />

& Ochmann, 2009). Friedman’s test <strong>and</strong> Kendall’s coefficient, useful <strong>in</strong><br />

analysis of small groups were applied to confirm the existence of the<br />

similarities <strong>in</strong> the data studied.<br />

Figure 1. Example of quantification of errors registered <strong>in</strong> angular displacement<br />

of the parameters studied<br />

With<strong>in</strong> the range of illustrated errors made by swimmers <strong>in</strong> the time cycle<br />

function (recorded dur<strong>in</strong>g swimm<strong>in</strong>g of each 100m section of a trial)<br />

a model analyz<strong>in</strong>g the value of parameters was <strong>in</strong>troduced. Information<br />

was obta<strong>in</strong>ed on the scale <strong>and</strong> structure of error <strong>in</strong> relation to the model.<br />

The range of errors were labeled <strong>and</strong> assigned to the relevant movement<br />

sequence. The errors were quantified by calculat<strong>in</strong>g the size of the fields<br />

estimated on the basis of the range of angles analyzed, which exceeded<br />

(or did not atta<strong>in</strong>) the boundary established by the model (Figure 1).<br />

The values of fields estimated <strong>in</strong> a given cycle were summed for each of<br />

the participants tested. In the next stage, the estimated ranges of errors<br />

were illustrated by the movement sequence registered previously. Next,<br />

these sequences were compared with sequences, which achieved the criteria<br />

of the model, or demonstrated a slight comparable difference. The<br />

juxtapositions supplemented <strong>in</strong>formation related to the range of errors<br />

committed, form<strong>in</strong>g the basis for the isolation of determ<strong>in</strong>ant movement<br />

sequences. The identification of these sequences, along with the<br />

results of analysis from the scale <strong>and</strong> structure of errors, allows the description<br />

of key elements <strong>in</strong> the movement structure of legs <strong>and</strong> monof<strong>in</strong>,<br />

<strong>in</strong> the occurrence of errors. The relation between errors committed<br />

<strong>and</strong> swimm<strong>in</strong>g speed was also exam<strong>in</strong>ed.<br />

results<br />

Based on <strong>in</strong>formation related to the scale <strong>and</strong> structure of errors committed<br />

by swimmers (Figure 2, Table 1) the follow<strong>in</strong>g generalizations<br />

were formulated: (1) the fastest swimmer made fewer errors, <strong>in</strong> terms<br />

of the parameters exam<strong>in</strong>ed, than the slowest; (2) movement errors deduced<br />

from the model were ma<strong>in</strong>ly related to angular displacement, with<br />

the exception of the ankle jo<strong>in</strong>t angle dur<strong>in</strong>g upbeat, performed by the<br />

slowest swimmer; (3) based on the average values of sum of errors it


may be assumed that the most difficult element of monof<strong>in</strong> swimm<strong>in</strong>g<br />

is the proper range of motion <strong>in</strong> the ankle jo<strong>in</strong>ts; (4) an analysis of the<br />

differences between value of errors performed, suggests the parameter<br />

most differentiat<strong>in</strong>g the fastest from the slowest swimmer, is the angle<br />

of bend of the feet <strong>in</strong> relation to the shanks (19.5%). The angle of attack<br />

of distal part of the f<strong>in</strong> (11.5%) placed second <strong>in</strong> the rank<strong>in</strong>g mentioned.<br />

The differences between values of errors <strong>in</strong> terms of the angle of bend <strong>in</strong><br />

the proximal part of the f<strong>in</strong> (7.3%) <strong>and</strong> angle of attack of the entire f<strong>in</strong><br />

(6.8%) was the lowest, even when most similar. (5) The errors estimated<br />

high correlated to swimm<strong>in</strong>g <strong>in</strong>tracycle velocity.<br />

Angular Displacement [deg]<br />

220<br />

200<br />

180<br />

160<br />

140<br />

M900 4 16 20 30<br />

ERROR ERROR<br />

M600 5 17 27 29<br />

ERROR ERROR<br />

120<br />

M300 4 21 24 33<br />

TIME [s] (Sampl<strong>in</strong>g frequency 50Hz)<br />

ERROR ERROR<br />

100<br />

1 3 5 7 9 11 13 15 17 19 21 23 25 27 29 31 33 35 37<br />

KAT1ER<br />

KAT6ER<br />

KAT1COR<br />

KAT6COR<br />

KAT3ER<br />

KAT9ER<br />

KAT3COR<br />

KAT9COR<br />

Ma M100 4<br />

ERROR<br />

17 19<br />

ERROR<br />

33<br />

M-HIGHEST SPEED<br />

SUMM OF ERRORS [%]<br />

M-LOWEST SPEED AVERAGE SD<br />

KAT<br />

58,1<br />

77.6<br />

71,5<br />

8,4<br />

ATM<br />

26,4<br />

33,7<br />

34,6<br />

6,1<br />

HME<br />

22,4<br />

33,6<br />

34,6<br />

6,1<br />

HTE<br />

29,8<br />

36,6<br />

42,5<br />

8,5<br />

Figure 2. Graph illustrat<strong>in</strong>g scope of errors (ER) <strong>in</strong> angle of the foot<br />

flexion <strong>in</strong> relation to shank (KAT) <strong>in</strong> time function. At left are sequences<br />

of movement illustrat<strong>in</strong>g the range of errors showed <strong>in</strong> the graph.<br />

Sum of errors by fastest <strong>and</strong> slowest swimmers compared to average<br />

value calculated for all swimmers.<br />

Table 1. Pearson’s correlation coefficients between value of error <strong>in</strong> cycle<br />

made by all subjects on 100-m sections, <strong>and</strong> average velocity (ranked by<br />

average velocity). (KAT) – angle of bend <strong>in</strong> foot at ankle jo<strong>in</strong>t; (ATM) –<br />

angle of bend <strong>in</strong> tail of monof<strong>in</strong>; (HME) – angle of attack of distal part<br />

of f<strong>in</strong>, (HTE) – angle of attack of entire surface of f<strong>in</strong>.<br />

SUBJECT KAT ATM HME HTE SUBJECT KAT ATM HME HTE<br />

M -0,94 -0,99 -0,62 -0,99 P -0,66 -0,88 -0,90 -0,89<br />

A -0,99 -0,55 -0,72 -1,00 S -0,79 -0,96 -0,85<br />

B -0,71 -0,94 -1,00 -0,70 N -0,77 -0,52<br />

The follow<strong>in</strong>g determ<strong>in</strong>ant movement sequences were estimated. The<br />

end of the downbeat movement, where the knee jo<strong>in</strong>ts straighten, the<br />

legs are straight, the feet are <strong>in</strong> their lowest downbeat position, the tail<br />

is at maximum bent at the maximum angle of attack of the entire surface<br />

of the f<strong>in</strong> (Table 2(1)). The change ankle jo<strong>in</strong>t angle <strong>and</strong> the angle<br />

between proximal part of the f<strong>in</strong> <strong>and</strong> the feet is dur<strong>in</strong>g the downbeat<br />

– beg<strong>in</strong>n<strong>in</strong>g of the phase where the legs are maximally flexed <strong>and</strong> the<br />

segments of the f<strong>in</strong> are more or less parallel (Table 2(3)) <strong>and</strong> f<strong>in</strong>ally, dur<strong>in</strong>g<br />

upbeat – the last part of upward movement, with legs straightened,<br />

just before flex<strong>in</strong>g at the knees, at the maximum bend of the tail of the<br />

f<strong>in</strong> (Table 2(2)). The determ<strong>in</strong>ant movement sequence referr<strong>in</strong>g to the<br />

change of angle of the distal part of the f<strong>in</strong> <strong>and</strong> its entire surface is <strong>in</strong> the<br />

downbeat - the second part of legs straighten<strong>in</strong>g at the knees, where the<br />

shanks are more or less parallel to the direction of swimm<strong>in</strong>g <strong>and</strong> the<br />

monof<strong>in</strong> is more or less straight <strong>in</strong> the maximum angle of attack (Table<br />

2(4)). Dur<strong>in</strong>g upbeat – the second part of the lifted legs straightened<br />

with the knees up, until the legs are placed more or less parallel to direction<br />

of swimm<strong>in</strong>g <strong>and</strong> the monof<strong>in</strong> is at maximum bend <strong>in</strong> the middle<br />

(Table 3(5)). The key elements <strong>in</strong> the movement structure of legs <strong>and</strong><br />

monof<strong>in</strong> were also described (Table 1).<br />

chaPter2.<strong>Biomechanics</strong><br />

Table 2. The determ<strong>in</strong>ant sequence of leg movements <strong>and</strong> monof<strong>in</strong><br />

(1,2,3,4,5) arranged with the key elements <strong>in</strong> the structure of monof<strong>in</strong><br />

<strong>and</strong> leg movements (A,B,C,D).related to occurrence of errors.<br />

dIscussIon<br />

Errors <strong>in</strong> propulsive movement structure <strong>and</strong> their impact on swimm<strong>in</strong>g<br />

speed, are relevant to the pr<strong>in</strong>ciple of equilibrium of momentum<br />

due to the <strong>in</strong>teraction between the water <strong>and</strong> swimmer. Without errors<br />

momentum transfer between the subsequent leg segments <strong>and</strong> the<br />

monof<strong>in</strong>, is most effective (Rejman, 2006). Therefore, the determ<strong>in</strong>ant<br />

sequence <strong>in</strong>itiated <strong>in</strong> the category of quality of momentum transfer, occurs<br />

between subsequent elements of the feet - parts of the monof<strong>in</strong>‘s<br />

cha<strong>in</strong>.<br />

The swimmers tested <strong>in</strong> this study show a low level of control over<br />

feet movement while execut<strong>in</strong>g propulsion actions. The angle of bent<br />

of the feet <strong>in</strong> relation to the shanks is the most difficult element of the<br />

movement structure (Figure 2). Additionally, chang<strong>in</strong>g this angle <strong>in</strong><br />

the function of time <strong>and</strong> layout of errors, demonstrates the least mutual<br />

similarity among the parameters tested. The dom<strong>in</strong>ant role of foot<br />

movement <strong>in</strong> generat<strong>in</strong>g propulsion is revealed <strong>in</strong> results ga<strong>in</strong>ed from<br />

the construction of a neural network (Rejman <strong>and</strong> Ochmann, 2009) as<br />

well as research on factors support<strong>in</strong>g ma<strong>in</strong>tenance of consistent high<br />

<strong>in</strong>fracycle monof<strong>in</strong> swimm<strong>in</strong>g velocity (Rejman, 2006). The aim of<br />

these suggestions was to avoid plac<strong>in</strong>g the f<strong>in</strong> parallel to the direction of<br />

swimm<strong>in</strong>g. The results confirmed that, the feet as an active (under total<br />

control of the swimmer) element <strong>in</strong> the biomechanical cha<strong>in</strong> are the<br />

f<strong>in</strong>al l<strong>in</strong>k of torque transfer from the legs to the surface of the f<strong>in</strong> (Rejman,<br />

2006). Hence, correct movement <strong>in</strong> this element of the sequence<br />

structure of propulsion seems to be important. Cognitive control of foot<br />

movement allows for self-correction of swimm<strong>in</strong>g technique. The tendency<br />

toward excessive plantar flexion of the feet (observed generally,<br />

not only <strong>in</strong> the research group) thus seems unjustified from the po<strong>in</strong>t of<br />

view of swimm<strong>in</strong>g efficiency<br />

An analysis of the value of sum of errors made by swimmers <strong>in</strong>dicated<br />

similarities between angle of bend <strong>in</strong> the tail of the monof<strong>in</strong><br />

(ATM) <strong>and</strong> angle of attack of the distal part of the f<strong>in</strong> (HME) (Figure<br />

2). Similarities were also noted when compar<strong>in</strong>g the values of difference<br />

between angle of bend <strong>in</strong> the tail of the monof<strong>in</strong> (ATM) <strong>and</strong> angle of<br />

attack of the entire surface of the f<strong>in</strong> (HTE) This may <strong>in</strong>dicate that<br />

the bend<strong>in</strong>g of the tail of the f<strong>in</strong>, <strong>in</strong>fluences the change <strong>in</strong> shape of the<br />

monof<strong>in</strong>’s surface. It is accepted that the tail is the place where transfer<br />

of torque, generated by the legs, to the surface of the f<strong>in</strong> is performed<br />

(Rejman, 2006). With this <strong>in</strong> m<strong>in</strong>d, the tail is the key element <strong>in</strong> analyz<strong>in</strong>g<br />

the biomechanical cha<strong>in</strong>, divid<strong>in</strong>g it <strong>in</strong>to parts consist<strong>in</strong>g of leg segments<br />

<strong>and</strong> monof<strong>in</strong> segments. Support<strong>in</strong>g this thesis are results show<strong>in</strong>g<br />

that the optimal plantar flexion dur<strong>in</strong>g downbeat, limits the bend of the<br />

tail, as a result optimiz<strong>in</strong>g the angle of attack of the proximal part of<br />

the f<strong>in</strong>. Optimal dorsal flexion of the feet dur<strong>in</strong>g upbeat causes greater<br />

tail bend<strong>in</strong>g <strong>and</strong> consequently, the angle of attack of the distal part <strong>and</strong><br />

entire f<strong>in</strong>, achieves optimum range <strong>in</strong> both phases of the cycle (Rejman<br />

<strong>and</strong> Ochmann, 2009). These suggestions are confirmed <strong>in</strong> the present<br />

work. Greater optimization of tail bend, with<strong>in</strong> limits established <strong>in</strong> the<br />

161


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

functional model (form<strong>in</strong>g an isolated sequence) leads to the appearance<br />

of reserves <strong>in</strong> swimm<strong>in</strong>g technique, support<strong>in</strong>g the achievement of<br />

maximum swimm<strong>in</strong>g speed (Rejman <strong>and</strong> Ochmann, 2009).<br />

Due to optimal mutual actions of the feet, tail <strong>and</strong> the parts of the<br />

f<strong>in</strong> with speed, the formation of vortices occurs. These become an additional<br />

source of propulsion. Stable vortex circulation creates additional<br />

momentum due to velocity changes of water mass, produced by the<br />

rotational velocity of the vortex (Colman et al., 1999). It seems that<br />

the efficient transfer of torque over the surface of the f<strong>in</strong>, no matter<br />

if directly from leg movements, is subord<strong>in</strong>ated to the hydrodynamic<br />

conditions of water flow over the surface of the f<strong>in</strong>. In this aspect, the<br />

dynamic transfer system, displayed as changes to the angle of attack of<br />

the monof<strong>in</strong>, changes the structure of water flow over its surface, <strong>and</strong><br />

appears to be a key to effective swimm<strong>in</strong>g. The results obta<strong>in</strong>ed correspond<br />

to the analysis of particular components of force generated on<br />

the surface of the f<strong>in</strong>, with respect to the change <strong>in</strong> <strong>in</strong>tracycle velocity<br />

(Colman et al., 1999; Rejman et al., 2006) (Table 2 - B, D) – <strong>in</strong> extreme<br />

upper <strong>and</strong> lower feet position, where the legs are straight at the ankle<br />

jo<strong>in</strong>t, the monof<strong>in</strong> bends at the tail, <strong>and</strong> its midsection is placed parallel<br />

to the direction of swimm<strong>in</strong>g. The research cited <strong>in</strong>dicates that the ma<strong>in</strong><br />

source of propulsion <strong>in</strong> this part of the cycle are drag <strong>and</strong> lift forces as<br />

well as accompany<strong>in</strong>g components due to vortex <strong>in</strong>duced momentum<br />

<strong>and</strong> the flexion of the f<strong>in</strong>. These same authors believe that ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g<br />

the velocity cited, plays a ma<strong>in</strong> role <strong>in</strong> plac<strong>in</strong>g the distal part of the f<strong>in</strong><br />

parallel to the direction of swimm<strong>in</strong>g (Table 2 – (A, C) - maximum<br />

bend of the distal part <strong>and</strong> entire surface of the f<strong>in</strong>, dur<strong>in</strong>g change of<br />

direction of edge movement). In the sequences described, the energy<br />

essential to swimmer propulsion emanates from both additional mass<br />

slides away from the edge <strong>and</strong> acceleration reaction.<br />

The diagnostic value of the parameters analyzed was confirmed <strong>in</strong> an<br />

earlier constructed model of functional swimm<strong>in</strong>g <strong>and</strong> monof<strong>in</strong> technique<br />

(Rejman <strong>and</strong> Ochmann, 2009). It was also confirmed that, the<br />

greater the <strong>in</strong>fluence of the parameter on swimm<strong>in</strong>g speed, the more difficult<br />

the performance of proper movement <strong>in</strong> relation to this parameter.<br />

The errors <strong>in</strong>dicated concern the fragments, which registered the highest<br />

<strong>in</strong>tracycle velocity (confirmed by correlation coefficients (Table 1)) suggest<strong>in</strong>g<br />

that, the achievement of maximum <strong>in</strong>tracycle speed, is a consequence<br />

of proper execution of the determ<strong>in</strong>ant sequence of movement.<br />

No difference was demonstrated <strong>in</strong> terms of the change <strong>in</strong> angular foot<br />

movement, <strong>in</strong> subjectively <strong>in</strong>terpreted conditions, ensu<strong>in</strong>g from fatigue<br />

dur<strong>in</strong>g swimm<strong>in</strong>g of subsequent distances of the trial. Therefore, there is<br />

a basis for the objective evaluation of the reliability of the errors, which<br />

occurred. The procedures outl<strong>in</strong><strong>in</strong>g determ<strong>in</strong>ant sequences, on the basis<br />

of errors analyzed, create an empirical foundation for treat<strong>in</strong>g this sequence<br />

as a tool for evaluat<strong>in</strong>g monof<strong>in</strong> swimm<strong>in</strong>g technique (Table 2).<br />

conclusIon<br />

Precise control of foot movement, alows for achiev<strong>in</strong>g a dynamic system<br />

transferr<strong>in</strong>g torque, as a basis of propulsion, which creates momentum,<br />

bend<strong>in</strong>g the tail of the f<strong>in</strong> dur<strong>in</strong>g transfer, thus chang<strong>in</strong>g the shape of the<br />

f<strong>in</strong> <strong>and</strong> the structure of water flow over its surface. This same proper sequence<br />

of propulsive movement creates conditions for us<strong>in</strong>g the surface<br />

of the monof<strong>in</strong> to achieve maximum speeds. Therefore, it is justified to<br />

assign key elements to monof<strong>in</strong> swimm<strong>in</strong>g technique, for the quantification<br />

of its quality, <strong>and</strong> for the anticipation <strong>and</strong> elim<strong>in</strong>ation of errors<br />

dur<strong>in</strong>g the technical tra<strong>in</strong><strong>in</strong>g.<br />

reFerences<br />

Colman V, Persyn U, Ungerechts BE. (1999). A mass of water added to<br />

swimmer’s mass to estimate the velocity <strong>in</strong> dolph<strong>in</strong>-like swimm<strong>in</strong>g<br />

bellow the water surface. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> of Swimm<strong>in</strong>g<br />

VIII. Kesk<strong>in</strong>en K, Komi P, Holl<strong>and</strong>er A. (eds.). Gummerus Pr<strong>in</strong>t<strong>in</strong>g,<br />

Jyvaskyla, (pp) 89 - 94.<br />

Persyn U, Colman V, Zhu JP. (1997). Scientific concept <strong>and</strong> educational<br />

transfer <strong>in</strong> undulat<strong>in</strong>g competitive strokes <strong>in</strong> Belgium. Koelner<br />

162<br />

Schwimmsporttage 1996, Sport-Fahnemann-Verlag, Boikenem, (pp<br />

34-40).<br />

Rejman M, Ochmann B. (2009). Model<strong>in</strong>g of monof<strong>in</strong> swimm<strong>in</strong>g technique:<br />

optimization of feet displacement <strong>and</strong> f<strong>in</strong> stra<strong>in</strong>. J.Applied Biomech,<br />

25: 340-350<br />

Rejman, M. (2006). Influenc<strong>in</strong>g of tim<strong>in</strong>g delay on monof<strong>in</strong> <strong>in</strong>tra-cycle<br />

swimm<strong>in</strong>g velocity. Vilas-Boas JP, Alves F, Marques A. (eds.). <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X. Portuguese Journal of Sport<br />

Sciences, 85–88.<br />

Richard A Schmidt RA Lee T. (2005). Motor control <strong>and</strong> learn<strong>in</strong>g. a behavioral<br />

emphasis - 4th Edition. Champaign: Human K<strong>in</strong>etics.<br />

Shup<strong>in</strong>g L <strong>and</strong> S<strong>and</strong>ers R. (2002). Mechanical properties of the f<strong>in</strong>.<br />

Scientific Proceed<strong>in</strong>gs of XX International Symposium on Biomechanice<br />

<strong>in</strong> Sports. Gianikellis K. (eds.) Caceres, (pp) 479-481.<br />

Wu Yao-Tsu T. (1971). Hydrodynamics of swimm<strong>in</strong>g propulsion. Part<br />

1. Swimm<strong>in</strong>g of a two-dimensional flexible plate at variable forward<br />

speeds <strong>in</strong> an <strong>in</strong>viscid fluid. J. Fluid Mech. 46, 337-355.


Evaluation of the Glid<strong>in</strong>g Capacity of a Swimmer<br />

roig, A.<br />

GIRSANE Research Group from Olympic Tra<strong>in</strong><strong>in</strong>g Centre, Barcelona,<br />

Spa<strong>in</strong><br />

Reduc<strong>in</strong>g resistance is probably the fastest way to improve performance<br />

<strong>and</strong> the most efficient to reduce energetic cost. Therefore, the aim of this<br />

study was twofold: (i) to give advice to coaches to re-orient their tra<strong>in</strong><strong>in</strong>g<br />

sessions towards reduction of resistance forces <strong>and</strong> suggest exercises<br />

for its improvement <strong>and</strong>, (ii) to develop <strong>and</strong> apply a new test for the<br />

evaluation of glid<strong>in</strong>g. The proposed glid<strong>in</strong>g test evaluated the maximum<br />

speed reached by the swimmer after push-off <strong>and</strong> the passive hydrodynamic<br />

resistance when glid<strong>in</strong>g through the water. A well-balanced<br />

solution between accuracy, validity <strong>and</strong> applicability for the evaluation<br />

of underwater glide was found.<br />

Key words: Glid<strong>in</strong>g coefficient, hydrodynamic position, resistance<br />

force, starts, turns<br />

IntroductIon<br />

The capacity to move its own body through the water with the lowest<br />

resistance should be <strong>in</strong>cluded among the most important qualities of a<br />

swimmer. Advanc<strong>in</strong>g through a liquid, the swimmer evacuates water <strong>and</strong><br />

occupies its place, caus<strong>in</strong>g the hydrodynamic resistance that acts <strong>in</strong> the<br />

same swimm<strong>in</strong>g direction but <strong>in</strong> the opposite sense.<br />

The underwater phase represents an important part of the entire race<br />

time (Chow, 1984). This is even more true <strong>in</strong> a 25m-pool race, where the<br />

number of turns is doubled.<br />

Dur<strong>in</strong>g the phases of pure glid<strong>in</strong>g, <strong>in</strong> starts or turns, the swimmer tries<br />

to ma<strong>in</strong>ta<strong>in</strong> the highest velocity of all race obta<strong>in</strong>ed after push-off<br />

(highest peak of speed <strong>in</strong> figure 1).<br />

Figure 1. Velocity graph of a breaststroker dur<strong>in</strong>g start.<br />

The higher the speed of the swimmer, the higher will be the resistance<br />

to overcome. Therefore, <strong>in</strong> those phases of the race, where velocity is<br />

<strong>in</strong>creased (start <strong>and</strong> turns), the swimmer will have to pay much more attention<br />

on reduc<strong>in</strong>g resistance forces. An accurate underwater technique<br />

comb<strong>in</strong>es the capacity to self-propel <strong>in</strong> the water <strong>and</strong> to reduce brak<strong>in</strong>g<br />

forces to the m<strong>in</strong>imum for a beneficial use of the generated propulsion.<br />

Both qualities coexist when a swimmer travels <strong>in</strong> the water <strong>and</strong> should<br />

be optimised to obta<strong>in</strong> the highest velocity.<br />

Many factors may determ<strong>in</strong>e the glid<strong>in</strong>g capacity of a body <strong>in</strong>side<br />

the water. One of them, the fluid density (water is about 1000 times<br />

more dense than air) is not controllable by the swimmer <strong>and</strong> is equal<br />

for all participants. Others, as frontal area, sk<strong>in</strong> <strong>and</strong> swimsuit friction, or<br />

body shape, can be modified <strong>and</strong> have to be improved <strong>in</strong> tra<strong>in</strong><strong>in</strong>g sessions.<br />

A slender <strong>and</strong> aligned body <strong>in</strong> the mov<strong>in</strong>g direction will produce<br />

a lower resistance. New swimsuits seem to slightly alter the parameters<br />

chaPter2.<strong>Biomechanics</strong><br />

that <strong>in</strong>crease the swimmers glid<strong>in</strong>g, modify<strong>in</strong>g buoyancy <strong>and</strong> alignment<br />

(slender the body shape <strong>and</strong> avoid feet fall<strong>in</strong>g) <strong>and</strong> reduc<strong>in</strong>g friction by<br />

means of remov<strong>in</strong>g seams <strong>and</strong> us<strong>in</strong>g new textile that m<strong>in</strong>imizes turbulence<br />

generation.<br />

Many authors like Clarys (1979), Maiello et al. (1998) <strong>and</strong> Lyttle et<br />

al. (2000) have studied the effect of depth of glide onto resistance forces,<br />

conclud<strong>in</strong>g with different op<strong>in</strong>ions, some of them even opposed.<br />

Dim<strong>in</strong>ish<strong>in</strong>g resistance is probably the fastest way to improve performance<br />

<strong>and</strong> the most efficient way to reduce energetic cost. It is for<br />

this reason that we pursued a double goal: To give advise to coaches<br />

to re-orient their tra<strong>in</strong><strong>in</strong>g sessions towards the reduction of resistance<br />

forces by suggest<strong>in</strong>g exercises for its improvement <strong>and</strong> to develop <strong>and</strong><br />

apply a new test for the evaluation of glid<strong>in</strong>g.<br />

Methods<br />

The proposed glid<strong>in</strong>g test is an adaptation of the one developed by<br />

Klauck et al. (1976) <strong>and</strong> evaluates simultaneously, the maximum speed<br />

reached by the swimmer after push-off from the wall <strong>and</strong> the passive<br />

hydrodynamic resistance when glid<strong>in</strong>g through the water. Glid<strong>in</strong>g test<br />

is be<strong>in</strong>g applied to swimmers tra<strong>in</strong><strong>in</strong>g at the Olympic Tra<strong>in</strong><strong>in</strong>g Centre<br />

<strong>in</strong> Barcelona, belong<strong>in</strong>g to a wide variety of performance levels, <strong>in</strong>clud<strong>in</strong>g<br />

Olympic, World <strong>and</strong> European Championships <strong>and</strong> Paralympics’<br />

swimmers.<br />

Three underwater cameras are placed at the pool’s sidewall at a distance<br />

of 2m between them (Figure 2). The first camera distance from the<br />

wall varies <strong>and</strong> is equivalent to the distance reached by the swimmer’s<br />

head with his feet extended. For example, if first camera was placed at<br />

a distance of 1.9 m, the follow<strong>in</strong>g ones were placed at 3.9 m <strong>and</strong> 5.9 m.<br />

A 4th travell<strong>in</strong>g “dolly” camera followed the swimmer along the pool’s<br />

sidewall.<br />

Figure 2. Camera <strong>and</strong> buoy placement for the evaluation of resistance<br />

factor.<br />

The swimmer pushed off from the wall <strong>and</strong> adopted the most hydrodynamic<br />

position until his body stopped. Two trials were recorded for each<br />

chosen body orientation: ventral (fac<strong>in</strong>g down), dorsal for backstrokers<br />

(fac<strong>in</strong>g up) <strong>and</strong> lateral position. In addition, the swimmer performed<br />

a turn, start<strong>in</strong>g 10 meters before the wall <strong>and</strong> glide, as done before, to<br />

maximum distance. This variant detects if push-off or glide were affected<br />

by previous swim or flip.<br />

Image review of the exercise permitted the detection of possible<br />

mistakes on technique. A list of <strong>in</strong>dicators were pre-def<strong>in</strong>ed for the<br />

analysis of power application aga<strong>in</strong>st the wall <strong>and</strong> resistance reduction<br />

while glid<strong>in</strong>g: feet gap, support surface of feet aga<strong>in</strong>st the wall, knee<br />

flexion, head with<strong>in</strong> arms, shoulder ris<strong>in</strong>g to lengthen the body, overlapp<strong>in</strong>g<br />

of h<strong>and</strong>s, extension of elbows, non-arched trunk <strong>and</strong> alignment of<br />

h<strong>and</strong>s, elbows, shoulders, hips, knees, feet <strong>and</strong> toes <strong>in</strong> the trajectory l<strong>in</strong>e<br />

of glide. The video images were also used for the calculation of time of<br />

head pass<strong>in</strong>g <strong>in</strong> front of each camera <strong>and</strong> the time spent to cover the<br />

distance of 2 meters between each pair.<br />

Signals from a velocity meter were recorded, also. This device, attached<br />

to the swimmer’s hip by a th<strong>in</strong> belt, registered the <strong>in</strong>stantaneous speed<br />

dur<strong>in</strong>g the exercise. The follow<strong>in</strong>g parameters were obta<strong>in</strong>ed from values<br />

of the velocity graph:<br />

163


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

– maximum speed after push-off (VMax) as a result of apply<strong>in</strong>g the<br />

maximum power aga<strong>in</strong>st the pool’s wall.<br />

– distance covered after glid<strong>in</strong>g time follow<strong>in</strong>g push-off. SL =<br />

VAVG * dT<br />

– glid<strong>in</strong>g resistance coefficient. Gc = 20 / dT * (1 / VF<strong>in</strong>al – 1 /<br />

VInitial), where:<br />

dT is Glid<strong>in</strong>g time, V Initial is Maximum velocity obta<strong>in</strong>ed after<br />

push-off <strong>and</strong> V F<strong>in</strong>al is Instant velocity at the end of dT<br />

Glid<strong>in</strong>g resistance coefficient Gc <strong>in</strong>cludes <strong>in</strong> a s<strong>in</strong>gle parameter,<br />

frontal area (A) <strong>and</strong> friction <strong>and</strong> shape coefficient (C d ) <strong>and</strong> derives<br />

from the follow<strong>in</strong>g formula that expla<strong>in</strong>s the resistance force of a<br />

body travell<strong>in</strong>g through a gas or liquid:<br />

164<br />

where:<br />

ρ = Density of fluid (water)<br />

v = Relative velocity of the swimmer with respect to water. Dur<strong>in</strong>g<br />

turns, water will be mov<strong>in</strong>g at a certa<strong>in</strong> velocity <strong>and</strong> at the<br />

same direction but opposite sense to the swimmer, because of his<br />

body’s approach to the wall before turn.<br />

C d = Resistance coefficient. Describes how slender the body of<br />

the swimmer is. It is ma<strong>in</strong>ly expla<strong>in</strong>ed by the resistance generated<br />

by friction of swimsuit <strong>and</strong> sk<strong>in</strong> aga<strong>in</strong>st the water <strong>and</strong> swimmer’s<br />

shape.<br />

A = Projected frontal area of the swimmers’ body.<br />

results<br />

When compar<strong>in</strong>g Klauck’s Resistance Factor Rf <strong>and</strong> proposed Glid<strong>in</strong>g<br />

Coefficient Gc, the observed F (154.64) was higher than the Critical F<br />

(4.05), mean<strong>in</strong>g that both coefficients evaluated loss of speed <strong>and</strong> are<br />

l<strong>in</strong>early related by the equation Rf = 0.0403 * Gc + 0,089 for the group<br />

of 48 swimmers (Determ<strong>in</strong>ation Coefficient R2 =0.771, St<strong>and</strong>ard Error<br />

of Estimation SEE=0,0213 <strong>and</strong> Critical T=2,3172). Therefore, the<br />

95% confidence <strong>in</strong>terval of estimated values of Rf from Gc is def<strong>in</strong>ed by<br />

equation Rf = 0.0403 * Gc + 0.089 ± 2.3172 * 0.0213.<br />

Personal reports (exemplified by Figures 3 & 4) for each swimmer<br />

conta<strong>in</strong>ed a description of errors <strong>in</strong> technique observed <strong>in</strong> video images<br />

<strong>and</strong> the related values from velocity curve: elapsed time to cover both<br />

2 m distances, resistance factor (Rf ), maximum <strong>in</strong>itial velocity, glided<br />

distance after period of time <strong>and</strong> glid<strong>in</strong>g coefficient (Gc).<br />

Figure 3. Body’s wrong alignment <strong>in</strong> respect to hip’s trajectory described<br />

dur<strong>in</strong>g glide.<br />

Figure 4. Result<strong>in</strong>g speed curve <strong>and</strong> calculations of a swimmers glid<strong>in</strong>g<br />

test.<br />

Range of values of the glid<strong>in</strong>g coefficients obta<strong>in</strong>ed from tested swimmers<br />

has been wide, because of gender, age, size, shape <strong>and</strong> expertise<br />

differences. A high push-off power will <strong>in</strong>itially enable the swimmer to<br />

travel faster <strong>and</strong> further, but will also be the cause of a higher resistance<br />

force to overcome (resistance force Fd <strong>in</strong>creases proportionally to the<br />

square of velocity as shown previously <strong>in</strong> formula). Once mov<strong>in</strong>g, two<br />

factors will be determ<strong>in</strong>ant: Body shape <strong>and</strong> size, <strong>and</strong> body position <strong>and</strong><br />

alignment (technique).<br />

As shown <strong>in</strong> figure 5, the best gliders obta<strong>in</strong>ed the lowest values of<br />

Gc, because of either a higher <strong>in</strong>itial velocity (2.87 m/s of upper curve<br />

vs. 2.42 m/s of lower curve) or a small lost of speed (top curve vs. middle<br />

curve). Lower <strong>in</strong>itial velocities <strong>and</strong> / or higher decelerations will lead to<br />

a higher value of Gc (7.01 of lower curve vs. 3.52 of upper curve) of a<br />

bad glider. Higher-level swimmers average better values of Gc than the<br />

less experienced, even though improvements on swimmers with lower<br />

tra<strong>in</strong><strong>in</strong>g experience have been very obvious so far.<br />

Figure 5. Behaviour of glid<strong>in</strong>g coefficient Gc on different glid<strong>in</strong>g tests<br />

When compar<strong>in</strong>g by gender, men obta<strong>in</strong> higher average values of <strong>in</strong>itial<br />

speed near 3m/s compared to women’s values closer to 2.5m/s.<br />

Both the Klauck’s Resistance Factor (Rf ) <strong>and</strong> Glid<strong>in</strong>g Coefficient<br />

(Gc), were calculated for every test <strong>and</strong> demonstrated a high correlation<br />

(Figure 6).<br />

dIscussIon<br />

Technique learn<strong>in</strong>g is a complex process. Every swimmer has its own<br />

characteristics <strong>and</strong> tries to reproduce technical patterns to reach the<br />

highest performance. Hav<strong>in</strong>g a better conscience of what is do<strong>in</strong>g, the<br />

proposed modifications <strong>and</strong> its results, will lead to an improvement of<br />

his technique. Videography offers a visual feedback of what the swimmer<br />

is do<strong>in</strong>g. The velocity meter evaluates the <strong>in</strong>crements of speed on<br />

propulsive actions <strong>and</strong> decelerations caused by hydrodynamic resistance.<br />

Graph<strong>in</strong>g velocities over video images will allow the swimmer to establish<br />

a direct relation between “what he/she feels” (sensations) with “what<br />

he/she does” (video images, execution) <strong>and</strong> “the result of what he/she<br />

does” (speed, deceleration, performance).<br />

Figure 6. Correlation between Resistance Factor (Rf ) <strong>and</strong> Glid<strong>in</strong>g Coefficient<br />

(Gc).


Both Resistance Factor (Rf ) <strong>and</strong> Glid<strong>in</strong>g Coefficient (Gc) measure loss<br />

of speed, but they present their own advantages. Klauck’s glid<strong>in</strong>g test<br />

methodology has the advantage of not hav<strong>in</strong>g a cable attached to the<br />

swimmer’s hip <strong>and</strong> the possibility to compare with trials preceded of a<br />

turn. The proposed methodology uses of a velocity meter <strong>and</strong> offers the<br />

possibility to calculate parameters like maximum speed, glided distance,<br />

<strong>in</strong>stantaneous velocity <strong>and</strong> glid<strong>in</strong>g coefficient Gc with<strong>in</strong> any chosen period<br />

of glid<strong>in</strong>g time. This peculiarity has been of great help to determ<strong>in</strong>e<br />

the precise <strong>in</strong>stant to quit glid<strong>in</strong>g <strong>and</strong> to start underwater kick<strong>in</strong>g on<br />

starts <strong>and</strong> turns.<br />

conclusIon<br />

Starts <strong>and</strong> turns can be cut-off <strong>and</strong> analysed by parts. As a result, experts<br />

are able to better def<strong>in</strong>e lacks on technique <strong>and</strong> establish priorities <strong>in</strong><br />

tra<strong>in</strong><strong>in</strong>g sessions to reach the best performance. A well-balanced solution<br />

between accuracy, validity <strong>and</strong> applicability for the evaluation of<br />

underwater glide has been found. Coaches have designed <strong>and</strong> <strong>in</strong>cluded<br />

specific exercises for the tra<strong>in</strong><strong>in</strong>g of the glide, starts <strong>and</strong> turns <strong>in</strong> everyday<br />

practice <strong>and</strong> sport science have <strong>in</strong>creased their presence <strong>in</strong> the<br />

everyday work of swimmers. When applied on young swimmers, the<br />

glid<strong>in</strong>g test seems to be of great use for talent detection.<br />

reFerences<br />

Chow J.W., Hay J.G., Wilson B.D. <strong>and</strong> Imel C. (1984). Turn<strong>in</strong>g technique<br />

of elite swimmers. Journal of Sports Sciences, 2. pp 241-255.<br />

Clarys J.P. (1979). Human morphology <strong>and</strong> hydrodynamics. International<br />

Series on Sport Science Vol 8: pp 3–41, University Park<br />

Press, Baltimore.<br />

Klauck J. <strong>and</strong> Daniel K. (1976). Determ<strong>in</strong>ation of man’s drag<br />

coefficients <strong>and</strong> effective propell<strong>in</strong>g forces <strong>in</strong> swimm<strong>in</strong>g by<br />

means of chronocyclography. In: P V Komi (ed.) <strong>Biomechanics</strong><br />

V B. Human K<strong>in</strong>etics Pubishers. pp 250-257.<br />

Lyttle A.D., Blanksby B.A.B., Elliott B.C. <strong>and</strong> Lloyd D.G.<br />

(1998). The effect of depth <strong>and</strong> velocity on drag dur<strong>in</strong>g the<br />

streaml<strong>in</strong>ed glide. Journal of Swimm<strong>in</strong>g Research. 13: pp15-<br />

22.<br />

Maiello D., Sabat<strong>in</strong>i A., Demarie S., Sardella F. <strong>and</strong> Dal Monte<br />

A. (1998). Passive drag on <strong>and</strong> under the water surface. Journal<br />

of Sports Sciences, 16(5), pp 420-421.<br />

AcKnoWledGeMents<br />

I would like to thank coaches from Spanish <strong>and</strong> Catalan Swimm<strong>in</strong>g<br />

Federation <strong>and</strong> Paralympic Committee, as well as my sport’s sciences<br />

colleagues from GIRSANE (Research Group from Olympic Tra<strong>in</strong><strong>in</strong>g<br />

Centre <strong>in</strong> Barcelona, Spa<strong>in</strong>).<br />

chaPter2.<strong>Biomechanics</strong><br />

Effects of a Blueseventy TM Bodysuit on Spatialtemporal<br />

<strong>and</strong> Coord<strong>in</strong>ative Parameters Dur<strong>in</strong>g<br />

an All-out 50-m Front Crawl<br />

silveira, r.P., Kanefuku, J.Y., Moré, F.c., castro, F.A.s.<br />

Universidade Federal do Rio Gr<strong>and</strong>e do Sul, Porto Alegre, Brazil<br />

The aim of this study was to establish the effects of us<strong>in</strong>g a shoulder<br />

to ankle bodysuit (Blueseventy TM ) on spatial-temporal <strong>and</strong> coord<strong>in</strong>ative<br />

parameters dur<strong>in</strong>g an all-out 50m front crawl swim. Six subjects (16.6<br />

± 2.0 yrs) performed two all-out 50m trials (with <strong>and</strong> without<br />

bodysuit). The arm stroke parameters <strong>and</strong> <strong>in</strong>dex of coord<strong>in</strong>ation<br />

were determ<strong>in</strong>ed by videography. A repeated measures ANOVA<br />

was performed, with ma<strong>in</strong> effects verified us<strong>in</strong>g LSD post-hoc<br />

for an α < 5 %. Us<strong>in</strong>g the bodysuit, swimm<strong>in</strong>g speed <strong>and</strong> stroke<br />

length were higher. The duration of the entry <strong>and</strong> catch phase<br />

<strong>and</strong> non-propulsive phase were shorter <strong>in</strong> the second 25 m split.<br />

No statistical differences <strong>in</strong> <strong>in</strong>dex of coord<strong>in</strong>ation were found.<br />

Wear<strong>in</strong>g the bodysuit significantly improves the swimm<strong>in</strong>g performance,<br />

mostly on the second half of the test.<br />

Key words: high-tech bodysuits, swimsuits, coord<strong>in</strong>ation, front crawl<br />

IntroductIon<br />

The implementation of new technology <strong>in</strong> order to enhance sports performance<br />

has resulted <strong>in</strong> a range of new equipment that can be used<br />

dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competition. Most prom<strong>in</strong>ent among these advances<br />

has been the development of highly technical bodysuits purported to<br />

improve swimm<strong>in</strong>g performance.<br />

The orig<strong>in</strong>al purpose of these swimsuits was to decrease drag by<br />

mimick<strong>in</strong>g sharksk<strong>in</strong>. The latest bodysuits, however, also appear to improve<br />

buoyancy <strong>and</strong> compress body parts (Benjanuvatra et al., 2009).<br />

The body suits have been further developed through the use of particular<br />

fabric <strong>and</strong> by the manner <strong>in</strong> which the suits are sewn. Indeed, the most<br />

advanced bodysuits have no sewed parts at all.<br />

The evolution of high technology bodysuits is almost certa<strong>in</strong>ly a major<br />

factor <strong>in</strong> the recent spate of new world records <strong>in</strong> swimm<strong>in</strong>g events.<br />

As a result, questions have been raised concern<strong>in</strong>g the fabric composition<br />

<strong>and</strong> availability as well as ethical <strong>and</strong> legal issues l<strong>in</strong>ked to wear<strong>in</strong>g<br />

these suits <strong>in</strong> competitions. FINA subsequently banned the bodysuits<br />

<strong>in</strong> <strong>in</strong>door competitions from January 2010. But the suits are free to be<br />

utilized <strong>in</strong> open water <strong>and</strong> triathlon events. Furthermore, there does not<br />

exist enough research on the effects of us<strong>in</strong>g bodysuits on swimm<strong>in</strong>g<br />

performance.<br />

Spatial-temporal parameters, as well as the <strong>in</strong>dex of coord<strong>in</strong>ation<br />

proposed by Chollet et al. (2000), appear to be dependent on restrictions<br />

of the organism, the environment <strong>and</strong> the task (Seifert et al., 2007).<br />

Thus, the purpose of this study was to establish the effects of us<strong>in</strong>g a<br />

bodysuit (Blueseventy TM ) on spatial-temporal <strong>and</strong> coord<strong>in</strong>ative parameters<br />

dur<strong>in</strong>g an all-out 50m front crawl performance. Consider<strong>in</strong>g<br />

the improvement <strong>in</strong> performance (Benjanuvatra et al., 2009), <strong>in</strong>creased<br />

stroke length <strong>and</strong> swimm<strong>in</strong>g velocity <strong>and</strong> a greater cont<strong>in</strong>uity <strong>in</strong> propulsion<br />

actions (<strong>in</strong>dex of coord<strong>in</strong>ation near zero) were expected wear<strong>in</strong>g<br />

the bodysuit.<br />

Methods<br />

Subjects: Six subjects, each competitive at Brazilian age group national<br />

level, took part <strong>in</strong> this <strong>in</strong>vestigation (age: 16.6 ± 2.0 yrs; body mass: 67.8<br />

± 5.9 kg). All participants signed a consent form prior to which the aims,<br />

risks <strong>and</strong> procedures associated with this trial had been fully expla<strong>in</strong>ed.<br />

The sample size was limited by the Blueseventy TM bodysuits availability.<br />

Trials: The subjects performed two all-out 50m trials <strong>in</strong> a 25 <strong>in</strong>door<br />

pool, start<strong>in</strong>g <strong>in</strong> the pool. One trial was performed with an ord<strong>in</strong>ary<br />

165


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

suit (short made by Lycra) <strong>and</strong> one us<strong>in</strong>g a BlueseventyTM bodysuit that<br />

covered from the shoulders to the ankles. The order of the trials was<br />

r<strong>and</strong>omized <strong>and</strong> the subjects rested for 20 m<strong>in</strong> between the trials. The<br />

subjects used their own bodysuits dur<strong>in</strong>g the trials.<br />

Video sampl<strong>in</strong>g <strong>and</strong> analysis: Two synchronized sub-aquatic video<br />

cameras (SANYO VPC-WH1), operat<strong>in</strong>g at 30 Hz, were used to acquire<br />

images <strong>in</strong> the sagittal plane of the swimmers. The cameras were<br />

positioned on the lateral sides of the pool <strong>and</strong> were carried manually<br />

us<strong>in</strong>g chariots on rails. To determ<strong>in</strong>e the stroke phases, two experienced<br />

researchers made a frame-by-frame analysis as reported before by Chollet<br />

et al. (2000) us<strong>in</strong>g the software VirtualDub v1.8.7.<br />

A third <strong>in</strong>dependent video camera operat<strong>in</strong>g at 25 Hz ( JVC, GR-<br />

DVL9800) was positioned 4 m above the water surface <strong>in</strong> the middle<br />

of the pool deck to measure race parameters. This camera allowed us to<br />

quantify swimm<strong>in</strong>g speed <strong>and</strong> stroke rate, from which stroke length was<br />

calculated. The analysis of the images was performed with the software<br />

Dgeme v.1.0.<br />

Index of coord<strong>in</strong>ation <strong>and</strong> arm stroke phases: Index of coord<strong>in</strong>ation<br />

(IdC) was taken to represent arm coord<strong>in</strong>ation, as proposed by Chollet<br />

et al. (2000). The <strong>in</strong>dex of coord<strong>in</strong>ation was expressed as a percentage of<br />

the duration of one arm stroke <strong>and</strong> represents the time between the end<br />

of propulsive action of one arm <strong>and</strong> the beg<strong>in</strong>n<strong>in</strong>g of propulsion with<br />

the other arm, consider<strong>in</strong>g the mean of both the right <strong>and</strong> left arms.<br />

Therefore it is possible to quantify a catch-up (IdC < 0%), an opposition<br />

(IdC = 0%) or a superposition coord<strong>in</strong>ation mode (IdC > 0%).<br />

The duration of the stroke phases were expressed <strong>in</strong> absolute values<br />

(s), divided <strong>in</strong>to four phases: (1) entry <strong>and</strong> catch: from the entry of the<br />

h<strong>and</strong> <strong>in</strong>to the water to the moment prior to the beg<strong>in</strong>n<strong>in</strong>g of its backwards<br />

movement relative to the body, (2) the pull: from the beg<strong>in</strong>n<strong>in</strong>g<br />

of h<strong>and</strong>’s backwards movement until the moment where the h<strong>and</strong> is<br />

<strong>in</strong> a plane vertical to the shoulder, (3) the push: from the po<strong>in</strong>t where<br />

the h<strong>and</strong> is below the shoulder until its release from the water <strong>and</strong> (4)<br />

the recovery: from the po<strong>in</strong>t of water release to the h<strong>and</strong> re-entry <strong>in</strong>to<br />

the water. The pull <strong>and</strong> push phases were considered the propulsive<br />

ones <strong>and</strong> the entry <strong>and</strong> catch <strong>and</strong> the recovery were considered the nonpropulsive<br />

phases of the stroke.<br />

Mean, st<strong>and</strong>ard error <strong>and</strong> deviation, normality <strong>and</strong> sphericity were<br />

calculated <strong>and</strong> verified for all the analyzed variables. To verify the effects<br />

of the bodysuit <strong>and</strong> the split of the trial (first or second 25 m split) on<br />

selected variables, a repeated measures ANOVA was performed (mixed<br />

model 2 x 2 – two suits <strong>and</strong> two 25 m splits), with ma<strong>in</strong> effects verified<br />

us<strong>in</strong>g LSD post-hoc. For the stroke phases where there was an <strong>in</strong>teraction<br />

between the split <strong>and</strong> suit condition, the Student-t test for paired<br />

samples was used. The level of significance was set at 95% (p


the ankles dur<strong>in</strong>g 25 to 800 m all-out trials. It is likely that the larger<br />

<strong>in</strong>crease <strong>in</strong> speed found <strong>in</strong> our study is due to the fabric composition<br />

of the suits from Bluesevnty TM , made of 75% nylon <strong>and</strong> 25% PU-CR<br />

(polyurethane that improves buoyancy), <strong>in</strong> contrary to the polyester <strong>and</strong><br />

lycra composition of the FastSk<strong>in</strong> TM .<br />

Parsons <strong>and</strong> Day (1986) <strong>and</strong> Corda<strong>in</strong> <strong>and</strong> Kopriva (1991) analyzed<br />

the effects of wetsuits, allowed <strong>in</strong> triathlon competitions <strong>and</strong> made of<br />

low-density material, which is similar to the bodysuits analyzed <strong>in</strong> our<br />

study. The authors suggested that the performance enhancement was directly<br />

related to the improved buoyancy offered by the suit. Accord<strong>in</strong>g to<br />

Benjanuvatra et al. (2002), improved buoyancy allows a smaller energetic<br />

cost to susta<strong>in</strong> an optimal body position, <strong>and</strong> therefore greater force can<br />

be applied on generat<strong>in</strong>g propulsion.<br />

In the present study, the <strong>in</strong>crease <strong>in</strong> speed was due to an <strong>in</strong>crease <strong>in</strong><br />

stroke length, s<strong>in</strong>ce there was no difference <strong>in</strong> the stroke rate when us<strong>in</strong>g<br />

the bodysuit. Roberts et al. (2003) found similar results when compar<strong>in</strong>g<br />

front crawl swimm<strong>in</strong>g us<strong>in</strong>g the Speedo Fastsk<strong>in</strong> TM to ord<strong>in</strong>ary suits.<br />

These authors, however, analyzed sub-maximal swimm<strong>in</strong>g <strong>in</strong>tensities.<br />

Chatard <strong>and</strong> Wilson (2008) found a significant decrease of the energetic<br />

cost associated with an <strong>in</strong>crease of the stroke length when us<strong>in</strong>g<br />

the Fastsk<strong>in</strong> TM body suit, which means improved swimm<strong>in</strong>g economy.<br />

Our subjects showed a shorter duration of the entry <strong>and</strong> catch phase<br />

dur<strong>in</strong>g the second split of the trial when us<strong>in</strong>g the bodysuits, result<strong>in</strong>g<br />

<strong>in</strong> a significant decrease <strong>in</strong> the duration of the non-propulsive stroke<br />

phase. This result took us to believe <strong>in</strong> a possible <strong>in</strong>fluence on the <strong>in</strong>dex<br />

of coord<strong>in</strong>ation, which was not confirmed. This result is <strong>in</strong> accordance<br />

with the ones presented by Hue et al. (2003) who found differences <strong>in</strong><br />

the <strong>in</strong>dex of coord<strong>in</strong>ation when us<strong>in</strong>g a triathlon wetsuit only when analyz<strong>in</strong>g<br />

long distance races, with no differences found dur<strong>in</strong>g swimm<strong>in</strong>g<br />

at velocities similar to the 100 m <strong>and</strong> 50 m races.<br />

Analyz<strong>in</strong>g the subjects <strong>in</strong>dividually, five subjects showed a similar<br />

<strong>in</strong>dex of coord<strong>in</strong>ation on both suit situations <strong>and</strong> one subject showed<br />

a greater cont<strong>in</strong>uity between the propulsive actions dur<strong>in</strong>g the first 25<br />

m split. Dur<strong>in</strong>g the second split four out of the six subjects showed a<br />

greater cont<strong>in</strong>uity of the propulsive phases us<strong>in</strong>g the suit <strong>and</strong> the other<br />

two did not change their <strong>in</strong>dex of coord<strong>in</strong>ation values. This suggests that<br />

the suit may have a greater <strong>in</strong>fluence on technique dur<strong>in</strong>g the f<strong>in</strong>al portion<br />

of the race.<br />

S<strong>in</strong>ce the suit did not <strong>in</strong>terfere with the duration of the propulsive<br />

phase of the stroke, the greater stroke length is probably as a result<br />

of more effective force application dur<strong>in</strong>g the phase probably due<br />

to a decrease <strong>in</strong> drag. The propulsive effectiveness is dependent on the<br />

comb<strong>in</strong>ation of a high displacement speed of the h<strong>and</strong> <strong>and</strong> its adequate<br />

trajectory dur<strong>in</strong>g the propulsive phase, generat<strong>in</strong>g higher peak forces<br />

(Toussa<strong>in</strong>t & Beek, 1992).<br />

It was not possible to evaluate the body compression caused by the<br />

suit, if any, <strong>and</strong> this is a limitation of this study. However, the subjects<br />

reported difficulties to put on the suits, tak<strong>in</strong>g a long time dress them<br />

properly. Ka<strong>in</strong>uma (2009) suggests that the compression of the LZR<br />

Racer TM from Speedo, can modify the physiological systems by an alternative<br />

mechanism, where the compression would affect the blood circulation,<br />

forc<strong>in</strong>g the use of anaerobic-glycolitic pathways. This would <strong>in</strong><br />

turn enable an <strong>in</strong>stantaneous <strong>in</strong>crement <strong>in</strong> force generation, which could<br />

have some <strong>in</strong>fluence on short distance, more high-speed races.<br />

Even though we r<strong>and</strong>omized the tests order <strong>and</strong> tried to verbally<br />

stimulate the athletes the same way on both trials, a possible placebo<br />

effect could not be controlled for.<br />

conclusIon<br />

Wear<strong>in</strong>g a full bodysuit, cover<strong>in</strong>g from the shoulders to the ankles, from<br />

Blueseventy TM , significantly improves the swimm<strong>in</strong>g speed dur<strong>in</strong>g an<br />

all-out 50 m front crawl swimm<strong>in</strong>g trial, mostly on the second half of<br />

the test. When wear<strong>in</strong>g the suits, the subjects showed a greater stroke<br />

length dur<strong>in</strong>g both 25 m splits <strong>and</strong> shorter duration of the non-propulsive<br />

phase of the arm stroke dur<strong>in</strong>g the second half of the test.<br />

chaPter2.<strong>Biomechanics</strong><br />

reFerences<br />

Benjanuvatra, N., Dawson, G., Blanksby, B.A., Elliott, B.C. (2002).<br />

Comparison of buoyancy, passive <strong>and</strong> net active drag forces between<br />

Fastsk<strong>in</strong> TM <strong>and</strong> st<strong>and</strong>ard swimsuits. J Sci Med Sport, 5(2):115-123.<br />

Chatard, J.C., Wilson, B. (2008). Effect of Fastsk<strong>in</strong> Suits on Performance,<br />

Drag, <strong>and</strong> Energy Cost of Swimm<strong>in</strong>g. Med Sci Sports Exerc,<br />

40(6): 1149-1154.<br />

Chollet, D., Chalies, S., Chatard, J.C. (2000). A new <strong>in</strong>dex of coord<strong>in</strong>ation<br />

for the crawl: description <strong>and</strong> usefulness. Int J Sports Med, 21(1):<br />

54-59.<br />

Corda<strong>in</strong>, L., Kopriva, R. (1991). Wet suits, body density <strong>and</strong> swimm<strong>in</strong>g<br />

performance. Br J Sports Med, 25: 31-33.<br />

Hue, O., Benavente, H., Chollet, D. (2003). The effect of wetsuit use by<br />

triathletes: An analysis of the different phases of arm movement. J<br />

Sports Sci, 21(12): 1025-1030.<br />

Ka<strong>in</strong>uma, E., Watanebe, M., Chikako, T.M., Inoue, M., Kuwano, Y.,<br />

Ren, H.W., Abo, T. (2009). Proposal of alternative mechanism responsible<br />

for the function of high-speed swimsuits. Biomed Res,<br />

30(1): 69-70.<br />

Mollendorf, J.C., Term<strong>in</strong>, A.C., Oppenheim, E., Pendergast, D.R.<br />

(2004). Effect of swim suit design on passive drag. Med Sci Sports<br />

Exerc, 36(6): 1029-1035.<br />

Parsons, L., Day, S.J. (1986). Do wet suit affect swimm<strong>in</strong>g speed? Br J<br />

Sports Med, 20: 129-131.<br />

Roberts, B.S., Kamel, K.S., Hedrick, C.E., McLean, S.P., Sharp, R.L.<br />

(2003). Effect of a fastsk<strong>in</strong> suit on submaximal freestyle swimm<strong>in</strong>g.<br />

Med Sci Sports Exerc, 35(3): 519-524.<br />

Seifert, L., Chollet, D., Rouard, A. (2007). Swimm<strong>in</strong>g constra<strong>in</strong>ts <strong>and</strong><br />

arm coord<strong>in</strong>ation. Hum Mov Sci, 26(1): 68-86.<br />

Toussa<strong>in</strong>t, H.M., Beek, P.J. (1992). <strong>Biomechanics</strong> of competitive front<br />

crawl swimm<strong>in</strong>g. Sports Med, 13(1): 08-24.<br />

AcKnoWledGeMents<br />

The authors want to express their gratitude to the athletes <strong>and</strong> coaches<br />

from Grêmio Náutico União, for the contribution <strong>in</strong> this study, <strong>and</strong> to<br />

Aquatic Sports Research group for their cooperation.<br />

167


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Fatigue Analysis of 100 Meters All-Out Front<br />

Crawl Us<strong>in</strong>g Surface EMG<br />

stirn, I. 1 , Jarm, t. 2 , Kapus, V. 1 , strojnik, V. 1<br />

1University of Ljubljana, Faculty of sports, Ljubljana, Slovenija<br />

2University of Ljubljana, Faculty of Electrical Eng<strong>in</strong>eer<strong>in</strong>g, Ljubljana,<br />

Slovenia<br />

The aim of the study was to estimate fatigue <strong>in</strong> arm propell<strong>in</strong>g muscles<br />

by analyz<strong>in</strong>g electromyographic (EMG) signal. Eleven male competitive<br />

swimmers performed a 100 meters all-out front crawl. Trials were<br />

recorded to obta<strong>in</strong> k<strong>in</strong>ematical data, lactate concentration after the<br />

swims were measured. EMG signals of latissimus dorsi (LD), pectoralis<br />

major (PM) <strong>and</strong> triceps brachii (TB) were recorded, also. Average lactate<br />

concentration was 14.1 ± 2.93 mmol.l -1 . Stroke length, stroke rate<br />

<strong>and</strong> swimm<strong>in</strong>g speed decreased. The EMG amplitude (ARV) for the<br />

lower part of LD <strong>and</strong> for TB <strong>in</strong>creased <strong>and</strong> the mean frequency (MNF)<br />

decreased for 20.5 ± 9.1 to 24.6 ± 8.4 % for all muscles under observation<br />

(P


ARV value of the fitted curve at the time of the first <strong>and</strong> the last stroke<br />

were computed. For the frequency analysis mean frequency (MNF) was<br />

calculated. The values of MNF were plotted as a function of time. L<strong>in</strong>ear<br />

regression analysis was applied to obta<strong>in</strong> the <strong>in</strong>itial value (the value of<br />

MNF at the time of the first stroke) <strong>and</strong> the f<strong>in</strong>al value (the value of<br />

MNF at the time of the last stroke), labelled MNF Sbeg <strong>and</strong> MNF Send respectively.<br />

In order to normalize results between subjects the f<strong>in</strong>al values<br />

were expressed as a percentage of the <strong>in</strong>itial values <strong>and</strong> labelled MNF n.<br />

Descriptive statistics <strong>and</strong> repeated measures ANOVA, with subsequent<br />

Tukey’s test for post-hoc analysis were used for multiple comparisons<br />

between the groups.<br />

results<br />

The average blood lactate values collected before <strong>and</strong> 1, 3 <strong>and</strong> 5 m<strong>in</strong>utes<br />

after the swim were 1.8 ± 0.6, 6.7 ± 1.47, 12.7 ± 2.2 <strong>and</strong> 14.1 ±<br />

2.93 mmol.l -1 respectively. The highest lactate value collected was 17.7<br />

mmol.l -1 .<br />

Stroke rate (SR), stroke length (SL) <strong>and</strong> SS (S) are shown <strong>in</strong> Table 1<br />

Table 1. Stroke length (SL), stroke rate (SR) <strong>and</strong> swimm<strong>in</strong>g speed SS<br />

(S)<br />

SL(m) SR(stroke*m<strong>in</strong>-1 ) S(m/s)<br />

Distance (m) av. SD av. SD av. SD<br />

25 2.00 0.13 50.56 4.15 1.68 0.08<br />

50 2.02 0.16 47.12 5.33 1.58 0.09<br />

75 1.94 0.14 46.32 4.54 1.49 0.06<br />

100 1.89 0.18 45.77 4.71 1.43 0.08<br />

The ARV calculated for LD2 <strong>and</strong> TB <strong>in</strong>creased significantly at the end<br />

of the swimm<strong>in</strong>g with respect to the beg<strong>in</strong>n<strong>in</strong>g of swimm<strong>in</strong>g as shown<br />

<strong>in</strong> Figure 2, left.<br />

Fig.2. Left: Comparison of the amplitude (ARV) of the EMG signal at<br />

the beg<strong>in</strong>n<strong>in</strong>g <strong>and</strong> the end of 100 m all-out swim. Right: Mean MNF<br />

values with SD of MNF Sbeg <strong>and</strong> MNF Send for all muscles *p < 0.05.<br />

The differences between the MNF Sbeg <strong>and</strong> the MNF Send , were significant<br />

for all muscles (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

conclusIon<br />

By us<strong>in</strong>g EMG amplitude <strong>and</strong> frequency analysis, the progression of<br />

muscle fatigue <strong>in</strong> arm propell<strong>in</strong>g muscles was clearly detected. No differences<br />

<strong>in</strong> the relative decrease of MNF between the muscles under<br />

observation were found. This suggests that these muscles fatigued to<br />

approximately the same extent dur<strong>in</strong>g all-out crawl, which may present<br />

significant <strong>in</strong>formation for the coaches <strong>in</strong> order to plan strength<br />

workouts.<br />

reFerences<br />

Aspenes, S., Kjendlie, P.L., Hoff, J., & Helgerud, J. (2009). Comb<strong>in</strong>ed<br />

strength <strong>and</strong> endurance tra<strong>in</strong><strong>in</strong>g <strong>in</strong> competitive swimmers. J Sports<br />

Sci Med 8, 357-365.<br />

Aujouannet, Y.A., Bonifazi, M., H<strong>in</strong>tzy, F., Vuillerme, N., & Rouard,<br />

A.H. (2006). Effects of a high-<strong>in</strong>tensity swim test on k<strong>in</strong>ematic parameters<br />

<strong>in</strong> high-level athletes. Appl Physiol Nutr Metabol 31:150-158.<br />

Bonifazi, M., Martelli, G., Marugo, L., Sardela, F., & Carli, G.(1993).<br />

Blood lactate acumulation <strong>in</strong> top level swimmers follow<strong>in</strong>g competition.<br />

J Sports Med Phys Fitness, 33(1) 13-18.<br />

Caty, V.Y., Rouard, A.H., H<strong>in</strong>tzy, F., Aujouannet, Y.A., Mol<strong>in</strong>ari, F.,<br />

& Knaflitz, M.(2006).Time-frequency parameters of wrist muscles<br />

EMG after an exhaustive freestyle test. Revista Portuguesa de Ciencias<br />

do Desporto 6:28-30.<br />

Clarys, J. P., Massez, C., Van der Broeck, M., Piette, G., & Robeaux,<br />

R.(1983). Total Telemetric Surface EMG of the Front Crawl. International<br />

Series on <strong>Biomechanics</strong> 5, 4A, p.p. 951-959. Human K<strong>in</strong>etics<br />

Publishers.<br />

Girold, S., Calmels, P., Maur<strong>in</strong>, D., Milhau, N., & Chatard, J.C. (2006).<br />

Assisted <strong>and</strong> resisted spr<strong>in</strong>t tra<strong>in</strong><strong>in</strong>g <strong>in</strong> swimm<strong>in</strong>g. J Strength Condit<br />

Res 20(3),547-554.<br />

Havriluk, R. (2004). H<strong>and</strong> force <strong>and</strong> swimm<strong>in</strong>g velocity. In: XVth Federation<br />

Internationale de Natation World Congress. Indianapolis. http://<br />

swimm<strong>in</strong>gtechnology.com/FINA2004.htm<br />

Kesk<strong>in</strong>en, K.L., & Komi, P.V. (1993). Strok<strong>in</strong>g characteristics of front<br />

crawl swimm<strong>in</strong>g dur<strong>in</strong>g exercise. J Appl Biomech 9:219–226.<br />

Maglischo, E. W. (2003). Swimm<strong>in</strong>g fastest. Champa<strong>in</strong>, IL: Human k<strong>in</strong>etics.<br />

Merletti, R., Lo Conte, R., & Orizio, C. (1991). Indices of muscle fatigue.<br />

J Electromyogr K<strong>in</strong>esiol 1:20-33.<br />

Miyashita, M. (1975). Arm action <strong>in</strong> the crawl stroke. In Lewillie L,<br />

Clarys JP (ed) Swimm<strong>in</strong>g II University Park Press, Baltimore, 167–<br />

173.<br />

Rouard, A.H., Billat, R.P., Deschodt, V., & Clarys, J.P. (1997) Muscular<br />

activations dur<strong>in</strong>g repetitions of scull<strong>in</strong>g movements up to exhaustion<br />

<strong>in</strong> swimm<strong>in</strong>g. Arch Physiol Biochem 105:655-662.<br />

Rouard, A.H., Schleihauf, R.E., & Troup, J.P. (1996). H<strong>and</strong> forces <strong>and</strong><br />

phases <strong>in</strong> freestyle stroke. In: Troup JP, Holl<strong>and</strong>er AP, Strasse D,<br />

Trappe SW, Cappaert JM, Trappe TA (ed) <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> swimm<strong>in</strong>g VII, Chapman & Hall, London, UK, 34-42.<br />

Seifert, L., Chollet, D., & Chatard, J.C. (2008) K<strong>in</strong>ematic changes dur<strong>in</strong>g<br />

a 100-m front crawl: effects of performance level <strong>and</strong> gender. Med<br />

Sci Sports Exerc 40(3):591.<br />

Schleihauf,R.E. (1979). A hydrodynamic analysis of swimm<strong>in</strong>g propulsion.<br />

In: Teraud J, Bed<strong>in</strong>gfield EW (eds) Swimm<strong>in</strong>g III, International<br />

Series of Sport Sciences. University Park Press, BaltimoreSeifert L,<br />

Chollet D, Chatard JC (2008) K<strong>in</strong>ematic changes dur<strong>in</strong>g a 100-m<br />

front crawl: effects of performance level <strong>and</strong> gender. <strong>Medic<strong>in</strong>e</strong> & Science<br />

<strong>in</strong> Sports & Exercise 40(3):591.<br />

Toussa<strong>in</strong>t, H.M., Carol, A., Kranenborg, H., & Truijens, M.J. (2006).<br />

Effect of fatigue on strok<strong>in</strong>g characteristics <strong>in</strong> an arms-only 100-m<br />

front-crawl race. Medic Sci Sports Exerc 38:1635-42.<br />

Wakayoshi, K., Moritani, T., Mutoh, Y., Miyashita, M. (1994). Electromyographic<br />

evidence of selective muscle fatigue dur<strong>in</strong>g competitive<br />

swimm<strong>in</strong>g. In: Miyashita M, Mutoh Y, Richardson AB (eds) <strong>Medic<strong>in</strong>e</strong><br />

<strong>and</strong> Sport Science 39:16-23.<br />

170<br />

Comparison Among Three Types of Relay Starts <strong>in</strong><br />

Competitive Swimm<strong>in</strong>g<br />

takeda, t. 1 , takagi, h. 1 , tsubakimoto, s. 1<br />

1 University of Tsukuba, Tsukuba, JAPAN<br />

The purpose of the present study was to evaluate the effectiveness of<br />

no-step, s<strong>in</strong>gle-step <strong>and</strong> double-step relay starts for swimmers. Eight<br />

male collegiate swimmers participated <strong>in</strong> the present study. For each<br />

type of start, each swimmer performed six trials of relay starts with maximum<br />

effort. Ground reaction forces were measured us<strong>in</strong>g a Kistler<br />

force plate to calculate the take-off velocity <strong>and</strong> take-off angle<br />

from the force data. Relay times were measured by count<strong>in</strong>g the<br />

number of video frames obta<strong>in</strong>ed by a high-speed camera. No<br />

significant difference <strong>in</strong> the horizontal take-off velocity was observed.<br />

The relay times decreased significantly <strong>in</strong> the order nostep,<br />

s<strong>in</strong>gle-step <strong>and</strong> double-step starts (P < 0.05). Eight trials<br />

among all the trials for the step starts resulted <strong>in</strong> <strong>in</strong>correct foot<br />

placement on the edge of the block. No-step starts resulted <strong>in</strong><br />

better performance than step starts.<br />

Key words: step start, relay time, performance<br />

IntroductIon<br />

In relay events, it is possible to record a time on the start<strong>in</strong>g block (block<br />

time) of zero second. The block time is the time that elapses between<br />

the <strong>in</strong>stant at which the start signal is given <strong>and</strong> the <strong>in</strong>stant at which<br />

the swimmer’s foot leaves the start<strong>in</strong>g block. In relay events, the first<br />

swimmer beg<strong>in</strong>s the race when the start signal is given, <strong>and</strong> swimmers<br />

to follow start after the previous swimmer has reached his or her f<strong>in</strong>ish<strong>in</strong>g<br />

po<strong>in</strong>t. Therefore, the time on the block of the swimmers to follow<br />

should ideally correspond to the <strong>in</strong>stant at which the previous swimmer<br />

reaches his or her f<strong>in</strong>ish<strong>in</strong>g po<strong>in</strong>t. The block time of an <strong>in</strong>dividual <strong>in</strong><br />

regular events ranges from approximately 0.6 to 0.8 s, as reported <strong>in</strong><br />

previous studies (Issur<strong>in</strong> & Verbitsky 2003, Takeda & Nomura 2006).<br />

The results of relay events depend upon the technique adopted while<br />

chang<strong>in</strong>g swimmers dur<strong>in</strong>g a relay. The sum of the block times <strong>in</strong> the<br />

three changeover swimmers represents approximately 2.4 s.<br />

There are two k<strong>in</strong>ds of start<strong>in</strong>g techniques <strong>in</strong> relay events. Their<br />

starts generate greater horizontal velocity upon take-off from the start<strong>in</strong>g<br />

block (McLean et al. 2000). The sw<strong>in</strong>g start <strong>in</strong>volves the sw<strong>in</strong>g of<br />

an arm. On the other h<strong>and</strong>, the step start <strong>in</strong>volves tak<strong>in</strong>g one or two<br />

steps before jump<strong>in</strong>g with both feet from the block. There have been a<br />

few studies on relay starts (Gambrel et al. 1991, McLean et al. 2000).<br />

McLean et al. (2000) <strong>in</strong>vestigated the effectiveness of step starts <strong>in</strong> the<br />

case of collegiate male swimmers who were given <strong>in</strong>struction on step<br />

starts over a four-week period. These researchers reported that step starts<br />

were effective relay starts. However, they did not consider the relay time<br />

when evaluat<strong>in</strong>g the start performance.<br />

The step start is considered a more difficult technique than a start<br />

<strong>in</strong>volv<strong>in</strong>g no steps (no-step start) because swimmers often place their<br />

foot on the edge of the start<strong>in</strong>g block by mistake. The swimmer cannot<br />

generate satisfactory horizontal velocity on the block if the foot placement<br />

is <strong>in</strong>correct. It is necessary to determ<strong>in</strong>e the best relay start by<br />

tak<strong>in</strong>g <strong>in</strong>to consideration the time taken to change swimmers dur<strong>in</strong>g the<br />

relay <strong>and</strong> the difficulty each swimmer faces <strong>in</strong> the step start. The purpose<br />

of the present study was to evaluate the effectiveness of the three types<br />

of relay starts <strong>in</strong> order to determ<strong>in</strong>e the relay start performance while<br />

consider<strong>in</strong>g the relay time <strong>and</strong> the difficulty faced dur<strong>in</strong>g step starts.<br />

Methods<br />

Eight well-tra<strong>in</strong>ed male college swimmers participated <strong>in</strong> this study.<br />

Their mean height, mean body weight <strong>and</strong> mean age were 177.9 ± 5.7


cm, 73.1 ± 6.4 kg <strong>and</strong> 20 ± 1.2 years, respectively. Before the experiment<br />

began, each swimmer received <strong>in</strong>struction on the no-step start <strong>and</strong> two<br />

types of step starts over a two-weeks; this was achieved by conduct<strong>in</strong>g<br />

daily tra<strong>in</strong><strong>in</strong>g sessions. In each trial of a relay start, swimmers were permitted<br />

to sw<strong>in</strong>g their arms <strong>and</strong> to perform counter-movement.<br />

In the trial, we select three relay starts: a no-step start (NS), s<strong>in</strong>glestep<br />

start (SS) <strong>and</strong> double-step start (DS) (Figure 1). For each start<br />

technique, each swimmer performed six trials with maximum effort; the<br />

trials were performed <strong>in</strong> r<strong>and</strong>om order. Each swimmer executed the relay<br />

start trial by tim<strong>in</strong>g it with the goal touch of the previous front crawl<br />

swimmer <strong>and</strong> then spr<strong>in</strong>ted 15 m by front crawl swimm<strong>in</strong>g.<br />

No-step start<br />

S<strong>in</strong>gle-step start start<br />

Double-step start start<br />

Figure 1. Three types of relay starts performed <strong>in</strong> this study.<br />

Two high-speed cameras (FAST-CAM PCI, Photron Inc., JAPAN)<br />

filmed the trials at 250 frames per second. Camera 1 was positioned<br />

such that its optical axes were perpendicular to the plane of motion.<br />

Camera 2 was positioned 2.5 m above the floor of the side pool deck <strong>and</strong><br />

filmed the scene at the <strong>in</strong>stant at which the <strong>in</strong>com<strong>in</strong>g swimmer touched<br />

his f<strong>in</strong>ish<strong>in</strong>g po<strong>in</strong>t <strong>and</strong> the outgo<strong>in</strong>g swimmer take-off from the start<strong>in</strong>g<br />

block. The relay time was def<strong>in</strong>ed as the time elapsed between the touch<br />

<strong>and</strong> take-off <strong>and</strong> was calculated by count<strong>in</strong>g the frames <strong>in</strong> the video image<br />

captured by Camera 2.<br />

Ground reaction forces dur<strong>in</strong>g the relay starts were sampled at 1000<br />

Hz by a waterproof force plate (5253B11, Kistler JAPAN Inc.) that was<br />

modified <strong>in</strong>to the start<strong>in</strong>g block. The force data were smoothed us<strong>in</strong>g a<br />

low-pass Butterworth digital filter with a low pass cutoff frequency of 40<br />

Hz. The velocity at take-off (take-off velocity) was calculated from the<br />

data on the ground reaction force by perform<strong>in</strong>g time <strong>in</strong>tegration until the<br />

time of take-off. The take-off angle was def<strong>in</strong>ed as the angle between the<br />

resultant take-off-velocity vector <strong>and</strong> horizontal l<strong>in</strong>e (upward direction:<br />

positive; downward direction: negative). The horizontal ground reaction<br />

forces were used to dist<strong>in</strong>guish the forces generated by steps or the body<br />

lean<strong>in</strong>g forward <strong>and</strong> the legs driv<strong>in</strong>g out. The force generated by legs driv<strong>in</strong>g<br />

forward was def<strong>in</strong>ed as the force after the time (t 1 ) when the horizontal<br />

ground reaction force reached over 30% of body weight. The force before<br />

t 1 was obta<strong>in</strong>ed was def<strong>in</strong>ed as the force by step or body lean<strong>in</strong>g forward<br />

(Figure 2). The horizontal reaction force generated by the legs driv<strong>in</strong>g was<br />

<strong>in</strong>tegrated with respect to time, <strong>and</strong> this value was used to calculate the velocity<br />

generated by the legs driv<strong>in</strong>g. A one-way repeated measure ANOVA<br />

was performed for the start type; this was followed by Bonferroni multiple<br />

comparison <strong>in</strong> each variable. The statistical significance was set at P < 0.05.<br />

Ground reaction force [N]<br />

Vertical<br />

+<br />

chaPter2.<strong>Biomechanics</strong><br />

horizontal<br />

+<br />

1400<br />

1200<br />

1000<br />

800<br />

Horizontal component<br />

600<br />

Force by<br />

400<br />

200<br />

0<br />

30% of subject’s body weght<br />

legs driv<strong>in</strong>g<br />

-200<br />

t1 -1.4 -1.3 -1.2 -1.1 -1 -0.9 -0.8 -0.7 -0.6 -0.5 -0.4 -0.3 -0.2 -0.1<br />

Time [sec]<br />

0<br />

Figure 2. The def<strong>in</strong>ition of the horizontal ground reaction force generated<br />

by tak<strong>in</strong>g steps <strong>and</strong> lean<strong>in</strong>g forward <strong>and</strong> the force generated by the<br />

legs driv<strong>in</strong>g.<br />

results<br />

Table 1 lists the mean horizontal take-off velocity, take-off angle <strong>and</strong> relay<br />

time <strong>in</strong> each trial. The relay times were <strong>in</strong>creased significantly <strong>in</strong> order of<br />

no-step start, s<strong>in</strong>gle-step start <strong>and</strong> double-step start. The horizontal velocity<br />

generated by legs driv<strong>in</strong>g <strong>in</strong> the no-step start was significantly greater<br />

than that <strong>in</strong> the double-step start. There was no significant difference <strong>in</strong><br />

the horizontal take-off velocity <strong>and</strong> take-off angle. Table 2 lists the mean<br />

values of the st<strong>and</strong>ard deviation <strong>in</strong> the six trials for each condition.<br />

Table 1. Mean values of horizontal take-off velocity, horizontal velocity<br />

by legs driv<strong>in</strong>g, take-off angle <strong>and</strong> relay time <strong>in</strong> each trial.<br />

Horizontal<br />

take-off velocity<br />

Horizontal<br />

velocity by legs driv<strong>in</strong>g<br />

Take-off angle Relay time<br />

(m/s) (m/s)<br />

(°)<br />

(s)<br />

No-Step 4.09 ± 0.34 3.50 ± 0.34 -11.92 ± 6.15 0.018 ± 0.029<br />

S<strong>in</strong>gle-Step 4.09 ± 0.31 3.28 ± 0.24 -13.18 ± 5.27 0.052 ± 0.044 *<br />

Double-Step 4.13 ± 0.32 3.22 ± 0.25 * -13.70 ± 4.80 0.087 ± 0.060 * †<br />

*: P < 0.05 <strong>in</strong> comparison with no-step start trials.<br />

†: P < 0.05 <strong>in</strong> comparison with s<strong>in</strong>gle-step start trials.<br />

Table 2. Mean st<strong>and</strong>ard deviations of horizontal take-off velocity, horizontal<br />

velocity generated by legs driv<strong>in</strong>g, take-off angle <strong>and</strong> relay time<br />

<strong>in</strong> each trial.<br />

Horizontal<br />

take-off velocity<br />

Horizontal<br />

velocity by legs driv<strong>in</strong>g<br />

Take-off angle Relay time<br />

(m/s) (m/s)<br />

(°)<br />

(s)<br />

No-Step 0.15 ± 0.08 0.10 ± 0.05 2.17 ± 1.58 0.054 ± 0.023<br />

S<strong>in</strong>gle-Step 0.25 ± 0.09 0.15 ± 0.05 2.11 ± 0.59 0.075 ± 0.031<br />

Double-Step 0.23 ± 0.09 0.13 ± 0.03 2.25 ± 1.08 0.077 ± 0.035<br />

Figure 3 shows the changes <strong>in</strong> the ground reaction force until take-off,<br />

as a typical example for Sub. A. Similar patterns were observed when the<br />

three trials <strong>in</strong>volv<strong>in</strong>g the other subjects were compared. For all subjects,<br />

there were a total of eight trials for each step start.<br />

dIscussIon<br />

McLean et al. (2000) reported that the horizontal take-off velocity after<br />

the double-step start was significantly greater than that after the no-step<br />

start. Our hypothesis was similar to the results of McLean’s study. However,<br />

there was no significant difference among the horizontal take-off<br />

velocities achieved by the three relay start techniques (see Table 1). The<br />

advantage of step starts is that horizontal forces are generated until the<br />

legs driv<strong>in</strong>g (See Figure 3). No-step starts were superior to step starts<br />

<strong>in</strong> terms of the horizontal force generated by the legs driv<strong>in</strong>g. The horizontal<br />

velocity generated by legs driv<strong>in</strong>g <strong>in</strong> the no-step start was significantly<br />

greater than that <strong>in</strong> the double-step start. In the step start, the<br />

swimmers had greater horizontal velocities before the legs started driv<strong>in</strong>g.<br />

It was difficult for the swimmer to generate a large horizontal force<br />

dur<strong>in</strong>g the leg drive <strong>in</strong> the step starts. In addition, the time required for<br />

the legs to drive decreased because the swimmer was already mov<strong>in</strong>g<br />

forward with a greater velocity before the legs began driv<strong>in</strong>g.<br />

171


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The mean values of the st<strong>and</strong>ard deviations for each trial were small.<br />

Participants <strong>in</strong> the present study adopted an effective technique <strong>in</strong> relay<br />

starts. Although there were significant differences <strong>in</strong> the relay times,<br />

these differences were not very large. They may be related to the time<br />

elapsed dur<strong>in</strong>g the step start until take-off, because the step starts <strong>in</strong>volve<br />

a greater number of movements associated with stepp<strong>in</strong>g to the<br />

edge, adjust<strong>in</strong>g the foot placement on the edge, <strong>and</strong> jump<strong>in</strong>g <strong>in</strong>to the<br />

pool. In eight trials among all the trials for all starts, the foot placement<br />

was <strong>in</strong>correct. This <strong>in</strong>dicates that the degree of difficulty of the step<br />

start is higher than that of the no-step start. Therefore, the no-step start<br />

is better for achiev<strong>in</strong>g consistent <strong>and</strong> superior performance <strong>in</strong> an relay<br />

event with<strong>in</strong> actual competition..<br />

However, a step start may help achieve greater horizontal take-off<br />

velocities. Swimmers should apply the technique aimed at generat<strong>in</strong>g a<br />

greater horizontal force with<strong>in</strong> a shorter duration of leg driv<strong>in</strong>g It is also<br />

advantageous to achieve a certa<strong>in</strong> amount of horizontal velocity by stepp<strong>in</strong>g,<br />

improve the accuracy while plac<strong>in</strong>g both feet <strong>and</strong> to achieve grip<br />

by us<strong>in</strong>g both feet correctly on the edge of start<strong>in</strong>g block.<br />

Force [N]<br />

172<br />

NS<br />

SS<br />

DS<br />

1400<br />

1200<br />

1000<br />

800<br />

Horizontal component<br />

600<br />

No-Step No-Step<br />

400<br />

S<strong>in</strong>gle-Step<br />

200<br />

0<br />

-200<br />

1400<br />

Double-Step<br />

1200<br />

1000<br />

800<br />

600<br />

400<br />

200<br />

0<br />

-200<br />

Vertical component<br />

-1.4 -1.2 -1 -0.8 -0.6 -0.4 -0.2 0<br />

Time [sec]<br />

Figure 3. Changes <strong>in</strong> ground reaction force until take-off, as a typical example<br />

for Sub. A. For the no-step start, the horizontal take-off velocity<br />

was 4.92 m/s <strong>and</strong> the take-off angle was -10.8°. For the s<strong>in</strong>gle-step start,<br />

the horizontal take-off velocity was 4.89 m/s <strong>and</strong> the take-off angle was<br />

-12.0°. For the double-step start, the horizontal take-off velocity was<br />

4.92 m/s <strong>and</strong> the take-off angle was -15.5°.<br />

conclusIon<br />

The take-off velocity generated by the step start was not higher than that<br />

achieved by the no-step start. In step starts, the time required to change<br />

swimmers <strong>in</strong> a relay was significantly longer than that <strong>in</strong> no-step starts<br />

<strong>and</strong> there were eight failed trials (SS, DS). Therefore, the no-step start is<br />

better than the step start s<strong>in</strong>ce it helps achieve consistent <strong>and</strong> superior<br />

relay start performance.<br />

reFFerences<br />

Gambrel DW, Blanke D, Thigp<strong>in</strong> K, Mellion M. (1991). A Biomehanical<br />

comparison of two relay starts <strong>in</strong> swimm<strong>in</strong>g. The Journal of Swimm<strong>in</strong>g<br />

Research, 7(2): 5-10.<br />

Issur<strong>in</strong> VB, Verbitsky O. (2003). Track Start vs grab Start; Evidence<br />

from the Sydney Olympic Games. Proceed<strong>in</strong>gs of the IXth World<br />

Symposium on <strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g. University<br />

of Sa<strong>in</strong>t-Etienne: 213-218.<br />

McLean SP, Holthe MJ, V<strong>in</strong>t PF, Beckett KD, H<strong>in</strong>richs RN. (2000).<br />

Addition of an approach to a swimm<strong>in</strong>g Relay Start. Journal of Applied<br />

<strong>Biomechanics</strong>, 16: 342-355.<br />

Roffer BJ (1972). The grab start is faster. Swimm<strong>in</strong>g technique, 8: 101-<br />

102.<br />

Takeda T, Nomura T. (2006). What are the differences between grab<br />

<strong>and</strong> track start? In: Vilas-Boas JP, Alves F. & Marques A. (Eds.),<br />

<strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g X. Portuguese Journal of<br />

Sport Sciences, Porto, 192-105.


A Study About the 3D Acceleration <strong>in</strong> Front Crawl<br />

<strong>and</strong> its Relation With Performance<br />

tella, V., Madera, J., colado, J.c., Mateu, J., García Massó, X.,<br />

González, l.M.<br />

Universidad de Valencia, Valencia, España<br />

The objective of this study was to analyze the acceleration of the hip<br />

generated dur<strong>in</strong>g front crawl. The swimmers (n=71) performed 25 meters<br />

at maximum speed. 3D acceleration was registered. Swimm<strong>in</strong>g time<br />

doma<strong>in</strong> acceleration signal was analysed. Root Mean Square (RMS)<br />

parameter was calculated <strong>in</strong> the three directions. Also, RMS <strong>in</strong>dexes<br />

were calculated to relate the directions <strong>in</strong> twos. The results showed differences<br />

between the different parameters. Speed correlated positively<br />

with the RMS values: anterior-posterior (X), medium-lateral (Y) <strong>and</strong><br />

superior-<strong>in</strong>ferior (Z) directions (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The velocity, as a parameter that determ<strong>in</strong>es the f<strong>in</strong>al swimm<strong>in</strong>g performance,<br />

showed a positive correlation with some of the studied statistical<br />

data of the acceleration (Table 3).<br />

Table 3. Correlation variables (r de Pearson), time doma<strong>in</strong> analysis,<br />

<strong>in</strong>dex <strong>and</strong> swimm<strong>in</strong>g velocity.<br />

v<br />

RMS z 0.51*<br />

RMS y 0.40*<br />

RMS x 0.60*<br />

IRMSX/Y 0.36*<br />

IRMSX/Z 0.43*<br />

IRMSZ/Y 0.03<br />

*p


Aquatic Space Activities – Practice Needs Theory<br />

ungerechts, B., Klauck, J².<br />

University of Bielefeld, Germany<br />

2 German Sport University Cologne, Germany<br />

Aquatic Space Activities (ASA) is a collective term for activities <strong>in</strong><br />

water such as: Competitive – Recreational – Masters swimm<strong>in</strong>g, F<strong>in</strong>swimm<strong>in</strong>g,<br />

Triathlon, Scuba-div<strong>in</strong>g or Water-exercises. ASA must obey<br />

flow physics. Traditionally, flow physics <strong>in</strong> aquatic sports is conf<strong>in</strong>ed to<br />

steady conditions assum<strong>in</strong>g that the flow velocity is constant <strong>and</strong> the<br />

body is rigid. It is not new <strong>in</strong>formation that this is not <strong>and</strong> was never the<br />

case <strong>in</strong> human swimm<strong>in</strong>g. The fact is that the limbs change motion <strong>in</strong><br />

all ASA which causes unsteady flow conditions. Unsteady flow dem<strong>and</strong>s<br />

closer consideration of water-motion <strong>in</strong>duced by motion of the limbs’.<br />

The purpose of this paper is to <strong>in</strong>troduce some challeng<strong>in</strong>g <strong>in</strong>formation<br />

concern<strong>in</strong>g unsteady flow conditions <strong>and</strong> consequences for practise.<br />

Key words: unsteady flow, momentum-<strong>in</strong>duced propulsion, jet-flow<br />

IntroductIon<br />

Aquatic Space Activities (ASA) focuses attention on the <strong>in</strong>teraction<br />

between the actively mov<strong>in</strong>g body (or its parts) <strong>and</strong> water-mass set <strong>in</strong><br />

motion. ASA also deals with the mutual effects of buoyancy <strong>and</strong> the<br />

reaction to <strong>in</strong>duced water-motion. Buoyancy is a natural reaction due to<br />

displacement of water-mass of any body, submerged <strong>in</strong> water. Induced<br />

water-motion or water flow is a physical reaction due to displacement<br />

of water-mass of any submerged body mov<strong>in</strong>g relative to the surround<strong>in</strong>g<br />

water.<br />

Reactions to <strong>in</strong>duced water-motion have some contra-<strong>in</strong>tuitive features.<br />

A simple drag approach suggested by most books on swimm<strong>in</strong>g<br />

does not expla<strong>in</strong> swimm<strong>in</strong>g speed sufficiently. The h<strong>and</strong>s’ actions are not<br />

most effective if water resistance is at a maximum (the term effective<br />

focuses on the result of an action). Intuition may tell us that e.g. a h<strong>and</strong><br />

is mov<strong>in</strong>g the same block of water either back or mov<strong>in</strong>g new blocks<br />

by chang<strong>in</strong>g h<strong>and</strong> motion. This is not the complete story. What really<br />

happens is (completely) different. Accord<strong>in</strong>g to the law of conservation<br />

of mass, <strong>in</strong> a flow, water cannot be pushed away <strong>in</strong> relation to the surround<strong>in</strong>g<br />

water-mass. Nevertheless it is true that, where there is one<br />

solid body (like a swimmer’s h<strong>and</strong>) there cannot be another body. However,<br />

where does mass of displaced water go? The aim of this paper is to<br />

<strong>in</strong>troduce some facts of flow physics, beyond our underst<strong>and</strong><strong>in</strong>g of the<br />

exist<strong>in</strong>g biomechanical aspects, <strong>and</strong> relevant for a better underst<strong>and</strong><strong>in</strong>g<br />

of aspects of aquatic space activities <strong>and</strong> the reaction of water-set-<strong>in</strong>motion.<br />

Methods<br />

Swimm<strong>in</strong>g text books mostly provide a chapter related to biomechanical<br />

background of activities <strong>in</strong> aquatic space. It is curious that over the<br />

decades, the content of this chapter, <strong>in</strong>clud<strong>in</strong>g pictures has not really<br />

changed from the very first publication of the author <strong>and</strong> coach “Doc”<br />

Counsilman. Obviously these text books were so conv<strong>in</strong>c<strong>in</strong>g worldwide<br />

that later authors had no reason to change this. In nearly the same<br />

decades numerous studies have been presented <strong>in</strong> the congress series of<br />

biomechanics <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g, it seems as if their outcome<br />

is of m<strong>in</strong>or relevance.<br />

Dur<strong>in</strong>g the same time period <strong>in</strong> parallel, much research was done <strong>in</strong><br />

the field of swimm<strong>in</strong>g animals. Researchers <strong>in</strong> this field, start<strong>in</strong>g with<br />

similar assumptions to their colleagues <strong>in</strong> human swimm<strong>in</strong>g, soon became<br />

aware that the steady flow approach was not helpful <strong>in</strong> answer<strong>in</strong>g<br />

their questions. The alternative approach, mostly based on concepts published<br />

by Lighthill, opened a quite new route to structur<strong>in</strong>g the research<br />

<strong>and</strong> to study unknown hydrodynamic features related to self-<strong>in</strong>duced<br />

chaPter2.<strong>Biomechanics</strong><br />

propulsion. Some of these results have held <strong>and</strong> can act as a guidel<strong>in</strong>e <strong>in</strong><br />

swimm<strong>in</strong>g literature, because the myths <strong>and</strong> the impact on swimm<strong>in</strong>g<br />

technique are considerable. Coaches <strong>and</strong> researchers may mislead their<br />

swimmers when still follow<strong>in</strong>g the ancient concepts.<br />

results<br />

Let’s consider the properties of water mass. It has long been known that<br />

aquatic space is characterized, like any body, by mass <strong>and</strong> other features.<br />

Firstly, water has the property to change shape. Any body, e.g. the h<strong>and</strong>s<br />

or feet, even when mov<strong>in</strong>g relative to water, displaces some water-mass.<br />

This means the motion of the water (<strong>in</strong> the vic<strong>in</strong>ity to the mov<strong>in</strong>g body)<br />

is changed <strong>and</strong> flow is created: if water is at rest (before it is displaced)<br />

this is also true: what counts is the relative change of motion. S<strong>in</strong>ce the<br />

relative motion between the body <strong>and</strong> water is essential, research on<br />

aquatic activities executed <strong>in</strong> a flume also applies to activities <strong>in</strong> a pool.<br />

Pressure is an important feature of water at rest <strong>and</strong> <strong>in</strong> motion: the<br />

weight of the water mass displaced by a body submerged <strong>in</strong> water exerts<br />

a force due to water pressure <strong>in</strong> an upward direction, called buoyancy.<br />

A body, submerged <strong>and</strong> mov<strong>in</strong>g relative to water produces a change<br />

of pressure <strong>and</strong> due to that change “some” particles are set <strong>in</strong>to motion.<br />

Based on the cont<strong>in</strong>uity-pressure-concept, the pressure causes <strong>and</strong><br />

ma<strong>in</strong>ta<strong>in</strong>s a flow, a cont<strong>in</strong>uous movement of the fluid from one place to<br />

another. Accord<strong>in</strong>g to Euler (1707 - 1783) particles-<strong>in</strong>-motion (i) possess<br />

mass, weight, acceleration, velocity, etc. <strong>and</strong> (ii) occupy some space<br />

<strong>in</strong> the vic<strong>in</strong>ity of the mov<strong>in</strong>g body (whereas the rest of the water-mass<br />

rema<strong>in</strong>s undisturbed).<br />

This space of particles-<strong>in</strong>-motion is full of vectors <strong>and</strong> scalars, form<strong>in</strong>g<br />

vector fields.<br />

Fig 1 Flow<strong>in</strong>g water: sketch by Leonardo Da V<strong>in</strong>ci, <strong>and</strong> today:<br />

cm.math.uniuc.edu/242syl.php<br />

Vector fields allow for transitional <strong>and</strong> rotational motion of the particles<br />

(the particle itself does not rotate, but follows a circular path), <strong>in</strong>dicat<strong>in</strong>g<br />

that vorteses form <strong>and</strong> the effects <strong>in</strong>duced by vortex forms are likely<br />

to occur. By <strong>in</strong>dependent variations <strong>in</strong> time <strong>and</strong> space, the flow is to a<br />

certa<strong>in</strong> extent “unpredictable” (also when the displac<strong>in</strong>g action causes<br />

“un-steady” flow conditions). From practical experience it is known that<br />

swimmers claim they sometimes feel a “different slip” although us<strong>in</strong>g the<br />

same biomechanical actions.<br />

Internal friction exists between particles, measured as viscosity,<br />

which is the cause of pressure change. The change of pressure is mediat<strong>in</strong>g<br />

between any displac<strong>in</strong>g action of any body <strong>and</strong> particles-<strong>in</strong>-motion;<br />

hence, the <strong>in</strong>teraction of the limbs <strong>and</strong> water-mass means pressurechange.<br />

In addition, viscosity causes repulsive actions. The reaction to<br />

this repulsive action is mostly measured by the established u²-law of resistance<br />

– provided that the flow rema<strong>in</strong>s unaffected by any body (called<br />

a steady situation).<br />

Momentum-<strong>in</strong>duced propulsion <strong>in</strong> aquatic space ie the act of displac<strong>in</strong>g<br />

a whole body <strong>in</strong> aquatic space, is related to a change of motion<br />

of water-mass. The change of motion of any mass is called momentum.<br />

Galileo (1565-1642) already po<strong>in</strong>ted out that momentum is the property<br />

by which the motive agency moves <strong>and</strong> the body resists. Newton<br />

(1642-1727) claimed that displacement means impart<strong>in</strong>g momentum to<br />

175


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

all particles set <strong>in</strong> motion. Momentum is a vector; the magnitude is the<br />

product of mass (m) times its velocity (v): [m*v] = kgm/s = Ns <strong>and</strong> its<br />

direction co<strong>in</strong>cides with the direction of the velocity.<br />

The momentum approach allows for application of the law of conservation<br />

of momentum (orig<strong>in</strong>al enunciation: René Descartes (1596-<br />

1650). Accord<strong>in</strong>g to this pr<strong>in</strong>ciple the total momentum is constant – provided<br />

a closed system is considered (which is not subject to external<br />

<strong>in</strong>fluence). If two (or more) masses belong to a closed system (Figure<br />

2) <strong>and</strong> one mass changes velocity, simultaneously the other masses will<br />

adapt their momentum (<strong>in</strong> the opposite direction), hence, any <strong>in</strong>teraction<br />

between body <strong>and</strong> surround<strong>in</strong>g water gives a reaction. The actions of<br />

(parts of ) any body <strong>in</strong> aquatic space transmit energy while chang<strong>in</strong>g the<br />

motion of water-mass over a period of time. The simultaneous reaction<br />

has an effect <strong>in</strong> <strong>and</strong> aga<strong>in</strong>st the swimm<strong>in</strong>g direction at the same time. If<br />

<strong>in</strong>creas<strong>in</strong>g speed of a whole body is observed, there will be a zero “nett”<br />

effect <strong>in</strong> swimm<strong>in</strong>g direction.<br />

The pr<strong>in</strong>ciple of momentum claims that if the momentum before<br />

<strong>and</strong> after an <strong>in</strong>teraction of limbs <strong>and</strong> water-mass differs this difference<br />

is <strong>in</strong>duced by the <strong>in</strong>teraction. This concept is elegantly applied to determ<strong>in</strong>e<br />

effects of a “displac<strong>in</strong>g” rigid total body on a flow of constant speed,<br />

either <strong>in</strong> steady or unsteady conditions. Based on the law of conservation<br />

of momentum it is evident that momentum <strong>in</strong> front of the whole<br />

body must be equal to the momentum <strong>in</strong> the wake plus all momentum<br />

changes produced by the <strong>in</strong>teraction between total body <strong>and</strong> particles<strong>in</strong>-motion.<br />

The difference <strong>in</strong> momentum over time <strong>in</strong> steady flow is called<br />

drag or propulsion (Figure 3).<br />

Figure 2 Momentum change due to the total body action of the fish<br />

result<strong>in</strong>g <strong>in</strong> thrust<br />

Jet-propulsion <strong>in</strong> aquatic space: In context with <strong>in</strong>duced water motion<br />

it was po<strong>in</strong>ted out that body actions change the motion of water-mass<br />

due to <strong>in</strong>teraction of the limbs <strong>and</strong> water-mass. The effect of the <strong>in</strong>teraction<br />

of limbs <strong>and</strong> water-mass is a change of momentum. From this it<br />

follows that the change of momentum of particles (m’*v’) are comb<strong>in</strong>ed<br />

with a change of momentum of the total body mass (m’’*v’’), <strong>in</strong> the opposite<br />

direction. From the swimmers view the reaction (m’’*v’’) provides<br />

components <strong>in</strong> <strong>and</strong> aga<strong>in</strong>st the swimm<strong>in</strong>g direction (called drag or<br />

thrust). If the momentum of particles (m’*v’) is totally directed aga<strong>in</strong>st<br />

the swimm<strong>in</strong>g direction of the total body, the reaction results <strong>in</strong> a 100<br />

% effect. Water mov<strong>in</strong>g backwards is thrust<strong>in</strong>g the whole body forward.<br />

However, this does not suggest that one should move the h<strong>and</strong> or leg<br />

backwards to ga<strong>in</strong> an effective thrust. The most effective <strong>and</strong> efficient<br />

way to ga<strong>in</strong> maximum thrust for a given energy-<strong>in</strong>put is a jet-flow, used<br />

by squids or jelly fish (Fig . 3).<br />

Figure 3 Vortex <strong>in</strong>duced jet by a jelly fish<br />

176<br />

Jet-flow is a powerful stream of mass carry<strong>in</strong>g high momentum. Jetpropulsion<br />

exists also <strong>in</strong> the swimm<strong>in</strong>g of the skilled human. Matsuuchi<br />

et al. (2004) published research data for the first time based on the PIVmethod<br />

(Particle Image Velocimetry), demonstrat<strong>in</strong>g the existence of<br />

<strong>in</strong>termittent jet-flow. Close scrut<strong>in</strong>y revealed that first a vortex-r<strong>in</strong>g had<br />

to be produced by the action of the swimmer’s h<strong>and</strong> <strong>and</strong> <strong>in</strong> its wake.<br />

The rotation of the vortex r<strong>in</strong>gs cause a particle drift <strong>in</strong> one direction.<br />

The shape <strong>and</strong> rotation of the vortex r<strong>in</strong>g determ<strong>in</strong>es the jet length-todiameter-ratio<br />

<strong>and</strong> thus the momentum. Hence, the orientation of the<br />

jet-flow relative to swimm<strong>in</strong>g direction determ<strong>in</strong>es the contribution<br />

to thrust<strong>in</strong>g the body.<br />

Figure 4 Vortex-<strong>in</strong>duced jet-flow of a h<strong>and</strong> while swimm<strong>in</strong>g freestyle<br />

dIscussIon<br />

Concentration on the <strong>in</strong>teraction of limbs <strong>and</strong> water-mass <strong>in</strong>stead of<br />

limit<strong>in</strong>g oneself to the mere action of limbs or bodies, augments the<br />

underst<strong>and</strong><strong>in</strong>g of reality. The act of underst<strong>and</strong><strong>in</strong>g is a dynamic process<br />

<strong>and</strong> prone to verification / falsification of theories. The say<strong>in</strong>g, noth<strong>in</strong>g<br />

is more practical than a good theory, is valid when theory mirrors reality.<br />

Sometimes a change <strong>in</strong> theory means that already exist<strong>in</strong>g, but not<br />

established concepts survive; e.g. Berger (1996, 95) found that high propulsive<br />

forces cannot be based solely on lift <strong>and</strong> drag of an act<strong>in</strong>g h<strong>and</strong><br />

<strong>and</strong> concluded “the key to produc<strong>in</strong>g effective propulsion at low energy<br />

cost may be the creation of vortices of a special form”.<br />

The research of jet-flow requires a water-related view of both the<br />

motion of the limbs <strong>and</strong> of the water-<strong>in</strong>-motion <strong>in</strong> aquatic space. Most<br />

of the exist<strong>in</strong>g studies on swimm<strong>in</strong>g use a body related approach focuss<strong>in</strong>g<br />

on the velocity of body actions. In most studies related to swimm<strong>in</strong>g<br />

the underst<strong>and</strong><strong>in</strong>g of the movement of the surround<strong>in</strong>g water is<br />

limited to the lift <strong>and</strong> drag approach, established <strong>in</strong> 1970 by Counsilman.<br />

Already <strong>in</strong> 1986 Counsilman said <strong>in</strong> personal communication: “I<br />

can’t help it if people still refer to my publications of the end of the<br />

sixties”. He was aware that the drag <strong>and</strong> lift approach was not applicable<br />

to an unsteady swimm<strong>in</strong>g situation. In that time the vortex <strong>in</strong>duced<br />

propulsion concept <strong>and</strong> <strong>in</strong>fluence of added mass to swimm<strong>in</strong>g<br />

bodies started to attract the <strong>in</strong>terest of (a few) swimm<strong>in</strong>g researchers.<br />

Ungerechts (1988) published the idea that breaststrokers’ leg actions<br />

lead to rotat<strong>in</strong>g water forms by which “momentum is transferred to the<br />

fluid <strong>and</strong> <strong>in</strong> reaction, its “impulse” accelerates the body.” Van Tilborg et<br />

al. (1988) presented data of “impulses”, measured <strong>in</strong> Ns, result<strong>in</strong>g from<br />

the difference between propulsion <strong>and</strong> resistance for different phases<br />

<strong>in</strong> breaststroke. They po<strong>in</strong>ted out that “impulses are more reliable than<br />

forces”. Ungerechts (1992), calculated momentum needed to change<br />

hip motion (Δv) dur<strong>in</strong>g the arm stroke <strong>in</strong>clud<strong>in</strong>g an <strong>in</strong>ertial term due<br />

to acceleration based on experimental data of eight breaststrokers <strong>and</strong><br />

compared the data with forces due to the h<strong>and</strong>s’ actions. It was shown<br />

that momentum =|16.5 – 45.9| Ns will expla<strong>in</strong> (Δv) = |0.27 – 0.76| m/s<br />

with 93 % confidence. Ungerechts & Klauck (2006) presented the flow<br />

physical laws which are relevant for unsteady flow <strong>in</strong> conjunction with<br />

added mass effects.<br />

A change of paradigm from a body related to a water related view


considers the effects due to displacement of water <strong>in</strong> addition to repulsive<br />

effects. The latter are not neglected but qualified. Humans can<br />

perform well <strong>in</strong> an aquatic space without know<strong>in</strong>g the details of flow<br />

physics. It is a different case however when <strong>in</strong>structors or coaches are<br />

not well <strong>in</strong>formed about the relevancy of the <strong>in</strong>teraction of limbs <strong>and</strong><br />

water-mass <strong>and</strong> its reaction. In particular the illiteracy of the momentum<br />

aspect, only about ten papers <strong>in</strong> 36 years of the Conference Series<br />

of <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> of Swimm<strong>in</strong>g have h<strong>and</strong>led this topic,<br />

is not helpful.<br />

The water related view also tackles the term<strong>in</strong>ology of rules of strok<strong>in</strong>g<br />

written for the referees <strong>in</strong> swimm<strong>in</strong>g. This term<strong>in</strong>ology still uses the<br />

concept of pull<strong>in</strong>g <strong>and</strong> push<strong>in</strong>g arms, whereas e.g. the BMS conference<br />

series revealed that scull<strong>in</strong>g actions of the h<strong>and</strong>s dom<strong>in</strong>ate all strokes.<br />

Of course each expert is free to select any term<strong>in</strong>ology. But a more appropriate<br />

term<strong>in</strong>ology supports the mental representation of strokes required<br />

to execute <strong>and</strong> control movements.<br />

conclusIons<br />

The <strong>in</strong>crease of knowledge of effects of ASA <strong>in</strong> the last decade is remarkable<br />

<strong>and</strong> resembles a change <strong>in</strong> paradigm. The traditional paradigm<br />

is body orientated <strong>and</strong> concentrates on the biomechanical aspects of<br />

body motion. ASA related sports like Recreational swimm<strong>in</strong>g, F<strong>in</strong>swimm<strong>in</strong>g,<br />

Triathlon, Scuba-div<strong>in</strong>g or Water-exercises seem still to be<br />

far from the water related view, still rely<strong>in</strong>g on the established u²-law of<br />

resistance. This approach is an acceptable pedagogical view, search<strong>in</strong>g<br />

for best solutions as to how to teach swimm<strong>in</strong>g <strong>and</strong> strok<strong>in</strong>g correctly.<br />

Bridg<strong>in</strong>g the gap <strong>and</strong> approach<strong>in</strong>g a water related view <strong>in</strong>clud<strong>in</strong>g unsteady<br />

features of flow seems to be difficult.<br />

The vortex-r<strong>in</strong>g like structure created by h<strong>and</strong>-action dem<strong>and</strong>s a<br />

turn<strong>in</strong>g around action of the h<strong>and</strong>, a k<strong>in</strong>d of sup<strong>in</strong>ation or pronation,<br />

dur<strong>in</strong>g the period of underwater action. S<strong>in</strong>ce all activities performed <strong>in</strong><br />

aquatic space will face more or less the same conditions, it is concluded<br />

that unsteady flow physics should become the basis of further research,<br />

<strong>in</strong>dependently of biomechanical or physiological issues. This cont<strong>in</strong>ued<br />

research needs also to be phrased <strong>in</strong> terms permitt<strong>in</strong>g it to be accepted<br />

by practitioners.<br />

reFerences<br />

Berger, M. (1995). Force generation <strong>and</strong> efficiency <strong>in</strong> front crawl swimm<strong>in</strong>g.<br />

Thesis Vrije Universiteit, Amsterdam.<br />

Counsilman, J. E. (1968). The Science of Swimm<strong>in</strong>g. Prentice Hall. New<br />

Jersey.<br />

Counsilman, J. E. & Counsilman, B (1994). The New Science of Swimm<strong>in</strong>g.<br />

Prentice Hall. New Jersey.<br />

Matsuuchi, K, Miwa, T., Nomura, T., Sakakibara, J., Sh<strong>in</strong>tan, H.. & Ungerechts,<br />

B.E, (2004). Unsteady flow measurement around a human<br />

h<strong>and</strong> <strong>in</strong> swimm<strong>in</strong>g us<strong>in</strong>g PIV. In: E v Praagh, J Coudert, N Fellmann,<br />

P Duché (eds.) Proceed<strong>in</strong>gs of 9 th Annual Congress of the ECSS,<br />

Clermont-Ferr<strong>and</strong>, 274.<br />

Tilborgh van, L., Willems E.J, & Persyn U. (1988). Estimation of<br />

breaststroke propulsion <strong>and</strong> resistance-resultant impulses from film<br />

analyses. In: B.E. Ungerechts, K. Wilke <strong>and</strong> K. Reischle (eds.), Swimm<strong>in</strong>g<br />

Science V, Human K<strong>in</strong>etics Publishers, Champaign, IL: 67- 71.<br />

Ungerechts, B.E., (1988). The relation of peak body acceleration <strong>and</strong><br />

phases of movements <strong>in</strong> swimm<strong>in</strong>g. In: B.E. Ungerechts, K. Wilke<br />

<strong>and</strong> K. Reischle (eds.), Swimm<strong>in</strong>g Science V, Human K<strong>in</strong>etics Publishers,<br />

Champaign, IL, 61-66.<br />

Ungerechts, B.E., (1992). The <strong>in</strong>terrelationship of hydrodynamical forces<br />

<strong>and</strong> swimm<strong>in</strong>g speed <strong>in</strong> breaststroke. In: D. MacLaren, T. Reilly &<br />

A. Lees (eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g -Swimm<strong>in</strong>g<br />

Science VI-. E. & FN Spon, London:69 - 73.<br />

Ungerechts, B. E. & Klauck J. (2006). Consequences of non-stationary<br />

flow effects for functional attribution of swimm<strong>in</strong>g strokes. In: J.P.<br />

chaPter2.<strong>Biomechanics</strong><br />

Vilas-Boas, F. Alves, A. Marques (eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g X. Portuguese Journal of Sport Sciences, 6, Suppl. 2, 109-<br />

111.<br />

AcKnoWledGMents<br />

The authors would like to thank Dr. Huub Toussa<strong>in</strong>t from Swimm<strong>in</strong>g<br />

Research Center Amsterdam, The Netherl<strong>and</strong>s, for valuable <strong>in</strong>formation<br />

<strong>and</strong> suggestions to accomplish this paper.<br />

177


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Analysis of Swim Turn<strong>in</strong>g, Underwater Glid<strong>in</strong>g<br />

<strong>and</strong> Stroke Resumption Phases <strong>in</strong> Top Division<br />

Swimmers us<strong>in</strong>g a Wearable Inertial Sensor Device<br />

Vannozzi, G. 1 , donati, M. 1 , Gatta G. 2 & cappozzo, A. 1<br />

1 Department of Human Movement <strong>and</strong> Sport Sciences, University of Rome<br />

“Foro Italico”, Italy<br />

2 Faculty of Exercise <strong>and</strong> Sport Science, University of Bologna, Italy<br />

Improv<strong>in</strong>g performance is a difficult task for élite swimmers. The study<br />

of turn<strong>in</strong>g, underwater glid<strong>in</strong>g <strong>and</strong> stroke resumption k<strong>in</strong>ematics may<br />

lead to the reduction of the relevant durations. Common video analysis<br />

is sometimes <strong>in</strong>adequate to <strong>in</strong>vestigate motor tasks. This work aimed<br />

at describ<strong>in</strong>g the mentioned phases <strong>in</strong> top division swimmers us<strong>in</strong>g a<br />

wearable <strong>in</strong>ertial device. Eight élite swimmers were selected so as to<br />

cover all the four swimm<strong>in</strong>g styles. The device was positioned on the<br />

lower trunk <strong>and</strong> a 50m trial at the maximum velocity was executed. The<br />

angular velocity about each axis was post-processed <strong>and</strong> both time <strong>and</strong><br />

k<strong>in</strong>ematic parameters were extracted for each phase, characteriz<strong>in</strong>g each<br />

swimm<strong>in</strong>g style. Strength po<strong>in</strong>ts of the approach are: simple description<br />

of the turn<strong>in</strong>g k<strong>in</strong>ematics; possibility to extract performance-related parameters;<br />

simplicity of use for the operator; the m<strong>in</strong>imal encumber for<br />

the athlete.<br />

KeY-Words: <strong>in</strong>ertial sensor, angular velocity, turn<strong>in</strong>g, k<strong>in</strong>ematics<br />

IntroductIon<br />

Improv<strong>in</strong>g athletic performance is one of the ma<strong>in</strong> goals of sport biomechanics,<br />

<strong>in</strong> general, <strong>and</strong> of swimm<strong>in</strong>g research, <strong>in</strong> particular. This goal<br />

is more difficult to obta<strong>in</strong> as the elite swimm<strong>in</strong>g level <strong>in</strong>creases, thus<br />

chances for improvement are relatively limited. However, closely exam<strong>in</strong><strong>in</strong>g<br />

swimm<strong>in</strong>g aspects such as turn<strong>in</strong>g, underwater glid<strong>in</strong>g <strong>and</strong> stroke<br />

resumption phases, <strong>and</strong> <strong>in</strong>vestigat<strong>in</strong>g how the relevant tim<strong>in</strong>g might be<br />

optimised for improv<strong>in</strong>g the overall swimmer performance, may provide<br />

valuable <strong>in</strong>formation to the coach. This circumstance was remarked by<br />

Lyttle et al. (1999) who stated that “little changes on the turn<strong>in</strong>g action<br />

performance can imply substantial improvements of the f<strong>in</strong>al event<br />

time”. The goal of deepen<strong>in</strong>g knowledge <strong>in</strong>to the mentioned swimm<strong>in</strong>g<br />

phase can be obta<strong>in</strong>ed if an accurate way to describe the k<strong>in</strong>ematics of<br />

the abovementioned swimm<strong>in</strong>g phases is made available.<br />

Among the mentioned swim phases, turn<strong>in</strong>g is one of the most critical<br />

to be analysed. Turn<strong>in</strong>g mechanics is usually described us<strong>in</strong>g force<br />

plates embedded <strong>in</strong> the pool wall (Takahashi et al., 1982), to obta<strong>in</strong><br />

forces <strong>and</strong> torques dur<strong>in</strong>g the push-off phase that follows the rotational<br />

phase. Both flip-turns <strong>and</strong> open turns are complex movements, usually<br />

<strong>in</strong>vestigated - with great difficulty - us<strong>in</strong>g video analysis. In fact, due to<br />

the aquatic environment, refraction of the water, as well as actions of<br />

several body segments, which are mov<strong>in</strong>g <strong>in</strong> different movement planes<br />

(Pereira et al., 2008), it is not rare to experience serious difficulties <strong>in</strong><br />

track<strong>in</strong>g the selected sk<strong>in</strong> markers. Moreover, video analysis usually<br />

requires a complex <strong>in</strong>strumental set-up <strong>and</strong> a massive computational<br />

effort to obta<strong>in</strong> the desired biomechanical quantities. For these reasons,<br />

this important phase of a swimm<strong>in</strong>g competition is scarcely dealt with<br />

<strong>in</strong> the scientific literature.<br />

Follow<strong>in</strong>g the recent trend of imply<strong>in</strong>g wearable <strong>in</strong>ertial devices <strong>in</strong><br />

human movement analysis, also swimm<strong>in</strong>g research recently started to<br />

<strong>in</strong>clude such sensors <strong>in</strong> experimental setups. Ohgi <strong>and</strong> colleagues (2003)<br />

used a tri-axial accelerometer positioned on the wrist to carry out a<br />

phase segmentation of breaststroke trials. The feasibility of us<strong>in</strong>g a 3D<br />

accelerometer mounted on the pelvis was demonstrated by Slawson et<br />

al. (2008), who succeeded <strong>in</strong> characteris<strong>in</strong>g pelvis l<strong>in</strong>ear accelerations <strong>in</strong><br />

different swimm<strong>in</strong>g styles. At this stage of research, the available applications<br />

dealt only with l<strong>in</strong>ear accelerations <strong>and</strong> there is no evidence<br />

178<br />

on how the mentioned swimm<strong>in</strong>g phases might be characterized us<strong>in</strong>g<br />

<strong>in</strong>ertial sensor devices.<br />

This work aimed at quantitatively describ<strong>in</strong>g the swim turn<strong>in</strong>g, underwater<br />

glid<strong>in</strong>g <strong>and</strong> stroke resumption phases <strong>in</strong> top division swimmers<br />

us<strong>in</strong>g a wearable <strong>in</strong>ertial device composed of a tri-axial accelerometer<br />

<strong>and</strong> gyroscope. This objective entailed the def<strong>in</strong>ition of appropriate<br />

parameters that could be effectively used by the coach to compare different<br />

swimm<strong>in</strong>g techniques towards total-time m<strong>in</strong>imisation.<br />

Methods<br />

Eight elite swimmers (four males <strong>and</strong> four females) volunteered to participate<br />

<strong>in</strong> the study. The athletes are part of a top division Italian team<br />

<strong>and</strong> were selected so as to cover the four swimm<strong>in</strong>g styles (freestyle,<br />

backstroke, breaststroke <strong>and</strong> butterfly).<br />

Participants wore the FreeSense device (Sensorize, Italy) which is<br />

a wearable measurement <strong>in</strong>strument equipped with a tri-axial accelerometer<br />

<strong>and</strong> two bi-axial gyroscopes, weigh<strong>in</strong>g 93g <strong>and</strong> fully portable<br />

(size: 8.8 x 5.1 x 2.5 cm), allow<strong>in</strong>g to perform the swimm<strong>in</strong>g task <strong>in</strong><br />

the most natural fashion (as depicted <strong>in</strong> Figure 1). Once water-proofed,<br />

the device was <strong>in</strong>corporated <strong>in</strong>to an elastic (neoprene) belt which was<br />

fastened around the participant’s waist, at the dorsal side of the trunk<br />

at the fourth lumbar vertebra level. In Fig.1 the device position<strong>in</strong>g is<br />

represented together with the def<strong>in</strong>ition of the local reference frame.<br />

The device output were three l<strong>in</strong>ear accelerations along the three local<br />

axes <strong>and</strong> three angular velocities (ω x , ω y <strong>and</strong> ω z ) about the same axes.<br />

Figure 1: Device position<strong>in</strong>g on a swimmer low trunk <strong>and</strong> def<strong>in</strong>ition of<br />

the local frame of reference.<br />

Data were collected with a sampl<strong>in</strong>g frequency of 100 Hz <strong>and</strong> were<br />

saved directly on board of the device. A commercial video camera <strong>and</strong><br />

a chronometer were also used to video-record each trial <strong>and</strong> to record<br />

the relevant time duration (t chr ), respectively. All data collection was performed<br />

<strong>in</strong> a 25m swimm<strong>in</strong>g pool.<br />

After familiarisation with the <strong>in</strong>strument, each participant was<br />

asked to perform a 50m trial at his/her maximum velocity as dur<strong>in</strong>g a<br />

real competition.<br />

In this study, temporal <strong>and</strong> k<strong>in</strong>ematic parameters were ma<strong>in</strong>ly obta<strong>in</strong>ed<br />

us<strong>in</strong>g angular velocities about the three axes of the local frame<br />

of reference. For each swimm<strong>in</strong>g style, the follow<strong>in</strong>g parameters were<br />

extracted for the different phases:<br />

� Glid<strong>in</strong>g phase - duration of first <strong>and</strong> second lap, respectively<br />

t glide25 <strong>and</strong> t glide50 ;<br />

� Stroke phase - duration of first <strong>and</strong> second lap, respectively<br />

t stroke25 <strong>and</strong> t stroke50 ;<br />

� turn<strong>in</strong>g phase - duration, t turn ; peaks of angular velocities<br />

- pω x , pω y <strong>and</strong> pω z ; time <strong>in</strong>terval between the ma<strong>in</strong> two<br />

angular velocity peaks, t pp .<br />

The parameter selection procedure is depicted <strong>in</strong> Figure 2 consider<strong>in</strong>g a<br />

r<strong>and</strong>omly selected backstroke trial that <strong>in</strong>cludes the execution of a flipturn<br />

technique. The same procedure was also reported <strong>in</strong> Figure 3 for a<br />

butterfly trial, <strong>in</strong>clud<strong>in</strong>g an open-turn<strong>in</strong>g execution. Even if only angular<br />

velocities were used <strong>in</strong> this paper, similar considerations can be made to<br />

extract appropriate parameters from measured local accelerations.


ω y (deg/s) ω x (deg/s)<br />

t glide25<br />

Parameter selection for a backstroke trial<br />

t stroke25<br />

t pp<br />

pω x<br />

t turn<br />

pω y<br />

t glide50<br />

t stroke50<br />

time (s)<br />

time (s)<br />

Figure 2: parameter selection for backstroke us<strong>in</strong>g its most descriptive<br />

angular velocities, ω x <strong>and</strong> ω y . The same parameter selection can be adopted<br />

for the further axis <strong>and</strong> for the other swimm<strong>in</strong>g styles. Apart from<br />

the start<strong>in</strong>g phase, it is possible to easily recognise the underwater glid<strong>in</strong>g<br />

<strong>and</strong> the stroke phase of the first 25m lap, the turn<strong>in</strong>g phase <strong>and</strong> the<br />

f<strong>in</strong>al lap with the relevant glid<strong>in</strong>g <strong>and</strong> stroke phases. Local peaks for<br />

each angular velocity, pω x <strong>and</strong> pω y , dur<strong>in</strong>g the turn<strong>in</strong>g phase were also<br />

highlighted, together with the t turn <strong>and</strong> t pp durations.<br />

ω z (deg/s) ω y (deg/s)<br />

t glide25<br />

Parameter selection for a butterfly trial<br />

t stroke25<br />

pω y<br />

pω z<br />

t turn<br />

t glide50<br />

t stroke50<br />

time (s)<br />

time (s)<br />

Figure 3: parameter selection for a butterfly trial us<strong>in</strong>g its most descriptive<br />

angular velocities, ω y <strong>and</strong> ω z . It is possible to outl<strong>in</strong>e several differences<br />

from the previous style, particularly <strong>in</strong> the stroke phase <strong>and</strong> <strong>in</strong> the<br />

turn<strong>in</strong>g phase, where the negative ω z peak specifically characterizes the<br />

open-turn technique executed by the butterfly swimmer.<br />

Start<strong>in</strong>g from the sensor output, the follow<strong>in</strong>g further parameters were<br />

def<strong>in</strong>ed. Accord<strong>in</strong>g to the literature, the stroke rate is def<strong>in</strong>ed for each<br />

lap (sr25 <strong>and</strong> sr50 ) as number of stroke cycles per m<strong>in</strong>ute. Furthermore,<br />

aim<strong>in</strong>g at outl<strong>in</strong><strong>in</strong>g the strategy undertaken by the swimmer <strong>in</strong> choos<strong>in</strong>g<br />

the duration of both glid<strong>in</strong>g <strong>and</strong> stroke phases for the two laps, the<br />

tglide<br />

synthetic <strong>in</strong>dices r25 <strong>and</strong> r50 were def<strong>in</strong>ed as follows: r = . An r <strong>in</strong>dex<br />

tstroke<br />

near 1 <strong>in</strong>dicates that the two phases have a similar duration (e.g. for<br />

backstroke), whereas values less than 0.5 are expected for breaststroke<br />

swimmers.<br />

chaPter2.<strong>Biomechanics</strong><br />

results<br />

Each swimmer completed the execution without problems <strong>and</strong> did not<br />

experience any difficulty <strong>in</strong> us<strong>in</strong>g the <strong>in</strong>strumental apparatus. Results for<br />

the eight swimmers are listed <strong>in</strong> Table 1. Positive <strong>and</strong> negative pω values<br />

are accord<strong>in</strong>g to the convention <strong>in</strong> Fig. 1.<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b<br />

Table 1. Results obta<strong>in</strong>ed for the four swimm<strong>in</strong>g styles for each selected<br />

parameter.<br />

Table 1. Results obta<strong>in</strong>ed for the four swimm<strong>in</strong>g styles for each selected parameter.<br />

pωx<br />

(deg/s)<br />

pωy<br />

(deg/s)<br />

pωz<br />

(deg/s)<br />

tpp<br />

(s)<br />

tturn<br />

(s)<br />

sr25<br />

(cycle/m<strong>in</strong>)<br />

r25<br />

sr50<br />

(cycle/m<strong>in</strong>)<br />

r50<br />

tchr<br />

(s)<br />

Free<br />

M<br />

F<br />

-241<br />

-310<br />

565<br />

324<br />

-111<br />

-69<br />

0.95<br />

0.92<br />

1.35<br />

1.48<br />

60.08<br />

55.17<br />

0.36<br />

0.44<br />

55.65<br />

51.60<br />

0.12<br />

0.11<br />

25.7<br />

27.8<br />

Back<br />

M<br />

F<br />

-352<br />

354<br />

344<br />

321<br />

-18<br />

-47<br />

1.02<br />

1.16<br />

2.15<br />

2.36<br />

67.67<br />

46.81<br />

0.99<br />

0.70<br />

56.07<br />

44.44<br />

0.65<br />

0.56<br />

26.7<br />

32.0<br />

Breast<br />

M<br />

F<br />

-205<br />

-140<br />

-379<br />

-296<br />

-330<br />

-128<br />

0.46<br />

0.42<br />

1.16<br />

1.26<br />

61.71<br />

52.82<br />

0.36<br />

0.29<br />

57.24<br />

44.02<br />

0.16<br />

0.26<br />

29.8<br />

35.8<br />

Fly<br />

M<br />

F<br />

-230<br />

-119<br />

-321<br />

-265<br />

-260<br />

-238<br />

0.54<br />

0.66<br />

1.24<br />

1.14<br />

60.26<br />

61.46<br />

0.41<br />

0.51<br />

59.29<br />

57.04<br />

0.28<br />

0.17<br />

25.6<br />

29.5<br />

DISCUSSION<br />

dIscussIon<br />

The present study verified the feasibility to use wearable <strong>in</strong>ertial sensor devices to<br />

characterise turn<strong>in</strong>g, glid<strong>in</strong>g <strong>and</strong> stroke resumption <strong>in</strong> swimm<strong>in</strong>g. The novelty of the<br />

approach is constituted by the use of gyroscopes to measure angular velocities <strong>and</strong> by<br />

the consequent easy description of swimm<strong>in</strong>g rotational movements. If used <strong>in</strong><br />

conjunction with the available measured l<strong>in</strong>ear accelerations, several biomechanical<br />

parameters can be extracted that <strong>in</strong>crease the knowledge about each swimm<strong>in</strong>g style<br />

<strong>and</strong>/or about the strategy adopted by each swimmer.<br />

Several quantitative parameters were selected from the sensor device output: the choice<br />

reflected the need to characterise each swimm<strong>in</strong>g style <strong>and</strong> offer possible parameters to<br />

describe the way each athlete executes his/her swimm<strong>in</strong>g exercise.<br />

Highest pωy were found for freestyle <strong>in</strong> both genders. This circumstance is directly<br />

related to the well-known highest velocities usually obta<strong>in</strong>ed <strong>in</strong> this swimm<strong>in</strong>g style at<br />

the end of the 25m lap. This parameter was higher for males than for females, as it<br />

happens usually for mean velocity, even if related differences are slighter than for l<strong>in</strong>ear<br />

velocity. In fact, the two parameters are l<strong>in</strong>ked by the equation - v = ω*R - be<strong>in</strong>g R the<br />

distance between the most external po<strong>in</strong>t <strong>and</strong> the rotational axis <strong>and</strong>, thus, related to the<br />

<strong>in</strong>dividual flexibility. Consider<strong>in</strong>g that females are usually more flexible than males,<br />

thus more able <strong>in</strong> reduc<strong>in</strong>g R, it is possible to argue that a higher R for female<br />

compensates the higher mean velocity usually obta<strong>in</strong>ed by male swimmers. The sign of<br />

the rotation depends upon the style turn<strong>in</strong>g technique: freestyle <strong>and</strong> backstroke use a<br />

ecutes flip-turn his/her technique, swimm<strong>in</strong>g thus <strong>in</strong>volv<strong>in</strong>g exercise. a positive rotation about the y axis, vice-versa<br />

breaststroke <strong>and</strong> butterfly use an open-turn that <strong>in</strong>volves a negative rotation about the<br />

same axis correspond<strong>in</strong>g to the recall of the leg before the push-off.<br />

Further peak angular velocities, pωx <strong>and</strong> pωz, characterised differently the other<br />

swimm<strong>in</strong>g styles. Highest pωx were found for the backstroke flip-turn that is first<br />

characterised by a sudden rotation about the cranio-caudal axis, consistently with its<br />

theoretical execution. For all styles, the negative peak <strong>in</strong>dicated that every athlete<br />

carried out the rotation lead<strong>in</strong>g the right arm, thus execut<strong>in</strong>g a clockwise rotation about<br />

the cranio-caudal axis. This is, <strong>in</strong> fact, a choice dependent upon the s<strong>in</strong>gle swimmer.<br />

Highest pωz, conversely, were found for both breaststroke <strong>and</strong> butterfly. This<br />

circumstance is consistent with the open-turn technique used for these two styles: after<br />

the feet contact on the pool wall, the swimmer suddenly turns the upper body lead<strong>in</strong>g<br />

the rotation us<strong>in</strong>g the right arm, thus generat<strong>in</strong>g a clockwise rotation about the z axis<br />

(negative pωz peak).<br />

The present study verified the feasibility to use wearable <strong>in</strong>ertial sensor<br />

devices to characterise turn<strong>in</strong>g, glid<strong>in</strong>g <strong>and</strong> stroke resumption <strong>in</strong><br />

swimm<strong>in</strong>g. The novelty of the approach is constituted by the use of<br />

gyroscopes to measure angular velocities <strong>and</strong> by the consequent easy<br />

description of swimm<strong>in</strong>g rotational movements. If used <strong>in</strong> conjunction<br />

with the available measured l<strong>in</strong>ear accelerations, several biomechanical<br />

parameters can be extracted that <strong>in</strong>crease the knowledge about each<br />

swimm<strong>in</strong>g style <strong>and</strong>/or about the strategy adopted by each swimmer.<br />

Several quantitative parameters were selected from the sensor device<br />

output: the choice reflected the need to characterise each swimm<strong>in</strong>g<br />

style <strong>and</strong> offer possible parameters to describe the way each athlete ex-<br />

Highest pωy were found for freestyle <strong>in</strong> both genders. This circumstance<br />

is directly related to the well-known highest velocities usually obta<strong>in</strong>ed<br />

<strong>in</strong> this swimm<strong>in</strong>g style at the end of the 25m lap. This parameter<br />

was higher for males than for females, as it happens usually for mean velocity,<br />

even if related differences are slighter than for l<strong>in</strong>ear velocity. In fact, the<br />

two parameters are l<strong>in</strong>ked by the equation - v = ω*R - be<strong>in</strong>g R the distance<br />

between the most external po<strong>in</strong>t <strong>and</strong> the rotational axis <strong>and</strong>, thus, related<br />

to the <strong>in</strong>dividual flexibility. Consider<strong>in</strong>g that females are usually more flexible<br />

than males, thus more able <strong>in</strong> reduc<strong>in</strong>g R, it is possible to argue that<br />

a higher R for female compensates the higher mean velocity usually obta<strong>in</strong>ed<br />

by male swimmers. The sign of the rotation depends upon the style<br />

turn<strong>in</strong>g technique: freestyle <strong>and</strong> backstroke use a flip-turn technique, thus<br />

<strong>in</strong>volv<strong>in</strong>g a positive rotation about the y axis, vice-versa breaststroke <strong>and</strong><br />

butterfly use an open-turn that <strong>in</strong>volves a negative rotation about the same<br />

axis correspond<strong>in</strong>g to the recall of the leg before the push-off.<br />

Further peak angular velocities, pωx <strong>and</strong> pωz , characterised differently<br />

the other swimm<strong>in</strong>g styles. Highest pωx were found for the backstroke<br />

flip-turn that is first characterised by a sudden rotation about<br />

the cranio-caudal axis, consistently with its theoretical execution. For all<br />

styles, the negative peak <strong>in</strong>dicated that every athlete carried out the rotation<br />

lead<strong>in</strong>g the right arm, thus execut<strong>in</strong>g a clockwise rotation about the<br />

cranio-caudal axis. This is, <strong>in</strong> fact, a choice dependent upon the s<strong>in</strong>gle<br />

swimmer. Highest pωz, conversely, were found for both breaststroke <strong>and</strong><br />

butterfly. This circumstance is consistent with the open-turn technique<br />

used for these two styles: after the feet contact on the pool wall, the<br />

swimmer suddenly turns the upper body lead<strong>in</strong>g the rotation us<strong>in</strong>g the<br />

right arm, thus generat<strong>in</strong>g a clockwise rotation about the z axis (negative<br />

pωz peak).<br />

Still focus<strong>in</strong>g on the turn<strong>in</strong>g phase, tpp <strong>and</strong> tturn were higher for backstroke,<br />

consistently with the backstroke turn<strong>in</strong>g technique that <strong>in</strong>cludes<br />

a rotation (positive if clockwise, negative if counter-clockwise) about<br />

the X-axis before the execution of the rotation about the Y-axis. Also, tpp value <strong>in</strong>dicates that flip-turns are characterised by two dist<strong>in</strong>ct rotations<br />

(about y <strong>and</strong> x axes), while open-turns are complex movements <strong>in</strong> which<br />

rotations follow each other <strong>in</strong> a faster way.<br />

165<br />

179


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The use of gyroscopes allowed us to describe, the strategy adopted by<br />

each athlete dur<strong>in</strong>g his/her swimm<strong>in</strong>g action, also. This was done us<strong>in</strong>g<br />

both sr <strong>and</strong> r parameters. Deal<strong>in</strong>g with stroke rates, sr 50 was consistently<br />

lower than sr 25 , circumstance that is presumably related to the appearance<br />

fatigue. This parameter was typically lower <strong>in</strong> females than males,<br />

except for butterfly where the female <strong>and</strong> male swimmers obta<strong>in</strong>ed similar<br />

sr values. This is due to l<strong>in</strong>ear relationship between velocity <strong>and</strong> stroke<br />

frequency: the female butterfly swimmer had a very good performance,<br />

thus approach<strong>in</strong>g the execution of the male athlete. Thus, the approach<br />

proposed <strong>in</strong> this paper allowed for the quantification of stroke frequency,<br />

but its application to performance analysis needs to be carried out <strong>in</strong><br />

presence of trials at a constant velocity, where differences could be attributed<br />

to a different strategy adopted by the swimmer. Focus<strong>in</strong>g on the<br />

ratio between glid<strong>in</strong>g <strong>and</strong> stroke phases, r 50 was consistently lower than<br />

r 25 , which <strong>in</strong>volves a longer glid<strong>in</strong>g phase after the rac<strong>in</strong>g start. Highest<br />

r 25 <strong>and</strong> r 50 were found for backstroke <strong>and</strong> butterfly, consistently with<br />

their theoretical style executions.<br />

conclusIon<br />

Inertial sensor devices <strong>in</strong>tegrat<strong>in</strong>g both accelerometers <strong>and</strong> gyroscopes<br />

represent a useful tool for performance evaluation <strong>in</strong> swimm<strong>in</strong>g research.<br />

Specifically, us<strong>in</strong>g gyroscopes represents a promis<strong>in</strong>g measurement technique<br />

for coaches to <strong>in</strong>vestigate how swim turn<strong>in</strong>g, underwater glid<strong>in</strong>g<br />

<strong>and</strong> stroke resumption phases are implemented <strong>in</strong> the different swimm<strong>in</strong>g<br />

styles. Strength po<strong>in</strong>ts of the approach are the simple description<br />

of the turn<strong>in</strong>g k<strong>in</strong>ematics, the possibility to extract multiple parameters<br />

useful for performance analysis, the simplicity of use for the operator,<br />

the m<strong>in</strong>imal encumber for the athlete. Future steps <strong>in</strong> this research will<br />

take <strong>in</strong>to account the <strong>in</strong>clusion of further athletes <strong>and</strong> the def<strong>in</strong>ition of<br />

further parameter (acceleration peaks, estimation of angles), eventually<br />

specific for each swimm<strong>in</strong>g styles.<br />

reFerences<br />

Lyttle AD, Blanksby BA, Elliott BC, Lloyd DG (1999). Optimis<strong>in</strong>g<br />

k<strong>in</strong>etics <strong>in</strong> the freestyle flip turn push-off. Journal of Applied <strong>Biomechanics</strong>,<br />

15: 242-52<br />

Ohgi Y, Ichikawa H, Homma M, Miyaji C (2003). Stroke phase discrim<strong>in</strong>ation<br />

<strong>in</strong> breaststroke swimm<strong>in</strong>g us<strong>in</strong>g a tri-axial acceleration<br />

sensor device. Sports Eng<strong>in</strong>eer<strong>in</strong>g, 6: 113–123.<br />

Pereira S, Vilar S, Goncaves P, Figueiredo P, Fern<strong>and</strong>es R, Roesler H,<br />

Vilas-Boas JP (2008). A comb<strong>in</strong>ed biomechanical analysis of the flip<br />

turn technique. Proceed<strong>in</strong>gs of the 26th ISBS Conference: 699-702.<br />

Slawson SE, Justham LM, West AA, Conway PP, Ca<strong>in</strong>e1 MP, Harrison<br />

R (2008). Accelerometer Profile Recognition of Swimm<strong>in</strong>g Strokes.<br />

The Eng<strong>in</strong>eer<strong>in</strong>g of Sport 7, 1: 81-88.<br />

Takahashi G, Yoshida A, Tsubakimoto S, Miyashita M (1982). Propulsive<br />

Forces Generated by Swimmers dur<strong>in</strong>g a Turn<strong>in</strong>g Motion.<br />

In Proc. of the Fourth International Symposium of <strong>Biomechanics</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g: 192-198. Champaign, Ill.: Human K<strong>in</strong>etic<br />

Publishers.<br />

180<br />

Influence of Swimm<strong>in</strong>g Start Styles on<br />

<strong>Biomechanics</strong> <strong>and</strong> Angular Momentum<br />

Vantorre, J. 1 , seifert, l. 1 , Bideau, B.²,nicolas, G.², Fern<strong>and</strong>es,<br />

r.J. 3 , Vilas-Boas, J.P. 3 , chollet, d. 1<br />

1 C.E.T.A.P.S. EA 3832, Faculty of Sports Sciences, University of Rouen,<br />

France<br />

2 M2S, University of Rennes 2, France<br />

3 CIFI2D, Faculty of Sport, University of Porto, Portugal<br />

The aim of this study was to analyze how the start style <strong>in</strong>fluences angular<br />

momentum. The durations of the block <strong>and</strong> flight phases, body<br />

angles at takeoff <strong>and</strong> entry, k<strong>in</strong>etic momentum, k<strong>in</strong>etics, <strong>and</strong> 15-m time<br />

were assessed. The sample was classified accord<strong>in</strong>g to start style. The flat<br />

start showed significantly lower angular momentum (H=14.7±2.92 vs.<br />

18.0±0.67 <strong>and</strong> 17.5±0.4 for pike <strong>and</strong> Volkov), shorter flight phase <strong>and</strong><br />

distance, <strong>and</strong> a smaller takeoff angle than the two other start styles. The<br />

analysis of angular momentum revealed two ma<strong>in</strong> strategies to achieve<br />

optimal performance: direct entry <strong>in</strong>to the water to reduce the temporal<br />

deficit <strong>and</strong> start swimm<strong>in</strong>g early (flat start), <strong>and</strong> the immediate generation<br />

of high velocity to achieve longer flight time <strong>and</strong> distance <strong>in</strong> order<br />

to compensate for the relative loss of time <strong>in</strong> the follow<strong>in</strong>g parts of the<br />

start (pike <strong>and</strong> Volkov).<br />

Key words: swimm<strong>in</strong>g start, start style, expertise, angular momentum<br />

IntroductIon<br />

Many studies have compared the different positions on the start block,<br />

but few have compared the aerial curve (def<strong>in</strong>ed as the takeoff <strong>and</strong> entry<br />

angles, <strong>and</strong> the body angles at takeoff <strong>and</strong> entry). The flat start <strong>and</strong> the<br />

pike start (also called the scoop, whip or hole start) have been described<br />

(e.g., Maglischo, 2003) but only a few studies have compared the two.<br />

Counsilman et al. (1988) showed a longer start time, greater takeoff <strong>and</strong><br />

entry angles, <strong>and</strong> a shorter distance to head entry for the pike start than<br />

for the flat start. However, this study was carried out <strong>in</strong> young swimmers<br />

from 10 to17 years old <strong>and</strong> not <strong>in</strong> elite spr<strong>in</strong>ters. In contrast, Wilson <strong>and</strong><br />

Mar<strong>in</strong>o (1983) showed <strong>in</strong> elite swimmers a shorter 10-m start time, a<br />

greater entry angle, a shorter distance to entry, <strong>and</strong> a greater hip angle at<br />

entry for the pike start than for the flat start. Kirner et al. (1989) had five<br />

tra<strong>in</strong><strong>in</strong>g sessions for swimmers <strong>in</strong> which they comb<strong>in</strong>ed grab/track starts<br />

<strong>and</strong> pike/flat entries <strong>and</strong> demonstrated that the grab start-flat entry had<br />

a shorter 8-m start time <strong>and</strong> a smaller entry angle than the grab start–<br />

pike entry. However, this study did not compare specialists of each start<br />

style but <strong>in</strong>stead imposed tra<strong>in</strong><strong>in</strong>g <strong>in</strong> <strong>and</strong> performance of the four styles;<br />

therefore, the 8-m start time may have been <strong>in</strong>fluenced by the preferential<br />

style of the swimmers. Seifert et al. (<strong>in</strong> press) studied 11 elite grab<br />

starters <strong>and</strong> front crawl spr<strong>in</strong>t specialists <strong>and</strong> dist<strong>in</strong>guished four aerial<br />

phase profiles. In addition to the flat start (upper limbs almost extended<br />

at takeoff <strong>and</strong> used for impulse <strong>in</strong> the block phase) <strong>and</strong> the pike start<br />

(greater arm sw<strong>in</strong>g <strong>and</strong> great takeoff <strong>and</strong> entry angles), they observed<br />

two other styles of aerial curve: the Volkov start (shoulders stretched<br />

upward <strong>and</strong> forward <strong>in</strong>stead of arms) <strong>and</strong> flight start (short block phase<br />

but long flight phase due to great leg power).<br />

McLean et al. (2000) calculated the angular momentum of the aerial<br />

phase, which is generated dur<strong>in</strong>g the block phase <strong>in</strong> order to quantify<br />

rotation. They analyzed several start relay techniques, with <strong>and</strong> without<br />

one or two steps before tak<strong>in</strong>g off from the block. Tak<strong>in</strong>g steps before<br />

leav<strong>in</strong>g the block resulted <strong>in</strong> greater takeoff <strong>and</strong> entry angles (like a pike<br />

start) <strong>and</strong> each step start was characterized by greater body rotation than<br />

the no-step start. Pike trajectory or arm sw<strong>in</strong>g dur<strong>in</strong>g the flight phase<br />

(Volkov style) thus has an effect on body rotation <strong>and</strong> consequently on<br />

the aerial part of the start. Indeed, the swim start cannot be reduced to<br />

generate the greatest forward impulse; the <strong>in</strong>itial position is a blocked


chaPter2.<strong>Biomechanics</strong><br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b 169<br />

forward unstead<strong>in</strong>ess. This unstead<strong>in</strong>ess permitted to obta<strong>in</strong> a couple<br />

of oppos<strong>in</strong>g forces <strong>and</strong> to <strong>in</strong>fluence the angular momentum. The aim<br />

of this study was to analyze how the start style <strong>in</strong>fluences the angular<br />

stretched upward <strong>and</strong> forward <strong>in</strong>stead of arms) <strong>and</strong> flight start (short block phase but<br />

momentum around the mediolateral axis, as this is an important char-<br />

long flight phase due to great leg power).<br />

acteristic McLean of et the al. start. (2000) calculated the angular momentum of the aerial phase, which is<br />

generated dur<strong>in</strong>g the block phase <strong>in</strong> order to quantify rotation. They analyzed several<br />

Methods<br />

start relay techniques, with <strong>and</strong> without one or two steps before tak<strong>in</strong>g off from the<br />

Five block. elite Tak<strong>in</strong>g male steps front-crawl before leav<strong>in</strong>g spr<strong>in</strong>ters the volunteered block resulted to <strong>in</strong> participate greater takeoff <strong>in</strong> this <strong>and</strong> entry angles<br />

(like a pike start) <strong>and</strong> each step start was characterized by greater body rotation than the<br />

study no-step (22±2 start. years; Pike 180±0.1 trajectory cm; or 74.7±7.9 arm sw<strong>in</strong>g kg; dur<strong>in</strong>g mean the time flight for phase a 100-m (Volkov style) thus<br />

front has crawl an effect <strong>in</strong> a on 50-m body pool: rotation 53.6±1.8 <strong>and</strong> consequently s). Each swimmer on the aerial performed part of the a start. Indeed,<br />

25-m the swim front start crawl cannot three times be reduced at the to 50-m generate race the pace greatest with the forward grab start impulse; the <strong>in</strong>itial<br />

position on is the a blocked block. A forward camera unstead<strong>in</strong>ess. (50 Hz) was This placed unstead<strong>in</strong>ess at the edge permitted of the to obta<strong>in</strong> a<br />

couple of oppos<strong>in</strong>g forces <strong>and</strong> to <strong>in</strong>fluence the angular momentum. The aim of this<br />

pool <strong>and</strong> videotaped the block phase to determ<strong>in</strong>e block phase duration,<br />

study was to analyze how the start style <strong>in</strong>fluences the angular momentum around the<br />

the mediolateral takeoff angle axis, (calculated as this is an from important the centre characteristic of gravity, of the foot start. extremity<br />

<strong>and</strong> horizontal axis), the wrist/shoulder/hip angle (body angle at takeoff<br />

METHODS ), <strong>and</strong> the duration <strong>and</strong> distance of the flight phase. A second camera<br />

(50 Five Hz) elite was male mounted front-crawl on a specially spr<strong>in</strong>ters volunteered designed support to participate placed <strong>in</strong> at this the study lat- (22±2 years;<br />

180±0.1 cm; 74.7±7.9 kg; mean time for a 100-m front crawl <strong>in</strong> a 50-m pool: 53.6±1.8<br />

eral wall 3 m from the edge of the pool deck to videotape the entry phase<br />

s). Each swimmer performed a 25-m front crawl three times at the 50-m race pace with<br />

(entry the grab angle, start calculated position from on the the block. centre A of camera gravity, (50 f<strong>in</strong>ger Hz) was extremity placed <strong>and</strong> at the edge of the<br />

horizontal pool <strong>and</strong> axis videotaped at water the contact). block A phase third to camera determ<strong>in</strong>e (50 block Hz) was phase placed duration, 15 the takeoff<br />

m angle from the (calculated edge of from the pool the centre deck to of determ<strong>in</strong>e gravity, foot the extremity moment the <strong>and</strong> swim- horizontal axis), the<br />

mer’s wrist/shoulder/hip head reached the angle 15-m (body mark angle (placed at takeoff), on the <strong>and</strong> swimm<strong>in</strong>g the duration l<strong>in</strong>e). <strong>and</strong> Im- distance of the<br />

flight phase. A second camera (50 Hz) was mounted on a specially designed support<br />

ages placed were at processed the lateral us<strong>in</strong>g wall Simi-Motion 3 m from the (Simi edge of Reality the pool Motion deck Systems to videotape the entry<br />

GmbH, phase (entry City, angle, Germany). calculated The from spatial the model centre of comprised gravity, f<strong>in</strong>ger 20 anatomical extremity <strong>and</strong> horizontal<br />

l<strong>and</strong>marks axis at water digitalized contact). <strong>in</strong> A each third frame, camera def<strong>in</strong><strong>in</strong>g (50 Hz) a 14-body was placed segment 15 m model from the edge of the<br />

(de pool Leva, deck 1996). to determ<strong>in</strong>e To compute the moment the angular the swimmer’s momentum head for reached each body the seg- 15-m mark (placed<br />

on the swimm<strong>in</strong>g l<strong>in</strong>e). Images were processed us<strong>in</strong>g Simi-Motion (Simi Reality<br />

ment, we evaluated the mechanical parameters such as the segment mass<br />

Motion Systems GmbH, City, Germany). The spatial model comprised 20 anatomical<br />

<strong>and</strong> l<strong>and</strong>marks <strong>in</strong>ertia. For digitalized this purpose, <strong>in</strong> each we frame, assumed def<strong>in</strong><strong>in</strong>g that each a 14-body body segment, segment ex- model (de Leva,<br />

cept 1996). the head, To compute could be the modelled angular momentum as a homogeneous for each cyl<strong>in</strong>der. body segment, The head we evaluated the<br />

was mechanical considered parameters as a sphere. such To obta<strong>in</strong> as the the segment body mass segment <strong>and</strong> <strong>in</strong>ertia, <strong>in</strong>ertia. we For used this purpose, we<br />

the assumed radius of that gyration each body computed segment, by except Zatsiorsky the head, <strong>and</strong> could Seluyanov be modelled (1983). as As a homogeneous<br />

cyl<strong>in</strong>der. The head was considered as a sphere. To obta<strong>in</strong> the body segment <strong>in</strong>ertia, we<br />

the motions were <strong>in</strong> two dimensions, we computed the angular momen-<br />

used the radius of gyration computed by Zatsiorsky <strong>and</strong> Seluyanov (1983). As the<br />

tum motions along the were transverse <strong>in</strong> two dimensions, axis as follows: we computed the angular momentum along the<br />

transverse axis as follows:<br />

i<br />

⎛<br />

L GZ / F * = [ Ii<br />

] wi<br />

z + mi⎜<br />

( GGix<br />

* VGiy<br />

/ F * ) − ( GGi<br />

y * VGix<br />

/ F *<br />

⎝<br />

⎞<br />

)⎟<br />

⎠<br />

where G is the centre of gravity of the whole body, mi is the mass of the ith segment, Gi<br />

where G is the centre of gravity of the whole body, m<br />

is the centre of mass of the ith segment, F* is the barycentric i is the mass of the<br />

frame, Ii is the <strong>in</strong>ertial<br />

i matrix of the ith segment, <strong>and</strong> wi is the angular velocity. The total angular momentum <strong>in</strong><br />

the global frame was then obta<strong>in</strong>ed by add<strong>in</strong>g the local angular momentum of each<br />

segment.<br />

Angular momentum was calculated at takeoff (H, kg.m²/s) <strong>and</strong> the mean st<strong>and</strong>ard<br />

deviation for H (∆H, kg.m²/s) was also calculated. For dynamic analysis, starts were<br />

th segment, Gi is the centre of mass of the results<br />

The takeoff angle differed significantly with the start styles <strong>and</strong> ranged<br />

from 19±3.3° for flat start to 27.8±2.4° for Volkov start (26.8±3.6° was<br />

measured for the pike start). Three swimmers used a flat start def<strong>in</strong>ed<br />

by a low takeoff angle (19±3.3°) <strong>and</strong> one swimmer used the pike start<br />

(26.8±3.6°). The body angle at takeoff (wrist/shoulder/hip) was significantly<br />

different between the three start styles. The Volkov start showed<br />

negative values because of the position of the arms beh<strong>in</strong>d the trunk.<br />

The entry angle was significantly greater for the pike start (34.3±3.9°,<br />

39.7 ±2.8° <strong>and</strong> 37±3.1°, respectively, for the flat, pike <strong>and</strong> Volkov starts).<br />

Although these differences were not statistically significant, greater entry<br />

angles were observed for the pike <strong>and</strong> Volkov vs. the flat start. No<br />

significant difference <strong>in</strong> performance to the 15-m mark was observed<br />

between the start style groups. The takeoff angle, flight distance, <strong>and</strong><br />

the total <strong>and</strong> st<strong>and</strong>ard deviation of the angular momentum were significantly<br />

lower for the flat start than for the two other start styles (with a<br />

significantly longer flight phase for the Volkov start <strong>in</strong> comparison with<br />

the two other starts). The time to 15-m was significantly <strong>and</strong> negatively<br />

correlated with the vertical impulse (r=-0.507) <strong>and</strong> positively correlated<br />

with <strong>Biomechanics</strong> ΔH (r=0.461) <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> (Table <strong>in</strong> Swimm<strong>in</strong>g 1). <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b 171<br />

Table 1. Start parameters as a function of start style<br />

Table 1. Start parameters as a function of start style<br />

Start Styles Flat Start (n=3) Pike Start (n=1) Volkov Start (n=2) Correlation<br />

with T15m<br />

Block Phase (s) 0.95±0.04 0.94±0.03 0.89±0.08<br />

Flight Phase (s) 0.26±0.02 0.32±0 a 0.38±0.03 a, b<br />

Flight Distance 3±0.06<br />

(m)<br />

Takeoff Angle 22.1±3.5<br />

(°)<br />

Entry Angle (°) 23.4±2.2<br />

3.2±0.01 a<br />

30.0±2.7 a<br />

24.6±4.8<br />

3.2±0.03 b<br />

34.6±5.2 b<br />

28.2±2.5<br />

Body Angle at<br />

Takeoff (°)<br />

Horizontal<br />

Impulse (N)<br />

Vertical<br />

Impulse (N)<br />

145.3 ±7.6<br />

788.4±48.7<br />

188.7±26.2<br />

27.1±10.5 a<br />

698.9±60.8<br />

171.5±21<br />

- 55.4±13.9 a, b<br />

829.2±61.9 a<br />

205.4±31 r= -0.507<br />

H Takeoff<br />

(kg.m²/s)<br />

∆H (kg.m²/s)<br />

14.7±2.92<br />

0.8±0.13<br />

18.0±0.67 a<br />

1.1±0.2 a<br />

17.5±0.4 b<br />

1.1±0.15 b r= 0.461<br />

Time to 15m (s) 6.5±0.2 6.6±0.08 6.6±0.07<br />

a: significantly different from the previous style on the table; b: significantly different<br />

ith segment, F* is the bary- a: from significantly the flat start different from the previous style on the table; b: significentric<br />

frame, Ii is the <strong>in</strong>ertial matrix of the ith segment, <strong>and</strong> wi is the cantly different from the flat start<br />

DISCUSSION<br />

angular velocity. The total angular momentum <strong>in</strong> the global frame was The aim of this study was to analyze how the start style <strong>in</strong>fluences angular momentum.<br />

then obta<strong>in</strong>ed by add<strong>in</strong>g the local angular momentum of each segment. dIscussIon<br />

The results regard<strong>in</strong>g the k<strong>in</strong>etic momentum showed that significantly less rotation<br />

generated dur<strong>in</strong>g impulsion <strong>in</strong>duced a flat aerial trajectory <strong>and</strong> permitted the swimmers<br />

Angular momentum was calculated at takeoff (H, kg.m²/s) <strong>and</strong> the The to enter aim the of water this more study quickly was (as to demonstrated analyze how by a significantly the start style shorter <strong>in</strong>fluences flight phase). an-<br />

mean st<strong>and</strong>ard deviation for H (ΔH, kg.m²/s) was also calculated. For<br />

dynamic analysis, starts were evaluated with a Bertec 4060-15 force plate<br />

gular The pike momentum. <strong>and</strong> Volkov starts The showed results significantly regard<strong>in</strong>g more the rotation. k<strong>in</strong>etic The momentum arm sw<strong>in</strong>g <strong>in</strong> showed the<br />

pike (forward) <strong>and</strong> Volkov (backward then forward) <strong>in</strong>creased the quantity of rotation.<br />

that In the significantly Volkov start, the less backward rotation sw<strong>in</strong>g generated dur<strong>in</strong>g impulse dur<strong>in</strong>g accelerated impulsion the forward <strong>in</strong>duced rotation a flat<br />

(Bertec Corp., Columbus OH, USA) mounted on a specially built support<br />

fixed to the pool wall to allow a start position that conformed with<br />

the FINA rules. The sampl<strong>in</strong>g rate was 1000 Hz. The analogue signal was<br />

transmitted to a PC through a Biopac A/D converter (Biopac Systems<br />

Inc., Goleta CA, USA). The start signal was <strong>in</strong> accordance with the swimm<strong>in</strong>g<br />

rules <strong>and</strong> was produced by the starter device (ProStart). After filter<strong>in</strong>g<br />

<strong>and</strong> smooth<strong>in</strong>g (Hamm<strong>in</strong>g, low pass, 80 Hz), the reaction time,<br />

impulse time <strong>and</strong> impulse values were obta<strong>in</strong>ed <strong>in</strong> 3D from the force<br />

plate. Only the horizontal <strong>and</strong> vertical axes were analyzed because they<br />

aerial of the body trajectory but the swimmer’s <strong>and</strong> permitted head was <strong>in</strong> the complete swimmers extension, to thus enter <strong>in</strong> opposition the water to the more<br />

arms. The opposite was observed for the pike start. The body angle at takeoff <strong>in</strong>dicated<br />

quickly that the arms (as were demonstrated <strong>in</strong> cont<strong>in</strong>uation by of the a body significantly for the flat style shorter (angle flight close to phase). 180° with The<br />

pike 145.3±7.6°). <strong>and</strong> Volkov The Volkov starts start showed significantly a negative value more due rotation. to the fact The that arm the arms sw<strong>in</strong>g<br />

were beh<strong>in</strong>d the trunk, <strong>and</strong> the values were low for the pike start (27.1±10.5°),<br />

<strong>in</strong> <strong>in</strong>dicat<strong>in</strong>g the pike that (forward) the swimmers <strong>and</strong> were Volkov able (backward to sw<strong>in</strong>g the then arms forward forward) dur<strong>in</strong>g <strong>in</strong>creased the flight the<br />

quantity phase. The of takeoff rotation. <strong>and</strong> entry In angles, the Volkov distance start, to h<strong>and</strong> the entry, backward <strong>and</strong> phase sw<strong>in</strong>g duration dur<strong>in</strong>g were <strong>in</strong> im-<br />

the range of the results provided by the literature: flight distance was 3.09±0.14 m <strong>in</strong><br />

pulse our study accelerated vs. 3.42±0.16 the m for forward McLean rotation et al. (2000), of the <strong>and</strong> the body angular but momentum the swimmer’s was<br />

head 16.2±2.5 was kg.m²/s <strong>in</strong> complete <strong>in</strong> our study extension, vs. 16.4±3.2 thus kg.m²/s <strong>in</strong> opposition for McLean et to al. the (2000). arms. The The<br />

vertical impulse was significantly <strong>and</strong> negatively correlated with time to 15-m,<br />

opposite <strong>in</strong>dicat<strong>in</strong>g that was an observed efficient vertical for the impulse pike needs start. to The be high body enough angle to ensure at takeoff that the <strong>in</strong>dicated<br />

flight distance that is the sufficiently arms were long <strong>in</strong> (this cont<strong>in</strong>uation variable was not of significantly the body for different the among flat style<br />

made up the plane <strong>in</strong> which the swimmer moved. The swimmers’ starts (angle close to 180° with 145.3±7.6°). The Volkov start showed a negative<br />

were classified accord<strong>in</strong>g to the four start styles presented by Seifert et al. value due to the fact that the arms were beh<strong>in</strong>d the trunk, <strong>and</strong> the values<br />

(<strong>in</strong> press). The parameters def<strong>in</strong><strong>in</strong>g the start styles were: block <strong>and</strong> flight were low for the pike start (27.1±10.5°), <strong>in</strong>dicat<strong>in</strong>g that the swimmers<br />

phases, takeoff angle (arms/trunk <strong>and</strong> body/horizontal axes), body angle were able to sw<strong>in</strong>g the arms forward dur<strong>in</strong>g the flight phase. The takeoff<br />

at takeoff (wrist/shoulder/hip), <strong>and</strong> entry angles (body/horizontal axis <strong>and</strong> entry angles, distance to h<strong>and</strong> entry, <strong>and</strong> phase duration were <strong>in</strong><br />

at h<strong>and</strong> entry). After verify<strong>in</strong>g the normality of the data (checked with the range of the results provided by the literature: flight distance was<br />

the Shapiro-Wilk test), ANOVA tests analyzed the variables that signifi- 3.09±0.14 m <strong>in</strong> our study vs. 3.42±0.16 m for McLean et al. (2000), <strong>and</strong><br />

cantly differentiated the start styles. Pearson correlation analysis was also the angular momentum was 16.2±2.5 kg.m²/s <strong>in</strong> our study vs. 16.4±3.2<br />

applied to study the relationships between the start parameters <strong>and</strong> the kg.m²/s for McLean et al. (2000). The vertical impulse was significantly<br />

total 15-m start time (T15m). Statistics were performed with M<strong>in</strong>itab <strong>and</strong> negatively correlated with time to 15-m, <strong>in</strong>dicat<strong>in</strong>g that an effi-<br />

14.10 (M<strong>in</strong>itab Inc., 2003) <strong>and</strong> the level of significance was set at p< 0.05 cient vertical impulse needs to be high enough to ensure that the flight<br />

181


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

distance is sufficiently long (this variable was not significantly different<br />

among the start styles). These elite swimmers had flight distances of at<br />

least 3 m. The mean st<strong>and</strong>ard deviation for the angular momentum was<br />

used to determ<strong>in</strong>e the transfer of angular momentum from the transverse<br />

axis to the two other axes, especially the sagittal axis with twist<strong>in</strong>g<br />

of the trunk. The results <strong>in</strong>dicated that the flat start (<strong>in</strong> grab start technique)<br />

<strong>in</strong>duced less angular momentum transfer. The transfer may have<br />

been affected <strong>in</strong> rotations <strong>in</strong> the sagittal axis (rotations of shoulders <strong>and</strong>/<br />

or hips), as shown by Benvanutra et al. (2004) through the measurement<br />

of the dissymmetry <strong>in</strong> the left <strong>and</strong> right foot impulses dur<strong>in</strong>g the grab<br />

(<strong>and</strong> track) start. This dissymmetry can produce a sagittal rotation of<br />

the hips <strong>and</strong> consequent twist<strong>in</strong>g of the trunk. The flat start showed<br />

less st<strong>and</strong>ard deviation, which <strong>in</strong>dicates that start performances with<br />

this style can be as efficient as with the two others. The flat start style<br />

<strong>in</strong> fact <strong>in</strong>dicates that some swimmers prefer to reduce a temporal deficit<br />

(lower mastery of the start technique) rather than try<strong>in</strong>g to travel greater<br />

distances <strong>in</strong> the air <strong>in</strong> order to keep higher velocity at water entry for<br />

the follow<strong>in</strong>g phases.<br />

conclusIon<br />

Expertise cannot be reduced to the efficient performance of a s<strong>in</strong>gle<br />

technique. Instead, it is demonstrated by the optimization of personal<br />

characteristics <strong>in</strong> order to achieve optimal performance. These expert<br />

swimmers displayed two means to obta<strong>in</strong> optimal performance: direct<br />

(<strong>and</strong> clean) entry <strong>in</strong>to the water to reduce the temporal deficit <strong>and</strong> start<br />

swimm<strong>in</strong>g early, <strong>and</strong> the immediate generation of high velocity with<br />

greater flight distances to compensate for the relative loss of time <strong>in</strong> the<br />

follow<strong>in</strong>g parts of the start (the glide phase, for example).<br />

reFerences<br />

Benjanuvatra, N., Lyttle, A., Blanksby, B., Lark<strong>in</strong>, D. (2004). Force development<br />

profile of the lower limbs <strong>in</strong> the grab <strong>and</strong> track start, <strong>in</strong><br />

swimm<strong>in</strong>g. X<strong>XI</strong>Ith International Symposium on <strong>Biomechanics</strong> <strong>in</strong><br />

Sports. Ottawa, Faculty of Health Sciences University of Ottawa:<br />

399-402<br />

Counsilman, J.E., Counsilman B.E., Nomura, T., Endo, M. (1988).<br />

Three types of grab starts for competitive swimm<strong>in</strong>g. In: Swimm<strong>in</strong>g<br />

Science V. B.E. Ungerechts, K. Wilke, <strong>and</strong> K. Reischle, eds. Champaign,<br />

Ill<strong>in</strong>ois, Human K<strong>in</strong>etics Publishers, 81-91<br />

De Leva, P. (1996). Adjustments to Zatsiorsky-Seluyanov’s segment <strong>in</strong>ertia<br />

parameters. J Appl Biomech, 29, 1223-1230<br />

Kirner, K.E., Bock, M.A., Welch, J.H. (1989). A comparison of four<br />

different start comb<strong>in</strong>ations. J Swim Res, 5, 5-11<br />

Maglischo, E.W. (2003). Swimm<strong>in</strong>g fastest, Champaign: Ill<strong>in</strong>ois, Human<br />

K<strong>in</strong>etics<br />

Ashby, B., Heegaard, J. (2002). Role of arm motion <strong>in</strong> the st<strong>and</strong><strong>in</strong>g long<br />

jump. J Biomech, 35, 1631-1637<br />

McLean, S.P., Holthe, M.J., V<strong>in</strong>t, P.F., Beckett, K.D., H<strong>in</strong>richs, R.N.<br />

(2000). Addition of an approach to swimm<strong>in</strong>g relay start. J Appl Biomech,<br />

16, 342-355<br />

Seifert, L., Vantorre, J., Lemaitre, F., Chollet, D., Toussa<strong>in</strong>t, H.M., Vilas-Boas,<br />

J.P. (2010) (<strong>in</strong> press). Different profiles of the aerial start<br />

phase <strong>in</strong> front crawl. J Strength Cond Res<br />

Wilson, D.S., Mar<strong>in</strong>o, G.W. (1983). K<strong>in</strong>ematic analysis of three starts.<br />

Swim Tech, 19: 30<br />

Zatsiorsky, Seluyanov (1983). The mass <strong>and</strong> <strong>in</strong>ertia characteristics of the<br />

ma<strong>in</strong> segments of the human body. In <strong>Biomechanics</strong> VIII, 8, 1152-<br />

1159<br />

182<br />

The Validity <strong>and</strong> Reliability of a Procedure for<br />

Competition Analysis <strong>in</strong> Swimm<strong>in</strong>g Based on<br />

Individual Distance Measurements<br />

Veiga, s. 1 , cala, A. 2 , González Frutos, P. 1 , navarro, e. 1<br />

1 Faculty of Physical Activity <strong>and</strong> Sport Sciences-INEF, Madrid, Spa<strong>in</strong><br />

2 New Zeal<strong>and</strong> Academy of Sport North Isl<strong>and</strong>, Auckl<strong>and</strong>, New Zeal<strong>and</strong><br />

In swimm<strong>in</strong>g, competition analyses have been frequently performed accord<strong>in</strong>g<br />

to three segments of the race, equal for all competitors. However,<br />

<strong>in</strong>dividual distance measurements dur<strong>in</strong>g start <strong>and</strong> turn race segments<br />

have been scarcely assessed. The aim of the present study was:<br />

1) to verify the validity <strong>and</strong> reliability of a 2D-DLT based system for<br />

competition analysis <strong>in</strong> swimm<strong>in</strong>g <strong>and</strong>, 2) to compare it with the commonly<br />

used technique. Higher values of accuracy (RMSE=0.05 m) <strong>and</strong><br />

reliability (CV


20 to 30 meter) <strong>and</strong> turn phase (from 35 to 50 meter). All cameras were<br />

connected to computers where the images were stored <strong>in</strong> real time. A<br />

light flash connected to the official tim<strong>in</strong>g system <strong>and</strong> captured by the<br />

camera film<strong>in</strong>g start phase provided the beg<strong>in</strong>n<strong>in</strong>g of the time code.<br />

The same camera system was used for both competition analyses: i)<br />

us<strong>in</strong>g a l<strong>in</strong>ear scale system, vertical l<strong>in</strong>es were overlaid on each camera<br />

view def<strong>in</strong><strong>in</strong>g the beg<strong>in</strong>n<strong>in</strong>g <strong>and</strong>/or end of the race segments dur<strong>in</strong>g the<br />

analysis process; ii) us<strong>in</strong>g 2D photogrammetry, computerized analysis of<br />

the frames was carried out with software Photo 23D (Cala et al., 2009);<br />

<strong>and</strong> the algorithm with 2D direct l<strong>in</strong>ear transformation (2D-DLT) was<br />

used (Abdel-Aziz <strong>and</strong> Karara, 1971).<br />

Forty control po<strong>in</strong>ts (8 calibration <strong>and</strong> 32 reconstruction) for each<br />

camera were uniformly distributed on the horizontal plane delimitated<br />

by the water surface. Control po<strong>in</strong>ts used for calibration purposes were<br />

pool-side build<strong>in</strong>g marks while reconstruction po<strong>in</strong>ts were colored<br />

buoys from the float<strong>in</strong>g lanes. Reference l<strong>in</strong>es connect<strong>in</strong>g the near <strong>and</strong><br />

far sides of the pool were used to place the colored buoys at exactly the<br />

appropriate distance.<br />

The accuracy of the 2D-DLT measurement system was assessed reconstruct<strong>in</strong>g<br />

the position of 32 control po<strong>in</strong>ts <strong>in</strong> the field of view of one<br />

camera; distance between the control po<strong>in</strong>ts was also reconstructed. Although<br />

these control po<strong>in</strong>ts used for reconstruction purposes were easily<br />

recognized <strong>in</strong> the image, as the accuracy of the competition analysis<br />

depends on how well the competitors can be identified. There is no way<br />

to directly evaluate the accuracy of every measurement dur<strong>in</strong>g competition<br />

(Challis, 1995), so sampl<strong>in</strong>g of the same action must be repeatedly<br />

checked for consistency.<br />

For that purpose, two actions at the beg<strong>in</strong>n<strong>in</strong>g <strong>and</strong> the end of the<br />

freestyle turn phase were repeatedly digitalized 30 times by the same<br />

experienced observer. The swimmer’s h<strong>and</strong> entry of the last stroke before<br />

the wall represented the beg<strong>in</strong>n<strong>in</strong>g of the turn; on the other h<strong>and</strong>, the<br />

mark where the swimmer´s head passes completely the water surface<br />

after the underwater swim represented the end of the turn phase. No<br />

technical actions other than freestyle turn were assessed s<strong>in</strong>ce both h<strong>and</strong><br />

entry or head emersion are used <strong>in</strong> all four strokes. The digitization process<br />

was repeated <strong>in</strong> each lane of the pool, represent<strong>in</strong>g the lane 1 the<br />

nearest side <strong>in</strong> the field of view. Horizontal total distance (m) of the turn<br />

phase was obta<strong>in</strong>ed us<strong>in</strong>g the 2D-DLT measurement system.<br />

F<strong>in</strong>ally, 32 times of each stroke <strong>and</strong> race segment were measured us<strong>in</strong>g<br />

the two procedures for competition analysis separately. The variables<br />

were identified when swimmer’s head pass every reference as follows:<br />

start time = start signal to 15 m mark; turn time = 7.5 m – 7.5 m before<br />

<strong>and</strong> after the wall; swim time = start time – turn time.<br />

Root mean square error (RMSE) (Allard et al., 1995), ratio maxto-RMSE,<br />

mean error <strong>and</strong> absolute error were measured to check the<br />

accuracy of the 2D-DLT measurement system. Coefficient of variation<br />

(CV) as an <strong>in</strong>dex of the absolute reliability (Atk<strong>in</strong>son <strong>and</strong> Nevill, 1998)<br />

<strong>and</strong> st<strong>and</strong>ard deviation (SD) were used to evaluate the consistency of<br />

30 repeated observations. F<strong>in</strong>ally, the two procedures for swimm<strong>in</strong>g<br />

competition analysis were compared with the Bl<strong>and</strong> <strong>and</strong> Altman’s 95%<br />

limits of agreement (Bl<strong>and</strong> <strong>and</strong> Altman, 1986); heteroscedasticity was<br />

previously checked us<strong>in</strong>g a Bl<strong>and</strong>-Altman plot.<br />

results<br />

The root mean square error of the 2D-DLT measurement system when<br />

reconstruct<strong>in</strong>g the position of 32 control po<strong>in</strong>ts was 0.050 meter, less<br />

than 0.5% of control space <strong>in</strong> x axis. Reconstruct<strong>in</strong>g the distance between<br />

the control po<strong>in</strong>ts, the RMSE was 0.046 meter, lower than 1.2%<br />

of the total distance. (Table 1)<br />

chaPter2.<strong>Biomechanics</strong><br />

Table 1: Accuracy (m) of the position <strong>and</strong> the <strong>in</strong>ter-control po<strong>in</strong>ts distance<br />

reconstruction’s us<strong>in</strong>g 2D-DLT procedure.<br />

Position Distance<br />

RMSE (root mean squared error) 0.050 0.046<br />

Ratio max-rmse 2.064 1.941<br />

Mean error 0.012 0.028<br />

Absolute error 0.045 0.031<br />

The consistency <strong>in</strong> the repeated digitization of the swimmer position<br />

dur<strong>in</strong>g the turn phase is shown <strong>in</strong> Table 2. Consider<strong>in</strong>g the total distance<br />

of the turn, differences <strong>in</strong> the measurements are consistently lower<br />

than 1%.<br />

Table 2: Consistency (m) of digitiz<strong>in</strong>g the beg<strong>in</strong>n<strong>in</strong>g (h<strong>and</strong> entry), the<br />

end (head emersion) <strong>and</strong> the total distance of freestyle turn us<strong>in</strong>g 2D-<br />

DLT procedure. (SD: st<strong>and</strong>ard deviation; CV: coefficient of variation)<br />

H<strong>and</strong> entry<br />

(SD)<br />

Head emersion (SD)<br />

Turn distance<br />

(SD)<br />

Turn distance<br />

(CV)<br />

Lane 1 0.0127 0.0092 0.0155 0.5292%<br />

Lane 2 0.0206 0.0109 0.0208 0.5906%<br />

Lane 3 0.0236 0.0159 0.0243 0.8487%<br />

Lane 4 0.0243 0.0143 0.0274 0.7267%<br />

Lane 5 0.0216 0.0192 0.0313 0.9343%<br />

Lane 6 0.0241 0.0188 0.0255 0.7857%<br />

Lane 7 0.0225 0.0178 0.0272 0.9247%<br />

Lane 8 0.0262 0.0214 0.0343 0.9338%<br />

The limits of agreement between the scal<strong>in</strong>g technique <strong>and</strong> the 2D-<br />

DLT photogrammetry <strong>in</strong> each segment of the swimm<strong>in</strong>g race are shown<br />

<strong>in</strong> Table 3. Maximum systematic differences between procedures occur<br />

dur<strong>in</strong>g freestyle <strong>and</strong> backstroke turn time (0.05 s), be<strong>in</strong>g r<strong>and</strong>om error<br />

higher <strong>in</strong> the breaststroke turn.<br />

Table 3: 95% limits of agreement (s) between 2D-DLT <strong>and</strong> scal<strong>in</strong>g<br />

technique dur<strong>in</strong>g competition analysis<br />

Stroke Start time Swim time Turn time<br />

Freestyle 0.0062 ± 0.0711 0.0344 ± 0.1231 0.0474 ± 0.1341<br />

Backstroke 0.0164 ± 0.0860 0.0208 ± 0.1088 0.0474 ± 0.1191<br />

Breaststroke 0.0164 ± 0.1553 0.0348 ± 0.2074 0.0192 ± 0.2365<br />

Butterfly 0.0167 ± 0.1223 0.0325 ± 0.2083 0.0128 ± 0.1479<br />

dIscussIon<br />

Application of 2D-DLT technique for analysis of swimm<strong>in</strong>g competition<br />

shows great accuracy. In comparison to studies analyz<strong>in</strong>g activities<br />

with a smaller field of view (Table 4), the 2D-DLT procedures <strong>in</strong><br />

swimm<strong>in</strong>g shows similar accuracy values, with errors reported around<br />

0.05 meter. The only study measur<strong>in</strong>g RMSE with 2D-DLT technique<br />

(Challis, 1998) reports similar values corrected to dimensions of the<br />

field of view. Even if the errors presented are concerned with easily identifiable<br />

po<strong>in</strong>ts <strong>in</strong> the image, <strong>and</strong> not anatomical l<strong>and</strong>marks, the protocol<br />

used provides an appropriate method for assess<strong>in</strong>g the accuracy of the<br />

reconstruction technique.<br />

183


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 4: Accuracy of reconstruct<strong>in</strong>g the position <strong>in</strong> x axis when analyz<strong>in</strong>g<br />

different activities with DLT procedures. RMSE corrected to the<br />

dimensions of the control space.<br />

STUDY ACTIVITY PROCEDURE RMSE<br />

Lauder et al. (2001) Swimm<strong>in</strong>g 3D Peak Performance 0.15%<br />

Payton et al. (2002) Swimm<strong>in</strong>g 3D-DLT 0.154%<br />

Challis <strong>and</strong> Kerv<strong>in</strong> (1992) Laboratory 3D-DLT 0.160%<br />

S<strong>and</strong>ers et al. (1998) Swimm<strong>in</strong>g 3D-DLT 0.273%<br />

Challis et al. (1998) Vertical jump 2D-DLT 0.3%<br />

Present study Swimm<strong>in</strong>g 2D-DLT 0.333%<br />

Cappaert et al. (1995) Swimm<strong>in</strong>g 3D-DLT 0.618%<br />

About the consistency of the digitization process, the identification of<br />

body l<strong>and</strong>marks <strong>in</strong> swimm<strong>in</strong>g competition with 2D-DLT technique<br />

shows high levels of <strong>in</strong>tra-rater reliability; even <strong>in</strong> the farthest side of<br />

the pool (lane 8) the coefficient of variation of the measured distances<br />

is less than 1%. It is suggested that no corrections are necessary if errors<br />

reported are less than 3% of the total distance (Blanksby et al., 2004).<br />

Two technical actions successfully tested dur<strong>in</strong>g the digitization process<br />

(h<strong>and</strong> entry <strong>and</strong> head emersion) allow multiple possibilities <strong>in</strong> the measurement<br />

of any variable dur<strong>in</strong>g competition.<br />

Although validity of DLT techniques has been confirmed <strong>in</strong> the video-analysis<br />

of underwater footages <strong>in</strong> two dimensions (Kwon, 1999) <strong>and</strong><br />

three dimensions (S<strong>and</strong>ers et al., 1998), no other studies applied DLT<br />

techniques to swimm<strong>in</strong>g competition analysis; most of the studies use<br />

the scal<strong>in</strong>g technique, superimpos<strong>in</strong>g digital l<strong>in</strong>es onto the video playback<br />

based on pool-side calibration mark<strong>in</strong>gs (Thompson et al., 2000);<br />

with this procedure the distance of the race segments is equal for every<br />

competitor. However, no <strong>in</strong>formation relat<strong>in</strong>g the validation of such a<br />

technique has been previously published.<br />

In this study, the measurement of the traditional race segments with<br />

both 2D-DLT <strong>and</strong> scal<strong>in</strong>g techniques showed systematic differences<br />

no longer than a frame of st<strong>and</strong>ard-speed video (0.04 s.). R<strong>and</strong>om error,<br />

however, rise to 0.20 s. <strong>in</strong> some strokes (breaststroke <strong>and</strong> butterfly)<br />

where the swimmer’s head moves underwater as part of the swim cycle;<br />

dur<strong>in</strong>g these frames, the identification of the swimmer’s position on<br />

the image seems to be difficult. S<strong>in</strong>ce the use of 2D-DLT technique<br />

is shown as accurate <strong>and</strong> reliable <strong>in</strong> this study, the differences with the<br />

scal<strong>in</strong>g technique could be acceptable for its practical use <strong>in</strong> competition<br />

analysis. However, precautions must be taken when measurements are<br />

made dur<strong>in</strong>g underwater parts of the race.<br />

conclusIon<br />

In summary, the application of 2D-DLT technique to the competition<br />

analysis <strong>in</strong> swimm<strong>in</strong>g shows to be highly accurate <strong>and</strong> reliable. Position<br />

of the swimmer <strong>and</strong> distance swam dur<strong>in</strong>g race segments can be measured<br />

with<strong>in</strong> ±0.05 m, allow<strong>in</strong>g the measurement <strong>and</strong> comparison of<br />

different factors <strong>in</strong>fluenc<strong>in</strong>g performance <strong>in</strong> competition. For practical<br />

implications, time measurements dur<strong>in</strong>g the different parts of the race<br />

us<strong>in</strong>g 2D-DLT can be compared with the traditional scal<strong>in</strong>g technique.<br />

reFerences<br />

Abdel-Aziz, Y. I., Karara, H. M. (1971). Direct l<strong>in</strong>ear transformation<br />

from comparator coord<strong>in</strong>ates <strong>in</strong>to space coord<strong>in</strong>ates <strong>in</strong> close range<br />

photogrammetry. In: American Society of Photogrammetry (Ed.),<br />

Proceed<strong>in</strong>gs of the Symposium on Close Range Photogrammetry. Falls-<br />

Church, E.E.U.U.<br />

Allard, P., Blanchi, J. P., Aissaoui, R. (1995). Bases of three-dimensional<br />

reconstruction. In: Allard, P. (ed.), Three-dimensional Analysis of Human<br />

Movement, 19-40. Champaign, Ill<strong>in</strong>ois.<br />

184<br />

Atk<strong>in</strong>son, G., Nevill, A. M. (1998). Statistical methods for assess<strong>in</strong>g<br />

measurement error (reliability) <strong>in</strong> variables relevant to sports medic<strong>in</strong>e.<br />

Sports <strong>Medic<strong>in</strong>e</strong>, 26(4), 217-238.<br />

Bl<strong>and</strong>, J. M., Altman, D. G. (1986). Statistical methods for assess agreement<br />

between two methods of cl<strong>in</strong>ical measurement. The Lancet, 307-<br />

11.<br />

Blanksby, B., Skender, S., Elliott, B., McElroy, K., L<strong>and</strong>ers, G. (2004).<br />

An analysis of the rollover backstroke turn by age-group swimmers.<br />

Sports <strong>Biomechanics</strong>, 3(1), 1-14.<br />

Cala, A., Veiga, S., Garcia, A., Navarro, E. (2009). Previous cycl<strong>in</strong>g does<br />

not affect runn<strong>in</strong>g efficiency dur<strong>in</strong>g a triathlon World Cup competition.<br />

Journal of Sport <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Physical Fitness, 49, 152-158.<br />

Challis, J. H. (1995). A multiphase calibration procedure for the direct<br />

l<strong>in</strong>ear transformation. Journal of Applied <strong>Biomechanics</strong>, 11(3), 351.<br />

Challis, J. H. (1998). An <strong>in</strong>vestigation of the <strong>in</strong>fluence of bi-lateral deficit<br />

on human jump<strong>in</strong>g. Human Movement Science, 17(3), 307.<br />

Chatard, J. C., Girold, S., Caudal, N., Cossor, J., Mason, B. (2003). Analysis<br />

of the 200m events <strong>in</strong> the Sydney Olympic games. <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX: 261-264. Sa<strong>in</strong>t-Etienne, France.<br />

Chow, J. W. C., Hay, J. G., Imel, C., Wilson, B. D. (1984). Turn<strong>in</strong>g techniques<br />

of elite swimmers. Journal of Sports Sciences, 2(3), 241-255.<br />

Hay, J. G., Reid, J. G. (1982). The anatomical <strong>and</strong> mechanical bases of human<br />

motion. New Jersey: Prentice-Hall.<br />

Hay, J. G., Guimaraes, A. C. S. (1983). A quantitative look at swimm<strong>in</strong>g<br />

biomechanics. Swimm<strong>in</strong>g Technique, 20(2), 11-12; 14-17.<br />

Kwon, Y. H. (1999). Object plane deformation due to refraction <strong>in</strong> twodimensional<br />

underwater motion analysis. Journal of Applied <strong>Biomechanics</strong>,<br />

15(4), 396.<br />

Mallo, J. (2009). Physical dem<strong>and</strong>s of top-class soccer assistant referee<strong>in</strong>g<br />

dur<strong>in</strong>g high-st<strong>and</strong>ard matches. International Journal of Sports<br />

<strong>Medic<strong>in</strong>e</strong>, 30(5), 331.<br />

Pai, Y., Hay, J. G., Wilson, B. D. (1984). Strok<strong>in</strong>g techniques of elite<br />

swimmers. Journal of Sports Sciences, 2(3), 225-239.<br />

S<strong>and</strong>ers, R. H., Cappaert, J. M., Pease, D. L. (1998). Wave characteristics<br />

of Olympic breaststroke swimmers. Journal of Applied <strong>Biomechanics</strong>,<br />

14(1), 40-51.<br />

Thompson, K. G., Halj<strong>and</strong>, R., MacLaren, D. P. (2000). An analysis of<br />

selected k<strong>in</strong>ematic variables <strong>in</strong> national <strong>and</strong> elite male <strong>and</strong> female<br />

100-m <strong>and</strong> 200-m breaststroke swimmers. Journal of Sports Sciences,<br />

18(6), 421-431.<br />

Thompson, K. G., Halj<strong>and</strong>, R., & L<strong>in</strong>dley, M. (2004). A comparison of<br />

selected k<strong>in</strong>ematic variables between races <strong>in</strong> national to elite male<br />

200 m breaststroke swimmers. Journal of Swimm<strong>in</strong>g Research, 16,<br />

6-10.


An Analysis of the Underwater Glid<strong>in</strong>g Motion <strong>in</strong><br />

Collegiate Competitive Swimmers<br />

Wada, t. 1 , sato, t. 2 , ohishi, K. 2 , tago, t. 3 , Izumi, t. 1 , Matsumoto,<br />

t. 1 , Yamamoto, n. 4 , Isaka, t. 5 , shimoyama, Y. 6<br />

1 Kokushikan University, Tokyo, Japan<br />

2 Nippon Sport Science University, Tokyo, Japan<br />

3 Tokushima Bunri University, Sanuki, Japan<br />

4 Japanese Red Cross Hokkaido College of Nurs<strong>in</strong>g, Kitami, Japan<br />

5 Ritsumeikan University, Kusatsu, Japan<br />

6 Niigata University of Health <strong>and</strong> Welfare, Niigata, Japan<br />

The purpose of this study was to analyze the underwater glid<strong>in</strong>g motion<br />

<strong>in</strong> collegiate competitive swimmers. Twelve male collegiate swimmers<br />

were monitored with a video camera (SK-2130, SONY, Japan) with a<br />

sampl<strong>in</strong>g frequency of 60Hz <strong>in</strong> the sagittal plane to measure the angular<br />

displacement of their different jo<strong>in</strong>ts. A motion analysis system<br />

(Frame-DIAS4, DKH, Japan) was used to digitize ten body l<strong>and</strong>marks.<br />

The follow<strong>in</strong>g results were obta<strong>in</strong>ed: the highest speed was ma<strong>in</strong>ta<strong>in</strong>ed<br />

dur<strong>in</strong>g the glid<strong>in</strong>g motion when the knee <strong>and</strong> the hip jo<strong>in</strong>t angles of 180<br />

degrees were ma<strong>in</strong>ta<strong>in</strong>ed from push off from the wall to 0.8sec (1.82m).<br />

In addition, swimm<strong>in</strong>g speed slowed down when the <strong>in</strong>voluntary movements<br />

of flexion-extension <strong>in</strong> the knee <strong>and</strong> the hip jo<strong>in</strong>ts were observed<br />

dur<strong>in</strong>g the glid<strong>in</strong>g motion.<br />

Key words: Motion analysis, underwater glid<strong>in</strong>g motion, competitive<br />

swimm<strong>in</strong>g<br />

IntroductIon<br />

In competitive swimm<strong>in</strong>g races, the improvement of swimm<strong>in</strong>g performance<br />

is related not only to the effect of strok<strong>in</strong>g but also to performance<br />

of the start <strong>and</strong> the turn phase. Furthermore, it is important that<br />

the momentum created by a swimmer <strong>in</strong> the forward swimm<strong>in</strong>g direction<br />

is larger than <strong>in</strong> the opposite direction.<br />

Passive drag is produced by measur<strong>in</strong>g the force necessary to tow a<br />

swimmer through the water at a constant speed with his body <strong>in</strong> a prone<br />

position (Adrian <strong>and</strong> Cooper 1995). The underwater glid<strong>in</strong>g motion<br />

dur<strong>in</strong>g the start <strong>and</strong> turn phases are important for the total race time<br />

<strong>in</strong> modern swimm<strong>in</strong>g (Mar<strong>in</strong>ho et al. 2009). Recently, the development<br />

of the swimsuit progressed rapidly. Previous studies suggested that this<br />

new model swimsuit had an effect on the body compression <strong>and</strong> the<br />

good streaml<strong>in</strong>ed posture (Chatard <strong>and</strong> Wilson 2008, Mollendorf et al.<br />

2004, Roberts et al. 2003), <strong>and</strong> could reduce the passive drag dur<strong>in</strong>g<br />

the underwater glid<strong>in</strong>g motion (Chatard <strong>and</strong> Wilson 2008, Mollendorf<br />

et al. 2004). Furthermore, many companies have been developed new<br />

product of fabrics. These swimsuits were called “high speed” swimsuits.<br />

However, most research done by these companies, focus<strong>in</strong>g on the effects<br />

of new fabrics, is not published.<br />

The “high speed” swimsuit were hypothesized to assist ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g<br />

the knee <strong>and</strong> hip jo<strong>in</strong>t angles of 180 degrees, consequently, swimmers<br />

could keep a better body position <strong>and</strong> higher speed dur<strong>in</strong>g the underwater<br />

glid<strong>in</strong>g motion.<br />

The purpose of this study was to analyze the underwater glid<strong>in</strong>g<br />

motion <strong>in</strong> collegiate competitive swimmers <strong>and</strong> to <strong>in</strong>vestigate whether<br />

wear<strong>in</strong>g “high speed” swimsuit could ma<strong>in</strong>ta<strong>in</strong> the knee <strong>and</strong> the hip<br />

jo<strong>in</strong>t angles of 180 degree.<br />

Methods<br />

Subjects <strong>and</strong> experimental procedures: Twelve healthy male collegiate<br />

swimmers (age 19.4±1.3yrs, height 170.0±5.0cm, body weight<br />

67.0±4.8kg, BMI 23.2±1.5) volunteered to participate <strong>in</strong> this study. The<br />

chaPter2.<strong>Biomechanics</strong><br />

subjects performed underwater glid<strong>in</strong>g motion as fast as possible after<br />

a pushoff from the pool wall. Dur<strong>in</strong>g the underwater phase of glid<strong>in</strong>g<br />

motion, the swimmer ma<strong>in</strong>ta<strong>in</strong>ed streaml<strong>in</strong>e position (Elipot et al.<br />

2009), <strong>and</strong> it was directed not to kick it. The head of the subjects were<br />

completely submerged dur<strong>in</strong>g glid<strong>in</strong>g. For each subject, only the fastest<br />

glid<strong>in</strong>g motion was analyzed.<br />

The subjects were monitored with an underwater video camera (SK-<br />

2130, SONY, Japan, Figure 1) with a sampl<strong>in</strong>g frequency of 60Hz <strong>in</strong><br />

the sagittal plane to measure the angular displacement of their different<br />

jo<strong>in</strong>ts. The underwater area covered by the camera ranged from the start<br />

wall to the 5-meter po<strong>in</strong>t.<br />

Figure 1. The underwater video camera (SK-2130, SONY, Japan)<br />

In this study, the subjects were asked to wear two different models of<br />

swimsuits: one is made of the conventional fabrics; the other is a newly<br />

developed, so-called “high speed” swimsuit (Figure 2 <strong>and</strong> 3, respectively).<br />

All subjects received a written <strong>and</strong> verbal explanation of the study<br />

<strong>and</strong> gave their written <strong>in</strong>formed consent for participation. Approval was<br />

granted from the <strong>in</strong>stitutional human ethics committee <strong>and</strong> the study<br />

was conducted <strong>in</strong> conformity with the Declaration of Hels<strong>in</strong>ki for medical<br />

research <strong>in</strong>volv<strong>in</strong>g human subjects.<br />

Figure 2. A conventional fabric swimsuit.<br />

The “high-speed” swimsuit: The Speedo Fastsk<strong>in</strong> LZR racer (LZR) is a<br />

fully bonded swimsuit (Figure 3). Its full-length bonded seams are ultrasonically<br />

welded together to elim<strong>in</strong>ate stitch<strong>in</strong>g, creat<strong>in</strong>g the most low<br />

profile silhouette <strong>and</strong> reduc<strong>in</strong>g sk<strong>in</strong> friction drag. The LZR is made from<br />

Speedo’s own LZR Pulse material the world’s lightest woven swimsuit<br />

fabric. It is highly compressive, water repellent, chlor<strong>in</strong>e resistant <strong>and</strong><br />

fast dry<strong>in</strong>g. The LZR is equipped with orig<strong>in</strong>al panels of ultra-th<strong>in</strong><br />

polyurethane membrane, precisely cut by laser, which are embedded<br />

<strong>in</strong>to the base LZR Pulse fabric. The LZR Pulse fabric was strategically<br />

placed on important parts of the body to create a Hydro Form Compression<br />

system that provides an optimum streaml<strong>in</strong>ed shape <strong>and</strong> drag<br />

reduction for the swimmer. This system also provides a core stabilizer<br />

built to support <strong>and</strong> hold the athlete (Speedo International Limited<br />

2009). However, these objective data were not published.<br />

185


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 3. The Speedo Fastsk<strong>in</strong> LZR racer (LZR) swimsuits.<br />

Digitiz<strong>in</strong>g <strong>and</strong> data analysis: A motion analysis system (Frame-DIAS4,<br />

DKH, Japan) was used to digitize ten body l<strong>and</strong>marks. The ten anatomical<br />

l<strong>and</strong>marks chosen <strong>and</strong> identified are as follows: f<strong>in</strong>ger tips, head,<br />

tragus (ear), acromions, elbow, wrist, large trochanter, knee(femoral condyles),<br />

lateral malleolus, toes. The angular displacement of the jo<strong>in</strong>ts are<br />

def<strong>in</strong>ed as <strong>in</strong>ternal jo<strong>in</strong>t angles (Figure 4).<br />

186<br />

Elbow jo<strong>in</strong>t<br />

angle<br />

Shoulder jo<strong>in</strong>t<br />

angle Hip jo<strong>in</strong>t<br />

anlge<br />

Knee jo<strong>in</strong>t<br />

angle<br />

Figure 4. The def<strong>in</strong>ition of the jo<strong>in</strong>t angular displacement.<br />

Ankle jo<strong>in</strong>t<br />

angle<br />

results<br />

Figure 5 <strong>in</strong>dicates the stick picture of a swimmer obta<strong>in</strong>ed by means of<br />

the motion analysis system. The swimm<strong>in</strong>g speed of the subject’s center<br />

of gravity wear<strong>in</strong>g a conventional swimsuit decreased when the flexionextension<br />

movement <strong>in</strong> the knee <strong>and</strong> the hip jo<strong>in</strong>ts were performed dur<strong>in</strong>g<br />

underwater glid<strong>in</strong>g motion (a typical example is shown <strong>in</strong> Figure 6).<br />

On the other h<strong>and</strong>, the swimm<strong>in</strong>g velocity of those wear<strong>in</strong>g an LZR<br />

swimsuit showed that the highest speed was ma<strong>in</strong>ta<strong>in</strong>ed dur<strong>in</strong>g the<br />

glid<strong>in</strong>g motion when the knee <strong>and</strong> the hip jo<strong>in</strong>t angles of 180 degrees<br />

were ma<strong>in</strong>ta<strong>in</strong>ed from the push-off from the wall to 0.8sec (1.82m) (a<br />

typical example is shown <strong>in</strong> Figure 7).<br />

The high-speed swimsuit ma<strong>in</strong>ta<strong>in</strong>ed a streaml<strong>in</strong>e <strong>in</strong> a knee jo<strong>in</strong>t <strong>and</strong><br />

a hip jo<strong>in</strong>t of 180 degrees <strong>in</strong> longer time (Table 1). In addition, duration of<br />

the swimm<strong>in</strong>g speed of the 90% equivalency of the best swimm<strong>in</strong>g speed<br />

was significantly longer wear<strong>in</strong>g high-speed swimsuit (Table 2).<br />

Figure 5. The stick picture of the swimmer.<br />

Angular displacement<br />

(degree)<br />

200<br />

190<br />

180<br />

170<br />

160<br />

150<br />

Subj.GY (Normal swimsuit)<br />

0 0.2 0.4 0.6 0.8 1<br />

Time (sec)<br />

Hip jo<strong>in</strong>t Knee jo<strong>in</strong>t Velocity of CG<br />

Figure 6. Relationship between the jo<strong>in</strong>t angle <strong>and</strong> the velocity for the<br />

normal swimsuit. This figure <strong>in</strong>dicates that the knee <strong>and</strong> hip jo<strong>in</strong>ts were<br />

performed flexion-extension movement from start to 0.8sec (1.2m).<br />

Angular displacement<br />

(degree)<br />

200<br />

190<br />

180<br />

170<br />

160<br />

150<br />

Subj.GY (High-speed swimsuit)<br />

0 0.2 0.4 0.6 0.8 1<br />

Time (sec)<br />

3<br />

2.5<br />

2<br />

1.5<br />

1<br />

0.5<br />

3<br />

2.5<br />

2<br />

1.5<br />

1<br />

0.5<br />

Hip jo<strong>in</strong>t Knee jo<strong>in</strong>t Velocity of CG<br />

Figure 7. Relationship between the jo<strong>in</strong>t angle <strong>and</strong> the velocity for the<br />

LZR swimsuit. This figure <strong>in</strong>dicates that the knee <strong>and</strong> hip jo<strong>in</strong>ts angle<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b were fixed about 180 degree from start to 0.8sec (1.2m).<br />

184<br />

Table <strong>Biomechanics</strong> 1. The <strong>and</strong> comparison <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g high-speed <strong>XI</strong> swimsuit Chapter <strong>and</strong> 2 <strong>Biomechanics</strong> normal swimsuit b 184 <strong>in</strong><br />

Table angular 1. displacement. The comparison (n=12) high-speed swimsuit <strong>and</strong> normal swimsuit <strong>in</strong> angular<br />

displacement. (n=12)<br />

Normal High-speed<br />

Table 1. The comparison high-speed swimsuit <strong>and</strong> swimsuit normal swimsuit <strong>in</strong> angular<br />

displacement. (n=12)<br />

Ave SD Ave SD<br />

Maximum hip jo<strong>in</strong>t angle(degree) 190.6 Normal 5.7<br />

swimsuit<br />

186.0 High-speed 4.3<br />

swimsuit<br />

p


dIscussIon<br />

The ma<strong>in</strong> aim of this study was to analyze the underwater glid<strong>in</strong>g motion<br />

<strong>in</strong> collegiate competitive swimmers <strong>and</strong> <strong>in</strong>vestigate whether wear<strong>in</strong>g<br />

“high speed” swimsuit could ma<strong>in</strong>ta<strong>in</strong> the knee <strong>and</strong> the hip jo<strong>in</strong>t<br />

angles of 180 degree. The underwater glid<strong>in</strong>g motion of the swimmer<br />

is said a significant role <strong>in</strong> the start <strong>and</strong> the turn phase. Dur<strong>in</strong>g these<br />

phases, reduc<strong>in</strong>g underwater resistance force leads to the improvement<br />

of the swimm<strong>in</strong>g performance.<br />

Dur<strong>in</strong>g the underwater glid<strong>in</strong>g motion, the swimmers have to hold a<br />

streaml<strong>in</strong>ed posture. This posture directly <strong>in</strong>fluences the modification of<br />

the hydrodynamic resistance created by the swimmer (Havriluk 2007).<br />

Elipot et al. (2009) showed that, to hold a streaml<strong>in</strong>ed position, a k<strong>in</strong>ematical<br />

synergy of the three pr<strong>in</strong>cipal jo<strong>in</strong>ts’ action is an essential. This<br />

synergy is characterized by a comb<strong>in</strong>ation of the three jo<strong>in</strong>ts, aim<strong>in</strong>g to<br />

stay <strong>in</strong> the best streaml<strong>in</strong>ed position, <strong>and</strong> to glide longer at high speed.<br />

The return to the water surface should rather be <strong>in</strong>itialized by a progressive<br />

<strong>and</strong> synchronize action of the three jo<strong>in</strong>ts (Elipot et al. 2009).<br />

The result of this study showed that the highest speed was ma<strong>in</strong>ta<strong>in</strong>ed<br />

dur<strong>in</strong>g the glid<strong>in</strong>g motion when the knee <strong>and</strong> the hip jo<strong>in</strong>t angles<br />

of 180 degrees were ma<strong>in</strong>ta<strong>in</strong>ed from the start to 0.8sec (Figure 7). In<br />

addition, swimm<strong>in</strong>g speed slowed down when the <strong>in</strong>voluntary movements<br />

of flexion-extension <strong>in</strong> the knee <strong>and</strong> the hip jo<strong>in</strong>ts were observed<br />

dur<strong>in</strong>g the glid<strong>in</strong>g motion. These results suggested that the subjects<br />

could not ma<strong>in</strong>ta<strong>in</strong> the knee <strong>and</strong> the hip jo<strong>in</strong>t angles of 180 degrees<br />

dur<strong>in</strong>g the glid<strong>in</strong>g motion, as the results, might try to ma<strong>in</strong>ta<strong>in</strong> the body<br />

balance by the flexion-extension movements <strong>in</strong> the knee <strong>and</strong> the hip<br />

jo<strong>in</strong>ts. Moreover, high-speed swimsuit would support ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the<br />

knee <strong>and</strong> the hip jo<strong>in</strong>t angles of 180 degrees dur<strong>in</strong>g the glid<strong>in</strong>g motion<br />

without the flexion-extension movements <strong>in</strong> the knee <strong>and</strong> the hip jo<strong>in</strong>ts.<br />

Therefore, dur<strong>in</strong>g the underwater phase dur<strong>in</strong>g starts <strong>and</strong> turns, it is a<br />

necessity that the swimmer ma<strong>in</strong>ta<strong>in</strong>s a streaml<strong>in</strong>ed posture.<br />

conclusIon<br />

The highest speed was ma<strong>in</strong>ta<strong>in</strong>ed dur<strong>in</strong>g the glid<strong>in</strong>g motion when the<br />

knee <strong>and</strong> the hip jo<strong>in</strong>t angles of 180 degrees were ma<strong>in</strong>ta<strong>in</strong>ed from push<br />

off from the wall to 0.8sec (1.82m). In addition, swimm<strong>in</strong>g speed slowed<br />

down when the <strong>in</strong>voluntary movements of flexion-extension <strong>in</strong> the knee<br />

<strong>and</strong> the hip jo<strong>in</strong>ts were observed dur<strong>in</strong>g the glid<strong>in</strong>g motion.<br />

reFerences<br />

Adrian M.J., J.M. Cooper. (1995). <strong>Biomechanics</strong> of Human Movement.<br />

Brown & Benchmark, Madison.<br />

Chatard J.C., B. Wilson. (2008). Effect of Fastsk<strong>in</strong> suits on performance,<br />

drag, <strong>and</strong> energy cost of swimm<strong>in</strong>g. Med Sci Sports Exerc. 40(6): 1149-<br />

1154.<br />

Elipot M., P. Hellard, R. Taiar, E. Boissiere, J.L. Rey, S. Lecat, N. Houel.<br />

(2009). Analysis of swimmers’ velocity dur<strong>in</strong>g the underwater glid<strong>in</strong>g<br />

motion. J Biomech, 42(9): 1367-1370.<br />

Havriluk R. (2007). Variability <strong>in</strong> measurement of swimm<strong>in</strong>g forces: a<br />

meta-analysis of passive <strong>and</strong> active drag. Research Quarterly for Exercise<br />

<strong>and</strong> Sport. 78: 32-39.<br />

Mar<strong>in</strong>ho D.A., V.M. Reis, F.B. Alves, J.P. Vilas-Boas, L. Machado, A.J.<br />

Silva, A.I. Rouboa. (2009). Hydrodynamic drag dur<strong>in</strong>g glid<strong>in</strong>g <strong>in</strong><br />

swimm<strong>in</strong>g. J Appl Biomech, 25(3): 253-257.<br />

Mollendorf J.C., A.C. Term<strong>in</strong> II, E. Oppenheim, D.R. Pendergast.<br />

(2004). Effect of swim suit design on passive drag. Med Sci Sports<br />

Exerc. 36(6): 1029-1035.<br />

Roberts B.S., K.S. Kamel, C.E. Hedrick, S.P. Mclean, R.L. Sharp.<br />

(2003). Effect of a Fastsk<strong>in</strong>TM suit on submaximal freestyle swimm<strong>in</strong>g.<br />

Med Sci Sports Exerc. 35(3): 519-524.<br />

Speedo International Limited. (2009). http://www.speedo.co.uk/en_uk/<br />

aqualab_ technologies/aqualab/<strong>in</strong>dex.html.<br />

chaPter2.<strong>Biomechanics</strong><br />

Head Out Swimm<strong>in</strong>g <strong>in</strong> Water Polo: a Comparison<br />

with Front Crawl <strong>in</strong> Young Female Players<br />

Zamparo, P., Falco, s.<br />

Faculty of Exercise <strong>and</strong> Sport Sciences, University of Verona, Italy<br />

The aim of this study was to measure heart rate (HR), arm stroke efficiency<br />

(ηp) <strong>and</strong> trunk <strong>in</strong>cl<strong>in</strong>e (TI) dur<strong>in</strong>g head out swimm<strong>in</strong>g (HOS)<br />

<strong>and</strong> front crawl swimm<strong>in</strong>g (FCS) <strong>in</strong> young female water polo players<br />

(12 <strong>and</strong> 16.5 years of age, 3.3 <strong>and</strong> 4.8 years of practice, respectively) at<br />

different speeds (from slow to maximal). The need of keep<strong>in</strong>g the head<br />

out of the water <strong>and</strong> the elbows high <strong>in</strong> HOS leads to a small (2%), albeit<br />

significant, reduction of the self select speed <strong>in</strong> comparison to FCS.<br />

Dur<strong>in</strong>g HOS the players have a larger (32%) TI while ηp is significantly<br />

reduced (21%) than dur<strong>in</strong>g FCS. Both factors (the <strong>in</strong>crease <strong>in</strong> TI <strong>and</strong><br />

the reduction <strong>in</strong> ηp) lead to an <strong>in</strong>crease of the energy requirement of this<br />

peculiar “form of locomotion <strong>in</strong> water” as confirmed, albeit <strong>in</strong>directly, by<br />

the higher HR (10%) observed <strong>in</strong> HOS at any given speed.<br />

Key words: water polo, arm stroke efficiency, hydrodynamic resistance,<br />

IntroductIon<br />

In water polo, dribbl<strong>in</strong>g is the technique of mov<strong>in</strong>g the ball, while swimm<strong>in</strong>g<br />

forward, <strong>in</strong> the wake created by alternat<strong>in</strong>g arm strokes. With this<br />

technique the players keep the elbows high (<strong>in</strong> order to stop oppos<strong>in</strong>g<br />

players from ga<strong>in</strong><strong>in</strong>g possession of the ball) <strong>and</strong> keep their head out of<br />

the water to see the rest of the pool <strong>and</strong> make the appropriate play.<br />

This “mode of locomotion <strong>in</strong> water” is expected to be quite expensive<br />

energetically s<strong>in</strong>ce the need of keep<strong>in</strong>g the head out of the water necessary<br />

means that the trunk is more <strong>in</strong>cl<strong>in</strong>ed <strong>in</strong> respect to the horizontal<br />

(<strong>and</strong> this should have an effect on the hydrodynamic resistance, W d )<br />

while keep<strong>in</strong>g the elbows high probably affects the propulsive efficiency<br />

of the arm stroke (η p ). Both W d <strong>and</strong> η p are known to affect the energy<br />

cost of aquatic locomotion (C, the energy expended to cover one unit<br />

distance):<br />

C = W d / (η p η m ) (1)<br />

where η m is the mechanical efficiency of swimm<strong>in</strong>g (e. g. Zamparo et al.,<br />

2008). Thus the hypothesized <strong>in</strong>crease <strong>in</strong> W d <strong>and</strong> decrease <strong>in</strong> η p should<br />

lead to a proportional <strong>in</strong>crease <strong>in</strong> C, <strong>in</strong> respect to the condition of a<br />

“st<strong>and</strong>ard” front crawl stroke.<br />

Whereas <strong>in</strong> the literature it is reported that water polo players are<br />

less economical <strong>in</strong> front crawl (head down) swimm<strong>in</strong>g compared to<br />

competitive swimmers (for a review see Smith, 1998) to our knowledge<br />

no one has <strong>in</strong>vestigated so far the energy cost of swimm<strong>in</strong>g dur<strong>in</strong>g head<br />

out swimm<strong>in</strong>g nor its determ<strong>in</strong>ants: i. e. the efficiency of the arm stroke<br />

<strong>and</strong>/or the hydrodynamic resistance.<br />

Moreover, as well as competitive swimmers learn how to swim efficiently<br />

(by improv<strong>in</strong>g swimm<strong>in</strong>g technique) also water polo players are<br />

expected to learn how to swim wit the head out <strong>in</strong> the most efficient<br />

<strong>and</strong> economical way. We can thus hypothesize that more expert water<br />

polo players would show a lower difference between head out swimm<strong>in</strong>g<br />

(HOS) <strong>and</strong> front crawl swimm<strong>in</strong>g (FCS) than younger, less expert ones.<br />

The aim of this study was, therefore, to <strong>in</strong>vestigate the trunk <strong>in</strong>cl<strong>in</strong>e<br />

<strong>and</strong> the propell<strong>in</strong>g efficiency of the arm stroke <strong>in</strong> two groups of young<br />

female water polo players (G-12: 12 years old <strong>and</strong> G-16: 16.5 years old)<br />

while swimm<strong>in</strong>g both styles (HOS <strong>and</strong> FCS) at different speeds (from<br />

slow to maximal).<br />

187


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Methods<br />

Twenty-one young female water polo players participated to the study.<br />

They were divided <strong>in</strong>to two groups: G-12: 11 players, their average age,<br />

stature <strong>and</strong> body mass were, respectively: 11.9 ± 1.4 years; 1.59 ± 0.07 m;<br />

48.4 ± 5.3 kg; <strong>and</strong> G-16: 10 players, their average age, stature <strong>and</strong> body<br />

mass were, respectively: 16.5 ± 1.3 years; 1.64 ± 0.04 m; 65.2 ± 9.5 kg.<br />

The G-12 players had a practice of water polo of 3.3 ± 0.5 years whereas<br />

the G-16 players of 4.8 ± 0.6 years. The subjects were <strong>in</strong>formed about<br />

the methods <strong>and</strong> aims of the study <strong>and</strong> gave their written <strong>in</strong>formed consent<br />

to participate; parental consent was obta<strong>in</strong>ed for under age subjects.<br />

The experiments were performed <strong>in</strong> an <strong>in</strong>door 25 m swimm<strong>in</strong>g pool.<br />

The subjects were requested to swim at constant speed <strong>and</strong> stroke rate<br />

start<strong>in</strong>g, without div<strong>in</strong>g, from the pool wall. The experiments were repeated<br />

at 4 speeds (self selected by the swimmers as slow, moderate, fast<br />

<strong>and</strong> maximal) <strong>and</strong> with the two styles (HOS: head out swimm<strong>in</strong>g <strong>and</strong><br />

FCS: front crawl swimm<strong>in</strong>g) <strong>in</strong> two separate days.<br />

In the central 10 m of the pool the average speed (V, m . s -1 ), the<br />

stroke frequency (SF, Hz) <strong>and</strong> the kick frequency (KF, Hz) were measured<br />

by means of a stopwatch. The stroke length (SL, m) was then calculated<br />

as V/ SF.<br />

The arm stroke efficiency was calculated accord<strong>in</strong>g to the simple<br />

model proposed by Zamparo et al. (2005). The model is based on the assumption<br />

that the arm is a rigid segment of length l, rotat<strong>in</strong>g at constant<br />

angular speed about the shoulder <strong>and</strong> yields the average efficiency for<br />

the underwater phase only, as follows:<br />

188<br />

η p = ((V . 0.9) / (2π . SF . l)) . (2 / π) (2)<br />

where V is the average speed of the swimmer, SF is the stroke frequency<br />

<strong>and</strong> l is the average shoulder to h<strong>and</strong> distance. In turn, l can be calculated<br />

trigonometrically by measur<strong>in</strong>g the upper limb length (0.49 ± 0.02 m<br />

<strong>in</strong> G-12 <strong>and</strong> 0.50 ± 0.02 m <strong>in</strong> G-16) <strong>and</strong> the average elbow angle (EA)<br />

dur<strong>in</strong>g the <strong>in</strong>-sweep of the arm pull. In this study, EA was not directly<br />

measured but calculated on the basis of the subject’s age based on data<br />

published by Zamparo (2006). F<strong>in</strong>ally, <strong>in</strong> equation 7, the speed was multiplied<br />

by 0.9 to take <strong>in</strong>to account that, <strong>in</strong> the front crawl, about 10% of<br />

forward propulsion is produced by the legs (e. g. Holl<strong>and</strong>er et al. 1988).<br />

For a detailed discussion about the pro <strong>and</strong> cons of this model the reader<br />

is referred to Zamparo et al. (2005) <strong>and</strong> Zamparo (2006).<br />

Dur<strong>in</strong>g the experiments video records were taken, with a sampl<strong>in</strong>g<br />

rate of 50 Hz, by means of a video-camera (TS-6031PSC, CANO-<br />

PUS, UK) positioned 0.5 m below the water surface, perpendicular to<br />

the swimmer’s direction (the subjects swam <strong>in</strong> the second lane, at a distance<br />

of 7-8 m from the camera). After the experiments, the data were<br />

downloaded to a PC <strong>and</strong> analyzed us<strong>in</strong>g a commercial software package<br />

(Tw<strong>in</strong> pro, SIMI, G). In FCS trunk <strong>in</strong>cl<strong>in</strong>e (TI, degrees) was measured<br />

from the angle with the horizontal of the segment between the shoulder<br />

(acromion) <strong>and</strong> the hip (great trochanter) whereas <strong>in</strong> HOS, <strong>in</strong>stead of<br />

the shoulder, the marg<strong>in</strong> of the axilla was marked <strong>in</strong>stead (s<strong>in</strong>ce the<br />

shoulder jo<strong>in</strong>t is outside the water <strong>in</strong> this condition). The measurement<br />

of TI was taken, for a s<strong>in</strong>gle passage, at the end of the <strong>in</strong>-sweep (when<br />

the h<strong>and</strong> is directly below the shoulder) s<strong>in</strong>ce <strong>in</strong> this position the rotation<br />

around the sagittal axis is the least <strong>and</strong> has the smaller <strong>in</strong>fluence on<br />

the degree of rotation (see also Kjendlie et al. 2004).<br />

F<strong>in</strong>ally, the subjects were equipped with a waterproof heart rate<br />

monitor<strong>in</strong>g system (RS800sd, Polar, Fi) so their heart rate (HR, bpm)<br />

at the end of each trial was recorded as well. These data should <strong>in</strong>dicate,<br />

albeit <strong>in</strong>directly, whether the differences <strong>in</strong> the k<strong>in</strong>ematical/biomechanical<br />

parameters between styles <strong>and</strong> groups do <strong>in</strong>deed lead to differences<br />

<strong>in</strong> the energetics of swimm<strong>in</strong>g.<br />

Statistical analysis was carried out by means of an ANOVA test<br />

(SPSS v17.0, SPSS Inc., Chicago Ill., USA) for repeated measures: two<br />

groups (G-12 <strong>and</strong> G-16), four speeds (V1 –V4) <strong>and</strong> two conditions<br />

(FCS: front crawl swimm<strong>in</strong>g <strong>and</strong> HOS: head out swimm<strong>in</strong>g).<br />

measurement of TI was taken, for a s<strong>in</strong>gle passage, at the end of the <strong>in</strong>-sweep (when the<br />

h<strong>and</strong> is directly below the shoulder) s<strong>in</strong>ce <strong>in</strong> this position the rotation around the sagittal<br />

axis is the least <strong>and</strong> has the smaller <strong>in</strong>fluence on the degree of rotation (see also<br />

Kjendlie et al. 2004).<br />

F<strong>in</strong>ally, the subjects were equipped with a waterproof heart rate monitor<strong>in</strong>g system<br />

(RS800sd, Polar, Fi) so their heart rate (HR, bpm) at the end of each trial was recorded<br />

as well. These data should <strong>in</strong>dicate, albeit <strong>in</strong>directly, whether the differences <strong>in</strong> the<br />

k<strong>in</strong>ematical/biomechanical parameters between styles <strong>and</strong> groups do <strong>in</strong>deed lead to<br />

results<br />

differences <strong>in</strong> the energetics of swimm<strong>in</strong>g.<br />

In tables 1 <strong>and</strong> 2 are reported the average ± 1 SD values of all the <strong>in</strong>ves-<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b<br />

tigated parameters for the two groups (Table 1: G-12; Table 2: G-16)<br />

at swimm<strong>in</strong>g). the four speeds <strong>and</strong> <strong>in</strong> the two conditions (FCS <strong>and</strong> HOS). In both<br />

conditions RESULTS (HOS <strong>and</strong> FCS) <strong>and</strong> for both groups (G-12 <strong>and</strong> G-16), with<br />

<strong>in</strong>creas<strong>in</strong>g speed (from V1: slow to V4: maximal) KF <strong>and</strong> SF <strong>in</strong>crease<br />

while SL <strong>and</strong> ηp decrease; moreover, with <strong>in</strong>creas<strong>in</strong>g speed TI decreases<br />

while HR <strong>in</strong>creases (ANOVA, F (3, 57) , p < 0.001 <strong>in</strong> all cases).<br />

Statistical analysis was carried out by means of an ANOVA test (SPSS v17.0, SPSS<br />

Inc., Chicago Ill., USA) for repeated measures: two groups (G-12 <strong>and</strong> G-16), four 188<br />

speeds (V1 –V4) <strong>and</strong> two conditions (FCS: front crawl swimm<strong>in</strong>g <strong>and</strong> HOS: head out<br />

were downloaded to a PC <strong>and</strong> analyzed us<strong>in</strong>g a commercial software package (Tw<strong>in</strong><br />

In pro, tables SIMI, 1 G). <strong>and</strong> In 2 FCS are trunk reported <strong>in</strong>cl<strong>in</strong>e the (TI, average degrees) ± was 1 SD measured values from of all the the angle <strong>in</strong>vestigated with the<br />

parameters horizontal for of the two segment groups between (Table 1: the G-12; shoulder Table 2: (acromion) G-16) at the <strong>and</strong> four the speeds hip <strong>and</strong> (great <strong>in</strong><br />

the trochanter) two conditions whereas (FCS <strong>in</strong> HOS, <strong>and</strong> HOS). <strong>in</strong>stead In of both the conditions shoulder, the (HOS marg<strong>in</strong> <strong>and</strong> FCS) of the <strong>and</strong> axilla for both was<br />

groups marked (G-12 <strong>in</strong>stead <strong>and</strong> (s<strong>in</strong>ce G-16), the with shoulder <strong>in</strong>creas<strong>in</strong>g jo<strong>in</strong>t speed is outside (from V1: the water slow to <strong>in</strong> V4: this maximal) condition). KF The <strong>and</strong><br />

SF<br />

measurement<br />

<strong>in</strong>crease while<br />

of TI<br />

SL<br />

was<br />

<strong>and</strong><br />

taken, for<br />

ηp decrease;<br />

a s<strong>in</strong>gle<br />

moreover,<br />

passage, at<br />

with<br />

the<br />

<strong>in</strong>creas<strong>in</strong>g<br />

end of the <strong>in</strong>-sweep<br />

speed TI<br />

(when<br />

decreases<br />

the<br />

while h<strong>and</strong> is HR directly <strong>in</strong>creases below (ANOVA, the shoulder) s<strong>in</strong>ce F(3, 57), p < 0.001 <strong>in</strong> this <strong>in</strong> position all cases). the rotation around the sagittal<br />

axis is the least <strong>and</strong> has the smaller <strong>in</strong>fluence on the degree of rotation (see also<br />

Table 1. Average values ± 1 SD of the <strong>in</strong>vestigated parameters for the<br />

Kjendlie et al. 2004).<br />

G-12 group<br />

Table 1. Average values ± 1 SD of the <strong>in</strong>vestigated parameters for the G-12 group<br />

V (m<br />

FCS<br />

. s -1 ) SF (Hz) SL (m ) KF(Hz) ηp TI (deg) HR (bpm)<br />

V1 0.94 ± 0.06 0.45 ± 0.12 2.22 ± 0.57 1.85 ± 0.37 0.45 ± 0.08 23.4 ± 3.99 149 ± 17<br />

V2 1.07 ± 0.11 0.59 ± 0.05 1.81 ± 0.21 1.86 ± 0.73 0.38 ± 0.04 21.0 ± 3.85 162 ± 12<br />

V3 1.15 ± 0.13 0.76 ± 0.10 1. 54 ± 0.18 2.01 ± 0.60 0.32 ± 0.04 18.1 ± 3.91 169 ± 11<br />

V4 1.25 ± 0.16 0.85 ± 0.13 1.49 ± 0.26 2.50 ± 0.60 0.31 ± 0.06 13.5 ± 4.51 165 ± 11<br />

V1 0.95 ± 0.09 0.69 ± 0.07 1.39 ± 0.18 1.56 ± 0.71 0.29 ± 0.04 33.7 ± 9.08 159 ± 14<br />

HOS V2 1.00 ± 0.12 0.73 ± 0.07 1.38 ± 0.20 1.76 ± 0.85 0.29 ± 0.04 28.7 ± 4.62 167 ± 15<br />

V3 1.12 ± 0.15 0.89 ± 0.15 1.30 ± 0.26 1.85 ± 0.84 0.27 ± 0.05 30.2 ± 4.97 174 ± 16<br />

V4 1.16 ± 0.18 0.93 ± 0.16 1.28 ± 0.25 2.04 ± 0.76 0.27 ± 0.05 22.2 ± 8.06 176 ± 16<br />

Table 2. Average values ± 1 SD of the <strong>in</strong>vestigated parameters for the G-16 group<br />

V (m . s -1 F<strong>in</strong>ally, the subjects were equipped with a waterproof heart rate monitor<strong>in</strong>g system<br />

(RS800sd, Polar, Fi) so their heart rate (HR, bpm) at the end of each trial was recorded<br />

as well. These data should <strong>in</strong>dicate, albeit <strong>in</strong>directly, whether the differences <strong>in</strong> the<br />

k<strong>in</strong>ematical/biomechanical parameters between styles <strong>and</strong> groups do <strong>in</strong>deed lead to<br />

differences <strong>in</strong> the energetics of swimm<strong>in</strong>g.<br />

Statistical analysis was carried out by means of an ANOVA test (SPSS v17.0, SPSS<br />

Inc., Chicago Ill., USA) for repeated measures: two groups (G-12 <strong>and</strong> G-16), four<br />

speeds (V1 –V4) <strong>and</strong> two conditions (FCS: front crawl swimm<strong>in</strong>g <strong>and</strong> HOS: head out<br />

swimm<strong>in</strong>g).<br />

RESULTS<br />

In tables 1 <strong>and</strong> 2 are reported the average ± 1 SD values of all the <strong>in</strong>vestigated<br />

parameters for the two groups (Table 1: G-12; Table 2: G-16) at the four speeds <strong>and</strong> <strong>in</strong><br />

the two conditions (FCS <strong>and</strong> HOS). In both conditions (HOS <strong>and</strong> FCS) <strong>and</strong> for both<br />

groups (G-12 <strong>and</strong> G-16), with <strong>in</strong>creas<strong>in</strong>g speed (from V1: slow to V4: maximal) KF <strong>and</strong><br />

SF <strong>in</strong>crease while SL <strong>and</strong> ηp decrease; moreover, with <strong>in</strong>creas<strong>in</strong>g speed TI decreases<br />

while HR <strong>in</strong>creases (ANOVA, F(3, 57), p < 0.001 <strong>in</strong> all cases).<br />

Table 2. Average values ± 1 SD of the <strong>in</strong>vestigated parameters for the<br />

G-16 <strong>Biomechanics</strong> group <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> Chapter 2 <strong>Biomechanics</strong> b 189<br />

) SF (Hz) SL (m ) KF(Hz) ηp TI (deg) HR (bpm)<br />

Table 1. Average values ± 1 SD of the <strong>in</strong>vestigated parameters for the G-12 group<br />

V (m . s -1 ) SF (Hz) SL (m ) KF(Hz) ηp TI (deg) HR (bpm)<br />

V1 0.94 1.01 ± 0.06 0.08 0.45 0.48 ± 0.12 0.07 2.22 2.13 ± 0.57 0.34 1.85 1.43 ± 0.37 0.48 0.45 0.43 ± 0.08 0.07 23.4 24.0 ± 3.99 5.62 149 131 ± 17 13<br />

V2 1.07 1.15 ± 0.11 0.08 0.59 ± 0.05 0.15 1.81 2.04 ± 0.21 0.56 1.86 1.82 ± 0.73 0.31 0.38 0.39 ± 0.04 0.07 21.0 21.4 ± 3.85 5.20 162 141 ± ± 12 8<br />

FCS<br />

FCS V3 1.15 1.27 ± 0.13 0.76 0.66 ± 0.10 0.12 1. 1.97 54 ± 0.18 0.32 2.01 2.03 ± 0.60 0.53 0.32 0.40 ± 0.04 0.06 18.1 20.0 ± 3.91 5.49 169 157 ± 11<br />

V4 1.25 1.37 ± 0.16 0.12 0.85 0.74 ± 0.13 0.10 1.49 1.88 ± 0.26 0.27 2.50 2.40 ± 0.60 0.31 0.38 ± 0.06 13.5 14.6 ± 4.51 3.71 165 166 ± ± 11 8<br />

V1 0.95 1.01 ± 0.09 0.12 0.69 0.60 ± 0.07 0.09 1.39 1.70 ± 0.18 0.23 1.56 1.30 ± 0.71 0.52 0.29 0.34 ± 0.04 0.05 33.7 34.4 ± 9.08 3.39 159 153 ± 14 15<br />

HOS V2 1.00 1.13 ± 0.12 0.09 0.73 0.70 ± 0.07 0.11 1.38 1.66 ± 0.20 0.33 1.76 1.55 ± 0.85 0.55 0.29 0.34 ± 0.04 0.07 28.7 27.6 ± 4.62 3.81 167 160 ± 15 14<br />

V3 1.12 1.24 ± 0.15 0.11 0.89 0.78 ± 0.15 0.08 1.30 1.62 ± 0.26 0.25 1.85 1.78 ± 0.84 0.69 0.27 0.33 ± 0.05 30.2 30.9 ± 4.97 3.33 174 165 ± 16 13<br />

V4 1.16 1.33 ± 0.18 0.13 0.93 0.84 ± 0.16 0.08 1.28 1.59 ± 0.25 0.23 2.04 2.10 ± 0.76 0.61 0.27 0.32 ± 0.05 22.2 ± 8.06 4.43 176 175 ± ± 16 9<br />

The comparison between styles (both groups considered, at all swim-<br />

Table 2. Average values ± 1 SD of the <strong>in</strong>vestigated parameters for the G-16 group<br />

V (m . s -1 The comparison between styles (both groups considered, at all swimm<strong>in</strong>g speeds)<br />

<strong>in</strong>dicates that all parameters are significantly different <strong>in</strong> the two conditions (HOS <strong>and</strong><br />

m<strong>in</strong>g FCS) (ANOVA, speeds) <strong>in</strong>dicates F(1, 19), p < that 0.05 all <strong>in</strong> all parameters cases). Swimm<strong>in</strong>g are significantly with the head different out leads <strong>in</strong> to a<br />

the small two (2%), conditions albeit ) significant, (HOS SF (Hz) reduction <strong>and</strong> SL (m FCS) ) of the (ANOVA, KF(Hz) self select speed F <strong>in</strong> comparison ηp TI (deg) HR to (bpm) FCS.<br />

(1, 19) , p < 0.05 <strong>in</strong> all<br />

Dur<strong>in</strong>g HOS the players have a larger (32%) <strong>in</strong>cl<strong>in</strong>ation of the trunk with the horizontal<br />

cases). Swimm<strong>in</strong>g with the head out leads to a small (2%), albeit signifi-<br />

<strong>and</strong> a higher heart rate (7%) compared to FCS. Moreover, <strong>in</strong> HOS, SL <strong>and</strong> ηp are<br />

cant, significantly reduction reduced of the (21% self <strong>in</strong> both select cases) speed whereas <strong>in</strong> comparison SF is <strong>in</strong>creased to (17%) FCS. <strong>in</strong> Dur<strong>in</strong>g respect to<br />

HOS FCS. F<strong>in</strong>ally, the players KF is 10% have lower a larger dur<strong>in</strong>g (32%) HOS than <strong>in</strong>cl<strong>in</strong>ation dur<strong>in</strong>g FCS. of the trunk with the<br />

The comparison between groups (both styles considered, at all swimm<strong>in</strong>g speeds)<br />

horizontal <strong>in</strong>dicates that <strong>and</strong> there a higher are no significant heart rate differences (7%) compared between groups to FCS. (G-12 Moreover, <strong>and</strong> G-16) <strong>in</strong> <strong>in</strong> TI<br />

<strong>and</strong> KF. However, players of G-12 swim at a significantly lower pace than those of G-<br />

HOS, SL <strong>and</strong> ηp are significantly reduced (21% <strong>in</strong> both cases) whereas<br />

SF is <strong>in</strong>creased (17%) <strong>in</strong> respect to FCS. F<strong>in</strong>ally, KF is 10% lower dur<strong>in</strong>g<br />

HOS than dur<strong>in</strong>g FCS.<br />

The comparison between groups (both styles considered, at all swim-<br />

16 (9%), with a lower SL (14%), a higher SF (8%) <strong>and</strong> a lower ηp (11%) (ANOVA, F(1,<br />

19), p < 0.05 <strong>in</strong> all cases). F<strong>in</strong>ally, HR is 5% lower <strong>in</strong> G-16 than <strong>in</strong> G-12 albeit this<br />

difference does not reach a significant level (p = 0.06).<br />

DISCUSSION<br />

m<strong>in</strong>g speeds) <strong>in</strong>dicates that there are no significant differences between<br />

Data reported <strong>in</strong> this study <strong>in</strong>dicate that HOS is characterized by relevant differences <strong>in</strong><br />

groups the biomechanics (G-12 <strong>and</strong> of swimm<strong>in</strong>g G-16) <strong>in</strong> <strong>in</strong> TI comparison <strong>and</strong> KF. with However, FCS. The players need of keep<strong>in</strong>g G-12 swim the head<br />

at out a of significantly the water does lower <strong>in</strong>deed pace lead than to an <strong>in</strong>crease those of G-16 TI (<strong>and</strong> (9%), thus to with an <strong>in</strong>crease a lower of frontal SL<br />

area <strong>and</strong> hydrodynamic resistance) whereas the need of keep<strong>in</strong>g the elbows high does<br />

(14%), <strong>in</strong>deed a lead higher to an SF <strong>in</strong>crease (8%) of <strong>and</strong> SF a <strong>and</strong> lower thus ηto p (11%) a reduction (ANOVA, of the distance F (1, 19) , covered p < 0.05 per<br />

<strong>in</strong> stroke all cases). (<strong>and</strong> of F<strong>in</strong>ally, the arm stroke HR is efficiency). 5% lower Both <strong>in</strong> needs G-16 do than <strong>in</strong>deed <strong>in</strong> result, G-12 as albeit hypothesized, this<br />

<strong>in</strong> an <strong>in</strong>crease of the energy requirement of this peculiar “form of locomotion <strong>in</strong> water”<br />

difference does not reach a significant level (p = 0.06).<br />

as confirmed, albeit <strong>in</strong>directly, by the higher HR <strong>in</strong> HOS than <strong>in</strong> FCS at any given<br />

speed.<br />

Interest<strong>in</strong>gly, KF is lower dur<strong>in</strong>g HOS than FCS <strong>and</strong> this suggests that these players<br />

are not able to contrast the larger trunk <strong>in</strong>cl<strong>in</strong>e with a more frequent/forceful leg kick.<br />

dIscussIon<br />

Moreover, KF <strong>and</strong> TI do not change with the years of practice (no differences are<br />

Data observed reported between <strong>in</strong> the this two study groups <strong>in</strong>dicate for these two that parameters) HOS is characterized <strong>and</strong> this suggests by that rel- more<br />

experienced swimmers essentially rely on a better arm stroke efficiency to overcome the<br />

evant differences <strong>in</strong> the biomechanics of swimm<strong>in</strong>g <strong>in</strong> comparison with<br />

challenges of this “swimm<strong>in</strong>g style”.<br />

FCS. The need of keep<strong>in</strong>g the head out of the water does <strong>in</strong>deed lead<br />

to an <strong>in</strong>crease of TI (<strong>and</strong> thus to an <strong>in</strong>crease of frontal area <strong>and</strong> hydrodynamic<br />

resistance) whereas the need of keep<strong>in</strong>g the elbows high does<br />

<strong>in</strong>deed lead to an <strong>in</strong>crease of SF <strong>and</strong> thus to a reduction of the distance<br />

covered per stroke (<strong>and</strong> of the arm stroke efficiency). Both needs do<br />

<strong>in</strong>deed result, as hypothesized, <strong>in</strong> an <strong>in</strong>crease of the energy requirement<br />

of this peculiar “form of locomotion <strong>in</strong> water” as confirmed, albeit <strong>in</strong>directly,<br />

by the higher HR <strong>in</strong> HOS than <strong>in</strong> FCS at any given speed.<br />

CONCLUSIONS<br />

This study suggests that while tra<strong>in</strong><strong>in</strong>g young water polo players is necessary to<br />

improve as much as possible the efficiency of the arm stroke. Moreover, it <strong>in</strong>dicates the<br />

importance to teach them how to perform a cont<strong>in</strong>uous <strong>and</strong> regular leg kick to raise, as


Interest<strong>in</strong>gly, KF is lower dur<strong>in</strong>g HOS than FCS <strong>and</strong> this suggests<br />

that these players are not able to contrast the larger trunk <strong>in</strong>cl<strong>in</strong>e with<br />

a more frequent/forceful leg kick. Moreover, KF <strong>and</strong> TI do not change<br />

with the years of practice (no differences are observed between the two<br />

groups for these two parameters) <strong>and</strong> this suggests that more experienced<br />

swimmers essentially rely on a better arm stroke efficiency to<br />

overcome the challenges of this “swimm<strong>in</strong>g style”.<br />

conclusIons<br />

This study suggests that while tra<strong>in</strong><strong>in</strong>g young water polo players is necessary<br />

to improve as much as possible the efficiency of the arm stroke.<br />

Moreover, it <strong>in</strong>dicates the importance to teach them how to perform a<br />

cont<strong>in</strong>uous <strong>and</strong> regular leg kick to raise, as much as possible, the trunk<br />

towards the horizontal. Furthermore, these data <strong>in</strong>dicate that tra<strong>in</strong><strong>in</strong>g<br />

practice <strong>in</strong> water polo has to be less <strong>in</strong>tense <strong>and</strong> with sufficient pauses<br />

to allow for a recovery <strong>in</strong> HR, due to its higher energy requirement <strong>in</strong><br />

comparison with FCS practice.<br />

reFerences<br />

Holl<strong>and</strong>er A.P., De Groot G., Van Ingen Schenau G.J., Kahman R.,<br />

Toussa<strong>in</strong>t H.M. (1988). Contribution of the legs to propulsion <strong>in</strong><br />

front crawl swimm<strong>in</strong>g. In: Ungherects B.E., Wilkie K., Reischle K.<br />

(eds). Swimm<strong>in</strong>g Science V (pp 39-42). Champaign, Ill, Human K<strong>in</strong>etics.<br />

Kjendlie P.L., Stallman R.K., Gunderson J.S. (2004). Passive <strong>and</strong> active<br />

float<strong>in</strong>g torque dur<strong>in</strong>g swimm<strong>in</strong>g. Eur J Appl Physiol 93: 75-81.<br />

Smith H.K. (1998). Applied physiology of water polo. Sports Med, 26:<br />

317-334<br />

Zamparo P., Pendergast D.R., Mollendorf J., Term<strong>in</strong> B., M<strong>in</strong>etti A.M.<br />

(2005). An energy balance of front crawl. Eur J Appl Physiol, 94: 134-<br />

144.<br />

Zamparo P. (2006). Effects of age <strong>and</strong> gender on the propell<strong>in</strong>g efficiency<br />

of the arm stroke. Eur J Appl Physiol, 97: 52-58.<br />

Zamparo P., Lazzer S., Antoniazzi C., Cedol<strong>in</strong> S., Avon R., Lesa C.<br />

(2008). The <strong>in</strong>terplay between propell<strong>in</strong>g efficiency, hydrodynamic<br />

position <strong>and</strong> energy cost of front crawl <strong>in</strong> 8 to19-year-old swimmers.<br />

Eur J Appl Physiol, 104: 689-699.<br />

chaPter2.<strong>Biomechanics</strong><br />

189


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

190


Chapter 3. Physiology <strong>and</strong> Bioenergetics


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Models of Vertical Swimm<strong>in</strong>g Abilities <strong>in</strong> Elite<br />

Female Senior Water Polo Players<br />

dopsaj, M.<br />

University of Belgrade Faculty of Sport <strong>and</strong> Physical Education, Serbia.<br />

This paper aims to def<strong>in</strong>e different models of vertical swimm<strong>in</strong>g abilities<br />

(VSA) <strong>in</strong> elite female senior water polo (WP) players with regard to all<br />

three energetic systems of swim effort. The study <strong>in</strong>cluded 30 female<br />

WP players, members of the Serbian senior national team. On the basis<br />

of raw data obta<strong>in</strong>ed through test<strong>in</strong>g (four different test loads: 10, 12,<br />

13.5 <strong>and</strong> 16 kg) the function of Power-Time equation was calculated<br />

for each subject apply<strong>in</strong>g the general equation y=a∙bx. All data are presented<br />

<strong>in</strong> absolute terms as Absolute Vertical Swim Abilities Model<br />

(ABSvswim), <strong>in</strong> relative terms as Relative Vertical Swim Abilities Model<br />

(RELvswim), <strong>and</strong> <strong>in</strong> terms of reached biological capacity as Capacity<br />

Vertical Swim Abilities Model (CAPvswim). The raw data were used to<br />

def<strong>in</strong>e the follow<strong>in</strong>g models of VSA <strong>in</strong> female WP players: ABSvswim,<br />

y = 30.4868x-0.2087, RELvswim, y = 47.8754x-0.2127, CAPvswim, y=<br />

91.9195x-0.1846, respectively.<br />

Key words: Vertical swimm<strong>in</strong>g abilities, water polo, female<br />

IntroductIon<br />

Although men’s water polo was <strong>in</strong>troduced at the modern Olympic<br />

Games <strong>in</strong> Paris <strong>in</strong> 1900, it was not until the Sydney Olympics <strong>in</strong> 2000<br />

that women’s water polo became an Olympic sport. This is one of the<br />

very reasons why sport research on women’s water polo is still scanty.<br />

Previous research has established two basic positions a water polo<br />

(WP) player assumes <strong>in</strong> the water dur<strong>in</strong>g the game: horizontal <strong>and</strong> vertical<br />

(Platanou, 2009). Available studies covered a variety of methods to<br />

assess horizontal swimm<strong>in</strong>g abilities <strong>in</strong> women players (Tan et al., 2009),<br />

laboratory tests were applied to def<strong>in</strong>e the physiological profile based on<br />

women players’ abilities (Radovanovic et al., 2007), there was research<br />

<strong>in</strong>to the changes of anthropomorphic <strong>and</strong> physiological characteristics<br />

caused by a year-round tra<strong>in</strong><strong>in</strong>g cycle (Marr<strong>in</strong> & Bampouras, 2008),<br />

<strong>and</strong> both general <strong>and</strong> specific test<strong>in</strong>g was conducted to compare the<br />

methods of assess<strong>in</strong>g women players’ abilities (Bampouras & Marr<strong>in</strong>,<br />

2009). Although the vertical position is dom<strong>in</strong>ant while perform<strong>in</strong>g the<br />

elements of the ball techniques, dual play, <strong>and</strong> offensive <strong>and</strong> defensive<br />

tactics (D’Auria & Gabbett, 2008), female players‘ vertical swimm<strong>in</strong>g<br />

abilities have yet to be studied comprehensively.<br />

This paper aims to def<strong>in</strong>e different models of vertical swimm<strong>in</strong>g<br />

abilities (VSA) <strong>in</strong> elite female senior WP players with regard to all three<br />

energetic systems of swim effort.<br />

Methods<br />

The study <strong>in</strong>cluded 30 female WP players, members of the Serbian national<br />

senior team (Age=21.6±3.3 yrs, BH=170.5±5.2 cm, BM=64.9±7.1<br />

kg, tra<strong>in</strong><strong>in</strong>g experience=7.7±3.3 yrs). The tests were conducted <strong>in</strong> the<br />

seasons of 2007 <strong>and</strong> 2008 us<strong>in</strong>g the st<strong>and</strong>ard procedure (Dopsaj & Thanopoulos,<br />

2006) at the beg<strong>in</strong>n<strong>in</strong>g of the national team‘s preparations for<br />

the summer season. On the basis of raw data obta<strong>in</strong>ed through test<strong>in</strong>g<br />

(four different test loads: 10, 12, 13.5 <strong>and</strong> 16 kg) the function of the Power-<br />

Time equation was calculated for each subject apply<strong>in</strong>g the general equation<br />

y = a ∙ b x . All data are presented <strong>in</strong> absolute terms as Absolute Vertical Swim<br />

Abilities Model (ABS vswim ) <strong>in</strong> kg of weight mass, <strong>in</strong> relative terms as Relative<br />

Vertical Swim Abilities Model (REL vswim ) <strong>in</strong> % of weight mass <strong>in</strong> relation<br />

to BM, <strong>and</strong> <strong>in</strong> terms of reached biological capacity as Capacity Vertical<br />

Swim Abilities Model (CAP vswim ) <strong>in</strong> added weight mass <strong>in</strong> relation to the<br />

b coefficient (calculated as extra load divided with coefficient b), which represents<br />

the maximal hypothetical work<strong>in</strong>g biological capacity load. All data<br />

192<br />

were calculated <strong>and</strong> presented for the follow<strong>in</strong>g n<strong>in</strong>e time <strong>in</strong>tervals: 5, 10 <strong>and</strong><br />

15 s - anaerobic alactic; 30, 60 <strong>and</strong> 120 s - anaerobic lactic; <strong>and</strong> 300, 600 <strong>and</strong><br />

1800 s – aerobic, as the time <strong>in</strong>tervals characteristic of estimat<strong>in</strong>g the <strong>in</strong>tensity,<br />

power <strong>and</strong> capacity of all three energetic systems (Gast<strong>in</strong>, 2001). All<br />

data underwent the descriptive statistical analysis <strong>and</strong> mathematical model<strong>in</strong>g<br />

through a method of fitt<strong>in</strong>g.<br />

results<br />

All basic descriptive statistics are shown <strong>in</strong> Table 1. The raw data were used<br />

to def<strong>in</strong>e the follow<strong>in</strong>g models of VSA <strong>in</strong> female WP players: ABS vswim , y<br />

= 30.4868x -0.2087 , REL vswim , y = 47.8754x -0.2127 , CAP vswim , y= 91.9195x -0.1846 ,<br />

respectively (Figures 1, 2 <strong>and</strong> 3, respectively).<br />

Table 1. Basic descriptive statistics<br />

Absolute Vertical Swim Abilities Model (ABSvswim ) results<br />

Time <strong>in</strong>tervals (<strong>in</strong> s) 5 10 15 30 45 120 300 600 1800<br />

MEAN (kg) 22.32 18.98 17.30 14.82 13.57 11.03 9.17 8.02 6.55<br />

SD (kg) 5.77 3.87 3.06 2.21 2.02 2.17 2.59 2.89 3.30<br />

cV % 25.86 20.38 17.71 14.94 14.87 19.71 28.24 36.08 50.33<br />

Relative Vertical Swim Abilities Model (RELvswim) results<br />

MEAN (% BM) 34.81 29.53 26.88 22.96 20.99 16.99 14.07 12.27 9.98<br />

SD (% BM) 9.67 6.40 4.96 3.23 2.69 2.64 3.27 3.75 4.38<br />

cV % 27.79 21.69 18.44 14.08 12.81 15.52 23.21 30.55 43.88<br />

Capacity Vertical Swim Abilities Model (CAPvswim) results<br />

MEAN (% b) 69.69 60.42 55.69 48.58 44.94 37.42 31.77 28.20 23.54<br />

SD (% b) 9.37 11.22 12.10 13.27 13.79 14.64 15.08 15.28 15.49<br />

cV % 13.45 18.56 21.73 27.32 30.68 39.11 47.47 54.19 65.78<br />

Extra load mass (kg)<br />

y = 30.4868x -0.2087<br />

R 2 24<br />

22<br />

20<br />

18<br />

Wat Females<br />

16<br />

14<br />

12<br />

10<br />

8<br />

6<br />

4<br />

= 0.9985<br />

0 250 500 750 1000<br />

Time (s)<br />

1250 1500 1750 2000<br />

Figure 1. Follow<strong>in</strong>g model of Absolute Vertical Swim Abilities Model<br />

(ABS vswim ).<br />

% of weight mass <strong>in</strong> relation to BM<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

y = 47.8754x -0.2127<br />

R 2 = 0.9986<br />

Wat Females<br />

5<br />

0 250 500 750 1000<br />

Time (s)<br />

1250 1500 1750 2000<br />

Figure 2. Follow<strong>in</strong>g model of Relative Vertical Swim Abilities Model<br />

(REL vswim ).


Capacity level (<strong>in</strong> %)<br />

75<br />

70<br />

65<br />

60<br />

55<br />

50<br />

45<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

y = 91.9195x -0.1846<br />

R 2 = 0.9986<br />

0 250 500 750 1000 1250 1500 1750 2000<br />

Time (s)<br />

Wat Females<br />

Figure 3. Follow<strong>in</strong>g model of Capacity Vertical Swim Abilities Model<br />

(CAP vswim ).<br />

dIscussIon<br />

The female WP players showed the follow<strong>in</strong>g VSA: they could susta<strong>in</strong><br />

the vertical position <strong>in</strong> water at all the energetic <strong>in</strong>tervals with the average<br />

load of 22.32, 18.98, 17.30, 14.82, 13.57, 11.03, 9.17, 8.02 <strong>and</strong> 6.55<br />

kg, respectively. The values obta<strong>in</strong>ed were at the levels of 34.81, 29.53,<br />

26.88, 22.96, 20.99, 16.99, 14.07, 12.27 <strong>and</strong> 9.98 % of BM, respectively.<br />

With respect to the capacity model, the players showed VSA at the follow<strong>in</strong>g<br />

capacity levels: 69.69, 60.42, 55.69, 48.58, 44.94, 37.42, 31.77, 28.20 <strong>and</strong><br />

23.54 % of the hypothetical maximum, respectively.<br />

Previous research has established that female water polo players have<br />

great anaerobic capacity <strong>and</strong> muscular strength of the upper body (peak<br />

power - 8.05±0.8 W·kg -1 , mean power - 6.5±0.4 W·kg -1 ), a very high<br />

level of aerobic endurance (VO 2 peak - 46.52±7.0 mL∙kg −1 ∙m<strong>in</strong> −1 ) on<br />

the arm ergometer tests, (VO 2 peak - 61.8±11.9 mL∙kg −1 ∙m<strong>in</strong> −1 ) on the<br />

leg ergometer tests, <strong>and</strong> high values of lung function parameters. The<br />

great strength of the upper body <strong>and</strong> pronounced aerobic endurance of<br />

the whole organism are dom<strong>in</strong>ant characteristics of elite female water<br />

polo players. Along with a relatively pronounced body height <strong>and</strong> a low<br />

percentage of fat tissue, these female athletes are very well predisposed<br />

for adaptation to great physical dem<strong>and</strong>s over the whole match (Radovanovic<br />

et al., 2007).<br />

With regard to Time-Motion analysis of <strong>in</strong>ternational women’s water<br />

polo match play, it was established that the average exercise bout<br />

duration was 7.4 ± 2.5 s <strong>and</strong> exercise to rest ratio with<strong>in</strong> play was 1:1.6<br />

± 0.6. The average pattern of exercise was represented by 64.0 ± 15.3%<br />

swimm<strong>in</strong>g, 13.1 ± 9.2% contested swimm<strong>in</strong>g, 14.0 ± 11.6% wrestl<strong>in</strong>g,<br />

<strong>and</strong> 8.9 ± 7.1% hold<strong>in</strong>g position. Significant differences existed between<br />

the outside <strong>and</strong> the center players for percentage time swimm<strong>in</strong>g<br />

(67.5 ± 14.0% vs 60.2 ± 13.3%, P = 0.002) <strong>and</strong> wrestl<strong>in</strong>g (9.9 ± 9.3%<br />

vs 18.4 ± 11.1%, P = 0.000). Also, a significant difference was found<br />

<strong>in</strong> the number (P = 0.017) <strong>and</strong> duration (P = 0.010) of high-<strong>in</strong>tensity<br />

activity (HIA) bouts performed <strong>in</strong> each quarter for the outside (1.8 ±<br />

2.2 bouts, 7.0 ± 3.4 s) <strong>and</strong> the center players (1.2 ± 1.5 bouts, 5.2 ± 3.4<br />

s). The authors concluded that <strong>in</strong>ternational women’s water polo match<br />

play was characterized by a highly <strong>in</strong>termittent activity. Swimm<strong>in</strong>g, particularly<br />

that of high <strong>in</strong>tensity, had greater significance for the outside<br />

players whereas wrestl<strong>in</strong>g had greater significance for the center players<br />

(D’Auria & Gabbett, 2008).<br />

Regard<strong>in</strong>g the data presented by D’Auria <strong>and</strong> Gabbett (2008), approximately<br />

40% of the <strong>in</strong>tensive duel play, i.e., wrestl<strong>in</strong>g, lasts between<br />

2 <strong>and</strong> 5 s, c. 19% lasts 5 – 10 s, while c. 8% lasts 10 – 15 s. In other words,<br />

about 67% (2/3) of a given situation is realized with sub-maximal <strong>and</strong><br />

maximal <strong>in</strong>tensity with<strong>in</strong> 2 to 15 s, i.e., <strong>in</strong> anaerobic-alactic energetic<br />

system of swim effort. Our study established that the players tested <strong>in</strong><br />

the above-mentioned time <strong>in</strong>tervals of 5, 10 <strong>and</strong> 15 s could susta<strong>in</strong> the<br />

vertical position with the respective additional loads of 34.81, 29.53<br />

<strong>and</strong> 26.88 % of their body mass (Table 1). Such data can <strong>in</strong>dicate the<br />

requirement for particular considerations <strong>in</strong> develop<strong>in</strong>g maximal <strong>and</strong><br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

repetitive strength or power <strong>in</strong> an anaerobic work<strong>in</strong>g regimen both <strong>in</strong><br />

basic water tra<strong>in</strong><strong>in</strong>g <strong>and</strong> additional l<strong>and</strong> tra<strong>in</strong><strong>in</strong>g of female water polo<br />

players so as to improve specific anaerobic endurance of the lower limbs<br />

(Bampouras & Marr<strong>in</strong>, 2009).<br />

When the results of this study on ABS vswim, REL vswim <strong>and</strong> CAP vswim<br />

values were used to calculate the Fatigue <strong>in</strong>dex (which is expressed as the<br />

extra weight load decl<strong>in</strong>e – that is, observed vertical swimm<strong>in</strong>g value results<br />

reached <strong>in</strong> 5 s as the peak power abilities m<strong>in</strong>us observed vertical<br />

swimm<strong>in</strong>g value results reached <strong>in</strong> 30 s as the m<strong>in</strong>imum power abilities<br />

– divided by the time <strong>in</strong>terval <strong>in</strong> seconds between the peak <strong>and</strong> the<br />

m<strong>in</strong>imum of the observed vertical swimm<strong>in</strong>g values, i.e. divided by 25),<br />

the follow<strong>in</strong>g was obta<strong>in</strong>ed: Fi aps = 0.30 kg -s , Fi rel = 0.47 %BM -s , <strong>and</strong><br />

Fi cap = 0.84 %b -s .<br />

The comparison of results <strong>in</strong> vertical swimm<strong>in</strong>g abilities between the<br />

present <strong>and</strong> the previous study (Dopsaj & Thanopoulos, 2006), which<br />

nevertheless tested male elite water polo players us<strong>in</strong>g the same methodology,<br />

the follow<strong>in</strong>g gender differences can be <strong>in</strong>ferred: a) With regard<br />

to absolute test results, the women players were able to susta<strong>in</strong> the vertical<br />

swimm<strong>in</strong>g position for the same time <strong>in</strong>tervals (5, 10, 15, 30, 45, 120,<br />

300, 600 <strong>and</strong> 1800 s) with less additional load of 14.11, 11.89, 10.78,<br />

9.13, 6.95, 6.61, 5.36, 4.57 <strong>and</strong> 3.56 kg, respectively. b) With regard to<br />

absolute test results, the women players were able to susta<strong>in</strong> the vertical<br />

swimm<strong>in</strong>g position for the same time <strong>in</strong>tervals (5, 10, 15, 30, 45, 120,<br />

300, 600 <strong>and</strong> 1800 s) with a lower percentage of additional load of 38.73,<br />

38.51, 38.38, 38.11, 33.88, 37.48, 36.91, 36.32 <strong>and</strong> 35.22 %, respectively.<br />

Generally speak<strong>in</strong>g, with regard to absolute additional load values<br />

the female players‘ abilities were lower (37.06 %) than the male players,<br />

i.e. their average abilities comprised 62.94 % of the comparative men‘s<br />

abilities.<br />

conclusIon<br />

For the water polo tra<strong>in</strong><strong>in</strong>g plan, consideration needs to be taken of<br />

the primary <strong>in</strong>formative sources, i.e. the physiological dem<strong>and</strong>s of the<br />

game based on the game duration <strong>and</strong> the different technical <strong>and</strong> tactical<br />

dem<strong>and</strong>s dur<strong>in</strong>g the game accord<strong>in</strong>g to player position. The result<strong>in</strong>g<br />

models should be used to control the fitness levels, as well as to assist the<br />

development of tra<strong>in</strong><strong>in</strong>g technology with WP female players.<br />

reFerences<br />

Bampouras, T. M. & Marr<strong>in</strong>, K. (2009). Comparison of two anaerobic<br />

water polo specific tests with the W<strong>in</strong>gate test. Journal of Strength<br />

<strong>and</strong> Condition<strong>in</strong>g Research, 23(1), 336-340.<br />

D’Auria, S. & Gabbett, T. (2008). A Time-Motion analysis of <strong>in</strong>ternational<br />

women’s water polo match play. International Journal of Sports<br />

Physiology <strong>and</strong> Performance, 3, 305-319.<br />

Dopsaj, M. & Thanopoulos, V. (2006). The structure of evaluation <strong>in</strong>dicators<br />

of vertical swimm<strong>in</strong>g work ability of top water polo players.<br />

Revista Portuguesa de Ciencias do Desporto (Portugese Journal of<br />

Sport Sciences), 6(2),124-126.<br />

Gast<strong>in</strong>, P. B. (2001). Energy system <strong>in</strong>teraction <strong>and</strong> relative contribution<br />

dur<strong>in</strong>g maximal exercise. Sports <strong>Medic<strong>in</strong>e</strong>, 31(10), 725-741.<br />

Marr<strong>in</strong>, K. & Bampouras, T. M. (2008). Anthropometric <strong>and</strong> physiological<br />

changes <strong>in</strong> elite female water polo players dur<strong>in</strong>g a tra<strong>in</strong><strong>in</strong>g year. Serbian Journal<br />

of Sports Sciences, 2(3), 75-83.<br />

Platanou, T. (2009). Cardiovascular <strong>and</strong> metabolic requirements of water<br />

polo. Serbian Journal of Sports Sciences, 3(3), 85-97.<br />

Radovanovic, D., Okicic, T. & Ignjatovic, A. (2007). Physiological profile<br />

of elite women water polo players. Acta Medica Medianae, 46(4),<br />

48-51.<br />

Tan, F., Polglaze, T. & Dawson, B. (2009). Comparison of progressive<br />

maximal swimm<strong>in</strong>g tests <strong>in</strong> elite female water polo players. International<br />

Journal of Sports Physiology <strong>and</strong> Performance, 4, 206-217.<br />

193


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Critical Velocity <strong>and</strong> the Velocity at Maximal Lactate<br />

Steady State <strong>in</strong> Swimm<strong>in</strong>g<br />

espada, M.A., Alves, F.B.<br />

Faculty of Human K<strong>in</strong>etics - Technical University of Lisbon, Portugal<br />

The purpose of this study was to compare critical velocity (CV) to the<br />

velocity at maximal lactate steady state (MLSSv) <strong>in</strong> swimm<strong>in</strong>g. Eighteen<br />

well-tra<strong>in</strong>ed male swimmers performed a maximal 400 m front<br />

crawl to estimate maximal aerobic velocity (V400) <strong>and</strong> two to three 30m<strong>in</strong><br />

constant velocity swims <strong>in</strong> order to directly determ<strong>in</strong>e MLSSv. CV,<br />

estimated from 200 m <strong>and</strong> 400 m maximal swims, was highly correlated<br />

to MLSSv (r = 0.94 <strong>and</strong> p < 0.01) <strong>and</strong> V400 (r = 0.95 <strong>and</strong> p < 0.01).<br />

However, CV was significantly faster than MLSSv, confirm<strong>in</strong>g that this<br />

parameter does not represent a steady metabolic rate <strong>in</strong> long distance<br />

swimm<strong>in</strong>g. Nevertheless, CV still seems to be a useful tool for aerobic<br />

condition<strong>in</strong>g evaluation, due to the simplicity of its determ<strong>in</strong>ation.<br />

Keywords: exercise; swimm<strong>in</strong>g; Maximal lactate steady state; critical<br />

Velocity<br />

IntroductIon<br />

The maximal tolerated duration of a constant-load high-<strong>in</strong>tensity swimm<strong>in</strong>g<br />

bout has been shown to be a hyperbolic function of the power (or<br />

velocity) of the exercise (Wakayoshi et al., 1992), similarly to other forms<br />

of human locomotion (for a review, see Morton, 2006). Accord<strong>in</strong>g to this<br />

model, the velocity-duration relationship has an asymptote on the velocity<br />

axis, termed the critical velocity (CV) that has been considered as a valid<br />

fatigue threshold <strong>and</strong> a marker of the transition between the heavy <strong>and</strong><br />

the severe <strong>in</strong>tensity doma<strong>in</strong>s (Poole et al., 1988), s<strong>in</strong>ce it has also been<br />

shown to be a close correlate of the highest metabolic rate associated with<br />

pulmonary oxygen uptake (VO2), acid-base status <strong>and</strong> blood lactate concentration<br />

that can be susta<strong>in</strong>ed for a certa<strong>in</strong> time at a constant level.<br />

The power output or the velocity correspond<strong>in</strong>g to the CV has also<br />

been considered as express<strong>in</strong>g the maximal lactate steady state (MLSS)<br />

(discussed <strong>in</strong> Pr<strong>in</strong>gle <strong>and</strong> Jones, 2002), although this equivalence has not<br />

been confirmed <strong>in</strong> many experimental studies, especially <strong>in</strong> swimm<strong>in</strong>g<br />

(Dekerle et al., 2005b).<br />

The MLSS corresponds to the highest workload or velocity that<br />

can be ma<strong>in</strong>ta<strong>in</strong>ed over time without a cont<strong>in</strong>uous blood lactate accumulation<br />

(Billat et al., 2003) <strong>and</strong> its measurement dem<strong>and</strong>s several<br />

subsequent constant load tests that have to be performed with different<br />

workloads on different days, until it is possible the determ<strong>in</strong>e an<br />

<strong>in</strong>dividual workload <strong>in</strong>tensity above which the rate of lactate production<br />

exceeds lactate clearance. However, the number of studies directly<br />

assess<strong>in</strong>g this parameter is surpris<strong>in</strong>g limited <strong>in</strong> swimm<strong>in</strong>g, due surely<br />

to the time-consum<strong>in</strong>g <strong>and</strong> cumbersome procedures required, when<br />

compared to the performance of an <strong>in</strong>cremental graded test for lactate<br />

threshold determ<strong>in</strong>ation.<br />

The purpose of this study was to compare critical velocity (CV), estimated<br />

by a two-component model, us<strong>in</strong>g 200 m <strong>and</strong> 400 m maximal<br />

swims, to the velocity at maximal lactate steady state (MLSSv) <strong>in</strong> welltra<strong>in</strong>ed<br />

swimmers.<br />

Methods<br />

Eighteen male national <strong>and</strong> <strong>in</strong>ternational level competitive swimmers<br />

volunteered for this study. They were aged 17.1 ± 2.8 years, with a height<br />

of 177.6 ± 5.7 cm, a body mass of 65.8 ± 9.1 kg <strong>and</strong> a% body fat of 10.1<br />

± 2.4%. Subjects have tra<strong>in</strong>ed regularly for at least 6 years <strong>and</strong> took no<br />

drugs or medicaments dur<strong>in</strong>g the study. Most of the swimmers were<br />

familiar with swimm<strong>in</strong>g pool exercise test<strong>in</strong>g procedures. They were <strong>in</strong>formed<br />

of the nature of the experiments <strong>and</strong> gave written consent to<br />

participate <strong>in</strong> this study.<br />

194<br />

Athletes were <strong>in</strong>structed to avoid exhaust<strong>in</strong>g exercise the day before<br />

the tests <strong>and</strong> to reta<strong>in</strong> their normal nutritional habits. A st<strong>and</strong>ardize<br />

warm-up of 600 m was completed <strong>in</strong> every test<strong>in</strong>g session. A maximal<br />

400 m front crawl was performed <strong>in</strong> order to use the average velocity<br />

between 50 m <strong>and</strong> the 350 m (V400) as an estimate of the maximal<br />

aerobic velocity (Lavoie <strong>and</strong> Leone, 1988).<br />

CV was calculated from the slope of the regression analysis between<br />

the averaged velocity of the 400 m trial previously referred to <strong>and</strong> a 200<br />

m front crawl maximal trial performed for this purpose.<br />

In a first round of test<strong>in</strong>g, six subjects performed 30-m<strong>in</strong> constant<br />

velocity swims at 75 <strong>and</strong> 80% of V400. The physiological impact of these<br />

bouts was clearly low so it was decided to cont<strong>in</strong>ue the study us<strong>in</strong>g higher<br />

<strong>in</strong>tensities. All eighteen subjects performed, then, <strong>in</strong> r<strong>and</strong>om order,<br />

30-m<strong>in</strong> at constant velocity at 85, 90 <strong>and</strong> 95% of V400. Split times for<br />

each 50 m were determ<strong>in</strong>ed <strong>and</strong> used by two <strong>in</strong>vestigators positioned at<br />

7.5 m <strong>and</strong> 17.5 m of the pool to control the athletes swimm<strong>in</strong>g pace. The<br />

swimmer was asked to ma<strong>in</strong>ta<strong>in</strong> the pre-established swim pace as long<br />

as possible. The test was <strong>in</strong>terrupted when the swimmer could no longer<br />

match the required swimm<strong>in</strong>g velocity. Each subject was stopped every<br />

400 m (30 to 45 seconds) for blood sample collection <strong>and</strong> record of the<br />

rate of perceived exertion (MLSSrpe) (6-20 scale).<br />

Maximal lactate steady state blood lactate concentration (MLSSc)<br />

was def<strong>in</strong>ed as the highest blood lactate concentration that <strong>in</strong>creased by<br />

no more than 1 mmol.L-1 dur<strong>in</strong>g the f<strong>in</strong>al 20-m<strong>in</strong> of a 30-m<strong>in</strong> constant<br />

workload (Beneke, 2003; Baron et al., 2005). When this criterion was<br />

not accomplished, the test was stopped. MLSSv was the <strong>in</strong>tensity associated<br />

with MLSS. Tests were conducted at similar times on separate<br />

days (1 day of total rest between tests) at a 25 m pool with the water<br />

temperature at 28.2º C. No polyurethane suits were used.<br />

Stroke rate (SR) was measured from three stroke cycles taken <strong>in</strong> the<br />

middle of the pool for every 50 m <strong>and</strong> stroke length (SL) calculated.<br />

Blood lactate concentrations were analyzed us<strong>in</strong>g a Lactate Pro LT device<br />

(Arkray, Kyoto, Japan). A Polar Sport Tester (S410) recorded the<br />

heart rate frequency every 5 seconds dur<strong>in</strong>g all tests.<br />

Paired-samples t-test was used to compare CV <strong>and</strong> MLSSv. Pearson’s<br />

l<strong>in</strong>ear coefficient was used to test correlations. Statistical significance<br />

was accepted at p < 0.05.<br />

results<br />

Mean <strong>and</strong> st<strong>and</strong>ard deviation of V400, MLSSv, CV <strong>and</strong> MLSSc are<br />

shown <strong>in</strong> Table 1. MLSSv corresponded to 89.7 ± 1.2% <strong>and</strong> CV to 94.0<br />

± 1.5% of V400. Only one swimmer achieved MLSS at 85% of V400. At<br />

95% of V400 no one achieved stabilization <strong>in</strong> blood lactate concentration,<br />

confirm<strong>in</strong>g that work bouts at this <strong>in</strong>tensity were performed above<br />

MLSS. Extreme values of 2.6 <strong>and</strong> 7.8 mmol.L -1 were found associated<br />

to MLSSv. Mean SR at MLSSv was 32.9 ± 4.3 (cycles.m<strong>in</strong> -1 ) <strong>and</strong> mean<br />

SL was 2.49 ± 0.34 (m.cycle -1 ). Mean heart rate frequency at MLSSv<br />

(MLSS HR ) was 177.0 ± 6.9 beats.m<strong>in</strong> -1 <strong>and</strong> the mean MLSSrpe expressed<br />

by the swimmers was 13.39 ± 1.33.<br />

Table 1. Mean <strong>and</strong> st<strong>and</strong>ard deviation of V400, MLSSv, CV <strong>and</strong><br />

MLSSc.<br />

N=18<br />

V400<br />

(m·s-1)<br />

MLSSv<br />

(m·s-1)<br />

CV<br />

(m·s-1)<br />

MLSSc<br />

(mmol·L-1)<br />

1.49 ± 0.07 1.34 ± 0.06 1.40 ± 0.08 5.3 ± 1.6<br />

CV was significantly faster than MLSSv (p < 0.01) <strong>and</strong> both expressed<br />

velocities significantly different from V400 (p < 0.01).


MLSSv (m.s -1 )<br />

1,50<br />

1,45<br />

1,40<br />

1,35<br />

1,30<br />

1,25<br />

y = 0.78x + 0.25<br />

r 2 = 0.89<br />

1,20<br />

1,25 1,30 1,35 1,40 1,45 1,50 1,55 1,60<br />

CV (m.s -1 )<br />

Figure 1. L<strong>in</strong>ear regression of MLSSv on CV (SSE = 0.02 m·s -1 ).<br />

MLSSv <strong>and</strong> CV were highly correlated (r = 0.94; p < 0.01). Both were<br />

associated with V400 (r = 0.97; p < 0.01 <strong>and</strong> r = 0.95; p < 0.01, respectively).<br />

Regression analysis of CV over MLSSv (SSE = 0.02 m·s -1 ) revealed<br />

that the latter can be predicted with reasonable accuracy from the<br />

200 m / 400 m swim trials CV. Stroke cycle parameters were unrelated<br />

to performance, MLSSv or CV.<br />

10<br />

0<br />

9<br />

+1.96 SD<br />

8<br />

7<br />

6<br />

8.8<br />

5<br />

Mean<br />

4<br />

3<br />

2<br />

4.8<br />

1<br />

-1.96 SD<br />

0<br />

0.8<br />

1.25 1.30 1.35 1.40 1.45 1.50 1.55<br />

Figure 2. Bl<strong>and</strong>-Altman plot show<strong>in</strong>g the bias <strong>and</strong> limits of agreement<br />

between CV <strong>and</strong> MLSSv. X axis: velocity of CV <strong>and</strong> MLSS (m/s) <strong>and</strong><br />

y-axis: CV-MLSS (%). The r<strong>and</strong>om scatter of po<strong>in</strong>ts between the upper<br />

<strong>and</strong> lower confidence limits is <strong>in</strong>dicative of a good fit.<br />

dIscussIon<br />

MLSS was determ<strong>in</strong>ed employ<strong>in</strong>g only two to three attempts of 30-m<strong>in</strong><br />

swims at constant velocity. In a study conducted with ten <strong>in</strong>ter-regional<br />

<strong>and</strong> national swimmers, Baron et al. (2005) <strong>in</strong>dicated that MLSSv corresponded<br />

to 86.5 ± 5.5% of V400. Our results (extreme values of 2.6<br />

<strong>and</strong> 7.8 mmol.L -1 ) are consistent with previous studies conducted with<br />

well-tra<strong>in</strong>ed athletes (i.e. Baron et al., 2003) <strong>and</strong> <strong>in</strong>dicate that it is impossible<br />

to l<strong>in</strong>k the true MLSS to a fixed lactate concentration.<br />

Dekerle et al. (2005a) found a decrease <strong>in</strong> stroke length at <strong>in</strong>tensities<br />

above MLSS. It has been suggested that this decrease <strong>in</strong> SL is related<br />

to local muscular fatigue <strong>and</strong> ris<strong>in</strong>g of blood lactate concentration. In<br />

the present study, SL was ma<strong>in</strong>ta<strong>in</strong>ed constant by all swimmers dur<strong>in</strong>g<br />

the 30-m<strong>in</strong> velocity swims at MLSS, evidenc<strong>in</strong>g that athletes were not<br />

under <strong>in</strong>creas<strong>in</strong>g metabolic imbalance.<br />

Wakayoshi et al. (1993) found that CV determ<strong>in</strong>ed by 200 m <strong>and</strong><br />

400m trials almost agreed with the exercise <strong>in</strong>tensity at MLSS. Our<br />

results confirm the f<strong>in</strong>d<strong>in</strong>g of Dekerle et al. (2005b) that CV over estimates<br />

MLSSv <strong>in</strong> swimmers. The use of a 2-parameter model may expla<strong>in</strong><br />

part of the difference between CV <strong>and</strong> MLSSv, s<strong>in</strong>ce this model<br />

provides higher estimates than the 3-paramater one, thought to be more<br />

accurate <strong>and</strong> closer to the MLSS velocity or power output (Billat et<br />

al., 2003; Morton, 2006). Another po<strong>in</strong>t is the variation of the swimm<strong>in</strong>g<br />

energy cost with velocity, tend<strong>in</strong>g to produce a faster CV when<br />

shorter distances are used (di Prampero et al., 2008). Bishop et al. (1998)<br />

showed that the shorter the predictive trials, the greater the slope of the<br />

distance-time regression, even <strong>in</strong> tasks where mechanical efficiency is<br />

rather constant throughout the range of <strong>in</strong>tensities used, attribut<strong>in</strong>g this<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

effect to the aerobic <strong>in</strong>ertia dependent on the primary phase of the VO2<br />

on-k<strong>in</strong>etics. Several studies have confirmed this shift to faster estimated<br />

swimm<strong>in</strong>g velocities when us<strong>in</strong>g shorter distances (Mart<strong>in</strong> <strong>and</strong> Whyte,<br />

2000; Toubekis et al., 2006; Reis <strong>and</strong> Alves, 2006; Costa et al., 2009).<br />

In this study, 200 m <strong>and</strong> 400 m swimm<strong>in</strong>g distances <strong>in</strong> the estimation<br />

of CV is recommended. This is ma<strong>in</strong>ly due to the usefulness of a<br />

simple enough test to be used frequently <strong>in</strong> tra<strong>in</strong><strong>in</strong>g conditions, <strong>in</strong> spite<br />

of be<strong>in</strong>g aware that us<strong>in</strong>g more trials would improve the accuracy of<br />

the calculation (Dekerle et al., 2005b), but also because these distances<br />

comply with the physiological requirements of the model (di Prampero,<br />

1999), correspond<strong>in</strong>g to effort durations that lie between limits with<strong>in</strong><br />

which the hyperbolic relationship appears to provide a good characterization<br />

of the physiological response.<br />

Exercise durations of less than 1-m<strong>in</strong> would fail, with strong probability,<br />

two criteria: the reach<strong>in</strong>g of maximal oxygen consumption (VO-<br />

2max) <strong>and</strong> the exhaustion of the available anaerobic energy. So, distances<br />

of 50 m should not be used for the estimation of CV, <strong>and</strong> it would<br />

be cautioned not to use 100 m trials as well, for the same reasons. The<br />

<strong>in</strong>clusion of a longer distance, of 600 to 800 m, would certa<strong>in</strong>ly lessen<br />

the tendency to overestimate a true steady metabolic rate power output<br />

(Bishop et al., 1998) but this would make the test<strong>in</strong>g much more timeconsum<strong>in</strong>g<br />

<strong>and</strong> less practical <strong>in</strong> a day-to-day basis. It is not advisable to<br />

<strong>in</strong>clude longer distances as well, not only would that <strong>in</strong>crease the variation<br />

<strong>in</strong> energy cost but also would <strong>in</strong>troduce another source of bias<strong>in</strong>g,<br />

s<strong>in</strong>ce the effort would be performed at a lower %VO2max.<br />

Therefore, it appears that CV <strong>in</strong> swimmers does not demarcate the<br />

transition from heavy to severe exercise <strong>and</strong> may not provide a direct<br />

non-<strong>in</strong>vasive measure of MLSSv. Differences <strong>in</strong> exercise <strong>in</strong>tensity of this<br />

magnitude have substantial effects on performance factors such as time to<br />

exhaustion, as well as the physiological dem<strong>and</strong>s of cont<strong>in</strong>uous exercises.<br />

However, our data also <strong>in</strong>dicates that MLSSv could be estimated from CV<br />

with enough accuracy to be used as a guidance to exercise prescription.<br />

conclusIon<br />

Our results confirm that the direct determ<strong>in</strong>ation of MLSSv rema<strong>in</strong>s<br />

the most accurate procedure for exercise prescription aim<strong>in</strong>g at aerobic<br />

load<strong>in</strong>g.<br />

This study also confirms previous observations that the CV, estimated<br />

from two repeated maximal swims, us<strong>in</strong>g a two-parameter model<br />

approach, overestimates MLSSv, correspond<strong>in</strong>g to an <strong>in</strong>tensity of exercise<br />

well <strong>in</strong>to the severe doma<strong>in</strong>.<br />

Swimm<strong>in</strong>g critical velocity is still a valuable tool to assess tra<strong>in</strong><strong>in</strong>g<br />

adaptations <strong>and</strong> could be used as an estimator of the MLSSv.<br />

reFerences<br />

Baron, B., Dekerle, J., Depretz, S., Lefevre, T., Pelayo, P. (2005). Self<br />

selected speed <strong>and</strong> maximal lactate steady state <strong>in</strong> swimm<strong>in</strong>g. J Sports<br />

Med Phys Fitness; 45 (1), 1-6.<br />

Baron, B., Dekerle, J., Rob<strong>in</strong>, S., Neviere, R., Dupont, L., Matran, R.,<br />

Vanvelcenaher, J., Rob<strong>in</strong>, H., Pelayo, P. (2003). Maximal lactate<br />

steady state does not correspond to a complete physiological steady<br />

state. Int J Sports Med; 24 (8), 582-587.<br />

Beneke, R. (2003). Methodological aspects of maximal lactate<br />

steady state-implications for performance test<strong>in</strong>g. Eur J Appl<br />

Physiol; 89, 95-99.<br />

Billat, V.L., Sirvent, P., Py, G., Koralszte<strong>in</strong>, J.P., Mercier, J. (2003). The<br />

concept of maximal lactate steady state: a bridge between biochemistry,<br />

physiology <strong>and</strong> sport science. Sports Med; 33 (6), 407-426.<br />

Bishop, D., Jenk<strong>in</strong>s, D.G., Howard, A. (1998). The critical power function<br />

is dependent on the duration of the predictive exercise tests chosen.<br />

Int J Sports Med; 19, 125-129.<br />

Costa, A.M., Silva, A.J., Louro, H., Reis, V.M., Garrido, N.D., Marques,<br />

M.C., Mar<strong>in</strong>ho, D.A. (2009). Can the curriculum be used to estimate<br />

critical velocity <strong>in</strong> young competitive swimmers. J Sports Sci & Med;<br />

8, 17-23.<br />

195


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Dekerle, J., Nesi, X., Lefevre, T., Depretz, S., Sidney, M., March<strong>and</strong>,<br />

F.H., Pelayo, P. (2005a). Strok<strong>in</strong>g parameters <strong>in</strong> front crawl swimm<strong>in</strong>g<br />

<strong>and</strong> maximal lactate steady state speed. Int J Sports Med; 26,<br />

53-58.<br />

Dekerle, J., Pelayo, P., Clipet, B., Depretz, S., Lefevre, T., Sidney, M.<br />

(2005b). Critical swimm<strong>in</strong>g speed does not represent the speed at<br />

maximal lactate steady state. Int J Sports Med; 26 (7), 524-530.<br />

Dekerle, J., Sidney, M., Hespel, J.M., Pelayo, P. (2002). Validity <strong>and</strong> reliability<br />

of critical speed, critical stroke rate, <strong>and</strong> anaerobic capacity<br />

<strong>in</strong> relation to front crawl swimm<strong>in</strong>g performances. Int J Sports Med;<br />

23, 93-98.<br />

di Prampero, P.E. (1999). The concept of critical velocity: a brief analysis.<br />

Eur J Appl Physiol Occup Physiol; 80 (2), 162-164.<br />

di Prampero, P.E., Dekerle, J., Capelli, C., Zamparo, P. (2008). The critical<br />

velocity <strong>in</strong> swimm<strong>in</strong>g. Eur J Appl Physiol; 102 (2),165-171.<br />

Lavoie, J.M. <strong>and</strong> Leone, M. (1988). Functional maximal aerobic power<br />

<strong>and</strong> prediction of swimm<strong>in</strong>g performances. J. Swimm<strong>in</strong>g Research; 4<br />

(4), 17-19.<br />

Mart<strong>in</strong>, L. <strong>and</strong> Whyte, G.P. (2000). Comparison of critical swimm<strong>in</strong>g<br />

velocity <strong>and</strong> velocity at lactate threshold <strong>in</strong> elite triathletes. Int J<br />

Sports Med; 21 (5), 366-368.<br />

Morton, R.H. (2006). The critical power <strong>and</strong> related whole-body bioenergetic<br />

models. Eur J Appl Physiol, 96 (4), 339-354.<br />

Poole, D.C., Ward, S.A., Gardner, G.W., Whipp, B.J. (1988). A metabolic<br />

<strong>and</strong> respiratory profile of the upper limit for prolonged exercise<br />

<strong>in</strong> man. Ergonomics; 31, 1265-1279.<br />

Pr<strong>in</strong>gle, J.S. <strong>and</strong> Jones, A.M. (2002). Maximal lactate steady state, critical<br />

power <strong>and</strong> EMG dur<strong>in</strong>g cycl<strong>in</strong>g. Eur J Appl Physiol; 88, 214-226.<br />

Reis, J. <strong>and</strong> Alves, F. (2006). Tra<strong>in</strong><strong>in</strong>g <strong>in</strong>duced changes <strong>in</strong> critical velocity<br />

<strong>and</strong> V4 <strong>in</strong> age group swimmers. In: Vilas-Boas, J.P., Alves, F.<br />

<strong>and</strong> Marques, A. (eds.). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X.<br />

Portuguese Journal of Sport Sciences; Porto, 311-313.<br />

Toubekis, A.G., Tsami, A.P., Tokmakidis, S.P. (2006). Critical velocity<br />

<strong>and</strong> lactate threshold <strong>in</strong> young swimmers. Int J Sports Med; 27<br />

(2),117-123.<br />

Wakayoshi, K., Yoshida, T., Udo, M., Kasai, T., Moritani, T., Mutoh,<br />

Y., Miyashita, M. (1992). A simple method for determ<strong>in</strong><strong>in</strong>g critical<br />

speed as swimm<strong>in</strong>g fatigue threshold <strong>in</strong> competitive swimm<strong>in</strong>g. Int J<br />

Sports Med; 13, 367-371.<br />

Wakayoshi, K., Yoshida, T., Udo, M., Harada, T., Moritani, T., Mutoh,<br />

Y., Miyashita, M. (1993). Does critical swimm<strong>in</strong>g velocity represent<br />

exercise <strong>in</strong>tensity at maximal lactate steady state? Eur J Appl Physiol<br />

Occup Physiol; 66, 90-95.<br />

AcKnoWledGeMents<br />

The first author gratefully acknowledges the ‘Fundação para a Ciência e<br />

Tecnologia, Portugal’ (‘The Foundation for Science <strong>and</strong> Technology’) for<br />

their doctoral fellowship award (SFRH/BD/41417/2007).<br />

196<br />

Modell<strong>in</strong>g the VO 2 Slow Component <strong>in</strong> Elite Long<br />

Distance Swimmers at the Velocity Associated with<br />

Lactate Threshold<br />

hellard, P. 1, 4 , dekerle, J. 2 , nesi, X. 2 , toussa<strong>in</strong>t, J.F. 4 , houel, n.<br />

1 , hausswirth, c. 3<br />

1Département recherche, Fédération Française de Natation, Paris France<br />

2Chelsea School, University of Brighton, Engl<strong>and</strong><br />

3Département des Sciences du Sport, INSEP, Paris, France<br />

4Institut de recherche en médec<strong>in</strong>e et en épidémiologie du sport, IRMES,<br />

Paris, France<br />

Seven elite male long-distance swimmers (Mean ± SD, age 21.4 ± 3.5<br />

yrs; weight 71 ± 5 kg ; height 180 ± 5 cm) participated <strong>in</strong> two experimental<br />

tests performed dur<strong>in</strong>g a one-week period. The first test consisted<br />

<strong>in</strong> a 6 x 300-m <strong>in</strong>cremental swimm<strong>in</strong>g exercise performed to exhaustion<br />

<strong>in</strong> order to determ<strong>in</strong>e lactate threshold (LT = 3.1 ± 1.2 mmol·L -1 ),<br />

<strong>and</strong> the velocity associated with LT (v LT = 1.45 ± 0.01 m·sec-1 = 97.3 ±<br />

5.6% of v · VO2 max ). The parameters of the · VO2 k<strong>in</strong>etics were calculated<br />

dur<strong>in</strong>g a 500-m <strong>in</strong>terval swum at v LT us<strong>in</strong>g a two- <strong>and</strong> one-term<br />

exponential model. The fit was statistically superior for the two-term<br />

model (r²= 0.62 ± 0.18 vs. 0.52 ± 0.21, P < 0.01). A slow component (A2 = 401.7 ± 129.9 ml·m<strong>in</strong>·kg -1 , Td 2 = 189.7 ± 63.3 s, 2<br />

τ = 64.5 ± 114.4 s)<br />

can be observed <strong>in</strong> elite male long-distance swimmers swimm<strong>in</strong>g at submaximal<br />

<strong>in</strong>tensities (vLT; 96.7 ± 0.5% of v · VO 2 max ).<br />

Key words: lactate threshold, Vo 2 k<strong>in</strong>etics, long distance swimmers,<br />

model<strong>in</strong>g<br />

IntroductIon<br />

The lactate threshold has been shown to represent an essential factor<br />

of high-level performance <strong>in</strong> endurance sports (marathon, Nordic ski<strong>in</strong>g,<br />

triathlon, cycl<strong>in</strong>g; Billat et al., 2001; Mahood et al., 2001). With<br />

tra<strong>in</strong><strong>in</strong>g, a reduction <strong>in</strong> blood lactate accumulation for a given <strong>in</strong>tensity<br />

would be the result of lower lactate production <strong>and</strong>/or <strong>in</strong>creased lactate<br />

clearance (Billat et al., 2001, Mahood et al., 2001) associated with lower<br />

energy cost (Billat et al., 2001).<br />

The oxygen response to constant load exercise can be characterized<br />

by three transient phases. Phase I is a rapid early rise <strong>in</strong> · VO 2 (last<strong>in</strong>g 15-<br />

30-s) <strong>and</strong> represents the circulatory transit delay between the exercis<strong>in</strong>g<br />

muscle <strong>and</strong> lungs (Whipp, 1996). Follow<strong>in</strong>g the phase I response, the<br />

phase II rise <strong>in</strong> · VO 2 is best characterized as an exponential function that<br />

atta<strong>in</strong>s a steady state with<strong>in</strong> 2-3 m<strong>in</strong>. If the <strong>in</strong>tensity of the exercise is<br />

performed above the lactate threshold a slowly develop<strong>in</strong>g component<br />

of <strong>in</strong>creas<strong>in</strong>g · VO 2 (termed the slow component of O2 uptake k<strong>in</strong>etics)<br />

can be observed (Gaesser et Poole, 1996). Cont<strong>in</strong>uous exercise performed<br />

at the lactate threshold is also thought to reduce the amplitude<br />

of the slow component after a period of tra<strong>in</strong><strong>in</strong>g (Carter et al., 2000;<br />

Gaesser et Poole, 1996; Whipp, 1996). The · VO 2 slow component appears<br />

to be more frequent among athletes hav<strong>in</strong>g a high fractional · VO 2<br />

at the lactate threshold (Billat, 2001) which is typical of ultra-endurance<br />

athletes (Billat et al., 2001; Lucia et al., 1998; Mahood et al., 2001). In<br />

high-level long-distance swimmers, it is hypothesized that a long swimm<strong>in</strong>g<br />

<strong>in</strong>terval <strong>in</strong>duces a greater slow component of · VO 2 .<br />

Methods<br />

Seven elite long-distance male swimmers participated <strong>in</strong> this study.<br />

Their performances over a 800-, 1500-, <strong>and</strong> 5000-meter front crawl test<br />

(V800, V1500, V5000) were recorded. They are expressed <strong>in</strong> percentage<br />

of the world record <strong>in</strong> Table 1.


TABLE 1. Performances dur<strong>in</strong>g competition events<br />

(5000-m, 1500-m, 800-m) expressed <strong>in</strong> real time <strong>and</strong> as<br />

percent of world record.<br />

S LP T5000-m<br />

(h:m<strong>in</strong>:s)<br />

T1500-m<br />

(m<strong>in</strong>:s)<br />

1500-m<br />

(% wr)<br />

T-800-m<br />

(m<strong>in</strong>:s)<br />

800-m<br />

(% wr)<br />

1 N 55:31 16:25 88.7 8 :31 89.7<br />

2 N 53:57 16:12 89.9 8 :17 92.2<br />

3 N 55:07 16:12 89.9 8 :32 89.6<br />

4 I 53:46 15:51 91.9 8 :12 93.1<br />

5 I 54:37 16:05 90.6 8 :28 90.3<br />

6 I 54:46 16:01 91.1 8 :16 92.4<br />

7 N 55:44 16:08 90.3 8 :22 91.3<br />

M 55:18 16:03 90:3 8 :37 91.2<br />

SE 00 :44 00 :15 1.1 0 :07 1.3<br />

All swimmers completed an <strong>in</strong>cremental test performed to exhaustion.<br />

This test was composed of five consecutive 300-m swims separated by<br />

30s of rest. The speed of each <strong>in</strong>crement was determ<strong>in</strong>ed from the best<br />

time performance of each swimmer <strong>in</strong> a 400-m freestyle event achieved<br />

dur<strong>in</strong>g the month preced<strong>in</strong>g the test. The speed for the first 300m was<br />

30s slower than the best 400-m time: this time was reduced by <strong>in</strong>crements<br />

of 5s for each consecutive 300m until the f<strong>in</strong>al 300m performed<br />

maximally. Swimm<strong>in</strong>g speeds were monitored with Aquapacer ‘Solo’<br />

(Challenge <strong>and</strong> Response, Inverurie, UK) so that each swimmer could<br />

match auditory signals with visual markers positioned every 12.5m<br />

along the border of the pool. Blood lactate level (expressed <strong>in</strong> mM/L)<br />

was determ<strong>in</strong>ed from a f<strong>in</strong>gertip blood sample which was analyzed immediately<br />

us<strong>in</strong>g a portable lactate analyzer (Lactate Pro, Arkray, Japan).<br />

Breath-by-breath respiratory data were collected with a portable gas<br />

analyzer (Cosmed K4b2, Rome, Italy) connected to an Aquatra<strong>in</strong>er<br />

snorkel (Cosmed, Rome, Italy). Heart rate (HR) was recorded dur<strong>in</strong>g<br />

the K 4 b 2 exercise us<strong>in</strong>g a belt system (Polar Electro, F<strong>in</strong>l<strong>and</strong>). The lactate<br />

threshold (LT) was mathematically determ<strong>in</strong>ed us<strong>in</strong>g the DMax<br />

method (Cheng et al., 1992). HRpeak (expressed <strong>in</strong> beats·m<strong>in</strong> -1 ) was<br />

def<strong>in</strong>ed as the highest 15-s averaged HR value.<br />

The <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g session consisted <strong>in</strong> a 500-m <strong>in</strong>terval set. The<br />

swimmers were <strong>in</strong>formed of their velocity us<strong>in</strong>g the protocol described<br />

above. Because they were wear<strong>in</strong>g a snorkel, the swimmers used open<br />

turns between 50-m bouts. Dur<strong>in</strong>g a pilot run, the time needed to execute<br />

a turn with the snorkel was estimated <strong>in</strong>dividually at 1±0.37 s compared<br />

with a conventional kick-off turn. Swimmers were <strong>in</strong>structed to perform<br />

an open turn, always performed to the same lateral wall side, without underwater<br />

glid<strong>in</strong>g <strong>and</strong> breath<strong>in</strong>g cont<strong>in</strong>ually. The velocity (m·s-1) was calculated<br />

by divid<strong>in</strong>g the length of the 500-m by the time with <strong>in</strong>dividual<br />

correction for number of turns. Expired gases collected breath-by-breath<br />

was monitored cont<strong>in</strong>uously <strong>and</strong> recorded every 5-s. Serum lactate level<br />

was measured at the end of the IT session. The parameters of · VO 2 k<strong>in</strong>etics<br />

were calculated for the first 500m of the IT6x500 session. S<strong>in</strong>ce the<br />

<strong>in</strong>tensity of the exercise was equal to LT, breath-by-breath data were fitted<br />

to two dist<strong>in</strong>ct models (Bell et al., 2001): a s<strong>in</strong>gle exponential model<br />

(equation 1) <strong>and</strong> a double-exponential model (equation 2).<br />

·<br />

VO 2 (t) = A 0 + A 1 × [1 – e – (t – TD 1 )/τ 1 )] (1)<br />

Where A 0 is the basel<strong>in</strong>e value (mL.m<strong>in</strong> -1 ), A 1 is the asymptotic amplitude<br />

for the exponential term (mL.m<strong>in</strong> -1 ), τ 1 is the time constant (sec),<br />

TD 1 is the time delay from the onset of exercise (sec)<br />

·<br />

VO 2 (t) = A 0 + A 1 × [1 – e – (t – TD 1 )/τ 1 )]*u 1 + A 2 × [1- e -(t – TD 2 )/<br />

τ 2 (2)<br />

·<br />

where A 1 is the basel<strong>in</strong>e value, TD 1 <strong>and</strong> τ 1 respectively the time delay<br />

<strong>and</strong> the time constant for the first exponential term which is the rapid<br />

phase of oxygen uptake adjustment <strong>and</strong> TD 2 (about 120 sec) <strong>and</strong> τ 2 are<br />

respectively the delay <strong>and</strong> the time constant for the second exponential<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

term which is the slow phase of oxygen uptake adjustment. S<strong>in</strong>ce the<br />

first phase is unaffected by cardiodynamic factors (Bell et al., 2001), it<br />

was not modeled <strong>in</strong> this study. As a consequence, the first 20sec of data<br />

record<strong>in</strong>g was removed from the analysis to ensure that the early <strong>in</strong>itial<br />

component would not <strong>in</strong>fluence the result (Bell et al., 2001). The parameters<br />

of the model were determ<strong>in</strong>ed by <strong>in</strong>teraction m<strong>in</strong>imization of<br />

the sum of the mean squares of the differences between modeled VO<br />

·<br />

2<br />

<strong>and</strong> measured · VO2 (Bell et al., 2001). The measured · VO2 values differ<strong>in</strong>g<br />

by more than three st<strong>and</strong>ard deviations from the modeled · VO2 were excluded from the analysis. This exclusion was performed before<br />

determ<strong>in</strong><strong>in</strong>g the f<strong>in</strong>al parameters for the model <strong>and</strong> accounted for only<br />

2.5% of collected data. If the amplitude of the slow component was 0,<br />

the second exponential term was removed <strong>and</strong> ·<br />

VO2 k<strong>in</strong>etics was modeled<br />

with the first exponential term (Bell et al., 2001). A Fisher test was<br />

used to determ<strong>in</strong>e the significance of the exponential model. L<strong>in</strong>ear <strong>and</strong><br />

non-l<strong>in</strong>ear regressions were used to analyze the distribution of residual<br />

errors between measured <strong>and</strong> modeled · VO2 over time. The determ<strong>in</strong>ation<br />

coefficient was calculated <strong>and</strong> the Cp score computed as comparison<br />

criteria to confirm accuracy <strong>and</strong> sensitivity of the model<strong>in</strong>g.<br />

results<br />

Swimm<strong>in</strong>g velocity (vLT), oxygen uptake ( · VO 2 LT), <strong>and</strong> blood lactate<br />

concentration ([La]b) at LT were 1.46 ± 0.01 m·sec -1 , 352 ± 17-s, 60.1<br />

± 6.4 mL·kg -1 .m<strong>in</strong> -1 <strong>and</strong> 3.1 ± 1.2 mmol·L -1 , respectively. · VO 2 LT was<br />

86.8 ± 1.7% of · VO 2 max <strong>and</strong> v LT was 96.7 ± 0.5% of v · VO 2 max . v · VO 2 max<br />

was 91.1 ± 1.4 m·sec -1 of the 400-m best performance (with div<strong>in</strong>g start,<br />

without snorkel <strong>and</strong> with kick-off turns). · VO 2 max , HR peak , RPE <strong>and</strong> [La]<br />

b obta<strong>in</strong>ed at v · VO 2 max dur<strong>in</strong>g the <strong>in</strong>crement test were 68.7 ± 5.2 mL·kg -1 .<br />

m<strong>in</strong> -1 , 196.3 ± 7.3 b·m<strong>in</strong> -1 , 18.4 ± 3.2 a.u., 6.9 ± 1.4 mmol·L -1 respectively.<br />

The fit was statistically superior for the two-term exponential model<br />

compared with the one-term model (r²= 0.62 ± 0.18 vs. 0.52 ± 0.21, P<br />

< 0.01). Furthermore, the Cp score was lower for the bi-exponential<br />

model <strong>in</strong>dicat<strong>in</strong>g a lesser prediction error (Cp=33.5±20.8 vs. 35.4±20.5,<br />

p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

<strong>in</strong>terval performed at lactate threshold, all seven swimmers exhibited a<br />

slow component of · VO2 lead<strong>in</strong>g to an atta<strong>in</strong>ment of 99% of · VO2 max.<br />

The present study demonstrated that the two-term exponential model<br />

fit performance better than the s<strong>in</strong>gle-term exponential model when applied<br />

to a population of seven elite swimmers swimm<strong>in</strong>g at a velocity correspond<strong>in</strong>g<br />

to LT (higher determ<strong>in</strong>ation coefficient <strong>and</strong> lower CP score).<br />

Bell et al. (2001) demonstrated that this method of model<strong>in</strong>g the · VO2 response (two-components model from 20 sec after exercise onset to the<br />

end) is more appropriate <strong>and</strong> accurate than previous methods, even if the<br />

description of phase 3 is still unsatisfy<strong>in</strong>g <strong>and</strong> if the physiological basis for<br />

fitt<strong>in</strong>g an exponential to this phase is still unclear. The determ<strong>in</strong>ation coefficient,<br />

r² = 0.62 ± 0.17 was slightly lower <strong>and</strong> the coefficients of variation<br />

equivalent to those observed <strong>in</strong> the ecological runn<strong>in</strong>g sett<strong>in</strong>g (Borrani<br />

et al., 2001). Us<strong>in</strong>g the same estimation method, these authors reported<br />

that the coefficient of variation for the amplitude of the slow component<br />

A2 was 47.8% with the same · VO2 k<strong>in</strong>etics model dur<strong>in</strong>g a limited time<br />

of runn<strong>in</strong>g at 100% v · VO2 max. The greater imprecision compared with<br />

laboratory studies such as reported by Borrani et al. (2001) who found<br />

coefficients of variation below 15% for all parameters of the model except<br />

TD1 could be expla<strong>in</strong>ed by mathematical <strong>and</strong> methodological differences.<br />

The number of data po<strong>in</strong>ts for breath-by-breath analysis (240<br />

± 36) would have to be greater to allow for more accurate adjustment of<br />

the two-component model with six parameters. S<strong>in</strong>ce the bi-exponential<br />

model is non-l<strong>in</strong>ear, <strong>in</strong>ference is based on asymptotic theory which, as recommended<br />

(Wetherill et al., 1986), would require 180 to 300 data po<strong>in</strong>ts<br />

for our study. Another source of variability would be greater variations <strong>in</strong><br />

exertion <strong>in</strong> the sett<strong>in</strong>g of ecological exercises (runn<strong>in</strong>g, swimm<strong>in</strong>g) compared<br />

with laboratory conditions. The fact that our swimmers controlled<br />

their velocity us<strong>in</strong>g the visual or auditory l<strong>and</strong>marks probably imposed a<br />

certa<strong>in</strong> degree of variability on muscle workload which was expressed by<br />

greater · VO2 variability. In addition, the turn<strong>in</strong>g phases with the imposed<br />

h<strong>and</strong>-turn created a pause <strong>in</strong> workload <strong>and</strong> certa<strong>in</strong>ly <strong>in</strong>duced a variable<br />

VO<br />

·<br />

2 response which would compromise the accuracy of the model us<strong>in</strong>g a<br />

complex set of parameters (Wetherill et al., 1986).<br />

The slow component recorded <strong>in</strong> this study (401.7 ± 129.9<br />

mlO2·m<strong>in</strong>-1 <strong>and</strong> 5.69 ± 1.96 ml·m<strong>in</strong>-1 ·kg-1 ) was equal if not greater than<br />

those reported <strong>in</strong> swimm<strong>in</strong>g at equivalent if not higher <strong>in</strong>tensity of exercise,<br />

but <strong>in</strong> less tra<strong>in</strong>ed swimmers (Bentley et al., 2005; Demarie et al.,<br />

2001; Fern<strong>and</strong>ez et al., 2003). Demarie et al., (2001) reported values of<br />

239 ± 194 mlO2·m<strong>in</strong>-1 when measured <strong>in</strong> six elite pentathletes exercis<strong>in</strong>g<br />

at above critical velocity but below v · VO2 peak (v = 1.22 ± 0.06<br />

m·sec-1 ; tlim =375 ± 38-s ). Fern<strong>and</strong>ez et al., (2008) reported values of<br />

274.11 ± 152.83 mlO2·m<strong>in</strong>-1 for a group of 15 elite swimmers perform<strong>in</strong>g<br />

a test to exhaustion at v · VO2 max (v = 1.46 ± 0.06 m·s-1 ; tlim =260.20<br />

± 60.73-s ) while Bentley et al., (2005) found a slow component (7.7±3.1<br />

mlO2·m<strong>in</strong>-1 ·kg-1 ) only <strong>in</strong> 5 of the 9 elite swimmers tested, when swimm<strong>in</strong>g<br />

at a velocity represent<strong>in</strong>g 25% of the difference between ventilatory<br />

threshold <strong>and</strong> · VO2 max (1.35±0.03 m·s-1 ) for 400-m. One study<br />

(Lucia et al., 1998) reports a slow component of 130 mlO2·m<strong>in</strong>-1 <strong>in</strong> 9<br />

professional road cyclists perform<strong>in</strong>g a 20-m<strong>in</strong> exercise above ventilatory<br />

threshold (~80% · VO2 max; [La]b < 3 mmol·l-1 ). In agreement with the<br />

work reported by Carter et al., 2000, the hypothesis of a cause <strong>and</strong> effect<br />

relationship between the slow component <strong>and</strong> lactate accumulation or<br />

lower pH would not appear to be confirmed by our data s<strong>in</strong>ce our athletes<br />

exhibited low serum lactate levels dur<strong>in</strong>g the IT6*500 sessions (4.1<br />

mmol·l-1 ) but with high slow component. This f<strong>in</strong>d<strong>in</strong>g supports the conclusions<br />

of several researches which associate the slow component with<br />

changes <strong>in</strong> fiber type recruitment pattern (Carter et al., 2000; Gaesser<br />

et Poole, 1996; Whipp, 1996). Indeed, <strong>in</strong> the case of muscle fatigue, additional<br />

motor units or muscles (possibly less efficient) will be recruited<br />

<strong>and</strong> the · VO2 will <strong>in</strong>crease <strong>in</strong> order to ma<strong>in</strong>ta<strong>in</strong> the work rate when power<br />

output of recruited motor unit is reduced. It could be hypothesized that<br />

<strong>in</strong> swimm<strong>in</strong>g such progressive muscular fatigue <strong>in</strong>duces a reduction <strong>in</strong><br />

propulsive efficiency requir<strong>in</strong>g a compensatory <strong>in</strong>crease <strong>in</strong> stroke rate to<br />

ma<strong>in</strong>ta<strong>in</strong> speed <strong>and</strong> consequently a delayed <strong>in</strong>crease <strong>in</strong> oxygen uptake.<br />

198<br />

Moreover high level endurance swimmers are characterized by a strong<br />

capacity to reduce muscle lactate accumulation, so allow<strong>in</strong>g them to<br />

ma<strong>in</strong>ta<strong>in</strong> a high fraction of the · VO 2 max at speeds correspond<strong>in</strong>g to the<br />

lactate threshold. Therefore high ventilatory responses led by the power<br />

of the exercise associated to the <strong>in</strong>spiratory breath<strong>in</strong>g resistance <strong>in</strong>crease<br />

due to the breath<strong>in</strong>g <strong>in</strong> a snorkel contribute certa<strong>in</strong>ly to the amplitude of<br />

the O2SC. Therefore, the characteristics of the slow component observed<br />

<strong>in</strong> the present study (high amplitude A2, long delay Td2, <strong>and</strong> low time<br />

constant π2) could be attributed by both the specificity of swimm<strong>in</strong>g <strong>and</strong><br />

high-level endurance of the swimmers.<br />

conclusIon<br />

Elite Long-distance swimmers atta<strong>in</strong>ed an exceptionally high percent<br />

of · VO 2 max when swimm<strong>in</strong>g at the velocity correspond<strong>in</strong>g to lactate<br />

threshold, with this velocity be<strong>in</strong>g very close to maximal speeds. All of<br />

the swimmers tested exhibited great amplitude of the slow component<br />

<strong>in</strong> their · VO 2 response.<br />

reFerences<br />

Bell C, Paterson DH, Kowalchuk JM, Padilla J, Cunn<strong>in</strong>gham DA<br />

(2001b). A comparison of modell<strong>in</strong>g techniques used to characterise<br />

oxygen uptake k<strong>in</strong>etics dur<strong>in</strong>g the on-transient of exercise. Exp<br />

Physiol, 86(5), 667-676, 2001(b).<br />

Bentley DJ, Roels B, Hellard P, Fauquet C, Libicz S, Millet GP (2005).<br />

Physiological responses dur<strong>in</strong>g submaximal <strong>in</strong>terval swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g:<br />

effects of <strong>in</strong>terval duration. J Sci Med Sport, 8(4), 392-402.<br />

Billat V, Demarle A, Slaw<strong>in</strong>ski J, Paiva M, Koralszte<strong>in</strong> JP (2001). Physical<br />

<strong>and</strong> tra<strong>in</strong><strong>in</strong>g characteristics of top-class marathon runners. Med<br />

Sci Sports Exerc, 33(12), 2089-2097.<br />

Borrani F, C<strong>and</strong>au R, Millet GY, Perrey S, Fuchslocher J, Rouillon JD<br />

(2001). Is the ·VO2 slow component dependent on progressive recruitment<br />

of fast-twitch fibers <strong>in</strong> tra<strong>in</strong>ed runners ? J Appl Physiol,<br />

90(6), 2212-2220.<br />

Carter H, Jones AM, Barstow TJ, Burnley M, Williams C, Doust JH<br />

(2000). Effect of endurance tra<strong>in</strong><strong>in</strong>g on oxygen uptake k<strong>in</strong>etics dur<strong>in</strong>g<br />

treadmill runn<strong>in</strong>g. J Appl Physiol, 89, 1744-1752.<br />

Cheng B., Kuipers H., Snyder A.C., Keizer H.A., Jeukendrup A., Hessel<strong>in</strong>k<br />

M (1992). A new approach for the determ<strong>in</strong>ation of ventilator<br />

<strong>and</strong> lactate thresholds. Int J Sports Med, 13, 518-522.<br />

Costill DL, Maglischo EW, Richardson AB. Swimm<strong>in</strong>g, Blackwell Science<br />

LTD, 1992.<br />

Demarie S, Sardella F, Billat V, Mag<strong>in</strong>i W, Fa<strong>in</strong>a M (2001). The ·VO2<br />

slow component <strong>in</strong> swimm<strong>in</strong>g. Eur J Appl Physiol 84, 95-99.<br />

Fern<strong>and</strong>es RJ, Cardoso CS, Soares SM, Ascensao A, Colaco PJ, Vilas-<br />

Boas JP (2003). Time limit <strong>and</strong> VO2 slow component at <strong>in</strong>tensities<br />

correspond<strong>in</strong>g to VO2max <strong>in</strong> swimmers. Int J Sports Med, 24(8),<br />

576-581.<br />

Gaesser GA, Poole DC (1996). The slow component of oxygen k<strong>in</strong>etics<br />

<strong>in</strong> human. Exerc. Sports Sc Rev, 24, 35-71.<br />

Krustrup P, Soderlund K, Mohr M, Bangsbo J (2004). The slow component<br />

of oxygen uptake dur<strong>in</strong>g <strong>in</strong>tense, sub-maximal exercise <strong>in</strong> man<br />

is associated with additional fibre recruitment. Pflugers Arch, 447(6),<br />

855-866.<br />

Lucia A, Pardo J, Durantez A, Hoyos J, Chicharro JL (1998). Physiological<br />

differences between professional <strong>and</strong> elite road cyclists. Int J<br />

Sports Med, 19(5), 342-348.<br />

Mahood NV, Kenefick RW, Kertzer R, Qu<strong>in</strong>n TJ (2001). Physiological<br />

determ<strong>in</strong>ants of cross-country ski rac<strong>in</strong>g performance. Med Sci<br />

Sports Exerc, 33(8), 1379-1384.<br />

Wetherill GB, Duncombe P, Kenward M. Regression analysis with applications.<br />

London,New York; 1986. p. 82-86; 102-104; 180-182;<br />

226-227; 240-246.<br />

Whipp BJ. Doma<strong>in</strong>s of aerobic function <strong>and</strong> their limit<strong>in</strong>g parameters.<br />

The Physiology <strong>and</strong> Pathophysiology of Exercise Tolerance, edited by<br />

Ste<strong>in</strong>acker <strong>and</strong> Ward. Plenum Press, New York, 1996.


The Impact of Tension <strong>in</strong> Abdom<strong>in</strong>al <strong>and</strong> Lumbar<br />

Musculature <strong>in</strong> Swimmers on Ventilatory <strong>and</strong><br />

Cardiovascular Functions<br />

henrich, t.W. 1 , Pankey, r.B. 2 , soukup, G.J. 1<br />

1 University of the Incarnate Word, San Antonio Texas, USA<br />

2 Texas State University, San Marcos, Texas, USA,<br />

Swimm<strong>in</strong>g performance is governed by the ability of the body to consume<br />

oxygen for energy production for most events, <strong>in</strong>crease the resistance<br />

on the propulsive surfaces, <strong>and</strong> decrease resistance on the nonpropulsive<br />

surfaces of the body. It has been proposed that the abdom<strong>in</strong>al<br />

<strong>and</strong> erector sp<strong>in</strong>ae muscles contract dur<strong>in</strong>g swimm<strong>in</strong>g to decrease form<br />

resistance or drag on the swimmers’ body to <strong>in</strong>crease speed. The hypothesis<br />

is that contract<strong>in</strong>g these muscle groups would negatively impact<br />

pulmonary functions <strong>and</strong> <strong>in</strong>crease oxygen consumption. Significantly<br />

lower pulmonary functions <strong>and</strong> higher rest<strong>in</strong>g oxygen consumption<br />

were observed while the abdom<strong>in</strong>al <strong>and</strong> erector sp<strong>in</strong>ae muscles were<br />

contracted. Contract<strong>in</strong>g the abdom<strong>in</strong>al <strong>and</strong> erector sp<strong>in</strong>ae muscles could<br />

cause decrements <strong>in</strong> crawl stroke swimm<strong>in</strong>g performance.<br />

Key Words: swimm<strong>in</strong>g, Ventilation, V0 2 , Propulsion, resistance<br />

IntroductIon<br />

Pulmonary function does not appear to place a limit on maximal exercise<br />

<strong>in</strong> most physical activities. However, <strong>in</strong> competitive swimm<strong>in</strong>g,<br />

the posture <strong>and</strong> movements required to properly execute the different<br />

strokes often impede <strong>and</strong> the ability of the body to ventilate the lungs<br />

<strong>and</strong> consume oxygen dur<strong>in</strong>g butterfly, breast stroke <strong>and</strong> crawl stroke<br />

where breath<strong>in</strong>g is restricted to the movement pattern of the arms <strong>and</strong><br />

legs <strong>and</strong> the swimmer’s face <strong>in</strong> the water.<br />

In competitive swimm<strong>in</strong>g, particularly dur<strong>in</strong>g the crawl stroke, the<br />

position of the head <strong>in</strong> the water <strong>and</strong> the sequence with<strong>in</strong> the stroke<br />

where the swimmer can breathe places some restrictions on pulmonary<br />

ventilation. In spite of these limitations, pulmonary ventilation has not<br />

been shown to limit the performances of competitive crawl stroke swimmers<br />

(Ingvar, 1974). The pulmonary functions of swimmers have been<br />

studied with regularity because some researchers consider the water<br />

pressure aga<strong>in</strong>st the rib cage a challenge to ventilation that results <strong>in</strong> an<br />

adaptation to exercise not shown <strong>in</strong> other sports. Clanton <strong>and</strong> Gadek et<br />

al. (1987) compared the effects of 12 weeks of <strong>in</strong>spiratory muscle tra<strong>in</strong><strong>in</strong>g,<br />

regular aerobic tra<strong>in</strong><strong>in</strong>g <strong>and</strong> 12 weeks of swim tra<strong>in</strong><strong>in</strong>g. Significant<br />

improvements <strong>in</strong> the swim tra<strong>in</strong><strong>in</strong>g group were noted for vital capacity p<br />

< 0.01, functional residual capacity p < 0.0001, <strong>and</strong> total lung capacity p<br />

< 0.0025 when compared to the regular aerobic tra<strong>in</strong><strong>in</strong>g group.<br />

Competitive swimmers can have greater total lung capacities than<br />

other athletes (Corda<strong>in</strong> <strong>and</strong> Tucker, et al. 1990) <strong>and</strong> greater forced expiratory<br />

volume (Courteix <strong>and</strong> Obert et al. 1997). Armour <strong>and</strong> Donnelly<br />

et al. (1993) compared pulmonary functions of age-matched swimmers<br />

<strong>and</strong> runners. Swimmers had significantly greater total lung capacity, vital<br />

capacity, maximal <strong>in</strong>spiratory capacity <strong>and</strong> forced vital capacity than<br />

runners when the data were normalized for age <strong>and</strong> body size. Therefore,<br />

swimmers’ breath<strong>in</strong>g mechanics <strong>and</strong> lung volumes should not necessarily<br />

limit their performances. These f<strong>in</strong>d<strong>in</strong>gs suggest that swimmers are<br />

not limited directly by ventilatory factors <strong>and</strong> because of either genetic<br />

<strong>and</strong>/or developmental reasons, appear to have better respiratory <strong>and</strong> pulmonary<br />

functions than athletes participat<strong>in</strong>g <strong>in</strong> other sports.<br />

In terms of bioenergetics, swimm<strong>in</strong>g performance is determ<strong>in</strong>ed<br />

by the swimmer’s ability to expend energy from both aerobic <strong>and</strong> nonaerobic<br />

sources depend<strong>in</strong>g on the events <strong>in</strong> which they compete. Biomechanically,<br />

the swimmer must <strong>in</strong>crease resistance on the propulsive<br />

surfaces of the body like the h<strong>and</strong>s, legs <strong>and</strong> perhaps the forearms to<br />

produce force. Conversely, they must also decrease resistance on the<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

non-propulsive surfaces of the body like the torso, head <strong>and</strong> hips (Counsilman<br />

& Counsilman, 1994). Sk<strong>in</strong>ner (2007) suggests that the posture<br />

of the body should be optimized while swimm<strong>in</strong>g the crawl stroke to<br />

decrease form drag <strong>and</strong> <strong>in</strong>crease speed. This change <strong>in</strong> posture <strong>in</strong>volves<br />

contract<strong>in</strong>g the abdom<strong>in</strong>al muscles to flatten the abdomen, <strong>and</strong> erector<br />

sp<strong>in</strong>ae muscles to flatten the lumbar portion of the sp<strong>in</strong>al column, which<br />

collectively produce a more streaml<strong>in</strong>ed body. This proposed change <strong>in</strong><br />

posture could <strong>in</strong>terfere with the coord<strong>in</strong>ation of movement between the<br />

abdom<strong>in</strong>al muscles <strong>and</strong> the diaphragm, <strong>and</strong> work <strong>in</strong> direct opposition<br />

to the accessory respiratory muscles limit<strong>in</strong>g the swimmer’s ability to<br />

ventilate air <strong>and</strong> consume oxygen. There seems to be no experimental<br />

data <strong>in</strong> the literature that contract<strong>in</strong>g these muscle groups decreases resistance<br />

on a swimmer. These muscular contractions are hypothesized to<br />

limit the swimmers’ ventilatory capacity <strong>and</strong> <strong>in</strong>crease oxygen consumption<br />

dur<strong>in</strong>g swimm<strong>in</strong>g.<br />

Methods<br />

Prior to <strong>in</strong>itiat<strong>in</strong>g a logistically complex study of swimmers <strong>in</strong> the water,<br />

a l<strong>and</strong>-based study was undertaken to determ<strong>in</strong>e if contracted muscles<br />

would negatively affect pulmonary functions measured <strong>in</strong> a controlled<br />

laboratory sett<strong>in</strong>g. Pulmonary functions <strong>and</strong> rest<strong>in</strong>g oxygen consumption<br />

were measured under control <strong>and</strong> experimental conditions. The<br />

non-contracted or control conditions (NC) <strong>in</strong>volved measurements<br />

made with subjects <strong>in</strong> a st<strong>and</strong>ard sitt<strong>in</strong>g position. The experimental<br />

or contracted condition (CC) <strong>in</strong>volved participants sitt<strong>in</strong>g upright <strong>in</strong><br />

a chair with their abdom<strong>in</strong>al <strong>and</strong> erector sp<strong>in</strong>ae muscles tensed. This<br />

condition was documented by hold<strong>in</strong>g a measur<strong>in</strong>g tape around the abdom<strong>in</strong>al<br />

area <strong>and</strong> the participants were <strong>in</strong>structed to ma<strong>in</strong>ta<strong>in</strong> a constant<br />

circumference. The participants ma<strong>in</strong>ta<strong>in</strong>ed an upright vertical position<br />

of the upper body that was documented by us<strong>in</strong>g a meter stick placed<br />

next to the trunk. The lumbar sp<strong>in</strong>e of the participants was flattened<br />

aga<strong>in</strong>st the back of the chair as close as possible accord<strong>in</strong>g to the recommendations<br />

of Sk<strong>in</strong>ner (2007) <strong>and</strong> the USA Swimm<strong>in</strong>g Sport Science<br />

Department. It is hypothesized that if vital capacity (VC), maximal<br />

voluntary ventilation (MVV), forced vital capacity (FVC 1 ) <strong>and</strong> rest<strong>in</strong>g<br />

oxygen consumption (RVO 2 ) <strong>and</strong> rest<strong>in</strong>g carbon dioxide production<br />

(VC0 2 ) were altered with the subject’s abdom<strong>in</strong>al <strong>and</strong> erector sp<strong>in</strong>ae<br />

muscles contracted <strong>in</strong> a seated posture, then maximal exercise could be<br />

impeded by the decreased ventilatory capacity <strong>and</strong> <strong>in</strong>creased oxygen<br />

consumption <strong>and</strong> place limits on the performance of the competitive<br />

crawl stroke swimmer.<br />

Thirteen participants <strong>in</strong>volved <strong>in</strong> swimm<strong>in</strong>g activities (8 males, 5 females)<br />

ages 22-60 years of age volunteered for evaluation of their VC,<br />

MVV, FVC1, RVO2 <strong>and</strong> VC02 under the two differ<strong>in</strong>g postural conditions<br />

NC <strong>and</strong> CC. Each participant was measured on a Spirometrics<br />

Flowmate III Spirometer for pulmonary functions <strong>and</strong> a metabolic cart<br />

for RVO2 <strong>and</strong> VC02. There were 3 m<strong>in</strong>utes of rest between counterbalanced<br />

trials for all measurements. All participants’ pulmonary functions<br />

were expressed relative to their age, body weight <strong>and</strong> height <strong>and</strong><br />

rest<strong>in</strong>g RVO2 relative to body weight.<br />

A one-way analysis of variance (ANOVA) was used to compare NC<br />

<strong>and</strong> CC conditions. The Bonferonni correction factor of 0.05/3 were<br />

used, which required a p value of less than 0.0167 for the correlated<br />

variables of VC, MVV, <strong>and</strong> FVC1. The variables of RVO2 <strong>and</strong> VC02<br />

were not significantly correlated <strong>and</strong> a 0.05 level of significance was used<br />

to test these hypotheses. To account for the percent of variance <strong>in</strong> the<br />

dependent variables related to the variance <strong>in</strong> the <strong>in</strong>dependent variable,<br />

the Omega Squared statistic was used (Tolson, 1980).<br />

results<br />

There were significant differences between all evaluations VC, MVV,<br />

FVC 1 , RVO 2 <strong>and</strong> RC0 2 between EC <strong>and</strong> CC. An Omega Squared computation<br />

showed the amounts of variance <strong>in</strong> the dependent variables<br />

that were accounted for by the variance <strong>in</strong> the <strong>in</strong>dependent variable or<br />

CC. Results are reported mean plus or m<strong>in</strong>us st<strong>and</strong>ard error.<br />

199


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 1. Vital capacity.<br />

VC measured under NC 5.21 + .27 liters <strong>and</strong> was 111% of the predicted<br />

volume. The CC was 4.17 + .26 liters which was 89% of the predicted<br />

volume. This difference was significant (F = 6.77, p< .01). For VC the<br />

Omega Squared was 0.63 <strong>in</strong>dicat<strong>in</strong>g that 62% of the variance was accounted<br />

for by the CC.<br />

MVV was 127 + 12.2 l·m<strong>in</strong>-1 NC conditions <strong>and</strong> was 109% of the<br />

predicted volume while CC conditions elicited a volume of 87.6 + 9.5<br />

l·m<strong>in</strong>-1 which was 89% of the predicted volume. This difference was significant<br />

(F = 6.44, p


eFerences<br />

Armour, J., Donnelly, P. <strong>and</strong> Bye, P. (1993). The large lungs of elite swimmers:<br />

An <strong>in</strong>creased alveolar number? Eur Respir J, 6, 237-247.<br />

Clanton, T. L., Dixon, G. F., Drake, J. <strong>and</strong> Gadek, J. E. (1987). Effects of<br />

swim tra<strong>in</strong><strong>in</strong>g on lung volumes <strong>and</strong> <strong>in</strong>spiratory muscle condition<strong>in</strong>g.<br />

J Appl Physiol, 62, 39-46.<br />

Corda<strong>in</strong>, L., Tucker, A., Moon, D. <strong>and</strong> Stager, J. (1990). Lung volumes<br />

<strong>and</strong> maximal respiratory pressures <strong>in</strong> collegiate swimmers <strong>and</strong> runners.<br />

Res Quart 61, 70-74.<br />

Counsilman, J.E. & Counsilman, B. E. (1994). The mechanical pr<strong>in</strong>ciples<br />

<strong>in</strong>volved <strong>in</strong> swimm<strong>in</strong>g. In J.E. Counsilman, J.E. & B.E. Counsilman.<br />

The new science of swimm<strong>in</strong>g. (p 5) New Jersey: Prentice Hall<br />

Publish<strong>in</strong>g Company.<br />

Courteix, D., Obert, P., Lecoq, A. M., Guenon, P. <strong>and</strong> Koch, G. (1997).<br />

Effect of <strong>in</strong>tensive swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g on lung volumes, airway resistance<br />

<strong>and</strong> on the maximal expiratory flow volume relationship <strong>in</strong><br />

pre-pubertal girls. Eur J of Appl Physiol, 76, 264-269.<br />

Gomez, C.L., Strongoli, L. <strong>and</strong> Coast, J.R. (2009). Repeated abdom<strong>in</strong>al<br />

exercise <strong>in</strong>duces respiratory muscle fatigue. J. Sport Sci 8, 543-547<br />

Harms, C., Babcock, M., McClaran, S., Pegelow, D., Nickele, G., Nelson,<br />

W., <strong>and</strong> Dempsey, J. (1997). Respiratory muscle work compromises<br />

leg blood flow dur<strong>in</strong>g maximal exercise. J Appl Physiol.82, 1573-1583<br />

Ingvar, H. (1974). Energy cost of arm stroke, leg kick <strong>and</strong> the whole<br />

stroke. . Eur J of Appl Physiol, 33, 105-118.<br />

Kar<strong>in</strong>e, J. Sarro, A Am<strong>and</strong>a P. Silvatti, Ricardo M. L. <strong>and</strong> Barros J.<br />

(2010). Coord<strong>in</strong>ation between ribs motion <strong>and</strong> thoracoabdom<strong>in</strong>al<br />

volumes <strong>in</strong> swimmers dur<strong>in</strong>g respiratory maneuvers. J. Sport Sci (<strong>in</strong><br />

press)<br />

Sk<strong>in</strong>ner, J. (2007). Trunk <strong>and</strong> vertebral column position <strong>and</strong> alignment<br />

dur<strong>in</strong>g swimm<strong>in</strong>g USA Swimm<strong>in</strong>g Sports Science Division, Personal<br />

Communication.<br />

Tolson, H. (1980). An adjustment to statistical significance: V 2 . Res<br />

Quart, 51, 580-584.<br />

Toshimasa, Y. (2004). Buoyancy is the primary source of generat<strong>in</strong>g<br />

body roll <strong>in</strong> front-crawl swimm<strong>in</strong>g. J Biomech 37(5), 606-612.<br />

AcKnoWledGeMents<br />

We would like to thank the reviewers for their detailed <strong>and</strong> conscientious<br />

work dur<strong>in</strong>g the revision of this manuscript <strong>and</strong> Jonty Sk<strong>in</strong>ner for<br />

his dialogue <strong>and</strong> exchange of ideas.<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

Relationship between Propell<strong>in</strong>g Efficiency <strong>and</strong><br />

Swimm<strong>in</strong>g Performance <strong>in</strong> Elite Swimmers.<br />

huang, Z. 1 , Kurobe, K. 1 , nishiwaki, M. 2 , ozawa, G. 1 , tanaka,<br />

t. 1 , taguchi, n. 1 , ogita, F. 1<br />

1 National Institute of Fitness <strong>and</strong> Sports, Kanoya, Japan<br />

2 Prefectural University of Kumamoto, Japan<br />

The relationship between propell<strong>in</strong>g efficiency (ep) <strong>and</strong> swimm<strong>in</strong>g performance<br />

was <strong>in</strong>vestigated for 9 elite swimmers <strong>in</strong>clud<strong>in</strong>g an Olympic<br />

gold medalist <strong>and</strong> a f<strong>in</strong>alist (age: 23±1 yrs). The ep was calculated as the<br />

ratio of the power to overcome drag (Pd) to the total power output (Po)<br />

us<strong>in</strong>g the MAD system. The swimm<strong>in</strong>g performance of each subject was<br />

evaluated by the respective average velocity of 50m, 100m, 200m <strong>and</strong><br />

400m maximal swimm<strong>in</strong>g. The <strong>in</strong>dividual ep (71±6%, range; 56 to 80%)<br />

values were significantly related to <strong>in</strong>dividual swimm<strong>in</strong>g performance<br />

<strong>in</strong> 200m <strong>and</strong> 400m (200m; r=0.72, P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The MAD system allowed the subjects to push-off from fixed pads at<br />

each stroke. Hence, power expended <strong>in</strong> giv<strong>in</strong>g the water a k<strong>in</strong>etic energy<br />

change was 0 (Pk=0) as <strong>in</strong> free swimm<strong>in</strong>g, <strong>and</strong> thus Po=Pd. The 15 pushoff<br />

pads were fixed 1.30m apart on a 23m horizontal rod 0.75m below<br />

the water surface, mak<strong>in</strong>g cont<strong>in</strong>uous swimm<strong>in</strong>g over the system possible.<br />

At one end of the swimm<strong>in</strong>g pool, one rod was connected to a force<br />

transducer. The force signal was processed <strong>and</strong> stored on the hard disk<br />

of the notebook computer. Throughout the measurement, the swimmers<br />

used their arms only; their legs were supported <strong>and</strong> fixed together by a<br />

small buoy (buoyant force 15.7N) (ARN-100, ARENA).<br />

The force signal was time-<strong>in</strong>tegrated, <strong>and</strong> yielded the average<br />

force. The mean swimm<strong>in</strong>g velocity was computed from the time needed<br />

to cover the distance between the second <strong>and</strong> fourteenth pads. The<br />

power used to overcome drag (Pd) was calculated from the product of<br />

the mean drag force <strong>and</strong> the mean velocity.<br />

For the measurement of propell<strong>in</strong>g efficiency (ep), each subject<br />

swam 300m 6 times us<strong>in</strong>g front crawl arm stroke only, 3 times us<strong>in</strong>g the<br />

MAD system, <strong>and</strong> 3 times <strong>in</strong> free swimm<strong>in</strong>g. The swimm<strong>in</strong>g velocities<br />

were set at 80%, 85%, <strong>and</strong> 90% of the average velocity of 400m maximal<br />

arm stroke swimm<strong>in</strong>g. These velocities were determ<strong>in</strong>ed by the need to<br />

ensure that all exercise was sub-maximal <strong>and</strong> also that subjects were<br />

able to ma<strong>in</strong>ta<strong>in</strong> normal swimm<strong>in</strong>g technique even at the lowest velocity.<br />

Dur<strong>in</strong>g the measurements, subjects were aided to keep a constant<br />

swimm<strong>in</strong>g velocity by a pac<strong>in</strong>g device consist<strong>in</strong>g of underwater lights<br />

that was set at the bottom of swimm<strong>in</strong>g pool (SWIMMING PACE<br />

MAKE MODEL PMS-103, TAKAGI). All measurements for each<br />

subject were made <strong>in</strong> one day, tak<strong>in</strong>g enough rest to prevent the subjects<br />

from becom<strong>in</strong>g fatigued.<br />

To determ<strong>in</strong>e energy expenditure, steady state oxygen uptake (VO 2 )<br />

dur<strong>in</strong>g the 300m swim was measured by the Douglas bag method. The<br />

face mask used for collect<strong>in</strong>g expired gas allowed unh<strong>in</strong>dered movement<br />

of the arms dur<strong>in</strong>g swimm<strong>in</strong>g. In an earlier study the “streaml<strong>in</strong><strong>in</strong>g”<br />

of this design was such that there was no measurable <strong>in</strong>crease <strong>in</strong><br />

drag (Toussa<strong>in</strong>t et al., 1987). The expired gas collection to measure VO 2<br />

was performed while the subject was swimm<strong>in</strong>g the f<strong>in</strong>al 50m (after<br />

at least 3 m<strong>in</strong> from beg<strong>in</strong>n<strong>in</strong>g of the trial), by which time VO 2 had<br />

reached a steady state. The O 2 <strong>and</strong> CO 2 fractions <strong>in</strong> the expired gas<br />

were determ<strong>in</strong>ed by an automatic gas analyzer (Vmax29c, Sensor medics<br />

Corporation, California, USA). Expired gas volume was measured by a<br />

dry gas meter (SHINAGAWA). The VO 2 was taken to reflect the rate<br />

of energy expenditure at the sub-maximal exercise level studied, which<br />

was confirmed by the observed respiratory exchange ratio (RER) values.<br />

The rate of energy expenditure (PVO2) <strong>in</strong> Watts was calculated by the<br />

oxygen uptake (l•m<strong>in</strong>-1, STPD) <strong>and</strong> RER follow<strong>in</strong>g the formula of<br />

Carby et al., 1987:<br />

PVO2=(4940RER+16040)•VO2/60 (Eq.1)<br />

The rate of energy expenditure (PVO2) measured dur<strong>in</strong>g swimm<strong>in</strong>g on<br />

the MAD system was related to the total power output (Po), which<br />

was equal to Pd, s<strong>in</strong>ce the push-off was aga<strong>in</strong>st the fixed pads (Pk=0).<br />

Hence, gross efficiency (eg) <strong>in</strong> this experiment was computed as follows<br />

(Toussa<strong>in</strong>t et al., 1990);<br />

eg=Po/ PVO2 (Eq.2)<br />

Furthermore, the total power output (Po) of the free swimm<strong>in</strong>g was<br />

calculated by the product of gross efficiency (eg) <strong>and</strong> energy expenditure<br />

(PVO2 <strong>in</strong> W) of free swimm<strong>in</strong>g.<br />

Po= PVO2•eg (Eq.3)<br />

The Propell<strong>in</strong>g efficiency (ep) is def<strong>in</strong>ed as the ratio of the propell<strong>in</strong>g<br />

power (used overcome drag, Pd) to the total power output (Po) (Toussa<strong>in</strong>t<br />

et al., 1988). Therefore, ep was calculated as Pd divided by Po <strong>in</strong><br />

free swimm<strong>in</strong>g at the same velocity.<br />

ep=Pd/Po=Pd/(Pd+Pk (Eq.4)<br />

202<br />

The time trials of 50m, 100m, 200m <strong>and</strong> 400m front crawl were performed<br />

on different days. Then, the average swimm<strong>in</strong>g velocity was<br />

computed from each performance time.<br />

results<br />

The swimm<strong>in</strong>g performance (average velocity) of each distance for each<br />

subject is presented <strong>in</strong> Table 1.<br />

Measurements for ep were taken dur<strong>in</strong>g free swimm<strong>in</strong>g <strong>and</strong> on the<br />

MAD system <strong>in</strong> a range of matched velocities (range; 1.22 to 1.46 m•s -1 ).<br />

PVO 2 calculated from the VO 2 data ranged from 388.5 to 917.7W (MAD<br />

system), <strong>and</strong> from 553.1 to 1367.0W (free swim).The power used to overcome<br />

drag (Pd) ranged from 40.7<br />

50m<br />

(m•s -1 100m<br />

) (m•s -1 200m<br />

) (m•s -1 400m<br />

) (m•s -1 Table 1. Swimm<strong>in</strong>g performance (velocity) of each<br />

distance<br />

)<br />

S.W. 1.82 1.71 1.61 1.55<br />

K.W. 1.88 1.71 1.56 1.48<br />

F.U. 1.89 1.71 1.47 1.4<br />

K.A. 1.82 1.72 1.62 1.56<br />

M.Y. 1.75 1.64 1.56 1.54<br />

M.U. 1.77 1.67 1.58 1.52<br />

S.K. 1.77 1.62 1.52 1.49<br />

A.S. 1.85 1.75 1.67 1.62<br />

E.T. 1.84 1.73 1.65 1.56<br />

mean 1.82 1.70 1.58 1.52<br />

SD 0.05 0.04 0.06 0.06<br />

to 76.5W, <strong>and</strong> the total power output (Po) <strong>in</strong> free swimm<strong>in</strong>g ranged<br />

from 54.1 to 103.4W. The mean value of eg calculated by the ratio of<br />

Po <strong>and</strong> PVO2 was 10±1% (range; 6 to 11%). F<strong>in</strong>ally, know<strong>in</strong>g the Po <strong>in</strong><br />

free swimm<strong>in</strong>g <strong>and</strong> Pd as determ<strong>in</strong>ed on the MAD system at the same<br />

velocity, the calculated ep was 71±6% (range; 56 to 80%) (Table 2).<br />

velocity<br />

(m・s -1 Table 2. Individual data dependent on velocity are given for power <strong>in</strong>put (PiMAD, <strong>and</strong> Pifree), power out<br />

(Pofree), drag force (Fd), power to overcome drag (PdAMD), power lost <strong>in</strong> mov<strong>in</strong>g water (Pk), the propell<strong>in</strong>g<br />

efficicency (ep), <strong>and</strong> gross efficiency (eg).<br />

PiMAD PdMAD Fd Pofree Pifree Pk ep eg<br />

) (W) (W) (N) (W) (W) (W) (%) (%)<br />

S.W. 1.38 525.3 60.1 43.5 82.6 722.8 22.6 73% 11%<br />

1.40 551.9 58.9 42.1 77.7 727.9 18.8 76% 11%<br />

1.43 630.4 63.8 44.6 83.5 824.6 19.7 76% 10%<br />

K.W. 1.22 388.5 41.2 33.8 63.1 595.0 21.9 65% 11%<br />

1.28 453.2 49.7 38.8 75.5 688.7 25.8 66% 11%<br />

1.32 491.0 51.8 39.3 77.9 738.6 26.1 66% 11%<br />

F.U. 1.25 542.0 52.8 42.2 76.0 781.1 23.3 69% 10%<br />

1.28 597.1 47.1 36.8 69.5 880.8 22.4 68% 8%<br />

1.31 917.7 53.3 40.7 79.4 1367.0 26.1 67% 6%<br />

K.A. 1.23 612.3 44.0 35.7 55.3 769.9 11.3 80% 7%<br />

1.29 610.9 47.3 36.7 65.4 844.9 18.1 72% 8%<br />

1.35 618.6 54.8 40.6 76.2 860.4 21.4 72% 9%<br />

M.Y. 1.23 558.9 40.7 33.1 54.1 743.7 13.4 75% 7%<br />

1.30 553.7 49.0 37.7 69.3 784.6 20.3 71% 9%<br />

1.36 566.4 54.2 39.9 73.2 765.8 19.0 74% 10%<br />

S.U. 1.23 441.8 45.3 36.8 56.7 553.1 11.4 80% 10%<br />

1.29 471.0 47.7 37.0 61.1 604.2 13.5 78% 10%<br />

1.35 491.6 53.8 39.8 95.3 871.6 41.6 56% 11%<br />

S.K. 1.23 421.1 43.5 35.3 58.8 570.0 15.4 74% 10%<br />

1.30 488.6 48.9 37.6 67.7 676.0 18.7 72% 10%<br />

1.36 556.5 55.5 40.8 93.2 934.2 37.7 60% 10%<br />

A.S. 1.39 528.7 57.9 41.7 89.2 726.3 24.3 73% 11%<br />

1.43 602.7 64.9 45.4 103.4 814.5 26.9 74% 11%<br />

1.46 773.2 76.5 52.4 103.3 1043.8 26.8 74% 10%<br />

E.T. 1.25 408.7 42.4 33.9 59.2 570.8 16.8 72% 10%<br />

1.28 420.2 47.1 36.8 64.2 573.2 17.2 73% 11%<br />

1.36 497.9 55.6 41.0 76.5 685.1 20.9 73% 11%<br />

mean 1.32 545.2 52.1 39.4 74.4 767.4 21.5 71% 10%<br />

SD 0.07 112.6 8.2 4.2 13.9 170.3 6.9 6% 1%<br />

When the relationship between ep <strong>and</strong> swimm<strong>in</strong>g performance for<br />

different distances was exam<strong>in</strong>ed, the <strong>in</strong>dividual ep values were significantly<br />

related to <strong>in</strong>dividual swimm<strong>in</strong>g performance <strong>in</strong> 200m <strong>and</strong> 400m<br />

(200m; r=0.72, P


propell<strong>in</strong>g efficiency(%)<br />

propell<strong>in</strong>g efficiency(%)<br />

propell<strong>in</strong>g efficiency(%)<br />

propell<strong>in</strong>g efficiency(%)<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

100m<br />

80 200m<br />

80 400m<br />

70<br />

70<br />

60<br />

y = 37.0x + 12.94 60<br />

y = 41.6x + 8.10<br />

r = 0.72, P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Effect of Increas<strong>in</strong>g Energy Cost on Arm<br />

Coord<strong>in</strong>ation at Different Exercise Intensities <strong>in</strong> Elite<br />

Spr<strong>in</strong>t Swimmers<br />

Komar, J. 1 , leprêtre, P.M. 2 , Alberty, M. 3 , Vantorre, J. 1 , Fern<strong>and</strong>es,<br />

r.J. 4 , hellard, P. 5,6 , chollet, d. 1 , seifert, l. 1<br />

1 Centre d’Etudes des Transformations des Activités Physiques et<br />

Sportives, Faculté des Sciences du Sport, Université de Rouen, France<br />

2 Laboratoire de Recherche Adaptations physiologiques à l’exercice et<br />

Réadaptation à l’Effort, Faculté des Sciences du Sport, Université de<br />

Picardie Jules Verne, Amiens, France<br />

3 Laboratoire d’Etude de Motricité Huma<strong>in</strong>e, EA-3608, Faculté des<br />

Sciences du Sport, Université de Lille, France<br />

4Centre of Research, Education, Innovation <strong>and</strong> Intervention <strong>in</strong><br />

Sport, Faculty of Sports, University of Porto, Portugal<br />

5 Département d’Etudes et Recherches, Fédération Française de Natation,<br />

Paris, France<br />

6 Laboratoire Vie Sportive, Tradition, Innovation et Intervention,<br />

Faculté des Sciences du Sport de Bordeaux 2, France<br />

The purpose of this study was to analyze the changes of the strok<strong>in</strong>g parameters<br />

<strong>and</strong> the coord<strong>in</strong>ation <strong>in</strong>duced by the <strong>in</strong>crease of energy cost (C)<br />

of aquatic locomotion. Six elite spr<strong>in</strong>t swimmers performed a 6 . 300-m<br />

<strong>in</strong>cremental swimm<strong>in</strong>g test. Strok<strong>in</strong>g parameters (stroke rate, SR; stroke<br />

length, SL) <strong>and</strong> arm coord<strong>in</strong>ation (measured by <strong>in</strong>dex of coord<strong>in</strong>ation,<br />

IdC) have been calculated from video data <strong>and</strong> the C by measur<strong>in</strong>g oxygen<br />

consumption <strong>and</strong> blood lactate. Results showed that an <strong>in</strong>crease <strong>in</strong><br />

C led to significant <strong>in</strong>creases <strong>in</strong> IdC, SR <strong>and</strong> a decrease <strong>in</strong> SL. L<strong>in</strong>ear<br />

regression between IdC <strong>and</strong> C, SR <strong>and</strong> C <strong>and</strong> SL <strong>and</strong> C suggested that a<br />

specific C corresponds to the emergence of a specific coord<strong>in</strong>ation <strong>and</strong><br />

SR/SL ratio. The <strong>in</strong>crease of the anaerobic part of C suggested that fatigue<br />

could also <strong>in</strong>fluence the emergence of motor organization.<br />

Key Words: Motor control, <strong>Biomechanics</strong>, swimm<strong>in</strong>g, energy cost<br />

IntroductIon<br />

In cyclic activities <strong>and</strong> especially <strong>in</strong> swimm<strong>in</strong>g, many constra<strong>in</strong>ts have<br />

been studied through their effects on the <strong>in</strong>ter-limb coord<strong>in</strong>ation <strong>and</strong><br />

strok<strong>in</strong>g parameters (e.g. effect of gender, speed, specialty, expertise <strong>and</strong><br />

laterality). In order to facilitate his locomotion, the <strong>in</strong>ter-limb coord<strong>in</strong>ation<br />

<strong>in</strong> swimm<strong>in</strong>g is managed by the swimmer to overcome the resistive<br />

forces <strong>in</strong>herent to the density of water. Accord<strong>in</strong>g to the def<strong>in</strong>ition of<br />

environmental constra<strong>in</strong>ts (i.e. forward resistance which is a function of<br />

the swimmer’s hydrodynamic coefficient but mostly of the speed squared<br />

required to overcome this resistance), the shift<strong>in</strong>g to a superposition mode<br />

is related to the high active drag that spr<strong>in</strong>ters must overcome to swim<br />

fast. Indeed, above a critical value of speed (1.8 m·s -1 ) <strong>and</strong> stroke rate (50<br />

stroke.m<strong>in</strong>ute -1 ), only the superposition coord<strong>in</strong>ation mode occurred <strong>in</strong><br />

elite spr<strong>in</strong>ters (Seifert et al. 2007). In swimm<strong>in</strong>g, several studies have also<br />

shown that the organismic constra<strong>in</strong>ts (i.e. gender, stroke specialty <strong>and</strong><br />

anthropometry) affected the arm coord<strong>in</strong>ation <strong>in</strong> front crawl. Concern<strong>in</strong>g<br />

task constra<strong>in</strong>ts, several studies have shown a shift<strong>in</strong>g of coord<strong>in</strong>ation with<br />

<strong>in</strong>creased race pace or when us<strong>in</strong>g paddles (Seifert et al., 2007).<br />

In accordance with Sparrow <strong>and</strong> Newell (1998), we supposed that<br />

modifications of coord<strong>in</strong>ation emerge <strong>in</strong> the <strong>in</strong>terest of energy efficiency.<br />

If the opposition mode leads to a greater propulsive cont<strong>in</strong>uity, <strong>in</strong> order to<br />

theoretically ma<strong>in</strong>ta<strong>in</strong> swimm<strong>in</strong>g speed, it would be <strong>in</strong>terest<strong>in</strong>g to <strong>in</strong>vestigate<br />

the effect of energy cost (C) <strong>in</strong>crease on the adopted aquatic propulsion<br />

mode, i.e. catch-up, opposition or superposition (Chollet et al., 2000).<br />

The purpose of this study was to assess the effects of the <strong>in</strong>teraction<br />

of both an environmental constra<strong>in</strong>t (<strong>in</strong>crease <strong>in</strong> speed between sets)<br />

<strong>and</strong> a task constra<strong>in</strong>t (the ma<strong>in</strong>tenance of this speed dur<strong>in</strong>g the 300m)<br />

on the strok<strong>in</strong>g parameters (stroke rate, SR <strong>and</strong> stroke length, SL)<br />

204<br />

<strong>and</strong> arm coord<strong>in</strong>ation <strong>in</strong> front crawl. We hypothesized that the motor<br />

organization is <strong>in</strong>fluenced by the C <strong>and</strong> that therefore its <strong>in</strong>crease would<br />

lead the swimmers to adapt their coord<strong>in</strong>ation <strong>and</strong> strok<strong>in</strong>g parameters.<br />

Methods<br />

Six French national swimmers, specialists <strong>in</strong> spr<strong>in</strong>t front crawl performed<br />

six consecutive 300-m swims separated by 30-s rest<strong>in</strong>g <strong>in</strong>tervals. Individual<br />

personal best 400-m freestyle performances recorded with<strong>in</strong> the<br />

month preced<strong>in</strong>g the test<strong>in</strong>g period were used to determ<strong>in</strong>e the pace of<br />

the <strong>in</strong>cremental stages. The pace of the first 300-m was 30-s slower than<br />

the time required to swim 300-m at the adjusted 400-m pace. This time<br />

was then reduced by 5-s for each consecutive 300-m until the f<strong>in</strong>al 300-m.<br />

Aerial <strong>and</strong> underwater (0.5 m) side-view cameras were superposed<br />

<strong>and</strong> fixed on the right side of the pool. A calibration frame of 5-m on the<br />

horizontal-axis <strong>and</strong> 2-m on the vertical axis was positioned on the floor<br />

of the swimm<strong>in</strong>g pool, orthogonally to the external side-view camera,<br />

that enabled us to measure the time over a distance of 5-m to obta<strong>in</strong><br />

the clean speed (v <strong>in</strong> m·s-1 ). The arm stroke rate (SR <strong>in</strong> stroke.m<strong>in</strong>-1 )<br />

was calculated from h<strong>and</strong> entry at the first stroke to h<strong>and</strong> entry at the<br />

second stroke. SL (m·stroke-1 ) was calculated from the average speed (v)<br />

<strong>and</strong> SR (stroke.m<strong>in</strong>-1 ):<br />

SL = v • SR/60 (1)<br />

Arm coord<strong>in</strong>ation was quantified us<strong>in</strong>g the <strong>in</strong>dex of coord<strong>in</strong>ation (IdC)<br />

(Chollet et al., 2000). The IdC was calculated for two strokes per 50-m<br />

taken <strong>in</strong> the 10-m central part of the pool, then averaged for the 3 laps<br />

of 50-m compos<strong>in</strong>g the last 150-m to correspond to the analysis of the<br />

oxygen uptake. The IdC was expressed as a percentage of complete arm<br />

stroke duration.<br />

Dur<strong>in</strong>g exercise, m<strong>in</strong>ute ventilation (VE ), oxygen uptake (VO2 ) <strong>and</strong><br />

carbon dioxide production (VCO2 ) were recorded breath-by-breath by<br />

the K4b² telemetric gas exchange system (Cosmed, Rome, Italy) us<strong>in</strong>g<br />

the St<strong>and</strong>ard K4b2 valve .The K4b2 system was calibrated accord<strong>in</strong>g<br />

to the manufacturer’s <strong>in</strong>structions before each test. A capillary blood<br />

sample was obta<strong>in</strong>ed from the f<strong>in</strong>ger at rest, <strong>and</strong> no more than 30-sec<br />

after the end of the first five sets <strong>and</strong> three m<strong>in</strong>utes after the last set<br />

<strong>and</strong> analyzed for blood lactate concentration (lactate Pro LT, Arkay Inc.,<br />

Kyoto, Japan). The energy cost per unit distance (C, mLO2 .kg-1 .m-1 ) was<br />

def<strong>in</strong>ed as:<br />

C = E � • v -1 (2)<br />

where E � is the total metabolic energy expenditure (aerobic <strong>and</strong> anaerobic<br />

pathways) expressed <strong>in</strong> mLO 2 .m<strong>in</strong> -1 .kg -1 <strong>and</strong> v, <strong>in</strong> m.m<strong>in</strong> -1 , is<br />

the swimm<strong>in</strong>g speed (di Prampero 1986) at sub-maximal <strong>and</strong> maximal<br />

<strong>in</strong>tensities. The aerobic part of swimm<strong>in</strong>g energy cost (C aero ) was equal<br />

to the ratio between VO 2 net (i.e. the difference between the VO 2 measured<br />

dur<strong>in</strong>g the last m<strong>in</strong>ute of each swimm<strong>in</strong>g stage <strong>and</strong> its value at<br />

rest) <strong>and</strong> the swimm<strong>in</strong>g speed (di Prampero 1986). Anaerobic glycolytic<br />

net energy cost (C anaero ) was estimated us<strong>in</strong>g blood lactate. Blood lactate<br />

measures (mmol) were converted to oxygen equivalent values as 3<br />

mLO 2 .kg -1 of bodyweight per mmol of blood lactate. Thus, C, calculated<br />

as the sum of C aero <strong>and</strong> C anaero , represented the energy expended to cover<br />

one unit of distance while swimm<strong>in</strong>g at a given speed <strong>and</strong> with a given<br />

stroke (anaerobic alactic energy sources seems to be neglected, or assumed<br />

to be reduced, when evaluat<strong>in</strong>g E � for 200-m or more events).<br />

F<strong>in</strong>ally, C is given <strong>in</strong> J.kg -1 .m -1 assum<strong>in</strong>g that 1 mLO 2 consumed by the<br />

human body yields 20.9 J (Fern<strong>and</strong>es et al., 2006).<br />

ANOVA <strong>and</strong> the Tukey Post-hoc test were used to analyse the differences<br />

between the different sets. L<strong>in</strong>ear regression tests studied the<br />

relationships among the physiological parameters (C), motor organisation<br />

(IdC), stroke rate (SR) <strong>and</strong> stroke length (SL). For all tests, the level<br />

of significance was fixed at P


evaluat<strong>in</strong>g for 200-m or more events). F<strong>in</strong>ally, C is given <strong>in</strong> J.kg -1 .m -1 E assum<strong>in</strong>g that<br />

1 mLO2 consumed by the human body yields 20.9 J (Fern<strong>and</strong>es et al., 2006).<br />

ANOVA <strong>and</strong> the Tukey Post-hoc test were used to analyse the differences between<br />

the different sets. L<strong>in</strong>ear regression tests studied the relationships among the<br />

physiological parameters (C), motor organisation (IdC), stroke rate (SR) <strong>and</strong> stroke<br />

length (SL). For all tests, the level of significance was fixed at P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Swimm<strong>in</strong>g <strong>and</strong> Respiratory Muscle Endurance<br />

Tra<strong>in</strong><strong>in</strong>g: A Case Study<br />

lemaître, F., chavallard, F., chollet, d.<br />

Centre d’Etudes des Transformations des Activités Physiques et Sportives<br />

(CETAPS, EA3832), France<br />

The aim of this case study was to <strong>in</strong>vestigate whether respiratory<br />

muscle endurance tra<strong>in</strong><strong>in</strong>g (RMET) would <strong>in</strong>crease performance<br />

<strong>in</strong> a long-distance swimmer. An expert long-distance<br />

swimmer tra<strong>in</strong>ed for 10 weeks <strong>in</strong> a RMET program (30 m<strong>in</strong>utes<br />

a day, 5 days a week) plus his usual swim tra<strong>in</strong><strong>in</strong>g. Maximal swim<br />

time trials, ventilatory function tests, maximal <strong>in</strong>spiratory <strong>and</strong><br />

expiratory pressure (MIP <strong>and</strong> MEP), <strong>and</strong> respiratory endurance<br />

tests (RET) were done. Ventilatory function parameters were not<br />

improved post-tra<strong>in</strong><strong>in</strong>g, but MIP, MEP, RET <strong>and</strong> swimm<strong>in</strong>g<br />

performance were <strong>in</strong>creased (+19%, +33%, +7 m<strong>in</strong>utes; 50 m:<br />

-5.4%; 200 m: -7.2% respectively). RMET may be thus a useful<br />

technique to improve performance <strong>in</strong> long-distance swimmers.<br />

Key words: endurance, respiratory muscle, performance<br />

IntroductIon<br />

The aim of this case study was to <strong>in</strong>vestigate whether respiratory muscle<br />

endurance tra<strong>in</strong><strong>in</strong>g (RMET) would <strong>in</strong>crease performance <strong>in</strong> a longdistance<br />

swimmer. Immersion <strong>in</strong> water <strong>in</strong>creases the pressure around the<br />

thorax, rais<strong>in</strong>g ventilatory constra<strong>in</strong>ts both at rest <strong>and</strong> dur<strong>in</strong>g physical effort.<br />

Until lately, ventilation was not considered to be a limit<strong>in</strong>g factor for<br />

sub-maximal or maximal effort. However, it was shown that this ventilatory<br />

limitation decreases maximal performance <strong>in</strong> healthy subjects <strong>and</strong><br />

athletes (Verges et al. 2007). It was thus suggested that tra<strong>in</strong><strong>in</strong>g might<br />

delay respiratory muscle fatigue <strong>and</strong> permit better distribution of blood<br />

flow to the work<strong>in</strong>g muscles. It has often been observed that swimmers<br />

have pulmonary volumes that are greater than both predicted values <strong>and</strong><br />

those of controls (Doherty et al., 1997). The improved pulmonary volumes<br />

<strong>in</strong> swimmers could be due to swim tra<strong>in</strong><strong>in</strong>g per se (Clanton et al.,<br />

1987), stronger respiratory muscles (Doherty et al., 1997), alveolar hyperplasia<br />

(Armour et al., 1993), or accelerated pulmonary growth (Courteix<br />

et al., 1993). Clanton et al. (1987) showed that pulmonary function,<br />

endurance <strong>and</strong> respiratory muscle force were improved after swim tra<strong>in</strong><strong>in</strong>g,<br />

whereas supplementary RMET did not lead to additional change.<br />

Similarly, Wells et al. (2005) showed that swim tra<strong>in</strong><strong>in</strong>g alone improved<br />

pulmonary function <strong>and</strong> respiratory muscle force to the same extent as<br />

RMT associated with swim tra<strong>in</strong><strong>in</strong>g. These f<strong>in</strong>d<strong>in</strong>gs seemed to be confirmed<br />

<strong>in</strong> a more recent study <strong>in</strong> high-level swimmers (Mickleborough et<br />

al., 2008). Moreover, it was recently reported that the impact on swimm<strong>in</strong>g<br />

performance seems to be limited (Kild<strong>in</strong>g et al., 2009).<br />

Methods<br />

An expert long-distance swimmer (21 years, 183 cm, 71 kg) tra<strong>in</strong>ed for<br />

10 weeks <strong>in</strong> a RMET program plus his usual swim tra<strong>in</strong><strong>in</strong>g. The athlete’s<br />

speciality was the 1,500-m event <strong>and</strong> he was a f<strong>in</strong>alist <strong>in</strong> the French<br />

national championships. His best performance time on this distance<br />

was thus expressed as a percentage of the current world record, <strong>and</strong> was<br />

93.4%. He was not asthmatic <strong>and</strong> consented to the study requirements<br />

<strong>in</strong> writ<strong>in</strong>g. The experimental procedures were conducted <strong>in</strong> accordance<br />

with the Declaration of Hels<strong>in</strong>ki <strong>and</strong> were approved by the local ethics<br />

committee. He was evaluated on two occasions: before (1 week) <strong>and</strong> just<br />

after the RMET program.<br />

Measurements of body mass <strong>and</strong> sk<strong>in</strong> folds were generally made between<br />

8.00 <strong>and</strong> 10.00 A.M.; the swimmer presented after tra<strong>in</strong><strong>in</strong>g <strong>in</strong><br />

a fasted state <strong>and</strong> all anthropometric parameters were measured by the<br />

same <strong>in</strong>vestigator. Height was measured to the nearest 0.5 cm (Tanita,<br />

206<br />

Tanita Corp., Arl<strong>in</strong>gton Heights, IL, USA). Body composition (fat mass:<br />

FM) was estimated with the sk<strong>in</strong>fold method of Durn<strong>in</strong> <strong>and</strong> Womersley<br />

(1974) us<strong>in</strong>g a calibrated sk<strong>in</strong>fold calliper (Model HSK-BI, Baty International,<br />

West Sussex, UK). Chest expansion was measured at the level<br />

of the xiphoid process us<strong>in</strong>g a tape measure. The subject was <strong>in</strong>structed<br />

to perform a maximal exhalation [to residual volume (RV)] <strong>and</strong> then<br />

an <strong>in</strong>halation to maximum <strong>in</strong>spiratory capacity (MIC). Chest expansion<br />

was calculated as the difference between circumferences at RV <strong>and</strong> MIC.<br />

The CV of test-retest measurements (with<strong>in</strong> the day) at the level of the<br />

xiphoid process was 0.7%. Buoyancy was evaluated by measur<strong>in</strong>g the hydrostatic<br />

lift (HL), which is the force that enables swimmers to float<br />

when they are immersed <strong>in</strong> forced <strong>in</strong>spiration. It was measured at the end<br />

of a maximal <strong>in</strong>spiration when the subject was float<strong>in</strong>g. The subject was<br />

<strong>in</strong> the fetal position, fac<strong>in</strong>g downward. A lead mass (0.1-1 kg) was placed<br />

on the swimmer’s back between the shoulder blades. The load needed to<br />

keep the subject just under the water was taken as the HL. For the glide<br />

distance measurement, the subject was asked to adopt a prone position<br />

with the arms completely extended at the elbows <strong>and</strong> wrists, to position<br />

the upper arms <strong>in</strong> contact with the sides of the head (one h<strong>and</strong> on top of<br />

the other), to ma<strong>in</strong>ta<strong>in</strong> the feet together with the ankles plantar flexed,<br />

to hold onto the wire, <strong>and</strong> to hold his breath after a maximal <strong>in</strong>spiration.<br />

For the passive torque time (Tt), which can be def<strong>in</strong>ed as the time it<br />

takes for the body to pass from horizontal to vertical position, the same<br />

researcher ma<strong>in</strong>ta<strong>in</strong>ed the swimmer <strong>in</strong> the horizontal position until a<br />

signal was given by another researcher, who then noted the time it took<br />

for the swimmer to get <strong>in</strong>to vertical position. The subject was asked to<br />

hold his breath after a maximal <strong>in</strong>spiration until the test ended. Each<br />

time (before <strong>and</strong> after RMET), three glide <strong>and</strong> three Tt measures are<br />

made <strong>in</strong> order to calculate <strong>and</strong> average the glide distance.<br />

Several parameters were measured for the pulmonary function tests:<br />

forced vital capacity (FVC), forced expiratory volume <strong>in</strong> 1 s (FEV1),<br />

<strong>and</strong> peak expiratory flow (PEF). For each parameter, the best value was<br />

chosen from at least three consecutive maneuvers differ<strong>in</strong>g by no more<br />

than 5% (Quanjer et al. 1993). All parameters were measured with a Microquark<br />

spirometer (Cosmed, Rome, Italy) <strong>in</strong> the same conditions, with<br />

the subject <strong>in</strong> a sitt<strong>in</strong>g position <strong>and</strong> breath<strong>in</strong>g through the mouthpiece<br />

with a nose-clip. The spirometer volume was calibrated twice daily with<br />

a 3-L calibrated syr<strong>in</strong>ge. The results were corrected to BTPS conditions<br />

<strong>and</strong> compared with predicted values (Quanjer et al. 1993). The maximal<br />

<strong>in</strong>spiratory <strong>and</strong> expiratory pressures (MIP <strong>and</strong> MEP) were measured<br />

<strong>in</strong> the sitt<strong>in</strong>g position at the end of a normal expiration <strong>and</strong> <strong>in</strong>spiration<br />

(MEPFRC, MIPFRC) us<strong>in</strong>g a small portable mouth pressure meter<br />

(ZAN 100 USB, ZAN Messgeräte GmbH, Germany). The subject was<br />

verbally encouraged to achieve maximal strength. All maneuvers were<br />

repeated at least twice.<br />

The respiratory endurance test (RET) was performed with the<br />

SpiroTiger® device. The subject was asked to susta<strong>in</strong> a given m<strong>in</strong>ute<br />

ventilation (VE) with a predeterm<strong>in</strong>ed tidal volume (VT) <strong>and</strong> respiratory<br />

frequency (fR) for as long as possible; that is, until he could no<br />

longer susta<strong>in</strong> either VT or fR despite three consecutive “warn<strong>in</strong>gs” by<br />

the experimenter. The RMET was performed 30 m<strong>in</strong>utes a day, 5 days<br />

a week, with the same specific device (SpiroTiger®) allow<strong>in</strong>g partial rebreath<strong>in</strong>g<br />

of CO2 <strong>and</strong> thus assur<strong>in</strong>g normocapnic hyperpnea. RMET<br />

consisted of voluntary normocapnic hyperpnea at a given VT <strong>and</strong> fR<br />

with a duty cycle of 0.5. The Spirotiger® provided breath-by-breath<br />

feedback of fR <strong>and</strong> VT. The size of the re-breath<strong>in</strong>g bag was set at 50-<br />

60% of vital capacity, <strong>and</strong> VE of the first tra<strong>in</strong><strong>in</strong>g session was set at 60%<br />

of the maximal voluntary ventilation. The swimmer was <strong>in</strong>structed to<br />

<strong>in</strong>crease fR after 25 m<strong>in</strong> of tra<strong>in</strong><strong>in</strong>g, if he felt he would not be exhausted<br />

by 30 m<strong>in</strong>. If he felt he could not susta<strong>in</strong> the target for 30 m<strong>in</strong>, he was<br />

to decrease the fR. The swimmer was <strong>in</strong>structed to <strong>in</strong>crease fR from<br />

one session to the next by 1-2 breaths/m<strong>in</strong> <strong>and</strong> was monitored by the<br />

experimenter at least once a week to verify compliance.<br />

The swimm<strong>in</strong>g performance was evaluated from the 50-m <strong>and</strong> 200m<br />

time trials (TT50m <strong>and</strong> TT200m) swum at maximal velocity <strong>and</strong> <strong>in</strong>


<strong>and</strong>omized order. In addition, at rest <strong>and</strong> 3 m<strong>in</strong>utes after the end of each<br />

swim trial, a 5-µL capillary blood sample was drawn from a f<strong>in</strong>ger <strong>and</strong> analyzed<br />

(Lactate proTM, LT-1710, Arkray, Inc. Japan). The rates of perceived<br />

exertion (RPE, Borg 6-20 scale) were also measured after each swim trial.<br />

results<br />

The parameters for the long-distance subject are shown <strong>in</strong> Table 1. Body<br />

mass, fat mass, hydrostatic lift, glide distance <strong>and</strong> torque time were all<br />

decreased after the RMET. Chest expansion was also <strong>in</strong>creased. Ventilatory<br />

function parameters (FVC, FEV 1 <strong>and</strong> PEF) were not improved after<br />

tra<strong>in</strong><strong>in</strong>g, whereas MIP, MEP, the RET <strong>and</strong> swimm<strong>in</strong>g performances<br />

<strong>in</strong>creased (+19%, +33%, +12 m<strong>in</strong>.; 50 m: -5.4%; 200 m: -7.2%). The rates<br />

of perceived exertion were decreased after the two swim trials (50 m <strong>and</strong><br />

200 m). Lactate concentrations were lower after the swim trials (50 m:<br />

-0.7 mmol·l -1 ; 200 m: -4.4 mmol·l -1 ).<br />

Table 1. Descriptive basel<strong>in</strong>e <strong>and</strong> post-tra<strong>in</strong><strong>in</strong>g characteristics of the<br />

long-distance swimmer.<br />

Before RMET After RMET<br />

Body mass (kg) 71.7 68.6<br />

Fat mass (%) 9.7 8.9<br />

Chest expansion (cm) 9.0 8.9<br />

HL (kg) 3.7 2.9<br />

Glide distance (m) 14.6 13.2<br />

Torque time (s) 7.4 6.8<br />

FVC (L) 7.00 7.07<br />

FEV1 (L) 5.13 5.56<br />

PEF (L.s-1) 11.33 11.24<br />

MIP (kPa) 7.66 9.13<br />

MEP (kPa) 4.00 5.32<br />

RET (m<strong>in</strong>) 16 28<br />

TT50m (s) 28.13 26.69<br />

TT200m (s) 128.02 119.41<br />

RPE50m 13 11<br />

RPE200m 17 16<br />

La50m (mmol·l-1) 4.1 3.4<br />

La200m (mmol·l-1) 10.2 5.8<br />

RMET: respiratory muscle endurance tra<strong>in</strong><strong>in</strong>g; HL: hydrostatic lift;<br />

FVC: forced vital capacity; FEV1 : forced expiratory volume <strong>in</strong> one second;<br />

PEF: peak expiratory flow; MIP <strong>and</strong> MEP: maximal <strong>in</strong>spiratory<br />

<strong>and</strong> expiratory pressure; RET: respiratory endurance test; TT: time trial.<br />

dIscussIon<br />

The ma<strong>in</strong> f<strong>in</strong>d<strong>in</strong>g was the improved performance <strong>in</strong> the swim trials after<br />

RMET tra<strong>in</strong><strong>in</strong>g <strong>and</strong> the improved endurance, respiratory muscle force<br />

<strong>and</strong> perceived exertion.<br />

The body mass, fat mass, hydrostatic lift, glide distance <strong>and</strong> torque<br />

time were all decreased after the RMET. These results <strong>in</strong>dicated that<br />

the swimmer had become th<strong>in</strong>ner dur<strong>in</strong>g the tra<strong>in</strong><strong>in</strong>g period, los<strong>in</strong>g fat<br />

mass, which probably reduced his buoyancy <strong>and</strong> may have modified his<br />

glide <strong>and</strong> Tt. These changes may also have had an impact on performance,<br />

especially for the 200 m.<br />

The f<strong>in</strong>d<strong>in</strong>gs were compared with previous RMET f<strong>in</strong>d<strong>in</strong>gs <strong>in</strong> swimmers.<br />

Greater changes <strong>in</strong> our swimmer’s performance for TT200m were<br />

found, whereas TT50m has never been tested before (Mickleborough<br />

et al., 2008; Kild<strong>in</strong>g et al., 2009). It is difficult to compare a case study<br />

with other studies to expla<strong>in</strong> why our performance effect was higher<br />

(TT200m), but it is noteworthy that our RMET was longer (10 weeks vs.<br />

6 weeks) <strong>and</strong> our subject was an expert long-distance swimmer. Long-distance<br />

swimmers, who undergo more endurance tra<strong>in</strong><strong>in</strong>g than other swim-<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

mers, are usually mixed <strong>in</strong> with other swim specialities (50 m to 400 m).<br />

It is thus difficult to expla<strong>in</strong> the effect of a specific RMET, such as<br />

<strong>in</strong>spiratory muscle tra<strong>in</strong><strong>in</strong>g (IMT), which may not be specific enough<br />

for a given swim speciality. RMET seems to be more specific for a<br />

long-distance swimmer than IMT. This po<strong>in</strong>t may expla<strong>in</strong> <strong>in</strong> part the<br />

differences <strong>in</strong> performance <strong>and</strong> respiratory muscle force observed <strong>in</strong> our<br />

study. In previous studies, the tendency toward reduced lactate did not<br />

always reach statistical significance (Kild<strong>in</strong>g et al., 2009; Romer et al.,<br />

2002). The lactate concentration was also more reduced after the 200-m<br />

trial <strong>and</strong> the RET also <strong>in</strong>crease. Decreased respiratory muscle work <strong>and</strong>/<br />

or improved leg blood flow could have reduced anaerobic metabolism <strong>in</strong><br />

respiratory <strong>and</strong>/or leg muscles. Thus, the RET <strong>and</strong> the lactate concentration<br />

changes <strong>in</strong>dicate that dur<strong>in</strong>g swimm<strong>in</strong>g the respiratory muscle<br />

work was probably decreased, <strong>and</strong> can <strong>in</strong> turn improve leg blood flow<br />

reduc<strong>in</strong>g anaerobic metabolism. Those parameters re<strong>in</strong>force the hypothesis<br />

of beneficial effects of specific respiratory tra<strong>in</strong><strong>in</strong>g for swimmers.<br />

conclusIon<br />

The present <strong>in</strong>dividual data suggest that RMET has a beneficial effect<br />

on swimm<strong>in</strong>g performance (50 m <strong>and</strong> 200 m), although 200-m performance<br />

seemed to be more improved. It may be <strong>in</strong>terest<strong>in</strong>g to compare<br />

the effects of respiratory tra<strong>in</strong><strong>in</strong>g with the respiratory device adapted<br />

to the swimm<strong>in</strong>g specialty (spr<strong>in</strong>t: force respiratory device vs. longdistance:<br />

endurance respiratory device). Respiratory muscle tra<strong>in</strong><strong>in</strong>g<br />

can therefore be considered a worthwhile ergogenic aid for competitive<br />

swimmers.<br />

reFerences<br />

Courteix D, Obert P, Lecoq AM, Guenon P, Koch G. (1997). Effect of<br />

<strong>in</strong>tensive swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g on lung volumes, airway resistance <strong>and</strong><br />

on the maximal expiratory flow-volume relationship <strong>in</strong> prepubertal<br />

girls. Eur J Appl Physiol Occup Physiol, 76, 264–269.<br />

Clanton TL, Dixon GF, Drake J, Gadek JE. (1987). Effects of swim<br />

tra<strong>in</strong><strong>in</strong>g on lung volumes <strong>and</strong> <strong>in</strong>spiratory muscle condition<strong>in</strong>g. J Appl<br />

Physiol, 62, 39–46.<br />

Doherty M, Dimitriou L. (1997). Comparison of lung volume <strong>in</strong> Greek<br />

swimmers, l<strong>and</strong> based athletes, <strong>and</strong> sedentary controls us<strong>in</strong>g allometric<br />

scal<strong>in</strong>g. Br J Sports Med, 31, 337–341.<br />

Durn<strong>in</strong> JV, Womersley J. (1974). Body fat assessed from total body density<br />

<strong>and</strong> its estimation from sk<strong>in</strong>fold thickness: measurements on 481<br />

men <strong>and</strong> women aged from 16 to 72 years. Br J Nutr, 32, 77-97.<br />

Kild<strong>in</strong>g AE, Brown S, McConnell AK. (2009). Inspiratory tra<strong>in</strong><strong>in</strong>g improves<br />

100 <strong>and</strong> 200 m swimm<strong>in</strong>g performance. Eur J Appl Physiol,<br />

[Epub ahead of pr<strong>in</strong>t].<br />

Lomax ME, McConnell AK. (2003). Inspiratory muscle fatigue <strong>in</strong><br />

swimmers after a s<strong>in</strong>gle 200 m swim. J Sports Sci, 21, 659–664.<br />

Mickleborough TD, Stager JM, Chatham K, L<strong>in</strong>dley MR, Ionescu IA.<br />

(2008). Pulmonary adaptations to swim <strong>and</strong> <strong>in</strong>spiratory muscle tra<strong>in</strong><strong>in</strong>g.<br />

Eur J Appl Physiol, 103, 635–646.<br />

Quanjer PH, Tammel<strong>in</strong>g GJ, Cotes JE, Pedersen OF, Pesl<strong>in</strong> R, Yernault<br />

JC. (1993). Lung volumes <strong>and</strong> forced ventilatory flows. Report<br />

Work<strong>in</strong>g Party St<strong>and</strong>ardization of Lung Function Tests, European<br />

Community for Steel <strong>and</strong> Coal. Official Statement of the European<br />

Respiratory Society. Eur Respir J, Suppl 16, 5-40.<br />

Romer LM, McConnell AK, Jones DA. (2002). Effects of <strong>in</strong>spiratory<br />

muscle tra<strong>in</strong><strong>in</strong>g upon recovery on time-trial performance <strong>in</strong> tra<strong>in</strong>ed<br />

cyclists. J Sports Sci, 20, 547-562.<br />

Verges S, Lenherr O, Haner AC, Schulz C, Spengler CM. (2007). Increased<br />

fatigue resistance of respiratory muscles dur<strong>in</strong>g exercise after<br />

respiratory muscle endurance tra<strong>in</strong><strong>in</strong>g. Am J Physiol, 292, R1246–<br />

R1253.<br />

Wells GD, Plyley M, Thomas S, Goodman L, Duff<strong>in</strong> J. (2005). Effects<br />

of concurrent <strong>in</strong>spiratory <strong>and</strong> expiratory muscle tra<strong>in</strong><strong>in</strong>g on respiratory<br />

<strong>and</strong> exercise performance <strong>in</strong> competitive swimmers. Eur J Appl<br />

Physiol, 94, 527-540.<br />

207


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Heart Rate Responses Dur<strong>in</strong>g Gradually Increas<strong>in</strong>g<br />

<strong>and</strong> Decreas<strong>in</strong>g Exercise <strong>in</strong> Water<br />

nishimura, K. 1 , nose, Y. 2 , Yoshioka, A. 2 , Kawano, h. 3 , onodera,<br />

s. 4 , takamoto, n. 1<br />

1Hiroshima Institute of Technology, Hiroshima, Japan<br />

2Graduate School of Kawasaki University of Medical Welfare, Kurashiki,<br />

Japan<br />

3Waseda University, Tokorozawa, Japan<br />

4Kawasaki University of Medical Welfare, Kurashiki, Japan<br />

The purpose of this study was to determ<strong>in</strong>e the heart rate (HR)<br />

responses dur<strong>in</strong>g <strong>and</strong> after gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g<br />

exercise <strong>in</strong> water <strong>and</strong> on l<strong>and</strong>. Eight healthy Japanese males volunteered<br />

for this study. Subjects performed arm crank<strong>in</strong>g exercise<br />

(calibration <strong>and</strong> triangular tests) for 32 -m<strong>in</strong> <strong>and</strong> recovered for<br />

1 -m<strong>in</strong>. HR <strong>and</strong> cardiac autonomic nervous system activity were<br />

cont<strong>in</strong>uously measured. The amplitude <strong>and</strong> phase lags at the top<br />

<strong>and</strong> bottom of the work rate were measured <strong>in</strong> each cycle. The<br />

results were as follows; 1) the HR phase response was shorter <strong>in</strong><br />

water than on l<strong>and</strong>, but there were no differences <strong>in</strong> amplitude,<br />

2) reactivation <strong>in</strong> cardiac parasympathetic nerve was greater <strong>in</strong><br />

water. Thus, exercise <strong>and</strong> recovery <strong>in</strong> water may enhance the stability<br />

of autonomic nervous activity, not only dur<strong>in</strong>g exercise but<br />

also after exercise.<br />

Key words: arm crank<strong>in</strong>g exercise, gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g<br />

exercise, water immersion, heart rate response, recovery after excise<br />

IntroductIon<br />

In water, humans have different physiological responses than on l<strong>and</strong><br />

due to the <strong>in</strong>fluence of the physical characteristics of water, such as water<br />

temperature (hydrostatic), water pressure, buoyancy <strong>and</strong> viscosity. Venous<br />

return is greater <strong>in</strong> water than on l<strong>and</strong>, which causes <strong>in</strong>creased<br />

stroke volume <strong>and</strong> cardiac output, decreased heart rate, <strong>and</strong> <strong>in</strong>creased<br />

cardiac parasympathetic nervous system modulation.<br />

Dur<strong>in</strong>g arm crank<strong>in</strong>g exercise, there are no significant differences of<br />

oxygen uptake between <strong>in</strong>-water <strong>and</strong> on-l<strong>and</strong> conditions, despite water<br />

immersion-<strong>in</strong>duced bradycardia (Kimura et al., 2001). In addition, the<br />

high frequency component <strong>in</strong> heart rate variability, an <strong>in</strong>dex of cardiac<br />

autonomic nervous system, is enhanced at the onset of arm crank<strong>in</strong>g<br />

exercise <strong>in</strong> water compared with the on l<strong>and</strong> response. These data suggest<br />

that dur<strong>in</strong>g exercise at the same work-load, heart rate responses<br />

<strong>in</strong>clud<strong>in</strong>g heart rate variability are different between on-l<strong>and</strong> <strong>and</strong> <strong>in</strong>water<br />

conditions. Heart rate k<strong>in</strong>etics (i.e., phase response <strong>and</strong> amplitude)<br />

dur<strong>in</strong>g s<strong>in</strong>usoidal exercise are affected by cardiopulmonary fitness<br />

(Fukuoka et al., 2002), physical fitness status (Fukuoka et al., 2002) <strong>and</strong><br />

low <strong>in</strong>tensity aerobic tra<strong>in</strong><strong>in</strong>g (Nabekura et al., 2007). In fact, the time<br />

delay of heart rate <strong>in</strong> response to s<strong>in</strong>usoidal exercise is shorter <strong>in</strong> highly<br />

fit <strong>in</strong>dividuals, suggest<strong>in</strong>g that heart rate k<strong>in</strong>etics <strong>in</strong> response to s<strong>in</strong>usoidal<br />

exercise may reflect physical fitness. However, the effects of environmental<br />

factors, <strong>in</strong> particular water immersion, on heart rate k<strong>in</strong>etics <strong>in</strong><br />

response to gradually <strong>in</strong>creased <strong>and</strong> decreased exercise workload, such as<br />

<strong>in</strong> s<strong>in</strong>usoidal or gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g exercise, are largely<br />

unknown.<br />

It has been shown that the time constant of heart rate decl<strong>in</strong>e for the<br />

first 30 second (T30) after exercise can serve as a specific <strong>in</strong>dex to assess<br />

post-exercise reactivation of cardiac parasympathetic nerve activity<br />

(Imai et al., 1994). Nishimura et al. suggested that sup<strong>in</strong>e float<strong>in</strong>g after<br />

exercise <strong>in</strong>duced a greater activation <strong>in</strong> the cardiac parasympathetic nervous<br />

system, via <strong>in</strong>crease of central venous pressure <strong>and</strong> cardiac output,<br />

<strong>and</strong> the subsequent arterial baroreflex response caused by greater venous<br />

208<br />

return, lead<strong>in</strong>g to bradycardia (Nishimura et al., 2006).<br />

Therefore, it was hypothesized that 1) the phase response <strong>and</strong> amplitude<br />

of heart rate dur<strong>in</strong>g gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g arm<br />

crank<strong>in</strong>g exercise <strong>in</strong> water exercise is higher than on l<strong>and</strong>, <strong>and</strong> 2) the<br />

activation of the cardiac parasympathetic nervous system after exercise<br />

<strong>in</strong> the water is greater than after on-l<strong>and</strong> exercise. To test these hypotheses,<br />

the present study was designed to determ<strong>in</strong>e the effects of heart<br />

rate response dur<strong>in</strong>g <strong>and</strong> after gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g arm<br />

crank<strong>in</strong>g exercise <strong>in</strong> the water <strong>and</strong> on l<strong>and</strong>.<br />

Methods<br />

Eight healthy Japanese males volunteered for this study. Their mean (±<br />

SD) age, height, body weight, <strong>and</strong> % body fat were 20.9 ± 0.6 years,<br />

175.3 ± 4.2 cm, 66.9 ± 4.7 kg, <strong>and</strong> 13.9 ± 2.8 %, respectively. All subjects<br />

signed an <strong>in</strong>formed consent form prior to participation <strong>in</strong> this study.<br />

Subjects performed arm crank<strong>in</strong>g exercise for 32 -m<strong>in</strong>utes <strong>and</strong> recovered<br />

for 1 -m<strong>in</strong>ute <strong>in</strong> a st<strong>and</strong><strong>in</strong>g position. Subjects performed two<br />

types of exercise, a calibration test <strong>and</strong> a triangular test. The calibration<br />

test consisted of three 4-m<strong>in</strong>ute bouts of exercise at 20, 60 <strong>and</strong> 40% of<br />

peak oxygen uptake (VO2peak) with a total duration of 12 -m<strong>in</strong>utes.<br />

The triangular test consider of 4-m<strong>in</strong>ute bouts of gradually <strong>in</strong>creas<strong>in</strong>g<br />

<strong>and</strong> decreas<strong>in</strong>g work load exercise between 20 <strong>and</strong> 60%VO2peak for<br />

20 -m<strong>in</strong>utes. Both experimental tests were performed on l<strong>and</strong> (L-condition)<br />

<strong>and</strong> <strong>in</strong> water (W-condition). Water temperature was 30 ºC <strong>and</strong><br />

water level was at the height of the iliac crest.<br />

Heart rate <strong>and</strong> cardiac autonomic nervous system activity were<br />

cont<strong>in</strong>uously measured under both conditions. Heart rate maximal <strong>and</strong><br />

m<strong>in</strong>imal values, amplitude (difference between maximal <strong>and</strong> m<strong>in</strong>imal<br />

values), <strong>and</strong> phase lags at the top <strong>and</strong> bottom of the work rate were<br />

measured <strong>in</strong> each exercise cycle. The cardiac autonomic nervous system<br />

activity was calculated us<strong>in</strong>g the Maximum Entropy Calculation (Mem-<br />

Calc) methodology. The heart rate variability frequency doma<strong>in</strong> spectrum<br />

was divided <strong>in</strong>to two parts: high frequency (HF; 0.15-0.40Hz)<br />

<strong>and</strong> low frequency (LF; 0.04-0.15Hz). The cardiac autonomic nervous<br />

system activity was transformed <strong>in</strong>to natural logarithmic values to obta<strong>in</strong><br />

a statistically normal distribution. The natural logarithm of HF was<br />

taken as an <strong>in</strong>dex of cardiac parasympathetic nervous system modulation.<br />

T30 reflected reactivation of cardiac parasympathetic was calculated<br />

by decrease of heart rate calculated from RR <strong>in</strong>tervals 30 seconds<br />

after exercise. All experiments were performed at the same time. All<br />

subjects fasted dur<strong>in</strong>g three hours prior to the experiments, <strong>and</strong> caffe<strong>in</strong>e<br />

<strong>in</strong>take was not allowed either dur<strong>in</strong>g that time. Room temperature <strong>and</strong><br />

humidity were 27.3 ± 1.2ºC <strong>and</strong> 64.9 ± 5.0%, respectively.<br />

All data are expressed as mean ± st<strong>and</strong>ard deviation. Two-way analysis<br />

of variance for repeated measurements (condition × time course)<br />

<strong>and</strong> paired t-tests were used to compare values obta<strong>in</strong>ed dur<strong>in</strong>g the Lcondition<br />

<strong>and</strong> the W-condition trials. The level of significance was set<br />

up at p< 0.05.<br />

Table 1. Changes <strong>in</strong> heart rate dur<strong>in</strong>g each work load both <strong>in</strong> the Wcondition<br />

<strong>and</strong> on the L-condition.<br />

work load(watt) L-condition(bpm) W-condition(bpm)<br />

Rest on l<strong>and</strong> 59.3±7.8 57.0±13.5<br />

Calibration 20 93.0±7.0 84.3±9.4 *<br />

Calibration 60 129.1±13.8 119.2±16.2 *<br />

Calibration 40 115.8±15.6 102.7±14.5 *<br />

Increas<strong>in</strong>g 40 114.7±16.1 99.6±14.5 *<br />

Increas<strong>in</strong>g 45 117.8±14.9 102.2±15.5 *<br />

Increas<strong>in</strong>g 50 120.7±14.9 104.9±15.0 *<br />

Increas<strong>in</strong>g 55 123.9±15.1 108.1±15.3 *<br />

Increas<strong>in</strong>g 60 128.1±14.4 110.8±15.3 *<br />

Decreas<strong>in</strong>g 55 130.6±15.3 112.6±15.3 *


work load(watt) L-condition(bpm) W-condition(bpm)<br />

Decreas<strong>in</strong>g 50 130.4±16.8 112.4±15.4 *<br />

Decreas<strong>in</strong>g 45 129.5±18.1 110.9±15.7 *<br />

Decreas<strong>in</strong>g 40 126.7±19.2 108.8±15.8 *<br />

Decreas<strong>in</strong>g 35 123.0±19.4 105.2±15.7 *<br />

Decreas<strong>in</strong>g 30 120.0±19.1 101.7±15.7 *<br />

Decreas<strong>in</strong>g 25 115.8±18.6 98.4±15.6 *<br />

Decreas<strong>in</strong>g 20 112.5±18.3 96.0±14.9 *<br />

Increas<strong>in</strong>g 25 111.7±17.0 94.7±14.8 *<br />

Increas<strong>in</strong>g 30 112.2±16.3 95.5±14.9 *<br />

Increas<strong>in</strong>g 35 113.2±16.5 97.4±14.5 *<br />

Increas<strong>in</strong>g 40 115.1±16.4 98.7±14.5 *<br />

ANOVA:p< 0.05, *;p< 0.05 L-condition vs W-condition<br />

Figure 1. The phase lags to (top) the top of the work rate <strong>and</strong> (bottom)<br />

the bottom of the work rate both <strong>in</strong> the W-condition <strong>and</strong> on the Lcondition.<br />

Figure 2. The amplitude of heart rate both conditions<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

Figure 3. The ln HF under arm cak<strong>in</strong>g exercise both conditions.<br />

Figure 4. Comparison of T30 <strong>in</strong> both conditions.<br />

Figure 5. The ln HF both condition dur<strong>in</strong>g 1 –m<strong>in</strong>ute after exercise.<br />

209


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

Table 1 shows changes <strong>in</strong> heart rate dur<strong>in</strong>g arm crank<strong>in</strong>g exercise dur<strong>in</strong>g<br />

gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g workload. Dur<strong>in</strong>g the calibration<br />

test (20, 60 <strong>and</strong> 40%VO 2peak ), heart rate <strong>in</strong> the W-condition was significantly<br />

lower than on the L-condition (p< 0.05, respectively). Heart<br />

rate <strong>in</strong> the W-condition was significantly lower than <strong>in</strong> the L-condition<br />

dur<strong>in</strong>g triangular exercise (ANOVA; p< 0.05). Figure 1 shows the mean<br />

response time of heart rate (phase lags) to (a) the top of the work rate<br />

<strong>and</strong> (b) the bottom of the work rate <strong>in</strong> both conditions. The phase lags to<br />

the top the work rate <strong>in</strong> the W-condition was significantly shorter than<br />

on the L-condition (p< 0.05). Furthermore, phase lags to the bottom of<br />

the work rate <strong>in</strong> the W-condition were significantly shorter than on the<br />

L-condition (p< 0.05). The amplitude (difference between maximal <strong>and</strong><br />

m<strong>in</strong>imal values) was no significant different <strong>in</strong> each condition (Figure<br />

2). The ln HF <strong>in</strong> the W-condition was significantly higher than on the<br />

L-condition dur<strong>in</strong>g triangular exercise (p< 0.05) (Figure 3). Figure 4<br />

shows T30 <strong>in</strong> both conditions. T30 <strong>in</strong> the W-condition was significantly<br />

lower than on the L-condition (p< 0.05). Dur<strong>in</strong>g 1 m<strong>in</strong>ute after exercise,<br />

the ln HF <strong>in</strong> the W-condition was significantly higher than on the Lcondition<br />

(p< 0.05) (figure 5).<br />

dIscussIon<br />

The results of the present study are as follows; 1) the heart rate phase<br />

response to gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g arm crank<strong>in</strong>g exercise<br />

was shorter <strong>in</strong> the water than on l<strong>and</strong>, but no differences <strong>in</strong> heart rate<br />

amplitude were observed, 2) the reactivation <strong>in</strong> cardiac parasympathetic<br />

tone after arm crank<strong>in</strong>g exercise was greater <strong>in</strong> water than on l<strong>and</strong>. These<br />

results may exp<strong>and</strong> our underst<strong>and</strong><strong>in</strong>g of heart rate responses modulated<br />

by the autonomic nervous system to gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g<br />

exercise <strong>in</strong> water.<br />

In the present study, heart rate <strong>in</strong> water exercise was significantly<br />

reduced as compared to l<strong>and</strong> exercise. This fact may depend on immersion-<strong>in</strong>duced<br />

bradycardia, <strong>and</strong> be caused by <strong>in</strong>creased venous return due<br />

to water pressure. It is thought that the heart rate response to exercise<br />

under the anaerobic threshold level is ma<strong>in</strong>ly due to the attenuation<br />

of cardiac parasympathetic nervous activity (Xenakis et al., 1975). In<br />

the present study, s<strong>in</strong>ce peak heart rate values <strong>in</strong> W-condition <strong>and</strong> Lcondition<br />

were 113 bpm <strong>and</strong> 131 bpm, respectively, it is speculated that<br />

exercise <strong>in</strong>tensity was below the anaerobic threshold level. Thereby, heart<br />

rate response to gradually <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g exercise can be also<br />

expla<strong>in</strong>ed by activation of the cardiac parasympathetic nervous system.<br />

Indeed, the ln HF (an <strong>in</strong>dex of cardiac parasympathetic nerve activity)<br />

was higher <strong>in</strong> the W-condition as compared with on the L-condition,<br />

support<strong>in</strong>g our speculation.<br />

Sone et al. (1997) have suggested that the contribution of the withdrawal<br />

of cardiac parasympathetic activity to the <strong>in</strong>crease <strong>in</strong> heart rate<br />

with <strong>in</strong>creas<strong>in</strong>g exercise <strong>in</strong>tensity was greater at lower heart rate, <strong>and</strong><br />

that the cardiac parasympathetic system was more activated dur<strong>in</strong>g<br />

heart rate decreases than dur<strong>in</strong>g heart rate <strong>in</strong>creases at the same heart<br />

rate. The density of the high frequency spectrum of heart rate dur<strong>in</strong>g<br />

light work rates is higher than dur<strong>in</strong>g heavier workloads (Nabekura et<br />

al., 2007). In this present study, the phase lags at the top <strong>and</strong> bottom<br />

of the work rate <strong>in</strong> the W-condition were significantly shorter than <strong>in</strong><br />

the L-condition, suggest<strong>in</strong>g that immersion-<strong>in</strong>duced bradycardia might<br />

have coursed an <strong>in</strong>crease <strong>in</strong> the phase lags at the top <strong>and</strong> bottom of the<br />

work rate.<br />

In the present study, T30 <strong>in</strong> W-condition was greater than <strong>in</strong> Lcondition<br />

suggest<strong>in</strong>g that the cardiac parasympathetic nervous system<br />

rapidly reactivates <strong>in</strong> the water. It has been reported that an <strong>in</strong>crease<br />

of central blood volume due to water immersion might accelerate the<br />

recovery process of cardio-respiratory system (Miyamoto et al., 2001).<br />

Given this, the <strong>in</strong>creased venous return shown <strong>in</strong> the present <strong>in</strong>vestigation<br />

may contribute to the rapid reactivation of the cardiac parasympathetic<br />

nervous system. In fact, the ln HF <strong>in</strong> the W-condition was<br />

significantly higher than <strong>in</strong> the L-condition 1 m<strong>in</strong>ute after exercise.<br />

210<br />

conclusIon<br />

The results of the present study suggest that the activation of the cardiac<br />

parasympathetic nervous system caused by water immersion may produce<br />

an attenuation of heart rate time response to gradually <strong>in</strong>creas<strong>in</strong>g<br />

<strong>and</strong> decreas<strong>in</strong>g exercise. This attenuation of the phase lags dur<strong>in</strong>g exercise<br />

<strong>in</strong> the water may contribute to a reactivation of cardiac parasympathetic<br />

nervous system after exercise. Thus, exercise <strong>and</strong> recovery <strong>in</strong> water<br />

may enhance the stability of the autonomic nervous activity not only<br />

dur<strong>in</strong>g exercise but also after exercise.<br />

reFerences<br />

Kimura M, Suzuki M, Yazawa M, <strong>and</strong> Muraoka I (2001). Effect of Water<br />

Immersion on Heart Rate Responses dur<strong>in</strong>g Arm Crank<strong>in</strong>g<br />

Exercise. Adv. Exerc. Sports Physiol., 8, 41-48.<br />

Fukuoka Y, Nakagawa Y, Ogoh K, Shiojiri T <strong>and</strong> Fukuba Y (2002).<br />

Dynamics of the heart rate response to s<strong>in</strong>usoidal work <strong>in</strong> humans:<br />

<strong>in</strong>fluence of physical activity <strong>and</strong> age. Cl<strong>in</strong> Sci, 102, 31-38.<br />

Nabekura Y, Yoshioka Y, Nakagaki K, Tsujimura S <strong>and</strong> Sengoku Y<br />

(2007). Effect of Short-term Tra<strong>in</strong><strong>in</strong>g on Heart Rate Response dur<strong>in</strong>g<br />

S<strong>in</strong>usoidal Exercise. Adv. Exerc. Sports Physiol., 14, 29-39.<br />

Imai K, Sato H, Hori M, Kusuoka H, Ozaki H, Yokoyama H, Takeda H,<br />

Inoue M <strong>and</strong> Kamada T (1994). Vagally mediated heart rate recovery<br />

after exercise is accelerated <strong>in</strong> athletes but blunted <strong>in</strong> patients with<br />

chronic heart failure. J Am Coll Cardiol., 24, 1529-1535.<br />

Nishimura K, Seki K, Ono K <strong>and</strong> Onodera S (2006). Effects of the Sup<strong>in</strong>e<br />

Float<strong>in</strong>g on Rectal Temperature <strong>and</strong> Cardiac Parasympathetic<br />

Nervous System Activity after Exercise with a Cycle Ergometer.<br />

Japanese Journal of Aerospace <strong>and</strong> Environmental <strong>Medic<strong>in</strong>e</strong>, 43, 11-18.<br />

Xenakis, A.P., Quarry, V.M. <strong>and</strong> Spodick, D.H. (1975). Immediate Cardiac<br />

response to exercise: physiologic <strong>in</strong>vestigation by systolic time<br />

<strong>in</strong>tervals at graded workloads. Am Heart J., 89, 178-185.<br />

Sone R, Yamazaki F, Fukuoka Y <strong>and</strong> Ikegami H (1997). Respiratory<br />

variability <strong>in</strong> R-R <strong>in</strong>terval dur<strong>in</strong>g S<strong>in</strong>usoidal exercise. Eur J Appl<br />

Physiol Occup Physiol., 75, 39-46.<br />

Miyamoto T, Nakanishi Y <strong>and</strong> K<strong>in</strong>oshita H (2001). Effects of Increased<br />

Central Blood Volume on Cardio-Respiratory <strong>and</strong> Metabolic Responses<br />

dur<strong>in</strong>g Recovery after Exercise. Descente Sports Science, 22,<br />

127-138.


Effects of Recently Developed Swimwear on Drag<br />

Dur<strong>in</strong>g Front Crawl Swimm<strong>in</strong>g<br />

ogita, F., huang, Z., Kurobe, K., ozawa, G., taguchi,t.,<br />

tanaka, t.<br />

National Institute of Fitness <strong>and</strong> Sports, Japan<br />

The effect on active drag of 3 new types of swimwear compared to conventional<br />

wear was <strong>in</strong>vestigated <strong>in</strong> 8 male subjects swimm<strong>in</strong>g at different<br />

velocities to establish the drag-velocity relationship. The active drag<br />

force was directly measured dur<strong>in</strong>g front crawl swimm<strong>in</strong>g us<strong>in</strong>g a system<br />

of underwater push-off pads <strong>in</strong>strumented with a force transducer.<br />

When mean drag values were estimated for a range of swimm<strong>in</strong>g speed<br />

(1.2 to 1.8 m•s-1 Figure 1. Swimwear<br />

A<br />

used <strong>in</strong> this<br />

B<br />

experiment.<br />

C D<br />

Figure 1. Swimwear<br />

A B<br />

used <strong>in</strong> this<br />

B C<br />

experiment.<br />

C D<br />

A;<br />

A;<br />

a<br />

conventional<br />

conventional<br />

swimwear<br />

swimwear<br />

B,<br />

B,<br />

C,<br />

C,<br />

D;<br />

D;<br />

new<br />

new<br />

types<br />

types<br />

of<br />

of<br />

swimwear<br />

swimwear<br />

developed<br />

developed<br />

<strong>in</strong><br />

<strong>in</strong><br />

2008<br />

2008<br />

by<br />

by<br />

different<br />

different<br />

manufactures<br />

manufactures<br />

Measurement of active drag; The measurements were performed with a modified<br />

MAD system similar to that described by Toussa<strong>in</strong>t et al. (1988b) (Figure 2). The<br />

Measurement system similar of to active that drag; described The measurements by Toussa<strong>in</strong>t et were al. performed (1988b) (Figure with 2). The<br />

essential aspects of the apparatus <strong>and</strong> the accuracy of the collected data have been<br />

), statistically non-significant drag reduction effects of a modified aspects of MAD the apparatus system similar <strong>and</strong> the to that accuracy described of the by collected Toussa<strong>in</strong>t data et al. have been<br />

previously described <strong>in</strong> detail (Ogita et al., 2004, 2006, Toussa<strong>in</strong>t et al., 1988b). The<br />

1-5 N (2-6%) were observed for the new types of swimwear. Even if no system<br />

(1988b) described<br />

allowed<br />

(Figure <strong>in</strong><br />

the swimmer<br />

2). detail The (Ogita<br />

to<br />

essential et al.,<br />

push off<br />

aspects 2004,<br />

from fixed<br />

of 2006, the<br />

pads<br />

apparatus Toussa<strong>in</strong>t<br />

at each stroke.<br />

<strong>and</strong> et al., the 1988b).<br />

The<br />

ac- The<br />

system allowed the swimmer to push off from fixed pads at each stroke. The 15 push-<br />

major differences <strong>in</strong> drag were found among swimwear, our results sugoff<br />

pads Figure curacy were 1. Swimwear of fixed the A<br />

1.30 collected used m <strong>in</strong> this apart<br />

Bdata experiment. on have a 23 been m<br />

C<br />

horizontal previously D<br />

rod, described <strong>and</strong> the <strong>in</strong> rod detail<br />

off pads were fixed 1.30 m apart on a 23 m horizontal rod, <strong>and</strong> the rod was mounted<br />

gest that the observed reduction, even if non significant, could <strong>in</strong>deed 0.75m (Ogita below A; a conventional the et al., water 2004, surface. swimwear 2006, The Toussa<strong>in</strong>t rod was et <strong>in</strong>strumented al., 1988b). with The system a force transducer allowed<br />

0.75m below at one<br />

B, C, the D; new water types surface. of swimwear The developed rod was <strong>in</strong> <strong>in</strong>strumented 2008 by different with manufactures a force transducer at one<br />

expla<strong>in</strong> the observed competitive advantage.<br />

end of the swimmer swimm<strong>in</strong>g to pool push to off measure from fixed the push-off pads at each forces. stroke. The The force 15 signal push-<br />

end of the swimm<strong>in</strong>g pool to measure the push-off forces. The force signal was lowpass<br />

Measurement filtered off pads (30-Hz were of active fixed cut-off drag; 1.30 frequency), The m apart measurements on on-l<strong>in</strong>e a 23 m digitized were horizontal performed at 100-Hz rod, with <strong>and</strong> sampl<strong>in</strong>g a the modified rod<br />

pass filtered (30-Hz cut-off frequency), on-l<strong>in</strong>e digitized at 100-Hz sampl<strong>in</strong>g rate, <strong>and</strong><br />

Key words: active drag, swimwear, MAd system, swimm<strong>in</strong>g perfor- MAD stored system<br />

stored was on the mounted similar hard disk to<br />

hard disk 0.75m that of the described<br />

of the below notebook the by water computer. Toussa<strong>in</strong>t<br />

computer. surface. et The The al. force (1988b)<br />

force rod was signal (Figure<br />

signal <strong>in</strong>strumented pushed 2). off The<br />

pushed off from the<br />

essential<br />

mance<br />

second with aspects to the a force last of the<br />

last (15th) transducer apparatus pad at was <strong>and</strong><br />

was one time the<br />

time end accuracy <strong>in</strong>tegrated, of the swimm<strong>in</strong>g of <strong>and</strong> the collected<br />

<strong>and</strong> yielded pool to the data<br />

the measure average have<br />

average the been force. The<br />

previously mean velocity described<br />

velocity was <strong>in</strong><br />

was computed detail (Ogita<br />

computed from et al.,<br />

from the 2004,<br />

the time 2006,<br />

time taken Toussa<strong>in</strong>t<br />

taken to cover et<br />

cover the al.,<br />

the distance 1988b).<br />

distance between The<br />

push-off forces. The force signal was low-pass filtered (30-Hz cut-off between the<br />

system allowed the swimmer to push off from fixed pads at each stroke. The 15 push- the<br />

IntroductIon<br />

second frequency), <strong>and</strong> last pad on-l<strong>in</strong>e (i.e.13 digitized x 1.3 = at 16.9 100-Hz m). sampl<strong>in</strong>g For the drag rate, <strong>and</strong> measurement, stored on the<br />

the subject<br />

off pads were fixed 1.30 m apart on a 23 m horizontal rod, <strong>and</strong> the rod was mounted subject<br />

performed only arm stroke (without leg kick<strong>in</strong>g), <strong>and</strong> the legs were supported <strong>and</strong> fixed<br />

Recently (2008-2009), numerous new world records were made <strong>in</strong> com0.75m<br />

performed below hard the only disk water arm of surface. the stroke notebook (without The rod computer. was leg <strong>in</strong>strumented kick<strong>in</strong>g), The force <strong>and</strong> with the signal a legs force pushed were transducer supported off from at one <strong>and</strong> fixed<br />

petitive swimm<strong>in</strong>g. The great success has been considered to be <strong>in</strong> part end of the the swimm<strong>in</strong>g second to pool the to last measure (15th) the pad push-off was time forces. <strong>in</strong>tegrated, The force <strong>and</strong> signal yielded was the low-<br />

attributed to a reduction <strong>in</strong> drag associated with advances <strong>in</strong> the quality pass filtered average (30-Hz force. cut-off The frequency), mean velocity on-l<strong>in</strong>e was digitized computed at 100-Hz from the sampl<strong>in</strong>g time taken rate, <strong>and</strong> to<br />

of swimwear.<br />

stored on cover the hard the disk distance of the between notebook the computer. second The <strong>and</strong> force last pad signal (i.e.13 pushed x 1.3 off from = 16.9 the<br />

second to<br />

Drag consists of sk<strong>in</strong> friction, pressure drag, <strong>and</strong> wave-mak<strong>in</strong>g resis- m). the For last the (15th) drag pad measurement, was time <strong>in</strong>tegrated, the subject <strong>and</strong> yielded performed the average only arm force. stroke The<br />

mean velocity was computed from the time taken to cover the distance between the<br />

tance, <strong>and</strong> total drag equals to the sum of those factors (Toussa<strong>in</strong>t et al., (without leg kick<strong>in</strong>g), <strong>and</strong> the legs were supported <strong>and</strong> fixed together by<br />

second <strong>and</strong> last pad (i.e.13 x 1.3 = 16.9 m). For the drag measurement, the subject<br />

2000). Previously, it was assumed that friction drag was negligible (5% the same pull buoy (buoyant force 15.7N).<br />

performed only arm stroke (without leg kick<strong>in</strong>g), <strong>and</strong> the legs were supported <strong>and</strong> fixed<br />

of total drag) given the high Reynolds numbers (>105) that occur dur<strong>in</strong>g<br />

swimm<strong>in</strong>g (Toussa<strong>in</strong>t et al., 1988b). However, later War<strong>in</strong>g (1999) sug- Figure<br />

Figure<br />

2.<br />

2.<br />

Schematic<br />

Schematic<br />

side<br />

side<br />

view<br />

view<br />

of<br />

of<br />

system<br />

system<br />

to<br />

to<br />

measure<br />

measure<br />

active<br />

active<br />

drag<br />

drag<br />

(MAD<br />

(MAD<br />

system)<br />

system)<br />

used<br />

used<br />

<strong>in</strong><br />

<strong>in</strong><br />

this<br />

this<br />

study.<br />

study.<br />

gested that a significant reduction <strong>in</strong> total drag could be accomplished<br />

by reduc<strong>in</strong>g pressure drag by the use of vortex generators m<strong>in</strong>imiz<strong>in</strong>g<br />

separated flow.<br />

Over the last decade, swimwear manufacturers have tried further<br />

development of special fabrics <strong>and</strong> surface treatments of swimwear<br />

which supposedly reduce drag. The manufacturer which has developed<br />

the swimwear used by the most swimmers <strong>in</strong> the Beij<strong>in</strong>g Olympics<br />

claimed that swimmers can reduce (passive) drag by 10% when wear<strong>in</strong>g<br />

the new type of swimwear. However, it is probably <strong>in</strong>correct to assume<br />

that results obta<strong>in</strong>ed by passive measurement are directly applicable to<br />

those by active measurement (Toussa<strong>in</strong>t et al., 2000). Therefore, <strong>in</strong> the<br />

present study, the total active drag obta<strong>in</strong>ed when wear<strong>in</strong>g new types of<br />

swimwear were compared to those evoked when wear<strong>in</strong>g conventional<br />

swimwear.<br />

Methods<br />

Subjects; The subjects were 8 well-tra<strong>in</strong>ed male college swimmers.Their<br />

mean (±SD) age, height, body mass, <strong>and</strong> maximal oxygen uptake (VO-<br />

2<br />

max) were 20(±1) yrs, 1.68 (±0.04) m, 64.0 (±5.2) kg, 4.17(±0.36)<br />

l•m<strong>in</strong> -1 , <strong>and</strong> 65.8 (±4.7) ml•kg -1 •m<strong>in</strong> -1 , respectively. Each subject was<br />

fully <strong>in</strong>formed of the purposes, protocol, <strong>and</strong> procedures of this experiment,<br />

<strong>and</strong> any risks, <strong>and</strong> voluntarily participated <strong>in</strong> this study.<br />

Swimwear; To evaluate the effects of differences <strong>in</strong> swimwear on total<br />

drag, a conventional swimwear (box type: A) <strong>and</strong> 3 new types of swimwear<br />

(long type: B, C, D) which was developed <strong>in</strong> 2008 were used <strong>in</strong> this<br />

experiment (see Figure 1).<br />

(±0.04) m, 64.0 (±5.2) kg, 4.17(±0.36) l•m<strong>in</strong><br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

-1 , <strong>and</strong> 65.8 (±4.7) ml•kg -1 •m<strong>in</strong> -1 age, height, body mass, <strong>and</strong> maximal oxygen uptake (VO2max) were 20(±1) yrs, 1.68<br />

(±0.04) m, 64.0 (±5.2) kg, 4.17(±0.36) l•m<strong>in</strong> ,<br />

respectively. Each subject was fully <strong>in</strong>formed of the purposes, protocol, <strong>and</strong> procedures<br />

of this experiment, <strong>and</strong> any risks, <strong>and</strong> voluntarily participated <strong>in</strong> this study.<br />

Swimwear; To evaluate the effects of differences <strong>in</strong> swimwear on total drag, a<br />

conventional swimwear (box type: A) <strong>and</strong> 3 new types of swimwear (long type: B, C,<br />

D) which was developed <strong>in</strong> 2008 were used <strong>in</strong> this experiment (see Figure 1).<br />

-1 , <strong>and</strong> 65.8 (±4.7) ml•kg -1 •m<strong>in</strong> -1 55 ,<br />

respectively. Each subject was fully <strong>in</strong>formed of the purposes, protocol, <strong>and</strong> procedures<br />

of this experiment, <strong>and</strong> any risks, <strong>and</strong> voluntarily participated <strong>in</strong> this study.<br />

drag obta<strong>in</strong>ed Swimwear; when To wear<strong>in</strong>g evaluate new the types effects of swimwear of differences were compared <strong>in</strong> swimwear to those on evoked total drag, a<br />

when conventional wear<strong>in</strong>g conventional swimwear swimwear. (box type: A) <strong>and</strong> 3 new types of swimwear (long type: B, C,<br />

D) which was developed <strong>in</strong> 2008 were used <strong>in</strong> this experiment (see Figure 1).<br />

METHODS<br />

Subjects; The subjects were 8 well-tra<strong>in</strong>ed male college . swimmers. Their mean (±SD)<br />

age, height, body mass, <strong>and</strong> maximal oxygen uptake (VO2max)<br />

were 20(±1) yrs, 1.68<br />

(±0.04) m, 64.0 (±5.2) kg, 4.17(±0.36) l•m<strong>in</strong> -1 , <strong>and</strong> 65.8 (±4.7) ml•kg -1 •m<strong>in</strong> -1 ,<br />

respectively. Each subject was fully <strong>in</strong>formed of the purposes, protocol, <strong>and</strong> procedures<br />

of this experiment, <strong>and</strong> any risks, <strong>and</strong> voluntarily participated <strong>in</strong> this study.<br />

Swimwear; To evaluate the effects of differences <strong>in</strong> swimwear on total drag, a<br />

conventional swimwear (box type: A) <strong>and</strong> 3 new types of swimwear (long type: B, C,<br />

D) which was developed <strong>in</strong> 2008 were used <strong>in</strong> this experiment (see Figure 1).<br />

Figure 2. Schematic side view of system to measure active drag (MAD system) used <strong>in</strong> this study.<br />

To measure drag <strong>and</strong> to establish the relationship between drag <strong>and</strong><br />

swimm<strong>in</strong>g velocity, the subjects were asked to swim 25 m more than<br />

10 times at different but constant velocities (range 0.80-1.90 m•s -1 ). At<br />

constant swimm<strong>in</strong>g velocity the mean propulsive force is equal to the<br />

mean drag force (Fd) (Toussa<strong>in</strong>t 1988b). On each trial, mean Fd <strong>and</strong><br />

mean swimm<strong>in</strong>g velocity (v) were calculated. These v <strong>and</strong> Fd data were<br />

least-squares fitted to the function:<br />

Fd = A•vn<br />

where, A <strong>and</strong> n are constants of proportionality, <strong>and</strong> were respectively<br />

adopted as drag coefficient <strong>and</strong> drag exponent <strong>in</strong> this study.<br />

All subjects used the same 4 types of swimwear (i.e. one conventional<br />

<strong>and</strong> 3 new, developed <strong>in</strong> 2008), <strong>and</strong> the order of test<strong>in</strong>g of each<br />

swimwear was r<strong>and</strong>omized. All measurements for each subject were<br />

completed <strong>in</strong> the same day.<br />

Evaluation of effect on drag; The A <strong>and</strong> n obta<strong>in</strong>ed with each swimwear<br />

were computed for each subject. These fitted functions were used<br />

to estimate the drag at three different velocities (1.2, 1.5, 1.8 m•s -1 ). The<br />

effect on drag was evaluated by compar<strong>in</strong>g the estimated drag among 4<br />

types of swimwear. Intra-<strong>in</strong>dividual differences (<strong>in</strong> %) with respect to<br />

the drag when wear<strong>in</strong>g conventional swimwear were also calculated at<br />

the three velocities studied.<br />

Statistics; All data were expressed by mean <strong>and</strong> SD or <strong>in</strong>dividual<br />

value. Two-way analysis of variance with repeated measures was used<br />

to test the difference <strong>in</strong> estimated drag values among 4 conditions by<br />

211


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

swimwear condition <strong>and</strong> velocity. Also one-way analysis of variance with<br />

repeated measures was used to test the difference <strong>in</strong> A <strong>and</strong> n among<br />

swimwear conditions. When <strong>in</strong>teractions reached statistical significance,<br />

then Scheffe’s post-hoc test was used to identify the difference <strong>in</strong> mean<br />

values among swimwear conditions. The 0.05 level of significant was<br />

used.<br />

results<br />

In Figure 3, the drag curves (group average) are presented. The drag<br />

curves when wear<strong>in</strong>g new types of swimwear were slightly lower than<br />

that when wear<strong>in</strong>g conventional swimwear, but no difference <strong>in</strong> drag<br />

was observed among new types swimwear. Statistics of the fitted curves<br />

for all subjects are presented <strong>in</strong> Table 1. From the fitted curves, estimations<br />

were made for the drag at velocities of 1.2, 1.5, <strong>and</strong> 1.8 m•s -1 . The<br />

results of parameters were presented <strong>in</strong> Table 2.<br />

Table 1. Table Statictics 1�DStatictics describ<strong>in</strong>g describ<strong>in</strong>g the fitted the curves fitted curves of the drag of the dependent drag dependent on velocity. on velocity.<br />

Subject<br />

A B<br />

A<br />

C D A B<br />

n<br />

C D<br />

TI 27.8 26.2 29.0 27.3 2.08 2.05 1.78 1.95<br />

HY 23.8 20.6 21.3 21.9 2.05 2.15 2.12 2.11<br />

JF 22.5 25.0 22.4 24.1 2.08 1.74 2.03 1.79<br />

KS 19.6 20.7 20.4 20.6 2.29 2.13 2.06 2.10<br />

AN 22.0 21.1 22.9 21.7 1.89 2.00 1.97 2.06<br />

YH 23.5 21.7 20.4 21.6 2.08 2.06 2.22 2.16<br />

HA 23.7 25.5 24.8 25.5 2.22 2.03 2.05 2.03<br />

SY 26.7 23.0 23.1 23.3 2.01 2.17 2.23 2.17<br />

mean 23.7 23.0 23.0 23.3 2.09 2.04 2.06 2.05<br />

SD 2.6 2.3 2.8 2.3 0.12 0.14 0.14 0.13<br />

212<br />

A = coeeficient of proportionality; n = power of the velocity<br />

A, B, C, D = sort of swimwear (see Figure 1)<br />

As the results show, neither A nor n differed significantly among<br />

swimwear conditions. Although the estimated values of drag at swimm<strong>in</strong>g<br />

velocities of 1.2, 1.5, <strong>and</strong> 1.8 m•s-1 were lower by 1-5 N (2-6%)<br />

<strong>in</strong> 3 new types of swimwear than those <strong>in</strong> conventional wear, the differences<br />

<strong>in</strong> drag were not statistically significant at all velocities among<br />

swimwear conditions, either. Therefore, no significant drag reduction<br />

effect of new types of swimwear could be detected. When compared,<br />

the estimated drag values at the same velocity among the new types of<br />

swimwear, the difference was quite small <strong>and</strong> less than 1.5%.<br />

Table 2. Mean values of estimated drag at velocities of 1.2, 1.5, <strong>and</strong> 1.8 m¥s -1 swimm<strong>in</strong>g with each swimwear<br />

1.2 m¥s -1<br />

1.5 m¥s -1<br />

1.8 m¥s -1<br />

swimwear<br />

drag % diff. drag % diff. drag % diff.<br />

A 34.7 ± 3.4 55.2 ± 5.7 80.8 ± 8.6<br />

B 33.7 ± 2.8 -3.6 ± 6.7 52.5 ± 4.7 -4.7 ± 4.1 76.2 ± 7.3 -5.5 ± 3.8<br />

C 33.5 ± 3.1 -3.3 ± 6.1 52.9 ± 4.4 -4.0 ± 5.2 76.9 ± 6.0 -4.4 ± 6.4<br />

D 33.5 ± 3.2 -2.4 ± 5.2 53.2 ± 4.4 -3.3 ± 4.2 77.3 ± 6.5 -4.0 ± 5.7<br />

(unit; Newtons)<br />

%diff. refers to difference between drag while swimm<strong>in</strong>g with swimwear A <strong>and</strong> drag while swimm<strong>in</strong>g with other<br />

swimwear (B,C,D)<br />

dIscussIon<br />

Several studies have <strong>in</strong>vestigated whether newly developed swimwear<br />

could br<strong>in</strong>g some advantage (i.e. a reduction of drag or energy expenditure)<br />

for competitive swimm<strong>in</strong>g performance. Some have shown a<br />

significant reduction <strong>in</strong> drag or energy expenditure by wear<strong>in</strong>g experimental<br />

swimwear (Benjanuvatra et al., 2002, Chatard <strong>and</strong> Wilson, 2008,<br />

Mollendorf et al., 2004), support<strong>in</strong>g the claim of the manufactures, but<br />

some have not (Ogita et al. 1996, Robert et al., 2003, Toussa<strong>in</strong>t et al.,<br />

2002). The f<strong>in</strong>d<strong>in</strong>gs of this experiment are <strong>in</strong> agreement with the latter<br />

results, <strong>in</strong>dicat<strong>in</strong>g that a drag reduction effect of only 2-6%, but not statistically<br />

significant, was observed for newly developed swimwear.<br />

In competitive swimm<strong>in</strong>g events, the difference between w<strong>in</strong> <strong>and</strong><br />

loss may be 0.01 s. Therefore, a small reduction <strong>in</strong> active drag would be<br />

very important for swimmers to improve their performance. The reduction<br />

<strong>in</strong> drag by wear<strong>in</strong>g newly developed swimwear was not significant,<br />

however, a drag reduction of 2-6% on average was observed. To what<br />

extent can such small difference <strong>in</strong> drag contribute to improve swimm<strong>in</strong>g<br />

performance?<br />

The rate of energy expenditure (E) dur<strong>in</strong>g swimm<strong>in</strong>g is a function<br />

of the power to overcome drag (Pd), gross efficiency (eg), <strong>and</strong> propell<strong>in</strong>g<br />

efficiency (ep) (Toussa<strong>in</strong>t <strong>and</strong> Holl<strong>and</strong>er 1994).<br />

E = Pd / (ep • eg) (Eq.1)<br />

In turn, Pd can be calculated from the product of drag (Fd) <strong>and</strong> velocity<br />

(v). Furthermore, Fd is given by;<br />

Fd = Avn (Eq.2)<br />

Therefore;<br />

E = Fd•v / (ep•eg) = Avn•v / (ep•eg) = Avn+1 / (ep•eg) (Eq.3)<br />

Integration of this equation gives the energy expenditure (E) to swim a<br />

certa<strong>in</strong> distance (d) at a given velocity or <strong>in</strong> a certa<strong>in</strong> time (t);<br />

E = Avn•d / (eg•ep) = Ad n+1 / (ep•eg•t n ) (Eq.4)<br />

The energy cost required to swim the 100, 200, <strong>and</strong> 400m was then calculated<br />

based on the values of A <strong>and</strong> n measured <strong>in</strong> this study (right side<br />

of Eq.4) <strong>and</strong> by assum<strong>in</strong>g eg <strong>and</strong> ep equal to 9% <strong>and</strong> 65%, respectively<br />

(Huang et al., 2007, Toussa<strong>in</strong>t et al., 1988a).<br />

Based on our previous results (Ogita 2003), the energy dem<strong>and</strong>s for<br />

the 100, 200, <strong>and</strong> 400m competitive races were assumed equal to 170%,<br />

120%, <strong>and</strong> 100%VO2max, respectively. The energy supply as a function<br />

of time for each competitive distance (left side of Eq.4) was computed<br />

by the product of swimm<strong>in</strong>g time <strong>and</strong> energy dem<strong>and</strong> for each competitive<br />

distance based on the VO2max of each subject (see Subjects section<br />

<strong>in</strong> Methods). F<strong>in</strong>ally, the best time to swim the competitive distances<br />

can be predicted by determ<strong>in</strong><strong>in</strong>g the <strong>in</strong>tersection of the time dependent<br />

energy cost to swim these distances (right side of Eq.4) with time dependent<br />

energy supply (left side of Eq.4). In this regard, <strong>in</strong>fluences of<br />

the dive <strong>and</strong> turn(s) on performance time are not considered for this<br />

calculation.<br />

Table 3 shows the predicted best times for each competitive distance<br />

when swimm<strong>in</strong>g with each swimwear. The best times predicted when<br />

swimm<strong>in</strong>g with new types of swimwear were faster by 0.7-1.0s <strong>in</strong> 100m,<br />

by 1.5-2.1 s <strong>in</strong> 200m, <strong>and</strong> 2.8-4.2 s <strong>in</strong> 400m than those when swimm<strong>in</strong>g<br />

with conventional swimwear. Of course, the time differences observed<br />

among swimwear were not statistically significant because there are no<br />

significant differences <strong>in</strong> the values of drag used for this calculation.<br />

However, when the average times for f<strong>in</strong>alists of 200m <strong>and</strong> 400m free<br />

style event both for men <strong>and</strong> women between World Championship <strong>in</strong><br />

2007 <strong>and</strong> <strong>in</strong> 2009 were compared, similar time differences were observed<br />

(200m; 2.0-2.2 s, 400m; 2.7-3.0 s). Therefore, the differences <strong>in</strong> the predicted<br />

best records seem to be quite reasonable results, suggest<strong>in</strong>g a large<br />

advantage of new types of swimm<strong>in</strong>g wear for swimm<strong>in</strong>g performance.<br />

Table 3. Estimated best times for the 100m, 200m, amd 400m when swimm<strong>in</strong>g with each swimwear.<br />

A B C D<br />

100m 57Ó9 ± 2"6 56"9 ± 2"3 57"1 ± 2"0 57"2 ± 2"3<br />

200m 2' 04"5 ± 5"5 2' 02"4 ± 4"7 2' 02"8 ± 4"1 2' 03"0 ± 4"7<br />

400m 4' 24"1 ± 11"5 4' 19"9 ± 9"5 4 '20"7 ± 8"5 4' 21"3 ± 9"7<br />

A: conventional swimwear, B, C, D,: new types of swimwear<br />

(m<strong>in</strong>' sec")<br />

conclusIon<br />

Even if no major differences <strong>in</strong> drag were found among swimwear, our<br />

results suggest that the observed 2-6% reduction, even if non significant,<br />

could <strong>in</strong>deed expla<strong>in</strong> the observed competitive advantage.<br />

reFerences<br />

Benjanuvatra, N., Dawson, G., Blanksby, B.A. & Elliott, B.C. (2002).<br />

Comparison of buoyancy, passive <strong>and</strong> net active drag forces between<br />

fastsk<strong>in</strong> <strong>and</strong> st<strong>and</strong>ard swimsuits. J Sci Med Sports, 5, 115-123.<br />

Chatard, J.-C. & Wilson B. (2008). Effect of Fastsk<strong>in</strong> suits on performance,<br />

drag, <strong>and</strong> energy cost of swimm<strong>in</strong>g. Med Sci Sports Exerc, 40,<br />

1149-1154.


Huang, Z., Tanaka, T. & Ogita, F. (2008). Propell<strong>in</strong>g efficiency <strong>in</strong> elite<br />

Japanese female swimmers. Proceed<strong>in</strong>gs of Annual meet<strong>in</strong>g of Japanese<br />

Society of Sciences <strong>in</strong> Swimm<strong>in</strong>g <strong>and</strong> Water Exercise, 70-73 (<strong>in</strong> Japanese).<br />

Mollendorf, J.C., Term<strong>in</strong>, A.C.,II, Oppenheim, E. & Pendergast D.R.<br />

(2004). Effect of swim suit design on passive drag. Med Sci Sports<br />

Exerc, 36, 1029 -1035.<br />

Ogita, F., Tanaka, T., Tamaki, H., Wagatsuma, A., Hamaoka, T. &<br />

Toussa<strong>in</strong>t H.M. (2006). Metabolic <strong>and</strong> mechanical characteristics<br />

of Olympic female gold medalist. In: Vilas-Boas J.P., Alves F., &<br />

Marques A. (eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X, Porto;<br />

Portuguese journal of sport sciences 6, Suppl 2, 194-197.<br />

Ogita, F, Tamaki, H., Wagatsuma, A. & Maeda, A. (2004). The determ<strong>in</strong>ants<br />

of swimm<strong>in</strong>g performance – from the mechanical <strong>and</strong> metabolic<br />

analysis with MAD system. Decent Sports Science, 25, 122-130.<br />

(<strong>in</strong> Japanese with English abstract)<br />

Ogita, F., Onodera, T., Tamaki, H., Toussa<strong>in</strong>t, H.M., Holl<strong>and</strong>er, A.P.<br />

& Wakayoshi K. (2003). Metabolic profile dur<strong>in</strong>g exhaustive arm<br />

stroke, leg kick, <strong>and</strong> whole body swimm<strong>in</strong>g last<strong>in</strong>g 15s to 10 m<strong>in</strong>.<br />

In: Chatard J.-C. (ed), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX, ,<br />

Sa<strong>in</strong>t-Etienne, 361-366.<br />

Ogita, F., Tanaka, T. & Taguchi, N. (1996). The effects of the difference<br />

of material, size <strong>and</strong> cutt<strong>in</strong>g type of swimm<strong>in</strong>g wear on energy<br />

expenditure dur<strong>in</strong>g swimm<strong>in</strong>g. Decent Sports Science, 17, 101-112. (<strong>in</strong><br />

Japanese with English abstract)<br />

Roberts, B.S., Kamel, K.S., Hedrick, C.E., Mclean, S.P. & Sharp R.L.<br />

(2003). Effect of a Fastsk<strong>in</strong> TM suit on submaximal freestyle swimm<strong>in</strong>g.<br />

Med Sci Sports Exerc, 35, 519-524.<br />

Toussa<strong>in</strong>t, H.M., Truijens, M., Elz<strong>in</strong>ga, M.-J., van de Ven A., de Best<br />

H., Snabel B. & de Groot G. (2002). Effect of a Fast-sk<strong>in</strong> TM ‘body’<br />

suit on drag dur<strong>in</strong>g front crawl swimm<strong>in</strong>g. Sports Biomech, 1,1-10.<br />

Toussa<strong>in</strong>t, H.M., Holl<strong>and</strong>er, A.P., van den Berg C. & Vorontsov, A.R.<br />

(2000). <strong>Biomechanics</strong> of swimm<strong>in</strong>g. In: Garret W.E., & Kirkendall<br />

D.T. (eds.), Exercise <strong>and</strong> Sports Science (pp, 639-660). Philadelphia:<br />

Lipp<strong>in</strong>cott, Williams <strong>and</strong> Wilk<strong>in</strong>s.<br />

Toussa<strong>in</strong>t, H.M. & Holl<strong>and</strong>er, A.P. (1994). Energetics of competitive<br />

swimm<strong>in</strong>g, Implications for tra<strong>in</strong><strong>in</strong>g programmes. Sports Med, 18,<br />

384-405.<br />

Toussa<strong>in</strong>t, H.M., Beelen, A., Rodenburg, A., Sargeant, A.J., de Groot,<br />

G., Holl<strong>and</strong>er A.P. & van Ingen Schenau G.J. (1988a). Propell<strong>in</strong>g<br />

efficiency of front-crawl swimm<strong>in</strong>g. J Appl Physiol, 65, 2506-2512.<br />

Toussa<strong>in</strong>t, H.M., de Groot, G., Savelberg H.H.C.M., Vervoorn, K.,<br />

Holl<strong>and</strong>er, A.P. & van Ingen Schenau, G.J. (1988b). Active drag related<br />

to velocity <strong>in</strong> male <strong>and</strong> female swimmers. J Biomech, 21, 435-<br />

438.<br />

War<strong>in</strong>g, J. (1999). Reduction of drag of a submerged swimmer us<strong>in</strong>g<br />

vortex generators. MSc. thesis, Carleton University, Ottawa, Ontario,<br />

Canada.<br />

AcKnoWledGeMents<br />

This study is partly supported by a Grant-<strong>in</strong>-Aid for THE DESCEN-<br />

TE AND ISHIMOTO MEMORIAL FOUNDATION FOR THE<br />

PROMOTION OF SPORTS SCIENCE.<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

Relationship between Heart Rate <strong>and</strong> Water Depth <strong>in</strong><br />

the St<strong>and</strong><strong>in</strong>g Position<br />

onodera, s. 1 , Yoshioka, A. 1 , Matsumoto, n. 1 , takahara, t. 1 ,<br />

nose, Y. 1 , hirao, M. 1 , seki, K. 2 , nishimura, K. 3 , Baik, W. 1 ,<br />

hara, h. 4 , Murakawa, t. 5<br />

1 Kawasaki University of Medical Welfare, Kurashiki City, Japan<br />

2 University of Market<strong>in</strong>g <strong>and</strong> Distribution Sciences, Kobe City, Japan<br />

3 Hirosima Institute of Technology, Hiroshima City, Japan<br />

4 Kokugaku<strong>in</strong> University, Yokohama City, Japan<br />

5 Tokai University, Hiratsuka City, Japan<br />

The purpose of this study was to clarify the relationship between heart<br />

rate <strong>and</strong> water depth dur<strong>in</strong>g st<strong>and</strong><strong>in</strong>g submersion. Seven volunteers participated<br />

<strong>in</strong> this study. Subjects were <strong>in</strong> a st<strong>and</strong><strong>in</strong>g position, <strong>in</strong> a test<br />

tank, for n<strong>in</strong>e conditions of water depth. The water temperature was<br />

34ºC. Heart rate significantly decreased dur<strong>in</strong>g <strong>in</strong>crease of water depth,<br />

<strong>and</strong> significantly <strong>in</strong>creased dur<strong>in</strong>g decrease of water depth. The changes<br />

<strong>in</strong> heart rate were statistically different (ANOVA, P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

Fig. 1 shows the k<strong>in</strong>etics of the heart rate <strong>in</strong> each condition of water<br />

depth. Heart rate significantly decreased dur<strong>in</strong>g <strong>in</strong>crease of water depth<br />

(on l<strong>and</strong>: 80 (SD: 9) b/m, knee jo<strong>in</strong>t: 73 (SD: 7) b/m, greater trochanter:<br />

70 (SD: 7) b/m, xiphoid process: 63 (SD: 7) b/m, under the collarbone:<br />

62 (SD: 9) b/m). In the other h<strong>and</strong>, heart rate significantly <strong>in</strong>creased<br />

dur<strong>in</strong>g decrease of water depth (xiphoid process: 62 (SD: 4) b/m, greater<br />

trochanter: 64 (SD: 9) b/m, knee jo<strong>in</strong>t: 68 (SD: 5) b/m, on l<strong>and</strong>: 77 (SD:<br />

8) b/m). The changes <strong>in</strong> heart rate were statistically different (ANOVA,<br />

P


Oxygen Uptake K<strong>in</strong>etics Around the Respiratory<br />

Compensation Po<strong>in</strong>t <strong>in</strong> Swimm<strong>in</strong>g<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

study was to describe VO2 k<strong>in</strong>etics throughout the heavy <strong>and</strong> severe<br />

exercise doma<strong>in</strong>s dur<strong>in</strong>g front-crawl swimm<strong>in</strong>g, consider<strong>in</strong>g RCP as the<br />

transition parameter between them.<br />

Pessôa Filho, d.M.<br />

215<br />

1 , reis, J.F. 2 , Alves, F.B. 2 , denadai, B.s. 1<br />

1Paulista State University, Brazil<br />

2Faculty of Human K<strong>in</strong>etics, Technical University of Lisbon, Portugal<br />

The purpose of this study was to describe VO2 k<strong>in</strong>etics throughout the<br />

heavy <strong>and</strong> severe doma<strong>in</strong>s dur<strong>in</strong>g swimm<strong>in</strong>g. N<strong>in</strong>e swimmers completed<br />

two swimm<strong>in</strong>g tests to measure the condition<strong>in</strong>g <strong>in</strong>dexes (ventilatory<br />

threshold (VT), respiratory compensation po<strong>in</strong>t (RCP), <strong>and</strong> VO2max )<br />

<strong>and</strong> VO2 k<strong>in</strong>etics (two trials <strong>in</strong>tensities set at 2.5% below <strong>and</strong> above the<br />

crawl velocity at RCP, last<strong>in</strong>g 420s). In both cases, a portable breathby-breath<br />

system connected to a respiratory snorkel <strong>and</strong> valve was used.<br />

The trial below RCP elicited only a sub-maximal rate (91.6±5.7%VO-<br />

2max ), with a slow component of 391ml·m<strong>in</strong>-1 beg<strong>in</strong>n<strong>in</strong>g after 154s. The<br />

trial above RCP showed a time delay of 188s for the slow component<br />

(399ml·m<strong>in</strong>-1 Method<br />

Subjects: N<strong>in</strong>e well-tra<strong>in</strong>ed male swimmers (21.0 ± 7.2 yr, 68.6 ± 9.2 kg,<br />

178.2 ± 6.4 cm, 13.2 ± 4.1% body fat, <strong>and</strong> ~4.0 ± 0.7 L.m<strong>in</strong><br />

), elicit<strong>in</strong>g a rate of 104.6±9.5%VO2max . Thus, expected<br />

VO2 k<strong>in</strong>etics for heavy <strong>and</strong> severe doma<strong>in</strong>s was characterized<br />

around RCP.<br />

Key-word: Vo2 k<strong>in</strong>etics, heavy <strong>and</strong> severe doma<strong>in</strong>s, respiratory compensation<br />

po<strong>in</strong>t<br />

IntroductIon<br />

The boundary between heavy <strong>and</strong> severe exercise denotes a considerable<br />

change <strong>in</strong> exercise tolerance. Accord<strong>in</strong>g to Jones & Poole (2005), the<br />

upper boundary for the heavy doma<strong>in</strong> is def<strong>in</strong>ed as the highest exercise<br />

<strong>in</strong>tensity <strong>in</strong> which oxygen uptake (VO2 ) <strong>and</strong> blood lactate concentration<br />

([lactate]) can be ma<strong>in</strong>ta<strong>in</strong>ed at an elevated but steady-state level.<br />

By def<strong>in</strong>ition, both critical power (CP: the asymptote of the power (P)<br />

–time (t) relationship, represents the limit<strong>in</strong>g parameter to the aerobic<br />

supply, compris<strong>in</strong>g the notion that if P ≤ CP, the anaerobic supply is<br />

never required, <strong>and</strong> endurance time is <strong>in</strong>f<strong>in</strong>itely long – Morton, 2006)<br />

<strong>and</strong> maximal lactate steady-state (MLSS: highest constant workload<br />

that can be ma<strong>in</strong>ta<strong>in</strong>ed over time without cont<strong>in</strong>uous blood lactate accumulation<br />

– Beneke, 2003) match the physiological responses encompassed<br />

<strong>in</strong> the upper boundary of the heavy doma<strong>in</strong>.<br />

However, CP <strong>in</strong>tensity cannot be ma<strong>in</strong>ta<strong>in</strong>ed without a substantial<br />

<strong>in</strong>crease <strong>in</strong> blood lactate concentration, <strong>and</strong> other physiological parameters<br />

(Pr<strong>in</strong>gle & Jones, 2002; Dekerle et al., 2003). Comparisons between<br />

the CP <strong>and</strong> power associated to MLSS suggest that both are different<br />

<strong>and</strong> should not be used <strong>in</strong>terchangeably (Pr<strong>in</strong>gle & Jones, 2002). Moreover,<br />

the critical swimm<strong>in</strong>g velocity (CV), correspond<strong>in</strong>g to the slope<br />

of the distance–time relationship (Sd–t), lies with<strong>in</strong> the severe <strong>in</strong>tensity<br />

doma<strong>in</strong> with the physiological responses characteriz<strong>in</strong>g the heavy <strong>and</strong><br />

severe <strong>in</strong>tensity doma<strong>in</strong>s when swimm<strong>in</strong>g 5% slower <strong>and</strong> 5% faster than<br />

Sd-t, respectively (Dekerle et al., 2009). The dependence of the P-t relationship<br />

on the choice of predictive trials may expla<strong>in</strong> the mis<strong>in</strong>terpretation<br />

of its mathematical def<strong>in</strong>ition as the highest work rate that can be<br />

ma<strong>in</strong>ta<strong>in</strong>ed for a very long time without fatigue (Dekerle et al., 2009).<br />

Exercis<strong>in</strong>g at 50% of the difference between the mode-specific LT<br />

<strong>and</strong> VO2max (50%ΔVO2) is an alternative <strong>in</strong>dex to the transition between<br />

heavy <strong>and</strong> severe doma<strong>in</strong>s ( Jones & Poole, 2005). Surpris<strong>in</strong>gly,<br />

whereas the LT has been estimated from gas-exchange responses as<br />

ventilatory threshold (VT: ris<strong>in</strong>g <strong>in</strong> the VE/VO2 curve with no change<br />

<strong>in</strong> the VE/VCO2 curve – Beaver et al., 1986), the respiratory compensation<br />

po<strong>in</strong>t (RCP: po<strong>in</strong>t <strong>in</strong> the plot of VE vs. VCO2 where VE rises<br />

more rapidly <strong>in</strong> a phase of relative hyperventilation - Beaver et al., 1986)<br />

for metabolic acidosis <strong>and</strong> buffer<strong>in</strong>g events <strong>in</strong> the tissues, has not clearly<br />

demarcated the upper boundary of the heavy doma<strong>in</strong>. Although no significant<br />

differences were obta<strong>in</strong>ed between VO2 <strong>and</strong> power output at<br />

CP <strong>and</strong> RCP <strong>in</strong> cycl<strong>in</strong>g (Dekerle et al., 2003). Thus, the purpose of this<br />

-1 VO2max )<br />

participated of this study. All subjects were advised to tests protocols<br />

<strong>and</strong> gave written consent. This research was approved by the local Ethics<br />

Committee.<br />

Experimental design: The subjects were required to perform three<br />

stages of experimentation. The first stage <strong>in</strong>volved the determ<strong>in</strong>ation<br />

of VT, RCP <strong>and</strong> VO2max . The second stage <strong>in</strong>volved two swimm<strong>in</strong>g<br />

sessions with the subjects perform<strong>in</strong>g two repetitions of square-wave<br />

transitions, from rest to one of two exercise <strong>in</strong>tensities set at 2.5% below<br />

(v-2.5% ) <strong>and</strong> above (v +2.5% ) the velocity at RCP, correspond<strong>in</strong>g to 36.3 ±<br />

7.0% <strong>and</strong> 74.1 ± 11.4% of the delta between velocity at VT <strong>and</strong> VO2max .<br />

No more than two transitions were completed <strong>in</strong> one day, with at least<br />

1h of recovery between transitions. All the procedures were not extended<br />

beyond 3–4 weeks for each subject, <strong>and</strong> the study was completed <strong>in</strong><br />

about eight weeks. All tests were performed <strong>in</strong> a 50-m <strong>in</strong>door swimm<strong>in</strong>g<br />

pool. Dur<strong>in</strong>g the exercise tests, pulmonary gas exchange was determ<strong>in</strong>ed<br />

breath-by-breath with a portable automated system (K4b2, Cosmed),<br />

which was calibrated before each test, <strong>and</strong> connected to the swimmer<br />

by a special respiratory snorkel <strong>and</strong> valve system, previously validated by<br />

Kesk<strong>in</strong>en et al. (2002).<br />

Incremental protocol: Subjects performed an <strong>in</strong>termittent <strong>in</strong>cremental<br />

test (300-m stages) to exhaustion. The velocity <strong>in</strong>crements were del<strong>in</strong>eated<br />

to four or five percentages designed to atta<strong>in</strong> the 400-m maximal swimm<strong>in</strong>g<br />

velocity at the last stage. The breath-by-breath VO2 responses were<br />

smoothed <strong>and</strong> averaged every 30s. VO2max was calculated as the highest<br />

30s value achieved dur<strong>in</strong>g the <strong>in</strong>cremental test. The swimm<strong>in</strong>g velocity<br />

related to the VO2max (vVO2max ) was def<strong>in</strong>ed as the lowest velocity that<br />

elicited VO2max (Demarie et al. 2001). The lower <strong>and</strong> upper boundary for<br />

heavy <strong>in</strong>tensity doma<strong>in</strong>s were determ<strong>in</strong>ed from gas exchange responses at<br />

VT <strong>and</strong> RPC respectively, follow<strong>in</strong>g the recommendations of Beaver et<br />

al. (1986). VT was exam<strong>in</strong>ed visually us<strong>in</strong>g plots of VE /VCO2 , VE /VO2 ,<br />

end-tidal PCO2 (PETCO2 ) <strong>and</strong> end-tidal PO2 (PETO2 ). The criteria used<br />

for determ<strong>in</strong>ation of VT <strong>and</strong> RCP were a non-l<strong>in</strong>ear <strong>in</strong>crease <strong>in</strong> VE/VO2 <strong>and</strong> PETO2 curves without a correspond<strong>in</strong>g change <strong>in</strong> VE/VCO2 <strong>and</strong><br />

PETCO2 curves; <strong>and</strong> an <strong>in</strong>crease <strong>in</strong> both VE/VO2 <strong>and</strong> VE/VCO2 <strong>and</strong> a<br />

decrease <strong>in</strong> PETCO2 , respectively. VT <strong>and</strong> RCP location po<strong>in</strong>t were estimated<br />

by two <strong>in</strong>dependent observers. The highest 30-s average VO2 for<br />

these steps was considered the VO2 at VT <strong>and</strong> RCP.<br />

VO2 k<strong>in</strong>etic model<strong>in</strong>g: Subjects performed two repetitions of squarewave<br />

transitions of 7 m<strong>in</strong> duration at the two exercise <strong>in</strong>tensities on<br />

separate days. After a 3-4 m<strong>in</strong> warm-up at a low swimm<strong>in</strong>g velocity<br />

followed by 5 m<strong>in</strong> of rest, the subjects were <strong>in</strong>structed to perform the<br />

required <strong>in</strong>tensity. Intensities were set at 2.5% below <strong>and</strong> above the velocity<br />

at RCP, which corresponded to 1.35 ± 0.05 m·s-1 <strong>and</strong> 1.28 ± 0.05<br />

m·s-1 67<br />

<strong>in</strong>structed to perform the required <strong>in</strong>tensity. Intensities were set at 2.5% below <strong>and</strong><br />

, respectively. For each exercise transition, the breath-by-breath<br />

above the velocity at RCP, which corresponded to 1.35 ± 0.05 m·s<br />

data were <strong>in</strong>terpolated to give second-by-second values. For every each<br />

<strong>in</strong>tensity, the transitions were then synchronized with the start of exercise<br />

<strong>and</strong> averaged to enhance the underly<strong>in</strong>g response characteristics.<br />

Nonl<strong>in</strong>ear regression techniques were used to fit VO2 data after the onset<br />

of exercise with a bi-exponential model (Equation 1) that provided<br />

an estimate of the on-transients: amplitudes (A1 <strong>and</strong> A2 ), time delays<br />

(TD1 <strong>and</strong> TD2 ) <strong>and</strong> time constants (t1 <strong>and</strong> t2 ). The <strong>in</strong>itial cardiodynamic<br />

component was not considered by elim<strong>in</strong>at<strong>in</strong>g the first 20s of data after<br />

the onset of exercise. The basel<strong>in</strong>e VO2 was def<strong>in</strong>ed as the average VO2 measured dur<strong>in</strong>g rest<strong>in</strong>g 30s before the start of each transition.<br />

(1)<br />

-1 <strong>and</strong> 1.28 ± 0.05<br />

m·s -1 , respectively. For each exercise transition, the breath-by-breath data were<br />

<strong>in</strong>terpolated to give second-by-second values. For every each <strong>in</strong>tensity, the transitions<br />

were then synchronized with the start of exercise <strong>and</strong> averaged to enhance the<br />

underly<strong>in</strong>g response characteristics. Nonl<strong>in</strong>ear regression techniques were used to fi<br />

VO2 data after the onset of exercise with a bi-exponential model (Equation 1) tha<br />

provided an estimate of the on-transients: amplitudes (A1 <strong>and</strong> A2), time delays (TD1 <strong>and</strong><br />

TD2) <strong>and</strong> time constants (t1 <strong>and</strong> t2). The <strong>in</strong>itial cardiodynamic component was no<br />

considered by elim<strong>in</strong>at<strong>in</strong>g the first 20s of data after the onset of exercise. The basel<strong>in</strong>e<br />

VO2 was def<strong>in</strong>ed as the average VO2 measured dur<strong>in</strong>g rest<strong>in</strong>g 30s before the start of<br />

each transition.<br />

⎛ −<br />

⎛ −<br />

⎡ −<br />

t TD1<br />

⎞ ⎤ ⎡ −<br />

t TD2<br />

⎞<br />

⎜ ⎟<br />

⎜ ⎟ ⎤<br />

⎝ τ1<br />

⎠<br />

⎝ τ 2 ⎠<br />

VO2 ( t)<br />

= VO2b<br />

+ A1<br />

⎢1<br />

− l ⎥ + A2<br />

⎢1<br />

− l ⎥<br />

⎣ ⎦ ⎣ ⎦<br />

(1)<br />

The physiologically relevant <strong>in</strong>crease <strong>in</strong> VO2 is the amplitude of phase I (A1’), or<br />

primary component, which was calculated from:<br />

⎛ ( )<br />

⎜<br />

⎛ −<br />

TD2−TD1<br />

⎟<br />

⎞<br />

'<br />

⎞<br />

⎝<br />

τ 1⎠<br />

A = ⎜ −<br />

⎟<br />

1 A1<br />

1 l<br />

⎝<br />

⎠<br />

(2)<br />

Because the asymptotic value (A2) may represent a higher value than that actually


average VO2 measured dur<strong>in</strong>g rest<strong>in</strong>g 30s before the start of<br />

g the first 20s of data after the onset of exercise. The basel<strong>in</strong>e<br />

average VO2 measured dur<strong>in</strong>g rest<strong>in</strong>g 30s before the start of<br />

⎡ ⎤ ⎡ ⎤<br />

= VO − l − l ⎥<br />

(1)<br />

<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

−<br />

⎛ t−TD1<br />

⎞<br />

−<br />

⎛ t−TD2<br />

⎞<br />

⎜ ⎟<br />

⎜ ⎟<br />

⎝ τ1<br />

⎠<br />

⎝ τ 2 ⎠<br />

2b<br />

+ A1<br />

⎢1<br />

⎥ + A2<br />

⎢1<br />

⎛ t−TD<br />

⎛ −<br />

⎡ − 1 ⎞ ⎤ ⎡ −<br />

t TD2<br />

⎞<br />

⎜ ⎟<br />

⎜ ⎟ ⎤<br />

+ ⎣ ⎝ τ1<br />

⎠ − + ⎦ −⎣<br />

⎝ τ 2 ⎠<br />

2b<br />

A1<br />

1 A2<br />

1<br />

) = VO ⎢ l ⎥ ⎢ l ⎥ ⎦ (1)<br />

The physiologically ⎣<br />

relevant ⎦ <strong>in</strong>crease ⎣ <strong>in</strong> VO2 is the ⎦ amplitude of phase I<br />

(A1’), or primary component, which was calculated from:<br />

h relevant was calculated <strong>in</strong>crease <strong>in</strong> from: VO2 is the amplitude of phase I (A1’), or<br />

ch was calculated<br />

⎛<br />

from: ( )<br />

⎜<br />

⎛ −<br />

TD2−TD1<br />

⎟<br />

⎞<br />

'<br />

⎞<br />

⎝<br />

τ 1⎠<br />

(2)<br />

= ⎜ −<br />

⎟<br />

1 A⎛1<br />

1 ( )<br />

⎜<br />

⎛ −<br />

TD2−TD1<br />

⎟<br />

⎞<br />

'<br />

⎞<br />

⎝<br />

τ 1⎠<br />

A ⎜<br />

⎜⎝<br />

⎟<br />

1 = A1<br />

1−<br />

l ⎠<br />

(2)<br />

⎝<br />

⎠<br />

Because the asymptotic value (A2) may represent a higher value than<br />

otic value<br />

that<br />

(A2)<br />

actually<br />

may<br />

reached<br />

represent<br />

at the end<br />

a higher<br />

of the exercise,<br />

value than<br />

the value<br />

that<br />

of<br />

actually<br />

the VO2<br />

exercise, slow the exponential value of term the at VO2 the end slow of exercise exponential was def<strong>in</strong>ed term as at (A2’): the end<br />

s (A2’):<br />

⎛ ( )<br />

⎜<br />

⎛ −<br />

ED−TD2<br />

⎟<br />

⎞<br />

' ⎛ ( )<br />

⎜<br />

⎛ −<br />

ED−TD2<br />

⎟<br />

⎞ ⎞ (3)<br />

'<br />

⎝ ⎞ τ 2 ⎠<br />

= ⎜ ⎝<br />

τ 2 ⎠<br />

A −<br />

⎟<br />

2 = A2<br />

⎜ 1−<br />

⎟<br />

2 A2<br />

1 l (3)<br />

⎝⎝<br />

⎠ ⎠<br />

duration. where ED is the exercise duration.<br />

relevant <strong>in</strong>crease <strong>in</strong> VO2 is the amplitude of phase I (A1’), or<br />

A l (2)<br />

tic value (A2) may represent a higher value than that actually<br />

exercise, the value of the VO2 slow exponential term at the end<br />

duration.<br />

A l (3)<br />

Statistical analysis: The values were expressed as mean ± SD. The normal-<br />

values were expressed as mean ± SD. The normality of data<br />

values were expressed as mean ± SD. The normality of data<br />

-Wilk test.<br />

ity of<br />

The<br />

data was<br />

statistical<br />

checked by<br />

difference<br />

Shapiro-Wilk<br />

between<br />

test. The<br />

two<br />

statistical<br />

means<br />

difference<br />

was<br />

-Wilk test. between The two statistical means was checked difference by a paired between Student’s t-test two (2-tailed). means was<br />

dent’s t-test (2-tailed). Bi-exponential analyses were performed<br />

ent’s t-test Bi-exponential<br />

duals method. (2-tailed). analyses<br />

The level of Bi-exponential were performed by<br />

significance was analyses the least squared<br />

set at p were residuals<br />

≤ 0.05. performed<br />

method. The level of significance was set at p ≤ 0.05. All statistical analy- All<br />

performed uals method. by utiliz<strong>in</strong>g The level software of significance SPSS 17.0. was set at p ≤ 0.05. All<br />

ses were performed by utiliz<strong>in</strong>g software SPSS 17.0.<br />

erformed by utiliz<strong>in</strong>g software SPSS 17.0.<br />

RESULTS<br />

Variables presented <strong>in</strong> Table 1 describe the physiological <strong>and</strong> perfor-<br />

able 1 describe the physiological <strong>and</strong> performance parameters<br />

delimit<strong>in</strong>g exercise doma<strong>in</strong>s. The RCP was observed to<br />

po<strong>in</strong>t between VT <strong>and</strong> VO2max, but substantial variability was<br />

ble 1.<br />

cremental test. n = 9.<br />

to BW Relative to Velocity<br />

1<br />

) VO2max (%) (m·s -1 able 1 describe the physiological <strong>and</strong> performance parameters<br />

delimit<strong>in</strong>g exercise doma<strong>in</strong>s. The RCP was observed to<br />

po<strong>in</strong>t between VT <strong>and</strong> VO2max, but substantial variability was<br />

able 1.<br />

ncremental test. n = 9.<br />

to BW Relative to Velocity<br />

-1<br />

) VO2max (%) (m·s<br />

Delta<br />

) (%∆)<br />

100 1.40 (±0.03) 100<br />

70.5 (±8.0) 1.21 (±0.06) 0<br />

-1 mance parameters related to the <strong>in</strong>dices delimit<strong>in</strong>g exercise doma<strong>in</strong>s.<br />

The RCP was observed to correspond with the midpo<strong>in</strong>t between VT<br />

<strong>and</strong> VO2max , but substantial variability was observed, as shown on Table<br />

1.<br />

Table 1: Parameters for <strong>in</strong>cremental test. n = 9.<br />

VO Delta<br />

2 relative to BW<br />

(ml ) (%∆)<br />

100 1.40 (±0.03) 100<br />

70.5 (±8.0) 1.21 (±0.06) 0<br />

86.0 (±4.9) 1.32 (±0.05) 51.0 (±16.5)<br />

. m<strong>in</strong>-1 .kg-1 Relative to Velocity<br />

) VO2max (%) (m·s-1 Delta<br />

) (%Δ)<br />

VO2max 58.0 (±5.1) 100 1.40 (±0.03) 100<br />

VT 41.1 (±7.3) 70.5 (±8.0) 1.21 (±0.06) 0<br />

RCP 49.9 (±5.5) 86.0 (±4.9) 1.32 (±0.05) 51.0 (±16.5)<br />

The trivial difference between predeterm<strong>in</strong>ed <strong>and</strong> performed trials above<br />

(1.35 ± 0.05 m·s<br />

86.0 (±4.9) 1.32 (±0.05) 51.0 (±16.5)<br />

-1 <strong>and</strong> 1.34 ± 0.05 m·s-1 , ρ = 0.54) <strong>and</strong> below (1.28 ± 0.05<br />

m·s-1 <strong>and</strong> 1.28 ± 0.05 m·s-1 , ρ = 0.78) RCP ensured the effective control<br />

of the velocity under the test condition. The velocity measured dur<strong>in</strong>g<br />

trials was closer to the def<strong>in</strong>ed velocity <strong>in</strong> both trials above (2.0 ± 1.2%)<br />

<strong>and</strong> below (-2.7 ± 0.8%) the RCP.<br />

Table 2: Parameters of VO2 on-k<strong>in</strong>etics around RCP. n = 9.<br />

2.5% below RCP 2.5% above RCP<br />

VO2Basel<strong>in</strong>e (ml.m<strong>in</strong>-1 ) 474.90 ± 91.24 523.78 ± 79.08<br />

TD1 (s) 17.6 ± 3.3 14.0 ± 5.6 †<br />

t1 (s) 17.8 ± 7.1 16.1 ± 4.9<br />

A’ 1 (ml·m<strong>in</strong>-1 ) 2.784.93 ± 616.02 3.247.04 ± 669.99 †<br />

R2 0.97 ± 0.02 0.93 ± 0.04<br />

TD2 (s) 153.8 ± 42.5 188.4 ± 97.2<br />

t2 (s) 99.5 ± 82.2 73.8 ± 67.4<br />

A’ 2 (ml·m<strong>in</strong>-1 ) 391.24 ± 236.61 399.40 ± 270.49<br />

R2 0.69 ± 0.26 0.66 ± 0.23<br />

EEVO2 (ml·m<strong>in</strong>-1 ) 3.176.17 ± 647.01 3.646.45 ± 823.11 †<br />

A’ 2 %EEVO2 12.4 ± 7.3 10.5 ± 5.3<br />

TotalVO2 (ml·m<strong>in</strong>-1 ) 3.651.07 ± 660.36 4.170.23 ± 810.11 †<br />

%VO2max atta<strong>in</strong>ed 92.0 ± 6.0 105.0 ± 9.5 †<br />

EEVO 2 is the <strong>in</strong>crease <strong>in</strong> VO 2 above basel<strong>in</strong>e at end of exercise. † Marked<br />

differences (p < 0.05) were observed <strong>in</strong> relation to 2.5% below RCP.<br />

216<br />

Time parameters of VO2 on-k<strong>in</strong>etics seems not to differ substantially<br />

between trials around RCP, with the exception of TD1 (p = 0.03) (Table<br />

2). This scenario suggests that the response for the primary component<br />

beg<strong>in</strong>s early while swimm<strong>in</strong>g above rather than below RCP. The amplitude<br />

parameters account for the noticeable differences between trials<br />

<strong>in</strong> each condition. Primary amplitude, end-exercise VO2 (EEVO2 ), <strong>and</strong><br />

entire VO2 (TotalVO2 ) showed difference for their paired values <strong>in</strong> each<br />

trial (p values of 0.001, 0.001, <strong>and</strong> 0.000, respectively) (Table 2). There<br />

was no tendency for the onset of the slow component (TDs) to occur<br />

earlier as exercis<strong>in</strong>g above (188.4s) <strong>and</strong> below (153.8s) RCP <strong>in</strong>tensity,<br />

neither to differ <strong>in</strong> amplitude (399.4 <strong>and</strong> 391.2 ml.m<strong>in</strong>-1 above <strong>and</strong> below<br />

RCP, respectively), or <strong>in</strong> relative contribution to the EEVO2 (10.5<br />

<strong>and</strong> 12.4% above <strong>and</strong> below RCP, respectively) (Table 2). None of the<br />

subjects reached the exhaustion <strong>in</strong> either trial (above <strong>and</strong> below RCP),<br />

however because of the slow component, TotalVO2 elicit<strong>in</strong>g 104.57 <strong>and</strong><br />

91.58% of VO2max while swimm<strong>in</strong>g above <strong>and</strong> below RCP, respectively.<br />

The on-transient for VO2 above <strong>and</strong> below RCP is illustrated for one<br />

swimmer <strong>in</strong> the Figure 1.<br />

VO2 (L x m<strong>in</strong> -1 )<br />

6.0<br />

5.0<br />

4.0<br />

3.0<br />

2.0<br />

1.0<br />

2.5%RCP<br />

VO2max<br />

RCP<br />

VT<br />

-100 0 100 200 300 400 500<br />

Time (s)<br />

Figure 1: On-transition oxygen uptake k<strong>in</strong>etics <strong>in</strong> the trials around RCP<br />

for subject 6. Basel<strong>in</strong>e VO 2 <strong>in</strong> each trials is showed for 30-s before exercise<br />

beg<strong>in</strong>n<strong>in</strong>g (at time zero).<br />

dIscussIon<br />

In swimm<strong>in</strong>g, heavy <strong>and</strong> severe doma<strong>in</strong>s of exercise <strong>in</strong>tensity have not<br />

been studied by means of pulmonary VO 2 on-k<strong>in</strong>etics. In a recent study,<br />

Dekerle et al. (2009) concluded that CV lies on the boundary between<br />

the heavy <strong>and</strong> severe <strong>in</strong>tensity doma<strong>in</strong>s with<strong>in</strong> a range of ± 5%, s<strong>in</strong>ce<br />

post exercise VO 2 (reach<strong>in</strong>g only 87 ± 14%VO 2peak ) <strong>and</strong> [lactate] rema<strong>in</strong>ed<br />

stable when swimm<strong>in</strong>g 5% below CV. In contrast, when swimm<strong>in</strong>g<br />

5% above, both a rapid <strong>in</strong>crease <strong>in</strong> [lactate] <strong>and</strong> quick atta<strong>in</strong>ment<br />

of peak VO 2 were observed. Data from the present study corroborates<br />

with these results <strong>in</strong> an even narrower range (less than 5% was the difference<br />

between slower <strong>and</strong> faster trials) around the RCP, by on-transient<br />

VO 2 k<strong>in</strong>etics. The trial ~2.7% below RCP was performed at v36.8 ±<br />

8.5%∆ (about 1.28 ± 0.05 m·s -1 or 91 ± 2% of vVO 2max ), elicit<strong>in</strong>g a submaximal<br />

VO 2 (about 92.0 ± 6.0%VO 2max ), after a delayed steady-state<br />

(154s) of an amplitude of 391 ml·m<strong>in</strong> -1 . The VO 2 <strong>in</strong> the trial above ~2%<br />

of RCP (v71.1 ± 17.1%Δ, about 1.3 ± 0.05 m·s -1 or 96.1 ± 2.4% of<br />

vVO 2max ) presented a delayed (188s) amplitude of 399 ml·m<strong>in</strong> -1 limited<br />

trunked at its maximum rate (105.0 ± 9.5%VO 2max ).<br />

Similar results were previously observed by Demarie et al. (2001)<br />

with pentathletes, whose VO2 slow component rose to 114 ± 10%VO-<br />

2peak when swimm<strong>in</strong>g at a velocity correspond<strong>in</strong>g to 96% of VO-<br />

2peak. Swimm<strong>in</strong>g at previously determ<strong>in</strong>ed vVO2max, high level male<br />

swimmers exhibited a VO2 slow component of 274.1 ± 152.8 ml·m<strong>in</strong> -1<br />

(Fern<strong>and</strong>es et al., 2003). These authors have analyzed the VO2 changes<br />

(ΔVO2) between the second m<strong>in</strong>ute to the end of exercise for determ<strong>in</strong><strong>in</strong>g<br />

the amplitude of VO2 slow component, argu<strong>in</strong>g that (1) onset<br />

of slow component has an earlier time delay <strong>in</strong> the severe than <strong>in</strong> the<br />

heavy doma<strong>in</strong>; (2) there is no consensus about the algorithm to fit VO2<br />

slow component k<strong>in</strong>etic; <strong>and</strong> (3) there is a high variability <strong>in</strong> the ampli-


tude <strong>and</strong> time delay of the slow component. In our study, low adjusted<br />

coefficients for the second exponential (fitt<strong>in</strong>g VO2 slow component<br />

k<strong>in</strong>etics) were observed to both trials above <strong>and</strong> below RCP. Despite<br />

high variability, this variable was <strong>in</strong> an acceptable range for the goodness<br />

of fit. There was observed a substantial variability for the most of<br />

the amplitude <strong>and</strong> time parameters of VO2 k<strong>in</strong>etics above <strong>and</strong> below<br />

RCP. Although, the accuracy of the estimation was not compromised<br />

<strong>and</strong> the on-k<strong>in</strong>etic response was described comprehensively across heavy<br />

<strong>and</strong> severe doma<strong>in</strong>s shift<strong>in</strong>g exercise <strong>in</strong>tensity slight above <strong>and</strong> below<br />

RCP. The ma<strong>in</strong> VO2 response shown <strong>in</strong> the two swim velocities were<br />

(a) patterns <strong>in</strong> the time constant for the primary <strong>and</strong> slow components<br />

rema<strong>in</strong>ed unchanged; (b) time delay was significantly shorter dur<strong>in</strong>g exercis<strong>in</strong>g<br />

at severe doma<strong>in</strong> only for primary component; <strong>and</strong> (c) although<br />

slow component was unchanged between heavy <strong>and</strong> severe doma<strong>in</strong>s,<br />

it lead to the atta<strong>in</strong>ment of VO2max when above RCP. Thus, some of<br />

trends reported to Carter et al. (2002) for changes <strong>in</strong> the amplitudes<br />

<strong>and</strong> k<strong>in</strong>etics of the VO2 response profiles on treadmill across heavy <strong>and</strong><br />

severe doma<strong>in</strong>s were also present <strong>in</strong> this study.<br />

The major f<strong>in</strong>d<strong>in</strong>g of this study is that VO2 k<strong>in</strong>etics <strong>in</strong> swimm<strong>in</strong>g<br />

around RCP gathers the pulmonary VO2 responses reflect<strong>in</strong>g heavy <strong>and</strong><br />

severe doma<strong>in</strong>s of exercise. Therefore, VO2 k<strong>in</strong>etics may be applied rather<br />

than CP to either dim<strong>in</strong>ish the tests used to access doma<strong>in</strong> boundaries<br />

or the protocol variability associated with the determ<strong>in</strong>ation of CP.<br />

Furthermore, if a challenge for coaches is to <strong>in</strong>duce a required profile<br />

of physiological responses from a given tra<strong>in</strong><strong>in</strong>g load, the study of VO2<br />

k<strong>in</strong>etics dur<strong>in</strong>g different swimm<strong>in</strong>g <strong>in</strong>tensities could provide a valuable<br />

<strong>in</strong>sight for tra<strong>in</strong><strong>in</strong>g prescription.<br />

reFerences<br />

Beaver W.L., Wasserman K., & Whipp B.J. (1986). A new method for<br />

detect<strong>in</strong>g threshold by gas exchange. J Appl Physiol, 60(6), 2020-2027.<br />

Beneke R. (2003). Maximal lactate steady state concentration (MLSS):<br />

experimental <strong>and</strong> modell<strong>in</strong>g approaches. Eur J Appl Physiol, 88, 361–<br />

369.<br />

Carter H., Pr<strong>in</strong>gle J.S.M., Jones A.M., & Doust J.H. (2002). Oxygen<br />

uptake k<strong>in</strong>etics dur<strong>in</strong>g treadmill runn<strong>in</strong>g across exercise <strong>in</strong>tensity doma<strong>in</strong>s.<br />

Eur J Appl Physiol, 86, 347–354.<br />

Dekerle J., Baron B., Dupont L., Vanvelcenaher J., & Pelayo P. (2003).<br />

Maximal lactate steady state, respiratory compensation threshold <strong>and</strong><br />

critical power. Eur J Appl Physiol, 89, 281–288.<br />

Dekerle J., Brickley G., Alberty M., & Pelayo P. (2009). Character<strong>in</strong>z<strong>in</strong>g<br />

the slope of the distance-time relationship <strong>in</strong> swimm<strong>in</strong>g. J Sci Med<br />

Sport, doi:10.1016/j.jsams.2009.05.007<br />

Demarie S., Sardella F., Billat V., Mag<strong>in</strong>i W., & Fa<strong>in</strong>a M. (2001). The<br />

VO 2 slow component <strong>in</strong> swimm<strong>in</strong>g. Eur J Appl Physiol, 84, 95-99.<br />

Fern<strong>and</strong>es R.J., Cardoso C.S., Soares S.M., Ascensão A., Colaço P.J.;<br />

& Vilas-Boas J.P. (2003) Time limit <strong>and</strong> VO 2 slow component at<br />

<strong>in</strong>tensities correspond<strong>in</strong>g to VO 2max <strong>in</strong> swimmers. Int J Sport Med,<br />

24, 576-581.<br />

Jones A.M., & Poole D.C. (2005). Introduction to oxygen uptake k<strong>in</strong>etics<br />

<strong>and</strong> historical development of the discipl<strong>in</strong>e. In Jones A.M., &<br />

Poole D.C. (eds) Oxygen uptake k<strong>in</strong>etics <strong>in</strong> sports, exercise <strong>and</strong> medic<strong>in</strong>e<br />

(pp: 03-36). Routledge: Ab<strong>in</strong>gdon.<br />

Kesk<strong>in</strong>en K.L., Rodríguez F.A., & Kesk<strong>in</strong>en O.P. (2003). Respiratory<br />

snorkel <strong>and</strong> valve system for breath-by-breath gas analysis <strong>in</strong> swimm<strong>in</strong>g.<br />

Sc<strong>and</strong> J Med Sci Sports, 13, 322–329.<br />

Morton R.H. (2006). The critical power <strong>and</strong> related whole-body bioenergetic<br />

models. Eur J Appl Physiol, 96, 339-354.<br />

Pr<strong>in</strong>gle J.S., & Jones A.M. (2002). Maximal lactate steady state, critical<br />

power <strong>and</strong> EMG dur<strong>in</strong>g cycl<strong>in</strong>g. Eur J Appl Physiol, 88, 214–226.<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

Hormonal, Immune, Autonomic <strong>and</strong> Mood State<br />

Variation <strong>in</strong> the Initial Preparation Phase of a W<strong>in</strong>ter<br />

Season, <strong>in</strong> Portuguese Male Swimmers<br />

rama, l. 1 , Alves, F. 2 , teixeira, A. 1<br />

1Research Centre for Sport <strong>and</strong> Physical Activity, University of Coimbra,<br />

Portugal<br />

2Faculty of Human K<strong>in</strong>etics, Technical University of Lisbon, Portugal<br />

At the <strong>in</strong>itial phase of seasonal preparation, swimmers are submitted<br />

to a sudden <strong>in</strong>crement of tra<strong>in</strong><strong>in</strong>g load. Because the amount of tra<strong>in</strong><strong>in</strong>g<br />

is normally less than the maximal that will be imposed later on <strong>in</strong> the<br />

season, coaches do not pay much attention to how athletes accommodate<br />

this <strong>in</strong>crement. This study aims to analyse at rest, the variation of<br />

serum <strong>and</strong> salivary cortisol <strong>and</strong> testosterone, salivary IgA, HRV <strong>and</strong> the<br />

Profile of Mood States (POMS) after the first meso-cycle of a w<strong>in</strong>ter<br />

swimm<strong>in</strong>g season <strong>in</strong> a sample of 13 male Portuguese swimmers<br />

of national level. In this study, the impact of the <strong>in</strong>itial phase of<br />

seasonal tra<strong>in</strong><strong>in</strong>g on the athlete’s adaptation <strong>in</strong> a multidimensional<br />

approach was <strong>in</strong>vestigated. Significant variation <strong>in</strong> hormonal,<br />

mood <strong>and</strong> autonomic variables were found, which justifies<br />

pay<strong>in</strong>g attention to athletes work tolerance, especially <strong>in</strong> the<br />

<strong>in</strong>itial phase.<br />

Key words: salivary IgA, heart rate variability, hormonal response,<br />

PoMs<br />

IntroductIon<br />

Swimm<strong>in</strong>g as an endurance sport is recognized as a sport where athletes<br />

are normally submitted to heavy tra<strong>in</strong><strong>in</strong>g loads. In seasonal plann<strong>in</strong>g the<br />

option at the beg<strong>in</strong>n<strong>in</strong>g of the season of a marked load <strong>in</strong> the tra<strong>in</strong><strong>in</strong>g<br />

volume is common, aim<strong>in</strong>g to hit as soon as possible, high volumes focus<strong>in</strong>g<br />

on aerobic adaptation (Pyne & Goldsmith, 2005). Because this<br />

does not correspond yet to the maximal requirements of the tra<strong>in</strong><strong>in</strong>g<br />

season, coaches do not always pay enough attention to the <strong>in</strong>ability of<br />

athletes to adapt to this sudden <strong>in</strong>crement of tra<strong>in</strong><strong>in</strong>g volume (Maglischo,<br />

2003). Although their performance capacity does not seem to be<br />

impaired, the high requirement of body resources often stresses the athlete’s<br />

adaptation capacity. This precarious balance between positive <strong>and</strong><br />

negative <strong>in</strong>fluence of the tra<strong>in</strong><strong>in</strong>g stimulus <strong>and</strong> the related fatigue, modulate<br />

tra<strong>in</strong><strong>in</strong>g adaptation. In the doma<strong>in</strong> of control of tra<strong>in</strong><strong>in</strong>g, researchers<br />

have put their efforts <strong>in</strong>to look<strong>in</strong>g for biological <strong>and</strong> psychological<br />

markers that can be used <strong>in</strong> an effective way to prevent <strong>in</strong>adequate adaptation<br />

(Norris & Smith, 2002).<br />

The hormonal response to tra<strong>in</strong><strong>in</strong>g is a recurrent strategy <strong>in</strong> the control<br />

of tra<strong>in</strong><strong>in</strong>g. Among the several markers used, the hormones testosterone<br />

<strong>and</strong> cortisol were among the most used to follow the response<br />

to tra<strong>in</strong><strong>in</strong>g load (Hooper, Mack<strong>in</strong>on et al, 1999). In brief, cortisol is<br />

considered because of its response to stress <strong>and</strong> catabolic action, while<br />

testosterone is used because is considered to be a marker of anabolic<br />

function. Look<strong>in</strong>g at the rest<strong>in</strong>g values of these hormones, the literature<br />

suggests that a decrease of testosterone <strong>and</strong> <strong>in</strong>crease of cortisol <strong>in</strong> endurance<br />

tra<strong>in</strong><strong>in</strong>g athletes is common (Duclos et al. 2001). Although the<br />

controversy persists, generally the reduction of cortisol is necessary as a<br />

pre-requisite for performance improvement (Bonifazi et al. 2000). The<br />

salivary content that corresponds to the free <strong>and</strong> biological active form<br />

of the hormones may constitute a less <strong>in</strong>vasive <strong>and</strong> preferable marker<br />

(Paccotti et al. 2005). It is accepted that salivary IgA is a mucosal immune<br />

marker that shows reduced values after long periods of tra<strong>in</strong><strong>in</strong>g<br />

which could compromise tra<strong>in</strong><strong>in</strong>g <strong>and</strong> performance capacity (Pyne et al.<br />

2000; Gleeson et al. 2000).<br />

Heart rate variability (HRV) has become a promiss<strong>in</strong>g <strong>and</strong> useful<br />

<strong>in</strong>dicator that reflects the autonomic response to tra<strong>in</strong><strong>in</strong>g. Autonomic<br />

217


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

imbalance associat<strong>in</strong>g <strong>in</strong>creased sympathetic activity <strong>and</strong> reduced vagal<br />

tone has been proposed as a marker of the negative impact of poorly<br />

tolerated tra<strong>in</strong><strong>in</strong>g load (Atlaoui et al. 2007). The <strong>in</strong>terest <strong>in</strong> HRV is also<br />

re<strong>in</strong>forced because of the non-<strong>in</strong>vasive approach as it is possible to assess<br />

it through the use of portable heart rate monitors able to record the<br />

R-R <strong>in</strong>terval.<br />

Mood states reflect the impact of tra<strong>in</strong><strong>in</strong>g as perceived by the swimmers,<br />

<strong>and</strong> is known to be affected by difficulties of accommodation to<br />

the requirements of the tra<strong>in</strong><strong>in</strong>g <strong>and</strong> often constitute the first signal of<br />

problems with load adaptation. The POMS questionnaire is one of the<br />

most applied <strong>in</strong>struments <strong>in</strong> sports to access alterations of athlete mood<br />

states <strong>in</strong>duced by tra<strong>in</strong><strong>in</strong>g (Morgan et al. 1988).<br />

In this study, the aim is to control the response of these variables <strong>in</strong><br />

rest<strong>in</strong>g condition just before the beg<strong>in</strong>n<strong>in</strong>g of tra<strong>in</strong><strong>in</strong>g season <strong>and</strong> after<br />

the first meso-cycle characterized by the susta<strong>in</strong>ed <strong>in</strong>creased volume.<br />

The ma<strong>in</strong> <strong>in</strong>terest is to focus on the chronic effect of tra<strong>in</strong><strong>in</strong>g.<br />

Methods<br />

The sample <strong>in</strong> this study consisted of 13 male swimmers of national<br />

Portuguese level (17.2± 1.3 years old, 174.9 ±5.8 cm, 65.8±6.8 kg of<br />

height <strong>and</strong> weight, respectively). All subjects were <strong>in</strong>formed <strong>and</strong> signed<br />

the <strong>in</strong>formed consent. Tra<strong>in</strong><strong>in</strong>g volume, <strong>in</strong>tensity <strong>and</strong> time spent <strong>in</strong> dry<br />

l<strong>and</strong> activities were controlled. Intensity is expressed <strong>in</strong> arbitrary units<br />

of load (Mujika et al. 1995). Blood <strong>and</strong> saliva samples were collected: 1)<br />

<strong>in</strong> the beg<strong>in</strong>n<strong>in</strong>g of the w<strong>in</strong>ter season, after an off tra<strong>in</strong><strong>in</strong>g period of 6<br />

weeks (t0) 2) after 7 weeks of tra<strong>in</strong><strong>in</strong>g (t1), by veno puncture, always at<br />

the same time of the day (between 15 <strong>and</strong> 17h. At (t1), a time lapse of 48<br />

hours of rest after the last tra<strong>in</strong><strong>in</strong>g session was respected.<br />

Serum cortisol <strong>and</strong> free testosterone were determ<strong>in</strong>ed by Electrochemi<br />

lum<strong>in</strong>escent immuno-assay with the Immulite® 2000 analyser.<br />

The salivary content of cortisol <strong>and</strong> testosterone were determ<strong>in</strong>ed by<br />

ELISA (Salimetrics® USA). Salivary IgA was determ<strong>in</strong>ed by ELISA as<br />

it was described elsewhere (Li & Gleeson, 2004). Salivary IgA secretion<br />

rate was calculated from salivary flow rate <strong>and</strong> the IgA concentration.<br />

For the HRV assessment, the swimmers lay 8 m<strong>in</strong>utes <strong>in</strong> the sup<strong>in</strong>e<br />

position, wear<strong>in</strong>g a heart rate monitor (Polar® S810) selected for<br />

RR <strong>in</strong>terval record<strong>in</strong>g. 5 m<strong>in</strong>utes were used for HRV analysis, exclud<strong>in</strong>g<br />

the first 2m<strong>in</strong> <strong>and</strong> the last m<strong>in</strong>ute. Dur<strong>in</strong>g heart rate record<strong>in</strong>g, the<br />

athletes were required to synchronize their breath pattern at 12 cycles<br />

per m<strong>in</strong>-1 with the help of a sound pacer, <strong>in</strong> order to avoid perturbation<br />

determ<strong>in</strong>ed by breath<strong>in</strong>g. The software Polar Performance SW®<br />

was used to transfer data from the monitors <strong>and</strong> to analyze <strong>and</strong> correct<br />

for ectopic <strong>and</strong> miss<strong>in</strong>g beats. The HRV analysis was done with<br />

the Kubios HRV Analysis Software (Kuopio, FIN). Time SDNN was<br />

used as a marker of global heart rate variability. The frequency analysis<br />

was done through fast Fourier transformation controll<strong>in</strong>g the LF power,<br />

HF power <strong>and</strong> LF/HF ratio upon the R-R <strong>in</strong>terval power spectra. The<br />

recommendations of the Task Force of the European Society of Radiology<br />

<strong>and</strong> North American Society Electrophysiology were respected.<br />

For the mood state assessment, the Portuguese version of the Profile<br />

of Mood States POMS short form was used. Statistical analysis us<strong>in</strong>g<br />

nom parametric Wilcoxon test was conducted (p


that the sudden <strong>in</strong>crease of the volume of tra<strong>in</strong><strong>in</strong>g causes significant<br />

alterations <strong>in</strong> several markers, namely the <strong>in</strong>crease <strong>in</strong> the concentration<br />

of the stress hormone cortisol, the autonomic imbalance through the<br />

re<strong>in</strong>forcement of sympathetic regulation. As previously found (Rietjens<br />

et al. 2005), the mood proves to be a sensitive marker of the impact of<br />

tra<strong>in</strong><strong>in</strong>g <strong>and</strong> its deterioration seems to <strong>in</strong>dicate problems <strong>in</strong> the adaptation<br />

to the tra<strong>in</strong><strong>in</strong>g process.<br />

These changes could correspond to the normal overload, but they<br />

should be considered carefully by coaches <strong>in</strong> order to optimize performance<br />

development. More precisely, monitor<strong>in</strong>g psychological adaptation<br />

to tra<strong>in</strong><strong>in</strong>g seems to be a good approach to prevent failure <strong>in</strong> the<br />

tolerance of <strong>in</strong>dividuals to workload. Our results seem to agree with<br />

those of Norris & Smith, (2002) who advocate an adequate plann<strong>in</strong>g<br />

of recovery strategies, that could contribute to avoid<strong>in</strong>g the negative<br />

impact of the sudden <strong>in</strong>crease of tra<strong>in</strong><strong>in</strong>g load especially at the <strong>in</strong>itial<br />

preparation phase.<br />

reFerences<br />

Atlaoui, D., Pichot, V., Lacoste, L., Barale, F., Lacour, J. R., & Chatard,<br />

J. C. (2007). Heart Rate Variability, Tra<strong>in</strong><strong>in</strong>g Variation <strong>and</strong> Performance<br />

<strong>in</strong> Elite Swimmers. International Journal of Sports <strong>Medic<strong>in</strong>e</strong>,<br />

28(5), 394-400.<br />

Bonifazi, M., Sardella, F., & Lupo, C. (2000). Preparatory versus ma<strong>in</strong><br />

competitions: differences <strong>in</strong> performances, lactate responses <strong>and</strong> precompetition<br />

plasma cortisol concentrations <strong>in</strong> elite male swimmers.<br />

European Journal of Applied Physiology, 82(5-6), 368-373.<br />

Duclos, M., Corcuff, J. B., Pehourcq, F., & Tabar<strong>in</strong>, A. (2001). Decreased<br />

pituitary sensitivity to glucocorticoids <strong>in</strong> endurance-tra<strong>in</strong>ed men.<br />

European Journal of Endocr<strong>in</strong>ology, 144(4), 363-368.<br />

Fry, A., & Kraemer, W. (1997). Resistance Exercise Overtra<strong>in</strong><strong>in</strong>g <strong>and</strong><br />

Overreach<strong>in</strong>g. Neuroendocr<strong>in</strong>e Responses. Sports <strong>Medic<strong>in</strong>e</strong>, 23(2),<br />

106-129.<br />

Gleeson, M., G<strong>in</strong>n, E., & Francis, J. (2000). Salivary immunoglobul<strong>in</strong><br />

monitor<strong>in</strong>g <strong>in</strong> an elite kayaker. Cl<strong>in</strong>ical Journal of Sport <strong>Medic<strong>in</strong>e</strong>,<br />

10(3), 206.<br />

Hooper, S. L., Mack<strong>in</strong>non, L. T., & Howard, A. (1999). Physiological<br />

<strong>and</strong> psychometric variables for monitor<strong>in</strong>g recovery dur<strong>in</strong>g taper<strong>in</strong>g<br />

for major competition. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports <strong>and</strong> Exercise,<br />

31(8), 1205-1210.<br />

Li, T. L., & Gleeson, M. (2004). The effect of s<strong>in</strong>gle <strong>and</strong> repeated bouts<br />

of prolonged cycl<strong>in</strong>g <strong>and</strong> circadian variation on saliva flow rate, immunoglobul<strong>in</strong><br />

A <strong>and</strong> alpha-amylase responses. Journal of Sports Sciences,<br />

22(11-12), 1015-1024.<br />

Maglischo, E. (2003). Swimm<strong>in</strong>g Fastest. The essential reference on<br />

technique, tra<strong>in</strong><strong>in</strong>g, <strong>and</strong> program design: Human K<strong>in</strong>etics<br />

Mack<strong>in</strong>non, L. (1997). Immunity <strong>in</strong> Athletes. Int J Sports Med, 18(Supl),<br />

s62-s68.<br />

Morgan, W. P., Costill, D. L., Flynn, M. G., Ragl<strong>in</strong>, J. S., & O’Connor,<br />

P. J. (1988). Mood disturbance follow<strong>in</strong>g <strong>in</strong>creased tra<strong>in</strong><strong>in</strong>g <strong>in</strong> swimmers.<br />

<strong>Medic<strong>in</strong>e</strong> & Science <strong>in</strong> Sports & Exercise, 20(4), 408-414.<br />

Mujika, I., Chatard, J. C., Busso, T., Geyssant, A., Barale, F., & Lacoste,<br />

L. (1995). Effects of tra<strong>in</strong><strong>in</strong>g on performance <strong>in</strong> competitive swimm<strong>in</strong>g.<br />

. Can J Appl Physiol, 20(4), 395-406.<br />

Mujika, I., Chatard, J. C., Padilla, S., Guezennec, C. Y., & Geyssant, A.<br />

(1996). Hormonal responses to tra<strong>in</strong><strong>in</strong>g <strong>and</strong> its taper<strong>in</strong>g off <strong>in</strong> competitive<br />

swimmers: relationships with performance. Eur J Appl Physiol<br />

Occup Physiol, 74(4), 361-366.<br />

Norris, S., & Smith, D. (2002). Plan<strong>in</strong>g, Periodization, <strong>and</strong> Sequenc<strong>in</strong>g<br />

of Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Competition: The rationale for a Competently<br />

Planned, Optimally Executed Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Competition Program,<br />

Supported by a Multidiscipl<strong>in</strong>ary Team. In M. Kellmann (Ed.), Enhanc<strong>in</strong>g<br />

recovery: Prevent<strong>in</strong>g underperformance <strong>in</strong> athletes. Champaign,<br />

IL: Human K<strong>in</strong>etics.<br />

Paccotti, P., M<strong>in</strong>etto, M., Terzolo, M., Ventura, M., Ganzit, G. P., Borrione,<br />

P., et al. (2005). Effects of high-<strong>in</strong>tensity isok<strong>in</strong>etic exercise on<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

salivary cortisol <strong>in</strong> athletes with different tra<strong>in</strong><strong>in</strong>g schedules: Relationships<br />

to serum cortisol <strong>and</strong> lactate. International Journal of Sports<br />

<strong>Medic<strong>in</strong>e</strong>, 26(9), 747-755.<br />

Pyne, D., McDonald, W., Gleeson, M., Flanagan, A., Clancy, R., &<br />

Fricker, P. (2001). Mucosal Immunity, Respiratory Illness, <strong>and</strong> Competitive<br />

Performance <strong>in</strong> Elite Swimmers. Med Sci Sports Exerc., 33(3),<br />

348-353.<br />

Pyne, D., & Goldsmith, W. (2005). Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> test<strong>in</strong>g of competitive<br />

swimmers. In J. M. Stager & D. A. Tanner (Eds.), H<strong>and</strong>book of Sports<br />

Medec<strong>in</strong>e <strong>and</strong> Science - Swimm<strong>in</strong>g (2th ed.): Blackwell<br />

Rietjens, G. J., Kuipers, H., Adam, J. J., Saris, W. H., van Breda, E.,<br />

van Hamont, D., et al. (2005 ). Physiological, biochemical <strong>and</strong> psychological<br />

markers of strenuous tra<strong>in</strong><strong>in</strong>g-<strong>in</strong>duced fatigue. Int J Sports<br />

Med 26(1), 16-26.<br />

AcKnoWledGeMents<br />

This project was f<strong>in</strong>anced by the Portuguese foundation for Science <strong>and</strong><br />

Technology (FCT PTDC/ DES/ 68647/ 2006).<br />

219


Fourteen highly tra<strong>in</strong>ed male swimmers were divided <strong>in</strong>to two groups (E (n = 7;<br />

22.7±2.7 yr.; 81.68 ±12.5 kg; 1.83 ± 0.10m <strong>and</strong> C (n=7; 18.8 ± 1.4 yr.; 69.1 ± 8.4 kg;<br />

<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

1.77 ± 0.04 m) gave written <strong>in</strong>formed consent to participate <strong>in</strong> the study, which was<br />

granted ethical approval by the Scientific Committee of the Faculty of Human K<strong>in</strong>etics<br />

of the Technical University of Lisbon. The Elite group consisted of swimmers who have<br />

represented the Portuguese National Team <strong>in</strong> International Competition <strong>in</strong> freestyle<br />

Oxygen Uptake K<strong>in</strong>etics <strong>and</strong> Performance <strong>in</strong> events (200 meter The subjects or above). were Club familiarised level swimmers with the test were procedures characterized <strong>and</strong> equip- as hav<strong>in</strong>g never<br />

Swimm<strong>in</strong>g<br />

represented ment their used country <strong>in</strong> the at experiment the senior <strong>and</strong> level, were but <strong>in</strong>structed all of the to subjects avoid strenuous underwent regular<br />

tra<strong>in</strong><strong>in</strong>g <strong>and</strong> exercise competed <strong>in</strong> the regularly 24 hours <strong>in</strong> preced<strong>in</strong>g National the Championships.<br />

test.<br />

The subjects Swimmers were familiarised were required with to report the test to the procedures pool on 3 <strong>and</strong> occasions equipment over a used <strong>in</strong> the<br />

reis, J.F., Alves, F.B.<br />

experiment 10 <strong>and</strong> day were period. <strong>in</strong>structed All the tests to were avoid <strong>in</strong>terspersed strenuous with exercise at least <strong>in</strong> 24-h the recovery. 24 hours preced<strong>in</strong>g<br />

the test. Subjects underwent a prelim<strong>in</strong>ary test compris<strong>in</strong>g 5 x 200 m with 30 s<br />

CIPER, Faculty of Human K<strong>in</strong>etics, Lisbon, Portugal<br />

Swimmers rest <strong>and</strong> were 5-10% required velocity to report <strong>in</strong>crements to the for pool determ<strong>in</strong>ation on 3 occasions of maximal over a oxy- 10 day period.<br />

All the tests gen were uptake <strong>in</strong>terspersed (VO2 max ) <strong>and</strong> with ventilatory at least threshold 24-h (VT). recovery. The last Subjects repetition underwent a<br />

The purpose of this study was to compare the VO2 k<strong>in</strong>etics <strong>in</strong> two<br />

prelim<strong>in</strong>ary<br />

sub-<br />

was test performed compris<strong>in</strong>g at maximal 5 x 200 velocity m with (vVO 30 s 2 rest ). VO<strong>and</strong> 2 max 5-10% was recorded velocity as the <strong>in</strong>crements for<br />

maximal <strong>in</strong>tensities <strong>in</strong> elite (E) <strong>and</strong> club-level (C) swimmers. After pre-<br />

determ<strong>in</strong>ation highest of maximal 30 s average oxygen <strong>and</strong> VT uptake was established ( VO2 maxus<strong>in</strong>g<br />

the V-slope method<br />

vious determ<strong>in</strong>ation of VO2 max <strong>and</strong> ventilatory threshold (VT), four-<br />

(Beaver al., 1986). On subsequent test days, the swimmers performed<br />

teen swimmers were divided <strong>in</strong>to two groups: E (n = 7; 22.7±2.7 yr) <strong>and</strong><br />

two 7-m<strong>in</strong> square-wave transitions from rest to 25%Δ [VT + 0.25 x<br />

C (n=7; 18.8 ± 1.4 yr) <strong>and</strong> performed two constant velocity swimm<strong>in</strong>g<br />

(VO2 max- VT)] (H) <strong>and</strong> 70%Δ (S) with at 1-h rest <strong>in</strong> between. The<br />

bouts at Δ25% (Heavy) [= VT + 0.25 x (VO2 max- VT)] <strong>and</strong> Δ70% (Se-<br />

subjects returned to the pool with<strong>in</strong> one week to repeat the procedure,<br />

vere) for determ<strong>in</strong>ation of VO2 k<strong>in</strong>etics. The E group presented a faster<br />

giv<strong>in</strong>g a total of two H <strong>and</strong> two S exercise transitions.<br />

time constant of the primary phase VO2 response than C <strong>in</strong> severe<br />

Heart Rate was recorded throughout each swimm<strong>in</strong>g bout <strong>and</strong> aver-<br />

swimm<strong>in</strong>g (13.3±3.4s <strong>and</strong> 18.4±4.6s, respectively, p>0.05) which<br />

aged every 5 s. Blood lactate concentration was determ<strong>in</strong>ed after each<br />

was also correlated with endurance performance, recorded as the<br />

square-wave transition (Lactate Pro (Arkray, Kyoto, Japan). All the tests<br />

time atta<strong>in</strong>ed <strong>in</strong> an official 400 freestyle event (r= 0.6, p


The E swimmers presented higher values for vVO 2 max than C, lower π p<br />

for S <strong>in</strong>tensity swimm<strong>in</strong>g <strong>and</strong> T400 (240.1±2.5s <strong>and</strong> 262.7±5.9s, respectively,<br />

p>0.01). Neither of the other VO 2 k<strong>in</strong>etics parameters differed<br />

between groups, nor did the heart rate response or the lactate concentration<br />

after each square-wave transition. When the entire group is considered,<br />

there was a positive correlation between T400 (251.4 ± 4.5s) <strong>and</strong><br />

π p <strong>in</strong> both H (15.7±4.8s, r=0.6; p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

recruitment of fast-twitch fibers <strong>in</strong> tra<strong>in</strong>ed runners? J Appl Physiol,<br />

90(6),2212-20.<br />

Carter H., Jones A.M., Barstow T.J., Burnley M., Williams C.A., Doust<br />

J.H. (2000). Oxygen uptake k<strong>in</strong>etics <strong>in</strong> treadmill runn<strong>in</strong>g <strong>and</strong> cycle<br />

ergometry: a comparison. J Appl Physiol, 89, 899-907.<br />

Carter H., Pr<strong>in</strong>gle J.S., Jones A.M., Doust J.A. (2002). Oxygen uptake<br />

k<strong>in</strong>etics dur<strong>in</strong>g treadmill runn<strong>in</strong>g across exercise <strong>in</strong>tensity doma<strong>in</strong>s.<br />

Eur J Appl Physiol, 86, 347-354.<br />

Davison, R.C., Someren, K.A., Jones A.M. (2009). Physiological<br />

monitor<strong>in</strong>g of the Olympic athlete. J Sports Sci, DOI:<br />

10.1080/02640410903045337.<br />

Demarie, S., Sardella, F., Billat, V., Mag<strong>in</strong>i, W., Fa<strong>in</strong>a, M. (2001) The<br />

VO 2 slow component <strong>in</strong> swimm<strong>in</strong>g. Eur J Appl Physiol, 84, 95-99.<br />

Fern<strong>and</strong>es R.J., Kesk<strong>in</strong>en K.L., Colaço P., Querido A.J., Machado L.J.,<br />

Morais P.A., Novais D.Q., Mar<strong>in</strong>ho D.A., Vilas Boas J.P. (2008).<br />

Time Limit at VO 2 max Velocity <strong>in</strong> Elite Crawl Swimmers. Int J<br />

Sports Med , 29, 145–50.<br />

Ingham S.A., Carter H., Whyte G., Doust J.H. (2007). Comparison of<br />

the oxygen uptake k<strong>in</strong>etics of Club <strong>and</strong> Olympic champion rowers.<br />

Med Sci Sports Exerc, 39(5), 865-71.<br />

Jones A.M., Koppo K. (2005). Effect of tra<strong>in</strong><strong>in</strong>g on O 2 k<strong>in</strong>etics <strong>and</strong> performance.<br />

In: Jones AM & Poole DC, editors. Oxygen Uptake K<strong>in</strong>etics<br />

<strong>in</strong> Sport, Exercise <strong>and</strong> <strong>Medic<strong>in</strong>e</strong>. Oxon: Routledge, p. 373-398.<br />

Koga S., Tomoyuki S., Kondo N., Barstow T. (1997). Effect of <strong>in</strong>creased<br />

muscle temperature on oxygen uptake k<strong>in</strong>etics dur<strong>in</strong>g exercise. J Appl<br />

Physiol,83(4), 1333-8.<br />

Poole D.C., Ward S.A., Gardner G.W., Whipp B.J. (1988). Metabolic<br />

<strong>and</strong> respiratory profile of the upper limit for prolonged exercise <strong>in</strong><br />

man. Ergonomics, 31, 1265–1279.<br />

Reis J.F., Millet G.P., Malatesta D., Roels B., Borrani F., Vleck V.E.,<br />

Alves F.B. (2010). Are oxygen uptake k<strong>in</strong>etics modified when us<strong>in</strong>g a<br />

respiratory snorkel? Int J Sports Physiol Perform, <strong>in</strong> press.<br />

Rodriguez F., Kesk<strong>in</strong>en K., Malvela M., Kesk<strong>in</strong>en O. (2003).<br />

Oxygen uptake k<strong>in</strong>etics <strong>in</strong> free swimm<strong>in</strong>g- a pilot study. In<br />

Chatard JC (eds). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX,<br />

Sa<strong>in</strong>t Etienne, Publications de l’Université de Sa<strong>in</strong>t-Etienne, 379-<br />

384.<br />

W<strong>in</strong>love M.A., Jones A.M., Welsman J.R. (2010) Influence of tra<strong>in</strong><strong>in</strong>g<br />

status <strong>and</strong> exercise modality on pulmonary O 2 uptake k<strong>in</strong>etics <strong>in</strong><br />

pre-pubertal girls. Eur J Appl Physiol , DOI: 10.1007/s00421-009-<br />

1320-2.<br />

ACKNOWLEDGEMENTS<br />

The first author gratefully acknowledges the ‘Fundação para a Ciência<br />

e Tecnologia, Portugal’ (‘The Foundation for Science <strong>and</strong> Technology’)<br />

for their doctoral fellowship award (reference number SFRH/<br />

BD/23351/2005).<br />

222<br />

Maximum Blood Lactate Concentration after two<br />

Different Specific Tests <strong>in</strong> Freestyle Swimm<strong>in</strong>g<br />

rozi, G. 1 , Thanopoulos, V. 1 , dopsaj, M. 2<br />

1Faculty of Physical Education <strong>and</strong> Sports Science, University of Athens,<br />

Greece<br />

2Faculty of Sport <strong>and</strong> Physical Education, University of Belgrade, Serbia<br />

The purpose of the present study was to compare the blood lactate concentrations<br />

after two tests of maximal <strong>in</strong>tensity: a) 2x100 freestyle swimm<strong>in</strong>g<br />

<strong>and</strong> b) 4x50m freestyle. Eight competitive swimmers participated<br />

<strong>in</strong> this study. Capillary blood samples were obta<strong>in</strong>ed the 3rd, 5th <strong>and</strong> 7th<br />

m<strong>in</strong> after the end of each test. Analysis of the results showed that there<br />

is a statistically significant correlation between the lactate concentration<br />

<strong>in</strong> the test of 2x100 <strong>and</strong> 4x50m freestyle swimm<strong>in</strong>g only for females<br />

(r=0.871). Moreover, no statistical significance was observed between<br />

the test of 4x50 or 2x100 concern<strong>in</strong>g lactic acid accumulation between<br />

male <strong>and</strong> female. The results obta<strong>in</strong>ed showed that the tested female<br />

swimmers swam at 4x50m more efficiently than their male counterparts.<br />

Key words: Freestyle swimm<strong>in</strong>g, maximum lactate concentration,<br />

gender<br />

IntroductIon<br />

Lactic acid constitutes a useful tool for the determ<strong>in</strong>ation of anaerobic<br />

capacity for researchers <strong>and</strong> tra<strong>in</strong>ers. The highest lactate levels have<br />

been recorded follow<strong>in</strong>g the swimm<strong>in</strong>g distances of 100 <strong>and</strong> 200 meters<br />

(Avlonitou 1996). The energy cost of swimm<strong>in</strong>g has been found<br />

to dependent on the drag of the athlete, efficiency of stroke mechanics<br />

<strong>and</strong> velocity of movement through the water. Competitive swimm<strong>in</strong>g<br />

requires <strong>in</strong>tense activity from a large muscle mass. This requirement favours<br />

<strong>in</strong>volvement of anaerobic energy release with the subsequent accumulation<br />

of lactate <strong>in</strong> the blood.<br />

The measurement of blood lactate concentration has become a<br />

common practice of swimm<strong>in</strong>g coaches for performance diagnosis<br />

<strong>and</strong> tra<strong>in</strong><strong>in</strong>g control <strong>in</strong> competitive swimm<strong>in</strong>g over the last few years<br />

(Pelayo et al. 1996; Avlonitou, E. 1996). For researchers <strong>and</strong> coaches,<br />

lactic acid constitutes a useful implement for the determ<strong>in</strong>ation of anaerobic<br />

capacity. Lactic acid is a useful marker of anaerobic capacity for<br />

researchers <strong>and</strong> tra<strong>in</strong>ers. Considerable emphasis has been given to the<br />

measurement of blood lactate dur<strong>in</strong>g sub-maximal <strong>and</strong> maximal swimm<strong>in</strong>g<br />

efforts. Muscle lactic levels are between 1 – 2 mmol/l <strong>in</strong> the blood<br />

dur<strong>in</strong>g rest <strong>and</strong> can <strong>in</strong>crease to between 10 -20 mmol/l dur<strong>in</strong>g all out<br />

effort (Maglischo 2003). The distances that are used to measure maximum<br />

lactic acid accumulation are 100m or 200m (Avlonitou, E. 1996).<br />

As a result, for the maximum production of lactic acid, efforts of 1 to 2<br />

m<strong>in</strong>utes of full <strong>in</strong>tensity are required. Rate of lactic acid production <strong>in</strong><br />

muscle fibers depends on swimm<strong>in</strong>g speed, rate of oxygen consumption<br />

<strong>and</strong> type of muscle fiber (Maglischo 2003). There is much <strong>in</strong>terest<br />

concern<strong>in</strong>g difference <strong>in</strong> blood lactate accumulation level <strong>in</strong> male <strong>and</strong><br />

female swimmers.<br />

Indeed, several studies have used the relationship between blood lactate<br />

concentration <strong>and</strong> swimm<strong>in</strong>g velocity to determ<strong>in</strong>e the appropriate<br />

exercise <strong>in</strong>tensities dur<strong>in</strong>g competition (Sawka et al. 1979; Chatard<br />

et al. 1988) or tra<strong>in</strong><strong>in</strong>g <strong>and</strong> to gauge swimmers adaptation to tra<strong>in</strong><strong>in</strong>g<br />

programs (Mader et al. 1978; Kesk<strong>in</strong>en et al. 1989; Ryan et al. 1990;<br />

Costill 1992).<br />

In their attempt to improve competition performance, swimmers<br />

perform large volumes <strong>and</strong>/or high <strong>in</strong>tensities of tra<strong>in</strong><strong>in</strong>g with, sometimes,<br />

<strong>in</strong>sufficient time to recover between workouts (Pelayo et al. 1996).<br />

There is little <strong>in</strong>formation for the comparison of different maximum<br />

efforts <strong>in</strong> order to determ<strong>in</strong>e the most adequate tra<strong>in</strong><strong>in</strong>g method for<br />

maximal accumulation <strong>and</strong> tolerance of lactic acid.


In addition, review of the scientific literature revealed that peak<br />

blood lactate levels are not significantly different between sexes, suggest<strong>in</strong>g<br />

that the capacity to produce high lactate levels <strong>in</strong> the blood is<br />

probably acquired through tra<strong>in</strong><strong>in</strong>g, rather than be<strong>in</strong>g sex related (Chatard<br />

et al. 1988; Jacobs et al.1983)<br />

The success <strong>in</strong> these tests seems to depend on the swimmer’s capacity<br />

to achieve higher velocities with lower blood lactate levels <strong>and</strong>/or<br />

utiliz<strong>in</strong>g a lower percentage of their VO2 max.(Ribeiro 1990).<br />

The purpose of the present study was to compare two specific tests<br />

for the determ<strong>in</strong>ation of maximum accumulation of lactic acid <strong>in</strong> blood,<br />

based on two distances of 2x100m <strong>and</strong> 4x50m freestyle of maximum<br />

<strong>in</strong>tensity <strong>and</strong> the same rest, compar<strong>in</strong>g: a) the two tests <strong>and</strong> b) the two<br />

genders.<br />

Methods<br />

In the present study 8 swimmers of competitive level participated (4<br />

males of 16.2±0.96 years, body mass 71.70±5.56kg <strong>and</strong> body stature<br />

181.12±7.86cm <strong>and</strong> 4 females of 15.5±2.08 years, body mass<br />

53.27±14.92kg <strong>and</strong> body stature 164.87±9.20cm). At the beg<strong>in</strong>n<strong>in</strong>g,<br />

they swam 2x100 meters freestyle with maximum <strong>in</strong>tensity <strong>and</strong> time<br />

performance <strong>and</strong> the blood lactate accumulation was measured. Five<br />

days later the same athletes were tested for 4x50 meters with 10 seconds<br />

rest between each effort of 50meters. In order to determ<strong>in</strong>e maximum<br />

concentration of lactic acid <strong>in</strong> the two different tests, capillary samples<br />

of blood were taken from the f<strong>in</strong>ger of 3rd, 5th, 7th <strong>and</strong> 10th m<strong>in</strong>ute of<br />

recovery time <strong>and</strong> analysed us<strong>in</strong>g the automatic analyzer Lactate Scout.<br />

For the comparison of mean values of blood lactate production <strong>in</strong> the<br />

two tests, the t - test for dependent samples was applied. Furthermore,<br />

the correlation coefficient was exam<strong>in</strong>ed between the two tests.<br />

results<br />

The average time performance of swimmers <strong>in</strong> 2x100 meters freestyle<br />

was 120.79±5.67sec <strong>and</strong> 146.32±5.26sec while <strong>in</strong> 4x50m it was<br />

120.43±5.96sec <strong>and</strong> 139.64±5.44sec <strong>in</strong> males <strong>and</strong> females respectively.<br />

Maximum accumulation of lactic acid <strong>in</strong> 2x100 meters freestyle was<br />

11.3±2.6 <strong>and</strong> 10.3±2.1 mmol/l <strong>in</strong> males <strong>and</strong> females respectively. In relation<br />

to the test of 4x50 it was 12.1±2.3 <strong>and</strong> 12.5±3.9 mmol/l <strong>in</strong> males<br />

<strong>and</strong> females, respectively. Significant correlation was found between the<br />

two tests <strong>in</strong> lactic acid accumulation only among the females (r=0.871;<br />

p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Can Blood Glucose Threshold be Determ<strong>in</strong>ed <strong>in</strong><br />

Swimmers Early <strong>in</strong> the Swimm<strong>in</strong>g Season?<br />

sengoku, Y. 1 , nakamura, K. 2 , takeda, t. 2 , nabekura, Y. 2 , tsubakimoto,<br />

s. 2<br />

1 Heisei International University, Saitama, Japan<br />

2 University of Tsukuba, Ibaraki, Japan<br />

The present study <strong>in</strong>vestigated whether blood glucose threshold (GT)<br />

could be determ<strong>in</strong>ed <strong>in</strong> swimmers early <strong>in</strong> the swimm<strong>in</strong>g season. Seven<br />

university swimmers participated <strong>in</strong> this study <strong>and</strong> performed an <strong>in</strong>cremental<br />

swimm<strong>in</strong>g test <strong>in</strong> a swimm<strong>in</strong>g flume. The test was conducted 4<br />

– 5 weeks after the w<strong>in</strong>ter season commencement. Blood glucose (Glu)<br />

<strong>and</strong> blood lactate (Bla) were measured after each swimm<strong>in</strong>g <strong>in</strong>cremental<br />

step, <strong>and</strong> the velocity correspond<strong>in</strong>g to GT <strong>and</strong> blood lactate threshold<br />

(LT) was calculated. A LT was observed <strong>in</strong> all swimmers. However,<br />

Glu tended to decrease as the test started <strong>and</strong> then did not<br />

<strong>in</strong>crease with swimm<strong>in</strong>g <strong>in</strong>tensity. The low Glu observed dur<strong>in</strong>g<br />

high <strong>in</strong>tensities may be due to high glucose uptake by the work<strong>in</strong>g<br />

muscles or low endurance capacity <strong>in</strong> the early season. A GT<br />

could not be observed for all swimmers.<br />

Key words: endurance capacity, <strong>in</strong>cremental swimm<strong>in</strong>g test, glucose<br />

metabolism<br />

IntroductIon<br />

Blood lactate concentration (Bla) is known to <strong>in</strong>crease rapidly at high<br />

exercise <strong>in</strong>tensity dur<strong>in</strong>g an <strong>in</strong>cremental test <strong>and</strong> the exercise <strong>in</strong>tensity<br />

where Bla starts to rise is recognized as lactate threshold (LT). LT is<br />

observed when lactate production surpasses the lactate removal rate <strong>and</strong><br />

thus this <strong>in</strong>tensity is considered to demonstrate the boundary of aerobic<br />

<strong>and</strong> anaerobic energy supply <strong>and</strong> is utilized as an <strong>in</strong>dicator of aerobic<br />

endurance performance (Hollman, 1985).<br />

Recently, Simões et al. (1999) reported that blood glucose (Glu)<br />

also <strong>in</strong>creases dur<strong>in</strong>g an <strong>in</strong>cremental runn<strong>in</strong>g test <strong>and</strong> a blood glucose<br />

threshold (GT) could be observed as for LT. It was reported that GT<br />

significantly correlates with LT, ventilation threshold (VT) <strong>and</strong> maximal<br />

lactate steady state (MLSS) (Simões et al., 1999; Simões et al., 2003;<br />

Sotero et al., 2009), thus GT may also be a good <strong>in</strong>dicator for the aerobic-anaerobic<br />

transition.<br />

Simões et al. (1999) speculated that the <strong>in</strong>crease of Glu when exercise<br />

became more <strong>in</strong>tense was due to activated catecholam<strong>in</strong>e <strong>and</strong> glucagon<br />

responses. It is considered that these hormonal activities will elevate<br />

when the exercise <strong>in</strong>tensity rises above the anaerobic threshold (AT) <strong>and</strong><br />

higher glucose production than glucose uptake by the skeletal muscle<br />

may lead to a Glu <strong>in</strong>crement. For these reasons, it could be suggested<br />

that Glu reflects the shift of glucose metabolism <strong>and</strong> the GT could be a<br />

new <strong>in</strong>dex for energy metabolism dur<strong>in</strong>g endurance exercise. However,<br />

observations of GT were reported only <strong>in</strong> runn<strong>in</strong>g (Simões et al., 1999;<br />

Simões et al., 2003; Sotero et al., 2009) <strong>and</strong> cycl<strong>in</strong>g ( Júnior et al., 2001)<br />

<strong>and</strong> there is no study <strong>in</strong>vestigat<strong>in</strong>g GT <strong>in</strong> competitive swimmers whose<br />

endurance capacity is supposed to be important. As a previous study<br />

reported that Glu is lower <strong>in</strong> swimm<strong>in</strong>g than runn<strong>in</strong>g after sub-maximal<br />

cont<strong>in</strong>uous exercise (Flynn et al., 1990), there are possibilities that different<br />

Glu response may occur even dur<strong>in</strong>g <strong>in</strong>cremental exercise.<br />

The purpose of the present study was to <strong>in</strong>vestigate Glu response<br />

dur<strong>in</strong>g an <strong>in</strong>cremental swimm<strong>in</strong>g test <strong>and</strong> verify whether GT could be<br />

determ<strong>in</strong>ed as <strong>in</strong> runn<strong>in</strong>g on l<strong>and</strong> early <strong>in</strong> the swimm<strong>in</strong>g season.<br />

Methods<br />

Seven male university swimmers specialized <strong>in</strong> middle <strong>and</strong> long distance<br />

freestyle (n = 3) or <strong>in</strong>dividual medley (n = 4) participated <strong>in</strong> this<br />

study (20.1 ± 0.9 years of age, 173.1 ± 4.3 cm height, 65.2 ± 2.6 kg<br />

224<br />

body weight, 4:02.1 ± 5.8 for best 400 m freestyle). All swimmers were<br />

compet<strong>in</strong>g at national level championships. The measurement was conducted<br />

4 – 5 weeks after the w<strong>in</strong>ter season commencement (Nov. 2009).<br />

The subjects were made fully aware of the risks, benefits <strong>and</strong> stresses of<br />

the study <strong>and</strong> their <strong>in</strong>formed consent was obta<strong>in</strong>ed.<br />

All <strong>in</strong>cremental swimm<strong>in</strong>g tests were conducted <strong>in</strong> a swimm<strong>in</strong>g<br />

flume at University of Tsukuba. The schematic representation of the<br />

test<strong>in</strong>g is presented <strong>in</strong> Fig. 1. Swimm<strong>in</strong>g velocity of the <strong>in</strong>cremental<br />

swimm<strong>in</strong>g test was <strong>in</strong>dividualized by each swimmer’s average swimm<strong>in</strong>g<br />

speed for their best 400 m freestyle (V400). After a 5 m<strong>in</strong> warm up at<br />

55% V400 <strong>and</strong> a 4 m<strong>in</strong> rest, the participants completed an <strong>in</strong>cremental<br />

swimm<strong>in</strong>g test consist<strong>in</strong>g of a series of seven 3 m<strong>in</strong> swimm<strong>in</strong>g steps<br />

with 2 m<strong>in</strong> <strong>in</strong>terval for blood sampl<strong>in</strong>g. The <strong>in</strong>tensity of each step was<br />

<strong>in</strong>creased from 55 % to 85% V400.<br />

W-up<br />

Time(m<strong>in</strong>) 0 5 9 12 14 17 19 22 24 27 29 32 34 37 39 42<br />

55%V400 55%V400 60%V400 65%V400 70%V400 75%V400 80%V400 85%V400<br />

Bla ↑ ↑ ↑ ↑ ↑ ↑ ↑ ↑ ↑<br />

Glu ↑ ↑ ↑ ↑ ↑ ↑ ↑ ↑ ↑<br />

Fig. 1 Schematic representation of the test<strong>in</strong>g sequence<br />

Before the test <strong>and</strong> right after each <strong>in</strong>cremental swimm<strong>in</strong>g step, blood<br />

samples were obta<strong>in</strong>ed from the f<strong>in</strong>ger tip <strong>and</strong> blood glucose (Glu; Glucocard,<br />

GT-1670, Arkray, Japan) <strong>and</strong> blood lactate (Bla; Lactate Pro,<br />

LT-1710, Arkray, Japan) were measured. The accuracy of the portable<br />

measurement devices are assessed <strong>in</strong> previous studies (Weitgasser et al.,<br />

1999; Tanner et al., 2010). Swimm<strong>in</strong>g velocity correspond<strong>in</strong>g to GT<br />

(VGT) <strong>and</strong> LT (VLT) were analyzed utiliz<strong>in</strong>g Blood Lactate Endurance<br />

Marker Software (Lactate-E) (Newell et al., 2007).<br />

The subjects were <strong>in</strong>structed to refra<strong>in</strong> from strenuous physical activity<br />

<strong>and</strong> caffe<strong>in</strong>e <strong>in</strong>take on the test<strong>in</strong>g day <strong>and</strong> f<strong>in</strong>ish their last meal 3 h<br />

before test<strong>in</strong>g. Only water <strong>in</strong>gestion was allowed after the f<strong>in</strong>al meal. All<br />

data are reported as mean ± SD.<br />

results<br />

Glu <strong>and</strong> Bla before the test were 5.5 ± 0.8 mmol·l -1 <strong>and</strong> 1.2 ± 0.4<br />

mmol·l -1 respectively. Result of the Glu <strong>and</strong> Bla measurements dur<strong>in</strong>g<br />

the <strong>in</strong>cremental swimm<strong>in</strong>g test are presented <strong>in</strong> Fig. 2. LT was observed<br />

<strong>in</strong> all swimmers <strong>and</strong> the average VLT was 1.24 ± 0.05 m·sec -1 . Glu<br />

tended to decrease as the test started <strong>and</strong> did not <strong>in</strong>crease at the higher<br />

swimm<strong>in</strong>g <strong>in</strong>tensity steps. Consequently, a GT threshold could not be<br />

determ<strong>in</strong>ed for all swimmers.<br />

Blood Lactate (mmol/l)<br />

Blood Glucose (mmol/l)<br />

12.0<br />

10.0<br />

8.0<br />

6.0<br />

4.0<br />

2.0<br />

0.0<br />

Bla Glu<br />

55 60 65 70 75 80 85<br />

%V 400<br />

Fig. 2 Blood glucose <strong>and</strong> blood lactate responses dur<strong>in</strong>g <strong>in</strong>cremental<br />

swimm<strong>in</strong>g test


dIscussIon<br />

The present study <strong>in</strong>tended to <strong>in</strong>vestigate Glu response dur<strong>in</strong>g an <strong>in</strong>cremental<br />

swimm<strong>in</strong>g test <strong>and</strong> verify whether GT could be determ<strong>in</strong>ed early<br />

<strong>in</strong> the swimm<strong>in</strong>g season. The ma<strong>in</strong> f<strong>in</strong>d<strong>in</strong>g of this study was the constant<br />

Glu level throughout the <strong>in</strong>cremental swimm<strong>in</strong>g test <strong>and</strong> that GT was<br />

not observed <strong>in</strong> competitive swimmers. The subjects <strong>in</strong> this study tra<strong>in</strong>ed<br />

on a daily basis as they were elite national level competitive swimmer.<br />

The physical activity preced<strong>in</strong>g this <strong>in</strong>vestigation was not controlled for,<br />

which is a limitation <strong>in</strong> this study. However, physical activity level <strong>and</strong><br />

nutritional state were controlled on the test<strong>in</strong>g day <strong>and</strong> the rest<strong>in</strong>g Glu<br />

<strong>and</strong> Bla were at a normal level (5.5 ± 0.8 mmol·l -1 <strong>and</strong> 1.2 ± 0.4 mmol·l -1 ,<br />

respectively).<br />

Previous studies reported that GT was observed dur<strong>in</strong>g an <strong>in</strong>cremental<br />

runn<strong>in</strong>g test on l<strong>and</strong> <strong>and</strong> GT significantly correlates with LT,<br />

VT <strong>and</strong> MLSS (Simões et al., 1999; Simões et al., 2003; Sotero et al.,<br />

2009). The possible mechanism for the GT observation is speculated to<br />

be affected by the activated catecholam<strong>in</strong>e <strong>and</strong> glucagon responses, thus<br />

the different hormonal response between swimm<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g could<br />

expla<strong>in</strong> the conflict<strong>in</strong>g results <strong>in</strong> this study. Unfortunately, runn<strong>in</strong>g <strong>and</strong><br />

hormone measurements were not performed <strong>in</strong> the present study.<br />

Flynn et al. (1990) <strong>in</strong>vestigated the Glu response dur<strong>in</strong>g 45 m<strong>in</strong> of<br />

swimm<strong>in</strong>g or runn<strong>in</strong>g (75% VO2max) <strong>and</strong> reported that a lower Glu<br />

level was observed after swimm<strong>in</strong>g than runn<strong>in</strong>g. In addition, this study<br />

demonstrated that ep<strong>in</strong>ephr<strong>in</strong>e levels was similar after both trials. However,<br />

the Glucagon to Insul<strong>in</strong> ratio (G:I ratio) was significantly higher<br />

for swimm<strong>in</strong>g than runn<strong>in</strong>g. Greater glucagon to <strong>in</strong>sul<strong>in</strong> ratio represents<br />

higher hepatic glucose production, therefore, it is suggested that the energy<br />

dem<strong>and</strong> of hepatic glycogen at the same relative exercise <strong>in</strong>tensity<br />

may differ between swimm<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g.<br />

An <strong>in</strong>creased reliance on carbohydrate dur<strong>in</strong>g swimm<strong>in</strong>g is also discussed<br />

<strong>in</strong> the work of Lavoie (1982). It is speculated that swimm<strong>in</strong>g may<br />

result <strong>in</strong> a preferential recruitment of type II fibers <strong>and</strong> thus <strong>in</strong>crease the<br />

dependence on glycolytic processes. Consider<strong>in</strong>g these studies, it is possible<br />

that glucose uptake was higher dur<strong>in</strong>g the <strong>in</strong>cremental swimm<strong>in</strong>g<br />

test than <strong>in</strong> runn<strong>in</strong>g <strong>and</strong> Glu did not <strong>in</strong>crease at the higher <strong>in</strong>tensity<br />

steps <strong>in</strong> the present study. Further <strong>in</strong>vestigation is needed to exam<strong>in</strong>e<br />

carbohydrate oxidation <strong>and</strong> hormonal response dur<strong>in</strong>g an <strong>in</strong>cremental<br />

swimm<strong>in</strong>g test to clarify the mechanism of the different Glu responses<br />

<strong>in</strong> swimm<strong>in</strong>g.<br />

On the other h<strong>and</strong>, the swimmer’s tra<strong>in</strong><strong>in</strong>g state dur<strong>in</strong>g this <strong>in</strong>vestigation<br />

may be another factor caus<strong>in</strong>g Glu not to <strong>in</strong>crease along<br />

with exercise <strong>in</strong>tensity <strong>in</strong>crement. Coggan et al. (1995) <strong>in</strong>vestigated<br />

the Glu response dur<strong>in</strong>g 30 m<strong>in</strong> at 80 % VO2max cycl<strong>in</strong>g compar<strong>in</strong>g<br />

endurance tra<strong>in</strong>ed cyclists <strong>and</strong> untra<strong>in</strong>ed subjects. They reported that<br />

rate of glucose disappearance dur<strong>in</strong>g exercise was 19 % lower <strong>in</strong> the<br />

tra<strong>in</strong>ed compared with the untra<strong>in</strong>ed subjects (27.0 ± 2.6 vs. 33.2 ± 1.5<br />

mumol·m<strong>in</strong>-1·kg-1; p< 0.001), consequently, dur<strong>in</strong>g exercise, plasma<br />

glucose concentration rose significantly <strong>in</strong> the tra<strong>in</strong>ed subjects but did<br />

not change <strong>in</strong> the untra<strong>in</strong>ed subjects. Thus, observation of GT dur<strong>in</strong>g<br />

an <strong>in</strong>cremental exercise test may reflect the endurance capacity level of<br />

the subject. The present study was conducted 4 – 5 weeks after the w<strong>in</strong>ter<br />

season commencement. Before the season, all subjects spent a one<br />

month rest<strong>in</strong>g period, so it could be that the endurance capacity of the<br />

present subject was not highly enhanced. As there is no study <strong>in</strong>vestigat<strong>in</strong>g<br />

the effect of endurance tra<strong>in</strong><strong>in</strong>g on GT, further study is warranted to<br />

exam<strong>in</strong>e Glu response dur<strong>in</strong>g an <strong>in</strong>cremental swimm<strong>in</strong>g test at higher<br />

levels of endurance, later <strong>in</strong> the season.<br />

conclusIon<br />

The present study was <strong>in</strong>tended to <strong>in</strong>vestigate Glu response dur<strong>in</strong>g an<br />

<strong>in</strong>cremental swimm<strong>in</strong>g test <strong>and</strong> verify whether GT could be determ<strong>in</strong>ed<br />

early <strong>in</strong> the swimm<strong>in</strong>g season. It was clarified that GT could not be<br />

determ<strong>in</strong>ed dur<strong>in</strong>g an <strong>in</strong>cremental swimm<strong>in</strong>g test. The fact that Glu did<br />

not <strong>in</strong>crease was speculated to be the different hormonal response dur<strong>in</strong>g<br />

swimm<strong>in</strong>g or the effect of the measurement period when swimmer’s<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

endurance capacity was not highly enhanced. Further research is needed<br />

to clarify the Glu response dur<strong>in</strong>g an <strong>in</strong>cremental swimm<strong>in</strong>g test by<br />

analyz<strong>in</strong>g the physiological responses more precisely.<br />

reFerences<br />

Coggan A.R., Raguso C.A., Williams B.D., Sidossis L.S., Gastaldelli A.<br />

(1995) Glucose k<strong>in</strong>etics dur<strong>in</strong>g high-<strong>in</strong>tensity exercise <strong>in</strong> endurancetra<strong>in</strong>ed<br />

<strong>and</strong> untra<strong>in</strong>ed humans. J. Appl. Physiol., 80,1073-1075.<br />

Flynn M.G., Costill D.L., Kirwan J.P., Mitchell J.B., Houmard J.A.,<br />

F<strong>in</strong>k W.J., Beltz J.D., D’Acquisto J. (1990) Fat storage <strong>in</strong> athlete:<br />

Metabolic <strong>and</strong> hormonal responses to swimm<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g. Int. J.<br />

Sports Med., 11, 433-440.<br />

Hollman L.H. (1985) Historical remarks on the development of the<br />

aerobic-anaerobic threshold up to 1966. Int. J. Sports Med., 6: 109-<br />

116.<br />

Júnior P.B., Neiva C.M., Denadai B.S. (2001) Effect of an acute betaadrenergic<br />

blockade on the blood glucose response dur<strong>in</strong>g lactate<br />

m<strong>in</strong>imum test. J. Sci. Med. Sport., 4, 257-265.<br />

Lavoie J.M. (1982) Blood metabolites dur<strong>in</strong>g prolonged exercise <strong>in</strong><br />

swimm<strong>in</strong>g <strong>and</strong> leg cycl<strong>in</strong>g. Eur. J. Appl. Physiol., 48, 127-133.<br />

Newell J., Higg<strong>in</strong>s D., Madden N., Cruickshank J., E<strong>in</strong>beck J., McMillan<br />

K., McDonald R. (2007) Software for calculat<strong>in</strong>g blood lactate<br />

endurance markers, J. Sports Sci., 25, 1403-1409.<br />

Simões H.G., Grubert Campbell C.S., Kokubun E., Denadai B.S.,<br />

Baldissera V. (1999) Blood glucose responses <strong>in</strong> humans mirror lactate<br />

responses for <strong>in</strong>dividual anaerobic threshold <strong>and</strong> for lactate m<strong>in</strong>imum<br />

<strong>in</strong> track tests. Eur. J. Appl. Physiol. Occup. Physiol., 80, 34-40.<br />

Simões H.G., Campbell C.S., Kushnick M.R., Nakamura A., Katsanos<br />

C.S., Baldissera V., Moffatt R.J. (2003) Blood glucose threshold <strong>and</strong><br />

the metabolic responses to <strong>in</strong>cremental exercise tests with <strong>and</strong> without<br />

prior lactic acidosis <strong>in</strong>duction. Eur. J. Appl. Physiol., 89, 603-611.<br />

Sotero R.C., Pardono E., L<strong>and</strong>wehr R., Campbell S.G., Simoes H.G.<br />

(2009) Blood glucose m<strong>in</strong>imum predicts maximal lactate steady state<br />

on runn<strong>in</strong>g. Int. J. Sports Med., 30, 643-646.<br />

Tanner R.K., Fuller K.L., Ross M.L. (2010) Evaluation of three portable<br />

blood lactate analysers: Lactate Pro, Lactate Scout <strong>and</strong> Lactate<br />

Plus. Eur. J. Appl. Physiol. [ahead of pr<strong>in</strong>t]<br />

Weitgasser R., Gappmayer B., Pichler M. (1999) Newer portable glucose<br />

meters – Analytical improvement compared with previous generation<br />

devices? Cl<strong>in</strong>. Chem., 45, 1821-1825.<br />

225


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The Effects of Rubber Swimsuits on Swimmers<br />

Us<strong>in</strong>g a Lactic Acid Curve Test<br />

shiraki, t. 1 , Wakayoshi, K. 1 , hata, h. 1 , Yamamoto, t. 2 , tomikawa,<br />

M. 3<br />

1 Biwako Seikei Sport College, Japan<br />

2 YAMAMOTO CORPORATION CO., LTD., Japan<br />

3 University of Tsukuba, Japan<br />

The rubber swimsuit, made from Neoprene rubber, was one of the causes<br />

of the swimm<strong>in</strong>g record rush <strong>in</strong> 2009. The benefits of wear<strong>in</strong>g a wetsuit<br />

on swimmers were widely reported. This study verified the <strong>in</strong>fluence of<br />

wear<strong>in</strong>g the rubber swimsuit on a swimm<strong>in</strong>g exercise load. Eight female<br />

university swimmers performed 4 x 200 m crawl swimm<strong>in</strong>g at <strong>in</strong>cremental<br />

speeds, set from the best record of each 200 m freestyle race<br />

(80%V 200 , 85% V 200 , 90% V 200 , 95% V 200 ). Four different suits (three<br />

types of rubber suits <strong>and</strong> a cloth swimsuit) were used <strong>and</strong> lactic acid<br />

curve tests were conducted. The blood lactate concentration after 90%<br />

V 200 <strong>and</strong> 95% V 200 trials with rubber swimsuits tended to be lower than<br />

those with a cloth swimsuit. An exam<strong>in</strong>ation of the trials revealed that<br />

the total number of arm strokes tended to decrease due to the use of the<br />

rubber swimsuits. It is suggested that the rubber swimsuits might improve<br />

propulsion efficiency <strong>and</strong> decreased the swimmer’s exercise load,<br />

<strong>in</strong>dicat<strong>in</strong>g that the rubber swimsuit may improve the race performance<br />

of swimmers.<br />

Key words: rubber swimsuit, lactic acid curve test<br />

IntroductIon<br />

Forty-three new world records were set <strong>in</strong> 13 th FINA World Championships<br />

<strong>in</strong> Rome 2009. It was not just a historical co<strong>in</strong>cidence that<br />

the 43 new world records were established <strong>in</strong> just one meet<strong>in</strong>g. These<br />

records were reached with new swimsuits with high technology. In fact,<br />

the rubber swimsuit was one of the causes of this record rush. Be<strong>in</strong>g<br />

similar to wetsuits, the rubber swimsuit was made from Neoprene rubber.<br />

So, rubber swimsuits probably present beneficial characteristics similar<br />

to wetsuits. The effects of us<strong>in</strong>g wetsuits on swimmers were widely<br />

reported:(i) triathletes are able to hold their bodies <strong>in</strong> a more horizontal<br />

position because of the added buoyancy (Chatard et al., 1996, Chatard<br />

et al., 1995, Toussa<strong>in</strong>t et al., 1989) <strong>and</strong> (ii) drag force is reduced by the<br />

smooth surface provided by a wetsuit (Chatard et al., 1995, Toussa<strong>in</strong>t<br />

et al., 1989).<br />

Additionally, Tomikawa et al. (2008) showed that swimm<strong>in</strong>g velocity<br />

at maximal oxygen consumption with a wetsuit was 5.4% higher than<br />

with a swimsuit, <strong>and</strong> that the swimm<strong>in</strong>g energy cost of swimm<strong>in</strong>g with<br />

a wetsuit was lower by 14.4% at 60% of the velocity correspond<strong>in</strong>g to<br />

VO 2 max <strong>and</strong> 7.5% at 80% of the velocity correspond<strong>in</strong>g to VO 2 max.<br />

These results suggest that the benefits of wear<strong>in</strong>g a wetsuit <strong>in</strong>clude not<br />

only the improvement <strong>in</strong> swimm<strong>in</strong>g propulsion efficiency, but also the<br />

reduction <strong>in</strong> energy consumption. While the thickness of a wetsuit is<br />

2-5mm, a rubber swimsuit is only 0.3mm thick, which seems to imply<br />

that the benefits of wear<strong>in</strong>g a rubber swimsuit might be less than those<br />

of us<strong>in</strong>g a wetsuit.<br />

A lactic acid curve test is usually used to determ<strong>in</strong>e the anaerobic<br />

threshold to monitor tra<strong>in</strong><strong>in</strong>g (Maglischo, 2003). The test is an <strong>in</strong>cremental<br />

one, allow<strong>in</strong>g that the values of blood lactate concentration be<br />

plotted on a graph <strong>in</strong> comb<strong>in</strong>ation with the swimm<strong>in</strong>g velocity. If the<br />

lactate-velocity curve will move to the right when wear<strong>in</strong>g a wetsuit,<br />

the swimm<strong>in</strong>g performance is improved. This study aimed to verify the<br />

<strong>in</strong>fluence of wear<strong>in</strong>g a rubber swimsuit on the swimm<strong>in</strong>g exercise load<br />

by us<strong>in</strong>g a lactic-velocity curve test.<br />

226<br />

Methods<br />

Eight female university swimmers participated <strong>in</strong> this study. The average<br />

of their best records for 200 m freestyle swimm<strong>in</strong>g was 129.8 ± 4.5 seconds.<br />

They attended the Japanese <strong>in</strong>ter-college swim meet 2009. Their<br />

age, height <strong>and</strong> weight were 19.8 ± 0.9 years, 160.8 ± 4.2 cm <strong>and</strong><br />

58.0 ± 2.8 kg, respectively, <strong>and</strong> they had a body fat % of 28.4 ± 3.6.<br />

Four types of suits were used <strong>in</strong> this study. Three rubber suits were<br />

made from Neoprene rubber: (i) rubber suit A was a commercially available<br />

suit: (ii) rubber suit B was made from Neoprene rubber, <strong>and</strong> metallic<br />

m<strong>in</strong>erals were conta<strong>in</strong>ed between rubber <strong>and</strong> back fabric layers: (iii)<br />

rubber suit C was also made from Neoprene rubber, <strong>in</strong> which titanium<br />

was <strong>in</strong>cluded <strong>in</strong> bond part between rubber <strong>and</strong> back fabric layers. Rubber<br />

suit B <strong>and</strong> C were not commercially available. The 4 th suit type was a<br />

cloth swimsuit, be<strong>in</strong>g a common water-repellent competitive swimsuit<br />

with. All swimsuits were the full-length type, cover<strong>in</strong>g from shoulder<br />

to ankle.<br />

Swimmers performed a 4 x 200 m <strong>in</strong>cremental swimm<strong>in</strong>g protocol,<br />

the speed of the four stages set from the best record of each 200 m<br />

freestyle race (80%V 200 , 85% V 200 , 90% V 200 , 95% V 200 ). The speed was<br />

controlled by a pace maker set on the bottom of pool. Blood from the<br />

f<strong>in</strong>gertip was taken at 0, 3 <strong>and</strong> 5 m<strong>in</strong> after each trial. The blood lactate<br />

concentration was determ<strong>in</strong>ed us<strong>in</strong>g Lactate Pro analyzer (ARKRAY,<br />

Inc.). Arm strokes <strong>in</strong> the trials were counted each 25 m (LAP 1 to 8).<br />

The mean <strong>and</strong> st<strong>and</strong>ard deviation were computed for all variables.<br />

ANOVA with repeated measures was used to compare the data obta<strong>in</strong>ed<br />

<strong>in</strong> the wetsuits <strong>and</strong> a swimsuit condition. A probability level of 5% was<br />

selected for tests of statistical significance.<br />

results<br />

The mean ± SD values of blood lactate concentrations <strong>in</strong> each trial are<br />

shown <strong>in</strong> Table 1. No significant differences were found <strong>in</strong> blood lactate<br />

concentration between different rubber suit conditions.<br />

Table 1. Means ± SD of Blood lactate concentration <strong>in</strong> each suit<br />

condition<br />

NS<br />

mmol·L -1<br />

RS-A<br />

mmol·L -1<br />

RS-B<br />

mmol·L -1<br />

RS-C<br />

mmol·L -1<br />

80%V200 1.49 ± 0.45 1.61 ± 0.54 1.54 ± 0.51 1.30 ± 0.47<br />

85%V200 2.11 ± 0.59 1.95 ± 0.88 1.83 ± 0.69 1.78 ± 0.61<br />

90%V200 3.89 ± 1.37 3.20 ± 1.73 2.89 ± 1.21 2.95 ± 1.45<br />

95%V200 10.46 ± 2.37 8.68 ± 2.66 9.35 ± 2.24 8.18 ± 2.98<br />

However, the blood lactate concentration after 90% V 200 <strong>and</strong> 95% V 200<br />

trials with rubber swimsuits tended to be lower than those with a cloth<br />

swimsuit (Figure 1). Especially, when wear<strong>in</strong>g rubber suit C, the blood<br />

lactate concentration tended to be lower than wear<strong>in</strong>g other suits. The<br />

blood lactate concentrations after 90% V 200 <strong>and</strong> 95% V 200 trials with the<br />

four suits were at the same level.<br />

Fig 1. The blood lactate concentration-Swimm<strong>in</strong>g velocity curve <strong>in</strong> an<br />

experimental suits conditions


The trials were controlled by a pace maker. When wear<strong>in</strong>g rubber swimsuits,<br />

most subjects could swim 2.0-2.9% faster than the velocity (95%<br />

V 200 trials) set by the pace maker (Fig1, Table 2).<br />

Table 2. Means <strong>and</strong> St<strong>and</strong>ard Deviations of Swimm<strong>in</strong>g velocity <strong>in</strong> each<br />

suit condition<br />

NS<br />

m·s-1 RS-A<br />

m·s-1 RS-B<br />

m·s-1 RS-C<br />

m·s-1 80%V200 1.24 ± 0.04 1.25 ± 0.04 1.25 ± 0.04 1.25 ± 0.04<br />

85%V200 1.32 ± 0.04 1.32 ± 0.04 1.32 ± 0.05 1.32 ± 0.05<br />

90%V200 1.39 ± 0.05 1.40 ± 0.05 1.40 ± 0.05 1.40 ± 0.05<br />

95%V200 1.49 ± 0.04 1.50 ± 0.04 1.51 ± 0.06 1.51 ± 0.06<br />

No significant differences were found <strong>in</strong> the number of arm strokes per<br />

25m between suit conditions. Conversely, an exam<strong>in</strong>ation of the trials<br />

revealed that the total number of arm strokes tended to decrease due to<br />

the use of the rubber swimsuits <strong>in</strong> 90%V200 <strong>and</strong> 95%V200 swimm<strong>in</strong>g<br />

(Fig2 <strong>and</strong> 3).<br />

Fig 2. The total number of arm strokes <strong>in</strong> 90%V 200 swimm<strong>in</strong>g <strong>in</strong> different<br />

suit condition<br />

Fig 3. The total number of arm strokes <strong>in</strong> 95% V 200 swimm<strong>in</strong>g <strong>in</strong> different<br />

suit condition<br />

dIscussIon<br />

No significant differences were found <strong>in</strong> blood lactate concentration<br />

between the suit conditions. However, Figure. 1 shows that the blood<br />

lactate concentration after 90% V 200 <strong>and</strong> 95% V 200 trials with rubber<br />

swimsuits tended to be lower by 1.1 to 2.2 mmol·L -1 than those with<br />

a cloth swimsuit. Even though the swimm<strong>in</strong>g velocity was controlled<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

by a pace maker on the bottom of the pool, some subjects could swim<br />

faster at 90% V 200 <strong>and</strong> 95% V 200 trials with rubber swimsuits. The results<br />

suggested that wear<strong>in</strong>g rubber swimsuits might improve the propulsion<br />

efficiency <strong>and</strong> reduce anaerobic energy consumption at a comparable<br />

swimm<strong>in</strong>g velocity. In previous studies, it was assumed that wear<strong>in</strong>g a<br />

wetsuit might reduce the exercise <strong>in</strong>tensity dur<strong>in</strong>g swimm<strong>in</strong>g (Bentley<br />

et al., 2002). Tomikawa et al. (2008) reported that even if triathletes have<br />

similar VO 2 <strong>in</strong> the wetsuit <strong>and</strong> swimsuit conditions, they swam 5.4%<br />

faster with a wetsuit. Given this result, it was considered that the effects<br />

of wear<strong>in</strong>g a rubber swimsuit were similar to those of wear<strong>in</strong>g a wetsuit,<br />

although a rubber swimsuit was th<strong>in</strong>ner than a wetsuit.<br />

When wear<strong>in</strong>g a wetsuit, s<strong>in</strong>ce triathletes float <strong>in</strong> a more horizontal<br />

position because of the added buoyancy, they are able to devote more<br />

energy to their arm propell<strong>in</strong>g motion, <strong>and</strong> to <strong>in</strong>crease their stroke<br />

rates with lengthen<strong>in</strong>g or reta<strong>in</strong><strong>in</strong>g stroke lengths (Chatard et al., 1995,<br />

Tomikawa et al., 2003). In this study, an exam<strong>in</strong>ation of the trials revealed<br />

that the total number of arm strokes tended to decrease due to<br />

the use of the rubber swimsuits (Figs. 2 <strong>and</strong> 3), while no significant differences<br />

were found <strong>in</strong> the total number of arm strokes between the suit<br />

conditions. It was suggested that swimmers could devote more energy<br />

to the propulsive force because of the added buoyancy, when wear<strong>in</strong>g<br />

rubber swimsuits.<br />

conclusIon<br />

The results showed that the beneficial characteristics of rubber swimsuits<br />

might be similar to wetsuits. S<strong>in</strong>ce rubber swimsuits were th<strong>in</strong>ner<br />

than wetsuits, the effects of wear<strong>in</strong>g a rubber swimsuit on swimmers<br />

were obviously smaller. Therefore, it is suggested that the rubber swimsuits<br />

might improve the propulsion efficiency <strong>and</strong> reduce the exercise<br />

<strong>in</strong>tensity dur<strong>in</strong>g swimm<strong>in</strong>g, <strong>in</strong>dicat<strong>in</strong>g that the rubber swimsuit may<br />

improve the race performance of swimmers.<br />

reFerences<br />

Bentley, D.J., Millet, G-P., Vlek, V-E. & McNaughton LR (2002). Specific<br />

aspect of contemporary triathlon: implications for physiological<br />

analysis <strong>and</strong> performance. Sports Med, 32, 345-59.<br />

Chatard, J.C. & Millet, G. (1996). Effects of wetsuit use <strong>in</strong> swimm<strong>in</strong>g<br />

events. Sports Med, 22, 70-75.<br />

Chatard, J.C., Senegas, X., Selles, M., Dreanot, P. & Geyssant A. (1995).<br />

Wetsuit effect: a comparison between competitive swimmers <strong>and</strong> triathletes.<br />

Med Sci Sports Exerc, 27(4), 580-86<br />

Maglischo, E.W. (2003). Swimm<strong>in</strong>g Fastest. Champaign: Human K<strong>in</strong>etics.<br />

Tomikawa, M. & Nomura T (2009). Relationships between swim performance,<br />

maximal oxygen uptake <strong>and</strong> peak power output when<br />

wear<strong>in</strong>g a wetsuit. Journal of Science & <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Sport, 12, 317-22.<br />

Tomikawa, M., Shimoyama, Y. & Nomura T (2008). Factors related<br />

to the advantageous effects of wear<strong>in</strong>g a wetsuit dur<strong>in</strong>g swimm<strong>in</strong>g<br />

at different submaximal velocity <strong>in</strong> triathletes. Journal of Science &<br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Sport, 11, 417-23.<br />

Tomikawa, M., Shimoyama, Y., Ichikawa, H. & Nomura T (2003). The<br />

effects of triathlon wetsuits on stroke parameters, physiological parameters<br />

<strong>and</strong> performance dur<strong>in</strong>g swimm<strong>in</strong>g. In: Chatard JC editor.<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> swimm<strong>in</strong>g, vol. Ⅸ. Sa<strong>in</strong>t-Etienne:<br />

University of Sa<strong>in</strong>t-Etienne, 517-22.<br />

Toussa<strong>in</strong>t, H.M., Bru<strong>in</strong><strong>in</strong>k, L., Coste,r R., De, Looze M, Van Rossem,<br />

B., Van Veenen R. & De Groot, G (1989). Effects of a triathlon wetsuit<br />

on drag dur<strong>in</strong>g swimm<strong>in</strong>g. Med Sci Sports Exerc, 21, 325-28.<br />

227


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Some Factors Limit<strong>in</strong>g Energy Supply <strong>in</strong> 200m Front<br />

Crawl Swimm<strong>in</strong>g<br />

strumbelj, B., usaj, A., Kapus, J., Bednarik, J.<br />

University of Ljubljana, Faculty of Sport, Ljubljana, Slovenia<br />

The aim of this research was to establish whether any measured factors<br />

could limit energy supply on 200 m front crawl swimm<strong>in</strong>g. Twelve<br />

male swimmers performed 4 swims of 200 m crawl at <strong>in</strong>tensities of 80%,<br />

90%, 100% <strong>and</strong> 110% (until exhaustion) on separate days with a swimm<strong>in</strong>g<br />

snorkel. Respiratory parameters (V E , Vo 2 ), blood parameters (pH,<br />

[LA - ]) <strong>and</strong> heart rate (HR) were measured. The results demonstrate that<br />

limitations <strong>in</strong> V E , Vo 2 <strong>and</strong> HR dur<strong>in</strong>g swimm<strong>in</strong>g occur dur<strong>in</strong>g supra<br />

maximal swims (no further <strong>in</strong>crease of measured maximal parameters<br />

<strong>and</strong> time constant parameters) <strong>in</strong> comparison to maximal swims. Limitations<br />

<strong>in</strong> obta<strong>in</strong>ed maximal [LA - ] <strong>and</strong> m<strong>in</strong>imal pH values were found.<br />

It is possible to conclude that <strong>in</strong>dividual limitations <strong>in</strong> V E , Vo 2 , HR<br />

<strong>and</strong> consequently acidosis could be limit<strong>in</strong>g factors of <strong>in</strong>dividual<br />

performance on 200 m front crawl because of energy supply limitations.<br />

Key words: swimm<strong>in</strong>g, front crawl, energetics, maximal, supra maximal<br />

performances<br />

IntroductIon<br />

Maximal performances <strong>in</strong> swimm<strong>in</strong>g depend on the maximal metabolic<br />

power of the athlete <strong>and</strong> on the economy of locomotion. The amount of<br />

metabolic energy spent <strong>in</strong> transport<strong>in</strong>g the body mass of the subject over<br />

a unit of distance has been def<strong>in</strong>ed as the energy cost of locomotion (di<br />

Prampero, 1986). Energy dur<strong>in</strong>g swimm<strong>in</strong>g is estimated as the sum of<br />

the energy derived from alactic (AnAl), lactic (AnL) <strong>and</strong> aerobic (Aer)<br />

processes. The amount of metabolic energy spent dur<strong>in</strong>g supra maximal<br />

swims (E, kilojoules) was assumed to be the sum of three terms:<br />

E = Ean + αVO2maxtp + αVO2max π(1 – e –t<br />

p π -1 )<br />

where α is the energy equivalent for O2 , assumed to be equal to 20.9<br />

kJ . l-1 , π is the time constant for the atta<strong>in</strong>ment of VO2max from the<br />

onset of exercise, Ean is the amount of energy derived from the use of<br />

anaerobic energy stores, tp is the performance time, <strong>and</strong> V O2max (litres<br />

per second) <strong>in</strong>cludes VO2 at rest (Capelli et al. 1998). Energy cost of<br />

front-crawl swimm<strong>in</strong>g (Capelli et al., 1998; Zamparo et al., 2000, Poujade<br />

et al., 2002) <strong>and</strong> factors affect<strong>in</strong>g energy cost at different <strong>in</strong>tensities<br />

of swimm<strong>in</strong>g were studied <strong>in</strong> many researches (Lavoie <strong>and</strong> Montpetit<br />

1986; Toussa<strong>in</strong>t <strong>and</strong> Holl<strong>and</strong>er 1994). However, little evidence was<br />

found that some of the before mentioned factors could represent limits<br />

<strong>in</strong> energy supply with <strong>in</strong>creas<strong>in</strong>g swimm<strong>in</strong>g velocity <strong>and</strong> consequently<br />

limits <strong>in</strong> performance.<br />

The aim of this study was to establish whether measured aerobic <strong>and</strong><br />

anaerobic lactate parameters could limit energy supply for 200m front<br />

crawl <strong>and</strong> consequently affect the performance dur<strong>in</strong>g supra maximal<br />

swimm<strong>in</strong>g.<br />

Methods<br />

Twelve male swimmers (age: 24 ± 3 yrs; height: 181 ± 9 cm; body mass:<br />

77 ± 13 kg) volunteered to participate <strong>in</strong> this study. All subjects had a<br />

m<strong>in</strong>imum of eight years competition swimm<strong>in</strong>g experience <strong>and</strong> considered<br />

front crawl their best stroke. The subjects were <strong>in</strong>formed of the risks<br />

<strong>in</strong>volved <strong>in</strong> the experiment before they agreed to participate.<br />

All swims were performed us<strong>in</strong>g the front crawl stroke <strong>in</strong> a 25 m<br />

<strong>in</strong>door swimm<strong>in</strong>g pool. The temperature of the water was 27° C. Each<br />

swimmer performed 4 swims of 200 m crawl at <strong>in</strong>tensities of 80%, 90%,<br />

100% <strong>and</strong> 110% (until exhaustion) on separate days with a swimm<strong>in</strong>g<br />

snorkel (Toussa<strong>in</strong>t et al. 1987). First, the swimmers performed a maximal<br />

200 m front crawl swim. Thereafter, they performed sub/maximal<br />

228<br />

swims with 80% <strong>and</strong> 90% of maximal 200 m front crawl velocity. F<strong>in</strong>ally,<br />

the swimmers performed a supra-maximal swim with 110 % velocity<br />

until exhaustion (on average they were able to swim 113.8 ± 17.0 m)..<br />

A light leader was used to keep even pace dur<strong>in</strong>g swimm<strong>in</strong>g with submaximal<br />

<strong>and</strong> supra-maximal <strong>in</strong>tensities.<br />

Arterial blood samples (20 µl) were collected from the earlobe after<br />

a warm up <strong>and</strong> at 1, 3 <strong>and</strong> 5 m<strong>in</strong>utes of recovery after swimm<strong>in</strong>g <strong>and</strong><br />

analyzed for blood lactate concentration ([LA-]) us<strong>in</strong>g a Kodak Ektachrome<br />

analyzer. At the same time, arterial blood samples (60 - 80 µl)<br />

were collected <strong>and</strong> analyzed for pH with an ABL5 analyzer (Radiometer<br />

Copenhagen). Calibration of the equipment was performed every<br />

six samples with st<strong>and</strong>ard lactate <strong>and</strong> pH solution, respectively. Maximal<br />

measured [LA-] <strong>and</strong> m<strong>in</strong>imal pH obta<strong>in</strong>ed values were analyzed.<br />

Ventilation (VE) <strong>and</strong> O2 uptake (VO2) were measured us<strong>in</strong>g a<br />

portable respiratory gas analyzer METAMAX 2 (Cortex, Germany)<br />

adapted to measurements with a swimm<strong>in</strong>g snorkel made by Toussa<strong>in</strong>t<br />

et al.(1987). Average data for every 10-s period were recorded after<br />

warm up, dur<strong>in</strong>g swimm<strong>in</strong>g <strong>and</strong> 5 m<strong>in</strong>utes after the end of each swim.<br />

The flow meter was calibrated with a syr<strong>in</strong>ge of known volume (3.0 l).<br />

The gas analyzer was calibrated by known st<strong>and</strong>ard gases.<br />

Heart rate (HR) was measured us<strong>in</strong>g heart rate monitors POLAR<br />

S-610 (Polar, F<strong>in</strong>l<strong>and</strong>). Average data for 10 –s period were recorded<br />

after warm up, dur<strong>in</strong>g swimm<strong>in</strong>g <strong>and</strong> 5 m<strong>in</strong>utes after the end of each<br />

swim. From all obta<strong>in</strong>ed data of heart rate values <strong>in</strong> the rest were excluded<br />

to observe relative change.<br />

Means <strong>and</strong> st<strong>and</strong>ard deviations were computed for all variables. Individual<br />

one-way repeated measures ANOVAs were employed to test<br />

for any significant differences between the measured parameters. Significance<br />

was accepted when p


Time (sec)<br />

Figure 1. VE k<strong>in</strong>etic responses of <strong>in</strong>terpolated data to value of 0 l.m<strong>in</strong> -1 dur<strong>in</strong>g<br />

swimm<strong>in</strong>g with different <strong>in</strong>tensities to the moment when all swimmers were able to<br />

perform the predef<strong>in</strong>ed load.<br />

With ANOVA significant changes were found between <strong>in</strong>terpolated<br />

values of VE from 10 to 80 seconds (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

were reached (Table 1.). Someth<strong>in</strong>g similar was observed with maximal<br />

heart rate values (Table 3.). Additionally, k<strong>in</strong>etics of HR frequency was<br />

similar at 110% <strong>in</strong>tensity to that at 100% <strong>in</strong>tensity (Figure 4.). From our<br />

results it could be concluded that the aerobic energy supply to work<strong>in</strong>g<br />

muscles could be limited by the cardiovascular system at supra-maximal<br />

<strong>in</strong>tensities (no further <strong>in</strong>crease of maximal heart rate <strong>and</strong> k<strong>in</strong>etic responses<br />

of heart rate). However at the beg<strong>in</strong>n<strong>in</strong>g of the swimm<strong>in</strong>g, swimmers<br />

were able to compensate the <strong>in</strong>sufficient energy supply by aerobic processes<br />

with <strong>in</strong>creased energy production by anaerobic lactic processes, s<strong>in</strong>ce<br />

<strong>in</strong>creased lactate production per unit of time was found with <strong>in</strong>creas<strong>in</strong>g<br />

<strong>in</strong>tensity of swimm<strong>in</strong>g (Figure 3.). However when the level of acidosis<br />

<strong>and</strong> lactate concentration at 110% <strong>in</strong>tensity was similar to that at 100%<br />

<strong>in</strong>tensity swimmers were no longer able to swim at that <strong>in</strong>tensity (Table<br />

2.). From the results it was not possible to demonstrate that <strong>in</strong>sufficient<br />

energy supply is the limit<strong>in</strong>g factor of maximal performance <strong>in</strong> front crawl<br />

swimm<strong>in</strong>g. However, when certa<strong>in</strong> levels of V E , Vo 2 , HR, pH <strong>and</strong> lactate<br />

concentration were reached, similar to those at maximal <strong>in</strong>tensity, swimmers<br />

were no longer able to swim at selected supra-maximal <strong>in</strong>tensity.<br />

conclusIon<br />

The energy cost of swimm<strong>in</strong>g <strong>in</strong>creases as a function of the speed. With<br />

<strong>in</strong>crease of swimm<strong>in</strong>g speed the sum of energy supply dur<strong>in</strong>g swimm<strong>in</strong>g<br />

should <strong>in</strong>crease from either alactic (AnAl), lactic (AnL) <strong>and</strong> aerobic<br />

(Aer) processes. It is concluded that <strong>in</strong>sufficient energy supply because<br />

limitations <strong>in</strong> aerobic <strong>and</strong> anaerobic lactic processes occur, could limit<br />

the maximal speed of swimmers for 200 m front crawl.<br />

However there is still the open question as to whether the swimmers<br />

studied need more aerobic tra<strong>in</strong><strong>in</strong>g or do they need more anaerobic<br />

tra<strong>in</strong><strong>in</strong>g to better their performances <strong>in</strong> the 200 m front crawl or do they<br />

need to improve their swimm<strong>in</strong>g technique.<br />

reFerences<br />

Capelli C., Pendergast D.R., Term<strong>in</strong> B. (2005). Energetics of swimm<strong>in</strong>g<br />

at maximal speeds <strong>in</strong> humans. Eur J Appl Physiol 78,385-393.<br />

Holmer I. (1974). Physiology of swimm<strong>in</strong>g man. Acta Physiologica Sc<strong>and</strong><strong>in</strong>avica<br />

supplementum 407, 1 – 55.<br />

Monpetit R., Lavoie J.M., Cazorla G. (1988). Energy expenditure dur<strong>in</strong>g<br />

front crawl swimm<strong>in</strong>g: a comparision between males <strong>and</strong> females.<br />

In: Ungerechts BE, Wilke K, Reisschee K. Swimm<strong>in</strong>g Science V. Human<br />

K<strong>in</strong>etics, Champaign III., pp 229-236.<br />

Prampero P.E. di. (1986). The energy cost of human locomotion on l<strong>and</strong><br />

<strong>and</strong> <strong>in</strong> water. Int J Sports Med 7,55-72.<br />

Toussa<strong>in</strong>t H.M., Beelen A., Rodenburg A., Sargeant A.J., de Groot G.,<br />

Hol<strong>and</strong>er P., Ingen Schenau AG van (1988). Propell<strong>in</strong>g efficenciy of<br />

front crawl swimm<strong>in</strong>g. J Appl Physiol 65, 2506-2512.<br />

Toussa<strong>in</strong>t H.M., Meulemans A., De Groot G., Holl<strong>and</strong>er A.P., Schreurs<br />

W., & Vervoorn K. (1987). Respiratory valve for oxygene uptake<br />

measurments dur<strong>in</strong>g swimm<strong>in</strong>g. Eur J Appl Physio. 56, 363-366.<br />

Zamparo P., Capelli C., Cautero M., Di N<strong>in</strong>o A. (2000). Energy cost<br />

of front crawl swimm<strong>in</strong>g at supra-maximal speeds <strong>and</strong> underwater<br />

torque <strong>in</strong> young swimmers. Eur J Appl Physiol 83,487-491.<br />

Zamparo P., Pendergast D.R., Mollendorf J., Term<strong>in</strong> A., M<strong>in</strong>etti E.A.<br />

(2005). An energy balance of front crawl. Eur J Appl Physiol 94,134-<br />

144.<br />

230<br />

Lactate Comparison Between 100m Freestyle <strong>and</strong><br />

Tethered Swimm<strong>in</strong>g of Equal Duration<br />

Thanopoulos, V., rozi, G., Platanou, t.<br />

Faculty of Physical Education <strong>and</strong> Sports Science, University of Athens,<br />

Greece<br />

The purpose of the present study was to compare the blood lactate<br />

concentrations after two tests of maximal <strong>in</strong>tensity: a) 100m freestyle<br />

swimm<strong>in</strong>g <strong>and</strong> b) tethered swimm<strong>in</strong>g of equal duration with the test of<br />

100m freestyle. Furthermore, the force produced <strong>in</strong> tethered swimm<strong>in</strong>g<br />

was measured. Twelve male competitive swimmers participated <strong>in</strong> this<br />

study. Capillary blood samples were obta<strong>in</strong>ed 3 o , 5 o <strong>and</strong> 7 o m<strong>in</strong> after<br />

the end of each test. Analysis of the results showed that there was no<br />

statistically significant difference between the lactate concentration <strong>in</strong><br />

the tethered swimm<strong>in</strong>g test <strong>and</strong> the test of 100m freestyle swimm<strong>in</strong>g.<br />

Moreover, there was correlation between performance <strong>in</strong> 100 m <strong>and</strong><br />

force <strong>in</strong> tethered swimm<strong>in</strong>g (r= -0.63). The results <strong>in</strong>dicate that when<br />

tethered swimm<strong>in</strong>g is used for spr<strong>in</strong>ters, it seems more adequate to<br />

analyze the values of mean force because as a mechanical characteristic,<br />

it better describes spr<strong>in</strong>ters achievements.<br />

Keywords: blood lactate, pull<strong>in</strong>g force, freestyle spr<strong>in</strong>ters, swimm<strong>in</strong>g<br />

performance<br />

IntroductIon<br />

Maximal swimm<strong>in</strong>g velocity, especially at spr<strong>in</strong>t distances, except for technical<br />

ability depends on pull<strong>in</strong>g force characteristics <strong>and</strong> maximal anaerobic<br />

lactic capacity that is proportional with maximum production of lactic<br />

acid. In order to determ<strong>in</strong>e maximum lactate accumulation, several middle<br />

distance tests are used as well as resistance swimm<strong>in</strong>g. The most common<br />

test for anaerobic capacity is 100m freestyle. Several researchers have also<br />

used tethered swimm<strong>in</strong>g. The test most widely used to measure pull<strong>in</strong>g<br />

force realized <strong>in</strong> swimm<strong>in</strong>g is the tethered swimm<strong>in</strong>g test (Kesk<strong>in</strong>en et<br />

al., 1989; Sidney et al., 1996; Maglischo, 2003). Furthermore, tethered<br />

swimm<strong>in</strong>g is one of the most famous types of tra<strong>in</strong><strong>in</strong>g for swimmers <strong>and</strong><br />

aims at <strong>in</strong>creas<strong>in</strong>g maximum speed <strong>and</strong> strength (Maglishco, 2003). The<br />

subject wears a special belt <strong>and</strong> swims at the same po<strong>in</strong>t (tethered swimm<strong>in</strong>g<br />

Bonen et al., 1980). Viewed k<strong>in</strong>ematically, swimm<strong>in</strong>g is a series of<br />

cyclic movements performed by alternation of arm <strong>and</strong> leg strokes. Each<br />

stroke results <strong>in</strong> a characteristic force, which pulls the swimmer forward<br />

<strong>and</strong> is realized by contract<strong>in</strong>g the muscles <strong>in</strong>volved.<br />

Many researchers suggested this mean of tra<strong>in</strong><strong>in</strong>g that helps <strong>in</strong> <strong>in</strong>creas<strong>in</strong>g<br />

maximum speed <strong>and</strong> improv<strong>in</strong>g strength for better preparation<br />

of swimmers. (Colw<strong>in</strong>; 1993; Counsilman, 1979; Hannula, 1995; Smith,<br />

2002; Maglischo, 2003).<br />

Some other reviewers found positive correlation between swimm<strong>in</strong>g<br />

performance <strong>and</strong> muscular strength that can be measured <strong>in</strong> several<br />

ways (Sharp et al., 1982; Costill et al., 1983; Hawley & Williams, 1991;<br />

Crowe et al., 1999). Previous research has focused only on the relationship<br />

between the maximal pull<strong>in</strong>g force or the average of maximal pull<strong>in</strong>g<br />

forces (Fmax or avgFmax) of a s<strong>in</strong>gle stroke realized <strong>in</strong> a time <strong>in</strong>terval<br />

of 10 seconds, <strong>and</strong> the swimm<strong>in</strong>g velocity achieved ma<strong>in</strong>ly at spr<strong>in</strong>t<br />

distances (Sidney et al., 1996, Dopsaj, 2000).<br />

In terms of measurements, Fmax or avgFmax conta<strong>in</strong>s <strong>in</strong>formation<br />

solely about the force peak po<strong>in</strong>t or the average of such po<strong>in</strong>ts achieved<br />

for the given s<strong>in</strong>gle strokes realized by tethered swimm<strong>in</strong>g. On the other<br />

h<strong>and</strong>, force as a measurable value which is a product of muscle contraction<br />

is def<strong>in</strong>ed by at least two more dimensions, i.e., by its <strong>in</strong>crement<br />

gradient/ its <strong>in</strong>crement <strong>in</strong> time (RFD – rate of force development) <strong>and</strong><br />

by the impulse of force (ImpF) (Zatsiorsky, 1995), the realization of<br />

which can be reliably measured <strong>in</strong> water dur<strong>in</strong>g tethered swimm<strong>in</strong>g<br />

(Dopsaj, 2000).


Besides, the methodology of establish<strong>in</strong>g the relationship <strong>and</strong>/or its<br />

quality between swimm<strong>in</strong>g velocity at a given distance <strong>and</strong> the characteristics<br />

of pull<strong>in</strong>g force realized by tethered swimm<strong>in</strong>g requires that the<br />

test lasts at least approximately as long as the distance covered. In that<br />

way it is possible to adjust the observed occurrences, i.e., the characteristics<br />

of pull<strong>in</strong>g force <strong>and</strong> the velocity of swimm<strong>in</strong>g (as criterion <strong>and</strong><br />

predictor variables), also tak<strong>in</strong>g <strong>in</strong>to consideration the load exerted on<br />

the same energy system (R<strong>in</strong>g et al., 1996).<br />

Accord<strong>in</strong>g to previous research, the question that occurs is with<br />

which of the two events, 100m freestyle or tethered swimm<strong>in</strong>g of equal<br />

duration to 100m, maximum accumulation of lactic acid <strong>in</strong> blood can<br />

be achieved. Also, if there is a relationship between maximal performance<br />

<strong>in</strong> 100m freestyle swimm<strong>in</strong>g (the level of competitor fitness) <strong>and</strong><br />

strength.<br />

The purpose of this study was to exam<strong>in</strong>e lactic acid accumulation<br />

<strong>in</strong> blood after two efforts of maximum <strong>in</strong>tensity <strong>and</strong> equal duration: a)<br />

100m freestyle swimm<strong>in</strong>g <strong>and</strong> b) tethered swimm<strong>in</strong>g, as well as to f<strong>in</strong>d<br />

differences between these two measurements concern<strong>in</strong>g lactate production<br />

<strong>and</strong> heart rate. Moreover, this study attempts to <strong>in</strong>vestigate the<br />

relationship between performance <strong>in</strong> 100m freestyle <strong>and</strong> the forces produced<br />

<strong>in</strong> tethered swimm<strong>in</strong>g. It was hypothesized that there are no significant<br />

differences <strong>in</strong> blood lactate accumulation after the two events.<br />

Methods<br />

In this study 12 active swimmers of national level participated<br />

(age = 21.50±0.68 years, Body stature =182.83±7.24 cm <strong>and</strong> Body<br />

mass=80.75±8.00) <strong>in</strong> freestyle swimm<strong>in</strong>g (Table 1). At the beg<strong>in</strong>n<strong>in</strong>g,<br />

they swam 100 meters freestyle with maximum <strong>in</strong>tensity <strong>and</strong> time performance<br />

<strong>and</strong> blood lactate accumulation were measured. Samples of<br />

blood were taken at 3 rd , 5 th <strong>and</strong> 7th m<strong>in</strong>ute of recovery time <strong>and</strong> analysed<br />

immediately us<strong>in</strong>g the reflectance photometry - enzymatic reaction<br />

method (Accusport, Boehr<strong>in</strong>ger, Germany) <strong>in</strong> order to determ<strong>in</strong>e maximum<br />

accumulation of lactic acid <strong>in</strong> 100m freestyle swimm<strong>in</strong>g.<br />

Two days later the same athletes were tested <strong>in</strong> tethered swimm<strong>in</strong>g, over<br />

an equal time to that achieved <strong>in</strong> the 100 meters swim. Blood samples<br />

were also taken <strong>in</strong> 3 rd , 5 th <strong>and</strong> 7 th m<strong>in</strong>ute of recovery time <strong>in</strong> order to<br />

determ<strong>in</strong>e maximum lactate accumulation <strong>and</strong> strength characteristics<br />

were measured (Kesk<strong>in</strong>en et al., 1989; Sidney et al., 1996), accord<strong>in</strong>g to<br />

the st<strong>and</strong>ardized procedure (Dopsaj, 2000).<br />

Table 1. Swimmers characteristics<br />

Age (years) Body Stature (cm) Body Mass (kg)<br />

Male (N=12) 21.50±0.68 182.83±7.24 80.75±8.00<br />

Before the test, the swimmers warmed up swimm<strong>in</strong>g <strong>in</strong>dependently up<br />

to 1000 m. After a 10-m<strong>in</strong>ute rest the measur<strong>in</strong>g started. On his turn,<br />

each swimmer put on a belted harness adjust<strong>in</strong>g it to his body dimensions<br />

(Figure 1). Then he hooked a 1cm-thick PVC rope to the belt<br />

at the back hip region. The other end of the 5m rope was attached to<br />

a water-resistant high-resolution (100 kHz) tensiometric dynamometer<br />

placed on a metal support fixed on the side of the pool (Figure 2).<br />

The dynamometer was connected to a PC. Hav<strong>in</strong>g entered the pool,<br />

the swimmer did a 10-second trial of tethered swimm<strong>in</strong>g at medium<br />

<strong>in</strong>tensity <strong>in</strong> order to get familiar with the equipment <strong>and</strong> the test<strong>in</strong>g<br />

procedure. After a 1m<strong>in</strong>ute rest the measur<strong>in</strong>g commenced.<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

Fig. 1. Swimmer with the belted harness adjust<strong>in</strong>g it to his body dimensions<br />

The swimmers started tethered swimm<strong>in</strong>g (full technique – arms <strong>and</strong><br />

legs stroke) at medium <strong>in</strong>tensity <strong>and</strong> after two to three strokes, at the<br />

whistle of the timekeeper, they swam at maximal <strong>in</strong>tensity for the same<br />

time as that achieved <strong>in</strong> 100m freestyle swimm<strong>in</strong>g. At the whistle, the<br />

assistant timekeeper, who operated the PC, started the program for<br />

measur<strong>in</strong>g <strong>and</strong> acquisition of data. The raw data were processed by software<br />

specially designed by ProIng to analyze the parameters relevant to<br />

pull<strong>in</strong>g force.<br />

Fig. 2. The support with the dynamometer used to measure tethered<br />

pull<strong>in</strong>g force<br />

After the time of 100m freestyle there was a second whistle as the signal<br />

to stop swimm<strong>in</strong>g. This procedure yielded the entire record<strong>in</strong>g of<br />

the pull<strong>in</strong>g force dur<strong>in</strong>g the achieved time of 100m freestyle. Swimmers<br />

were told to follow the breath<strong>in</strong>g pattern they would normally apply<br />

dur<strong>in</strong>g a race. The test was done <strong>in</strong> the <strong>in</strong>door swimm<strong>in</strong>g pool of the<br />

Physical Education Faculty of Athens Kapodistrian University a week<br />

before the summer national senior championships.<br />

All results are expressed as means <strong>and</strong> st<strong>and</strong>ard deviations. For the<br />

comparison of mean values of blood lactate production <strong>and</strong> of heart rate<br />

<strong>in</strong> the two tests, t - test with depended samples was applied. In addition,<br />

Pearson’s correlation coefficient was used to calculate the relationships<br />

between time of performance <strong>in</strong> 100m freestyle <strong>and</strong> strength produced<br />

<strong>in</strong> tethered swimm<strong>in</strong>g, as well as their relationship with lactic acid accumulation<br />

<strong>in</strong> both events. Statistical significance was set at p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

results<br />

The performance time for 100m freestyle was 58.74±2.33, <strong>and</strong> was the<br />

time that they also swam <strong>in</strong> tethered swimm<strong>in</strong>g. The comparison <strong>in</strong><br />

maximum accumulation of lactic acid <strong>and</strong> heart rate after the two tests<br />

are presented <strong>in</strong> table 2. Pared correlations showed that there were no<br />

statistical significant differences.<br />

Table 2. Performance time, maximum blood lactate accumulation<br />

(mmol/l) <strong>and</strong> heart rate of swimmers after the tests.<br />

Tests<br />

100m freestyle<br />

(m/s)<br />

Tethered swimm<strong>in</strong>g<br />

232<br />

Perf. time<br />

(sec)<br />

58.74±2.33<br />

58.74±2.33<br />

Mean force<br />

(N)<br />

-<br />

131.51±27.8<br />

Lactate<br />

(mmol/l)<br />

11.09±4.2<br />

10.27±3.3<br />

Heart rate<br />

(beat/m<strong>in</strong>) P


swimm<strong>in</strong>g power <strong>and</strong> dryl<strong>and</strong> power to spr<strong>in</strong>t freestyle performance:<br />

A mul-tiple regression approach. Journal of Swimm<strong>in</strong>g Research, 9,<br />

10-14.<br />

Kesk<strong>in</strong>en, K., Tilli, L., & Komi, P. (1989). Maximum velocity swimm<strong>in</strong>g:<br />

Interrelationships of strok<strong>in</strong>g characteristics, force production<br />

<strong>and</strong> anthropometric variables. Sc<strong>and</strong><strong>in</strong>avian Journal of Sports Science,<br />

11(2), 87-92.<br />

Konstantaki, M., Trowbridge, E. A., & Swa<strong>in</strong>e, I. L. (1998). The relationship<br />

between blood lactate <strong>and</strong> heart rate responses to swim<br />

bench exer-cise <strong>and</strong> women’s competitive water polo. Journal of Sports<br />

Sciences, 16, 251-256.<br />

Konstantaki M. & Swa<strong>in</strong>e I. L. (1999). Lactate <strong>and</strong> cardiopulmonary<br />

responses to simulated arm-pull<strong>in</strong>g <strong>and</strong> leg-kick<strong>in</strong>g <strong>in</strong> collegiate <strong>and</strong><br />

recreational swimmers. International Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 20,<br />

118-121.<br />

Maglischo E. W. (2003). Swimm<strong>in</strong>g Fastest. Champaign IL: Human<br />

K<strong>in</strong>etics.<br />

Mitchell J. B. & Huston J. S. (1993). The effect of high <strong>and</strong> low <strong>in</strong>tensity<br />

warm-up on the physiological responses to a st<strong>and</strong>ardized swim<br />

<strong>and</strong> tethered swimm<strong>in</strong>g performance. Journal of Sports Sciences, 11,<br />

159-165.<br />

Pluto R., Cruze S. A., Weiss M., Hotz T., M<strong>and</strong>el P., & Weicker H.<br />

(1988). Cardiocirculatory, hormonal, <strong>and</strong> metabolic reactions to various<br />

forms of ergometric tests. International Journal of Sports <strong>Medic<strong>in</strong>e</strong>,<br />

9, S79-S88.<br />

R<strong>in</strong>ehardt, K. F., Kraemer, R. R, Gormely, S., Colan, S. (1991). Comparison<br />

of Maximal Oxygen Uptakes from the Tethered, the 183 <strong>and</strong><br />

457Meter Unimpeded Supramaximal Freestyle Swims International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>, 12, 6-9<br />

R<strong>in</strong>g, S., Mader, A., Wirtz, W., & Wilke, K. (1996) Energy metabolism<br />

dur<strong>in</strong>g spr<strong>in</strong>t swimm<strong>in</strong>g, In J.P. Troup, A.P. Holl<strong>and</strong>er, D. Strasse,<br />

Biomehanics <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VII, (pp. 177-183). UK: E<br />

& FN Spon.<br />

Sharp, R. L., Troup, J. P., & Costill, D. L. (1982). Relationship between<br />

power <strong>and</strong> spr<strong>in</strong>t freestyle swimm<strong>in</strong>g. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports<br />

<strong>and</strong> Exercise, 14, 53-56.<br />

Smith, D. J., Norris, S. R., & Hogg, J. M. (2002). Performance evaluation<br />

of swimmers: scientific tools. Sports <strong>Medic<strong>in</strong>e</strong>, 32, 539-554.<br />

Tanaka H., Costill D. L., Thomas R., F<strong>in</strong>k W. J., & Widrick J. J. (1993).<br />

Dry l<strong>and</strong> resistance tra<strong>in</strong><strong>in</strong>g for competitive swimm<strong>in</strong>g. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong><br />

Science <strong>in</strong> Sports <strong>and</strong> Exercise, 25, 952-959.<br />

Thanopoulos, V., Platanou, Rozi, G. (2009). Maximum accumulation<br />

of lactic acid <strong>in</strong> freestyle <strong>and</strong> tethered swimm<strong>in</strong>g. 11 th International<br />

Conference of Sport K<strong>in</strong>etics. Abstract book. p. 201<br />

Ueda T., Kurokawa T. (1995). Relationships between perceived exertion<br />

<strong>and</strong> physiological variables dur<strong>in</strong>g swimm<strong>in</strong>g. International<br />

Journal of Sports <strong>Medic<strong>in</strong>e</strong>. Aug 16(6) 385-9.<br />

Zatsiorsky V. (1995). Science <strong>and</strong> practice of strength tra<strong>in</strong><strong>in</strong>g. Champaign,<br />

II, U.S.A.: Human K<strong>in</strong>etics.<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

Blood Lactate Concentration <strong>and</strong> Clearance <strong>in</strong> Elite<br />

Swimmers Dur<strong>in</strong>g Competition<br />

Vescovi, J.d. 1,3 , Falenchuk, o. 4 , Wells G.d. 1,2<br />

1Canadian Sport Centre Ontario, Toronto, Canada<br />

2Faculty of <strong>Medic<strong>in</strong>e</strong>, University of Toronto, Toronto, Canada<br />

3School of K<strong>in</strong>esiology <strong>and</strong> Health Science, York University, Toronto, Canada<br />

4Ontario Institute of Secondary Educ., University of Toronto, Toronto, Canada<br />

Blood lactate [BLa] concentrations after swimm<strong>in</strong>g events may be <strong>in</strong>fluenced<br />

by demographic features <strong>and</strong> characteristics of the swim race,<br />

whereas active recovery (AR) enhances [BLa] removal. Our aims were to<br />

exam<strong>in</strong>e how sex, age, race distance, <strong>and</strong> swim stroke <strong>in</strong>fluenced [BLa]<br />

after competitive swimm<strong>in</strong>g events <strong>and</strong> to develop a model based on AR<br />

swim distance to help optimize [BLa] removal. Post-race [BLa] from<br />

100 swimmers compet<strong>in</strong>g <strong>in</strong> the f<strong>in</strong>als at the Canadian Swim Championships<br />

were retrospectively anaysed. [BLa] was also assessed repeatedly<br />

dur<strong>in</strong>g AR. Post-race [BLa] was highest after 100 <strong>and</strong> 200 m events<br />

<strong>and</strong> lowest after 50 <strong>and</strong> 1500 m races. There was a negligible effect of<br />

age on post-race [BLa]. The follow<strong>in</strong>g model can be used to estimate<br />

the change <strong>in</strong> [BLa] dur<strong>in</strong>g AR: Δ[BLa] after AR = –3.374 + 1.162<br />

(male=0;female=1) + 0.789 *post-race [BLa]+ 0.003 * AR distance.<br />

Key Words: blood lactate, active recovery, sex differences, swimm<strong>in</strong>g<br />

IntroductIon<br />

Short duration bouts of high <strong>in</strong>tensity exercise rely largely on nonoxidative<br />

energy metabolism, result<strong>in</strong>g <strong>in</strong> the accumulation of muscle<br />

<strong>and</strong> blood lactate. Peak blood lactate concentrations ([BLa]) follow<strong>in</strong>g<br />

maximal exercise has a direct relationship with performance <strong>in</strong> swim<br />

events rang<strong>in</strong>g between 100 <strong>and</strong> 800 m (Benelli et al., 2007; Bonifazi et<br />

al., 1993). Evaluation of [BLa] follow<strong>in</strong>g competitive races also provides<br />

evidence of the physiological stress for an <strong>in</strong>dividual swimmer <strong>in</strong> a given<br />

event. Thus, the utility of assess<strong>in</strong>g [BLa] for swimmers is important for<br />

a variety of tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competitive purposes.<br />

Swimm<strong>in</strong>g provides an ideal model for characteriz<strong>in</strong>g [BLa] response<br />

with events rang<strong>in</strong>g from ~20 s (50 m freestyle) to 15 m<strong>in</strong> (1500<br />

m freestyle). Swimmers commonly compete <strong>in</strong> multiple events throughout<br />

a s<strong>in</strong>gle day, which requires them to recover from <strong>and</strong> prepare for<br />

several races. Strategies that <strong>in</strong>crease the return rate of post-race [BLa]<br />

to rest<strong>in</strong>g values are often used by coaches <strong>in</strong> an effort to optimize subsequent<br />

performance. In an effort to expedite blood lactate removal<br />

while maximiz<strong>in</strong>g energy conservation between swimm<strong>in</strong>g events it<br />

would be of practical use to know if there is an optimal distance or time<br />

to recommend for active recovery (Toubekis et al., 2008).<br />

Research on the effect of sex, age <strong>and</strong> race characteristics on postrace<br />

[BLa] dur<strong>in</strong>g competitive swim events rema<strong>in</strong>s equivocal. Additionally,<br />

sport scientists, coaches <strong>and</strong> swimmers cont<strong>in</strong>ually search for<br />

practical strategies to maximize recovery after an event <strong>in</strong> preparation<br />

for subsequent heat or f<strong>in</strong>al races. The aims of this study were to exam<strong>in</strong>e<br />

how sex, age, race distance, <strong>and</strong> swim stroke <strong>in</strong>fluenced [BLa] after<br />

competitive swimm<strong>in</strong>g events <strong>and</strong> to develop a practical model based on<br />

recovery swim distance to help optimize blood lactate removal.<br />

Methods<br />

Post-race [BLa] after the f<strong>in</strong>al races <strong>in</strong> male <strong>and</strong> female swimmers compet<strong>in</strong>g<br />

<strong>in</strong> the 2009 Canadian National Swimm<strong>in</strong>g Championships were<br />

assessed. The effect of active recovery distance on [BLa] disappearance<br />

<strong>and</strong> a model that could be used by coaches as a practical tool dur<strong>in</strong>g<br />

competitions was also exam<strong>in</strong>ed. Data from one hundred swimmers<br />

(n=50 male <strong>and</strong> n=50 females) were <strong>in</strong>cluded <strong>in</strong> this analysis. Multiple<br />

races from the same person were <strong>in</strong>cluded <strong>and</strong> thus data from 156 races<br />

233


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

were collected, however because of miss<strong>in</strong>g data the f<strong>in</strong>al analysis <strong>in</strong>cluded<br />

149 f<strong>in</strong>als races swam by 98 swimmers. The age of the swimmers<br />

ranged between 14 <strong>and</strong> 29 years. Race results were collected from the<br />

host organiz<strong>in</strong>g committee <strong>and</strong> used to determ<strong>in</strong>e FINA po<strong>in</strong>ts.<br />

Blood samples were collected with<strong>in</strong> three to five m<strong>in</strong>utes after complet<strong>in</strong>g<br />

the race. Samples were obta<strong>in</strong>ed from f<strong>in</strong>ger stick <strong>and</strong> analyzed<br />

with a Lactate ProTM (Arkray Lt., Japan). Swimmers then proceeded<br />

to the recovery pool <strong>and</strong> performed their own coach-directed active recovery.<br />

[BLa] was repeatedly assessed until it was below 2 mmol•L-1.<br />

The distance of each active recovery segment as well as the total active<br />

recovery distance <strong>and</strong> the change <strong>in</strong> [BLa] from post-race to the lowest<br />

concentration achieved follow<strong>in</strong>g the active recovery were recorded.<br />

Several swimmers competed <strong>in</strong> more than one f<strong>in</strong>al race <strong>and</strong> had<br />

data from multiple races <strong>in</strong>cluded <strong>in</strong> the analysis, therefore the assumption<br />

of <strong>in</strong>dependence was violated. To evaluate the relationship between<br />

post-race [BLa] <strong>and</strong> swimmers characteristics (age <strong>and</strong> sex) <strong>and</strong> the races<br />

(stroke <strong>and</strong> distance) the Generalized Estimat<strong>in</strong>g Equations (GEE)<br />

technique was used (Hard<strong>in</strong> & Hilbe, 2002), which accommodates for<br />

a violation of the <strong>in</strong>dependence assumption. To evaluate active recovery<br />

distance on [BLa] disappearance an exploratory model build<strong>in</strong>g approach<br />

was used with [BLa] follow<strong>in</strong>g active recovery as the dependent<br />

variable, while sex was entered <strong>in</strong> the model as a two-level factor. Age,<br />

post-race [BLa], <strong>and</strong> active recovery distance were entered as covariates.<br />

The maximal model was developed, then non-significant effects were<br />

removed until the most parsimonious model was achieved. Each model<br />

was compared with the previous us<strong>in</strong>g Quasi Likelihood under Independence<br />

Model Criterion (QIC) <strong>in</strong>dex to determ<strong>in</strong>e whether removal<br />

of non-significant parameters improved the fit of the model. Values are<br />

expressed as mean ± SD <strong>and</strong> statistical significance was set at p


found. This pattern has previously been described (Avlonitou, 1996;<br />

Bonifazi et al., 1993) <strong>and</strong> reflects the energetic dem<strong>and</strong>s for each distance.<br />

Because of the short duration of 50 m races (~20 s) the ATP-PC<br />

system is able to supply a substantial proportion of the energy needed<br />

for these events, thus blood lactate concentration was lower <strong>in</strong> comparison<br />

to 100-800 m events. With<strong>in</strong> the 50 m events, post-race [BLa]<br />

was lowest for breaststroke <strong>and</strong> highest for butterfly. Our f<strong>in</strong>d<strong>in</strong>gs that<br />

the highest post-race [BLa] were observed follow<strong>in</strong>g the 100 <strong>and</strong> 200<br />

m races was not surpris<strong>in</strong>g as other researchers have reported similar<br />

outcomes <strong>in</strong> elite (Bonifazi et al., 1993; Bonifazi et al., 2000) <strong>and</strong> college<br />

swimmers (Sawka et al., 1979). Thus, even though it is estimated that a<br />

large proportion of the energy supplied for events of this duration comes<br />

from oxidative metabolism substantial blood lactate accumulation occurs<br />

dur<strong>in</strong>g these events.<br />

Table 2. Suggested active recovery distances<br />

Event<br />

Freestyle<br />

Men Women<br />

50 1000-1200 600-800<br />

100 1300-1500 800-1000<br />

200 1300-1500 800-1000<br />

400 1300-1500 800-1000<br />

800 1000-1200 600-800<br />

1500<br />

Backstroke<br />

800-1000 600-800<br />

50 1000-1200 600-800<br />

100 1300-1500 1000-1200<br />

200<br />

Breaststroke<br />

1300-1500 1000-1200<br />

50 800-1000 500-800<br />

100 1200-1400 800-1000<br />

200<br />

Butterfly<br />

1200-1400 800-1000<br />

50 1200-1400 700-900<br />

100 1200-1400 800-1000<br />

200<br />

Individual Med.<br />

1200-1400 800-1000<br />

200 1200-1400 800-1000<br />

400 1200-1400 800-1000<br />

Sex differences <strong>in</strong> post-race [BLa] have been reported for top level<br />

(Bonifazi et al., 1993) <strong>and</strong> age group (Avlonitou, 1996) swimmers, but<br />

not all events display a substantial disparity between men <strong>and</strong> women<br />

(Avlonitou, 1996; Bonifazi et al., 1993). The post-race [BLa] distribution<br />

curve is shifted to the right for males compared to females (Bonifazi<br />

et al., 1993) <strong>and</strong> [BLa] tends to be about 1 mmol•L -1 higher <strong>in</strong> most<br />

events for men (Avlonitou, 1996). A sex difference existed <strong>in</strong> post-race<br />

[BLa] only follow<strong>in</strong>g freestyle events with male swimmers achiev<strong>in</strong>g a<br />

greater [BLa] compared to women. Only female swimmers competed<br />

<strong>in</strong>, <strong>and</strong> were subsequently evaluated after, the 1500 m freestyle event,<br />

which had the lowest mean post-race [BLa]. However the sex difference<br />

persisted even when the outcomes from the 1500 m freestyle event were<br />

removed from the analysis.<br />

Previous research has reported post-race [BLa] tend to be greater<br />

follow<strong>in</strong>g IM events, whereas breaststroke tends to result <strong>in</strong> lower [BLa]<br />

regardless of age or sex (Avlonitou, 1996; Bonifazi et al., 1993; Sawka et<br />

al., 1979). Interest<strong>in</strong>gly, our male swimmers had similar post-race [BLa]<br />

across all swim strokes. In contrast, the female swimmers displayed a<br />

7-21% greater post-race [BLa] for IM events compared to freestyle,<br />

breaststroke <strong>and</strong> butterfly races. The lack of difference between strokes<br />

for males is unclear, however the observed relative difference between<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

IM <strong>and</strong> other strokes for females is similar, albeit on the lower end,<br />

to others who demonstrated a 25-60% greater post-race [BLa] for IM<br />

compared to other strokes of equal distance <strong>in</strong> age group (Avlonitou,<br />

1996) <strong>and</strong> college (Sawka et al., 1979) swimmers.<br />

Swimmers <strong>in</strong> the current study completed an active recovery accord<strong>in</strong>g<br />

to their <strong>in</strong>dividual coach’s assigned protocol. While not experimentally<br />

optimal, it reflects the reality of swim meets, <strong>and</strong> thus the recovery<br />

distances recommended <strong>in</strong> this paper may be more widely implemented<br />

than if the protocols were rigidly controlled. As an example of the utility<br />

of our model, if a female swimmer competed <strong>in</strong> the 200 m freestyle f<strong>in</strong>al<br />

<strong>and</strong> had a post-race [BLa] of 12.5 mmol•L -1 , an active recovery of 600<br />

m or 1200 m would be expected to reduce [BLa] by 9.5 mmol•L -1 <strong>and</strong><br />

11.3 mmol•L -1 , respectively, which would result <strong>in</strong> a post active recovery<br />

[BLa] of 3.0 mmol•L -1 or 1.3 mmol•L -1 . Taken together with the f<strong>in</strong>d<strong>in</strong>gs<br />

of Greenwood et al. (Greenwood et al., 2008)<strong>and</strong> subsequent swimm<strong>in</strong>g<br />

performance, coaches can now specify the distance <strong>and</strong> <strong>in</strong>tensity of<br />

the active recovery to maximize blood lactate clearance.<br />

conclusIon<br />

The results of a comprehensive analysis of blood lactate levels across a<br />

range of swimm<strong>in</strong>g events are reported. Furthermore, an estimate of lactate<br />

clearance by gender <strong>and</strong> event which is a practical tool for coaches<br />

is presented.<br />

reFerences<br />

Avlonitou, E. (1996). Maximal lactate values follow<strong>in</strong>g competitive performance<br />

vary<strong>in</strong>g accord<strong>in</strong>g to age, sex <strong>and</strong> swimm<strong>in</strong>g style. J Sports<br />

Med Phys Fitness, 36(1), 24-30.<br />

Benelli, P., Ditroilo, M., Forte, R., De Vito, G., & Stocchi, V. (2007). Assessment<br />

of post-competition peak blood lactate <strong>in</strong> male <strong>and</strong> female<br />

master swimmers aged 40-79 years <strong>and</strong> its relationship with swimm<strong>in</strong>g<br />

performance. Eur J Appl Physiol, 99(6), 685-693.<br />

Bonifazi, M., Martelli, G., Marugo, L., Sardella, F., & Carli, G. (1993).<br />

Blood lactate accumulation <strong>in</strong> top level swimmers follow<strong>in</strong>g competition.<br />

J Sports Med Phys Fitness, 33(1), 13-18.<br />

Bonifazi, M., Sardella, F., & Lupo, C. (2000). Preparatory versus ma<strong>in</strong><br />

competitions: differences <strong>in</strong> performances, lactate responses <strong>and</strong> precompetition<br />

plasma cortisol concentrations <strong>in</strong> elite male swimmers.<br />

Eur J Appl Physiol, 82(5-6), 368-373.<br />

Greenwood, J. D., Moses, G. E., Bernard<strong>in</strong>o, F. M., Gaesser, G. A.,<br />

& Weltman, A. (2008). Intensity of exercise recovery, blood lactate<br />

disappearance, <strong>and</strong> subsequent swimm<strong>in</strong>g performance. J Sports Sci,<br />

26(1), 29-34.<br />

Hard<strong>in</strong>, J. W., & Hilbe, J. M. (2002). Generalized Estimat<strong>in</strong>g Equations.<br />

Boca Raton: Chapman & Hall/CRC.<br />

Sawka, M. N., Knowlton, R. G., Miles, D. S., & Critz, J. B. (1979). Postcompetition<br />

blood lactate concentrations <strong>in</strong> collegiate swimmers. Eur<br />

J Appl Physiol Occup Physiol, 41(2), 93-99.<br />

Toubekis, A. G., Tsolaki, A., Smilios, I., Douda, H. T., Kourtesis, T., &<br />

Tokmakidis, S. P. (2008). Swimm<strong>in</strong>g performance after passive <strong>and</strong><br />

active recovery of various durations. Int J Sports Physiol Perform, 3(3),<br />

375-386.<br />

AcKnoWledGeMents<br />

Fund<strong>in</strong>g provided by Canadian Sport Centre Ontario. Thanks to R.<br />

Rupf, E. Fern<strong>and</strong>ez, C. Dalc<strong>in</strong>, T. Zochowski, S Farra.<br />

235


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Determ<strong>in</strong>ation <strong>and</strong> Validity of Critical Velocity <strong>in</strong><br />

Front Crawl, Arm Stroke <strong>and</strong> Leg Kick as an Index of<br />

Endurance Performance <strong>in</strong> Competitive Swimmers<br />

Wakayoshi, K. 1 , shiraki, t. 1 , ogita, F. 2 , Kitajima, M. 3<br />

1 Biwako Seikei Sport College, Japan<br />

2 National <strong>in</strong>stitute of Fitness <strong>and</strong> Sports, Japan<br />

3 Hyogo High School, Japan<br />

The purposes of this study were to determ<strong>in</strong>e critical velocity (Vcri) <strong>in</strong><br />

swim, pull <strong>and</strong> kick tests, <strong>and</strong> also to exam<strong>in</strong>e whether Vcri correspond<br />

to the exercise <strong>in</strong>tensity at maximal lactate steady state (MLSS) for each<br />

stroke. Fourteen male tra<strong>in</strong>ed college swimmers volunteered for this<br />

study. A regression analysis of swimm<strong>in</strong>g distance on time calculated<br />

for each swimmer showed l<strong>in</strong>ear relationships (r 2 =0.998, p


RESULTS<br />

Table 1 shows the physical characteristics, Vcri <strong>and</strong> correlation coefficient<br />

<strong>in</strong> swim, pull <strong>and</strong> kick for each subject.<br />

The experimental plots used to determ<strong>in</strong>e Vcri of subject 1 are shown<br />

<strong>in</strong> Fig. 1 as an example. The relations between distance (D) <strong>and</strong> time (T) <strong>in</strong><br />

swim, pull <strong>and</strong> kick were expressed <strong>in</strong> the general form, D = a + b x T, with<br />

r2 value (goodness of fit) show<strong>in</strong>g higher than 0.998 (p0.998) <strong>in</strong> all strokes for every subject,<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

so that the relationship D = a x T + b, was remarkably l<strong>in</strong>ear. These<br />

f<strong>in</strong>d<strong>in</strong>gs mean that the concept of Vcri is applicable to pull <strong>and</strong> kick as<br />

well as swim, <strong>and</strong> the obta<strong>in</strong>ed Vcri-p <strong>and</strong> Vcri-k could be also useful<br />

assessment for endurance capacity <strong>in</strong> arm stroke <strong>and</strong> leg kick, which can<br />

obta<strong>in</strong> without requir<strong>in</strong>g blood sampl<strong>in</strong>g or the use of highly expensive<br />

equipment.<br />

Wakayoshi et al. (1992a, 1992b, 1993) revealed that Vcri observed<br />

<strong>in</strong> swimm<strong>in</strong>g significantly correlated with several <strong>in</strong>dices for endurance<br />

capacity, such as oxygen consumption at anaerobic threshold, the<br />

swimm<strong>in</strong>g velocity at the onset of blood lactate accumulation <strong>and</strong> the<br />

mean velocity of 400 m freestyle. Moreover, they have suggested that<br />

Vcri, which is calculated by the times of 200m <strong>and</strong> 400m <strong>in</strong> the normal<br />

pool, would correspond approximately to the exercise <strong>in</strong>tensity at<br />

MLSS. Support<strong>in</strong>g those previous f<strong>in</strong>d<strong>in</strong>gs, all subjects <strong>in</strong> this experiment<br />

could ma<strong>in</strong>ta<strong>in</strong> the Vcri for 20 m<strong>in</strong> <strong>in</strong> all strokes, <strong>and</strong> the values of<br />

BL showed almost a steady state while the MLSS test, that is, there was<br />

no significant difference among the mean values of BL after each stage<br />

<strong>in</strong> each stroke. Furthermore, the values of BL at each stage were not<br />

significantly different among strokes. The results of this study suggest<br />

that the Vcri determ<strong>in</strong>ed by pull <strong>and</strong> kick as well as swim correspond<br />

approximately to the <strong>in</strong>tensity of MLSS <strong>and</strong> that those measurements<br />

could provide useful guidel<strong>in</strong>e for sett<strong>in</strong>g an appropriate <strong>in</strong>tensity for<br />

endurance tra<strong>in</strong><strong>in</strong>g for arm pull <strong>and</strong> leg kick.<br />

Interest<strong>in</strong>gly, Vcri-p observed <strong>in</strong> this experiment was almost equal or<br />

rather higher when compared to Vcri-s. This might be expla<strong>in</strong>ed by the<br />

use of pull-buoys while pull<strong>in</strong>g thus enabl<strong>in</strong>g more efficient strok<strong>in</strong>g <strong>in</strong><br />

Vcri-p as compared to Vcri-s.<br />

S<strong>in</strong>ce Vcri is a certa<strong>in</strong> <strong>in</strong>dex for endurance capacity, this result implies<br />

that the propulsion for whole stroke is generated mostly by the<br />

arm action as the swimm<strong>in</strong>g distance becomes longer. This conjecture<br />

is <strong>in</strong> l<strong>in</strong>e with the results of BL <strong>in</strong> MLSS tests, that is, the values of<br />

BL <strong>in</strong> pull were almost equal to those <strong>in</strong> swim (4-5 mmol•l-1), but<br />

those <strong>in</strong> kick (6-7 mmol•l-1) tended to be higher, suggest<strong>in</strong>g that the<br />

metabolic dem<strong>and</strong> for leg muscles dur<strong>in</strong>g swim should be much lower<br />

than that dur<strong>in</strong>g leg kick. On the other h<strong>and</strong>, maximal speed <strong>in</strong> swim is<br />

generally higher than that <strong>in</strong> pull. Therefore, leg kick should contribute<br />

the generation of the total propulsion of the swim, especially <strong>in</strong> spr<strong>in</strong>t<br />

event. Actually, <strong>in</strong> the short last<strong>in</strong>g exhaustive swimm<strong>in</strong>g (


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

kick, <strong>and</strong> whole body swimm<strong>in</strong>g last<strong>in</strong>g 15s to 10 m<strong>in</strong>. In Chatard<br />

J.C. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX, eds., , Sa<strong>in</strong>t-Etienne,<br />

361-366.<br />

Scheen A, Juchmes J, Cession-Fossion A (1981) Critical analysis of the<br />

“Anaerobic Threshold” dur<strong>in</strong>g exercise at constant workloads. Eur. J.<br />

Appl. Physiol. 46, 367-377.<br />

Stegmann H, K<strong>in</strong>dermann W (1982) Comparison of prolonged exercise<br />

tests at the <strong>in</strong>dividual anaerobic threshold <strong>and</strong> fixed anaerobic threshold<br />

of 4 mmol/l lactate. Int. J. Sports Med. 3, 105-110.<br />

Wakayoshi K, Ikuta K, Yoshida T, Udo M, Moritani T, Mutoh Y, Miyashita<br />

M (1992a) The determ<strong>in</strong>ation <strong>and</strong> validity of critical speed<br />

as swimm<strong>in</strong>g performance <strong>in</strong>dex <strong>in</strong> the competitive swimmer. Eur. J.<br />

Appl. Physiol. 64, 153-157.<br />

Wakayoshi K, Yoshida T, Udo M, Kasai T, Moritani T, Mutoh Y <strong>and</strong><br />

Miyashita M (1992b) The simple method for determ<strong>in</strong><strong>in</strong>g critical<br />

speed as swimm<strong>in</strong>g fatigue threshold <strong>in</strong> competitive swimm<strong>in</strong>g. Int.<br />

J Sports Med. 13, 367-371.<br />

Wakayoshi K, Yoshida T, Udo M, Harada T, Moritani T, Mutoh Y <strong>and</strong><br />

Miyashita M (1993) Does critical swimm<strong>in</strong>g velocity represent exercise<br />

<strong>in</strong>tensity at maximal lactate steady state? Eur. J. Appl. Physiol.<br />

66, 90-95.<br />

238<br />

Differences In Methods Determ<strong>in</strong><strong>in</strong>g The Anaerobic<br />

Threshold Of Triathletes In The Water<br />

Zoretić, d. 1 , Wertheimer, V. 2 , leko, G. 1<br />

1 Faculty of K<strong>in</strong>esiology, University of Zagreb<br />

2 Croatian Academic Swimm<strong>in</strong>g Club „MLADOST“<br />

The goal of this research is to exam<strong>in</strong>e the differences between three<br />

various methods for determ<strong>in</strong><strong>in</strong>g the anaerobic threshold, i.e. differences<br />

<strong>in</strong> heart frequencies with regard to the anaerobic threshold (FSanp-1,<br />

FSanp-2, FSanp-3). 13 Croatian triathletes swam a progressive <strong>in</strong>terval<br />

test of 7 x 200 meters. The evaluation of functional ability was measured<br />

by: maximum heart frequency, maximum speed, maximum lactate, anaerobic<br />

threshold FS <strong>and</strong> anaerobic threshold lactate, for three different<br />

methods. Results showed high correlation (r=0.91) between FSanp-1<br />

(„<strong>in</strong>tersection“ method) <strong>and</strong> FSanp-3 (D-max method), while the t-test<br />

for dependant samples showed that no statistically significant differences<br />

exist, the same demonstrat<strong>in</strong>g that those two different measures<br />

for determ<strong>in</strong><strong>in</strong>g the anaerobic threshold are reliable <strong>in</strong> evaluat<strong>in</strong>g the<br />

anaerobic threshold <strong>in</strong> swimmers.<br />

Key words: „Intersection” method, 4 mmol/l method <strong>and</strong> d-max<br />

method, swimm<strong>in</strong>g<br />

IntroductIon<br />

The ma<strong>in</strong> problem <strong>in</strong> test<strong>in</strong>g swimmers <strong>and</strong> triathletes is the implementation<br />

of a protocol <strong>in</strong> the water where ventilation parameters can’t be monitored<br />

requir<strong>in</strong>g tests that <strong>in</strong>clude monitor<strong>in</strong>g metabolic parameters. Test<strong>in</strong>g<br />

these athletes outside the water does not ensure adequate <strong>and</strong> reliable<br />

results due to the specificity of water tra<strong>in</strong><strong>in</strong>g: decreased body temperature,<br />

higher pressure volume of the heart, lower maximum heart frequency<br />

<strong>and</strong> lower energy consumption (Maglischo, 2003). Various methods exist<br />

for determ<strong>in</strong><strong>in</strong>g the anaerobic threshold based on the speed-lactate curve.<br />

One of the methods used for establish<strong>in</strong>g the anaerobic threshold is the<br />

fixed lactate model proposed by K<strong>in</strong>dermann (1979), <strong>and</strong> upgraded by<br />

Sjod<strong>in</strong> <strong>and</strong> Jacobs (1981) by <strong>in</strong>troduc<strong>in</strong>g the OBLA (Onset of blood lactate<br />

accumulation). Based on that <strong>in</strong>itial model, the anaerobic threshold<br />

was fixed at 4mmol/l, while the aerobic threshold precedes it at 2mmol/l.<br />

A special <strong>in</strong>terpretation of the lactate threshold arose after the existence<br />

of <strong>in</strong>dividual differences <strong>in</strong> the blood lactate concentration, at the lactate<br />

anaerobic threshold, was confirmed. The orig<strong>in</strong>al method by Stegmann<br />

<strong>and</strong> Associates (1981), def<strong>in</strong><strong>in</strong>g the <strong>in</strong>dividual anaerobic threshold (IAT)<br />

as the exercise <strong>in</strong>tensity at which the speed-lactate curve changes its shape<br />

from a curve to a straight l<strong>in</strong>ear (Maglischo, 2003). This method is also<br />

known as the <strong>in</strong>tersection method. Cheng <strong>and</strong> Kuipers have, <strong>in</strong> 1992, described<br />

a new procedure, they call the D-max method, for determ<strong>in</strong><strong>in</strong>g the<br />

anaerobic threshold, us<strong>in</strong>g a start<strong>in</strong>g <strong>and</strong> term<strong>in</strong>at<strong>in</strong>g curve po<strong>in</strong>t. The l<strong>in</strong>e<br />

is set by the basic course of variable change. Thereafter, a po<strong>in</strong>t is set on the<br />

curve that is the farthest from the l<strong>in</strong>e. Said po<strong>in</strong>t represents a change <strong>in</strong><br />

trend <strong>and</strong> the authors believe it corresponds with the anaerobic threshold<br />

(Maglischo, 2003).<br />

The purpose of this paper is to determ<strong>in</strong>e whether statistically significant<br />

differences exist between 3 various methods of anaerobic threshold<br />

determ<strong>in</strong>ation (the „Intersection” method, the 4 mmol/l method <strong>and</strong> the<br />

D-max method), i.e. differences <strong>in</strong> heart frequencies at the anaerobic<br />

threshold level (FSanp-1, FSanp-2, FSanp-3) dur<strong>in</strong>g the swimmers’<br />

progressive test. The importance of the anaerobic threshold determ<strong>in</strong>ant<br />

lies <strong>in</strong> the subsequent simplicity <strong>in</strong> establish<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g zones <strong>and</strong><br />

achiev<strong>in</strong>g planned tra<strong>in</strong><strong>in</strong>g goals.<br />

Methods<br />

The subjects were a group of 13 Croatian triathletes of a recreational <strong>and</strong><br />

national level, of which there were 10 male <strong>and</strong> 3 female triathletes, at an


average age of 27.1 ± 5.9 years. When select<strong>in</strong>g subjects, the prerequisite<br />

was to have at least one year of tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competitive experience <strong>in</strong><br />

triathlon, as well as be<strong>in</strong>g of satisfactory health.<br />

Table 1: Descriptive parameters<br />

AS±SD (m<strong>in</strong>-max)<br />

AGE (yrs) 27.1 ± 5.9 (18-39)<br />

body height (cm) 174.85 ± 7.28 (165.0-187.0)<br />

body mass (kg) 72.65 ± 11.18 (58.7-92.7)<br />

%BF (%) 13.4 ± 7.72 (4.0-26.2)<br />

AGE – years, body height (cm) , body mass (kg), %BF - Subcutaneous<br />

Body Fat<br />

Sample of Variables<br />

a) A set of variables for evaluat<strong>in</strong>g anthropometric characteristics<br />

Measurement of exam<strong>in</strong>ees’ morphological characteristics was carried<br />

out <strong>in</strong> accordance with the guidel<strong>in</strong>es of the International Biological<br />

Program (IBP, Mišigoj-Duraković 2008). Basic morphological variables<br />

were measured <strong>in</strong> order to determ<strong>in</strong>e the exam<strong>in</strong>ees’ morphological status.<br />

With the help of anthropometric <strong>in</strong>struments <strong>and</strong> a medical scale,<br />

the variables of body mass <strong>and</strong> body height were measured, while the<br />

subcutaneous body fat was established based on the method of biological<br />

impedance, us<strong>in</strong>g the Tanita BC-418 (TANITA, USA) scale. Eight<br />

electrodes (4 for the arms, 4 for the feet) are used to send a weak electric<br />

signal through the entire body. In those locations where the resistance,<br />

i.e. impedance is higher, the signal needs more time to travel, <strong>in</strong>dicat<strong>in</strong>g<br />

a higher content of subcutaneous body fat.<br />

b) Set of variables for evaluat<strong>in</strong>g functional abilities<br />

1)FS max (BPM ) - Maximum Heart Frequency, 2) V max (m/s) Maximum<br />

Speed, 3) LAC max (mmol/l) - Maximum Lactates, 4) FS anp-1 (BPM)<br />

- Anaerobic Threshold Heart Frequency („<strong>in</strong>tersection method“), 5)<br />

FS anp-2 (BPM) - Anaerobic Threshold Heart Frequency („4 mmol/l“),<br />

6) FS anp-3 (BPM) - Anaerobic Threshold Heart Frequency („D-max<br />

method“), 7) LAC anp-1 (mmol/l) - Anaerobic Threshold Lactates („<strong>in</strong>tersection<br />

method“), 8) LAC anp-2 (mmol/l) - Anaerobic Threshold<br />

Lactates („4 mmol/l“), 9) LAC anp-3 ( mmol/l) - Anaerobic Threshold<br />

Lactates („D-max method“).<br />

Specified parameters were measured dur<strong>in</strong>g one test protocol, while the<br />

variables were determ<strong>in</strong>ed based on three various methods.<br />

Prior to test<strong>in</strong>g, the exam<strong>in</strong>ees were acqua<strong>in</strong>ted with the test<strong>in</strong>g protocol<br />

which, with regard to the swimm<strong>in</strong>g test, consists of seven (7) 200<br />

meter sections with a 5 m<strong>in</strong>ute active rest regime <strong>in</strong> a small swimm<strong>in</strong>g<br />

pool. Each section is covered by apply<strong>in</strong>g a faster swimm<strong>in</strong>g pace, up<br />

to the maximum <strong>and</strong> at an even pace. How fast each exam<strong>in</strong>ee swam<br />

through a certa<strong>in</strong> section was determ<strong>in</strong>ed based on the best 200 meter<br />

result, the same be<strong>in</strong>g tested a few days prior to the swimm<strong>in</strong>g test. The<br />

obta<strong>in</strong>ed result was <strong>in</strong>creased by 5 seconds <strong>in</strong> order to get the fastest<br />

seventh section. Every previous section is also <strong>in</strong>creased by 5 seconds <strong>in</strong><br />

order to get the swimm<strong>in</strong>g pace for each set section which the swimmer<br />

must comply with. An example of calculat<strong>in</strong>g swimm<strong>in</strong>g speed for each<br />

of the set sections is shown <strong>in</strong> Table 6. Specified swimm<strong>in</strong>g pace was<br />

dictated by an assistant by the pool, us<strong>in</strong>g a whistle every 12.5 m, <strong>and</strong><br />

if the exam<strong>in</strong>ee was swimm<strong>in</strong>g at a set pace, then the assistant would<br />

whistle every 25 or 50 m. Dur<strong>in</strong>g test<strong>in</strong>g, the exam<strong>in</strong>ees wore a pulse<br />

meter (Polar RS 400, F<strong>in</strong>l<strong>and</strong>) the whole time, <strong>and</strong> at each section’s end,<br />

the concentration of lactates <strong>in</strong> the blood was measured with a Lactate<br />

Scout device (SensLab, Germany). Immediately prior to start<strong>in</strong>g a new<br />

section (about 15-30 seconds prior), the exam<strong>in</strong>ee would enter the pool<br />

<strong>and</strong> prepare for start. In order for the transmitter of the pulse meter to<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

be attached to the exam<strong>in</strong>ees’ chests, all the exam<strong>in</strong>ees wore swimsuits.<br />

Results obta<strong>in</strong>ed by measurement procedures were processed by a data<br />

analysis software system Statistic version 8.0. In order to determ<strong>in</strong>e statistically<br />

significant differences between various methods used to establish the<br />

anaerobic threshold of the subjects, the t-test was used for dependent samples.<br />

results<br />

Assessed means, st<strong>and</strong>ard deviation, m<strong>in</strong>imal <strong>and</strong> maximal results,<br />

skewness <strong>and</strong> kurtosis for certa<strong>in</strong> variables is presented <strong>in</strong> Table 2. Ttest<br />

for dependant variables showed that there is no statistical significant<br />

difference between FS anp-1 <strong>and</strong> FS anp-3 (Table 3).<br />

Table 2: Descriptive Values of Certa<strong>in</strong> Variables<br />

Valid N Mean M<strong>in</strong>imum Maximum Std.Dev. Skewness Kurtosis<br />

FSmax 13 180.15 170 192 7.50 0.065 -1.342<br />

LACmax 13 11.31 6.6 19.2 2.99 1.236 4.098<br />

Vmax 13 1.13 0.96 1.36 0.11 0.415 0.139<br />

LACanp-1 13 4.63 3.3 6 0.80 0.015 -0.705<br />

LACanp-2 13 4.00 4 4 0.00 -- --<br />

LACanp-3 13 4.98 3.3 7.3 1.15 0.521 0.006<br />

Table 3: T-test <strong>and</strong> Correlation Results<br />

FSanp-1<br />

FSanp-2<br />

FSanp-3<br />

P < .05000 FSanp-1 FSanp-2 FSanp-3<br />

R 1 0.88 0.91<br />

t (p) 3.87 (0.0022) -1.95 (0.07)<br />

R 0.88 1 0.74<br />

t (p) 3.87 (0.0022) -3.92 (0.0020)<br />

R 0.91 0.74 1<br />

t (p) -1.95 (0.07) -3.92 (0.0020)<br />

High correlation values (Table 3) are <strong>in</strong>dicative of a l<strong>in</strong>k between FS anp-1<br />

<strong>and</strong> FS anp-2 which shows that the purpose of measurement is the same<br />

<strong>and</strong> that predict<strong>in</strong>g results by us<strong>in</strong>g the D-max method based on the<br />

„<strong>in</strong>tersection” method is 82% successful, while predict<strong>in</strong>g results through<br />

the D-max method based on the 4 mmol/l method is much less successful,<br />

i.e. 54%.<br />

dIscussIon<br />

Large differences between maximum values of lactate <strong>in</strong> the blood suggest<br />

various degrees <strong>in</strong> which the body is able to react to acidosis. Naturally,<br />

those values are conditioned by tra<strong>in</strong><strong>in</strong>g as well, <strong>and</strong> if look<strong>in</strong>g at<br />

each exam<strong>in</strong>ee separately, it is noticeable that exam<strong>in</strong>ees that are more<br />

tra<strong>in</strong>ed are able to <strong>in</strong>crease speed one section after another, regardless<br />

of the rise of blood lactate <strong>and</strong> the decrease of pH value. Said values of<br />

maximum blood lactateise a generally accepted aerobic capacity parameter<br />

<strong>and</strong> the buffer<strong>in</strong>g ability of the muscles.<br />

Values of the maximum heart frequency <strong>in</strong> this test are the highest<br />

value achieved <strong>in</strong> a test, but the maximum. In order to achieve maximum<br />

heart frequency values, the test must be shorter, without <strong>in</strong>tervals <strong>and</strong><br />

more <strong>in</strong>tense.<br />

It would be logical that there are no statistically significant differences<br />

between all these measures because the object measured is the<br />

same. Table 3 shows a high correlation (r=0.91) between FSanp-1 („<strong>in</strong>tersection“<br />

method) <strong>and</strong> FSanp-3 (D-max method), while the t-test for<br />

dependant samples showed (Table 3) that no statistically significant differences<br />

exist, the same demonstrat<strong>in</strong>g that those two different measures<br />

for determ<strong>in</strong><strong>in</strong>g the anaerobic threshold are reliable <strong>in</strong> evaluat<strong>in</strong>g the<br />

anaerobic threshold <strong>in</strong> swimmers.<br />

239


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Furthermore, Table 3 shows that a statistically significant difference<br />

exists between FSanp-2 (4 mmol/l method) with FSanp-1 <strong>and</strong><br />

FSanp-3, thereby prov<strong>in</strong>g it to be a deviat<strong>in</strong>g measure, mean<strong>in</strong>g that it<br />

does not target the same qualities.<br />

Accord<strong>in</strong>g to Stegmann <strong>and</strong> associates, 1981, it is impossible to fix<br />

the threshold at 4mmol/l for everyone (FSanp-2), so therefore it is necessary<br />

to determ<strong>in</strong>e the so called IAT – <strong>in</strong>dividual anaerobic threshold<br />

(FSanp-1). In their research, Stegman <strong>and</strong> K<strong>in</strong>dermann have shown<br />

that the <strong>in</strong>dividual anaerobic threshold is different <strong>in</strong> relation to the<br />

threshold obta<strong>in</strong>ed by a fixed concentration of lactates at 4mmol/l. The<br />

„Intersection” method, i.e. the <strong>in</strong>dividual anaerobic threshold represents<br />

a reliable way of evaluat<strong>in</strong>g the lactate anaerobic threshold (Urhausen,<br />

1993), <strong>and</strong> if carried out carefully it provides overall consistent results<br />

with athletes or with<strong>in</strong> the cl<strong>in</strong>ical population (Svedahl <strong>and</strong> MacIntosh,<br />

2003). Establish<strong>in</strong>g the anaerobic threshold at 4mmol/l has its advantages,<br />

consider<strong>in</strong>g the objectivity of determ<strong>in</strong>ation, but also a great disadvantage<br />

due to ignor<strong>in</strong>g <strong>in</strong>dividual differences <strong>and</strong> <strong>in</strong>dividual lactate<br />

k<strong>in</strong>etics. That is, not all exam<strong>in</strong>ees show a significant <strong>in</strong>crease of lactate<br />

at 4 mmol/l, but this range is much wider, spann<strong>in</strong>g from 3-6 mmol/l,<br />

up to as much as 9 mmol/l (MacIntosh <strong>and</strong> Assoc., 2002.; Billat <strong>and</strong><br />

Assoc.2003).<br />

Figure 1: Comparison of FSanp Percentage Values from FSmax Obta<strong>in</strong>ed by Three Different Methods<br />

Figure 1: Comparison of FSanp Percentage Values from FSmax Ob-<br />

It ta<strong>in</strong>ed is important by Three to Different know that, Methods on average, untra<strong>in</strong>ed persons will exceed the threshold at<br />

only 50-60% of maximum load, while top athletes <strong>in</strong> aerobic sports do the same at 85-<br />

95% It is important of maximum to load know (Janssen, that, on 2001). average, The untra<strong>in</strong>ed percentage persons values will of exceed FSanp <strong>in</strong>cidence are<br />

very the threshold high <strong>and</strong> at should only 50-60% not be taken of maximum literally, load, s<strong>in</strong>ce while unfortunately top athletes maximum <strong>in</strong> values of<br />

heart aerobic frequency sports do have the same not been at 85-95% obta<strong>in</strong>ed. of Accord<strong>in</strong>g maximum load to Maglischo, ( Janssen, 2003, 2001). the maximum<br />

heart frequency value for swimmers must be tested <strong>in</strong> the water, while an additional<br />

The percentage values of FSanp <strong>in</strong>cidence are very high <strong>and</strong> should not<br />

prerequisite of obta<strong>in</strong><strong>in</strong>g maximum heart frequency values is read<strong>in</strong>g the values dur<strong>in</strong>g<br />

or be immediately taken literally, after s<strong>in</strong>ce maximum unfortunately performance maximum last<strong>in</strong>g values between of heart one <strong>and</strong> frequen- two m<strong>in</strong>utes.<br />

cy have not been obta<strong>in</strong>ed. Accord<strong>in</strong>g to Maglischo, 2003, the maximum<br />

CONCLUSION<br />

heart frequency value for swimmers must be tested <strong>in</strong> the water, while an<br />

Today, additional there prerequisite are several of def<strong>in</strong>itions obta<strong>in</strong><strong>in</strong>g maximum of the term heart anaerobic frequency threshold. values is The anaerobic<br />

threshold is considered to be the <strong>in</strong>tensity at which the oxygen supply system activates<br />

read<strong>in</strong>g the values dur<strong>in</strong>g or immediately after maximum performance<br />

the mechanism of anaerobic glycolysis <strong>in</strong> a more significant way, <strong>and</strong> at which the<br />

accumulation last<strong>in</strong>g between of one lactic <strong>and</strong> acid two is m<strong>in</strong>utes. equal to its breakdown. The method most often used <strong>in</strong><br />

practice is the ventilation method, but its application <strong>in</strong> water is almost impossible,<br />

whereas conclusIon the second mostly used method is the heart frequency deflection po<strong>in</strong>t that can<br />

be Today, determ<strong>in</strong>ed there are on several a heart def<strong>in</strong>itions frequency of curve the term obta<strong>in</strong>ed anaerobic from threshold. a cont<strong>in</strong>uous The test. For that<br />

reason,<br />

anaerobic<br />

test<strong>in</strong>g<br />

threshold<br />

<strong>in</strong> the<br />

is<br />

water<br />

considered<br />

is significantly<br />

to be the<br />

more<br />

<strong>in</strong>tensity<br />

difficult,<br />

at which<br />

thereby<br />

the<br />

mak<strong>in</strong>g<br />

oxygen<br />

the anaerobic<br />

threshold determ<strong>in</strong>ation more difficult as well. In the course of this research, three<br />

methods supply system were used activates to determ<strong>in</strong>e the mechanism the anaerobic of anaerobic threshold: glycolysis 1) the <strong>in</strong> „<strong>in</strong>tersection” a more method<br />

(IAT), significant 2) the way, 4mmol/l <strong>and</strong> at which method, the <strong>and</strong> accumulation the 3) D-max of lactic method. acid is Both equal the to „Intersection”<br />

method its breakdown. <strong>and</strong> the The D-max method method most have often been used shown <strong>in</strong> practice to be a is reliable the ventilation manner of evaluat<strong>in</strong>g<br />

the method, anaerobic but its threshold, application <strong>and</strong> <strong>in</strong> if water applied is almost carefully impossible, they provide whereas generally the consistent<br />

results second <strong>in</strong> mostly swimmers. used method is the heart frequency deflection po<strong>in</strong>t that<br />

can be determ<strong>in</strong>ed on a heart frequency curve obta<strong>in</strong>ed from a cont<strong>in</strong>uous<br />

test. For that reason, test<strong>in</strong>g <strong>in</strong> the water is significantly more difficult,<br />

thereby mak<strong>in</strong>g the anaerobic threshold determ<strong>in</strong>ation more dif-<br />

240<br />

85,00<br />

80,00<br />

75,00<br />

%FSanp‐1<br />

%FSanp‐2<br />

%FSanp‐3<br />

ficult as well. In the course of this research, three methods were used to<br />

determ<strong>in</strong>e the anaerobic threshold: 1) the „<strong>in</strong>tersection” method (IAT),<br />

2) the 4mmol/l method, <strong>and</strong> the 3) D-max method. Both the „Intersection”<br />

method <strong>and</strong> the D-max method have been shown to be a reliable<br />

manner of evaluat<strong>in</strong>g the anaerobic threshold, <strong>and</strong> if applied carefully<br />

they provide generally consistent results <strong>in</strong> swimmers.<br />

reFerences<br />

Billat, L.V., Sirvent, P., Py, G., Koralszte<strong>in</strong> J., Mercier, J. (2003). The<br />

Concept of Maximal Lactate Steady State. Sports Med 33(6), 407-<br />

426.<br />

Janssen, P. (2001). Lactate Threshold Tra<strong>in</strong><strong>in</strong>g. Human K<strong>in</strong>etics. USA.<br />

K<strong>in</strong>dermann, W., Simon, G., <strong>and</strong> Keul, J. (1979). The significance of the<br />

aerobic-anaerobic transition for the determ<strong>in</strong>ation of work load <strong>in</strong>tensities<br />

dur<strong>in</strong>g endurance tra<strong>in</strong><strong>in</strong>g. Eur. J. Appl. Physiol. 42, 25-34.<br />

MacIntosh, B.R., Esau, S., Svedahl, K. (2002). The lactate m<strong>in</strong>imum test<br />

for cycl<strong>in</strong>g: Estimation of the maximal lactate steady state. Can. J. Appl.<br />

Physiol, 27, 232-249.<br />

Maglischo, 127 E. (2003). Swimm<strong>in</strong>g Fastest. Human K<strong>in</strong>etics, UK.<br />

Mišigoj-Duraković M. K<strong>in</strong>antropologija. Biološki aspekti tjelesnog<br />

vježbanja (K<strong>in</strong>anthropology. Biological Aspects of Physical Exer-<br />

range is much wider, spann<strong>in</strong>g from 3-6 mmol/l, up to as much as 9 mmol/l (MacIntosh cise). Faculty of K<strong>in</strong>esiology, University of Zagreb, 2008; 130-150<br />

<strong>and</strong> A graphical Assoc., 2002.; overview Billat of <strong>and</strong> FSAssoc.2003). anp values shows that the lowest values of Sjod<strong>in</strong>, B., Jacobs, I., <strong>and</strong> Karlsson, J. (1981). Onset of blood lactate ac-<br />

FSanp-2 , i.e. heart frequency were determ<strong>in</strong>ed by the 4 mmol/l method. cumulation <strong>and</strong> marathon runn<strong>in</strong>g performance. Int. J. Sports Med. 2,<br />

A graphical overview of FSanp values shows that the lowest values of FSanp-2, i.e. heart<br />

frequency A higher similarity were determ<strong>in</strong>ed of <strong>in</strong>cidence by the <strong>and</strong> 4 mmol/l higher values method. between A higher FSsimilarity anp-1 <strong>and</strong> of <strong>in</strong>cidence 23-26.<br />

<strong>and</strong> FSanp-3 higher are values also clearly between visible. FSanp-1 <strong>and</strong> FSanp-3 are also clearly visible. Stegmann H, K<strong>in</strong>derman W, Schnabel A. (1981). Lactate k<strong>in</strong>etics <strong>and</strong> the<br />

<strong>in</strong>dividual anaerobic threshold. International Journal of Sports Medi-<br />

100,00<br />

c<strong>in</strong>e. 2, 160-165.<br />

Swedahl K., MacIntosh B.R. (2003). Anaerobic threshold: The concept <strong>and</strong><br />

95,00<br />

methods of measurement. Can. J. Appl. Physiol. 28 (2), 229-323.<br />

Urhausen, A., Coen, B., Weiler, B., <strong>and</strong> K<strong>in</strong>dermann, W. (1993). In-<br />

90,00<br />

dividual anaerobic threshold <strong>and</strong> maximum lactate steady state. Int. J.<br />

Sports Med, 14, 134-139.


Chapter 4. Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Performance


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Physiological Responses <strong>and</strong> Performance<br />

Characteristics of 200m Cont<strong>in</strong>uous Swimm<strong>in</strong>g <strong>and</strong><br />

4x50m ‘’Broken Swimm<strong>in</strong>g’’ with Different Rest<br />

Intervals<br />

Beidaris, n., Botonis, P. <strong>and</strong> Platanou, t.<br />

Faculty of Physical Education <strong>and</strong> Sport Science, University of Athens, Greece<br />

The purpose of the present study was to <strong>in</strong>vestigate the physiological responses<br />

<strong>and</strong> performance characteristics of ‘’broken’’ swimm<strong>in</strong>g (4x50m)<br />

with different rest <strong>in</strong>tervals (5, 10 <strong>and</strong> 20s) compared with those of cont<strong>in</strong>uous<br />

swimm<strong>in</strong>g (200m) dur<strong>in</strong>g maximum <strong>in</strong>tensity free-style swimm<strong>in</strong>g.<br />

Twelve voluntary swimmers of competitive level (aged: 14-17<br />

years) were tested. Significant differences were observed <strong>in</strong> performance<br />

time <strong>and</strong> heart rate between cont<strong>in</strong>uous <strong>and</strong> «broken» swimm<strong>in</strong>g with<br />

rest<strong>in</strong>g <strong>in</strong>terval of 20s (F=4.27, P=0.009 <strong>and</strong> F=3.31, P=0.03, respectively).<br />

However, no differences were found <strong>in</strong> blood lactate <strong>and</strong> oxygen<br />

consumption. In conclusion, it seems that even if the physiological<br />

responses were similar between conditions, the performance<br />

characteristics were higher <strong>in</strong> the condition of broken swimm<strong>in</strong>g<br />

with 20s rest<strong>in</strong>g <strong>in</strong>terval.<br />

Key words: Vo 2 , lactate, heart rate, performance, speed, number of<br />

strokes<br />

IntroductIon<br />

In swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g, various methods have been employed for the<br />

improvement of swimm<strong>in</strong>g endurance <strong>and</strong> speed. ‘’Broken’’ swimm<strong>in</strong>g<br />

is a mode of <strong>in</strong>terval <strong>and</strong> repeated tra<strong>in</strong><strong>in</strong>g for ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g high rate<br />

<strong>and</strong> speed of swimm<strong>in</strong>g of a distance with maximum <strong>in</strong>tensity (“broken”<br />

swim, Maglischo 1993). Accord<strong>in</strong>g to this method, the total swimm<strong>in</strong>g<br />

distance is divided <strong>in</strong>to smaller distances with short rest <strong>in</strong>tervals dur<strong>in</strong>g<br />

which athletes swim to their limits, ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the highest speed<br />

possible. The rest <strong>in</strong>tervals between swims could be either long (20 s) or<br />

short (5 s), dur<strong>in</strong>g which swimmers ma<strong>in</strong>ta<strong>in</strong> the same rate <strong>and</strong> speed<br />

throughout the total distance. The total time is estimated by subtract<strong>in</strong>g<br />

the rest <strong>in</strong>terval time from the total time of the total distance. Additionally,<br />

the above method is ma<strong>in</strong>ly used as a test of performance <strong>in</strong> a given<br />

distance before competition.<br />

The physiological responses <strong>and</strong> the performance characteristics are<br />

very important for a coach who needs to analyze the tra<strong>in</strong><strong>in</strong>g data <strong>and</strong> to<br />

ga<strong>in</strong> feedback for the results of a method as a way for achiev<strong>in</strong>g the competition<br />

goals. It is known that heart rate is an exercise <strong>in</strong>tensity <strong>in</strong>dex as<br />

are blood lactate <strong>and</strong> maximal oxygen consumption. In particular, dur<strong>in</strong>g<br />

high <strong>in</strong>tensity exercise, the heart rate <strong>and</strong> heart muscle contractility are<br />

<strong>in</strong>creased to deliver more blood to exercis<strong>in</strong>g muscles. Heart rate is considered<br />

as a ma<strong>in</strong> tra<strong>in</strong><strong>in</strong>g guide by many researchers (Chen et al. 2002,<br />

Niewiadomski et al. 2007).<br />

Moreover, lactic acid is produced dur<strong>in</strong>g exercise <strong>and</strong> it is well established<br />

that dur<strong>in</strong>g high <strong>in</strong>tensity exercise, the lactate production is<br />

raised. Dur<strong>in</strong>g the first stages of exercise, O 2 deficit is evident, <strong>and</strong> as<br />

a result lactic acid is <strong>in</strong>creased for energy production. The blood lactate<br />

concentration is another ma<strong>in</strong> <strong>in</strong>dex of exercise <strong>in</strong>tensity (Billat 1996).<br />

Oxygen consumption is also an <strong>in</strong>dex of exercise <strong>in</strong>tensity <strong>and</strong> can be<br />

used to evaluate the contribution of aerobic energy dur<strong>in</strong>g exercise (Fern<strong>and</strong>ez<br />

et al., 2003). It shows the cardiovascular <strong>and</strong> muscle ability of<br />

the body to consume O 2 per unit time. The <strong>in</strong>crement of oxygen consumption<br />

is l<strong>in</strong>ear <strong>and</strong> is related to the exercise <strong>in</strong>tensity.<br />

However it is not known, if the physiological responses <strong>and</strong> performance<br />

characteristics are similar between <strong>in</strong>terval <strong>and</strong> cont<strong>in</strong>uous<br />

tra<strong>in</strong><strong>in</strong>g. The purpose of this study was to <strong>in</strong>vestigate: 1) the physiological<br />

responses of ‘’broken’’ swimm<strong>in</strong>g (4x50m) with different rest<strong>in</strong>g <strong>in</strong>tervals<br />

compared with those of cont<strong>in</strong>uous swimm<strong>in</strong>g (200m) dur<strong>in</strong>g<br />

242<br />

maximum <strong>in</strong>tensity free-style swimm<strong>in</strong>g <strong>and</strong> 2) which rest<strong>in</strong>g <strong>in</strong>terval<br />

<strong>in</strong> ‘’broken’’ swimm<strong>in</strong>g, contributes to the development of higher swimm<strong>in</strong>g<br />

speed with similar physiological dem<strong>and</strong>s compared to those of<br />

cont<strong>in</strong>uous swimm<strong>in</strong>g. The hypotheses <strong>in</strong> this study are that 1) the maximum<br />

lactate concentration <strong>and</strong> oxygen consumption would be similar<br />

at the end of the 200m swimm<strong>in</strong>g, regardless of the rest<strong>in</strong>g <strong>in</strong>terval<br />

between the 50m swims. 2) The heart rate dur<strong>in</strong>g the 200m swimm<strong>in</strong>g<br />

would be expected to be different because the <strong>in</strong>tensity of exercise would<br />

be dependent on the previous rest<strong>in</strong>g <strong>in</strong>terval <strong>and</strong> 3) the performance<br />

related characteristics <strong>in</strong> ‘’broken’’ swimm<strong>in</strong>g would be expected to be<br />

different. It is expected that a long rest<strong>in</strong>g <strong>in</strong>terval would contribute to a<br />

higher swimm<strong>in</strong>g performance.<br />

Methods<br />

Twelve swimmers (aged: 14-17 years) with at least five years of tra<strong>in</strong><strong>in</strong>g<br />

age were tested <strong>in</strong> 4 exercise conditions: <strong>in</strong> 200m <strong>and</strong> <strong>in</strong> 4x50m of<br />

free-style swimm<strong>in</strong>g with 5, 10 <strong>and</strong> 20 s rest <strong>in</strong>tervals between swims. In<br />

all sets, A) Physiological parameters: 1. oxygen consumption (VO2000<br />

Breeze Lite, MedGraphics, USA) 2. blood lactate concentration (Accusport,<br />

Boehr<strong>in</strong>ger, Germany) 3. Heart rate (Polar, Vantage NV, F<strong>in</strong>l<strong>and</strong>)<br />

B) Performance characteristics: record<strong>in</strong>g of performance time,<br />

mean speed <strong>and</strong> number of strokes. C) Rate of perceived exertion (Borg<br />

scale), were measured.<br />

In the beg<strong>in</strong>n<strong>in</strong>g, a VO 2 max test (400m free style swimm<strong>in</strong>g) was<br />

conducted <strong>in</strong> order to estimate the oxygen consumption as a percentage<br />

(%) of VO 2 max by backward extrapolation. The reliability <strong>and</strong> validity<br />

of backward extrapolation has been previously tested (Leger et al. 1980,<br />

Montpetit 1981). Accord<strong>in</strong>g to that method, the air is collected at the<br />

end of exercise <strong>in</strong> 4 different times of 20 s <strong>and</strong> then a l<strong>in</strong>ear backward<br />

regression curve is conducted. Afterwards, each participant swam 200m<br />

<strong>and</strong> on a separate day 4x50m free style swimm<strong>in</strong>g of maximum <strong>in</strong>tensity<br />

with 5, 10 <strong>and</strong> 20 s rest<strong>in</strong>g <strong>in</strong>terval between swims <strong>in</strong> a r<strong>and</strong>om order.<br />

At the end of each condition the O 2 deficit was calculated by measur<strong>in</strong>g<br />

the exhaled air for 2-m<strong>in</strong> dur<strong>in</strong>g recovery. Immediately after the<br />

swimm<strong>in</strong>g test, the participants expired directly <strong>in</strong>to a respiratory valve<br />

that was connected to the metabolic card. Dur<strong>in</strong>g each test, heart rate<br />

was recorded every 5 seconds. The rate of perceived exertion which is<br />

considered as a fatigue <strong>in</strong>dex was measured at the end of the test by the<br />

Borg scale. Blood samples for lactate concentration measurement were<br />

taken at 3, 5 <strong>and</strong> 7 m<strong>in</strong>utes of recovery. Moreover, the performance time<br />

was recorded for each 50m swim <strong>and</strong> for the total distance by a h<strong>and</strong><br />

chronometer.<br />

All results are expressed as mean values (±SD). One way ANOVA<br />

for dependent samples was used to def<strong>in</strong>e the overall differences <strong>in</strong> each<br />

variable. Furthermore, one way ANOVA for dependent samples with<br />

repeated measurements was used to def<strong>in</strong>e differences <strong>in</strong> each variable<br />

between 50m swims. A Tukey test was employed to assign specific differences<br />

<strong>in</strong> the analysis of variance. Statistical significance was set at<br />

P


Table 1. Physiological <strong>and</strong> performance variables <strong>in</strong> 200m <strong>and</strong> 4x50m of<br />

free style swimm<strong>in</strong>g with 5, 10 <strong>and</strong> 20s rest <strong>in</strong>tervals for all participants<br />

(n=13).<br />

Performance (s)<br />

H.R (beat·m<strong>in</strong> -1 )<br />

Lactate (Mmol·l -1 )<br />

Strokes number (rep.)<br />

Mean speed (m·s -1 )<br />

VO 2 peak (ml . kg -1 ·m<strong>in</strong> -1 )<br />

l·m<strong>in</strong> -1<br />

% VO 2 peak at VO 2 max<br />

RPE<br />

200m 4x50 m p<br />

5 s 10 s 20 s<br />

149.33±9.27<br />

184.23±5.26<br />

7.58±2.51<br />

189.07±20.03<br />

1.33±0.08<br />

45.45±15.14<br />

2.81±0.85<br />

99.1±28.86<br />

17.69±0.85<br />

144.38±8.52<br />

190.61±9.47<br />

7.30±2.15<br />

194.92±22.95<br />

1.38±0.08<br />

39.76±14.05<br />

2.45±0.74<br />

86.6±42.40<br />

17.61±0.76<br />

141.60±8.47<br />

189.53±8.42<br />

7.38±1.82<br />

192.92±21.30<br />

1.41±0.09<br />

44.72±12.43<br />

2.79±0.82<br />

98.6±45.56<br />

17.38±0.96<br />

137.12±7.78*<br />

195.38±11.87*<br />

7.53±1.61<br />

190.53±21.14<br />

1.45±0.09 *<br />

44.47±13.03<br />

2.77±0.89<br />

97.9±32.29<br />

17.76±0.72<br />

0.004<br />

0.015<br />

n.s.<br />

n.s.<br />

0.004<br />

n.s.<br />

n.s.<br />

n.s.<br />

n.s.<br />

Values are means ± SD. VO 2 : oxygen uptake, HR: heart rate, RPE: rate<br />

of perceived exertion, VO 2 peak: peak oxygen consumption at 50m. (*)<br />

significant difference between 200m <strong>and</strong> 4x50m with 20 s rest<strong>in</strong>g <strong>in</strong>terval,<br />

p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Accord<strong>in</strong>g to our results, the rest<strong>in</strong>g <strong>in</strong>terval between swims, <strong>in</strong> the<br />

4x50m ‘’broken’’ swim, should be great enough to partly replenish energy<br />

sources. Additionally, <strong>in</strong> ‘’broken’’ swimm<strong>in</strong>g the high speed ma<strong>in</strong>tenance<br />

capacity is improved when the swimm<strong>in</strong>g speed between swims<br />

is high <strong>and</strong> rema<strong>in</strong>s constant throughout sets with similar physiological<br />

responses as those <strong>in</strong> cont<strong>in</strong>uous swimm<strong>in</strong>g. However, the rest<strong>in</strong>g<br />

<strong>in</strong>terval needed for improv<strong>in</strong>g the high speed ma<strong>in</strong>tenance capacity<br />

may depend on athlete’s fitness level. In this study, the 20 s rest<strong>in</strong>g time<br />

between swims was adequate while the shorter rest<strong>in</strong>g <strong>in</strong>tervals were<br />

not enough to ma<strong>in</strong>ta<strong>in</strong> the <strong>in</strong>tensity <strong>and</strong> the swimm<strong>in</strong>g speed <strong>in</strong> levels<br />

higher than that of cont<strong>in</strong>uous swimm<strong>in</strong>g. Consequently, if the <strong>in</strong>terval<br />

time between swims is very short, the concrete tra<strong>in</strong><strong>in</strong>g target of ‘’broken’’<br />

swim can not be accomplished. However, shorter rest<strong>in</strong>g <strong>in</strong>tervals<br />

could be used to overload the swimmers with relatively higher <strong>in</strong>tensity<br />

than straight 200m.<br />

The results verified the hypotheses while <strong>in</strong> some circumstances<br />

were differentiated depend<strong>in</strong>g on the rest <strong>in</strong>terval. Regardless of the rest<br />

<strong>in</strong>terval between swims <strong>in</strong> ‘’broken’’ swimm<strong>in</strong>g, the maximum lactate<br />

concentration <strong>and</strong> O 2 deficit were similar at the end of each condition.<br />

The heart rate <strong>in</strong> the condition of 20 s rest <strong>in</strong>terval was higher than <strong>in</strong><br />

conditions of shorter rest <strong>in</strong>terval due to the greater exercise <strong>in</strong>tensity.<br />

On the contrary, no differences were observed for heart rate, when the<br />

rest<strong>in</strong>g <strong>in</strong>terval was short (10 <strong>and</strong> 5 s.). Based on our results, performance<br />

improvement <strong>in</strong> ‘’broken’’ swimm<strong>in</strong>g needed the concrete <strong>in</strong>terval<br />

time of 20 s.<br />

The pr<strong>in</strong>ciple limitation of the present study is the sample size.<br />

12 male, young swimmers (14-17 years) participated. The conclusions<br />

drawn by the present study can not be generalized for elite swimmers,<br />

women <strong>and</strong> for different swimm<strong>in</strong>g style <strong>and</strong> distance, given the fact<br />

that 200m distance <strong>and</strong> free style swimm<strong>in</strong>g were employed.<br />

conclusIons<br />

The present study has <strong>in</strong>vestigated the physiological responses of ‘’broken’’<br />

swimm<strong>in</strong>g (4x50m) with different rest<strong>in</strong>g <strong>in</strong>terval compared with<br />

those of cont<strong>in</strong>uous method (200m) dur<strong>in</strong>g free-style swimm<strong>in</strong>g of<br />

maximum <strong>in</strong>tensity. Moreover, the present study exam<strong>in</strong>ed which specific<br />

rest<strong>in</strong>g <strong>in</strong>terval <strong>in</strong> ‘’broken’’ swimm<strong>in</strong>g, contributes to the development<br />

of higher swimm<strong>in</strong>g speed with similar physiological dem<strong>and</strong>s<br />

compared to those of cont<strong>in</strong>uous swimm<strong>in</strong>g. Our f<strong>in</strong>d<strong>in</strong>gs suggest that<br />

the physiological responses of the two methods are similar <strong>and</strong> ‘’broken’’<br />

swimm<strong>in</strong>g with short rest<strong>in</strong>g <strong>in</strong>terval does not give any benefit for<br />

swimm<strong>in</strong>g speed improvement. Different benefits could be ga<strong>in</strong>ed from<br />

shorter rest<strong>in</strong>g <strong>in</strong>tervals. However, it was found that swimmers <strong>in</strong> ‘’broken’’<br />

swimm<strong>in</strong>g derived a significant benefit from swimm<strong>in</strong>g with 20<br />

s rest<strong>in</strong>g <strong>in</strong>terval between swims. Particularly, it seems that swimm<strong>in</strong>g<br />

performance <strong>in</strong> ‘’broken’’ swimm<strong>in</strong>g needs 20 s rest<strong>in</strong>g <strong>in</strong>terval between<br />

swims to be developed.<br />

reFerences<br />

Billat, V. & Koralszte<strong>in</strong>, J.P. (1996). Significance of the velocity at VO-<br />

2max <strong>and</strong> time to exhaustion at this velocity. Sports Med. 22 (2), 90-<br />

108.<br />

Borg, A.G. (1982). Pshychophysical bases of perceived exertion. Med Sci<br />

Sports Exerc. 14 (5), 377-381.<br />

Chen, M.J., Fan X. & Moe S. T. (2002). Criterion-related validity of<br />

the Borg rat<strong>in</strong>gs of perceived exertion scale <strong>in</strong> healthy <strong>in</strong>dividuals: a<br />

meta-analysis. J Sports Sci. 20, 873-899.<br />

Di Prampero, P.E., Davies, C.T.M., Cerretelli, P. & Margaria, R. (1970).<br />

An analysis of O2 debt contracted <strong>in</strong> submaximal exercise. J Appl<br />

Physiol. 29 (5), 547-551.<br />

Fern<strong>and</strong>es, R.J., Cardoso, C.S., Soares, S.M., Ascensão, A., Colaço, P.J.<br />

& Vilas-Boas J.P. (2003). Time limit <strong>and</strong> VO2 slow component at<br />

<strong>in</strong>tensities correspond<strong>in</strong>g to VO2max <strong>in</strong> swimmers. Int J Sports Med.<br />

24, 576-581.<br />

244<br />

Leger, L.A., Seliger, V. & Brassard, L. (1980). Backward extrapolation<br />

of VO2max values from the O2 recovery curve. Med Sci Sports Exerc.<br />

12 (1), 24-27.<br />

Maglischo, E.W. (1993). Swimm<strong>in</strong>g Even Faster, Mayfield Pub. Co.,<br />

Chapter 13. pp. 417-450.<br />

Montpetit, R.R., Leger, L.A., Lavoie, J.M. & Cazorla, G. (1981). VO2<br />

peak dur<strong>in</strong>g free swimm<strong>in</strong>g us<strong>in</strong>g the backward extrapolation of the<br />

O2 recovery curve. Eur J Appl. Physiol & Occup Physiol. 47, 385-391.<br />

Niewiadomski, W., Gasiorowska, A., Krauss, B., Mroz, A. & Cybulski,<br />

G. (2007). Suppression of heart rate variability after supramaximal<br />

exertion. Cl<strong>in</strong> Physiol Funct Imag<strong>in</strong>g. 27, 309-319.


General Indexes of Crawl Swimm<strong>in</strong>g Velocity of<br />

Junior Water Polo Players <strong>in</strong> a Match<br />

Bratusa, F.Z. 1 , Perisic, s.M. 2 , dopsaj, J.M. 1<br />

1Faculty of Sport <strong>and</strong> Physical Education, University of Belgrade, Belgrade,<br />

Serbia<br />

2UFK Sports Recreational Center Tasmajdan, Belgrade, Serbia<br />

The aim of this research is to def<strong>in</strong>e crawl swimm<strong>in</strong>g velocity realized<br />

by junior water polo players dur<strong>in</strong>g a match. Over a four year period,<br />

35 water polo players have been observed at the age of 16 years. It was<br />

established that there is no statistically significant difference of crawl<br />

technique swimm<strong>in</strong>g velocity between the quarters of a match (F=1.903,<br />

p =0.127). It was also determ<strong>in</strong>ed that there are no differences of swimm<strong>in</strong>g<br />

velocity distribution with regard to quarters (F=5.269, p = 0.153).<br />

The given fact can be a consequence of adaptation to the applied tra<strong>in</strong><strong>in</strong>g<br />

load of dom<strong>in</strong>antly aerobic type, but also to the tactical choices dur<strong>in</strong>g<br />

play. The obta<strong>in</strong>ed results should not be generalized <strong>and</strong> it does not<br />

mean that the same results would be obta<strong>in</strong>ed if this category were to be<br />

observed on the <strong>in</strong>ternational level.<br />

Key words: water polo, crawl technique, swimm<strong>in</strong>g velocity<br />

IntroductIon<br />

Water polo is among those sports with predom<strong>in</strong>antly non stereotypical<br />

movements <strong>and</strong> situations, with a constant change of dynamic <strong>and</strong><br />

motor behaviour. Water polo has swimm<strong>in</strong>g efforts that are predom<strong>in</strong>ant<br />

<strong>in</strong> the course of a match (swimm<strong>in</strong>g volume, <strong>in</strong>tensity, comb<strong>in</strong>ation<br />

of different swimm<strong>in</strong>g techniques <strong>and</strong> different swimm<strong>in</strong>g distances),<br />

conditions that require elite water polo players to have developed well<br />

all three energy systems, aerobic, alactate <strong>and</strong> lactate (P<strong>in</strong>n<strong>in</strong>gton et al.,<br />

1988; Dopsaj <strong>and</strong> Matković, 1994; Smith, H. 1999).<br />

A water polo game is not represented only by basic movements<br />

(swimm<strong>in</strong>g) but also by a great number of specific movements <strong>in</strong> the<br />

water performed <strong>in</strong> a horizontal <strong>and</strong> a vertical position. In these positions,<br />

a great number of elements of technique with the ball are performed<br />

(pass<strong>in</strong>g, receiv<strong>in</strong>g, shoot<strong>in</strong>g on goal), without the ball (pass over, jumps<br />

out, blocks), contacts with the opponent player (duels), without contact<br />

with opponent player (basic position), (Bratusa at al 2003). All of this <strong>in</strong>dicates<br />

the complexity of water polo as well as of the tra<strong>in</strong><strong>in</strong>g process itself,<br />

regard<strong>in</strong>g better technical <strong>and</strong> tactical preparation of water polo players.<br />

In the course of a match a water polo player spends around 37% of<br />

overall play<strong>in</strong>g time <strong>in</strong> the horizontal position, <strong>and</strong> for around 90% of<br />

the swims the crawl technique is used (Dopsaj <strong>and</strong> Matković, 1994).<br />

This <strong>in</strong>dicates that the horizontal position is a less represented activity<br />

dur<strong>in</strong>g a match compared to others. The horizontal position, i.e. movement<br />

parallel with the water surface, <strong>in</strong>cludes swimm<strong>in</strong>g by us<strong>in</strong>g crawl,<br />

backstroke <strong>and</strong> breaststroke <strong>and</strong> comb<strong>in</strong>ations of these techniques.<br />

The aim of this study is to def<strong>in</strong>e the swimm<strong>in</strong>g velocity of players <strong>in</strong> a<br />

horizontal position, i.e. crawl technique swimm<strong>in</strong>g velocity, realized by<br />

junior water polo players dur<strong>in</strong>g a match, as it is the most represented<br />

technique.<br />

Method<br />

The motor activity of each selected player was monitored at matches<br />

played <strong>in</strong> the state championship or cup. Only one player was monitored<br />

dur<strong>in</strong>g each match.<br />

By video analysis, all swimm<strong>in</strong>g movement phases were registered<br />

dur<strong>in</strong>g a water polo match. By chronometry, the duration of each swim<br />

per effort was recorded. The length of the covered distances were determ<strong>in</strong>ed<br />

by the analysis of video record<strong>in</strong>gs <strong>and</strong> use of markers placed<br />

along the outl<strong>in</strong>e of the play<strong>in</strong>g area at 2 nd , 4 th , 7 th , 10 th , 15 th , 20 th , 23 rd<br />

<strong>and</strong> 28 th meter.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

The sample consisted of 35 junior water polo players. The players<br />

were monitored at the f<strong>in</strong>al competitions of championship <strong>and</strong> cup<br />

of Serbia <strong>and</strong> Montenegro from March 2004 to April 2008. The test<br />

encompassed four generations of the junior category (the age of 16).<br />

The players were members of the follow<strong>in</strong>g clubs: Water polo clubs: VK<br />

“Partizan”: N=9, VK “Crvena Zvezda”: N=6, VK “Beograd”: N=7, VK<br />

“Primorac”: N=3, VK “Vojvod<strong>in</strong>a”: N=3, VK “Zemun”: N=2, VK “Nis”:<br />

N=2, VK “Becej”: N=1, VK “Jadran”: N=1. <strong>and</strong> VK “Student” N=1. The<br />

criteria for selection were that they were regularly players of the first<br />

formation of their teams, playmakers, successful water polo players,<br />

<strong>and</strong> played the most m<strong>in</strong>utes per match. The majority of the players<br />

monitored are now members of youth national teams. The variables <strong>in</strong><br />

this research covered the structure of the crawl technique. The follow<strong>in</strong>g<br />

variables were observed: 1) Average swimm<strong>in</strong>g velocity dur<strong>in</strong>g the<br />

match (V M-crawl – average crawl technique swimm<strong>in</strong>g velocity realized<br />

by a player dur<strong>in</strong>g the match expressed <strong>in</strong> m·s -1 ) . 2) Average swimm<strong>in</strong>g<br />

velocity per quarter (V Q-crawl) - average crawl technique swimm<strong>in</strong>g<br />

velocity realized by a player dur<strong>in</strong>g the each quarter expressed <strong>in</strong> m·s -1 ).<br />

3) Distribution of swimm<strong>in</strong>g velocity dur<strong>in</strong>g the match (DV M-crawl ) –<br />

the swims realized by a player at low, moderate, medium, near maximal<br />

or maximal velocity dur<strong>in</strong>g the match, expressed <strong>in</strong> percentages. 4)<br />

Distribution of swims per quarter accord<strong>in</strong>g to the swimm<strong>in</strong>g velocity<br />

(DV Q-crawl ) – covered sections realized by a player at low, moderate, medium,<br />

near maximal or maximal velocity dur<strong>in</strong>g the each quarter, expressed<br />

<strong>in</strong> percentages.<br />

The results were elaborated by descriptive statistical analysis <strong>and</strong><br />

ANOVA <strong>in</strong> order to establish differences of the observed variables between<br />

the quarters (Hair et al. 1995).<br />

Table 1. Descriptive statistics<br />

N Mean SD cV<br />

Quarters m·s- 1 m·s- 1 (%)<br />

95% Confidence<br />

Interval for Mean<br />

Lower<br />

Bound<br />

Upper<br />

Bound<br />

M<strong>in</strong> Max<br />

m·s- 1 m·s- 1<br />

1.00 500 1.385 .358 25.86 1.354 1.416 .667 3.226<br />

2.00 398 1.343 .363 27.00 1.307 1.379 .605 3.008<br />

3.00 425 1.353 .357 26.42 1.319 1.387 .595 2.979<br />

4.00 359 1.331 .328 24.67 1.297 1.365 .660 2.727<br />

Total 1682 1.356 .353 26.06 1.339 1.372 .595 3.226<br />

results<br />

Table 1 displays the values of basic descriptive statistics of average<br />

swimm<strong>in</strong>g velocity dur<strong>in</strong>g the match <strong>and</strong> per quarter. The average<br />

swimm<strong>in</strong>g velocity realized by the observed water polo players dur<strong>in</strong>g<br />

the match was 1.356±0.353 m·s -1 , <strong>and</strong> per quarter – <strong>in</strong> the first quarter<br />

1.385±0.350 m·s -1 , <strong>in</strong> the second quarter 1.343±0.362 m·s -1 ; <strong>in</strong> the third<br />

quarter 1.353±0.357 m·s -1 <strong>and</strong> <strong>in</strong> the fourth quarter 1.331±0.328 m·s -1<br />

(Figure 1)<br />

Figure 1 .Average swimm<strong>in</strong>g velocities per quarter by <strong>in</strong>tensity category<br />

245


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 2. Reliability <strong>in</strong>terval<br />

246<br />

<strong>in</strong>tensity Interval velocity<br />

maximal 1.886 <strong>and</strong> faster<br />

near maximal 1.533 1.885<br />

medium 1.179 1.532<br />

moderate 0.826 1.178<br />

low 0.825 <strong>and</strong> slower<br />

With regard to the structure of swimm<strong>in</strong>g velocity <strong>in</strong> the match, the<br />

results <strong>in</strong>dicated that the players observed realized maximal velocity for<br />

2.3% of the swims (at >1.886m/s -1 ) (Figure 2), at near maximal velocity<br />

30.6% of the swims (at >1.533m/s -1 1.179 1.179


Bench Press <strong>and</strong> Leg Press Strength <strong>and</strong> its<br />

Relationship with In-Water Force <strong>and</strong> Swimm<strong>in</strong>g<br />

Performance when Measured <strong>in</strong>-season <strong>in</strong> Male <strong>and</strong><br />

Female Age-group Swimmers<br />

carl, d.l., leslie, n., dickerson, t., Griff<strong>in</strong>, B., Markste<strong>in</strong>er, A.<br />

University of C<strong>in</strong>c<strong>in</strong>nati, C<strong>in</strong>c<strong>in</strong>nati Ohio, USA<br />

The purpose of this study was to determ<strong>in</strong>e if two st<strong>and</strong>ard measurements<br />

of dry l<strong>and</strong> strength would correlate with the ability to generate<br />

<strong>in</strong>-water force. Participants were 25 male <strong>and</strong> female age-group swimmers.<br />

One repetition max lifts were established for the Bench Press (BP)<br />

<strong>and</strong> Leg Press (LP) <strong>and</strong> correlated with <strong>in</strong>-water force generation as<br />

measured dur<strong>in</strong>g tethered swimm<strong>in</strong>g (TeS). They were also correlated<br />

with swimm<strong>in</strong>g performance us<strong>in</strong>g a timed 22.9-m (25y) swim. A significant<br />

correlation existed between BP strength <strong>and</strong> both TeS <strong>and</strong> 25y<br />

tests (r = 0.82 <strong>and</strong> 0.84 respectively, p< 0.01) A m<strong>in</strong>or correlation existed<br />

between LP <strong>and</strong> 25y (R = 0.70, p< 0.01). No significant correlation existed<br />

between LP <strong>and</strong> TeS (r= 0.50, p< 0.01). In addition, males demonstrated<br />

stronger correlations than females <strong>in</strong> all cases. In conclusion,<br />

BP strength may be an appropriate alternative to established methods as<br />

an <strong>in</strong>dicator of <strong>in</strong>-water force generation <strong>and</strong> swimm<strong>in</strong>g performance <strong>in</strong><br />

older age-group swimmers.<br />

Key words: swimm<strong>in</strong>g, tethered swimm<strong>in</strong>g, Bench Press, leg Press<br />

IntroductIon<br />

In recent years, USA-Swimm<strong>in</strong>g launched a series of educational programs<br />

<strong>and</strong> databases designed to quickly <strong>and</strong> efficiently dissem<strong>in</strong>ate<br />

<strong>in</strong>formation to their entire coach<strong>in</strong>g membership. One such program<br />

is the L<strong>and</strong> / Water Strength Test (LWST; Sokolovas, 2007 <strong>and</strong> USA-<br />

Swimm<strong>in</strong>g, 2007) database. The purpose of the LWST is to assess<br />

swimm<strong>in</strong>g-specific strength on l<strong>and</strong> <strong>and</strong> to determ<strong>in</strong>e how effectively<br />

it transfers <strong>in</strong>to the generation of force while <strong>in</strong> the water. Depend<strong>in</strong>g<br />

upon the relationship observed, a coach could make personalized adjustments<br />

<strong>in</strong> the swimmers strength tra<strong>in</strong><strong>in</strong>g program <strong>and</strong> or their stroke efficiency.<br />

If the relationship is high between l<strong>and</strong> <strong>and</strong> water strength then<br />

it might be suggested that the coach design a resistance tra<strong>in</strong><strong>in</strong>g program<br />

to enhance overall strength <strong>in</strong> an effort to improve performance.<br />

Conversely, if the relationship is low it would be desirable for the coach<br />

<strong>and</strong> athlete to focus on correct<strong>in</strong>g stroke efficiency, more so, than the<br />

overall strength of the swimmer.<br />

To assess dry l<strong>and</strong> strength, USA-Swimm<strong>in</strong>g recorded maximum<br />

effort strength dur<strong>in</strong>g isometric contractions on a Vasa Tra<strong>in</strong>er swim<br />

bench. To our knowledge, additional test<strong>in</strong>g measures have not been<br />

conducted to determ<strong>in</strong>e whether other forms of l<strong>and</strong> strength are equally<br />

beneficial <strong>in</strong> establish<strong>in</strong>g discrepancies between l<strong>and</strong> <strong>and</strong> <strong>in</strong>-water<br />

strength measurements. Therefore, it was the purpose of this study to<br />

determ<strong>in</strong>e if two st<strong>and</strong>ard measurements of dry l<strong>and</strong> strength, bench<br />

press (BP) <strong>and</strong> leg press (LP), would correlate with the ability to generate<br />

force <strong>in</strong> water, as measured dur<strong>in</strong>g tethered swimm<strong>in</strong>g, <strong>and</strong> whether<br />

they would correlate with spr<strong>in</strong>t swimm<strong>in</strong>g performance as measured by<br />

a timed 22.9m swim.<br />

Methods<br />

Twenty five (10 male, 15 females) highly competitive age-group swimmers<br />

rang<strong>in</strong>g from National qualifiers to High School competitors volunteered<br />

to participate <strong>in</strong> the study. Their mean (+ SD) age, weight <strong>and</strong><br />

height were 16.6 + 1.3 years, 71.6 + 17.3 kg, <strong>and</strong> 181.6 + 3.8 cm for males<br />

<strong>and</strong> 16.3 + 0.9 years, 62.0 + 2.9 kg, <strong>and</strong> 168.2 + 4.6 cm for females respectively.<br />

Each participant <strong>in</strong> the study tra<strong>in</strong>ed on a year-round basis. The<br />

study was approved by the <strong>in</strong>stitutional review board at the University of<br />

C<strong>in</strong>c<strong>in</strong>nati with all subjects complet<strong>in</strong>g an <strong>in</strong>formed consent document.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

Each subject completed a s<strong>in</strong>gle day test<strong>in</strong>g session that consisted<br />

of a r<strong>and</strong>omized distribution of the follow<strong>in</strong>g activities:<br />

Swim Tra<strong>in</strong><strong>in</strong>g: Prior to the <strong>in</strong>-water test<strong>in</strong>g, each subject completed<br />

a st<strong>and</strong>ardized 1371-m warm-up. Completion of the 2 <strong>in</strong>-water tests<br />

was completed <strong>in</strong> r<strong>and</strong>omized order. 22.9-m Swim Test: Each subject<br />

completed two 22.9-m maximal effort swims from the start<strong>in</strong>g block.<br />

Each swim was separated by a m<strong>in</strong>imum of 5 m<strong>in</strong>utes. Active recovery<br />

swimm<strong>in</strong>g was allowed at the discretion of each subject. Times were<br />

recorded to the 100 th of a second <strong>and</strong> the two trials were averaged for<br />

best time <strong>and</strong> recorded. Tethered maximal effort swim: Each subject completed<br />

two <strong>in</strong>-water tethered maximal force generation swims (Digital<br />

Force Gauge, IMADA, Inc). Each subject was <strong>in</strong>structed to go all out<br />

from a push for 10 seconds. Maximal force generated was recorded <strong>in</strong><br />

Newton’s <strong>and</strong> the two trials averaged for best effort <strong>and</strong> recorded. Each<br />

trial was separated by a m<strong>in</strong>imum of 1 m<strong>in</strong>ute rest.<br />

Resistance Tra<strong>in</strong><strong>in</strong>g: Prior to the l<strong>and</strong> test<strong>in</strong>g each subject participated<br />

<strong>in</strong> some light lift<strong>in</strong>g for the benefit of warm<strong>in</strong>g up. Completion of the<br />

two l<strong>and</strong> strength tests was completed <strong>in</strong> r<strong>and</strong>omized order. Bench Press:<br />

Subjects completed a st<strong>and</strong>ard barbell chest press to determ<strong>in</strong>e a one<br />

repetition maximum (1RM). The follow<strong>in</strong>g protocol was established.<br />

Each subject began with a warm up set consist<strong>in</strong>g of light weight for<br />

10-15 repetitions. Subjects then completed a set of moderate weight for<br />

10 repetitions followed by a m<strong>in</strong>imum of 2 m<strong>in</strong>utes rest. The weight was<br />

<strong>in</strong>creased by 10-20 % <strong>and</strong> another set of 10 repetitions was completed.<br />

This procedure was cont<strong>in</strong>ued until the subject was unable to complete<br />

ten full repetitions. 1RM BP was estimated us<strong>in</strong>g the follow<strong>in</strong>g equation<br />

(Brzycki 1993): Lift<strong>in</strong>g weight (<strong>in</strong> pounds) / (1.0278-(.0278 x no.<br />

of reps)). Leg Press: To establish a 1RM LP, subjects completed a bilateral<br />

seated leg press follow<strong>in</strong>g the same established protocol (Brzycki<br />

1993) that was used for the 1RM BP.<br />

Descriptive statistics (mean <strong>and</strong> SD) were calculated for subjects<br />

characteristics (age, height, <strong>and</strong> weight). Pearson’s product moment correlation<br />

coefficient (r) was used to explore the relationships among different<br />

variables. The level of significance was set at p ≤ 0.01.<br />

results<br />

Table 1 summarizes the correlation coefficients for each of the variables<br />

measured. A significant correlation was found to exist between BP<br />

strength <strong>and</strong> both the TeS <strong>and</strong> the 22.9m swim respectively (r = 0.82 &<br />

0.84). The relationship between BP <strong>and</strong> TeS <strong>and</strong> between BP <strong>and</strong> 22.9m<br />

swim time is shown <strong>in</strong> figures 1 <strong>and</strong> 2 respectively.<br />

The correlation between LP <strong>and</strong> the 22.9-m swim time was not as<br />

strong as the BP (r = 0.70). In addition, no significant correlation existed<br />

between LP <strong>and</strong> TeS force generated. However, further analyses revealed<br />

that when the males were separated from the females, significant<br />

correlations were found between all variables measured <strong>in</strong> both test<strong>in</strong>g<br />

sessions <strong>in</strong>clud<strong>in</strong>g LP vs TeS (Table 1).<br />

Table 1. Mid season r-values for correlation between l<strong>and</strong> strength <strong>and</strong><br />

<strong>in</strong>-water force generation measurements. P < 0.01; BP bench press, LP<br />

leg press, 25 22.9-m swim, TeS tethered swim. Bold <strong>in</strong>dicates significant<br />

correlation.<br />

Correlation Comb<strong>in</strong>ed Males Females<br />

LP vs 25 0.702409 0.752053 0.232553<br />

LPrel vs 25 0.279929<br />

LP vs TeS 0.504378 0.708448 0.282953<br />

LPrel vs TeS 0.0782<br />

BP vs TeS 0.819576 0.732068 0.560393<br />

BPrel vs TeS 0.694141<br />

BP vs 25 0.841623 0.871575 0.387719<br />

BPrel vs 25 0.813758<br />

247


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

dIscussIon<br />

The relationship between various power measurements <strong>and</strong> swimm<strong>in</strong>g<br />

performance has been well established (Sharp et al., 1982; Hawley et<br />

al., 1992 & Swa<strong>in</strong>e (1994). Often measured us<strong>in</strong>g a modification of the<br />

W<strong>in</strong>gate Anaerobic test, what has not been established to our knowledge<br />

is the relationship between swimm<strong>in</strong>g performance <strong>and</strong> more<br />

practical forms of general strength. Follow<strong>in</strong>g the protocols established<br />

by USA-Swimm<strong>in</strong>g’s L<strong>and</strong> / Water Strength Test<strong>in</strong>g, a common measurement<br />

of strength, the 1RM BP, can be used with success when address<strong>in</strong>g<br />

imbalances between l<strong>and</strong> strength <strong>and</strong> swimm<strong>in</strong>g performance.<br />

With the relative ease associated with the measurement of a 1RM BP,<br />

this protocol may be more readily useable for a majority of swimm<strong>in</strong>g<br />

programs.<br />

Although the correlation data for the 1RM leg press was not as strong as<br />

the bench press it too may be useful <strong>in</strong> develop<strong>in</strong>g an overall <strong>in</strong>dividualized<br />

picture of a swimmer. The comb<strong>in</strong>ation of the two measurements<br />

would allow a coach to look at both upper <strong>and</strong> lower body strength<br />

separately <strong>and</strong> <strong>in</strong> comb<strong>in</strong>ation as they translate to swimm<strong>in</strong>g performance.<br />

Although not a part of this study, the USA-Swimm<strong>in</strong>g protocol<br />

<strong>in</strong>cludes a kick<strong>in</strong>g component <strong>and</strong> therefore the measurement of LP<br />

strength warrants further <strong>in</strong>vestigation <strong>in</strong>to its potential effectiveness.<br />

Interest<strong>in</strong>gly, when separat<strong>in</strong>g the females from the males <strong>in</strong> this study,<br />

weaker correlations were observed for all measurements taken. It is believed<br />

that this discrepancy may have been the result of the males hav<strong>in</strong>g<br />

a greater amount of muscle mass than their female counterparts (Carter<br />

& Ackl<strong>and</strong> 1994). In addition, there may have been more familiarity<br />

with strength tra<strong>in</strong><strong>in</strong>g for the males than the females <strong>and</strong> this may have<br />

had an effect on the measurements of each subject’s 1RM’s. Also, this<br />

could have been due to greater homogeneity with<strong>in</strong> each group. Participant<br />

group heterogeneity/homogeneity can affect the correlations like<br />

these.<br />

In addition, the data revealed similarity between the mid season<br />

<strong>and</strong> the post season test<strong>in</strong>g sessions for all measurements taken. It is our<br />

belief that this lends support to the usefulness of this type of strength<br />

test<strong>in</strong>g. This may <strong>in</strong>dicate that regardless of the stress levels associated<br />

with tra<strong>in</strong><strong>in</strong>g, the relationship between l<strong>and</strong> strength <strong>and</strong> <strong>in</strong>-water force<br />

generation is strong <strong>and</strong> is relevant throughout the entire swimm<strong>in</strong>g<br />

season <strong>in</strong>clud<strong>in</strong>g through the taper period.<br />

Figure 1. The relationship between BP <strong>and</strong> timed 22.9m swim comb<strong>in</strong>ed<br />

for males <strong>and</strong> females. (r = 0.84, p ≤ 0.01)<br />

248<br />

Tethered Swim (kg.)<br />

60<br />

55<br />

50<br />

45<br />

40<br />

35<br />

30<br />

25<br />

y = 0.3144x + 21.374<br />

20<br />

30 40 50 60 70 80 90 100<br />

Bench Press (kg)<br />

Figure 2. The relationship between BP <strong>and</strong> TeS for comb<strong>in</strong>ed males <strong>and</strong><br />

females. (r = 0.82, p ≤ 0.01)<br />

Limitations to this study <strong>in</strong>clude the relatively small number of subjects<br />

<strong>in</strong>volved. This potential issue was heightened when the males <strong>and</strong><br />

females were separated <strong>and</strong> the subject numbers were even smaller. The<br />

second limitation to our study is the methods used for the determ<strong>in</strong>ation<br />

of the 1RM’s. Although a widely accepted approach to the measurement<br />

of 1RM, the protocol is still susceptible to error <strong>in</strong> prediction.<br />

conclusIon<br />

In conclusion, bench press strength may be an appropriate alternative to<br />

the established USA-swimm<strong>in</strong>g methods, for measur<strong>in</strong>g strength as an<br />

<strong>in</strong>dicator of discrepancy between swimm<strong>in</strong>g-related strength <strong>and</strong> either<br />

<strong>in</strong>-water force generation or spr<strong>in</strong>t swimm<strong>in</strong>g performance.<br />

reFerences<br />

Brzycki, M. (1993) Strength test<strong>in</strong>g: Predict<strong>in</strong>g a one-rep max from<br />

reps-to-fatigue. JOPERD 64, 88-90.<br />

Carter, J. E. & Ackl<strong>and</strong>, T.R. (1994). K<strong>in</strong>anthropometry <strong>in</strong> aquatic<br />

sports. A study of world class athletes. In: Carter JE, Ackl<strong>and</strong> TR,<br />

eds. Human K<strong>in</strong>etics Sport Science Monograph Series, vol. 5. Chanpa<strong>in</strong>g,<br />

IL, Human K<strong>in</strong>etics.<br />

Hawley, J.A., Williams, M.M., Vickovic, M.M. & H<strong>and</strong>cock, P.J.<br />

(1992). Muscle power predicts freestyle swimm<strong>in</strong>g performance. Br J<br />

Sports Med. Sep;26(3), 151-5.<br />

L<strong>and</strong> / Water Strength Test. USA Swimm<strong>in</strong>g Web site. http://www.<br />

usaswimm<strong>in</strong>g.org/ USASWeb/ViewMiscArticle.aspx?TabId=977<br />

&Alias=Ra<strong>in</strong>bow&Lang=en&mid=2811&ItemId=2445. Accessed<br />

January 11, 2010.<br />

Sharp, R.L., Troup, J.P. & Costill, D.L. (1982). Relationship between<br />

power <strong>and</strong> spr<strong>in</strong>t freestyle swimm<strong>in</strong>g. Med Sci Sports Exerc, 14(1),<br />

53-6.<br />

Sokolovas, G. (2007). Personal communication.<br />

Swa<strong>in</strong>e, I.L. (1994). The relationship between physiological variables<br />

from a swim bench ramp test <strong>and</strong> middle-distance swimm<strong>in</strong>g performance.<br />

Journal of Swimm<strong>in</strong>g Res 10, 41-48


Effect of Start Time Feedback on Swimm<strong>in</strong>g Start<br />

Performance.<br />

de la Fuente, B. 1 <strong>and</strong> Arellano, r. 2<br />

1Sierra Nevada High Performance Altitude Tra<strong>in</strong><strong>in</strong>g Centre, Monachil,<br />

Spa<strong>in</strong>.<br />

2University of Granada, Granada, Spa<strong>in</strong>.<br />

The start is a significant component <strong>in</strong> competitive swimm<strong>in</strong>g performance,<br />

particularly <strong>in</strong> the short events. This relevance is confirmed when<br />

the differences <strong>in</strong> the start times are greater than the differences <strong>in</strong> the<br />

event’s f<strong>in</strong>al times. The purpose of this study was to determ<strong>in</strong>e how start<br />

time feedback dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g would improve a swimmer’s start performance.<br />

A group (n=42) of regional swimmers <strong>and</strong> P. E. Students (former<br />

competitive swimmers), participated <strong>in</strong> the study. The ma<strong>in</strong> group was<br />

equally divided related to 15m performance <strong>and</strong> gender <strong>in</strong>to experimental<br />

<strong>and</strong> control groups. After ten sessions of specific start tra<strong>in</strong><strong>in</strong>g, both<br />

groups improved their start<strong>in</strong>g times (average improvements: EG: 0.30<br />

s vs CG 0.11 s). However, greater improvements were produced with<strong>in</strong><br />

the experimental group (15m: p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 1. Specifically designed structure to support the electronic<br />

ALGE touchpad (TPI), to be placed at any distance from the wall on<br />

either side of the 25 m or 50 m pool.<br />

results<br />

The change <strong>in</strong> start times did not display significant differences between<br />

groups. However, data showed that both groups reduced their start<strong>in</strong>g<br />

times, even the group that did not receive feedback after the effort (Average<br />

improvements: EG: 0.30 s vs CG 0.11 s). The fact that the CG<br />

group improved due to practice without feedback may expla<strong>in</strong> the lack<br />

of significant differences between the improvements <strong>in</strong> the EG <strong>and</strong> CG.<br />

However, the improvements were greater with<strong>in</strong> the EG (5.2%) than<br />

control (2.2%), where the swimmers received TKR after the practice. In<br />

order to check the significance of the improvement with<strong>in</strong> each group, a<br />

related samples t-Test was performed. Results showed significant differences<br />

<strong>in</strong> both groups, with a greater significance level <strong>in</strong> the EG, at the<br />

four distances analyzed (Table 2).<br />

At the previous video record<strong>in</strong>g, most swimmers emerged to the<br />

surface before 10 m. For that reason, the decision was made to focus<br />

the tra<strong>in</strong><strong>in</strong>g on 10 m rather than 15m, <strong>in</strong> order to avoid an erroneous<br />

start measurement related to the swim phase after surfac<strong>in</strong>g. Tak<strong>in</strong>g <strong>in</strong>to<br />

account the total number of repetitions, the performance improvement<br />

was greater at the more practiced distances (start followed by freestyle<br />

swimm<strong>in</strong>g up to 10m <strong>and</strong> start followed by underwater dolph<strong>in</strong> kick<strong>in</strong>g<br />

up to 10m) (Table 2).<br />

Table 2. Differences between pre-test <strong>and</strong> post-test <strong>in</strong> both groups (Experimental<br />

– EG <strong>and</strong> control group CG). Results from related samples<br />

t-Test.<br />

Pre-test Post-Test<br />

Mean (s) SD Mean (s) SD t-test<br />

15 m free<br />

EG<br />

1 8.02 0.78 7.87 0.79 **<br />

10 m DK2 10 m free<br />

5.68<br />

4.84<br />

0.75<br />

0.53<br />

5.38<br />

4.58<br />

0.73<br />

0.49<br />

***<br />

***<br />

10 m glide 3 7.18 1.11 7.04 1.09 **<br />

15 m free 8.17 0.81 8.07 0.81 *<br />

CG<br />

10 m DK1 10 m free<br />

5.84<br />

4.95<br />

0.81<br />

0.57<br />

5.73<br />

4.84<br />

0.81<br />

0.58<br />

**<br />

**<br />

10 m glide 7.41 1.11 7.31 1.10 *<br />

1. Free. Start followed by freestyle swim until 15m 2. DK: Underwater<br />

dolph<strong>in</strong> kick<strong>in</strong>g. 3. Start + Glid<strong>in</strong>g until h<strong>and</strong>s contact (TPI) at 10m.<br />

To represent the effectiveness of the experimental tra<strong>in</strong><strong>in</strong>g, the start improvement<br />

as a percentage between the times achieved before <strong>and</strong> after<br />

the tra<strong>in</strong><strong>in</strong>g sessions was calculated. As a result, the improvement percentage<br />

was 3% greater <strong>in</strong> the experimental group, with greater differences<br />

on the more practiced distances (Figure 2). This seems to <strong>in</strong>dicate<br />

250<br />

that giv<strong>in</strong>g accurate feedback related to the start duration produces more<br />

significant effects than just systematic repetition.<br />

Figure 2. Percentage improvement <strong>in</strong> start times before <strong>and</strong> after tra<strong>in</strong><strong>in</strong>g<br />

<strong>in</strong> the experimental <strong>and</strong> control groups.<br />

As a consequence of the statistical results, the data for <strong>in</strong>dividual swimmers<br />

were analysed. The start<strong>in</strong>g times as a function of the number of<br />

tra<strong>in</strong><strong>in</strong>g sessions for two subjects; the one with greatest improvement<br />

<strong>and</strong> the one with the least improvement for both groups were exam<strong>in</strong>ed<br />

(Figure 3). Compar<strong>in</strong>g times, (Figure 4) it was seen that performance<br />

tended to be more consistent with<strong>in</strong> the EG (lower differences between<br />

the best time <strong>and</strong> the average time among the sessions). Similar times<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g Page 25<br />

seem to <strong>in</strong>dicate a more constant <strong>and</strong> uniform performance at the end<br />

of the tra<strong>in</strong><strong>in</strong>g period.<br />

10m Free Swim (s)<br />

5,2<br />

5<br />

4,8<br />

4,6<br />

4,4<br />

4,2<br />

6,8<br />

6,6<br />

6,4<br />

6,2<br />

6<br />

Experimental Group (Subject 39)<br />

Best<br />

Average<br />

1 2 3 4 5 6 7 8 9 10<br />

S E S S I ON S<br />

Control Group (Subject 21)<br />

Best<br />

Avera<br />

5 8<br />

Figure 3. Individual performance evolution (10m Free) along the sessions.<br />

Dif. Before Dif. After<br />

Figure 0,4 3. Individual performance evolution (10m Free) along the ses-<br />

sions.<br />

Dif. between Best & Average (s)<br />

0,35<br />

0,3<br />

0,25<br />

0,2<br />

0,15<br />

0,1<br />

0,05<br />

0<br />

S21 S16 S09 S73 S39 S15 S75 S25<br />

Control Group Experimental Group


Figure 4. Examples from four subjects of each group. Differences between<br />

best time <strong>and</strong> average time trial before <strong>and</strong> after the practice.<br />

dIscussIon<br />

Results suggest that the systematic repetition of the start leads to improvement<br />

<strong>in</strong> performance <strong>and</strong> that provid<strong>in</strong>g feedback to the swimmer<br />

resulted <strong>in</strong> greater improvement. This should be taken <strong>in</strong>to account <strong>in</strong><br />

tra<strong>in</strong><strong>in</strong>g by <strong>in</strong>creas<strong>in</strong>g the practice of start<strong>in</strong>g with<strong>in</strong> the year’s plann<strong>in</strong>g.<br />

Different studies had shown that jump<strong>in</strong>g ability was not related<br />

to the total start performance (Fuente, et al., 2003) nor is n<strong>in</strong>e weeks of<br />

strength tra<strong>in</strong><strong>in</strong>g (Breed, et al., 2003). There seems to be no direct transfer<br />

of strength or jump<strong>in</strong>g skills to the swim starts. This f<strong>in</strong>d<strong>in</strong>g further<br />

supports the need to adapt the motor control mechanisms of the div<strong>in</strong>g<br />

techniques by practic<strong>in</strong>g them <strong>in</strong> parallel with resistance tra<strong>in</strong><strong>in</strong>g (Bobbert,<br />

et al., 1994). Furthermore it is recomended to <strong>in</strong>crease the total<br />

number of start repetitions dur<strong>in</strong>g the tra<strong>in</strong><strong>in</strong>g sessions.<br />

Importantly, giv<strong>in</strong>g the swimmers accurate knowledge of results<br />

produces greater performance improvements than merely systematic<br />

repetition. At the end of the movement, swimmer’s propioceptive <strong>in</strong>formation<br />

is contrasted with the external data <strong>in</strong>put (start time or distance)<br />

to improve <strong>and</strong> to optimize the motor schema. Information obta<strong>in</strong>ed as<br />

a result of the start times can then be compared to the expected objectives<br />

of the swimmer <strong>and</strong> to ref<strong>in</strong>e future skill development (Oña, et al.,<br />

1999). The <strong>in</strong>formation about the start duration offered by the system,<br />

by itself, seems to be useful for the swimmers, so that they can <strong>in</strong>ternally<br />

compare their execution with the result <strong>and</strong> for ref<strong>in</strong><strong>in</strong>g the future start<br />

skill. In addition, the system seems to be more effective for the <strong>in</strong>dividual,<br />

mak<strong>in</strong>g the start performance more consistent. This is important<br />

when consider<strong>in</strong>g the performance expected at important competitions.<br />

F<strong>in</strong>ally, as Mason suggests, the coach should ensure appropriate tra<strong>in</strong><strong>in</strong>g<br />

with similar conditions to competition (Mason, 1999).<br />

conclusIon<br />

The systematic <strong>and</strong> controlled repetition of the start technique produces<br />

an improvement <strong>in</strong> performance. This should be taken <strong>in</strong>to account by<br />

<strong>in</strong>creas<strong>in</strong>g the start practic<strong>in</strong>g time with<strong>in</strong> the whole year’s plann<strong>in</strong>g.<br />

Moreover, the system developed for giv<strong>in</strong>g accurate <strong>in</strong>formation about<br />

the start’s duration dur<strong>in</strong>g the practice seems to be more effective <strong>in</strong><br />

reduc<strong>in</strong>g the start<strong>in</strong>g times than the st<strong>and</strong>ard repetition.<br />

Accurate <strong>and</strong> precise knowledge of results at the end of the execution<br />

made the <strong>in</strong>dividual performance more consistent, reduc<strong>in</strong>g the differences<br />

between trials <strong>and</strong> tend<strong>in</strong>g to decrease the start<strong>in</strong>g times. These<br />

data suggest that <strong>in</strong>creas<strong>in</strong>g the start practice time with<strong>in</strong> the year’s<br />

plann<strong>in</strong>g would benefit the swimmer.<br />

reFerences<br />

Arellano, R. (1990). El entrenamiento técnico. In F. E. d. Natación<br />

(Ed.), Natación (1 ed., Vol. 2, pp. 35-62). Madrid, Spa<strong>in</strong>: Comité<br />

Olímpico Español.<br />

Bobbert, M. F., & Van Soest, A. J. (1994). Effects of muscle strengthen<strong>in</strong>g<br />

on vertical jump height: a simulation study. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science<br />

<strong>in</strong> Sports <strong>and</strong> Exercise, 26, 1012-1020.<br />

Breed, R. V. P., & Young, W. B. (2003). The effect of a resistance tra<strong>in</strong><strong>in</strong>g<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

programme on the grab, track <strong>and</strong> sw<strong>in</strong>g starts <strong>in</strong> swimm<strong>in</strong>g. Journal<br />

of Sport Sciences, 21, 213-220.<br />

Fuente, B. D. L., García, F., & Arellano, R. (2003). Are the Forces Applied<br />

Dur<strong>in</strong>g Vertical Countermovement Jump Related to the Forces<br />

Applied Dur<strong>in</strong>g the Swimm<strong>in</strong>g Start? In J.-C. Chatard (Ed.), <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX (Vol. 1, pp. 207-212). Sa<strong>in</strong>t-<br />

Etienne (France): Publications de l’Université Sant-Etienne.<br />

Halj<strong>and</strong>, R. (2002). European Swimm<strong>in</strong>g Championships Berl<strong>in</strong> 2002.<br />

Retrieved August 2002<br />

Knapp, B. (1963). Skill <strong>in</strong> sport: The atta<strong>in</strong>ment of proficiency. London:<br />

Routledge & Kegan Paul.<br />

Mason, B. (1999). Where are races won (<strong>and</strong> lost)? Paper presented at<br />

the SWIMMING: Applied Proceed<strong>in</strong>gs of the XVII International<br />

Symposium on <strong>Biomechanics</strong> <strong>in</strong> Sports., Perth: Western Australia.<br />

Miller, M. K., Allen, D., & Pe<strong>in</strong>, R. (2002, 21-23 June 2002). A k<strong>in</strong>etic<br />

<strong>and</strong> k<strong>in</strong>ematic comparison of the grab <strong>and</strong> track starts <strong>in</strong> swimm<strong>in</strong>g.<br />

Paper presented at the IXth World Symposium <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g, Sa<strong>in</strong>t -Etienne.<br />

Oña, A., Martínez, M., Moreno, F., & Ruiz, L. M. (1999). Control y<br />

Aprendizaje Motor. Madrid: Síntesis.<br />

Zatsiorsky, V. M., Bulgakova, N. Z., & Chapl<strong>in</strong>sky, N. M. (1979). Biomechanical<br />

Analysis of Start<strong>in</strong>g Techniques <strong>in</strong> Swimm<strong>in</strong>g. Paper<br />

presented at the Third International Symposium of <strong>Biomechanics</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g, Edmonton,Canada.<br />

251


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Predictors of Performance <strong>in</strong> Pre-Pubertal <strong>and</strong><br />

Pubertal Male <strong>and</strong> Female Swimmers<br />

douda, h.t. 1 , toubekis, A.G. 2 , Georgiou, ch. 1 , Gourgoulis, V. 1 ,<br />

<strong>and</strong> tokmakidis, s.P. 1<br />

1 Democritus University of Thrace, Komot<strong>in</strong>i, Greece<br />

2 Kapodistrian University of Athens, Athens, Greece<br />

The predictors of the 50 m front-crawl performance were exam<strong>in</strong>ed <strong>in</strong><br />

72 pre-pubertal <strong>and</strong> pubertal swimmers. They underwent a battery of<br />

anthropometric, body composition <strong>and</strong> muscle strength measurements.<br />

A Pr<strong>in</strong>cipal Component Analysis showed that the Component-1 [Anthropometric-Tethered<br />

Swimm<strong>in</strong>g Force (TSF)] expla<strong>in</strong>ed 65.1% of the<br />

total variance, Component-2 [Body Composition] 14.6% <strong>and</strong> Component-3<br />

[Body Dimension] 8.2% respectively. Also, Component 1 was significantly<br />

correlated with performance (r=-0.71, p


age tethered swimm<strong>in</strong>g force <strong>in</strong> the total sample (Figure 1a) for both<br />

pre-pubertal (Figure 1b) <strong>and</strong> pubertal athletes (Figure 1c). In addition,<br />

the majority of anthropometric variables were significantly related to<br />

performance <strong>in</strong> pubertal swimmers.<br />

From the PCA analysis, three components were extracted <strong>and</strong> were<br />

labelled <strong>in</strong> the follow<strong>in</strong>g order: Component-1: Anthropometric-Tethered<br />

Swimm<strong>in</strong>g Force (TSF), Component-2: Body Composition <strong>and</strong><br />

Component-3: Body Dimension. Variables were well def<strong>in</strong>ed <strong>and</strong> their<br />

communalities ranged between 0.70 <strong>and</strong> 0.98. In addition, based on the<br />

load<strong>in</strong>g of variables on the three components, the percentage of cumulative<br />

variance expla<strong>in</strong>ed the 88% of the performance score. A multiple<br />

regression procedure was used to determ<strong>in</strong>e which components were<br />

significant predictors of the maximal 50-m front-crawl swimm<strong>in</strong>g score<br />

(Table 2). Correlation coefficients between the above three factors <strong>and</strong><br />

the performance swimm<strong>in</strong>g score revealed that, <strong>in</strong> the total sample, the<br />

anthropometric <strong>and</strong> TSF were significantly correlated with performance<br />

(r=-0.71, p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

mance. Indeed, body structure appears to be useful <strong>in</strong> expla<strong>in</strong><strong>in</strong>g differences<br />

<strong>in</strong> swimm<strong>in</strong>g performance-score. For example, when swimmers<br />

of equal ability meet <strong>in</strong> competition, the one with the most favourable<br />

physical characteristics may w<strong>in</strong> the race. In addition, excess body mass is<br />

a disadvantage. In this respect, morphological characteristics are important<br />

elements because are they <strong>in</strong>fluence the quality of the performance<br />

(Jurimae et al., 2007). Therefore, simple anthropometric <strong>in</strong>dicators may be<br />

elaborated for biological supervision.(Bénéfice et al., 1990).<br />

conclusIon<br />

It is important to po<strong>in</strong>t out that these f<strong>in</strong>d<strong>in</strong>gs must be taken <strong>in</strong>to consideration<br />

especially by coaches <strong>and</strong> may have practical implications for both<br />

tra<strong>in</strong><strong>in</strong>g <strong>and</strong> talent identification <strong>in</strong> swimm<strong>in</strong>g. Moreover, the measurement<br />

of TSF should be a useful <strong>in</strong>dicator for monitor<strong>in</strong>g pre-pubertal<br />

<strong>and</strong> pubertal male <strong>and</strong> female swimmers performance <strong>and</strong> could be used<br />

to evaluate the tra<strong>in</strong><strong>in</strong>g process. TSF, arm-span <strong>and</strong> arm circumference<br />

appear to be the major determ<strong>in</strong>ants of the 50 m front-crawl performance<br />

<strong>in</strong> young swimmers.<br />

reFerences<br />

Bailey, D & Mirwald,R. (1988). The Effects of Tra<strong>in</strong><strong>in</strong>g on the Growth<br />

<strong>and</strong> Development of the Child. In: Mal<strong>in</strong>a R, (ed), Young Athletes: Biological,<br />

Phychological, <strong>and</strong> Educational Perspectives (pp 33-48). Champaign:<br />

Human K<strong>in</strong>etics.<br />

Bloomfield, J. J., Blanskby, B. A., Ackl<strong>and</strong>, T. R. & Elliot, B. C. (1986). The<br />

mechanical <strong>and</strong> physiological characteristics of preadolescent swimmers,<br />

tennis players <strong>and</strong> non-competitors. In: Day J.A.P (ed.), Perspectives<br />

<strong>in</strong> K<strong>in</strong>anthropometry (pp 165-170). Champaign: Human K<strong>in</strong>etics.<br />

Benefice, E., Mercier, J., Guer<strong>in</strong>, M. J. & Prefaut, C. (1990). Differences<br />

<strong>in</strong> Aerobic <strong>and</strong> Anthropometric Characteristics Between Peripubertal<br />

Swimmers <strong>and</strong> Non-Swimmers. Int J Sports Med, 11, 456-460.<br />

Caldarone, G., Leglise, M., Giampietro, M. G. & Berlutti, G. (1986). Anthropometric<br />

measurements, body composition, biological maturation<br />

<strong>and</strong> growth predictions <strong>in</strong> young female gymnasts of high agonistic<br />

level. J Sports Med, 26, 263-273.<br />

Douda, H., Laparidis, K. & Tokmakidis, S. P. (2002). Long-term tra<strong>in</strong><strong>in</strong>g<br />

<strong>in</strong>duces specific adaptations on physique of rhythmic sports <strong>and</strong> female<br />

artistic gymnasts. Eur J Sport Sci, 2, 1-14.<br />

Espaρa-Romero, V., Artero, E.G., Santaliestra-Pasias A.M., Gutierrez,<br />

A., Castillo, M. J. & Ruiz, J. R. (2008). H<strong>and</strong> Span Influences Optimal<br />

Grip Span <strong>in</strong> Boys <strong>and</strong> Girls Aged 6 to 12 Years. J H<strong>and</strong> Surg, 33A,<br />

378-384.<br />

Geladas, N. D., Nassis, G.P. & Pavlicevic, S. (2005). Somatic <strong>and</strong> physical<br />

traits affect<strong>in</strong>g spr<strong>in</strong>t swimm<strong>in</strong>g performance <strong>in</strong> young swimmers. Int<br />

J of Sports Med, 26, 139-144.<br />

Jürimäe, J., Haljaste, K., Cicchella, A., Lätt, E., Purge, P., Leppik, A. &<br />

Jürimäe, T. (2007). Analysis of swimm<strong>in</strong>g performance from physical,<br />

physiological, <strong>and</strong> biomechanical parameters <strong>in</strong> young swimmers. Pediatr<br />

Exerc Sci, 19, 70-81.<br />

Lohman, T. G., Roche, F. A. & Martorell, R. (1988). Anthropometric St<strong>and</strong>ardization<br />

Reference Manual, (pp 3-54). Champaign, IL: Human<br />

K<strong>in</strong>etics.<br />

Mal<strong>in</strong>a, R. (1986). Physical Activity & Well-be<strong>in</strong>g: Physical Growth <strong>and</strong><br />

Maturation. American Alliance for Health, Physical Education, Recreation,<br />

<strong>and</strong> Dance (AAHPERD) (pp. 3-38), Virg<strong>in</strong>ia.<br />

Pyne, D. B., Anderson, M. E. & Hopk<strong>in</strong>s, W. G. (2006). Monitor<strong>in</strong>g<br />

Changes <strong>in</strong> Lean Mass of Elite Male <strong>and</strong> Female Swimmers, Int J<br />

Sports Physiol Perf, 1, 14-26.<br />

Slaughter, M. H., Lohman, T. G., Boileau, R. A., Horswill, C. A., Stillman,<br />

R. J., Van Loan, M. D. & Bemben, D. A. (1988). Sk<strong>in</strong>fold equations<br />

for estimation of body fatness <strong>in</strong> children <strong>and</strong> youth. Human Biology,<br />

60, 709-723.<br />

Yeater, R., Mart<strong>in</strong>, B., White, M. & Gilson, K. (1981). Tethered swimm<strong>in</strong>g<br />

forces <strong>in</strong> the crawl, breast <strong>and</strong> back strokes <strong>and</strong> their relationship<br />

to competitive performance. J <strong>Biomechanics</strong>, 14, 527-537.<br />

254<br />

Changes of Competitive Performance, Tra<strong>in</strong><strong>in</strong>g<br />

Load <strong>and</strong> Tethered Force Dur<strong>in</strong>g Taper<strong>in</strong>g <strong>in</strong> Young<br />

Swimmers<br />

drosou, e. 1 , toubekis, A.G. 2 , Gourgoulis, V. 1 , Thomaidis, s. 1 ,<br />

douda, h. 1 , tokmakidis, s.P. 1<br />

1 Democritus University of Thrace, Komot<strong>in</strong>i, Greece,<br />

2 Kapodistrian University of Athens, Athens, Greece,<br />

Dur<strong>in</strong>g a four-week tra<strong>in</strong><strong>in</strong>g period clos<strong>in</strong>g with a two-week taper<br />

before a National competition (NC) the tra<strong>in</strong><strong>in</strong>g load (TL) of twelve<br />

young swimmers (age: 14.2±1.3 yrs) was calculated by the product of<br />

the session-RPE score with the tra<strong>in</strong><strong>in</strong>g duration. Tethered swimm<strong>in</strong>g<br />

force (TF), h<strong>and</strong>-grip strength (HG) <strong>and</strong> body fat (BF) evaluated 34,<br />

20 <strong>and</strong> 6 days before the NC were unchanged (p>0.05). The TL difference<br />

of week 4 vs. week 1 before the NC was related to percent performance<br />

change (0.11±1.6%, p>0.05; r=0.63, p0.05). The TL<br />

changes alone accounted for 40% (r 2 =0.4, SEE=1.37%, p


<strong>and</strong> backstroke events, <strong>and</strong> one swimmer <strong>in</strong> butterfly. All swimmers had<br />

followed regular tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competitive participation dur<strong>in</strong>g the previous<br />

four to six years.<br />

The swimmers’ tra<strong>in</strong><strong>in</strong>g was recorded daily <strong>and</strong> the tra<strong>in</strong><strong>in</strong>g load<br />

was calculated multiply<strong>in</strong>g the 10-po<strong>in</strong>t rat<strong>in</strong>g of the perceived exertion<br />

scale (RPE) score with the tra<strong>in</strong><strong>in</strong>g duration <strong>in</strong> m<strong>in</strong>utes (Wallace et al.,<br />

2009). The tra<strong>in</strong><strong>in</strong>g duration <strong>in</strong> m<strong>in</strong>utes was recorded by the experimenters<br />

<strong>and</strong> the RPE scale was shown to each swimmer 30 m<strong>in</strong>utes after<br />

the end of each tra<strong>in</strong><strong>in</strong>g session. This time was selected to ensure the<br />

report of a global RPE for each session as has been suggested by Wallace<br />

et al., (2009). The daily load was summarized to a weekly tra<strong>in</strong><strong>in</strong>g load.<br />

The weekly session-RPE load was calculated the four weeks before the<br />

NC (week 1: the last before NC). All swimmers were familiarised with<br />

the use of the RPE scale fifteen days before the exam<strong>in</strong>ation period.<br />

Thirty-four days (TEST 1), twenty days (TEST 2) <strong>and</strong> six<br />

days (TEST 3) before the NC each swimmer’s tethered swimm<strong>in</strong>g force<br />

dur<strong>in</strong>g a 15 s maximum effort test, the h<strong>and</strong>-grip strength (HG) <strong>and</strong> the<br />

percentage of body fat (BF) were evaluated. H<strong>and</strong>-Grip strength was selected<br />

because it has been shown to correlate with performance <strong>in</strong> young<br />

swimmers (Geladas et al., 2005), while BF may show body composition<br />

changes that have been reported dur<strong>in</strong>g the taper period (Mujika et al.,<br />

2004). Tethered swimm<strong>in</strong>g force was measured us<strong>in</strong>g a piezoelectric<br />

force transducer <strong>in</strong>terfaced to an analog to digital converter (Muscle-<br />

Lab, Ergotest). Swimmers were familiarized with the procedure a week<br />

before the first test <strong>and</strong> followed the same warm-up before each test.<br />

The procedure had previously been tested for its reliability (ICC=0.985,<br />

p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

scale, swimmers expressed the general feel<strong>in</strong>g of fatigue after tra<strong>in</strong><strong>in</strong>g. It<br />

has been shown that significant improvement of psychometric parameters<br />

dur<strong>in</strong>g a taper may be related to performance of swimmers (Hooper<br />

et al., 1999). It seems that calculation of tra<strong>in</strong><strong>in</strong>g load with this method<br />

takes <strong>in</strong>to account the “global” feel<strong>in</strong>g of fatigue of the swimmers.<br />

It has been shown that tra<strong>in</strong><strong>in</strong>g load should be reduced more than<br />

50% (Mujika <strong>and</strong> Padilla, 2003) <strong>and</strong> tra<strong>in</strong><strong>in</strong>g distance by 41 to 60% for<br />

an effective taper (Bosquet et al., 2007). In the present study the taper<br />

planned by the coaches failed to meet these criteria s<strong>in</strong>ce tra<strong>in</strong><strong>in</strong>g load<br />

<strong>and</strong> distance were decreased only by 30% <strong>and</strong> 35% respectively from<br />

week 4 to the last week of taper. It should be noted that five of the six<br />

swimmers who improved their performance showed the greatest difference<br />

<strong>in</strong> tra<strong>in</strong><strong>in</strong>g load between week 4 <strong>and</strong> week 1 (Figure 2). Although<br />

not significant, this 1.3% improvement <strong>in</strong> performance of six swimmers<br />

may be important for improv<strong>in</strong>g the plac<strong>in</strong>g <strong>in</strong> a race.<br />

It is likely that the swimmers were not overloaded enough the weeks<br />

preced<strong>in</strong>g the taper (weeks 3 <strong>and</strong> 4). In fact, the calculated tra<strong>in</strong><strong>in</strong>g load<br />

was somewhat reduced dur<strong>in</strong>g week 3 before a local competition. This<br />

occurred because the coaches decided to reduce the tra<strong>in</strong><strong>in</strong>g distance of<br />

week 3 aim<strong>in</strong>g to <strong>in</strong>crease the number of <strong>in</strong>dividual qualify<strong>in</strong>g events<br />

for the NC. Whatever the case, it has been reported that performance<br />

may improve more after taper with prior <strong>in</strong>creased tra<strong>in</strong><strong>in</strong>g overload<strong>in</strong>g,<br />

than without prior overload<strong>in</strong>g (Thomas et al., 2008). A likely less than<br />

necessary overload before the taper or the small percentage decrease of<br />

tra<strong>in</strong><strong>in</strong>g load <strong>and</strong> distance from week 4 to week 1 before the NC may<br />

partly expla<strong>in</strong> the failure to improve performance <strong>in</strong> this group of swimmers.<br />

It is also likely that given the absence of overload tra<strong>in</strong><strong>in</strong>g before<br />

the taper, a shorter than fifteen days taper duration may be required for<br />

an effective performance outcome <strong>in</strong> this group of young swimmers.<br />

The performance of NC was compared to the best performance of<br />

the year <strong>in</strong> the present study. Previous studies compared performance<br />

changes after a taper with performance after an <strong>in</strong>tensified tra<strong>in</strong><strong>in</strong>g<br />

period <strong>and</strong> this may have caused a greater reported percent improvement<br />

(Hooper et al., 1998; Papoti et al., 2007; Tr<strong>in</strong>ity et al., 2008). Furthermore,<br />

the swimmers participated <strong>in</strong> a local competition at the start<br />

of the taper after a reduction of tra<strong>in</strong><strong>in</strong>g distance <strong>and</strong> load (Figure 1)<br />

<strong>and</strong> some of them achieved personal best performance time dur<strong>in</strong>g this<br />

competition (after week 3). This may have decreased the chance for a<br />

further improvement of performance, s<strong>in</strong>ce it was possibly difficult to<br />

achieve a better performance <strong>in</strong> the NC after the two weeks of taper<strong>in</strong>g.<br />

Although the tra<strong>in</strong><strong>in</strong>g distance <strong>and</strong> load reduction dur<strong>in</strong>g week 3 was<br />

not characterised as a taper<strong>in</strong>g, it cannot be overlooked that it may have<br />

had an impact on the follow<strong>in</strong>g taper <strong>and</strong> subsequent NC performance.<br />

It has been shown that after reduction of tra<strong>in</strong><strong>in</strong>g load for a conferance<br />

competition, the performance achieved <strong>in</strong> a follow<strong>in</strong>g taper is reduced<br />

(Tr<strong>in</strong>ity et al., 2008).<br />

Force (N)<br />

256<br />

200<br />

180<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

40<br />

20<br />

0<br />

TEST 1 TEST 2 TEST 3<br />

*<br />

*<br />

*<br />

* *<br />

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15<br />

Time (s)<br />

Figure 1. Changes of tethered force dur<strong>in</strong>g the 15 s tests performed<br />

thirty-four (TEST 1), twenty (TEST 2) <strong>and</strong> six days (TEST 3) before<br />

the National competition. * p


Perceived Exertion at Different Percents of The<br />

Critical Velocity <strong>in</strong> Front Crawl<br />

Franken, M. 1 , diefenthaeler, F. 1,2 , de souza castro, F.A. 1<br />

1 Federal University of Rio Gr<strong>and</strong>e do Sul, Porto Alegre, Brazil.<br />

2 Federal University of Santa Catar<strong>in</strong>a, Florianópolis, Brazil.<br />

The aim of the present study was to compare <strong>and</strong> correlate the perceived<br />

exertion (PE) behaviour at different percents of the critical velocity<br />

(CV) <strong>in</strong> front crawl. Ten tra<strong>in</strong>ed male swimmers (19.4 ± 2.2 years)<br />

performed five trials of 200 m at different percents of the CV (90, 95,<br />

100, 103 <strong>and</strong> 105%), <strong>in</strong> r<strong>and</strong>om order, 90 s of passive rest. PE presented<br />

significant differences (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 2: Comparison between percent values of the prescribed critical<br />

velocity (CV P ) <strong>and</strong> real swimm<strong>in</strong>g velocity (SV R ) <strong>and</strong> with percent immediately<br />

above (n=10).<br />

VC P (%)<br />

SC R (%)<br />

(mean ± SD)<br />

P (CV P x<br />

CV R )<br />

p (SV R x %<br />

immediately<br />

above)<br />

90 91.91 ± 1.04 0.000* 0.000*<br />

95 96.29 ± 1.88 0.040* 0.000*<br />

100 101.07 ± 1.57 0.002* 0.028*<br />

103 104.12 ± 1.80 0.093 -<br />

105 106.20 ± 1.76 0.063 -<br />

*significant difference (p


Ribeiro, L. F. P. R., Lima, M. C. V. & Gobatto, C. A. (2010). Changes<br />

<strong>in</strong> physiological <strong>and</strong> strok<strong>in</strong>g parameters dur<strong>in</strong>g <strong>in</strong>terval sw<strong>in</strong>s at the<br />

slope of the d-t relationship. J Sci Med Sport, 13(1), 141-145.<br />

Suzuki, F. G., Okuno, N. M., Lima-Silva, A. E., Per<strong>and</strong><strong>in</strong>i L. A. B.,<br />

Kokubun E. & Nakamura F. Y. (2007). Perceived exertion dur<strong>in</strong>g <strong>in</strong>terval<br />

tra<strong>in</strong><strong>in</strong>g <strong>in</strong> swimm<strong>in</strong>g at <strong>in</strong>tensities below <strong>and</strong> above the critical<br />

speed. Port Jf Sports Scien, 7(3), 299-307.<br />

St Clair Gibson A., Baden, B. A., Lambert, M. I., Lambert, E. V., Harley,<br />

Y. X., Hampson, D., Russell, V. A. & Noakes, T. D. (2003). The<br />

conscious perception of sensation of fatigue. Sports Med, 33, 167-176.<br />

Ueda, T. & Kurokawa, T. (1995). Relationships between perceived exertion<br />

<strong>and</strong> physiological variables dur<strong>in</strong>g swimm<strong>in</strong>g. Int J Sports Med,<br />

16, 385-9.<br />

Ulmer, H. V. (1996). Concept of an extracellular regulation of muscular<br />

metabolic rate dur<strong>in</strong>g heavy exercise <strong>in</strong> humans by psychophysiological<br />

feedback. Experientia, 52, 416-420.<br />

Wakayoshi, K., Ilkuta, K., Yoshida, T., Udo, M., Moritani, T. & Mutoh,<br />

Y. (1992). Determ<strong>in</strong>ation <strong>and</strong> validity of critical velocity as an <strong>in</strong>dex<br />

of swimm<strong>in</strong>g performance <strong>in</strong> the competitive swimmer. Eur J Appl<br />

Physiol, 64, 153-7.<br />

AcKnoWledGeMents<br />

The authors are grateful for Daniel Geremia <strong>and</strong> Caio Baganholo Contador<br />

<strong>and</strong> athletes; Grupo de Pesquisa em Esportes Aquáticos – GPEA;<br />

Grupo de Pesquisa em Biomecânica e C<strong>in</strong>esiologia – GPBIC, Universidade<br />

Federal do Rio Gr<strong>and</strong>e do Sul (UFRGS).<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

Ventilatory <strong>and</strong> Biomechanical Responses <strong>in</strong> Short<br />

vs. Long Interval Tra<strong>in</strong><strong>in</strong>g <strong>in</strong> Elite Long Distance<br />

Swimmers.<br />

hellard, P. 1,4 , dekerle, J. 2 , nesi, X. 2 , toussa<strong>in</strong>t, J.F. 4 , houel, n. 1 ,<br />

hausswirth, c. 3<br />

1Département recherche, Fédération Française de Natation, Paris France.<br />

2Chelsea, School, University of Brighton, Engl<strong>and</strong>.<br />

3Département des Sciences du Sport, INSEP, Paris, France.<br />

4Institut de recherche en médec<strong>in</strong>e et en épidémiologie du sport, IRMES,<br />

Paris, France.<br />

The objective of this study was to compare <strong>in</strong> seven elite male longdistance<br />

swimmers (Mean ± SD, age 21.4±3.5 yrs; weight 71±5 kg ;<br />

height 180±5 cm), physiological responses (mean oxygen uptake ( VO2 �<br />

mean ), carbon dioxide production ( VCO 2<br />

�<br />

mean ) , ventilation ( E V� mean ) ,<br />

heart rate (HRmean ) , time susta<strong>in</strong>ed above 90% of 2 O V� max , (T90%),<br />

blood lactate concentration (BL ), stroke rate (SFmean ), <strong>and</strong> stroke length<br />

(SL mean )) dur<strong>in</strong>g two different <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g sets (6x500 m (IT6x500 )<br />

<strong>and</strong> 30x100 (IT30x100 )) performed <strong>in</strong> r<strong>and</strong>om order at the velocity at<br />

Lactate Threshold (vLT) with the same work-to-rest ratio (60 vs. 15 s).<br />

Compared with the IT30x100 set, the IT6x500 set displayed greater ventilatory<br />

responses but with shorter stroke length to ma<strong>in</strong>ta<strong>in</strong> a given<br />

sub-maximal speed. Short-<strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g can be used to develop the<br />

distance per stroke while long <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g allows tra<strong>in</strong><strong>in</strong>g to prevent<br />

the deterioration of stroke mechanics dur<strong>in</strong>g high oxygen consumption<br />

regimens.<br />

Key words: Interval tra<strong>in</strong><strong>in</strong>g, physiological responses, lactate threshold.<br />

IntroductIon<br />

The impact of a tra<strong>in</strong><strong>in</strong>g set can be modulated by vary<strong>in</strong>g the duration,<br />

<strong>in</strong>tensity, <strong>and</strong> the number of repetitions <strong>and</strong> rest periods between tra<strong>in</strong><strong>in</strong>g<br />

<strong>in</strong>tervals (Astr<strong>and</strong> et al., 1960; Bentley et al., 2005; Billat, 2001;<br />

Essen et al., 1977; MacDougall <strong>and</strong> Sale, 1981; Olbrecht et al., 1985).<br />

Changes <strong>in</strong> the parameters of a tra<strong>in</strong><strong>in</strong>g set also has an effect on the<br />

amount of time the athlete tra<strong>in</strong>s at a given percent of 2 O V� max <strong>and</strong><br />

thus affects long-term physiological adaptations <strong>in</strong> long distance tra<strong>in</strong><strong>in</strong>g<br />

(Astr<strong>and</strong> et al., 1960; Bentley et al., 2005; Billat, 2001; Essen et al.,<br />

1977; MacDougall <strong>and</strong> Sale, 1981; Olbrecht et al., 1985). Intermittent<br />

bouts with long <strong>in</strong>tervals <strong>in</strong>-between, swum at velocities close to maximum<br />

lactate steady state (vMLSS) <strong>and</strong> VO2 �<br />

max (v VO2 �<br />

max ) enables<br />

athletes to ma<strong>in</strong>ta<strong>in</strong> higher speeds (Bentley et al., 2005; Billat, 2001; Essen<br />

et al., 1977; MacDougall <strong>and</strong> Sale, 1981; Olbrecht et al., 1985). This<br />

range of speeds is associated with preferential catabolism of lipid substrates<br />

via the attenuator effect of citrate produced by glycolysis dur<strong>in</strong>g<br />

the <strong>in</strong>tervals of rest (Essen et al., 1977). This leads to less pronounced<br />

serum lactate concentrations for equivalent or higher 2 O V� than reached<br />

dur<strong>in</strong>g cont<strong>in</strong>uous tra<strong>in</strong><strong>in</strong>g performed at lower speeds (Billat, 2001;<br />

Olbrecht et al., 1985). Because of the short periods of recovery <strong>in</strong>between<br />

repetitions, <strong>in</strong>termittent tra<strong>in</strong><strong>in</strong>g also enables the restitution<br />

of myoglob<strong>in</strong>-bound oxygen stocks <strong>and</strong> higher muscular concentrations<br />

of adenos<strong>in</strong>e triphosphate (ATP) <strong>and</strong> creat<strong>in</strong>e phosphate (CP) so that<br />

dur<strong>in</strong>g the first phase of a subsequent work, ß-oxydation is favored over<br />

glycolysis. Lesser accumulation of lactate at a given VO2 � , appears to<br />

be even more attractive <strong>in</strong> swimm<strong>in</strong>g as the stroke efficiency seems to<br />

deteriorate pass<strong>in</strong>g the anaerobic threshold pace. This is thought to be a<br />

consequence of a greater local fatigue (Dekerle et al., 2005). Moreover,<br />

<strong>in</strong>termittent tra<strong>in</strong><strong>in</strong>g would enable the swimmer to ma<strong>in</strong>ta<strong>in</strong> speeds<br />

close to those of competition, which is useful for speed-specific neuromuscular<br />

<strong>and</strong> coord<strong>in</strong>ation adaptations (Billat, 2001; Essen, 1977; Olbrecht<br />

et al., 1985). It is hypothesized that <strong>in</strong> high-level long-distance<br />

259


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

swimmers, very long tra<strong>in</strong><strong>in</strong>g <strong>in</strong>tervals (repetitions of 500 m) swum at<br />

lactate threshold would lead to greater oxygen uptake, higher stroke rate,<br />

<strong>and</strong> shorter stroke length than those observed dur<strong>in</strong>g <strong>in</strong>tervals of shorter<br />

distance (repetitions of 100 m).<br />

Methods<br />

Seven long-distance male swimmers compet<strong>in</strong>g at the national <strong>and</strong> <strong>in</strong>ternational<br />

level participated <strong>in</strong> this study.<br />

Table 1. Individual anthropometric characteristics <strong>and</strong> tra<strong>in</strong><strong>in</strong>g content.<br />

S<br />

260<br />

Age<br />

(Y)<br />

Weight<br />

(kg)<br />

Height<br />

(cm)<br />

v LT-<br />

(km)<br />

v LT+<br />

(km)<br />

1 23 61 176 2100 380<br />

2 22 74 188 1900 290<br />

3 20 75 185 2050 370<br />

4 21 69 175 2200 303<br />

5 20 76 182 2200 320<br />

6 29 69 174 2350 352<br />

7 20 76 182 2200 330<br />

M 22 71 180 2143 335<br />

SE 3.2 5.5 5.4 143 34<br />

v LT-, annual tra<strong>in</strong><strong>in</strong>g volume at low <strong>in</strong>tensity below the lactate threshold.<br />

v LT+, annual tra<strong>in</strong><strong>in</strong>g volume at high <strong>in</strong>tensity above the lactate<br />

threshold .<br />

All participants completed three experimental sessions <strong>in</strong> a 50-m open<br />

pool (26°C) dur<strong>in</strong>g one week of st<strong>and</strong>ardized tra<strong>in</strong><strong>in</strong>g. The first tra<strong>in</strong><strong>in</strong>g<br />

test consisted <strong>in</strong> a progressive <strong>in</strong>cremental test to exhaustion. The<br />

other tests were two r<strong>and</strong>omized <strong>in</strong>terval sessions – 6 x 500 m (IT6x500 )<br />

or 30x100 m (IT30x100 ) – performed at the velocity correspond<strong>in</strong>g to<br />

lactate threshold (vLT). Dur<strong>in</strong>g each IT session, the time spent at 90%<br />

above 2 O V� max <strong>and</strong> 90% above maximal heart rate (HRpeak ) were determ<strong>in</strong>ed<br />

retrospectively. The <strong>in</strong>cremental test <strong>in</strong>cluded five consecutive<br />

300-m swims separated by 30s of rest. The speed of each <strong>in</strong>crement was<br />

determ<strong>in</strong>ed from the best performance of each swimmer <strong>in</strong> the 400m<br />

freestyle event measured dur<strong>in</strong>g the month preced<strong>in</strong>g the test. The<br />

speed for the first 300-m was 30-s slower than the average 300-m pace<br />

over the 400-m best performance <strong>and</strong> this time was then reduced by<br />

<strong>in</strong>crements of 5 s for each consecutive 300-m until the f<strong>in</strong>al 300-m at<br />

the swimmer’s fastest speed. Swimm<strong>in</strong>g speeds were monitored with<br />

Aquapacer ‘Solo’ (Challenge <strong>and</strong> Response, Inverurie, UK) so that each<br />

swimmer could match auditory signals with visual markers positioned<br />

every 12.5 m along the border of the pool. Blood lactate level (expressed<br />

<strong>in</strong> mM/L) was determ<strong>in</strong>ed from a f<strong>in</strong>gertip blood sample which was<br />

analyzed immediately us<strong>in</strong>g a portable lactate analyzer (Lactate Pro,<br />

Arkray, Japan). Breath-by-breath respiratory data were collected with<br />

a portable gas analyzer (Cosmed K4b2, Rome, Italy) connected to an<br />

Aquatra<strong>in</strong>er snorkel (Cosmed, Rome, Italy). Heart rate (HR) was recorded<br />

us<strong>in</strong>g a belt system (Polar Electro, F<strong>in</strong>l<strong>and</strong>). The lactate threshold<br />

(LT) was determ<strong>in</strong>ed by two <strong>in</strong>dependent observers us<strong>in</strong>g the first<br />

<strong>in</strong>flexion method applied to the l<strong>in</strong>ear relationship between lactate level<br />

<strong>and</strong> velocity associated with a 1mmol·l-1 <strong>in</strong>crease <strong>in</strong> serum lactate above<br />

the basel<strong>in</strong>e level. HRpeak (expressed <strong>in</strong> beats·m<strong>in</strong>-1 ) was def<strong>in</strong>ed as the<br />

mean highest HR measured over 15s dur<strong>in</strong>g the test.<br />

Dur<strong>in</strong>g the <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g (IT), the swimmers were kept <strong>in</strong>formed<br />

of their velocity us<strong>in</strong>g the protocol described above. Swimmers were<br />

encouraged orally to susta<strong>in</strong> their velocity despite <strong>in</strong>creas<strong>in</strong>g exhaustion<br />

throughout the set. Swim times (s) were systematically recorded for<br />

each 500 <strong>and</strong> 100-m repetition. Because the swimmers were wear<strong>in</strong>g a<br />

snorkel, they used open turns. Dur<strong>in</strong>g a pilot run, the time needed to execute<br />

a turn with the snorkel was estimated <strong>in</strong>dividually with an average<br />

time of 1±0.37 s compared with a conventional tumble turn. The velocity<br />

(m·s-1 ) was calculated by divid<strong>in</strong>g the length of each repetition (100-m<br />

or 500-m) by the time with <strong>in</strong>dividual correction for number of turns.<br />

The actual velocity for each 5x100m workout was averaged for a comparison<br />

with IT6x500 . Mean stroke rate (SR) (cycle·m<strong>in</strong>-1 ) was measured<br />

<strong>in</strong> a 25-m central zone us<strong>in</strong>g a base 3 chronometer (Seiko, base 3, Japan).<br />

Stroke length (SL) was calculated for each 50 m by divid<strong>in</strong>g the mean<br />

velocity by SR. Expired gases collected breath-by-breath were monitored<br />

cont<strong>in</strong>uously <strong>and</strong> recorded every 5 s. VO2 �<br />

mean for the two IT6x500 <strong>and</strong> IT30*100 sessions were calculated as was the time of swimm<strong>in</strong>g above<br />

90% of VO2 � max (T>90%). Breath samples were then averaged over 30<br />

s <strong>and</strong> 2 O V� peak <strong>and</strong> HR peak were measured <strong>and</strong> expressed <strong>in</strong> % of VO2 �<br />

max. Serum lactate level was measured at the end of eat IT session.<br />

results<br />

Stroke length was longer dur<strong>in</strong>g IT 30x100 than IT 6*500 (2.45 ± 0.16 vs.<br />

2.30 ± 0.16 m, P < 0.05) (Figure 1) <strong>and</strong> stroke rate tended to be lower<br />

(35.4 ± 3.3 vs. 37.8 ± 3.2, s·mn -1 , P = 0.08).<br />

SL (m)<br />

2,8<br />

2,7<br />

2,6<br />

2,5<br />

2,4<br />

2,3<br />

2,2<br />

2,1<br />

2<br />

1 2 3 4 5 6<br />

Figure 1. Mean ± SE Stroke length (SL) (m·stroke -1 ) dur<strong>in</strong>g each<br />

stage of the 30 x 100-m (IT 30x100 ) (Broken l<strong>in</strong>e with white diamonds<br />

shaped) <strong>and</strong> 6 x 500-m (IT 6x500 ) IT sessions (Cont<strong>in</strong>uous l<strong>in</strong>e with<br />

black squares). Stroke length was higher (P < 0.05) for (IT 30x100 ) than<br />

for (IT 6x500 ).<br />

There was no significant difference <strong>in</strong> swimm<strong>in</strong>g velocity between<br />

IT6*500 <strong>and</strong> IT30*100 for each 500 m. Expressed <strong>in</strong> % v VO2 �<br />

max <strong>and</strong> %<br />

vLT, swimm<strong>in</strong>g velocities were 96.4 ± 3.4 <strong>and</strong> 99.2 ± 3.6% for IT6*500 <strong>and</strong> 96.7 ± 3.4 <strong>and</strong> 99.4 ± 4.4% for IT30*100 respectively. Although the<br />

swimm<strong>in</strong>g velocity was similar dur<strong>in</strong>g IT6*500 <strong>and</strong> IT30*100, VO2 �<br />

mean ,<br />

VE �<br />

mean , BL <strong>and</strong> RPE were greater for IT6*500 than IT30*100 (63.8±3.9 vs.<br />

57.3±3.1 mL.kg-1 ·m<strong>in</strong>-1 ; 79.6±18.8 vs. 73.2±10.5 mL·kg-1 ·m<strong>in</strong>-1 ; 4.1±1.2<br />

vs. 3.2±1.4 mmol·L-1 ; 17.3±2.4 vs. 14.7±3.1 a.u. P < 0.05). T>90% was<br />

greater for IT6*500 (1357 ± 288 vs. 562 ± 326 s, P < 0.05) (Table 2).<br />

dIscussIon<br />

The major f<strong>in</strong>d<strong>in</strong>g of this study is that the long <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g set<br />

(IT6*500m ) which was performed at vLT displayed higher physiological<br />

responses <strong>and</strong> longer time susta<strong>in</strong>ed above 90% VO2 �<br />

max compared with<br />

the shorter <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g (IT30*100m ). This is <strong>in</strong> agreement with the<br />

pioneer work on physiological response to <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g conducted<br />

by Astr<strong>and</strong> et al., (1960) who demonstrated that for exercise performed<br />

at 98% of the workload correspond<strong>in</strong>g to VO 2<br />

�<br />

max , long <strong>in</strong>terval exercise<br />

allowed athletes to atta<strong>in</strong> VO 2<br />

�<br />

max whereas short-<strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g<br />

led to sub-maximal response (63% VO 2<br />

�<br />

max ). Conversely, our results are<br />

not <strong>in</strong> agreement with those reported by Bentley et al. (2005) who compared,<br />

<strong>in</strong> eight elite swimmers, two <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g sessions compris<strong>in</strong>g<br />

4 repetitions of 400m or 16 repetitions of 100m completed at a velocity<br />

represent<strong>in</strong>g 25% of the difference between ventilatory threshold <strong>and</strong><br />

VO2 �<br />

max (Δ25%). They were unable to f<strong>in</strong>d any significant difference<br />

<strong>in</strong> the physiological responses. The apparent discordance with our data<br />

might be attributed to the shorter <strong>in</strong>tervals (400 vs. 500 m), the smaller<br />

exercise volume (1600 vs. 3000 m).<br />

For elite long-distance swimmers, tra<strong>in</strong><strong>in</strong>g at vLT over long <strong>in</strong>tervals<br />

would probably be particularly useful as has already been reported


There was no significant difference <strong>in</strong> swimm<strong>in</strong>g velocity between IT6*500 <strong>and</strong> IT30*100<br />

for each 500 m. Expressed <strong>in</strong> % v 2 O V& max <strong>and</strong> % vLT, swimm<strong>in</strong>g velocities were 96.4 ±<br />

3.4 <strong>and</strong> 99.2 ± 3.6% for IT6*500 <strong>and</strong> 96.7 ± 3.4 <strong>and</strong> 99.4 ± 4.4% for IT30*100 respectively.<br />

Although the swimm<strong>in</strong>g velocity was similar dur<strong>in</strong>g IT6*500 <strong>and</strong> IT30*100, VO2 & mean,<br />

VE & mean, BL <strong>and</strong> RPE were greater for IT6*500 than IT30*100 (63.8±3.9 vs. 57.3±3.1<br />

mL.kg -1 ·m<strong>in</strong> -1 ; 79.6±18.8 vs. 73.2±10.5 mL·kg -1 ·m<strong>in</strong> -1 ; 4.1±1.2 vs. 3.2±1.4 mmol·L -1 ;<br />

17.3±2.4 vs. 14.7±3.1 a.u. P < 0.05). T>90% was greater for IT6*500 (1357 ± 288 vs. 562<br />

Table 2. Maximal <strong>and</strong> peak physiological variables obta<strong>in</strong>ed <strong>in</strong> the<br />

(ITE6x300) ± 326 s, P < 0.05) <strong>in</strong>cremental (Table 2). test to exhaustion (ITE6x300-m) <strong>and</strong> mean<br />

physiological values obta<strong>in</strong>ed <strong>in</strong> the 30x100-m (IT30x100 ) <strong>and</strong> 6x500-m<br />

(IT6x500 ) IT sessions.<br />

Table 2. Maximal <strong>and</strong> peak physiological variables obta<strong>in</strong>ed <strong>in</strong> the (ITE6x300)<br />

<strong>in</strong>cremental test to exhaustion (ITE6x300-m) <strong>and</strong> mean physiological values obta<strong>in</strong>ed <strong>in</strong><br />

the 30x100-m (IT30x100) <strong>and</strong> 6x500-m (IT6x500) IT sessions.<br />

Incremental<br />

Interval tra<strong>in</strong><strong>in</strong>g sets.<br />

test.<br />

Mean values.<br />

Maximal values.<br />

6*300 IT30*100 IT6*500<br />

V (m·s -1 ) 1.51 ± 0.02 1.46 ± 0.06 1.45 ± 0.06<br />

%v 2 O V& max 100 96.7 ± 3.6 95.9 ± 3.2<br />

VO 2<br />

& (mL·kg -1 ·m<strong>in</strong> -1 ) 69.2 ± 6.5 57.3 ± 3.1* 63.8 ± 3.9<br />

% VO2 & max 100 82.8 ± 3.7* 91.3 ± 3.6<br />

VCO2 & (mL·kg -1 ·m<strong>in</strong> -1 ) 62.1 ± 5.7 48.6 ± 6.3* 54.8 ± 2.4<br />

% VCO2 & max 100 78.3 ± 7.7* 88.2 ± 9.7<br />

VE & (mL·kg -1 ·m<strong>in</strong> -1 ) 1749 ± 166 1281 ± 193* 1392 ± 207<br />

% VE & max 100 73.2 ± 10.5* 79.6 ± 17.8<br />

Lactate (mmol·L -1 ) 6.9 ± 1.4 3.2 ± 1.4* 4.1 ± 1.2<br />

RPE (a.u.) 18.4 ± 3.1 14.7 ± 3.1* 17.3 ± 2.4<br />

QR 0.98 ± 0.09 0.86 ± 0.09 0.86 ± 0.09<br />

%QR max 87.9 ± 9.1 87.9 ± 8.1<br />

HR (b·m<strong>in</strong> -1 ) 196 ± 7.3 175 ± 9.8 180 ± 6.2<br />

% HR max 89.3 ± 3.8 91.8 ± 3.6<br />

DISCUSSION<br />

The major f<strong>in</strong>d<strong>in</strong>g of this study is that the long <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g set (IT6*500m) which was<br />

performed at vLT displayed higher physiological responses <strong>and</strong> longer time susta<strong>in</strong>ed<br />

above 90% VO2 & for moderately to highly tra<strong>in</strong>ed or even elite athletes (Billat, 2001). The<br />

use of cont<strong>in</strong>uous max compared or long-<strong>in</strong>terval with the shorter tra<strong>in</strong><strong>in</strong>g <strong>in</strong>terval sessions tra<strong>in</strong><strong>in</strong>g when (IT30*100m). performed This at is <strong>in</strong><br />

<strong>in</strong>tensities close to the lactate threshold has been suggested to be particularly<br />

good for reduc<strong>in</strong>g energy cost (Billat, 2001; Jones, 1998), for<br />

an enhancement of the capacity of ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g a larger proportion of<br />

VO � max over long periods of time. Nevertheless, the results of the<br />

2<br />

present study also suggest that <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g sessions similar to the<br />

IT 30*100 protocol could be useful for develop<strong>in</strong>g stroke length while<br />

complet<strong>in</strong>g a large volume of tra<strong>in</strong><strong>in</strong>g without metabolic overload (Olbrecht<br />

et al., 1985). In agreement, MacDougall <strong>and</strong> Sale (1981) who<br />

demonstrated that 30-s exercise periods alternated with 30-s rest solicited<br />

the aerobic metabolism less than 2-3 m<strong>in</strong> exercise periods which<br />

produced a higher level of hypoxia. Dur<strong>in</strong>g the short <strong>in</strong>tervals, Medbo<br />

et al. (1992) found that a large quantity of oxygen was stored <strong>in</strong> muscle<br />

myoglob<strong>in</strong> dur<strong>in</strong>g the rest periods (10% of maximal cumulative oxygen<br />

debt) m<strong>in</strong>imiz<strong>in</strong>g depletion dur<strong>in</strong>g the exercise time <strong>and</strong> thus spar<strong>in</strong>g<br />

the glycolytic pathway dur<strong>in</strong>g exercise. The fall <strong>in</strong> phosphocreat<strong>in</strong>e dur<strong>in</strong>g<br />

the course of the exercise would be followed by resynthesis dur<strong>in</strong>g<br />

recovery lead<strong>in</strong>g to lesser accumulation of lactate <strong>in</strong> the muscles compared<br />

with cont<strong>in</strong>uous work. The lower levels of glycolysis <strong>in</strong> both motor<br />

<strong>and</strong> ventilatory muscles dur<strong>in</strong>g IT 30*100 would probably contribute to<br />

the lesser muscle fatigue (MacDougall <strong>and</strong> Sale, 1981), enabl<strong>in</strong>g the<br />

athlete to ma<strong>in</strong>ta<strong>in</strong> longer stroke lengths. It could be suggested that this<br />

would enhance, long term, motor efficiency, an essential factor of fast<br />

swimm<strong>in</strong>g performance (Dekerle et al., 2005).<br />

conclusIon<br />

To conclude, dur<strong>in</strong>g long <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g performed at lactate threshold,<br />

elite swimmers exhibited large amplitude of the 2 O V� slow component<br />

<strong>and</strong> an <strong>in</strong>crease <strong>in</strong> the ventilatory response that is l<strong>in</strong>ked to an<br />

<strong>in</strong>crease <strong>in</strong> stroke rate. Moreover, responses observed dur<strong>in</strong>g the short<strong>in</strong>terval<br />

tra<strong>in</strong><strong>in</strong>g (IT 30*100 ) were characterized by a better technical<br />

efficiency accompanied with a lower ventilatory <strong>and</strong> metabolic stress.<br />

Short-<strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g can be used to develop the distance per stroke<br />

while long <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g allows tra<strong>in</strong><strong>in</strong>g aga<strong>in</strong>st the deterioration of<br />

stroke mechanics dur<strong>in</strong>g high oxygen consumption regimens.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

reFerences<br />

Astr<strong>and</strong>, I., Astr<strong>and</strong>, P., Christensen, E. & Hedman, R. (1960). Intermitent<br />

muscular work. Acta Physiol Sc<strong>and</strong>, 50, 443-453.<br />

Bentley, D.J., Roels, B., Hellard, P., Fauquet, C., Libicz, S. & Millet,<br />

G.P. (2005). Physiological responses dur<strong>in</strong>g submaximal <strong>in</strong>terval<br />

swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g: effects of <strong>in</strong>terval duration. J Sci Med Sport, 8(4),<br />

392-402, 2005.<br />

Billat, V (2001a). Interval tra<strong>in</strong><strong>in</strong>g for performance: a scientific <strong>and</strong><br />

empirical practice. Part 1: Aerobic Interval Tra<strong>in</strong><strong>in</strong>g. Sports Med, 31,<br />

13-31.<br />

Dekerle, J., Nesi X., Lefevre T., Depretz S., Sidney M., March<strong>and</strong> F.H.<br />

& Pelayo P (2005). Strok<strong>in</strong>g parameters <strong>in</strong> front crawl swimm<strong>in</strong>g<br />

<strong>and</strong> maximal lactate steady state speed. Int J Sports Med, 26(1), 53-58.<br />

Essen, B., Hagenfeldt, L. & Kaijser, L. (1977). Utilization of bloodborne<br />

<strong>and</strong> <strong>in</strong>tramuscular substrates dur<strong>in</strong>g cont<strong>in</strong>uous <strong>and</strong> <strong>in</strong>termittent<br />

exercise <strong>in</strong> man. J Physiol, 265(2), 489-506.<br />

MacDougall, D. & Sale, D. (1981). Cont<strong>in</strong>uous vs. <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g: a<br />

review for the athlete <strong>and</strong> the coach. Can J Appl Sport Sci, 6(2), 93-97.<br />

Medbo, J.I., Mohn A.C., Tabata I., Bahr R., Vaage O. & Sejersted O.M<br />

(1992). Anaerobic capacity determ<strong>in</strong>ed by maximal accumulated O2<br />

deficit. J Appl Physiol, 73(3), 1207-1209.<br />

Olbrecht, J., Madsen, O., Mader, A., Liesen, H. & Hollmann, W. (1985).<br />

Relationship between swimm<strong>in</strong>g velocity <strong>and</strong> lactic concentration<br />

dur<strong>in</strong>g cont<strong>in</strong>uous <strong>and</strong> <strong>in</strong>termittent tra<strong>in</strong><strong>in</strong>g exercises. Int J Sports<br />

Med, 6(2), 74-77.<br />

261


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Talent Prognosis <strong>in</strong> Young Swimmers<br />

hohmann, A. 1 , seidel, I. 2<br />

1 Institute of Sport Science, University of Bayreuth, Bayreuth, Germany<br />

2 Karlsruhe Institute of Technology, Karlsruhe, Germany<br />

In talent selection a high level of competitive performance, <strong>and</strong> also of<br />

performance prerequisites are of <strong>in</strong>terest. Furthermore, the tra<strong>in</strong>ability<br />

<strong>and</strong> utilization of the performance prerequisites, <strong>and</strong> also psychological<br />

factors have to be <strong>in</strong>cluded. As the different components of the early<br />

talent make-up not only change over time, but also mutually suppress<br />

or enhance each other, talent development is a complex non-l<strong>in</strong>ear process.<br />

L<strong>in</strong>ear models like discrim<strong>in</strong>ate analysis can only predict the talent<br />

development with<strong>in</strong> a small range of the future performance outcome.<br />

Therefore, non-l<strong>in</strong>ear neural network methods turned out to be appropriate<br />

tools for talent detection purposes. By recogniz<strong>in</strong>g dist<strong>in</strong>ct patterns<br />

<strong>in</strong> the <strong>in</strong>dividual dispositions, the Self-organiz<strong>in</strong>g Kohonen Feature<br />

Map allowed for better predictions of the future success of talented<br />

swimmers.<br />

Key words: talent prognosis, swimm<strong>in</strong>g, discrim<strong>in</strong>ate analyses, neural<br />

network<br />

IntroductIon<br />

Recent theoretical contributions to the theory of talent <strong>in</strong> sport have<br />

clearly shown that a complex <strong>and</strong> longitud<strong>in</strong>al framework is necessary to<br />

successfully address talent identification <strong>and</strong> the talent promotion issue<br />

<strong>in</strong> most sports (Gagnè, 1985; Abbot & Coll<strong>in</strong>s, 2002; 2004). Consequently,<br />

the early diagnosis of juvenile competition performances <strong>and</strong><br />

performance prerequisites has to be complimented by a f<strong>in</strong>al follow-up<br />

search for the <strong>in</strong>dividual best performance of each adult athlete at the<br />

end of his/her career (Willimczik, 1982; Schneider, et al., 1993).<br />

As talent development is a complex non-l<strong>in</strong>ear process, <strong>and</strong> the different<br />

components of early talent make-up not only change over time,<br />

but can also mutually suppress or enhance each other, l<strong>in</strong>ear models like<br />

discrim<strong>in</strong>ate analysis can only approximate the non-l<strong>in</strong>ear talent development<br />

with<strong>in</strong> a very small range of the future performance output.<br />

Because of this, neural networks also seem to be appropriate tools for<br />

talent detection purposes (Philippaerts, et al., 2008). Due to their pattern<br />

detection ability, such methods as e.g. the Self-organiz<strong>in</strong>g Kohonen<br />

Feature Map may allow to predict the future success of talents by reveal<strong>in</strong>g<br />

dist<strong>in</strong>ct patterns <strong>in</strong> the <strong>in</strong>dividual sets of sport specific dispositions.<br />

The purpose of this paper is to compare the quality of l<strong>in</strong>ear <strong>and</strong><br />

non-l<strong>in</strong>ear talent predictions, which are both based on prognostic valid<br />

talent criteria <strong>in</strong> swimm<strong>in</strong>g. Specifically, it shall be demonstrated that<br />

the talent development outcome can be better modeled by means of the<br />

non-l<strong>in</strong>ear Self-organiz<strong>in</strong>g Kohonen Feature Map (SOFM) network.<br />

Methods<br />

The Magdeburg Talent study on Elite Sport Schools (MATASS;<br />

Hohmann, 2009) is a six year longitud<strong>in</strong>al study on the development<br />

of talented children <strong>and</strong> adolescents. It was conducted at the two Elite<br />

Sport Schools <strong>in</strong> Magdeburg, Germany, <strong>and</strong> was based on a sequential<br />

slid<strong>in</strong>g populations design (Regnier, et al., 1993) with three test waves <strong>in</strong><br />

the years 1997, 1999 <strong>and</strong> 2001. In each test wave all pupils of the swimm<strong>in</strong>g<br />

classes 5 to 12 were <strong>in</strong>cluded. They were added by pre-selected<br />

young athletes from class 4 of the elementary schools <strong>and</strong> the graduates<br />

of the last year before the tests (see Fig.1).<br />

262<br />

Cohort 3<br />

Cohort 4<br />

Cohort 5<br />

Cohort 6<br />

Cohort 7<br />

Cohort 2<br />

Cohort 1<br />

1997 1999 2001<br />

Wave 1 Wave 2 Wave 3<br />

Classes 4 & 5<br />

Classes 6 & 7<br />

Classes 8 & 9<br />

Classes 10 &11<br />

Classes 12 & 13<br />

Figure 1. The longitud<strong>in</strong>al study design of the MATASS<br />

The data for these analyses of swimm<strong>in</strong>g were collected from 1997 to<br />

2001 from a total of N = 290 male (n = 172, M<strong>in</strong> = 128 months, Max<br />

= 276 months, M = 171.24 months, SD = 42.52) <strong>and</strong> female swimmers<br />

(n = 118, M<strong>in</strong> = 116 months, Max = 282 months, M = 159.25 months,<br />

SD = 39.02). The f<strong>in</strong>al competition performance data was recorded <strong>in</strong><br />

the year 2006 for all male swimmers (n = 130, M = 254.51 months,<br />

SD = 37.99) <strong>and</strong> female swimmers (n = 113, M = 236.47 months, SD<br />

= 36.29) that were at least 16 years old. Thus, the diagnosis of the adult<br />

competition results took place about seven years after their personal best<br />

test results (males: M = 81.67 months, SD = 19.68; females: M = 76.98<br />

months, SD = 17.95).<br />

Twenty one elementary physical <strong>and</strong> technical performance components<br />

of the swimm<strong>in</strong>g performance were measured. Elementary speed:<br />

(1) Reactive fall <strong>in</strong>to the wall (wall contact time), (2) Reactive drop jump<br />

(ground contact time), (3) Foot tapp<strong>in</strong>g speed, (4) Accoustic reaction<br />

time, (5) Arm crank<strong>in</strong>g speed. Complex speed: (6) Isok<strong>in</strong>etic arm pull<br />

(speed level 1), (7) Isok<strong>in</strong>etic arm pull (speed level 9), (8) Maximum<br />

rate of force development (isok<strong>in</strong>etic arm pull, level 1), (9) St<strong>and</strong><strong>in</strong>g<br />

high jump, (10) St<strong>and</strong><strong>in</strong>g long jump, (11) 7.5-m-start (<strong>in</strong>to the water),<br />

(12) 5-m-fly<strong>in</strong>g spr<strong>in</strong>t (<strong>in</strong> the water). Technique <strong>and</strong> coord<strong>in</strong>ation:<br />

(13) Crawl swimm<strong>in</strong>g technique, (14) Complex coord<strong>in</strong>ation (swimm<strong>in</strong>g<br />

with obstacles <strong>in</strong> the water), (15) Maximum pull<strong>in</strong>g frequency<br />

(<strong>in</strong> the water). Strength: (16) Isometric maximum strength of the arms<br />

(bench press), (17) Maximum rate of force development of the arms<br />

(bench press). Anthropometric variables (body structure): (18) Arm<br />

span width, (19) H<strong>and</strong> size, (20) Shoulder flexibility, (21) Broca <strong>in</strong>dex.<br />

These variables were complemented by four psychological (achievement<br />

motivation, volition, stress stability, concentration) <strong>and</strong> four sociological<br />

(school support, family support, tra<strong>in</strong><strong>in</strong>g environment, tra<strong>in</strong><strong>in</strong>g load)<br />

performance components, which were collected via questionnaire. The<br />

best competition performance of each athlete <strong>in</strong> each of the three survey<br />

periods (1997, 1999, 2001) was also assessed. F<strong>in</strong>ally, at the end of the<br />

study <strong>in</strong> the year 2006, the adult (peak) performance up to then of all<br />

athletes aged 16 years <strong>and</strong> older was recorded.<br />

In a first step, the 21 physical <strong>and</strong> technical performance components<br />

were analysed by factor analysis (SPSS 14.0, SPSS Inc., Chicago,<br />

Ill.). Us<strong>in</strong>g this procedure, six complex <strong>and</strong> one-dimensional performance<br />

prerequisites were extracted by orthogonal factor analysis. In<br />

swimm<strong>in</strong>g, these factors were (1) body structure, (2) maximum strength,<br />

(3) general <strong>and</strong> (4) swim specific speed strength, (5) technique <strong>and</strong> coord<strong>in</strong>ation,<br />

<strong>and</strong> (6) elementary speed (Hohmann, 1999).<br />

In a second step, the (1) juvenile competition performance <strong>and</strong> (2)<br />

the factor values of the six complex performance prerequisites served<br />

as well as talent predictors as the (3) speed of performance development,<br />

(4) speed of development of the performance prerequisites, (5)<br />

utilization (Kupper, 1980; Hohmann & Seidel, 2003), <strong>and</strong> (6) psychological<br />

stress stability. This set of six complex predictors was <strong>in</strong>cluded<br />

<strong>in</strong> the talent prediction model that was used to determ<strong>in</strong>e the f<strong>in</strong>al tal-


ent outcome at the adult age of the participants. To def<strong>in</strong>e a criterion<br />

variable, all athletes were categorized <strong>in</strong>to three different talent groups<br />

accord<strong>in</strong>g to their personal best adult competition performance up to<br />

the year 2006. So, the best adult swimmers tak<strong>in</strong>g part <strong>in</strong> <strong>in</strong>ternational<br />

championships were assigned to the category of extremely high talented<br />

athletes, the national calibre athletes were assigned to the category of<br />

highly talented swimmers, <strong>and</strong> the regional starters were labelled as normal<br />

talents.<br />

In a third step, the six juvenile talent criteria described above (of the<br />

earlier time period 1997-2001) were used to predict the three f<strong>in</strong>al adult<br />

talent groups (of the year 2006). For the prediction of the f<strong>in</strong>al adult talent<br />

group two methods were used: firstly, a discrim<strong>in</strong>ate analysis (DA),<br />

<strong>and</strong> secondly, the neural network of a Self-organiz<strong>in</strong>g Kohonen Feature<br />

Map (SOFM; DataEng<strong>in</strong>e, MIT Inc., Aachen, Germany).<br />

To obta<strong>in</strong> a “true” prognosis, the talent forecasts on the basis of the<br />

discrim<strong>in</strong>ate analyses <strong>and</strong> on the basis of the neural network method<br />

have to follow a cross-validation procedure. In the case of the discrim<strong>in</strong>ate<br />

analyses, 50 percent of the total number of cases was used to compute<br />

the discrim<strong>in</strong>ate functions that were then used to determ<strong>in</strong>e the<br />

talent outcome of the rema<strong>in</strong><strong>in</strong>g 50 percent of cases.<br />

In the two specific SOFM models for the male <strong>and</strong> the female<br />

swimmers, the talent forecasts were validated by the “leave-one-out”procedure.<br />

Therefore, one less than the total number of the data sets<br />

of the talents (n-1) were used to tra<strong>in</strong> the network (consist<strong>in</strong>g of a 5x5<br />

neuron layer) with 5 000 tra<strong>in</strong><strong>in</strong>g steps. The rema<strong>in</strong><strong>in</strong>g data set of the<br />

one s<strong>in</strong>gle athlete was then presented to the neural network to calculate<br />

a prognosis of his personal adult peak performance category. After<br />

that, the predicted future talent category was compared with the real,<br />

already known adult performance category. This procedure was repeated<br />

for each s<strong>in</strong>gle data set, so that the total number of correctly predicted<br />

cases represents the quality of the talent prediction models for the male<br />

<strong>and</strong> the female swimmers.<br />

results<br />

For talent identification purposes it is essential to know the early performance<br />

prerequisites that form the structure of the current, <strong>and</strong> also the<br />

future adult peak performance (e.g. for the female swimmers see Fig. 2).<br />

Juvenile performance prerequisites <strong>in</strong> 16-20 years old female swimmers (1997-2001)<br />

R = .74; R2 = .55; R2adj = .41; F (22;72) = 4.02; p = 0.001<br />

Psychological V.<br />

Technique &<br />

Coord<strong>in</strong>ation<br />

Condition<br />

Anthropometric<br />

variables<br />

Extr<strong>in</strong>sic<br />

motivation<br />

Action orientation<br />

(after failure)<br />

Psychological<br />

stress stability<br />

Arm movement<br />

frequency<br />

Spr<strong>in</strong>t<strong>in</strong>g power<br />

Strok<strong>in</strong>g power<br />

Shoulder<br />

flexibility<br />

H<strong>and</strong> size<br />

.77 .001<br />

.42<br />

Spr<strong>in</strong>t<strong>in</strong>g speed<br />

(71 %)<br />

.071 .74 .001<br />

.014<br />

.40<br />

.37 .099<br />

.77 .021<br />

.61 .049<br />

.51 .045<br />

.33 .055<br />

Swimm<strong>in</strong>g<br />

coord<strong>in</strong>ation<br />

(64 %)<br />

.79 .071<br />

.60 .039<br />

.44<br />

Adult<br />

Competition<br />

Performance<br />

(2006)<br />

50-m-Crawl<br />

(41 %)<br />

.005<br />

.43 .089<br />

Figure 2. Path analysis on the prognostic relevance of different performance<br />

prerequisites of young female swimmers for the future competition<br />

performance <strong>in</strong> 50 m spr<strong>in</strong>t swimm<strong>in</strong>g (Hohmann, 2009)<br />

The comparison of the real adult performance groups with the predicted<br />

future groups of the talented swimmers at adult age led to far better<br />

predictions, when the neural network method was applied. The percentages<br />

of correctly predicted cases by discrim<strong>in</strong>ate analysis (females: 69.0<br />

percent; males: 50.0 percent) are much lower than those delivered by<br />

SOFM (females: 87.9 percent; males: 68.3 percent; Fig. 3).<br />

Extreme<br />

Talents<br />

100.0 %<br />

High<br />

Talents<br />

77.3 %<br />

Normal<br />

Talents<br />

88.9 %<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

Extreme<br />

Talents<br />

100.0 %<br />

High<br />

Talents<br />

74.2 %<br />

Normal<br />

Talents<br />

33.3 %<br />

Figure 3. Results of the talent prognosis <strong>in</strong> female (left) <strong>and</strong> male (right)<br />

swimmers on the basis of the nonl<strong>in</strong>ear model of the Self-organiz<strong>in</strong>g<br />

Kohonen Feature Map (s<strong>in</strong>gle <strong>and</strong> double arrows symbolize light resp.<br />

severe classification errors). Extreme talents: Participants <strong>in</strong> Olympic<br />

Games, World Championships, European Championships, <strong>and</strong> German<br />

Championship f<strong>in</strong>als. High talents: European Youth Championships.<br />

Normal talents: German Youth Championships<br />

dIscussIon<br />

This paper aimed at f<strong>in</strong>d<strong>in</strong>g out whether the talent development outcome<br />

can be better modeled by means of the nonl<strong>in</strong>ear mathematical<br />

method of artificial neural networks or by l<strong>in</strong>ear methods such as discrim<strong>in</strong>ate<br />

analyses. The percentages of correctly modeled performances<br />

<strong>in</strong> the l<strong>in</strong>ear discrim<strong>in</strong>ate analysis were comparably lower than <strong>in</strong> the<br />

non-l<strong>in</strong>ear neural network procedure. Thus, the results support the assumption<br />

of Philippaerts et al. (2008) that neural networks are excellent<br />

tools to model <strong>and</strong> to predict future competitive performance categories<br />

on the basis of juvenile talent make-up data.<br />

S<strong>in</strong>ce there is no guarantee that such model<strong>in</strong>g <strong>and</strong> talent prediction<br />

will lead to similar results <strong>in</strong> other groups, the validation procedure has<br />

to be applied to data sets of other swimmers. Based on the results of<br />

this procedure it must be decided whether the neural network is a good<br />

or poor model of talent development <strong>in</strong> swimm<strong>in</strong>g. To obta<strong>in</strong> a good<br />

model, it may require changes <strong>in</strong> some of the tra<strong>in</strong><strong>in</strong>g parameters.<br />

conclusIon<br />

The better results of the neural network analysis compared with the<br />

poorer results of the discrim<strong>in</strong>ate analysis support the <strong>in</strong>terpretation<br />

that the adaptive behaviour of the athlete is a non-l<strong>in</strong>ear complex problem.<br />

This supports a dynamic systems approach to talent development <strong>in</strong><br />

which the young athlete unfolds a performance development process <strong>in</strong><br />

a self-organized way, which is <strong>in</strong>fluenced by various personal <strong>and</strong> contextual<br />

moderator variables (Gagnè, 1985; Heller & Hany, 1986; Heller,<br />

et al., 2005; Cote, et al., 2003).<br />

As neural networks are able to recognize global patterns of different<br />

talent make-ups, they are a worthwhile tool <strong>in</strong> the detection of talents<br />

under the condition of the non-l<strong>in</strong>ear talent development. Hence, from<br />

a dynamical systems po<strong>in</strong>t of view, a successful neural network model<strong>in</strong>g<br />

may be <strong>in</strong>terpreted as a representation of deviations of the different<br />

states of the system from equi-probability, <strong>in</strong> our case the identification<br />

of different patterns of juvenile athletic performance. This is a very <strong>in</strong>terest<strong>in</strong>g<br />

aspect of the model<strong>in</strong>g of competitive performances, because<br />

the non-l<strong>in</strong>ear dynamic systems perspective is rapidly emerg<strong>in</strong>g as one<br />

of the dom<strong>in</strong>ant meta-theories <strong>in</strong> the natural sciences, <strong>and</strong> there is also<br />

reason to believe that <strong>in</strong> the future it will eventually provide a more<br />

general <strong>in</strong>tegrative underst<strong>and</strong><strong>in</strong>g <strong>in</strong> tra<strong>in</strong><strong>in</strong>g science, as well.<br />

reFerences<br />

Abbot, A. & Coll<strong>in</strong>s, D (2002). A theoretical <strong>and</strong> empirical analysis of<br />

a `State of the Art` talent identification model. High Ability Studies,<br />

13(2), 157-78.<br />

Abbot, A. & Coll<strong>in</strong>s, D (2004) Elim<strong>in</strong>at<strong>in</strong>g the dichotomy between<br />

theory <strong>and</strong> practice <strong>in</strong> talent identification <strong>and</strong> development: consider<strong>in</strong>g<br />

the role of psychology. Journal of Sport Sciences, 22(5), 395-408.<br />

Cotè, J., Baker, J. & Abernethy, B. (2003). From Play to Practice. A<br />

Developmental Framework for the Acquisition of Expertise <strong>in</strong> Team<br />

263


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Sport. In Starkes, JL, Ericsson, KA (eds.). Expert Performance <strong>in</strong><br />

Sports. Champaign, IL: Human K<strong>in</strong>etics, 89-110.<br />

Gagnè, F. (1985). Giftedness <strong>and</strong> talent: Reexam<strong>in</strong><strong>in</strong>g a reexam<strong>in</strong>ation<br />

of the def<strong>in</strong>itions. Gifted Child Quarterly, 19, 103-112.<br />

Hohmann, A. (2009). Entwicklung sportlicher Talente an sportbetonten<br />

Schulen, Schwimmen – Leichtathletik – H<strong>and</strong>ball. [Development of<br />

talents at elite schools, swimm<strong>in</strong>g – track <strong>and</strong> field - h<strong>and</strong>ball.] Petersberg:<br />

Imhof.<br />

Hohmann, A. & Seidel, I. (2003). Scientific Aspects of Talent Development.<br />

International Journal of Physical Education, 40(1), 9-20.<br />

Kupper, K. (1980). Zur Vervollkommnung der Eignungsbeurteilung im<br />

Nachwuchsleistungssport der DDR. [On the perfection of the suitability<br />

assessment <strong>in</strong> young elite athletes <strong>in</strong> the GDR.] Theorie und<br />

Praxis des Leistungssports, 18(6), 3-34.<br />

Philippaerts, R.M., Coutts, A. & Vaeyens, R (2008). Physiological Perspectives<br />

on the Identification <strong>and</strong> Development of Talented Performers<br />

<strong>in</strong> Sport. In Fisher, R, Bailey, R (eds.). Talent Identification<br />

<strong>and</strong> Development. The Search for Sport<strong>in</strong>g Excellence. Berl<strong>in</strong>: IC-<br />

SSPE, 49-67.<br />

Regnier, G., Salmela, J., Russell, S.J. (1993). Talent detection <strong>and</strong> development<br />

<strong>in</strong> sport. In S<strong>in</strong>ger, RN, Murphy, M, Tennant, LK (eds.).<br />

H<strong>and</strong>book of Research <strong>in</strong> Sport Psychology. New York: Wiley, 290-313.<br />

Schneider, W., Bös, K. & Rieder, H. (1993). Leistungsprognose bei jugendlichen<br />

Spitzensportlern. [Performance prediction <strong>in</strong> young elite<br />

athletes]. In Beckmann, J, Strang, H, Hahn, E (eds.). Aufmerksamkeit<br />

und Energetisierung. Facetten von Konzentration und Leistung. Gött<strong>in</strong>gen:<br />

Hogrefe, 277-99.<br />

Vaeyens, R., Mal<strong>in</strong>a, R.M., Janssens, M., van Renterghem, B., Burgois,<br />

J. & Vrijens, J., et al. (2006). A multidiscipl<strong>in</strong>ary selection model for<br />

youth soccer : the Ghent Youth Soccer Project. British Journal of<br />

Sports <strong>Medic<strong>in</strong>e</strong>, 40(11), 928-934.<br />

Willimczik, K. (1982). Determ<strong>in</strong>anten der sportmotorischen Leistungsfähigkeit<br />

im K<strong>in</strong>desalter. Konzeption und Zwischenergebnisse e<strong>in</strong>es<br />

Forschungsprojektes. [Determ<strong>in</strong>ants of sport-motor performance <strong>in</strong><br />

childhood. Design <strong>and</strong> <strong>in</strong>termediate results of a research project.]<br />

In Howald, H, Hahn, E (eds.). K<strong>in</strong>der im Leistungssport. Stuttgart:<br />

Birkhäuser, 141-153.<br />

AcKnoWledGeMents<br />

This study was supported by the Federal Institute of Sports Science<br />

(BISp), Bonn, Germany<br />

264<br />

Determ<strong>in</strong>ation of Lactate Threshold with Four<br />

Different Analysis Techniques for Pool Test<strong>in</strong>g <strong>in</strong><br />

Swimmers<br />

Kesk<strong>in</strong>en, K.L. 1,2 , Kesk<strong>in</strong>en, O.P. 2 , Pöyhönen, T. 3<br />

1F<strong>in</strong>nish Society of Sport Sciences, Hels<strong>in</strong>ki, F<strong>in</strong>l<strong>and</strong>,<br />

2Department of Biology of Physical Activity, University of Jyväskylä, Jyväskylä,<br />

F<strong>in</strong>l<strong>and</strong>,<br />

3Kymenlaakso Central Hospital, Kotka, F<strong>in</strong>l<strong>and</strong><br />

Pool test<strong>in</strong>g us<strong>in</strong>g the blood lactate versus swimm<strong>in</strong>g velocity relationship<br />

is a st<strong>and</strong>ard <strong>in</strong> performance diagnostics of swimmers. The reliability<br />

of four techniques designed to determ<strong>in</strong>e the lactate threshold (LT)<br />

were exam<strong>in</strong>ed. The subjects were 15 female <strong>and</strong> 15 male swimmers.<br />

Mean ± SD for age was 16.7 ± 3.3 years, stature 1.70 ± 0.08 m <strong>and</strong> body<br />

mass 61.8 ± 6.6 kg. They performed a set of ten 100 meter swims twice<br />

<strong>in</strong> three days. LT was analyzed from the blood lactate - velocity association<br />

by two experienced analysts. L<strong>in</strong>ear regressions (R 2 ), <strong>in</strong>traclass correlation<br />

coefficients (ICC) with two-way ANOVA, <strong>and</strong> t-tests showed<br />

that both test-retest reliability <strong>and</strong> comparability between mathematical<br />

curve fitt<strong>in</strong>g <strong>and</strong> visual l<strong>in</strong>ear estimation methods were very high (R 2 =<br />

0.85-0.96; ICC = 0.96-0.99; t-tests = N.S.).<br />

Key words: pool test<strong>in</strong>g, analysis techniques, reliability<br />

IntroductIon<br />

Blood lactate concentration (BLa) is one of the most commonly measured<br />

parameters <strong>in</strong> both cl<strong>in</strong>ical exercise test<strong>in</strong>g <strong>and</strong> dur<strong>in</strong>g performance<br />

test<strong>in</strong>g of athletes. In healthy subjects a normal physiological<br />

response to physical stra<strong>in</strong> is an elevated BLa. In response to progressive<br />

<strong>in</strong>cremental exercise BLa-test<strong>in</strong>g offers a convenient tool to observe<br />

its systematic behavior dependent on the <strong>in</strong>tensity of exercise. Under<br />

low work rates BLa either rema<strong>in</strong>s at its <strong>in</strong>itial lowest concentration or<br />

slowly <strong>in</strong>creases. As the exercise becomes more <strong>in</strong>tense, the BLa eventually<br />

<strong>in</strong>creases exponentially. This is recognized as the lactate threshold<br />

(LT) (Stegmann et al. 1981). As a s<strong>in</strong>gle work rate, illustrat<strong>in</strong>g the curvil<strong>in</strong>ear<br />

BLa versus exercise <strong>in</strong>tensity response, determ<strong>in</strong>ation of LT is a<br />

st<strong>and</strong>ard procedure <strong>in</strong> both predict<strong>in</strong>g athletic performances as well as<br />

<strong>in</strong> diseased conditions (Goodw<strong>in</strong> et al., 2007).<br />

Even though the status of the LT as a powerful predictor of performance<br />

is well accepted the velocity at which LT appears depends<br />

on the pool test protocol applied. Kesk<strong>in</strong>en et al. (1987) found that LT<br />

was different between 2·400 (Mader et al., 1978), n·100 (Gullstr<strong>and</strong> et<br />

Holmer, 1980) <strong>and</strong> n·300 m (Simon et al., 1982) swimm<strong>in</strong>g tests with<br />

different BLa values <strong>in</strong> each case. Evidently there is also a different reference<br />

po<strong>in</strong>t for LT when the def<strong>in</strong>ition is made us<strong>in</strong>g a frequently used<br />

n·200-m protocol (Pyne et al., 1992).<br />

In addition to different test<strong>in</strong>g protocols, different analysis techniques<br />

have also been used. Mader et al. (1978) def<strong>in</strong>ed LT as a swimm<strong>in</strong>g<br />

velocity correspond<strong>in</strong>g to fixed 4 mmol·l -1 <strong>in</strong> BLa (V 4 ) from a<br />

two-speed test. Due to its feasability this test has s<strong>in</strong>ce served as the<br />

reference for LT <strong>in</strong> several <strong>in</strong>stances (Svedahl & MacIntosh, 2003).<br />

In a practical sense, the BLa-velocity association has traditionally<br />

been plotted <strong>and</strong> the LT visually determ<strong>in</strong>ed as the orig<strong>in</strong> of the exponential<br />

<strong>in</strong>crement. The concept of an <strong>in</strong>dividual LT was presented by<br />

Stegmann et al. (1981) with an <strong>in</strong>cremental field protocol. Cheng et<br />

al. (1992) proposed a mathematical procedure to determ<strong>in</strong>e ventilatory<br />

threshold <strong>and</strong> LT as an objective <strong>and</strong> reliable method for threshold determ<strong>in</strong>ation,<br />

which can be applied to various ventilatory or metabolic<br />

variables.<br />

There is only limited <strong>in</strong>formation available <strong>in</strong> the scientific literature<br />

about the comparability <strong>and</strong> repeatability of the methods used


for determ<strong>in</strong>ation of LT. This study was thus designed to test whether<br />

commonly used analysis techniques were reliable <strong>in</strong> both test-retest <strong>and</strong><br />

analysis-to-analysis comparisons.<br />

Methods<br />

A total of 30 swimmers, female (n=15) <strong>and</strong> male (n=15) volunteered <strong>and</strong><br />

gave their consent to serve as subjects (Table 1). Each subject performed<br />

a st<strong>and</strong>ardized pool test of ten 100 meter swims twice <strong>in</strong> a three-day<br />

period (Gullstr<strong>and</strong> & Holmer, 1980). Pace-lights were placed l<strong>in</strong>early<br />

along on the bottom of a 50 meter pool for visually adjust<strong>in</strong>g swimm<strong>in</strong>g<br />

velocity. The <strong>in</strong>itial velocity of the exercise was 0.45 m·s -1 less than the<br />

<strong>in</strong>dividual maximum velocity. Velocity was <strong>in</strong>creased by 0.05 m·s -1 with<br />

each 100 meter swim until the test ended <strong>in</strong> exhaustion. The rest <strong>in</strong>terval<br />

between the 100 meter swims was 90 seconds. Time for the 100 meter<br />

swims, as well as for 50 meter laps were taken by h<strong>and</strong> held watches<br />

to calculate mean velocity. Blood samples (20µl) were taken from the<br />

ear lobe immediately after each swim to obta<strong>in</strong> BLa (Boehr<strong>in</strong>ger-<br />

Mannheim: test-fibel).<br />

Table 1. Physical characteristics of the subjects (mean ± st<strong>and</strong>ard deviation).<br />

Age<br />

(years)<br />

Stature<br />

(m)<br />

Body mass<br />

(kg)<br />

BMI<br />

(kg/m 2 )<br />

T100*<br />

(s)<br />

Pooled (n=30) 16.7 ± 3.3 1.70 ± 0.08 61.8 ± 6.6 21.3 ± 1.1 65.2 ± 5.7<br />

Females (n=15) 17.3 ± 3.7 1.68 ± 0.06 60.7 ± 5.9 21.5 ± 1.0 67.3 ± 4.2<br />

Males (n=15) 16.0 ± 2.7 1.72 ± 0.09 62.8 ± 7.1 21.2 ± 1.1 62.8 ± 6.3<br />

*Time for best personal performance <strong>in</strong> 100 meter freestyle swimm<strong>in</strong>g<br />

Two experienced analysts were used to def<strong>in</strong>e the LT from each test. The<br />

results from the analyses were compared between the two analysts. The<br />

BLa-velocity graphs were plotted, <strong>and</strong> subsequently the four different<br />

approaches were applied to def<strong>in</strong>e the LT. Figure 1 shows an example<br />

on how the determ<strong>in</strong>ation was performed us<strong>in</strong>g the mathematical technique<br />

presented by Cheng et al. (1992). First the BLa-velocity plots<br />

were fitted with 3 rd power polynomial. Then the two ends of the polynomial<br />

were <strong>in</strong>terpolated with a straight l<strong>in</strong>e. F<strong>in</strong>ally, the po<strong>in</strong>t of maximal<br />

distance (D max ) between the straight l<strong>in</strong>e perpendiculars to the polynomial<br />

was calculated. The velocity correspond<strong>in</strong>g to the D max was used as<br />

the LT. The l<strong>in</strong>ear estimation model was used to detect <strong>in</strong>dividual LT so<br />

that two l<strong>in</strong>ear l<strong>in</strong>es were formed. The first l<strong>in</strong>e was parallel to the x-axis<br />

connect<strong>in</strong>g the BLa-velocity plots at low <strong>in</strong>tensities without significant<br />

<strong>in</strong>crease <strong>in</strong> BLa. The second l<strong>in</strong>e was drawn between the rapidly <strong>in</strong>creas<strong>in</strong>g<br />

BLa values <strong>in</strong> the latter part of the exercise neglect<strong>in</strong>g those values at<br />

around the exponential phase of <strong>in</strong>creas<strong>in</strong>g BLa-velocity association. LT<br />

was def<strong>in</strong>ed as the velocity correspond<strong>in</strong>g to the <strong>in</strong>tersection of the two<br />

l<strong>in</strong>es. Third analysis mode was the V 4 as described earlier by Mader et al.<br />

(1978). Fourth analysis was the V correspond<strong>in</strong>g to a 1 mmol·l -1 <strong>in</strong>crease<br />

<strong>in</strong> BLa above the lowest level (V ∆1 ) dur<strong>in</strong>g the exercise.<br />

The mean (± SD) are presented as descriptive statistics. Coefficients<br />

<strong>and</strong> equations of l<strong>in</strong>ear regression were computed between the<br />

parameters. Intraclass correlation coefficients (ICC) were calculated <strong>in</strong><br />

connection with two-way ANOVA to <strong>in</strong>dicate the test-retest reliability.<br />

T-test between paired observations was used to test the statistical significance<br />

of differences (p < 0.05).<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

Figure 1. D max analysis for subject no 26 shows that the velocity at LT<br />

≈ 1.43 m·s -1<br />

results<br />

Test-retest comparison between the measured velocity <strong>in</strong> the two test<br />

sessions demonstrated a very high repeatability (y = 1.0023x + 0.0035,<br />

R 2 0.994) be<strong>in</strong>g near to equal between the test sessions. Test-retest reliability<br />

for BLa was also very high (y = 0.9913x + 0.1365, R 2 0.909). The<br />

swimmers’ ability to follow the pace-lights were very high (y = 0.9603x +<br />

0.0519, R 2 0.987). Inter-rater reliability was very high <strong>in</strong> three of the four<br />

analyses (D max , V 4 <strong>and</strong> V ∆1 ) where the LT was detected automatically.<br />

L<strong>in</strong>ear estimation technique repeated the LT values with >99% accuracy.<br />

Thus, mean values were calculated only for the l<strong>in</strong>ear estimation method.<br />

Test-retest comparison <strong>in</strong> D max analysis demonstrated a very high<br />

reliability as shown by Figure 2. However the same was true for the rest<br />

of the analysis methods also. The closest association between different<br />

analysis techniques was found <strong>in</strong> D max versus l<strong>in</strong>ear estimation as shown<br />

by Figure 3. Less consistent results as shown by Table 2 were obta<strong>in</strong>ed<br />

between D max <strong>and</strong> V 4 , <strong>and</strong> D max <strong>and</strong> V ∆1 relations as well as <strong>in</strong> l<strong>in</strong>ear<br />

estimation <strong>and</strong> V 4 <strong>and</strong> D max <strong>and</strong> V ∆1 comparisons. The relationship between<br />

V 4 <strong>and</strong> V ∆1 was high even though the velocities were significantly<br />

higher <strong>in</strong> V 4 as expected.<br />

Table 2. The associations between the analysis methods (slope, <strong>in</strong>tercept,<br />

R2 ).<br />

Slope Intercept R2 <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g<br />

Dmax <strong>and</strong> l<strong>in</strong>ear estimation 0.9902 + 0.0153 0.928***<br />

Dmax Dmax <strong>and</strong> Vl<strong>in</strong>ear 4 estimation 0.9902 0.7094 + 0.0153 + 0.4005 0.928*** 0.802***<br />

Dmax D <strong>and</strong> V4<br />

max <strong>and</strong> V∆1 Dmax <strong>and</strong> VΔ1<br />

V4 V4 <strong>and</strong> l<strong>in</strong>ear estimation<br />

0.7094 0.6632<br />

0.6632<br />

1.1396 1.1396<br />

+ 0.4005 + 0.3832 0.802*** 0.712***<br />

+ 0.3832 0.712***<br />

− 0.2012 − 0.2012 0.771*** 0.771***<br />

V4 V4 <strong>and</strong> VΔ1 V∆1 VΔ1 <strong>and</strong> l<strong>in</strong>ear estimation<br />

*** V∆1 <strong>and</strong> p


Figure 2. Repeatability of the LT<strong>in</strong>d by Dmax analysis <strong>in</strong> two 10·100 meter swims.<br />

<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

reFerences<br />

Cheng, B., Kuipers H., Snyder A.C., Keizer H.A., Jeukendrup A. &<br />

Hessel<strong>in</strong>k M. (1992). A new approach for the determ<strong>in</strong>ation of ventilatory<br />

<strong>and</strong> lactate threshold. Int J Sports Med, 13, 518-522.<br />

Goodw<strong>in</strong>, M.L., Harris, J.E., Hernándes, A. & Gladden, L.B. (2007).<br />

Blood lactate measurements <strong>and</strong> analysis dur<strong>in</strong>g exercise: a guide for<br />

cl<strong>in</strong>icians. J Diabetes Sci Tech, 1(4), 558-69.<br />

Kesk<strong>in</strong>en, K.L., Komi, P.V. & Rusko, H. (1987). A comparative study<br />

of blood lactate tests <strong>in</strong> swimm<strong>in</strong>g. Int J Sports Med, 10(3), 197201.<br />

Gullstr<strong>and</strong>, L. & Holmer, I. (1980) Fysiologiska tester av l<strong>and</strong>slagssimmare:<br />

Anaerob energi-leveransmätn<strong>in</strong>gen av blodmjölksyra [Physiological<br />

tests for national team swimmers: Measurement of anaerobic<br />

Figure 3. Comparison between Dmax <strong>and</strong> l<strong>in</strong>ear estimation methods <strong>in</strong> energy metabolism by blood lactate] Simsport, 3, 1517.<br />

Figure def<strong>in</strong><strong>in</strong>g 3. LT. Comparison between Dmax <strong>and</strong> l<strong>in</strong>ear estimation methods <strong>in</strong> Mader, def<strong>in</strong><strong>in</strong>g A., LT. Heck, H. & Hollmann, W. (1978). Evaluation of lactic acid<br />

anaerobic energy contribution by determ<strong>in</strong>ation of post-exercise lac-<br />

DISCUSSION<br />

dIscussIon<br />

tic acid concentration of ear capillary blood <strong>in</strong> middle-distance run-<br />

The present study was designed to to test test whether whether the the four four analysis analysis tech- techniques ners would <strong>and</strong> swimmers. show In: L<strong>and</strong>ry F. & Orban W.A.R., Exercise Physiol-<br />

results niques would reliably show <strong>in</strong> results both reliably test-retest <strong>in</strong> both <strong>and</strong> test-retest analysis-to-analysis <strong>and</strong> analysis-to- comparisons. ogy, 4, The 187200. major Symposia specialists, Miami, Florida.<br />

f<strong>in</strong>d<strong>in</strong>g analysis was comparisons. that the n·100-m The major pool f<strong>in</strong>d<strong>in</strong>g test<strong>in</strong>g was protocol that the (Gullstr<strong>and</strong> n·100-m pool & Holmer, Pyne, 1980) D.B., Lee can H. be & Swanwick K.M. (2001). Monitor<strong>in</strong>g the lactate<br />

repeated test<strong>in</strong>g protocol with a (Gullstr<strong>and</strong> very high & reliability, Holmer, 1980) thus confirm<strong>in</strong>g can be repeated the with hypothesis. a This threshold is the <strong>in</strong> world most ranked swimmers. Med Sci Sports Exerc, 33(2), 291<br />

important very high reliability, determ<strong>in</strong>ant thus for confirm<strong>in</strong>g successful the hypothesis. test<strong>in</strong>g <strong>and</strong> This fulfills is the most the basic – requirement 297. of<br />

reliable measurement. As shown by Pyne et al. (2001), st<strong>and</strong>ardized Simon, blood G., Thiesmann, lactate M., Clas<strong>in</strong>g, D. & Frohberger, V. (1982). Ergometrie<br />

im Wasser - e<strong>in</strong>e neue Methode der Leistungsdiagnostik<br />

[Ergometry <strong>in</strong> water – a new method for performance evaluation]. In:<br />

Sport: Leistung und Gesundheit, 1, 38-43. Köln, BRD.<br />

Stegmann, H., K<strong>in</strong>dermann, W. & Schnabel, A. (1981). A lactate k<strong>in</strong>etics<br />

<strong>and</strong> <strong>in</strong>dividual anaerobic threshold. Int J Sports Med, 2, 160 – 165.<br />

Svedahl, K. & MacIntosh, B.R. (2003). Anaerobic threshold: the concept<br />

<strong>and</strong> methods of measurement. Can J Appl Physiol, 28, 299 – 323.<br />

important determ<strong>in</strong>ant for successful test<strong>in</strong>g <strong>and</strong> fulfills the basic requirement<br />

of reliable measurement. As shown by Pyne et al. (2001),<br />

st<strong>and</strong>ardized blood lactate test<strong>in</strong>g can be used successfully <strong>in</strong> monitor<strong>in</strong>g<br />

changes <strong>in</strong> swimm<strong>in</strong>g performance over a tra<strong>in</strong><strong>in</strong>g year. The strength<br />

of our study was that the swimm<strong>in</strong>g velocity was accurately controlled<br />

with pace-lights. In turn<strong>in</strong>g the swimmers were advised to regulate their<br />

speed dur<strong>in</strong>g the push-off from the turn<strong>in</strong>g wall.<br />

The second requirement for reliable test<strong>in</strong>g is that the test results can<br />

be analyzed objectively. Our two experienced analysts showed identical<br />

results <strong>in</strong> three out of four methods (D max , V 4 <strong>and</strong> V ∆1 ), which constitutes<br />

the reliability of these <strong>in</strong>vestigations. L<strong>in</strong>ear estimation which required<br />

visual <strong>in</strong>spection <strong>and</strong> a subjective decision, revealed a smaller degree of<br />

reliability although the reliability still was significant <strong>and</strong> very high. It is<br />

therefore suggested that mathematical h<strong>and</strong>l<strong>in</strong>g of the analysis should be<br />

preferred to keep subjective <strong>in</strong>fluence to a m<strong>in</strong>imum. The analysis method<br />

suggested by Cheng et al. (1992) seems to be the method of choice when<br />

determ<strong>in</strong><strong>in</strong>g LT from the BLa-velocity association.<br />

F<strong>in</strong>ally, for the test to be applicable to regular tra<strong>in</strong><strong>in</strong>g practice<br />

it must also be valid. Previously Kesk<strong>in</strong>en et al. (1987) observed that<br />

the n·100 meter test (Gullstr<strong>and</strong> & Holmer, 1980) could be compared<br />

to both the n·300 meter (Simon et al. 1982) <strong>and</strong> the 2·400 meter test<br />

(Mader et al., 1978). Kesk<strong>in</strong>en et al. (1987) found that when compared<br />

with the V 4 of the 2∙400 meter test the same velocity <strong>in</strong> the n∙100 meter<br />

test was found at 0.5 mmol·l -1 <strong>in</strong>crease <strong>in</strong> blood lactate above the <strong>in</strong>itial<br />

lowest level. Similar velocity was found <strong>in</strong> the n∙300 meter test at 1.5<br />

mmol·l -1 <strong>in</strong>crease <strong>in</strong> blood lactate above the basic level.<br />

The present results showed that the LT as analyzed by both D max<br />

<strong>and</strong> l<strong>in</strong>ear estimation techniques corresponded well between each other,<br />

but there were significant differences to both V 4 <strong>and</strong> V ∆1 . Conclusively,<br />

even though the determ<strong>in</strong>ation of LT can be done similarly <strong>in</strong> various<br />

test<strong>in</strong>g protocols, each protocol has its own dist<strong>in</strong>ctives to be taken<br />

<strong>in</strong>to account. Cautiousness must therefore be practiced when exercise<br />

prescription is applied to athletes. Both over- <strong>and</strong> under-estimation of<br />

tra<strong>in</strong><strong>in</strong>g speeds may deteriorate balanced development of the athlete.<br />

conclusIons<br />

It is concluded that the test-retest reliability of the n·100 meter swimm<strong>in</strong>g<br />

test was high <strong>in</strong>dicat<strong>in</strong>g that the method itself was repeatable <strong>and</strong><br />

is a useful means of monitor<strong>in</strong>g changes <strong>in</strong> <strong>in</strong>dicators of physical fitness<br />

<strong>in</strong> swimm<strong>in</strong>g. Also, the analyses offered reliable results which can be<br />

used for prescription of tra<strong>in</strong><strong>in</strong>g. From the analysis-to-analysis comparisons<br />

the necessity to underst<strong>and</strong> their specific characters must be emphasized.<br />

The orig<strong>in</strong>al speed at which the LT appear depends specifically<br />

on the protocol be<strong>in</strong>g used.<br />

266<br />

AcKnoWledGeMents<br />

We greatly acknowledge the swimmers <strong>and</strong> coaches who participated <strong>in</strong><br />

perform<strong>in</strong>g this study. We also want to thank the parents of the swimmers<br />

who gave their support to the research team. The personnel of the<br />

Aalto Alvari Swimm<strong>in</strong>g facility provided proper work conditions to run<br />

the experiments.


Competitive Systematization <strong>in</strong> Age-group<br />

Swimm<strong>in</strong>g: An Evaluation of Performances,<br />

Maturational Considerations, <strong>and</strong> International<br />

Paradigms<br />

Kojima, K. 1 <strong>and</strong> stager, J.M. 1<br />

1 Indiana University, USA<br />

The most appropriate method for group<strong>in</strong>g youth swimmers to assure<br />

fair competition has been debated for decades with little progress be<strong>in</strong>g<br />

made. The present study evaluates the age classification utilized at the<br />

2 nd FINA World Youth Swimm<strong>in</strong>g Championships <strong>and</strong> those used by<br />

swimm<strong>in</strong>g federations around the world. Our results illustrate a greater<br />

proportion of older participants <strong>and</strong> older f<strong>in</strong>alists at the <strong>in</strong>ternational<br />

event. No universal age-group<strong>in</strong>g system is evident among the various<br />

swimm<strong>in</strong>g federations. We conclude that most age-group<strong>in</strong>g systems,<br />

particularly those us<strong>in</strong>g a multi-age group paradigm, unduly <strong>in</strong>fluence<br />

participation <strong>and</strong> bias competition outcomes. More effective agegroup<strong>in</strong>gs<br />

are hypothesized. From these research f<strong>in</strong>d<strong>in</strong>gs, cont<strong>in</strong>ued<br />

<strong>in</strong>ternational discussion on this topic appears to be warranted.<br />

Key words: youth swimm<strong>in</strong>g, age classification, growth <strong>and</strong> maturation,<br />

fairness <strong>in</strong> competition<br />

IntroductIon<br />

Competitive youth swimmers are commonly separated by sex <strong>and</strong> then<br />

stratified <strong>in</strong>to competitive groups based on chronological age (CA). This<br />

is done regardless of the differences <strong>in</strong> maturational tim<strong>in</strong>g <strong>and</strong> tempo<br />

or physical size among the swimmers that may exist with<strong>in</strong> a given CA<br />

(Mal<strong>in</strong>a et al., 2004). Implement<strong>in</strong>g maturation- or size-based assessments<br />

for a more fair group<strong>in</strong>g system is not logistically practicable.<br />

Such assessments are complex, costly, <strong>in</strong>vasive, potentially unsafe, <strong>and</strong> at<br />

times, unreliable. However, given the variation <strong>in</strong> maturity status with<strong>in</strong><br />

a s<strong>in</strong>gle CA, collaps<strong>in</strong>g CAs <strong>in</strong>to multi-age categories does not assure<br />

competitive fairness <strong>and</strong> equity. Kojima et al. (2009) demonstrated the<br />

age-related differences <strong>in</strong> swim performance of the top 100 U.S. swimmers<br />

<strong>and</strong> confirmed the hypothesis that younger swimmers with<strong>in</strong> the<br />

st<strong>and</strong>ard multi-age-groups used by USA Swimm<strong>in</strong>g are competitively<br />

disadvantaged. Whether or not this is true at the <strong>in</strong>ternational level of<br />

competition rema<strong>in</strong>s to be determ<strong>in</strong>ed.<br />

With the <strong>in</strong>tention of provid<strong>in</strong>g future World <strong>and</strong> Olympic level<br />

athletes with greater competitive <strong>and</strong> more <strong>in</strong>tercultural experiences,<br />

the Fédération Internationale de Natation (FINA) hosted the second<br />

edition of the FINA World Youth Swimm<strong>in</strong>g Championships <strong>in</strong> July,<br />

2008. Only one age-group was provided for each sex, comb<strong>in</strong><strong>in</strong>g 14-17<br />

year-old girls <strong>and</strong> 15-18 year-old boys at the Youth Championships.<br />

However, consider<strong>in</strong>g the magnitude of our recent f<strong>in</strong>d<strong>in</strong>gs (Kojima et<br />

al., 2009), it was hypothesized that older swimmers with<strong>in</strong> the multiage-groups<br />

might represent the majority (or at least a greater proportion)<br />

of the f<strong>in</strong>alists at this event. Furthermore, the age-group<strong>in</strong>g system<br />

that comb<strong>in</strong>ed four CAs <strong>in</strong>to a s<strong>in</strong>gle group is likely to have resulted <strong>in</strong><br />

age-related (also potentially maturation-based) competitive outcomes<br />

which might differ <strong>in</strong> the girls as compared to the boys. The goals of<br />

this study were 1) to evaluate the appropriateness of the age-groups at<br />

the 2nd FINA World Youth Swimm<strong>in</strong>g Championships <strong>and</strong> 2) to discuss<br />

age-group<strong>in</strong>g systems used by countries <strong>in</strong> the world as a means of<br />

ga<strong>in</strong><strong>in</strong>g a better <strong>in</strong>sight <strong>in</strong>to the most appropriate age-group stratification<br />

paradigm.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

Methods<br />

The 2nd FINA World Youth Swimm<strong>in</strong>g Championships: All data (i.e., meet<br />

results) were acquired from the official website of FINA (www.f<strong>in</strong>a.org).<br />

The s<strong>in</strong>gle age-group<strong>in</strong>g for each sex was composed of four CAs (ages<br />

14-17 years for girls <strong>and</strong> ages 15-18 for boys). The Championships<br />

<strong>in</strong>cluded 17 <strong>in</strong>dividual events for both sexes: 50-, 100-, 200-, 400-, 800-,<br />

<strong>and</strong> 1500-m freestyle, 50-, 100-, <strong>and</strong> 200-m backstroke, breaststroke,<br />

<strong>and</strong> butterfly, <strong>and</strong> 200- <strong>and</strong> 400-m <strong>in</strong>dividual medley. In addition, there<br />

were three relays: 400- <strong>and</strong> 800-m freestyle relays <strong>and</strong> 400-m medley<br />

relay. To <strong>in</strong>vestigate the <strong>in</strong>fluence of the age-group<strong>in</strong>gs on the swimmers<br />

qualify<strong>in</strong>g for prelim<strong>in</strong>aries <strong>and</strong> f<strong>in</strong>als, a frequency distribution of<br />

all competitors <strong>and</strong> the top 8 f<strong>in</strong>ishers <strong>in</strong> the 17 events was exam<strong>in</strong>ed<br />

for each of the four CAs. A relative frequency distribution of all competitors<br />

<strong>and</strong> f<strong>in</strong>alists was calculated <strong>and</strong> averaged over the 17 events. To<br />

exam<strong>in</strong>e the <strong>in</strong>fluence of the age-group<strong>in</strong>gs on ‘chance of participation’<br />

<strong>in</strong> the Youth Championships <strong>and</strong> selection at the trials of each country,<br />

the relative frequency distribution of relay members of the top 8<br />

countries was exam<strong>in</strong>ed. All data were analyzed us<strong>in</strong>g PASW Statistics<br />

17.0 (SPSS <strong>in</strong>c., Chicago, Ill<strong>in</strong>ois). Chi-square tests were performed<br />

to determ<strong>in</strong>e whether or not there was a significant difference between<br />

the expected frequencies (a quarter of the total frequency for age) <strong>and</strong><br />

the observed frequencies with<strong>in</strong> the age-groups. One-way analysis of<br />

variance (ANOVA) with Tukey’s post-hoc test <strong>and</strong> Pearson product<br />

moment correlation coefficients were also used to test the research hypotheses.<br />

The level of significance was set at p < 0.05.<br />

International age-group<strong>in</strong>g systems: Information regard<strong>in</strong>g age-group<strong>in</strong>g<br />

systems of FINA swimm<strong>in</strong>g federations was collected from the website<br />

of each national federation. The follow<strong>in</strong>g countries were selected for<br />

this study due to the lack of a common language: Australia, Brita<strong>in</strong>,<br />

Canada, Ch<strong>in</strong>a (Hong Kong & Macau), Germany, Japan, New Zeal<strong>and</strong>,<br />

Spa<strong>in</strong>, Taiwan, <strong>and</strong> the USA. Phone correspondence was also made<br />

to obta<strong>in</strong> more details of each federation’s rationale <strong>and</strong> <strong>in</strong>tent <strong>in</strong> their<br />

age-group<strong>in</strong>g systems.<br />

results<br />

The 2nd FINA World Youth Swimm<strong>in</strong>g Championships: The total number<br />

of swims <strong>in</strong> the 17 <strong>in</strong>dividual events was 754 for the girls <strong>and</strong> 943<br />

for the boys. When expressed by age categories, <strong>in</strong> girls there were 66<br />

swims (8.8%) by fourteen year olds, 148 (19.6%) by fifteen year olds, 218<br />

(28.9%) by sixteen year olds, <strong>and</strong> 322 (42.7%) by seventeen year olds. In<br />

boys, there were 46 swims (4.9%) by fifteen year olds, 152 (16.1%) by<br />

sixteen year olds, 259 (27.5%) by seventeen year olds, <strong>and</strong> 486 (51.5%)<br />

by eighteen year olds. A significant difference was found between the<br />

observed <strong>and</strong> expected values <strong>in</strong> both sexes, <strong>in</strong>dicat<strong>in</strong>g an uneven distribution<br />

of swims across age categories.<br />

Figures 1 <strong>and</strong> 2 illustrate the relative frequency distributions (%) of<br />

the top 8 swimmers over the 17 events <strong>and</strong> relay members of the top 8<br />

countries. Significant differences <strong>in</strong> the mean relative frequency among<br />

CAs were found <strong>in</strong> both sexes (Table 1). The oldest CA <strong>in</strong> both sexes<br />

(age 17 for girls <strong>and</strong> age 18 for boys) had a significantly greater proportion<br />

compared with all other age categories. The younger CAs had fewer<br />

swims <strong>in</strong> the f<strong>in</strong>als <strong>and</strong> represented a smaller proportion of the total distribution.<br />

The age-related differences were more evident <strong>in</strong> boys. There<br />

was only one 15-year-old f<strong>in</strong>alist (100-m butterfly) <strong>in</strong> boys, <strong>and</strong> he was<br />

the only swimmer under the age of 17 who competed <strong>in</strong> a relay f<strong>in</strong>al.<br />

267


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Proportion of swimmers<br />

Proportion of swimmers<br />

268<br />

100%<br />

90%<br />

80%<br />

70%<br />

60%<br />

50%<br />

40%<br />

30%<br />

20%<br />

10%<br />

0%<br />

100%<br />

90%<br />

80%<br />

70%<br />

60%<br />

50%<br />

40%<br />

30%<br />

20%<br />

10%<br />

0%<br />

Girls<br />

1st 2nd 3rd 4th 5th 6th 7th 8th Total<br />

Place at f<strong>in</strong>als<br />

Boys<br />

1st 2nd 3rd 4th 5th 6th 7th 8th Total<br />

Place at F<strong>in</strong>als<br />

age 14<br />

age 15<br />

age 16<br />

age 17<br />

age 15<br />

age 16<br />

age 17<br />

age 18<br />

Figure 1. The relative frequency distributions (%) of the top 8 swimmers<br />

(1 st –8 th ) <strong>and</strong> the total swims <strong>in</strong> f<strong>in</strong>als (Total, N = 136) over 17 events for<br />

the four age categories.<br />

Proportion of swimmers<br />

Proportion of swimmers<br />

100%<br />

90%<br />

80%<br />

70%<br />

60%<br />

50%<br />

40%<br />

30%<br />

20%<br />

10%<br />

0%<br />

100%<br />

90%<br />

80%<br />

70%<br />

60%<br />

50%<br />

40%<br />

30%<br />

20%<br />

10%<br />

0%<br />

Girls<br />

400-m MR 400-m FR 800-m FR Total<br />

Boys<br />

400-m MR 400-m FR 800-m FR Total<br />

14 yrs<br />

15 yrs<br />

16 yrs<br />

17 yrs<br />

15 yrs<br />

16 yrs<br />

17 yrs<br />

18 yrs<br />

Figure 2. The relative frequency distributions (%) of the top 8 relay<br />

members <strong>and</strong> the total f<strong>in</strong>alists of three relays (Total, N = 96) for the<br />

four age categories.<br />

MR, medley relay; FR, freestyle relay<br />

Table 1. Mean relative frequency distributions (%) of the top 8 swimmers<br />

<strong>and</strong> the top 8 relay members over all events for the four age categories.<br />

Girls Boys<br />

Age (yrs) Age (yrs)<br />

17 47.8 ± 14.2 ‡ 55.2 ± 6.5 ‡ 18 64.7 ± 8.9 ‡ 74.0 ± 7.9 ‡<br />

16 31.6 ± 10.9 ‡ 26.0 ± 9.0 ¶ 17 27.2 ± 6.2 ‡ 25.0 ± 8.3 ‡<br />

15 11.8 ± 7.0 † 13.5 ± 4.8 * 16 7.4 ± 8.8 † 0 ± 0 †<br />

14 8.8 ± 19.0 † 5.2 ± 6.5 † 15 0.7 ± 2.1 † 1.0 ± 1.8 †<br />

IE f<strong>in</strong>alists Relay members IE f<strong>in</strong>alists Relay members<br />

IE, <strong>in</strong>dividual event<br />

‡ Significantly different from all other age categories (p < 0.05).<br />

† Significantly different from two oldest age categories (p < 0.05).<br />

¶ Significantly different from the youngest <strong>and</strong> oldest age categories<br />

(p < 0.05).<br />

* Significantly different from the oldest age category (p < 0.05).<br />

To <strong>in</strong>vestigate the chance to advance to the f<strong>in</strong>als <strong>and</strong> therefore to score,<br />

i.e., chance of success, for swimmers <strong>in</strong> each CA category, the ratio of the<br />

number of top 8 swimmers to total competitors <strong>in</strong> each event was exam<strong>in</strong>ed<br />

(Table 2). No significant difference <strong>in</strong> the mean ratio for the 17 <strong>in</strong>dividual<br />

events among CAs was found <strong>in</strong> girls, while the mean ratio <strong>in</strong> boys<br />

was significantly different (p < 0.01) <strong>and</strong> related to age (r = 0.59, p < 0.01).<br />

Table 2. The mean ratio of the number of f<strong>in</strong>alists to the total competitors<br />

over 17 events by age category.<br />

Girls Boys<br />

Age (yrs) Mean ratio Age (yrs) Mean ratio<br />

17 0.21 ± 0.10 18 0.20 ± 0.06 ‡<br />

16 0.21 ± 0.14 17 0.16 ± 0.07 †<br />

15 0.11 ± 0.11 16 0.08 ± 0.11<br />

14 0.16 ± 0.18 15 0.03 ± 0.12<br />

‡ Significantly different from the two youngest age categories (p < 0.05)<br />

† Significantly different from the youngest age category (p < 0.05)<br />

dIscussIon<br />

The hypothesis that older swimmers with<strong>in</strong> the designated age-groups represent<br />

the majority of swims <strong>in</strong> the f<strong>in</strong>als <strong>and</strong> that of competition at large<br />

was supported by the analyses. There were a greater number of older participants<br />

<strong>and</strong> f<strong>in</strong>alists <strong>in</strong> both sexes. Furthermore, the odds of advanc<strong>in</strong>g to<br />

the f<strong>in</strong>als for boys were significantly greater for the oldest swimmers at the<br />

Championships. By comb<strong>in</strong><strong>in</strong>g four ages <strong>in</strong>to a s<strong>in</strong>gle competitive cohort,<br />

participation was <strong>in</strong>fluenced <strong>and</strong> thus performance outcomes at the FINA<br />

Youth Championships were nearly predeterm<strong>in</strong>ed. Although “fairness” was<br />

not a goal at this <strong>in</strong>ternational event, the age-group<strong>in</strong>g system employed did<br />

not provide the younger swimmers with<strong>in</strong> age-groups with an equal chance<br />

of experienc<strong>in</strong>g a higher level of competition or any competitive success.<br />

Age-related variations <strong>in</strong> physiological parameters related to sports<br />

performance dur<strong>in</strong>g adolescence are well documented (Mal<strong>in</strong>a et al.,<br />

2004). These variations are attributable ma<strong>in</strong>ly to maturity status <strong>and</strong><br />

size differences (e.g., limb length, height, <strong>and</strong> muscle mass) <strong>and</strong> become<br />

more apparent dur<strong>in</strong>g <strong>and</strong> after the growth spurt, especially <strong>in</strong> boys. One<br />

marker of maturation is the age at peak height velocity (PHV: on average,<br />

age 12 <strong>in</strong> girls <strong>and</strong> age 14 <strong>in</strong> boys). Regard<strong>in</strong>g swim performance data,<br />

Pelayo et al. (1997) reported age-related differences <strong>in</strong> the performance<br />

of non-skilled students aged 11 to 17 years. Also, Kojima et al. (2009)<br />

recently demonstrated age-related differences <strong>in</strong> the swim times of the top<br />

100 U.S. swimmers from age 5 to 20 years. Both studies found significant<br />

differences <strong>in</strong> swim performance between 14- <strong>and</strong> 17-year-old girls, while<br />

swim performance of boys <strong>in</strong> 15 to 17 year-old categories was significantly<br />

different from each other. In each case, younger swimmers were slower<br />

than older swimmers. Girls reach a po<strong>in</strong>t where age (<strong>and</strong> maturity) is less<br />

of an issue about two years earlier than boys.<br />

In the present study, younger swimmers typically placed lower than<br />

older swimmers (Figure 1). N<strong>in</strong>e 14 <strong>and</strong> 15 year-old girls (out of 51,


17%) f<strong>in</strong>ished with<strong>in</strong> the top 3 <strong>in</strong> any of the 17 events. In the boys, no<br />

15 or 16-year-olds f<strong>in</strong>ished <strong>in</strong> the top 3, <strong>and</strong> only ten 16-year-olds f<strong>in</strong>ished<br />

<strong>in</strong> the 4-8 th places. There was only one 15-year-old f<strong>in</strong>alist, <strong>and</strong> he<br />

f<strong>in</strong>ished 8 th <strong>in</strong> his event. This might lead to the conclusion that age (<strong>and</strong><br />

thus maturation) might be more important among boys than among<br />

girls, at least <strong>in</strong> this age range.<br />

With<strong>in</strong> the relays, the majority of the f<strong>in</strong>alists (81.2% <strong>in</strong> girls <strong>and</strong><br />

99.0% <strong>and</strong> <strong>in</strong> boys) were swimmers <strong>in</strong> the two oldest age categories<br />

(Figure 2 <strong>and</strong> Table 1). Moreover, the mean ratio of chance to advance<br />

to the f<strong>in</strong>als over 17 events is presented by age categories <strong>in</strong> Table 2<br />

(note that the ratio does not reflect the absolute number of swimmers,<br />

rather, swims). Significant differences <strong>in</strong> the ratios among CAs were revealed<br />

<strong>in</strong> the boys, while there was no significant difference <strong>in</strong> girls. This<br />

<strong>in</strong>dicated that the age-group<strong>in</strong>g systems comb<strong>in</strong><strong>in</strong>g plural ages together<br />

would clearly <strong>in</strong>fluence competition <strong>and</strong> the chance of success, especially<br />

<strong>in</strong> boys due <strong>in</strong> part to their greatly varied maturational nature among<br />

these CAs. The data perta<strong>in</strong><strong>in</strong>g to the girls (similar ratios) imply that<br />

the difference <strong>in</strong> the number of f<strong>in</strong>alists among CAs might possibly be<br />

reduced if the number of participants at each CA was equal.<br />

International age-group<strong>in</strong>g systems: Accord<strong>in</strong>g to FINA, each national<br />

federation is allowed to adopt their own competitive age-group<strong>in</strong>gs.<br />

Thus, there are a wide variety of age-group<strong>in</strong>g systems <strong>in</strong> swimm<strong>in</strong>g<br />

currently <strong>in</strong> use around the world (Table 3). Each of the ten countries<br />

exam<strong>in</strong>ed <strong>in</strong> this study uses a different system to classify swimmers, from<br />

as few as four to as many as eight age-groups. Some federations adopt<br />

sex-specific age-groups where CAs <strong>in</strong> the girls are pooled <strong>in</strong> a different<br />

manner from the boys. Others provide the same age-groups for both<br />

sexes. Brita<strong>in</strong> <strong>and</strong> Japan use s<strong>in</strong>gle-age-based qualification times for national<br />

youth championships, although some age categories are comb<strong>in</strong>ed<br />

<strong>in</strong>to competitive groups for the actual competition. Ch<strong>in</strong>a <strong>and</strong> USA<br />

entrust age-group<strong>in</strong>g systems <strong>and</strong> rules to each prov<strong>in</strong>cial swimm<strong>in</strong>g association<br />

or local swimm<strong>in</strong>g committee, so there may not be a common<br />

age-group<strong>in</strong>g system across these countries.<br />

Table <strong>Biomechanics</strong> 3. Age-group<strong>in</strong>g <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> systems Swimm<strong>in</strong>g <strong>in</strong> <strong>XI</strong> representative / Chapter 4 Tra<strong>in</strong><strong>in</strong>g swimm<strong>in</strong>g countries Page 71<br />

(federations).<br />

Table 3. Age-group<strong>in</strong>g systems <strong>in</strong> representative swimm<strong>in</strong>g countries (federations).<br />

Country Sex < 8 9 10 11 12 13 14 15 16 17 18 19 < 20 Σ<br />

Australia unisex � � � � � 5<br />

Brita<strong>in</strong><br />

Canada<br />

Girls � � � � � 5<br />

Boys � � � � � � 6<br />

QT � � � � � � � � 8<br />

Girls � � � � � 5<br />

Boys � � � � � 5<br />

Ch<strong>in</strong>a* unisex � � � � � 5<br />

Hong Kong unisex � � � � 4<br />

Macau unisex � � � � � � � 6<br />

Germany<br />

Japan<br />

Girls � � � � � � 6<br />

Boys � � � � � � 6<br />

unisex � � � � 4<br />

QT � � � � � � � � � � 10<br />

New Zeal<strong>and</strong> unisex � � � � � � � � 8<br />

Spa<strong>in</strong><br />

Girls � � � � � � 6<br />

Boys � � � � � 5<br />

Taiwan unisex � � � � 4<br />

USA* unisex � � � � 4<br />

Unisex, the same age-groups are adopted for girls <strong>and</strong> boys; QT, qualification time<br />

for national or state youth (age-group) championships; Σ, total age-groups; *Agegroup<strong>in</strong>g<br />

systems differ among local swimm<strong>in</strong>g committees or prov<strong>in</strong>cial swimm<strong>in</strong>g<br />

associations.<br />

Unisex, the same age-groups are adopted for girls <strong>and</strong> boys; QT, qualification<br />

time for national or state youth (age-group) championships; Σ,<br />

total age-groups; *Age-group<strong>in</strong>g systems differ among local swimm<strong>in</strong>g<br />

committees or prov<strong>in</strong>cial swimm<strong>in</strong>g associations.<br />

The fact that FINA does not stipulate particular rules for age-group<strong>in</strong>g provides notable<br />

characteristics of age-group<strong>in</strong>g systems among federations, such as 1) the number of<br />

age-groups, 2) sex-dependent or <strong>in</strong>dependent groups, 3) s<strong>in</strong>gle-age-based qualification<br />

times regardless of age-groups, <strong>and</strong> 4) local/prov<strong>in</strong>cial organization-determ<strong>in</strong>ed<br />

systems. These are conceivably derived as a means of re<strong>in</strong>forcement <strong>and</strong> enlivenment<br />

of youth swimmers. For <strong>in</strong>stance, comb<strong>in</strong><strong>in</strong>g multi-ages <strong>in</strong>to groups appears to be an<br />

attempt to provide a higher competitive field for swimmers although the multi-agegroup<strong>in</strong>g<br />

reduces the chance of success for younger swimmers with<strong>in</strong> age-groups.<br />

Moreover, s<strong>in</strong>ce girls, on average, reach maturity sooner than boys, <strong>and</strong> therefore<br />

potentially have less variation <strong>in</strong> sports performance among older <strong>in</strong>dividuals (Mal<strong>in</strong>a et<br />

al., 2004), they could be classified <strong>in</strong>to a multi-age-group at an earlier age than boys.<br />

Us<strong>in</strong>g multi-age classification addresses the issue of younger swimmers be<strong>in</strong>g<br />

discouraged until they “age up.” It is not uncommon for young swimmers to term<strong>in</strong>ate<br />

their competitive swimm<strong>in</strong>g careers when they move up to older multi-age-groups: thus<br />

be<strong>in</strong>g at the “bottom of their age-group,” where they feel they can no longer compete<br />

successfully. This co<strong>in</strong>cides with a greater time dem<strong>and</strong> for academics <strong>and</strong> schoolwork.<br />

Lack of success at higher levels of competition causes swimmers to reevaluate their<br />

The fact that FINA does not stipulate particular rules for age-group<strong>in</strong>g<br />

provides notable characteristics of age-group<strong>in</strong>g systems among federations,<br />

such as 1) the number of age-groups, 2) sex-dependent or <strong>in</strong>dependent<br />

groups, 3) s<strong>in</strong>gle-age-based qualification times regardless of age-<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

groups, <strong>and</strong> 4) local/prov<strong>in</strong>cial organization-determ<strong>in</strong>ed systems. These<br />

are conceivably derived as a means of re<strong>in</strong>forcement <strong>and</strong> enlivenment of<br />

youth swimmers. For <strong>in</strong>stance, comb<strong>in</strong><strong>in</strong>g multi-ages <strong>in</strong>to groups appears<br />

to be an attempt to provide a higher competitive field for swimmers although<br />

the multi-age-group<strong>in</strong>g reduces the chance of success for younger<br />

swimmers with<strong>in</strong> age-groups. Moreover, s<strong>in</strong>ce girls, on average, reach<br />

maturity sooner than boys, <strong>and</strong> therefore potentially have less variation<br />

<strong>in</strong> sports performance among older <strong>in</strong>dividuals (Mal<strong>in</strong>a et al., 2004), they<br />

could be classified <strong>in</strong>to a multi-age-group at an earlier age than boys.<br />

Us<strong>in</strong>g multi-age classification addresses the issue of younger swimmers<br />

be<strong>in</strong>g discouraged until they “age up.” It is not uncommon for young<br />

swimmers to term<strong>in</strong>ate their competitive swimm<strong>in</strong>g careers when they<br />

move up to older multi-age-groups: thus be<strong>in</strong>g at the “bottom of their agegroup,”<br />

where they feel they can no longer compete successfully. This co<strong>in</strong>cides<br />

with a greater time dem<strong>and</strong> for academics <strong>and</strong> schoolwork. Lack of<br />

success at higher levels of competition causes swimmers to reevaluate their<br />

<strong>in</strong>terests. In light of these logistic <strong>and</strong> maturational factors, Kojima et al.<br />

(2009) have suggested an alternative age-group<strong>in</strong>g system: 1) us<strong>in</strong>g s<strong>in</strong>gle<br />

CA category (at least, up to age 14 years <strong>in</strong> girls <strong>and</strong> 16 years <strong>in</strong> boys), 2)<br />

sex-dependent group<strong>in</strong>gs, <strong>and</strong> 3) a s<strong>in</strong>gle unisex group for girls <strong>and</strong> boys<br />

aged 7 years <strong>and</strong> under. These ideas may not address all <strong>in</strong>herent issues of<br />

group<strong>in</strong>g adolescent swimmers by CA, but may better ensure fairness <strong>and</strong><br />

equality <strong>in</strong> competition than the current paradigms <strong>in</strong> use today.<br />

Lastly, that FINA does not control worldwide age-group<strong>in</strong>g rules may<br />

be logically appropriate. From the po<strong>in</strong>t of view of documented ethnic<br />

variation <strong>in</strong> tim<strong>in</strong>g of growth <strong>and</strong> maturation (Eveleth & Tanner, 1990;<br />

Mal<strong>in</strong>a et al., 2004), it would be unreasonable to adopt a universal agegroup<strong>in</strong>g<br />

paradigm. Data have shown that maturational events occur at<br />

early ages <strong>in</strong> Asian <strong>and</strong> Black-American children when compared with<br />

European <strong>and</strong> American Caucasian children. There seems to be approximately<br />

a 1-year difference <strong>in</strong> the age at PHV between these ethnic groups.<br />

The mean age of Asian <strong>and</strong> European/North American swimmers at the<br />

2nd FINA Youth Championships was 15.7 ± 1.1 years for Asians girls <strong>and</strong><br />

16.2 ± 0.9 years for Caucasians girls (p < 0.05). The Asian boy swimmers<br />

were also younger (16.9 ± 1.0 years vs. 17.6 ± 0.6 years, p < 0.05). Due to<br />

maturation-related competitive advantages <strong>in</strong> early maturers over late <strong>and</strong>/<br />

or average maturers (Mal<strong>in</strong>a et al., 2004), the ethnic differences may be an<br />

<strong>in</strong>terest<strong>in</strong>g consideration <strong>in</strong> predict<strong>in</strong>g performance outcomes at <strong>in</strong>ternational<br />

competitive events.<br />

conclusIon<br />

Age classification systems clearly <strong>in</strong>fluence participation <strong>and</strong> competition<br />

outcomes <strong>in</strong> competitive youth swimm<strong>in</strong>g. The number of swimmers qualify<strong>in</strong>g<br />

for competitive events <strong>and</strong> then qualify<strong>in</strong>g for f<strong>in</strong>als at <strong>in</strong>ternational<br />

events is significantly greater for swimmers who are the oldest <strong>in</strong> their agegroups.<br />

Group<strong>in</strong>g swimmers by the use of broad CAs is not the optimal way<br />

to encourage younger competitors. With today’s comput<strong>in</strong>g power <strong>and</strong> software<br />

sophistication, novel strategies are available to group swimmers without<br />

affect<strong>in</strong>g the meet timel<strong>in</strong>e or expense. These new <strong>in</strong>novative strategies may<br />

act to enhance competition <strong>and</strong> encourage participation.<br />

reFerences<br />

Eveleth, P. B. & Tanner, J. M. (1990). Worldwide Variation <strong>in</strong> Human<br />

Growth. 2nd Edition. Cambridge: University Press.<br />

Fédération Internationale de Natation: http://www.f<strong>in</strong>a.org<br />

Kojima, K., Jamison, P. L., Brammer, C. L. & Stager, J. M. (2009). Age<br />

classification <strong>in</strong> USA Swimm<strong>in</strong>g: are current competitive age-groups<br />

appropriate? <strong>Medic<strong>in</strong>e</strong> & Science <strong>in</strong> Sports & Exercise, 41(5), 148.<br />

Mal<strong>in</strong>a, R. M., Bouchard, C. & Bar-Or, O. (2004). Growth, Maturation,<br />

<strong>and</strong> Physical Activity. 2 nd Edition. Champaign, IL: Human K<strong>in</strong>etics.<br />

Pelayo, P., Wille, F., Sidney, M., Bertho<strong>in</strong>, S. & Lavoie, J. M. (1997).<br />

Swimm<strong>in</strong>g performances <strong>and</strong> strok<strong>in</strong>g parameters <strong>in</strong> non skilled<br />

grammar school pupils: relation with age, gender <strong>and</strong> some anthropometric<br />

characteristics. Journal of Sports <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Physical Fitness,<br />

37, 187-93.<br />

269


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Effects of Reduced Knee-bend on 100 Butterfly<br />

Performance: A Case Study Us<strong>in</strong>g the Men’s Asian<br />

<strong>and</strong> Japanese Record Holder<br />

Ide, t. 1 , Yoshimura, Y. 2 , Kawamoto, K. 3 , takise, s. 1 , Kawakami,<br />

t. 1<br />

1 Osaka University of Health <strong>and</strong> Sport Sciences, Osaka, Japan.<br />

2 Chuo University, Tokyo, Japan.<br />

3 Phoenix Swim Club, Phoenix, Arizona, USA<br />

This article analyzed the 30 year old Asian <strong>and</strong> Japanese record holder<br />

of the men’s 100 meter butterfly. In 2002, Kohei Kawamoto’s best time<br />

was 53.22 seconds, <strong>and</strong> he improved his time to 51.00 seconds <strong>in</strong> 2009.<br />

The most significant difference between Kohei <strong>in</strong> 2002 <strong>and</strong> 2009 was<br />

the focus on a straight leg butterfly kick technique. When compar<strong>in</strong>g<br />

his 2005 stroke to his 2009 stroke, we found that the extent of the<br />

straightness of his butterfly kick improved from 39% to 55% (of >170<br />

degrees knee-bend<strong>in</strong>g). Additionally, this swimmer improved his speed<br />

from 2.5m·s -1 to 2.7m·s -1 , <strong>and</strong> <strong>in</strong>creased his distance per stroke from<br />

1.894m±0.062 to 2.204m±0.131.<br />

Key words: tra<strong>in</strong><strong>in</strong>g, Asian <strong>and</strong> Japanese national record,<br />

Butterfly, straight kick, coach<strong>in</strong>g, swimm<strong>in</strong>g speed Meter.<br />

IntroductIon<br />

Butterfly swimmers should keep their body as horizontal as possible<br />

dur<strong>in</strong>g the propulsive phase of the arm stroke (Maglischo, 2003). In<br />

general, coaches use the technique of ‘wave butterfly’ ( Japan Swimm<strong>in</strong>g<br />

Federation, 2006), <strong>and</strong> the dolph<strong>in</strong> kick technique of bend<strong>in</strong>g the knees.<br />

The wave butterfly arises from body movement, arm-stroke tim<strong>in</strong>g <strong>and</strong><br />

kick tim<strong>in</strong>g (Yoshimura, 1996). Bend<strong>in</strong>g the knees dur<strong>in</strong>g the butterfly<br />

kick <strong>in</strong>creases the undulation of ‘wave butterfly’. Coaches still use the<br />

technique of bend<strong>in</strong>g the knees dur<strong>in</strong>g the butterfly kick, with the purpose<br />

of push<strong>in</strong>g back the water (Fig.2).<br />

S<strong>in</strong>ce 2006, we coached Kawamoto to change his butterfly technique,<br />

employ<strong>in</strong>g a straighter leg-kick. The result was a more horizontal<br />

stroke. Kawamoto’s <strong>in</strong>itial butterfly kick technique used a bend<strong>in</strong>g butterfly<br />

kick. We changed this to a straighter kick with less knee-bend<br />

(Yoshimura, 2008), which is imag<strong>in</strong>ed as ‘hold<strong>in</strong>g the water to the bottom<br />

the pool’ (Fig. 1).<br />

Figure 1. Straight kick.<br />

270<br />

Figure 2. Bend<strong>in</strong>g kick.<br />

Methods<br />

Kohei Kawamoto, 30 years old Asian <strong>and</strong> Japanese record holder of the<br />

men’s 100 meter butterfly (height; 174 cm, body weight; 64kg) volunteered<br />

to participate <strong>in</strong> this study. A comparison was made of Kawamoto’s<br />

performance <strong>in</strong> 2009 to his previous performance <strong>in</strong> 2005. He<br />

performed 4 times 25 meter butterfly swims, whilst be<strong>in</strong>g filmed, from<br />

a push start. The first 15 meters were completed under water us<strong>in</strong>g the<br />

butterfly kick <strong>and</strong> the f<strong>in</strong>al 10 meters swimm<strong>in</strong>g all out butterfly stroke.<br />

A Swimm<strong>in</strong>g Speed Meter (V<strong>in</strong>e, VMS-003, AC100V, 1/500s, 0.2mm/<br />

pulse) us<strong>in</strong>g a wire attached to the swimmer, exported the analogue signals<br />

via an RS232C post to a computer. These signals were used to calculate<br />

swimm<strong>in</strong>g speed (Microsoft W<strong>in</strong>dows Excel; Yoshimura, 2007).<br />

The wire l<strong>in</strong>e of the speed meter was attached to the swimmer by a<br />

belt <strong>and</strong> <strong>in</strong>tracyclic velocity changes were recorded precisely for several<br />

stroke cycles while swimm<strong>in</strong>g at maximum speed. The average velocity<br />

changes for one stroke cycle were calculated with data from all successive<br />

stroke curves. The average number of stroke cycles were compared<br />

(for the 2009 stroke <strong>and</strong> 2005 stroke). A Swimm<strong>in</strong>g Speed Meter, registered<br />

velocity when the subject was at maximum speed with<strong>in</strong> one<br />

stroke cycle, which is dur<strong>in</strong>g the second kick phase. Then comes the<br />

wave phase, <strong>and</strong> first kick phase, <strong>in</strong>sweep phase. Dur<strong>in</strong>g swimm<strong>in</strong>g, the<br />

subject was monitored from the side plane us<strong>in</strong>g an underwater video<br />

camera at a sampl<strong>in</strong>g frequency of 60Hz (Underwater monitor system<br />

2, YAMAHA, Shizuoka, Japan). The angle of the knee bend <strong>and</strong> upper<br />

body movement. were analyzed with the DartTra<strong>in</strong>er.<br />

results<br />

The Swimm<strong>in</strong>g Speed Meter showed that swimm<strong>in</strong>g speeds <strong>in</strong>creased<br />

from 2.5m·s -1 for 2005 to 2.7m·s -1 <strong>in</strong> 2009 (dur<strong>in</strong>g the second kick<br />

phase). Distance per stroke (DPS) <strong>in</strong>creased to 2.204m±0.131 for 2009,<br />

from 1.894m±0.062 <strong>in</strong> 2005 (m) Wicoxon.: p=0.006061, 1 stroke (velocity)<br />

Wicoxon.: p=0.7748) (Figure 3.). Four phases of the 2009 <strong>and</strong><br />

2005’s velocity results were not significantly different (the first kick<br />

phase Wilcoxon: p=0.64850, <strong>in</strong>sweep phase Wilcoxon: p=0.16360, upsweep<br />

<strong>and</strong> second kick phase Wilcoxon: p=0.00606, wave phase Wilcoxon:<br />

0.10910.


The Swimm<strong>in</strong>g Speed Meter showed that swimm<strong>in</strong>g speeds <strong>in</strong>creased from 2.5m·s for<br />

2005 to 2.7m·s -1 <strong>in</strong> 2009 (dur<strong>in</strong>g the second kick phase). Distance per stroke (DPS)<br />

<strong>in</strong>creased to 2.204m±0.131 for 2009, from 1.894m±0.062 <strong>in</strong> 2005 (m) Wicoxon.:<br />

p=0.006061, 1 stroke (velocity) Wicoxon.: p=0.7748) (Figure 3.). Four phases of the<br />

2009 <strong>and</strong> 2005’s velocity results were not significantly different (the first kick phase<br />

Wilcoxon: p=0.64850, <strong>in</strong>sweep phase Wilcoxon: p=0.16360, upsweep <strong>and</strong> second kick<br />

phase Wilcoxon: p=0.00606, wave phase Wilcoxon: 0.10910.<br />

Vel oci t y ( m/ sec)<br />

1. 2 1. 4 1. 6 1. 8 2. 0 2. 2 2. 4<br />

first kick phase <strong>in</strong>sweep phase<br />

upsweep <strong>and</strong> second<br />

kick phase<br />

| | | | | | | |<br />

Figure 3. Four phase of velocity 2005 <strong>and</strong> 2009 us<strong>in</strong>g the Wilcoxon.<br />

wave phase<br />

2005 2008 2005 2008 2005 2008 2005 2008<br />

Figure 3. Four phase of velocity 2005 <strong>and</strong> 2009 us<strong>in</strong>g the Wilcoxon.<br />

Table 1. Knee-bend<br />

2009 2005<br />

Straight knee (+170 degrees) 55%(39/71) 39%(26/66)<br />

Bent knee (-170 degrees) 45%(32/71) 61%(40/66)<br />

In 2006, Kawamoto changed his stroke technique to a straighter knee<br />

angle ,def<strong>in</strong>ed as 170 degrees to 180 degrees (+170 degrees) <strong>and</strong> 55% of<br />

the stroke cycle was spent with<strong>in</strong> this ‘degree of bend’ for 2009 whereas<br />

it was only 39% <strong>in</strong> 2005 (Table 1.). Therefore, 2009’s stroke, with the<br />

straight knee technique, decreased the resistance dur<strong>in</strong>g his stroke <strong>and</strong><br />

as a result, <strong>in</strong>creased his distance per stroke <strong>and</strong> maximum speed.<br />

dIscussIon<br />

Based on the above evidence it is clear the most preferred butterfly<br />

technique is to use a straight knee kick. The men’s 100 butterfly world<br />

record holder, Michael Phelps employed this stroke technique with the<br />

straighter knee (+170 degrees) <strong>and</strong> 49.6% of the stroke cycle was spent<br />

with<strong>in</strong> these ‘degrees of bend’. Mike Cavic, 2nd <strong>in</strong> the men’s 100 butterfly<br />

2008 Olympic Games, employed the straight knee kick <strong>and</strong> 55% of<br />

his stroke cycle was at >170 degrees knee-bend. The men’s 100 butterfly<br />

former world record holder, Ian Croker employed showed 48% of his<br />

stroke cycle t be at >170 degrees knee-bend. S<strong>in</strong>ce 2006, we employed<br />

a four step tra<strong>in</strong><strong>in</strong>g plan <strong>in</strong> practice <strong>and</strong> <strong>in</strong> swimm<strong>in</strong>g competition<br />

(Ide, 2009). In the first step, we imag<strong>in</strong>ed the straighter kick on l<strong>and</strong>.<br />

On l<strong>and</strong>, we focused on the butterfly straight leg kick, stretch<strong>in</strong>g the<br />

tendon of the tibialis anterior muscle rather than us<strong>in</strong>g the quadriceps<br />

muscles (Huij<strong>in</strong>g, 1992). When Kawamoto used this stretched tendon<br />

<strong>in</strong> a similar way <strong>in</strong> the butterfly straight leg kick, the kick frequency was<br />

much more rapid (Hosokawa, 2009). The second step was to utilize the<br />

straight leg kick <strong>in</strong> the pool, <strong>and</strong> this <strong>in</strong>volved slow speed drills dur<strong>in</strong>g<br />

tra<strong>in</strong><strong>in</strong>g. We changed his technique dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g, so these drills <strong>in</strong>volved<br />

swimm<strong>in</strong>g no more than 3500m. If he swam more than 3500m<br />

he had a tendency to bend the knees <strong>and</strong> move the upper body too<br />

much. Also, these sessions were performed just once a day. The third step<br />

was to test the technique <strong>in</strong> a m<strong>in</strong>or meet. After the race, we checked<br />

these techniques by the video camera. Then we would check these techniques<br />

from the m<strong>in</strong>or meet <strong>and</strong> <strong>in</strong>sure they are correct <strong>in</strong> preparation<br />

for the next step. The fourth step was the major meet, which will be the<br />

Olympic Trials, World Championship Trials, Japan Nationals, World<br />

Championship, East Asian Games or Japan Open. His tra<strong>in</strong><strong>in</strong>g partner<br />

won <strong>and</strong> set a meet record at the 2009 US Junior Nationals men 100Fly.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

conclusIon<br />

This study analyzed the butterfly stroke technique of Japan’s 100 meter<br />

butterfly record holder. Kawamoto improved his performances, due<br />

to three possible reasons: 1. <strong>in</strong>creased maximum speed, from 2.5m·s -<br />

1 to 2.7 m·s -1 . 2. <strong>in</strong>creased distance per stroke, from 1.894m±0.062 to<br />

2.204m±0.131 . 3. Use of the straight knee dolph<strong>in</strong> kick.<br />

reFerences<br />

Huij<strong>in</strong>g P. A. (1992). Mechanical muscle models. In: Strength <strong>and</strong> power<br />

<strong>in</strong> sport (Komi P. V. ed.). Blackwell Scientific Publications, Oxford.<br />

Hosokawa K., Takise M., Kawakami T., Matsumoto K., Ito S., Koshiba<br />

Y., Ide T., (2009). Effect of the Tendon Hold to Rat Rear Reg. The<br />

64th Annual Meet<strong>in</strong>g of the Japanese Society of Physical Fitness <strong>and</strong><br />

Sports <strong>Medic<strong>in</strong>e</strong>, Niigata, Japan.<br />

Ide T., Yoshimura Y., Kawamoto K., Takise M., Kawakami T., (2009).<br />

How to Coach Butterfly. 2009 Japan Society of Sciences <strong>in</strong> Swimm<strong>in</strong>g<br />

<strong>and</strong> Water Exercise, Kanagawa, Japan.<br />

Japan Swimm<strong>in</strong>g Federation, Japan Swimm<strong>in</strong>g Club Association<br />

(2006). Coach<strong>in</strong>g Manual, Taishuukann sho-ten.<br />

Loebbecke, A. V., Mittal, R., Fish, F., Mark, R. (2009) A Comparison<br />

of the K<strong>in</strong>ematics of the Dolph<strong>in</strong> Kick <strong>in</strong> Humans <strong>and</strong> Cetaceans.<br />

Human Movement Science 28, 99-112.<br />

Maglischo EW (2003). Swimm<strong>in</strong>g Fastest. Champaign: Human K<strong>in</strong>etics.<br />

Yoshimura Y., Kosuge T. (2008). Science of Swimm<strong>in</strong>g. NHK books, 75-<br />

76<br />

Yoshimura Y., Takahashi Y. (1996). Swimm<strong>in</strong>g. Ikeda-shoten, 60-61<br />

Yoshimura Y., Tanaka T., Oishi K., Yasukawa M., Matsuo A. (2007).<br />

Characteristics of Butterfly Strok<strong>in</strong>g Skill <strong>in</strong> Elite Swimmers Detected<br />

by Means of a Speed Meter. ACSM 54th annual meet<strong>in</strong>g.<br />

AcKnoWledGeMents<br />

I would like to express my heartfelt appreciation to the many people who<br />

supported this research. Thanks to the Tokyo Institute of Swimm<strong>in</strong>g<br />

Science, who allowed us to use Kawamoto’s data s<strong>in</strong>ce 2005. They had<br />

control of the Swimm<strong>in</strong>g Speed Meter. Also Mr. Tetsuya Tanaka, who<br />

was calculated Kawamoto’s data with the Wicoxon Signed Ranked Test.<br />

And Hamamatsu Photonics K.K. (Hamamatsu Swim Stroke Watcher)<br />

Mr. Takehiro Kurono, who had supported Kawamoto’s race data.<br />

271


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Stability <strong>and</strong> Prediction of 100-m Breaststroke<br />

Performance Dur<strong>in</strong>g The Careers of Elite Swimmers<br />

costa, M.J. 1,4 ; Mar<strong>in</strong>ho, d.A. 2,4 ; reis, V.M. 3,4 ; silva, A.J. 3,4 ;<br />

Bragada, J.A. 1,4 ; Barbosa, t.M. 1,4<br />

1 Polytechnic Institute of Bragança, Bragança, Portugal<br />

2 University of Beira Interior, Covilhã, Portugal<br />

3 University of Trás-os-Montes <strong>and</strong> Alto Douro, Vila Real, Portugal<br />

4 Research Centre <strong>in</strong> Sports, Health <strong>and</strong> Human Development, Vila Real,<br />

Portugal<br />

The aim of this study was to track <strong>and</strong> analyze the 100-m Breaststroke<br />

performance stability throughout elite swimmers’ careers. 35 Portuguese<br />

male top-50 swimmers were analyzed for seven consecutive seasons<br />

between the ages of 12 <strong>and</strong> 18 years old. Best performances were collected<br />

from rank<strong>in</strong>g tables. Longitud<strong>in</strong>al assessment was performed<br />

based on two approaches: (i) mean stability was analyzed by descriptive<br />

statistics <strong>and</strong> ANOVA repeated measures for each season followed by<br />

a post-hoc test (Bonferroni test), (ii) normative stability was analyzed<br />

with self-correlation (Mal<strong>in</strong>a, 2001) <strong>and</strong> the Cohen’s Kappa track<strong>in</strong>g<br />

<strong>in</strong>dex (L<strong>and</strong>is <strong>and</strong> Koch, 1977). There was a 100-m Breaststroke performance<br />

enhancement from child to adult age. The overall career performance<br />

prediction was low. The change from 13 to 14 years can be a<br />

milestone, where the ability to predict the f<strong>in</strong>al swimmer’s performance<br />

level strongly <strong>in</strong>creases.<br />

Keywords: stability, prediction, track<strong>in</strong>g, breaststroke<br />

IntroductIon<br />

Swimm<strong>in</strong>g seems to be one of the most studied sports <strong>in</strong> the Sport<br />

Sciences community. Researchers are constantly try<strong>in</strong>g to identify <strong>and</strong><br />

underst<strong>and</strong> the factors that can better predict swimm<strong>in</strong>g performance.<br />

However, the majority of the studies <strong>in</strong> swimm<strong>in</strong>g “science” have a crosssectional<br />

character. Indeed, they do not consider the performance stability<br />

<strong>and</strong> change as the result of <strong>in</strong>dividual development, new tra<strong>in</strong><strong>in</strong>g<br />

methods <strong>and</strong>/or technological sophistication.<br />

The longitud<strong>in</strong>al approaches regard<strong>in</strong>g competitive swimm<strong>in</strong>g are<br />

few. Even so, most of the papers published have a strong focus on physiological<br />

<strong>and</strong>/or biomechanical issues <strong>and</strong> less on the swimm<strong>in</strong>g performance<br />

itself. Swimm<strong>in</strong>g performance is expressed by the time spent to<br />

cover the event distance. The longitud<strong>in</strong>al performance assessment is<br />

important to help coaches to def<strong>in</strong>e realistic goals <strong>and</strong> tra<strong>in</strong><strong>in</strong>g methods.<br />

These longitud<strong>in</strong>al assessments can be developed track<strong>in</strong>g the performance<br />

of elite swimmers, analyz<strong>in</strong>g its progression between competitions<br />

<strong>and</strong>/or seasons. The ma<strong>in</strong> advantages are that it is possible to: (i)<br />

describe <strong>and</strong> estimate the progression <strong>and</strong> the variability of performance<br />

dur<strong>in</strong>g <strong>and</strong> between seasons; (ii) f<strong>in</strong>d hypothetical chronological po<strong>in</strong>t<br />

determ<strong>in</strong>ants to predict swimmer’s performance throughout his/her<br />

career or a given time frame <strong>and</strong>; (iii) determ<strong>in</strong>e swimmer’s chance to<br />

reach f<strong>in</strong>als or w<strong>in</strong> medals <strong>in</strong> important competitions. Pyne et al. (2004),<br />

<strong>in</strong> a 12 month study, made an attempt to underst<strong>and</strong> the performance<br />

behaviour lead<strong>in</strong>g up to the 2000 Olympic Games by analyz<strong>in</strong>g the 50m,<br />

100-m, 200-m, 400-m, 800-m (females only) <strong>and</strong> 1500-m (males<br />

only) freestyle events; two backstroke, breaststroke <strong>and</strong> butterfly events<br />

over 100-m <strong>and</strong> 200-m, <strong>and</strong> the 200-m <strong>and</strong> 400-m <strong>in</strong>dividual medley<br />

events. They reported that to stay <strong>in</strong> contention for a medal, a Sydney<br />

2000 Olympic swimmer should improve his/her performance by approximately<br />

1 % with<strong>in</strong> a competition <strong>and</strong> by approximately 1 % with<strong>in</strong><br />

the year lead<strong>in</strong>g up to the Olympics. The authors also stated that presumably<br />

an additional enhancement of approximately 0.4 % would substantially<br />

<strong>in</strong>crease the swimmer’s chances of a medal.<br />

So far, any research analyz<strong>in</strong>g the change <strong>and</strong> stability of swimmer’s<br />

breaststroke performance dur<strong>in</strong>g his/her career us<strong>in</strong>g the track<strong>in</strong>g ap-<br />

272<br />

proach does not appear to exist. Therefore, the purpose of this study was<br />

to track <strong>and</strong> analyze the 100-m male breaststroke performance stability<br />

throughout the elite swimmer’s career, from childhood to adult age.<br />

Methods<br />

An overall of 35 Portuguese male swimmers <strong>and</strong> 905 race times were<br />

analyzed for seven consecutive seasons between 12 <strong>and</strong> 18 years old. The<br />

Portuguese male top-50 rank<strong>in</strong>gs <strong>in</strong> the 100-m Breaststroke event, <strong>in</strong><br />

the 2007-2008 season was consulted to identify the swimmers <strong>in</strong>cluded.<br />

Exclusion criteria were def<strong>in</strong>ed as: (i) authors do not have access to the<br />

season best performance <strong>in</strong> seven consecutive seasons <strong>and</strong> (ii) swimmer<br />

did not swim the 100-m breaststroke event at least once per season for<br />

some reason. Best performances from official competitions, <strong>in</strong> a short<br />

course pool (regional, national or <strong>in</strong>ternational level), dur<strong>in</strong>g the career<br />

seasons, were collected from rank<strong>in</strong>g tables. The rank<strong>in</strong>gs tables were<br />

provided by the Portuguese National Swimm<strong>in</strong>g Federation, <strong>and</strong> when<br />

suitable or appropriate were also consulted from a public swimm<strong>in</strong>g database<br />

(www.swimrank<strong>in</strong>gs.net, November 2009).<br />

Longitud<strong>in</strong>al assessment was performed based on two approaches:<br />

(i) mean stability; (ii) normative stability. For mean stability, quartiles,<br />

means plus st<strong>and</strong>ard deviations were computed for each chronological<br />

age. Data variation was analyzed with ANOVA repeated measures<br />

followed by a post-hoc test (Bonferroni test). Normative stability was<br />

analyzed with Pearson Correlation Coefficient between paired performances<br />

throughout the seven seasons. Qualitatively stability was considered<br />

to be: (i) high if r ≥ 0.60; (ii) moderate if 0.30 < r < 0.60 <strong>and</strong>;<br />

(iii) low if r < 0.30, as suggested by Mal<strong>in</strong>a (2001). The Cohen’s Kappa<br />

track<strong>in</strong>g <strong>in</strong>dex (K) plus one st<strong>and</strong>ard deviation, with a confidence <strong>in</strong>terval<br />

of 95 % was also calculated. The qualitative <strong>in</strong>terpretation of K<br />

was made accord<strong>in</strong>g to L<strong>and</strong>is <strong>and</strong> Koch (1977) suggestion, where the<br />

stability is: (i) excellent if K > 0.75; (ii) moderate if 0.40 < K < 0.75 <strong>and</strong>;<br />

(iii) low if K < 0.40.<br />

All statistical procedures were computed with SPSS software (v.<br />

13.0, Apache Software Foundation, Chicago, IL, USA). However, the<br />

K value was computed with the Longitud<strong>in</strong>al Data Analysis software (v.<br />

3.2, Dallas, USA). The level of statistical significance was set at P ≤ 0.05.<br />

results<br />

Figure 1 presents the variation of swimm<strong>in</strong>g performance throughout<br />

swimmer’s career. ANOVA repeated measures revealed significant<br />

variations <strong>in</strong> the 100-m Breaststroke swimm<strong>in</strong>g performance [F (1.34)<br />

= 353.57; P < 0.01, power = 1.00]. Bonferroni post-hoc tests verified<br />

significant differences (P < 0.01) between all seasons analyzed. The only<br />

exception was for the pair wise comparison between the sixth <strong>and</strong> the<br />

seventh seasons that was not significant. From the age of 12 to the age<br />

of 18, median values ranged between 80.70 s (12 years) <strong>and</strong> 66.55 s (18<br />

years). So, there was an obvious performance enhancement dur<strong>in</strong>g the<br />

swimmer’s career.<br />

Figure 1: Diagram of 100-m Breaststroke swimm<strong>in</strong>g performance, median<br />

extremes <strong>and</strong> quartiles from childhood to adult age.


The K value, express<strong>in</strong>g the stability throughout the overall swimmer’s<br />

career, was moderate (K = 0.38 ± 0.05) with 0.33 < K < 0.43 for a 95 %<br />

confidence <strong>in</strong>terval. So, based on overall values of the seven consecutive<br />

seasons, a low swimm<strong>in</strong>g performance stability <strong>and</strong> prediction can be<br />

considered.<br />

Table 1 presents the self-correlation values for pairwised ages<br />

throughout swimmer’s career. Self-correlations were significant <strong>in</strong><br />

all situations (P < 0.05), except between the 16 <strong>and</strong> 17 years. Overall,<br />

throughout swimmers career, self-correlation ranged between a moderate<br />

<strong>and</strong> a high stability (0.30 < r < 0.60). Indeed, most of the pair wise<br />

self-correlations were r ≥ 0.60. Stability becomes high (r = 0.644) from<br />

14 until 18 years old.<br />

Table 1: Pearson Correlation Coefficients from children to adult age <strong>in</strong><br />

the 100-m Breaststroke event.<br />

Age 12 13 14 15 16 17<br />

13 0.863* 1<br />

14 0.610* 0.850* 1<br />

15 0.459* 0.727* 0.867* 1<br />

16 0.300 0.582* 0.741* 0.728* 1<br />

17 0.300 0.505* 0.696* 0.678* 0.802* 1<br />

18 0.398* 0.485* 0.644* 0.598* 0.730* 0.839*<br />

* P < 0.05<br />

dIscussIon<br />

The aim of this study was to track <strong>and</strong> analyze the 100-m Breaststroke<br />

performance stability throughout the elite swimmer’s career. Ma<strong>in</strong> data<br />

suggests an obvious performance enhancement <strong>in</strong> the 100-m Breaststroke<br />

event, from children to adult age. Analyz<strong>in</strong>g the overall track<strong>in</strong>g<br />

values, the prediction of adult swimmer’s performance level, based on<br />

childhood performance is moderate. When more strict time frames are<br />

used, swimm<strong>in</strong>g performance stability <strong>and</strong> prediction <strong>in</strong>creases start<strong>in</strong>g<br />

at the age of 14. It seems that the change from 13 to 14 years can be a<br />

milestone, were the ability to predict the swimmer’s performance level<br />

strongly <strong>in</strong>creases.<br />

The trend for performance enhancement throughout swimmer’s career<br />

might be associated to some scientific improvements <strong>and</strong> <strong>in</strong>novations<br />

that along with the normal <strong>in</strong>dividual development process, allow<br />

swimmers to obta<strong>in</strong> better performances. As swimm<strong>in</strong>g performance is<br />

determ<strong>in</strong>ed by different parameters, the <strong>in</strong>dividual development will affect<br />

the energy cost of swimm<strong>in</strong>g (Kjendlie et al., 2003). Changes <strong>in</strong> anthropometric<br />

characteristics, like body length <strong>and</strong> body mass, are identified<br />

as causes to <strong>in</strong>crease energy cost (Chatard et al., 1985). Along with<br />

these morphological changes, development shows an <strong>in</strong>crease <strong>in</strong> swimmers<br />

muscular strength. It appears that hormonal development that occurs<br />

dur<strong>in</strong>g maturation has a determ<strong>in</strong>ant role <strong>in</strong> <strong>in</strong>creas<strong>in</strong>g muscle size<br />

<strong>and</strong> strength (Matos <strong>and</strong> W<strong>in</strong>sley, 2007). Furthermore, the sequence<br />

<strong>in</strong> which tra<strong>in</strong><strong>in</strong>g loads or volumes are applied, as a series of tra<strong>in</strong><strong>in</strong>g<br />

blocks, is critical to enhance performance. The model of tra<strong>in</strong><strong>in</strong>g load<br />

reduction adopted before important competitions has a high effect on<br />

the athlete’s performance (Mujika et al., 2002). This type of tra<strong>in</strong><strong>in</strong>g<br />

reduction is not common <strong>in</strong> younger ages.<br />

Another explanation for this career improvement is the technological<br />

sophistication of the swimm<strong>in</strong>g suits. The type of material (e.g. polyurethane),<br />

the ways to sew the fabric pieces, suit types <strong>and</strong> sizes, the<br />

effect of swim suits upon wobbl<strong>in</strong>g body mass, <strong>and</strong> body compression<br />

might expla<strong>in</strong> the major advantages of wear<strong>in</strong>g these recently developed<br />

suits lead<strong>in</strong>g better performances <strong>in</strong> adult ages (Mar<strong>in</strong>ho et al., 2009).<br />

However, despite this performance improvement dur<strong>in</strong>g the swimmers<br />

career, a slight “break<strong>in</strong>g effect” start<strong>in</strong>g at the age of 16 (Figure 1)<br />

can be observed. This fact may be associated with: (i) a maximal level of<br />

external tra<strong>in</strong><strong>in</strong>g load reached by the swimmers, which is more difficult<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

to overcome; (ii) a decrease <strong>in</strong> physiological functional capacity with age<br />

or; (iii) a slowdown or stagnation <strong>in</strong> the development of anthropometric<br />

characteristics.<br />

The self-correlation values (Table 1) ranged between moderate <strong>and</strong><br />

high stability throughout the swimmer’s career. The <strong>in</strong>itial sharp <strong>in</strong>crease<br />

<strong>in</strong> stability can be observed dur<strong>in</strong>g the change from 13 to 14 years old.<br />

This can be expla<strong>in</strong>ed by: i) maturational process, that provides greater<br />

availability for tra<strong>in</strong><strong>in</strong>g process, <strong>in</strong> order to obta<strong>in</strong> more ambitious performances,<br />

ii) consolidation of values <strong>and</strong> culture of swimm<strong>in</strong>g performance<br />

acquired throughout swimmer’s career.<br />

The K value, express<strong>in</strong>g the stability throughout the overall swimmer’s<br />

career, was low (K = 0.38 ± 0.05). Based on such long careers, it<br />

is clear that swimmers performance stability is difficult to ma<strong>in</strong>ta<strong>in</strong> on<br />

a high level. Moreover, there are several episodes that can <strong>in</strong>fluence the<br />

performance stability, such as illness or an acute/chronic <strong>in</strong>jury. When<br />

more strict time frames are used, performance stability <strong>and</strong> prediction<br />

<strong>in</strong>creases.<br />

conclusIon<br />

The prediction of adult performance level, based on childhood performance<br />

is low, when consider<strong>in</strong>g the swimmer’s overall career. When<br />

more strict time frames are used, swimm<strong>in</strong>g performance stability <strong>and</strong><br />

prediction <strong>in</strong>creases start<strong>in</strong>g at the age of 14. It seems that the change<br />

from 13 to 14 years can be a milestone, where the ability to predict the<br />

f<strong>in</strong>al swimmer’s performance level strongly <strong>in</strong>creases.<br />

reFerences<br />

Chatard, J.C., Padilla, S., Carzorla, G. & Lacour, J.R. (1985). Influence<br />

of body height, weight, hydrostatic lift <strong>and</strong> tra<strong>in</strong><strong>in</strong>g on the energy<br />

cost of the front crawl. NZL Sports Med, 13, 82-84<br />

Kjendlie, P.L., Ingjer F., Madsen, O., Stallman, R.K. & Stray-Gundersen,<br />

J. (2003). Differences <strong>in</strong> the energy cost between children <strong>and</strong><br />

adults dur<strong>in</strong>g front crawl swimm<strong>in</strong>g. Eur J Appl Physiol. 91, 473-480<br />

L<strong>and</strong>is, J.R. & Koch, G.G. (1977). The measurement of observer agreement<br />

for categorical data. Biometrics, 37, 439-446.<br />

Mal<strong>in</strong>a, R.M. (2001). Adherence to physical activity from childhood to<br />

adulthood: a perspective forma track<strong>in</strong>g studies. Quest, 53, 346-355.<br />

Mar<strong>in</strong>ho, D.A., Barbosa, T.M., Kjendlie, P.L., Vilas-Boas, J.P., Alves,<br />

F.B., Rouboa, A.I. & Silva, A.J. (2009). In: M. Peters, ed. Swimm<strong>in</strong>g<br />

simulation: a new tool for swimm<strong>in</strong>g research <strong>and</strong> practical applications.<br />

Lecture Notes <strong>in</strong> Computational Science <strong>and</strong> Eng<strong>in</strong>eer<strong>in</strong>g – Computational<br />

Fluid Dynamics for Sport Simulation. Berl<strong>in</strong>: Spr<strong>in</strong>ger.<br />

Matos, N. & W<strong>in</strong>sley, R.L. (2007). Tra<strong>in</strong>ability of young athletes <strong>and</strong><br />

overtra<strong>in</strong><strong>in</strong>g. J Sport Science, 6, 353-367<br />

Mujika, I., Padilla, S., Pyne, D. (2002). Swimm<strong>in</strong>g performance changes<br />

dur<strong>in</strong>g the f<strong>in</strong>al 3 weeks of tra<strong>in</strong><strong>in</strong>g lead<strong>in</strong>g to the Sydney 2000<br />

Olympic Games. Int J Sports Med, 23(8), 582-587.<br />

Pyne, D., Trew<strong>in</strong>, C. & Hopk<strong>in</strong>s W. (2004). Progression <strong>and</strong> variability<br />

of competitive performance of Olympic swimmers. J Sports Sci. 22(7),<br />

613-20.<br />

AcKnoWledGMents<br />

Mário J. Costa would like to acknowledge to the Portuguese Science<br />

<strong>and</strong> Technology Foundation (FCT) for the PhD grant (SFRH/<br />

BD/62005/2009).<br />

273


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Effect of Subjective Effort on Stroke Tim<strong>in</strong>g <strong>in</strong><br />

Breaststroke Swimm<strong>in</strong>g<br />

ohba, M. 1 , sato, s. 1 , shimoyama, Y. 2 , sato, d. 2<br />

1 Niigata University, Niigata, Japan<br />

2 Niigata University of Health <strong>and</strong> Welfare, Niigata, Japan<br />

This study exam<strong>in</strong>ed the relationship between stroke tim<strong>in</strong>g <strong>and</strong> subjective<br />

effort dur<strong>in</strong>g breaststroke swimm<strong>in</strong>g (BR) <strong>in</strong> comparison with<br />

front crawl swimm<strong>in</strong>g (FC). Eight 25-m swim trials were conducted,<br />

consist<strong>in</strong>g of two styles (FC <strong>and</strong> BR) <strong>and</strong> four levels of subjective effort.<br />

The levels were four steps from 70–100% effort with the same clearance<br />

for one’s maximal effort. A significant positive correlation was found<br />

between subjective effort <strong>and</strong> SV. Increas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g the swimm<strong>in</strong>g<br />

velocity depends remarkably upon SR, not only for FC but also for<br />

BR. However, a significant <strong>in</strong>teraction was found for SV. No significant<br />

<strong>in</strong>teraction was found for SR. Both strokes have the same ratio of SR<br />

<strong>in</strong>crease as stepp<strong>in</strong>g up the subjective effort, but not the same ratio of<br />

SV <strong>in</strong>crease. Results show that the degree of SV <strong>in</strong>crease by SR <strong>in</strong>crease<br />

<strong>in</strong> BR is less than <strong>in</strong> FC, which might be attributed to technical characteristics.<br />

Key words: subjective effort, breaststroke, grad<strong>in</strong>g, output <strong>in</strong>tensity<br />

IntroductIon<br />

It is important for competitive swimmers to subjectively control their<br />

output. To do so, they must have the capacity of chang<strong>in</strong>g swimm<strong>in</strong>g<br />

speed. It is difficult for athletes to control their own motion because they<br />

attempt to control their own motion depend<strong>in</strong>g on subjective sensations.<br />

They might be surprised by the difference between actual motion <strong>and</strong><br />

imag<strong>in</strong>g when they confirm their motion displayed on a monitor. Such<br />

a difference might engender poor results <strong>in</strong> competitive swimm<strong>in</strong>g. The<br />

relation between subjective sensations <strong>and</strong> the actual output <strong>in</strong>tensity<br />

is strongly associated with the ability to grade. Some reports of studies<br />

of grad<strong>in</strong>g for swimm<strong>in</strong>g (Goya et al. 2005, 2008) have described that<br />

the subjective effort was correlated significantly with objective <strong>in</strong>tensity<br />

at given conditions dur<strong>in</strong>g 50 m crawl swimm<strong>in</strong>g <strong>in</strong> male <strong>and</strong> female<br />

subjects. However, no reports <strong>in</strong> the literature describe the effects of<br />

subjective effort <strong>in</strong> the tim<strong>in</strong>g of breaststroke swimm<strong>in</strong>g. This study was<br />

undertaken to exam<strong>in</strong>e the relation between stroke tim<strong>in</strong>g <strong>and</strong> subjective<br />

effort dur<strong>in</strong>g BR <strong>in</strong> comparison with FC.<br />

Methods<br />

Subjects<br />

In this study, 22 well-tra<strong>in</strong>ed college swimmers (11 male, 11 female)<br />

participated after giv<strong>in</strong>g their consent. Their ma<strong>in</strong> characteristics were<br />

the follow<strong>in</strong>g: age, 19.5±0.7 y; height, 176.5±5.0 cm; mass, 69.4±4.0 kg;<br />

<strong>and</strong> age, 20.2±0.5y; height, 163.6±5.3 cm; mass, 59.3±5.2 kg.<br />

Experimental schema<br />

Figure 1 presents the experimental design. After 30 m<strong>in</strong> free warm-up,<br />

each was asked to swim at an imposed subjective effort of “maximal”.<br />

Eight 25-m swim trials were conducted <strong>in</strong> all, which consisted of two<br />

swimm<strong>in</strong>g styles (FC <strong>and</strong> BR) <strong>and</strong> four levels of subjective effort. The<br />

levels were four steps––from 70% to 100% effort. The maximal effort<br />

trial was conducted on the fourth trial with each style. Other levels of<br />

effort were selected arbitrarily. Subjects were given 5–6 m<strong>in</strong> rest between<br />

trials.<br />

Subjects were <strong>in</strong>structed as follows: 1) Swim with your subjective<br />

feel<strong>in</strong>g only. 2) Do not speak about your own or another subject’s performance.<br />

3) Swim with your highest concentration. Subjects were not<br />

<strong>in</strong>formed of their swimm<strong>in</strong>g time after each trial.<br />

274<br />

Figure 1. Experimental design of this study<br />

Measurement methods<br />

Two experienced timers hold<strong>in</strong>g the swimm<strong>in</strong>g coach license, recorded<br />

the trial times us<strong>in</strong>g a stopwatch, enabl<strong>in</strong>g calculation of the swimm<strong>in</strong>g<br />

speed (SV, m/s). A digital camcorder (Sony Corp.) placed on the pool<br />

deck videotaped <strong>and</strong> timed the swimmers over all distances from a side<br />

view, enabl<strong>in</strong>g calculation of the stroke rates (SR, strokes/m<strong>in</strong>) for three<br />

strokes (from 3 rd to 5 th ). The stroke length (SL, m/stroke) was computed<br />

from SV <strong>and</strong> SR values. A second camcorder (Sony Corp.) <strong>in</strong> a waterproof<br />

case (Sony Corp.) was placed underwater to record the swimmers<br />

for at least one complete stroke cycle, enabl<strong>in</strong>g analyses of the stroke<br />

phases. After be<strong>in</strong>g downloaded on a PC, the pictures were analyzed<br />

us<strong>in</strong>g motion analysis software (Fram Dias 4.0; DKH Corp.).<br />

Figure 2 portrays def<strong>in</strong>itions of stroke phases dur<strong>in</strong>g respective swimm<strong>in</strong>g<br />

styles as follows. Phase 1, from the 1 st po<strong>in</strong>t to the 2 nd po<strong>in</strong>t, <strong>in</strong>cluded<br />

the glide phase. Phase 2, from the 2 nd po<strong>in</strong>t to the 3 rd po<strong>in</strong>t,<br />

<strong>in</strong>cluded the propulsion phase. Phase 3, from the 3 rd po<strong>in</strong>t to the next 1 st<br />

po<strong>in</strong>t, <strong>in</strong>cluded the recovery phase.<br />

Figure 2. Def<strong>in</strong>itions of stroke phases of each swimm<strong>in</strong>g style.<br />

Statistical analysis<br />

Data, as the mean ± st<strong>and</strong>ard deviation (SD), were analyzed us<strong>in</strong>g computer<br />

software (SPSS v.15; SPSS Inc.). Stroke × grad<strong>in</strong>g level (2 × 4)<br />

repeated measures ANOVA was used to analyze the significance of<br />

changes with grad<strong>in</strong>g level between strokes. Tukey’s post hoc test was<br />

used. The level of significance was set to p


Figure 3. SV <strong>and</strong> SR of respective strokes <strong>in</strong> each subjective effort.<br />

Table 1 shows the SV <strong>and</strong> SR of both strokes for each grad<strong>in</strong>g level.<br />

Significant <strong>in</strong>teraction was apparent <strong>in</strong> SV, but no significant <strong>in</strong>teraction<br />

was found for SR. The second f<strong>in</strong>d<strong>in</strong>g is that both strokes have the same<br />

ratio of SR <strong>in</strong>crease when stepp<strong>in</strong>g up the subjective effort, but not the<br />

same ratio of SV <strong>in</strong>crease. Results show that the degree of SV <strong>in</strong>crease<br />

by <strong>in</strong>creas<strong>in</strong>g SR <strong>in</strong> BR was less than <strong>in</strong> FC, which might be attributed<br />

to technical characteristics: the difference between the alternate arm<br />

stroke <strong>in</strong> FC <strong>and</strong> the simultaneous arms stroke <strong>in</strong> BR.<br />

Table 1. SV <strong>and</strong> SR of both strokes for each grad<strong>in</strong>g level, <strong>in</strong> % of max<br />

Effort(%) FC-SV(%) BR-SV(%) <strong>in</strong>teraction FC-SR(%) BR-SR(%) <strong>in</strong>teraction<br />

70 89.3±4.8 93.5±4.2 74.4±5.8 76.6±9.1<br />

80 93.7±3.6 96.3±2.9 84.2±6.3 85.5±6.4<br />

90 97.5±2.4 98.8±1.8 92.2±3.3 93.3±4.5<br />

100 100 100 p = 0.011 100 100 p = 0.821<br />

Note. SV, swimm<strong>in</strong>g velocity; SR, stroke rate;<br />

FC, front crawl stroke; BR, breaststroke<br />

Figure 4 presents the respective contribution of stroke phases of the<br />

whole stroke duration. The FC showed almost identical percentages for<br />

the three phases. With an <strong>in</strong>crease of the grad<strong>in</strong>g level <strong>in</strong> FC, Phase 1<br />

tended to decrease (from 39.1% to 33.2%), although Phase 2 <strong>in</strong>creased<br />

(from 37.1% to 42.9%). The percentage of Phase 3 (about 24%) did not<br />

change at each grad<strong>in</strong>g level. These results might be attributable to alternate<br />

stroke<strong>in</strong>g <strong>in</strong> FC. In contrast, BR showed an especially large Phase<br />

1 <strong>and</strong> a small Phase 2. With an <strong>in</strong>creased grad<strong>in</strong>g level <strong>in</strong> BR, Phase 1<br />

(from 59.9% to 51.0%) tended to decrease greatly, although both Phase<br />

2 (from 13.8% to 16.8%) <strong>and</strong> Phase 3 (from 26.3% to 32.2%) <strong>in</strong>creased.<br />

These results might expla<strong>in</strong> why BR gets more propulsion from kick<strong>in</strong>g<br />

than from arm strokes with simultaneous arm <strong>and</strong> leg motion.<br />

Figure 4. Ratio of the time of each stroke phase to the whole stroke<br />

duration.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

conclusIon<br />

In conclusion, <strong>in</strong>creas<strong>in</strong>g <strong>and</strong> decreas<strong>in</strong>g the swimm<strong>in</strong>g velocity depends<br />

mostly upon SR, not only <strong>in</strong> FC but also <strong>in</strong> BR. However, the degree<br />

of SV <strong>in</strong>crease by SR <strong>in</strong>crease <strong>in</strong> BR is expected to be less than <strong>in</strong> FC.<br />

These results suggest that chang<strong>in</strong>g the swim speed by chang<strong>in</strong>g the<br />

subjective effort <strong>in</strong> a race or <strong>in</strong> tra<strong>in</strong><strong>in</strong>g can be considered a change of<br />

coord<strong>in</strong>ation (style).<br />

reFerences<br />

Goya, T., Nomura, T. & Sugiura, K. (2005). The relationship between<br />

stroke motion <strong>and</strong> output <strong>in</strong>tensity for velocity dur<strong>in</strong>g 50 m crawl<br />

swimm<strong>in</strong>g <strong>in</strong> female. The Japan Journal of Sport Methodology, 18(1),<br />

75-83.<br />

Goya, T., Nomura, T. & Matsui, A. (2008). The relationship between<br />

stroke motion <strong>and</strong> output <strong>in</strong>tensity for velocity dur<strong>in</strong>g 50 m crawl<br />

swimm<strong>in</strong>g <strong>in</strong> male. Journal of Tra<strong>in</strong><strong>in</strong>g Science for Exercise <strong>and</strong> Sport,<br />

20(1), 33-42.<br />

Leblanc, H. Seifert, L. & Chollet, D. (2009). Arm-leg coord<strong>in</strong>ation <strong>in</strong><br />

recreational <strong>and</strong> competitive breaststroke swimmers. Journal of Science<br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Sport, 12, 352-356.<br />

Takagi, H. Sugimoto, S Miyashita, M, Nomura, T. Wakayoshi, K. Okuno,<br />

K. Ogita, F. Ikuta, Y. & Wilson, B. (2002). Arm <strong>and</strong> leg coord<strong>in</strong>ation<br />

dur<strong>in</strong>g breast stroke: Analysis of 9th F<strong>in</strong>a World Swimm<strong>in</strong>g<br />

Championships, Fukuoka 2001. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g,<br />

IX, 301-306.<br />

275


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Models for Assess<strong>in</strong>g General Horizontal Swimm<strong>in</strong>g<br />

Abilities of Junior Water Polo Players Accord<strong>in</strong>g to<br />

Play<strong>in</strong>g Position<br />

Özkol, Z. 1 , dopsaj, M. 2 , Thanopoulos, V. 3 , Bratusa, Z. 2<br />

1Ege University Physical Education <strong>and</strong> Sport Department, Izmir, Türkiye.<br />

2University of Belgrade Faculty of Sport <strong>and</strong> Physical Education, Belgrade,<br />

Serbia.<br />

3University of Athens Faculty of Physical Education <strong>and</strong> Sports Sciences,<br />

Athens, Greece.<br />

The aim of this study was to identify general level of horizontal swim<br />

abilities of junior water polo players accord<strong>in</strong>g to play<strong>in</strong>g position. The<br />

subjects were 71 players, members of national junior teams. The players<br />

were divided <strong>in</strong> three ma<strong>in</strong> play<strong>in</strong>g position groups; peripherals (P), center<br />

defenders (CD) <strong>and</strong> center players (C). The follow<strong>in</strong>g six swimm<strong>in</strong>g<br />

tests were performed, crawl; 15m, 25m, 50m, 200m, 25m crawl with<br />

head up <strong>and</strong> 25m crawl with ball. The results of these tests were analyzed<br />

us<strong>in</strong>g a confirmative model of factor analysis for the determ<strong>in</strong>ation of<br />

the factor scores <strong>and</strong> mathematical multidimensional procedures were<br />

determ<strong>in</strong>ed for creat<strong>in</strong>g models. There were no statistical differences<br />

(p>0.05) between general level of basic horizontal swim abilities accord<strong>in</strong>g<br />

to position.<br />

Key words: Waterpolo, play<strong>in</strong>g position, junior, model assessment,<br />

swim test.<br />

IntroductIon<br />

Tactical, technical, physical dem<strong>and</strong>s <strong>and</strong> also play<strong>in</strong>g position differences<br />

of water polo players are very important factors for competitive<br />

success. For the plann<strong>in</strong>g of water polo tra<strong>in</strong><strong>in</strong>g, the primary <strong>in</strong>formative<br />

sources need to be taken <strong>in</strong>to consideration, the physiological dem<strong>and</strong>s<br />

of the game, based on the differences <strong>in</strong> game duration, the period of the<br />

game, the level of competitiveness of the players, the level of competitiveness<br />

of the teams <strong>and</strong> the different player positions (Lozov<strong>in</strong>a, 1983;<br />

Lozov<strong>in</strong>a et al., 2009; Platanou, 2009; Tsekouras et al., 2005).<br />

Certa<strong>in</strong> activities are performed more frequently <strong>and</strong> with an <strong>in</strong>creased<br />

overall duration by the center forwards compared to attackers<br />

<strong>and</strong> defenders (Platanou, 2009). However, very few studies have been<br />

published about the anthropometrical, physical <strong>and</strong> physiological parameters<br />

of water polo players at various ages. Bratusa (2000) found that<br />

water polo tra<strong>in</strong><strong>in</strong>g affects basic motor skill improvement <strong>in</strong> prepubescent<br />

children. Matković et al. (1999) suggest us<strong>in</strong>g specific tests on l<strong>and</strong><br />

<strong>and</strong> <strong>in</strong> the water. Through tra<strong>in</strong><strong>in</strong>g <strong>and</strong> selection, an early specialization<br />

takes place <strong>and</strong> those boys who are more skillful <strong>in</strong> specific situations<br />

st<strong>and</strong> out. Falk et al. (2004) recommend us<strong>in</strong>g fewer swimm<strong>in</strong>g tests <strong>in</strong><br />

the selection process of young water polo players. In high profile water<br />

polo, us<strong>in</strong>g manifest anthropometric <strong>and</strong> motor skills variables, it is possible<br />

to make a prognosis of how successful any defense/offence will be<br />

(Lozov<strong>in</strong>a, 1983).<br />

However, there is little data about horizontal swimm<strong>in</strong>g abilities<br />

accord<strong>in</strong>g to play<strong>in</strong>g position <strong>in</strong> the younger categories, especialy cross<br />

culturally. There is also a lack of research on how to identify horizontal<br />

swimm<strong>in</strong>g abilities accord<strong>in</strong>g to play<strong>in</strong>g position differences of water<br />

polo players. Therefore the aim of this study was to identify the general<br />

level of horizontal swim abilities of junior water polo players accord<strong>in</strong>g<br />

to play<strong>in</strong>g position <strong>and</strong> to improve our underst<strong>and</strong><strong>in</strong>g of the positional<br />

differences of water polo players.<br />

Methods<br />

The subjects consisted of 71 players aged 15-16, members of national<br />

junior teams from: Slovenia, Türkiye, Serbia <strong>and</strong> Greece. For the play-<br />

276<br />

<strong>in</strong>g positions, players were divided three ma<strong>in</strong> play<strong>in</strong>g position group,<br />

peripherals (P, n=41), center defenders (CD, n=20) <strong>and</strong> center players<br />

(C, n=13). Each team has been tested us<strong>in</strong>g by the same procedures<br />

(3) <strong>and</strong> <strong>in</strong> the same tra<strong>in</strong><strong>in</strong>g period at the start of the national precompetition<br />

period.<br />

The follow<strong>in</strong>g six swimm<strong>in</strong>g tests were performed: 15m crawl, 25m<br />

crawl, 50mcrawl, 200m crawl, 25m crawl with head up <strong>and</strong> 25m crawl<br />

with ball (25mcrawlHUP, 25mcrawlWB). All tests were performed <strong>in</strong> a<br />

50m swimm<strong>in</strong>g pool. The players started from <strong>in</strong> the water at the signal<br />

of the timekeeper, <strong>and</strong> tracks of 25m were measured by stopp<strong>in</strong>g the<br />

stopwatch when the head crossed the imag<strong>in</strong>ary l<strong>in</strong>e of the f<strong>in</strong>ish.<br />

Data obta<strong>in</strong>ed were processed by st<strong>and</strong>ard descriptive statistics, calculations<br />

<strong>in</strong>cluded arithmetic mean (X), st<strong>and</strong>ard deviation (SD) <strong>and</strong><br />

coefficient of variation (cV%). Multivariate tests were performed to determ<strong>in</strong>e<br />

the level of statistical significance between the play<strong>in</strong>g positions.<br />

Then results of these tests were analyzed us<strong>in</strong>g confirmative models<br />

of factor analysis for the determ<strong>in</strong>ation of the factor scores. Follow<strong>in</strong>g<br />

this analysis, the mathematical multi-dimensional procedures were determ<strong>in</strong>ed<br />

for creat<strong>in</strong>g models for assess<strong>in</strong>g the horizontal swim score<br />

(HSS) equations for three different play<strong>in</strong>g positions; for the peripherals<br />

HSS (P) , for the central defenders HSS (CD) <strong>and</strong> for the center players<br />

HSS (C) . The results of HSS for three different play<strong>in</strong>g positions was<br />

expressed numerically (from a hypothetical m<strong>in</strong>imum of zero to a hypothetical<br />

maximum of 100, where 50 represents an average swim score).<br />

For this process, multiple regression model analysis has been used to<br />

determ<strong>in</strong>e predictor system <strong>in</strong>fluence on the criterion variable. The level<br />

of significance was set at p0.05 (p=0.305), there are no statistical<br />

Wilks’ differences Lambda between statistics basic horizontal found swim that abilities the accord<strong>in</strong>g p was >0.05 to position. (p=0.305), It seems that there<br />

are the no process statistical of specialization differences is not yet between strong <strong>in</strong> basic 16 yrs horizontal old water polo swim players abilities from these ac-<br />

four countries (Slovenia, Türkiye, Serbia <strong>and</strong> Greece).<br />

cord<strong>in</strong>g to position. It seems that the process of specialization is not<br />

yet strong <strong>in</strong> 16 yrs old water polo players from these four countries<br />

(Slovenia, Türkiye, Serbia <strong>and</strong> Greece).<br />

Table 2. The results of tests of between-subjects effects.<br />

Dependent Variable Type III Sum of Squares df Mean Square F Sig.<br />

m15crawl .043 2 .022 .078 .925<br />

m25crawl .363 2 .181 .209 .812<br />

m50crawl 1.434 2 .717 .253 .777<br />

m200crawl 61.343 2 30.671 .641 .530<br />

m25crawlHUP .626 2 .313 .390 .678<br />

m25crawlWB .068 2 .034 .027 .974<br />

Beside the fact that statistically significant differences were not found (Table 2)<br />

between these observed groups (P,CD,C) for the variables (Table 2); 15m crawl<br />

(F=0.078, p=0.925), 25m crawl (F=0.209, p=0.812), 50m crawl (F=0.253, p=0.777),<br />

200m crawl (F=0.641, p=0.530), 25m crawlHUP (F=0.390, p=0.678), 25m crawlWB<br />

(F=0.027, p=0.974) three different multidimensional models for prediction of basic<br />

horizontal swimm<strong>in</strong>g abilities for 16 yrs old water polo players were created, as<br />

Horizontal Swim Score (HSS).<br />

The ANOVA regression analysis results show that the separated set of 6 predict<strong>in</strong>g


Table 2. The results of tests of between-subjects effects.<br />

Dependent<br />

Variable<br />

Type III Sum of<br />

Squares<br />

df<br />

Mean<br />

Square<br />

F Sig.<br />

m15crawl .043 2 .022 .078 .925<br />

m25crawl .363 2 .181 .209 .812<br />

m50crawl 1.434 2 .717 .253 .777<br />

m200crawl 61.343 2 30.671 .641 .530<br />

m25crawlHUP .626 2 .313 .390 .678<br />

m25crawlWB .068 2 .034 .027 .974<br />

Beside the fact that statistically significant differences were not found<br />

(Table 2) between these observed groups (P,CD,C) for the variables<br />

(Table 2); 15m crawl (F=0.078, p=0.925), 25m crawl (F=0.209, p=0.812),<br />

50m crawl (F=0.253, p=0.777), 200m crawl (F=0.641, p=0.530), 25m<br />

crawlHUP (F=0.390, p=0.678), 25m crawlWB (F=0.027, p=0.974) three<br />

different multidimensional models for prediction of basic horizontal<br />

swimm<strong>in</strong>g abilities for 16 yrs old water polo players were created, as<br />

Horizontal Swim Score (HSS).<br />

The ANOVA regression analysis results show that the separated set<br />

of 6 predict<strong>in</strong>g variables statistically significantly describes the HSS (P) ,<br />

HSS (CD) <strong>and</strong> HSS (C) at the level p=0.000. The model expla<strong>in</strong>s 100%<br />

of all three play<strong>in</strong>g positions, variability with values of st<strong>and</strong>ard estimation<br />

error of ±0.00307%, ±0.00213% <strong>and</strong> ±0.00255% of horizontal<br />

swimm<strong>in</strong>g abilitiy, respectively. It can be considered that the calculated<br />

model is useful <strong>and</strong> reliable s<strong>in</strong>ce the st<strong>and</strong>ard estimation error is lower<br />

than the st<strong>and</strong>ard error (SD) HSS (P) =17.48%, HSS (CD) =16.28% <strong>and</strong><br />

HSS (C) =15.81%.<br />

Table 3. Function of equations of mathematical models of predict<strong>in</strong>g<br />

HSS.<br />

Model predict<strong>in</strong>g equations<br />

Peripherals Horizontal Swim SCORE; HSS (P) = 349.882<br />

- (m15crawl*5.681) - (m25crawl*3.555) - (m50crawl*1.893) -<br />

(m200crawl*0.408) - (m25crawlHUP*3.608) - (m25crawlWB*2.844)<br />

Center Defenders Horizontal Swim SCORE; HSS (CD) = 349.872<br />

- (m15crawl*5.682) - (m25crawl*3.559) - (m50crawl*1.893) -<br />

(m200crawl*0.408) - (m25crawlHUP*3.603) - (m25crawlWB*2.845)<br />

Center Horizontal Swim SCORE; HSS (C) = 349.938 - (m15crawl*5.679)<br />

- (m25crawl*3.557) - (m50crawl*1.893) - (m200crawl*0.408) - (m25crawl-<br />

HUP*3.607) - (m25crawlWB*2.845)<br />

Table 3 shows the results of multiple regression analysis for variables<br />

which by regression model method, def<strong>in</strong>ed the model of the mathematical<br />

regression equation. From this model the set of 6 variables<br />

which make up the complex of horizontal swimm<strong>in</strong>g abilities, (which<br />

<strong>in</strong>tegrally <strong>and</strong> on the statistically significant level, describes HSS of<br />

three play<strong>in</strong>g positions) were extracted.<br />

dIscussIon<br />

Competitive water polo can be characterized as a physiologically dem<strong>and</strong><strong>in</strong>g<br />

<strong>in</strong>termittent activity, ma<strong>in</strong>ly rely<strong>in</strong>g on players’ aerobic power<br />

<strong>and</strong> lactate threshold (Hohmann <strong>and</strong> Frase, 1992; Platanou <strong>and</strong> Geladas,<br />

2006) <strong>and</strong> a sport that requires a variety of technical skills <strong>and</strong> athletic<br />

abilities that depend on each player’s positional role (Smith, 1998).<br />

However, Hohmann <strong>and</strong> Frase (1992) reported no significant differences<br />

<strong>in</strong> the swimm<strong>in</strong>g <strong>in</strong>tensity or the distance covered among various<br />

field positions among senior players.<br />

Our f<strong>in</strong>d<strong>in</strong>gs po<strong>in</strong>t out no swimm<strong>in</strong>g ability differences between<br />

players who play three different positions. Based on the analysis made,<br />

no statistical differences were found between peripherals, defenders <strong>and</strong><br />

centers <strong>in</strong> HSS. Although there were mathematical differences <strong>in</strong> HSS<br />

between players play<strong>in</strong>g three different positions, HSS figures were still<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

very close to each other. As expected the best scores <strong>in</strong> HSS belonged to<br />

peripherals followed by centers <strong>and</strong> then center defenders.<br />

Prior to our analysis, it was estimated that peripherals would perform<br />

much better when compared to the other two positions but our<br />

f<strong>in</strong>d<strong>in</strong>gs did not confirm this. Peripherals usually st<strong>and</strong> out with their<br />

ability play a faster game, better reflexes, better swimm<strong>in</strong>g performance,<br />

more drives <strong>in</strong> the pool. Tak<strong>in</strong>g <strong>in</strong>to account all of this, it was expected<br />

that their scores would be much better than centers <strong>and</strong> center defenders.<br />

The latter two are accoustomed to do more one-on-one battle due to<br />

their position <strong>in</strong> the game <strong>and</strong> this builds up power <strong>and</strong> strength for the<br />

players <strong>in</strong> these positions.<br />

However the f<strong>in</strong>d<strong>in</strong>gs did not entirely follow the hypotheses <strong>and</strong><br />

theory. Especially when look<strong>in</strong>g at their alactic swimm<strong>in</strong>g skills, there<br />

were no major differences between these three position. In fact, the center<br />

defenders showed better performance on the alactic swimm<strong>in</strong>g ability<br />

than the peripherals.<br />

Based on all of the f<strong>in</strong>d<strong>in</strong>gs above, it was found that players do not<br />

exhibit specific swimm<strong>in</strong>g charcateristics associated with their position<br />

at the youth national team level.<br />

On the other h<strong>and</strong> Bratusa <strong>and</strong> Dopsaj (2006) reported that there<br />

def<strong>in</strong>itely are differences <strong>in</strong> swimm<strong>in</strong>g features of the players <strong>in</strong> different<br />

positions of junior Slovenian players.<br />

A greater number of swimm<strong>in</strong>g efforts (Dopsaj <strong>and</strong> Matkovic, 1994;<br />

Sarmento, 1994; Smith, 1998) <strong>in</strong> the w<strong>in</strong>g positions <strong>and</strong> a greater number<br />

of duels particularly <strong>in</strong> center <strong>and</strong> back positions caused the greatest<br />

differences exactly between these positions (Bratusa et al., 2003; Sarmento,<br />

1994; Smith, 1998).<br />

Different positions <strong>in</strong> water polo have their specificities that should<br />

be responded to by the players who play <strong>in</strong> those positions (Bratusa <strong>and</strong><br />

Dopsaj, 2006).<br />

conclusIon<br />

In this study analyz<strong>in</strong>g horizontal swimm<strong>in</strong>g abilities of players <strong>in</strong> different<br />

positions, the results show no differences between these observed<br />

groups. It seems that the process of specialization is not yet strong<br />

among 16 years old water polo players from these four countries. The def<strong>in</strong>ed<br />

models of mathematical regression equations, the models of HSS<br />

prediction of the three positions (Table 3), can be used as a model, as a<br />

test<strong>in</strong>g procedure for check<strong>in</strong>g the horizontal swimm<strong>in</strong>g abilities of the<br />

young water polo players <strong>and</strong> the present study provided effective <strong>in</strong>formation<br />

on the horizontal swimm<strong>in</strong>g performance of elite young water<br />

polo players accord<strong>in</strong>g to play<strong>in</strong>g position. Def<strong>in</strong>ed equations can be<br />

used by coaches as an effective <strong>and</strong> easy to apply method for test<strong>in</strong>g the<br />

actual level of horizontal swimm<strong>in</strong>g ability of junior water polo players.<br />

reFerences<br />

Bratuša, Z. (2000). Speed abilities development of young school age<br />

boys under <strong>in</strong>fluence of specific water polo tra<strong>in</strong><strong>in</strong>gs. Unpublished<br />

master thesis, Belgrade, Faculty of Physical Education.<br />

Bratuša, Z., Matkovic, I. & Dopsaj, M. (2003). Model characteristics of<br />

water polo players’ activities <strong>in</strong> vertical position dur<strong>in</strong>g a match. In:<br />

Chatard J.C. (ed.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX. Sa<strong>in</strong>t-Etienne:<br />

Publications de L’Universite de Sa<strong>in</strong>t-Etienne, 481-486.<br />

Bratuša, Z. & Dopsaj, M. (2006). Difference between general <strong>and</strong> specific<br />

swimm<strong>in</strong>g abilities of junior top water polo players based on their<br />

position with<strong>in</strong> the team. Rev Port Cien Desp, 6, Supl.2, 285-324.<br />

Dopsaj M. & Matkovic I. (1994). Motor activities dur<strong>in</strong>g the game.<br />

Physical Culture, 48, 4, 339 – 347.<br />

Falk B., Lidor R., L<strong>and</strong>er Y. & L<strong>and</strong> B. (2004). Talent identification<br />

<strong>and</strong> early development of elite water polo players: a 2-year follow-up<br />

study. Journal of Sports Sciences, 4, 347-355.<br />

Hohmann A. & Frase R. (1992). Analysis of swimm<strong>in</strong>g speed <strong>and</strong> energy<br />

metabolism <strong>in</strong> competition water polo games. In: MacLaren D.,<br />

277


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Reilly T., Lees A. (eds.), Swimm<strong>in</strong>g science VI: <strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e<br />

<strong>in</strong> swimm<strong>in</strong>g (pp. 313 – 319). London: E & F N Spon.<br />

Lozov<strong>in</strong>a, V. (1983). Influence of morphological characteristics <strong>and</strong> motorical<br />

abilities <strong>in</strong> swimm<strong>in</strong>g on success of water polo players. Unpublished<br />

doctoral dissertation, Zagreb: Faculty of Physical Education.<br />

Lozov<strong>in</strong>a, M., Durovic, N. & Katic, R. (2009). Position specific morphological<br />

characteristics of elite water polo players. Coll Antropol, 33,<br />

3, 781–789.<br />

Matković, I., Gavrilović, P., Jovović D. & Thanopoulos V. (1999). Specific<br />

abilities test of top Yugoslav water polo players <strong>and</strong> its validation.<br />

In: Kesk<strong>in</strong>en K.L., Komi P.V., Pitkanen P.L. (eds.), <strong>Biomechanics</strong> <strong>and</strong><br />

Swimm<strong>in</strong>g VIII (pp. 259-264). Juvaskyla: University of Jyvaskyla.<br />

Platanou, T. & Geladas, N. (2006). The <strong>in</strong>fluence of game duration <strong>and</strong><br />

play<strong>in</strong>g position on <strong>in</strong>tensity of exercise dur<strong>in</strong>g match-play <strong>in</strong> elite<br />

water polo players. Journal of Sports Sciences, 24, 11, 1173 – 1181.<br />

Platanou, T. (2009). Cardiovascular <strong>and</strong> metabolic requirements of water<br />

polo. Serb. J. Sports. Sci, 3, 4, 85-97.<br />

Sarmento, P. (1994). Physiological <strong>and</strong> morphological task related profiles<br />

of Portuguese water polo players. II. International Symposium on<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, Atlanta.<br />

Smith, H. (1998). Applied physiology of water polo. Sports <strong>Medic<strong>in</strong>e</strong>,<br />

26, 317 – 334.<br />

Tsekouras, Y.E., Kavouras, S.A., Campagna, A., Kotsis, S.A., Syntosi<br />

S.S., Papazoglou, K. & Sidossis, L. (2005). The anthropometrical <strong>and</strong><br />

physiological characteristics of water polo players. European Journal of<br />

Applied Physiology, 95, 35-41.<br />

278<br />

A Markov Cha<strong>in</strong> Model of Elite Water Polo<br />

Competition<br />

Pfeiffer, M., hohmann, A., siegel, A., Böhnle<strong>in</strong>, s.<br />

Institute of Sport Science, University of Bayreuth, Bayreuth, Germany<br />

When it comes to water polo, performance diagnostics offers many<br />

different methods to analyze a game. In this context, problems mostly<br />

occur <strong>in</strong> adequately modell<strong>in</strong>g the game, <strong>in</strong> part because the various<br />

approaches lack scope for uniform performance criteria. In this study<br />

the concept of match-play analysis through mathematical simulation by<br />

means of the Markov-cha<strong>in</strong> model was applied to water polo <strong>and</strong> used<br />

to analyse the performance relevance of tactical behaviour patterns at<br />

the World League F<strong>in</strong>al 2007 (Berl<strong>in</strong>) with focus on the German <strong>and</strong><br />

Serbian teams. The results suggest that <strong>in</strong> <strong>in</strong>ternational-level water polo,<br />

the performance relevance of “Turn over to counter attack” <strong>and</strong> “Turn over<br />

to One-center-attack” were the most worthwhile tactical behaviour<br />

patterns. No significant differences between Germany <strong>and</strong> Serbia<br />

could be found.<br />

Key words: game analysis, water polo, tactical behaviour, simulation,<br />

Markov cha<strong>in</strong><br />

IntroductIon<br />

From a performance diagnostic po<strong>in</strong>t of view, the key task of notational<br />

analysis is to analyze the game structure <strong>and</strong> f<strong>in</strong>d determ<strong>in</strong><strong>in</strong>g factors,<br />

<strong>in</strong> this case tactics, of performance. A look at the literature shows that<br />

a large number of methods have been developed – based on rapid technological<br />

developments <strong>in</strong> the area of computers, video etc. – to analyse<br />

the structure of game sports by game observation, <strong>in</strong> order to identify<br />

performance <strong>in</strong>dicators (Hughes & Bartlett, 2002). A comprehensive<br />

review of the evolution of notational analysis <strong>in</strong> sports games is given<br />

by Hughes <strong>and</strong> Franks (2004), Hughes (2008) <strong>and</strong> Hughes <strong>and</strong> Bartlett<br />

(2008). Most of these methods use structure-oriented observation models,<br />

which enable the researcher to register isolated elementary actions<br />

<strong>in</strong> a match, but do not allow for the obta<strong>in</strong><strong>in</strong>g of data on the <strong>in</strong>teraction<br />

process itself.<br />

Consider<strong>in</strong>g a sports game as a dynamic system or an <strong>in</strong>teractionprocess,<br />

different stochastic models have been developed. The models of<br />

the f<strong>in</strong>ite Markov cha<strong>in</strong> were successfully applied to describe <strong>and</strong> predict<br />

play<strong>in</strong>g profiles or patterns (McGarry & Franks, 1994; McGarry & Perl,<br />

2004), <strong>and</strong> to determ<strong>in</strong>e the performance relevance of tactical behaviour<br />

(Hirotsu, Miyaji, Ezake, Shigenaga & Taguchi, 2004; Hohmann, Zhang<br />

& Koth, 2004; Lames, 1991; Zhang, 2003). In the game analysis approach<br />

of Lames (Lames, 1991; Lames & McGarry, 2007), comparable<br />

quantitative values for the performance relevance of selected tactical<br />

patterns are determ<strong>in</strong>ed by the method of simulation. The concept of<br />

performance analysis through mathematical simulation by means of the<br />

Markov cha<strong>in</strong> model was first established <strong>in</strong> the area of return games<br />

<strong>and</strong> successfully transferred to <strong>in</strong>vasion games (e.g. h<strong>and</strong>ball <strong>and</strong> soccer;<br />

Pfeiffer, 2004; Pfeiffer, 2005; Pfeiffer & Hohmann, 2008). In this study,<br />

the same approach was applied to water polo to analyse the relevance of<br />

specific tactical behaviour to performance <strong>in</strong> general <strong>and</strong> with focus on<br />

the German <strong>and</strong> Serbian Water Polo teams at the World League F<strong>in</strong>al<br />

2007 <strong>in</strong> Berl<strong>in</strong>.<br />

Methods<br />

Observation model: The water polo match is described as a system that<br />

gradually moves through different states. The start<strong>in</strong>g po<strong>in</strong>t of our observation<br />

model was the possession of the ball (state “Turn over”). The<br />

offensive play was modelled on the basis of all offensive attempts, which<br />

were characterized by 16 different states of the game. These states represent<br />

different player positions <strong>in</strong> even-man offense (6-6; position at-


tack <strong>and</strong> double-center attack) <strong>and</strong> one man-up offense (6-5) as well as<br />

specific game situations (turn over, driv<strong>in</strong>g-<strong>in</strong>, <strong>and</strong> goal/penalty) (Table<br />

1). The f<strong>in</strong>al state of “goal/penalty” is def<strong>in</strong>ed as the criterion of performance,<br />

necessary for judg<strong>in</strong>g the performance relevance of all other tactical<br />

behaviour. The typical tactical behaviour of the teams is expressed<br />

<strong>in</strong> the transition between two subsequent states (“tactical patterns”).<br />

Table 1. State model used for game analysis <strong>in</strong> water polo (for both<br />

teams)<br />

No. State Abbrev.<br />

Turn over TO<br />

Counter-attack CA<br />

One-center-attack OCA<br />

Back-position <strong>in</strong> OCA BPOCA<br />

Flanker-position OCA FPOCA<br />

Center-position <strong>in</strong> OCA CPOCA<br />

Driv<strong>in</strong>g-<strong>in</strong> DI<br />

Double-center-attack DCA<br />

Back-position <strong>in</strong> double-center attack BPDCA<br />

Flanker-position <strong>in</strong> double-center attack FPDCA<br />

Center-position <strong>in</strong> double-center attack CPDCA<br />

Man-up-Attack MUA<br />

Back-position man-up (BPMUA) BPMUA<br />

Flanker-position man-up (FPMUA) FPMUA<br />

Center-position man-up (CPMUA) CPMUA<br />

Goal/penalty G<br />

Stochastic model: The transition probabilities between two states describe the<br />

water polo match as a process that can be understood as a first order Markov<br />

cha<strong>in</strong>, when the follow<strong>in</strong>g two properties are given: (1) the probability<br />

for the next state depends only on the current state (Markov-property), <strong>and</strong><br />

(2) the transition probability from one state to another is <strong>in</strong>dependent of<br />

their chronological position <strong>in</strong> the match process (cha<strong>in</strong>-property).<br />

The transition probabilities between the states can be transformed<br />

<strong>in</strong>to a two dimensional transition matrix. Each element of this matrix<br />

has the property p ij (n) ≥ 0 <strong>and</strong> the l<strong>in</strong>e sum is equal to 1. In the theory<br />

of a Markov cha<strong>in</strong>, several k<strong>in</strong>ds of states are dist<strong>in</strong>guished. Absorb<strong>in</strong>g<br />

states are important, because the process ends <strong>in</strong> these states, <strong>and</strong> a new<br />

process starts. For our purpose of performance diagnosis, the state “goal/<br />

penalty” is def<strong>in</strong>ed as the absorb<strong>in</strong>g state. The transition probability to<br />

the absorb<strong>in</strong>g state is called the goal probability (GP). The GP can be<br />

calculated for both opponents by multiplication of a start vector (distribution<br />

of the states) with the observed (empirical) transition matrix. Inso-do<strong>in</strong>g,<br />

the probabilities for the absorb<strong>in</strong>g condition of “goal/penalty”<br />

are atta<strong>in</strong>ed for both teams.<br />

Simulation to quantify the performance relevance of tactical behaviour<br />

patterns: Based on the empirical transition matrix of a water polo<br />

match, it is also possible to calculate the GP on the basis of a numerically<br />

manipulated (simulated) transition matrix. In order to determ<strong>in</strong>e<br />

the performance relevance of a tactical behaviour pattern of <strong>in</strong>terest,<br />

the empirical transition probability between these two states was manipulated<br />

by a certa<strong>in</strong> percentage <strong>in</strong> each observed match. After this the<br />

goal probability was once more calculated <strong>and</strong> def<strong>in</strong>ed the performance<br />

relevance (δGP) of a tactical behaviour pattern as the difference between<br />

the goal probability (GP) as calculated by the orig<strong>in</strong>al (observed) transition-matrix<br />

<strong>and</strong> the goal probability as calculated by the manipulated<br />

transition-matrix.<br />

With reference to this simulation method there are two special<br />

problems: 1. to f<strong>in</strong>d the adequate quantitative size of the manipulation<br />

of the <strong>in</strong>vestigated transition probability, <strong>and</strong> 2. to establish an algorithm<br />

that determ<strong>in</strong>es how the other (not manipulated) transition probabilities<br />

have to be changed, so that the stochastic character of the matrix<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

(sum of each row equals 1.00) is preserved. Regard<strong>in</strong>g (1): accord<strong>in</strong>g to<br />

Lames (1991), the function to deflect the transition probabilities is: δTP<br />

(TP) = C+B∙4∙TP (1-TP). TP is the transition probability <strong>and</strong> δTP the<br />

change of the transition probability of the <strong>in</strong>vestigated tactical pattern.<br />

The constant values applied <strong>in</strong> the present study were C = 1 <strong>and</strong> B = 5,<br />

which were also determ<strong>in</strong>ed by Lames (1991) <strong>and</strong> thoroughly tested<br />

by Pfeiffer (2004, 2005). Regard<strong>in</strong>g (2): each compensation procedure<br />

was based on a proportional compensation of all other transition probabilities,<br />

as no a priori <strong>in</strong>formation existed to justify any targeted compensation:<br />

δTP yi = -(T yi /(1-TP)) ∙δTP x . Figure 1 demonstrates how the<br />

performance relevance (δGP) of a tactical behaviour is calculated by a<br />

simulation on the basis of a st<strong>and</strong>ardized manipulation of the transition<br />

probability.<br />

Figure 1. Part of a transition matrix of a water polo match with an example<br />

of the simulative calculation of the performance relevance (δGP)<br />

of the tactical pattern “back position <strong>in</strong> position attack” to “driv<strong>in</strong>g-<strong>in</strong>”<br />

(BPPA 1 – DI 1) of team 1.<br />

The <strong>in</strong>crease of the transition probability between the states “back position<br />

<strong>in</strong> position attack” to “driv<strong>in</strong>g-<strong>in</strong>” of team 1 by 2.48 % elevates the<br />

GP by 0.6 % (Figure 1). This value documents the performance relevance<br />

(δGP) of the manipulated tactical behaviour pattern. Thus, the<br />

performance relevance (δGP) of any tactical pattern is quantified by the<br />

scale <strong>in</strong> which the goal probability (GP) changes after the transition<br />

matrix has been modified <strong>in</strong> terms of the tactical behaviour <strong>in</strong> question.<br />

results<br />

In the present study, eleven matches of the World League F<strong>in</strong>al 2007<br />

<strong>in</strong> Berl<strong>in</strong> were analysed <strong>in</strong> regard to eleven tactical patterns (transition<br />

probabilities) (Table 2).<br />

Table 2. Analysed tactical patterns (<strong>in</strong> each case for both teams)<br />

No. Tactical pattern (transition) Abbrev.<br />

Turn over – Counter-attack TO-CA<br />

Turn over – One-center-attack TO-OCA<br />

Back-position – Center-position (both “One-center-attack”) BPOCA-CPOCA<br />

Back-position (One-center-attack) – Driv<strong>in</strong>g-<strong>in</strong> BPOCA-DI<br />

Back-position (One-center-attack) – Double-center attack BPOCA-DCA<br />

Back-position (One-center-attack) – Man-up-attack BPOCA-MUA<br />

Flanker-position – Center-position (both “One-centerattack”)<br />

FPOCA-CPOCA<br />

Flanker-position (One-center-attack) – Driv<strong>in</strong>g-<strong>in</strong> FPOCA-DI<br />

Flanker-position (One-center-attack) – Double-centerattack<br />

FPOCA-DCA<br />

Flanker-position (One-center-attack) – Man-up-attack FPOCA-MUA<br />

Center-position (One-center-attack) – Man-up-attack CPOCA-MUA<br />

The differences between the German <strong>and</strong> Serbian teams were analyzed<br />

by t-test (<strong>in</strong>dependent two-sample). In all tests, p < 0.05 was accepted<br />

as significant.<br />

279


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Objectivity of the game observation model: The <strong>in</strong>strumental consistency<br />

of the observation model (objectivity) was exam<strong>in</strong>ed by the <strong>in</strong>ter-rater<br />

consistency (Cohen’s Kappa) of two observers. Three different games<br />

(SRB-ROM, SRB-GER, SRB-HUN) were selected for this purpose.<br />

The Cohen’s Kappa value of the observation model varied between .80<br />

< κ < .86, which represents an “excellent” classification (Robson, 2002).<br />

Performance relevance of tactical patterns: Due to the small number of<br />

games <strong>in</strong>vestigated <strong>and</strong> to the high variance <strong>in</strong> the empirical match data<br />

of the observed teams <strong>in</strong> the Water Polo World League F<strong>in</strong>al 2007, no<br />

significant differences between the performance relevance of the different<br />

tactical behaviour patterns of Germany <strong>and</strong> Serbia could be found.<br />

Nevertheless, the differences reported below at least exhibited a clear<br />

tendency (p < 0.10).<br />

The descriptive results showed that the performance relevance of the<br />

“Turn over to counter attack” (TO-CA) <strong>in</strong> general was the most worthwhile<br />

tactical pattern <strong>in</strong> the observed <strong>in</strong>ternational water polo matches.<br />

Especially <strong>in</strong> the German team this specific transition was much more<br />

important than <strong>in</strong> the Serbian <strong>and</strong> all other teams (M GER = 1.39+0.81<br />

[n = 3] vs. M SRB = 0.45+0.99 [n = 6] resp. M ALL = 0.43+0.1.41; [n =<br />

15]). Furthermore, <strong>in</strong> the w<strong>in</strong>n<strong>in</strong>g teams the transition from w<strong>in</strong>n<strong>in</strong>g<br />

the ball <strong>in</strong>to swimm<strong>in</strong>g a fast break was much more effective than for<br />

the losers (M WIN = 0.70+1.18 [n = 10] vs. M LOS = 0.33+1.70 [n = 7]). In<br />

addition to that, the w<strong>in</strong>n<strong>in</strong>g teams also showed a higher effectiveness<br />

when turn<strong>in</strong>g over the w<strong>in</strong> of the ball <strong>in</strong>to a more static position attack.<br />

This can be seen by the transition from “Turn over to One-center-attack”<br />

(TO-OCA), which was only positive <strong>in</strong> the w<strong>in</strong>ners of the observed<br />

games (M WIN = 0.32+0.1.08 [n = 12] vs. M LOS = –0.34+1.21 [n = 12]).<br />

Concern<strong>in</strong>g the position attack itself, the performance relevance of the<br />

tactical pattern to pass the ball from the “Back-position <strong>in</strong> the One-center<br />

position attack to the Center-position” (BPOCA-CPOCA) is positive <strong>in</strong><br />

all teams, but by far highest <strong>in</strong> the German team (M GER = 1.34+1.07 [n<br />

= 6] vs M SRB = 0.27+1.34 [n = 6]). On the other h<strong>and</strong>, for the w<strong>in</strong>ners<br />

this k<strong>in</strong>d of center play was much less relevant than for the defeated<br />

teams (M WIN = 0.60+1.14 [n = 12] vs. M LOS = 1.70+3.04 [n = 12]).<br />

Also important <strong>in</strong> water polo is the tactical manoeuvre from the<br />

position attack to the man-up situation, when an opposition player has<br />

been excluded from a period of play. So, the transition from ball possession<br />

<strong>in</strong> the “Back-position <strong>in</strong> the One-center position attack to the man-up<br />

attack” (BPOCA-MUA) was also positive <strong>in</strong> all <strong>in</strong>vestigated teams, <strong>and</strong><br />

aga<strong>in</strong> highest <strong>in</strong> the German team (M GER = 1.39+1.58 [n = 6] vs M SRB<br />

= 0.49+1.05 [n = 6]). But as already seen above, this k<strong>in</strong>d of advantage<br />

was less relevant for the w<strong>in</strong>ners than for the losers (M WIN = 0.55+0.74<br />

[n = 12] vs. M LOS = 1.86+2.71 [n = 12]). The reason for the latter two,<br />

somewhat surpris<strong>in</strong>g f<strong>in</strong>d<strong>in</strong>gs might result from the fact that the w<strong>in</strong>n<strong>in</strong>g<br />

teams seem to put more emphasis on play<strong>in</strong>g fast polo, i.e. on counter<br />

attacks <strong>and</strong> also on the pattern of “driv<strong>in</strong>g-<strong>in</strong>” <strong>in</strong>to the area <strong>in</strong> front<br />

of goal. So, the transition from hold<strong>in</strong>g the ball <strong>in</strong> the “back-position to<br />

driv<strong>in</strong>g-<strong>in</strong>” (BPOCA-DI) is much more effective <strong>in</strong> the w<strong>in</strong>n<strong>in</strong>g teams<br />

than <strong>in</strong> the losers, where it even had a negative effect on the total score<br />

(M WIN = 0.20+0.69 [n = 12] vs. M LOS = –0.22+1.06 [n = 12]).<br />

dIscussIon<br />

In this study, performance diagnosis <strong>in</strong> water polo by stochastic path<br />

simulation was used for the first time. In comparison with traditional<br />

notational analysis methods <strong>in</strong> water polo (Bratusa, Matkovic & Dopsaj,<br />

2003; Dopsaj & Matkovic, 1999; Hohmann, 1992; Platanou & Nikopopoulos,<br />

2003), the ma<strong>in</strong> advantage of this approach is that it delivers not<br />

only a statistical description of the analyzed tactical behaviour, but is also<br />

capable of: (a) analyz<strong>in</strong>g the performance relevance of the various tactical<br />

behaviour patterns, <strong>and</strong> (b) provid<strong>in</strong>g a prognosis on the probable effects<br />

of certa<strong>in</strong> modifications to the tactical behaviour of <strong>in</strong>terest, based on a<br />

mathematical simulation of the <strong>in</strong>teractive game process. Performance<br />

diagnosis through stochastic path simulation by means of the Markovcha<strong>in</strong><br />

model, hence, is a worthwhile performance diagnostic procedure <strong>in</strong><br />

water polo, allow<strong>in</strong>g the calculation of optimal tactical behaviour.<br />

280<br />

reFerences<br />

Bratusa, Z. F., Matkovic, I. Z. & Dopsaj, M. J. (2003). Model characteristics<br />

of water polo players movements <strong>in</strong> the vertical position<br />

dur<strong>in</strong>g competition. In J. C. Chatard (Ed.). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g IX (pp. 481-486). Sa<strong>in</strong>t-Étienne: l´Université de<br />

Sa<strong>in</strong>t-Étienne.<br />

Dopsaj, M. & Matkovic, I. Z. (1999). The structure of technical <strong>and</strong><br />

tactical activities of water polo players <strong>in</strong> the first Yugoslav league<br />

dur<strong>in</strong>g the game. In K. L. Kesk<strong>in</strong>en, P. V. Komi, & A. P. Holl<strong>and</strong>er<br />

(Eds.). <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII (pp. 435-438).<br />

Jyväskylä: Gummerus Pr<strong>in</strong>t<strong>in</strong>g House.<br />

Hirotsu, N., Miyaji, C., Ezake, N., Shigenaga, T. & Taguchi, A. (2004).<br />

A model for f<strong>in</strong>d<strong>in</strong>g optimal tactics <strong>in</strong> volleyball us<strong>in</strong>g Markov decision<br />

processes. The Eng<strong>in</strong>eer<strong>in</strong>g of Sports, 5(2), 447-453.<br />

Hohmann, A. (1992). Analysis of delayed tra<strong>in</strong><strong>in</strong>g effects <strong>in</strong> the preparation<br />

of the West-German water polo team for the Olympic games<br />

1988. In D. MacLaren, T. Reilly & A. Lees (Eds.). Swimm<strong>in</strong>g Science<br />

VI (pp. 213-217). London: E & F Spon.<br />

Hohmann, A., Zhang, H. & Koth, A. (2004). Performance diagnosis<br />

through mathematical simulation <strong>in</strong> table tennis <strong>in</strong> left <strong>and</strong> right<br />

h<strong>and</strong>ed shakeh<strong>and</strong> <strong>and</strong> penholder players. In A. Lees, J. F. Kahn, A.<br />

Maynard (Eds.). Science <strong>and</strong> Racket Sports III (pp. 220-226). London:<br />

Routledge.<br />

Hughes, M. (2008). An Overview of the Development of Notational<br />

Analysis. In M. Hughes & M. Franks (Eds.). The essentials of performance<br />

analysis - an Introduction (pp. 51-84). Chippenham: Routledge.<br />

Hughes, M. & Bartlett, R. M. (2008). What is Performance Analysis? In<br />

M. Hughes & M. Franks (Eds.). The essentials of performance analysis -<br />

an Introduction (pp. 8-20). Chippenham: Routledge.<br />

Hughes, M. & Franks, I. (2004). Notational analysis of sport. New York:<br />

Routledge.<br />

Hughes, M. & Bartlett, R. M. (2002). The use of performance <strong>in</strong>dicators<br />

<strong>in</strong> performance analysis. Journal of Sports Sciences, 20(10), 739-754.<br />

Lames, M. (1991). Leistungsdiagnostik durch Computersimulation [Performance<br />

diagnosis by computer simulation]. Frankfurt am Ma<strong>in</strong>: Harri<br />

Deutsch.<br />

Lames, M. & McGarry, T. (2007). On the search for reliable performance<br />

<strong>in</strong>dicators <strong>in</strong> game sports. International Journal of Performance<br />

Analysis <strong>in</strong> Sport, 5(1), 62-79.<br />

McGarry, T. & Franks, I. M. (1994). A stochastic approach to predict<strong>in</strong>g<br />

competition squash match-play. Journal of Sports Sciences, 12(6),<br />

573-584.<br />

McGarry, T. & Perl, J. (2004). Models of sports contests - Markov processes,<br />

dynamical systems <strong>and</strong> neural networks. In M. Hughes & M.<br />

Franks (Eds.). Notational analysis of sport (2 ed.) (pp. 227-242). New<br />

York: Routledge.<br />

Pfeiffer, M. (2004). Computer Simulation to Evaluate the Performance<br />

Relevance of Tactical Behaviour <strong>in</strong> H<strong>and</strong>ball. In F. Seifritz, M. Mester,<br />

J. Perl, O. Spaniol, & J. Wiemeyer (Eds.). 1st International Work<strong>in</strong>g<br />

Conference IT <strong>and</strong> Sport & 5th Conference dvs-Section Computer<br />

Science <strong>in</strong> Sport (pp. 56-59). Cologne: German Sport University.<br />

Pfeiffer, M. (2005). Leistungsdiagnostik im Nachwuchstra<strong>in</strong><strong>in</strong>g der Sportspiele.<br />

[Performance diagnosis <strong>in</strong> the game sport tra<strong>in</strong><strong>in</strong>g of young athletes].<br />

Köln: Sport & Buch Strauß.<br />

Pfeiffer, M. & Hohmann, A. (2008). Performance Diagnostics of tactical<br />

behaviour at the FIFA World Cup 2006. In International Convention<br />

on Science, Education <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Sport (vol. 1) (p.175).<br />

Guangzhou: People’s Sports Publish<strong>in</strong>g House.<br />

Platanou, T. & Nikopopoulos, G. (2003). Assessment of sport orientation<br />

<strong>in</strong> the field of water polo. In J. C. Chatard (Ed.). <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX (pp. 493-498). Sa<strong>in</strong>t-Étienne: l´Université<br />

de Sa<strong>in</strong>t-Étienne.<br />

Robson, C. (2002). Real world research. Oxford: Blackwell Publishers.<br />

Zhang, H. (2003). Leistungsdiagnostik im Tischtennis [Performance diagnosis<br />

<strong>in</strong> table tennis]. Hamburg: Dr. Kovac.


Throw<strong>in</strong>g Accuracy of Water Polo Players of Different<br />

Tra<strong>in</strong><strong>in</strong>g Age <strong>and</strong> Fitness Levels <strong>in</strong> a Static Position<br />

<strong>and</strong> after Previous Swimm<strong>in</strong>g<br />

Platanou, t. <strong>and</strong> Botonis, P.<br />

Faculty of Physical Education <strong>and</strong> Sport Science, University of Athens, Greece<br />

The aim of the present study was to compare throw<strong>in</strong>g accuracy <strong>in</strong> a<br />

static position to after previous swimm<strong>in</strong>g <strong>in</strong> relation to tra<strong>in</strong><strong>in</strong>g age<br />

<strong>and</strong> fitness level. Fifty (50) water polo players (aged: 11-17 yrs) were<br />

tested. Significant differences were observed <strong>in</strong> throw<strong>in</strong>g accuracy<br />

between the static position <strong>and</strong> after previous swimm<strong>in</strong>g<br />

(F=58.05, P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 1. Throw<strong>in</strong>g accuracy <strong>in</strong> a static position <strong>and</strong> after swimm<strong>in</strong>g <strong>in</strong><br />

relation to tra<strong>in</strong><strong>in</strong>g age<br />

282<br />

Variables<br />

Static accuracy<br />

Static accuracy (%)<br />

Accuracy pr. swimm<strong>in</strong>g<br />

Accuracy pr. swimm<strong>in</strong>g (%)<br />

Difference accuracy<br />

Difference accuracy (%)<br />

First group<br />

(2-3 years)<br />

1.7±0.9*<br />

35.0 ±13.9*<br />

0.6 ± 0.5*<br />

11.7 ±9.8*<br />

1.2 ±1.0<br />

23.3 ±20.6<br />

Second group<br />

(4-5 years)<br />

2.7 ± 1.3**<br />

53.8 ±22.4**<br />

1.7 ±1.0**<br />

34.6 ±20.0**<br />

1.0 ±0.9<br />

19.2 ± 19.0<br />

Third group<br />

(6-8 years)<br />

4.0 ± 0.7***<br />

80.0 ±14.7***<br />

2.7 ±0.8***<br />

53.3 ±15.6***<br />

1.3 ±0.9<br />

26.7 ±19.7<br />

(*) significant difference between the first <strong>and</strong> second group, (**) significant<br />

difference between the second <strong>and</strong> the third group, (***) significant<br />

difference between the first <strong>and</strong> the third group (P31.9<br />

3.8±0.7***<br />

76.7±14.1***<br />

2.7±0.8***<br />

53.3±15.3***<br />

1.2±1.0<br />

23.3±19.7<br />

*significant difference between 1st <strong>and</strong> 2nd group, ** significant difference<br />

between 2nd <strong>and</strong> 3rd group,*** significant difference between 1st<br />

<strong>and</strong> 3rd group, (p


correctly executed, <strong>in</strong> order for the whole to be effective. It is possible<br />

that <strong>in</strong>efficient swimm<strong>in</strong>g technique has a negative effect on shoot<strong>in</strong>g<br />

accuracy. Effective swimm<strong>in</strong>g technique is one of the ma<strong>in</strong> factors that<br />

determ<strong>in</strong>es swimm<strong>in</strong>g performance <strong>in</strong> a given distance. One other ma<strong>in</strong><br />

factor is the fitness level. In the present study, the participants of higher<br />

swimm<strong>in</strong>g performance had greater shoot<strong>in</strong>g accuracy than participants<br />

with lower swimm<strong>in</strong>g performance. Accord<strong>in</strong>g to our results, it was revealed<br />

that fitness level is a significant predictor of accuracy either <strong>in</strong><br />

shoot<strong>in</strong>g <strong>in</strong> a static position or after previous swimm<strong>in</strong>g. However, Δ<br />

values <strong>in</strong> accuracy between shot <strong>in</strong> a static position <strong>and</strong> after previous<br />

swimm<strong>in</strong>g were not different <strong>in</strong> relation to fitness level.<br />

Significantly high correlation was observed <strong>in</strong> swimm<strong>in</strong>g performance<br />

<strong>and</strong> tra<strong>in</strong><strong>in</strong>g age. Moreover, tra<strong>in</strong><strong>in</strong>g age <strong>and</strong> swimm<strong>in</strong>g performance<br />

were significantly correlated with shoot<strong>in</strong>g accuracy either <strong>in</strong> a<br />

static position or after previous swimm<strong>in</strong>g. It seems that yearly tra<strong>in</strong><strong>in</strong>g<br />

improves shoot<strong>in</strong>g accuracy. The swimm<strong>in</strong>g performance, also, which<br />

can be considered not only as a fitness level <strong>in</strong>dex but as an <strong>in</strong>dex of<br />

adequate swimm<strong>in</strong>g technique, strongly affects shoot<strong>in</strong>g accuracy. Accord<strong>in</strong>g<br />

to our f<strong>in</strong>d<strong>in</strong>gs, our hypothesis that shots <strong>in</strong> a static position<br />

would be more accurate than after previous swimm<strong>in</strong>g <strong>and</strong> that waterpolo<br />

players of greater tra<strong>in</strong><strong>in</strong>g age <strong>and</strong> those with better swimm<strong>in</strong>g<br />

performance would be more accurate compared with <strong>in</strong>experienced<br />

water-polo players, of lower fitness level, was verified.<br />

conclusIon<br />

The present study is the first to <strong>in</strong>vestigate shoot<strong>in</strong>g accuracy <strong>in</strong> a static<br />

position <strong>and</strong> after previous swimm<strong>in</strong>g of water-polo players differ<strong>in</strong>g<br />

<strong>in</strong> tra<strong>in</strong><strong>in</strong>g age <strong>and</strong> swimm<strong>in</strong>g performance. These results suggest that<br />

shots <strong>in</strong> a static position are more accurate than shots after previous<br />

swimm<strong>in</strong>g. Additionally, shoot<strong>in</strong>g accuracy is highly dependent on<br />

tra<strong>in</strong><strong>in</strong>g age. The <strong>in</strong>experienced water-polo players were less accurate<br />

than players of greater tra<strong>in</strong><strong>in</strong>g age. Accord<strong>in</strong>g to our results, it seems<br />

that shoot<strong>in</strong>g accuracy is highly dependent on swimm<strong>in</strong>g performance.<br />

The water-polo players of lower swimm<strong>in</strong>g performance had a significantly<br />

lower percentage of accurate shots than players of greater swimm<strong>in</strong>g<br />

performance.There is no difference <strong>in</strong> accuracy between shot <strong>in</strong> a<br />

static position <strong>and</strong> after previous swimm<strong>in</strong>g as Δ values, <strong>in</strong> relation to<br />

tra<strong>in</strong><strong>in</strong>g age or swimm<strong>in</strong>g performance. Previous swimm<strong>in</strong>g has a negative<br />

effect on shoot<strong>in</strong>g accuracy, regardless of the tra<strong>in</strong><strong>in</strong>g age.<br />

The data of this study should be applied to athletes of similar level <strong>and</strong><br />

could provide water polo coaches with guidel<strong>in</strong>es for tra<strong>in</strong><strong>in</strong>g.<br />

reFerences<br />

Bloomfield, J., Blanksby B.A. & Ackl<strong>and</strong> T. (1990). The <strong>in</strong>fluence of<br />

strength tra<strong>in</strong><strong>in</strong>g on overhead throw<strong>in</strong>g velocity of elite water polo<br />

players. Aus J Sci Med Sport. 22, 63-67.<br />

Erquli, F. & Supej, M. (2009). Impact of fatigue on the position of the<br />

release arm <strong>and</strong> shoulder girdle over a longer shoot<strong>in</strong>g distance for an<br />

elite basketball player. J. Strength Cond Res. 23(3), 1029-1036.<br />

Feltner, M.E. & Nelson, S.T. (1996). Three-dimensional k<strong>in</strong>ematics of<br />

the throw<strong>in</strong>g arm dur<strong>in</strong>g the penalty throw <strong>in</strong> water polo. J Applied<br />

Biomech. 12, 359-382.<br />

Triplett, T., Fleck, S.J., & Smith, S.L. (1991). Isok<strong>in</strong>etic torque <strong>and</strong><br />

throw<strong>in</strong>g velocity <strong>in</strong> water polo. Med Sci Sports Exer. 23, 11-14.<br />

Royal, K.A., Farrow, D., Mujica, I., Halson, S.L., Pyne, D. & Abernethy,<br />

B. (2006). The effects of fatigue on decision mak<strong>in</strong>g <strong>and</strong> shoot<strong>in</strong>g skill<br />

performance <strong>in</strong> water polo players. J. Sport Sci. 24(8), 807-815.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

The Effect of Cognition-Based Technique Tra<strong>in</strong><strong>in</strong>g on<br />

Stroke Length <strong>in</strong> Age-Group Swimmers<br />

schmidt, A.c. 1 , ungerechts, B.e. 2 , Buss, W. 1 & schack, t. 2<br />

1University of Gött<strong>in</strong>gen, Department of Society <strong>and</strong> Tra<strong>in</strong><strong>in</strong>g, Germany<br />

2University of Bielefeld, Department of Neurocognition <strong>and</strong> Action – <strong>Biomechanics</strong>,<br />

Germany<br />

This study deals with a specific <strong>and</strong> <strong>in</strong>novative aspect of long-term performance-plann<strong>in</strong>g<br />

<strong>in</strong> swimm<strong>in</strong>g: cognition-based technique tra<strong>in</strong><strong>in</strong>g.<br />

Based on the studies of Thomas Schack on the cognitive architecture<br />

of movements, the cognition-based technique tra<strong>in</strong><strong>in</strong>g method was developed<br />

<strong>and</strong> proved the first time <strong>in</strong> swimm<strong>in</strong>g. The study applies the<br />

program ‚Split’, which has already been successfully used <strong>in</strong> other sports.<br />

Split uses distance scal<strong>in</strong>g between the elements of a system of concepts<br />

to measure conceptual structures. To evaluate the potential <strong>in</strong>troduction<br />

of cognition-based technique tra<strong>in</strong><strong>in</strong>g <strong>in</strong> long-term performanceplann<strong>in</strong>g<br />

of swimmers, biomechanical criteria were used.<br />

Key words: age-group swimmers, crawl, representational structure,<br />

stroke distance, stroke rate<br />

IntroductIon<br />

Highly skilled swimmers aspire to cover as much distance per stroke<br />

as possible. Accord<strong>in</strong>g to Reischle (1988) <strong>and</strong> Arellano et al. (1991) an<br />

improved swimm<strong>in</strong>g technique results <strong>in</strong> a longer stroke length. Therefore<br />

it is likely that the athlete swims the same race-distance with fewer<br />

strokes <strong>and</strong> probably <strong>in</strong> less time. In the case of less time <strong>and</strong> <strong>in</strong>creased<br />

stroke length, the so-called stroke-<strong>in</strong>dex (speed squared <strong>and</strong> multiplied<br />

by stroke length) will also be <strong>in</strong>creased.<br />

Know<strong>in</strong>g this, it is obviously important to <strong>in</strong>crease the stroke length<br />

of any swimmer. To ga<strong>in</strong> more effective underwater-movement, the<br />

swimmer could <strong>in</strong>crease his power (without technical tra<strong>in</strong><strong>in</strong>g this<br />

might be limited soon) <strong>and</strong> / or try to optimize his motion sequence<br />

<strong>in</strong> relationship to the water. In contrast to most other sport<strong>in</strong>g activities,<br />

swimmers do not have a fixed base to push off. Swimmers, <strong>in</strong>stead,<br />

produce propulsion due to <strong>in</strong>teraction of body <strong>and</strong> water-mass. Therefore<br />

it is very important to educate swimmers at the beg<strong>in</strong>n<strong>in</strong>g of long<br />

term performance plann<strong>in</strong>g on how to work with water properly while<br />

execut<strong>in</strong>g regular strokes. To reach this, emphasis should be placed on<br />

how strok<strong>in</strong>g is mentally represented by swimmers, even age-group<br />

swimmers.<br />

Advanced age-group swimmers, <strong>in</strong> order to improve the efficacy of<br />

their strok<strong>in</strong>g actions, have to control the stroke-technique mentally as<br />

a prerequisite to optimize details of motion sequences. In this context a<br />

cognitive <strong>in</strong>tervention can be used which is based on the Structural Dimension<br />

Analysis of Motor Memory (SDA-M) accord<strong>in</strong>g to SCHACK<br />

(2003). UNGERECHTS/SCHACK (2006) did a first study of the<br />

representation of butterfly-swimmers us<strong>in</strong>g SDA-M <strong>and</strong> described the<br />

method.<br />

SDA-M is used to describe mental representation structures <strong>and</strong> it<br />

enables statements about the cognitive architecture of complex movements<br />

<strong>in</strong> the long-term memory. This means, <strong>in</strong>terpret<strong>in</strong>g the results,<br />

one can underst<strong>and</strong> how the swimmer is th<strong>in</strong>k<strong>in</strong>g about his movements,<br />

which parts (nodes) he connects closely <strong>and</strong> where there are large distances<br />

or connections, which – biomechanically – are not reasonable.<br />

So the major cause of problems of (strok<strong>in</strong>g) actions can be localized <strong>in</strong><br />

a way which fits with the dem<strong>and</strong> of effective communication between<br />

coach <strong>and</strong> athlete. The purpose of this paper is to exam<strong>in</strong>e the effect of<br />

cognition-based technique tra<strong>in</strong><strong>in</strong>g on the strok<strong>in</strong>g ability of age-group<br />

swimmers.<br />

283


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Method<br />

The empirical study was carried out on three test days. A test group <strong>and</strong><br />

a control group with 23 <strong>and</strong> 24 age-group swimmers, respectively, were<br />

<strong>in</strong>volved <strong>in</strong> the study. Between the first <strong>and</strong> second test day the test<br />

group performed specific workouts for six weeks. On the test days the<br />

program ‘Split’ (SCHACK et al., 2000) was used to evaluate the representational<br />

structure <strong>and</strong> the swimmers also performed a swimm<strong>in</strong>g<br />

test of 2 x 25 meters crawl stroke at full speed. The control group only<br />

performed the swimm<strong>in</strong>g test. To evaluate the long-term educational<br />

effects of the cognition-based tra<strong>in</strong><strong>in</strong>g, the swimmers of both groups<br />

tra<strong>in</strong>ed for another 12 weeks. The study was concluded by a f<strong>in</strong>al swimm<strong>in</strong>g<br />

test for both groups <strong>and</strong> the test group also used ‘Split’ aga<strong>in</strong>.<br />

Dur<strong>in</strong>g the spr<strong>in</strong>ts on the test days a) the time over a 10m distance<br />

– from 10 to 20 m – <strong>and</strong> b) the stroke rate were measured <strong>and</strong> f<strong>in</strong>ally<br />

the stroke length <strong>and</strong> the stroke <strong>in</strong>dex were calculated (the data of the<br />

two trials were averaged). “Split” was used to sort out “basic action concepts”,<br />

called nodes, represent<strong>in</strong>g arm/h<strong>and</strong> actions dur<strong>in</strong>g crawl stroke.<br />

The nodes were established by the coach <strong>in</strong> close relation to how he/<br />

she normally describes strok<strong>in</strong>g, however <strong>in</strong> a more structured manner.<br />

After sort<strong>in</strong>g out all nodes accord<strong>in</strong>g to the criteria, if they belong<br />

to the anchor node or not, as result one gets an impression of the mental<br />

representation, which the swimmer has of its motion sequence (<strong>in</strong><br />

this example of the crawl arm stroke). By means of this computer programme,<br />

the so-called split technique is used <strong>in</strong> order to achieve the<br />

data of proximity.<br />

“The SDA-M consists of four steps: First, a special split procedure <strong>in</strong>volv<strong>in</strong>g<br />

a multiple sort<strong>in</strong>g task delivers a distance scal<strong>in</strong>g between the BACs<br />

of a suitably predeterm<strong>in</strong>ed set. Second, a hierarchical cluster analysis is used<br />

to transform the set of BACs <strong>in</strong>to a hierarchical structure. Third, a factor<br />

analysis reveals the dimensions <strong>in</strong> this structured set of BACs, <strong>and</strong> fourth,<br />

the cluster solutions are tested for non-variance with<strong>in</strong>- <strong>and</strong> between-groups<br />

(for psychometric details, see Schack, 2001, 2002” (BLÄSING et al. 2009).<br />

The mental representation is described by a so-called dendrogram <strong>and</strong><br />

clusters (groups of <strong>in</strong>dividual nodes). Analyz<strong>in</strong>g the dendrograms <strong>and</strong><br />

the clusters special tra<strong>in</strong><strong>in</strong>g-programs were created (theoretical <strong>and</strong><br />

practical), which were performed dur<strong>in</strong>g the six week tra<strong>in</strong><strong>in</strong>g period.<br />

The <strong>in</strong>dividual strok<strong>in</strong>g <strong>in</strong>structions were <strong>in</strong>ferred from the results of the<br />

SDA-M tests. The communication between coach <strong>and</strong> athlete was based<br />

on def<strong>in</strong>ed notes. Dur<strong>in</strong>g the workouts established drills were used <strong>in</strong><br />

another context, deal<strong>in</strong>g with one or more BAC <strong>and</strong> their connection<br />

to each other. First the coach expla<strong>in</strong>ed to the athlete (a) the results of<br />

split <strong>and</strong> <strong>in</strong> most of the cases (b) aga<strong>in</strong> all the nodes <strong>and</strong> their impact<br />

<strong>in</strong> the strok<strong>in</strong>g action, especially the ‘problem-nodes’ of the athlete. This<br />

was the basis of the workouts cover<strong>in</strong>g each node with drills <strong>and</strong> then<br />

later on groups of nodes <strong>and</strong> especially the ‘problem’ nodes. So <strong>in</strong> each<br />

workout (after one or more drills) by us<strong>in</strong>g the nodes, the connection of<br />

one node to the neighbor-nodes or a group of nodes to each other was<br />

discussed. Dur<strong>in</strong>g strok<strong>in</strong>g the swimmer had to concentrate on what<br />

he was do<strong>in</strong>g <strong>and</strong> on his feel<strong>in</strong>gs (e.g. strok<strong>in</strong>g, propulsion) tell<strong>in</strong>g this<br />

later to his coach.<br />

As an example, the BACs of one of the tra<strong>in</strong><strong>in</strong>g groups are shown here:<br />

F<strong>in</strong>gers enter water (1), Shrugg<strong>in</strong>g shoulders (2), Roll<strong>in</strong>g to side of action<br />

(3), Downwards (4), Pronation (5), Elbow extension (6), Roll<strong>in</strong>g<br />

back (7), Slic<strong>in</strong>g h<strong>and</strong> (8), Breath<strong>in</strong>g (9), H<strong>and</strong> forward (10).<br />

results<br />

The follow<strong>in</strong>g figures show the representational structure of one swimmer<br />

at test 1, 2 <strong>and</strong> 3.<br />

284<br />

Fig. 2 Dendrogram of one swimmer (test 1) without any cluster <strong>and</strong><br />

without a real regularity of the nodes. The distances between the nodes<br />

are quite large, therefore do not cluster.<br />

Fig. 3 Dendrogram of the same swimmer after the six week tra<strong>in</strong><strong>in</strong>g<br />

period (test 2) with three clusters (all nodes are <strong>in</strong>tegrated <strong>in</strong> clusters<br />

<strong>and</strong> are <strong>in</strong> biomechanical regularity)<br />

Fig. 4 Dendrogram of the same swimmer after 18 weeks (six weeks specific<br />

tra<strong>in</strong><strong>in</strong>g <strong>and</strong> 12 weeks ‘normal’ tra<strong>in</strong><strong>in</strong>g (data 3). The dendrogram<br />

shows four clusters, regularity of nodes, but also partly <strong>in</strong>creased distances<br />

between nodes.<br />

At test 1 the structure is not really sorted, the distances between the BACs<br />

are quite large (it does not have any clusters). After the tra<strong>in</strong><strong>in</strong>g period


(test 2), however, all BACs are <strong>in</strong>tegrated <strong>in</strong> clusters, the distances are<br />

smaller <strong>and</strong> the nodes are <strong>in</strong> regularity. After the twelve weeks tra<strong>in</strong><strong>in</strong>g<br />

period (test 3) the structure is quite stabilized, some distances are once<br />

aga<strong>in</strong> reduced (p. E. 9 <strong>and</strong> 10, 5 <strong>and</strong> 6) but also some (p. e. 3 <strong>and</strong> 4, 7 <strong>and</strong><br />

8) <strong>in</strong>creased.<br />

The follow<strong>in</strong>g schedule shows a way to transfer the structure of the dendrograms<br />

above <strong>in</strong>to a schedule to compare it directly. Each dendrogram<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g Page 111<br />

shows 2 ma<strong>in</strong> groups, but only test (2) <strong>and</strong> (3) shows 3 <strong>and</strong> 4 clusters.<br />

At test (2) there are 6 nodes (2 clusters) <strong>in</strong> the ma<strong>in</strong> group 1, at test (3)<br />

7 nodes (3 clusters). Accord<strong>in</strong>g to ma<strong>in</strong> group 1 are <strong>in</strong> ma<strong>in</strong> group 2 at<br />

test The follow<strong>in</strong>g (2) 4 nodes schedule (1 cluster) shows a way <strong>and</strong> to at transfer test the (3) structure 3 nodes of (1 the cluster). dendrograms The above real<br />

<strong>in</strong>to <strong>Biomechanics</strong> a schedule <strong>and</strong> to compare <strong>Medic<strong>in</strong>e</strong> it <strong>in</strong> directly. Swimm<strong>in</strong>g Each <strong>XI</strong> dendrogram / Chapter shows 4 Tra<strong>in</strong><strong>in</strong>g 2 ma<strong>in</strong> groups, Page but only 111<br />

distances test (2) <strong>and</strong> between (3) shows 3 the <strong>and</strong> s<strong>in</strong>gle 4 clusters. nodes At test cannot (2) there be are shown 6 nodes <strong>in</strong> (2 the clusters) schedule, <strong>in</strong> the<br />

these ma<strong>in</strong> group details 1, at are test only (3) 7 visible nodes (3 directly clusters). <strong>in</strong> Accord<strong>in</strong>g the dendrograms. to ma<strong>in</strong> group 1 are <strong>in</strong> ma<strong>in</strong><br />

group 2 at test (2) 4 nodes (1 cluster) <strong>and</strong> at test (3) 3 nodes (1 cluster). The real<br />

distances between the s<strong>in</strong>gle nodes cannot be shown <strong>in</strong> the schedule, these details are<br />

Tab. The follow<strong>in</strong>g 1 Schedule schedule of representational shows a way to transfer<br />

only visible directly <strong>in</strong> the dendrograms. structure the structure for one of the swimmer dendrograms at above<br />

<strong>Biomechanics</strong> three<br />

<strong>in</strong>to a schedule <strong>and</strong> to <strong>Medic<strong>in</strong>e</strong> compare <strong>in</strong> it directly. Swimm<strong>in</strong>g Each <strong>XI</strong> dendrogram / Chapter 4 Tra<strong>in</strong><strong>in</strong>g shows 2 ma<strong>in</strong> groups, Page but 111 only<br />

tests test (2) <strong>and</strong> (3) shows 3 <strong>and</strong> 4 clusters. At test (2) there are 6 nodes (2 clusters) <strong>in</strong> the<br />

Tab. 1 Schedule of representational structure for one swimmer at three tests<br />

ma<strong>in</strong> group 1, at test (3) 7 nodes (3 clusters). Accord<strong>in</strong>g to ma<strong>in</strong> group 1 are <strong>in</strong> ma<strong>in</strong><br />

Number of Number of<br />

group Test 2 at test (2) 4 nodes (1 cluster) BAC <strong>and</strong> ma<strong>in</strong> at test group (3) 1 3 nodes BAC (1 ma<strong>in</strong> cluster). group The 2 real<br />

ma<strong>in</strong> groups Cluster<br />

The distances<br />

Test follow<strong>in</strong>g between<br />

1 2 schedule the shows s<strong>in</strong>gle<br />

0 a nodes way to cannot<br />

1,2,4 transfer be the shown structure <strong>in</strong> the of schedule,<br />

5,8,9,10,7,3 the dendrograms these details above are<br />

<strong>in</strong>to only<br />

Test a schedule visible directly<br />

2 2 to compare <strong>in</strong> the<br />

3 it dendrograms. directly. Each {9,10} dendrogram {1,2,3,4} shows {5,6,7,8} 2 ma<strong>in</strong> groups, but only<br />

test Test (2) 3 <strong>and</strong> 2 (3) shows 3 <strong>and</strong> 4 4 clusters. {8,9,10}{1,2}{3,4} At test (2) there are 6 nodes {5,6,7} (2 clusters) <strong>in</strong> the<br />

ma<strong>in</strong> Tab. group 1 Schedule 1, at test of representational (3) 7 nodes (3 structure clusters). for Accord<strong>in</strong>g one swimmer to ma<strong>in</strong> at three group tests 1 are <strong>in</strong> ma<strong>in</strong><br />

group<br />

The Test improvement 2 at Number test (2) of<br />

<strong>in</strong> 4 mental nodes Number (1 representation cluster) of<br />

improvement <strong>in</strong> mental representation BAC <strong>and</strong> shown ma<strong>in</strong> at test group as (3) example 3<br />

shown 1 nodes BAC for (1<br />

as one example ma<strong>in</strong> cluster). swimmer group The<br />

for 2 above real<br />

one<br />

distances also led between ma<strong>in</strong> groups<br />

to improvements the s<strong>in</strong>gle Cluster<br />

<strong>in</strong> nodes the swimm<strong>in</strong>g cannot be parameters shown <strong>in</strong> the (also schedule, shown for these one details swimmer are<br />

only swimmer Test<br />

below). visible 1 2<br />

Accord<strong>in</strong>g directly above <strong>in</strong> also to the REISCHLE dendrograms. led 0 to improvements 1,2,4<br />

(1988) <strong>and</strong> Arellano <strong>in</strong> the et swimm<strong>in</strong>g 5,8,9,10,7,3<br />

al. (1991) the parameters follow<strong>in</strong>g<br />

Test 2 2 3 {9,10} {1,2,3,4} {5,6,7,8}<br />

(also parameters shown were for selected one swimmer to demonstrate below). technical Accord<strong>in</strong>g progress: to REISCHLE first, stroke length (1988) <strong>and</strong><br />

Tab. Test<br />

second, 1 Schedule 3 2<br />

stroke <strong>in</strong>dex of representational 4<br />

which comb<strong>in</strong>es structure {8,9,10}{1,2}{3,4}<br />

stroke for length one swimmer <strong>and</strong> swimm<strong>in</strong>g at {5,6,7} three speed. tests<br />

<strong>and</strong> Arellano<br />

The follow<strong>in</strong>g Number schedule of et al. Number (1991)<br />

lists the of the follow<strong>in</strong>g parameters were selected to<br />

Test<br />

time (10 metres) (t), speed (v), stroke rate (sr), length<br />

demonstrate The improvement<br />

(d) <strong>and</strong> the stroke technical <strong>in</strong> mental<br />

<strong>in</strong>dex (si) of progress: representation BAC ma<strong>in</strong><br />

the example first, shown group<br />

swimmer. stroke as example 1 BAC<br />

length for ma<strong>in</strong><br />

<strong>and</strong> one second, swimmer group 2<br />

ma<strong>in</strong> groups Cluster<br />

stroke above<br />

Test also 1 led 2 to improvements 0 <strong>in</strong> the swimm<strong>in</strong>g 1,2,4 parameters (also 5,8,9,10,7,3 shown for one swimmer<br />

Test <strong>in</strong>dex below). which comb<strong>in</strong>es stroke length <strong>and</strong> swimm<strong>in</strong>g speed.<br />

Tab. 2 Biomechanical 2 Accord<strong>in</strong>g to REISCHLE<br />

data 3 (1988)<br />

of one swimmer {9,10} at {1,2,3,4} <strong>and</strong> Arellano et<br />

test (1), (2) <strong>and</strong> {5,6,7,8} al. (1991) the follow<strong>in</strong>g<br />

(3)<br />

Test The parameters 3 follow<strong>in</strong>g 2 were<br />

Test 1 schedule selected 4 to lists demonstrate the {8,9,10}{1,2}{3,4} Test time technical<br />

2 (10 metres) progress: {5,6,7} (t), first, speed stroke<br />

Test 3 (v), length stroke <strong>and</strong><br />

second, stroke <strong>in</strong>dex which comb<strong>in</strong>es stroke length <strong>and</strong> swimm<strong>in</strong>g speed.<br />

rate t (sr), v length sr d (d) <strong>and</strong> si the t stroke v sr <strong>in</strong>dex d (si) si of the t example v sr swimmer. d si<br />

The The<br />

6.52 improvement follow<strong>in</strong>g schedule<br />

1.53 53 <strong>in</strong> 1.76 mental lists<br />

4.08 representation the time (10<br />

6.64 1.51 47 shown metres)<br />

1.92 as (t), example speed (v),<br />

4.36 6.66for stroke<br />

1.50 one swimmer rate (sr),<br />

48 1.88 above length<br />

4.23<br />

also (d)<br />

6.64 led <strong>and</strong><br />

1.49 to the improvements stroke <strong>in</strong>dex (si)<br />

50 1.81 4.10 <strong>in</strong> of the the<br />

6.22 swimm<strong>in</strong>g example swimmer.<br />

1.57 46 parameters 2.04 5.02 (also 6.64 shown 1.51 for 48 one 1.88 swimmer 4.27<br />

below). Tab. 2 Accord<strong>in</strong>g Biomechanical to REISCHLE data of (1988) one swimmer <strong>and</strong> Arellano at test et al. (1), (1991) (2) <strong>and</strong> the follow<strong>in</strong>g (3)<br />

parameters Tab. 2 Biomechanical<br />

From test 1 were to test selected data<br />

2 (tra<strong>in</strong><strong>in</strong>g to of demonstrate one swimmer at test (1), (2) <strong>and</strong> (3)<br />

period) the technical average progress: speed <strong>in</strong>creased first, stroke a little, length the stroke <strong>and</strong><br />

second, Test 1 Test 2 Test 3<br />

length clearly, stroke <strong>in</strong>dex while which the stroke comb<strong>in</strong>es rate decreased. stroke length Thus, <strong>and</strong> the swimm<strong>in</strong>g stroke-<strong>in</strong>dex speed. also <strong>in</strong>creased. At<br />

The t v sr d si t v sr d si t v sr d si<br />

test follow<strong>in</strong>g 3 the average schedule speed lists decreased the time a bit. (10 The metres) stroke (t), rate, speed the (v), stroke stroke length rate <strong>and</strong> (sr), the length stroke<br />

(d) 6.52 1.53 53 1.76 4.08 6.64 1.51 47 1.92 4.36 6.66 1.50 48 1.88 4.23<br />

<strong>in</strong>dex <strong>and</strong> were the stroke stabilized <strong>in</strong>dex on (si) a level of the between example test swimmer. (1) <strong>and</strong> test (2).<br />

6.64 1.49 50 1.81 4.10 6.22 1.57 46 2.04 5.02 6.64 1.51 48 1.88 4.27<br />

The follow<strong>in</strong>g table shows the mean data of relevant parameters (test 1, 2 <strong>and</strong> 3) of the<br />

Tab. test 2 group. Biomechanical data of one swimmer at test (1), (2) <strong>and</strong> (3)<br />

From test Test 1 to 1 1 to test test 2 (tra<strong>in</strong><strong>in</strong>g 2 (tra<strong>in</strong><strong>in</strong>g period) Test the period) 2 average the speed average <strong>in</strong>creased speed Test a little, 3 <strong>in</strong>creased the stroke a<br />

little, length clearly, while the stroke rate decreased. Thus, the stroke-<strong>in</strong>dex also <strong>in</strong>creased. At<br />

Tab. t 3 v the Statistical stroke sr data d length for si test clearly, group t v while sr the d stroke si rate t decreased. v sr d Thus, si the<br />

6.52 test 3 the average speed decreased a bit. The stroke rate, the stroke length <strong>and</strong> the stroke<br />

Parameter 1.53 53 1.76 4.08 Test 6.64 1 (mean, 1.51std) 47<br />

stroke-<strong>in</strong>dex Test 1.922 4.36 (mean, 6.66 std) 1.50 Test 48 3 (mean, 1.88 4.23 std)<br />

<strong>in</strong>dex were stabilized also <strong>in</strong>creased. on a level between At test test 3 (1) the <strong>and</strong> average test (2). speed decreased a bit.<br />

6.64 Speed 1.49 50 1.81 4.10 1.53 6.22 ± 0.09 1.57 m/s 46 1.52 2.04 ± 5.02 0.11 6.64 m/s 1.51 1.49 48 ± 1.88 0.09 m/s 4.27<br />

The follow<strong>in</strong>g table shows the mean data of relevant parameters (test 1, 2 <strong>and</strong> 3) of the<br />

Stroke stroke rate rate, the 49.61 stroke ± length 4.2 /m<strong>in</strong> <strong>and</strong> 47.81 the stroke ± 3.26 <strong>in</strong>dex /m<strong>in</strong> were 46.70 stabilized ± 4.18 /m<strong>in</strong> on<br />

From test group.<br />

a Stroke level test length between 1 to test 2 test (tra<strong>in</strong><strong>in</strong>g 1.85 (1) <strong>and</strong> ± period) 0.16 test m the (2). average 1.92 speed ± 0.19 <strong>in</strong>creased m 1.93 a little, ± 0.20 the stroke m<br />

length Stroke clearly, <strong>in</strong>dex while the stroke 4.36 ± rate 0.72 decreased. 4.50 Thus, ± the 1.01 stroke-<strong>in</strong>dex 4.34 also ± <strong>in</strong>creased. 0.80 At<br />

test The Tab. 3 the follow<strong>in</strong>g 3 Statistical average speed data table for decreased shows test group the a bit. mean The stroke data rate, of relevant the stroke length parameters <strong>and</strong> the (test stroke 1,<br />

<strong>in</strong>dex Parameter Test 1 (mean, std) Test 2 (mean, std) Test 3 (mean, std)<br />

2 The <strong>and</strong> speed were 3) stabilized of rema<strong>in</strong>ed the test on nearly a group. level the between same over test (1) the <strong>and</strong> 3 tests. test (2). Compar<strong>in</strong>g the stroke length,<br />

The Speed 1.53 ± 0.09 m/s 1.52 ± 0.11 m/s 1.49 ± 0.09 m/s<br />

however, follow<strong>in</strong>g an <strong>in</strong>crease table shows of approx. the mean 0.07 data m (60 of strokes relevant = parameters 4.20 m) <strong>and</strong> (test aga<strong>in</strong> 1, 2 1 <strong>and</strong> cm to 3) test of the (3).<br />

test Stroke rate 49.61 ± 4.2 /m<strong>in</strong> 47.81 ± 3.26 /m<strong>in</strong> 46.70 ± 4.18 /m<strong>in</strong><br />

The group. stroke rate decreased by approx. 2 <strong>and</strong> 1 strokes per m<strong>in</strong>ute. The stroke <strong>in</strong>dex<br />

Tab. Stroke length 1.85 ± 0.16 m 1.92 ± 0.19 m 1.93 ± 0.20 m<br />

<strong>in</strong>creased 3 Statistical from test data 1 to test for 2 test <strong>and</strong> group decreased to test 3. Although there are small<br />

Tab. Stroke 3 Statistical <strong>in</strong>dex data for 4.36 test group ± 0.72 4.50 ± 1.01 4.34 ± 0.80<br />

Parameter Test 1 (mean, std) Test 2 (mean, std) Test 3 (mean, std)<br />

Speed The speed rema<strong>in</strong>ed nearly 1.53 ± 0.09 the same m/s over 1.52 the 3 ± tests. 0.11 m/s Compar<strong>in</strong>g 1.49 the ± stroke 0.09 m/s length,<br />

Stroke however, rate an <strong>in</strong>crease of 49.61 approx. ± 4.2 0.07 /m<strong>in</strong> m (60 strokes 47.81 = ± 4.20 3.26 m) /m<strong>in</strong> <strong>and</strong> aga<strong>in</strong> 46.70 1 ± cm 4.18 to test /m<strong>in</strong> (3).<br />

Stroke The stroke length rate decreased 1.85 ± by 0.16 approx. m 2 <strong>and</strong> 1.92 1 strokes ± 0.19 per m m<strong>in</strong>ute. 1.93 The ± 0.20 stroke m <strong>in</strong>dex<br />

Stroke <strong>in</strong>creased <strong>in</strong>dex from test 1 4.36 to ± test 0.72 2 <strong>and</strong> decreased 4.50 ± to 1.01 test 3. Although 4.34 ± there 0.80 are small<br />

The speed rema<strong>in</strong>ed nearly the same over the 3 tests. Compar<strong>in</strong>g the<br />

stroke length, however, an <strong>in</strong>crease of approx. 0.07 m (60 strokes = 4.20<br />

m) <strong>and</strong> aga<strong>in</strong> 1 cm to test (3). The stroke rate decreased by approx. 2 <strong>and</strong><br />

1 strokes per m<strong>in</strong>ute. The stroke <strong>in</strong>dex <strong>in</strong>creased from test 1 to test 2 <strong>and</strong><br />

decreased <strong>Biomechanics</strong> to <strong>and</strong> test <strong>Medic<strong>in</strong>e</strong> 3. Although <strong>in</strong> Swimm<strong>in</strong>g there <strong>XI</strong> are / Chapter small 4 <strong>in</strong>creases, Tra<strong>in</strong><strong>in</strong>g only the Page stroke 112<br />

rate changed significantly (shown by the Wilcoxon signed-rank test).<br />

The speed rema<strong>in</strong>ed nearly the same over the 3 tests. Compar<strong>in</strong>g the stroke length,<br />

however, an <strong>in</strong>crease of approx. 0.07 m (60 strokes = 4.20 m) <strong>and</strong> aga<strong>in</strong> 1 cm to test (3).<br />

The stroke rate decreased by approx. 2 <strong>and</strong> 1 strokes per m<strong>in</strong>ute. The stroke <strong>in</strong>dex<br />

<strong>in</strong>creased from test 1 to test 2 <strong>and</strong> decreased to test 3. Although there are small<br />

<strong>in</strong>creases, only the stroke rate changed significantly (shown by the Wilcoxon signed-<br />

The rank test). follow<strong>in</strong>g table shows the mean data of relevant parameters (test 1,<br />

2 <strong>and</strong> 3) of the control group.<br />

The follow<strong>in</strong>g table shows the mean data of relevant parameters (test 1, 2 <strong>and</strong> 3) of the<br />

control group.<br />

Tab. 4 Statistical data for control group<br />

Tab. 4 Statistical data for control group<br />

Parameter Test 1 (mean, std) Test 2 (mean, std) Test 3 (mean, std)<br />

Speed 1.38 ± 0.10 m/s 1.30 ± 0.11 m/s 1.28 ± 0.08 m/s<br />

Stroke rate 49.63 ± 3.62 /m<strong>in</strong> 48.65 ± 3.87 /m<strong>in</strong> 48.80 ± 4.62 /m<strong>in</strong><br />

Stroke length 1.68 ± 0.15 m 1.62 ± 0.16 m 1.57 ± 0.18 m<br />

Stroke <strong>in</strong>dex 3.23 ± 0.66 2.81 ± 0.70 2.60 ± 0.56<br />

In contrast with the test group, the control group does not show any <strong>in</strong>creases. Rather<br />

the speed <strong>and</strong> the stroke distance decreased, while the stroke rate nearly rema<strong>in</strong>ed at the<br />

same level.<br />

DISCUSSION<br />

Compar<strong>in</strong>g the test-group-results of the three tests after six weeks tra<strong>in</strong><strong>in</strong>g <strong>in</strong>clud<strong>in</strong>g a<br />

SDA-M based <strong>in</strong>tervention the <strong>in</strong>crease of stroke length at a similar speed is obvious.<br />

This can also be shown for the stroke <strong>in</strong>dex (test 1 to 2, which is based on speed <strong>and</strong> the<br />

stroke length. Longer stroke length is an <strong>in</strong>dicator of an <strong>in</strong>creased effect of the strok<strong>in</strong>g<br />

action. In comb<strong>in</strong>ation with lower stroke rate a total <strong>in</strong>crease of efficiency is obvious.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

In contrast with the test group, the control group does not show any<br />

<strong>in</strong>creases. Rather the speed <strong>and</strong> the stroke distance decreased, while the<br />

stroke rate nearly rema<strong>in</strong>ed at the same level.<br />

dIscussIon<br />

Compar<strong>in</strong>g the test-group-results of the three tests after six weeks<br />

tra<strong>in</strong><strong>in</strong>g <strong>in</strong>clud<strong>in</strong>g a SDA-M based <strong>in</strong>tervention the <strong>in</strong>crease of stroke<br />

length at a similar speed is obvious. This can also be shown for the stroke<br />

<strong>in</strong>dex (test 1 to 2, which is based on speed <strong>and</strong> the stroke length. Longer<br />

stroke length is an <strong>in</strong>dicator of an <strong>in</strong>creased effect of the strok<strong>in</strong>g action.<br />

In comb<strong>in</strong>ation with lower stroke rate a total <strong>in</strong>crease of efficiency is obvious.<br />

However, without the specific workouts the test group also could<br />

not stabilize the high level reached at test 2. The chosen parameters also<br />

decreased a bit, but reached at test 3 a level between test 1 <strong>and</strong> test 2.<br />

In contrast of the test group, the control group rema<strong>in</strong>ed on the level<br />

of test 1 or the results decreased. Without us<strong>in</strong>g Split or do<strong>in</strong>g the specific<br />

technique tra<strong>in</strong><strong>in</strong>g, they did not show the same changes as the test<br />

group.<br />

Even though the changes were mostly not statistically significant,<br />

the <strong>in</strong>tervention made an impact: the participat<strong>in</strong>g swimmers <strong>in</strong>creased<br />

their cognitive ability <strong>and</strong> thus enhanced their own power to optimize<br />

their aquatic space activities. But this seems to be a first, small step –<br />

without the specific tra<strong>in</strong><strong>in</strong>g the changes could not be stabilized at the<br />

high level of test 2. Either the <strong>in</strong>tervention-time was too short or it<br />

might be important to repeat the specific workouts for better stabilization.<br />

Presumably, if the SDA-M based strok<strong>in</strong>g <strong>in</strong>structions causes<br />

large-sale changes, the concerned swimmers were not able to automate<br />

the new motion sequence <strong>in</strong> the short time of the <strong>in</strong>tervention. Especially<br />

when they try to swim at maximal speed, they did not manage<br />

to cont<strong>in</strong>uously produce the motion sequence at an optimized level or<br />

they did not reach maximal speed, they swam more slowly than on the<br />

pre-test.<br />

conclusIon<br />

The elected method st<strong>and</strong>s the test, although it will be important <strong>in</strong> the<br />

future to study aga<strong>in</strong> this type of tra<strong>in</strong><strong>in</strong>g <strong>in</strong> the doma<strong>in</strong> of motor control<br />

<strong>and</strong> motor learn<strong>in</strong>g, for example dur<strong>in</strong>g a longer <strong>in</strong>tervention. In the<br />

future, technique tra<strong>in</strong><strong>in</strong>g offers great potential for more effective tra<strong>in</strong><strong>in</strong>g<br />

of age-group swimmers. In long term performance plann<strong>in</strong>g, more<br />

time should therefore be spent on the education of motor competence<br />

start<strong>in</strong>g early <strong>in</strong> the swimmer’s education. With advanced swimmers the<br />

cognition based technique tra<strong>in</strong><strong>in</strong>g can be used to work systematically<br />

on the cognitive representation of the motion <strong>in</strong> theory <strong>and</strong> practice.<br />

However, this requires better education of the swimmers <strong>in</strong> the theoretical<br />

background of the different strokes.<br />

reFerences<br />

Arellano, R & Pardollp, S. (1991). An evaluation of changes <strong>in</strong> the<br />

crawl-stroke techniques dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g periods <strong>in</strong> a swimm<strong>in</strong>g season.<br />

In D. Mac Laren, T. Reilly, A. Lees (eds.), Swimm<strong>in</strong>g Science VI<br />

(S. 143-149). London.<br />

Bläs<strong>in</strong>g, B., Tenenbaum, G. & Schack, T. (2009). The cognitive structure<br />

of movements <strong>in</strong> classical dance. Psychology of Sport <strong>and</strong> Exercise, 10,<br />

350-360.<br />

Engel, F. & Schack, T. (2001), Das Coach<strong>in</strong>gkonzept ProMent <strong>in</strong> der<br />

Praxis.<br />

Reischle, k., 1988: Biomechanik des Schwimmens. Bockenem.<br />

Schack, T. (2002). Kognitive Architektur von Bewegungsh<strong>and</strong>lungen. Unveröffentlichte<br />

Habil. Köln.<br />

Schmidt, A. C. (2009). Kognitionsbasiertes Bewegungstra<strong>in</strong><strong>in</strong>g und Talentförderung.<br />

E<strong>in</strong>e Interventionsstudie zur Kraularmbewegung. Gött<strong>in</strong>gen.<br />

285


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Assess<strong>in</strong>g Mental Workload at Maximal Intensity <strong>in</strong><br />

Swimm<strong>in</strong>g Us<strong>in</strong>g the NASA-TLX Questionnaire<br />

schnitzler, c. 1 , seifert, l. 1 , chollet, d. 1<br />

1 CETAPS EA 3832, Faculty of Sports Sciences, University of Rouen, France<br />

The sensitivity of the NASA-TLX questionnaire to gender, age <strong>and</strong> expertise<br />

was <strong>in</strong>vestigated. Fifty subjects performed a 400-m front crawl at maximal<br />

velocity. Then, 100-, 200- <strong>and</strong> 300-m trials at the same velocity were performed.<br />

Mental workload was assessed. The results showed that total subjective<br />

workload (TWL) <strong>in</strong>creased gradually with the distance (p


Part (ii): Table 3 presents the results for the highly tra<strong>in</strong>ed population that<br />

performed 100-m, 200-m <strong>and</strong> 300-m trials at the speed of the previous<br />

400-m.<br />

Table 3. Distance effect on physiological <strong>and</strong> NASA-TLX (highlytra<strong>in</strong>ed<br />

population)<br />

Distance<br />

(m)<br />

HR<br />

(Bpm)<br />

[La-]<br />

(mmol.l -1 )<br />

TWL<br />

(/100)<br />

Mental Physical Temporal<br />

dem<strong>and</strong> dem<strong>and</strong> dem<strong>and</strong><br />

Own Frustraperfortionmance<br />

Effort<br />

100 168.0±10.7 3.5±0.6c, d 32±28c, d 24±28 21±22c,d 31±20 55±37 27±28 32±16c,d 200 176.0±7.8 6.4±0.9 39±24 26±21 33±27 37±13 60±27 32±24 47±20<br />

300 180.4±8.3 7.8±1.6 a 49±24 a 40±21 56±28 a 53±25 61±25 31±16 52±21 a<br />

400 186.1±7.2 10.4±1.8 a 50±28 a 38±21 65±29 a 46±28 53±32 34±28 63±19 a<br />

* * * * *<br />

* Significant change with distance swum, with p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

these subjects s<strong>in</strong>ce test<strong>in</strong>g occurred at the beg<strong>in</strong>n<strong>in</strong>g of re-tra<strong>in</strong><strong>in</strong>g. After<br />

three months of <strong>in</strong>tensive tra<strong>in</strong><strong>in</strong>g, however, these athletes were probably<br />

able to accurately estimate the gap between their current best competitive<br />

performance <strong>and</strong> that of the present experiment. More surpris<strong>in</strong>g,<br />

then, is the lower “frustration” level found <strong>in</strong> the second test. This is only<br />

speculative, but it may have been because these athletes knew what they<br />

were capable of <strong>in</strong> competitive situations at that time <strong>and</strong> did not worry<br />

that their performance <strong>in</strong> the experimental conditions was far from what<br />

they did <strong>in</strong> competition.<br />

F<strong>in</strong>ally, it is <strong>in</strong>terest<strong>in</strong>g to note that <strong>in</strong> the different experimental conditions,<br />

a difference <strong>in</strong> TWL was accompanied by an <strong>in</strong>crease <strong>in</strong> [La-]<br />

level <strong>in</strong> the comparisons of gender, age <strong>and</strong> distance swum. But whether<br />

these changes were concomitant or the lactate <strong>in</strong>crease was the consequence<br />

of the change <strong>in</strong> TWL goes beyond the scope of this article.<br />

conclusIon<br />

The multi-dimensionality of the NASA-TLX questionnaire provides an<br />

<strong>in</strong>sight <strong>in</strong>to sport performance. It might be a useful tool to determ<strong>in</strong>e the<br />

characteristics of specific populations or to monitor change due to tra<strong>in</strong><strong>in</strong>g<br />

with more precision.<br />

reFerences<br />

Borg, G. (1998). Borg’s perceived exertion <strong>and</strong> pa<strong>in</strong> scales. Champaign, IL:<br />

Human K<strong>in</strong>etics.<br />

Craig, A. b., Skehan, P. L., Pawelczyk, J. A., & Boomer, W. L. (1985).<br />

Velocity, stroke rate <strong>and</strong> distance per stroke dur<strong>in</strong>g elite swimm<strong>in</strong>g<br />

competition. Med Sci Sports Exerc, 17(6), 625-634.<br />

Garc<strong>in</strong>, M. & Billat, V. (2001). Perceived exertion scales attest to both<br />

<strong>in</strong>tensity <strong>and</strong> exercise duration. Percept Mot Skills, 93(3), 661-671.<br />

Hart, S. & Stavel<strong>and</strong>, L. (1988). Development of the NASA-TLX: Results<br />

of empirical <strong>and</strong> theoretical research. In P. A. Hancock & N.<br />

Meshkati (Eds.), Human mental workload (pp. 139-195). Amsterdam:<br />

North Holl<strong>and</strong>.<br />

Koltyn, K. F., O’Connor, P. J. & Morgan, W. P. (1991). Perception of effort<br />

<strong>in</strong> female <strong>and</strong> male competitive swimmers. Int J Sports Med, 12(4),<br />

427-429.<br />

Medbo, J., Mohn, A., Tabata, I., Bahr, R., Vaage, O. & Sejersted, O.<br />

(1988). Anaerobic capacity determ<strong>in</strong>ed by maximal accumulated O2<br />

deficit. J Appl Physiol, 64(1), 50-60.<br />

Naughton, G., Farpour-Lambert, N. J., Carlson, J., Bradney, M. & Van<br />

Praagh, E. (2000). Physiological issues surround<strong>in</strong>g the performance of<br />

adolescent athletes. Sports Med, 30(5), 309-325.<br />

Newell, K. M. (1986). Constra<strong>in</strong>ts on the development of coord<strong>in</strong>ation. In<br />

M. G. Wade & H. T. A. Whit<strong>in</strong>g (Eds.), Motor development <strong>in</strong> children:<br />

aspect of coord<strong>in</strong>ation <strong>and</strong> control (pp. 341-360). Nijhoff: Dordrecht.<br />

Reid, G. & Nygren, T. (1988). The subjective workload assessment technique:<br />

a scal<strong>in</strong>g procedure for measur<strong>in</strong>g mental workload. In P. A.<br />

Hancock & N. Meshkati (Eds.), Human Mental Workload. Amsterdam:<br />

North Holl<strong>and</strong>: 185-218.<br />

Schnitzler, C. Ernwe<strong>in</strong>, V., Seifert, L., & Chollet, D. (2007). Comparison<br />

of spatio-temporal, metabolic, <strong>and</strong> psychometric responses <strong>in</strong> recreational<br />

<strong>and</strong> highly tra<strong>in</strong>ed swimmers dur<strong>in</strong>g <strong>and</strong> after a 400-m freestyle<br />

swim. Int J Sports Med, 28(2), 164-171.<br />

Toussa<strong>in</strong>t, H. M. & Truijens, M. (2005). Biomechanical aspects of peak<br />

performance <strong>in</strong> human swimm<strong>in</strong>g. Animal Biology, 55(1), 17-40.<br />

288<br />

Does the Y-Intercept of a Regression L<strong>in</strong>e <strong>in</strong> the<br />

Critical Velocity Concept Represent the Index for<br />

Evaluat<strong>in</strong>g Anaerobic Capacity?<br />

shimoyama, Y. 1 , okita, K. 1 , Baba,Y. 1 , sato, d. 1<br />

1 Niigata University of Health <strong>and</strong> Welfare, Niigata, JAPAN<br />

The purpose of the present study was to <strong>in</strong>vestigate whether the y<strong>in</strong>tercept<br />

of a regression l<strong>in</strong>e <strong>in</strong> the critical velocity concept could be<br />

utilized as an <strong>in</strong>dex for evaluat<strong>in</strong>g anaerobic capacity. Twenty-one welltra<strong>in</strong>ed<br />

college swimmers performed a maximum effort swim over 50,<br />

100, 200 <strong>and</strong> 400m for model<strong>in</strong>g the distance-time (D-T) relationship<br />

<strong>and</strong> measur<strong>in</strong>g peak blood lactate concentration ([La]), <strong>and</strong> a 30-s allout<br />

W<strong>in</strong>gate Anaerobic Test (WAnT) performed with arms <strong>and</strong> legs.<br />

The y-<strong>in</strong>tercept was significantly related to highest [La], the mean <strong>and</strong><br />

the peak power of the WAnT performed with both arms <strong>and</strong> legs. These<br />

results suggest that the y-<strong>in</strong>tercept is a valuable <strong>in</strong>dex for evaluat<strong>in</strong>g anaerobic<br />

capacity us<strong>in</strong>g a non-<strong>in</strong>vasive method <strong>in</strong> competitive swimm<strong>in</strong>g.<br />

Key words: critical velocity concept, anaerobic capacity, y-<strong>in</strong>tercept<br />

IntroductIon<br />

The accurate monitor<strong>in</strong>g of both aerobic <strong>and</strong> anaerobic capacities is required<br />

to make a tra<strong>in</strong><strong>in</strong>g program effective (Maglischo 2003). Therefore,<br />

several test<strong>in</strong>g procedures have been presented <strong>in</strong> the literature to<br />

measure [La] at sub-maximum <strong>in</strong>tensities <strong>and</strong> VO 2 max (Bosquet et al.<br />

2002) for evaluat<strong>in</strong>g the aerobic capacity, <strong>and</strong> to measure the highest<br />

[La] (Lacour et al. 1990) <strong>and</strong> the maximal oxygen deficit (Ogita et al.<br />

1996) for the anaerobic capacity. However, it is difficult to measure these<br />

<strong>in</strong>dices <strong>in</strong> the field, because they rely on the use of expensive equipment<br />

<strong>and</strong> their method are <strong>in</strong>vasive.<br />

A l<strong>in</strong>ear relationship is observed between the total work performed<br />

dur<strong>in</strong>g an exhaustive maximal test <strong>and</strong> the time to exhaustion. In the<br />

2-parameter model, the slope of the l<strong>in</strong>ear regression l<strong>in</strong>e has been<br />

referred to as critical power (Monod <strong>and</strong> Scherrer 1965), which was<br />

def<strong>in</strong>ed as the theoretical maximum power that could be ma<strong>in</strong>ta<strong>in</strong>ed<br />

without exhaustion for a long time. This critical power concept was applied<br />

by Wakayoshi (1992) <strong>in</strong> swimm<strong>in</strong>g (the critical swimm<strong>in</strong>g velocity<br />

concept). Wakayoshi et al.(1992) suggested that the slope of the l<strong>in</strong>ear<br />

regression l<strong>in</strong>e between distance (D) <strong>and</strong> time required to cover it (T)<br />

at maximal speed could be a critical velocity (CV). Further, there was a<br />

positive correlation between the CV <strong>and</strong> 30-m<strong>in</strong>ute maximum swimm<strong>in</strong>g<br />

velocity (Dekerle et al. 2002), LT (Mart<strong>in</strong> et al. 2000), <strong>and</strong> the<br />

velocity at [La] of 4 mmol.L -1 (V@OBLA; Wakayoshi et al. 1993). It<br />

was therefore suggested that CV was a valuable <strong>in</strong>dex for evaluat<strong>in</strong>g the<br />

aerobic capacity of swimmers us<strong>in</strong>g a non-<strong>in</strong>vasive method.<br />

On the other h<strong>and</strong>, the y-<strong>in</strong>tercept of the regression l<strong>in</strong>e <strong>in</strong> the<br />

critical power concept (Monod <strong>and</strong> Scherrer 1965) was called the anaerobic<br />

work capacity (AWC) (V<strong>and</strong>ewalle et al. 1997). In previous studies,<br />

AWC has been shown to be related to the highest [La] measured at the<br />

end of exhaust<strong>in</strong>g runn<strong>in</strong>g exercise (V<strong>and</strong>ewalle et al. 1997), the total<br />

amount of work dur<strong>in</strong>g the WAnT (V<strong>and</strong>ewalle et al. 1989) <strong>and</strong> the<br />

maximal oxygen deficit (Miura et al. 2002). Therefore, it was suggested<br />

that the y-<strong>in</strong>tercept of the regression l<strong>in</strong>e <strong>in</strong> the critical power concept<br />

would represent an <strong>in</strong>dex of anaerobic capacity.<br />

In the critical swimm<strong>in</strong>g velocity concept, Oshita et al. (2009)<br />

found a highly positive correlation between the y-<strong>in</strong>tercept <strong>and</strong> the<br />

residual error obta<strong>in</strong>ed from the relationship between 1500-m performance<br />

<strong>and</strong> CV <strong>in</strong> F<strong>in</strong>-swimm<strong>in</strong>g. Besides, when model<strong>in</strong>g the energetic<br />

contribution <strong>in</strong> swimm<strong>in</strong>g, di Prampero et al. (2008) assumed that the y-


<strong>in</strong>tercept would correspond to the distance covered at the expense of the<br />

anaerobic energy stores. However, no study has yet directly evaluated the<br />

relationship between the y-<strong>in</strong>tercept of the D-T relationship <strong>and</strong> <strong>in</strong>dices<br />

of anaerobic capacity <strong>in</strong> swimm<strong>in</strong>g. In this study it was hypothesized<br />

that the y-<strong>in</strong>tercept of the regression l<strong>in</strong>e <strong>in</strong> the critical swimm<strong>in</strong>g velocity<br />

concept might represent an <strong>in</strong>dex of anaerobic capacity. The purpose<br />

of the present study was to <strong>in</strong>vestigate whether this parameter could<br />

be utilized as an <strong>in</strong>dex for evaluat<strong>in</strong>g anaerobic capacity <strong>in</strong> competitive<br />

swimm<strong>in</strong>g.<br />

Methods<br />

Subjects: Twenty one well-tra<strong>in</strong>ed college swimmers (11 males <strong>and</strong> 10<br />

females) participated <strong>in</strong> this study. They were varsity swim team members<br />

who tra<strong>in</strong>ed for an average of 2–3 h per session, eight times per<br />

week. They took part <strong>in</strong> national level competitions. Their respective<br />

mean height, body mass, <strong>and</strong> body fat percentage were 1.70 ± 0.07 m,<br />

64.2 ± 5.6 kg, <strong>and</strong> 17.8 ± 6.6 %. They were <strong>in</strong>formed of the risks of the<br />

study <strong>and</strong> signed an <strong>in</strong>formed consent form.<br />

Experimental design: All tests were performed <strong>in</strong> front crawl <strong>in</strong> a 25-m<br />

swimm<strong>in</strong>g pool. A st<strong>and</strong>ardized warm-up, which consisted of approximately<br />

2000m for 30m<strong>in</strong>, was performed prior to each test. With<strong>in</strong> one<br />

week, each subject performed a) a maximum swimm<strong>in</strong>g effort (50m,<br />

100m, 200m <strong>and</strong> 400m), b) a 300-m <strong>in</strong>termittent progressive swimm<strong>in</strong>g<br />

test, <strong>and</strong> c) a 30-s all-out W<strong>in</strong>gate Anaerobic Test (WAnT) performed<br />

with arms <strong>and</strong> legs.<br />

Determ<strong>in</strong>ation of CV <strong>and</strong> the y-<strong>in</strong>tercept: Fig.1 gives an example of the<br />

relationship between D <strong>and</strong> T for a given swimmer. The l<strong>in</strong>ear relationship<br />

was drawn, the slope (CV) <strong>and</strong> the y-<strong>in</strong>tercept were determ<strong>in</strong>ed<br />

from the regression l<strong>in</strong>e between D <strong>and</strong> T.<br />

Determ<strong>in</strong>ation of V@OBLA: Each subject performed a 300-m <strong>in</strong>termittent<br />

progressive swimm<strong>in</strong>g test, which consisted of five repetitions of<br />

300m with a 25-m<strong>in</strong>ute rest period. Swimm<strong>in</strong>g velocities were 60, 70,<br />

80, 90 <strong>and</strong> 100 % of their maximum effort. [La] was taken from a f<strong>in</strong>-<br />

gertip immediately after completion of each trial. Blood was analyzed<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g Page 123<br />

us<strong>in</strong>g a blood lactate analyzer (Lactate Pro; ARKRAY). V@OBLA for<br />

each subject was determ<strong>in</strong>ed from the velocity-[La] curve.<br />

Fig.1 An example of the l<strong>in</strong>ear regression l<strong>in</strong>e between time (T) <strong>and</strong><br />

distance (D) <strong>in</strong> the case of one subject.<br />

Fig.1 An example of the l<strong>in</strong>ear regression l<strong>in</strong>e between time (T) <strong>and</strong> distance (D) <strong>in</strong><br />

the case of one subject.<br />

Determ<strong>in</strong>ation of the highest [La]<br />

The highest [La] was determ<strong>in</strong>ed from the [La] values recorded follow<strong>in</strong>g a<br />

maximum Determ<strong>in</strong>ation 100-m <strong>and</strong> of the 200-m highest swimm<strong>in</strong>g [La]: test. The Capillary highest samples [La] were was collected determ<strong>in</strong>ed at<br />

m<strong>in</strong>ute from 1, the 3, [La] 5 <strong>and</strong> values 7 of the recorded recovery period, follow<strong>in</strong>g <strong>and</strong> the a maximum highest value 100-m was def<strong>in</strong>ed <strong>and</strong> as 200-m the<br />

highest swimm<strong>in</strong>g [La]. test. Capillary samples were collected at m<strong>in</strong>ute 1, 3, 5 <strong>and</strong> 7<br />

30-s all-out W<strong>in</strong>gate Anaerobic Test (WAnT)<br />

Subjects of the recovery the WAnT period, performed <strong>and</strong> with the both highest arms value <strong>and</strong> legs was us<strong>in</strong>g def<strong>in</strong>ed a bicycle as the ergometer highest<br />

(Power [La]. Max V-II ; COMBI). Accord<strong>in</strong>g to a previous study (Bar-Or, 1987), the<br />

resistance load for the arms was set at 6.2 % per kg body weight (male) <strong>and</strong> 4.8 %<br />

30-s all-out W<strong>in</strong>gate Anaerobic Test (WAnT): Subjects the WAnT per-<br />

(female), <strong>and</strong> the load for the legs were 7.5 % <strong>and</strong> 7.5% for male <strong>and</strong> female,<br />

respectively. formed with The both mean arms power <strong>and</strong> peak legs power us<strong>in</strong>g were a bicycle measured ergometer <strong>and</strong> associated (Power with Max an<br />

<strong>in</strong>dex V-II of ; anaerobic COMBI). capacity. Accord<strong>in</strong>g to a previous study (Bar-Or, 1987), the re-<br />

Statistical analysis<br />

The sistance observed load data for are the presented arms as was mean set ± at st<strong>and</strong>ard 6.2 % deviation per kg (SD). body All weight analyses (male) were<br />

performed <strong>and</strong> 4.8 % us<strong>in</strong>g (female), the computer <strong>and</strong> the software load for (Statcel2; the legs OMS). were The 7.5 Pearson's % <strong>and</strong> correlation 7.5% for<br />

coefficient male <strong>and</strong> was female, used to exam<strong>in</strong>e respectively. the relationship The mean between power the <strong>and</strong> variables. peak The power significance were<br />

was accepted to be at p < 0.05 level.<br />

RESULTS<br />

Mean ± SD for CV <strong>and</strong> the y-<strong>in</strong>tercept were 1.42 ± 0.09 m·s -1 <strong>and</strong> 15.54 ± 2.92 m,<br />

respectively.<br />

CV was significantly correlated with the V@OBLA (r = 0.94, p < 0.05).<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

measured <strong>and</strong> associated with an <strong>in</strong>dex of anaerobic capacity.<br />

Statistical analysis: The observed data are presented as mean ± st<strong>and</strong>ard<br />

deviation (SD). All analyses were performed us<strong>in</strong>g the computer software<br />

(Statcel2; OMS). The Pearson’s correlation coefficient was used to<br />

exam<strong>in</strong>e the relationship between the variables. The significance was accepted<br />

to be at p < 0.05 level.<br />

results<br />

Mean ± SD for CV <strong>and</strong> the y-<strong>in</strong>tercept were 1.42 ± 0.09 m·s-1 <strong>and</strong><br />

15.54 ± 2.92 m, respectively. CV was significantly correlated with the<br />

V@OBLA (r = 0.94, p < 0.05).<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g Page 124<br />

Fig.2 <strong>in</strong>dicates the relationship between the y-<strong>in</strong>tercept <strong>and</strong> the highest<br />

[La]. A positive significant relationship (r = 0.63, p < 0.05) was found<br />

between the two.<br />

positive significant relationship (r = 0.63, p < 0.05) was found between the two.<br />

The y-<strong>in</strong>tercept was also significantly related to the mean power of<br />

the WAnT performed with the arms (r = 0.51, p < 0.05) as well as with<br />

the legs (r = 0.54, p < 0.05), <strong>and</strong> to the peak power of both tests (arms: r<br />

respectively.<br />

= 0.50, p < 0.05; legs: r = 0.52, p < 0.05), respectively.<br />

Fig.2 <strong>in</strong>dicates the relationship between the y-<strong>in</strong>tercept <strong>and</strong> the highest [La]. A<br />

The y-<strong>in</strong>tercept was also significantly related to the mean power of the WAnT<br />

performed with the arms (r = 0.51, p < 0.05) as well as with the legs (r = 0.54, p < 0.05),<br />

<strong>and</strong> to the peak power of both tests (arms: r = 0.50, p < 0.05; legs: r = 0.52, p < 0.05),<br />

Fig.2 Relationship between y-<strong>in</strong>tercept of D-T relationship <strong>and</strong> highest [La]<br />

Fig.2 Relationship between y-<strong>in</strong>tercept of D-T relationship <strong>and</strong> highest<br />

[La]<br />

DISCUSSION<br />

The present study <strong>in</strong>vestigated whether the y-<strong>in</strong>tercept of a regression l<strong>in</strong>e between D<br />

dIscussIon<br />

<strong>and</strong> T could be utilized as an <strong>in</strong>dex for evaluat<strong>in</strong>g anaerobic capacity <strong>in</strong> competitive<br />

The swimm<strong>in</strong>g. present The study y-<strong>in</strong>tercept <strong>in</strong>vestigated was significantly whether related the y-<strong>in</strong>tercept to highest [La], of <strong>and</strong> a regression the mean <strong>and</strong><br />

l<strong>in</strong>e peak between power of the D <strong>and</strong> WAnT T performed could be with utilized the arms as an or <strong>in</strong>dex the legs. for This evaluat<strong>in</strong>g is the first anstudy<br />

that evaluates directly the relationship between the y-<strong>in</strong>tercept <strong>and</strong> <strong>in</strong>dices of anaerobic<br />

aerobic capacity <strong>in</strong> competitive swimm<strong>in</strong>g. The y-<strong>in</strong>tercept was signifi-<br />

capacity. This demonstrates the usefulness of determ<strong>in</strong><strong>in</strong>g the y-<strong>in</strong>tercept to evaluate the<br />

cantly anaerobic related capacity to of highest swimmers [La], <strong>in</strong> the <strong>and</strong> field. the mean <strong>and</strong> peak power of the<br />

WAnT In the performed present study, with the y-<strong>in</strong>tercept arms or the of the legs. D-T This relationship is the first was study significantly that<br />

correlated with the highest [La] <strong>and</strong> the mean <strong>and</strong> peak power of the WAnT whether the<br />

evaluates directly the relationship between the y-<strong>in</strong>tercept <strong>and</strong> <strong>in</strong>dices of<br />

test was performed with the arms or the legs. It has been suggested that the highest [La]<br />

anaerobic <strong>and</strong> mean <strong>and</strong> capacity. peak power This of demonstrates the WAnT were the effective usefulness <strong>in</strong>dices of determ<strong>in</strong><strong>in</strong>g of anaerobic capacity, the<br />

y-<strong>in</strong>tercept <strong>and</strong> these <strong>in</strong>dices to evaluate were significantly the anaerobic related capacity to spr<strong>in</strong>t swimm<strong>in</strong>g of swimmers performance <strong>in</strong> the (Lacour field. et<br />

al. 1990, Maglischo 2003, Hawley et al. 1992, Bar-Or 1987). In the critical power<br />

In the present study, the y-<strong>in</strong>tercept of the D-T relationship was<br />

concept, the y-<strong>in</strong>tercept called AWC, was found to be related to highest [La] measured<br />

significantly at the end of exhaust<strong>in</strong>g correlated runn<strong>in</strong>g with exercise the highest (V<strong>and</strong>ewalle [La] <strong>and</strong> et al. the 1997), mean the total <strong>and</strong> amount peak of<br />

power of the WAnT whether the test was performed with the arms or<br />

the legs. It has been suggested that the highest [La] <strong>and</strong> mean <strong>and</strong> peak<br />

power of the WAnT were effective <strong>in</strong>dices of anaerobic capacity, <strong>and</strong><br />

these <strong>in</strong>dices were significantly related to spr<strong>in</strong>t swimm<strong>in</strong>g performance<br />

(Lacour et al. 1990, Maglischo 2003, Hawley et al. 1992, Bar-Or 1987).<br />

In the critical power concept, the y-<strong>in</strong>tercept called AWC, was found<br />

to be related to highest [La] measured at the end of exhaust<strong>in</strong>g runn<strong>in</strong>g<br />

exercise (V<strong>and</strong>ewalle et al. 1997), the total amount of work of the<br />

WAnT (V<strong>and</strong>ewalle et al. 1989), <strong>and</strong> the maximal oxygen deficit (Miura<br />

et al. 2002). Thus, AWC could provide a measurement of the anaerobic<br />

capacity, <strong>and</strong> be related to the ability to perform high-<strong>in</strong>tensity exercise<br />

(Dekerle et al. 2002). In the critical swimm<strong>in</strong>g velocity concept, di<br />

Prampero et al. (2008) assumed that the y-<strong>in</strong>tercept would correspond<br />

to the distance covered at the expense of the anaerobic energy stores<br />

by apply<strong>in</strong>g a model to calculate the energetic contributions of various<br />

swimm<strong>in</strong>g performances. Further, Oshita et al. (2009) demonstrated a<br />

289


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

highly significant correlation between the y-<strong>in</strong>tercept <strong>and</strong> the residual<br />

error obta<strong>in</strong>ed from the relationship between 1500-m performance <strong>and</strong><br />

CV <strong>in</strong> F<strong>in</strong>-swimm<strong>in</strong>g. These f<strong>in</strong>d<strong>in</strong>gs from previous <strong>and</strong> present studies<br />

suggest that the y-<strong>in</strong>tercept of a regression l<strong>in</strong>e between D <strong>and</strong> T <strong>in</strong><br />

competitive swimm<strong>in</strong>g is a valuable <strong>in</strong>dex of anaerobic capacity that can<br />

be therefore assessed us<strong>in</strong>g a non-<strong>in</strong>vasive method.<br />

The f<strong>in</strong>d<strong>in</strong>gs of this study suggest that apply<strong>in</strong>g the CV concept<br />

<strong>in</strong> swimm<strong>in</strong>g would enable both aerobic <strong>and</strong> anaerobic capacities to be<br />

evaluated at once without us<strong>in</strong>g <strong>in</strong>vasive methods or expensive equipment.<br />

Thus, it would provide a simple <strong>and</strong> effective tool for coaches <strong>and</strong><br />

swimmers <strong>in</strong> the field.<br />

conclusIon<br />

The y-<strong>in</strong>tercept of the D-T relationship <strong>in</strong> swimm<strong>in</strong>g is significantly<br />

correlated with various <strong>in</strong>dices of anaerobic capacity, such as the highest<br />

[La], the mean <strong>and</strong> peak power of the WAnT. From these results, it is<br />

suggested that the y-<strong>in</strong>tercept of a regression l<strong>in</strong>e <strong>in</strong> the critical velocity<br />

concept could represent a good <strong>in</strong>dex of anaerobic capacity, determ<strong>in</strong>able<br />

without any <strong>in</strong>vasive measurements.<br />

reFerences<br />

Bar-Or, O. (1987). The W<strong>in</strong>gate anaerobic test. An update on methodology,<br />

reliability <strong>and</strong> validity. Sports Med 4(6), 381-94.<br />

Bosquet, L., Leger, L. & Legros P. (2002). Methods to determ<strong>in</strong>e aerobic<br />

endurance. Sports Med 32(11), 675-700.<br />

Dekerle, J., Sidney, M., Hespel, J.M. & Pelayo P. (2002). Validity <strong>and</strong><br />

reliability of critical speed, critical stroke rate, <strong>and</strong> anaerobic capacity<br />

<strong>in</strong> relation to front crawl swimm<strong>in</strong>g performances. Int J Sports Med<br />

23(2), 93-8.<br />

di Prampero, P.E., Dekerle, J., Capelli, C. & Zamparo P. (2008). The<br />

critical velocity <strong>in</strong> swimm<strong>in</strong>g. Eur J Appl Physiol 102(2), 165-71.<br />

Hawley, J.A., Williams, M.M., Vickovic, M.M. & H<strong>and</strong>cock PJ. (1992).<br />

Muscle power predicts freestyle swimm<strong>in</strong>g performance. Br J Sports<br />

Med 26(3), 151-5.<br />

Lacour, J.R., Bouvat, E. & Barthelemy, J.C. (1990). Post-competition<br />

blood lactate concentrations as <strong>in</strong>dicators of anaerobic energy expenditure<br />

dur<strong>in</strong>g 400-m <strong>and</strong> 800-m races. Eur J Appl Physiol Occup<br />

Physiol 61(3-4), 172-6.<br />

Maglischo, E.W. (2003). Swimm<strong>in</strong>g fastest. Champaign: Human K<strong>in</strong>etics.<br />

Mart<strong>in</strong>, L. & Whyte GP. (2000). Comparison of critical swimm<strong>in</strong>g velocity<br />

<strong>and</strong> velocity at lactate threshold <strong>in</strong> elite triathletes. Int J Sports<br />

Med 21(5), 366-8.<br />

Miura, A., Endo, M., Sato, H., Sato, H., Barstow, T.J. & Fukuba Y.<br />

(2002). Relationship between the curvature constant parameter of the<br />

power-duration curve <strong>and</strong> muscle cross-sectional area of the thigh for<br />

cycle ergometry <strong>in</strong> humans. Eur J Appl Physiol 87(3), 238-44.<br />

Monod, H. & Scherrer, J. (1965). The work capacity of synergic muscle<br />

group. Ergonomics 8, 329-38.<br />

Ogita, F., Hara, M. & Tabata I. (1996). Anaerobic capacity <strong>and</strong> maximal<br />

oxygen uptake dur<strong>in</strong>g arm stroke, leg kick<strong>in</strong>g <strong>and</strong> whole body swimm<strong>in</strong>g.<br />

Acta Physiol Sc<strong>and</strong> 157(4), 435-41.<br />

Oshita, K., Ross, M., Koizumi, K., Kashimoto, S., Yano, S., Takahashi,<br />

K. & Kawakami, M. (2009). The critical velocity <strong>and</strong> 1500-m surface<br />

performances <strong>in</strong> F<strong>in</strong>swimm<strong>in</strong>g. Int J Sports Med 30(8), 598-601.<br />

V<strong>and</strong>ewalle, H., Kapitaniak, B., Grun, S., Raveneau, S. & Monod H.<br />

(1989). Comparison between a 30-s all-out test <strong>and</strong> a time-work test<br />

on a cycle ergometer. Eur J Appl Physiol Occup Physiol 58(4), 375-81.<br />

V<strong>and</strong>ewalle, H., Vautier, J.F., Kachouri, M., Lechevalier, J.M. & Monod,<br />

H. (1997). Work-exhaustion time relationships <strong>and</strong> the critical power<br />

concept. A critical review. J Sports Med Phys Fitness 37(2), 89-102.<br />

Wakayoshi, K., Ikuta, K., Yoshida, T., Udo, M., Moritani, T., Mutoh,<br />

Y. & Miyashita, M. (1992). Determ<strong>in</strong>ation <strong>and</strong> validity of critical<br />

290<br />

velocity as an <strong>in</strong>dex of swimm<strong>in</strong>g performance <strong>in</strong> the competitive<br />

swimmer. Eur J Appl Physiol Occup Physiol 64(2), 153-7.<br />

Wakayoshi, K., Yoshida, T., Udo, M., Harada, T., Moritani, T., Mutoh,<br />

Y. & Miyashita M. (1993). Does critical swimm<strong>in</strong>g velocity represent<br />

exercise <strong>in</strong>tensity at maximal lactate steady state? Eur J Appl Physiol<br />

Occup Physiol 66(1), 90-5.


Evaluation of Force Production <strong>and</strong> Fatigue us<strong>in</strong>g<br />

an Anaerobic Test Performed by Differently Matured<br />

Swimmers<br />

soares, s., silva, r., Aleixo, I., Machado, l., Fern<strong>and</strong>es, r.J.,<br />

Maia, J., Vilas-Boas, J.P.<br />

University of Porto, Faculty of Sport, Cifi2d, Porto, Portugal<br />

The purpose of this research was to characterize fatigue determ<strong>in</strong><strong>in</strong>g<br />

thresholds <strong>in</strong> force-to-time curves produced dur<strong>in</strong>g 30 second tethered<br />

swimm<strong>in</strong>g efforts. N<strong>in</strong>ety swimmers of three maturational groups took<br />

part <strong>in</strong> the study. Values of maximal, mean, <strong>and</strong> m<strong>in</strong>imum force were determ<strong>in</strong>ed,<br />

as well as the variation coefficient of the mean force. The anaerobic<br />

fatigue thresholds were determ<strong>in</strong>ed on the <strong>in</strong>dividual force-totime<br />

curves, <strong>and</strong> typical stroke cycles were determ<strong>in</strong>ed before <strong>and</strong> after<br />

the fatigue occurrence. Typical force cycles were quantitatively analysed.<br />

It was possible to conclude that force tends to <strong>in</strong>crease with maturation<br />

<strong>in</strong> males. In females, tethered force seems to stabilize after puberty.<br />

Key words: anaerobic performance, fatigue, force, tethered swimm<strong>in</strong>g<br />

IntroductIon<br />

Delay<strong>in</strong>g fatigue is a desire <strong>in</strong> competitive swimm<strong>in</strong>g. In swimm<strong>in</strong>g,<br />

the use of the anaerobic threshold concept has lead to the growth of<br />

scientific knowledge applied to swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g <strong>and</strong> seems to keep<br />

up with performance evolution. That threshold establishes the border<br />

between balanced <strong>and</strong> unbalanced lactate production <strong>and</strong> removal (maximal<br />

full aerobic <strong>and</strong> partially anaerobically supported energy production).<br />

Fatigue studies of anaerobic function <strong>and</strong> high power production<br />

resisted exercises are not so well developed. It is not clear when fatigue<br />

significantly emerges <strong>in</strong> those efforts <strong>and</strong> how to get useful <strong>in</strong>formation<br />

for control <strong>and</strong> plann<strong>in</strong>g of anaerobic swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g. In a previous<br />

study from our group (Soares et al., 2003), we were able to study fatigue<br />

<strong>and</strong> determ<strong>in</strong>e fatigue thresholds on velocity-to-time curves obta<strong>in</strong>ed <strong>in</strong><br />

30 second maximal efforts. Those f<strong>in</strong>d<strong>in</strong>gs made it possible to improve<br />

the control over swimm<strong>in</strong>g plann<strong>in</strong>g <strong>and</strong> tra<strong>in</strong><strong>in</strong>g <strong>in</strong> the anaerobic doma<strong>in</strong>.<br />

The purpose of the present study was to <strong>in</strong>vestigate fatigue <strong>and</strong><br />

determ<strong>in</strong>e fatigue thresholds <strong>in</strong> force-to-time curves produced dur<strong>in</strong>g<br />

30 second bouts of tethered swimm<strong>in</strong>g.<br />

Methods<br />

A total of 90 swimmers (Table 1) divided <strong>in</strong>to three maturational groups<br />

accord<strong>in</strong>g to Tanner (Tanner, Whitehouse et al., 1962) performed a 30<br />

second maximal tethered swimm<strong>in</strong>g test attached by a non-elastic cable<br />

to a stra<strong>in</strong>-gauge system (Globus, Italy). Previously to the start<strong>in</strong>g signal,<br />

swimmers adopted a horizontal position with the cable fully extended<br />

start<strong>in</strong>g the data collection only after the first stroke cycle was completed.<br />

This procedure was used to avoid the <strong>in</strong>ertial effect of the cable<br />

extension usually produced immediately before or dur<strong>in</strong>g the first arm<br />

action. The end of the test was <strong>in</strong>dicated by an acoustic signal. Video<br />

images were captured dur<strong>in</strong>g all the tests us<strong>in</strong>g a JVC camera (JVC GR-<br />

<strong>Biomechanics</strong> SX1EG SVHSC), <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> <strong>in</strong>dividual <strong>in</strong> Swimm<strong>in</strong>g force-to-time <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g curves [F(t)] were Page pro- 128<br />

duced for each session.<br />

us<strong>in</strong>g a JVC camera (JVC GR-SX1EG SVHSC), <strong>and</strong> <strong>in</strong>dividual force-to-time curves<br />

[F(t)] Table were 1. Anthropometric produced for each session. characteristics (mean±SD) <strong>and</strong> maturational<br />

status.<br />

Table 1. Anthropometric characteristics (mean±SD) <strong>and</strong> maturational status.<br />

Swim level Pre-pub. - Pre-Competition Pub. - National Post-pub - Interational<br />

M (n=15) F (n=15) M (n=15) F (n=15) M (n=15) F (n=15)<br />

Age, years 9.42±0.82 8.45±0.94 13.51±0.65 12.65±0.98 18.18±2.35 16.54±2.35<br />

Weight, kg 34.20±7.21 28.20±3.22 55.28±7.04 47.47±5.66 69.88±7.03 58.47±7.22<br />

Height, cm 136.47±4.73 131.33±4.84 165.53±8.06 160.00±5.18 176.27±7.49 165.80±3.32<br />

Ts: g - b 1.00±0.00 1.00±0.00 3.80±0.41 3.20±0.77 3.87±0.36 4.27±0.70<br />

Ts: ph 1.00±0.00 1.00±0.00 4.13±0.64 4.00±1.00 4.73±0.46 4.80±0.68<br />

Pre-pub: pre-pubertal; Pub: pubertal; Post-pub: post pubertal; M: males;<br />

F: females; Ts: g – b: Tanner stage for genitalia or breast; Ts: ph: Tanner<br />

stage for pubic hair.<br />

The maximal (Fmax), mean (Fmean) <strong>and</strong> m<strong>in</strong>imum (Fm<strong>in</strong>) force values were obta<strong>in</strong>ed<br />

directly from the F(t) curve <strong>and</strong> normalized to body weight. The variation coefficient<br />

(VC) of Fmean was calculated for each maturational group. Data treatment for fatigue<br />

was performed us<strong>in</strong>g a rout<strong>in</strong>e based on a wavelet analysis, written by our research<br />

group, <strong>in</strong> the MatLab software. The complete rout<strong>in</strong>e has already been described by<br />

Soares et al. (2006). Before runn<strong>in</strong>g the rout<strong>in</strong>e, the first 2 seconds of the test were<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

The maximal (Fmax), mean (Fmean) <strong>and</strong> m<strong>in</strong>imum (Fm<strong>in</strong>) force values<br />

were obta<strong>in</strong>ed directly from the F(t) curve <strong>and</strong> normalized to body<br />

weight. The variation coefficient (VC) of Fmean was calculated for each<br />

maturational group. Data treatment for fatigue was performed us<strong>in</strong>g a<br />

rout<strong>in</strong>e based on a wavelet analysis, written by our research group, <strong>in</strong><br />

the MatLab software. The complete rout<strong>in</strong>e has already been described<br />

by Soares et al. (2006). Before runn<strong>in</strong>g the rout<strong>in</strong>e, the first 2 seconds<br />

of the test were removed <strong>in</strong> order to elim<strong>in</strong>ate the <strong>in</strong>itial peak force.<br />

The rout<strong>in</strong>e allowed the determ<strong>in</strong>ation of fatigue thresholds <strong>in</strong> each<br />

<strong>in</strong>dividual F(t) curve <strong>and</strong> the time of occurrence. The <strong>in</strong>tracyclic variation<br />

of the force expressed through typical force cycles was established.<br />

Typical force cycles were quantitatively analysed through: (i) total cycle<br />

duration time (tcycle); (ii) stroke frequency (SF); (iii) mean cycle force<br />

(FmeanC), <strong>and</strong> (iv) FmeanC VC. Due to technical problems, data of<br />

<strong>in</strong>tracyclic force variations are presented for pre-pubertal <strong>and</strong> pubertal<br />

groups only.<br />

Comparison of means between maturational groups was performed<br />

through an ANOVA test for <strong>in</strong>dependent groups. Gender comparisons<br />

were performed us<strong>in</strong>g a t-test for <strong>in</strong>dependent groups. Normal distribution<br />

of data was verified. Significance level was 5%.<br />

results<br />

The Fmax, Fmean <strong>and</strong> Fm<strong>in</strong> values obta<strong>in</strong>ed for the male <strong>and</strong> female<br />

swimmers of the three maturational groups studied can be observed <strong>in</strong><br />

Table 2. The forces produced dur<strong>in</strong>g anaerobic tethered efforts seemed<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g Page 129<br />

to <strong>in</strong>crease with maturation, <strong>in</strong> contrast to VC which tends to decrease.<br />

Table 2. Mean±st<strong>and</strong>ard deviation of maximal, mean <strong>and</strong> m<strong>in</strong>imum<br />

force values obta<strong>in</strong>ed dur<strong>in</strong>g the 30 second tethered swimm<strong>in</strong>g test.<br />

Table 2. Mean±st<strong>and</strong>ard deviation of maximal, mean <strong>and</strong> m<strong>in</strong>imum force values<br />

obta<strong>in</strong>ed dur<strong>in</strong>g the 30 second tethered swimm<strong>in</strong>g test.<br />

Fmax Fmean Fm<strong>in</strong> VC of Fmean<br />

(%)<br />

pre-pub M 0.74±0.27 0.63±0.22 0.55±0.22 66.57±17.55<br />

Pre-pub F 0.66±0.21 0.56±0.18 0.46±0.16<br />

pub M 1.50±0.14 a 1.32±0.11 a 1.16±0.10 a<br />

52.86±11.36 a<br />

pub F 1.34±0.40 1.20±0.36 a 1.06±0.32 a<br />

post-pub M 1.82±0.23 *,a,b 1.62±0.20 *,a,b 1.43±0.19 *,a,b<br />

46.53±7.67 a<br />

Post-pub F 1.31±0.23 a 1.19±0.20 a 1.06±0.17 a<br />

*<br />

Significantly different from females at p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

A<br />

(%)<br />

292<br />

50<br />

Males<br />

pre-pubertal pubertal post-pubertal<br />

I<br />

50<br />

D1<br />

<strong>Biomechanics</strong> * <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 40 4 Tra<strong>in</strong><strong>in</strong>g 50<br />

40<br />

D2 Page 130<br />

100<br />

30<br />

20<br />

30<br />

20<br />

0Pre-pubertal<br />

(second)<br />

50<br />

40<br />

E1<br />

50<br />

40<br />

E2<br />

40<br />

30<br />

Pubertal One (second) threshold Two 13.60±3.87 thresholds<br />

Post-pubertal (second)<br />

30<br />

20<br />

10<br />

0<br />

0 0.2<br />

30<br />

20<br />

10<br />

0<br />

0.4 0.6 0.8 1 0 0.2 0.4 0.6<br />

t t<br />

norm<br />

norm<br />

0.8 1<br />

20<br />

10<br />

0<br />

0<br />

t<br />

B<br />

Females<br />

III<br />

IV<br />

D1<br />

D2<br />

150<br />

150<br />

100<br />

100<br />

pre-pubertal pubertal post-pubertal<br />

50<br />

50<br />

0<br />

0<br />

0 0.2 0.4 0.6 0.8 1 0 0.2 0.4 0.6 0.8 1<br />

*<br />

t t<br />

norm<br />

norm<br />

100<br />

*<br />

E1<br />

E2<br />

150<br />

150<br />

150<br />

100<br />

50<br />

0<br />

0<br />

150<br />

0.5<br />

t<br />

norm<br />

100<br />

100<br />

100<br />

50<br />

50<br />

50<br />

50<br />

0<br />

0<br />

0 0.2 0.4 0.6 0.8 1 0 0.2 0.4 0.6 0.8 1<br />

0<br />

0 0.5<br />

t t<br />

norm<br />

norm<br />

t<br />

norm<br />

0<br />

One threshold Two thresholds<br />

Figure 2. Mean cycles of <strong>in</strong>tyracyclic variation of the for<br />

the left (E) arms. Mean cycles are of the first <strong>and</strong> se<br />

Figure 1. Number of swimmers who achieved one or two thresholds <strong>in</strong> def<strong>in</strong>ed by the thresholds. I <strong>and</strong> II show the typical cyc<br />

percentage. Results are presented for swimmers of different gender <strong>and</strong><br />

maturational status.<br />

Panels III <strong>and</strong> IV show the correspondent cycles for post<br />

b<br />

14.54±2.60 c<br />

9.44±1.51 e,(*)<br />

9.25±0.50 f,(*)<br />

17.44±2.30 (*),(**)<br />

19.25±2.36 (*),(**)<br />

X±SD 14.21±3.08 9.72±1.84 (*) 18.60±2.94 (*),(**)<br />

*Significantly different from threshold of the curves with one threshold at<br />

p


Table 5. Mean±st<strong>and</strong>ard deviation values (X±SD) of the total swimm<strong>in</strong>g<br />

time (t), mean duration of each cycle (tcycle), stroke frequency<br />

(SF), cycle mean force (FmeanC) <strong>and</strong> variation coefficient of FmeanC<br />

(VC). Values for time <strong>in</strong>tervals def<strong>in</strong>ed by the fatigue thresholds of postpubertal<br />

swimmers.<br />

t total (s)<br />

One threshold*<br />

Two thresholds**<br />

tcycle (s)<br />

One threshold*<br />

Two thresholds**<br />

SF (cycles.s-1 )<br />

One threshold*<br />

Two thresholds**<br />

FmeanC(m·s-1 )<br />

One threshold*<br />

Two thresholds**<br />

VC (%)<br />

One threshold*<br />

Two thresholds**<br />

First time <strong>in</strong>terval<br />

11.89±2.79<br />

6.90±0.76<br />

1.19±0.11 a<br />

1.07±0.08 b<br />

0.84±0.08 a<br />

0.94±0.07 b<br />

105.29±32.81 a<br />

86.60±34.73 b<br />

43.58±7.52 a<br />

38.75±14.24<br />

Second time<br />

<strong>in</strong>terval<br />

Third time<br />

<strong>in</strong>terval<br />

13.90±2.85<br />

8.86±2.24 9.36±1.79<br />

1.28±0.11<br />

1.13±0.08 1.19±0.09<br />

0.79±0.07<br />

0.89±0.07 0.85±0.07<br />

86.21±26.66<br />

76.66±27.64 67.11±24.05<br />

47.08±8.81<br />

37.00±8.98 41.50±8.10<br />

a Significantely different from second time <strong>in</strong>terval at p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Identification of a Bias <strong>in</strong> the Natural Progression of<br />

Swim Performance<br />

stager, J.M. 1 , Brammer, c.l. 1 , tanner, d.A. 1<br />

1 Indiana University, Bloom<strong>in</strong>gton, USA<br />

The longitud<strong>in</strong>al progression of athletic records has been described by<br />

best fit curves which can be used to extrapolate future athletic performances.<br />

Any subsequent significant deviations from these curves would<br />

suggest compell<strong>in</strong>g evidence of cataclysmic changes <strong>in</strong>troduced <strong>in</strong>to<br />

the sport. We evaluated recent elite swim performances to determ<strong>in</strong>e if<br />

bias can be identified with<strong>in</strong> competitive swimm<strong>in</strong>g. Predictions of the<br />

2008 Olympic swimm<strong>in</strong>g competition were calculated for each event<br />

<strong>and</strong> compared to actual performances. 17/26 events <strong>in</strong> 2008 were significantly<br />

faster than predicted (p


was calculated for each year <strong>and</strong> averaged with<strong>in</strong> each event. This number<br />

was used to estimate the st<strong>and</strong>ard deviation of the predicted time for<br />

each event us<strong>in</strong>g the formula 1.25*(mean percent difference)*(predicted<br />

value)/100. This st<strong>and</strong>ard deviation was used to establish the 95% confidence<br />

<strong>in</strong>terval for that event (predicted time ± 2 st<strong>and</strong>ard deviations).<br />

The mean time of the f<strong>in</strong>alists of the 2008 Olympics were compared to<br />

this 95% confidence <strong>in</strong>terval <strong>and</strong> actual times that fall outside the <strong>in</strong>terval<br />

were concluded to be significantly faster or slower than predicted.<br />

To exam<strong>in</strong>e each Olympic year as a whole, a count was made of the<br />

number of events for which the actual time was above or below the correspond<strong>in</strong>g<br />

prediction curve. A b<strong>in</strong>omial test of statistical significance<br />

was used to test whether or not the likelihood of the number of events<br />

be<strong>in</strong>g either faster or slower than our predictions was different than<br />

50%. This table of event counts was tested to determ<strong>in</strong>e whether or not a<br />

particular year was faster or slower, <strong>in</strong> general, than predicted.<br />

To test the repeatability of this prediction method, the same calculations<br />

were performed to compare actual versus predicted performances of<br />

the 2004 Games us<strong>in</strong>g data from 1972 through 2000 only. These procedures<br />

were repeated for all Olympic Games 1988-2000 (us<strong>in</strong>g data s<strong>in</strong>ce 1972).<br />

results<br />

Prediction Analysis: For the 2008 Olympic Games, 10/13 (77%) men’s<br />

<strong>and</strong> 7/13 (54%) women’s events recorded mean times for the eight f<strong>in</strong>alists<br />

that were significantly faster than the predicted outcome values.<br />

Only 34% of the events <strong>in</strong> the 2008 Games were successfully predicted.<br />

Between 1988 <strong>and</strong> 2004, 10/61 (16%) men’s events were significantly<br />

faster <strong>and</strong> 1 (2%) event was significantly slower than predicted. For the<br />

women, 1/61 (2%) events was significantly faster <strong>and</strong> 9 (15%) events<br />

were significantly slower than predicted. That is, 87% of all events were<br />

successfully predicted. These data are presented <strong>in</strong> Table 1 <strong>and</strong> Figure 2.<br />

Table 1. Comparisons between predicted <strong>and</strong> actual Olympic f<strong>in</strong>al performance<br />

for all men’s events from 2000, 2004, <strong>and</strong> 2008. Predictions were<br />

based on the mean of top 8 performances for each event beg<strong>in</strong>n<strong>in</strong>g <strong>in</strong> 1972<br />

up to the Olympics prior. For example, to predict the 100 Free <strong>in</strong> 2000, top<br />

8 means from 1972, ’76, ’80, ’84, ’88, ’92, <strong>and</strong> ’96 were plotted <strong>and</strong> regressed<br />

us<strong>in</strong>g a power function. † denotes significantly faster than predicted.<br />

2000 2004 2008<br />

Men's Predicted Actual ƀ<br />

Act-Pred Predicted Actual ƀ<br />

Act-Pred Predicted Actual ƀ<br />

Act-Pred<br />

Event Mean (s) Mean (s) (S.D.) Mean (s) Mean (s) (S.D.) Mean (s) Mean (s) (S.D.)<br />

50 Free 22.28 22.19 0.85 22.10 22.11 -0.12 22.00 21.57 5.46†<br />

100 Free 49.28 48.95 1.17 49.00 48.80 0.74 48.79 47.77 3.36†<br />

200 Free 107.58 107.43 0.19 107.13 106.49 0.96 106.61 105.81 1.23<br />

400 Free 227.10 226.21 0.59 225.90 225.92 -0.01 225.09 223.72 1.13<br />

1500 Free 899.22 901.67 -0.26 896.68 898.05 -0.16 894.18 888.61 0.63<br />

100 Back 55.03 54.85 0.39 54.76 54.52 0.57 54.50 53.28 3.04†<br />

200 Back 119.79 118.43 1.75 118.97 117.98 1.17 118.31 115.54 3.44†<br />

100 Breast 61.47 61.25 0.66 61.14 61.15 -0.02 60.91 59.64 4.45†<br />

200 Breast 132.86 132.85 0.02 132.21 131.14 1.32 131.34 129.44 2.06†<br />

100 Fly 53.16 52.53 2.16† 52.77 51.98 2.41† 52.38 51.23 3.29†<br />

200 Fly 117.54 116.69 1.37 116.92 115.89 1.51 116.33 113.86 3.87†<br />

200 IM 121.26 121.13 0.42 120.74 119.71 3.55† 120.02 117.88 5.46†<br />

400 IM 255.79 256.74 -1.49 255.00 254.71 0.42 253.99 250.54 5.45†<br />

% of Total Events<br />

Predictive Success Rate of All Olympic Events (1988-2008)<br />

100<br />

90<br />

80<br />

70<br />

Men<br />

60<br />

Women<br />

50<br />

Comb<strong>in</strong>ed M & W<br />

40<br />

30<br />

20<br />

1988 1992 1996 2000 2004 2008<br />

Figure 2. Percent of total events successfully predicted (with<strong>in</strong> 95% C.I.)<br />

for each Olympic Games (1988-2008) for men, women, <strong>and</strong> comb<strong>in</strong>ed<br />

men <strong>and</strong> women categories.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

When all events are “pooled,” the 2008 Games deviated from our predictions<br />

significantly more than any previous Games, with the average<br />

event offset be<strong>in</strong>g faster than statistical models by nearly 3 st<strong>and</strong>ard deviations<br />

(Figure 3). From 1988 until 2004, only one other Games was<br />

significantly different from other Games. In that case (1996), however,<br />

the swimmers were slower than predicted, not faster. Additionally, unlike<br />

2008, the events of the 1996 Games were, on average, not statistically<br />

different than predicted outcomes (with<strong>in</strong> 1.96 st<strong>and</strong>ard deviations).<br />

St<strong>and</strong>ard deviations<br />

3<br />

2<br />

1<br />

0<br />

-1<br />

1988 1992 1996 2000 2004 2008<br />

*<br />

-2<br />

Figure 3. Average difference, <strong>in</strong> st<strong>and</strong>ard deviations, between actual <strong>and</strong><br />

predicted performances of Olympic swimm<strong>in</strong>g events (1988-2008). A<br />

positive value denotes the average of actual event means were faster than<br />

the predicted event means. * denotes significant difference compared to<br />

all other groups.<br />

B<strong>in</strong>omial Analysis: F<strong>in</strong>ally, the results of b<strong>in</strong>omial tests of statistical significance<br />

are presented <strong>in</strong> Table 2. At the 2008 Games, all 26 events<br />

(13 men <strong>and</strong> 13 women) were faster than our predictions. That is, all<br />

events lay below the prediction curve, but were not necessarily significantly<br />

faster than predicted. As a result, the b<strong>in</strong>omial test of statistical<br />

significance revealed that the 2008 Olympic swimm<strong>in</strong>g event was, as a<br />

whole, significantly faster than expected (p < 0.05). For prior Olympics<br />

(1988-2004), the performances of the women were significantly slower<br />

than expected (p < 0.05) <strong>in</strong> 1992 <strong>and</strong> 1996. Dur<strong>in</strong>g the Olympic Games<br />

<strong>in</strong> 1988, 2000 <strong>and</strong> 2004, however, women swimmers performed as expected.<br />

Meanwhile, performances of the men were significantly faster<br />

than expected <strong>in</strong> 2000 (p < 0.05). However, the Games <strong>in</strong> 1988, 1992,<br />

1996 <strong>and</strong> 2004 were as expected. The men <strong>and</strong> women comb<strong>in</strong>ed swam<br />

significantly slower than expected (p < 0.05) <strong>in</strong> 1996, significantly faster<br />

than expected <strong>in</strong> 2000 (p < 0.05), <strong>and</strong> as expected <strong>in</strong> 1988, 1992 <strong>and</strong><br />

2004.<br />

Table 2. Count of events that were faster or slower than our predictions<br />

(above or below the regression l<strong>in</strong>e) for men, women, <strong>and</strong> comb<strong>in</strong>ed<br />

men <strong>and</strong> women categories for each Olympic Games (1988-2008). The<br />

results of the b<strong>in</strong>omial test of statistical significance shows the probability<br />

that this many events will be slower (†) or faster (*) than predicted is<br />

less than 5% (p < 0.05).<br />

Men Women Total<br />

Slower Faster Slower Faster Slower Faster<br />

1988 2 9 4 7 6 16<br />

1992 4 8 10† 2 14 10<br />

1996 8 4 12† 0 20† 4<br />

2000 2 11* 4 9 6 20*<br />

2004 4 9 7 6 11 15<br />

2008 0 13* 0 13* 0 26*<br />

*<br />

295


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

dIscussIon<br />

The results of the 2008 swimm<strong>in</strong>g competition were, <strong>in</strong> general, exceptionally<br />

fast <strong>and</strong> do not fit the expectations of our mathematical modell<strong>in</strong>g<br />

<strong>and</strong> based upon prior performances. With the exception of the<br />

1996 Games (which resulted <strong>in</strong> performances that were significantly<br />

slower than expected), there is little to no evidence to suggest any pervasive<br />

performance enhanc<strong>in</strong>g bias existed before 2008 for men or women.<br />

The exception (us<strong>in</strong>g b<strong>in</strong>omial analysis) might be 2000 when the full<br />

body suits were first <strong>in</strong>troduced. Until now, our predictive modell<strong>in</strong>g<br />

was largely successful <strong>in</strong> describ<strong>in</strong>g swim performance at the elite level.<br />

We would conclude that this bias had a dom<strong>in</strong>ant role <strong>in</strong> enhanc<strong>in</strong>g<br />

performance <strong>in</strong> a manner <strong>in</strong>consistent with the natural progression of<br />

swim performance observed over the last half century.<br />

Personal communication with coaches <strong>and</strong> athletes at this level<br />

has not provided any evidence of <strong>in</strong>novation other than perhaps the<br />

<strong>in</strong>troduction of new technology suits <strong>in</strong>to the sport. Due to the nature<br />

of commerce <strong>and</strong> claims of “proprietary” knowledge, very little specific<br />

data exist identify<strong>in</strong>g the magnitude (if any) of the effect of the newest<br />

generation suits on swim performance. While the current study does<br />

not directly measure the effect of the new technology swim suits, the<br />

athletes <strong>and</strong> their performances suggest that these suits (which did not<br />

exist prior to 2008) have <strong>in</strong>troduced unnatural rates of improvement<br />

<strong>in</strong>to the sport.<br />

F<strong>in</strong>ally, if the great leap <strong>in</strong> performance is not due to the <strong>in</strong>troduction<br />

of the suits <strong>and</strong> due to better coach<strong>in</strong>g or enhanced coach<strong>in</strong>g techniques,<br />

then the “bias” should persist <strong>in</strong> future performances. If not, this<br />

leads to the hypothesis that future analyses of swim performance will<br />

show a correction such that 2012 will be slower than predictions suggest.<br />

The slope <strong>in</strong> the progression of performance will be similar to what<br />

existed prior to 2008 <strong>and</strong> 2008 will be judged as anomalous. Ultimately,<br />

the progression <strong>in</strong> times will slow as swimmers approach the <strong>in</strong>escapable<br />

limits of human performance.<br />

reFerences<br />

Berthelot, G., Thibault, V., Tafflet, M., Escolano, S., El Helou, N., Jouven,<br />

X., Herm<strong>in</strong>e, O., & Toussa<strong>in</strong>t, J.F. (2008). The citius end: world<br />

records progression announces the completion of a brief ultra-physiological<br />

quest. PLoS ONE, 3, e1552.<br />

Frucht, A.H. & Jokl, E. (1964). Parabolic extrapolation of Olympic performance<br />

growth s<strong>in</strong>ce 1900. J Sports Med Phys Fitness, 4, 142-152.<br />

Nevill, A.M. & Whyte, G. (2005). Are there limits to runn<strong>in</strong>g world<br />

records? Med Sci Sports Exerc, 37, 1785-88.<br />

Seiler, S., De Kon<strong>in</strong>g, J. & Foster, C. (2007). The fall <strong>and</strong> rise of the<br />

gender difference <strong>in</strong> elite anaerobic performance 1952-2006. Med Sci<br />

Sports Exerc, 39, 534-40.<br />

Whipp, B.J. & Ward, S.A. (1992). Will women soon outrun men? Nature,<br />

355, 25.<br />

AcKnoWledGeMents<br />

The authors are <strong>in</strong>debted to the graduate students of the Counsilman<br />

Center for the Science of Swimm<strong>in</strong>g at Indiana University.<br />

296<br />

Tethered Swimm<strong>in</strong>g as an Evaluation Tool of S<strong>in</strong>gle<br />

Arm-Stroke Force<br />

toubekis, A.G. 1 , Gourgoulis, V. 2 , tokmakidis, s.P. .2<br />

1 Kapodistrian University of Athens, Athens, Greece,<br />

2 Democritus University of Thrace, Komot<strong>in</strong>i, Greece,<br />

Eight competitive swimmers performed a series of maximum <strong>in</strong>tensity<br />

tethered swimm<strong>in</strong>g tests us<strong>in</strong>g full-stroke, arms only, right <strong>and</strong> left arm<br />

only. In all tests, the force of each arm-stroke was determ<strong>in</strong>ed. The validity<br />

of each arm-stroke separation was tested <strong>in</strong> advance us<strong>in</strong>g overwater<br />

<strong>and</strong> underwater video record<strong>in</strong>gs (ICC=0.939, <strong>and</strong> 0.974, p


was used <strong>in</strong> addition to arm-strokes. Dur<strong>in</strong>g the ARM test a float<strong>in</strong>g<br />

device was used to keep legs together <strong>in</strong> a horizontal position. A zero<br />

velocity was ma<strong>in</strong>ta<strong>in</strong>ed <strong>in</strong> all tests.<br />

The force for SW <strong>and</strong> ARM tests was averaged for 15 s. In addition,<br />

the force for each right <strong>and</strong> each left arm-stroke was measured for the<br />

first five stroke cycles dur<strong>in</strong>g the SW <strong>and</strong> ARM tests <strong>and</strong> dur<strong>in</strong>g five<br />

strokes of the 1ARM-R <strong>and</strong> 1ARM-L tests. Additionally, a qualitative<br />

representation of force variation dur<strong>in</strong>g the fourth stroke cycle of the<br />

SW <strong>and</strong> ARM test was applied. All tests were applied at maximum<br />

<strong>in</strong>tensity <strong>and</strong> completed with<strong>in</strong> two consecutive days. Each test started<br />

with slow swimm<strong>in</strong>g <strong>and</strong> with countdown from three. The swimmers<br />

applied maximum <strong>in</strong>tensity after the exam<strong>in</strong>er’s comm<strong>and</strong>s <strong>and</strong> the start<br />

always co<strong>in</strong>cided with the entry of the right h<strong>and</strong> <strong>in</strong> the water, while us<strong>in</strong>g<br />

the front crawl style <strong>in</strong> all tests. A st<strong>and</strong>ard warm-up was applied before<br />

each test (400-m swim, 4x50-m progressively <strong>in</strong>creas<strong>in</strong>g <strong>in</strong>tensity,<br />

2x6s tethered swimm<strong>in</strong>g spr<strong>in</strong>ts). All swimmers had been familiarized<br />

with the procedures on a previous day.<br />

Dur<strong>in</strong>g tethered swimm<strong>in</strong>g tests a piezoelectric force transducer<br />

connected to an analog to digital (A/D) converter system (MuscleLab,<br />

Ergotest) with a sampl<strong>in</strong>g frequency 100Hz was used for force measurement.<br />

A trigger was used to <strong>in</strong>sert a signal synchronized with force<br />

record<strong>in</strong>gs <strong>in</strong>to the system, <strong>and</strong> separated the arm-strokes. The button of<br />

the h<strong>and</strong>-held trigger was pressed by the experimenter at the moment<br />

of each arm-stroke entry <strong>in</strong> the water. In a separate experiment a female<br />

swimmer performed 10x20-arm-stroke trials videotaped above water<br />

<strong>and</strong> 6x20-arm-stroke trials videotaped underwater <strong>in</strong> order to validate<br />

the accuracy of stroke separation us<strong>in</strong>g the h<strong>and</strong>-held trigger. Us<strong>in</strong>g<br />

a small LED emitt<strong>in</strong>g light, the signal of the h<strong>and</strong>-held trigger was<br />

synchronized with a camera (Sony DCR-HC14 E, Sony Corporation,<br />

Japan) operat<strong>in</strong>g <strong>in</strong> <strong>in</strong>terlaced scan mode (50Hz), which was located<br />

perpendicular to the swimmer. A different group of swimmers (n=7, age:<br />

13.8±1.5 years, body mass: 58.5±7.6 kg, height: 1.67±0.08 m) was used<br />

to test the reliability of force output for each arm-stroke. The swimmers<br />

performed a 15 s spr<strong>in</strong>t with the same procedure as described above (test<br />

1) <strong>and</strong> repeated the test with<strong>in</strong> seven days (test 2). The force of the first<br />

ten arm-strokes of the two tests was compared.<br />

Analysis of variance for repeated measures on two factors (tests x<br />

arms) was used to exam<strong>in</strong>e force differences between tests <strong>and</strong> between<br />

arms. Differences between means were located us<strong>in</strong>g a Tukey post-hoc<br />

test. The Pearson correlation coefficient was used to test the relationship<br />

between variables <strong>and</strong> the <strong>in</strong>traclass correlation coefficient (ICC) was<br />

used to exam<strong>in</strong>e the reliability of the procedures. The results are presented<br />

as mean±SD <strong>and</strong> the accepted level of significance was set at p0.05). The<br />

R <strong>and</strong> L arm-stroke ICC confirmed the reliable force reproduction <strong>in</strong><br />

each arm-stroke (R arm-stroke, ICC=0.985; L arm-stroke, ICC=0.975<br />

p0.05, Figure 1). The average time to complete<br />

each arm-stroke calculated by video record<strong>in</strong>g, by the LED emitt<strong>in</strong>g<br />

time <strong>and</strong> by the h<strong>and</strong>-held trigger was no different (video time overwater:<br />

0.752±0.065 s, LED time: 0.748±0.070 s, h<strong>and</strong>-held trigger time:<br />

0.747±0.069 s, p>0.05). In addition, the reliability of the h<strong>and</strong>-held trigger<br />

use was confirmed with the over-water <strong>and</strong> underwater video record<strong>in</strong>gs<br />

(ICC=0.939 <strong>and</strong> 0.974, p0.05). The absolute difference between video-recorded stroke time<br />

(under-water <strong>and</strong> over-water) versus the trigger h<strong>and</strong>-held time measure<br />

was not significant (under-water video recorded stroke time vs. h<strong>and</strong>-held<br />

trigger time: 0.024±0.026 s <strong>and</strong> over-water video recorded stroke time vs.<br />

h<strong>and</strong>-held trigger time: 0.018±0.022 s, p>0.05).<br />

Force (N)<br />

180<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

R<br />

Test1 Test 2<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

L R L R L R L R L<br />

1 2 3 4 5 6 7 8 9 10<br />

Arm-stroke number<br />

Figure 1. The force produced by each arm-stroke dur<strong>in</strong>g 10 front-crawl<br />

strokes dur<strong>in</strong>g two successive tests performed with<strong>in</strong> a week. R <strong>and</strong> L:<br />

right <strong>and</strong> left arm-stroke.<br />

The mean force produced dur<strong>in</strong>g the 15 s spr<strong>in</strong>t SW was higher compared<br />

to ARM test (SW: 93±6, ARM: 68±4 N, p


-ARM<br />

*<br />

5<br />

<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Force (N)<br />

298<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

40<br />

20<br />

0<br />

B<br />

*<br />

*<br />

SW ARM 1-ARM<br />

*<br />

1 2 3 4 5<br />

Left arm strokes<br />

Figure 3. Force measured <strong>in</strong> the right (A) <strong>and</strong> left (B) arm-stroke dur<strong>in</strong>g 40<br />

five arm-strokes of each test. SW: full-stroke, ARM: arms only, 1ARM: 20<br />

us<strong>in</strong>g one arm test.<br />

dIscussIon<br />

The f<strong>in</strong>d<strong>in</strong>gs of the present study <strong>in</strong>dicate that a reliable measurement<br />

of swimm<strong>in</strong>g force for each arm can be achieved us<strong>in</strong>g tethered swimm<strong>in</strong>g.<br />

The procedure used for the separation of arm-strokes dur<strong>in</strong>g front<br />

crawl was proved to be valid when it was compared with over-water <strong>and</strong><br />

under-water video record<strong>in</strong>gs. Us<strong>in</strong>g three different tethered swimm<strong>in</strong>g<br />

tests (full-stroke, arms only, s<strong>in</strong>gle arm) no differences were observed<br />

between right <strong>and</strong> left arm-stroke force.<br />

Previous studies have shown a high reliability for the measurement of<br />

the maximum swimm<strong>in</strong>g force <strong>in</strong> a 10 s tethered swimm<strong>in</strong>g test (Kjendlie<br />

& Thorsvald 2006). However, there are no data concern<strong>in</strong>g the reliability<br />

of measur<strong>in</strong>g the force output dur<strong>in</strong>g a s<strong>in</strong>gle arm-stroke dur<strong>in</strong>g tethered<br />

swimm<strong>in</strong>g. In order to measure the force of each arm-stroke <strong>in</strong>dependently<br />

dur<strong>in</strong>g a test, a valid separation of the strokes is required. In the<br />

present study the time calculated to complete each arm-stroke from a<br />

video <strong>and</strong> from a h<strong>and</strong>-held trigger was similar (p>0.05). This means that<br />

the <strong>in</strong>put of the electrical signal us<strong>in</strong>g a h<strong>and</strong>-held trigger can separate<br />

arm-strokes with validity (ICC=0.974 <strong>and</strong> 0.939). In practice, the force<br />

variation with<strong>in</strong> this time frame can be measured. Apply<strong>in</strong>g these procedures<br />

with a group of young swimmers, the force was measured with reliability<br />

(ICC=0.985 <strong>and</strong> 0.975, p


Takagi, H. & Wilson, B. (1999). Calculat<strong>in</strong>g hydrodynamic force by<br />

us<strong>in</strong>g pressure differences <strong>in</strong> swimm<strong>in</strong>g. In: Kesk<strong>in</strong>en K, Komi P,<br />

Holl<strong>and</strong>er P. (eds), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII. (pp<br />

101-106). University of Jyväskylä, Jyväskylä, F<strong>in</strong>l<strong>and</strong>.<br />

Vorontsov, A., Popov, O., B<strong>in</strong>evsky, D. & Dyrko, V. (2006). The assessment<br />

of specific strength <strong>in</strong> well-tra<strong>in</strong>ed male athletes dur<strong>in</strong>g tethered<br />

swimm<strong>in</strong>g <strong>in</strong> the swimm<strong>in</strong>g flume. Port J of Sport Sci, 6(S2), 275-277.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

Blood Lactate Responses Dur<strong>in</strong>g Interval Tra<strong>in</strong><strong>in</strong>g<br />

Correspond<strong>in</strong>g to Critical Velocity <strong>in</strong> Age-Group<br />

Female Swimmers<br />

tsalis, G. 1 , toubekis, A.G. 2 , Michailidou, d. 1 , Gourgoulis, V. 3 ,<br />

douda, h. 3 , tokmakidis, s.P. 3<br />

1 Aristotle University, Thessaloniki, Greece,<br />

2 Kapodistrian University of Athens, Athens, Greece<br />

3 Democritus University of Thrace, Komot<strong>in</strong>i, Greece<br />

The present study exam<strong>in</strong>ed the blood lactate responses of female swimmers<br />

at <strong>in</strong>tensity correspond<strong>in</strong>g to critical velocity (CV). Eight children<br />

(C), eleven youth (Y) <strong>and</strong> seven adults (A) were timed <strong>in</strong> distances of 50,<br />

100, 200, 400 m for the CV calculation. On a follow<strong>in</strong>g day the C performed<br />

5x300 m <strong>and</strong> the Y <strong>and</strong> A 5x400 m repetitions with 30-40 s <strong>in</strong>terval,<br />

at CV. Blood lactate concentration ([La]) was similar between groups<br />

<strong>and</strong> ma<strong>in</strong>ta<strong>in</strong>ed steady with<strong>in</strong> a range of 3.5±1.2 to 5.1±1.6 mmol·L -1<br />

(p>0.05). RPE <strong>and</strong> RPE/[La] ratio were no different between groups<br />

(p>0.05) <strong>and</strong> <strong>in</strong>creased after the second <strong>and</strong> third repetition respectively<br />

<strong>in</strong> all groups (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

allowed between tests. Swimmers were not tested if they didn’t feel completely<br />

recovered after the first tested distance.<br />

On a follow<strong>in</strong>g day swimmers performed five repetitions of 400 m<br />

or 300 m with an <strong>in</strong>terval of 30-40 s (5x400 m, Y <strong>and</strong> A groups; 5x300<br />

m, C group). Dur<strong>in</strong>g the set the swimmers were guided to ma<strong>in</strong>ta<strong>in</strong> CV.<br />

The 300-m distance was used for children swimmers <strong>in</strong> order to keep<br />

the duration of each repetition similar among groups. A capillary blood<br />

sample was taken from a f<strong>in</strong>ger-tip after each 400 or 300 m repetition. The<br />

short rest<strong>in</strong>g <strong>in</strong>terval between repetitions was used for blood sampl<strong>in</strong>g<br />

(30-40 s). The blood sample was immediately mixed with 10 volumes of<br />

0.3 mol·l -1 perchloric acid <strong>and</strong> centrifuged at 1500 x g. The supernatant<br />

was stored <strong>and</strong> later analysed spectrophotometrically at 340 nm wavelength<br />

us<strong>in</strong>g reagents commercially available (Sigma, St Louis, MO). The<br />

RPE was reported after each 300 or 400 m repetition on a 10-po<strong>in</strong>t scale.<br />

A two-way analysis of variance for repeated measures (group x repetitions)<br />

<strong>and</strong> the Tukey post-hoc test were used for statistical analysis.<br />

The Pearson correlation coefficient was used to exam<strong>in</strong>e the relationship<br />

between variables. The results are presented as mean±SD <strong>and</strong> the level<br />

of significance was set at p0.05). Additionally,<br />

the susta<strong>in</strong>ed actual velocity dur<strong>in</strong>g the <strong>in</strong>terval swimm<strong>in</strong>g set<br />

of repetitions was not different from the CV, for all groups (Figure<br />

1, p>0.05). The average time required to cover the 300 or 400 m distance<br />

repetitions (C: 5.2±0.2 vs. Y: 5.8±0.4 <strong>and</strong> A: 5.6±0.3 m<strong>in</strong>, p


0-m<br />

*<br />

A: adult<br />

5<br />

Horton, 2001). A reduced carbohydrate utilisation may decrease the<br />

[La] levels <strong>in</strong> females compared to males exercis<strong>in</strong>g at the same relative<br />

<strong>in</strong>tensity (Deschenes et al., 2006). The relative <strong>in</strong>tensity <strong>in</strong> the present<br />

study (96% of 400 m velocity) was similar to previous studies calculat<strong>in</strong>g<br />

the CV with the same comb<strong>in</strong>ation of distances <strong>in</strong> males (Filipatou<br />

et al., 2006). It is also important to note that the time to complete each<br />

distance is shorter <strong>in</strong> male swimmers than female swimmers while us<strong>in</strong>g<br />

the same distances for CV calculation. This may underestimate the<br />

slope of the distance vs. time relationship, while the lower [La] may<br />

overestimate the boundary between moderate <strong>and</strong> severe exercise <strong>in</strong>tensity<br />

doma<strong>in</strong>s for females. Thus, it may be easier for female swimmers<br />

to complete a series of repetitions at this velocity s<strong>in</strong>ce they swim with<br />

decreased metabolic stress. As a consequence, a steady [La] dur<strong>in</strong>g the<br />

5x400 or 5x300 m repetitions was evident.<br />

Blood lactate (mmol*L -1 )<br />

8.0<br />

7.0<br />

6.0<br />

5.0<br />

4.0<br />

3.0<br />

2.0<br />

1.0<br />

0.0<br />

C: children Y: young A: adult<br />

rest 1 2 3 4 5<br />

Repetitions of 300 or 400-m<br />

Figure 2. Blood lactate responses of each group dur<strong>in</strong>g the 5x300 or<br />

5x400 m repetitions.<br />

RPE<br />

RPE / La ratio<br />

10<br />

9<br />

8<br />

7<br />

6<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

6<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

3B<br />

3A<br />

*<br />

*<br />

C: chlildren Y: young A: adult<br />

1 2 3 4 5<br />

Repetitions of 300 or 400-m<br />

*<br />

1 2 3 4 5<br />

Repetitions of 300 or 400-m<br />

*<br />

*<br />

*<br />

C: chlildren<br />

Y: young<br />

A: adult<br />

*<br />

RPE / La ratio<br />

Figure 3. The RPE changes (3A) <strong>and</strong> RPE to [La] ratio (3B) dur<strong>in</strong>g the<br />

5x300 or 5x400 m repetitions. * p8 <strong>in</strong> the 10-po<strong>in</strong>t scale). It is <strong>in</strong>terest<strong>in</strong>g to note that eight<br />

of the swimmers (four <strong>in</strong> the C group) reached “maximal” values <strong>in</strong> the<br />

RPE scale. Increased RPE to [La] ratio after the third repetition may<br />

be a sign of fatigue caused by the exercise duration when the <strong>in</strong>tensity<br />

rema<strong>in</strong>s constant.<br />

conclusIon<br />

Critical velocity calculated by slope of the distance vs. time relationship<br />

us<strong>in</strong>g distances of 50, 100, 200, 400 m, can be susta<strong>in</strong>ed dur<strong>in</strong>g <strong>in</strong>termittent<br />

swimm<strong>in</strong>g for 28 to 31 m<strong>in</strong>utes <strong>in</strong> female swimmers of eleven to<br />

n<strong>in</strong>eteen years of age. Irrespective of the age-group, female swimmers<br />

display steady-state <strong>and</strong> similar blood lactate responses dur<strong>in</strong>g <strong>in</strong>termittent<br />

swimm<strong>in</strong>g at a velocity correspond<strong>in</strong>g to critical velocity, <strong>and</strong> this is<br />

<strong>in</strong> contrast to previous f<strong>in</strong>d<strong>in</strong>gs <strong>in</strong> male swimmers.<br />

301


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

reFerences<br />

Beneke, R., Hütler, M., Jung, M. & Leithäuser R. M. (2005). Model<strong>in</strong>g<br />

the blood lactate k<strong>in</strong>etics at maximal short-term exercise conditions<br />

<strong>in</strong> children, adolescents, <strong>and</strong> adults. J Appl Physiol, 99, 499-504.<br />

Braun B. & Horton T. (2001). Endocr<strong>in</strong>e regulation of exercise substrate<br />

utilization <strong>in</strong> women compared to men. Exerc Sport Sci Rev,<br />

29, 149-154.<br />

Deschenes, M. R., Hillard, M. N., Wilson J. A., Dub<strong>in</strong>a M. I. & Eason<br />

M. K. (2006). Effects of gender on physiological responses dur<strong>in</strong>g<br />

sumbaximal exercise <strong>and</strong> recovery. Med Sci Sports Exerc, 38, 1304-<br />

1310.<br />

Dekerle, J., Brickley, G., Alberty, M. & Pelayo P. (2009). Characteriz<strong>in</strong>g<br />

the slope of the distance-time relationship <strong>in</strong> swimm<strong>in</strong>g. J Sci<br />

Med Sport, doi:10.1016/j.jsams.2009.05.007.<br />

Fawkner, S. & Armstrong N. (2003). Oxygen uptake k<strong>in</strong>etic response to<br />

exercise <strong>in</strong> children. Sports Med, 33, 651-669.<br />

Fern<strong>and</strong>es, R. & Vilas-Boas J. P. (1999). Critical velocity as a criterion<br />

for estimat<strong>in</strong>g aerobic tra<strong>in</strong><strong>in</strong>g pace for juvenile swimmers. In Kesk<strong>in</strong>en<br />

K. Komi P. Holl<strong>and</strong>er P. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g<br />

VIII, (pp 233-238). University of Jyväskylä, Juväskylä, F<strong>in</strong>l<strong>and</strong>.<br />

Fillipatou, E., Toubekis, A., Douda, H., Pilianidis, T. & Tokmakidis, S.<br />

P. (2006). Lactate <strong>and</strong> heart rate responses dur<strong>in</strong>g swimm<strong>in</strong>g at 95%<br />

<strong>and</strong> 100% of the critical velocity <strong>in</strong> children <strong>and</strong> young swimmers.<br />

Port J Sp Sci, 6(S2), 132-134.<br />

Greco, C. C. & Denadai, B. S. (2005). Critical speed <strong>and</strong> endurance<br />

capacity <strong>in</strong> young swimmers: effects of gender <strong>and</strong> age. Pediatr Exerc<br />

Sci, 17, 353-363<br />

Ribeiro, L. F., Lima, M. C. & Gobatto, C. A. (2008). Changes <strong>in</strong> physiological<br />

<strong>and</strong> strok<strong>in</strong>g parameters dur<strong>in</strong>g <strong>in</strong>terval swims at the slope of<br />

the d-t relationship. J Sci Med Sport, doi:10.1016/j.jsams.2008.10.001.<br />

Takahashi, S., Wakayoshi, K., Hayashi, A., Sakaguchi, Y. & Kitagawa,<br />

K. (2009). A method for determ<strong>in</strong><strong>in</strong>g critical swimm<strong>in</strong>g velocity. Int<br />

J Sports Med, 30, 119-123.<br />

Tanner, J. H. & Whitehouse, R. H. (1976). Cl<strong>in</strong>ical longitud<strong>in</strong>al st<strong>and</strong>ards<br />

for height, weight, height velocity, weight velocity <strong>and</strong> the<br />

stages of puberty. Arch Dis Child, 51, 170-179.<br />

Toubekis, A. G., Tsami, A. P. & Tokmakidis S. P. (2006). Critical velocity<br />

<strong>and</strong> lactate threshold <strong>in</strong> young swimmers. Int J Sports Med, 27,<br />

117-123.<br />

Wakayoshi, K., Yoshida, T., Udo, M., Harada, T., Moritani, T., Mutoh,<br />

Y. & Miyashita M. (1993). Does critical swimm<strong>in</strong>g velocity represent<br />

exercise <strong>in</strong>tensity at maximal lactate steady state? Eur J Appl Physiol,<br />

66, 90-95.<br />

Williams, C. A., Dekerle, J., McGawley, K., Bertho<strong>in</strong>, S. & Carter H.<br />

(2008). Critical power <strong>in</strong> adolescent boys <strong>and</strong> girls – an exploratory<br />

study. Appl Physiol Nutr Metab, 33, 1105-1111.<br />

302<br />

Monitor<strong>in</strong>g Swim Tra<strong>in</strong><strong>in</strong>g Based on Mean Intensity<br />

Stra<strong>in</strong> <strong>and</strong> Individual Stress Reaction of an Elite<br />

Swimmer<br />

ungerechts, B.e. 1 , steffen, r. 2 , <strong>and</strong> Vogel, K. 3<br />

1 University of Bielefeld, Germany,<br />

2 Coaches Academy Cologne, Germany,<br />

3 German Sport University Cologne, Germany<br />

Swim coaches prescribe tra<strong>in</strong><strong>in</strong>g to enhance the properties required for<br />

a person to swim the same distance <strong>in</strong> less time. Monitor<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g<br />

stra<strong>in</strong> may give a clue to the relationship between tra<strong>in</strong><strong>in</strong>g <strong>and</strong> race performance.<br />

Mujika (1996) monitored a tra<strong>in</strong><strong>in</strong>g season reduc<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g<br />

components to one MITS-value (mean <strong>in</strong>tensity of a tra<strong>in</strong><strong>in</strong>g season).<br />

S<strong>in</strong>ce tra<strong>in</strong><strong>in</strong>g stra<strong>in</strong> is modulated by personal traits <strong>in</strong>to an <strong>in</strong>ternal<br />

fatigu<strong>in</strong>g impulse, cooperation by the athlete is essential to monitor<br />

the perceived stress at the end of a day <strong>and</strong> the next morn<strong>in</strong>g, respectively.<br />

The difference of both items, called delayed perceived fatigue, <strong>and</strong><br />

MITS-value of a world level female swimmer was registered for 144<br />

days: MITS = 2.01 ± 0.12 <strong>and</strong> the delayed perceived fatigue = -1.31 ±<br />

1.81 arbitrary units, respectively. The <strong>in</strong>crease of the race performance<br />

was 2.8%.<br />

Key words: tra<strong>in</strong><strong>in</strong>g <strong>in</strong>tensity, perceived stress, tra<strong>in</strong><strong>in</strong>g monitor<strong>in</strong>g,<br />

elite swimmer<br />

IntroductIon<br />

Swim coaches prescribe tra<strong>in</strong><strong>in</strong>g to enhance the properties required of<br />

a person to swim the same distance <strong>in</strong> less time. Occasionally coaches<br />

are <strong>in</strong>terested <strong>in</strong> different concepts after e.g. realis<strong>in</strong>g that tra<strong>in</strong><strong>in</strong>g pr<strong>in</strong>ciples<br />

do not really tell how tra<strong>in</strong><strong>in</strong>g loads are related to reactions of the<br />

biological systems or when work<strong>in</strong>g with elite swimmers, which was the<br />

case here. Coach, swimmer <strong>and</strong> consultant realized that <strong>in</strong> the past the<br />

daily tra<strong>in</strong><strong>in</strong>g rout<strong>in</strong>e served to cause adaptations but a causal predication<br />

about the impact of tra<strong>in</strong><strong>in</strong>g volume <strong>and</strong> <strong>in</strong>tensity <strong>and</strong> the race performance<br />

or e.g. blood parameters could not be <strong>in</strong>dentified (Nissen et.<br />

al., 2007). They started mutual reason<strong>in</strong>g concern<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g contents<br />

<strong>and</strong> efficient monitor<strong>in</strong>g <strong>and</strong> were <strong>in</strong>terested <strong>in</strong> what scientists who had<br />

long worked <strong>in</strong> swimm<strong>in</strong>g research, recommended <strong>in</strong> the literature.<br />

Start<strong>in</strong>g with physiologists, Costill (1999) po<strong>in</strong>ted out that Olympic<br />

swimmers do not dist<strong>in</strong>guish themselves physiologically, it is biomechanics<br />

which counts <strong>and</strong> Holmer (1983) summed up that tra<strong>in</strong><strong>in</strong>g<br />

develops power, but the swimm<strong>in</strong>g speed is determ<strong>in</strong>ed by technique. In<br />

human swimm<strong>in</strong>g energy-rate research is not well established like e.g.<br />

<strong>in</strong> studies of swimm<strong>in</strong>g animals (Schultz & Webb, 2002). Consider<strong>in</strong>g<br />

an energy-rate approach might give a better underst<strong>and</strong><strong>in</strong>g of the <strong>in</strong>teraction<br />

of physiological <strong>and</strong> biomechanical parameters. Bremer (2003)<br />

measured oxygen uptake, lactate accumulation <strong>and</strong> efficiency factors of<br />

swimmers <strong>and</strong> reported that the propell<strong>in</strong>g power of a person amounts<br />

to 1800 Watts achiev<strong>in</strong>g a speed of approx 1.8 m/s but only 450 Watts<br />

for cruis<strong>in</strong>g a speed of approx. 1.1 m/s. This demonstrates how closely<br />

<strong>in</strong>tensity <strong>and</strong> duration are related, <strong>and</strong> that speed tra<strong>in</strong><strong>in</strong>g, requir<strong>in</strong>g<br />

high <strong>in</strong>tensity, short duration <strong>and</strong> longer rest periods is just part of a<br />

cont<strong>in</strong>uum of a “power field”.<br />

The studies concern<strong>in</strong>g importance of tra<strong>in</strong><strong>in</strong>g volume were also<br />

considered. Chartard (1999) reported that swimmers of squads with<br />

tra<strong>in</strong><strong>in</strong>g loads of 9 km/day do not race faster than squads with 5 km/d.<br />

Furthermore those squads which did some seasons at 8 km/d <strong>and</strong><br />

changed to 5 km/d, <strong>in</strong>creased speed <strong>in</strong> competition. Mujika, Chatard,<br />

Busco, Geyssant, Barale, Lacoste (1995) were able to demonstrate that<br />

a tra<strong>in</strong><strong>in</strong>g regime at high mean <strong>in</strong>tensity over a period of 6 weeks, characterized<br />

by exhaust<strong>in</strong>g loads between 1 <strong>and</strong> 2 m<strong>in</strong> accompanied by anaerobic<br />

energy release between 60 % to 35 %, will result <strong>in</strong> a ga<strong>in</strong> of 10


% anaerobic capacity; thus for elite swimmers mean tra<strong>in</strong><strong>in</strong>g <strong>in</strong>tensity<br />

is the determ<strong>in</strong><strong>in</strong>g component of enhanced performance <strong>and</strong> not volume<br />

or frequency (which might be different <strong>in</strong> age group swimmers). In<br />

addition it was shown that swimmers who improved their performace<br />

significantly <strong>in</strong> a season were primarily those who managed to swim the<br />

first races of a new season at relatively higher speed (<strong>in</strong> % of their personal<br />

best). Concern<strong>in</strong>g high <strong>in</strong>tensity tra<strong>in</strong><strong>in</strong>g regimes, costill, Kovaleski,<br />

Porter, Kirwan, Field<strong>in</strong>g, K<strong>in</strong>g published already <strong>in</strong> 1985 that elite<br />

athletes might possess a stimulus threshold requir<strong>in</strong>g HIT conditions,<br />

result<strong>in</strong>g <strong>in</strong> higher power output <strong>and</strong> faster race times.<br />

The coach also decided to consider this activity as a psycho-physical<br />

issue. An activity is a necessary condition which is modulated by personal<br />

traits result<strong>in</strong>g <strong>in</strong> an <strong>in</strong>ternal fatigu<strong>in</strong>g impulse (Mujika, Busso,<br />

Geyssant, Chatard, Barale, Lacoste, 1996) <strong>and</strong> becomes the sufficient<br />

determ<strong>in</strong><strong>in</strong>g condition for biological adaptation. Ulmer (1986) po<strong>in</strong>ted<br />

out that delayed stress triggers adaptation on the cellular level caus<strong>in</strong>g<br />

changes <strong>in</strong> biological mass, like mitochondria, enzymes, vessels, <strong>in</strong>clud<strong>in</strong>g<br />

energy delivery or power systems us<strong>in</strong>g exist<strong>in</strong>g genetical pathways.<br />

The effect of the daily tra<strong>in</strong><strong>in</strong>g rout<strong>in</strong>es must not be separated from<br />

the daily <strong>in</strong>duced stress of everyday life circumstances, like amount of<br />

sleep or psychological stress may <strong>in</strong>dividually <strong>in</strong>fluence <strong>in</strong>ternal thresholds<br />

related to effects of the fatigu<strong>in</strong>g impulse. It was decided to separate<br />

tra<strong>in</strong><strong>in</strong>g load (stra<strong>in</strong>) from <strong>in</strong>dividually perceived effects (stress) <strong>and</strong> to<br />

monitor both aspects for tra<strong>in</strong><strong>in</strong>g steer<strong>in</strong>g purpose (the say<strong>in</strong>g “no pa<strong>in</strong><br />

no ga<strong>in</strong>” can be understood as the importance of the <strong>in</strong>dividual reaction<br />

because a given load is not felt to be pa<strong>in</strong>ful by all members of the<br />

squad). The stress level perceived by the athlete can be recorded us<strong>in</strong>g a<br />

def<strong>in</strong>ed scale.<br />

Tra<strong>in</strong><strong>in</strong>g documentation formats, used so far, were replaced by a<br />

more <strong>in</strong>telligent format <strong>in</strong>troduced by Mujika et. al. (1996), called MITS<br />

(mean <strong>in</strong>tensity of a tra<strong>in</strong><strong>in</strong>g season). MITS is an easy way to represent<br />

tra<strong>in</strong><strong>in</strong>g components - <strong>in</strong>tensity, volume <strong>and</strong> frequency - <strong>in</strong> a s<strong>in</strong>gle value<br />

<strong>in</strong>stead of data <strong>in</strong> abundance. Tra<strong>in</strong><strong>in</strong>g loads are dist<strong>in</strong>guished <strong>in</strong> five<br />

load<strong>in</strong>g zones which are characterized by established <strong>in</strong>tensity <strong>in</strong>dex.<br />

MITS is calculated by multiply<strong>in</strong>g the volume data <strong>and</strong> stress <strong>in</strong>dex,<br />

respectively, summm<strong>in</strong>g up the products – <strong>in</strong>clud<strong>in</strong>g a dryl<strong>and</strong> tra<strong>in</strong><strong>in</strong>g<br />

equivalent- <strong>and</strong> divid<strong>in</strong>g the sum by the total meter sum dur<strong>in</strong>g<br />

the tra<strong>in</strong><strong>in</strong>g period taken <strong>in</strong>to consideration. The dryl<strong>and</strong> equivalent was<br />

described by Mujika et al. (1996) “ … it was empirically considered that<br />

1 h of dryl<strong>and</strong> tra<strong>in</strong><strong>in</strong>g was equivalent to 1 km swum at <strong>in</strong>tensity I, 0.5<br />

km at <strong>in</strong>tensity IV <strong>and</strong> 0.5 km at <strong>in</strong>tensity V.” How MITS-level effects<br />

the organism is unknown <strong>in</strong> detail. However, each coach would appreciate<br />

when the number of <strong>in</strong>fluenc<strong>in</strong>g parameters –which are likely to be<br />

related to each other <strong>in</strong> a still unknown way- is reduced.<br />

The purpose of this case study is to report the MITS-values <strong>and</strong> the<br />

perceived delayed stress-values based on be<strong>in</strong>g fatigued.<br />

Methods<br />

This is a case study. An elite female swimmer of 14 years of regular tra<strong>in</strong><strong>in</strong>g<br />

experience <strong>and</strong> 1:10.57 for 100 m breaststroke gave her consent to<br />

document twice a day the perceived level of fatigue a) directly after the<br />

workouts <strong>and</strong> b) on the follow<strong>in</strong>g morn<strong>in</strong>g accord<strong>in</strong>g to an exhaustion<br />

scale. A stress scale was negotiated between coach <strong>and</strong> athlete before<br />

start<strong>in</strong>g the monitor<strong>in</strong>g period. The details were: totally refreshed = 1,<br />

recovered = 2 – 3, relaxed = 4 – 5, reposed = 6, flagged = 7, tired = 8 – 9,<br />

nerveless = 10 -11, exhausted = 12 – 13, sick = 14. The values of i) <strong>and</strong> ii)<br />

were substracted from each other. The difference between both perceived<br />

fatigue values was calculated <strong>and</strong> called delayed perceived fatigue.<br />

Over a period of 144 days MITS-values per day were calculated based<br />

on the recorded tra<strong>in</strong><strong>in</strong>g components; MITS-values are placed between<br />

1 <strong>and</strong> 3 <strong>and</strong> values near to 3 represent most stra<strong>in</strong><strong>in</strong>g situations (Mujika<br />

et al., 1996). Five <strong>in</strong>tensity zones were def<strong>in</strong>ed accord<strong>in</strong>g to blood lactate<br />

<strong>and</strong> comb<strong>in</strong>ed with stress <strong>in</strong>dex: I1: < 2 mmol/l � 1, I2: 4 mmol/l � 2,<br />

I3: 6 mmol/l � 3, I4: 10 mmol/l � 5, I5: spr<strong>in</strong>t � 8. The calculation of<br />

MITS as a representative stra<strong>in</strong> factor was as follows.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

1. multiply the distance swum per tra<strong>in</strong><strong>in</strong>g load zone times the appropriate<br />

stress factor<br />

2. convert dry l<strong>and</strong> tra<strong>in</strong><strong>in</strong>g duration <strong>in</strong>to stress factor (here a constant<br />

factor: 4.5)<br />

3. add (a) 1 + 2 <strong>and</strong> (b) total tra<strong>in</strong><strong>in</strong>g volume (km per day)<br />

4. divide (a) by (b) to get MITS-Values<br />

MITS = (n kmI1)*1 + (n kmI2)*2 + (n kmI3)*3 + (n kmI4)*5 + (n kmI5)*8 + 4.5)<br />

total km<br />

results<br />

The elite female swimmer improved her best time by 2.8 % after this<br />

macro cycle over a period of 144 days or 288 half days, respectively. In<br />

this case study data of the tra<strong>in</strong><strong>in</strong>g components were: tra<strong>in</strong><strong>in</strong>g volume<br />

= 605 km, tra<strong>in</strong><strong>in</strong>g frequency = 188 half days, dryl<strong>and</strong> tra<strong>in</strong><strong>in</strong>g = 552<br />

m<strong>in</strong> <strong>and</strong> 100 half days of rest. The mean distance / day was 3.2 km. The<br />

percentages of the total distance covered at each <strong>in</strong>tensity level were: I1<br />

= 13.07 %, I2 = 75.52 %, I3 = 6.38 %, I4 = 1.24 % <strong>and</strong> I5 = 3.80 %. The<br />

calculated MITS-value (mean <strong>in</strong>tensity of a tra<strong>in</strong><strong>in</strong>g season) was 2.01<br />

± 0.12 arbitrary units. For a macro cycle of 16 weeks the distribution of<br />

MITS-values per week is presented (Fig 1).<br />

MITS<br />

2,30<br />

2,10<br />

1,90<br />

1,70<br />

1,50<br />

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16<br />

Weeks<br />

Fig 1 MITS (mean <strong>in</strong>tensity of a tra<strong>in</strong><strong>in</strong>g season) <strong>in</strong> arbitrary units<br />

over a period of 16 weeks; the stars <strong>in</strong>dicate competitions.<br />

The representation of weekly MITS- values show a trend towards somewhat<br />

more <strong>in</strong>tensive tra<strong>in</strong><strong>in</strong>g loads.<br />

The data of the perceived status of fatigue recorded directly after all<br />

workout sessions were: mean = 6.38 units, SD = ± 1.57 <strong>and</strong> variance =<br />

2.58 followed the next morn<strong>in</strong>g by mean = 5.02, SD = ± 1.97 <strong>and</strong> variance<br />

= 3.90. The differences between the two situations are presented <strong>in</strong><br />

Figure 2 over 144 days. The level of perceived fatigue after the tra<strong>in</strong><strong>in</strong>g<br />

sessions is generally higher than the level after sleep<strong>in</strong>g, the morn<strong>in</strong>g of<br />

the next day, <strong>in</strong>dicat<strong>in</strong>g recovery due to rest at night.<br />

Fig. 2 Perceived delayed fatigue data <strong>in</strong> arbitrary units over a period of<br />

144 days 0.00 means: no difference between perceived fatigue due to<br />

sleep<strong>in</strong>g, m<strong>in</strong>us means: the perceived value after sleep<strong>in</strong>g is lower than<br />

after tra<strong>in</strong><strong>in</strong>g the day before<br />

303


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Fig. 3 Representation of MITS-values (black l<strong>in</strong>es) per day <strong>and</strong> delayed<br />

perceived fatigue level data (grey l<strong>in</strong>es) over a period of 144 days; stars<br />

<strong>in</strong>dicate competitions<br />

The mutual representation of daily MITS-values <strong>and</strong> delayed perceived<br />

fatigue show two <strong>in</strong>dependant patterns. Delayed perceived fatigue data<br />

seem to more <strong>in</strong>fluenced by everyday life circumstances.<br />

dIscussIon<br />

The last improvement of the personal best happened some years before,<br />

while after this macro cycle it was 2.8 %. The caculated MITS of 2.01<br />

± 0.12 units seems to be fairly high when compared to results of 1.53<br />

± 0.06 units published by Mujika et al. (1996). The MITS-value of this<br />

case study <strong>in</strong>dicates a trend towards higher tra<strong>in</strong><strong>in</strong>g <strong>in</strong>tensity which was<br />

achieved predom<strong>in</strong>antly due to some new methods of dryl<strong>and</strong> tra<strong>in</strong><strong>in</strong>g.<br />

The work with the dryl<strong>and</strong>-tra<strong>in</strong><strong>in</strong>g equivalent approach led to new reflections<br />

about the <strong>in</strong>fluence of all activities of an athlete on the mental<br />

<strong>and</strong> physical fitness. Treat<strong>in</strong>g a dryl<strong>and</strong> tra<strong>in</strong><strong>in</strong>g equivalent as a summ<strong>and</strong><br />

of daily tra<strong>in</strong><strong>in</strong>g components seems noth<strong>in</strong>g particular; try<strong>in</strong>g to<br />

relate this component to tra<strong>in</strong><strong>in</strong>g volume is someth<strong>in</strong>g else. A bridge<br />

could be that the organism is not “count<strong>in</strong>g” meters to check the external<br />

stra<strong>in</strong> but is <strong>in</strong>ternally react<strong>in</strong>g to <strong>in</strong>tensity over time <strong>and</strong> the conversion<br />

of <strong>in</strong>tersity to volume is like (not similar) convert<strong>in</strong>g <strong>in</strong>tensity to power<br />

dem<strong>and</strong>.<br />

Expecially <strong>in</strong> swimm<strong>in</strong>g, the tra<strong>in</strong><strong>in</strong>g of fitness as such is <strong>in</strong>complete<br />

without shap<strong>in</strong>g the propell<strong>in</strong>g efficiency of each stroke cycle. Consequently<br />

the swimmer’s competence to adapt the breaststroke technique<br />

to the needs to swim faster was also <strong>in</strong>troduced <strong>in</strong>to the tra<strong>in</strong><strong>in</strong>g concept<br />

us<strong>in</strong>g the approach described by Ungerechts <strong>and</strong> Schack (1996). Elite<br />

swimmers can <strong>in</strong>crease their distance per stroke due to unsteady aspects<br />

of the flow around the cruis<strong>in</strong>g body (Ungerechts & Klauck, 1996),<br />

among others by decreas<strong>in</strong>g a swimmer’s active drag.<br />

The selection of the scale for perceived fatigue was <strong>in</strong>stalled after<br />

the co-workers discussed this issue thoroughly. The daily calculated <strong>in</strong>dividual<br />

delayed fatigue values were of great value to lower the risk of<br />

over tra<strong>in</strong><strong>in</strong>g. Especially the athlete appreciated the <strong>in</strong>dividualisation of<br />

the tra<strong>in</strong><strong>in</strong>g regime as a means to trigger adaptation. Recogniz<strong>in</strong>g that<br />

the recovery from fatigue while sleep<strong>in</strong>g can be expressed <strong>in</strong> terms of decreas<strong>in</strong>g<br />

perceived stress-factors was a challenge. The curves seem to be<br />

more <strong>in</strong>fluenced by everyday life circumstances. The coach <strong>and</strong> the athlete<br />

had to learn how to reason about the tra<strong>in</strong><strong>in</strong>g of a particular person<br />

which is always comb<strong>in</strong>ed with reason<strong>in</strong>g about <strong>in</strong>dividual (expected)<br />

properties, traits <strong>and</strong> personality. A unique route to improve success is<br />

not really known. The question of whether the value can be bettered by<br />

sophisticated methods, which was resolved by the fact that the adult<br />

swimmer can f<strong>in</strong>ally tell best what the needs will be, provided the person<br />

can rehearse, is still an open question.<br />

conclusIons<br />

The new approach <strong>in</strong>tensified the motivation of everybody tak<strong>in</strong>g part <strong>in</strong><br />

this cooperation. Swimm<strong>in</strong>g as a techno-motoric sport discipl<strong>in</strong>e with<br />

a strong psycho-physical endurance component is considered to be a<br />

304<br />

complex sports to deal with. Tra<strong>in</strong><strong>in</strong>g frames, -methods <strong>and</strong> –means<br />

should be elements of a systematic concerted <strong>in</strong>tervention which target<br />

on fitness, condition, effective strokes <strong>and</strong> stable mental processes.<br />

Monitor<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g, <strong>in</strong>clud<strong>in</strong>g the <strong>in</strong>dividually perceived stress levels<br />

is a modern approach dem<strong>and</strong><strong>in</strong>g close cooperation with the athletes<br />

because they know best their aims, <strong>in</strong>tentions or how to get <strong>in</strong>volved <strong>in</strong><br />

the external steer<strong>in</strong>g of his/her life (by coaches). Each athlete will react<br />

differently to a given tra<strong>in</strong><strong>in</strong>g load, based on <strong>in</strong>dividual biological factors<br />

<strong>and</strong> on everyday life circumstances. Successful coaches consider this<br />

when prescrib<strong>in</strong>g various tra<strong>in</strong><strong>in</strong>g loads. Although a bluepr<strong>in</strong>t tell<strong>in</strong>g<br />

how much is necessary <strong>and</strong> sufficient to ensure success is still miss<strong>in</strong>g,<br />

a better <strong>in</strong>teraction of humans based on certa<strong>in</strong> data will help <strong>and</strong> is<br />

highly recommended.<br />

reFerences<br />

Chartard, J.C. & Mujika, I. (1999). Tra<strong>in</strong><strong>in</strong>g load <strong>and</strong> performance<br />

<strong>in</strong> swimm<strong>in</strong>g. In: K.L. Kesk<strong>in</strong>en, P.V. Komi, A.P. Holl<strong>and</strong>er (eds.)<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII. Gummerus Pr<strong>in</strong>t<strong>in</strong>g,<br />

Jyväskylä, 429-434.<br />

Costill, DL, Kovaleski, J, Porter, D, Kirwan, J, Field<strong>in</strong>g, R & K<strong>in</strong>g, D.<br />

(1985) Energy expenditure dur<strong>in</strong>g front crawl swimm<strong>in</strong>g: predict<strong>in</strong>g<br />

success <strong>in</strong> middle-distance events. Int J Sports Med 6, 266-270<br />

Costill, D.L. (1999). Tra<strong>in</strong><strong>in</strong>g adaptation for optimal performance. In:<br />

K.L. Kesk<strong>in</strong>en, P.V. Komi, A.P. Holl<strong>and</strong>er (eds.) <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII. Gummerus Pr<strong>in</strong>t<strong>in</strong>g, Jyväskylä, 381-390.<br />

Holmer, I. (1983). Energetics <strong>and</strong> mencanical work <strong>in</strong> swimm<strong>in</strong>g. In:<br />

A.P. Holl<strong>and</strong>er, P. Huij<strong>in</strong>g <strong>and</strong> G. de Groot (eds.), <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g, Human K<strong>in</strong>etics Publishers, Champaign, IL,<br />

154-164.<br />

Mujika, I., Chatard, J-C., Busso, T., Geyssant, A., Barale, F. & Lacoste,<br />

L. (1995). Effects of tra<strong>in</strong><strong>in</strong>g on performance <strong>in</strong> competitive swimm<strong>in</strong>g.<br />

Can. J. Appl. Physiol. 20, 395-406.<br />

Mujika, I., Busso, T., Geyssant, A., Chatard, J-C., Barale, F. & Lacoste,<br />

L. (1996). tra<strong>in</strong><strong>in</strong>g content <strong>and</strong> its effects on performance <strong>in</strong> 100 <strong>and</strong><br />

200 m swimmers. J.P. Troup, A.P. Holl<strong>and</strong>er, D. Strass, S.W. Trappe,<br />

J.M. Cappaert, T.A. Trappe (Eds.) <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g VII. E & FN Spon, London: 201-207.<br />

Niessen, M. Hartmann, U., Schulz, H., Heck, H., Grabow, V. & Platen,<br />

P. (2007). Selektive Blutparameter im Tra<strong>in</strong><strong>in</strong>gsprozess von Langstreckenläufern.<br />

In: U. Hartmann, M Niessen, P. Spitzenpfeil (Hrsg.)<br />

Ausdauer und Ausdauertra<strong>in</strong><strong>in</strong>g. Köln: Sportverlag Strauss, 195.<br />

Schultz, W.W. & Webb, P. W. (2002). Power Requirements of Swimm<strong>in</strong>g:<br />

Do New Methods Resolve Old Questions? Integrative <strong>and</strong><br />

Comparative Biology. 42(5), 1018–1025.<br />

Ungerechts, B. E. & Klauck J. (2006). Consequences of non-stationary<br />

flow effects for functional attribution of swimm<strong>in</strong>g strokes. In: J.P.<br />

Vilas-Boas, F. Alves, A. Marques (eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g X. Portuguese Journal of Sport Sciences, Vol. 6, Suppl. 2,<br />

109-111.<br />

Ungerechts, B. E. & Schack, T. (2006). Mental representation of swimm<strong>in</strong>g<br />

strokes. In: J.P. Vilas-Boas, F. Alves, A. Marques (eds.), <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X. Portuguese Journal of Sport<br />

Sciences, Vol. 6,Suppl. 2, 346-348.<br />

Ulmer, H.-V. (1986). Perceived exertion as a part of a feedback system<br />

<strong>and</strong> its <strong>in</strong>teraction with tactical behaviour <strong>in</strong> endurance sports. In:<br />

Borg, G., Ottoson, D. (eds.): The perception of exertion <strong>in</strong> physical<br />

work. Wenner-Gren Int. Symp. Ser., vol 46, MacMillan Press LTD,<br />

Houndmills, Bas<strong>in</strong>gstoke, Hampshire, London:317-326.


Accelerometry as a Means of Quantify<strong>in</strong>g Tra<strong>in</strong><strong>in</strong>g<br />

Distance <strong>and</strong> Speed <strong>in</strong> Competitive Swimmers.<br />

Wright, B.V. , h<strong>in</strong>man, M.G. , stager, J.M.<br />

Counsilman Center for the Science of Swimm<strong>in</strong>g, Indiana University,<br />

Bloom<strong>in</strong>gton, IN, USA<br />

The purpose of this study was to exam<strong>in</strong>e the potential relationships between<br />

accelerometer output (AO) <strong>and</strong> swim distance (S dist ), <strong>and</strong> AO <strong>and</strong><br />

swim speed (S speed ). Fifty-three competitive swimmers (age: 17.7 ±3.13<br />

yrs.) were fitted with two accelerometers <strong>and</strong> completed two swim sets<br />

to develop prediction equations for swim bout distance (m) <strong>and</strong> swim<br />

bout speed (m·s -1 ). Significant correlations <strong>and</strong> regression equations<br />

were found for accelerometer output <strong>and</strong> swim bout distance (Correlation:<br />

r = 0.90, R 2 = 0.81, p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Pearson correlation coefficients exam<strong>in</strong><strong>in</strong>g the relationship between AO<br />

vs S dist (r =0.90, R 2 = 0.81, SEE= 59.4m, p


present data, other recent studies have similarly exam<strong>in</strong>ed competitive<br />

swim tra<strong>in</strong><strong>in</strong>g <strong>and</strong> report encourag<strong>in</strong>g data support<strong>in</strong>g the further use<br />

of accelerometers. For example, prelim<strong>in</strong>ary experiments conducted by<br />

the Counsilman Center for the Science of Swimm<strong>in</strong>g us<strong>in</strong>g the Actical<br />

activity monitor displayed data that are <strong>in</strong> support of the relationships<br />

between swim bout distance, swimm<strong>in</strong>g speed, <strong>and</strong> accelerometer output<br />

reported <strong>in</strong> the present study (Wright et al., 2007, <strong>and</strong> H<strong>in</strong>man et<br />

al., 2008). The current study more thoroughly explored the validity of<br />

predict<strong>in</strong>g swim bout distance <strong>and</strong> swimm<strong>in</strong>g speed from accelerometer<br />

output. Furthermore, the data from Wright et al. (2007) suggest that<br />

when a swimmer is <strong>in</strong>structed to swim fast, there is a larger contribution<br />

from kick<strong>in</strong>g that is evident from the subsequent greater leg accelerometer<br />

output. This appears to <strong>in</strong>dicate that <strong>in</strong> addition to swim speed<br />

<strong>and</strong> swim distance a swimmer’s relative effort from day to day or set to<br />

set, might be reflected <strong>in</strong> the comparative outputs of the appropriately<br />

placed accelerometers.<br />

Although, the f<strong>in</strong>d<strong>in</strong>gs from the current study support the use of accelerometers<br />

as a non-<strong>in</strong>vasive means to monitor a swimmer’s adherence<br />

to <strong>and</strong> effort <strong>in</strong> a competitive swim tra<strong>in</strong><strong>in</strong>g session, the application of a<br />

s<strong>in</strong>gle regression equation to predict swimm<strong>in</strong>g distance <strong>and</strong> speed for<br />

different types of swimm<strong>in</strong>g <strong>and</strong> or swimmers of different skill levels<br />

is limited. It is recommended, albeit more time consum<strong>in</strong>g, to create<br />

<strong>in</strong>dividual regression equations (e.g. for distance <strong>and</strong> speed) for each<br />

swimmer. This may provide stronger algorithms. In addition the use of<br />

an accelerometer with a shorter epoch length would also be ideal. This<br />

would produce a greater detailed set of data from which an experimenter<br />

or coach may exam<strong>in</strong>e tra<strong>in</strong><strong>in</strong>g sessions.<br />

In conclusion, this study displayed a significant relationship between<br />

swim bout distance, swimm<strong>in</strong>g speed, <strong>and</strong> accelerometer output (i.e. Actical<br />

activity monitor). The study also showed that accelerometers have<br />

the ability to accurately measure swim bout distance <strong>and</strong> mean swim<br />

bout speed. Future suggestions <strong>in</strong>clude the use of accelerometers dur<strong>in</strong>g<br />

actual competition, as well as, the development of computer software<br />

that will allow for the immediate display <strong>and</strong> <strong>in</strong>terpretation of accelerometer<br />

output upon the completion of a tra<strong>in</strong><strong>in</strong>g session.<br />

reFerences<br />

Banister, E.W. & Calvert, T.W. (1980). Plann<strong>in</strong>g for the future: Implications<br />

for long term tra<strong>in</strong><strong>in</strong>g. Can J Appl Sport Sci, 5, 170-176.<br />

H<strong>in</strong>man, M.G., Wright, B.V., Scofield, E.W. & Lundgren, E.A. (2008).<br />

Use of Accelerometers<br />

as a means of quantify<strong>in</strong>g swim tra<strong>in</strong><strong>in</strong>g load. Med Sci Sports Exerc,<br />

40, S382.<br />

Hopk<strong>in</strong>s, W. (1991). Quantification of tra<strong>in</strong><strong>in</strong>g <strong>in</strong> competitive sports.<br />

Sports Med, 12, 161-183.<br />

Ichikawa, H., Oghi, Y. & Miyaji, C. (1999). Analysis of stroke of the<br />

freestyle swimm<strong>in</strong>g us<strong>in</strong>g<br />

accelerometer.<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII, Gummerus<br />

Pr<strong>in</strong>t<strong>in</strong>g House, Jyväskylä, F<strong>in</strong>l<strong>and</strong>, 159-164.<br />

Johnston, J.D. & Stager, J.M. (2005). Estimate of swimm<strong>in</strong>g energy expenditure<br />

utiliz<strong>in</strong>g omnidirectional accelerometer <strong>and</strong> swim performance<br />

measures. Med Sci Sports Exerc, 37, 112.<br />

Mujika, I., Busso, T., Lacoste, L., Barale, F., Geyssant, A. & Chatard,<br />

J.C. (1996). Modeled responses to tra<strong>in</strong><strong>in</strong>g <strong>and</strong> taper <strong>in</strong> competitive<br />

swimmers. Med Sci Sports Exerc, 28, 251-258.<br />

Ohgi, Y., Ichikawa, H. & Miyaji, C. (2002). Microcomputer-based acceleration<br />

sensor device for swimm<strong>in</strong>g stroke monitor<strong>in</strong>g. Jpn Int J<br />

Mech Eng, 45, 960-966.<br />

Wright, B.V., Cornett, A.C., McKenzie, J.M., Johnston, J.D., Stager,<br />

J.M. (2007). Quantify<strong>in</strong>gtra<strong>in</strong><strong>in</strong>g load through the use of accelerometry<br />

<strong>in</strong> competitive swimmers. Med Sci Sports Exerc, 39, S115.<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

Critical Swimm<strong>in</strong>g Speed Obta<strong>in</strong>ed by the 200-400<br />

Meters Model <strong>in</strong> Young Swimmers<br />

Zacca, r. 1 , castro, F.A.s. 1<br />

1 Universidade Federal do Rio Gr<strong>and</strong>e do Sul (UFRGS), Brasil.<br />

The aim of the study was to compare the critical swimm<strong>in</strong>g speed<br />

(CSS) obta<strong>in</strong>ed by the 200-400m (CSS 10 ) vs 14 different comb<strong>in</strong>ations<br />

of CSS <strong>and</strong> vs 1500m velocity (V 1500 ) <strong>in</strong> 11 young spr<strong>in</strong>t swimmers<br />

(male) of national competitive level. CSS 1 (50-100m) was the comb<strong>in</strong>ation<br />

that most overestimated CSS 10 . The lowest error on the estimation<br />

of CSS was observed for the CSS 3 (50-400m) (-0.5%) <strong>and</strong> CSS 7 (100-<br />

400m) (0.8%). CSS 10 overestimated V 1500 by 3.5%. This might suggest<br />

studies to measure the level of agreement between CSS 10 vs the other<br />

comb<strong>in</strong>ations <strong>and</strong> between CSS 10 vs V 1500 to check whether this level<br />

of agreement will be ma<strong>in</strong>ta<strong>in</strong>ed until adulthood.<br />

Keywords: swimm<strong>in</strong>g, Performance, tra<strong>in</strong><strong>in</strong>g <strong>and</strong> test<strong>in</strong>g, critical<br />

swimm<strong>in</strong>g speed.<br />

IntroductIon<br />

The critical swimm<strong>in</strong>g speed (CSS) method has been proposed for predict<strong>in</strong>g<br />

swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g velocity because it is simple <strong>and</strong> can be applied<br />

with several swimmers at the same time dur<strong>in</strong>g the tra<strong>in</strong><strong>in</strong>g session.<br />

Furthermore, the CSS is an attractive tool to assess the evolution or that<br />

occurs with tra<strong>in</strong><strong>in</strong>g <strong>in</strong> a given period of time (VILAS-BOAS et al. 1997).<br />

CSS obta<strong>in</strong>ed from the model<strong>in</strong>g of the distance-time relationship us<strong>in</strong>g<br />

the two-parameter model is def<strong>in</strong>ed as the angular coefficient of the l<strong>in</strong>ear<br />

regression between the distance (x axis) <strong>and</strong> the time (y axis) of different<br />

swimm<strong>in</strong>g distance trials (Ettema, 1966). CSS represents the highest <strong>in</strong>tensity<br />

that is susta<strong>in</strong>able for a prolonged duration, without elicit<strong>in</strong>g maximal<br />

oxygen uptake (VO 2max ), i.e, the lower boundary of the severe <strong>in</strong>tensity<br />

doma<strong>in</strong> (Dekerle et al., 2008). CSS has been def<strong>in</strong>ed based on different<br />

sets of race distances (Dekerle et al., 2002; Wakayoshi et al., 1992b, 1992c,<br />

1993; Wrigth <strong>and</strong> Smith, 1994). However, previous research showed that<br />

different comb<strong>in</strong>ations of distance can result <strong>in</strong> different CSS (Greco et<br />

al., 2003) because of the “aerobic <strong>in</strong>ertia” (Wilkie 1980; V<strong>and</strong>ewalle et al.<br />

1989), related to the cardiorespiratory tun<strong>in</strong>g to the oxygen uptake which<br />

reaches its steady or maximal state. In addition, predict<strong>in</strong>g CSS from the<br />

200 <strong>and</strong> 400-m swimm<strong>in</strong>g performances were proposed as optimal for<br />

swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g (Wakayoshi et al., 1993; Dekerle et al., 2002) with a<br />

prediction of the “onset of blood lactate accumulation” (OBLA) of +3.3%<br />

(Wakayoshi et al., 1993) (Heck et al., 1985) <strong>and</strong> +3.2% higher when<br />

try<strong>in</strong>g to predict the velocity over a 30-m<strong>in</strong> test (Dekerle et al. 2002).<br />

Moreover, several studies have focused on the comparison between CSS<br />

obta<strong>in</strong>ed from the 200 <strong>and</strong> 400-m comb<strong>in</strong>ation (CSS 10 ) <strong>and</strong> other comb<strong>in</strong>ations<br />

of race distances to predict CSS <strong>in</strong> young swimmers. Regardless<br />

of the distances swum, the ability to calculate values of CSS obta<strong>in</strong>ed with<br />

performances <strong>in</strong> competition could make the CSS an even more attractive<br />

tool for coaches <strong>and</strong> swimmers. Hav<strong>in</strong>g access to <strong>in</strong>formation of possible<br />

differences between CSS 10 <strong>and</strong> other comb<strong>in</strong>ations for predict<strong>in</strong>g CSS<br />

seems important when for some reason the coach needs to calculate the<br />

CSS with other distances. Thus, coaches could make the necessary corrections<br />

to obta<strong>in</strong> CSS values of the comb<strong>in</strong>ation of 200-400m <strong>and</strong> use<br />

it <strong>in</strong> the tra<strong>in</strong><strong>in</strong>g prescription. The primary aim of the present study was<br />

to compare CSS us<strong>in</strong>g the 200 <strong>and</strong> 400-m race distance with another 14<br />

comb<strong>in</strong>ations of distances rang<strong>in</strong>g from 50 m to 1500-m <strong>in</strong> young swimmers.<br />

The secondary aim was to compare these CSS with the 1500-m<br />

best performance velocity (V 1500 ).<br />

Methods<br />

Participants: 11 young spr<strong>in</strong>t swimmers (male) of national competitive<br />

level (Age: 14.4 ± 0.5 years old; Body Mass: 60.6 ± 7kg; Height: 175 ±<br />

307


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

5cm; Arm Span: 182 ± 5cm; Competitive experience: 5 ± 1 years old)<br />

participated <strong>in</strong> the study. All swimmers tra<strong>in</strong>ed while perform<strong>in</strong>g the<br />

test<strong>in</strong>g (high volume; low to moderate <strong>in</strong>tensity level). They swam six<br />

to eight tra<strong>in</strong><strong>in</strong>g sessions per week (six to eight km per session). Prior<br />

to the commencement of the test<strong>in</strong>g, the person <strong>in</strong> charge of the swimmers<br />

signed <strong>in</strong>formed consents, the study be<strong>in</strong>g approved for the Ethics<br />

Committee of the University.<br />

Protocol: Maximal swimm<strong>in</strong>g trials (front crawl) were over 6 distances<br />

(50, 100, 200, 400, 800 <strong>and</strong> 1500-m) with<strong>in</strong> 16 days with a m<strong>in</strong>imum<br />

of 48 hours between each trial. The order of the trials was r<strong>and</strong>omized.<br />

A 50-m pool of controlled temperature (28 ± 0.5 ºC) was used. All trials<br />

were conducted at the same time of the day (8:00 am) with a prior<br />

warm up performed <strong>in</strong> free style at moderate <strong>in</strong>tensity for 2000-m. Each<br />

swimmer was <strong>in</strong>structed to perform as best as they could dur<strong>in</strong>g each<br />

trial. Performance times were measured by three experienced coaches<br />

who used a manual chronometer.<br />

Data analysis: The average performance time collected from each<br />

of the three measures were manually typed <strong>in</strong>to a spreadsheet for the<br />

estimative of the various CSS. CSS was computed for the follow<strong>in</strong>g<br />

comb<strong>in</strong>ations of distances: CSS 1 (50-100m), CSS 2 (50-200m), CSS 3<br />

(50-400m), CSS 4 (50-800m), CSS 5 (50-1500m), CSS 6 (100-200m),<br />

CSS 7 (100-400m), CSS 8 (100-800m), CSS 9 (100-1500m), CSS 10 (200-<br />

400m), CSS 11 (200-800m), CSS 12 (200-1500m), CSS 13 (400-800m),<br />

CSS 14 (400-1500m) <strong>and</strong> CSS 15 (800-1500m).<br />

Statistical analysis: To address the first aim of the study, different<br />

comb<strong>in</strong>ations for predict<strong>in</strong>g CSS were compared. Mean <strong>and</strong> st<strong>and</strong>ard<br />

deviation were selected to present the data after normality <strong>and</strong> sphericity<br />

analysis by the Shapiro Wilk <strong>and</strong> Mauchly tests, respectively. The<br />

t-test for pared sample was used for the comparison between CSS 10 vs<br />

all others 14 CSS comb<strong>in</strong>ations <strong>and</strong> between CSS 10 vs V 1500 . Significant<br />

results were selected when Type I error was rejected for a threshold<br />

level of 5%. SPSS software was employed for the aforementioned tests.<br />

The levels of agreement between the several predictions of CSS were<br />

analyzed us<strong>in</strong>g Bl<strong>and</strong> <strong>and</strong> Altman analysis (Bl<strong>and</strong> <strong>and</strong> Altman, 1986).<br />

The results were presented based on the differences between each CSS<br />

predictions (i.e. CSS 10 vs the all others 14 CSS comb<strong>in</strong>ations) <strong>and</strong> between<br />

CSS 10 <strong>and</strong> V 1500 .<br />

results<br />

Mean <strong>and</strong> st<strong>and</strong>ard deviation of performance time (s) <strong>in</strong> each distance<br />

are shown <strong>in</strong> Table 1. The results of comparisons between CSS 10 with<br />

the other predictions <strong>and</strong> with V 1500 are shown <strong>in</strong> Table 2.<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g Page 168<br />

Table 1: Mean <strong>and</strong> st<strong>and</strong>ard deviation of performance time (s) for each<br />

distance (50, 100, 200, 400, 800 <strong>and</strong> 1500-m).<br />

Table 1: Mean <strong>and</strong> st<strong>and</strong>ard deviation of performance time (s) for each distance (50,<br />

100, <strong>Biomechanics</strong> 200, 400, 800 <strong>and</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> 1500-m). <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong> / Chapter 4 Tra<strong>in</strong><strong>in</strong>g Page 168<br />

n 50 m 100 m 200 m 400 m 800 m 1500 m<br />

11 29.36 ± 1.67 65.64 ± 3.50 146.55 ± 7.57 305.09 ± 16.65 643.55 ± 36.75 1230.91 ± 88.58<br />

Table 2: Comparison between CSS10 with the other predictions <strong>and</strong> V1500 by the t test<br />

<strong>and</strong> the level of agreement expressed <strong>in</strong> absolute <strong>and</strong> percentage results.<br />

Comparison between CSS10<br />

(1.27 m·s<br />

308<br />

-1 Agreement (Bl<strong>and</strong> <strong>and</strong> Altman)<br />

T test<br />

Limits (95%)<br />

) <strong>and</strong> . . .<br />

Significance Bias<br />

- 1.96 SD + 1.96 SD<br />

CSS1 (50-100m) (1.39 m·s -1 ) 0.0004* -0.119 (-8.9%) -0.268(-19.3%) 0.028 (1.5%)<br />

-1<br />

CSS2 (50-200m) (1.28 m·s ) 0.5253 -0.016 (-1.4%) -0.181 (-14.6%) 0.148 (11.9%)<br />

CSS3 (50-400m) (1.27 m·s -1 ) 0.5928 -0.005 (-0.5%) -0.074 (-6.1%) 0.062 (5.1%)<br />

-1<br />

CSS4 (50-800m) (1.23 m·s ) 0.0410* 0.042 (3.3%) -0.075 (-6.2%) 0.159 (12.8%)<br />

-1<br />

CSS5 (50-1500m) (1.21 m·s ) 0.0229* 0.054 (4.4%) -0.077 (-6.3%) 0.186 (15.2%)<br />

CSS6 (100-200m) (1.24 m·s -1 ) 0.4356 0.026 (2.1%) -0.186 (-15.3%) 0.240 (19.4%)<br />

-1<br />

CSS7 (100-400m) (1.26 m·s ) 0.3389 0.010 (0.8%) -0.060 (-5.0%) 0.082 (6.6%)<br />

-1<br />

CSS8 (100-800m) (1.22 m·s ) 0.0200* 0.052 (4.1%) -0.070 (-5.8%) 0.175 (14.1%)<br />

CSS9 (100-1500m) (1.21 m·s -1 ) 0.0160* 0.059 (4.9%) -0.074 (-6.1%) 0.194 (15.9%)<br />

-1<br />

CSS11 (200-800m) (1.21 m·s ) 0.0096* 0.055 (4.5%) -0.057 (-4.8%) 0.169 (13.7%)<br />

-1<br />

CSS12 (200-1500m) (1.21 m·s ) 0.0114* 0.062 (5.1%) -0.068 (-5.6%) 0.193 (15.7%)<br />

CSS13 (400-800m) (1.19 m·s -1 ) 0.0095* 0.080 (6.5%) -0.083 (-7.0%) 0.244 (20.0%)<br />

-1<br />

CSS14 (400-1500m) (1.20 m·s ) 0.0117* 0.072 (5.9%) -0.080(-6.6%) 0.224 (18.5%)<br />

-1<br />

CSS15 (800-1500m) (1.20 m·s ) 0.0311* 0.065 (5.5%) -0.104 (-8.7%) 0.236 (197%)<br />

V1500 (1.22 m·s -1 ) 0.0605 0.040 (3.5%) -0.090 (-7.2%) 0.170 (14.2%)<br />

* = p < 0.05<br />

Compar<strong>in</strong>g the proposed comb<strong>in</strong>ations used <strong>in</strong> this study with CSS10, CSS1 showed the<br />

highest difference (p = 0.0004) <strong>and</strong> worst level of agreement (-0.119 m·s -1 ; -8.9%). The<br />

lowest error on the estimation of CSS was observed from CSS3 (-0.005 m·s -1 ; -0.5%)<br />

<strong>and</strong> CSS7 (0.010 m·s -1 Table 1: Mean <strong>and</strong> st<strong>and</strong>ard deviation of performance time (s) for each distance (50,<br />

100, 200, 400, 800 <strong>and</strong> 1500-m).<br />

Table n 2: 50 Comparison m 100 m between 200 m CSS10 400 with m the other 800 m predictions 1500 m <strong>and</strong><br />

11 29.36 ± 1.67 65.64 ± 3.50 146.55 ± 7.57 305.09 ± 16.65 643.55 ± 36.75 1230.91 ± 88.58<br />

V1500 by the t test <strong>and</strong> the level of agreement expressed <strong>in</strong> absolute <strong>and</strong><br />

percentage Table 2: Comparison results. between CSS10 with the other predictions <strong>and</strong> V1500 by the t test<br />

<strong>and</strong> the level of agreement expressed <strong>in</strong> absolute <strong>and</strong> percentage results.<br />

Comparison between CSS10 (1.27 m·s<br />

; 0.8%) both <strong>in</strong>clud<strong>in</strong>g the 400-m trial <strong>in</strong> their calculation.<br />

Furthermore, the limits of agreement were very similar (CSS3: -6.1 to 5.1%; CSS7: -5.0<br />

to 6.6%). CSS10 overestimated V1500 by +3.5%.<br />

DISCUSSION<br />

The method used to calculate CSS (two-parameter model) has many advantages as a)<br />

ease of application, b) analysis of large numbers of athletes can be carried out dur<strong>in</strong>g<br />

tra<strong>in</strong><strong>in</strong>g sessions without the use of expensive equipment or blood collection, <strong>and</strong> c)<br />

easy to assess the evolution or that occurs with tra<strong>in</strong><strong>in</strong>g <strong>in</strong> a given period of time. This<br />

-1 Agreement (Bl<strong>and</strong> <strong>and</strong> Altman)<br />

T test<br />

Limits (95%)<br />

) <strong>and</strong> . . .<br />

Significance Bias<br />

- 1.96 SD + 1.96 SD<br />

CSS1 (50-100m) (1.39 m·s -1 ) 0.0004* -0.119 (-8.9%) -0.268(-19.3%) 0.028 (1.5%)<br />

-1<br />

CSS2 (50-200m) (1.28 m·s ) 0.5253 -0.016 (-1.4%) -0.181 (-14.6%) 0.148 (11.9%)<br />

CSS3 (50-400m) (1.27 m·s -1 ) 0.5928 -0.005 (-0.5%) -0.074 (-6.1%) 0.062 (5.1%)<br />

-1<br />

CSS4 (50-800m) (1.23 m·s ) 0.0410* 0.042 (3.3%) -0.075 (-6.2%) 0.159 (12.8%)<br />

-1<br />

CSS5 (50-1500m) (1.21 m·s ) 0.0229* 0.054 (4.4%) -0.077 (-6.3%) 0.186 (15.2%)<br />

CSS6 (100-200m) (1.24 m·s -1 ) 0.4356 0.026 (2.1%) -0.186 (-15.3%) 0.240 (19.4%)<br />

-1<br />

CSS7 (100-400m) (1.26 m·s ) 0.3389 0.010 (0.8%) -0.060 (-5.0%) 0.082 (6.6%)<br />

-1<br />

CSS8 (100-800m) (1.22 m·s ) 0.0200* 0.052 (4.1%) -0.070 (-5.8%) 0.175 (14.1%)<br />

CSS9 (100-1500m) (1.21 m·s -1 ) 0.0160* 0.059 (4.9%) -0.074 (-6.1%) 0.194 (15.9%)<br />

-1<br />

CSS11 (200-800m) (1.21 m·s ) 0.0096* 0.055 (4.5%) -0.057 (-4.8%) 0.169 (13.7%)<br />

-1<br />

CSS12 (200-1500m) (1.21 m·s ) 0.0114* 0.062 (5.1%) -0.068 (-5.6%) 0.193 (15.7%)<br />

CSS13 (400-800m) (1.19 m·s -1 ) 0.0095* 0.080 (6.5%) -0.083 (-7.0%) 0.244 (20.0%)<br />

-1<br />

CSS14 (400-1500m) (1.20 m·s ) 0.0117* 0.072 (5.9%) -0.080(-6.6%) 0.224 (18.5%)<br />

-1<br />

CSS15 (800-1500m) (1.20 m·s ) 0.0311* 0.065 (5.5%) -0.104 (-8.7%) 0.236 (197%)<br />

V1500 (1.22 m·s -1 ) 0.0605 0.040 (3.5%) -0.090 (-7.2%) 0.170 (14.2%)<br />

* = p < 0.05<br />

Compar<strong>in</strong>g the proposed comb<strong>in</strong>ations used <strong>in</strong> this study with CSS10, CSS1 showed the<br />

highest difference (p = 0.0004) <strong>and</strong> worst level of agreement (-0.119 m·s -1 ; -8.9%). The<br />

lowest error on the estimation of CSS was observed from CSS3 (-0.005 m·s -1 ; -0.5%)<br />

<strong>and</strong> CSS7 (0.010 m·s -1 * = p < 0.05<br />

; 0.8%) both <strong>in</strong>clud<strong>in</strong>g the 400-m trial <strong>in</strong> their calculation.<br />

Furthermore, the limits of agreement were very similar (CSS3: -6.1 to 5.1%; CSS7: -5.0<br />

to 6.6%). CSS10 overestimated V1500 by +3.5%.<br />

DISCUSSION<br />

The method used to calculate CSS (two-parameter model) has many advantages as a)<br />

Compar<strong>in</strong>g the proposed comb<strong>in</strong>ations used <strong>in</strong> this study with CSS 10 ,<br />

CSS 1 showed the highest difference (p = 0.0004) <strong>and</strong> worst level of<br />

agreement (-0.119 m·s -1 ; -8.9%). The lowest error on the estimation of<br />

CSS was observed from CSS 3 (-0.005 m·s -1 ; -0.5%) <strong>and</strong> CSS 7 (0.010<br />

m·s -1 ; 0.8%) both <strong>in</strong>clud<strong>in</strong>g the 400-m trial <strong>in</strong> their calculation. Furthermore,<br />

the limits of agreement were very similar (CSS 3: -6.1 to 5.1%;<br />

CSS 7 : -5.0 to 6.6%). CSS 10 overestimated V 1500 by +3.5%.<br />

dIscussIon<br />

The method used to calculate CSS (two-parameter model) has many advantages<br />

as a) ease of application, b) analysis of large numbers of athletes<br />

can be carried out dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g sessions without the use of expensive<br />

equipment or blood collection, <strong>and</strong> c) easy to assess the evolution or that<br />

occurs with tra<strong>in</strong><strong>in</strong>g <strong>in</strong> a given period of time. This eases the test<strong>in</strong>g,<br />

especially for swimmer populations such as children <strong>and</strong> adolescents.<br />

Hav<strong>in</strong>g access to <strong>in</strong>formation of possible differences between CSS10 <strong>and</strong><br />

other comb<strong>in</strong>ations for predict<strong>in</strong>g CSS seems important when for some<br />

reason the coach needs to calculate the CSS with other distances.<br />

The first result of the present study was that the highest difference<br />

recorded <strong>in</strong> this study was that between CSS10 <strong>and</strong> CSS1 . However, a<br />

level of agreement is a more sensitive tool for test<strong>in</strong>g the accuracy of a<br />

method to predict a s<strong>in</strong>gle parameter. The substantial contribution of the<br />

anaerobic metabolism <strong>in</strong> the 50 <strong>and</strong> 100-m races (Gast<strong>in</strong>, 2001) could<br />

expla<strong>in</strong> this high difference between CSS10 <strong>and</strong> CSS1 (bias: -0.119 m·s- 1 ; -8.9%).<br />

The lowest error <strong>in</strong> the estimation of CSS10 was observed for CSS3 (-0.005 m·s-1 ; -0.5%) <strong>and</strong> CSS7 (0.010 m·s-1 ; 0.8%) both of them <strong>in</strong>clud<strong>in</strong>g<br />

the 400-m performance <strong>and</strong> one short distance (50 or 100-m) <strong>in</strong> the<br />

model<strong>in</strong>g. In addition, the limits of agreement were very similar (CSS3: -6.1 to 5.1%; CSS7 : -5.0 to 6.6%). Gast<strong>in</strong> (2001) used mathematical<br />

model<strong>in</strong>g techniques <strong>and</strong> suggested that performances lower than 75-s<br />

(under maximal <strong>in</strong>tensity) need more contribution of anaerobic than<br />

aerobic metabolism. However, there is a lower concentration of glycolytic<br />

enzymes <strong>and</strong> an <strong>in</strong>creased concentration of aerobic enzymes <strong>in</strong> adolescents<br />

compared with adults. Adolescents have a lower concentration<br />

of steroid hormones, which will <strong>in</strong>crease with the maturation process<br />

<strong>and</strong> therefore <strong>in</strong>crease muscle mass <strong>and</strong> anaerobic capacity (Dipla et al.,<br />

2009). Thus, probably the low anaerobic capacity of the swimmers is responsible<br />

for the similarity between CSS10 , CSS3 <strong>and</strong> CSS7 because the<br />

distances of 50 <strong>and</strong> 100-m do not seem to have <strong>in</strong>creased the value of<br />

CSS obta<strong>in</strong>ed by CSS3 <strong>and</strong> CSS7 . For females, it has been observed that<br />

muscle power reaches an earlier steady state, i.e soon after 14-15 years<br />

(Dipla et al., 2009). This might suggest studies to measure the level of<br />

agreement between CSS10 <strong>and</strong> the other comb<strong>in</strong>ations <strong>in</strong> young female<br />

<strong>and</strong> male swimmers (14-15 years), also to check whether this level of<br />

agreement will be ma<strong>in</strong>ta<strong>in</strong>ed until adulthood.<br />

Third, the results showed that the level of agreement between<br />

CSS10 <strong>and</strong> the comb<strong>in</strong>ations that use the distance of 800-m, 1500-m<br />

or both, can underestimate CSS10 <strong>in</strong> young swimmers. In our study,<br />

the underestimation of CSS10 was established between - 3.3 to 6.5%.<br />

The greater contribution of aerobic metabolism of the total energy required<br />

to travel distances of 800 <strong>and</strong> 1500-m (800-m: 643.55 ± 36.75<br />

s, 1500-m: 1230.91 ± 88.58 s) seems to have been the ma<strong>in</strong> reason for<br />

these f<strong>in</strong>d<strong>in</strong>gs (Gast<strong>in</strong>, 2001). In addition, although they are swimmers<br />

with a considerable level of experience, the application of extensive tests<br />

(800 <strong>and</strong> 1500-m) <strong>in</strong> young swimmers <strong>in</strong> the swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g situation<br />

rather than a competitive situation may dim<strong>in</strong>ish their motivation<br />

which would affect the performance of the test. Moreover, as they are<br />

spr<strong>in</strong>t swimmers, some of them probably did not have sufficient experience<br />

with longer events.<br />

F<strong>in</strong>ally, CSS10 (200-400m) was higher than V1500 (+3.5%) with performances<br />

over this distance rang<strong>in</strong>g from 19.5 to 22-m<strong>in</strong> (1231 ± 88 s)<br />

<strong>in</strong> young swimmers. This difference was similar to that found bewteen<br />

CSS10 <strong>and</strong> the speed of 30-m<strong>in</strong> test by Dekerle et al. (2002), which<br />

suggested a correction of - 3.2% to establish the swimm<strong>in</strong>g velocity over


a 30-m<strong>in</strong> test by the CSS 10 <strong>in</strong> adult male swimmers (18.6 ± 1.9 years).<br />

Studies also found that the speed of a 20-m<strong>in</strong> test <strong>in</strong> adolescents or<br />

a 2000-m test <strong>in</strong> adults was similar to the speed at Lactate threshold<br />

(Greco et al., 2003; Matsunami et al., 1999). However, further studies<br />

are needed to check whether or not it would be erroneous to use a<br />

s<strong>in</strong>gle correction factor to predict the velocity over a 30-m<strong>in</strong> test or V 1500<br />

through CSS 10 both <strong>in</strong> adolescence <strong>and</strong> adulthood, as these differences<br />

seem to vary dur<strong>in</strong>g the development of swimmers (Dipla et al., 2009).<br />

conclusIon<br />

Css 1 (50-100m) was the model that most overestimated css 10 (200-<br />

400m). The lowest error <strong>in</strong> the estimation of css 10 was observed with<br />

css 3 (-0.5%) <strong>and</strong> css 7 (0.8%). Css 10 overestimated v 1500 by +3.5%. Css 10<br />

(200-400 m) was higher than v 1500 (+3.5%) with performances over<br />

this distance rang<strong>in</strong>g from 19.5 to 22-m<strong>in</strong> (1231 ± 88 s) <strong>in</strong> young male<br />

swimmers. Hav<strong>in</strong>g access to <strong>in</strong>formation of possible differences between<br />

css 10 <strong>and</strong> other comb<strong>in</strong>ations for predict<strong>in</strong>g css seems important when<br />

for some reason the coach needs to calculate css with other distances. It<br />

might suggest studies to measure the level of agreement between css 10 vs<br />

the other comb<strong>in</strong>ations <strong>and</strong> between css 10 vs v 1500 to check whether this<br />

level of agreement will be ma<strong>in</strong>ta<strong>in</strong>ed until adulthood.<br />

reFerences<br />

Bishop, D., Jenk<strong>in</strong>s, D.G. & Howard, A. (1998). The critical power function<br />

is dependent on the duration of the predictive exercise tests chosen.<br />

Int J Sports Med 19, 125–129.<br />

Bl<strong>and</strong>, J.M. & Altman, D.G. (1986). Statistical methods for assess<strong>in</strong>g<br />

agreement between two methods of cl<strong>in</strong>ical measurement. Lancet 8,<br />

307-310.<br />

Dekerle, J., Vanhatalo, A. & Burnley M. (2008). Determ<strong>in</strong>ation of critical<br />

power from a s<strong>in</strong>gle test. Science & Sports 23(5), 231-8.<br />

Dekerle, J., Sidney, M., Hespel, J.M. & Pelayo, P. (2002). Validity <strong>and</strong><br />

reliability of critical speed, critical stroke rate <strong>and</strong> anaerobic capacity<br />

<strong>in</strong> relation to front crawl swimm<strong>in</strong>g performances. Int J Sports Med,<br />

23, 93-8.<br />

Dipla, K., Tsir<strong>in</strong>i, T., Zafeiridis, A., Manou, V., Dalamitros, A., Kellis, E.<br />

& Kellis, S. (2009). Fatigue resistence dur<strong>in</strong>g high-<strong>in</strong>tensity <strong>in</strong>termittent<br />

exercise from childhood to adulthood <strong>in</strong> males <strong>and</strong> females. Eur<br />

J Appl Physiol 106, 645-653.<br />

Ettema, J.H. (1966). Limits of human performance <strong>and</strong> energy production.<br />

Int Z Ang Physiol E<strong>in</strong>schl Arbeitphysiol. 22, 45-54.<br />

Gast<strong>in</strong>, P.B. (2001). Energy system <strong>in</strong>teraction <strong>and</strong> relative contribution<br />

dur<strong>in</strong>g maximal exercise. Sport Med 31 (10), 725 – 741.<br />

Greco, C.C., Denadai, B.S., Pellegr<strong>in</strong>otti, I.L., Freitas, A.D.B. & Gomide<br />

E. (2003). Anaerobic threshold <strong>and</strong> critical speed determ<strong>in</strong>ed with<br />

different distances <strong>in</strong> swimmers aged 10 to 15 years: relationship with<br />

the performance <strong>and</strong> blood lactate response dur<strong>in</strong>g endurance tests.<br />

Rev. Bras. Med. Esporte; vol. 9 nº 1 - jan/dez pg 02- 08.<br />

Heck, H., Mader, A. & Hess, G. (1985). Justification of the 4 mmol/L<br />

Lactate Threshold. Int J Sports Med 6, 117-30.<br />

Matsunami, M., Taguchi, M., Taimura, A., Suyama, M., Suga, M. &<br />

Shimonagata S., et al. (1999). Comparison of swimm<strong>in</strong>g speed <strong>and</strong><br />

exercise <strong>in</strong>tensity dur<strong>in</strong>g non-<strong>in</strong>vasive test <strong>and</strong> <strong>in</strong>vasive test <strong>in</strong> competitive<br />

swimm<strong>in</strong>g. In: Kesk<strong>in</strong>en K, Komi PV, Holl<strong>and</strong>er AP, editors.<br />

<strong>Biomechanics</strong> <strong>and</strong> medic<strong>in</strong>e <strong>in</strong> swimm<strong>in</strong>g VIII. Jyväskylä: Gummerus<br />

Pr<strong>in</strong>t<strong>in</strong>g; p. 245-8.<br />

V<strong>and</strong>ewalle, H., Kapitaniak. B., Grun. S., Raveneau. S. & Monod H.<br />

(1989). Comparison between a 30-s all-out test <strong>and</strong> a time-work test<br />

on a cycle ergometer. Eur J Appl Physiol Occup Physiol. 58(4), 375.<br />

Vilas-Boas J. & Lamares J.P. (1997). Velocidade Crítica: Critério para a<br />

Avaliação do Nadador e para a Def<strong>in</strong>ição de Objetivos. XX Congresso<br />

Técnico Científico da Associação Portuguesa dos Técnicos de Natação. 25 a<br />

27 Abril – Setúbal-Portugal.<br />

Wakayoshi, K., Yoshida, T., Udo, M., Harada, T., Morianti, T., Mutoh, Y.<br />

& Miyashita, M. (1993). Does critical swimm<strong>in</strong>g velocity represent<br />

chaPter4.tra<strong>in</strong><strong>in</strong>g<strong>and</strong>Performance<br />

exercise <strong>in</strong>tensity at maximal lactate steady state? Eur J Appl Physiol<br />

66, 90-5.<br />

Wakayoshi, K.,Yoshida, T., Kasai, T., Moritani, T., Mutoh, Y. &Miyashita<br />

M. (1992c). Validity of critical velocity as swimm<strong>in</strong>g fatigue<br />

threshold <strong>in</strong> the competitive swimmer. Annals of Physiological Anthropology<br />

11, 301-307.<br />

Wakayoshi, K., Yoshida, T., Udo, M., Kasai, T., Moritani, T., Mutoh,<br />

Y. Miyashita, M. (1992b). A simple method for determ<strong>in</strong><strong>in</strong>g critical<br />

speed as swimm<strong>in</strong>g fatigue threshold <strong>in</strong> competitive swimm<strong>in</strong>g.<br />

International Journal of Sports <strong>Medic<strong>in</strong>e</strong> 13, 367-371.<br />

Wilkie, D.R. (1980). Equations describ<strong>in</strong>g power <strong>in</strong>put by humans as<br />

a function of duration of exercise. In: Cerretelli P, Whipp B (eds)<br />

Exercise bioenergetics <strong>and</strong> gas exchange. Elsevier North Holl<strong>and</strong>s, Amsterdam,<br />

pp 75-80.<br />

Wright, B. & Smith, D.J. (1994). A protocol for the determ<strong>in</strong>ation of<br />

critical speed as an <strong>in</strong>dex of swimm<strong>in</strong>g endurance performance. In:<br />

Miyashita M, Mutoh Y, Richardson AB, eds. Med Sport Science 39,<br />

55-9.<br />

AcKnoWledGeMent<br />

The authors would like to thank Cristiano Klaser, Ricardo Peterson Silveira<br />

<strong>and</strong> Rodrigo B<strong>in</strong>i for their <strong>in</strong>volvement <strong>in</strong> this study.<br />

309


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi


Chapter 5. Education, Advice <strong>and</strong> Biofeedback


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

The Evolution of Swimm<strong>in</strong>g Science Research:<br />

Content analysis of the “<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g” Proceed<strong>in</strong>gs Books from 1971 to<br />

2006<br />

Barbosa, t.M. 1,4 , P<strong>in</strong>to, e. 1 , cruz, A.M. 1,4 , Mar<strong>in</strong>ho, d.A. 2,4 ,<br />

silva, A.J. 3,4 , reis, V.M. 3,4 , costa, M.J. 1,4 , Queirós ,t.M. 1<br />

1 Polytechnic Institute of Bragança, Bragança, Portugal<br />

2 University of Beira Interior, Covilhã, Portugal<br />

3 University of Trás-os-Montes <strong>and</strong> Alto Douro, Vila Real, Portugal<br />

4 Research Centre <strong>in</strong> Sports, Health <strong>and</strong> Human Development, Vila Real,<br />

Portugal<br />

The aim of this study was to analyze the evolution of swimm<strong>in</strong>g science<br />

research based on the content analysis of the “<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g” Proceed<strong>in</strong>gs book series from 1971 to 2006 (i.e.,<br />

a total of 622 full papers). There was an <strong>in</strong>creas<strong>in</strong>g number of papers<br />

published with<strong>in</strong> the period of time analyzed (rang<strong>in</strong>g from 23 papers<br />

<strong>in</strong> 1971 to 145 manuscripts <strong>in</strong> 2006). Compar<strong>in</strong>g the sub-categories<br />

related to “Aquatic activity” most research done was clearly on “competitive<br />

swimm<strong>in</strong>g”. In the last decade there is a slight but <strong>in</strong>creas<strong>in</strong>g<br />

<strong>in</strong>terest <strong>in</strong> “head-out aquatic exercises” Analyz<strong>in</strong>g the ma<strong>in</strong> “scientific<br />

area” of study, “<strong>Biomechanics</strong>” was the most often assessed area, followed<br />

by “Physiology”. S<strong>in</strong>ce 2003 an <strong>in</strong>creas<strong>in</strong>g trend <strong>in</strong> “<strong>in</strong>terdiscipl<strong>in</strong>ary assessment”<br />

manuscripts was verified.<br />

Key words: research, content analysis, aquatic activities, sport sciences,<br />

IntroductIon<br />

Swimm<strong>in</strong>g seems to be one of the most studied sports with<strong>in</strong> the Sport<br />

Sciences research community. More than a decade ago, Clarys (1996)<br />

conducted an analysis about swimm<strong>in</strong>g research. The author analyzed<br />

the content of 685 papers related to swimm<strong>in</strong>g based on 12 knowledge<br />

areas. The scientific area with most papers was “<strong>Biomechanics</strong>” represent<strong>in</strong>g<br />

20 % of total manuscripts, followed by “Physiology” represent<strong>in</strong>g<br />

18 %, “<strong>Medic<strong>in</strong>e</strong>/Cl<strong>in</strong>ics” represent<strong>in</strong>g 16 %, “Hydrodynamics” represent<strong>in</strong>g<br />

9 % <strong>and</strong> “Electromyography” represent<strong>in</strong>g 8 %.<br />

In these last 14 years there have been several developments <strong>in</strong> the<br />

aquatic activities doma<strong>in</strong>. It was hypothesized that the Clarys (1996)<br />

report could be updated. New highlights <strong>and</strong> technologic evolutions<br />

were <strong>in</strong>troduced <strong>in</strong> “swimm<strong>in</strong>g science”. Major updates happened <strong>in</strong><br />

the “state of the art” of swimm<strong>in</strong>g. In the past, “swimm<strong>in</strong>g research” was<br />

dedicated almost exclusively to competitive swimm<strong>in</strong>g. Nowadays there<br />

are several other aquatic activities be<strong>in</strong>g practiced <strong>in</strong> aquatic centres,<br />

such as head-out aquatic exercises, aquatic rehabilitation <strong>and</strong> <strong>in</strong>fant<br />

swimm<strong>in</strong>g. Swimm<strong>in</strong>g research is also dedicated to analyze <strong>and</strong> underst<strong>and</strong><br />

all these aquatic activities. Moreover, characteriz<strong>in</strong>g the evolution<br />

of research <strong>in</strong> these different aquatic activities has never been attempted.<br />

The “International Symposium on <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g” (BMS) is a scientific meet<strong>in</strong>g of aquatic activities researchers.<br />

The symposium happens every 4 years <strong>and</strong> is supported by<br />

UNESCO, among other organizations, gather<strong>in</strong>g all ma<strong>in</strong> research<br />

groups dedicated to these sports. The first meet<strong>in</strong>g was held <strong>in</strong> 1970<br />

(Brussels, Belgium) <strong>and</strong> titled “1st International Symposium of <strong>Biomechanics</strong><br />

<strong>in</strong> Swimm<strong>in</strong>g”. In 1986 (Bielefeld, Germany) the def<strong>in</strong>itive<br />

name of “International Symposium on <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g” was adopted. All ma<strong>in</strong> conferences, oral communications<br />

<strong>and</strong> poster presentations are collected, reviewed <strong>and</strong> published <strong>in</strong> a proceed<strong>in</strong>g<br />

book that nowadays is titled “<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g”. In this sense, BMS can be considered as representative of<br />

the work conducted by the ma<strong>in</strong> groups dedicated to aquatic activities<br />

research <strong>in</strong> a given historic time frame.<br />

312<br />

The aim of this study was to analyze the evolution of “swimm<strong>in</strong>g<br />

science” research <strong>in</strong> the last decades based on the BMS proceed<strong>in</strong>gs<br />

books.<br />

Methods<br />

The content of all the 622 papers published <strong>in</strong> the proceed<strong>in</strong>gs books<br />

of the “International Symposium on <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Swimm<strong>in</strong>g” series edited from 1971 to 2006 were analyzed. An observation<br />

grid for the manuscript analysis was developed. This <strong>in</strong>strument<br />

was composed by observational categories previously def<strong>in</strong>ed by the researchers.<br />

Two ma<strong>in</strong> categories were def<strong>in</strong>ed: (i) the “aquatic activity”<br />

studied <strong>in</strong> each paper analyzed <strong>and</strong>; (ii) the ma<strong>in</strong> “scientific area” applied<br />

for the assessment.<br />

The ma<strong>in</strong> category “aquatic activity” <strong>in</strong>cluded the follow<strong>in</strong>g subcategories:<br />

(i) Competitive swimm<strong>in</strong>g; (ii) Water Polo; (iii) Synchronized<br />

Swimm<strong>in</strong>g; (iv) Div<strong>in</strong>g; (v) Hydrotherapy; (vi) Infant Swim; (vii)<br />

Head-out Aquatic Exercises; (viii) F<strong>in</strong> Swimm<strong>in</strong>g <strong>and</strong>; (ix) others. The<br />

ma<strong>in</strong> “scientific area” <strong>in</strong>cluded the follow<strong>in</strong>g sub-categories (adapted<br />

from Clarys, 1996): (i) <strong>Biomechanics</strong>; (ii) Psychology; (ii) Sociology;<br />

(iii) Pedagogy/Teach<strong>in</strong>g; (iv) Biochemistry; (v) Physiology; (vi) Thermoregulation;<br />

(vii) Hydrodynamics; (viii) Electromyography; (ix) Anthropometry;<br />

(x) Equipment/Methodology; (xi) Cl<strong>in</strong>ical <strong>Medic<strong>in</strong>e</strong>/<br />

Traumatology <strong>and</strong>; (xii) Interdiscipl<strong>in</strong>ary assessment.<br />

For identification of each sub-category the follow<strong>in</strong>g steps were used:<br />

a) read the abstract, identify<strong>in</strong>g the aquatic activity studied, as well, the<br />

scientific area of assessment; b) whenever necessary or appropriate read<br />

the full paper; c) if the paper was not able to be <strong>in</strong>serted <strong>in</strong> any of the<br />

sub-categories def<strong>in</strong>ed for the ma<strong>in</strong> category “aquatic activity” it would be<br />

identified as “others” (e.g., life sav<strong>in</strong>g, recreational games, etc).<br />

The absolute frequency for the number of papers <strong>in</strong> each edition<br />

of the proceed<strong>in</strong>g s was registered. Relative frequency for each subcategory<br />

<strong>in</strong> a given edition <strong>and</strong> for full period of time between 1971 <strong>and</strong><br />

2006 was considered.<br />

results<br />

Figure 1 presents the number of papers published between 1971 <strong>and</strong><br />

2006. There was an <strong>in</strong>creas<strong>in</strong>g number of papers published with<strong>in</strong> the<br />

period of time analyzed (rang<strong>in</strong>g from 23 papers <strong>in</strong> 1971 to 145 manuscripts<br />

<strong>in</strong> 2006). The only exception to the <strong>in</strong>creas<strong>in</strong>g trend was the 1996<br />

edition.<br />

Figure 1. Evolution <strong>in</strong> the number of papers published between 1971<br />

<strong>and</strong> 2006.<br />

Figure 2 presents the partial contribution of each sub-category, for both<br />

ma<strong>in</strong> categories, <strong>in</strong> the period of time from 1971 to 2006 consider<strong>in</strong>g<br />

overall data. For the “scientific area”, ma<strong>in</strong> <strong>in</strong>terest was <strong>in</strong> “<strong>Biomechanics</strong>”<br />

(37.8 %), “Physiology” (17.20 %) <strong>and</strong> “Interdiscipl<strong>in</strong>ary assessment” (8.52<br />

%). Related to the “aquatic activity”, the sport with the greatest number<br />

of papers, by far, was “Competitive swimm<strong>in</strong>g” (87.46 %), followed by<br />

“Water polo” (3.22 %) <strong>and</strong> “Head-out aquatic activities (2.57 %).


Figure 3 presents the evolution <strong>in</strong> the relative frequency of each subcategory<br />

with<strong>in</strong> the 1971-2006 time frame. About the “scientific area”<br />

it is possible to verify that at any given moment there is a major <strong>in</strong>terest<br />

about one or a couple of specific issues, besides “<strong>Biomechanics</strong>” <strong>and</strong><br />

“Physiology”. For example, <strong>in</strong> 1983 there were several papers published<br />

about “Hydrodynamics”, <strong>in</strong> 1988 “Biochemistry”, <strong>in</strong> 1992 “Anthropometry”<br />

<strong>and</strong> <strong>in</strong> 2006 “Interdiscipl<strong>in</strong>ary assessment”. For the “aquatic activity”<br />

“Competitive swimm<strong>in</strong>g” was always on top. However, start<strong>in</strong>g <strong>in</strong><br />

1999 there was an <strong>in</strong>creas<strong>in</strong>g <strong>in</strong>terest for “Head-out aquatic exercises”<br />

<strong>and</strong> “F<strong>in</strong> swimm<strong>in</strong>g”.<br />

Figure 2. Partial contribution of each sub-category for “swimm<strong>in</strong>g science”<br />

<strong>in</strong> the period of time from 1971 to 2006.<br />

Figure 3. Evolution of sub-categories <strong>in</strong> each proceed<strong>in</strong>g book edition<br />

between 1971 <strong>and</strong> 2006.<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

dIscussIon<br />

There was an <strong>in</strong>creas<strong>in</strong>g number of papers published with<strong>in</strong> the period<br />

of time analyzed (rang<strong>in</strong>g from 23 papers <strong>in</strong> 1971 to 145 manuscripts<br />

<strong>in</strong> 2006). So, “swimm<strong>in</strong>g science” seems to be <strong>in</strong>creas<strong>in</strong>g s<strong>in</strong>ce 1971, as<br />

the number of research groups focused <strong>in</strong> this sport is <strong>in</strong>creas<strong>in</strong>g, as well<br />

as, the number of research projects developed by each group. The 1996<br />

book was the only one that did not present a greater number of papers<br />

<strong>in</strong> comparison to the previous edition. From the 80 studies presented<br />

at the VII th Symposium <strong>in</strong> <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g,<br />

only 36 were selected to be published. This means that from the 1992<br />

edition (with 64 papers published/presented) to the 1996 edition there<br />

was actually an <strong>in</strong>crease <strong>in</strong> the number of studies presented.<br />

Compar<strong>in</strong>g the sub-categories related to “Aquatic activity” the one<br />

with most research conducted was clearly “Competitive swimm<strong>in</strong>g”<br />

(rang<strong>in</strong>g from 78.8 % <strong>in</strong> 1971 to 100 % <strong>in</strong> 1996). In the last decade there<br />

is a slight but <strong>in</strong>creas<strong>in</strong>g <strong>in</strong>terest <strong>in</strong> “Head-out aquatic exercises” (e.g.,<br />

the second most studied aquatic activity <strong>in</strong> 2006 with 6.9 %). Aquatic<br />

activity was for a long time synonymous with swimm<strong>in</strong>g. Added to this,<br />

“Water polo” was also specially under the BMS scope, as is verified by<br />

the name of the 1971 proceed<strong>in</strong>g book: “First International Symposium<br />

on <strong>Biomechanics</strong> <strong>in</strong> Swimm<strong>in</strong>g, Water Polo <strong>and</strong> Div<strong>in</strong>g”. Nowadays<br />

“Head-out aquatic exercises” are gather<strong>in</strong>g a large part of the persons<br />

practic<strong>in</strong>g physical activity <strong>in</strong> aquatic centres. Indeed, these facilities<br />

provide services that are complementary to “traditional” competitive<br />

sports, such as “Head-out aquatic activities”. This is related to the <strong>in</strong>creas<strong>in</strong>g<br />

importance of aquatic activity for health. Start<strong>in</strong>g <strong>in</strong> 1999 there<br />

was also an <strong>in</strong>creas<strong>in</strong>g <strong>in</strong>terest <strong>in</strong> “F<strong>in</strong> swimm<strong>in</strong>g”. “F<strong>in</strong> swimm<strong>in</strong>g” now<br />

has a more consistent position among the aquatic competitive sports.<br />

“F<strong>in</strong> swimm<strong>in</strong>g” has competitions at all levels, <strong>in</strong>clud<strong>in</strong>g <strong>in</strong>ternational<br />

<strong>and</strong> media attention is <strong>in</strong>creas<strong>in</strong>g <strong>in</strong> some countries.<br />

Analyz<strong>in</strong>g the ma<strong>in</strong> “scientific area” of study, “<strong>Biomechanics</strong>” was the<br />

most common area (rang<strong>in</strong>g from 27.3 % <strong>in</strong> 1988 to 60 % <strong>in</strong> 1979), followed<br />

by “Physiology”. As “<strong>Biomechanics</strong>” <strong>and</strong> “Physiology” were with<strong>in</strong><br />

the orig<strong>in</strong>s of this scientific meet<strong>in</strong>g, it is logical that they are the largest<br />

sub-categories. It is consensual that biomechanical <strong>and</strong> physiological<br />

profiles of a swimmer are determ<strong>in</strong>ant factors for his/her performance<br />

enhancement. S<strong>in</strong>ce 2003 an <strong>in</strong>creas<strong>in</strong>g trend <strong>in</strong> “Interdiscipl<strong>in</strong>ary assessment”<br />

manuscripts is verified. There is now a trend to underst<strong>and</strong> not only<br />

how each scientific area determ<strong>in</strong>es performance, but also how they <strong>in</strong>terplay.<br />

At certa<strong>in</strong> periods of the history of BMS the major area of <strong>in</strong>terest <strong>in</strong><br />

addition to “<strong>Biomechanics</strong>” <strong>and</strong> “Physiology” (e.g., <strong>in</strong> 1983 the “Hydrodynamics”,<br />

<strong>in</strong> 1988 the “Biochemistry”, <strong>in</strong> 1992 the “Anthropometry” <strong>and</strong><br />

<strong>in</strong> 2006 the “Interdiscipl<strong>in</strong>ary assessment”). It seems there are some topics<br />

that are deeply explored <strong>in</strong> a given moment by several research groups.<br />

conclusIon<br />

As a conclusion, there is a significant <strong>in</strong>crease <strong>in</strong> scientific production regard<strong>in</strong>g<br />

aquatic activities throughout the 1971-2006 period. Concern<strong>in</strong>g<br />

the scientific area the ma<strong>in</strong> <strong>in</strong>terests are related to “<strong>Biomechanics</strong>”<br />

<strong>and</strong> “Physiology”. Recently there is a trend <strong>in</strong> “Interdiscipl<strong>in</strong>ary assessment”.<br />

“Competitive swimm<strong>in</strong>g” is the ma<strong>in</strong> aquatic activity studied.<br />

In the last proceed<strong>in</strong>gs, the tendency for a higher <strong>in</strong>terest <strong>in</strong> “Head-out<br />

aquatic activities” was verified.<br />

reFerences<br />

Clarys, J.P. (1996). The historical perspective of swimm<strong>in</strong>g science.<br />

Foreword to the <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VII. In:<br />

Troup J.P., Holl<strong>and</strong>er A.P., Strasse D., Trappe S.W., Cappaert J.M.,<br />

Trappe T.A. (eds), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VII (pp<br />

xi-xxxiv). London: E & FN Spon.<br />

AcKnoWledGMents<br />

Ana M. Cruz would like to acknowledge the Portuguese Science <strong>and</strong><br />

Technology Foundation (Research Integration Grant BII - CIDESD/<br />

UTAD).<br />

313


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Quantitative Data Supplements Qualitative<br />

Evaluations of Butterfly Swimm<strong>in</strong>g<br />

Becker, t.J. 1 , havriluk, r. 2<br />

1 Everett Pacific Industrial Rehabilitation, Seattle, USA<br />

2 Swimm<strong>in</strong>g Technology Research, Tallahassee, USA<br />

As mechanical advantage <strong>in</strong>creases with both shoulder extension <strong>and</strong><br />

elbow flexion dur<strong>in</strong>g the beg<strong>in</strong>n<strong>in</strong>g of the butterfly pull, it was hypothesized<br />

that h<strong>and</strong> force would significantly <strong>in</strong>crease with two events: 1)<br />

when the h<strong>and</strong>s first submerge below the level of the shoulders <strong>and</strong><br />

2) when elbow flexion beg<strong>in</strong>s. Female swimmers (n = 23) from three<br />

university teams were tested with Aquanex+Video, swimm<strong>in</strong>g butterfly<br />

over a 20 m course. As hypothesized, there was a significant (p


<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong><br />

Chapter 5 Education, Advice <strong>and</strong> Biofeedback<br />

Elbow Flexion Beg<strong>in</strong>s 36.4±15.6 51.0±13.5 1.00


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

the completion of the entry phase (Figure 5). While these adjustments<br />

are primarily designed to avoid shoulder <strong>in</strong>jury <strong>and</strong> <strong>in</strong>crease average<br />

h<strong>and</strong> force, stroke rate will also <strong>in</strong>crease. Once the entry is complete,<br />

elbow flexion can immediately beg<strong>in</strong>.<br />

The lack of significant <strong>in</strong>crease <strong>in</strong> force for two of the key events<br />

can be expla<strong>in</strong>ed. The angle at the elbow was already 90° when the h<strong>and</strong>s<br />

became medial to the elbows, so no force <strong>in</strong>crease due to mechanical<br />

<strong>Biomechanics</strong> advantage <strong>and</strong> could <strong>Medic<strong>in</strong>e</strong> be expected. <strong>in</strong> Swimm<strong>in</strong>g When <strong>XI</strong> the h<strong>and</strong>s passed perpendicularly<br />

Chapter below 5 Education, the shoulders, Advice any <strong>and</strong> potential Biofeedback <strong>in</strong>crease <strong>in</strong> mechanical advantage is<br />

tempered by a slowdown <strong>in</strong> h<strong>and</strong> speed due to the change <strong>in</strong> musculature<br />

from pull<strong>in</strong>g to push<strong>in</strong>g (Richardson, 1986).<br />

Figure 5. Butterfly arm entry that m<strong>in</strong>imizes shoulder stress <strong>and</strong> maximizes mechanical<br />

advantage. Figure 5. Butterfly arm entry that m<strong>in</strong>imizes shoulder stress <strong>and</strong> maximizes<br />

mechanical advantage.<br />

Logistics often make it difficult for a coach to collect quantitative data on technique<br />

dur<strong>in</strong>g Logistics a tra<strong>in</strong><strong>in</strong>g often session. make it Qualitative difficult for observations a coach to to collect determ<strong>in</strong>e quantitative when the data h<strong>and</strong>s<br />

submerge below the level of the shoulders <strong>and</strong> when elbow flexion beg<strong>in</strong>s, however, are<br />

entirely on technique possible. Track<strong>in</strong>g dur<strong>in</strong>g a these tra<strong>in</strong><strong>in</strong>g two events session. is Qualitative critical to m<strong>in</strong>imize observations the time to de- that the<br />

arms term<strong>in</strong>e are <strong>in</strong> a position when the likely h<strong>and</strong>s to stress submerge the shoulders below the <strong>and</strong> level maximize of the the shoulders time that <strong>and</strong> the arms<br />

are <strong>in</strong> when a mechanically elbow flexion advantageous beg<strong>in</strong>s, however, position are for force entirely generation. possible. Track<strong>in</strong>g these<br />

two events is critical to m<strong>in</strong>imize the time that the arms are <strong>in</strong> a position<br />

CONCLUSION<br />

Based likely on the to quantitative stress the shoulders results, coaches <strong>and</strong> maximize can qualitatively the time evaluate that the swimmers arms are to <strong>in</strong> ensure<br />

they a elim<strong>in</strong>ate mechanically the wasted advantageous time that their position h<strong>and</strong>s for are force above generation. the shoulders at the beg<strong>in</strong>n<strong>in</strong>g<br />

of the butterfly pull by adjust<strong>in</strong>g the entry angle. A downward entry angle will result <strong>in</strong><br />

a stronger conclusIon<br />

arm position, a faster stroke rate, <strong>and</strong> less shoulder stress. Coaches can also<br />

encourage swimmers to beg<strong>in</strong> elbow flexion as soon as the entry is complete. In<br />

addition Based to improv<strong>in</strong>g on the quantitative performance, results, these coaches technique can adjustments qualitatively will evaluate be helpful <strong>in</strong><br />

reduc<strong>in</strong>g swimmers the onset to of ensure shoulder they <strong>in</strong>jury. elim<strong>in</strong>ate the wasted time that their h<strong>and</strong>s are<br />

above the shoulders at the beg<strong>in</strong>n<strong>in</strong>g of the butterfly pull by adjust<strong>in</strong>g<br />

REFERENCES the entry angle. A downward entry angle will result <strong>in</strong> a stronger arm<br />

Becker, T.J. (1986). The athletic tra<strong>in</strong>er <strong>in</strong> swimm<strong>in</strong>g. Cl<strong>in</strong>ics <strong>in</strong> Sports <strong>Medic<strong>in</strong>e</strong>. 5(1),<br />

10. position, a faster stroke rate, <strong>and</strong> less shoulder stress. Coaches can also<br />

Becker, encourage T. & Havriluk, swimmers R. (2006). to beg<strong>in</strong> Bilateral elbow <strong>and</strong> flexion anterior-posterior as soon as the muscular entry is imbalances com-<br />

<strong>in</strong> plete. swimmers. In addition In J. P. to Vilas-Boas, improv<strong>in</strong>g F. performance, Alves, A. Marques these (Eds.), technique <strong>Biomechanics</strong> adjust- <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> ments will <strong>in</strong> be Swimm<strong>in</strong>g helpful <strong>in</strong> X. reduc<strong>in</strong>g Portuguese the Journal onset of Sport shoulder Sciences, <strong>in</strong>jury. 6(Suppl. 2), 327-<br />

328.<br />

Havriluk, R. (2003). Performance level differences <strong>in</strong> swimm<strong>in</strong>g drag coefficient. Paper<br />

presented reFerences at the VIIth IOC Olympic World Congress on Sport Sciences, Athens.<br />

Becker, T.J. (1986). The athletic tra<strong>in</strong>er <strong>in</strong> swimm<strong>in</strong>g. Cl<strong>in</strong>ics <strong>in</strong> Sports<br />

<strong>Medic<strong>in</strong>e</strong>. 5(1), 10.<br />

Becker, T. & Havriluk, R. (2006). Bilateral <strong>and</strong> anterior-posterior<br />

muscular imbalances <strong>in</strong> swimmers. In J. P. Vilas-Boas, F. Alves, A.<br />

Marques (Eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X. Portuguese<br />

Journal of Sport Sciences, 6(Suppl. 2), 327-328.<br />

Havriluk, R. (2003). Performance level differences <strong>in</strong> swimm<strong>in</strong>g drag coefficient.<br />

Paper presented at the VIIth IOC Olympic World Congress<br />

on Sport Sciences, Athens.<br />

Havriluk, R. (2004). H<strong>and</strong> force <strong>and</strong> swimm<strong>in</strong>g velocity. Paper presented<br />

at the XVth FINA World Sports <strong>Medic<strong>in</strong>e</strong> Congress, Indianapolis,<br />

IN.<br />

Havriluk, R. (2006a). Analyz<strong>in</strong>g h<strong>and</strong> force <strong>in</strong> swimm<strong>in</strong>g: Three typical<br />

limit<strong>in</strong>g factors. American Swimm<strong>in</strong>g Magaz<strong>in</strong>e, 2006(3), 14-18.<br />

Havriluk, R. (2006b). Magnitude of the effect of an <strong>in</strong>structional <strong>in</strong>tervention<br />

on swimm<strong>in</strong>g technique <strong>and</strong> performance. In J. P. Vilas-Boas,<br />

316<br />

F. Alves, A. Marques (Eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g<br />

X. Portuguese Journal of Sport Sciences, 6(Suppl. 2), 218-220.<br />

Havriluk, R. (2010). Performance level differences <strong>in</strong> swimm<strong>in</strong>g: Relative<br />

contributions of strength <strong>and</strong> technique. In Kjendlie, Stallman &<br />

Cabri. <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong>, <strong>in</strong> press.<br />

Richardson, A.B. (1986). The biomechanics of swimm<strong>in</strong>g: The shoulder<br />

<strong>and</strong> knee. In J.V. Ciullo (Ed.), Cl<strong>in</strong>ics <strong>in</strong> Sports <strong>Medic<strong>in</strong>e</strong> (pp. 103-<br />

14 114). Philadelphia: W.B. Saunders.


The Effect of Restrict<strong>in</strong>g the Visual Perceptual Task<br />

<strong>in</strong> the Temporal Organization of Crawl Swimm<strong>in</strong>g:<br />

Surface Characteristics<br />

Brito, c.A.F. 1 , Belvis, W.c. 2 , oliveira, M. 2<br />

1 Municipal University of São Caetano do Sul (USCS), São Caetano do Sul,<br />

Brazil<br />

2 Competitive Team DETUR, São Caetano do Sul, Brazil<br />

The objective of this study was to observe how disturb<strong>in</strong>g swimm<strong>in</strong>g<br />

skill execution can <strong>in</strong>fluence the superficial parameters of front crawl.<br />

There was mixed r<strong>and</strong>om-systematic sampl<strong>in</strong>g among 5% of high-ability<br />

swimmers from São Caetano do Sul, enrolled with DETUR <strong>in</strong> 2008<br />

(n=106). Disturbance was carried out by light shone onto the ret<strong>in</strong>a,<br />

form<strong>in</strong>g a configuration accord<strong>in</strong>g to the degree of complexity. The subjects<br />

swam at a natural rhythm. Data were analyzed us<strong>in</strong>g Mauchly’s<br />

Test of Sphericity <strong>and</strong> repeated measures ANOVA (Contrast). Probability<br />

was 5% (p


• Without restriction;<br />

• Bl<strong>in</strong>ded, lower field;<br />

• Bl<strong>in</strong>ded, upper field;<br />

• Completely bl<strong>in</strong>dfolded on the dom<strong>in</strong>ant side, but breath<strong>in</strong>g on the opposite side;<br />

<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

• Bl<strong>in</strong>dfolded, but keep<strong>in</strong>g a small open<strong>in</strong>g (foramen) – with convergence<br />

• Bl<strong>in</strong>dfolded, but keep<strong>in</strong>g a small open<strong>in</strong>g (foramen) – with divergence<br />

For statistical analysis, parametric statistics was used, after determ<strong>in</strong><strong>in</strong>g normality by<br />

the Kolmogorov-Smirnov test. Data were analyzed by Mauchly's Test of Sphericity <strong>and</strong><br />

for ANOVA time, was when used compared for repeated to without measures restriction (Contrast). If (21.68±2.69; the <strong>in</strong>teraction 21.51±2.5; effect was<br />

significant, the effect of each ma<strong>in</strong> factor was analyzed by contrasts with<strong>in</strong> of the levels<br />

22.73±3.31 s vs. 20.33±1.92 s, respectively) <strong>and</strong> lower values for speed,<br />

of the other factor. Data were analyzed by us<strong>in</strong>g the program SPSS (version 13.0), <strong>and</strong><br />

P values≤0.05 were considered as significant.<br />

when compared to without restriction (1.17±0.15; 1.18±0.14; 1.12±0.15<br />

m·s-1 vs. 1.24±0.12m·s-1 , respectively, p


Analyses of Instruction for Breath Control While<br />

Swimm<strong>in</strong>g the Breaststroke<br />

hara, h. 1 , Yoshioka, A. 2 , Matsumoto, n. 2 , nose, Y. 2 , Watanabe,<br />

r. 3 , shibata, Y. 4 , onodera, s. 2<br />

1 Kokugaku<strong>in</strong> University, Faculty of Human Development, Yokohama, Japan<br />

2 Kawasaki University of Medical Welfare, Kurashiki, Okayama, Japan<br />

3 Atomi University, Faculty of Literature, Saitama, Japan<br />

4 Tokyo Gakugei University, Department of Sports & Health Science, Tokyo,<br />

Japan<br />

The purpose of this research was to clarify the important factors prevent<strong>in</strong>g<br />

swimm<strong>in</strong>g apnea. We conducted the experiment with seven subjects<br />

us<strong>in</strong>g four pressure transducers simultaneously. These were connected to<br />

the control unit <strong>and</strong> the data were analyzed to detect pressure changes<br />

with the face <strong>in</strong> three different positions. We verified that tra<strong>in</strong>ed swimmers<br />

vary the amount of air blown out of the nose <strong>and</strong> mouth <strong>in</strong>dependently.<br />

There was an <strong>in</strong>terval between exhal<strong>in</strong>g from the nose to exhal<strong>in</strong>g<br />

from the mouth. In the case of <strong>in</strong>struction for beg<strong>in</strong>ners, <strong>in</strong> order to<br />

prevent swimm<strong>in</strong>g apnea it is effective if the <strong>in</strong>structor has the learner<br />

pronounce “Mnn” with the nose, then once that is completed, pronounce<br />

“Pha” or “Pa” from the mouth to blow out.<br />

Key words: swimm<strong>in</strong>g apnea, <strong>in</strong>halation, nasal pressure, pronounc<strong>in</strong>g,<br />

oral pressure<br />

IntroductIon<br />

One of the difficulties while develop<strong>in</strong>g swimm<strong>in</strong>g technique is how<br />

to control breath<strong>in</strong>g. Breath control is important for the acquisition of<br />

swimm<strong>in</strong>g skills such as stroke movement of arms <strong>and</strong> legs, <strong>and</strong> swimm<strong>in</strong>g<br />

faster <strong>in</strong> the various swimm<strong>in</strong>g strokes.<br />

However, it is not clear what the trigger for <strong>in</strong>halation is while<br />

swimm<strong>in</strong>g. In the exhalation phase, water pressure helps exhalation.<br />

Otherwise, <strong>in</strong>halation is more arduous than on l<strong>and</strong> because water pressure<br />

works to resist the enlarg<strong>in</strong>g of chest volume. Even tra<strong>in</strong>ed swimmers<br />

occasionally take <strong>in</strong> water dur<strong>in</strong>g <strong>in</strong>halation while swimm<strong>in</strong>g. Why<br />

are these k<strong>in</strong>ds of mistakes occurr<strong>in</strong>g?<br />

It is the purpose of this study to clarify the important factors prevent<strong>in</strong>g<br />

swimm<strong>in</strong>g apnea, or the un<strong>in</strong>tentional water-blockage of the<br />

airways.<br />

Methods<br />

The design of this experiment was approved by the Department of General<br />

Plann<strong>in</strong>g, Research Cooperation Section of Kokugaku<strong>in</strong> University.<br />

We expla<strong>in</strong>ed the purpose <strong>and</strong> methods of this study to the subjects<br />

<strong>in</strong> verbal <strong>and</strong> written form, <strong>and</strong> <strong>in</strong>formed consent was obta<strong>in</strong>ed from<br />

all. The seven subjects who voluntarily participated <strong>in</strong> this study were<br />

healthy university students; four students were tra<strong>in</strong>ed <strong>in</strong> swimm<strong>in</strong>g but<br />

three were not skilled swimmers. The only female subject was a tra<strong>in</strong>ed<br />

swimmer <strong>and</strong> other six students were male. We measured nasal cavity<br />

<strong>and</strong> oral cavity pressure while simulat<strong>in</strong>g the breaststroke motion,<br />

us<strong>in</strong>g four pressure transducers (SPC-464; Miller Instruments) simultaneously.<br />

These were connected to the control unit (TCB-500; Miller<br />

Instruments) by cables (TEC-10D; Miller Instruments). The equipment<br />

had been tested <strong>and</strong> verified <strong>in</strong> earlier work (3). One transducer<br />

was placed just beside the nose to measure water depth pressure at the<br />

nostril level (Channel: 1). The second was <strong>in</strong>side the nasal passage for<br />

measur<strong>in</strong>g nasal cavity pressure (Ch: 2). The third was placed on the<br />

cheek at the level of the mouth to measure water depth pressure at this<br />

level (Ch: 3). The fourth was placed <strong>in</strong> the mouth for measur<strong>in</strong>g oral<br />

cavity pressure (Ch: 4). Data were recorded on LogWorx (Distributed<br />

Design Corporation) program with the Recorder (EFA400; Distributed<br />

Design Corporation).<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

The data were analyzed to detect the pressure changes <strong>in</strong> three<br />

positions of the face. Position 1: Nose above the water surface but<br />

the mouth was <strong>in</strong> the water. Position 2: Nose <strong>and</strong> a mouth were both<br />

immersed <strong>in</strong> water. Position 3: Face was ris<strong>in</strong>g up <strong>and</strong> immers<strong>in</strong>g down<br />

<strong>in</strong>to water, simulat<strong>in</strong>g swimm<strong>in</strong>g the breaststroke.<br />

results<br />

Position 1: The nasal pressure <strong>and</strong> oral pressure did not change at the<br />

same time <strong>in</strong> the case of exhal<strong>in</strong>g except for one subject, who was not<br />

a skilled swimmer. His nasal pressure changed with oral pressure. But<br />

after blow<strong>in</strong>g out from the mouth <strong>in</strong> the water, almost all nasal pressures<br />

rose momentarily.<br />

Position 2: In the case of strong exhal<strong>in</strong>g from the nose, the nasal pressure<br />

<strong>and</strong> oral pressure changed simultaneously. On the other h<strong>and</strong>, at<br />

the moment of strong exhalation from the mouth, the nasal pressure did<br />

not elevate. (Fig.1)<br />

Exhalation<br />

from mouse <strong>in</strong><br />

water<br />

Water depth pressure curve at nostril level<br />

Nasal cavity pressure curve<br />

Water depth pressure curve at mouth level<br />

Oral cavity pressure curve<br />

Exhalation<br />

from mouse <strong>in</strong><br />

water<br />

Figure 1. The data obta<strong>in</strong>ed from Position 2: At the moment of strong<br />

exhalation from mouth, the nasal pressure (Ch2) did not rise. In this<br />

experiment, the pressure curves were not correlated between nasal <strong>and</strong><br />

oral spaces (Ch4).<br />

Position 3: We verified, us<strong>in</strong>g pressure sensors attached simultaneously <strong>in</strong><br />

nose <strong>and</strong> mouth, that tra<strong>in</strong>ed swimmers vary <strong>in</strong>dependently the amount<br />

of air blown out of the nose <strong>and</strong> mouth airways. There was some timelag<br />

between exhal<strong>in</strong>g from the nose to exhal<strong>in</strong>g from the mouth, <strong>and</strong><br />

this occurred while swimmers were face up above the surface of the water.<br />

In Position 3, the end of positive oral pressure was delayed 0.38sec.<br />

(Average) from the end of nasal positive pressure <strong>in</strong> tra<strong>in</strong>ed subjects, <strong>and</strong><br />

<strong>in</strong> untra<strong>in</strong>ed subjects, the delayed time was 0.11sec. (Ave.).<br />

Exhalation from<br />

nose <strong>in</strong> water<br />

Exhalation<br />

from mouse <strong>in</strong><br />

water<br />

Interval between<br />

nose to mouse<br />

exhalation<br />

Figure 2. The data obta<strong>in</strong>ed from Case.3 (Simulation of breaststroke<br />

swimm<strong>in</strong>g) <strong>in</strong> this experiment by the tra<strong>in</strong>ed subject: The nose was ris<strong>in</strong>g<br />

from water surface just before the mouth. After the nose has risen,<br />

delayed exhalation from the mouth was observed (Ch4), <strong>and</strong> nasal pressure<br />

(Ch2) did not reta<strong>in</strong> high values.<br />

319


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

dIscussIon<br />

Usually swimmers breathe out from the nose while the face is <strong>in</strong> the water.<br />

We detected that nasal pressure adapted to water depth pressure automatically<br />

(Hara H., et al., 1998). To study effects on nasal pressure, the<br />

nostrils were covered with film while subjects did the breaststroke. In this<br />

case, of shutt<strong>in</strong>g down the nose, a person might not be able to feel pressure<br />

changes <strong>in</strong> that area (Hara H, et al., 2006). This disturbed the <strong>in</strong>halation<br />

tim<strong>in</strong>g <strong>and</strong> resulted <strong>in</strong> swimm<strong>in</strong>g apnea. Experimentation <strong>in</strong> this form of<br />

nose-block<strong>in</strong>g has been carried out earlier (Hara H., et al., 2002).<br />

In the present study, the airway changes from nose to mouth were<br />

def<strong>in</strong>ed, when four tra<strong>in</strong>ed subjects were swimm<strong>in</strong>g simulated breaststroke.<br />

The nose pressure suddenly decreased when the nose broke the<br />

surface of the water. We th<strong>in</strong>k such a change of nasal pressure stopped<br />

exhalation from the nose. This also br<strong>in</strong>gs about a large blow-out from<br />

the mouth. The strong exhalation from the mouth needs a clos<strong>in</strong>g of<br />

the airways to the nose. Pronounc<strong>in</strong>g “Mnn” facilitates exhal<strong>in</strong>g from<br />

the nose, while pronounc<strong>in</strong>g “Pa” or “Pha” will shut the nasal airways<br />

lead<strong>in</strong>g to exhalation from the mouth. Tra<strong>in</strong>ed swimmers breathe out of<br />

the nose while their faces are <strong>in</strong> the water. In the case of <strong>in</strong>struction for<br />

beg<strong>in</strong>ners, to prevent swimm<strong>in</strong>g apnea it is effective if the <strong>in</strong>structor has<br />

the learner pronounce “Mnn” with the nose, then once that is completed,<br />

pronounce “Pha” or “Pa” from the mouth to blow out.<br />

The ventilation volume from the nose is smaller than from the mouth.<br />

However, the flow volume sensor <strong>in</strong> the nose is more sensitive than that<br />

<strong>in</strong> the mouth (Thubone H. 1990). Moreover, because the diameter of<br />

the nasal airways is smaller than the mouth’s, flow volume <strong>and</strong> pressure<br />

might be useful for provid<strong>in</strong>g <strong>in</strong>formation for breath control. This is the<br />

reason for us<strong>in</strong>g the nasal passages while swimm<strong>in</strong>g (Wheatly, JR., et<br />

al., 1991).<br />

In the case of sleep apnea, airway condition is very important for<br />

breath<strong>in</strong>g (Amal MO, et al., 2004). Airway conditions are controlled<br />

by the autonomic nervous system. When attempt<strong>in</strong>g to pronounce a<br />

word, one controls the palate movement, <strong>in</strong>tentionally. To prevent swimm<strong>in</strong>g<br />

apnea it is important for novice swimmers to acquire appropriate<br />

breath<strong>in</strong>g skills <strong>in</strong> their swimm<strong>in</strong>g skill progression.<br />

conclusIon<br />

In conclusion, it was verified that tra<strong>in</strong>ed swimmers vary the amount<br />

of air blown out of the nose <strong>and</strong> mouth, <strong>in</strong>dependently. In swimm<strong>in</strong>g,<br />

to protect from apnea, blow out from nose <strong>and</strong> stop breath<strong>in</strong>g, then<br />

feel non water pressure <strong>in</strong> nostrils. After that, change the airway to the<br />

mouth for large volume exhalation. This process is developed through<br />

palate control. We f<strong>in</strong>d that to acquire this <strong>in</strong>tentional airway control,<br />

word pronounc<strong>in</strong>g is appropriate.<br />

reFerences<br />

Amal MO, et al. (2004). Posthypoxic ventilatory decl<strong>in</strong>e dur<strong>in</strong>g NREM<br />

sleep: Influence of sleep apnea. J. Appl. Physiol., 96, 2220-2225<br />

Hara H., et al. (1999). The development of measur<strong>in</strong>g nasal pressure <strong>in</strong><br />

water, In Kesk<strong>in</strong>en K., Komi P. & Holl<strong>and</strong>er A.P. <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g VIII, 135-139<br />

Hara H., Watanabe R, et al. (2003). A study on nasal pressure <strong>in</strong>fluenced<br />

by swimm<strong>in</strong>g speed <strong>in</strong> breaststroke. In Chatard, J.C. <strong>Biomechanics</strong> <strong>and</strong><br />

<strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g IX, 63-67<br />

Hara H, et al. (2006). The function of nasal pressure for breath<strong>in</strong>g <strong>in</strong> the<br />

breaststroke. In Vilas-Boas J.P. Alves F. & Marques A. <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X, 137-139<br />

Thubone H., (1990). Nasal ‘pressure’ receptors. Jpn J Vet Sci, 52(2), 225-<br />

232<br />

Wheatly, JR., et al. (1991). Relationship between alae nasi activation<br />

<strong>and</strong> breath<strong>in</strong>g route dur<strong>in</strong>g exercise <strong>in</strong> humans. J Appl Physiol, 71(1),<br />

118-124<br />

320<br />

AcKnoWledGeMents<br />

The study was supported <strong>in</strong> part by Kokugaku<strong>in</strong> University, Specially<br />

Promoted Research, 2007. We acknowledge the students at Kokugaku<strong>in</strong><br />

University <strong>and</strong> Kawasaki University of Medical Welfare for their participation<br />

<strong>in</strong> this study.


Performance Level Differences <strong>in</strong> Swimm<strong>in</strong>g:<br />

Relative Contributions of Strength <strong>and</strong> Technique<br />

havriluk, r.<br />

Swimm<strong>in</strong>g Technology Research, Tallahassee, USA<br />

The purpose of this study was to compare the relative contributions of<br />

strength (measured by force, F) <strong>and</strong> technique (measured by the active<br />

drag coefficient, Cd) to swimm<strong>in</strong>g performance. Male (n = 40) <strong>and</strong> female<br />

(n = 40) swimmers were tested with Aquanex+Video swimm<strong>in</strong>g<br />

four trials (one of each stroke) over a 20 m course. Underwater video,<br />

h<strong>and</strong> force data, <strong>and</strong> swim time were collected over the last 10 m. The<br />

magnitude of the difference between faster <strong>and</strong> slower swimmers <strong>in</strong><br />

both F <strong>and</strong> Cd was calculated as an effect size (ES). The mean ES for the<br />

Cd was almost double the ES for F, <strong>in</strong>dicat<strong>in</strong>g that the advantage faster<br />

swimmers have over slower swimmers is derived more from technique<br />

than strength. Coaches can use this <strong>in</strong>formation to implement the most<br />

appropriate <strong>in</strong>terventions for cont<strong>in</strong>ued improvement.<br />

Key words: strength, technique, h<strong>and</strong> force, active drag coefficient,<br />

biomechanics<br />

IntroductIon<br />

The drag equation expla<strong>in</strong>s swimm<strong>in</strong>g performance as: v ≈ √(F/C d ),<br />

where v is swimm<strong>in</strong>g velocity, F is force, <strong>and</strong> C d is the active drag coefficient.<br />

Consistent with this equation, previous research found that v <strong>in</strong>creases<br />

with √F (Havriluk, 2004), <strong>and</strong> that faster swimmers have a lower<br />

C d than slower swimmers (Havriluk, 2003). Other test<strong>in</strong>g protocols (e.g.<br />

Takagi et al., 1983; Toussa<strong>in</strong>t et al., 1988; White & Stager, 2004) also<br />

reported significant relationships of F <strong>and</strong> C d with v.<br />

The importance of both strength (as measured by F) <strong>and</strong> technique<br />

(as measured by C d ) to swimm<strong>in</strong>g performance (as measured by<br />

v) is well established both theoretically <strong>and</strong> empirically. The relative contributions<br />

of F <strong>and</strong> C d to performance, however, have not been determ<strong>in</strong>ed.<br />

The purpose of this study was to determ<strong>in</strong>e how faster swimmers<br />

perform better than slower swimmers due to the relative contributions<br />

of strength (F) <strong>and</strong> technique (C d ), so that coaches can implement the<br />

most appropriate <strong>in</strong>terventions for cont<strong>in</strong>ued improvement.<br />

Method<br />

Swimmers from 21 teams volunteered to participate <strong>in</strong> the study. Male<br />

(n = 40) <strong>and</strong> female (n = 40) swimmers were tested with Aquanex+Video,<br />

swimm<strong>in</strong>g four trials (one of each stroke) over a 20 m course. The st<strong>and</strong>ard<br />

Aquanex test<strong>in</strong>g protocol as described <strong>in</strong> previous research (e.g.<br />

Havriluk, 2003, 2004, 2006b) was used (see Figure 1).<br />

Informed consent was obta<strong>in</strong>ed. Descriptive statistics for the male<br />

swimmers <strong>in</strong>clude: age <strong>in</strong> yrs (M = 18.0, SD = 1.3), height <strong>in</strong> cm (M =<br />

180, SD = 7.7), mass <strong>in</strong> kg (M = 74.2, SD = 8.5) <strong>and</strong> for the females:<br />

age <strong>in</strong> yrs (M = 17.7, SD = 1.0), height <strong>in</strong> cm (M = 168, SD = 6.0), mass<br />

<strong>in</strong> kg (M = 62.1, SD = 6.5). Underwater video, h<strong>and</strong> force data, <strong>and</strong><br />

swim time were collected over the last 10 m of each trial. The C d was<br />

calculated as: C d = F/(.5ρXv 2 ), where F is the average normal h<strong>and</strong> force,<br />

r is the mass density of water, X is the cross-sectional area of the body,<br />

<strong>and</strong> v is swimm<strong>in</strong>g velocity. Previous research found an almost perfect<br />

correlation between normal <strong>and</strong> propulsive force (r = .98) with a m<strong>in</strong>or<br />

overestimation (6 N) of propulsive force (Havriluk, 2006b).<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

Figure 1. Captured screen of an Aquanex+Video image of swimmer T09<br />

at .53 sec <strong>in</strong> the second stroke of butterfly. The vertical l<strong>in</strong>es on the force<br />

curves are synchronized with the video image.<br />

results<br />

Regression analyses found significant (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

322<br />

Butterfly<br />

0.0<br />

0 20 40 60 80 100 120 140<br />

Average H<strong>and</strong> Force (N)<br />

Males Reg Females Reg<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

Backstroke<br />

0.0<br />

0 20 40 60 80 100 120 140<br />

Average H<strong>and</strong> Force (N)<br />

Males Reg Females Reg<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

Breaststroke<br />

0.0<br />

0 20 40 60 80 100 120 140<br />

Average H<strong>and</strong> Force (N)<br />

Males Reg Females Reg<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

Freestyle<br />

0.0<br />

0 20 40 60 80 100 120 140<br />

Average H<strong>and</strong> Force (N)<br />

Males Reg Females Reg<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

Swimm<strong>in</strong>g Velocity (m/sec)<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

Butterfly<br />

0.0<br />

0.0 0.5 1.0 1.5 2.0<br />

Active Drag Coefficient<br />

Males Reg Females Reg<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

Backstroke<br />

0.0<br />

0.0 0.5 1.0 1.5 2.0<br />

Active Drag Coefficient<br />

Males Reg Females Reg<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

Breaststroke<br />

0.0<br />

0.0 0.5 1.0 1.5 2.0 2.5 3.0<br />

Active Drag Coefficient<br />

Males Reg Females Reg<br />

2.0<br />

1.5<br />

1.0<br />

0.5<br />

Freestyle<br />

0.0<br />

0.0 0.5 1.0 1.5 2.0<br />

Active Drag Coefficient<br />

Males Reg Females Reg<br />

Figure 2. Graphs of swimm<strong>in</strong>g velocity vs h<strong>and</strong> force <strong>and</strong> active drag<br />

coefficient.<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong><br />

Chapter 5 Education, Advice <strong>and</strong> Biofeedback<br />

Table 1. Mean (M) values for active drag coefficient (Cd), average h<strong>and</strong><br />

force (F), <strong>and</strong> swimm<strong>in</strong>g velocity (SV) for faster <strong>and</strong> slower groups. Differences<br />

between groups are listed as effect sizes (ES).<br />

Table 1. Mean (M) values for active drag coefficient (Cd), average h<strong>and</strong> force (F), <strong>and</strong><br />

swimm<strong>in</strong>g velocity (SV) for faster <strong>and</strong> slower groups. Differences between groups are<br />

listed as effect sizes (ES).<br />

Males (n = 40) Females (n = 40)<br />

Faster Slower Faster Slower<br />

M M SD ES M M SD ES<br />

Cd<br />

Butterfly .89 1.16 .23 -1.17 .93 1.10 .21 -.81<br />

Backstroke 1.10 1.35 .22 -1.14 1.11 1.23 .20 -.60<br />

Breaststroke 1.44 1.83 .40 -.98 1.36 1.68 .33 -.97<br />

Freestyle<br />

F (N)<br />

.92 1.07 .23 -.71 .92 1.07 .19 -.79<br />

Butterfly 85.9 81.4 17.8 .25 59.9 54.5 11.1 .49<br />

Backstroke 77.5 65.7 15.0 .79 51.6 43.5 9.7 .84<br />

Breaststroke 75.4 69.8 15.4 .36 52.3 48.1 10.2 .41<br />

Freestyle<br />

SV (m/sec)<br />

94.7 81.7 21.3 .61 60.8 54.3 11.4 .57<br />

Butterfly 1.56 1.37 .12 1.58 1.41 1.26 .10 1.50<br />

Backstroke 1.34 1.14 .12 1.67 1.19 1.06 .08 1.63<br />

Breaststroke 1.16 1.00 .10 1.60 1.10 .95 .10 1.50<br />

Freestyle 1.62 1.44 .12 1.50 1.42 1.28 .09 1.56<br />

H<strong>and</strong> Force Effect Size<br />

-1.2 -1.0 -0.8 -0.6 -0.4 -0.2 0.0<br />

Active Drag Coefficient Effect Size<br />

Figure 3. Graph of the differences between faster <strong>and</strong> slower swimmers (expressed as<br />

effect sizes) <strong>in</strong> active drag coefficient <strong>and</strong> average h<strong>and</strong> force for 8 gender/stroke<br />

comb<strong>in</strong>ations. The diagonal l<strong>in</strong>e represents an equal effect from both variables.<br />

DISCUSSION<br />

A previously conducted meta-analysis reported a wide range of values for the freestyle<br />

Cd – from less than .5 to greater than 2.5 (Havriluk, 2007). Cd values varied based on<br />

the test<strong>in</strong>g protocol <strong>and</strong> associated sources of systematic error. As systematic error is so<br />

1.2<br />

1.0<br />

0.8<br />

0.6<br />

0.4<br />

0.2<br />

0.0<br />

29<br />

H<strong>and</strong> Force Effect Size<br />

-1.2 -1.0 -0.8 -0.6 -0.4 -0.2 0.0<br />

Active Drag Coefficient Effect Size<br />

Figure 3. Graph of the differences between faster <strong>and</strong> slower swimmers<br />

(expressed as effect sizes) <strong>in</strong> active drag coefficient <strong>and</strong> average h<strong>and</strong><br />

force for 8 gender/stroke comb<strong>in</strong>ations. The diagonal l<strong>in</strong>e represents an<br />

equal effect from both variables.<br />

dIscussIon<br />

A previously conducted meta-analysis reported a wide range of values<br />

for the freestyle C d – from less than .5 to greater than 2.5 (Havriluk,<br />

2007). C d values varied based on the test<strong>in</strong>g protocol <strong>and</strong> associated<br />

sources of systematic error. As systematic error is so far unavoidable<br />

when measur<strong>in</strong>g C d , it is appropriate to identify known sources. The C d<br />

values for the present study were about 1.0 <strong>and</strong> have m<strong>in</strong>or systematic<br />

error due to measurement of normal h<strong>and</strong> force as opposed to propulsive<br />

h<strong>and</strong> force (Havriluk, 2006b).<br />

The significant curvil<strong>in</strong>ear relationships of v with √F <strong>and</strong> √(1/C d ) are<br />

consistent with the drag equation. The graphs <strong>in</strong> Figure 2 show the importance<br />

of both strength <strong>and</strong> technique to performance. These graphs<br />

also show proportionally smaller performance improvements with <strong>in</strong>creases<br />

<strong>in</strong> F <strong>and</strong> proportionally larger improvements with decreases <strong>in</strong><br />

C d , <strong>in</strong>dicat<strong>in</strong>g that no matter how effective a swimmer’s technique, there<br />

is reason to cont<strong>in</strong>ue to focus on improvement.<br />

The performance level differences <strong>in</strong> F <strong>and</strong> C d were expected, as was<br />

the gender difference <strong>in</strong> F <strong>and</strong> the lack of a gender difference <strong>in</strong> C d .<br />

The mean performance level ES for the C d was almost double the ES<br />

for F, <strong>in</strong>dicat<strong>in</strong>g that the advantage faster swimmers have over slower<br />

swimmers is derived more from technique than strength. Slower swimmers<br />

can become more like faster swimmers by improv<strong>in</strong>g technique<br />

to reduce the magnitude of the effect. While the data show that faster<br />

swimmers have already benefitted from their technique, they can still<br />

improve. Because of the large ga<strong>in</strong>s <strong>in</strong> v that result from small decreases<br />

<strong>in</strong> C d , additional technique improvements are critical for even the fastest<br />

swimmers.<br />

S<strong>in</strong>ce there is a smaller performance level difference <strong>in</strong> F than C d ,<br />

faster swimmers may <strong>in</strong>crease the difference <strong>in</strong> F by <strong>in</strong>creas<strong>in</strong>g their<br />

strength. Because most competitive swimmers already strength tra<strong>in</strong>,<br />

however, additional ga<strong>in</strong>s may be difficult. A more productive approach<br />

may be to exam<strong>in</strong>e how swimmers apply their strength to the water as<br />

revealed by variations <strong>in</strong> h<strong>and</strong> force throughout the stroke cycle.<br />

H<strong>and</strong> force analysis identified wasted motion <strong>and</strong> force losses <strong>in</strong><br />

even the fastest swimmers (Havriluk, 2006a). Recent research found<br />

that a group of college females wasted over 40% of the underwater butterfly<br />

arm motion with their arms <strong>in</strong> a mechanically disadvantageous<br />

position at the beg<strong>in</strong>n<strong>in</strong>g of the pull (Becker & Havriluk, 2010). (Co<strong>in</strong>cidentally,<br />

mechanically disadvantageous arm positions usually stress<br />

the shoulder <strong>in</strong> a manner that can cause <strong>in</strong>jury.) Force losses of over 80<br />

N have been measured on Olympians. These studies show that faster<br />

swimmers can benefit by m<strong>in</strong>imiz<strong>in</strong>g wasted motion <strong>and</strong> force losses so<br />

that they use their strength more effectively.<br />

1.2<br />

1.0<br />

0.8<br />

0.6<br />

0.4<br />

0.2<br />

0.0


Synchronized underwater video <strong>and</strong> h<strong>and</strong> force data shows swimmers<br />

<strong>and</strong> coaches exactly where <strong>in</strong> the stroke cycle that wasted motion<br />

<strong>and</strong> force losses occur. For example, the swimmer <strong>in</strong> the left image of<br />

Figure 4 shows .2 sec of wasted motion at the beg<strong>in</strong>n<strong>in</strong>g of the butterfly<br />

pull <strong>and</strong> the swimmer <strong>in</strong> the right image shows a major force loss as the<br />

arms pass under the shoulders. Armed with this <strong>in</strong>formation, the coach<br />

can suggest technique adjustments to m<strong>in</strong>imize these limit<strong>in</strong>g factors.<br />

When a quantitative analysis is not feasible, coaches can qualitatively<br />

evaluate swimmers to identify wasted motion (as shown by excess lateral<br />

h<strong>and</strong> motion) <strong>and</strong> force losses (as shown by sudden changes <strong>in</strong> h<strong>and</strong><br />

path). Coaches can then target control of the h<strong>and</strong> path angle to help a<br />

swimmer overcome these limitations. A quantitative analysis, however,<br />

is the most def<strong>in</strong>itive way to identify limitations, confirm the effect of<br />

technique adjustments, provide numerical feedback to swimmers, <strong>and</strong><br />

ensure that swimmers make the precise changes to optimize performance.<br />

Figure 4. Captured screens of Aquanex+Video images show<strong>in</strong>g butterfly<br />

swimmers with wasted motion (top) <strong>and</strong> a major force loss (bottom). In<br />

each screen, the vertical l<strong>in</strong>es on the force curves are synchronized with<br />

the video image.<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

conclusIons<br />

Coaches can help slower swimmers improve by emphasiz<strong>in</strong>g technique<br />

<strong>in</strong>struction <strong>and</strong> regularly measur<strong>in</strong>g their C d . Because of the large ga<strong>in</strong>s<br />

<strong>in</strong> v that result from small decreases <strong>in</strong> C d , even the fastest swimmers<br />

can cont<strong>in</strong>ue to benefit from improv<strong>in</strong>g technique. Faster swimmers can<br />

also ga<strong>in</strong> a greater advantage over slower swimmers from a more effective<br />

use of strength. With a detailed h<strong>and</strong> force analysis, a coach can<br />

identify wasted motion <strong>and</strong> force losses to provide options that <strong>in</strong>crease<br />

average force <strong>and</strong> achieve maximum performance potential.<br />

reFerences<br />

Becker, T.J., & Havriluk, R. (2010). Quantitative Data Supplements<br />

Qualitative Evaluations of Butterfly Swimm<strong>in</strong>g. In Kjendlie P.L.,<br />

Stallman R.K. <strong>and</strong> Cabri J. (eds): <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g<br />

<strong>XI</strong> (<strong>in</strong> press).<br />

Havriluk, R. (2003). Performance level differences <strong>in</strong> swimm<strong>in</strong>g drag coefficient.<br />

Paper presented at the VIIth IOC Olympic World Congress<br />

on Sport Sciences, Athens.<br />

Havriluk, R. (2004). H<strong>and</strong> force <strong>and</strong> swimm<strong>in</strong>g velocity. Paper presented<br />

at the XVth FINA World Sports <strong>Medic<strong>in</strong>e</strong> Congress, Indianapolis,<br />

IN.<br />

Havriluk, R. (2006a). Analyz<strong>in</strong>g h<strong>and</strong> force <strong>in</strong> swimm<strong>in</strong>g: Three typical<br />

limit<strong>in</strong>g factors. American Swimm<strong>in</strong>g Magaz<strong>in</strong>e, 2006(3), 14-18.<br />

Havriluk, R. (2006b). Magnitude of the effect of an <strong>in</strong>structional <strong>in</strong>tervention<br />

on swimm<strong>in</strong>g technique <strong>and</strong> performance. In J. P. Vilas-Boas,<br />

F. Alves, A. Marques (Eds.), <strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g<br />

X. Portuguese Journal of Sport Sciences, 6(Suppl. 2), 218-220.<br />

Havriluk, R. (2007). Variability <strong>in</strong> measurement of swimm<strong>in</strong>g forces: A<br />

meta-analysis of passive <strong>and</strong> active drag. Research Quarterly for Exercise<br />

<strong>and</strong> Sport, 78(2), 32-39.<br />

Takagi, H., Shimizu, Y., Onogi, H., & Kusagawa, Y. (1998). The relationship<br />

between coefficients of drag <strong>and</strong> swimm<strong>in</strong>g performance. II Australia<br />

<strong>and</strong> New Zeal<strong>and</strong> Society of <strong>Biomechanics</strong> Conference (Abstract),<br />

56.<br />

Toussa<strong>in</strong>t, H.M., de Groot, G., Savelberg, H.H.C.M., Vervoorn, K.,<br />

Holl<strong>and</strong>er, A. P., & van Ingen Schenau, G. J. (1988). Active drag related<br />

to velocity <strong>in</strong> male <strong>and</strong> female swimmers. Journal of <strong>Biomechanics</strong>,<br />

21, 435-438.<br />

White, J.C. & Stager, J.M. (2004). The relationship between drag forces<br />

<strong>and</strong> velocity for the four competitive swimm<strong>in</strong>g strokes. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong><br />

Science <strong>in</strong> Sports <strong>and</strong> Exercise, 36(5), S9.<br />

323


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Evaluation of K<strong>in</strong>aesthetic Differentiation Abilities <strong>in</strong><br />

Male <strong>and</strong> Female Swimmers<br />

Invernizzi, P.l., longo, s., scurati, r., Michielon, G.<br />

Università degli Studi di Milano, Facoltà di Scienze Motorie, Milan, Italy<br />

Events longer than 50 meters require some tactical skills <strong>in</strong> order to<br />

manage the <strong>in</strong>crease of fatigue, such as distribut<strong>in</strong>g the effort evenly<br />

over the whole distance. K<strong>in</strong>aesthetic differentiation skills are required<br />

to achieve a very high precision of the movements. The repeatability of<br />

two procedures, aimed to measure the k<strong>in</strong>aesthetic differentiation abilities<br />

of swimmers was studied <strong>and</strong> the correlations between the actual<br />

performances <strong>and</strong> the expected performances with respect to gender <strong>and</strong><br />

to the degree of change <strong>in</strong> velocity, were observed. Collect<strong>in</strong>g the data<br />

<strong>in</strong> a s<strong>in</strong>gle day <strong>and</strong> dur<strong>in</strong>g four days runn<strong>in</strong>g resulted <strong>in</strong> reliable results.<br />

Male swimmers seem to differentiate better than females <strong>and</strong> show a<br />

generally higher coefficient of correlation between the actual <strong>and</strong> the<br />

expected performance.<br />

Key words: k<strong>in</strong>aesthetic differentiation, sensory perception, motor<br />

control<br />

IntroductIon<br />

Physiological factors such as strength <strong>and</strong> power, <strong>and</strong> technique <strong>and</strong><br />

the ability to reduce drag, are the ma<strong>in</strong> factors determ<strong>in</strong><strong>in</strong>g swimm<strong>in</strong>g<br />

performance.<br />

Furthermore, any event longer than 50 meters requires that swimmers<br />

employ some tactical skills, such as distribut<strong>in</strong>g effort evenly over<br />

the whole distance, <strong>in</strong> order to manage <strong>in</strong>creas<strong>in</strong>g fatigue. Even highlevel<br />

athletes tend to swim too fast the first part of the event compromis<strong>in</strong>g<br />

the whole performance (Maglischo, 2003), especially dur<strong>in</strong>g<br />

short distance events.<br />

The control of swimm<strong>in</strong>g pace largely depends on coord<strong>in</strong>ative <strong>and</strong><br />

on sensory-perceptive abilities. The <strong>in</strong>teraction between feedback <strong>and</strong><br />

sensory-perceptive <strong>in</strong>formation allows full control of the movement.<br />

Furthermore, thanks to motor memory, the movement’s regulatory<br />

system can precisely differentiate <strong>and</strong> manage the <strong>in</strong>tensity of effort<br />

(Bernste<strong>in</strong>, 1975). K<strong>in</strong>aesthetic differentiation abilities seem to have a<br />

progressive development with age, a plateau dur<strong>in</strong>g puberty, an <strong>in</strong>crease<br />

from 16 years with a peak between 19 <strong>and</strong> 21 years, depend<strong>in</strong>g on gender<br />

(Hirtz, 1988).<br />

K<strong>in</strong>aesthetic differentiation skills are thus important to perfect the<br />

swim. Thanks to these abilities, swimmers can achieve a very high precision<br />

of movement, hav<strong>in</strong>g good control even when no visual feedback<br />

is allowed, br<strong>in</strong>g<strong>in</strong>g the execution of the movement closer to the ideal<br />

(Schicke, 1982), improv<strong>in</strong>g the “feel<strong>in</strong>g of the water” <strong>and</strong> thus perform<strong>in</strong>g<br />

better propulsive actions or better reduc<strong>in</strong>g drag forces (Colw<strong>in</strong>, 2002).<br />

This study aimed to verify the repeatability of measur<strong>in</strong>g <strong>and</strong> evaluat<strong>in</strong>g<br />

the k<strong>in</strong>aesthetic differentiation abilities <strong>in</strong> good-level swimmers by<br />

two different procedures based on simply swimm<strong>in</strong>g at different speeds.<br />

The correlations between the actual performances <strong>and</strong> the expected performances<br />

were also observed with respect to gender <strong>and</strong> to the degree<br />

of change <strong>in</strong> speed.<br />

Methods<br />

Eighteen swimmers aged 13 to 19 years, of regional to national level,<br />

participated <strong>in</strong> this study: 8 male swimmers (mean±SD, age 15.38±1.84<br />

years, height 168.9±11.7 cm, weight 57.6±13.3 kg, BMI 20.0±2.4 kg·m -<br />

2 ) <strong>and</strong> 10 female swimmers (mean±SD, age 15.75±1.39 years, height<br />

167.8±6.0 cm, weight 57.9±8.8 kg, BMI 20.5±2.8 kg·m -2 ).<br />

To measure their k<strong>in</strong>aesthetic differentiation ability, the subjects<br />

performed a number of 25m front crawl trials at different paces correspond<strong>in</strong>g<br />

to 50% <strong>and</strong> 80% of the maximum speed.<br />

324<br />

Each trial started without push<strong>in</strong>g-off the wall, the swimmer be<strong>in</strong>g<br />

supported <strong>in</strong> a streaml<strong>in</strong>ed, prone position. First, the swimmers<br />

performed a 25m front crawl trial at maximum speed (25m 100% ). The<br />

speed correspond<strong>in</strong>g to 50% <strong>and</strong> 80% of maximum was immediately<br />

calculated by an MsExcel worksheet <strong>and</strong> communicated to the swimmer.<br />

Afterwards they were asked to perform a total of eight 25m swims<br />

as closely as possible to the requested speed (4 trials at 50% <strong>and</strong> 4 trials<br />

at 80% respectively).<br />

The time of each 25m performance <strong>and</strong> the time for the central 10<br />

meters (from 7.5m to 17.5m) were recorded.<br />

Feedback was given after each trial: the swimmers were advised of<br />

their performance on a scale of 1 to 10, 10 correspond<strong>in</strong>g to the 100%<br />

(maximum), 8 for the 80% effort, <strong>and</strong> 5 for the 50% effort. This was done<br />

<strong>in</strong> order to make the perception of speed easier for the younger swimmers.<br />

Two different procedures were employed: i. Procedure 8/1, execut<strong>in</strong>g<br />

the protocol <strong>in</strong> a s<strong>in</strong>gle day; ii. Procedure 8/4, execut<strong>in</strong>g the protocol<br />

over four days.<br />

8/1: The swimmers performed 4 consecutive 25m front crawl trials<br />

at 50% of the maximum followed by 4 consecutive 25m front crawl<br />

trials at 80% of maximum on the same day. Full recovery was allowed<br />

between trials <strong>and</strong> feedback from the previous performance was given,<br />

as expla<strong>in</strong>ed above.<br />

8/4: The swimmers performed two trials per day, over four days.<br />

Each day, a 25m front crawl trial at 50% of maximum <strong>and</strong> after full recovery<br />

one at 80% of maximum, were performed. Feedback of the results<br />

from the previous day was provided before start<strong>in</strong>g.<br />

Statistical analysis was carried out us<strong>in</strong>g SPSS 13.0 software. The<br />

normal distribution of the data was verified by the Shapiro-Wilk test<br />

<strong>and</strong> parametric statistics were applied. Test validity was analyzed by the<br />

Intraclass Correlation Coefficient (ICC). Afterwards, by both gender<br />

<strong>and</strong> procedure (8/1 <strong>and</strong> 8/4), the Pearson’s Correlation Coefficient between<br />

the actual <strong>and</strong> the expected performance was calculated.<br />

results<br />

The validity <strong>and</strong> the repeatability of the procedures employed <strong>in</strong> this<br />

study are shown <strong>in</strong> Table 1.<br />

Table 1. Validity of the test (ICC)<br />

Group 1<br />

%<br />

Changes <strong>in</strong> the mean 2.36<br />

Typical error 5.92<br />

Intraclass r (ICC) 0.77<br />

The ability of the swimmers to perform 25m front crawl at a given speed<br />

correspond<strong>in</strong>g to 50% <strong>and</strong> 80% of their maximum is illustrated <strong>in</strong> Tables<br />

2 <strong>and</strong> 3: correlations with the 25m 100% front crawl trials are shown. Both<br />

procedures (all trials <strong>in</strong> a s<strong>in</strong>gle day <strong>and</strong> two trials <strong>in</strong> four days runn<strong>in</strong>g)<br />

have been considered.<br />

Table 2. Correlation (Pearrson’s) by gender <strong>in</strong> the 8/1 procedure between<br />

the performance <strong>and</strong> the expected speed at 50%max <strong>and</strong> 80%max. Values<br />

refer to the whole distance (25m) <strong>and</strong> to 7.5m to 17.5m (10m). * =<br />

p


Table 3. Correlation (Pearson’s r) by gender <strong>in</strong> the 8/4 procedure between<br />

the performance <strong>and</strong> the expected speed at 50%max <strong>and</strong> 80%max.<br />

Values refer to the whole distance (25m) <strong>and</strong> to 7.5m to 17.5m (10m).<br />

* = p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Swimm<strong>in</strong>g <strong>in</strong> Eyesight Deprivation: Relationships<br />

with Sensory-Perception, Coord<strong>in</strong>ation <strong>and</strong> laterality<br />

Invernizzi, P.l., longo, s., tad<strong>in</strong>i, F., scurati, r.<br />

Università degli Studi di Milano, Facoltà di Scienze Motorie, Milan, Italy<br />

Ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g control of direction dur<strong>in</strong>g displacement is important <strong>in</strong><br />

swimm<strong>in</strong>g, particularly for backstroke <strong>and</strong> open water events. Sensoryperception,<br />

coord<strong>in</strong>ation <strong>and</strong> laterality can relate to the ability to swim<br />

straight. This study aimed to analyze these relationships <strong>in</strong> front crawl,<br />

backstroke <strong>and</strong> breaststroke swum <strong>in</strong> a condition of eyesight deprivation.<br />

High correlation was found between the sensory-perception abilities<br />

<strong>and</strong> the ability <strong>in</strong> bl<strong>in</strong>d straight swimm<strong>in</strong>g. A crossed dom<strong>in</strong>ance<br />

right arm - left leg seems to be related to a better ability to manage the<br />

swimm<strong>in</strong>g direction <strong>in</strong> breaststroke, but neither <strong>in</strong> front crawl nor <strong>in</strong><br />

backstroke.<br />

Key words: sensory-perception, coord<strong>in</strong>ation, glid<strong>in</strong>g<br />

IntroductIon<br />

Previous studies on technical <strong>and</strong> coord<strong>in</strong>ative skills <strong>and</strong> on sensoryperception<br />

abilities po<strong>in</strong>ted out the importance of k<strong>in</strong>aesthetic differentiation<br />

skills <strong>and</strong> of the ability to reduce the drag forces <strong>in</strong> swimm<strong>in</strong>g<br />

performance.<br />

We wondered about the role of k<strong>in</strong>aesthetic differentiation <strong>and</strong> coord<strong>in</strong>ation<br />

<strong>in</strong> keep<strong>in</strong>g control of the swim direction, manag<strong>in</strong>g straight<br />

swimm<strong>in</strong>g. Usually athletes do not focus on it, thanks to the unconscious<br />

collection of <strong>in</strong>formation through eyesight (e.g. the lane l<strong>in</strong>e, the<br />

lane ropes, the walls). Swimmers should have good sensory-perception<br />

<strong>and</strong> k<strong>in</strong>aesthetic differentiation skills because these abilities allow them<br />

to perform the propulsive actions hav<strong>in</strong>g good control even with no visual<br />

feedback. Moreover they would be able to execute optimal swimm<strong>in</strong>g<br />

close to a theoretical model (Schicke, 1982). This is important<br />

<strong>in</strong> order to best manage the swimm<strong>in</strong>g direction, particularly <strong>in</strong> events<br />

such as backstroke or open water.<br />

The sensory-perception abilities are also essential to build “feel<strong>in</strong>g<br />

for the water” <strong>and</strong> they can be improved anytime by practice (Colw<strong>in</strong>,<br />

2002). Furthermore they are closely related to coord<strong>in</strong>ation (Me<strong>in</strong>el et<br />

al., 1984) <strong>and</strong> to balance, both dur<strong>in</strong>g swimm<strong>in</strong>g <strong>and</strong> outside the water.<br />

Visual feedback is closely related to balance, to sensory-perception improvement<br />

<strong>and</strong> to the control of direction dur<strong>in</strong>g displacement (Danion<br />

et al., 2000). Relationships are also found between coord<strong>in</strong>ation <strong>and</strong> laterality<br />

(h<strong>and</strong> dom<strong>in</strong>ance) (Oberbeck, 1989).<br />

The evaluation of coord<strong>in</strong>ation can be accomplished through a test<br />

based on the measurement of the maximal rotation on the longitud<strong>in</strong>al<br />

axis the athlete performs (Starosta, 2004). The laterality of subjects<br />

(h<strong>and</strong> dom<strong>in</strong>ance) could be calculated through the Hildreth <strong>in</strong>dex (Cilia<br />

et al., 1996), from the frequency of the favourite side used while perform<strong>in</strong>g<br />

a number of simple tasks.<br />

The ability to reduce drag, connected to swimm<strong>in</strong>g specific sensoryperception<br />

abilities, can be evaluated by a glid<strong>in</strong>g or a dive <strong>and</strong> glide test<br />

(Cazorla, 1993; Invernizzi et al., 2007).<br />

The aim of this study was to analyze the relationships among sensory-perception<br />

abilities, eyesight, coord<strong>in</strong>ation <strong>and</strong> laterality <strong>in</strong> ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g<br />

a straight swim dur<strong>in</strong>g the front crawl, the backstroke <strong>and</strong> the<br />

breaststroke, <strong>in</strong> young swimmers aged 8 to 14 years.<br />

326<br />

Methods<br />

Twenty-eight young swimmers participated <strong>in</strong> this study (mean±SD,<br />

age 10.8±1.3 years, height 146.2±11.3 cm, weight 37.7±8.8 kg, BMI<br />

16.9±2.2 kg·m -2 , arm span 148.7±13.5 cm).<br />

To evaluate the trajectory of the swim without the support of visual<br />

feedback, the swimmers were asked to swim wear<strong>in</strong>g dark goggles<br />

(Novàk, 1982). A total of 9 bl<strong>in</strong>d-trials were performed: strokes were repeated<br />

three times <strong>in</strong> the sequence 25m front crawl, 25m backstroke <strong>and</strong><br />

25m breaststroke to avoid any condition<strong>in</strong>g effect due to the protocol.<br />

Subjects swam <strong>in</strong> the middle of a double lane area, start<strong>in</strong>g <strong>in</strong> a<br />

prone or sup<strong>in</strong>e position, push<strong>in</strong>g off the wall with both legs. They were<br />

asked to perform the swim as straight as possible, feel<strong>in</strong>g the water displacement<br />

only through k<strong>in</strong>aesthetic <strong>and</strong> vestibular sensory perception<br />

feedback.<br />

Scores (-5 to 5) were assigned depend<strong>in</strong>g on where the swimmers<br />

touched the lane rope or the end wall (Figure 1). Assistants guaranteed<br />

the safety of the subjects <strong>and</strong> the survey was supported by videorecord<strong>in</strong>g.<br />

Positive scores <strong>in</strong>dicated a deviation to the left whereas negative<br />

scores <strong>in</strong>dicated a deviation to the right. The scores have been <strong>in</strong>verted<br />

for backstroke <strong>in</strong> order to have the same mean<strong>in</strong>g of the direction of<br />

deviation with respect to the swimmer’s body.<br />

Swimmers performed the front crawl stroke breath<strong>in</strong>g every three<br />

armstrokes (alternat<strong>in</strong>g the side of breath<strong>in</strong>g).<br />

Figure 1. Experimental sett<strong>in</strong>g for the “bl<strong>in</strong>d swimm<strong>in</strong>g” evaluation.<br />

The swimmers’ coord<strong>in</strong>ation was evaluated through a Coord<strong>in</strong>ation test<br />

as suggested by Starosta (2004). Subjects had to jump on a 1 square<br />

meter base (Figure 2), execut<strong>in</strong>g the maximal possible rotation on the<br />

longitud<strong>in</strong>al axis dur<strong>in</strong>g the flight. Athletes could make free use of upper<br />

limbs. The degree of rotation was collected from the position of the feet<br />

after l<strong>and</strong><strong>in</strong>g. Two trials were performed for each direction of rotation.<br />

The preferred direction to rotate was also detected from the results.


Figure 2. Experimental sett<strong>in</strong>g for the evaluation of the coord<strong>in</strong>ation.<br />

The Hildreth <strong>in</strong>dex (Cilia et al., 1996) was employed <strong>in</strong> order to evaluate<br />

the laterality of the subjects (h<strong>and</strong> dom<strong>in</strong>ance). Accord<strong>in</strong>g to the<br />

protocol, twelve actions for each part (e.g. h<strong>and</strong>, foot, eye) are selected<br />

<strong>and</strong> the preferred side employed dur<strong>in</strong>g the test is recorded. The <strong>in</strong>dex<br />

was calculated as follows: (nr of trials executed on the right – nr of trials<br />

executed on the left) · 12 -1 . Based on the results (-100 to 100) it is<br />

possible to def<strong>in</strong>e the side <strong>and</strong> the degree of the laterality. In our study<br />

the twelve actions us<strong>in</strong>g the h<strong>and</strong>s were selected <strong>and</strong> the frequency of<br />

employment <strong>in</strong> the action requested was surveyed.<br />

The ability to “feel the water” strictly depends on sensory-perceptive<br />

skills, hence the “dive <strong>and</strong> glide” test was applied to evaluate it (Cazorla,<br />

1993; Invernizzi et al., 2007). The distance reached by the swimmers<br />

after glid<strong>in</strong>g was measured. Neither movements nor propulsive actions<br />

were allowed dur<strong>in</strong>g the glid<strong>in</strong>g phase.<br />

The relationships observed were: bl<strong>in</strong>d swimm<strong>in</strong>g <strong>and</strong> swimm<strong>in</strong>g<br />

style, bl<strong>in</strong>d swimm<strong>in</strong>g <strong>and</strong> coord<strong>in</strong>ation, bl<strong>in</strong>d swimm<strong>in</strong>g <strong>and</strong> glid<strong>in</strong>g.<br />

Results were also discussed with respect to the swimmers laterality.<br />

Statistical analyses were carried out by SPSS 13.0® software, us<strong>in</strong>g<br />

p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 4 – Correlations between coord<strong>in</strong>ation (sum of the degrees of the<br />

trials performed) <strong>and</strong> the deviation (sum of the absolute score values) <strong>in</strong><br />

bl<strong>in</strong>d swimm<strong>in</strong>g.<br />

Figure 5 – Correlations between the deviation (sum of the absolute<br />

score values) <strong>in</strong> bl<strong>in</strong>d swimm<strong>in</strong>g <strong>and</strong> glid<strong>in</strong>g.<br />

The Hildreth test showed that 96.4% of the subjects were right h<strong>and</strong><br />

(RH) dom<strong>in</strong>ant (27 subjects out of 28). The Starosta test showed that<br />

66.6% of our subjects were left leg (LL) dom<strong>in</strong>ant, the rema<strong>in</strong><strong>in</strong>g be<strong>in</strong>g<br />

right leg (RL) dom<strong>in</strong>ant. Hence, 66.6% had the cross laterality comb<strong>in</strong>ation<br />

RH-LL. When compar<strong>in</strong>g the absolute score values between the<br />

RH-LL <strong>and</strong> RH-RL subjects, that is, how much the deviation from the<br />

straight l<strong>in</strong>e was regardless of the direction, no significant difference <strong>in</strong><br />

bl<strong>in</strong>d front crawl or backstroke were found. In breaststroke, a significant<br />

difference was found (po<strong>in</strong>ts±SD, 7.88±2.49 versus 9.88±1.90, p


Progression <strong>in</strong> Teach<strong>in</strong>g Beg<strong>in</strong>n<strong>in</strong>g Swimm<strong>in</strong>g: Rank<br />

Order by Degree of Difficulty<br />

Junge, M. 1,3 , Blixt, t. 2 , stallman, r.K, 1,2<br />

1 Norwegian School of Sport Science,<br />

2 Norwegian Swimm<strong>in</strong>g Federation,<br />

3 University of Oslo<br />

”Teach first th<strong>in</strong>gs first”! But what comes first? Where do we start? Also,<br />

children are different <strong>and</strong> no progression will suit all. It should be possible<br />

to a) agree on content <strong>and</strong> b) f<strong>in</strong>d a progression that suits a majority.<br />

Children 5-6 yrs of age (N=146) received 18 hrs of <strong>in</strong>struction, <strong>in</strong><br />

small groups. A theoretical progression of 19 skills was created from the<br />

<strong>in</strong>ternational literature, exam<strong>in</strong><strong>in</strong>g course content of lead<strong>in</strong>g educational<br />

organizations. A s<strong>in</strong>gle head <strong>in</strong>structor coord<strong>in</strong>ated all teach<strong>in</strong>g. Evaluation<br />

of progress <strong>and</strong> record<strong>in</strong>g of criterion success on the 19 skills was<br />

overseen by the same head <strong>in</strong>structor. The number of children succeed<strong>in</strong>g<br />

on each skill was deemed a reflection of the degree of difficulty. The<br />

actual rank order of skills derived from these learners was correlated to<br />

the theoretical rank order us<strong>in</strong>g Spearman’s rank order correlation. Rho<br />

proved to be 0.97. Among other results, all (paired) skills on the front<br />

proved easier than the correspond<strong>in</strong>g skill on the back. Arguments are<br />

presented to defend reta<strong>in</strong><strong>in</strong>g the theoretical rank order as well as arguments<br />

for adjust<strong>in</strong>g the rank order. When <strong>in</strong>dividualis<strong>in</strong>g teach<strong>in</strong>g, there<br />

seems to be an optimal progression for each child, albeit slightly different<br />

from one child to another. It was surmised that degree of difficulty<br />

may not be the only criterion to be used when creat<strong>in</strong>g a progression.<br />

Key words: learn to swim, progression, rank order, degree of difficulty<br />

IntroductIon<br />

There rema<strong>in</strong>s disagreement among experts <strong>and</strong> organizations as to both<br />

content <strong>and</strong> rank<strong>in</strong>g of skills by degree of difficulty <strong>in</strong> teach<strong>in</strong>g beg<strong>in</strong>n<strong>in</strong>g<br />

swimm<strong>in</strong>g. If one attempts to ”teach first th<strong>in</strong>gs first” several factors<br />

must be considered. Before organiz<strong>in</strong>g skills accord<strong>in</strong>g to degree<br />

of difficulty, what skills to <strong>in</strong>cluded must first be considered. As stated<br />

above, there is as of 2010, no broad agreement. Traditionally however,<br />

such general statements as the follow<strong>in</strong>g have been broadly accepted:<br />

”Swimm<strong>in</strong>g, <strong>in</strong> contrast to other physical activities has a clear survival<br />

value” ( Junge, 1984)<br />

”Learn<strong>in</strong>g to swim should be part of every persons general education”<br />

(Langendorfer & Bruya, 1995)<br />

”The teach<strong>in</strong>g of swimm<strong>in</strong>g should produce <strong>in</strong>dependence/self dependence<br />

<strong>in</strong> the water”<br />

”The aim of swimm<strong>in</strong>g lessons is to help to prevent drown<strong>in</strong>g”<br />

”The ability to swim is reflected <strong>in</strong> how far one can move the body<br />

through the water”<br />

”Breath control is the key to water safety” (American Red Cross,<br />

1951; Lanoe, 1963)<br />

”A person who can swim is one who can cope with an unexpected<br />

submersion <strong>in</strong> the water” (Whit<strong>in</strong>g, 1971)<br />

We could go on with such statements; there are many. They may <strong>in</strong>deed<br />

be necessary as aims for organized teach<strong>in</strong>g <strong>and</strong> would be difficult to<br />

disagree with. They have become platitudes <strong>and</strong> will not take us to the<br />

next step.<br />

There does appear to be a trend among researchers <strong>and</strong> educational<br />

organizations l<strong>in</strong>k<strong>in</strong>g content <strong>in</strong> learn to swim with the causes of<br />

drown<strong>in</strong>g (Stallman, et al, 2008). The issue rema<strong>in</strong>s complex because of<br />

the discussion (among others) of the use of flotation devices. Inherent<br />

<strong>in</strong> this discussion is the philosophy one uses, i.e. how does one def<strong>in</strong>e<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

swimm<strong>in</strong>g, how does one th<strong>in</strong>k of swimm<strong>in</strong>g. Those who perceive swimm<strong>in</strong>g<br />

to be the use of the arms <strong>and</strong> legs to propel ones self forward<br />

may believe that the use of flotation devices allows earlier attention to<br />

the learn<strong>in</strong>g of propell<strong>in</strong>g movements. Those who believe swimm<strong>in</strong>g to<br />

be much more than only propulsion are normally <strong>in</strong> no hurry to start<br />

these ”correct swimm<strong>in</strong>g movements”. There is <strong>in</strong>creased agreement on<br />

breath control, buoyancy control, glid<strong>in</strong>g <strong>and</strong> postural control <strong>and</strong> strok<strong>in</strong>g<br />

skills. Also, all around development (watermanship) has enjoyed a<br />

revitalization with the concepts of ”aquatic read<strong>in</strong>ess” <strong>and</strong> ”water competence”.<br />

(Langendorfer & Bruya, 1995).<br />

The aims of this study were a) to create a theoretical progression of<br />

skills by implied degree of difficulty <strong>and</strong> b) to evaluate the rank order of<br />

these skills aga<strong>in</strong>st the actual rank order as demonstrated by the achievement<br />

of selected learners.<br />

Methods<br />

A progression of 19 skills was created by synthesiz<strong>in</strong>g the progressions<br />

of several well established national organizations, accord<strong>in</strong>g to implied<br />

degree of difficulty. These skills were categorized as follows:<br />

a. Breath hold<strong>in</strong>g, breath<strong>in</strong>g, breath control <strong>and</strong> submersion<br />

b. Float<strong>in</strong>g, buoyancy control, postural control<br />

c. Glid<strong>in</strong>g, posture <strong>and</strong> position control, feel<strong>in</strong>g motion <strong>and</strong> resistance<br />

d. Propulsive skills, feel<strong>in</strong>g grip (resistance on propulsive surfaces)<br />

Included <strong>in</strong> each of these categories, often as supplementary or <strong>in</strong>termediate<br />

goals <strong>and</strong> teach<strong>in</strong>g exercises, were skills of orientation, balance<br />

<strong>and</strong> rotation.<br />

Pre-school children, aged 5 & 6 years were selected from 13 k<strong>in</strong>dergartens.<br />

Inclusion criteria were a) m<strong>in</strong>imum height 1.15m, b) previous<br />

experience <strong>in</strong> k<strong>in</strong>dergarten, c) could not swim 5m. Of the 146 children<br />

who started the program, 116 met the 4th criterion of a m<strong>in</strong>imum of<br />

50% participation <strong>and</strong> were <strong>in</strong>cluded <strong>in</strong> the analysis for degree of difficulty.<br />

The <strong>in</strong>structional period consisted of 18 hrs., some groups meet<strong>in</strong>g<br />

once per week, others twice per week. The data for these two groups<br />

were pooled when subsequent analysis showed no difference <strong>in</strong> learn<strong>in</strong>g<br />

progress. Instruction was given <strong>in</strong> small groups with 6-8 children <strong>and</strong><br />

no more than 3 groups <strong>in</strong> the pool simultaneously. A s<strong>in</strong>gle head <strong>in</strong>structor<br />

controlled all teach<strong>in</strong>g <strong>and</strong> especially the record<strong>in</strong>g of successful<br />

completion of each test criterion skill.<br />

The actual rank order of skills by degree of difficulty as shown by<br />

these learners progress was deemed reflected <strong>in</strong> the number of children<br />

who succeeded on each skill. The theoretical rank order of skills was<br />

compared to the actual rank order us<strong>in</strong>g Spearman’s rank order correlation.<br />

results<br />

Table 1 shows the theoretical rank order of skills <strong>in</strong> column one. Column<br />

2 shows the actual rank order as reflected <strong>in</strong> the total number of<br />

children (<strong>in</strong> parentheses) who mastered each skill.<br />

The rank correlation between these two progressions was Rho = 0.97,<br />

<strong>in</strong>dicat<strong>in</strong>g a very strong relationship. While the difference appears to be<br />

m<strong>in</strong>imal, there were <strong>in</strong> fact 7 of the 19 skills which differ <strong>in</strong> rank order<br />

from the theoretical progression.<br />

The first example of deviation is found already <strong>in</strong> steps 1-3 where<br />

submerg<strong>in</strong>g the head <strong>and</strong> hold<strong>in</strong>g the breath for 10 sec. seems to be<br />

more difficult than both rhythmic breath<strong>in</strong>g <strong>and</strong> jump <strong>and</strong> submerge.<br />

The next notable deviation was that it appears that front glide was easier<br />

<strong>and</strong> front kick glide was at least as easy as float on the back. Roll<strong>in</strong>g from<br />

front to back <strong>and</strong> vice versa was more difficult than both front glide <strong>and</strong><br />

back glide.<br />

329


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 1 Theoretical <strong>and</strong> Actual Rank Order<br />

Progressive Skills & Criterion, Theoretical rank order Actual Order (n)<br />

1. Head under water, 10 sec 3 (97)<br />

2. Rhythmic breath<strong>in</strong>g, 10 reps 1.5 (102)<br />

3.Jump to head under water 1.5 (102)<br />

4. Float on front, 15 sec 4 (90)<br />

5. Float on back, 15 sec 6.5 (64)<br />

6. Roll front to back <strong>and</strong> vice versa 9 (60)<br />

7. Front glide, 5 m 5 (79)<br />

8. Back glide, 5 m 8 (61)<br />

9. Kick glide (front or back), 5 m 6.5 (64)<br />

10. Front kick glide, 10 m 10 (50)<br />

11. Back kick glide,10 m 12 (34)<br />

12. Jump <strong>and</strong> float up (front & back) 11 (36)<br />

13. Beg<strong>in</strong>n<strong>in</strong>g armstroke on front10 m 13 (29)<br />

14. Beg<strong>in</strong>n<strong>in</strong>g armstroke on back10 m 14.5 (26)<br />

15. Beg<strong>in</strong>n<strong>in</strong>g swim on front with rhythmic breath<strong>in</strong>g10m 14.5 (26)<br />

16. Beg<strong>in</strong>n<strong>in</strong>g swim on back with rhythmic breath<strong>in</strong>g10 m 16 (24)<br />

17. Change direction, L & R, Front & Back 17 (23)<br />

18. Rest <strong>in</strong> deep water (Fr & bk, m<strong>in</strong>imal movement. 30 sec 18.5 (17)<br />

19. Comb<strong>in</strong>ed test ( Jump, 12.5 fr; rest 30 sec; turn, 12.5 back 18.5 (17)<br />

In every case where the skills are paired front <strong>and</strong> back (Nrs. 4 & 5, 7 &<br />

8, 10 & 11, 13 & 14, 15 & 16) execut<strong>in</strong>g the skill on the front was easier<br />

than the same skill on the back.<br />

Lastly, when consider<strong>in</strong>g the proportional success on the above<br />

named paired skills, the most dramatic was that 84% learned to float<br />

on the front first <strong>and</strong> later on the back. The apparent relative ease of the<br />

prone position dim<strong>in</strong>ished <strong>in</strong> the follow<strong>in</strong>g paired skills systematically<br />

<strong>and</strong> was virtually non existent by 15 & 16, beg<strong>in</strong>n<strong>in</strong>g swim on the front<br />

<strong>and</strong> back (10m).<br />

dIscussIon<br />

The Rho of 0.97 suggests that there may be no statistical need to alter<br />

the theoretical rank order. Such a high Rho must however, be taken<br />

cautiously. One of the variables was fixed <strong>in</strong> ascend<strong>in</strong>g order. Other<br />

confound<strong>in</strong>g factors may have <strong>in</strong>fluenced the results. The deviations described<br />

also <strong>in</strong>vite discussion regard<strong>in</strong>g possible adjustments for pedagogical<br />

reasons. Extremely <strong>in</strong>terest<strong>in</strong>g arguments for <strong>and</strong> aga<strong>in</strong>st can<br />

be made. There may be several factors which should be debated <strong>in</strong> this<br />

<strong>in</strong>stance.<br />

First <strong>and</strong> most important, children are so different that no progression<br />

will suit all. Us<strong>in</strong>g the example of float<strong>in</strong>g, the theoretical rank order<br />

proved to be correct for 84 % of the children tested. It was not correct<br />

for the rema<strong>in</strong><strong>in</strong>g 16%. For these children it was entirely normal to learn<br />

to float on the back first. For them, the rank order was <strong>in</strong> fact, adjusted<br />

by these children themselves. They showed the way. Thus, while less frequent,<br />

this development is by no means abnormal. The consequence of<br />

this situation is simply that the <strong>in</strong>structor would be well advised to start<br />

with front float but immediately when some have difficulty, suspect that<br />

they may belong to the 16% <strong>and</strong> give back float a try.<br />

The second factor is the concept of build<strong>in</strong>g blocks or aquatic read<strong>in</strong>ess<br />

(Langendorfer & Bruya, 1995). Here the first 3 skills <strong>and</strong> their relationship<br />

to both 4 & 5, as well as the rema<strong>in</strong><strong>in</strong>g paired skills may best<br />

exemplify this concept. Item 1 appeared to be more difficult than both<br />

2 <strong>and</strong> 3. It may be that the difficulty lies not <strong>in</strong> the relaxed submerg<strong>in</strong>g<br />

but <strong>in</strong> the 10 sec. criterion. If breath hold<strong>in</strong>g for 10 sec or even longer<br />

330<br />

may <strong>in</strong> some ways be a prerequisite for what comes later, perhaps one<br />

needs simply to spend more time on this item until it is more thoroughly<br />

mastered, before proceed<strong>in</strong>g. It is entirely possible that both rhythmic<br />

breath<strong>in</strong>g <strong>and</strong> jump <strong>and</strong> submerge would have reached a higher level<br />

had more time been spent on breath hold<strong>in</strong>g. Also to master float<strong>in</strong>g<br />

on the front for 15 sec. one has a good start if mak<strong>in</strong>g sure that 10 sec.<br />

along the way is easily manageable. Note that several of the follow<strong>in</strong>g<br />

paired skills are also dependent on breath hold<strong>in</strong>g/breath control. We<br />

might also speculate that the apparent difficulty with back float was <strong>in</strong><br />

some way connected with the level of competence atta<strong>in</strong>ed on the first<br />

four items. When the <strong>in</strong>structor is faced with a learner who struggles a<br />

bit with front or back float, it may not be the relationship between these<br />

two that is the problem but <strong>in</strong>sufficient mastery of the first three skills.<br />

The same could be said for roll<strong>in</strong>g from front to back <strong>and</strong> vice versa (nr.<br />

6). F<strong>in</strong>ally, when both front <strong>and</strong> back glide were easier than roll<strong>in</strong>g over,<br />

it can be assumed that tra<strong>in</strong><strong>in</strong>g on the glide also improved those factors<br />

upon which roll<strong>in</strong>g depends. The question then is simply, should one<br />

dwell a bit longer on front <strong>and</strong> back float, present them <strong>in</strong> greater variety<br />

or delay roll<strong>in</strong>g from front to back until after glid<strong>in</strong>g has been mastered?<br />

The third factor which presents the opportunity for reflection is the<br />

concept of balanced progress. Skills are normally acquired <strong>in</strong> an overlapp<strong>in</strong>g<br />

fashion. It is recommended to work on several skills at a time. This<br />

also allows greater flexibility for the learners to f<strong>in</strong>d their own way, their<br />

own correct progression. If one were to strictly follow the rank order as<br />

shown by the subjects <strong>in</strong> this study, one would move from front float<br />

to front glide <strong>and</strong> to front kick glide, all of which appeared to be easier<br />

than back float. An argument <strong>in</strong> favor of this might be that they are sufficiently<br />

related that they <strong>in</strong>vite transfer of learn<strong>in</strong>g <strong>and</strong> that this order<br />

would be easily understood by learners. If one followed such a course,<br />

one would then do the same on the back. A counter argument might be<br />

that if one could stop the clock <strong>in</strong> a learners progress, one might ask ”at<br />

this po<strong>in</strong>t <strong>in</strong> time, what comb<strong>in</strong>ation of skills would make our learner<br />

most safe?” One answer might be that hav<strong>in</strong>g some similar degree of<br />

proficiency on both back <strong>and</strong> front, at any given time, has a specific<br />

survival value.<br />

conclusIons<br />

It is possible to f<strong>in</strong>d the optimal progression for any learner. S<strong>in</strong>ce learners<br />

differ considerably, the <strong>in</strong>structor must be prepared for <strong>in</strong>dividualization.<br />

This is most easily done if the learners themselves are <strong>in</strong>volved <strong>in</strong><br />

certa<strong>in</strong> decision mak<strong>in</strong>g. When work<strong>in</strong>g on several related skills or skills<br />

of similar difficulty at the same time, the child will show the way. It is<br />

also well known that participation is greater when the child is <strong>in</strong>volved<br />

<strong>in</strong> decid<strong>in</strong>g. It is not a burden to cater to such <strong>in</strong>dividualization. It may<br />

<strong>in</strong> fact, make our job easier, by <strong>in</strong>creas<strong>in</strong>g motivation <strong>and</strong> by help<strong>in</strong>g<br />

each <strong>in</strong>dividual child f<strong>in</strong>d their own optimal progression. F<strong>in</strong>ally, other<br />

factors than simply degree of difficulty may be important <strong>in</strong> construct<strong>in</strong>g<br />

a progression.<br />

reFerences<br />

American Red Cross (1951). ARC Water Safety: Information brochure.<br />

Wash<strong>in</strong>gton D.C.<br />

Junge, M., (1984). Begynneropplær<strong>in</strong>g I svømm<strong>in</strong>g [Teach<strong>in</strong>g swimm<strong>in</strong>g].<br />

Unpublished MSc. Thesis. Norwegian School of Sport Science,<br />

Oslo<br />

Langendorfer, S.J., Bruya, L.D. (1995). Aquatic read<strong>in</strong>ess, Champaign,<br />

IL: Human K<strong>in</strong>etics<br />

Lanoe, F. (1963). Drownproof<strong>in</strong>g, Englewood Cliffs, NJ: Prentis-Hall<br />

Stallman, R.K., Junge, M., Blixt, T. (2008). The teach<strong>in</strong>g of swimm<strong>in</strong>g<br />

based on a model derived from the causes of drown<strong>in</strong>g. Int. J of<br />

Aquatic Research <strong>and</strong> Education, 2(4), 372-382.<br />

Whit<strong>in</strong>g, H.T.A., (1971). The persistent non-swimmer, London, Museum<br />

Press


The Construct Validity of a Traditional 25m Test of<br />

Swimm<strong>in</strong>g Competence<br />

Junge, M. 1,3 , Blixt, t. 2 , stallman, r.K. 1,4<br />

1 Norwegian School of Sport Science,<br />

2 Norwegian Swimm<strong>in</strong>g Federation,<br />

3 University of Oslo,<br />

4 Norwegian Life Sav<strong>in</strong>g Association<br />

A universal def<strong>in</strong>ition of the ability to swim has yet to be agreed upon.<br />

Some believe that “how far” one swims is the most important criterion.<br />

The number of meters is controversial. Some use a traditional def<strong>in</strong>ition<br />

of from 25m to 200m, often as the only criterion of “can swim”. In fact,<br />

this is not the po<strong>in</strong>t. A conceptual model emphasizes broader competence.<br />

The result of this model is a comb<strong>in</strong>ed test <strong>in</strong>clud<strong>in</strong>g more than only distance.<br />

This comb<strong>in</strong>ed test was used as the criterion to test the construct validity<br />

of a traditional test. When these two tests were compared they were<br />

found to be very different, thus measur<strong>in</strong>g different qualities. Among<br />

children already declared able to swim by the traditional test, only 5.7%<br />

satisfied the conditions of the conceptual test. It was concluded that the<br />

traditional test was not a valid measure of the ability to swim.<br />

Key words: evaluation, swimm<strong>in</strong>g competence, validity, distance test<br />

IntroductIon<br />

Learn to swim programs rema<strong>in</strong> dramatically different <strong>in</strong> their content<br />

<strong>and</strong> <strong>in</strong> the manner <strong>in</strong> which the learner’s progress is evaluated, <strong>in</strong> other<br />

words, by which criteria a child is judged “able to swim”. There is fortunately,<br />

grow<strong>in</strong>g agreement among researchers <strong>and</strong> educators on the<br />

importance of a) breath hold<strong>in</strong>g, breath control, b) float<strong>in</strong>g, buoyancy<br />

control, c) glid<strong>in</strong>g <strong>and</strong> postural control, <strong>and</strong> d) strok<strong>in</strong>g <strong>and</strong> directional<br />

control, as well as orientation, balance <strong>and</strong> rotation (Stallman, et al,<br />

2008). These are seen as essential, core elements. There rema<strong>in</strong> however,<br />

many ideas about how <strong>and</strong> what a child should learn. The less experienced<br />

person (school teacher who is not a swimm<strong>in</strong>g <strong>in</strong>structor, parent,<br />

significant other) is more prone to fall prey to misconceptions. In<br />

a recent Sc<strong>and</strong><strong>in</strong>avian questionnaire <strong>in</strong>vestigation, it was revealed that<br />

almost every primary school head master had her/his own def<strong>in</strong>ition<br />

(Directory of Education, Norway, 2008).<br />

There also rema<strong>in</strong>s a traditional notion that the number of meters<br />

achieved is the only or most important criterion for def<strong>in</strong><strong>in</strong>g the ability<br />

to swim. This is especially true among parents but sadly, rema<strong>in</strong>s common<br />

also among certa<strong>in</strong> swimm<strong>in</strong>g <strong>in</strong>structors. A common compla<strong>in</strong>t<br />

is that “we don’t have enough time”. The result is often a s<strong>in</strong>gle selected<br />

stroke <strong>and</strong> a pre-determ<strong>in</strong>ed distance (Directory of Education, Norway,<br />

2008). The notion that some form of all around development is more<br />

important than simply a certa<strong>in</strong> number of meters seems to have escaped<br />

closer scrut<strong>in</strong>y. A number of well known <strong>and</strong> respected national<br />

agencies (e.g. The American Red Cross, The German Life Sav<strong>in</strong>g Association,<br />

etc.) have long emphasized all-around development as essential<br />

<strong>in</strong> drown<strong>in</strong>g prevention. The concepts of “watermanship” or “aquatic<br />

competence” are well known (S<strong>in</strong>clair & Henry, 1893, Langendorfer &<br />

Bruya 1995). Both Cureton (1943) <strong>and</strong> the USA Navy (1943), emphasized<br />

that drown<strong>in</strong>g can take many forms, <strong>and</strong> that these are unpredictable.<br />

Therefore, many solutions (all-around development) are necessary<br />

to solve many possible life threaten<strong>in</strong>g situations.<br />

When consider<strong>in</strong>g the ultimate negative outcome of an aquatic “episode”<br />

(death by drown<strong>in</strong>g) it is clear that a variety of skills is required to<br />

cope with the wide variety of possible situations <strong>in</strong> which an unsuspect<strong>in</strong>g<br />

person might f<strong>in</strong>d themselves – <strong>in</strong> the water. It surely is obvious<br />

then that, one stroke or one distance is not sufficient. Unfortunately,<br />

some still appear to believe it is. And the discussion goes on, 25m, 100m,<br />

200m? And of course, whatever conclusions one reaches about skills, we<br />

also tend to neglect knowledge, attitude <strong>and</strong> judgment.<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

The motive for this study was thus to exam<strong>in</strong>e the idea that it is not<br />

how far but how one swims that really matters. The aim of this study is<br />

thus, to exam<strong>in</strong>e the construct validity of a 25m test of swimm<strong>in</strong>g competence<br />

by compar<strong>in</strong>g it with a criterion comb<strong>in</strong>ed test, ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the<br />

same overall distance on both. It was also assumed that the same results<br />

would appear if a different distance had been chosen. For example, that<br />

a traditional test of 200m with s<strong>in</strong>gle stroke is not the same as a 200m<br />

comb<strong>in</strong>ed test with the same pattern as the shorter comb<strong>in</strong>ed test.<br />

Method<br />

From among 200 primary school children, age 9&10 years, taught <strong>in</strong> a<br />

s<strong>in</strong>gle school term, 70 succeeded <strong>in</strong> the local traditional test of negotiat<strong>in</strong>g<br />

25m with no other criteria. These 70 were declared “able to swim”, awarded<br />

a p<strong>in</strong> <strong>and</strong> the parents were notified that their child could swim. These<br />

children (N=70) constituted the subjects of this study. By perform<strong>in</strong>g a<br />

second test, with<strong>in</strong> 3 days of the first, they served as their own controls.<br />

The criterion “comb<strong>in</strong>ed test” consisted of: a) jump or dive <strong>in</strong>to deep<br />

water (3m), level off, b) swim 12.5 m <strong>in</strong> the prone position c) turn 180<br />

degrees, d) roll over e) rest for 30 sec with m<strong>in</strong>imal movement, f ) swim<br />

back to the start<strong>in</strong>g po<strong>in</strong>t <strong>in</strong> the sup<strong>in</strong>e position. Div<strong>in</strong>g was awarded<br />

two po<strong>in</strong>ts, jump one po<strong>in</strong>t <strong>and</strong> 0 for those who refused both jump <strong>and</strong><br />

dive. Each of the other elements was awarded two po<strong>in</strong>ts. The maximum<br />

possible score was thus 12 po<strong>in</strong>ts. The total distance was the same for<br />

both tests but the criterion test was obviously more comprehensive, <strong>in</strong>cluded<br />

a more balanced skill profile.<br />

The children were motivated by be<strong>in</strong>g offered a second, new award.<br />

No mention was made of the second test be<strong>in</strong>g a test of swimm<strong>in</strong>g ability<br />

nor was it implied that the first test was anyth<strong>in</strong>g other than what<br />

they had believed it to be. To any direct question, the second test was<br />

simply referred to as a “new” test, <strong>and</strong> new award; swim or swim better.<br />

The children were tested by their own teacher to avoid bias by alter<strong>in</strong>g<br />

the atmosphere. The observers who evaluated the performance were<br />

known to the children. The children were tested four at a time <strong>and</strong> each<br />

of two observers was assigned to two children. The same observers evaluated<br />

all of the subjects. Pilot test<strong>in</strong>g was conducted to tra<strong>in</strong> the observers.<br />

Discussions were held to ensure that both observers used the same criteria.<br />

A head <strong>in</strong>structor coord<strong>in</strong>ated all evaluation <strong>and</strong> made the f<strong>in</strong>al decision<br />

<strong>in</strong> any case not obvious <strong>in</strong> its outcome. Each element was scored <strong>and</strong> the<br />

total score was recorded. The results were tabulated by frequency distribution<br />

<strong>and</strong> both the number <strong>and</strong> percent of subjects succeed<strong>in</strong>g on each<br />

element was recorded. The total scores were also recorded<br />

The criterion test was the result of a construct, i.e. a conceptual construction<br />

based on the logical arguments cited above. If these two tests<br />

gave similar results, the traditional test would be accepted as hav<strong>in</strong>g<br />

construct validity. If the two tests differed they would be considered to<br />

measure different qualities <strong>and</strong> the traditional test would be considered<br />

not to have construct validity.<br />

results<br />

Table 1 shows the results by element. The results clearly show that all<br />

but the one element reproduced also on the first test, were not mastered<br />

by many of the children.<br />

Table 1 Success by element on the comb<strong>in</strong>ed criterion test<br />

Test Item Number (n = 70) %<br />

1. Dive 16 23<br />

Jump 36 51<br />

Start <strong>in</strong> water 18 26<br />

2. Swim 12.5m prone 70 100<br />

3. Change direction 1800 63 90<br />

4. Roll over 40 57<br />

5. Stop & rest 30 sec. 4 6<br />

6. Swim 12.5m sup<strong>in</strong>e 36 51<br />

331


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

As would be expected, 100% of the children who had already swum<br />

25m on the front, succeeded <strong>in</strong> swimm<strong>in</strong>g 12.5m on the front. However<br />

from that po<strong>in</strong>t on, fewer managed the other elements. Twenty six<br />

percent refused to either jump or dive <strong>in</strong>to deep water, ask<strong>in</strong>g to start <strong>in</strong><br />

the water. Ten percent did not manage to change direction. Forty three<br />

percent were unable to roll over. Forty n<strong>in</strong>e percent were unable to swim<br />

on the back. And lowest of all, only 5.7% managed to stop <strong>and</strong> rest, even<br />

for only 30 seconds.<br />

The range of total scores was from 4 to 12. Only four of these pupils<br />

scored 11 or 12 po<strong>in</strong>ts, i.e. by the criterion test, could swim.<br />

dIscussIon<br />

The real issues here are, how do we evaluate whether a child can swim<br />

or not, <strong>and</strong> can a simple distance test serve the need to evaluate. To<br />

return to the idea that it is how one swims rather than how far, we<br />

must forsake traditional ideas of any given distance. Some <strong>in</strong>sist on 25m,<br />

some on 200m, others are somewhere <strong>in</strong> between. It can be remembered<br />

that the Scout<strong>in</strong>g movement has long operated with a 200yd (ca 180m)<br />

m<strong>in</strong>imum before permitt<strong>in</strong>g boat<strong>in</strong>g activities (Scout H<strong>and</strong>book, 1956).<br />

Several national life sav<strong>in</strong>g organizations also have a tradition of focus<strong>in</strong>g<br />

on 200m or 200 yds. In some cases, no other criteria are used. Can it<br />

be that one who can swim 200m but not 201m, can swim? How safe is<br />

this person? How are they prepared for the many possible scenarios one<br />

might be victim to <strong>in</strong> an <strong>in</strong>voluntary submersion?<br />

The results of this study show clearly that the two tests considered,<br />

measure different qualities. Be<strong>in</strong>g able to swim 25m non-stop on the<br />

front does not automatically give one the ability to swim <strong>in</strong> the back,<br />

turn, roll over, stop <strong>and</strong> rest or jump or dive <strong>in</strong>to the water. (if an emergency<br />

required one to swim on the back or to stop <strong>and</strong> rest (gather<br />

ones wits, catch the breath, settle down, re-orient oneself ) as it might<br />

well do, these subjects would be <strong>in</strong> serious difficulty. They are clearly,<br />

not <strong>Biomechanics</strong> as safe as they <strong>and</strong> might <strong>Medic<strong>in</strong>e</strong> have <strong>in</strong> been Swimm<strong>in</strong>g if they <strong>XI</strong> had mastered the criterion<br />

54<br />

Chapter 5 Education, Advice <strong>and</strong> Biofeedback<br />

test. Consider the statistic cited by Golden <strong>and</strong> Tipton (2002), that ><br />

40% of drown<strong>in</strong>gs <strong>in</strong> the UK happen with<strong>in</strong> 3m of safety. The logically<br />

match<strong>in</strong>g give one scenario the ability would to swim require <strong>in</strong> the back, victim turn, to turn roll over, around stop <strong>and</strong> <strong>and</strong> make rest or jump or dive<br />

their <strong>in</strong>to way the water. back to (if safety. an emergency Cold shock required also first one described to swim clearly on the by back these or to stop <strong>and</strong> rest<br />

same<br />

(gather<br />

authors,<br />

ones wits,<br />

operat<strong>in</strong>g<br />

catch<br />

with<strong>in</strong><br />

the breath,<br />

seconds<br />

settle<br />

of submersion<br />

down, re-orient<br />

<strong>and</strong> dramatically<br />

oneself) as it might well do,<br />

these subjects would be <strong>in</strong> serious difficulty. They are clearly, not as safe as they might<br />

rais<strong>in</strong>g the respiration rate, reduc<strong>in</strong>g air exchange <strong>and</strong> rais<strong>in</strong>g the HR,<br />

have been if they had mastered the criterion test. Consider the statistic cited by Golden<br />

requires <strong>and</strong> Tipton clearly (2002), the quality that > 40% of be<strong>in</strong>g of drown<strong>in</strong>gs able to stop, <strong>in</strong> the rest, UK take happen stock, with<strong>in</strong> catch 3m of safety. The<br />

the logically breath, match<strong>in</strong>g etc. It rema<strong>in</strong>s scenario a mystery would to require us that the the victim ability to to turn stop around <strong>and</strong> rest <strong>and</strong> make their way<br />

is back so often to safety. ignored Cold or underestimated.<br />

shock also first described clearly by these same authors, operat<strong>in</strong>g<br />

with<strong>in</strong> To accommodate seconds of submersion the desire <strong>and</strong> to keep dramatically some semblance rais<strong>in</strong>g the of distance respiration as rate, reduc<strong>in</strong>g air<br />

a exchange useful skill <strong>and</strong> (attitude?), rais<strong>in</strong>g the it HR, is only requires logical clearly to suggest the quality that of the be<strong>in</strong>g criterion able to stop, rest, take<br />

comb<strong>in</strong>ed stock, catch test the exam<strong>in</strong>ed breath, etc. <strong>in</strong> this It rema<strong>in</strong>s study, can a mystery easily be to exp<strong>and</strong>ed us that the to ability greater to stop <strong>and</strong> rest is<br />

so often ignored or underestimated.<br />

distance while reta<strong>in</strong><strong>in</strong>g the same pattern. An example might be a total<br />

To accommodate the desire to keep some semblance of distance as a useful skill<br />

of (attitude?), 100m (50 it + 50) is only with logical a 60 sec. to rest suggest <strong>and</strong> perhaps that the a criterion more dem<strong>and</strong><strong>in</strong>g comb<strong>in</strong>ed way test exam<strong>in</strong>ed <strong>in</strong> this<br />

to study, fall <strong>in</strong>to can the easily water, be or exp<strong>and</strong>ed 200m (100 to greater + 100) distance with a 3 while m<strong>in</strong> rest. reta<strong>in</strong><strong>in</strong>g Cloth<strong>in</strong>g the same pattern. An<br />

could example (<strong>and</strong> might should) be be a total added of to 100m <strong>in</strong>crease (50 the + 50) challenge. with a 60 Stallman, sec. rest et <strong>and</strong> al. perhaps a more<br />

(2008) dem<strong>and</strong><strong>in</strong>g <strong>in</strong>troduced way to the fall idea <strong>in</strong>to that the “Can water, Swim” or 200m is not (100 a sharp + 100) demarcation with a 3 m<strong>in</strong> rest. Cloth<strong>in</strong>g<br />

from could “Cannot (<strong>and</strong> should) Swim” be but added rather to <strong>in</strong>crease a zone <strong>in</strong> the which challenge. we can Stallman, describe et can al. (2008) <strong>in</strong>troduced<br />

swim the idea at a that m<strong>in</strong>imal “Can level Swim” <strong>and</strong> is progressively not a sharp at demarcation higher levels. from Can “Cannot <strong>and</strong> Can Swim” but rather a<br />

Better.<br />

zone <strong>in</strong><br />

See<br />

which<br />

Fig 1.<br />

we can describe can swim at a m<strong>in</strong>imal level <strong>and</strong> progressively at higher<br />

levels. Can <strong>and</strong> Can Better. See Fig 1.<br />

T-shirt shirt trousers shirt & trousers etc<br />

2 strokes 3 strokes 4 strokes 5 strokes, etc<br />

30 sec rest 1m<strong>in</strong> rest 2 m<strong>in</strong> rest 3 m<strong>in</strong> rest, etc<br />

25m 50m 100m 200m etc<br />

Fig.<br />

Fig.<br />

1 A graded<br />

graded<br />

approach<br />

approach<br />

to<br />

to<br />

“Can<br />

“Can<br />

Swim”<br />

Swim”<br />

In Northern Europe there exists a certa<strong>in</strong> feel<strong>in</strong>g about swimm<strong>in</strong>g on the back,<br />

<strong>in</strong>sist<strong>in</strong>g for example that <strong>in</strong> a 200m test, only 50 need be on the back. This is to<br />

332 denigrate the value of a life preserv<strong>in</strong>g skill. And often no other criteria are used. The<br />

comb<strong>in</strong>ed test approach presented here as a construct, is a balanced one.<br />

To focus on any distance is to avoid the issue. It is not a question of how far or<br />

which stroke. The child who is relaxed <strong>in</strong> the water <strong>and</strong> uses their natural buoyancy, is<br />

In Northern Europe there exists a certa<strong>in</strong> feel<strong>in</strong>g about swimm<strong>in</strong>g on<br />

the back, <strong>in</strong>sist<strong>in</strong>g for example that <strong>in</strong> a 200m test, only 50 need be on<br />

the back. This is to denigrate the value of a life preserv<strong>in</strong>g skill. And<br />

often no other criteria are used. The comb<strong>in</strong>ed test approach presented<br />

here as a construct, is a balanced one.<br />

To focus on any distance is to avoid the issue. It is not a question of<br />

how far or which stroke. The child who is relaxed <strong>in</strong> the water <strong>and</strong> uses<br />

their natural buoyancy, is able to control breath<strong>in</strong>g, is able to stop <strong>and</strong><br />

rest, is safer at 25m than the child who can swim 100m but does so only<br />

non-stop <strong>and</strong> with great effort. The first named child can swim 25, stop<br />

<strong>and</strong> rest, swim 25 more, etc <strong>and</strong> soon accumulates a greater distance<br />

than her/his counterpart. Those who focus on distance only, see only the<br />

result <strong>and</strong> lose sight of the process. Here the reader is rem<strong>in</strong>ded that a<br />

common attitude among less experienced <strong>in</strong>structors is that technique<br />

is not important, most children never become competitive swimmers.<br />

The real issue however is that economy of effort is often a matter of life<br />

<strong>and</strong> death. Technique <strong>in</strong> fact, when we consider sav<strong>in</strong>g energy by more<br />

efficient movement, not overcom<strong>in</strong>g the powers of nature but work<strong>in</strong>g<br />

<strong>in</strong> harmony with them, is the most valuable of survival skills.<br />

There can be little doubt that the ability to swim 200m <strong>in</strong>doors <strong>in</strong> a<br />

warm quiet pool, is no guarantee that one can swim the same distance<br />

outdoors, <strong>in</strong> colder <strong>and</strong> restless, open water, <strong>and</strong> perhaps fully clothed.<br />

But at what ever distance one arrests the learner’s progress, <strong>in</strong> a laboratory<br />

slice of life to be exam<strong>in</strong>ed under the microscope, the pattern of<br />

versatility should be reta<strong>in</strong>ed. Each element would then be <strong>in</strong>creased to<br />

a higher level of challenge.<br />

conclusIons<br />

The distance test of 25m, with no other criteria, measures different qual-<br />

ities than the slightly more comprehensive comb<strong>in</strong>ed criterion test. If we<br />

accept the construct validity of the criterion test, the traditional test is<br />

necessarily judged not to have construct validity.<br />

reFerences<br />

Cureton, T.K. (1943). Warfare Aquatics, Champaign, IL, Stipes Pub.<br />

Directory of Education, M<strong>in</strong>istry of Education, Norway (2008). The<br />

Teach<strong>in</strong>g of Swimm<strong>in</strong>g <strong>and</strong> Life Sav<strong>in</strong>g; Support materials for teachers<br />

<strong>and</strong> <strong>in</strong>structors <strong>in</strong> the primary school. Oslo, Norway<br />

Golden, F. <strong>and</strong> Tipton, M. (2002). The Essentials of Sea Survival, Champaign,<br />

IL. Human K<strong>in</strong>etics<br />

Higg<strong>in</strong>s J., et al. (1943). Swimm<strong>in</strong>g <strong>and</strong> Div<strong>in</strong>g. The United States Navy.<br />

United States naval Institute, Annapolis, MD<br />

H<strong>in</strong>es, F. (ed) (1978). The Scout H<strong>and</strong>book, Boy Scouts of America, N.Y.<br />

Hurt, H.W. (ed) (1910). H<strong>and</strong>book for Boys, Boy Scouts of America, N.Y.<br />

Langendorfer, S.J. <strong>and</strong> Bruya, L.D. (1995). Aquatic read<strong>in</strong>ess. Champaign,<br />

IL, Human K<strong>in</strong>etics<br />

S<strong>in</strong>clair A. <strong>and</strong> Henry W. (1893). Swimm<strong>in</strong>g, London, Longmans<br />

Stallman R.K., Junge M., Blixt T., (2008). The teach<strong>in</strong>g of swimm<strong>in</strong>g<br />

based on a model derived from the causes of drown<strong>in</strong>g. Int J of Aquatic<br />

Research <strong>and</strong> Educ, 2(4), 372-382


Us<strong>in</strong>g a Scalogram to Identify an Appropriate<br />

Instructional Order for Swimm<strong>in</strong>g Items<br />

langendorfer, s.J. 1 , chaya, J.A. 2<br />

1 Bowl<strong>in</strong>g Green State University<br />

2 University of Toledo<br />

Scalogram, first proposed by Guttman (1950), is a descriptive order<strong>in</strong>g<br />

technique used <strong>in</strong> the social sciences to <strong>in</strong>vestigate how heterogeneous<br />

behavioral items may relate to one another <strong>in</strong> time. In the present study,<br />

we explored whether there was a predictable order of acquisition among<br />

selected swim skill items used <strong>in</strong> the <strong>in</strong>struction of swimm<strong>in</strong>g. If so, we<br />

might identify a preferred order <strong>in</strong> which to teach these swim skills.<br />

A convenience sample of thirty-one college students enrolled <strong>in</strong> University<br />

<strong>in</strong>structional swimm<strong>in</strong>g classes performed each of the items <strong>in</strong><br />

r<strong>and</strong>om order while <strong>in</strong>vestigators videotaped each performance. After<br />

establish<strong>in</strong>g <strong>in</strong>ter-observer objectivity exceed<strong>in</strong>g P > 0.80, the <strong>in</strong>vestigators<br />

observed each video trial <strong>and</strong> scored each item for each participant<br />

as pass-fail us<strong>in</strong>g pre-established criteria based on the American Red<br />

Cross Swimm<strong>in</strong>g <strong>and</strong> Water Safety learn-to-swim program (Red Cross,<br />

2004). The Red Cross order for teach<strong>in</strong>g the tested skills was confirmed<br />

as the best order identified by the scalogram for young adult participants<br />

with a coefficient of reproducibility of CR = 0.93. Limitations <strong>in</strong> the<br />

procedures <strong>and</strong> results suggested the need for several future studies to<br />

identify whether the order applied to other ages <strong>and</strong> ability levels as well<br />

as how susceptible the scalogram technique is to vary<strong>in</strong>g <strong>in</strong>structional<br />

experiences of participants.<br />

Keywords: swim <strong>in</strong>struction, swimm<strong>in</strong>g skills, scalogram, developmental<br />

sequences<br />

IntroductIon<br />

The order <strong>in</strong> which different human behaviors are acquired has a long<br />

history of scholarly <strong>in</strong>terest. Charles Darw<strong>in</strong>, <strong>in</strong> his “Biography of a<br />

Baby,” chronicled the behaviors <strong>and</strong> ages he observed his son acquire<br />

typical “motor milestones” (Darw<strong>in</strong>, 1877). Jean Piaget, the noted developmental<br />

psychologist <strong>and</strong> epistemologist, provided detailed descriptions<br />

of the order <strong>in</strong> which his own three children acquired various<br />

psychomotor, cognitive, <strong>and</strong> social behaviors dur<strong>in</strong>g childhood (Piaget,<br />

1973). Dur<strong>in</strong>g the heyday of <strong>in</strong>fant motor development, developmental<br />

researchers such as Arnold Gesell (1940), Mary Shirley (1931), <strong>and</strong><br />

Myrtle McGraw (1939; 1963; 1975) all proposed different sequences of<br />

<strong>in</strong>fant behaviors. McGraw, specifically, focused on the description <strong>and</strong><br />

order <strong>in</strong> which <strong>in</strong>fant swimm<strong>in</strong>g behavior changes progressively over<br />

time (McGraw, 1939).<br />

The order with which <strong>in</strong>dividuals acquire different skills has implications<br />

<strong>and</strong> importance to different cl<strong>in</strong>icians <strong>and</strong> practitioners such as<br />

teachers <strong>and</strong> coaches. The logic is that easier tasks should be <strong>in</strong>troduced<br />

or taught first. The basis for the developmental task analysis (Herkowitz,<br />

1978; Roberton, 1989) or constra<strong>in</strong>ts-based task analysis approach<br />

(Haywood & Getchell, 2009) uses a similar logic for structur<strong>in</strong>g motor<br />

skills. Developmental task analysis separates motor task factors <strong>and</strong><br />

then organizes them accord<strong>in</strong>g to the levels of complexity. In the developmental<br />

task analysis scheme, <strong>in</strong>experienced performers encounter<br />

the least complex movement task factors first <strong>and</strong> then progressively<br />

experience more complicated levels to improve the success of movers.<br />

Presumably the acquisition of easier tasks serves to build foundational<br />

competence <strong>in</strong> learners as well as enhance their sense of self-confidence<br />

<strong>and</strong> success.<br />

Guttman (1950) proposed an <strong>in</strong>terest<strong>in</strong>g technique called the scalogram<br />

for exam<strong>in</strong><strong>in</strong>g the robustness of order of acquisition for series of<br />

different behaviors. He proposed to discern item difficulty by exam<strong>in</strong><strong>in</strong>g<br />

a heterogeneous sample of <strong>in</strong>dividuals who attempted a series of items<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

which were measured on a pass-fail (or dichotomous) basis. The reason<strong>in</strong>g<br />

beh<strong>in</strong>d the validity of the scalogram technique is that the easiest or<br />

least difficult items should be mastered by the most <strong>in</strong>dividuals because<br />

they are acquired first. As item difficulty <strong>in</strong>creases, fewer <strong>and</strong> fewer <strong>in</strong>dividuals<br />

should be able to master the task. Consequently, the most difficult<br />

<strong>and</strong> presumably the last items <strong>in</strong> a series to be mastered will be able<br />

to be demonstrated by the fewest <strong>in</strong>dividuals. Us<strong>in</strong>g a matrix-like table,<br />

Guttman (1950) proposed a “coefficient of reproducibility” which represents<br />

the average ratio between the total successful responses (or passed<br />

items) <strong>and</strong> the total possible number of responses (or product of items<br />

times participants). Like similar association coefficients, the coefficient<br />

can range from 0.0 to 1.0. A higher ratio produces a stronger coefficient<br />

of reproducibility which <strong>in</strong>dicates a more predictable acquisition order<br />

across the items under study.<br />

Guttman’s scalogram technique has been used to exam<strong>in</strong>e the order<br />

of difficulty <strong>and</strong> acquisition for several types of motor behaviors. DeOreo<br />

(1976) studied the order that children acquire balance task items.<br />

Prior to the current study, Harrod (Harrod, 1990; Harrod & Langendorfer,<br />

1991) was the only <strong>in</strong>dividual to exam<strong>in</strong>e the order of acquisition<br />

for swimm<strong>in</strong>g skills, specifically beg<strong>in</strong>ner swim items. Harrod undertook<br />

her study to test whether a traditional order of beg<strong>in</strong>ner skills proposed<br />

by the American Red Cross (1981) was, <strong>in</strong> fact, the optimal order<br />

<strong>in</strong> which to <strong>in</strong>troduce those swim items. One important result <strong>in</strong>cluded<br />

the discovery that the ten-second breath hold<strong>in</strong>g item (American Red<br />

Cross, 1981) was one of the hardest beg<strong>in</strong>ner skills <strong>and</strong> should either be<br />

shortened or be taught much later to beg<strong>in</strong>ners. She also identified that<br />

front <strong>and</strong> back glid<strong>in</strong>g skills were passed by more children than were<br />

front <strong>and</strong> back float items, suggest<strong>in</strong>g that for children it was easier to<br />

move <strong>and</strong> glide than to float motionless. As a result of Harrod’s work,<br />

the American Red Cross did revise the order <strong>in</strong> which some beg<strong>in</strong>ner<br />

swimm<strong>in</strong>g skills (e.g., breath hold<strong>in</strong>g) were taught (American Red<br />

Cross, 1992).<br />

The purpose for the current study was to replicate the f<strong>in</strong>d<strong>in</strong>gs of<br />

Harrod (1990; Harrod & Langendorfer, 1991) with an older age sample<br />

<strong>and</strong> with slightly different swimm<strong>in</strong>g items. The study was conducted<br />

because the American Red Cross was once aga<strong>in</strong> <strong>in</strong> the midst of revis<strong>in</strong>g<br />

the learn-to-swim program. The organization has made a commitment<br />

to base their practices more closely on evidence-based literature.<br />

Method<br />

College students already enrolled <strong>in</strong> academic credit-bear<strong>in</strong>g <strong>in</strong>structional<br />

swimm<strong>in</strong>g classes at Bowl<strong>in</strong>g Green State University were recruited to<br />

participate <strong>in</strong> our study. From the approximately sixty students enrolled<br />

<strong>in</strong> the courses while we conducted the study, thirty-eight students <strong>in</strong>itially<br />

volunteered <strong>and</strong> thirty-one (n f = 17 females; n m = 14 males) completed<br />

test<strong>in</strong>g for all thirteen skill items. Because test<strong>in</strong>g occurred across multiple<br />

days, several orig<strong>in</strong>al volunteers completed only some of the tasks due to<br />

absenteeism <strong>and</strong> were elim<strong>in</strong>ated from the data analysis.<br />

Before beg<strong>in</strong>n<strong>in</strong>g data collection for the study, the authors submitted<br />

a proposal <strong>and</strong> received approval from the University’s <strong>in</strong>stitutional research<br />

review board, called the Human Subjects Review Board (HSRB).<br />

Prior to participation <strong>in</strong> the study, each student completed an <strong>in</strong>formed<br />

consent form <strong>and</strong> <strong>in</strong>vestigators answered any of questions. Specifically,<br />

each student was rem<strong>in</strong>ded that participation was completely voluntary,<br />

would not <strong>in</strong>fluence their grade <strong>in</strong> the course, <strong>and</strong> they could end participation<br />

at any time with no penalties or consequences.<br />

The thirteen specific swimm<strong>in</strong>g skill items tested <strong>and</strong> performance<br />

criteria are identified <strong>in</strong> Table 1. They ranged from several typical beg<strong>in</strong>ner<br />

skills (Red Cross Levels 1 <strong>and</strong> 2) such as breath hold<strong>in</strong>g, prone <strong>and</strong><br />

sup<strong>in</strong>e floats <strong>and</strong> glid<strong>in</strong>g to perform<strong>in</strong>g more advanced strokes (Levels<br />

3, 4, 5) such as front <strong>and</strong> back crawl, breaststroke, elementary backstroke,<br />

<strong>and</strong> sidestroke. The specific performance criteria employed <strong>in</strong> judg<strong>in</strong>g<br />

the successful achievement of each skill were those described by the<br />

American Red Cross <strong>in</strong> their Swimm<strong>in</strong>g <strong>and</strong> Water Safety Instructor’s<br />

Manual (2004).<br />

333


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 1. List of swimm<strong>in</strong>g skill items tested <strong>in</strong> the current study <strong>and</strong><br />

their criterion st<strong>and</strong>ards.<br />

Swim Test Item Abbr. Criterion St<strong>and</strong>ard<br />

Breath hold<strong>in</strong>g Breath<br />

Submerge entire head <strong>and</strong> rema<strong>in</strong> submerged<br />

a m<strong>in</strong>imum of 3 seconds<br />

Prone float P float<br />

Float on your front for as long as possible, at<br />

least 5 seconds<br />

Prone glide P glide<br />

Push off on your front <strong>and</strong> glide forward at<br />

least two body lengths<br />

Back float B float<br />

Float on your back for as long as possible, at<br />

least 5 seconds<br />

Back glide B glide<br />

Push off on your back <strong>and</strong> glide forward at<br />

least two body lengths<br />

Comb<strong>in</strong>ed stroke<br />

alternat<strong>in</strong>g arm action<br />

334<br />

Comb Alt<br />

Dolph<strong>in</strong> kick Dol Kck<br />

Comb<strong>in</strong>ed stroke<br />

simultaneous arm<br />

action<br />

Comb Sim<br />

Front crawl Fr Crwl<br />

Back crawl Bk Crwl<br />

Elementary backstroke El Back<br />

Breaststroke Brst<br />

Sidestroke Side<br />

Swim on your front kick<strong>in</strong>g your feet <strong>and</strong><br />

pull<strong>in</strong>g with your arms, alternat<strong>in</strong>g (tak<strong>in</strong>g<br />

turns) for 10 yds<br />

Hold on to this kick board <strong>and</strong> kick us<strong>in</strong>g<br />

up-down dolph<strong>in</strong> kick for 10 yards<br />

Swim on your front kick<strong>in</strong>g your feet <strong>and</strong><br />

pull<strong>in</strong>g with your arms at the same time for<br />

10 yards<br />

Swim the front crawl (freestyle) with rotary<br />

breath<strong>in</strong>g for 15 yards<br />

Swim the back crawl (backstroke) for 15<br />

yards<br />

Swim the elementary backstroke with a whip<br />

kick <strong>and</strong> glide for 15 yards<br />

Swim the breaststroke us<strong>in</strong>g pull, breathe,<br />

kick, glide for 15 yards<br />

Swim the sidestroke with alternat<strong>in</strong>g arms,<br />

scissors kick, <strong>and</strong> glide for 15 yards<br />

The test<strong>in</strong>g occurred dur<strong>in</strong>g regular class times on Tuesday <strong>and</strong> Thursday<br />

morn<strong>in</strong>gs over a three week period dur<strong>in</strong>g the middle of a fall academic<br />

semester. The <strong>in</strong>structor of the swim classes who was also the assistant<br />

coach for the women’s varsity competitive swim team encouraged students<br />

to participate <strong>in</strong> our study <strong>and</strong> allowed them to come <strong>in</strong> pairs or<br />

threesomes to the shallow end (~ 1 yard (or 0.91m) depth) of the <strong>in</strong>door<br />

50 meter (54.7 yards) x 25 yard (22.86 m) University swimm<strong>in</strong>g pool<br />

while the rema<strong>in</strong>der of the class participated <strong>in</strong> normal class activities <strong>in</strong><br />

the middle <strong>and</strong> deep ends of the pool. The pool water temperatures were<br />

held constant at 26.7o C. Air temperature was a consistent 29.4o C.<br />

The shallow end of the large swimm<strong>in</strong>g pool was set up as three test<strong>in</strong>g<br />

stations to which participants rotated <strong>in</strong> pairs or threesomes. Station<br />

one <strong>in</strong>cluded breath hold<strong>in</strong>g, prone float, prone glide, sup<strong>in</strong>e float, <strong>and</strong><br />

sup<strong>in</strong>e glide items. Station two tested comb<strong>in</strong>ed stroke on the front us<strong>in</strong>g<br />

alternat<strong>in</strong>g arms, comb<strong>in</strong>ed stroke on the front us<strong>in</strong>g simultaneous<br />

arms, dolph<strong>in</strong> kick with a kick board for 10 yards, plus front <strong>and</strong> back<br />

crawl strokes for 15 yards. At station three students were asked to perform<br />

the breaststroke, elementary backstroke, <strong>and</strong> side stroke, each for<br />

at least 15 yards. Test adm<strong>in</strong>istrators asked each student to attempt each<br />

skill three times for purpose of establish<strong>in</strong>g reliability. If students passed<br />

their first two attempts, the third attempt was omitted.<br />

Performance of the skills at each station were recorded by a video<br />

camcorder (either SONY or Panasonic models) affixed to a tripod<br />

that allowed the tester to pan the camera to follow participants as<br />

they moved. Each video camcorder recorded the swimm<strong>in</strong>g skills on a<br />

m<strong>in</strong>iDV tape for later replay on a video recorder <strong>and</strong> large screen monitor.<br />

Video capture rate was 30 frames per second with the electronic<br />

shutter on the automatic sett<strong>in</strong>g.<br />

Student participants started at any of the three stations <strong>and</strong> rotated<br />

to the next open station. A set order of test<strong>in</strong>g purposefully was not followed<br />

to ensure that no test<strong>in</strong>g order affect occurred. If students became<br />

fatigued while perform<strong>in</strong>g any skill, they were permitted as much time<br />

as necessary to recover. If necessary, they were allowed to complete skills<br />

dur<strong>in</strong>g the next class period two or five days later to elim<strong>in</strong>ate the potential<br />

impact of fatigue on the results.<br />

Upon completion of the data collection, the <strong>in</strong>vestigators created<br />

a content analysis for each of the m<strong>in</strong>iDV videotapes that served as<br />

an <strong>in</strong>dex to locate <strong>in</strong>dividual students. Both <strong>in</strong>vestigators then sampled<br />

approximately 10 trials of each skill item <strong>and</strong> <strong>in</strong>dependently observed<br />

<strong>and</strong> classified the performance as successful (pass) or unsuccessful (fail)<br />

accord<strong>in</strong>g to the American Red Cross (2004) criteria (Table 1). We<br />

compared results <strong>and</strong> calculated the proportion of exact agreement to<br />

ensure that we were <strong>in</strong> agreement more than P = 0.80, or 80% exact<br />

agreement. When those levels of <strong>in</strong>ter-rater objectivity were assured, the<br />

second <strong>in</strong>vestigator viewed all the trials for all 31 participants <strong>and</strong> classified<br />

them as either successful or unsuccessful. Subsequently, successful<br />

performances (on at least two out of three trials) were recorded <strong>in</strong> a<br />

spreadsheet as ones (1). Unsuccessful attempts (at least two of three trials<br />

that did not reach the criterion st<strong>and</strong>ard) were placed <strong>in</strong> the spreadsheet<br />

as zeros (0).<br />

results<br />

Guttman’s (1950) scalogram matrix orders both participants <strong>and</strong> test<br />

items accord<strong>in</strong>g to the number of successful completions. In other<br />

words, the least successful (<strong>and</strong> presumably least skilled <strong>and</strong> experienced)<br />

participant was that <strong>in</strong>dividual who completed the fewest skill<br />

items. The most successful participant was the person who successfully<br />

performed the most items. Conversely, the easiest item was that which<br />

was completed by the most participants <strong>and</strong> the most difficult item was<br />

the one completed by the fewest participants.<br />

The swimm<strong>in</strong>g skill items passed most frequently by the current<br />

sample of college students were breath hold<strong>in</strong>g, comb<strong>in</strong>ed stroke on the<br />

front with alternat<strong>in</strong>g arms, <strong>and</strong> front crawl which were passed by all<br />

participants. The swimm<strong>in</strong>g skill items that were passed least frequently<br />

(by only 81-84% of the participants) were the prone <strong>and</strong> sup<strong>in</strong>e glides,<br />

elementary backstroke, <strong>and</strong> sidestroke. Slightly more than half (16)<br />

of the participants successfully passed all items. Only one participant<br />

passed fewer than ten items (i.e., n<strong>in</strong>e). On average, participants passed<br />

12.2 of the 13 items. The overall coefficient of reproducibility for the order<br />

of items was CR = 0.93.<br />

dIscussIon<br />

The results of the scalogram analysis performed <strong>in</strong> the current study<br />

<strong>in</strong>dicated that this selected set of thirteen swimm<strong>in</strong>g skill items could<br />

be quite reliably performed <strong>in</strong> the order proposed by the 2004 American<br />

Red Cross learn-to-swim program because of the relatively high coefficient<br />

of reproducibility <strong>in</strong> which CR = 0.93. This means that three<br />

second breath hold<strong>in</strong>g, front <strong>and</strong> back float<strong>in</strong>g for five seconds, followed<br />

by a 10 yard comb<strong>in</strong>ed stroke on the front us<strong>in</strong>g alternat<strong>in</strong>g arms are<br />

the least difficult swimm<strong>in</strong>g items that can be <strong>in</strong>troduced first, at least<br />

to young adult swimmers. Front crawl stroke also can be <strong>in</strong>troduced<br />

reasonably early <strong>in</strong> the learn-to-swim process for young adults. Other<br />

strokes appear to be more difficult, <strong>in</strong>clud<strong>in</strong>g the rest<strong>in</strong>g strokes of elementary<br />

backstroke <strong>and</strong> sidestroke. Described <strong>in</strong> developmental terms,<br />

these thirteen swimm<strong>in</strong>g items identified a reasonably robust <strong>in</strong>ter-test<br />

developmental sequence. In Harrod’s (1990; Harrod & Langendorfer,<br />

1991) previous scalogram study that tested some of these same items<br />

(albeit us<strong>in</strong>g 1981 Red Cross item descriptions) with elementary-aged<br />

children, the range of coefficients of reproducibility was CR = 0.64 to<br />

0.81. At least for the young adult sample tested <strong>in</strong> the current study, no<br />

higher coefficient of reproducibility could be obta<strong>in</strong>ed by alter<strong>in</strong>g the<br />

proposed order.<br />

The primary difference between the results of the current study<br />

<strong>and</strong> those of Harrod (1990; Harrod & Langendorfer, 1991) was that<br />

the prone (front) <strong>and</strong> sup<strong>in</strong>e (back) float<strong>in</strong>g items were <strong>in</strong>deed accomplished<br />

more successfully by the young adults than they were by the<br />

children. Harrod discovered that children appeared to more easily perform<br />

a front <strong>and</strong> back glide <strong>in</strong> which they could move their arms <strong>and</strong>


legs than they could float motionless on their front or back. Despite<br />

Harrod’s f<strong>in</strong>d<strong>in</strong>gs, the Red Cross never did <strong>in</strong>troduce glid<strong>in</strong>g skills prior<br />

to float<strong>in</strong>g <strong>in</strong> their learn-to-swim program (American Red Cross, 1992).<br />

At least with adults, it appears that float<strong>in</strong>g probably can be taught prior<br />

to <strong>in</strong>troduc<strong>in</strong>g the glid<strong>in</strong>g skills. Interest<strong>in</strong>gly, the two glid<strong>in</strong>g skill items<br />

were as difficult for the current sample to perform as were the elementary<br />

backstroke <strong>and</strong> sidestroke. This difficulty is somewhat surpris<strong>in</strong>g<br />

s<strong>in</strong>ce both front <strong>and</strong> back glid<strong>in</strong>g nom<strong>in</strong>ally would appear to be much<br />

less complicated <strong>and</strong> difficult items than the two rest<strong>in</strong>g strokes.<br />

Based upon these results, the authors could not suggest to the American<br />

Red Cross that there was any evidence-based support to alter the<br />

order <strong>in</strong> which the thirteen selected skill items ought to be presented<br />

<strong>in</strong> the revised 2009 American Red Cross learn-to-swim program. The<br />

study obviously did not test all pert<strong>in</strong>ent skill items <strong>in</strong>volved <strong>in</strong> the Red<br />

Cross’ learn-to-swim program <strong>and</strong> therefore the results should not be<br />

<strong>in</strong>terpreted to apply to the validity of the order for skills <strong>in</strong> the entire<br />

learn-to-swim program. Because the current sample was limited to a relatively<br />

small convenience sample of normally-abled young adult college<br />

students, it also is not possible to suggest that even the order of these<br />

items with the strong coefficient of reproducibility actually applies to<br />

other <strong>in</strong>dividuals such as preschool or elementary-age children or to <strong>in</strong>dividuals<br />

who may be differently-abled. Samples drawn from other specific<br />

populations would be required to underst<strong>and</strong> whether this order of<br />

acquisition, <strong>and</strong> by extension, <strong>in</strong>structional order, should be considered<br />

to be universal or whether the order is unique to different age <strong>and</strong> ability<br />

groups. Underst<strong>and</strong><strong>in</strong>g how much variability <strong>in</strong> order is associated with<br />

different ages <strong>and</strong> ability groups would be crucial pieces of <strong>in</strong>formation<br />

to support future evidence-based revisions to learn-to-swim programs<br />

such as the American Red Cross.<br />

The study <strong>and</strong> its results have some very def<strong>in</strong>ite limitations. A sample<br />

size of thirty-one was relatively small which limited the statistical<br />

power with which the descriptive scalogram could identify variability<br />

<strong>in</strong> the order of item difficulty. We <strong>in</strong>itially had <strong>in</strong>tended to test all sixty<br />

class participants, but some students did not volunteer while others were<br />

absent some days <strong>and</strong> did not complete all items. The sample was def<strong>in</strong>itely<br />

a convenience sample which meant that some of the less skilled<br />

<strong>in</strong>dividuals opted not to participate, skew<strong>in</strong>g the participant skill levels<br />

as evidenced by the high average number of successful item completions.<br />

A scalogram relies upon test<strong>in</strong>g a truly heterogeneous sample that<br />

should <strong>in</strong>clude persons who are capable of pass<strong>in</strong>g few if any of the<br />

items. The current sample of young adults was def<strong>in</strong>itely skewed toward<br />

a more homogeneous <strong>and</strong> skilled sample which is not surpris<strong>in</strong>g given<br />

that they were recruited from <strong>in</strong>structional swimm<strong>in</strong>g classes of college<br />

students.<br />

Because the test<strong>in</strong>g occurred dur<strong>in</strong>g the middle <strong>in</strong>stead of the beg<strong>in</strong>n<strong>in</strong>g<br />

of the semester of study, it is probable that previous <strong>in</strong>struction<br />

biased the sample toward greater skillfulness. It also appears that the<br />

<strong>in</strong>dividual swim <strong>in</strong>structor who was an assistant swim coach emphasized<br />

learn<strong>in</strong>g <strong>and</strong> practice of the competitive swim strokes of front <strong>and</strong> back<br />

crawl, breaststroke, <strong>and</strong> butterfly <strong>and</strong> not rest<strong>in</strong>g strokes of elementary<br />

backstroke <strong>and</strong> sidestroke. Presumably this expla<strong>in</strong>s the lower success<br />

rate observed <strong>in</strong> performance of the elementary backstroke <strong>and</strong> sidestroke<br />

items. Many students appeared puzzled <strong>and</strong> had never heard of<br />

these two strokes when presented with them as test items <strong>in</strong> the study.<br />

The <strong>in</strong>structional bias also presents a challenge to the potential utility<br />

of the scalogram <strong>and</strong> <strong>in</strong>terpretation of the robustness of the coefficient<br />

of reproducibility. It was generally presumed by Guttman (1950)<br />

that item difficulty possessed some <strong>in</strong>herently <strong>in</strong>variant task qualities<br />

<strong>and</strong> characteristics not substantively <strong>in</strong>fluenced by <strong>in</strong>tervention <strong>and</strong> <strong>in</strong>struction.<br />

In the current sample, it appeared fairly clear that familiarity<br />

with competitive strokes <strong>and</strong> lack of familiarity with rest<strong>in</strong>g strokes<br />

<strong>in</strong>fluenced the degree of success demonstrated by some participants.<br />

This def<strong>in</strong>itely could have <strong>in</strong>fluenced the order of item acquisition. The<br />

authors have personal <strong>in</strong>structional experience that both the elementary<br />

backstroke <strong>and</strong> sidestroke can be effectively <strong>in</strong>troduced prior to front<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

<strong>and</strong> back crawl strokes. The current results tend to negate those personal<br />

observations.<br />

The observation of potential <strong>in</strong>struction or <strong>in</strong>tervention bias means<br />

that further studies us<strong>in</strong>g a scalogram should be conducted under experimental<br />

conditions. Samples with well def<strong>in</strong>ed differences <strong>in</strong> experiences<br />

<strong>and</strong> <strong>in</strong>struction need to be compared to clarify the degree to which the<br />

coefficient of reproducibility is altered. For example if the first author<br />

<strong>and</strong> the assistant coach <strong>in</strong>structor of the classes <strong>in</strong> the current study<br />

both taught similar groups of young adults, one emphasiz<strong>in</strong>g acquisition<br />

of rest<strong>in</strong>g strokes <strong>and</strong> the other focus<strong>in</strong>g on the competitive strokes,<br />

would different orders <strong>and</strong> coefficients of reproducibility result? There<br />

are def<strong>in</strong>itely pedagogical <strong>and</strong> methodological questions that should <strong>and</strong><br />

could be addressed.<br />

conclusIon<br />

The current study employed Guttman’s (1950) descriptive scalogram<br />

technique to exam<strong>in</strong>e the validity of swim skill item order of acquisition<br />

<strong>in</strong> a small convenience sample of young adults. The <strong>in</strong>structional order of<br />

thirteen swimm<strong>in</strong>g skills used by the 2004 American Red Cross learnto-swim<br />

program was tested us<strong>in</strong>g a scalogram. The Red Cross order<br />

of the thirteen swimm<strong>in</strong>g items produced a very strong coefficient of<br />

reproducibility (CR = 0.93) <strong>and</strong> provided some evidence-based support<br />

for the Red Cross to cont<strong>in</strong>ue present<strong>in</strong>g those swimm<strong>in</strong>g items <strong>in</strong> a<br />

similar order <strong>in</strong> their learn-to-swim programs. The results of the study<br />

revealed several limitations <strong>in</strong> the conduct of the study (e.g., relatively<br />

small convenience sample, limited skill <strong>and</strong> age range of participants) as<br />

well as raised questions about the robustness of the scalogram technique<br />

itself <strong>and</strong> the <strong>in</strong>terpretation of the coefficient of reproducibility. The authors<br />

have proposed several subsequent studies to clarify the technique<br />

<strong>and</strong> <strong>in</strong>terpretation of the results.<br />

reFerences<br />

American National Red Cross. (1981). Swimm<strong>in</strong>g <strong>and</strong> aquatics safety.<br />

Wash<strong>in</strong>gton, D.C.<br />

American Red Cross. (1992). Water Safety Instructor Manual. St. Louis:<br />

Mosby Year Book.<br />

American Red Cross. (2004). Water Safety Instructor’s Manual. Yardley,<br />

PA: StayWell.<br />

American Red Cross. (2009). Water Safety Instructor’s Manual (r.09).<br />

Yardley, PA: StayWell.<br />

Darw<strong>in</strong>, C. (1877, July). A biographical sketch of an <strong>in</strong>fant. M<strong>in</strong>d, 285-<br />

294.<br />

DeOreo, K. (1976). Dynamic balance <strong>in</strong> preschool children: Quantify<strong>in</strong>g<br />

qualitative data. Research Quarterly, 47, 526-531.<br />

Erbaugh, S.J. (1978). Assessment of swimm<strong>in</strong>g performance of preschool<br />

children. Perceptual <strong>and</strong> Motor Skills, 47, 1179-1182.<br />

Erbaugh, S. (1980). The development of swimm<strong>in</strong>g skills of preschool<br />

children. In C. Nadeau, K. Newell, G. Roberts, & W. Halliwell (Eds.),<br />

Psychology of motor behavior <strong>and</strong> sport-1979 (pp. 324-335). Champaign,<br />

IL: Human K<strong>in</strong>etics.<br />

Gesell, A. (1940). The first five years of life. New York: Harper <strong>and</strong> Row.<br />

Guttman, L.L. (1950). The basis for scalogram analysis. In S.A. Stouffer,<br />

L. Guttman, E. Suchman, P. Lazerfeld, S. Star, & J. Clausen (Eds.),<br />

Measurement <strong>and</strong> prediction (pp. 60-90). Pr<strong>in</strong>ceton, NJ: Pr<strong>in</strong>ceton<br />

University Press.<br />

Harrod, D. (1990). A scalogram analysis of the American Red Cross Beg<strong>in</strong>ner<br />

swimm<strong>in</strong>g skill items. Unpublished Master’s thesis, Kent State<br />

University, Kent, OH.<br />

Harrod, D., & Langendorfer, S.J. (1991). A scalogram analysis of American<br />

Red Cross Beg<strong>in</strong>ner swimm<strong>in</strong>g skill items. National Aquatics<br />

Journal, 6, 10-16.<br />

Haywood, K.M., & Getchell, N. (2009). LifeSpan Motor Development<br />

(5 th Ed.). Champaign, IL: Human K<strong>in</strong>etics.<br />

Herkowitz, J. (1978). Developmental task analysis: The design of movement<br />

experiences <strong>and</strong> evaluation of motor development status. In<br />

335


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

M.V. Ridenour (Ed.), Motor development: Issues <strong>and</strong> applications (pp.<br />

139-164). Pr<strong>in</strong>ceton, NJ: Pr<strong>in</strong>ceton Book Co.<br />

Langendorfer, S.J., & Bruya, L.D. (1995). Aquatic read<strong>in</strong>ess: Develop<strong>in</strong>g<br />

aquatic competence <strong>in</strong> young children. Champaign, IL: Human K<strong>in</strong>etics.<br />

McGraw, M.B. (1939). Swimm<strong>in</strong>g behavior of the human <strong>in</strong>fant. Journal<br />

of Pediatrics, 15(4), 485-490.<br />

McGraw, M.B. (1963). Neuromuscular maturation of the human <strong>in</strong>fant.<br />

New York: Hafner. (Orig<strong>in</strong>ally published 1943 by Columbia University<br />

Press).<br />

McGraw, M.B. (1975). Growth: A study of Johnny <strong>and</strong> Jimmy. New York:<br />

Arno. (Orig<strong>in</strong>ally published 1935 by Appleton-Century.<br />

Piaget, J. (1973). The orig<strong>in</strong> of <strong>in</strong>telligence <strong>in</strong> children (M. Cook, trans.).<br />

New York: Norton.<br />

Roberton, M.A. (1989). Development sequence <strong>and</strong> developmental task<br />

analysis. In J. Sk<strong>in</strong>ner, et al. (Eds.), Future directions <strong>in</strong> exercise <strong>and</strong><br />

sport science research (pp. 369-381). Champaign, IL: Human K<strong>in</strong>etics.<br />

Shirley, M.M. (1931). The first two years. A study of 25 babies: Postural<br />

<strong>and</strong> locomotor development (Vol. 1). M<strong>in</strong>neapolis: University of M<strong>in</strong>nesota<br />

Press.<br />

AcKnoWledGeMents<br />

The data for this research study were collected as part of KNS 470, Independent<br />

Study <strong>in</strong> K<strong>in</strong>esiology, conducted while the second author was a<br />

student at Bowl<strong>in</strong>g Green State University. Both authors acknowledge<br />

resources <strong>and</strong> support provided by the BGSU Center for Undergraduate<br />

Research <strong>and</strong> Scholarship (CURS) that partially funded this study.<br />

336<br />

Imagery Tra<strong>in</strong><strong>in</strong>g <strong>in</strong> Young Swimmers: Effects on the<br />

Flow State <strong>and</strong> on Performance<br />

scurati, r., Michielon, G., longo, s., Invernizzi, P.l.<br />

Università degli Studi di Milano, Facoltà di Scienze Motorie, Milan, Italy<br />

Imagery tra<strong>in</strong><strong>in</strong>g is the ability to develop mental images that can <strong>in</strong>crease<br />

human resources <strong>and</strong> performances. Flow is one of the peak<br />

moments correspond<strong>in</strong>g to a state of optimal experience. This study <strong>in</strong><br />

young swimmers aimed to observe the effects of specific imagery tra<strong>in</strong><strong>in</strong>g<br />

on flow state <strong>and</strong> on swimm<strong>in</strong>g performance. Eight young swimmers<br />

completed a specific mental tra<strong>in</strong><strong>in</strong>g program us<strong>in</strong>g imagery as a<br />

supplement to three weeks of regular swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g. A Flow State<br />

Scale questionnaire was filled out before <strong>and</strong> after the tra<strong>in</strong><strong>in</strong>g as well<br />

as the performance on 100m front crawl stroke was surveyed. The imagery<br />

tra<strong>in</strong><strong>in</strong>g focused on improv<strong>in</strong>g three phases of the front crawl swim<br />

stroke <strong>and</strong> seemed to <strong>in</strong>duce a trend to vary the flow state of the participants.<br />

Imagery tra<strong>in</strong><strong>in</strong>g did not have effects on swimm<strong>in</strong>g performance.<br />

Key words: Flow, Imagery, mental tra<strong>in</strong><strong>in</strong>g<br />

IntroductIon<br />

Exercise is related to physical fitness, perception of wellness <strong>and</strong> quality<br />

of life. Positive attitudes, self-esteem <strong>and</strong> lower<strong>in</strong>g of stress are also <strong>in</strong>duced<br />

by sports activities, where psychophysical energies can be focused<br />

on a specific target with the maximum of concentration <strong>and</strong> attention<br />

(e.g. <strong>in</strong> tra<strong>in</strong><strong>in</strong>g or events), <strong>in</strong> the so called “peak moments” (Berger et al.,<br />

2001). Flow is one of these peak moments, correspond<strong>in</strong>g to a state of<br />

optimal experience, with a complete attention to the action <strong>and</strong> a strong<br />

balance between challenges <strong>and</strong> skills (Csikszentmihalyi, 1990). Flow<br />

is not necessarily dependent on best performance, be<strong>in</strong>g a preparatory<br />

phase of it (Muzio et al., 1999).<br />

Flow state can be measured through the Flow State Scale (FSS)<br />

questionnaire ( Jackson, 1996), based on 36 items evaluated us<strong>in</strong>g a 5<br />

po<strong>in</strong>t Likert scale, related to the 9 fundamentals or dimensions (4 items<br />

each) <strong>in</strong> which the Flow state can be subdivided (Csikszentmihalyi,<br />

1990).<br />

Dimensions <strong>in</strong> the FSS (Muzio et al., 1999) are: D1, balance between<br />

the perceived challenge <strong>and</strong> the perceived personal skills required<br />

to act; D2, union between action <strong>and</strong> awareness (athlete is fully focused<br />

on the task, no panic or effort, there is only naturalness); D3, clarity of<br />

targets (athlete can visualize <strong>in</strong> advance the performance); D4, <strong>in</strong>stantaneous<br />

feedback (<strong>in</strong>ner or outer); D5, concentration on the task avoid<strong>in</strong>g<br />

distractions; D6, Sense of control (management of the self-esteem<br />

improv<strong>in</strong>g confidence, quiet <strong>and</strong> empowerment <strong>and</strong> reduc<strong>in</strong>g the fear<br />

of failure); D7, lack of ones self awareness; D8, destructur<strong>in</strong>g of time<br />

(athlete perceives the time exp<strong>and</strong><strong>in</strong>g or condens<strong>in</strong>g); D9, the autotelic<br />

experience (athlete is motivated <strong>in</strong> do<strong>in</strong>g the activity just for pleasure,<br />

for fun or because it is excit<strong>in</strong>g).<br />

Imagery tra<strong>in</strong><strong>in</strong>g is the ability to develop mental images that can<br />

<strong>in</strong>crease human resources <strong>and</strong> performances exert<strong>in</strong>g a great effect on<br />

m<strong>in</strong>d, feel<strong>in</strong>gs <strong>and</strong> behaviours (Hogg, 2000). Images built dur<strong>in</strong>g the<br />

mental tra<strong>in</strong><strong>in</strong>g have to be very precise, clear <strong>and</strong> detailed <strong>and</strong> they can<br />

be obta<strong>in</strong>ed through the aid of the k<strong>in</strong>aesthetic abilities. An <strong>in</strong>ner or an<br />

outer vision can be built: <strong>in</strong> the <strong>in</strong>ner vision, the k<strong>in</strong>aesthetic acuity leads<br />

athletes <strong>in</strong> imag<strong>in</strong>g the actions as really performed; <strong>in</strong> the outer vision,<br />

the athlete watches himself act<strong>in</strong>g as through the eyes of a third person<br />

or as <strong>in</strong> a movie.<br />

Mental tra<strong>in</strong><strong>in</strong>g can transform negative images <strong>in</strong>to positive ones,<br />

aid<strong>in</strong>g athletes to overcome anxiety, stress, technical <strong>and</strong> tactical troubles,<br />

difficulty <strong>in</strong> concentration on the performance (e.g. visualiz<strong>in</strong>g<br />

dur<strong>in</strong>g the mental tra<strong>in</strong><strong>in</strong>g some memories of a situation experienced<br />

dur<strong>in</strong>g a previous event).


Because the visualization of a movement triggers activities <strong>in</strong> some<br />

areas of the bra<strong>in</strong>’s motor cortex, repeated imagery tra<strong>in</strong><strong>in</strong>g (movements<br />

or specific images closely related to the movements) could <strong>in</strong>duce improvements<br />

<strong>in</strong> the performance.<br />

This study <strong>in</strong> young swimmers aimed to observe the effects of a specific<br />

imagery tra<strong>in</strong><strong>in</strong>g on the flow state <strong>and</strong> on their swimm<strong>in</strong>g performance.<br />

Method<br />

Sixteen young swimmers (7 females <strong>and</strong> 9 males) volunteered for the<br />

study. Participants were divided <strong>in</strong>to two homogeneous groups (eight<br />

participants each) r<strong>and</strong>omly assigned to the Experimental or Control<br />

group: i. Experimental group (mean±SD, age 13.0±0.53 years, weight<br />

52.5±6.5 kg, height 161±7 cm, BMI 20.19±1.21 kg·m -2 ); ii. Control<br />

group (mean±SD, age 13.25±1.04 years, weight 55.38±7.95 kg, height<br />

165±8 cm, BMI 20.21±1.66 kg·m -2 ).<br />

Experimental participants were first <strong>in</strong>troduced to the imagery tra<strong>in</strong><strong>in</strong>g<br />

by means of a preparatory explanation <strong>and</strong> an <strong>in</strong>formation leaflet.<br />

Follow<strong>in</strong>g the <strong>in</strong>structions <strong>in</strong> the leaflet, they self-practiced a number of<br />

exercises at home for 10 days aimed to manage the imagery abilities <strong>and</strong><br />

the ability to overcome a negative situation (e.g.: to visualize a friend<br />

sitt<strong>in</strong>g <strong>in</strong> front of you <strong>and</strong> practice focus<strong>in</strong>g on a number of details <strong>and</strong><br />

emotions; to imag<strong>in</strong>e a weak lamp hang <strong>in</strong> front of you, <strong>in</strong>creas<strong>in</strong>g <strong>and</strong><br />

reduc<strong>in</strong>g <strong>in</strong> <strong>in</strong>tensity; to select an object <strong>and</strong> to focus on it through an<br />

<strong>in</strong>ner or an outer perspective; to focus on a technical swimm<strong>in</strong>g action,<br />

on muscular feel<strong>in</strong>gs, try<strong>in</strong>g to imag<strong>in</strong>e the same action at the maximum<br />

expected power dur<strong>in</strong>g events; to visualize the same fellow of the first<br />

exercise walk<strong>in</strong>g around the room <strong>and</strong> speak<strong>in</strong>g to the people <strong>and</strong> to<br />

yourself ). Subjects were also asked to watch the illustrations (Figure 1)<br />

of three very important movements of swimm<strong>in</strong>g events: the start phase<br />

(div<strong>in</strong>g <strong>in</strong> the fastest <strong>and</strong> most reactive way like a dolph<strong>in</strong>), the swimm<strong>in</strong>g<br />

phase (swimm<strong>in</strong>g to escape from a shark) <strong>and</strong> the turns (<strong>in</strong>vert<strong>in</strong>g<br />

the swimm<strong>in</strong>g direction as fast as possible like a missile).<br />

Figure 1. Illustrations aimed to drill the imagery associated with the<br />

important phases of swimm<strong>in</strong>g conta<strong>in</strong>ed <strong>in</strong> the leaflet for the Experimental<br />

subjects<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

After this preparatory period, the experimental subjects conducted specific<br />

mental tra<strong>in</strong><strong>in</strong>g on imagery to supplement the swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g.<br />

They were <strong>in</strong>vited to cont<strong>in</strong>ue to practice imagery at home <strong>and</strong> an additional<br />

imagery exercise was carried out dur<strong>in</strong>g swimm<strong>in</strong>g sessions: 20<br />

to 30 m<strong>in</strong>utes per session, subjects were lead by the coach <strong>in</strong> rehears<strong>in</strong>g<br />

the illustrations. They were also asked to perform at the maximum level<br />

the elements of the weekly swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g that were scheduled as:<br />

starts (on Monday), swimm<strong>in</strong>g speed (on Tuesday), turns (on Wednesday),<br />

starts <strong>and</strong> swimm<strong>in</strong>g (on Thursday), start, swimm<strong>in</strong>g <strong>and</strong> turns (on<br />

Friday).<br />

The swimmers attended a three week tra<strong>in</strong><strong>in</strong>g program, for two<br />

hours per day. The control group performed the same volume <strong>and</strong> tra<strong>in</strong><strong>in</strong>g<br />

program as the experimental group, but no sort of mental tra<strong>in</strong><strong>in</strong>g<br />

was carried out.<br />

The Flow State Scale questionnaire was filled out by subjects before<br />

<strong>and</strong> after the three weeks of swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g as well as the performance<br />

on 100m front crawl stroke was surveyed.<br />

Statistical analyses were carried out by SPSS 13.0® software, sett<strong>in</strong>g<br />

p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 3. Pre-post comparison of the Flow State Scale results <strong>in</strong> the<br />

Control subjects. Mean data are shown, grouped by FSS dimensions.<br />

Dimensions <strong>in</strong> brackets <strong>in</strong>dicate answers show<strong>in</strong>g low reliability.<br />

dIscussIon<br />

The results showed effects due to the imagery tra<strong>in</strong><strong>in</strong>g. The graph referr<strong>in</strong>g<br />

to the pre-post tra<strong>in</strong><strong>in</strong>g of the Experimental swimmers (Figure 2)<br />

compared to the one related to the Control swimmers (Figure 3) evidence<br />

the flow state variations after the Imagery tra<strong>in</strong><strong>in</strong>g.<br />

In particular, a significant relevance was found <strong>in</strong> the flow dimensions<br />

D3 (clarity of targets) <strong>and</strong> D6 (sense of control). Imagery tra<strong>in</strong><strong>in</strong>g<br />

aided athletes <strong>in</strong> identify<strong>in</strong>g a specific target <strong>in</strong> order to <strong>in</strong>crease the<br />

motivation <strong>in</strong> reach<strong>in</strong>g it. A low or a lack of motivation leads to an excessive<br />

relaxation often caus<strong>in</strong>g absence of energy <strong>and</strong> anxiety. Similarly,<br />

the mental tra<strong>in</strong><strong>in</strong>g could have improved the sense of control of the<br />

Experimental subjects that allow them to better focus on their goals <strong>and</strong><br />

to manage their self-esteem.<br />

The negative variations <strong>in</strong> the D7 (lack of ones self awareness) <strong>and</strong><br />

D9 (the autotelic experience) could be due to the fact that the specific<br />

imagery tra<strong>in</strong><strong>in</strong>g employed <strong>in</strong> this study would have forced the swimmers<br />

to a voluntary execution of the technical movement illustrated<br />

<strong>in</strong>stead of to execute automatic actions. A peculiarity of automatic<br />

movements is the lack of central control, with a high <strong>in</strong>tensity of the<br />

performances <strong>and</strong> a low level of conscious control (Logan, 1985).<br />

Referr<strong>in</strong>g to the lack of the repeatability found <strong>in</strong> the answers related<br />

to the dimension D5 (concentration on the task avoid<strong>in</strong>g distractions)<br />

of the FSS, it was hypothesized that young swimmers could have<br />

difficulties <strong>in</strong> concentration <strong>and</strong> could be quite liable to disturbance.<br />

In swimm<strong>in</strong>g performance no significant differences were found<br />

between the Experimental subjects <strong>and</strong> the Control or between the<br />

pre- <strong>and</strong> post- tra<strong>in</strong><strong>in</strong>g <strong>in</strong> the <strong>in</strong>tra-group comparisons. Even if the relative<br />

short time period of imagery tra<strong>in</strong><strong>in</strong>g (three weeks daily) would be<br />

suitable to <strong>in</strong>duce effects on the performance as a result of technical<br />

<strong>and</strong> c<strong>in</strong>ematic improvements, imagery tra<strong>in</strong><strong>in</strong>g did not affect swimm<strong>in</strong>g<br />

performance probably because flow <strong>and</strong> performance are not necessarily<br />

proportional (Muzio et al, 1999). Moreover, the age of the subjects could<br />

have relationships with the effects on imagery tra<strong>in</strong><strong>in</strong>g.<br />

conclusIon<br />

In young swimmers, three weeks of imagery tra<strong>in</strong><strong>in</strong>g focused on improv<strong>in</strong>g<br />

three phases of a front crawl swim shows that some flow dimensions<br />

vary <strong>in</strong> the flow state of subjects. Imagery tra<strong>in</strong><strong>in</strong>g did not<br />

have an effect on swimm<strong>in</strong>g performance (100m front crawl stroke). An<br />

extended tra<strong>in</strong><strong>in</strong>g over a longer period <strong>and</strong> with swimmers of different<br />

ages is advised <strong>in</strong> order to complete the results of this study.<br />

338<br />

reFerences<br />

Berger B.G., Molt R. (2001). Physical activity <strong>and</strong> quality of life. In: S<strong>in</strong>ger<br />

RN, Hausenblas H.A., Janelle C.M. H<strong>and</strong>book of Sport Psychology.<br />

New York: Wiley & Sons Inc.<br />

Csikszentmihalyi M. (1990). Flow. The Psychology of Optimal Experience.<br />

New York: Harper <strong>and</strong> Row.<br />

Hogg J.M. (2000). Mental Skills for Competitive Swimmers. Edmonton,<br />

Anversa: Sport Excel Publish<strong>in</strong>g Inc., 65.<br />

Jackson S.A., Marsh H. (1996). Development <strong>and</strong> Validation of a Scale<br />

to Measure Optimal Experience: the Flow State Scale. Journal of<br />

Sports & Exercise Psychology, 18, 17-35.<br />

Logan G.D. (1985). Skill <strong>and</strong> automaticity: relation, implication <strong>and</strong><br />

future directions. Can J Psychol, 39, 367–386.<br />

Muzio M., Nitro G. (1999) (a cura di) Atti del convegno “Flow e peak<br />

performance: discipl<strong>in</strong>e a confronto”, Milano, 23 ottobre 1999. Centro<br />

Studi e Formazione <strong>in</strong> Psicologia dello Sport, Milano.


Shallow or Deep Water for Adjustment? A Study <strong>in</strong><br />

Children Aged 3 to 6 Years<br />

scurati, r., Michielon, G., longo, s., Invernizzi, P.l.<br />

Università degli Studi di Milano, Facoltà di Scienze Motorie, Milan, Italy<br />

In a learn-to-swim programme, the question of what is the best environmental<br />

condition for aquatic adjustment. The choice could depend<br />

on the depth of the swimm<strong>in</strong>g facilities or on the swimm<strong>in</strong>g teach<strong>in</strong>g<br />

methodology. This study aimed to compare the outcomes of water adjustment<br />

carried out <strong>in</strong> deep or shallow water <strong>in</strong> 3 to 6 year old children.<br />

Children practic<strong>in</strong>g the learn<strong>in</strong>g programme <strong>in</strong> deep water obta<strong>in</strong>ed a<br />

higher mean score, but not significantly different than the children hav<strong>in</strong>g<br />

a shallow water adjustment programme. The depth of the swimm<strong>in</strong>g<br />

pool seems to not significantly affect the results. Children can approach<br />

guided experiences equally either <strong>in</strong> shallow or deep water to learn the<br />

swimm<strong>in</strong>g basic skills <strong>and</strong> <strong>in</strong>dependence <strong>in</strong> the water, with no differences<br />

<strong>in</strong> the rate of acquisition or <strong>in</strong> the quality of the skills.<br />

Key words: motor learn<strong>in</strong>g, water adjustment, beg<strong>in</strong>ners, deep water,<br />

aquatic skills<br />

IntroductIon<br />

Among more frequent questions swimm<strong>in</strong>g teachers have to answer<br />

when plann<strong>in</strong>g learn-to-swim programme is, “what is the best environmental<br />

condition for teach<strong>in</strong>g beg<strong>in</strong>ners? Frequently, teachers have no<br />

alternative <strong>and</strong> have to adapt to the swimm<strong>in</strong>g facilities they are work<strong>in</strong>g<br />

<strong>in</strong>, but if the environmental conditions allow it, which choice between<br />

start<strong>in</strong>g a swimm<strong>in</strong>g experience <strong>in</strong> deep or shallow water is the best one?<br />

In the literature there are several studies <strong>and</strong> theories about swimm<strong>in</strong>g<br />

teach<strong>in</strong>g methods. Referr<strong>in</strong>g to the best age for start<strong>in</strong>g swimm<strong>in</strong>g<br />

learn<strong>in</strong>g, the age of five to six years seems to be suitable for teach<strong>in</strong>g<br />

swimm<strong>in</strong>g front crawl stroke (Blanksby et al., 1995). At 4 years of age,<br />

children show adequate abilities to acquire good levels of water confidence<br />

or basic aquatic locomotion skills, whereas earlier water experience<br />

does not necessarily lead to a faster ga<strong>in</strong> of specific basic skills<br />

(Parker et al., 1997).<br />

The <strong>in</strong>fluence of aids on water first experiences has also been studied.<br />

No differences were found <strong>in</strong> learn<strong>in</strong>g <strong>and</strong> improv<strong>in</strong>g the front crawl<br />

kick<strong>in</strong>g either us<strong>in</strong>g just a kickboard or employ<strong>in</strong>g multiple various aids<br />

(Blanksby et al., 1999). Moreover, <strong>in</strong> advanced beg<strong>in</strong>ners flotation suits<br />

do not show evidence of <strong>in</strong>fluence on float<strong>in</strong>g or on glid<strong>in</strong>g abilities<br />

(Kjendlie, 2009a) as well as on the enhancement of the swimm<strong>in</strong>g abilities<br />

(Kjendlie, 2009b).<br />

Authors considered at first the depth of the water <strong>and</strong> advanced<br />

learn-to-swim programmes based on activities <strong>in</strong> shallow water (Langendorfer<br />

& Bruya, 1995; Bucher, 1995) or <strong>in</strong> deep water (Schmitt,<br />

1992; Cesary et al., 1998).<br />

The aim of this study was to compare the outcomes <strong>in</strong> 3 to 6 year<br />

old children of water adjustment carried out <strong>in</strong> deep or shallow water.<br />

Methods<br />

Twenty-two children were selected among the participants of the learnto-swim<br />

programmes <strong>in</strong> a swimm<strong>in</strong>g pool of a village near Milan. Criteria<br />

for selection were: i. real age; ii. anthropometric characteristics; iii.<br />

swimm<strong>in</strong>g skills.<br />

The participants were divided <strong>in</strong>to two groups: group A (mean ±<br />

SD, age 4.8 ± 0.7 years, weight 16.76 ± 1.63 kg, height 108 ± 7 cm, BMI<br />

14.23 ± 1.42 kg·m -2 ), group B (mean ± SD, age 5.3 ± 1.4 years, weight<br />

17.23 ± 3.38 kg, height 110 ± 11 cm, BMI 14.07 ± 1.22 kg·m -2 ).<br />

Swimm<strong>in</strong>g skills were the same for all subjects: no previous experience<br />

<strong>in</strong> learn-to-swim programmes, no specific swimm<strong>in</strong>g abilities, no evidence<br />

of preexist<strong>in</strong>g conditions caus<strong>in</strong>g problems dur<strong>in</strong>g water activities.<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

Each group was assigned to a learn-to-swim programme aimed at<br />

a first experience <strong>and</strong> adjustment to water activities correspond<strong>in</strong>g to<br />

the first level of a learn to swim programme (Table 1), accord<strong>in</strong>g to<br />

the progression showed <strong>in</strong> the Table 2, practiced <strong>in</strong> the shallow or deep<br />

water condition: group A <strong>in</strong> shallow water (SW), group B <strong>in</strong> deep water<br />

(DW).<br />

Sixteen classes 60-m<strong>in</strong>utes long were attended by the children. Each<br />

class was structured as follows: 5 to 10 m<strong>in</strong>utes of warm-up <strong>in</strong> a gym<br />

us<strong>in</strong>g simple games or exercises; 40 to 45 m<strong>in</strong>utes of various targeted<br />

games <strong>and</strong> practices with an open multi-lateral approach <strong>in</strong> order to<br />

ma<strong>in</strong>ta<strong>in</strong> high attention <strong>and</strong> motivation <strong>and</strong> to achieve the maximum<br />

educational effect (sometimes more than one step at a time, see Table<br />

2 ); 5 to 10 m<strong>in</strong>utes of free games, jumps <strong>and</strong> dives. Flotation supports<br />

were employed when necessary.<br />

The SW group transferred <strong>in</strong>to the deep water dur<strong>in</strong>g the two last<br />

classes for a short period of adaptation to the new environment because<br />

the f<strong>in</strong>al evaluation had to be executed <strong>in</strong> the deep water.<br />

Scores were assigned accord<strong>in</strong>g to the presence of level 1 <strong>in</strong>dicators<br />

<strong>in</strong> Table 3.<br />

Table 1. Complete learn to swim program.<br />

Level Target<br />

1 Comfort <strong>and</strong> <strong>in</strong>dependence <strong>in</strong> the water<br />

Displac<strong>in</strong>g by kick<strong>in</strong>g on the back <strong>and</strong> manag<strong>in</strong>g the side<br />

2<br />

breath<strong>in</strong>g <strong>in</strong> prone position<br />

3 Elementary front crawl <strong>and</strong> backstroke swimm<strong>in</strong>g<br />

Front crawl <strong>and</strong> backstroke with cont<strong>in</strong>uity <strong>and</strong> breaststroke<br />

4<br />

leg kick<strong>in</strong>g.<br />

5 Complete breaststroke <strong>and</strong> elementary turns<br />

6 All strokes <strong>and</strong> competitive starts <strong>and</strong> turns<br />

Table 2. Targets of the 1st level of the swimm<strong>in</strong>g program.<br />

Progression Target<br />

Discover<strong>in</strong>g the aquatic environment <strong>and</strong> first contact<br />

1<br />

with the water<br />

2 Displac<strong>in</strong>g with supports / holds<br />

3 Head submerg<strong>in</strong>g (with closed <strong>and</strong> open eyes)<br />

4 Breath<strong>in</strong>g <strong>in</strong> static <strong>and</strong> dynamic attitudes<br />

5 Static <strong>and</strong> dynamic float<strong>in</strong>g, with or without aids<br />

Static <strong>and</strong> dynamic float<strong>in</strong>g, with or without aids, add<strong>in</strong>g<br />

6<br />

breath<strong>in</strong>g<br />

7 Propell<strong>in</strong>g with <strong>and</strong> without floatation supports<br />

8 Jump<strong>in</strong>g <strong>and</strong> div<strong>in</strong>g<br />

Table 3. Table of evaluation of the complete swimm<strong>in</strong>g learn<strong>in</strong>g program.<br />

Level Sub-level Check-list (test) Score<br />

1 +<br />

Swimm<strong>in</strong>g lean<strong>in</strong>g on a float<strong>in</strong>g support, by kick<strong>in</strong>g <strong>in</strong><br />

prone position <strong>and</strong> immers<strong>in</strong>g the face.<br />

Swimm<strong>in</strong>g with a kickboard (or similar), by kick<strong>in</strong>g <strong>in</strong><br />

1<br />

++ prone or sup<strong>in</strong>e position <strong>and</strong> immers<strong>in</strong>g the face manag<strong>in</strong>g<br />

an elementary breath<strong>in</strong>g.<br />

Full <strong>in</strong>dependence <strong>in</strong> the water. Short displacement <strong>in</strong> prone<br />

2<br />

+++<br />

<strong>and</strong> sup<strong>in</strong>e position without any float<strong>in</strong>g support. Cont<strong>in</strong>uous<br />

breath<strong>in</strong>g at the border. Dropp<strong>in</strong>g <strong>and</strong> div<strong>in</strong>g <strong>in</strong> free<br />

techniques.<br />

3<br />

2 +<br />

Glid<strong>in</strong>g <strong>in</strong> prone position <strong>and</strong> <strong>in</strong> sup<strong>in</strong>e position (arms<br />

along the body) by correct kick<strong>in</strong>g.<br />

Perform<strong>in</strong>g a series of front crawl arm strokes breath<strong>in</strong>g<br />

1<br />

++ <strong>and</strong> roll<strong>in</strong>g on the back. Perform<strong>in</strong>g 25m on the back, arms<br />

along the body.<br />

2<br />

+++<br />

Kick<strong>in</strong>g with a kickboard or a float<strong>in</strong>g aid, no arm stroke,<br />

breath<strong>in</strong>g on the side. Backstroke keep<strong>in</strong>g the arms straight.<br />

3<br />

339


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Level Sub-level Check-list (test) Score<br />

3 +<br />

Swimm<strong>in</strong>g front crawl with a floatation aid; backstroke with<br />

alternate arm stroke; div<strong>in</strong>g from a kneel<strong>in</strong>g position.<br />

Swimm<strong>in</strong>g font crawl for a little while without supports,<br />

1<br />

++ alternate arm stroke <strong>and</strong> side breath<strong>in</strong>g; backstroke paus<strong>in</strong>g<br />

over the head.<br />

2<br />

+++<br />

Elementary front crawl stroke, one side breath<strong>in</strong>g; elementary<br />

backstroke.<br />

Elementary front crawl stroke, both sides breath<strong>in</strong>g; alter-<br />

3<br />

4 + nate <strong>and</strong> simultaneous backstroke. Div<strong>in</strong>g from a kneel<strong>in</strong>g<br />

position.<br />

1<br />

++<br />

Swimm<strong>in</strong>g alternat<strong>in</strong>g four arm strokes on front crawl <strong>and</strong><br />

backstroke<br />

2<br />

+++<br />

25m complete <strong>and</strong> cont<strong>in</strong>uous front crawl <strong>and</strong> backstroke.<br />

Breaststroke kicks with a kickboard.<br />

25m complete <strong>and</strong> cont<strong>in</strong>uous front crawl <strong>and</strong> backstroke.<br />

3<br />

5 + Breaststroke kick<strong>in</strong>g both <strong>in</strong> prone <strong>and</strong> sup<strong>in</strong>e position<br />

without kickboards.<br />

1<br />

++<br />

25m complete <strong>and</strong> cont<strong>in</strong>uous front crawl <strong>and</strong> backstroke.<br />

Complete breaststroke. Start<strong>in</strong>g with dive.<br />

2<br />

+++<br />

Complete front crawl, backstroke <strong>and</strong> breaststroke with<br />

elementary turns.<br />

Complete front crawl, backstroke <strong>and</strong> breaststroke; coordi-<br />

3<br />

6 +<br />

nation exercises (e.g. arms like <strong>in</strong> breaststroke <strong>and</strong> legs like<br />

<strong>in</strong> front crawl). Prone <strong>and</strong> sup<strong>in</strong>e undulat<strong>in</strong>g butterfly kicks;<br />

arms without breath<strong>in</strong>g <strong>and</strong> with front crawl kick<strong>in</strong>g.<br />

1<br />

++<br />

Complete swimm<strong>in</strong>g front crawl, backstroke, breaststroke<br />

<strong>and</strong> butterfly. Front crawl <strong>and</strong> backstroke flip turns.<br />

2<br />

+++ 100 relays with start dive <strong>and</strong> turns. 3<br />

Statistical analyses were carried out us<strong>in</strong>g SPSS 13.0® software. Mann-<br />

Whitney non-parametric statistics was applied <strong>in</strong> order to compare the<br />

results between SW <strong>and</strong> DW.<br />

results<br />

The results of the evaluation of the abilities children acquired <strong>in</strong> SW or<br />

DW learn-to-swim activities are reported <strong>in</strong> the Figure 1. No significant<br />

differences were found (p=0.20).<br />

Figure 1. Comparison between water adjustment carried out through<br />

SW or DW aquatic activities. No significant differences were found<br />

(p=0.20).<br />

dIscussIon<br />

Children practic<strong>in</strong>g the learn<strong>in</strong>g program <strong>in</strong> the deep water obta<strong>in</strong>ed<br />

a higher mean score, but not significantly different than the children<br />

hav<strong>in</strong>g a shallow water adjustment program. Probably this little difference<br />

could be due to the fact that SW children have to get acqua<strong>in</strong>ted<br />

to the new environment (they moved <strong>in</strong>to the deep swimm<strong>in</strong>g pool only<br />

two classes before the f<strong>in</strong>al evaluation was carried out <strong>in</strong> deep water),<br />

whereas DW children performed the test <strong>in</strong> the same situation they<br />

managed s<strong>in</strong>ce the first class. Authors claim<strong>in</strong>g the suitability of the<br />

deep water adjustment (Schmitt, 1992; Cesary et al., 1998) po<strong>in</strong>t out<br />

that children do not have to switch from a simple situation (shallow<br />

water) to a more difficult one, start<strong>in</strong>g the adjustment process aga<strong>in</strong>.<br />

340<br />

Children experienced <strong>in</strong> the shallow water could need a readjustment<br />

adaptation of their aquatic motor skills when transferred to deep water,<br />

<strong>and</strong> occasionally even suffer a regression.<br />

Shallow water activities led to similar results as deep water adjustment,<br />

support<strong>in</strong>g authors assert<strong>in</strong>g that this experience occurs <strong>in</strong> a simple<br />

condition with more stable supports <strong>and</strong> with the possibility to do<br />

more dynamic exercises (Langendorfer & Bruya, 1995; Bucher, 1995).<br />

Thus, deep water would be an unfriendly environment, where <strong>in</strong>stability<br />

of support, <strong>and</strong> a more adverse psychological situation could represent<br />

different issues.<br />

All authors agree with similar progressions of the complete swimm<strong>in</strong>g<br />

evolution as reported <strong>in</strong> Table 1. In particular, they largely agree<br />

with the sequence <strong>in</strong> Table 2 referr<strong>in</strong>g to the first level of aquatic skills<br />

acquisition, whatever the preferred environment for start<strong>in</strong>g the water<br />

activities is.<br />

As po<strong>in</strong>ted out by Magill (1988), the maturation level of children<br />

<strong>and</strong> the motivation are very important elements <strong>in</strong> learn<strong>in</strong>g the motor<br />

skills, which may apply to the current situation.<br />

conclusIon<br />

In children 3 to 6 years old, the depth of the swimm<strong>in</strong>g pool does not<br />

affect the learn<strong>in</strong>g of the first level of aquatic skills (adjustment <strong>and</strong><br />

<strong>in</strong>dependence <strong>in</strong> the water).<br />

Guided experiences both <strong>in</strong> shallow <strong>and</strong> deep water can lead to basic<br />

swimm<strong>in</strong>g skills with no differences <strong>in</strong> the rate of learn<strong>in</strong>g <strong>and</strong> improv<strong>in</strong>g<br />

skills or <strong>in</strong> the quality of the skills.<br />

reFerences<br />

Blanksby B.A., Parker H.E., Bradley S., Ong V. (1995). Children’s read<strong>in</strong>ess<br />

for learn<strong>in</strong>g front crawl swimm<strong>in</strong>g. Aust J Sci Med Sport, 27(2),<br />

34-7.<br />

Kjendlie P.L. (2009a). No effect of us<strong>in</strong>g flotation suits <strong>in</strong> glid<strong>in</strong>g <strong>and</strong> float<strong>in</strong>g<br />

abilities of advanced beg<strong>in</strong>ners <strong>in</strong> swimm<strong>in</strong>g teach<strong>in</strong>g. 14th annual<br />

ECSS Congress Oslo/Norway, June 24-27.<br />

Kjendlie P.L. (2009b). Swimm<strong>in</strong>g abilities are not enhanced by us<strong>in</strong>g a<br />

flotation suit for advanced beg<strong>in</strong>ners <strong>in</strong> deep water swimm<strong>in</strong>g teach<strong>in</strong>g.<br />

14th annual ECSS Congress Oslo/Norway, June 24-27.<br />

Langendorfer S.J., Bruya L.D. (1995). Aquatic read<strong>in</strong>ess. Develop<strong>in</strong>g water<br />

competence <strong>in</strong> young children. Champaign, IL: Human K<strong>in</strong>etics.<br />

Magill R.A. (1988). Critical Periods of Optimal Read<strong>in</strong>ess Learn<strong>in</strong>g<br />

Sports Skill. In: Magill R.A., Ash M.J. (ed.). Children <strong>in</strong> sport.<br />

Champaign, IL: Human K<strong>in</strong>etics.<br />

Parker, H.E & Blanksby, B.A. (1997). Start<strong>in</strong>g age <strong>and</strong> aquatic skill<br />

learn<strong>in</strong>g <strong>in</strong> young children: mastery of prerequisite water confidence<br />

<strong>and</strong> basic aquatic locomotion skills. Aust J Sci Med Sport, 29(3),83-7.<br />

Schmitt P. (1992). Nager de la Découverte à la Performance. Paris: Vigot.


The Effect of a Target Sound Made by a Model<br />

Swimmer’s Dolph<strong>in</strong> Kick Movement on Another<br />

Swimmer’s Dolph<strong>in</strong> Kick Performance<br />

shimojo, h. 1 , Ichikawa, h. 2 , tsubakimoto, s. 1 , takagi, h. 1<br />

1 Graduate School of Comprehensive Human Sciences, University of Tsukuba,<br />

Tsukuba City, Japan<br />

2 Department of Sports Information, Japan Institute of Sports Sciences, Tokyo,<br />

Japan<br />

The aim of this study was to determ<strong>in</strong>e the effect of a target sound made<br />

by a model swimmer’s dolph<strong>in</strong> kick movement on another swimmer’s<br />

dolph<strong>in</strong> kick performance. Fifteen competitive swimmers participated<br />

<strong>in</strong> this study. Subjects were required to swim us<strong>in</strong>g a dolph<strong>in</strong> kick while<br />

listen<strong>in</strong>g to the target sound as closely as possible. The aim of the task<br />

was to determ<strong>in</strong>e whether the tim<strong>in</strong>g <strong>and</strong> displacement of their dolph<strong>in</strong><br />

kick would change, <strong>and</strong> the degree to which the change would<br />

be reta<strong>in</strong>ed without the sound. After swimm<strong>in</strong>g with sound, subjects<br />

experienced a decrease <strong>in</strong> tim<strong>in</strong>g error relative to their performance<br />

without sound for up to 300 s, but displacement error did not decrease<br />

significantly. The results also suggested that with auditory models, which<br />

have been particularly effective for tim<strong>in</strong>g patterns, it would be hard to<br />

recognize displacement differences.<br />

Key words: dolph<strong>in</strong> kick, motor learn<strong>in</strong>g, auditory model<br />

IntroductIon<br />

In swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g, the swimmer must enhance power <strong>and</strong> endurance<br />

for good performance, which <strong>in</strong>volves efficient movement. Such<br />

high performance movement must be achieved through effective motor<br />

learn<strong>in</strong>g.<br />

Many motor learn<strong>in</strong>g <strong>and</strong> motor control studies were conducted <strong>in</strong><br />

sports psychology <strong>and</strong> neuroscience. Target track<strong>in</strong>g tasks, require the<br />

subject to move a cursor utiliz<strong>in</strong>g a mouse to track mov<strong>in</strong>g target po<strong>in</strong>t<br />

on display. The trajectory error of trials was used to evaluate performance.<br />

Yamamoto et al. (2007) reported target track<strong>in</strong>g tasks utiliz<strong>in</strong>g an auditory<br />

model, where the movement target on display was synchronized<br />

with stereo sounds express<strong>in</strong>g right or left by sound volume control. The<br />

subject was required to control the mouse to get close to the mov<strong>in</strong>g target<br />

follow<strong>in</strong>g auditory model with the eyes closed. They suggested that<br />

the auditory model could be used <strong>in</strong> real world sports tra<strong>in</strong><strong>in</strong>g.<br />

Baudry et al. (2006) reported that an auditory concurrent feedback<br />

on cyclic movement was effective <strong>in</strong> motor learn<strong>in</strong>g <strong>and</strong> performance.<br />

Wang <strong>and</strong> Hart (2005) reported that an auditory model that was an<br />

effective method to enhance the learn<strong>in</strong>g of swimm<strong>in</strong>g movement tim<strong>in</strong>g<br />

<strong>in</strong> beg<strong>in</strong>ner classes. But an auditory model has not been attempted<br />

<strong>in</strong> expert swimmers. If an auditory model could affect motor learn<strong>in</strong>g<br />

to create the skilled movement required for high performance <strong>in</strong> competitive<br />

swimm<strong>in</strong>g, coaches <strong>and</strong> swimmers could use such a method to<br />

enable swimmers to improve each other’s performance <strong>in</strong> tra<strong>in</strong><strong>in</strong>g. The<br />

purpose of this study, therefore, was to determ<strong>in</strong>e the effect of a target<br />

sound produced by a model swimmer’s dolph<strong>in</strong> kick movement on another<br />

swimmer’s dolph<strong>in</strong> kick performance.<br />

Method<br />

Fifteen competitive swimmers (ten males <strong>and</strong> five females) participated<br />

<strong>in</strong> this study. They were aged 22.1 ± 4.7 years <strong>and</strong> all subjects had more<br />

than ten years of experience <strong>in</strong> competitive swimm<strong>in</strong>g <strong>and</strong> had normal<br />

hear<strong>in</strong>g. An <strong>in</strong>formed consent was obta<strong>in</strong>ed from all subjects before<br />

their participation <strong>in</strong> this study.<br />

Before this study, one model swimmer swam with the dolph<strong>in</strong> kick<br />

<strong>in</strong> the pool at sub-maximal speed (1 m/s) for gett<strong>in</strong>g two-dimensional<br />

coord<strong>in</strong>ates by film<strong>in</strong>g. After a s<strong>in</strong>gle kick phase was chosen, coord<strong>in</strong>ates<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

of the swimmer’s vertical range were exchanged to relative coord<strong>in</strong>ates<br />

(% height). We created a “target sound” that <strong>in</strong>dicat<strong>in</strong>g displacement<br />

differences expressed as sound frequency scales <strong>in</strong> the range of 300~900<br />

Hz converted by the coord<strong>in</strong>ates. Because “Concert A” or “Middle A” is<br />

the 440 Hz tone that serves as the st<strong>and</strong>ard for musical pitch <strong>and</strong> is used<br />

<strong>in</strong> <strong>in</strong>strument tun<strong>in</strong>g, the range of 300~900 Hz was adopted with an<br />

average of 440Hz for the “target sound”. Prior to this study, it had been<br />

confirmed whether the model swimmer could replay the same movement<br />

while listen<strong>in</strong>g to the target sound <strong>in</strong> the pretest.<br />

After it was expla<strong>in</strong>ed to subjects what the target sound <strong>in</strong>dicated,<br />

the subjects were required to swim with the dolph<strong>in</strong> kick after a wall<br />

push start to a distance of 10m while listen<strong>in</strong>g to the target sound, <strong>and</strong><br />

to “track” the target swimmer’s movement. The task was to swim “track<strong>in</strong>g”<br />

the movement of the target as well as possible. After the normal<br />

dolph<strong>in</strong> kick test that required the subject to swim at 80 % or less effort,<br />

there were two tasks. The aim of Task 1 was to see whether difference of<br />

sound scale would affect the displacement of a swimmer’s dolph<strong>in</strong> kick.<br />

The 75% range (375~825 Hz) <strong>and</strong> the 50% range (450~750 Hz) target<br />

sound, <strong>in</strong>dicat<strong>in</strong>g that the height of toe displacement <strong>in</strong> the dolph<strong>in</strong> kick<br />

was narrow, were obta<strong>in</strong>ed from the target sound. Task 1 was conducted<br />

the 75% <strong>and</strong> the 50% target sound were used r<strong>and</strong>omly for ten trials,<br />

<strong>and</strong> the effect was <strong>in</strong>vestigated from differences between pre 1 <strong>and</strong> post<br />

1 trials with target sound.<br />

The aim of Task 2 was to see whether the swimmer’s dolph<strong>in</strong> kick<br />

would reta<strong>in</strong> any improvements without the target sound. Task 2 was<br />

conducted with the target sound for ten sessions. The effect was <strong>in</strong>vestigated<br />

from differences between pre2, post2, post3 (60 s later), post4 (120<br />

s later) <strong>and</strong> post5 (300 s later) with no sound requir<strong>in</strong>g the subjects to<br />

reproduce the same dolph<strong>in</strong> kick movement as <strong>in</strong> Task 1. Figure 1 shows<br />

the study protocol.<br />

Figure 1. Protocol followed <strong>in</strong> which subjects were required to use the<br />

dolph<strong>in</strong> kick <strong>in</strong> every trial.<br />

Data collection was undertaken <strong>in</strong> an <strong>in</strong>door swimm<strong>in</strong>g pool whose<br />

depth ranged 1.3 m to 1.8 m. Every trial was recorded us<strong>in</strong>g four cameras<br />

(TK-C1381 Victor Inc., Japan) through an underwater poolside<br />

w<strong>in</strong>dow. Data sampl<strong>in</strong>g set 60 Hz. The two-dimensional coord<strong>in</strong>ates<br />

of the swimmers’ vertical toe displacement were obta<strong>in</strong>ed by a two-dimensional<br />

DLT method us<strong>in</strong>g motion analysis software (Frame-DIAS<br />

4, DKH Inc., Japan), <strong>and</strong> were exchanged to relative coord<strong>in</strong>ates (%<br />

height) for comparison with the model swimmer. The sound was generated<br />

utiliz<strong>in</strong>g underwater speakers (MT-70 Toyoonkyo Corp., Japan)<br />

that were synchronized with the underwater cameras. Figure 2 shows<br />

the evaluation from data collected.<br />

341


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 2. Experiment sett<strong>in</strong>g <strong>and</strong> evaluation for performance from data<br />

collected.<br />

Two approaches to evaluation were used. One approach applied the idea<br />

of Tim<strong>in</strong>g Error (TE). The target cycle time was 0.6 s (i.e. the kick phase<br />

time). The TE obta<strong>in</strong>ed was compared with the trial cycle time <strong>and</strong> the<br />

target cycle time. The second approach employed Displacement Error<br />

(DE). The vertical displacement range of the target dolph<strong>in</strong> kicks were<br />

evaluated on a scale of 0 % to 100 %. DE was evaluated by relative Root<br />

Mean Square Error (rRMSE) by the displacement of each kick follow<strong>in</strong>g<br />

Fusco <strong>and</strong> Crétual (2008). Follow<strong>in</strong>g auditory perception, there is<br />

a delay before humans <strong>in</strong>itiate movement (Charles et al., 2001). The<br />

DE evaluation was divided <strong>in</strong>to an upward kick <strong>and</strong> a downward kick<br />

without match time. TE <strong>and</strong> DE were obta<strong>in</strong>ed as:<br />

TE (s) = A kick cycle time – the target cycle time (0.6 s)<br />

N<br />

DE (%) = rRMSE = 1 2<br />

∑= ei<br />

N i 1<br />

The closer that the value of TE <strong>and</strong> DE were to zero, the closer the<br />

movement of the subjects were to the target movement. The mean of TE<br />

<strong>and</strong> DE for all trials were compared us<strong>in</strong>g one-way repeated measures<br />

ANOVA followed by the Bonferroni multiple comparison.<br />

results<br />

Task 1: Time differences between target cycle time <strong>and</strong> subject cycle<br />

time on the last five trials <strong>and</strong> total average was calculated by TE. The<br />

result of total average of TE <strong>in</strong> the normal trial was 0.07 ± 0.03 s, pretest<br />

1 was 0.01 ± 0.01 s <strong>and</strong> post-test 1 was 0.01 ± 0.01 s. There were<br />

significant differences between normal <strong>and</strong> pre-test 1 (p < .01), normal<br />

<strong>and</strong> post-test 1 (p < .01), but no difference between pre-test 1 <strong>and</strong> posttest<br />

1. Relative displacement differences between target <strong>and</strong> subject on<br />

last five kick trials <strong>and</strong> total average was calculated by DE. The result of<br />

DE of total average <strong>in</strong> normal was 14.8 ± 1.39 %, pre-test 1 was 10.74<br />

± 1.00 % <strong>and</strong> post-test 1 was 10.87 ± 0.61 %. There were significant differences<br />

between normal <strong>and</strong> pre-test 1 (p < .01), normal <strong>and</strong> post-test 1<br />

(p < .01), but no difference between pre-test 1 <strong>and</strong> post-test 1. Figure 3<br />

shows the mean ± st<strong>and</strong>ard deviation of TE (left) <strong>and</strong> DE (right) of the<br />

last five dolph<strong>in</strong> kick trials <strong>and</strong> the total mean values.<br />

342<br />

TE (s)<br />

0.12<br />

0.10<br />

0.08<br />

0.06<br />

0.04<br />

0.02<br />

0.00<br />

-0.02<br />

-0.04<br />

-0.06<br />

normal TE pre1 TE post1<br />

1 2 3 4 5 total<br />

Dolph<strong>in</strong> kick (cycle)<br />

20.0<br />

18.0<br />

16.0<br />

14.0<br />

12.0<br />

10.0<br />

8.0<br />

6.0<br />

4.0<br />

2.0<br />

0.0<br />

normal DE pre1 DE post1<br />

1 2 3 4 5<br />

Dolph<strong>in</strong> kick (cycle)<br />

total<br />

Figure 3. TE (left) <strong>and</strong> DE (right) shows the mean ± st<strong>and</strong>ard deviation<br />

of each last five kick of all subjects <strong>and</strong> the total mean with sound. Fpor<br />

statistical significance, please refer to the text.<br />

DE (%)<br />

Task 2: Time differences between target cycle time <strong>and</strong> subject cycle<br />

time for the last five trials <strong>and</strong> total average was calculated by TE. The<br />

result of TE of total average <strong>in</strong> pre 2 was 0.02 ± 0.01 s, post 2 was 0.02<br />

± 0.03 s, post 3 was 0.01 ± 0.02 s, pos 4 was 0.02 ± 0.01 s <strong>and</strong> post 5 was<br />

0.01 ± 0.02 s. There were no differences between trials. Relative displacement<br />

differences between target <strong>and</strong> subject for the last five trials <strong>and</strong><br />

total average was calculated by DE. The result of DE of total average <strong>in</strong><br />

pre 2 was 12.1 ± 0.9 %, post 2 was 12.3 ± 0.9 %, post 3 was 13.0 ± 2.7 %,<br />

post 4 was 11.3 ± 1.9 % <strong>and</strong> post 5 was 10.45 ± 0.6 %. There were significant<br />

differences between pre 2 <strong>and</strong> post 5 (p < .01), post2 <strong>and</strong> post5<br />

(p < .01), post3 <strong>and</strong> post5 (p < .05). Figure4 shows the mean of TE (left)<br />

<strong>and</strong> DE (right) of each last five dolph<strong>in</strong> kick <strong>and</strong> the total mean values.<br />

TE (s)<br />

DE (%)<br />

0.12<br />

0.10<br />

0.08<br />

0.06<br />

0.04<br />

0.02<br />

0.00<br />

-0.02<br />

20.0<br />

18.0<br />

16.0<br />

14.0<br />

12.0<br />

10.0<br />

8.0<br />

6.0<br />

4.0<br />

2.0<br />

0.0<br />

TE pre2 TE post2<br />

TE post3 (60s) TE post4 (120s)<br />

TE post5 (300s)<br />

1 2 3 4 5 total<br />

Dolph<strong>in</strong> kick (cycle)<br />

DE pre2 DE post2<br />

DE post3 (60 s) DE post4 (120 s)<br />

DE post5 (300 s)<br />

1 2 3 4 5 total<br />

Dolph<strong>in</strong> kick (cycle)<br />

Figure 4. TE (top) <strong>and</strong> DE (bottom) shows the mean of each last five<br />

kick of all subjects <strong>and</strong> the total mean with sound. ns: no significant difference<br />

between trials. * significant difference between trials for multiple<br />

comparison (*p < .05, **p < .01).


dIscussIon<br />

Task 1: The difference between normal <strong>and</strong> pre-test 1 on tim<strong>in</strong>g <strong>and</strong> displacement<br />

<strong>in</strong>dicated that the swimmer could change the movement immediately<br />

while listen<strong>in</strong>g to the sound (see Figure 3). After Task 1, there was<br />

no significant difference between pre-test 1 <strong>and</strong> post-test 1. Although DE<br />

values <strong>in</strong> pre 1 <strong>and</strong> post 1 both were lower than the normal, our expectation<br />

was that DE value would decl<strong>in</strong>e more <strong>in</strong> post-test 1 than pre-test 1 because<br />

variable sound scales (i.e. 75 % <strong>and</strong> 50 % sound) could tra<strong>in</strong> relative hear<strong>in</strong>g<br />

(Miyazaki, 1993) <strong>and</strong> thus affect the vertical displacement, approximat<strong>in</strong>g<br />

the target movement. Task 1 would <strong>in</strong>dicate that chang<strong>in</strong>g sound scale<br />

r<strong>and</strong>omly (mean<strong>in</strong>g chang<strong>in</strong>g height of dolph<strong>in</strong> kick displacement) has no<br />

effect for dolph<strong>in</strong> kick movement.<br />

Task 2: The results of TE on post2, post3, post4 <strong>and</strong> post5 <strong>in</strong>dicated that the<br />

subjects reta<strong>in</strong>ed the approximate dolph<strong>in</strong> kick tim<strong>in</strong>g to the target without<br />

the sound (see Figure 4). The auditory model has been a quite effective<br />

aid for tim<strong>in</strong>g patterns (Charles et al., 2001). If a coach wishes to change a<br />

swimmer’s movement, a target sound could have an effect on his/her tim<strong>in</strong>g<br />

or help to create a constant tempo dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g. The result of DE, <strong>in</strong><br />

spite of the displacement of the target swimmer movement expressed on a<br />

sound scale, there was no difference after Task 2. There were, however, significant<br />

differences between three trials (see Figure 4). It would appear that<br />

the subject’s concentration on sound retention <strong>in</strong> Task 2 did not <strong>in</strong>fluence<br />

his/her performance <strong>in</strong> post2, but a non-auditory environment made the<br />

swimmer focus on receiv<strong>in</strong>g k<strong>in</strong>esthetic feedback. They could later reproduce<br />

the movement facilitated by the target sound.<br />

This study <strong>in</strong>dicates that an auditory model can be useful to set a swimm<strong>in</strong>g<br />

pace or to immediately coord<strong>in</strong>ate tim<strong>in</strong>g. The dolph<strong>in</strong> kick, however,<br />

is but one parameter of movement. In the real world of tra<strong>in</strong><strong>in</strong>g, the coord<strong>in</strong>ation<br />

<strong>and</strong> tim<strong>in</strong>g of strokes is based upon several parameters (e.g. kick <strong>and</strong><br />

arm coord<strong>in</strong>ation, arm f<strong>in</strong>ish <strong>and</strong> breath, etc.). A study of the use of auditory<br />

models <strong>in</strong> swimm<strong>in</strong>g should focus on parameters that could be coord<strong>in</strong>ated.<br />

In this study, displacement of the toe of the model swimmer was expressed<br />

on a sound scale. But the swimmer’s displacement error decl<strong>in</strong>e from<br />

the target appeared a few m<strong>in</strong>ute later without the sound (see DE graph<br />

on Figure 4). It seems that retention <strong>and</strong> reproduction of movement were<br />

sequential steps accord<strong>in</strong>g to the motor learn<strong>in</strong>g cognitive process (Schmidt,<br />

1991). Listen<strong>in</strong>g to the sound scale change <strong>and</strong> feel<strong>in</strong>g his/her toe displacement<br />

from k<strong>in</strong>esthetic sensation at the same time, for detection of error<br />

would be very hard for the swimmer underwater.<br />

conclusIon<br />

The target sound was effective for skilled swimmers learn<strong>in</strong>g movement tim<strong>in</strong>g.<br />

Learn<strong>in</strong>g displacement was difficult utiliz<strong>in</strong>g sound but would be more<br />

effective with the learn<strong>in</strong>g steps of retention <strong>and</strong> reproduction <strong>in</strong> the correct<br />

sequence.<br />

reFerences<br />

Charles H.S., Gabriele W., J<strong>in</strong>-hoon P. & Briana, G. (2001). Effects of an<br />

auditory model on the learn<strong>in</strong>g of relative <strong>and</strong> absolute tim<strong>in</strong>g. Journal of<br />

Motor Behavior, 33(2), 127-138.<br />

Fusco, N. & Crétual, A. (2008). Instantaneous treadmill speed determ<strong>in</strong>ation<br />

us<strong>in</strong>g subject’s k<strong>in</strong>ematic data. Gait & Posture, 28(4), 663-667.<br />

L<strong>in</strong>, W. & Melanie A.H. (2005). Influence of auditory modell<strong>in</strong>g on learn<strong>in</strong>g<br />

a swimm<strong>in</strong>g skill. Perceptual <strong>and</strong> Motor Skills, 100, 640-648.<br />

Seifert, L., David, L., Ragis, T. & Chollet, D.. (2006). Auditory concurrent<br />

feedback benefits on the circle performed <strong>in</strong> gymnastics. Journal of Sports<br />

Sciences, February, 24(2), 149-156.<br />

Miyazaki, K. (1993). Absolute pitch as an <strong>in</strong>ability: Identification of musical<br />

<strong>in</strong>tervals <strong>in</strong> a tonal context. Music Perception, 11, 55-72.<br />

Schmidt R.A. (1991). Motor learn<strong>in</strong>g <strong>and</strong> performance, Champaign, IL: Human<br />

K<strong>in</strong>etics.<br />

Yamamoto, M. (2007). Support of motor learn<strong>in</strong>g by auditory feedback. Unpublished<br />

master’s thesis, University of Electro Communications, Chofu<br />

City, Tokyo, Japan.<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

Tendencies <strong>in</strong> Natural Selection of High Level Young<br />

Swimmers<br />

timakovat.s., Klyuchnikova M.V.<br />

All-Russian Scientific Research Institute of Physical Culture <strong>and</strong> Sport,<br />

Moscow, Russia<br />

High performance levels <strong>in</strong> modern sport require great physical <strong>and</strong><br />

psychological effort from young athletes. Some specialists conduct the<br />

early orientation for children with unusual abilities <strong>and</strong> gifted young<br />

ones. This problem has difficulties not only <strong>in</strong> search of such criteria<br />

but also <strong>in</strong> some social <strong>and</strong> moral aspects. The aim of the study was to<br />

f<strong>in</strong>d out facts of change <strong>in</strong> young swimm<strong>in</strong>g leaders, <strong>and</strong> to discover the<br />

reasons of this replacement. The retrospective <strong>in</strong>vestigation was done,<br />

us<strong>in</strong>g data of young swimmers demonstrat<strong>in</strong>g high age group performance<br />

levels. The analyses have shown a clear tendency to change selection<br />

criteria accord<strong>in</strong>g to age group. Also the differences <strong>in</strong> biological<br />

maturity between swimmers of both sexes were revealed. The greatest<br />

variance <strong>in</strong> age development typology was observed <strong>in</strong> the age groups<br />

of 13-14 years.<br />

Key words: age group, biological age, high level, natural selection,<br />

generation.<br />

IntroductIon<br />

Over the last 30 years sport has often been criticized for be<strong>in</strong>g both<br />

<strong>in</strong>stitutionalised <strong>and</strong> for the premature specialisation of children <strong>and</strong><br />

youth sports. The lower age threshold of children’s entry <strong>in</strong>to “organised”<br />

sport has dropped from 6-8 to 4-6 years. So an early <strong>in</strong>troduction to<br />

tra<strong>in</strong><strong>in</strong>g <strong>and</strong> competition occurs more frequently <strong>and</strong> <strong>in</strong> a similar format<br />

to the adult paradigm (Schmidt 2001).<br />

Accord<strong>in</strong>g to expert op<strong>in</strong>ion (Brettschneider, 2001, Schmidt 2001)<br />

this contributes to the development of early mental fatigue <strong>and</strong> children’s<br />

exit from sport. Some researchers feel the need to have different<br />

development models of activity for children, such as: a holistic focus <strong>and</strong><br />

special programs for future champions (Brettschneider 2001). However,<br />

when adopt<strong>in</strong>g this approach we must employ serious scientific estimation<br />

methods <strong>in</strong> order to assess the potential of each child <strong>and</strong> teenager.<br />

Obviously, early talent identification <strong>and</strong> an appropriate orientation towards<br />

elite sport will avoid a misguided <strong>in</strong>tensification for the majority<br />

of youth.<br />

Our research confirms the presence of phenotype features of swimmers<br />

with different levels of achievement. However, we believe <strong>in</strong> the<br />

necessity of establish<strong>in</strong>g prognostic criteria for the talent search with<strong>in</strong><br />

sports. In our op<strong>in</strong>ion the ma<strong>in</strong> task of prepar<strong>in</strong>g young athletes consists<br />

of the clear <strong>and</strong> suitable match<strong>in</strong>g of the proposed tra<strong>in</strong><strong>in</strong>g loads to the<br />

possibilities of the develop<strong>in</strong>g young organism. This primarily concerns<br />

problems around the optimization of sports preparation (Bulgakova &<br />

Tchebotareva 1999, Klyuchnikova 2000, Timakova 1985).<br />

In this article the research material is presented to display the necessity<br />

of mak<strong>in</strong>g allowances for features of biological development.<br />

This permits qualitative management of the selection (talent hunt) <strong>and</strong><br />

preparation of young swimmers.<br />

Methods<br />

Retrospective analysis of the best swimmers’ research data <strong>in</strong> different<br />

age groups was done. In total 210 girls <strong>and</strong> 216 boys cover<strong>in</strong>g the age<br />

ranges of 12 to 19 years were surveyed. The data were analysed accord<strong>in</strong>g<br />

to their placement <strong>in</strong> different generations of the country’s national<br />

swimm<strong>in</strong>g teams. One generation of swimmers is from the decade of the<br />

1990s; the other from the first decade of the new century.<br />

Programs of test<strong>in</strong>g <strong>in</strong>cluded: 1) Anthropometry <strong>and</strong> the def<strong>in</strong>ition<br />

of biological age; 2) Swimmers’ bio-energetic parameters <strong>and</strong> functional<br />

343


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

abilities <strong>in</strong> a swimm<strong>in</strong>g flume. 3) Special strength tra<strong>in</strong><strong>in</strong>g parameters.<br />

The biological age of the swimmers (BA) was def<strong>in</strong>ed by the authors’<br />

own methods (Timakova 1985, 2006) Depend<strong>in</strong>g on a difference between<br />

chronologic age (CA) <strong>and</strong> BA, all swimmers were distributed <strong>in</strong>to<br />

5 groups: R 1 - 1-2 years of retardation on rates of maturation; R 2 – more<br />

than 2 years retardation; N - age norm; А 1 - 1-2 years acceleration on<br />

rates of maturation; А 2 - acceleration of more than 2 years. Investigation<br />

results were processed us<strong>in</strong>g st<strong>and</strong>ard statistical methods <strong>and</strong> correlation<br />

analysis. Methods of factor-typological description of objects were<br />

also used.<br />

results<br />

The materials <strong>in</strong> table 1 belong to the cont<strong>in</strong>gent of swimmers which<br />

displayed the peak of sport achievement <strong>in</strong> the middle of the 1990s. As<br />

we can see, the majority of tested swimmers belong to the 13-14 year<br />

age group. With advanc<strong>in</strong>g age the number of surveyed girls decreased,<br />

whereas the boys did not decrease to the same extent. The most essential<br />

differences <strong>in</strong> this age cont<strong>in</strong>gent of girls <strong>and</strong> boys are shown <strong>in</strong> the<br />

character of biological development.<br />

The norm age development of swimmers across all age groups<br />

dom<strong>in</strong>ates. However, <strong>in</strong> the girls’ aged 13-14 we mark the general shift<br />

towards delays <strong>in</strong> puberty. In male groups the trend of shift, on the contrary,<br />

is clearly visible as age acceleration. It is characteristic that <strong>in</strong> cases<br />

of acceleration of development this is not found <strong>in</strong> the senior girls’ age<br />

groups at all. Among the high level swimmers of senior age groups the<br />

shift <strong>in</strong> selection related to the tendency of puberty delay is recognized.<br />

Table 1. Swimmer age distribution <strong>in</strong> relation to personal rates of biological<br />

development <strong>in</strong> %<br />

Age<br />

girls<br />

n R2 R1 N A1 A2 tot.<br />

12 4 - - 3.6 1.2 - 4.8<br />

13 19 3.6 4.8 9.6 4.8 - 22.9<br />

14 37 6.0 16.3 1928 3.0 - 44.6<br />

15 10 3.6 6.0 2.4 - - 12.1<br />

16 8 1.2 3.6 4.8 - - 9.6<br />

17 5 - 2.4 3.6 - - 6.0<br />

total<br />

boys<br />

83 14.5 33.1 43.4 9.1 - 100<br />

13 21 - 2.7 4.4 5.3 6.2 18.6<br />

14 35 - 3.5 8.0 8.9 10.6 31.0<br />

15 17 - 0.9 9.7 3.5 0.9 15.0<br />

16 15 - - 10.6 1.8 0.9 13.3<br />

17 13 0.9 1.8 6.2 2.7 - 11.5<br />

18 12 1.7 0.9 3.6 4.4 - 10.6<br />

total 113 2.6 9.7 42.5 26.4 18.6 100<br />

Tables 2 <strong>and</strong> 3 give the percentage distribution of swimmers <strong>in</strong> age<br />

groups among their top ranked representatives. Data <strong>in</strong> these tables emphasises<br />

essentially different trends of a natural selection of girls <strong>and</strong><br />

boys. Among the strongest representatives of the age groups, female<br />

types with normal <strong>and</strong> slowed rate of development dom<strong>in</strong>ate. On the<br />

contrary, for the best representatives of the male groups a more complicated<br />

picture of distribution of the rate of biological development<br />

was shown, though the above mentioned tendencies of natural selection<br />

prevailed.<br />

344<br />

Table 2. Distribution of biological development types among top ranked<br />

girl swimmers (1990s Generation, n = 109), %<br />

Age,<br />

Years<br />

n %<br />

Biological Development Type<br />

R2 R1 N A1<br />

12 9 8.26 11.11 33.33 22.22 33.33<br />

13 24 22.02 8.33 41.67 50.0 ¾<br />

14 49 44.95 12.24 40.82 46.94 ¾<br />

15 24 22.02 4.17 45.83 50.0 ¾<br />

16 3 2.75 66.67 33.33 ¾ ¾<br />

Table 3. Distribution of biological development types among top ranked<br />

boy swimmers<br />

(1990s Generation, n = 63), %<br />

Age,<br />

Years<br />

n %<br />

Biological Development Type<br />

R2 R1 N A1 A2<br />

13 11 17.47 9.09 9.09 ¾ 45.46 36.36<br />

14 28 44.44 7.14 35.71 14.29 35.72 7.14<br />

15 14 22.22 ¾ 7.14 50.0 42.86 ¾<br />

16 10 15.87 ¾ ¾ 60.0 30.0 10.0<br />

Table 4. Distribution of 2000s swimmers Generation on biological development<br />

type, %<br />

Age, Girls (n=25) Boys (n=35)<br />

Years R2 R1 N R2 R1 N A1 13 33.3 33.3 33.3 – – – –<br />

14 12.5 25.0 62.5 – – – –<br />

15 18.2 18.2 63.6 – – – 100.0<br />

16 66.7 – 33.3 – 17.1 60.7 22.2<br />

17 – – – 21.4 35.7 28.6 14.3<br />

18-19 – – – 33.33* 33.3 33.3 ¾<br />

* At the age of 18 years <strong>and</strong> older <strong>in</strong> groups with R2 development there<br />

are cases with delay rates of puberty of more than 2 <strong>and</strong> 3 years.<br />

In table 4, data of swimmers with achievement peaks <strong>in</strong> the first decade of<br />

the 2000s are presented. Some of these swimmers competed as members<br />

of the national team at the Beij<strong>in</strong>g Olympic Games. The characteristic<br />

feature of this generation is a representation shift to the senior age groups.<br />

Only at the age of 13 years <strong>in</strong> girls are all three types of biological development<br />

equally represented. At the age of 14 <strong>and</strong> 15 years, the majority of<br />

girls correspond to their age norm <strong>in</strong> terms of development. However, at<br />

the age of 16 years the number of girls with a delay of processes of puberty<br />

is <strong>in</strong>creased. In the young men, with the <strong>in</strong>crease of years the variety of<br />

types of development grows; moreover the shift towards a delay <strong>in</strong> tempo<br />

of puberty strengthens. With the aim to reveal the reasons of such different<br />

dynamics of sport achievement growth <strong>in</strong> swimmers after 14 years<br />

of age, we have carried out an auto-classification of all tested parameters.<br />

In table 5 the average values of parameters of the largest numerical<br />

classes of swimmers are given. The featured particularity of girls <strong>in</strong><br />

comparison with boys is a higher parameter of sport achievement level.<br />

At the same time they do not differ on age, parameters of biological<br />

maturity <strong>and</strong> swimm<strong>in</strong>g career duration. As well, girls come short on<br />

morpho-functional parameters <strong>and</strong> especially on <strong>in</strong>tegrated characteristics<br />

of capacity <strong>and</strong> efficiency of the aerobic mechanism of power supply,<br />

compared with boys. However the ECG analysis of girls before the test<br />

was identical to the boys, but girls had higher parameters of cardiovascular<br />

system adaptation after test<strong>in</strong>g to the po<strong>in</strong>t of exhaustion (<strong>in</strong> a<br />

flume). We want to emphasize that at a later stage, none of the female<br />

swimmers from this class reached the level of elite competition.


are given. The featured particularity of girls <strong>in</strong> comparison with boys is a higher<br />

parameter of sport achievement level. At the same time they do not differ on age,<br />

parameters of biological maturity <strong>and</strong> swimm<strong>in</strong>g career duration. As well, girls come<br />

short on morpho-functional parameters <strong>and</strong> especially on <strong>in</strong>tegrated characteristics of<br />

capacity <strong>and</strong> efficiency of the aerobic mechanism of power supply, compared with<br />

boys. However the ECG analysis of girls before the test was identical to the boys, but<br />

girls had higher parameters of cardiovascular system adaptation after test<strong>in</strong>g to the po<strong>in</strong>t<br />

of exhaustion (<strong>in</strong> a flume). We want to emphasize that at a later stage, none of the<br />

female swimmers from this class reached the level of elite competition.<br />

Table 5. Mean values of parameters <strong>in</strong> classes of the strongest swimmers<br />

at the age of 14 years (M <strong>and</strong> SD)<br />

Table 5. Mean values of parameters <strong>in</strong> classes of the strongest swimmers at the age of<br />

14 years (M <strong>and</strong> SD)<br />

Parameters<br />

Classes<br />

Girls, n = 21 Boys, n = 22<br />

Qualification, nom<strong>in</strong>al units 4.21 ± 0.55 3.38 ± 0.99<br />

CA, months 167.05 ± 3.11 168.71 ± 3.09<br />

ВA, po<strong>in</strong>ts 4.99 * ± 0.79 4.94 ± 1.01<br />

CA– ВA, years -0.37 ± 0.53 0.82 ± 0.99<br />

Tra<strong>in</strong><strong>in</strong>g experience, years 6.07 ± 0.73 6.00 ± 1.15<br />

Height, сm 166.94 ± 5.72 174.97 ± 7.53<br />

Weight, kg 55.56 ± 5.20 61.68 ± 7.42<br />

Chest circumference, сm 83.67 ± 3.21 90.10 ± 3.67<br />

Biceps circumference, сm 24.86 ± 1.73 26.69 ± 1.78<br />

H<strong>and</strong> strength, kg 28.95 ± 4.34 42.48 ± 6.38<br />

Lung Capacity, l 3.58 ± 0.42 5.07 ± 0.74<br />

Bone mass, kg 9.88 ± 0.91 12.84 ± 1.50<br />

Muscle mass, kg 24.37 ± 2.68 30.25 ± 4.21<br />

Fat mass, kg 10.16 ± 2.18 8.37 ± 1.84<br />

Brachium-pelvic <strong>in</strong>dex 1.39 ± 0.10 1.45 ± 0.08<br />

VO2 max, l / m 2.98 ± 0.59 4.61 ± 0.46<br />

LV, l 92.84 ± 22.72 117.44 ± 18.16<br />

O2P, ml /beats/m<strong>in</strong> 16.23 ± 3.76 25.40 ± 3.15<br />

ECG before load, n.u. 4.67 ± 0.56 4.65 ± 0.53<br />

<strong>Biomechanics</strong> <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g <strong>XI</strong><br />

84<br />

Chapter * 5 Biological Education, age Advice <strong>in</strong> girls <strong>and</strong> Biofeedback = 5 po<strong>in</strong>ts correspond<strong>in</strong>g to the first menses age.<br />

ECG after In load, table n.u. 6 the different ways 4.89 of categoriz<strong>in</strong>g ± 0.29 the 4.43 athletes ± 0.83 are presented.<br />

* Biological Among age <strong>in</strong> representatives girls = 5 po<strong>in</strong>ts correspond<strong>in</strong>g of these classes to the there first menses are swimmers age. who per-<br />

In table formed 6 the different at a later ways date of as national categoriz<strong>in</strong>g swimm<strong>in</strong>g the athletes team are members presented. at Among the <strong>in</strong>-<br />

representatives ternational of these level. classes Parameter there are comparison swimmers who testifies performed that at the a later Class date of as 11<br />

national girls-swimmers swimm<strong>in</strong>g team generally members at do the not <strong>in</strong>ternational differ from level. the Parameter above class comparison analysis<br />

testifies that the Сlass of 11 girls-swimmers generally do not differ from the above class<br />

analysis concern<strong>in</strong>g concern<strong>in</strong>g chronologic chronologic <strong>and</strong> <strong>and</strong> biological biological age. Nevertheless, age. Nevertheless, they have they greater have<br />

body height greater <strong>and</strong> body also height more athletic <strong>and</strong> also constitution more athletic characteristics. constitution However, characteristics. the most<br />

important However, difference the for most them (from important a class difference of girls <strong>in</strong> table for them 5) is that (from they a already class of at girls the<br />

age of 14 years had more appreciably dimension of physiological characteristics (VO2<br />

<strong>in</strong> table 5) is that they already at the age of 14 years had more appre-<br />

max; O2P; LV, etc.). Boys of a class n=16 also have greater height <strong>and</strong> are biologically<br />

more mature. ciably At dimension the same time of physiological on body proportions characteristics they have a (VO less 2 strong-build max; O2P; <strong>and</strong> LV,<br />

less relative etc.). subcutaneous Boys of a class fat. n=16 also have greater height <strong>and</strong> are biologically<br />

more mature. At the same time on body proportions they have a less<br />

Table 6. Mean values of analysed parameters <strong>in</strong> classes of 14 years swimmers of<br />

vary<strong>in</strong>g strong-build characteristics <strong>and</strong> (M <strong>and</strong> less SD) relative subcutaneous fat.<br />

Parameters Classes<br />

Girls, n = 11 Boys, n = 16<br />

Qualification, nom<strong>in</strong>al units 4.18 ± 0.39 3.68 ± 0.41<br />

CA, months 167.91 ± 2.58 168.01 ± 1.98<br />

BA, po<strong>in</strong>ts 4.89 ± 0.93 5.44 ± 1.31<br />

CA – BA, years - 0.42 ± 0.61 1.02 ± 0.79<br />

Tra<strong>in</strong><strong>in</strong>g Experience, years 5.64 ± 0.98 5.77 ± 1.15<br />

Height, cm 170.50 ± 3.30 180.94 ± 4.39<br />

Weight, kg 56.03 ± 4.64 66.89 ± 4.99<br />

Chest circumference, сm 85.91 ± 4.30 92.50 ± 2.44<br />

Biceps circumference, сm 25.06 ± 1.53 27.46 ± 1.84<br />

H<strong>and</strong> strength, kg 28.95 ± 6.41 43.31 ± 7.18<br />

Lung Capacity, l 3.77 ± 0.46 5.69 ± 0.24<br />

Bone mass, kg 9.88 ± 0.91 13.81 ± 0.95<br />

Muscle mass, kg 25.83 ± 3.32 33.29 ± 3.23<br />

Fat mass, kg 10.61 ± 2.52 8.57 ± 1.80<br />

Brachium-pelvic <strong>in</strong>dex, n.u. 1.38 ± 0.08 1.41 ± 0.08<br />

VO2 max, l / m 3.79 ± 0.32 ⎯<br />

LV, l 102.43 ± 27.35 ⎯<br />

O2P, ml /beats/m<strong>in</strong> 20.85 ± 2.76 ⎯<br />

DISCUSSION Table 6. Mean values of analysed parameters <strong>in</strong> classes of 14 years swim-<br />

The analysis carried out reveals a complex process of the best performers chang<strong>in</strong>g <strong>in</strong><br />

their development mers of vary<strong>in</strong>g while characteristics <strong>in</strong> junior swimm<strong>in</strong>g. (M <strong>and</strong> The SD) f<strong>in</strong>d<strong>in</strong>gs show that swimmers of<br />

different characteristics at the age of 13-14 years can achieve success <strong>in</strong> this sport.<br />

Among girls, swimmers ga<strong>in</strong> advantage over others, through optimum body<br />

parameters <strong>and</strong> excellent adaptation possibilities of their cardiovascular system. It<br />

dIscussIon<br />

allows them to start <strong>in</strong>tensive tra<strong>in</strong><strong>in</strong>g early which does not lead to the necessary<br />

development The analysis of the carried aerobic out power reveals supply a complex mechanisms. process In of a the quantitative best performers sense<br />

chang<strong>in</strong>g <strong>in</strong> their development while <strong>in</strong> junior swimm<strong>in</strong>g. The f<strong>in</strong>d<strong>in</strong>gs<br />

show that swimmers of different characteristics at the age of 13-14 years<br />

can achieve success <strong>in</strong> this sport.<br />

Among girls, swimmers ga<strong>in</strong> advantage over others, through optimum<br />

body parameters <strong>and</strong> excellent adaptation possibilities of their car-<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

diovascular system. It allows them to start <strong>in</strong>tensive tra<strong>in</strong><strong>in</strong>g early which<br />

does not lead to the necessary development of the aerobic power supply<br />

mechanisms. In a quantitative sense <strong>in</strong>dependently of the different<br />

age-groups <strong>and</strong> generations the girls with retardation of biological maturity<br />

prevailed. Due to peculiarities of their body type <strong>and</strong> biological<br />

development they are <strong>in</strong>cl<strong>in</strong>ed to swim <strong>in</strong> tra<strong>in</strong><strong>in</strong>g regimes at a more<br />

moderate speed. That helps to boost aerobic capability.(tab.5). There is a<br />

further explanation of the preference of select<strong>in</strong>g swimmers with a body<br />

weight deficit <strong>and</strong> a retardation of puberty signs <strong>in</strong> girls. Only at the age<br />

of 16-17 years the tendency to prevalence of a somatotype accord<strong>in</strong>g to<br />

requirements of modern sports is observed. However the representation<br />

of swimmers <strong>in</strong> these age categories is already at a m<strong>in</strong>imum.<br />

The 12 years of <strong>in</strong>vestigation of the same high level swimmers have<br />

revealed a decrease <strong>in</strong> a selection tendency of swimmers with <strong>in</strong>adequate<br />

typology of age-related development for sports aim<strong>in</strong>g at high level<br />

achievement. The change <strong>in</strong> selection trends occurred aga<strong>in</strong>st an age<br />

<strong>in</strong>crease of swimmers of the reserves of the country national team. Accord<strong>in</strong>gly,<br />

we have observed a growth of the number of swimmers with<br />

optimum body parameters concern<strong>in</strong>g requirements for this particular<br />

sport.<br />

Table 6 shows that girls who moved forward at a later age <strong>in</strong> their<br />

sport results did not differ from the strongest swimmers at the age of 14<br />

years. But features of their physical development (tallness, body weight<br />

deficit) did not allow cop<strong>in</strong>g with high <strong>in</strong>tensity tra<strong>in</strong><strong>in</strong>g loads. Tra<strong>in</strong><strong>in</strong>g<br />

<strong>in</strong> more optimal regimes was reflected <strong>in</strong> an advantage <strong>in</strong> aerobic<br />

development possibilities. Thus, research has confirmed the necessity of<br />

account<strong>in</strong>g for age development features <strong>and</strong> the orientation of tra<strong>in</strong><strong>in</strong>g<br />

for peak achievements at a later age.<br />

conclusIons<br />

The competitive activity success at a juvenile age is def<strong>in</strong>ed often<br />

by a choice of the sports preparation strategy <strong>and</strong> the <strong>in</strong>fluence<br />

of swimmer phenotype, <strong>in</strong>clud<strong>in</strong>g features of biological development.<br />

At the age of decisive hormonal shifts (13-14 years) athletes<br />

with a certa<strong>in</strong> typology have the advantage. They co<strong>in</strong>cide<br />

with the age norm regard<strong>in</strong>g the pace of puberty <strong>and</strong> possess<br />

high adaptive capacities of the cardiovascular system. However,<br />

their ability to endure a high <strong>in</strong>tensity tra<strong>in</strong><strong>in</strong>g load is negatively reflected<br />

<strong>in</strong> their aerobic development possibilities. Such a situation<br />

further affects the dynamics of sport achievement growth. Features of<br />

athlete physical development, particularly growth <strong>in</strong> body height connected<br />

with asthenisation does not at this age allow tra<strong>in</strong><strong>in</strong>g at high<br />

<strong>in</strong>tensity. Accord<strong>in</strong>gly, these swimmers reach their best results at<br />

a later age. Their advantage <strong>in</strong> the development of aerobic power<br />

supply mechanisms also promotes this. Therefore, this provides<br />

them with the best adaptation to tra<strong>in</strong><strong>in</strong>g at higher <strong>in</strong>tensity at a<br />

more mature age. These revealed tendencies are more precisely shown<br />

<strong>in</strong> the comparative analysis of the high level young swimmers’ data of<br />

different generations.<br />

reFerences<br />

Brettschneider, W.D. (2001) Involvement of organized sports <strong>and</strong> adolescent<br />

development. In: Book of Abstracts, 6-th Annual Congress of the<br />

European College of Sport Science: ”Perspectives <strong>and</strong> Profiles”. Cologne,<br />

July 24-28, 2001. p. 16<br />

Bulgakova, N.Z. & I.V. Tchebotareva (1999). Analysis of the concepts<br />

<strong>and</strong> the effectiveness of prepar<strong>in</strong>g the sports reserve <strong>in</strong> swimm<strong>in</strong>g for<br />

the period of seventies – n<strong>in</strong>eties. In: “Wychowanie Fizyczne i Sport”.<br />

Proceed<strong>in</strong>g of the 3 rd International Scientific Congress on Modern Olympic<br />

Sport, vol. XLIII, Warszawa, p. 77-78.<br />

Klyuchnikova, M.V. (2000). Ispolzovanie kriteriev biologicheskogo razvitiya<br />

v upravlenii podgotovkoi yunykh sportsmenov (na primere sportivnogo<br />

plavaniya) [The use of biological development criteria <strong>in</strong> management of<br />

young sportsmen preparation (at example of competitive swimm<strong>in</strong>g)].<br />

Ph.D. Thesis <strong>in</strong> Educational Science: Moscow, VNIIFK, 170 p<br />

345


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Schmidt, W. (2001) Changes <strong>and</strong> trends <strong>in</strong> children’s sport career <strong>in</strong><br />

Germany. In: Book of Abstracts // 6-th Annual Congress of the European<br />

College of Sport Science: ”Perspectives <strong>and</strong> Profiles”. Cologne, July<br />

24-28. p 59<br />

Timakova, T.S.(1985) Mnogoletnyaya podgotovka plovtsa i ee <strong>in</strong>dividualizatsia<br />

(biologicheskie aspekty) [The Multi-year swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g<br />

<strong>and</strong> its <strong>in</strong>dividualization (biological aspects)] , Moskva : FiS., 144 p.<br />

(<strong>in</strong> Russian)<br />

Tiimakova, T.S. (2006) Podgotovka yunikh plovtsov v aspektakh ontogeneza<br />

(Metodicheskoe posobie) [Young swimmers tra<strong>in</strong><strong>in</strong>g <strong>in</strong> aspects of<br />

ontogeny (Textbook of methodics)]. Moscow, “Semilia”,- 132 p. (<strong>in</strong><br />

Russian)<br />

346<br />

The Cognitive Interplay Between Sensory <strong>and</strong><br />

Biomechanical Features While Execut<strong>in</strong>g Flip Turns<br />

Wear<strong>in</strong>g Different Swim Suits<br />

Vieluf, s. 1 3 , ungerechts, B.e. 1 , toussa<strong>in</strong>t, h.M. 2 , lex, h. 1 ,<br />

schack, t. 1<br />

1 Bielefeld University, Bielefeld, Germany<br />

2 Free University Amsterdam, Amsterdam, Netherl<strong>and</strong>s<br />

3 Jacobs University Bremen, Bremen, Germany<br />

A flip turn is a motor action due to a comb<strong>in</strong>ation of the established<br />

competence match<strong>in</strong>g features of postures <strong>and</strong> situational <strong>in</strong>fluences. In<br />

general, movements are organized at different cognitive levels <strong>in</strong>clud<strong>in</strong>g<br />

their sensory effects. Every movement is formed by cognitive units,<br />

called Basic Action Concepts. The purpose of this study is to elucidate<br />

the <strong>in</strong>fluence of sensory effects on the biomechanical outcome of the<br />

flip turn technique under two different conditions: regular <strong>and</strong> high tech<br />

full swim suit. Methods were biomechanical analysis for the flip turn,<br />

a questionnaire for exam<strong>in</strong><strong>in</strong>g the strength of sensory effects, <strong>and</strong> two<br />

sets for the structure dimension analysis–motorics. The results revealed<br />

a close connection between the cognitive representation of the sensory<br />

based effects of flip turn technique <strong>and</strong> their biomechanical structure.<br />

Keywords: flip turn, biomechanics, mental representation, swim suit<br />

IntroductIon<br />

Swimm<strong>in</strong>g is the result of displaced water mass which cause buoyancy<br />

<strong>and</strong> momentum, when set <strong>in</strong> motion by body movements. Body movements<br />

are controlled through cognitive <strong>and</strong> physiological frameworks.<br />

This holds true for activities <strong>in</strong> aquatic space where the <strong>in</strong>teraction between<br />

the body <strong>and</strong> the surround<strong>in</strong>g water mass is of importance for<br />

an underst<strong>and</strong><strong>in</strong>g beyond a simple biomechanical approach. Swimm<strong>in</strong>g<br />

experts know about the relevance of this <strong>in</strong>teraction, but there is only<br />

modest scientific evidence concern<strong>in</strong>g the connection of perception <strong>and</strong><br />

action. Follow<strong>in</strong>g Bernste<strong>in</strong> (1967) voluntary movements:<br />

• are stored <strong>in</strong> memory at different levels as a structure subdivided<br />

<strong>in</strong>to details –as an idea or image- but not as cha<strong>in</strong>s of details <strong>and</strong><br />

organized <strong>in</strong> long term memory as perceptual-cognitive (mental)<br />

representations.<br />

• are the result of perceptible events through a mental representation<br />

of anticipated characteristic (e.g. sensory) effects.<br />

• means that goals <strong>and</strong> effects of a movement are stored together<br />

<strong>and</strong> thus each volitional movement is stored effect-coded to<br />

achieve movement aims. .<br />

• are realisations of action goals or images.<br />

Follow<strong>in</strong>g the hierarchical movement organization of Schack (2004),<br />

voluntary movements are represented <strong>in</strong> the long term memory, <strong>in</strong>clud<strong>in</strong>g<br />

their <strong>in</strong>ternal <strong>and</strong> external effects <strong>in</strong> units, characterized as Basic<br />

Action Concepts (BACs), which are represented at the level of mental<br />

control. These BACs are <strong>in</strong>tegrated <strong>in</strong> a hierarchical cognitive architecture.<br />

In this context, movements are realiz<strong>in</strong>g action goals evoked by<br />

motivation, cognition, <strong>and</strong> emotion, which are grounded on auditory,<br />

visual, or k<strong>in</strong>aesthetic cues (Schack, 2004). Accord<strong>in</strong>g to this cognitive<br />

architecture, motor actions are activated <strong>and</strong> composed of BACs. The<br />

<strong>in</strong>ternal <strong>and</strong> external features of BACs are triggered by an image of the<br />

voluntary executed movement. Therefore, <strong>in</strong>formation from the environment<br />

is needed to perform adequately. L<strong>in</strong>ks between sensory effects of<br />

a movement <strong>and</strong> correspond<strong>in</strong>g motor comm<strong>and</strong>s will be established<br />

while execut<strong>in</strong>g an action <strong>and</strong>, moreover, create a specific expertise. In<br />

other words, a more adequate image will be created.<br />

A study of the cognitive representation of a swimm<strong>in</strong>g technique,<br />

<strong>in</strong>clud<strong>in</strong>g their sensory effects <strong>and</strong> biomechanics, needs to use an established<br />

technique, which <strong>in</strong> the present study is the flip-turn executed un-


der different conditions (i.e. different swim suits). The general reason<strong>in</strong>g<br />

is as follows: Accord<strong>in</strong>g to the statements of companies advertis<strong>in</strong>g high<br />

tech full swim suits (which were not banned before 2010) the speed will<br />

<strong>in</strong>crease <strong>and</strong> the feel<strong>in</strong>g will be altered. This is supported by statements<br />

of elite swimmers like: “swimm<strong>in</strong>g downhill”, “swim like a rocket”, “You<br />

lie on top of the water; don’t die <strong>in</strong> the last metres; you have no pa<strong>in</strong>” or<br />

“swim as on a hover cushion”. These statements show that biomechanical<br />

changes may not be effects simply due to physical enhancement of<br />

the swim suit properties, because they <strong>in</strong>dicate the importance of sensory<br />

aspects. Accord<strong>in</strong>g to the hierarchical movement organization theory<br />

(Schack, 2004), differences of the motor outcome can be caused by differences<br />

of the cognitive representation. Flip turns are important part of<br />

every race <strong>and</strong> differences <strong>in</strong> the biomechanics of flip turns are expected<br />

depend<strong>in</strong>g on the swim suit type. Here we <strong>in</strong>vestigate to what extent<br />

these differences co<strong>in</strong>cide with sensory changes. The question is whether<br />

sensory effects can <strong>in</strong>fluence the execution of motor programs <strong>in</strong>itiated<br />

by mental representation <strong>in</strong> long term memory, or not.<br />

The purpose of this study is to elucidate the <strong>in</strong>fluence of sensory effects<br />

on the biomechanical outcome of the flip turn technique under two<br />

different conditions: wear<strong>in</strong>g a regular or a full swim suit (cover<strong>in</strong>g the<br />

whole body surface <strong>and</strong> possess<strong>in</strong>g slight float<strong>in</strong>g properties).<br />

Methods<br />

Elite swimmers (N=8: 4 female, 4 male, mean age 19.6 years), members<br />

of national or youth national team participat<strong>in</strong>g <strong>in</strong> approx. 10 workouts<br />

per week were <strong>in</strong>formed about the test procedures <strong>and</strong> gave their<br />

consent to participate <strong>in</strong> this study. They were asked to br<strong>in</strong>g their own<br />

regular <strong>and</strong> competitive high tech swim suits <strong>and</strong> <strong>in</strong>structed to execute<br />

their flip turns as usual.<br />

The study consisted of 4 parts. First a k<strong>in</strong>ematic analysis of 10 flip<br />

turns with subjects wear<strong>in</strong>g both k<strong>in</strong>ds of swim suits was conducted<br />

(a). Subsequently, they executed the Structure Dimension Analysis-Motorics<br />

procedure (SDA-M, Schack, 2004) with biomechanical BACs (b).<br />

Thirdly, they answered a questionnaire regard<strong>in</strong>g their sensory impressions<br />

(c), <strong>and</strong> f<strong>in</strong>ally they executed the SDA-M procedure with sensory<br />

movement features (d).<br />

The SDA-M procedure reveals mental representations of movements,<br />

basically consist<strong>in</strong>g of three steps, <strong>and</strong> was <strong>in</strong>troduced already <strong>in</strong><br />

2006 <strong>in</strong> swimm<strong>in</strong>g research by Ungerechts <strong>and</strong> Schack. First, the participants<br />

make similarity judgements regard<strong>in</strong>g all BACs. Afterwards, the<br />

cognitive representation of the movement is illustrated via dendrograms<br />

as the result of a hierarchical unweighted pair-group average cluster<br />

analysis. At the end, all result<strong>in</strong>g cluster structures can be compared via<br />

an <strong>in</strong>variance measure.<br />

Dur<strong>in</strong>g the similarity judgements participants make an implicit<br />

statement about their movement organization by mak<strong>in</strong>g decisions<br />

based on their own mental representation. Basically there are two options<br />

to study the mental representation, either tak<strong>in</strong>g biomechanically<br />

based BACs or offer<strong>in</strong>g sensory movement features (remember<strong>in</strong>g that<br />

BACs are functionally closely related to the biomechanics as well as<br />

to sensory effects <strong>and</strong> stored together). The biomechanical BACs used<br />

were: fix h<strong>and</strong>s, head on chest, <strong>in</strong>itial butterfly kick, bend<strong>in</strong>g legs, feet<br />

hit wall, push-off, streaml<strong>in</strong>e position, glid<strong>in</strong>g, rotate hip/legs, rotate<br />

stomach, <strong>and</strong> leg movement (BxB splitt<strong>in</strong>g procedure). These eleven<br />

keywords also represent the allocations used <strong>in</strong> the B x B approach.<br />

The 23 sensory movement features were selected due to feel for own<br />

body (rush<strong>in</strong>g of water, look at the pool bottom, estimate distance to<br />

the wall, pressure on stomach, pressure on the soles <strong>in</strong>creases, vibration<br />

of muscles, vibration of sk<strong>in</strong>, tension <strong>in</strong> neck muscles, keep equilibrium,<br />

leg extension, pressure on shanks, pressure on both sides of the legs, alternatively),<br />

feel for speed (keep speed, rotational speed <strong>in</strong>creases, maximum<br />

change of body speed, renewed speed <strong>in</strong>creases, glid<strong>in</strong>g velocity<br />

decreases) <strong>and</strong> reactions of the water (wave drag, drag effects start, drag<br />

effects release, lowest drag, push<strong>in</strong>g water mass, buoyancy). They formed<br />

the keywords for the BxF splitt<strong>in</strong>g procedure.<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

Dur<strong>in</strong>g the splitt<strong>in</strong>g procedure the participants judge whether the<br />

two presented BACs (respectively the presented BAC <strong>and</strong> the sensory<br />

movement feature) are related to each other, or not. Us<strong>in</strong>g a BxB approach,<br />

eleven BACs <strong>and</strong> eleven biomechanical allocations are presented.<br />

Us<strong>in</strong>g a BxF approach the swimmers were asked to relate all of 23<br />

sensory movement features to eleven established BACs. The decisions<br />

form the basis for the hierarchical unweighted pair-group average cluster<br />

analysis which results <strong>in</strong> <strong>in</strong>dividual dendrograms. A comparison of<br />

the dendrograms via an <strong>in</strong>variance measure revealed similarities <strong>in</strong> the<br />

functional equivalence of biomechanical <strong>and</strong> sensory based movement<br />

constra<strong>in</strong>ts.<br />

results<br />

Biomechanical items show substantial differences; four of six are significantly<br />

different (e.g. Table 1). Consequently, <strong>in</strong> this test situation there<br />

is a trend towards an established difference of biomechanical items due<br />

to the <strong>in</strong>fluence of swim suits.<br />

Table 1. Biomechanical parameters of the flip turn for both conditions.<br />

Test item Regular swim suit Full swim suit<br />

speed <strong>in</strong>to the wall (m/s) 1.68 (0.26) 1.81 (0.25)<br />

speed of rotation (º/s) 291 (27.60) 284 (37.50)<br />

speed push off (m/s) 2.48 (0.30) 2.58 (0.33)<br />

time of leg extension (s) 0.286 (0.06) 0.294 (0.06)<br />

drag coefficient (s) 2.85 (0.07) 2.70 (0.08)<br />

Time total turn (s) 2.98 (0.32) 2.85 (0.25)<br />

The sensory questionnaire reveals the follow<strong>in</strong>g trends regard<strong>in</strong>g substantial<br />

differences between the two test situations. In 15 of 23 cases<br />

the sensory movement features were judged to be different; three of 15<br />

differences are statistically significant at the level of p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Figure 1. Grouped dendrogram of the flip turn <strong>in</strong> full suits accord<strong>in</strong>g<br />

to BxB; marked gray areas represent cluster structures; numbers on the<br />

right are (Euclidian distances); the lower the distances between these<br />

BACs, the stronger the connection <strong>in</strong> the LTM. Keywords: 1 fix h<strong>and</strong>s;<br />

2 head on chest; 3 <strong>in</strong>itial butterfly kick ;4 bend<strong>in</strong>g legs; 5 feet hit wall;<br />

6 push-off; 7 streaml<strong>in</strong>e position; 8 glid<strong>in</strong>g; 9 rotate hip/legs; 10 rotate<br />

stomach; 11 leg movement<br />

Figure 2. Grouped dendrogram of the flip turn <strong>in</strong> full suits accord<strong>in</strong>g to<br />

BxF. Keywords: 1 fix h<strong>and</strong>s; 2 head on chest; 3 <strong>in</strong>itial butterfly kick ;4<br />

bend<strong>in</strong>g legs; 5 feet hit wall; 6 push-off; 7 streaml<strong>in</strong>e position; 8 glid<strong>in</strong>g;<br />

9 rotate hip/legs; 10 rotate stomach; 11 leg movement<br />

dIscussIon<br />

This study is a first attempt to check experimentally via the cognitive<br />

representation of the flip turn technique how sensory effects <strong>in</strong>fluence<br />

the motor outcome under two different conditions: wear<strong>in</strong>g a regular or<br />

a full swim suit. The different swim suits changed the representation of<br />

the sensory based effects, <strong>and</strong> thus <strong>in</strong>fluenced the postures of the flipturn<br />

accord<strong>in</strong>g to the conditions.<br />

The particular mental representation was visualized by dendrograms<br />

(represent<strong>in</strong>g the cognitive representation) which give <strong>in</strong>sight as to how<br />

Basic Action Concepts are related to each other. The dendrograms, when<br />

based on action allocations, are well structured <strong>and</strong> valid for experts execut<strong>in</strong>g<br />

such a movement. The dendrograms, when based on sensory<br />

movement features, show similar patterns. A comparison of the group<br />

dendrograms us<strong>in</strong>g a full swim suit revealed that sensory based representations<br />

are closely related to the biomechanical structure of the flip<br />

turn. A cross over comparison showed that different swim suits changed<br />

the sensory effects <strong>and</strong> thus <strong>in</strong>fluences the postures of the flip-turn. This<br />

change was manifested <strong>in</strong> the mental representations. This change leads<br />

to the question whether there is one mental representation <strong>in</strong> the longterm-memory<br />

that needs to be modified for different conditions, or if<br />

there are different ones for the different conditions.<br />

The experiments revealed that sensory effects are strongly related to<br />

348<br />

action keywords <strong>in</strong> the cognitive representation of a movement stored <strong>in</strong><br />

LTM. This outcome is very promis<strong>in</strong>g for the work on technical aspects<br />

<strong>in</strong> swimm<strong>in</strong>g for elite swimmers. In striv<strong>in</strong>g for improvements related to<br />

the <strong>in</strong>teraction of limb movement <strong>and</strong> water motion, the sensory movement<br />

features should be the tra<strong>in</strong><strong>in</strong>g focus.<br />

conclusIon<br />

Any volitional or mentally controlled movement requires the encod<strong>in</strong>g<br />

of the <strong>in</strong>tended goal which pr<strong>in</strong>cipally acts as the trigger for subsequent<br />

cognitive processes establish<strong>in</strong>g a mental model of the future on which<br />

mental control processes can depend. The transfer of the anticipated action<br />

<strong>in</strong>to motor actions, executed at a mental representational level, is<br />

organized conceptually us<strong>in</strong>g cognitive compilation units, called BACs<br />

which f<strong>in</strong>ally serve to control actions effectively at lowest cognitive <strong>and</strong><br />

energetic costs. Each BAC can be regarded as an <strong>in</strong>variant movement<br />

posture that is related to its sensory effects (Schack, 2004). All of the<br />

<strong>in</strong>variant movement postures need to be achieved to successfully perform<br />

the movement. Suppose that, whether or not a movement position<br />

is reached is decided by compar<strong>in</strong>g actual perceptions to certa<strong>in</strong> target<br />

perceptions. As soon as one BAC is accomplished sensory control is<br />

used to <strong>in</strong>itiate the transition of the body to the next BAC. So the whole<br />

movement is under perceptive control. The structure of the movement<br />

<strong>and</strong> its effects <strong>and</strong> subsequently reached goals are stored together <strong>in</strong> the<br />

long-term-memory as a part of the motor repertoire.<br />

Movements performed consciously or subconsciously change the<br />

position of the body <strong>in</strong> space <strong>and</strong> time <strong>and</strong> evoke a change <strong>in</strong> the environment.<br />

So the movement is <strong>in</strong>itiated by the <strong>in</strong>tention to evoke a<br />

certa<strong>in</strong> change <strong>in</strong> the environment. Ma<strong>in</strong>ly subconsciously the needed<br />

movement is selected from the motor repertoire <strong>and</strong> adjusted to the<br />

situational <strong>in</strong>fluences. Thereby learned <strong>and</strong> automated movements can<br />

be accessed more easily.<br />

F<strong>in</strong>ally, after it has been shown that these keywords are of equivalent<br />

value, the research to f<strong>in</strong>d appropriate sensory based keywords for the<br />

various technical aspects <strong>in</strong> aquatic space is recommended.<br />

reFerences<br />

Bernste<strong>in</strong>, (1967). The co-ord<strong>in</strong>ation <strong>and</strong> regulation of movements. Oxford:<br />

Pergamon Press.<br />

Schack, T. (2004). The Cognitive Architecture of Complex Movement.<br />

International Journal of Sport <strong>and</strong> Exercise Psychology, 2 (4), 403-438.<br />

Ungerechts, B. E. & Schack T, (2006). Mental representation of swimm<strong>in</strong>g<br />

strokes. In: J.P. Vilas-Boas, F. Alves, A. Marques (eds.), <strong>Biomechanics</strong><br />

<strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong> Swimm<strong>in</strong>g X. Portuguese Journal of Sport<br />

Sciences Vol. 6,Suppl. 2, 346-348.<br />

AcKnoWledGeMents<br />

We thank the swimmers of the NZA for their participation, M. Truijens<br />

/ Amsterdam for his support <strong>and</strong> C. Schütz / Bielefeld for technical<br />

advice.


The Role of Verbal Information about Sensory<br />

Experience from Movement Apparatus <strong>in</strong> the<br />

Process of Swimm<strong>in</strong>g Economization<br />

Zatoń, K.<br />

The University School of Physical Education <strong>in</strong> Wrocław, Wrocław, Pol<strong>and</strong><br />

The way <strong>in</strong>formation is transferred <strong>and</strong> received <strong>in</strong> the process of learn<strong>in</strong>g<br />

motor swimm<strong>in</strong>g activities directly determ<strong>in</strong>es the effectiveness of<br />

the process. An effective way to improve the economization of the actions<br />

is through constant master<strong>in</strong>g of muscle tension regulation. This<br />

is only possible when a learner can receive <strong>in</strong>formation from the water<br />

environment, which affects his/her receptors <strong>in</strong> a conscious way. The aim<br />

of this study is to determ<strong>in</strong>e the impact of verbal <strong>in</strong>formation, which<br />

makes the learner aware of the k<strong>in</strong>aesthetic experience <strong>and</strong> which, <strong>in</strong><br />

effect, decreases the physiological cost of work.<br />

Key words: swimm<strong>in</strong>g, movement economization, word<br />

IntroductIon<br />

The ma<strong>in</strong> condition of learn<strong>in</strong>g <strong>in</strong> physical education, as <strong>in</strong> any form of<br />

education, is the work of stimuli on specialized reception organs (receptors).<br />

In these receptors alertness is generated which <strong>in</strong>itiates nervous<br />

processes whose different degree of <strong>in</strong>tensity reflects various <strong>in</strong>tensity<br />

of the stimuli (Arnold, 1988; Cox et al., 1988). This <strong>in</strong>itiates central<br />

nervous system, which is a precondition to further cognition stages, i.e.<br />

sens<strong>in</strong>g, impression <strong>and</strong> perception (Sadowski et al., 2000). Sens<strong>in</strong>g is<br />

the most basic <strong>and</strong> general impression related to stimulat<strong>in</strong>g receptors<br />

whose specifics are connected with a selected organ.<br />

In the process of learn<strong>in</strong>g about mov<strong>in</strong>g one’s own body, which ensures<br />

an easy use of motor skills, certa<strong>in</strong> <strong>in</strong>formation seems necessary;<br />

ma<strong>in</strong>ly the <strong>in</strong>formation com<strong>in</strong>g from a teacher <strong>and</strong> related to qualitative<br />

categories of movement. Here, it seems as if the only effective form of<br />

<strong>in</strong>formation is a word, thanks to which a teacher may, together with a<br />

student, assess senses/sensory experience (e.g. muscle receptors). Mak<strong>in</strong>g<br />

a student aware of those receptors seems only possible through the<br />

use of language.<br />

Verbal <strong>in</strong>formation becomes especially valuable <strong>in</strong> a situation where<br />

a new set of movement solutions is <strong>in</strong>troduced. Such sets may become a<br />

background for further success <strong>in</strong> sports, theatre or creative <strong>in</strong>spiration.<br />

Research to date suggests that teachers of physical education neglect<br />

the importance of verbal <strong>in</strong>formation <strong>in</strong> a teach<strong>in</strong>g <strong>and</strong> learn<strong>in</strong>g process<br />

(Zatoń, 1988; Zatoń, 1999). They seem to consider that the basis for<br />

the creation of an image of a certa<strong>in</strong> movement is through presentation.<br />

Verbal <strong>in</strong>formation serves only for the purposes of determ<strong>in</strong><strong>in</strong>g conditions<br />

for perform<strong>in</strong>g certa<strong>in</strong> movements, as a means of warn<strong>in</strong>g aga<strong>in</strong>st<br />

danger or for organizational purposes. However, as it has been proven<br />

<strong>in</strong> numerous studies deal<strong>in</strong>g with the impact of verbal <strong>in</strong>formation on<br />

the effectiveness of learn<strong>in</strong>g, an effective educational process of learn<strong>in</strong>g<br />

movements should be generally based on a verbal message, not only <strong>in</strong><br />

acquir<strong>in</strong>g <strong>in</strong>formation, but also <strong>in</strong> ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g balance of <strong>in</strong>formation<br />

(sensoristasis) (Arnold, 1988; Strath et al., 2000; Zatoń, 1999). It is by<br />

means of verbal communication that <strong>in</strong>formation flow may be directed,<br />

its hierarchy <strong>and</strong> specifics determ<strong>in</strong>ed. This refers particularly to those<br />

situations <strong>in</strong> which cognition takes place through stimulation of exteroreceptors<br />

<strong>and</strong> <strong>in</strong>ter-receptors <strong>in</strong> real time (Zatoń, 1999; Zatoń, 2002).<br />

The perception of senses com<strong>in</strong>g from this may, <strong>and</strong> <strong>in</strong> some situations<br />

should, be predeterm<strong>in</strong>ed by competent verbal <strong>in</strong>formation (Zatoń,<br />

2002).<br />

In the process of learn<strong>in</strong>g to swim, where the water environment<br />

requires a special pedagogical approach by a teacher, verbal <strong>in</strong>formation<br />

transferred by the teacher is of great significance. We are talk<strong>in</strong>g<br />

here about <strong>in</strong>formation provided by the teacher <strong>and</strong> reach<strong>in</strong>g a student<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

that expla<strong>in</strong>s the crucial ideas about perceived stimuli. This allows a<br />

learner to prepare for the <strong>in</strong>formation to come <strong>in</strong> such a way that it can<br />

be perceived effectively <strong>and</strong> selectively. The perception of senses from<br />

the movement apparatus dur<strong>in</strong>g the process of learn<strong>in</strong>g <strong>and</strong> master<strong>in</strong>g<br />

swimm<strong>in</strong>g technique may be h<strong>and</strong>led by way of proper verbal <strong>in</strong>struction.<br />

A conscious perception by the receptors translates <strong>in</strong>to better underst<strong>and</strong><strong>in</strong>g<br />

of one’s body position <strong>in</strong> space, <strong>and</strong> <strong>in</strong> effect a more optimal<br />

muscle tension. This may have an impact on faster <strong>and</strong> more economical<br />

learn<strong>in</strong>g of movement <strong>in</strong> water (Arnold, 1988; Fitts, 1996; Zatoń, 2002).<br />

From the physiological view po<strong>in</strong>t <strong>in</strong> a situation where the mechanism<br />

of steer<strong>in</strong>g the movement is improved, <strong>and</strong> energy is ga<strong>in</strong>ed (which occurs<br />

as a result of physical exercises) the physiological cost of work is<br />

decreased. This is commonly known as economization of effort. Physiological<br />

cost of work is – <strong>in</strong> turn – every <strong>in</strong>stance where homeostasis is<br />

disturbed due to effort (Abbis et al., 2005; Bentley et al., 2007; Kubukeli<br />

et al., 2002).<br />

The aim of this study is to determ<strong>in</strong>e the impact of verbal <strong>in</strong>formation<br />

on sensory experience from the movement apparatus (k<strong>in</strong>aesthetic)<br />

on economization of effort.<br />

Methods<br />

48 students of the first year at the University School of Physical Education<br />

<strong>in</strong> Wrocław were the subjects <strong>in</strong> this study (24 men <strong>and</strong> 24 women).<br />

An average height of the men was 186 cm, their average mass was 87 kg.<br />

The average height of women was 168 cm <strong>and</strong> their average mass was<br />

56 kg. The research was done <strong>in</strong> the second semester of the academic<br />

year 2007/2008 <strong>in</strong> the Laboratory of Movement <strong>in</strong> the Natural Environment<br />

at the Department of Swimm<strong>in</strong>g, which has certificate no<br />

1374-d/1/2007 ISO 9001:2001. The research was done at the same time<br />

of day for all the subjects, <strong>in</strong> rooms with similar conditions (similar temperature<br />

<strong>and</strong> humidity). The students had been <strong>in</strong>formed about the purpose<br />

of the experiment, its course <strong>and</strong> of what was expected from them.<br />

To secure a homogenous group, those subjects who tra<strong>in</strong>ed <strong>in</strong> sport<br />

professionally were elim<strong>in</strong>ated.<br />

The test group was divided r<strong>and</strong>omly <strong>in</strong>to three groups (control <strong>and</strong><br />

two experimental). Before embark<strong>in</strong>g on a proper experiment <strong>and</strong> before<br />

the groups were divided all the people that had been qualified to certa<strong>in</strong><br />

tests were subjected to a process of assess<strong>in</strong>g their entry level ability to<br />

differentiate k<strong>in</strong>etically. This allowed us to determ<strong>in</strong>e the <strong>in</strong>dividual level<br />

of k<strong>in</strong>aesthetic differentiat<strong>in</strong>g.<br />

The basic assumption of the experiment was to gauge the impact of<br />

verbal <strong>in</strong>formation provided by the researcher on the effort economization<br />

(physiological cost). This led to creat<strong>in</strong>g three groups: (1) control<br />

group – 16 people; (2) experimental group I – 16 people; (3) experimental<br />

group II – 16 people.<br />

The first group performed movement tasks on the swim ergometer<br />

without verbal <strong>in</strong>formation that could have prepared them to perceive<br />

sensory experience from the movement apparatus. In experimental<br />

group I, while perform<strong>in</strong>g tasks on the ergometer, a verbal message was<br />

prepared, transferred <strong>and</strong> verified, so that the tested <strong>in</strong>dividuals could<br />

consciously prepare themselves for the <strong>in</strong>formation they were gett<strong>in</strong>g<br />

from the movement apparatus. This lasted as long as the cost of physiological<br />

effort could be observed as ma<strong>in</strong>ta<strong>in</strong>ed at a constant low level.<br />

The experimental group II, while perform<strong>in</strong>g identical tasks on the<br />

ergometer, received verbal <strong>in</strong>formation previously prepared <strong>and</strong> tested<br />

with the experimental group I.<br />

The assessment of the level of k<strong>in</strong>aesthetic differentiation was performed<br />

us<strong>in</strong>g a method of muscle force movements repetition for elbow<br />

jo<strong>in</strong>ts extensors <strong>in</strong> the lab of the Swimm<strong>in</strong>g Department. A detailed<br />

description of the method can be read <strong>in</strong> the publication by Zatoń <strong>and</strong><br />

Klarowicz (Zatoń et al., 2001).<br />

The assessment of the effort economization (physiological cost)<br />

was performed with the use of the swim ergometer (Swim Ergometer<br />

– Weba Sport und Med. – Artikel CmbH) (Figure 1). It consisted of<br />

perform<strong>in</strong>g arms movements imitat<strong>in</strong>g crawl, <strong>in</strong> a given rhythm, with<br />

349


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

the help of a metronome. The duration of the test was 5 m<strong>in</strong>utes (this<br />

is the effort time when 95% of oxygen changes take place <strong>in</strong> the organism)<br />

(Abbis et al., 2005; Bentley et al., 2007; Costill 1966; Kubukeli et<br />

al., 2002).<br />

Figure 1. Swim Ergometer.<br />

Dur<strong>in</strong>g the experiment the follow<strong>in</strong>g were noted:<br />

movement frequency (Hz),<br />

force that the person subject to the test was us<strong>in</strong>g aga<strong>in</strong>st the arms of the<br />

ergometer <strong>in</strong> each pull movement cycle (separately for each arm) (N),<br />

distance that the upper limbs covered <strong>in</strong> the movement cycle (m),<br />

pulse dur<strong>in</strong>g the test <strong>and</strong> restitution time.<br />

The purpose of the test was to observe differences occurr<strong>in</strong>g <strong>in</strong> the<br />

movement economization (physiological cost) of effort before <strong>and</strong> after<br />

perform<strong>in</strong>g the task, by measur<strong>in</strong>g arm work frequency (5 m<strong>in</strong>). The<br />

measure of the economization was the sum of heart rate frequency <strong>and</strong><br />

rest time. It was assumed here that the change <strong>in</strong> the physiological cost<br />

is best shown by the sum of restitution frequency of heart rate accord<strong>in</strong>g<br />

to the formula proposed by Klarowicz (1970). It was documented on<br />

many occasions that after effort the restitution effectiveness is important<br />

<strong>in</strong>formation on the level of tiredness (Abbis et al., 2005; Bentley et al.,<br />

2007; Cox et al., 1988; Kubukeli et al., 2002).<br />

After the group was r<strong>and</strong>omly selected (experimental group I) a<br />

verification of <strong>in</strong>formation contents was performed. Its purpose was to<br />

attune the test persons to a conscious perception of stimuli from the<br />

movement apparatus. The verification consisted <strong>in</strong> <strong>in</strong>dividual transmission<br />

of <strong>in</strong>formation while work<strong>in</strong>g on the swim ergometer. The researcher<br />

was look<strong>in</strong>g for such verbal expressions that could directly translate to<br />

the decrease of effort. The experiment lasted as long as the tested person<br />

could receive an optimal version of the verbal <strong>in</strong>formation that would<br />

have a direct bear<strong>in</strong>g on mak<strong>in</strong>g his/her work more economical while<br />

perform<strong>in</strong>g the task on the swim ergometer (Zatoń et al., 2001).<br />

The f<strong>in</strong>al version of the verbal <strong>in</strong>formation used <strong>in</strong> the proper experiment<br />

(experimental group II).<br />

Lie on the bench so that you do not feel tension <strong>in</strong> any part of the<br />

body.<br />

Position your arms <strong>in</strong> a slightly bent position <strong>in</strong> elbow jo<strong>in</strong>ts (10<br />

– 15˚).<br />

Dur<strong>in</strong>g stroke movement slightly bend palms of h<strong>and</strong>s (articulatio<br />

radiocarpea) (5 – 10˚).<br />

Perform the movement fluently (do not move abruptly). Dur<strong>in</strong>g<br />

the experiment concentrate on feel<strong>in</strong>g steady pressure of the surface of<br />

“gauges” on the h<strong>and</strong> surface.<br />

While feel<strong>in</strong>g the pressure of “the gauges” on the palm receptors, try<br />

to regulate the pressure you are apply<strong>in</strong>g so that dur<strong>in</strong>g the pull movement<br />

you will feel a maximum pressure, while perform<strong>in</strong>g the recovery<br />

movement, m<strong>in</strong>imum pressure.<br />

350<br />

translate to the decrease of effort. The experiment lasted as long as the tested person<br />

could receive an optimal version of the verbal <strong>in</strong>formation that would have a direct<br />

bear<strong>in</strong>g on mak<strong>in</strong>g his/her work more economical while perform<strong>in</strong>g the task on the<br />

swim ergometer (Zatoń et al., 2001).<br />

The f<strong>in</strong>al version of the verbal <strong>in</strong>formation used <strong>in</strong> the proper experiment<br />

(experimental group II).<br />

Lie on the bench so that you do not feel tension <strong>in</strong> any part of the body.<br />

Position your arms <strong>in</strong> a slightly bent position <strong>in</strong> elbow jo<strong>in</strong>ts (10 – 15�).<br />

Dur<strong>in</strong>g stroke movement slightly bend palms of h<strong>and</strong>s (articulatio radiocarpea) (5 –<br />

results<br />

10�).<br />

To determ<strong>in</strong>e the relationship between verbal <strong>in</strong>formation on perception<br />

concentrate from the on feel<strong>in</strong>g movement steady pressure apparatus of the <strong>and</strong> surface effort of economization, “gauges” on the h<strong>and</strong> basic surface. statistical<br />

methods were used. Arithmetic average was measured, as well<br />

as pressure, st<strong>and</strong>ard while deviation, perform<strong>in</strong>g Student’s the recovery t-test movement, for dependent m<strong>in</strong>imum pressure. tests (with<strong>in</strong> the<br />

same RESULTS groups) <strong>and</strong> also a simple correlation between the tested features.<br />

Statistical significance was set at the confidence level, p ≤ 0.05.<br />

Perform the movement fluently (do not move abruptly). Dur<strong>in</strong>g the experiment<br />

While feel<strong>in</strong>g the pressure of “the gauges” on the palm receptors, try to regulate the<br />

pressure you are apply<strong>in</strong>g so that dur<strong>in</strong>g the pull movement you will feel a maximum<br />

To determ<strong>in</strong>e the relationship between verbal <strong>in</strong>formation on perception from the<br />

movement apparatus <strong>and</strong> effort economization, basic statistical methods were used.<br />

Arithmetic average was measured, as well as st<strong>and</strong>ard deviation, Student’s t-test for<br />

dependent tests (with<strong>in</strong> the same groups) <strong>and</strong> also a simple correlation between the<br />

Table 1. Change <strong>in</strong> the amount of work (∑ work) <strong>and</strong> the sum of restitution<br />

tested heart features. pulse Statistical (∑ HR significance rest), <strong>in</strong> two was set groups at the confidence (Control level, <strong>and</strong> Experimental<br />

p ≤ 0.05.<br />

I, II) before <strong>and</strong> after the end of the experiment <strong>and</strong> the significance of<br />

differences (t). (nK = 16, nE = 16).<br />

Table 1. Change <strong>in</strong> the amount of work (∑ work) <strong>and</strong> the sum of restitution heart pulse<br />

(∑ HR rest), <strong>in</strong> two groups (Control <strong>and</strong> Experimental I, II) before <strong>and</strong> after the end of<br />

the experiment <strong>and</strong> the significance of differences (t). (nK = 16, nE = 16).<br />

Group<br />

Feature<br />

Control<br />

group<br />

test 1<br />

Control<br />

group<br />

test 2<br />

t Experimental<br />

group I<br />

test 1<br />

Experimenta<br />

l group II<br />

test 2<br />

∑ work X 3089 3022 -0.11 3111 3481 3.11*<br />

KJ S 248.12 312.30 298.62 333.18 –<br />

∑ HR X 202 201 -0.02 212 109 -4.10*<br />

rest S 23.14 20.17 22.30 12.33 –<br />

Table 1 shows the results of the experiment. The conclusion is that <strong>in</strong><br />

the experimental group II, where the tested person work<strong>in</strong>g on the ergometer<br />

was provided with verbal <strong>in</strong>formation attun<strong>in</strong>g the person to<br />

conscious perception of senses from the movement apparatus, statistically<br />

relevant differences were achieved. These differences demonstrated<br />

the effectiveness of after effort restitution (significantly better <strong>in</strong> the<br />

experimental group II).<br />

dIscussIon<br />

Calculation of correlation coefficients proves that there is a relationship<br />

between verbal <strong>in</strong>formation <strong>and</strong> movement economization (Bentley<br />

et al., 2007; Klarowicz, 1970; Kubukeli et al., 2002; Zatoń 2002).<br />

Therefore, the conclusion can be drawn that, the <strong>in</strong>formation expressed<br />

verbally on how to perform a movement, which should provide certa<strong>in</strong><br />

impressions, given by the researcher before, dur<strong>in</strong>g <strong>and</strong> directly after the<br />

test, may make the tested person aware of the need to properly coord<strong>in</strong>ate<br />

the action (Cox et al., 1988; Zatoń, 1999). Receptors <strong>in</strong> muscles,<br />

tendons <strong>and</strong> jo<strong>in</strong>ts provide the central nervous system with the <strong>in</strong>formation<br />

on the movements <strong>and</strong> limb positions as well as positions of the<br />

other body parts (Arnold, 1988; Kubukeli et al., 2002; Sadowski et al.,<br />

2000). Ligaments transmitt<strong>in</strong>g these stimuli constitute a part of the so<br />

called movement neurons. Thanks to the <strong>in</strong>formation received from the<br />

nervous system, contractions of s<strong>in</strong>gle muscles or muscle groups are coord<strong>in</strong>ated,<br />

giv<strong>in</strong>g harmonious, subtle <strong>and</strong> effective movements. An <strong>in</strong>telligent<br />

teacher – possess<strong>in</strong>g an <strong>in</strong>herent feature of elim<strong>in</strong>at<strong>in</strong>g excessive<br />

<strong>in</strong>formation – may create a hierarchy of verbal <strong>in</strong>formation, consciously<br />

draw<strong>in</strong>g learner’s attention to selected fragments of this <strong>in</strong>formation. In<br />

the case of this experiment it was our <strong>in</strong>tention to draw the reader’s attention<br />

to a conscious preparation on the part of the learner to perform<br />

selected elements of movements (proper hierarchization of movement<br />

actions <strong>and</strong> contraction) (Abbis et al., 2005; Arnold, 1988; Bentley et<br />

al., 2007; Cox et al., 1988; Sadowski et al., 2000). It can be stated that<br />

the major role <strong>in</strong> the movement optimization (economization) is played<br />

by verbal <strong>in</strong>formation that allows the learner to become aware of the<br />

essence of actions through self-control (Zatoń 1999; Zatoń et al., 1999;<br />

Zatoń et al., 2001; Zatoń 2002). We are aware, however, that this conclusion<br />

requires further research. Mov<strong>in</strong>g certa<strong>in</strong> parts of the body <strong>in</strong> a<br />

proper way <strong>and</strong> <strong>in</strong> a certa<strong>in</strong> sequence requires <strong>in</strong>itiat<strong>in</strong>g th<strong>in</strong>k<strong>in</strong>g processes,<br />

i.e. perception, analysis, remember<strong>in</strong>g, etc. as skeletal muscles are<br />

subject to conscious decisions. (Abbis et al., 2005; Arnold 1988; Cox et<br />

al., 1988; Fitts 1996; Strath et al., 2000; Zatoń et al., 2001).<br />

t


conclusIon<br />

Self control, which is a conscious act of position<strong>in</strong>g limbs <strong>in</strong> relation<br />

to one another, to the body, head, <strong>and</strong> hence the structure of muscle<br />

tension <strong>and</strong> their sequence, may directly affect the decrease of the physiological<br />

cost of work. The results obta<strong>in</strong>ed show significant correlations<br />

between the verbal <strong>in</strong>formation used <strong>in</strong> the experiment <strong>and</strong> economy<br />

of movement.<br />

reFerences<br />

Abbis, C.R. & Laursen, P.B. (2005). Models to expla<strong>in</strong> fatigue dur<strong>in</strong>g<br />

prolonged endurance cycl<strong>in</strong>g. Sports <strong>Medic<strong>in</strong>e</strong>, 35(10), 865-898.<br />

Arnold, P.J. (1988). K<strong>in</strong>esthetic perception <strong>and</strong> sports skills: some empirical<br />

f<strong>in</strong>d<strong>in</strong>gs <strong>and</strong> philosophical considerations. In: Ross S., Charett<br />

L. (ed.) Persons M<strong>in</strong>ds <strong>and</strong> Bodies. University Press of Canada, North<br />

York, Ontario, 51-59.<br />

Bentley, D.J., Newell, U.J. & Bishop, D. (2007). Incremental exercise<br />

test design <strong>and</strong> analysis: implications for performance diagnostics <strong>in</strong><br />

endurance athletes. Sports <strong>Medic<strong>in</strong>e</strong>, 37(7), 575-586.<br />

Costill, D.L. (1966). Use of a swimm<strong>in</strong>g ergometer <strong>in</strong> physiological research.<br />

Research Qartarly, 37, 564-565.<br />

Cox, R. & Walkuski, J. (1988). K<strong>in</strong>esthetic Sensitivity <strong>and</strong> Stages of<br />

Motor Learn<strong>in</strong>g. Journal of Human Movement Study, 1, 1-10.<br />

Fitts, R.H. (1996). Muscle fatigue: the cellular aspects. American Journal<br />

of Sports <strong>Medic<strong>in</strong>e</strong>, 24, 9-13.<br />

Klonowicz, S. (1970). Metody badań fizjologicznych w zakładzie przemysłowym.<br />

PZWL, Warszawa.<br />

Kubukeli, Z.N., Noakes, T.D. & Dennis, S.C. (2002). Tra<strong>in</strong><strong>in</strong>g techniques<br />

to improve endurance exercise performances. Sports <strong>Medic<strong>in</strong>e</strong>,<br />

32(8), 489-509.<br />

Sadowski, B., Chmurzyński, J.A. (2000). Biological mechanisms of behavior<br />

(In Polish). PWN, Warszawa.<br />

Strath, J.S., Swarz, A.M., Dawid, R. & Basset, J.R. (2000). Evaluation<br />

of heart rate as a method for assess<strong>in</strong>g moderate <strong>in</strong>tensity physical<br />

activity. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports <strong>and</strong> Exercise, International<br />

Life Sciences Institute, 465-469.<br />

Zatoń, K. (1988). The effectiveness of verbal <strong>in</strong>formation <strong>in</strong> the process<br />

of learn<strong>in</strong>g motor function <strong>in</strong> swimm<strong>in</strong>g (In Polish). Rozprawy Naukowe<br />

AWF Wrocław, XVI, 217-283.<br />

Zatoń, K. (1999). Speech as a way of didactic communication dur<strong>in</strong>g<br />

physical education. VII ICHPER European Congress, Prague, 516-<br />

521.<br />

Zatoń, K. & Zatoń, M. (1999). Changes <strong>in</strong> heart rate <strong>in</strong>duced by exertion,<br />

accord<strong>in</strong>g to different discursive strategies employed <strong>in</strong> teach<strong>in</strong>g<br />

swimm<strong>in</strong>g (<strong>in</strong> French). Pelayo P., Sidney M. (eds). LEMH–LRN-<br />

F.S.S.E.P. LILLE 2–U.F.R.S.T.A.P.S. d’ARTOIS, Liev<strong>in</strong>.<br />

Zatoń, K. & Klarowicz, A. (2001). Effect of verbal <strong>in</strong>structions on the<br />

level of mastery of the art sports <strong>and</strong> differentiation k<strong>in</strong>aesthetic<br />

ability <strong>in</strong> children younger school age (In Polish). In: Migasiewicz<br />

J, Zatoń K (ed.) Sport pływacki i lekkoatletyczny w szkole. AWF,<br />

Wrocław, 5-11.<br />

Zatoń, K. (2002). Importance of verbal expressions <strong>in</strong> teach<strong>in</strong>g <strong>and</strong><br />

practic<strong>in</strong>g motor activities. 7 th International Scientific Conference of the<br />

International Association of Sport K<strong>in</strong>etics, University of Tartu, 44-48.<br />

chaPter5.education,advice<strong>and</strong>BiofeedBack<br />

351


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi


Chapter 6. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Water Safety


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Crucial F<strong>in</strong>d<strong>in</strong>gs from the 4W Model of Drown<strong>in</strong>g for<br />

Practical <strong>and</strong> Teach<strong>in</strong>g Applications<br />

Avramidis, s. 1,2,3 McKenna, J., 1 long, J., Butterly, r., 1 llewellyn,<br />

J.d. 4<br />

1 Leeds Metropolitan University, UK<br />

2 Hellenic Center for Disease Control <strong>and</strong> Prevention, Greece<br />

3 Irish Lifesav<strong>in</strong>g Foundation, Irel<strong>and</strong><br />

4 University of Cambridge, UK<br />

This study aimed to suggest practical <strong>and</strong> teach<strong>in</strong>g applications of the<br />

4W model of drown<strong>in</strong>g. A major literature review of quantitative research<br />

was undertaken to identify potential risk factors of drown<strong>in</strong>g<br />

<strong>and</strong> qualitative content analysis was used to analyze publicly available<br />

drown<strong>in</strong>g <strong>in</strong>cident videos (n = 41, M = 345.0, SD = 2.8), <strong>and</strong> 34 <strong>in</strong>dividuals<br />

<strong>in</strong>volved <strong>in</strong> drown<strong>in</strong>g <strong>in</strong>cidents were <strong>in</strong>terviewed (30 males age<br />

16–65 years, M = 28.4, SD = 11.3; 4 female age 19–65 years, M = 37.5,<br />

SD = 19.5). Results confirmed that test criteria such as a 100 m run–50<br />

m swim–100 m run for open water <strong>and</strong> a 50 m run–20 m swim–50 m<br />

run for pool/water parks could be more useful for assess<strong>in</strong>g speed comb<strong>in</strong>ed<br />

with an ‘early approach’ to the victim than any currently <strong>in</strong> operation.<br />

The ‘early approach’ criterion would be established to test the ability<br />

of the lifeguard to be able to rema<strong>in</strong> alert, to have good vision, to recognize<br />

the casualty’s <strong>in</strong>st<strong>in</strong>ctive drown<strong>in</strong>g response, to <strong>in</strong>itiate a rescue<br />

ignor<strong>in</strong>g the byst<strong>and</strong>er’s lack of response <strong>and</strong> to reassure the drown<strong>in</strong>g<br />

victim. Drown<strong>in</strong>gs <strong>and</strong> their rescue <strong>in</strong>terventions should be perceived as<br />

3-dimensional problems.<br />

Key words: lifesav<strong>in</strong>g, lifeguard<strong>in</strong>g, 4W model, drown<strong>in</strong>g, water<br />

safety, teach<strong>in</strong>g.<br />

IntroductIon<br />

Drown<strong>in</strong>g is a serious social <strong>and</strong> health problem worldwide but most<br />

research focuses on epidemiologic <strong>and</strong> forensic aspects. Limited models<br />

<strong>and</strong> teach<strong>in</strong>g theories have been suggested <strong>and</strong> implemented <strong>in</strong> the<br />

context of tra<strong>in</strong><strong>in</strong>g, risk assessment, risk management <strong>and</strong> risk prevention<br />

of drown<strong>in</strong>g (e.g. Griffiths, 2000; Pia, 1984; Connolly, 2004; Ellis<br />

& Associates, 1994). Because most of these theories <strong>and</strong> models were<br />

not scientifically established their effectiveness has been questioned (see<br />

Pia, 2007; DeRosa, 2008; Ellis <strong>and</strong> Associates & Poseidon Technologies,<br />

2001).<br />

Contrary to previous empirical published work, the 4W model on<br />

drown<strong>in</strong>g was a research-based proposed theoretical framework aim<strong>in</strong>g<br />

to offer an alternative way to underst<strong>and</strong> the antecedents of drown<strong>in</strong>g<br />

<strong>and</strong> assist teach<strong>in</strong>g <strong>in</strong> the field of water safety (Avramidis, 2009). More<br />

precisely, this model suggested that when there is a human activity <strong>in</strong>,<br />

on, around, near or above an aquatic environment then a drown<strong>in</strong>g <strong>in</strong>cident<br />

may occur to whomever, wherever <strong>and</strong> under whatever circumstances<br />

(Avramidis et al, 2007). Later, us<strong>in</strong>g novel practices, research<br />

attempts were made to break the problem down <strong>in</strong>to its basic build<strong>in</strong>g<br />

blocks (e.g. each one of the 4 W’s) <strong>in</strong> an effort to better describe who<br />

is more likely to be the rescuer (Avramidis et al., 2009a), who is more<br />

likely to be the casualty (Avramidis et al., 2009b), where (Avramidis et<br />

al., 2009c) <strong>and</strong> under what circumstances it is more likely a drown<strong>in</strong>g<br />

<strong>in</strong>cident may occur (Avramidis et al., 2009d). Therefore, the purpose of<br />

this study was to reassemble these basic build<strong>in</strong>g blocks <strong>in</strong>to the 4W<br />

model <strong>and</strong> to suggest practical applications for enhanc<strong>in</strong>g teach<strong>in</strong>g of<br />

drown<strong>in</strong>g prevention <strong>and</strong> effective rescue.<br />

Method<br />

Consideration of debate about different paradigms (e.g. Morgan, 2007),<br />

their strengths <strong>and</strong> limitations (see Hoshm<strong>and</strong>, 2003; Johnson & Onwuegbuzie,<br />

2004), led to the decision to undertake a mixed methods<br />

354<br />

approach ( Johnson & Onwuegbuzie, 2004) <strong>in</strong>volv<strong>in</strong>g three studies. The<br />

first study was a review of quantitative studies, aim<strong>in</strong>g to support the<br />

development of the theoretical framework of a 4W model. This model<br />

would conta<strong>in</strong> all the potential variables present dur<strong>in</strong>g a drown<strong>in</strong>g<br />

<strong>in</strong>cident (e.g. rescuer characteristics, casualty characteristics, place <strong>and</strong><br />

circumstances of occurrence of a drown<strong>in</strong>g <strong>in</strong>cident). The second study<br />

based on observations of video recorded drown<strong>in</strong>g rescues, aimed at assess<strong>in</strong>g<br />

whether or not the variables from the first study were present<br />

<strong>and</strong> whether other variables emerged. The third study was based on <strong>in</strong>terviews,<br />

aim<strong>in</strong>g to assess whether or not the variables found <strong>in</strong> the first<br />

study were present, <strong>and</strong> f<strong>in</strong>d<strong>in</strong>g possible emerg<strong>in</strong>g variables, but also to<br />

give <strong>in</strong>sights <strong>in</strong>to questions that were left unanswered by the second<br />

study. F<strong>in</strong>ally, the variables that were present <strong>in</strong> all three specific sets of<br />

data were synthesized to formulate a framework for drown<strong>in</strong>g prevention.<br />

This methodological procedure aimed to achieve multiple triangulation.<br />

A more detailed explanation of the above will be given below.<br />

STUDY 1<br />

The first study was an extensive review of the literature on quantitative<br />

studies. It was important that this type of research came first <strong>in</strong> the<br />

current research design because the <strong>in</strong>itial aim for the development of<br />

the drown<strong>in</strong>g prevention framework was to identify as many variables<br />

related to drown<strong>in</strong>g as possible. This could better be achieved by review<strong>in</strong>g<br />

a broad range of quantitative studies that had already exam<strong>in</strong>ed the<br />

drown<strong>in</strong>g problem <strong>and</strong> located a number of related variables than by undertak<strong>in</strong>g<br />

a quantitative or qualitative study with a limited sample. The<br />

terms ‘drown’, ‘aquatic emergency’, ‘risk factors’, ‘lifeguard’, ‘water safety’,<br />

‘lifesav<strong>in</strong>g’ <strong>and</strong> ‘rescue’ were used as key words <strong>in</strong> a search undertaken to<br />

identify literature with variables that might be <strong>in</strong>volved <strong>in</strong> a drown<strong>in</strong>g<br />

<strong>in</strong>cident. The search used academic <strong>and</strong> professional aquatic safety textbooks<br />

that are rout<strong>in</strong>ely available <strong>in</strong> libraries, electronic databases typically<br />

available <strong>in</strong> academic libraries (e.g. Medl<strong>in</strong>e, Sport Discuss, Sport<br />

Discuss with Full Text, PsychINFO <strong>and</strong> PubMed) <strong>and</strong> search eng<strong>in</strong>es<br />

(e.g. Google <strong>and</strong> Yahoo) cover<strong>in</strong>g studies that assessed the epidemiology<br />

<strong>and</strong> risk factors of drown<strong>in</strong>g. The available literature was limited to those<br />

available <strong>and</strong> published <strong>in</strong> Greek <strong>and</strong> English. Those qualitative data<br />

that were generated (i.e. variables related to drown<strong>in</strong>g) were clustered <strong>in</strong><br />

four pre-determ<strong>in</strong>ed clusters namely ‘rescuer’, ‘casualty’, ‘place of drown<strong>in</strong>g’<br />

<strong>and</strong> ‘circumstances of drown<strong>in</strong>g <strong>in</strong>cident’. In an effort to identify<br />

as many variables related to drown<strong>in</strong>g as possible, this review study <strong>in</strong>cluded<br />

<strong>in</strong> the clusters not only variables that were well documented <strong>in</strong><br />

the literature but also variables that appeared to be related to drown<strong>in</strong>g<br />

<strong>in</strong> case studies. This ensured that possible contribut<strong>in</strong>g variables that<br />

might have been neglected from the water safety related literature would<br />

not be missed <strong>and</strong> would be given an equal chance of be<strong>in</strong>g <strong>in</strong>cluded <strong>in</strong><br />

the theoretical framework of the study.<br />

STUDY 2<br />

Data Sources: The exact data sources <strong>and</strong> procedures have been reported<br />

earlier (Avramidis, et al., 2007; 2009a; 2009b; 2009c; 2009d). A criterion-sampl<strong>in</strong>g<br />

method obta<strong>in</strong>ed drown<strong>in</strong>g-<strong>in</strong>cident videos (N = 41) that<br />

were freely available <strong>in</strong> the public doma<strong>in</strong>. This method facilitated the<br />

identification of variables <strong>and</strong> their relationships that otherwise might<br />

not be available for fatal or non-fatal traumatic drown<strong>in</strong>gs. These visual<br />

narratives ranged <strong>in</strong> length from 30 to 720 s (M = 345.0, SD = 2.8).<br />

Apparatus <strong>and</strong> Procedures: The authors observed the videos on st<strong>and</strong>ard<br />

equipment <strong>and</strong> software to perform appropriate qualitative analyses<br />

(QSR, 2002). To deal with the various disadvantages <strong>and</strong> bias, the objective<br />

<strong>and</strong> subjective audio <strong>and</strong> visual content of the video were observed<br />

without unsupported assumptions <strong>and</strong> editorial comments. The audiovisual<br />

content was transcribed twice with<strong>in</strong> a period of three months.<br />

This text was <strong>in</strong>serted <strong>in</strong>to the computer software NVIVO (version<br />

2002) for content analysis. A number of codes were identified with<strong>in</strong><br />

the text. F<strong>in</strong>ally, frequencies were measured.


STUDY 3<br />

Participants: A comb<strong>in</strong>ation of convenience <strong>and</strong> snowball sampl<strong>in</strong>g, located<br />

participants who were water safety or aquatic professionals (e.g.,<br />

lifeguards, lifesavers, scuba divers, <strong>and</strong> athletes of aquatic sports (N=34)<br />

who could describe a drown<strong>in</strong>g episode (Table 1).<br />

Table 1.Demographic <strong>in</strong>formation of the participants <strong>in</strong> the <strong>in</strong>terview<br />

(n=34).<br />

30 males (age 16–65 years, M = 28.4, SD =<br />

11.3)<br />

Gender<br />

4 female (age 19–65 years, M = 37.5, SD =<br />

19.5)<br />

Greece (n = 25, 71.4%)<br />

United K<strong>in</strong>gdom (n = 2, 5.7%)<br />

Nationality<br />

United States (n = 1, 2.8%)<br />

Cyprus (n = 6, 17.1%)<br />

Place of Reported<br />

Drown<strong>in</strong>g<br />

Sea (above the water surface) (n = 23, 67.6%)<br />

Sea (under the surface of the water surface) (n<br />

= 5, 14.7%)<br />

Lake (n = 2, 5.9%)<br />

Swimm<strong>in</strong>g pool or water park (n = 4, 11.8%)<br />

Apparatus <strong>and</strong> Procedures: The same procedure as <strong>in</strong> the previous study<br />

(that exam<strong>in</strong>ed observation of video recorded rescues) <strong>and</strong> past published<br />

work was followed (Avramidis et al., 2007; 2009a; 2009b; 2009c;<br />

2009d). Anonymity <strong>and</strong> confidentiality were ma<strong>in</strong>ta<strong>in</strong>ed. The participants<br />

received <strong>and</strong> read participant <strong>in</strong>formation sheet <strong>and</strong>, after hav<strong>in</strong>g<br />

any questions about their <strong>in</strong>volvement answered to their satisfaction,<br />

signed an <strong>in</strong>formed consent form. The semi-structured <strong>in</strong>terview schedule<br />

<strong>in</strong>cluded open-ended questions. The <strong>in</strong>terview was transcribed <strong>and</strong><br />

<strong>in</strong>serted <strong>in</strong>to the computer software NVIVO for content analysis.<br />

results And dIscussIon<br />

The aim of the present mixed methods research approach was to suggest<br />

practical applications for drown<strong>in</strong>g prevention <strong>and</strong> demonstrate the efficacy<br />

of the proposed 4W model. A number of crucial f<strong>in</strong>d<strong>in</strong>gs therefore<br />

need to be discussed.<br />

Distance from Safety <strong>and</strong> the 3-Dimensions of Drown<strong>in</strong>g <strong>and</strong> Rescue Intervention:<br />

The video <strong>and</strong> <strong>in</strong>terview analyses showed that the distance from<br />

safety was a component of each drown<strong>in</strong>g <strong>in</strong>cident (Avramidis, 2009).<br />

In particular, it was shown that the distance of drown<strong>in</strong>g episodes from<br />

safety ranged from 1-9 m up to many miles. Consider<strong>in</strong>g that distance<br />

from safety is one of the components that affected the speed of rescue<br />

<strong>and</strong> also that speed equals time, then there was a need to locate spatially<br />

the activity prior to the <strong>in</strong>cident <strong>and</strong> the location of drown<strong>in</strong>g to underst<strong>and</strong><br />

its antecedents. Consequently, depict<strong>in</strong>g a drown<strong>in</strong>g victim <strong>in</strong><br />

a geometric model at the centre of 3-dimensional space yielded crucial<br />

f<strong>in</strong>d<strong>in</strong>gs. Drown<strong>in</strong>g was the outcome not only of engagement <strong>in</strong> aquatic<br />

activities (e.g. swimm<strong>in</strong>g, boat<strong>in</strong>g, scuba div<strong>in</strong>g etc.) but also of activities<br />

occurr<strong>in</strong>g <strong>in</strong> the air (e.g. parachute <strong>and</strong> bungee jumps, air <strong>and</strong> space<br />

flights above the sea etc.) <strong>and</strong> on l<strong>and</strong> (e.g. driv<strong>in</strong>g or walk<strong>in</strong>g <strong>in</strong> flooded<br />

areas or frozen lakes). Therefore, <strong>in</strong> the exam<strong>in</strong>ed sample <strong>in</strong> terms of<br />

distance, the drown<strong>in</strong>g problem as well as the consequent rescue <strong>in</strong>tervention,<br />

was not a 1-dimensional but rather a 3-dimensional problem<br />

<strong>and</strong> task respectively (e.g. length, height or depth <strong>and</strong> width).<br />

Drown<strong>in</strong>g <strong>in</strong>cidents <strong>in</strong> the video <strong>and</strong> <strong>in</strong>terview studies occurred <strong>in</strong><br />

all 3-dimensions. The first dimension of length represented the distance<br />

between the location of drown<strong>in</strong>g <strong>and</strong> the shore or the poolside of such<br />

activities as swimm<strong>in</strong>g, boat<strong>in</strong>g, sail<strong>in</strong>g etc. The second dimension of<br />

height or depth represented the distance between the location of drown<strong>in</strong>g<br />

from the water surface of such activities as air flight, space ship mission,<br />

parachute <strong>and</strong> bungee jump, as well as scuba div<strong>in</strong>g, spear fish<strong>in</strong>g<br />

<strong>and</strong> snorkell<strong>in</strong>g respectively. The third dimension of width represented<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

the distance between the location of drown<strong>in</strong>g <strong>in</strong> <strong>in</strong>l<strong>and</strong> water from the<br />

l<strong>and</strong> <strong>in</strong> such activities as walk<strong>in</strong>g or driv<strong>in</strong>g <strong>in</strong> flooded areas <strong>and</strong> frozen<br />

lakes etc. In other words, this showed that lifeguards, professional rescuers<br />

<strong>and</strong> amateur lifesavers had to respond to drown<strong>in</strong>g episodes whose<br />

start<strong>in</strong>g po<strong>in</strong>t was one of the previously described dimensions at various<br />

distances from safety. Therefore, people became drown<strong>in</strong>g victims<br />

regardless of whether or not the distance of their undertaken activity<br />

was far from the water.<br />

A rescue <strong>in</strong>tervention <strong>in</strong> the videos <strong>and</strong> <strong>in</strong>terviews was a 3-dimensional<br />

task. Rescues rarely occurred exactly <strong>in</strong> front of the eyes of the rescuer<br />

on a perpendicular plane to allow a 1-dimensional <strong>in</strong>tervention. For<br />

example, the <strong>in</strong>terviewee lifeguards from Greece who supervised 600<br />

m <strong>and</strong> were positioned <strong>in</strong> the middle of a beach, had to run across the<br />

beach a number of metres (e.g. dimension of width), attempt a swimm<strong>in</strong>g<br />

approach from the shortest distance (e.g. dimension of length) <strong>and</strong><br />

possibly cont<strong>in</strong>ue with an underwater search for the unconscious submerged<br />

drown<strong>in</strong>g victim (e.g. dimension of depth). Similarly, <strong>in</strong> other<br />

rescues from the video analysis a rescuer had to run to the place where<br />

the helicopter was parked (e.g. dimension of width), fly to the place<br />

where the victim was drown<strong>in</strong>g (e.g. dimension of length) <strong>and</strong> attempt<br />

a rescue which required the rescue swimmer jump<strong>in</strong>g <strong>in</strong>to the water<br />

<strong>and</strong> the eventual lift, together with the victim, <strong>in</strong>to the helicopter (e.g.<br />

dimension of height). This showed that lifeguards, professional rescuers<br />

<strong>and</strong> amateur lifesavers had to respond to drown<strong>in</strong>g episodes cover<strong>in</strong>g a<br />

distance from safety to the place of the event <strong>in</strong> more than one dimension.<br />

All these po<strong>in</strong>ts suggested that perceiv<strong>in</strong>g drown<strong>in</strong>g <strong>and</strong> the consequent<br />

attempted rescue as a 3-dimensional problem <strong>and</strong> task respectively<br />

had a number of implications. First, it revealed a number of ‘hidden’<br />

drown<strong>in</strong>g <strong>in</strong>cidents that contemporary <strong>in</strong>jury epidemiology would classify<br />

under different codes, underestimat<strong>in</strong>g the burden of drown<strong>in</strong>g <strong>and</strong><br />

therefore the magnitude of the problem, with negative consequences <strong>in</strong><br />

decision mak<strong>in</strong>g to fund research <strong>and</strong> education <strong>in</strong> terms of prevention,<br />

rescue <strong>and</strong> treatment (e.g. E830, accident to watercraft caus<strong>in</strong>g submersion;<br />

E832, other accidental submersion or drown<strong>in</strong>g <strong>in</strong> water transport<br />

accident; E984, submersion [drown<strong>in</strong>g] undeterm<strong>in</strong>ed whether accidentally<br />

or purposely <strong>in</strong>flicted). Second, it stressed the need, from an<br />

educational po<strong>in</strong>t of view, for better public awareness regard<strong>in</strong>g water<br />

safety prevention <strong>in</strong> people who engage not only <strong>in</strong> aquatic activities but<br />

also <strong>in</strong> non-aquatics <strong>in</strong>, on or around the water, for them to know how<br />

to swim <strong>and</strong> be able to survive <strong>in</strong> an aquatic emergency.<br />

Third, it showed that the 400 m swim for open water rescue <strong>and</strong> the<br />

50 m swim for pool/water park rescue on their own were not adequate<br />

teach<strong>in</strong>g <strong>and</strong> test requirements to ensure a speedy approach because they<br />

assessed speed <strong>in</strong> only one dimension. Instead, test criteria such as a 100<br />

m run–50 m swim–100 m run for open water <strong>and</strong> a 50 m run–20 m<br />

swim–50 m run for pool/water parks could be more useful for assess<strong>in</strong>g<br />

speed <strong>in</strong> relation to distance.<br />

F<strong>in</strong>ally, the presence of each dimension <strong>and</strong> the number of metres<br />

between the rescuer <strong>and</strong> the casualty of each of those dimensions posed<br />

an additional number of obstacles that had to be overcome. For example,<br />

a lifeguard who attempted a 1-dimensional rescue at a certa<strong>in</strong> distance<br />

from safety was concerned with fewer variables (e.g. distance from safety,<br />

weather <strong>and</strong> environmental conditions etc.) than a rescuer who attempted<br />

a 3-dimensional rescue who was concerned with all variables related<br />

to width (e.g. run, likelihood of gett<strong>in</strong>g <strong>in</strong>jured), length (e.g. swim, need<br />

to fuel <strong>and</strong> operate a power boat or a helicopter etc.) <strong>and</strong> possibly height<br />

(e.g. knowledge of h<strong>and</strong>l<strong>in</strong>g a specialized rescue, concern about weather<br />

conditions etc.) or depth (e.g. knowledge about mar<strong>in</strong>e life dangers, underwater<br />

currents, water temperature etc.). Therefore, this stressed the<br />

need for further education from the rescuer’s po<strong>in</strong>t of view.<br />

Early Approach: A crucial f<strong>in</strong>d<strong>in</strong>g of this research was that when approach<strong>in</strong>g<br />

the drown<strong>in</strong>g victim, an early approach was required by<br />

amateur <strong>and</strong> professional rescuers <strong>in</strong> the video <strong>and</strong> <strong>in</strong>terview samples<br />

355


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

(Avramidis , 2009). The review study revealed that many organizations<br />

across the world often l<strong>in</strong>ked the early approach to the drown<strong>in</strong>g victim<br />

with the swimm<strong>in</strong>g speed that a lifeguard should have. However,<br />

many of the <strong>in</strong>cidents <strong>in</strong> the two qualitative studies requir<strong>in</strong>g lifeguard<br />

<strong>in</strong>tervention were less than 10 m from safety but also <strong>in</strong> water depths<br />

little deeper than the victim’s height. This shows that early approach was<br />

needed for a rescue <strong>and</strong>, therefore, this element should have also been<br />

taught <strong>and</strong> tested <strong>in</strong> lifeguard certifications. To be able to approach a<br />

drown<strong>in</strong>g victim quickly, it was more important to rema<strong>in</strong> alert, have<br />

good vision, recognize the casualty’s <strong>in</strong>st<strong>in</strong>ctive drown<strong>in</strong>g response, run<br />

up to the po<strong>in</strong>t on l<strong>and</strong> that would allow the shortest swimm<strong>in</strong>g distance<br />

or wade approach <strong>and</strong> <strong>in</strong>itiate a rescue ignor<strong>in</strong>g the byst<strong>and</strong>er’s lack of<br />

response. Therefore, the term ’early approach’ may be a valid <strong>and</strong> multidimensional<br />

teach<strong>in</strong>g <strong>and</strong> test requirement; this is because it seems that<br />

it should be based not only on speed of swimm<strong>in</strong>g but on the speed that<br />

could be achieved <strong>in</strong> all the previously described elements that occurred,<br />

from the moment the casualty was spotted until the moment they were<br />

approached at distances up to 50 m. When the distance was greater than<br />

50 m, a different rescue method may be used (e.g. rescue board, Jet Ski or<br />

power boat) rather than a swimm<strong>in</strong>g approach.<br />

conclusIons<br />

A number of conclusions arose from the synthesis of the present 3 studies.<br />

First, teach<strong>in</strong>g prerequisites <strong>and</strong> test criteria like a 100 m run–50<br />

m swim–100 m run for open water <strong>and</strong> a 50 m run–20 m swim–50 m<br />

run for pool/water park lifeguard<strong>in</strong>g could be useful for assess<strong>in</strong>g speed<br />

comb<strong>in</strong>ed with an ‘early approach’ to the victim. Second, the ‘early approach’<br />

teach<strong>in</strong>g <strong>and</strong> assessment criteria establish importance of the<br />

ability of the lifeguard to be able to rema<strong>in</strong> alert, to have good vision, to<br />

recognize the casualty’s <strong>in</strong>st<strong>in</strong>ctive drown<strong>in</strong>g response, to <strong>in</strong>itiate a rescue<br />

ignor<strong>in</strong>g the byst<strong>and</strong>er’s lack of response <strong>and</strong> to reassure the drown<strong>in</strong>g<br />

victim. F<strong>in</strong>ally, drown<strong>in</strong>g <strong>in</strong>cidents <strong>and</strong> their rescue <strong>in</strong>terventions<br />

should be perceived as 3-dimensional issues.<br />

reFerences<br />

Avramidis, S. (2009). The 4W Model of Drown<strong>in</strong>g for Lifesav<strong>in</strong>g of<br />

Non-Aquatic <strong>and</strong> Swimm<strong>in</strong>g Activities. PhD thesis. Leeds Metropolitan<br />

University.<br />

Avramidis, S., Butterly, R., & Llewellyn, D.J. (2007). The 4W Model<br />

of Drown<strong>in</strong>g. International Journal of Aquatic Research <strong>and</strong> Education,<br />

1(3), 221-230.<br />

Avramidis, S., Butterly, R., & Llewellyn, D.J. (2009a). Drown<strong>in</strong>g Incident<br />

Rescuer Characteristics: Encod<strong>in</strong>g the First Component of the<br />

4W Model. International Journal of Aquatic Research <strong>and</strong> Education,<br />

3(1), 66-82.<br />

Avramidis, S., Butterly, R., & Llewellyn, D.J. (2009b). Who Drowns?<br />

Encod<strong>in</strong>g the Second Component of the 4W Model. International<br />

Journal of Aquatic Research <strong>and</strong> Education, 3(3), 224-235.<br />

Avramidis, S., Butterly, R., & Llewellyn, D.J. (2009c). Where do People<br />

Drown? Encod<strong>in</strong>g the Third Component of the 4W Model. International<br />

Journal of Aquatic Research <strong>and</strong> Education, 3(3), 236-254.<br />

Avramidis, S., Butterly, R., & Llewellyn, D.J. (2009d). Under What Circumstances<br />

Do People Drown? Encod<strong>in</strong>g the Fourth Component of<br />

the 4W Model. International Journal of Aquatic Research <strong>and</strong> Education,<br />

3(4), 406-421.<br />

Connolly, J. (2004). C-Zones the Connolly Framework. In: S. Avramidis,<br />

E. Avramidou & J. Tritaki (Eds.) 1st International Lifeguard Congress<br />

(p. 12). Piraeus: European Lifeguard Academy.<br />

DeRosa, S.P. (2008). Demystify<strong>in</strong>g the protection rule 10/20. In: S. Avramidis,<br />

(ed.) H<strong>and</strong>book on safety <strong>and</strong> lifesav<strong>in</strong>g (pp. 81-83). Greece:<br />

Stamoulis Publish<strong>in</strong>g.<br />

Ellis <strong>and</strong> Associates & Poseidon Technologies (2001). First on-site study<br />

of vigilance shows lifeguards can’t possibly see everyth<strong>in</strong>g all of the time.<br />

Bologne, France: Ellis <strong>and</strong> Associates & Poseidon Technologies.<br />

356<br />

Ellis, J., & White, J. (1994). National pool <strong>and</strong> waterpark lifeguard /CPR<br />

tra<strong>in</strong><strong>in</strong>g. Massachusetts: Jones <strong>and</strong> Bartlett Publishers.<br />

Griffiths, T. (2000, March). Five-m<strong>in</strong>ute scan. Aquatics International, 12.<br />

Griffiths, T. (2001, March). Swim at your own risk. Aquatics International,<br />

14.<br />

Hoshm<strong>and</strong>, L.T. (2003). Can lessons of history <strong>and</strong> logical analysis<br />

ensure progress <strong>in</strong> psychological science? Theory <strong>and</strong> Psychology, 13,<br />

39–44.<br />

Johnson, R.B., & Onwuegbuzie, A.J. (2004). Mixed methods research:<br />

a research paradigm whose time has come. Educational Research, 33,<br />

14–26.<br />

Morgan, D.L. (2007). Paradigms lost <strong>and</strong> pragmatism rega<strong>in</strong>ed: methodological<br />

implications of comb<strong>in</strong><strong>in</strong>g qualitative <strong>and</strong> quantitative<br />

methods. Journal of Mixed Methods Research, 1, 48–76.<br />

Pia, F. (1984). The RID factor as a cause of drown<strong>in</strong>g. Parks <strong>and</strong> Recreation,<br />

19(6), 52-55; 67.<br />

Pia, F. (2007). What can science teach us about lifesav<strong>in</strong>g <strong>and</strong> drown<strong>in</strong>g<br />

prevention? In N. Farmer, <strong>and</strong> S. Beerman, (Eds.) World Water Safety<br />

Conference & Exhibition 2007 (p. 12), Oporto, Portugal: Associação<br />

de Nadadores Salvadores <strong>and</strong> International Life Sav<strong>in</strong>g Federation.<br />

Pia, F. (2008). Inst<strong>in</strong>ctive drown<strong>in</strong>g response. In S. Avramidis (ed.).<br />

H<strong>and</strong>book on safety <strong>and</strong> lifesav<strong>in</strong>g (pp. 77-78). Greece: Stamoulis<br />

Publish<strong>in</strong>g.<br />

QSR. (2002). NVIVO, Gett<strong>in</strong>g Started <strong>in</strong> NVIVO. Australia: QSR International<br />

Pty Ltd.


Swimm<strong>in</strong>g, Cycl<strong>in</strong>g, Runn<strong>in</strong>g <strong>and</strong> Cardiovascular<br />

Health<br />

Bagheri, A.B. 1 , Mohebbi, h.d. 2 , Azizi, M.h. 3 , saiiari, A.r. 3<br />

1 Islamic Azad University-Dezful Branch, Dezful, Iran<br />

2 University of Guilan, Rasht, Iran<br />

3 Islamic Azad University-Abadan Branch, Abadan, Iran<br />

A number of epidemiological studies have proved the benefits of regular<br />

physical activity for the prevention of CHD. Exercise recommendations<br />

for health can be obta<strong>in</strong>ed from extrapolation between different modes<br />

of exercise. Forty non-athlete male youth participated <strong>in</strong> this study for<br />

the comparative effects of swimm<strong>in</strong>g, cycl<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g on lipid <strong>and</strong><br />

lipoprote<strong>in</strong>s serum. In this study, after aerobic tra<strong>in</strong><strong>in</strong>g, HDL-c <strong>in</strong>creased<br />

<strong>and</strong> LDL-c decreased; so TC <strong>and</strong> TG decreased. The f<strong>in</strong>d<strong>in</strong>gs<br />

suggest that moderate tra<strong>in</strong><strong>in</strong>g performed over many weeks <strong>in</strong>duces<br />

positive changes <strong>in</strong> the plasma lipid <strong>and</strong> lipoprote<strong>in</strong>s concentration <strong>in</strong><br />

youth. However, there were differences between the three groups. Swimm<strong>in</strong>g,<br />

runn<strong>in</strong>g <strong>and</strong> cycl<strong>in</strong>g are positive for health, although this study<br />

suggested that they have different effects.<br />

Key words: swimm<strong>in</strong>g, cycl<strong>in</strong>g, runn<strong>in</strong>g, aerobic tra<strong>in</strong><strong>in</strong>g, tc, tG,<br />

ldl-c, hdl-c<br />

IntroductIon<br />

Cardiovascular diseases (CVD) are also reported to be the lead<strong>in</strong>g cause<br />

of death <strong>in</strong> the eastern Mediterranean region <strong>in</strong>clud<strong>in</strong>g Iran. Epidemiological<br />

studies have shown that a sedentary life <strong>and</strong> obesity are related<br />

to coronary heart disease (CHD) (Andersen et al., 1995). In numerous<br />

studies, <strong>in</strong>verse associations have been demonstrated between physical<br />

activity, obesity <strong>and</strong> CHD (Daniel J. G, 2008. Kl<strong>in</strong>e et al., 1987. K<strong>in</strong>g<br />

et al., 1995). A number of epidemiological studies have proved the benefits<br />

of regular physical activity for the prevention of CHD. Despite the<br />

fact that exercise is crucial <strong>in</strong> weight management, the obese are found<br />

to have reduced exercise tolerance compared with the non-obese <strong>and</strong> are,<br />

<strong>in</strong> fact, less active. Fat is the major source of energy dur<strong>in</strong>g low-<strong>in</strong>tensity<br />

exercise, <strong>and</strong> as the <strong>in</strong>tensity <strong>in</strong>creases, the proportional contribution of<br />

fat decreases. Nonetheless, at 75-80% of VO 2 max, total fat oxidation is<br />

markedly above the rest<strong>in</strong>g value because the proportional contribution<br />

of fat oxidation is not great, the total rate of energy expenditure is high.<br />

Plasma fatty acids are the major source of energy dur<strong>in</strong>g mild to moderate<br />

energy expenditure. Exercise recommendations for health can be<br />

obta<strong>in</strong>ed from extrapolation between different modes of exercise.<br />

Methods<br />

Subjects: Forty non-athletic men (Age 22.56 ± 2.77 yr) with overweight<br />

(BMI >25 kg·m -2 ) participated <strong>in</strong> this study. Subjects were made fully<br />

aware of the risks, benefits <strong>and</strong> stresses of the study <strong>and</strong> were given both<br />

verbal <strong>and</strong> written <strong>in</strong>structions outl<strong>in</strong><strong>in</strong>g the experimental procedure,<br />

<strong>and</strong> their <strong>in</strong>formed consent was obta<strong>in</strong>ed before screen<strong>in</strong>g. The personal<br />

<strong>and</strong> medical <strong>in</strong>formation of the participants was obta<strong>in</strong>ed, as well as<br />

previous exercise history by questionnaire. A pre-participatory exercise<br />

screen<strong>in</strong>g questionnaire [Physical Activity Read<strong>in</strong>ess questionnaire<br />

(PARQ)] was adm<strong>in</strong>istered (Chisholm et al., 1975). All participants<br />

were asymptomatic <strong>and</strong> were not tak<strong>in</strong>g any form of medication known<br />

to affect the lipoprote<strong>in</strong> profile. Before the tra<strong>in</strong><strong>in</strong>g program (basel<strong>in</strong>e),<br />

accord<strong>in</strong>g to the National Cholesterol Education Program (NCEP; 26)<br />

classification of risk, no participants had ‘’borderl<strong>in</strong>e’’ or ‘’ undesirable’’<br />

concentrations of either TC <strong>and</strong> LDL-C. These youth were all classified<br />

as hav<strong>in</strong>g ‘’desirable’’ concentrations of TC <strong>and</strong> LDL-c at basel<strong>in</strong>e.<br />

Subjects were divided <strong>in</strong>to four groups r<strong>and</strong>omly; that <strong>in</strong>cluded ten per-<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

sons each. Three groups were assigned tra<strong>in</strong><strong>in</strong>g regimens (swimm<strong>in</strong>g,<br />

runn<strong>in</strong>g, <strong>and</strong> cycl<strong>in</strong>g), <strong>and</strong> completed the exercise tra<strong>in</strong><strong>in</strong>g program. Ten<br />

subjects served as controls.<br />

Measurements: Body weight (BW) was measured through calibrated<br />

cl<strong>in</strong>ical scale <strong>and</strong> height was measured through stadiometer while the<br />

participants wear<strong>in</strong>g light cloth<strong>in</strong>g with no shoes. Body Mass Index<br />

(BMI) was calculated as weight <strong>in</strong> kilograms divided by height <strong>in</strong> meters<br />

squared (kg·m -2 ). Five ml of venous blood sample were collected after a<br />

12-14 hours fast <strong>in</strong>to vacationer tubes without anticoagulant <strong>in</strong> pre-test<br />

<strong>and</strong> post test. Blood was allowed to clot at room temperature for 30<br />

m<strong>in</strong> before be<strong>in</strong>g centrifuged. Serum <strong>and</strong> red blood cells were separated<br />

by centrifuge at 1500gr for 20 m<strong>in</strong>. serum was transferred <strong>and</strong> stored<br />

at-80º for analysis of lipids <strong>and</strong> lipoprote<strong>in</strong>s. Total cholesterol (TC)<br />

measured by the CHOD-PAP method. TG by the GPO-PAP method,<br />

high density cholesterol (HDL) was determ<strong>in</strong>ed after separation with<br />

phosphotungstic acid <strong>and</strong> magnesium chloride, all us<strong>in</strong>g established kit<br />

methods from Boehr<strong>in</strong>ger (Mannnheim, Germany). Low density lipoprote<strong>in</strong>s<br />

(LDL) was then estimated by us<strong>in</strong>g the Friedeweald equation<br />

(Friedewald et al., 1972).<br />

Swimm<strong>in</strong>g Tra<strong>in</strong><strong>in</strong>g: Ten non-athlete male volunteers used swimm<strong>in</strong>g<br />

tra<strong>in</strong><strong>in</strong>g three times per week (t/wk) consecutively for 16 weeks.<br />

Technique tra<strong>in</strong><strong>in</strong>g (crawl) was provided to the subjects before start<strong>in</strong>g.<br />

The swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g program consisted of submaximal crawl 30 m<strong>in</strong><br />

pr day (m<strong>in</strong>/d) (5 m<strong>in</strong> activity <strong>and</strong> 2 m<strong>in</strong> rest), 2d/wk with 50 – 60<br />

percentage of each subject’s predicted maximal heart rate (max HR)<br />

<strong>in</strong>tensity <strong>in</strong> first <strong>and</strong> second month. Throughout the rema<strong>in</strong>der of the<br />

month, subjects tra<strong>in</strong>ed at 30 m<strong>in</strong>/d (5 m<strong>in</strong> activity <strong>and</strong> 1 m<strong>in</strong> rest), 2d/<br />

wk, approximately 70 – 80 percentage of maxHR. Dur<strong>in</strong>g this study, the<br />

subjects conducted to warm-up <strong>and</strong> cool-down (static stretch<strong>in</strong>g <strong>and</strong><br />

low <strong>in</strong>tensity exercise).<br />

Runn<strong>in</strong>g Tra<strong>in</strong><strong>in</strong>g: Ten non-athlete subjects performed runn<strong>in</strong>g exercise<br />

three t/wk dur<strong>in</strong>g 16 weeks. They tra<strong>in</strong>ed at 30 m<strong>in</strong>/d (5 m<strong>in</strong><br />

activity <strong>and</strong> 2 m<strong>in</strong> rest), 2d/wk with 50 –60 percentage of each subject’s<br />

max HR <strong>in</strong>tensity <strong>in</strong> first <strong>and</strong> second week. Almost all subjects were<br />

work<strong>in</strong>g at approximately 70 – 80 percentage of maxHR <strong>in</strong> throughout<br />

the rema<strong>in</strong>der of the weeks.<br />

Cycl<strong>in</strong>g Tra<strong>in</strong><strong>in</strong>g: Ten non-athlete male ended cycl<strong>in</strong>g (ergometer)<br />

exercise three t/wk consecutively for 16 weeks. Subjects tra<strong>in</strong>ed at 30<br />

m<strong>in</strong>/d (5 m<strong>in</strong> activity <strong>and</strong> 2 m<strong>in</strong> rest), 2d/wk with 50 –60 percentage<br />

of each subject’s predicted max HR <strong>in</strong>tensity <strong>in</strong> first <strong>and</strong> second week.<br />

Almost all subjects were work<strong>in</strong>g at approximately 70 – 80 percentage<br />

of maxHR <strong>in</strong> throughout the rema<strong>in</strong>der of the weeks.<br />

Statistical Analysis: Before hypothesis test<strong>in</strong>g, data were assessed for<br />

normality of distribution <strong>and</strong> homogeneity of variance. SPSS (V 15)<br />

<strong>and</strong> Microsoft office Excel (V 2007) was utilized for statistical analysis<br />

<strong>and</strong> graphic presentation. Ma<strong>in</strong> effects of tra<strong>in</strong><strong>in</strong>g modality <strong>and</strong> time<br />

(pre <strong>and</strong> post-exercise), were assessed us<strong>in</strong>g One-Way Analysis of Variance.<br />

Statistical significance was conferred at P ≤ 0.05. Tukey test was<br />

used for post hoc comparisons, when ma<strong>in</strong> effects were detected.<br />

results<br />

After 16 week of swimm<strong>in</strong>g, cycl<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g exercise, there were<br />

differences between experimental groups <strong>and</strong> control for TC (P ≤ 0.05)<br />

(Figure 1) . (Control Group = 155.78 ± 35.3 vs. 157.35 ± 35.4, Swimm<strong>in</strong>g<br />

Group (SG) = 155.76 ± 33 vs. 136.41 ± 35.9; Cycl<strong>in</strong>g Group<br />

(CG) = 154.93 ± 36 vs. 140.03 ± 21.8; Runn<strong>in</strong>g Group (RG) = 156.34 ±<br />

34.7 vs. 139.25 ± 35.8). Total Cholesterol <strong>in</strong> three groups decreased; SG:<br />

12.42%, CG: 9.61%, RG: 10.93%. Comparison with Tukey test showed<br />

that no significant differences between Control Group <strong>and</strong> CG (p =<br />

0.530) so RG (p= 0.317); but there were significant differences between<br />

control group <strong>and</strong> SG (p = 0.012).<br />

357


etween experimental groups <strong>and</strong> control for TC (P ≤ 0.05) (Figure 1) . (Control Group<br />

35.9; Cycl<strong>in</strong>g Group (CG) = 154.93 ± 36 vs. 140.03 ± 21.8; Runn<strong>in</strong>g Group (RG) =<br />

= 155.78 ± 35.3 vs. 157.35 ± 35.4, Swimm<strong>in</strong>g Group (SG) = 155.76 ± 33 vs. 136.41<br />

Figure<br />

±<br />

4). (Control Group: = 40.2 ± 17.8 vs. 39.98 ± 15.4; SG =; 40.33 ± 7.9 vs.<br />

156.34 ± 34.7 vs. 139.25 ± 35.8). Total Cholesterol <strong>in</strong> three groups decreased; SG:<br />

35.9; Cycl<strong>in</strong>g Group (CG) = 154.93 ± 36 vs. 140.03 ± 21.8; Runn<strong>in</strong>g Group (RG) 50.01±8.4; = CG = 40.46 ± 3.5 vs. 48.40 ± 3.2; RG = 42.84 ± 6.1 vs. 51.14 ± 9.6). HDL-c<br />

12.42%, CG: 9.61%, RG: 10.93%. Comparison with Tukey test showed that no<br />

<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

156.34 ± 34.7 vs. 139.25 ± 35.8). Total Cholesterol <strong>in</strong> three groups decreased; SG: <strong>in</strong>creased: SG: 24.00%, CG: 19.62%, RG: 19.37%). Comparison with Tukey test<br />

significant<br />

12.42%, CG:<br />

differences<br />

9.61%,<br />

between<br />

RG: 10.93%.<br />

Control<br />

Comparison<br />

Group <strong>and</strong><br />

with<br />

CG (p<br />

Tukey<br />

= 0.530)<br />

test<br />

so<br />

showed<br />

RG (p=<br />

that<br />

0.317);<br />

no showed that no significant differences between Control Group <strong>and</strong> CG (p = 0.217) so<br />

but<br />

significant<br />

there were<br />

differences<br />

significant<br />

between<br />

differences<br />

Control<br />

between<br />

Group<br />

control<br />

<strong>and</strong> CG<br />

group<br />

(p = 0.530)<br />

<strong>and</strong> SG<br />

so<br />

(p<br />

RG<br />

= 0.012).<br />

(p= 0.317); RG (p= 0.191); but there were differences between control group <strong>and</strong> SG (p = 0.010).<br />

but there were significant differences between control group <strong>and</strong> SG (p = 0.012).<br />

TC content<br />

HDL-c Content<br />

mg/dl<br />

mg/dl<br />

250<br />

200 250<br />

150 200<br />

100 150<br />

100 50<br />

TC content<br />

1 WK<br />

1 16 WKWk<br />

16 Wk<br />

80<br />

mg/dl 60<br />

40<br />

20<br />

1 WK<br />

16 Wk<br />

50 0<br />

0<br />

0 Control Swimm<strong>in</strong>g Cycl<strong>in</strong>g Runn<strong>in</strong>g<br />

Control Swimm<strong>in</strong>g Cycl<strong>in</strong>g Runn<strong>in</strong>g<br />

Control Swimm<strong>in</strong>g Cycl<strong>in</strong>g Runn<strong>in</strong>g<br />

Figure 1. 1. Comparison the the effect effect of swimm<strong>in</strong>g, of swimm<strong>in</strong>g, cycl<strong>in</strong>g cycl<strong>in</strong>g on subject’s on subject’s TC. TC.<br />

Figure 1. Comparison the effect of swimm<strong>in</strong>g, cycl<strong>in</strong>g on subject’s TC.<br />

Figure 4. 4. Comparison the the effect effect of swimm<strong>in</strong>g, of swimm<strong>in</strong>g, cycl<strong>in</strong>g cycl<strong>in</strong>g on subject’s on subject’s HDL-c.<br />

HDL-c.<br />

There were differences between the experimental group <strong>and</strong> <strong>and</strong> the the control group DISCUSSION<br />

for<br />

Triglyceride group<br />

There were<br />

for Triglyceride (P differences ≤ 0.05) (Figure between<br />

(P ≤ 2). 0.05)<br />

the (Control experimental<br />

(Figure group 2). = (Control<br />

group 146.1 ± <strong>and</strong> 29.9 group<br />

the vs. control<br />

= 144.4 146.1<br />

group ± 2.1; SG for Several dIscussIon<br />

= CHD risk factors are associated with obesity (Gregory et al, 2008). Physical<br />

143.4 ±<br />

Triglyceride<br />

29.9 ± 26 vs. vs. 144.4<br />

(P 126.3 ≤ 0.05)<br />

± 2.1; ± (Figure 14.6; SG CG =<br />

2).<br />

143.4 = (Control 142.7 ± 26 ± group 24 vs. vs. 126.3<br />

= 146.1 130 ± ±<br />

14.6; 38.0; 29.9<br />

CG<br />

vs. RG= 144.4<br />

= 145.1 142.7<br />

± 2.1; ± 28. SG 3 activity Several = vs. can CHD reduce risk CHD factors mortality are associated (Thompson with et obesity al., 2003). (Gregory Many et studies al, have shown a<br />

130.5 143.4<br />

± 24 ±<br />

vs. 41.4). 26 vs.<br />

130 ± TG 126.3<br />

38.0; <strong>in</strong> ± three 14.6;<br />

RG= groups CG = 142.7<br />

145.1 decreased; ± 24<br />

± 28. 3 vs. SG: vs. 130<br />

130.5 11.92%, ± 38.0;<br />

± 41.4). CG: RG=<br />

TG 8.89%, 145.1<br />

<strong>in</strong> three RG: ± 28. 10.06%. 3 vs.<br />

positive 2008). Physical effect of activity regular can physical reduce activity CHD on mortality blood lipid (Thompson metabolism, et al., especially aerobic<br />

Comparison 130.5 ± 41.4).<br />

groups decreased;<br />

with TG Tukey <strong>in</strong> three<br />

SG:<br />

test groups<br />

11.92%,<br />

showed decreased;<br />

CG:<br />

that<br />

8.89%,<br />

no SG: significant 11.92%,<br />

RG: 10.06%.<br />

differences CG: 8.89%,<br />

Comparison<br />

between RG: 10.06%. Control exercise 2003). Many (Heyward, studies 2002). have There shown are a some positive studies effect that of showed regular TC physical decreased <strong>in</strong> exercise<br />

Group Comparison<br />

with Tukey<br />

<strong>and</strong> CG with<br />

test<br />

(p Tukey<br />

showed<br />

= 0.380) test<br />

that<br />

so showed<br />

no<br />

RG<br />

significant<br />

(p= that 0.221); no significant<br />

differences<br />

but there differences<br />

between<br />

were differences between Control<br />

Control<br />

between<br />

control Group<br />

Group<br />

group <strong>and</strong> CG<br />

<strong>and</strong> CG<br />

<strong>and</strong> (p<br />

(p<br />

SG =<br />

=<br />

(p 0.380)<br />

0.380)<br />

= 0.009). so RG (p= 0.221); but there were differences between<br />

as activity <strong>in</strong> this on study blood (Merrill lipid metabolism, et al., 1990). especially Total aerobic cholesterol exercise reductions (Heyward, are associated with<br />

control group <strong>and</strong> SG (p = 0.009). so RG (p= 0.221); but there were differences body 2002). weight, There are percentage some studies of body that fat, showed <strong>and</strong> TC dietary decreased fat reductions. <strong>in</strong> exercise (Bounds as <strong>in</strong> R et al., 200,<br />

between control group <strong>and</strong> SG (p = 0.009).<br />

Merrill this study et al., (Merrill 1990, et Gerald al., 1990). F., 1997. Total Tanaka cholesterol H. et reductions al., 1997, are Susanne associat- R., 2006). The rise<br />

TG content<br />

TG content<br />

210<br />

190 210<br />

170 190<br />

mg/dl 150 170<br />

mg/dl 1 WK<br />

130 150<br />

1 WK<br />

110 130<br />

16 Wk<br />

110 90<br />

16 Wk<br />

70<br />

90<br />

50 70<br />

50<br />

Control Swimm<strong>in</strong>g Cycl<strong>in</strong>g Runn<strong>in</strong>g<br />

Control Swimm<strong>in</strong>g Cycl<strong>in</strong>g Runn<strong>in</strong>g<br />

Figure Figure 2. 2. Comparison Comparison the effect of of swimm<strong>in</strong>g, swimm<strong>in</strong>g, cycl<strong>in</strong>g cycl<strong>in</strong>g on on subject’s subject’s TG. TG.<br />

BMS Figure <strong>XI</strong> 2. Comparison Chapter the effect 6. <strong>Medic<strong>in</strong>e</strong>, of swimm<strong>in</strong>g, Rehabilitation cycl<strong>in</strong>g <strong>and</strong> Prevention on subject’s TG.<br />

ed with body weight, percentage of body fat, <strong>and</strong> dietary fat reductions.<br />

(Bounds R et al., 200, Merrill et al., 1990, Gerald F., 1997. Tanaka H. et<br />

al., 1997, Susanne R., 2006). The rise <strong>in</strong> plasma TC among apparently<br />

healthy young men <strong>and</strong> its fall <strong>in</strong> the elderly are significantly associated<br />

with similar trends for obesity (Wilson P et al., 1994). Triglyceride has<br />

relationship with activity (Ritakari et al., 1997). TG decreased <strong>in</strong> three<br />

groups but SG had a greater decrease. Our data <strong>in</strong>dicated that swimm<strong>in</strong>g<br />

effected TC <strong>and</strong> TG more than cycl<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g.<br />

LDL-C decreased significantly for exercise <strong>in</strong> SG, CG <strong>and</strong> RG;<br />

however, it was significant compared to the control group. This f<strong>in</strong>d<strong>in</strong>g<br />

agrees with others (Tanaka H. et al., 1997) <strong>and</strong> aga<strong>in</strong>st some other<br />

(Bounds et al., 2000). Widely believed that tra<strong>in</strong><strong>in</strong>g <strong>in</strong>creases HDL-c<br />

13<br />

(Andersen et al., 1996, Susanne R. et al., 2006), but some studies have<br />

not shown this result (Kantor et al., 1987). A 2-year study also showed<br />

There were no differences between experimental groups for LDL-C a slight <strong>in</strong>crease <strong>in</strong> HDL cholesterol levels with exercise (k<strong>in</strong>g et al.,<br />

There (P > 0.05) were (Figure no 3). differences (Control group between = 124.1±40.6 experimental vs. 124.8±49.5; groups SG = for LDL-C 1995). Those studies that do show <strong>in</strong>creased HDL generally <strong>in</strong>volved<br />

(P 123.53±37.9 > 0.05) (Figure vs. 102.33±39.0; 3). (Control group CG = = 125.6±36.8 124.1±40.6 vs. vs. 107.24±16.5; 124.8±49.5; SG RG = 123.53±37.9 more rigorous tra<strong>in</strong><strong>in</strong>g regimens, although there is some disagreement<br />

vs. 124.7±36.2 102.33±39.0; vs. 101.18±28.3). CG = 125.6±36.8 LDL-C decreased vs. 107.24±16.5; <strong>in</strong> swimmers RG (17.16%), = 124.7±36.2 on this vs. po<strong>in</strong>t as well (Barr S. et al., 1991). Among exercisers, the <strong>in</strong>crease<br />

101.18±28.3). Cyclist (14.61%) LDL-C <strong>and</strong> decreased runners (18.86%), <strong>in</strong> swimmers but <strong>in</strong> (17.16%), comparison Cyclist with (14.61%) control <strong>and</strong> runners <strong>in</strong> HDL-c cholesterol concentrations was significantly greater <strong>in</strong> men<br />

(18.86%), group there but were <strong>in</strong> comparison no differences. with control group there were no differences. with low HDL than <strong>in</strong> those with normal-to-high HDL at entry (Williams<br />

P. et al., 1994). The key determ<strong>in</strong>ants of a decl<strong>in</strong>e <strong>in</strong> HDL-C are<br />

LDL-c Content<br />

an <strong>in</strong>crease <strong>in</strong> obesity <strong>and</strong> advanc<strong>in</strong>g age itself <strong>in</strong> HDL with swimm<strong>in</strong>g,<br />

cycl<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g. There was a greater <strong>in</strong>crease for the SG<br />

200<br />

than the CG <strong>and</strong> RG. Our data <strong>and</strong> data from other studies (Smutok,<br />

1993) suggest that aerobic tra<strong>in</strong><strong>in</strong>g of sufficient <strong>in</strong>tensity <strong>and</strong> duration is<br />

150<br />

mg/dl<br />

100<br />

50<br />

1 WK<br />

16 Wk<br />

effective <strong>in</strong> elevat<strong>in</strong>g HDL levels.<br />

conclusIon<br />

In this study after aerobic tra<strong>in</strong><strong>in</strong>g, HDL-c <strong>in</strong>creased <strong>and</strong> LDL-c de-<br />

0<br />

Control Swimm<strong>in</strong>g Cycl<strong>in</strong>g Runn<strong>in</strong>g<br />

creased; so TC <strong>and</strong> TG decreased. The f<strong>in</strong>d<strong>in</strong>gs suggest that moderate<br />

tra<strong>in</strong><strong>in</strong>g performed over many weeks <strong>in</strong>duces positive changes <strong>in</strong> the<br />

plasma lipid <strong>and</strong> lipoprote<strong>in</strong> concentration <strong>in</strong> youth. However, there<br />

Figure 3. 3. Comparison the effect the effect of swimm<strong>in</strong>g, of swimm<strong>in</strong>g, cycl<strong>in</strong>g cycl<strong>in</strong>g on subject’s on subject’s LDL-c. were differences between the three groups. Swimm<strong>in</strong>g, runn<strong>in</strong>g <strong>and</strong> cy-<br />

LDL-c.<br />

cl<strong>in</strong>g are best type of exercise for health, although this study suggested<br />

Follow<strong>in</strong>g 16 week of swimm<strong>in</strong>g, cycl<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g, there were significant that they are not the same.<br />

differences<br />

Follow<strong>in</strong>g 16<br />

between<br />

week of<br />

the<br />

swimm<strong>in</strong>g,<br />

experimental<br />

cycl<strong>in</strong>g<br />

groups<br />

<strong>and</strong><br />

<strong>and</strong><br />

runn<strong>in</strong>g,<br />

control<br />

there<br />

group<br />

were<br />

for HDL-c<br />

signif-<br />

(P ≤ 0.05) (<br />

Figure<br />

icant differences<br />

4). (Control<br />

between<br />

Group:<br />

the<br />

=<br />

experimental<br />

40.2 ± 17.8 vs.<br />

groups<br />

39.98<br />

<strong>and</strong><br />

±<br />

control<br />

15.4; SG<br />

group<br />

=; 40.33<br />

for<br />

± 7.9 reFrences<br />

vs.<br />

50.01±8.4;<br />

HDL-c (P<br />

CG<br />

≤ 0.05)<br />

= 40.46<br />

( Figure<br />

± 3.5 vs.<br />

4).<br />

48.40<br />

(Control<br />

± 3.2;<br />

Group:<br />

RG =<br />

=<br />

42.84<br />

40.2<br />

±<br />

6.1<br />

17.8<br />

vs.<br />

vs.<br />

51.14<br />

39.98<br />

± 9.6). HDL-c Andersen. L. B., et al. (1996). Coronary heart disease risk factors, Physi-<br />

<strong>in</strong>creased: SG: 24.00%, CG: 19.62%, RG: 19.37%). Comparison with Tukey test<br />

± 15.4; SG =; 40.33 ± 7.9 vs. 50.01±8.4; CG = 40.46 ± 3.5 vs. 48.40 ± cal activity <strong>and</strong> fitness <strong>in</strong> Young dances, Med Sci Sports Exerc 27, 158showed<br />

that no significant differences between Control Group <strong>and</strong> CG (p = 0.217) so<br />

3.2; RG = 42.84 ± 6.1 vs. 51.14 ± 9.6). HDL-c <strong>in</strong>creased: SG: 24.00%, 163.<br />

RG (p= 0.191); but there were differences between control group <strong>and</strong> SG (p = 0.010).<br />

CG: 19.62%, RG: 19.37%). Comparison with Tukey test showed that Barr S., Costill D., F<strong>in</strong>k W., et al. (1991) .Effect of <strong>in</strong>creased tra<strong>in</strong><strong>in</strong>g<br />

no significant differences between Control Group <strong>and</strong> CG (p = 0.217) volume on blood lipids <strong>and</strong> lipoprote<strong>in</strong>s <strong>in</strong> male collegiate swimmers.<br />

so RG (p= 0.191); but there HDL-c were Content differences between control group <strong>and</strong><br />

SG (p = 0.010).<br />

80<br />

Med Sci Sports Exerc, 23, 795-800.<br />

mg/dl 60<br />

358 40<br />

20<br />

0<br />

1 WK<br />

16 Wk


Bounds. R. G., et al. (2000). Diet <strong>and</strong> Short term plasma lipoprote<strong>in</strong><br />

lipid changes after exercise <strong>in</strong> tra<strong>in</strong>ed men, Int J Sport Nutr Exerc<br />

Metab 10, 114-127.<br />

Daniel J. G., Gerry O., Michael J. Joyner, <strong>and</strong> Nigel T. Cable (2008). Exercise<br />

<strong>and</strong> cardiovascular risk reduction: Time to update the rationale<br />

for exercise? J Appl Physiol 105, 766-768.<br />

Dong S. H., et al. (1998).Regular Physical Activity <strong>and</strong> coronary risk<br />

factors <strong>in</strong> Japanese Men, American health association<br />

Edward. T. H. (2001). Type of Activity. Med Sci 33, 364-369.<br />

Fagard. R. H. (2001). Exercise Characteristic <strong>and</strong> Blood pressure, Med<br />

Sci 33, 484-492.<br />

Gerald F. Fletcher. (1997). How to Implement Physical Activity <strong>in</strong> Primary<br />

<strong>and</strong> Secondary Prevention. Circulation 96, 355-357.<br />

Henry Z., Nicola O., Janaki A., Alicja et al. (2009) Quantify<strong>in</strong>g the<br />

dose-response of walk<strong>in</strong>g <strong>in</strong> reduc<strong>in</strong>g coronary heart disease risk:<br />

meta-analysis. Eur J Epidemiology 24(4), 181-192.<br />

Heyward. V. H (2002). Advanced Fitness Assessment & Exercise Prescription.<br />

Fourth Edition.<br />

Kantar. M. A, et al. (1987). HDL-c <strong>and</strong> lipoprote<strong>in</strong> lipase activity <strong>in</strong><br />

tra<strong>in</strong>ed <strong>and</strong> untra<strong>in</strong>ed men, Metab 36, 188-192,<br />

K<strong>in</strong>g .C., William L. Haskell, D. R. Young, Roberta K. Oka, DNSc;<br />

Marcia 15.<br />

Merrill. G. F, et al. (1990).plasma lipid concentration <strong>in</strong> college students<br />

perform<strong>in</strong>g Self-selected Exercise, J Am Coll Nutr 9(3), 226-230.<br />

Hamer M., Chida Y. (2008).Walk<strong>in</strong>g <strong>and</strong> primary prevention: a metaanalysis<br />

of prospective cohort studies, Br J Sports Med; 42, 238-243<br />

Paul. D., et al. (2001).The Acuat Versus the Chronic Response. Med<br />

Sci 33, 438-445,<br />

Ritakari. O. et al. (1997).Assosiation between Physical activity <strong>and</strong> risk<br />

factors for coronary heart disease: the cardiovascular risk <strong>in</strong> young<br />

F<strong>in</strong>ns study. Med Sci Sports Exerc 29(8), 1055<br />

Skoumas. J, et al. (2003).Physical activity, High-density lipoprote<strong>in</strong> cholesterol<br />

<strong>and</strong> other lipids levels <strong>in</strong> men <strong>and</strong> women from ATTICA<br />

Study. Lipids Health Dis. 12 (1): 3.<br />

Smutok, M. A., Reece. C., et al. (1993). Aerobic versus strength tra<strong>in</strong><strong>in</strong>g<br />

for risk factor <strong>in</strong>tervention <strong>in</strong> middle-aged men at high risk for<br />

coronary heart disease. Metabolism 42(2): 177-84.<br />

Susanne R. D., Bernhard P., et al. (2006). The effect of physical activity<br />

<strong>and</strong> physical fitness on plasma adiponect<strong>in</strong> <strong>in</strong> adults with predisposition<br />

to metabolic syndrome. Eur J Applied Physiol 98(5), 472-481.<br />

Tanasescu .M., Eitzmann M., Rimm .E., et al. (2002). Exercise Type<br />

<strong>and</strong> Intensity <strong>in</strong> Relation to Coronary Heart Disease <strong>in</strong> Men. JAMA<br />

288, 16, 1994-2000<br />

Thompson. P. D, L. V., (2003). Physical activity <strong>in</strong> the prevention of<br />

Atherosclerotic coronary Heart Disease. Cadiovasc Med 5(4), 279-<br />

285.<br />

Tanaka H., Baseett D., Howley E. (1997). Effects of swim tra<strong>in</strong><strong>in</strong>g on<br />

body weight, carbohydrate metabolism, lipid <strong>and</strong> lipo prote<strong>in</strong> profile.<br />

Cl<strong>in</strong> Physiol 17, 347-59.<br />

Todd D. M., Gary J. B. <strong>and</strong> Gerald F. (1997). Exercise <strong>and</strong> its role <strong>in</strong><br />

the prevention <strong>and</strong> rehabilitation of cardiovascular disease, Annals of<br />

Behavioral <strong>Medic<strong>in</strong>e</strong>; 19(3), 220-229.<br />

Williams P., Stefanick M., Vranizan K., Wood P. (1994).The effects of<br />

weight loss by exercise or by diet<strong>in</strong>g on plasma high-density lipoprote<strong>in</strong><br />

(HDL) levels <strong>in</strong> men with low, <strong>in</strong>termediate, <strong>and</strong> normal-tohigh<br />

HDL at basel<strong>in</strong>e. Metabolism 43(7), 917-24.<br />

Wilson P., Anderson K., et al. (1994). Determ<strong>in</strong>ants of Change <strong>in</strong> Total<br />

Cholesterol <strong>and</strong> HDL-C with Age: The Fram<strong>in</strong>gham Study. Journal<br />

of Gerontology. 49(6), M252-M257.<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

Analysis of Aerobic/Anaerobic Performance <strong>in</strong><br />

Functionally Disabled Swimmers: Low Classes vs<br />

High Classes<br />

de Aymerich, J. 1 , Benavent, J. 2 , tella, V. 2 , colado, J.c. 2 ,<br />

González, l.M. 2 , García-Massó, X. 2 , Madera, J. 2<br />

1 Universidad País Vasco, Vitoria, España<br />

2 Universidad de Valencia, Valencia, España<br />

The ma<strong>in</strong> aim of this study was to exam<strong>in</strong>e whether there are differences<br />

<strong>in</strong> the LA accumulation <strong>in</strong> disabled swimmers belong<strong>in</strong>g to the lower<br />

classes, higher classes <strong>and</strong> those without functional disability. The sample<br />

was made up of 38 swimmers, 10 disabled swimmers from classes 1<br />

to 5 (G1), 9 swimmers from classes 6 to 10 (G2) <strong>and</strong> 10 swimmers without<br />

functional disability (G3). The swimmers performed two bouts of<br />

swimm<strong>in</strong>g: one anaerobic <strong>and</strong> the other aerobic-anaerobic. The Anova<br />

showed significant differences between the groups (p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Methods<br />

The sample consisted of 29 swimmers, 10 of them were disabled swimmers<br />

of functional classes 1 to 5 (G1), 9 disabled swimmers of functional<br />

classes 6 to 10 (G2) <strong>and</strong> 10 able swimmers (G3). The descriptive average<br />

values of the swimmers characteristics were (mean±st<strong>and</strong>ard error of<br />

the mean) height 163.8±6.17 cm, weight 56.83±2.39 kg <strong>and</strong> age 27±2.04<br />

years for G1; 170.67±5.39 cm, 62.72±5.67 kg <strong>and</strong> 27.44±3.5 years for G2;<br />

<strong>and</strong> 174.72±2.3 cm, 66.87±2.68 kg <strong>and</strong> 17.5±0.8 years for G3. Table 1<br />

presents <strong>in</strong>formation about the disability of the G1 <strong>and</strong> G2 swimmers.<br />

Table 1. Type of disability, <strong>and</strong> number of subjects affected by each disability<br />

of the Groups 1 <strong>and</strong> 2<br />

Disability Group 1 (n=10) Group 2 (n=9)<br />

Focamelia 1 3<br />

Arthrogryposis 1 0<br />

Paraplegia 3 1<br />

Amputee 1 1<br />

Cerebral palsy 4 0<br />

Brachial plexus lesion 0 1<br />

Perthes 0 1<br />

Sp<strong>in</strong>al cord disorder 0 1<br />

Muscular atrophy 0 1<br />

All the swimmers of G1 <strong>and</strong> G2 belonged to the national swimm<strong>in</strong>g team<br />

that competed at the Paralympic Games <strong>in</strong> Beij<strong>in</strong>g. G3 group subjects<br />

were national level swimmers without disability from different clubs. The<br />

subjects signed an <strong>in</strong>formed consent form before start<strong>in</strong>g the protocol,<br />

this be<strong>in</strong>g checked by the Research Commission of the Department of<br />

Physical Education <strong>and</strong> Sports at the University of Valencia (Spa<strong>in</strong>). All<br />

procedures described <strong>in</strong> this section comply with the requirements listed<br />

<strong>in</strong> the 1975 Declaration of Hels<strong>in</strong>ki <strong>and</strong> its later amendment <strong>in</strong> 2008.<br />

With the aim of verify<strong>in</strong>g whether the lactate accumulation after a<br />

maximum anaerobic effort (R1) <strong>and</strong> another aerobic-anaerobic effort (R2)<br />

differ between disabled swimmers (high <strong>and</strong> low classes) <strong>and</strong> non disabled<br />

swimmers, each subject performed one set of each test (R1 <strong>and</strong> R2). The<br />

subjects did the tests us<strong>in</strong>g their competition stroke. Table 2 shows the<br />

number of swimmers for each stroke. The subjects did two series. The<br />

objectives of these series were to reach the maximum LA concentration<br />

after an anaerobic effort (R1) <strong>and</strong> an aerobic-anaerobic effort (R2). After<br />

f<strong>in</strong>ish<strong>in</strong>g each test, LA level was registered at five po<strong>in</strong>ts (i.e. 1, 3, 5, 7 <strong>and</strong><br />

9 m<strong>in</strong>utes after the test). Before test R1, rest<strong>in</strong>g LA was taken (mean±<br />

SEM) (G1: 1.38±0.09, G2: 1.48±0.10, G3: 1.41±0.11). Although rest<strong>in</strong>g<br />

LA value before R2 was not registered, R2 was not started until the LA<br />

value was similar to rest<strong>in</strong>g LA before R1. One m<strong>in</strong>ute after f<strong>in</strong>ish<strong>in</strong>g each<br />

series, a blood sample for LA level, was taken every two m<strong>in</strong>utes till the<br />

highest LA peak was reached (i.e. 1, 3, 5, 7,… m<strong>in</strong>utes). The highest lactate<br />

peak was the one used for later analysis.<br />

Table 2. Number of subjects that used each swimm<strong>in</strong>g stroke <strong>in</strong> the three<br />

groups.<br />

Group 1 (n=10) Group 2 (n=9) Group 3 (n=10)<br />

Freestyle 3 5 8<br />

Butterfly 1 0 0<br />

Backstroke 3 1 0<br />

Breaststroke 3 3 2<br />

All the subjects did the R1 series first at the maximum <strong>in</strong>tensity. After a 30<br />

m<strong>in</strong>ute rest, they did R2 series to the maximum <strong>in</strong>tensity. R1 distance for<br />

each subject was the one that allowed (depend<strong>in</strong>g on the swimmer’s disability<br />

<strong>and</strong> or performance level) to complete as many laps (i.e. 25 meters)<br />

each as near 60 seconds as possible. To calculate the swimm<strong>in</strong>g distance of<br />

R2, approximately 240 seconds was the length to complete. Average time<br />

360<br />

(mean±st<strong>and</strong>ard error of the mean, SEM) for R1 was 73.23±3.15 seconds<br />

<strong>and</strong> for R2 was 224.48±11.3 seconds, without differences between groups.<br />

Lactate level for each subject was registered after the test. 5 µl of capillary<br />

blood was exam<strong>in</strong>ed with the lactate exam<strong>in</strong>er Lactate-Pro.<br />

Statistical analysis was carried out us<strong>in</strong>g SPSS software version 17<br />

(SPSS <strong>in</strong>c., Chicago, IL, USA). It was checked that all the variables complied<br />

with the assumption of normality (K-S normality test) before analyz<strong>in</strong>g<br />

the data. St<strong>and</strong>ard statistical methods were used to obta<strong>in</strong> the mean<br />

as a measurement of the central trend <strong>and</strong> the st<strong>and</strong>ard error of the mean<br />

(SEM) as a measurement of dispersion. A mixed model 3(group) x 2 (test)<br />

ANOVA was performed to discover differences between the exercises <strong>and</strong><br />

groups. For those variables where the ANOVA showed significant differences,<br />

post hoc analysis were requested us<strong>in</strong>g Bonferroni adjustment to<br />

determ<strong>in</strong>e between which exercises these differences appeared. The level<br />

of statistical significance was set at p


m<strong>in</strong>utes, thereby determ<strong>in</strong><strong>in</strong>g the maximum lactic acid concentration at<br />

an <strong>in</strong>tensity whose ma<strong>in</strong> source of energy was supplied by the anaerobic<br />

lactate as well as the aerobic system (Zamparo et al., 2000; Capelli et al.,<br />

1998). In this way, the swimmers did the R2 over a distance of 150 to 200<br />

meters, or 300 to 400 meters, accord<strong>in</strong>g to their swimm<strong>in</strong>g speed.<br />

In the same way, the duration of 60 seconds was selected for every<br />

swimmer <strong>in</strong> R1 to swim at maximum effort <strong>and</strong> so determ<strong>in</strong>e the maximum<br />

LA concentration at an <strong>in</strong>tensity whose ma<strong>in</strong> source was supplied<br />

by the anaerobic lactate system (Zamparo et al., 2000; Capelli et al., 1998).<br />

Thus the swimmers carried out R1 over a distance of 50 to 100 meters<br />

accord<strong>in</strong>g to their swimm<strong>in</strong>g speed.<br />

This decision meant that there were no significant differences<br />

(p>0.05) <strong>in</strong> the swimm<strong>in</strong>g time between groups <strong>in</strong> R2 (G1=212.82” ±<br />

57.96; G2=248.02” ± 66.60; G3= 208.95” ± 67.33) y en R1 (G1=76.76” ±<br />

16.61; G2=75.90” ± 21.02; G3= 67.33” ± 9.02)<br />

Roi & Cerriza (1992) studied the difference between disabled <strong>and</strong><br />

non-disabled swimmers over the same distance for both groups (50 meters).<br />

The results obta<strong>in</strong>ed do not account for the fact that disabled swimmers<br />

required a swimm<strong>in</strong>g time of approximately 129% of the non disabled<br />

(26.66” vs 61.29”). One of the contributions of our study is to show<br />

the necessity of equat<strong>in</strong>g the swimm<strong>in</strong>g times <strong>and</strong> <strong>in</strong>tensity, as opposed<br />

to select<strong>in</strong>g the same distance, when compar<strong>in</strong>g the performance between<br />

swimmers with <strong>and</strong> without disabilities.<br />

The swimmers with disabilities showed similar values (G2) or lower<br />

(G1) to the swimmers without disability (G3). However, Pelayo et al.<br />

(1995) present higher LA concentration values <strong>in</strong> swimmers with disabilities<br />

than the swimmers without disabilities on <strong>in</strong>tensities related to<br />

the maximum aerobic speed (similar to our R2), evidenc<strong>in</strong>g the difference<br />

<strong>in</strong> tra<strong>in</strong><strong>in</strong>g programs for the swimmers with <strong>and</strong> without disabilities.<br />

If the LA accumulation depends on the musculature engaged dur<strong>in</strong>g<br />

the effort (Ohkuma & Itoh, 1992), it seems reasonable to th<strong>in</strong>k that the<br />

characteristics of the different disabilities of the swimmers from lower<br />

classes, would limit the neuromuscular activation relative to the swimmers<br />

from higher classes <strong>and</strong> swimmers without disabilities. For example G1<br />

was formed by 4 cerebral palsy <strong>and</strong> 3 paraplegic swimmers.<br />

Another aspect to analyze is the differences <strong>in</strong> LA between R1 <strong>and</strong> R2<br />

<strong>in</strong> the different groups. Although the results obta<strong>in</strong>ed do not show differences<br />

between repetitions, the analysis for each swimmer shows whether<br />

the maximum LA concentration can be found <strong>in</strong> R1 or <strong>in</strong> R2 (Table 4).<br />

Table 4. Individual blood lactate levels for groups <strong>and</strong> conditions.<br />

Group 1 (n=10) Group 2 (n=9) Group 3 (n=10)<br />

R1 vs R2 (mmol/LA) R1 vs R2 (mmol/LA) R1 vs R2 (mmol/LA)<br />

7.3 6.8 11.3 9.2 12.2 10.8<br />

8.9 6.9 8.9 9.9 11 11.1<br />

11 7.6 11 8.4 12.7 7<br />

8.6 5.7 14.2 12.1 10.7 11.7<br />

12 9.2 14.2 11.7 10.7 11.8<br />

12 7 10.4 8.1 13.4 10.1<br />

9 9.7 10.8 10 14.1 12<br />

6.4 3.4 13.6 9 14.7 10<br />

14 12 13 9.6 11.7 11.3<br />

6.4 5.2 - - 10.1 9.7<br />

As Table 4 shows, four swimmers obta<strong>in</strong>ed similar values between R1 <strong>and</strong><br />

R2 (≤0.5 mmol/LA), three swimmers obta<strong>in</strong>ed greater values <strong>in</strong> R2 (>0.5<br />

mmol/LA), while the rest of the swimmers obta<strong>in</strong>ed greater values <strong>in</strong> R1<br />

(>0.5 mmol/LA).<br />

The LA concentration <strong>in</strong> aerobic-anaerobic <strong>in</strong>tensities can vary as a<br />

function of the tra<strong>in</strong><strong>in</strong>g carried out on the aerobic or anaerobic system, as<br />

<strong>in</strong>dicated <strong>in</strong> the latest scientific results (Kirsten et al., 2008). Thus the concentration<br />

of LA <strong>in</strong> R1 with respect to R2 could be due to the physiological<br />

adaptations produced by the type of tra<strong>in</strong><strong>in</strong>g; whether aerobic or anaerobic.<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

conclusIon<br />

To conclude, at anaerobic <strong>and</strong> aerobic-anaerobic <strong>in</strong>tensities, the swimmers<br />

of the lower classes have a lower LA accumulation than the swimmers<br />

from higher classes <strong>and</strong> the swimmers without any functional impairment.<br />

However, the swimmers from the higher classes have a similar LA<br />

accumulation to those swimmers without functional disability.<br />

reFerences<br />

Avlonitou, E. (1996). Maximal lactate values follow<strong>in</strong>g competitive performance<br />

vary<strong>in</strong>g accord<strong>in</strong>g to age, sex <strong>and</strong> swimm<strong>in</strong>g style. J Sports<br />

Med Phys Fitness, 36, 24-30.<br />

Capelli C, Pendergast DR, Term<strong>in</strong> B. (1998). Energetics of swimm<strong>in</strong>g at<br />

maximal speeds <strong>in</strong> humans. Eur J Appl Physiol, 78, 385-93.<br />

Ch<strong>in</strong> T, Sawamura S, Fujita H, Nakajima S, Ojima I, Oyabu H, Nagakura<br />

Y, Otsuka H, Nakagawa A. (2001). Effect of endurance tra<strong>in</strong><strong>in</strong>g program<br />

based on anaerobic threshold (AT) for lower limb amputees. J<br />

Rehabil Res Dev 38, 7-11.<br />

De Aymerich, J. (2007). Paralympic swimmers tra<strong>in</strong><strong>in</strong>g: Case study.<br />

“Swimm<strong>in</strong>g Science I”. Editorial Universidad de Granada. Granada<br />

ISBN: 978-84-338-4789-8<br />

Denadai, S.B. (2002). Determ<strong>in</strong>ação do limiar anaeróbio em jogadores<br />

de futebol com paralisia cerebral e nadadores participantes da Paraolimpíada<br />

de Sidney 2000. Rev Bras Med Esporte, Vol. 8, Nº 3 – May/<br />

Jun, 117-121<br />

Esau, SP & Mac<strong>in</strong>tosh, BR. (2006). Post-race lactate levels <strong>and</strong> classification<br />

<strong>in</strong>ternational level physically disabled swimmers. VISTA Conference<br />

2006 Congress IPC: Classification <strong>and</strong> Solutions for the future. Boon:<br />

Federal M<strong>in</strong>istry of Interior<br />

Foster, C., Fitzgerald, D.J., Spatz, P. (1999). Stability of the blood lactate,<br />

heart rate relationship <strong>in</strong> competitive athletes. Med Sci Sports Exerc, 31,<br />

578 – 582.<br />

Garatachea, N., Abad, O., García-Isla, F.J., Sarasa, F.J., Bresciani, G.,<br />

González-Gallego, J., De Paz, J.A. (2006). Determ<strong>in</strong>ation <strong>and</strong> validity<br />

of critical swimm<strong>in</strong>g velocity <strong>in</strong> elite physically disabled swimmers.<br />

Disability <strong>and</strong> Rehabilitation, 28(24), 1551 – 1556<br />

Hellw<strong>in</strong>g, T., Liesen, H., Mader, A., Hollmann, W. (1988). Possible means<br />

of spr<strong>in</strong>t –specific performance diagnostics <strong>and</strong> tra<strong>in</strong><strong>in</strong>g support us<strong>in</strong>g<br />

blood lactate concentrations. Abstract. International Journal oj Sports<br />

<strong>Medic<strong>in</strong>e</strong>, 9 (5), 87 – 388<br />

Burgomaster, K.A., Howarth, K.R., Phillips, S.M., Rakobowchuk, M.,<br />

MacDonald, M.J., McGee, S.L., Gibala, M.J. (2008). Similar metabolic<br />

adaptations dur<strong>in</strong>g exercise after low volume spr<strong>in</strong>t <strong>in</strong>terval <strong>and</strong><br />

traditional endurance tra<strong>in</strong><strong>in</strong>g <strong>in</strong> humans. J Physiol 586 (1), 151–160.<br />

Marliss, E. B., Kreisman, S.H., Manzon, A., Halter, J.B., Vranic, M., Nessim,<br />

S.J. (2000). Gender differences <strong>in</strong> glucoregulatory responses to<br />

<strong>in</strong>tense exercise. J. Appl. Physiol, 88, 457–466.<br />

Ohkuma, T., Itoh, H. (1992). Blood lactate, glycerol <strong>and</strong> catecholam<strong>in</strong>e<br />

<strong>in</strong> arm strokes, leg kicks <strong>and</strong> whole crawl strokes. J Sports Med Phys<br />

Fitness, 32, 32 – 38.<br />

Pelayo, P., Moretto, P., Rob<strong>in</strong>, H., Sidney, M., Gerbeaux, M.; Latour,<br />

M.G., Lavoie, J.M. (1995). Adaptation of maximal aerobic <strong>and</strong> anaerobic<br />

tests for disabled swimmers Eul J Appl Physiol, 71, 512-517<br />

Roi, G.S., Cerizza, C. (1992). Post-competition blood lactate <strong>in</strong> disabled<br />

swimmers. In: D. MacLaren, Thomas Reilly, A. Lees Eds. <strong>Biomechanics</strong><br />

<strong>and</strong> medic<strong>in</strong>e <strong>and</strong> swimm<strong>in</strong>g VI, 257–259.<br />

Telford, R.D., Hahn, A.G., Catchpole, E.A., Parker, A.R., Sweetenham,<br />

W.F. (1988). Post competition blood lactate concentration <strong>in</strong> highly<br />

ranked Australian swimmers. In: Swimm<strong>in</strong>g Science V Ungerechts,<br />

B.E.,Wilke, K., <strong>and</strong> Reischle, K., eds. Champaign, IL: Human K<strong>in</strong>etics<br />

Publishers,. pp. 277–283.<br />

Zamparo, P., Capelli, C., Cautero, M., Di N<strong>in</strong>o, A. (2000). Energy cost<br />

of front-crawl swimm<strong>in</strong>g at supra-maximal speeds <strong>and</strong> underwater<br />

torque <strong>in</strong> young swimmers. Eur J Appl Physiol, 83, 487–91.<br />

361


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Athletic Rehabilitation of a Platform Diver for Return<br />

to Competition after a Shoulder Dislocation<br />

Fuj<strong>in</strong>awa, o. 1,2 , Kondo, Y. 3 , tachikawa, K. 1,3 , Jigami, h. 1,4 , hirose,<br />

K. 2 , Matsunaga, h. 5<br />

1Medical Science Committee of Niigata Swimm<strong>in</strong>g Federation, Nagaoka,<br />

Japan<br />

2Saitama Prefectural University, Koshigaya, Japan<br />

3Yuyukenkomura Hospital, Nagaoka, Japan<br />

4Niigata University of Health <strong>and</strong> Welfare, Niigata, Japan<br />

5Himeji Dokkyo University, Himeji, Japan<br />

A high-school male diver was diagnosed with tend<strong>in</strong>itis of the left suprasp<strong>in</strong>atus<br />

secondary to shoulder dislocation dur<strong>in</strong>g the water-entry<br />

stage of a 10-m dive. L<strong>and</strong>-based athletic rehabilitation consist<strong>in</strong>g of<br />

15 sessions was <strong>in</strong>itiated at a hospital on the 5 th day after the <strong>in</strong>jury. After<br />

treatment with anti-<strong>in</strong>flammatory medication <strong>and</strong> immobilization<br />

by us<strong>in</strong>g a chest b<strong>and</strong>, the patient performed stabiliz<strong>in</strong>g exercise of the<br />

glenohumeral jo<strong>in</strong>t <strong>and</strong> scapula abduction-adduction exercises from the<br />

13 th to the 22 nd day. Aquatic rehabilitation (total, 6 times) was started on<br />

the 17 th day; jo<strong>in</strong>t mobilization of the glenohumeral jo<strong>in</strong>t <strong>and</strong> mobilization<br />

with movements <strong>and</strong> motor control exercises were applied until just<br />

before competition. He started div<strong>in</strong>g practice on the 21 st day; then, he<br />

returned to the National Sports Festival competition <strong>and</strong> won the 2 nd<br />

prize for the 10-m platform dive on the 26 th day after <strong>in</strong>jury.<br />

Key words: mobilization with movement, jo<strong>in</strong>t mobilization, PnF,<br />

imp<strong>in</strong>gement, motor learn<strong>in</strong>g<br />

IntroductIon<br />

Div<strong>in</strong>g-related <strong>in</strong>juries among children <strong>and</strong> adolescents younger than<br />

20 years were comprehensively exam<strong>in</strong>ed, <strong>and</strong> the research showed that<br />

the percentage of upper-extremity <strong>in</strong>juries was 9.5% (Day et al., 2008).<br />

Accord<strong>in</strong>g to their report, the frequency of div<strong>in</strong>g-related extremity <strong>in</strong>juries<br />

was relatively low. In this study, we describe the treatment <strong>and</strong><br />

rehabilitation protocol for a high-school diver with an <strong>in</strong>jury to the<br />

left suprasp<strong>in</strong>atus tendon secondary to shoulder dislocation dur<strong>in</strong>g the<br />

water-entry stage of a 10-m dive. He started athletic rehabilitation on<br />

day 5 after the <strong>in</strong>jury, <strong>and</strong> he tried to dive on the 21 st day; then, he returned<br />

to the National Sports Festival <strong>in</strong> Japan <strong>and</strong> won the 2 nd prize for<br />

10-m platform div<strong>in</strong>g on the 26 th day after <strong>in</strong>jury. The objective of this<br />

case study is to retrospectively analyze the rehabilitation program <strong>and</strong><br />

to suggest effective physical therapy (PT) procedures with regard to the<br />

biomechanical aspect.<br />

Methods<br />

The patient’s medical records, <strong>in</strong>clud<strong>in</strong>g magnetic resonance imag<strong>in</strong>g<br />

(MRI) scans, were evaluated, <strong>and</strong> the PT records for hospital <strong>and</strong> poolside<br />

rehabilitation were retrospectively analyzed with regard to the biomechanical,<br />

anatomical, <strong>and</strong> k<strong>in</strong>esiologic aspects. This study program<br />

was approved by the Saitama Prefectural University Ethical Committee.<br />

results<br />

History. The male patient, who was 17 years of age, experienced shoulder<br />

dislocation dur<strong>in</strong>g div<strong>in</strong>g practice for the Inter-High School Championships<br />

held outside his native city. He dislocated his left shoulder<br />

due to abduction of the arm dur<strong>in</strong>g entry <strong>in</strong>to the water. When a coach<br />

raised him from a sup<strong>in</strong>e to a sitt<strong>in</strong>g position to apply a sl<strong>in</strong>g at pool<br />

side, the dislocated shoulder was spontaneously reduced. He was admitted<br />

for emergency care to a local hospital because of jo<strong>in</strong>t swell<strong>in</strong>g<br />

<strong>and</strong> severe pa<strong>in</strong>. After the championship, he visited the orthopaedic<br />

department of a hospital <strong>in</strong> his native city <strong>and</strong> commenced l<strong>and</strong>-based<br />

362<br />

rehabilitation (Table 1).<br />

Diagnosis <strong>and</strong> Medication. He was diagnosed with suprasp<strong>in</strong>atus tend<strong>in</strong>itis,<br />

<strong>and</strong> MRI <strong>in</strong>dicated swell<strong>in</strong>g of the suprasp<strong>in</strong>atus tendon <strong>and</strong><br />

glenohumeral hydrarthrosis (fig. 1). Anti-<strong>in</strong>flammatory medication <strong>and</strong><br />

immobilization by a chest b<strong>and</strong> were prescribed.<br />

L<strong>and</strong>-based rehabilitation at a hospital commenced on the 5th day<br />

after <strong>in</strong>jury <strong>and</strong> was completed on the 22nd day (15 visits total). Dur<strong>in</strong>g<br />

the immobilization period (from the 5th to the 12th day), PT programs<br />

consisted of the sound side <strong>and</strong> general condition<strong>in</strong>g exercises. From the<br />

13th to the 22nd 24<br />

BMS <strong>XI</strong> Chapter 6. <strong>Medic<strong>in</strong>e</strong>, Rehabilitation <strong>and</strong> Prevention<br />

aspects. This study program was approved by the Saitama Prefectural University Ethical<br />

Committee.<br />

RESULTS<br />

History. The male patient, who was 17 years of age, experienced shoulder dislocation<br />

dur<strong>in</strong>g div<strong>in</strong>g practice for the Inter-High School Championships held outside his native<br />

city. He dislocated his left shoulder due to abduction of the arm dur<strong>in</strong>g entry <strong>in</strong>to the<br />

water. When a coach raised him from a sup<strong>in</strong>e to a sitt<strong>in</strong>g position to apply a sl<strong>in</strong>g at<br />

pool side, the dislocated shoulder was spontaneously reduced. He was admitted for<br />

emergency care to day, a local the hospital PT programs because of jo<strong>in</strong>t <strong>in</strong>troduced swell<strong>in</strong>g <strong>and</strong> stabilization severe pa<strong>in</strong>. After exercises the<br />

of championship, the left glenohumeral he visited the orthopaedic jo<strong>in</strong>t us<strong>in</strong>g department isometric of a hospital rotator <strong>in</strong> his cuff native exercises city <strong>and</strong> <strong>and</strong><br />

commenced l<strong>and</strong>-based rehabilitation (Table 1).<br />

scapula Diagnosis abduction-adduction <strong>and</strong> Medication. He was exercises. diagnosed Concentric with suprasp<strong>in</strong>atus <strong>and</strong> eccentric tend<strong>in</strong>itis, <strong>and</strong> rotator<br />

MRI cuff <strong>in</strong>dicated exercises swell<strong>in</strong>g of the of the glenohumeral suprasp<strong>in</strong>atus tendon jo<strong>in</strong>t <strong>and</strong> us<strong>in</strong>g glenohumeral a rubber hydrarthrosis b<strong>and</strong> were<br />

(fig. 1). Anti-<strong>in</strong>flammatory medication <strong>and</strong> immobilization by a chest b<strong>and</strong> were<br />

also prescribed. used. The objectives of the scapula abduction-adduction exercises<br />

were L<strong>and</strong>-based to ga<strong>in</strong> rehabilitation optimal scapular at a hospital mobility commenced <strong>and</strong> on stability the 5 for normal scapulohumeral<br />

rhythm <strong>and</strong> to prevent glenohumeral jo<strong>in</strong>t dysfunctions, such<br />

as abnormal stresses to the anterior capsular structures, <strong>in</strong>creased possibility<br />

of rotator cuff compression, <strong>and</strong> decreased performance. Isometric,<br />

concentric, <strong>and</strong> eccentric rotator cuff exercises were applied to keep the<br />

optimal position of the glenohumeral jo<strong>in</strong>t <strong>and</strong> to improve adequate<br />

balance of <strong>in</strong>ternal <strong>and</strong> external rotator muscle strength (Niederbracht<br />

et al., 2008).<br />

th day after <strong>in</strong>jury <strong>and</strong> was<br />

completed on the 22 nd day (15 visits total). Dur<strong>in</strong>g the immobilization period (from the<br />

5 th to the 12 th day), PT programs consisted of the sound side <strong>and</strong> general condition<strong>in</strong>g<br />

exercises. From the 13 th to the 22 nd day, the PT programs <strong>in</strong>troduced stabilization<br />

exercises of the left glenohumeral jo<strong>in</strong>t us<strong>in</strong>g isometric rotator cuff exercises <strong>and</strong><br />

scapula abduction-adduction exercises. Concentric <strong>and</strong> eccentric rotator cuff exercises<br />

of the glenohumeral jo<strong>in</strong>t us<strong>in</strong>g a rubber b<strong>and</strong> were also used. The objectives of the<br />

scapula abduction-adduction exercises were to ga<strong>in</strong> optimal scapular mobility <strong>and</strong><br />

stability for normal scapulohumeral rhythm <strong>and</strong> to prevent glenohumeral jo<strong>in</strong>t<br />

dysfunctions, such as abnormal stresses to the anterior capsular structures, <strong>in</strong>creased<br />

possibility of rotator cuff compression, <strong>and</strong> decreased performance. Isometric,<br />

concentric, <strong>and</strong> eccentric rotator cuff exercises were applied to keep the optimal<br />

position of the glenohumeral jo<strong>in</strong>t <strong>and</strong> to improve adequate balance of <strong>in</strong>ternal <strong>and</strong><br />

external rotator muscle strength (Niederbracht et al., 2008).<br />

Table 1. Process of Athletic Rehabilitation.<br />

Table 1. Process of Athletic Rehabilitation.<br />

Day* Situations Conditions F<strong>in</strong>d<strong>in</strong>gs <strong>and</strong> Programs**<br />

5 th L<strong>and</strong>-based Immobilizatio -General condition<strong>in</strong>g exercises such as stretch<strong>in</strong>g<br />

rehabilitation at n<br />

<strong>and</strong> strength tra<strong>in</strong><strong>in</strong>g of the neck, trunk, <strong>and</strong><br />

a hospital<br />

extremities except the affected left arm<br />

13 th Detachment of -Left shoulder passive ROM: Flex 120, Abd 90, ER<br />

the<br />

20, IR 35<br />

immobiliz<strong>in</strong>g -Pa<strong>in</strong> <strong>in</strong> the suprasp<strong>in</strong>atus <strong>and</strong> middle deltoid area<br />

brace <strong>and</strong> -Program: 1) Stabilization of the glenohumeral jo<strong>in</strong>t<br />

exercises of<br />

the affected<br />

arm<br />

with isometric exercise; 2) Scapula Abd-Add exercise<br />

15 th Swimm<strong>in</strong>g Walk<strong>in</strong>g <strong>in</strong> the -Passive ROM: Flex 145, ER 30, IR 30<br />

team tra<strong>in</strong><strong>in</strong>g pool -Program: 3) Concentric <strong>and</strong> eccentric rotator cuff<br />

camp<br />

exercises by us<strong>in</strong>g a rubber b<strong>and</strong><br />

17 th Aquatic Breast<br />

F<strong>in</strong>d<strong>in</strong>gs <strong>and</strong> programs after camp tra<strong>in</strong><strong>in</strong>g 25<br />

BMS <strong>XI</strong> rehabilitation at Chapter swimm<strong>in</strong>g 6. <strong>Medic<strong>in</strong>e</strong>, -Rest<strong>in</strong>g Rehabilitation pa<strong>in</strong> <strong>in</strong> <strong>and</strong> the Prevention anterior aspect of the shoulder<br />

pool side<br />

-Active movements: pa<strong>in</strong> with Abd 90, ER 30, IE 80,<br />

Horiz Add 60<br />

-Passive movements: Abd 90 with pa<strong>in</strong> <strong>and</strong> restricted<br />

at 120 by pa<strong>in</strong> <strong>and</strong> muscle guard<strong>in</strong>g<br />

-Jo<strong>in</strong>t mobility test: could not be performed because<br />

of pa<strong>in</strong><br />

<strong>and</strong> muscle guard<strong>in</strong>g<br />

-Palpation: muscle spasms <strong>and</strong> tenderness <strong>in</strong> all<br />

rotator cuff muscles<br />

-MWMS with postero<strong>in</strong>ferior glide: full Flex-Abd-<br />

ER without pa<strong>in</strong><br />

-Program: 4) MWMS; 5) Tap<strong>in</strong>g at the rotator cuff<br />

18 th 2 nd Aquatic<br />

rehabilitation<br />

-Program: 6) Self MWMS<br />

21 st 3 rd Aquatic Div<strong>in</strong>g -Pa<strong>in</strong> condition: no pa<strong>in</strong> experienced dur<strong>in</strong>g front<br />

rehabilitation<br />

dive; pa<strong>in</strong> experienced dur<strong>in</strong>g back dive<br />

-Program: 4) MWMS with a 300-g weight; 6) Self<br />

MWMS with a 300-g weight; 7) PNF (slow reversal,<br />

repeated contraction)<br />

22 nd Completed l<strong>and</strong>based<br />

rehabilitation<br />

-Passive ROM: Flex 170, ER 60, IR 70<br />

23 rd 4 th Aquatic<br />

-Rapid Abd-ER causes pa<strong>in</strong><br />

rehabilitation<br />

-Program: 4) MWMS with a 500-g weight; 6) Self<br />

MWMS with a 500-g weight; 7) PNF; 8) TFM <strong>and</strong><br />

functional massage<br />

25 th 5 th Aquatic 1 day before -The same programs were cont<strong>in</strong>ued<br />

rehabilitation the<br />

competition<br />

26 th 6 th Aquatic Before the -No shoulder pa<strong>in</strong><br />

rehabilitation competition -Same programs were cont<strong>in</strong>ued<br />

*, Day after onset of the <strong>in</strong>jury; ** Abbreviations: ROM, range of motion (numbers represent<br />

degrees); Flex, flexion; Abd, abduction; Add, adduction; ER, external rotation; IR, <strong>in</strong>ternal<br />

*, rotation; Day after Horiz onset Add, horizontal of the <strong>in</strong>jury; adduction; ** MWMS, Abbreviations: mobilization with ROM, movements; range PNF, of motion<br />

proprioceptive neuromuscular facilitation; TFM, transverse friction massage<br />

(numbers represent degrees); Flex, flexion; Abd, abduction; Add, adduc-<br />

tion; ER, external rotation; IR, <strong>in</strong>ternal rotation; Horiz Add, horizontal<br />

adduction; MWMS, mobilization with movements; PNF, proprioceptive<br />

neuromuscular facilitation; TFM, transverse friction massage<br />

Figure 1. MRI f<strong>in</strong>d<strong>in</strong>gs of the left Shoulder


Figure 1. MRI f<strong>in</strong>d<strong>in</strong>gs of the left Shoulder<br />

Figure 2. Checked tap<strong>in</strong>g on rotator cuff muscles by us<strong>in</strong>g a 4-mm wide<br />

non-elastic tape<br />

Aquatic rehabilitation at the pool side dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g camp commenced<br />

on the 17 th day after <strong>in</strong>jury (6 visits total). Jo<strong>in</strong>t mobilization of<br />

posterior capsule <strong>and</strong> mobilization with movements (MWMS) <strong>in</strong> active<br />

flexion-abduction-external rotation with the humeral head postero<strong>in</strong>ferior<br />

glid<strong>in</strong>g (Mulligan, 2004) were applied on the 17 th <strong>and</strong> 18 th day.<br />

Stretch<strong>in</strong>g rotator cuff muscles, tap<strong>in</strong>g at suprasp<strong>in</strong>atus, <strong>in</strong>frasp<strong>in</strong>atus,<br />

<strong>and</strong> teres m<strong>in</strong>or (fig. 2), <strong>and</strong> education of scapula <strong>and</strong> humeral head<br />

position<strong>in</strong>g were also performed. In this period, the humeral head still<br />

deviated anteriorly, <strong>and</strong> a pa<strong>in</strong>ful arc occurred dur<strong>in</strong>g elevation of the<br />

arm. Jo<strong>in</strong>t mobility test<strong>in</strong>g <strong>in</strong>dicated limitation of posterior glide of the<br />

humeral head because of the tight posterior capsule. Therefore, jo<strong>in</strong>t mobilization<br />

was applied <strong>and</strong> MWMS was used to try to correct dynamic<br />

alignment <strong>and</strong> to avoid imp<strong>in</strong>gement of the suprasp<strong>in</strong>atus tendon dur<strong>in</strong>g<br />

elevation. After correction of humeral head position, checked tap<strong>in</strong>g<br />

was applied on the rotator cuff muscles by us<strong>in</strong>g a 4-mm wide non-elastic<br />

tape to ma<strong>in</strong>ta<strong>in</strong> the correct position. Self MWMS was also taught<br />

to keep good position of the humeral head on the glenoid dur<strong>in</strong>g elevation<br />

of the arm. On the 21 st day, the PT programs were supplemented<br />

with MWMS with a 300-g weight (us<strong>in</strong>g 300 mL of water <strong>in</strong> a plastic<br />

bottle) <strong>and</strong> proprioceptive neuromuscular facilitation (PNF) (Myers <strong>and</strong><br />

Lephart, 2000). At this time, elevation of the arm dur<strong>in</strong>g front dive did<br />

not cause shoulder pa<strong>in</strong>; however, rapid elevation <strong>and</strong> elevation dur<strong>in</strong>g<br />

back dive caused pa<strong>in</strong>. Therefore, MWMS with a light weight <strong>and</strong> PNF<br />

were applied to improve proprioceptive stimulation for motor learn<strong>in</strong>g.<br />

From the 23 rd to the 26 th day, MWMS with a 500-g weight was used,<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

<strong>and</strong> soft-tissue mobilization such as transverse friction massage (TFM)<br />

(Cyriax <strong>and</strong> Cyriax, 1993) <strong>and</strong> functional massage (Evjenth <strong>and</strong> Hamberg,<br />

1984) were added. The reason for <strong>in</strong>creas<strong>in</strong>g the weight dur<strong>in</strong>g<br />

MWMS was to <strong>in</strong>crease proprioceptive stimulation for motor learn<strong>in</strong>g.<br />

Palpation <strong>in</strong>dicated muscle spasm of the rotator cuff muscles, especially<br />

subscapularis. Reaction to the palpation at the suprasp<strong>in</strong>atus tendon <strong>in</strong>dicated<br />

that the tend<strong>in</strong>itis would improve <strong>in</strong> the recovery stage. Therefore,<br />

soft-tissue mobilization was applied <strong>in</strong> these muscles.<br />

dIscussIon<br />

Rehabilitation <strong>in</strong> this case study <strong>in</strong>volved immobilization dur<strong>in</strong>g the<br />

acute stage (2 weeks), followed by stability exercises for the glenohumeral<br />

jo<strong>in</strong>t <strong>and</strong> scapula, <strong>and</strong> f<strong>in</strong>ally movement toward a functional approach.<br />

The rehabilitation program commenced the 5 th day after <strong>in</strong>jury;<br />

the affected area needed to be rested <strong>and</strong> other areas tra<strong>in</strong>ed to keep<br />

good condition. On the 13 th day, the immobiliz<strong>in</strong>g brace was detached,<br />

<strong>and</strong> passive treatments for limited range of motion (ROM), stabiliz<strong>in</strong>g<br />

exercises for the affected glenohumeral jo<strong>in</strong>t, <strong>and</strong> scapulothoracic<br />

exercises were applied. At this stage, the PT program commenced stabilization<br />

exercises for the glenohumeral jo<strong>in</strong>t to prevent imp<strong>in</strong>gement<br />

of the rotator cuff. In addition, concentric <strong>and</strong> eccentric exercises for the<br />

rotator cuff were <strong>in</strong>cluded to <strong>in</strong>duce optimal muscle recruitment dur<strong>in</strong>g<br />

overhead activities of the arm. The scapula plays an important role <strong>in</strong><br />

facilitat<strong>in</strong>g adequate shoulder function to produce efficient movement.<br />

The scapular muscles must be dynamically positioned <strong>in</strong> the glenoid so<br />

that efficient glenohumeral movement can occur; therefore, the scapular<br />

muscles should be tra<strong>in</strong>ed optimally.<br />

Be<strong>in</strong>g <strong>in</strong> the subacute stage dur<strong>in</strong>g the first day of the aquatic rehabilitation,<br />

the subject compla<strong>in</strong>ed slightly of rest<strong>in</strong>g pa<strong>in</strong> after elevat<strong>in</strong>g<br />

the arm <strong>and</strong> had positive sign of pa<strong>in</strong>ful arc. Maneuvers of MWMS<br />

applied postero<strong>in</strong>ferior force on the humeral head <strong>and</strong> mechanically<br />

avoided imp<strong>in</strong>gement of suprasp<strong>in</strong>ous tendon under the coracoacromial<br />

arch dur<strong>in</strong>g active elevation of the arm. MWMS with a light weight<br />

(Mulligan, 2004) <strong>and</strong> PNF facilitated proprioception to ga<strong>in</strong> good motor<br />

control of arm movements (Myers <strong>and</strong> Lephart, 2000). Self MWMS<br />

with a light weight was used to ga<strong>in</strong> proper movement patterns of the<br />

arm dur<strong>in</strong>g abduction <strong>and</strong> adduction. The checked tap<strong>in</strong>g was not strong<br />

enough to mechanically restrict anterior movement of the humeral<br />

head; however, the tape stimulated sk<strong>in</strong> <strong>and</strong> muscles as light compression<br />

dur<strong>in</strong>g anterior deviation of the humeral head. The tape also stimulated<br />

receptors of the sk<strong>in</strong> <strong>and</strong> the proprioceptors dur<strong>in</strong>g movements.<br />

Although he did not compla<strong>in</strong> of shoulder pa<strong>in</strong> dur<strong>in</strong>g div<strong>in</strong>g on the<br />

day before competition <strong>and</strong> the day of competition, he was still <strong>in</strong> the<br />

recovery stage. It was evident that he had learned the correct movements<br />

of the glenohumeral jo<strong>in</strong>t <strong>and</strong> scapulothoracic junction. Because<br />

divers hold extremely elevated positions of the glenohumeral jo<strong>in</strong>ts <strong>and</strong><br />

shoulder girdle dur<strong>in</strong>g the water-entry stage, they can avoid imp<strong>in</strong>gement<br />

at the middle <strong>and</strong> f<strong>in</strong>al range of elevation by us<strong>in</strong>g an appropriate<br />

movement pattern <strong>and</strong> congruous articular position dur<strong>in</strong>g movements.<br />

This rehabilitation program for div<strong>in</strong>g is very sports specific; however,<br />

the program could be applied to some sports with a throw<strong>in</strong>g stage, such<br />

as w<strong>in</strong>d-up <strong>and</strong> cock<strong>in</strong>g.<br />

conclusIon<br />

The rehabilitation program for a div<strong>in</strong>g-related shoulder <strong>in</strong>jury was<br />

as follows: (1) dur<strong>in</strong>g the immobilization stage, general condition<strong>in</strong>g<br />

exercises, such as stretch<strong>in</strong>g <strong>and</strong> strength tra<strong>in</strong><strong>in</strong>g of the neck, trunk,<br />

<strong>and</strong> extremities (not <strong>in</strong>clud<strong>in</strong>g the affected left arm), were applied; (2)<br />

after the immobilization stage, jo<strong>in</strong>t mobility was addressed, especially<br />

posterior capsule <strong>and</strong> short <strong>and</strong> tight muscles, then rotator cuff muscles<br />

<strong>and</strong> scapula muscles were strengthened; <strong>and</strong> (3) an appropriate movement<br />

pattern <strong>and</strong> congruous articular position were achieved dur<strong>in</strong>g<br />

movements by MWMS, PNF, <strong>and</strong> motor learn<strong>in</strong>g.<br />

363


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

reFerences<br />

Cyriax, J.H. & Cyriax JP (1993). Cyriax’s Illustrated Manual of Orthopaedic<br />

<strong>Medic<strong>in</strong>e</strong>, 2 nd ed. Oxford: Butterworth He<strong>in</strong>emann<br />

Day, C., Stolz, U., Mehan, T.J., Smith, G.A. & McKenzie, L.B (2008).<br />

Div<strong>in</strong>g-related <strong>in</strong>juries <strong>in</strong> children


BMS <strong>XI</strong> Chapter 6. <strong>Medic<strong>in</strong>e</strong>, Rehabilitation <strong>and</strong> Prevention<br />

BMS <strong>XI</strong> Chapter 6. <strong>Medic<strong>in</strong>e</strong>, Rehabilitation <strong>and</strong> Prevention<br />

Table 3. Changes of physical characteristics pre- to post-physical activity <strong>in</strong>tervention.<br />

time<br />

mean (SD ) mean (SD) mean (SD) mean (SD ) p p<br />

Body weight (kg) 67.3 (2.6) 64.4 (2.0) 61.5 (2.7) 59.4 (3.5) 0.03 * 0.56<br />

Body mass <strong>in</strong>dex (kg/m 2 WPI group(n=4) LPI group(n=4)<br />

pre post pre post<br />

<strong>in</strong>teraction<br />

) 26.3 (2.0) 25.1 (2.1) 25.7 (1.6) 24.6 (1.8) 0.00 * 0.77<br />

%Fat (%) Total 34.3 (10.3) 31.1 (10.6) 36.9 (2.5) 34.7 (2.5) 0.00 * 0.25<br />

%Fat (%) upper limbs 31.1 (11.5) 28.2 (11.3) 34.2 (2.8) 32.3 (2.9) 0.00 * 0.35<br />

%Fat (%) lower limbs 34.7 (9.1) 33.1 (9.5) 37.4 (1.4) 35.9 (1.7) 0.00 * 0.03<br />

%Fat (%) trunk 34.7 (10.8) 30.4 (7.2) 37.1 (3.2) 34.4 (3.1) 0.00 * 0.17<br />

LBM (kg) Total 44.4 (8.5) 44.4 (7.5) 38.8 (3.0) 38.8 (2.5) 0.95 0.91<br />

LBM (kg) upper limbs 2.3 (0.6) 2.4 (0.5) 1.9 (0.1) 1.9 (0.1) 0.36 0.15<br />

LBM (kg) lower limbs 7.6 (1.7) 7.6 (1.4) 6.8 (0.3) 6.9 (0.3) 0.86 0.86<br />

LBM (kg) trunk 24.7 (4.0) 24.6 (3.7) 21.5 (2.5) 21.4 (2.3) 0.48 0.86<br />

Walk<strong>in</strong>g steps (step/day) 13145 (3179) 13163 (1593) 9752 (3858) 13610 (2148) 0.03 * 0.03 *<br />

VO2max (ml/kg/m<strong>in</strong>) 22.0 (3.9) 21.9 (2.5) 18.3 (4.4) 22.1 (5.9) 0.10 0.09<br />

* P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Estimation Method for Energy Expenditure by<br />

Acceleration of Human Head dur<strong>in</strong>g Water Walk<strong>in</strong>g<br />

Kaneda, K. 1 , ohgi, Y. 2 , tanaka, c. 3<br />

1 Research Fellow of the Japan Society for the Promotion of Science, Japan<br />

2 Keio University, Japan<br />

3 J. F. Oberl<strong>in</strong> University, Japan<br />

This study aimed at estimat<strong>in</strong>g energy expenditure (EE) by accelerations<br />

of human head dur<strong>in</strong>g water walk<strong>in</strong>g (WW). Fifty Japanese males (n =<br />

29, age: 27 to 73) <strong>and</strong> females (n = 21, age: 33 to 70) participated <strong>in</strong> this<br />

study. They conducted WW at three walk<strong>in</strong>g speeds of 25 m/m<strong>in</strong>, 30 m/<br />

m<strong>in</strong> <strong>and</strong> 35 m/m<strong>in</strong>. Dur<strong>in</strong>g the WW, an accelerometer was attached to<br />

the occipital region of the subjects <strong>and</strong> recorded three-dimensional accelerations<br />

at 100 Hz. We developed estimation equation for EE (kcal/<br />

m<strong>in</strong>/kg) <strong>in</strong>clud<strong>in</strong>g three components of the rest<strong>in</strong>g metabolic rate, <strong>in</strong>ternal<br />

energy expenditure for mov<strong>in</strong>g his/her body <strong>and</strong> energy expenditure<br />

aga<strong>in</strong>st for water drag force. The correlation coefficients were high <strong>in</strong><br />

both males (r = 0.79) <strong>and</strong> females (r = 0.77). theoretical estimation equations<br />

for EE dur<strong>in</strong>g WW was developed.<br />

Key words: energy expenditure, estimation, Accelerometer, Water<br />

Walk<strong>in</strong>g<br />

IntroductIon<br />

There are many studies <strong>and</strong> devices estimat<strong>in</strong>g energy expenditure (EE)<br />

dur<strong>in</strong>g l<strong>and</strong> walk<strong>in</strong>g, jogg<strong>in</strong>g or daily life activities (Kumahara et al.,<br />

2004; Scott et al., 2006; Tanaka et al., 2007). Due to its availability, those<br />

studies mostly used accelerometers attached to human body (e.g. waist,<br />

wrist <strong>and</strong> ankle). They reported good estimation expla<strong>in</strong>ed by high correlation<br />

coefficient (Scott et al., 2006). However, those studies <strong>and</strong> devices<br />

cannot apply to water exercise because water has specific characteristics<br />

compared to air, most prom<strong>in</strong>ently water resistance <strong>and</strong> buoyancy.<br />

Dur<strong>in</strong>g exercis<strong>in</strong>g <strong>in</strong> water, the gravitational stress at the lower extremity<br />

jo<strong>in</strong>t is reduced <strong>and</strong> greater exert force required for mov<strong>in</strong>g (Miyoshi et<br />

al., 2005). The metabolic responses dur<strong>in</strong>g water exercise were different<br />

from exercise on l<strong>and</strong> (Masumoto et al., 2008). Until now, we <strong>in</strong>vestigated<br />

metabolic responses dur<strong>in</strong>g water walk<strong>in</strong>g (WW) for a wide range<br />

of Japanese males <strong>and</strong> females, <strong>and</strong> cleared that the metabolic responses<br />

dur<strong>in</strong>g the WW were <strong>in</strong>fluenced by mostly the walk<strong>in</strong>g speed other than<br />

the human body size <strong>and</strong> sex (Kaneda et al., 2009a). Therefore, it is important<br />

to develop specific estimation equation for EE dur<strong>in</strong>g WW for<br />

health promotion water exercise. The hypothesis was that the energy<br />

expenditure dur<strong>in</strong>g walk<strong>in</strong>g <strong>in</strong> water was estimated by three components<br />

of the rest<strong>in</strong>g metabolic rate, <strong>in</strong>ternal energy expenditure for mov<strong>in</strong>g<br />

his/her body <strong>and</strong> energy expenditure aga<strong>in</strong>st for water drag force. We<br />

tried to develop estimation equations for EE by accelerations of human ¾<br />

head dur<strong>in</strong>g WW, <strong>and</strong> this study <strong>in</strong>troduces these methodologies. The<br />

future goal is to develop an underwater activity monitor by us<strong>in</strong>g an<br />

accelerometer.<br />

Methods<br />

Fifty Japanese males (n = 29, age: 27 to 73) <strong>and</strong> females (n = 21, age:<br />

33 to 70) participated <strong>in</strong> this study. The mean characteristics of the subjects<br />

are shown <strong>in</strong> Table 1. They provided a written <strong>in</strong>formed consent<br />

to participate <strong>in</strong> this study, <strong>and</strong> their health status was exam<strong>in</strong>ed from<br />

screen<strong>in</strong>g of medical history <strong>and</strong> measured blood pressure before each<br />

subject’s experiment. This study was approved by the Ethics Committee<br />

of Shonan-Fujisawa Campus at Keio University.<br />

The subjects conducted WW at three walk<strong>in</strong>g speeds of 25 m/m<strong>in</strong>,<br />

30 m/m<strong>in</strong> <strong>and</strong> 35 m/m<strong>in</strong> (some subjects executed from 20 m/m<strong>in</strong> ¾ <strong>and</strong><br />

¾<br />

366<br />

40 m/m<strong>in</strong> depend<strong>in</strong>g on their physical condition), <strong>and</strong> exercised over 5<br />

m<strong>in</strong>utes at each walk<strong>in</strong>g speed. In order to ma<strong>in</strong>ta<strong>in</strong> the walk<strong>in</strong>g speed<br />

steady, a pace-maker walked with the subject on the pool-side. The each<br />

wak<strong>in</strong>g trial was separated by more than 5 m<strong>in</strong>utes rest period to recover<br />

the subject’s condition. The experiment was carried out at the <strong>in</strong>door<br />

swimm<strong>in</strong>g pool (17.2 m length, 5 m width <strong>and</strong> 1.1 m depth) (Figure 1).<br />

Dur<strong>in</strong>g the each exercise bout, an accelerometer was attached onto<br />

the occipital region of the subject <strong>and</strong> recorded three-dimensional accelerations<br />

at 100Hz. The metabolic responses (VO 2 , l/m<strong>in</strong>/kg <strong>and</strong> VCO 2,<br />

l/m<strong>in</strong>/kg) were measured by the Douglas bag method us<strong>in</strong>g a portable<br />

gas analyzer (AR-1 O2-ro, Arcosystem Inc., Japan) <strong>and</strong> a dry gas meter<br />

(DCDA-2C-M, Sh<strong>in</strong>agawa Corp., Japan). Furthermore <strong>in</strong>terval times<br />

between mid 15 m by stopwatch were also measured at the each bout.<br />

All analyzed data were selected from last 2 round trips of the each walk<strong>in</strong>g<br />

trial. The energy expenditure (EE, kcal/m<strong>in</strong>/kg) was calculated by<br />

follow<strong>in</strong>g equation (Weir, 1949) for develop<strong>in</strong>g estimation equation<br />

from acceleration data:<br />

EE (kcal/m<strong>in</strong>/kg) = 3.9 × VO 2 (l/m<strong>in</strong>/kg) + 1.1 ×VCO 2 (l/m<strong>in</strong>/kg) (1)<br />

Table 1. Characteristics of the subjects, mean±SD.<br />

Age (yr) Height (cm) Weight (kg) BMI<br />

Male (n = 29) 55.0 ± 14.9 170.9 ± 6.1 69.2 ± 9.0 23.7 ± 3.0<br />

Female (n = 21) 57.4 ± 10.7 156.8 ± 4.6 54.2 ± 5.6 22.1 ± 2.6<br />

Fig. 1. Pool condition <strong>in</strong> this study.<br />

results<br />

A total of 160 samples (males: 97 samples, females: 63 samples) were<br />

obta<strong>in</strong>ed <strong>and</strong> used for analysis. We considered three components <strong>in</strong> the<br />

estimation equation for the EE (kcal/m<strong>in</strong>/kg): rest<strong>in</strong>g metabolic rate<br />

(RMR, kcal/m<strong>in</strong>/kg), <strong>in</strong>ternal energy expenditure for mov<strong>in</strong>g his/her<br />

body (jo<strong>in</strong>t energy expenditure: EE j ) <strong>and</strong> energy expenditure for water<br />

drag force (EE wd ):<br />

EE(kcal /m<strong>in</strong>/kg) = α 0 + α 1 RMR + α 2 EE j + α 3 EE wd (2)<br />

The RMR was calculated by sex, age <strong>and</strong> weight based on the basal<br />

metabolic rate (BMR) equations <strong>in</strong> the Dietary Reference Intakes for<br />

Japanese (M<strong>in</strong>istry of Health, Labour <strong>and</strong> Welfare, Japan, 2010) <strong>and</strong><br />

multiplied 1.2 for the RMR by Numagiri et al. (1970):<br />

RMR(<br />

kcal / m<strong>in</strong>/ kg ) = BMR(<br />

kcal / m<strong>in</strong>/ kg ) × 1.<br />

2<br />

The EEj was assumed to the square root of the sum of squared of both<br />

the sagittal ( Ay') <strong>and</strong> vertical ( A z ′ ) accelerations. For elim<strong>in</strong>at<strong>in</strong>g gravity<br />

effect, the acceleration data was corrected by head <strong>in</strong>cl<strong>in</strong>ation angle<br />

(Figure 2):<br />

A ¾ z ′ = Az − gcosϑ ¾<br />

(4)<br />

Ay'= Ay − gs<strong>in</strong>ϑ (5)<br />

(3)


¾<br />

¾<br />

¾<br />

Fig. 2. Correction of head <strong>in</strong>cl<strong>in</strong>ation.<br />

When calculat<strong>in</strong>g the EE j , the dimensions of the each component must<br />

to be equivalent to the mechanical power, <strong>and</strong> a w<strong>in</strong>dow of data was<br />

set at 5 sec (= Δt) for the purpose of <strong>in</strong>clud<strong>in</strong>g one cycle dur<strong>in</strong>g WW<br />

(Kaneda et al., 2009b). Therefore, the EE j was calculated as follows:<br />

EE j = (Az' 2 +Ay' 2 t +∆t<br />

∫ ) /∆tdt × weight(kg) × v(m /m<strong>in</strong>)/weight(kg) (6)<br />

t<br />

where v is the walk<strong>in</strong>g speed measured by stopwatch.<br />

The EEwd was regarded as the anterior-posterior acceleration ( Aap). From the equation (4) <strong>and</strong> (5), the Aap is expressed as (Figure 2):<br />

Aap = Az's<strong>in</strong>ϑ + Ay'cosϑ<br />

¾<br />

(7)<br />

Therefore, the EEwd was calculated as follows:<br />

t +∆t<br />

2<br />

EEwd = ∫ Aap /∆tdt × weight(kg) × v(m /m<strong>in</strong>)/weight(kg) (8)<br />

t<br />

The acceleration data was averaged <strong>in</strong> the last 20 sec of the each trial<br />

to develop the estimation equation for the EE. The data of the each<br />

component was Z-scored.<br />

The results of this estimation equation for the males <strong>and</strong> females showed<br />

<strong>in</strong> Table 2 <strong>and</strong> Figure 3, <strong>and</strong> Figure 4 showed the results of the residual<br />

analysis. The correlation coefficients were high <strong>in</strong> both males (r = 0.79)<br />

<strong>and</strong> females (r = 0.77).<br />

Table 2. Coefficients of the each component <strong>and</strong> correlation coefficients<br />

<strong>in</strong> each sex.<br />

Sex α 0 α 1 α 2 α 3 adj r 2 r<br />

Male 0.06206 -0.00044 0.02202 0.00773 0.630 0.794<br />

Female 0.06928 0.00071 0.02042 -0.00639 0.598 0.773 ¾<br />

Fig. 3. Comparison between the estimated <strong>and</strong> measured EE.<br />

¾<br />

¾<br />

¾<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

Fig. 4. Relative error of the estimated EE from measured EE.<br />

dIscussIon<br />

This study conducted water walk<strong>in</strong>g (WW) with wide range of Japanese<br />

males <strong>and</strong> females. Energy expenditure were measured <strong>and</strong> threedimensional<br />

accelerations with a triaxial accelerometer to develop an<br />

estimation equation for energy expenditure (EE) dur<strong>in</strong>g WW by us<strong>in</strong>g<br />

acceleration data. For the purpose to adopt wide range of subjects, <strong>and</strong><br />

with the EE <strong>in</strong>fluenced by the walk<strong>in</strong>g speed rather than the body size<br />

<strong>and</strong> sex (Kaneda et al., 2009a), the swimm<strong>in</strong>g pool depth of the WW<br />

(1.1m) was selected as general.<br />

There are many studies estimat<strong>in</strong>g EE dur<strong>in</strong>g l<strong>and</strong> walk<strong>in</strong>g, jogg<strong>in</strong>g<br />

<strong>and</strong> other life style activities (Kumahara et al., 2004; Scott et al., 2006;<br />

Tanaka et al., 2007), <strong>in</strong> which the r 2 values reported by Scott et al. (2006)<br />

were from 0.436 to 0.719. The r 2 values <strong>in</strong> the present study were 0.630<br />

for the males <strong>and</strong> 0.598 for the females. It was considered that we could<br />

develop the estimation equation for the WW as a good manner. In this<br />

study, the estimation equation was composed three items that were rest<strong>in</strong>g<br />

metabolic rate (RMR), <strong>in</strong>ternal energy expenditure for mov<strong>in</strong>g his/<br />

her body (jo<strong>in</strong>t energy expenditure: EE j ) <strong>and</strong> energy expenditure aga<strong>in</strong>st<br />

for water drag force (EE wd ). This estimation equation is orig<strong>in</strong>al because<br />

we have to consider water drag force for water exercise that ord<strong>in</strong>ary<br />

need not to consider <strong>in</strong> l<strong>and</strong> exercise. In the WW, the EE is <strong>in</strong>fluenced<br />

by dom<strong>in</strong>antly the walk<strong>in</strong>g speed rather than the body size <strong>and</strong> sex<br />

(Kaneda et al., 2009a), <strong>and</strong> the gravitational stress at the lower extremity<br />

jo<strong>in</strong>t was reduced <strong>and</strong> greater exert force required for mov<strong>in</strong>g (Miyoshi<br />

et al., 2005). Those studies would <strong>in</strong>dicate that we have to consider the<br />

effect of water drag force rather than the gravity stress for the EE <strong>in</strong> the<br />

WW. Indeed, approximately 65% to 70% of the body weight was offset<br />

<strong>in</strong> the subjects of this study. Even if we consider about gravity effect, we<br />

cannot estimate <strong>and</strong> measure buoyancy correctly because it is cont<strong>in</strong>uously<br />

chang<strong>in</strong>g.<br />

The EE <strong>in</strong> this study was per unit time. In the view po<strong>in</strong>t of mechanics,<br />

the EE per unit time can be said as the mechanical power. The<br />

mechanical power (P) is expressed as follows:<br />

P = Fv (9)<br />

where F is mechanical force <strong>and</strong> v is velocity. The mechanical force is<br />

expressed as follows:<br />

F = ma (10)<br />

∴ P = mav (11)<br />

where m is mass of the object <strong>and</strong> a is acceleration. Therefore, we multiplied<br />

the body weight <strong>and</strong> the measured walk<strong>in</strong>g speed to the acceleration.<br />

And f<strong>in</strong>ally, the values were divided by body weight for elim<strong>in</strong>at<strong>in</strong>g<br />

the effect of the weight bear<strong>in</strong>g. Until now, we could not f<strong>in</strong>d out<br />

any previous study adopt<strong>in</strong>g such a theoretical estimation method even<br />

<strong>in</strong> l<strong>and</strong> activities. Though the correlation coefficients of the developed<br />

equation <strong>in</strong> this study were high (males: r = 0.79, females: r = 0.77),<br />

residual analysis showed large estimation errors, over 30%. We have to<br />

cont<strong>in</strong>ue consider<strong>in</strong>g about much reliable method for estimat<strong>in</strong>g EE<br />

dur<strong>in</strong>g WW. Moreover, future study about estimation of EE <strong>in</strong> various<br />

water exercise form will be useful for health promotion water exercise.<br />

367


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

If an activity monitor that estimates <strong>and</strong> show EE dur<strong>in</strong>g water exercise<br />

like activity monitors on l<strong>and</strong> walk<strong>in</strong>g, jogg<strong>in</strong>g <strong>and</strong> life activities (Kumahara<br />

et al., 2004; Scott et al., 2006; Tanaka et al., 2007) is developed,<br />

water exercise <strong>in</strong>structors <strong>and</strong>/or athletes can underst<strong>and</strong> their EE easily<br />

<strong>and</strong> precisely.<br />

conclusIon<br />

This study tried to develop specific estimation equation for energy expenditure<br />

dur<strong>in</strong>g water walk<strong>in</strong>g. The equation composed three items of<br />

rest<strong>in</strong>g metabolic rate, <strong>in</strong>ternal energy expenditure for mov<strong>in</strong>g his/her<br />

body <strong>and</strong> energy expenditure aga<strong>in</strong>st for water drag force. The correlation<br />

coefficients of the estimation equation developed <strong>in</strong> this study were<br />

high (males: r = 0.79, females: r = 0.77). The future study was needed to<br />

develop much reliable estimation equation for energy expenditure dur<strong>in</strong>g<br />

water exercise, although we could develop the theoretical estimation<br />

equation. Our future goal to develop an underwater activity monitor<br />

by us<strong>in</strong>g accelerometer will useful for health promotion water exercise.<br />

reFerences<br />

Dietary Reference Intakes for Japanese 2010. (2010). M<strong>in</strong>istry of Health,<br />

Labour <strong>and</strong> Welfare, Japan.<br />

Kaneda, K., Ohgi, Y. & Tanaka C. (2009a). Cardio-respiratory Responses<br />

<strong>and</strong> Relationship to Walk<strong>in</strong>g Speed dur<strong>in</strong>g Free Water Walk<strong>in</strong>g <strong>in</strong><br />

Japanese Adults. 2009 Australian Conference of Science <strong>and</strong> <strong>Medic<strong>in</strong>e</strong> <strong>in</strong><br />

Sport. Brisbane, Australia, 10.<br />

Kaneda, Km., Sato, D., Wakabayashi, H. & Nomura T. (2009b). EMG<br />

activity of hip <strong>and</strong> trunk muscles dur<strong>in</strong>g deep-water runn<strong>in</strong>g. J Electromyogr<br />

K<strong>in</strong>esiol, 19, 1064–1070.<br />

Kumahara, H., Schuts, Y., Ayabe, M., Yoshioka, M., Yoshitake, Y.,<br />

Sh<strong>in</strong>do, M., Ishii ,K. & Tanaka H. (2004). The use of uniaxial accelerometry<br />

for the assessment of physical-activity-related energy expenditure:<br />

a validation study aga<strong>in</strong>st whole-body <strong>in</strong>direct calorimetry.<br />

Br J Nutr, 91, 235-243.<br />

Masumoto, K., Shono, T., Hotta, N. & Fujishima K. (2008). Muscle activation,<br />

cardiorespiratory response, <strong>and</strong> rat<strong>in</strong>g of perceived exertion<br />

<strong>in</strong> older subjects while walk<strong>in</strong>g <strong>in</strong> water <strong>and</strong> on dry l<strong>and</strong>. J Electromyogr<br />

K<strong>in</strong>esiol, 18(4), 581-590.<br />

Miyoshi, T., Takashi, S., Yamamoto, S., Nakazawa, K. & Akai M. (2005).<br />

Functional roles of lower-limb jo<strong>in</strong>t moments while walk<strong>in</strong>g <strong>in</strong> water.<br />

Cl<strong>in</strong> Biomech, 20(2), 194-201.<br />

Numajiri, K. & Sh<strong>in</strong>do H. (1970). Energy expenditure of <strong>in</strong>dustrial<br />

workers <strong>in</strong> Japan. J Sci Labour, 46(6), 383-388.<br />

Scott, E.C., James, R.C., David, R.B. (2006). Estimationg energy expenditure<br />

us<strong>in</strong>g accelerometers. Eur J Appl Physiol, 98, 601-612.<br />

Tanaka, C., Tanaka, S., Kawahara, J. & Midorikawa T. (2007). Triaxial<br />

accelerometry for assessment physical activity <strong>in</strong> young children.<br />

Obesity, 15(5): 1233-1241.<br />

Weir, J.B. (1949). New methods for calculat<strong>in</strong>g metabolic rate with special<br />

reference to prote<strong>in</strong> metabolism. J Physiol, 109(1-2), 1-9.<br />

AcKnoWledGeMents<br />

The authors acknowledge to the Medical Fitness Club, Fureai Machida<br />

Hospital for their agreement <strong>and</strong> cooperation with successful experiment<br />

of this study.<br />

368<br />

Real <strong>and</strong> Perceived Swimm<strong>in</strong>g Competency, Risk<br />

Estimation, <strong>and</strong> Prevent<strong>in</strong>g Drown<strong>in</strong>g among New<br />

Zeal<strong>and</strong> Youth<br />

Moran, K. 1<br />

1 The University of Auckl<strong>and</strong>, New Zeal<strong>and</strong><br />

Little is known about youth swimm<strong>in</strong>g competency or of their perceptions<br />

of their risk of drown<strong>in</strong>g. This study reports the New Zeal<strong>and</strong><br />

f<strong>in</strong>d<strong>in</strong>gs of an <strong>in</strong>ternational project entitled the Can You Swim Project?<br />

The subjects (n = 68) were assessed <strong>in</strong> a two-part study us<strong>in</strong>g an <strong>in</strong>itial<br />

questionnaire survey to provide self-estimates of swimm<strong>in</strong>g competency<br />

<strong>and</strong> risk perception, followed by a practical test of seven swimm<strong>in</strong>g competencies.<br />

Self-estimates of swimm<strong>in</strong>g compared well with actual measurements.<br />

Similar proportions were obta<strong>in</strong>ed for those who thought<br />

they could swim more than 300m (estimated 41%; actual 43%). No significant<br />

gender differences <strong>in</strong> real or perceived swimm<strong>in</strong>g competency<br />

were found. Significantly more males estimated lower risk of drown<strong>in</strong>g<br />

associated with a series of aquatic scenarios. The implications of these<br />

f<strong>in</strong>d<strong>in</strong>gs on drown<strong>in</strong>g prevention <strong>and</strong> the need for further <strong>in</strong>vestigation<br />

are discussed.<br />

Key words: swimm<strong>in</strong>g competency, risk perception, drown<strong>in</strong>g prevention,<br />

water safety<br />

IntroductIon<br />

In New Zeal<strong>and</strong>, an isl<strong>and</strong> nation with more than 15 000 kilometres of<br />

coastl<strong>in</strong>e, opportunities to engage <strong>in</strong> aquatic recreation abound. Whilst<br />

participation <strong>in</strong> recreational aquatic activity is generally perceived as a<br />

positive <strong>in</strong>dicator of a healthy lifestyle, it does have attendant risks. In<br />

the five years from 2003 -2007, a total of 41 New Zeal<strong>and</strong>ers aged 15-<br />

19 years were fatally drowned. Of these, 66% of victims were male, most<br />

<strong>in</strong>cidents occurred <strong>in</strong> rivers (n = 23; 56%) or at beaches/tidal waters (n =<br />

9; 22%), <strong>and</strong> most of the fatal <strong>in</strong>cidents (n = 30; 73%) were recreationrelated<br />

(Drownbase, Water Safety New Zeal<strong>and</strong>, 2009). Surf lifesav<strong>in</strong>g<br />

rescue statistics further illustrate the potential for even greater loss<br />

of young lives. Dur<strong>in</strong>g that same 5-year period, 1132 <strong>in</strong>cidents necessitat<strong>in</strong>g<br />

rescue from the surf were recorded among 16-20-year-olds (SL-<br />

SNZ Rescue Statistics, 2009). Males comprised the greater proportion<br />

of these rescues (n = 701; 62%).<br />

Swimm<strong>in</strong>g has been identified as the activity most frequently engaged<br />

<strong>in</strong> prior to drown<strong>in</strong>g <strong>in</strong> New Zeal<strong>and</strong> (Child <strong>and</strong> Youth Mortality<br />

Review Committee, 2005). Not surpris<strong>in</strong>gly then, the ability to<br />

swim has long been promoted by water safety organisations as critical<br />

to drown<strong>in</strong>g prevention. However, there is a lack of consensus among<br />

water safety experts as to what constitutes swimm<strong>in</strong>g competency <strong>in</strong> the<br />

context of drown<strong>in</strong>g prevention (Brenner, Moran et al., 2006), or what<br />

swimm<strong>in</strong>g-related competencies are important <strong>in</strong> drown<strong>in</strong>g prevention<br />

(Stallman, Junge et al., 2008). While the ability to swim may appear axiomatic<br />

<strong>in</strong> prevent<strong>in</strong>g drown<strong>in</strong>g, some have claimed that the protective<br />

effect of be<strong>in</strong>g able to swim might be offset by the <strong>in</strong>creased exposure<br />

to aquatic risk <strong>in</strong>herent <strong>in</strong> utilis<strong>in</strong>g that skill (Baker, O’Neil et al., 1992).<br />

Further complicat<strong>in</strong>g the association between swimm<strong>in</strong>g competency<br />

<strong>and</strong> risk of drown<strong>in</strong>g are the possible underestimation of risk of<br />

drown<strong>in</strong>g <strong>and</strong> overestimation of ability to cope with that risk. Several<br />

New Zeal<strong>and</strong> studies have identified a male propensity to take risks dur<strong>in</strong>g<br />

aquatic activities (McCool et al., 2009, 2008; Moran, 2008) <strong>and</strong> have<br />

postulated that this propensity for risk tak<strong>in</strong>g rather than differences <strong>in</strong><br />

risk exposure or swimm<strong>in</strong>g competency may help expla<strong>in</strong> why males<br />

are overrepresented <strong>in</strong> the New Zeal<strong>and</strong> drown<strong>in</strong>g statistics. However,<br />

no studies have explored the relationship between perceived <strong>and</strong> real<br />

swimm<strong>in</strong>g ability, <strong>and</strong> perceptions of drown<strong>in</strong>g risk. The purpose of this<br />

paper is therefore threefold: 1)To assess the swimm<strong>in</strong>g competency of


a group of young New Zeal<strong>and</strong> adults, 2) Compare these assessed skills<br />

with preconceived estimates of these abilities, <strong>and</strong> 3) To ascerta<strong>in</strong> selfestimated<br />

perceptions of the risk of drown<strong>in</strong>g.<br />

Method<br />

University students newly enrolled <strong>in</strong> a four-year professional degree<br />

<strong>in</strong> physical education were <strong>in</strong>vited to voluntarily participate <strong>in</strong> a study<br />

entitled the Can you swim project The study consisted of two phases of<br />

data gather<strong>in</strong>g, an <strong>in</strong>itial self-complete questionnaire survey followed by<br />

practical swimm<strong>in</strong>g assessment prior to the commencement of study <strong>in</strong><br />

2008. The study received ethics clearance from the University of Auckl<strong>and</strong><br />

Human Participants Ethics Committee (case no.2007/447).<br />

The self-complete questionnaire conta<strong>in</strong>ed 20 questions, <strong>and</strong> was<br />

designed to take 10-15 m<strong>in</strong>utes to complete. The written survey sought<br />

<strong>in</strong>formation on swimm<strong>in</strong>g-related competencies, <strong>and</strong> perceptions of<br />

drown<strong>in</strong>g risk. Student estimates of their swimm<strong>in</strong>g competency were<br />

<strong>in</strong>cluded <strong>in</strong> two questions, the first of which provided 5 categories which<br />

best described their capacity from non-swimmer to excellent swimmer,<br />

the second of which asked students to estimate the distance they<br />

thought they could swim non-stop, us<strong>in</strong>g distance categories from 300 metres.<br />

Practical aquatic competency was tested <strong>in</strong> a 25 metre outdoor<br />

heated pool with a 2 metre deep end, us<strong>in</strong>g seven tests of aquatic skills<br />

<strong>in</strong>clud<strong>in</strong>g:<br />

◊ Distance swum non-stop <strong>in</strong> a 25-metre outdoor heated swimm<strong>in</strong>g<br />

pool<br />

◊ Stationary float<strong>in</strong>g <strong>in</strong> deep-water with m<strong>in</strong>imal swimm<strong>in</strong>g motion<br />

◊ Swim 100m non-stop on back<br />

◊ Dive headfirst entry <strong>in</strong>to deep water<br />

◊ Surface dive to deep end of the pool<br />

◊ Swim underwater a maximum of 25 metres<br />

◊ Contact rescue tow 25 metres<br />

Perceptions of risk of drown<strong>in</strong>g was assessed via five water-related scenarios<br />

depict<strong>in</strong>g differ<strong>in</strong>g levels of danger us<strong>in</strong>g four response categories<br />

rang<strong>in</strong>g from no risk to extreme risk (for example, How would you rate<br />

the risk to your life <strong>in</strong> the follow<strong>in</strong>g situation: tipped upside down <strong>in</strong> a canoe<br />

100m from the shore of a lake,).<br />

Data from the completed questionnaires were statistically analysed us<strong>in</strong>g<br />

SPSS Version 16.0 <strong>in</strong> W<strong>in</strong>dows. Descriptive statistics were used to<br />

report differences <strong>in</strong> student estimates of swimm<strong>in</strong>g competency, <strong>and</strong><br />

risk perceptions. Mann-Whitney U tests were used to determ<strong>in</strong>e significant<br />

differences between dependent (such as swimm<strong>in</strong>g competency)<br />

<strong>and</strong> <strong>in</strong>dependent variables (such as gender).<br />

results<br />

The study <strong>in</strong>cluded 68 first year students from an <strong>in</strong>take of 72 enrolments<br />

(four were excluded because they were older than 29 years) prior<br />

to their commencement of a 4-year undergraduate degree. Of these students,<br />

53% were male (n = 36), <strong>and</strong> two thirds were aged 17-19 years<br />

(69%; n = 47), 22% were aged 20-24 years (n = 15), <strong>and</strong> 9% were aged<br />

20-29 years (n = 6).<br />

i) Self-estimates of aquatic competency:Students were asked how they<br />

would categorise their aquatic competency <strong>and</strong> to estimate their swimm<strong>in</strong>g<br />

competency <strong>in</strong> five distance categories (See Table 1). One half<br />

considered they were good/very good (n = 28; 41%) or excellent swimmers<br />

(n = 6; 9%), one third considered themselves to be average swimmers (n<br />

= 25; 37%). One third of the students estimated that they could swim<br />

less than 100 m (n = 21; 32%).<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

Table 1. Student Self-estimated Aquatic Competency by Gender<br />

Total Male Female Mann-<br />

Swimm<strong>in</strong>g competency<br />

n % n % n %<br />

Whitney<br />

U<br />

p<br />

how would you describe your swimm<strong>in</strong>g competency?<br />

Non swimmer 2 2.9 0 0.0 2 6.3<br />

Weak/very weak swimmer 7 7.4 2 5.6 5 15.7<br />

Average swimmer 25 36.8 16 44.4 9 28.1 574.000 .980<br />

Good/very good swimmer 28 41.2 15 41.7 13 40.7<br />

Excellent swimmer<br />

how far do you th<strong>in</strong>k you could swim?<br />

6 8.8 3 8.3 3 9.4<br />

300m<br />

could you do this <strong>in</strong> open deep water?<br />

28 41.2 13 36.1 15 46.9<br />

Complete with difficulty<br />

Complete easily<br />

Can you swim 100 m on your back?<br />

16<br />

52<br />

23.5<br />

76.5<br />

8<br />

28<br />

22.2<br />

77.8<br />

8<br />

24<br />

25.0<br />

75.0<br />

554.000 .758<br />

Yes, can swim 100m on back<br />

No, can’t swim 100m on back<br />

58<br />

10<br />

85.3<br />

14.7<br />

33<br />

3<br />

91.7<br />

8.3<br />

25<br />

7<br />

78.1<br />

21.9<br />

498.000 .118<br />

If Yes, could you do this <strong>in</strong> open deep water?<br />

Complete with difficulty<br />

Complete easily<br />

can you swim 25 m underwater?<br />

11<br />

48<br />

16.1<br />

86.7<br />

3<br />

30<br />

8.3<br />

90.9<br />

8<br />

18<br />

30.8<br />

69.2<br />

339.000 .133<br />

Yes, can swim underwater<br />

No, can’t swim underwater<br />

If Yes, how do you feel about this task?<br />

45<br />

23<br />

66.2<br />

33.8<br />

25<br />

11<br />

69.4<br />

30.6<br />

20<br />

12<br />

62.5<br />

37.5<br />

536.000 .549<br />

Complete with difficulty<br />

Complete easily<br />

27<br />

19<br />

39.7<br />

27.9<br />

5<br />

21<br />

19.2<br />

80.8<br />

14<br />

6<br />

60.0<br />

40.0<br />

120.000 ≤.001*<br />

Total 68 100.0 36 100.0 32 100.0<br />

*Significant at the 1% level (2-tailed)<br />

More than one quarter of students estimated that they could swim between<br />

100-300 m (n = 19; 28%) <strong>and</strong> 41% thought that they could swim<br />

> 300 m (n = 28). Most students (n = 52; 76%) reported that they could<br />

achieve their estimate easily <strong>in</strong> open, deep water. No significant differences<br />

were evident when estimates of aquatic competency were analysed<br />

by gender, the exception be<strong>in</strong>g able to swim 25m underwater, where significantly<br />

more males than females thought they could easily complete<br />

the task (U = 120.000, p = ≤ .001).<br />

ii) Practical swimm<strong>in</strong>g assessment: Students completed seven swimm<strong>in</strong>grelated<br />

tasks comparable to the items they had been asked to provide<br />

estimates of their perceived competencies <strong>in</strong> the written questionnaire<br />

that was completed before the pool tests.<br />

369


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 2. Student Aquatic Competencies by Gender<br />

370<br />

Total<br />

n %<br />

Male<br />

n %<br />

Female<br />

n %<br />

Mann-<br />

Whitney<br />

U<br />

Swimm<strong>in</strong>g competency<br />

< 50 m 9 13.3 3 8.3 6 18.8<br />

50-100 m 14 20.6 8 22.2 6 18.8<br />

101-200 m 9 13.2 8 22.2 1 3.1 522.000 .616<br />

201-300 m 6 8.8 4 11.1 2 6.3<br />

>300m<br />

Float<strong>in</strong>g competency<br />

29 42.6 12 33.3 19 53.1<br />

< 2 m<strong>in</strong>utes 5 7.3 2 5.6 3 9.4<br />

< 6 m<strong>in</strong>utes<br />

< 15 m<strong>in</strong>utes<br />

8<br />

6<br />

11.7<br />

8.9<br />

7<br />

3<br />

19.5<br />

8.3<br />

1<br />

3<br />

3.1<br />

9.4<br />

492.000 .283<br />

> 15 m<strong>in</strong>utes<br />

100 m swim on back<br />

48 70.6 23 63.9 25 78.1<br />

Did not complete 14 20.6 8 22.2 6 18.8<br />

Completed with difficulty 23 33.9 11 30.5 12 37.5 526.500 .664<br />

Completed easily<br />

Dive <strong>in</strong>to pool (2 m depth)<br />

30 44.2 16 44.5 14 43.8<br />

Did not complete 7 10.3 2 5.6 5 15.6<br />

Completed with difficulty 12 17.6 8 22.3 4 12.5 487.000 .428<br />

Completed easily<br />

Swim 25 m underwater<br />

47 69.1 24 66.7 23 71.9<br />

Did not complete 24 35.3 10 27.8 14 43.8<br />

Completed with difficulty 16 23.5 12 33.4 4 12.5 527.000 .821<br />

Completed easily<br />

Surface dive 2 m<br />

26 38.3 12 33.3 14 43.8<br />

Did not complete 9 13.2 3 8.3 6 18.8<br />

Completed with difficulty 18 26.5 12 33.3 6 18.8 448.000 .202<br />

Completed easily<br />

Rescue contact tow 25 m<br />

39 57.4 19 52.7 20 62.5<br />

Did not complete 19 27.9 11 30.6 8 25.0<br />

Completed with difficulty 19 27.9 12 33.3 7 21.9 371.000 .077<br />

Completed easily 25 36.8 14 38.9 15 46.9<br />

Table 2 shows that almost half of the students (n = 29; 43%) could swim<br />

more than 300m non-stop <strong>in</strong> the 15 m<strong>in</strong>utes time slot allowed. Most<br />

students could perform the stationary float<strong>in</strong>g task for more than 15<br />

m<strong>in</strong>utes (n = 48; 70%), the headfirst dive entry <strong>in</strong>to deep water (n =47;<br />

69%) <strong>and</strong> the surface dive to two metres depth (n = 39; 57%).<br />

Less than half easily completed the 100m back swim on back (n =<br />

30; 44%), the underwater swim of 25m (n = 26; 38%), or the contact<br />

rescue tow of 25m (n = 25; 37%). As was the case with all but one of<br />

the self-estimated swimm<strong>in</strong>g competencies, no significant differences<br />

were found <strong>in</strong> actual swimm<strong>in</strong>g-related competencies among male <strong>and</strong><br />

female students.<br />

iii) Perceptions of drown<strong>in</strong>g risk: Significant differences were evident<br />

when the estimates of risk of drown<strong>in</strong>g associated with five hypothetical<br />

water-related scenarios were analysed by gender (see Table 3). Males<br />

were more likely than females to perceive lower risk of drown<strong>in</strong>g. For example,<br />

whereas most females rated fall<strong>in</strong>g <strong>in</strong>to a deep river fully clothed<br />

as an extreme/high risk situation (females 69%, males 6%), most males<br />

considered this to be a low/no risk situation (males 94%, females 31%).<br />

p<br />

Table 3. Perceptions of Risk of Drown<strong>in</strong>g by Gender<br />

Risk scenario<br />

Extreme/High<br />

Risk<br />

Male Female<br />

n(%) n(%)<br />

Slight/No Risk Mann-<br />

Whitney<br />

Male Female U<br />

n(%) n(%)<br />

Capsized canoe 100 metres<br />

offshore<br />

Caught <strong>in</strong> rip current at<br />

surf beach<br />

Chased toy <strong>in</strong>to deep end of<br />

swimm<strong>in</strong>g pool<br />

Fell <strong>in</strong>to deep river when<br />

fully clothed<br />

Swept off isolated rocks<br />

whilst fish<strong>in</strong>g<br />

4<br />

(11.1%)<br />

16<br />

(44.4%)<br />

0<br />

2<br />

(5.6%)<br />

29<br />

(80.6%)<br />

14<br />

(43.8%)<br />

23<br />

(71.9%)<br />

3<br />

(9.4%)<br />

22<br />

(68.8%)<br />

28<br />

(87.5%)<br />

* Significant at the 1% level (2-tailed)<br />

33<br />

(88.9%)<br />

20<br />

(55.6%)<br />

36<br />

(100%)<br />

34<br />

(94.4%)<br />

7<br />

(19.4%)<br />

18<br />

340.000 .001*<br />

(56.3%)<br />

9<br />

406.000 .027*<br />

(23.3%)<br />

29<br />

418.000 .009*<br />

(90.6%)<br />

10<br />

238.000 6 m<strong>in</strong>utes. Similar concerns<br />

have been raised among high school students with


competency might accurately reflect their ability to cope with risk of<br />

drown<strong>in</strong>g. Not withst<strong>and</strong><strong>in</strong>g these limitations, the lesser estimations of<br />

risk among males <strong>in</strong> the study does suggest that education aimed at<br />

enhanc<strong>in</strong>g male youth assessment of drown<strong>in</strong>g risk might help address<br />

the over-representation of males <strong>in</strong> youth drown<strong>in</strong>g <strong>and</strong> rescue statistics.<br />

conclusIon<br />

This paper reports on the first part of an <strong>in</strong>ternational study that attempts<br />

to identify the relationship between real <strong>and</strong> perceived swimm<strong>in</strong>g<br />

competency, <strong>and</strong> perceptions of risk of drown<strong>in</strong>g. The results suggest<br />

that participants <strong>in</strong> this study were realistic <strong>in</strong> self-estimates of their<br />

swimm<strong>in</strong>g competency <strong>and</strong> no significant differences were evident <strong>in</strong><br />

perceived or actual competency by gender or ethnicity. Males were more<br />

likely to underestimate the risk associated with aquatic activity re<strong>in</strong>forc<strong>in</strong>g<br />

previous research f<strong>in</strong>d<strong>in</strong>gs. Further <strong>in</strong>vestigation us<strong>in</strong>g similar methodology<br />

is required to determ<strong>in</strong>e whether these f<strong>in</strong>d<strong>in</strong>gs are replicated<br />

<strong>in</strong> other populations (without a background <strong>in</strong> physical education) to<br />

ascerta<strong>in</strong> whether others can accurately assess their swimm<strong>in</strong>g competency<br />

or whether they are likely to overestimate their ability to cope<br />

with the dangers <strong>in</strong>herent <strong>in</strong> any water-based activity thereby plac<strong>in</strong>g<br />

themselves at greater risk of drown<strong>in</strong>g.<br />

reFerences<br />

Baker, S.P., O’Neil, B., G<strong>in</strong>sburg, M.J. & Li, G. (1992). The <strong>in</strong>jury fact<br />

book. New York: Oxford University Press.<br />

Brenner, R.A., Moran, K., Stallman, R., Gilchrist, J. & McVan, J.T.<br />

(2005). Swimm<strong>in</strong>g ability, water safety education <strong>and</strong> drown<strong>in</strong>g prevention.<br />

In: J.J.L.M. Bierens (Ed.). H<strong>and</strong>book of drown<strong>in</strong>g (pp.112-<br />

116). Heidelberg: Spr<strong>in</strong>ger.<br />

Child <strong>and</strong> Youth Mortality Review Committee. (2005). Circumstances<br />

surround<strong>in</strong>g drown<strong>in</strong>g <strong>in</strong> those under 25 <strong>in</strong> New Zeal<strong>and</strong> (1980-2002).<br />

Well<strong>in</strong>gton: WSNZ.<br />

McCool, J.P., Ameratunga, S., Moran, K. & Rob<strong>in</strong>son, E. (2009). Tak<strong>in</strong>g<br />

a risk perceptions approach to improv<strong>in</strong>g beach swimm<strong>in</strong>g safety.<br />

International Journal of Behavioural <strong>Medic<strong>in</strong>e</strong> 16(4), 360-66.<br />

McCool, J.P., Moran, K., Ameratunga, S. & Rob<strong>in</strong>son, E. (2008). New<br />

Zeal<strong>and</strong> beachgoers’ swimm<strong>in</strong>g behaviours, swimm<strong>in</strong>g abilities <strong>and</strong><br />

perception of drown<strong>in</strong>g risk. International Journal of Aquatic Research<br />

& Education, 2(1), 7-15.<br />

Moran, K. (2008). Will they s<strong>in</strong>k or swim? New Zeal<strong>and</strong> youth water<br />

safety knowledge <strong>and</strong> skills. International Journal of Aquatic Research<br />

& Education, 2(2), 114-127.<br />

Quan L. & Cumm<strong>in</strong>gs, P. (2003). Characteristics of drown<strong>in</strong>g by different<br />

age groups. Injury Prevention, 9(2), 163-6.<br />

Stallman, R.S., Junge, M. & Blixt, T. (2008). The teach<strong>in</strong>g of swimm<strong>in</strong>g<br />

based on a model derived from the causes of drown<strong>in</strong>g. International<br />

Journal of Aquatic Research & Education, 2(4), 372-382.<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

Keep<strong>in</strong>g the Safety Messages Simple: The<br />

International Task Force on Open-Water Recreational<br />

Drown<strong>in</strong>g Prevention<br />

Quan, l. 1 , Bennett, e. 2 , Moran, K. 3 (co-chairs)<br />

1 Seattle Children’s Hospital/University of Wash<strong>in</strong>gton, USA<br />

2 Seattle Children’s Hospital, USA<br />

3 The University of Auckl<strong>and</strong>, New Zeal<strong>and</strong><br />

International task Force Members:<br />

Beerman S (Canada), Bennett E (USA), Bierens J (Netherl<strong>and</strong>s), Brewster<br />

BC (USA), Connelly J (Irel<strong>and</strong>), Farmer N (Australia), Frankl<strong>in</strong> R<br />

(Australia), George P (Australia), Kania J (Kenya), Matthews B (Australia),<br />

Moran K (New Zeal<strong>and</strong>), Quan L (USA), Rahman A (Bangladesh),<br />

Stallman R (Norway), Stanley T (New Zeal<strong>and</strong>), Szpilman D<br />

(Brazil), Tan RMK (S<strong>in</strong>gapore), Tipton M (UK).<br />

Secretariat: Tansik M (USA).<br />

Globally, many organizations addressed the risk of drown<strong>in</strong>g associated<br />

with aquatic recreation by promot<strong>in</strong>g a plethora of drown<strong>in</strong>g prevention<br />

messages. Prelim<strong>in</strong>ary discussion among drown<strong>in</strong>g prevention advocates<br />

suggested that messages could be conta<strong>in</strong>ed with<strong>in</strong> simplified generic<br />

messages applicable to all sett<strong>in</strong>gs. Us<strong>in</strong>g a modified Delphi technique<br />

to harness expert op<strong>in</strong>ion, the Task Force f<strong>in</strong>ally agreed on 16 key messages<br />

that would foster open water drown<strong>in</strong>g prevention. Messages were<br />

categorized <strong>in</strong>to Care of self <strong>and</strong> on the Care of others. Learn<strong>in</strong>g swimm<strong>in</strong>g<br />

<strong>and</strong> water safety survival skills was the dom<strong>in</strong>ant message <strong>in</strong> both<br />

categories. It is hoped that by provid<strong>in</strong>g simple <strong>and</strong> consistent prioritised<br />

safety messages that are applicable to a range of communities <strong>and</strong><br />

sett<strong>in</strong>gs, the ultimate goal of sav<strong>in</strong>g lives will be achieved.<br />

Key words: water safety, drown<strong>in</strong>g prevention, recreational drown<strong>in</strong>g,<br />

open water<br />

IntroductIon<br />

Drown<strong>in</strong>g as a consequence of aquatic recreation is a significant cause<br />

of un<strong>in</strong>tentional death worldwide. In many developed countries, aquatic<br />

recreation is an <strong>in</strong>tegral part of the lifestyle, especially where there is<br />

easy access to a wide range of water environments such as beaches, rivers,<br />

lakes, <strong>and</strong> other waterways. While participation <strong>in</strong> aquatic recreation<br />

is generally viewed as <strong>in</strong>dicative of a healthy lifestyle, there are attendant<br />

risks of drown<strong>in</strong>g <strong>and</strong> other water-related <strong>in</strong>juries (Moran, 2008).<br />

In many countries, the highest proportion of drown<strong>in</strong>g deaths occurs<br />

<strong>in</strong> open waters. For example, <strong>in</strong> Australia, a country renowned for its<br />

aquatic leisure pursuits, one third (33%) of the 370 fatalities from 1999-<br />

2004 occurred <strong>in</strong> natural bodies of water, more than half (55%) had been<br />

engaged <strong>in</strong> leisure activity, <strong>and</strong> swimm<strong>in</strong>g had been the activity prior to<br />

drown<strong>in</strong>g <strong>in</strong> one third (33%) of cases (Australian Institute of Health<br />

<strong>and</strong> Welfare, 2008).<br />

Globally, many organizations have attempted to address the risk of<br />

drown<strong>in</strong>g associated with aquatic recreation <strong>in</strong> open water by promot<strong>in</strong>g<br />

a diverse plethora of drown<strong>in</strong>g prevention messages. This diversity<br />

reflects the multifaceted nature of the drown<strong>in</strong>g problem <strong>and</strong> has <strong>in</strong>variably<br />

resulted <strong>in</strong> specific water safety advice relative to particular environments<br />

(such as surf beaches or rivers) or specific activities (such as<br />

swimm<strong>in</strong>g or surf<strong>in</strong>g). Some organizations (such as the International<br />

Lifesav<strong>in</strong>g Federation [ILS] at an <strong>in</strong>ternational level, or the Royal Life<br />

Sav<strong>in</strong>g Society [RLSS] at a national level) have dissem<strong>in</strong>ated <strong>in</strong>formation<br />

<strong>and</strong> advice on a wide range of water safety issues. Other organisations<br />

have developed expertise <strong>in</strong>, <strong>and</strong> engaged <strong>in</strong> the promotion<br />

of, specific aspects of water safety (such as Surf Life Sav<strong>in</strong>g Australia<br />

[SLSA] for surf safety or New Zeal<strong>and</strong> Coastguard [NZC] for boat<br />

371


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

safety), while others have focused on particular at-risk groups (such as<br />

Safe Kids, for children).<br />

While site-, activity-, <strong>and</strong> group-specific water safety messages are<br />

valued components of any targeted promotion, their multiplicity has<br />

the potential to obfuscate critical messages or confuse <strong>in</strong>tended recipients.<br />

Prelim<strong>in</strong>ary discussion among drown<strong>in</strong>g prevention advocates at a<br />

workshop <strong>in</strong> the World Water Safety Conference <strong>in</strong> Oporto, Portugal,<br />

<strong>in</strong> 2007 suggested that essential advice to the public <strong>in</strong> general <strong>and</strong> those<br />

<strong>in</strong> care of others around water might be better promoted primarily with<strong>in</strong><br />

simplified generic messages applicable to all open water recreational<br />

sett<strong>in</strong>gs, all swimm<strong>in</strong>g-related activities, <strong>and</strong> all population groups. As a<br />

consequence of this <strong>in</strong>itial discussion, a group of like-m<strong>in</strong>ded drown<strong>in</strong>g<br />

prevention experts established the International Task Force on Open<br />

Water Recreational Drown<strong>in</strong>g Prevention <strong>in</strong> 2008. It was the purpose<br />

of this Task Force to establish simplified guidel<strong>in</strong>es for the promotion<br />

of key public water safety messages related to open water recreational<br />

drown<strong>in</strong>g prevention.<br />

Method<br />

The process of develop<strong>in</strong>g the generic open water drown<strong>in</strong>g prevention<br />

messages was evolutionary, the <strong>in</strong>itial session was held with approximately<br />

35 people from the Wash<strong>in</strong>gton State Drown<strong>in</strong>g Prevention<br />

Network. It focused on the need to develop water safety messag<strong>in</strong>g for<br />

recreational open water sett<strong>in</strong>gs for parents <strong>and</strong> families. In addition,<br />

the discussion also focused on <strong>in</strong>-water, swimm<strong>in</strong>g-related activity (such<br />

as swimm<strong>in</strong>g <strong>and</strong> play<strong>in</strong>g <strong>in</strong> water) rather than aquatic sports (such as<br />

fish<strong>in</strong>g or div<strong>in</strong>g) or craft-related activity (such as boat<strong>in</strong>g or surf<strong>in</strong>g).<br />

The bra<strong>in</strong>storm<strong>in</strong>g technique was replicated <strong>in</strong> a workshop dur<strong>in</strong>g the<br />

World Water Safety Conference 2007 <strong>in</strong> Oporto, Portugal. In response<br />

to <strong>in</strong>terest from the <strong>in</strong>ternational water safety community who shared a<br />

collective concern about the ambiguity <strong>and</strong> <strong>in</strong>consistency of water safety<br />

messag<strong>in</strong>g, drown<strong>in</strong>g prevention advocates were <strong>in</strong>vited to take part<br />

<strong>in</strong> a task force that would prioritize <strong>and</strong> provide coherent <strong>and</strong> consistent<br />

safety messages to reduce the risk of drown<strong>in</strong>g dur<strong>in</strong>g open water<br />

aquatic recreation.<br />

From the prelim<strong>in</strong>ary workshops <strong>and</strong> <strong>in</strong>itial rounds of teleconferenc<strong>in</strong>g<br />

among Task Force members, a list of water safety messages was<br />

compiled <strong>in</strong> a central database. Messages specific to water sites (such as<br />

river currents) were separated out of the ma<strong>in</strong> list. The messages were<br />

then divided <strong>in</strong>to two categories: Care of Self <strong>and</strong> Care of Others. As a<br />

consequence of this process, 65 messages were <strong>in</strong>cluded <strong>in</strong> the Care of<br />

Self database <strong>and</strong> 66 <strong>in</strong> the Care of Others database. Us<strong>in</strong>g the Delphi<br />

technique to distill the op<strong>in</strong>ions of experts (Brown, 1968), Task Force<br />

members were asked to rate the two lists of items by assign<strong>in</strong>g a total of<br />

100 po<strong>in</strong>ts for messages related to Care of Self <strong>and</strong> another 100 po<strong>in</strong>ts<br />

for Care of Others. After the first round, po<strong>in</strong>ts were totaled <strong>and</strong> only the<br />

top 50% of messages were reta<strong>in</strong>ed. The messages were then reviewed<br />

<strong>and</strong> similar messages were comb<strong>in</strong>ed. Members were asked for feedback<br />

on word<strong>in</strong>g, rationale <strong>and</strong> any other comments related to the rema<strong>in</strong><strong>in</strong>g<br />

messages prior to the second round of vot<strong>in</strong>g. Dur<strong>in</strong>g the second round,<br />

messages were ordered by number of po<strong>in</strong>ts <strong>in</strong> the first round <strong>and</strong> all<br />

members were able to see the number of po<strong>in</strong>ts allocated dur<strong>in</strong>g the<br />

first round. After the second round of scor<strong>in</strong>g, the top 50% of messages<br />

were chosen.<br />

Two subsequent rounds of vot<strong>in</strong>g occurred to approve the word<strong>in</strong>g,<br />

comb<strong>in</strong><strong>in</strong>g messages, delet<strong>in</strong>g messages due to lack of support<strong>in</strong>g <strong>in</strong>formation<br />

<strong>and</strong> the f<strong>in</strong>al list of messages. All f<strong>in</strong>al messages received at least<br />

80% approval by Task Force members <strong>and</strong> two f<strong>in</strong>al rounds of draft documents<br />

were sent for review <strong>and</strong> feedback. F<strong>in</strong>ally, a brief reader friendly<br />

rationale <strong>and</strong> a set of critical actions were developed for messages based<br />

on content developed dur<strong>in</strong>g the message generation process. Full details<br />

of the rationale <strong>and</strong> key actions support<strong>in</strong>g these key messages are<br />

conta<strong>in</strong>ed <strong>in</strong> a user friendly version of the f<strong>in</strong>d<strong>in</strong>gs available at: www.<br />

drown<strong>in</strong>g-prevention.org<br />

372<br />

results<br />

As a consequence of the multiple rounds of distillation of drown<strong>in</strong>g<br />

prevention messages previously described, a total of eight messages for<br />

each category- Care for self <strong>and</strong> Care for others-were ultimately approved<br />

(see Tables 1 <strong>and</strong> 2).<br />

Table 1: Key messages of open-water Drown<strong>in</strong>g Prevention: Care of self<br />

1. Learn swimm<strong>in</strong>g <strong>and</strong> water safety survival skills<br />

2. Always swim with others<br />

3. Obey all safety signs <strong>and</strong> warn<strong>in</strong>g flags<br />

4. Never go <strong>in</strong> the water after dr<strong>in</strong>k<strong>in</strong>g alcohol<br />

5. Know how <strong>and</strong> when to use a life jacket<br />

6. Swim <strong>in</strong> areas with lifeguards<br />

7.<br />

Know the weather <strong>and</strong> water conditions before gett<strong>in</strong>g <strong>in</strong> the<br />

water<br />

8. Always enter shallow <strong>and</strong> unknown water feet first<br />

Table 1 shows, <strong>in</strong> descend<strong>in</strong>g order of priority, the eight statements that<br />

were identified as the most important messages related to Care of self<br />

dur<strong>in</strong>g swimm<strong>in</strong>g-related activities <strong>in</strong> open water environments. Learn<strong>in</strong>g<br />

swimm<strong>in</strong>g <strong>and</strong> water safety survival skills was seen as paramount<br />

<strong>in</strong> keep<strong>in</strong>g one’s self safe <strong>in</strong> open water swimm<strong>in</strong>g-related recreation.<br />

Beh<strong>in</strong>d this dom<strong>in</strong>ant message, a cluster of three messages were well<br />

supported by Task Force members, they <strong>in</strong>cluded: always swimm<strong>in</strong>g<br />

with others, obey<strong>in</strong>g all safety signs <strong>and</strong> warn<strong>in</strong>g flags, <strong>and</strong> never go<strong>in</strong>g<br />

<strong>in</strong> the water after dr<strong>in</strong>k<strong>in</strong>g alcohol. Other messages to receive moderate<br />

support <strong>in</strong> the f<strong>in</strong>al round of distillation <strong>in</strong>cluded: know<strong>in</strong>g how <strong>and</strong><br />

when to use a life jacket, swimm<strong>in</strong>g <strong>in</strong> areas with lifeguards, know<strong>in</strong>g<br />

the weather <strong>and</strong> water conditions before go<strong>in</strong>g <strong>in</strong> the water, <strong>and</strong> always<br />

enter<strong>in</strong>g shallow <strong>and</strong> water of unknown depth, feet first.<br />

Table 2 shows that, as was the case with Care of self messages, the<br />

learn<strong>in</strong>g of swimm<strong>in</strong>g <strong>and</strong> water safety survival skills was aga<strong>in</strong> the<br />

dom<strong>in</strong>ant message to prevent drown<strong>in</strong>g when car<strong>in</strong>g for others. Other<br />

messages to receive strong support <strong>in</strong> the Care of Others category all related<br />

to safe supervision <strong>and</strong> <strong>in</strong>cluded the need to swim under lifeguard<br />

supervision, to set <strong>and</strong> follow rules when car<strong>in</strong>g for others <strong>in</strong> <strong>and</strong> around<br />

water, <strong>and</strong> when supervis<strong>in</strong>g young children, to always provide close <strong>and</strong><br />

constant attention without distraction. Knowledge of the use <strong>and</strong> application<br />

of life jackets <strong>and</strong> the acquisition of first aid <strong>and</strong> CPR skills were<br />

also strongly advocated. Other messages to receive moderate support <strong>in</strong><br />

the f<strong>in</strong>al round of prioritisation <strong>in</strong>cluded the need to learn safe ways to<br />

rescue others without putt<strong>in</strong>g yourself <strong>in</strong> danger <strong>and</strong> obey<strong>in</strong>g all safety<br />

signs <strong>and</strong> warn<strong>in</strong>g flags.


Table 2: Key messages of open-water Drown<strong>in</strong>g Prevention: Care of<br />

Others<br />

1.<br />

Help <strong>and</strong> encourage others, especially children, to learn swimm<strong>in</strong>g<br />

<strong>and</strong> water safety survival skills<br />

2. Swim <strong>in</strong> areas with lifeguards<br />

3. Set water safety rules<br />

4.<br />

5.<br />

Always provide close <strong>and</strong> constant attention to children you are<br />

supervis<strong>in</strong>g <strong>in</strong> or near water<br />

Know how <strong>and</strong> when to use a life jacket, especially with children<br />

<strong>and</strong> weak swimmers<br />

6. Learn first aid <strong>and</strong> CPR<br />

7.<br />

Learn safe ways of rescu<strong>in</strong>g others without putt<strong>in</strong>g yourself <strong>in</strong><br />

danger<br />

8. Obey all safety signs <strong>and</strong> warn<strong>in</strong>g flags<br />

dIscussIon<br />

From an orig<strong>in</strong>al database conta<strong>in</strong><strong>in</strong>g over 60 messages related to care of<br />

self <strong>and</strong> care of others dur<strong>in</strong>g swimm<strong>in</strong>g-related, open water recreation,<br />

the Task Force agreed on 16 key messages that would most foster drown<strong>in</strong>g<br />

prevention. Learn<strong>in</strong>g swimm<strong>in</strong>g <strong>and</strong> water safety survival skills was<br />

the dom<strong>in</strong>ant message <strong>in</strong> both Care of self <strong>and</strong> Care of others categories.<br />

The collective reason<strong>in</strong>g support<strong>in</strong>g this dom<strong>in</strong>ance was that be<strong>in</strong>g able<br />

to swim reduced the chance of a serious <strong>in</strong>cident <strong>in</strong> or near the water, but<br />

the Task Force reiterated that swimm<strong>in</strong>g ability alone was no guarantee<br />

of safety. Most people learned to swim <strong>in</strong> a pool or calm water sett<strong>in</strong>g,<br />

but this does not fully prepare swimmers for open waters such lakes, rivers<br />

or beaches <strong>and</strong> even good swimmers can encounter life-threaten<strong>in</strong>g<br />

problems. Swimm<strong>in</strong>g safely <strong>in</strong> any open water therefore requires special<br />

caution s<strong>in</strong>ce different types of open water have chang<strong>in</strong>g risks such as<br />

cold, currents <strong>and</strong> high waves (Golden & Tipton, 2002).<br />

Task Force members concurred <strong>in</strong> the belief that swimmers should<br />

never underestimate the risk of drown<strong>in</strong>g or overestimate their ability<br />

to cope with those risks dur<strong>in</strong>g aquatic activity (Michalsen, 2006). Thus<br />

water safety was deemed to be more than just swimm<strong>in</strong>g competency;<br />

it was also about hav<strong>in</strong>g the knowledge <strong>and</strong> attitudes to be safe <strong>in</strong> <strong>and</strong><br />

around water. In the case of car<strong>in</strong>g for others, it was further reasoned<br />

that encourag<strong>in</strong>g others, especially children, to learn swimm<strong>in</strong>g <strong>and</strong> water<br />

safety survival skills was a prime responsibility, especially for parents<br />

<strong>and</strong> caregivers.<br />

Another strongly supported message <strong>in</strong> both Care of self <strong>and</strong> Care of<br />

others categories related to swimm<strong>in</strong>g with lifeguard supervision (ranked<br />

second <strong>and</strong> sixth respectively). While recogniz<strong>in</strong>g that no water is ever<br />

completely free from risk, evidence of the efficacy of lifeguard supervision<br />

<strong>in</strong> drown<strong>in</strong>g prevention is compell<strong>in</strong>g (for example, Branche &<br />

Stewart, 2001). Lifeguards are tra<strong>in</strong>ed to promote safe behavior around<br />

the water <strong>and</strong> to prevent drown<strong>in</strong>g by help<strong>in</strong>g those <strong>in</strong> distress through<br />

the provision of rescue <strong>and</strong> medical assistance. A key part of the safety<br />

actions advised by the Task Force was for people to check with the lifeguards<br />

for safety advice about the location before enter<strong>in</strong>g the water.<br />

They also noted that, when car<strong>in</strong>g for others even at a life-guarded location,<br />

the onus of supervisory care was still primarily that of the parent or<br />

caregiver. Furthermore, that supervision should be close, constant, <strong>and</strong><br />

without distraction.<br />

Several important messages focused on the personal application of<br />

safety rules <strong>in</strong> the Care of self category. These <strong>in</strong>cluded: always swim with<br />

others (ranked second), obey all safety signs <strong>and</strong> warn<strong>in</strong>g flags (ranked<br />

third), never mix swimm<strong>in</strong>g with alcohol (ranked fourth), <strong>and</strong> know the<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

weather <strong>and</strong> water conditions before gett<strong>in</strong>g <strong>in</strong> the water (ranked seventh).<br />

The safety value of swimm<strong>in</strong>g with others was predicated on the<br />

knowledge that many drown<strong>in</strong>g deaths <strong>in</strong>volve people swimm<strong>in</strong>g alone<br />

<strong>and</strong> that immediate assistance <strong>in</strong> the event of difficulty <strong>and</strong> the ability<br />

of others to signal or call for help would m<strong>in</strong>imize the risk of drown<strong>in</strong>g.<br />

The fourth-placed rank<strong>in</strong>g given to never mix<strong>in</strong>g alcohol with swimm<strong>in</strong>g<br />

reflected the <strong>in</strong>cidence of alcohol-related drown<strong>in</strong>g fatalities, <strong>and</strong><br />

because alcohol exacerbates cold water immersion effects, <strong>and</strong> impairs<br />

judgment.<br />

The message to obey all safety signs <strong>and</strong> warn<strong>in</strong>g flags (ranked third<br />

<strong>in</strong> Care of self <strong>and</strong> eighth <strong>in</strong> Care of others) was grounded <strong>in</strong> the importance<br />

of <strong>in</strong>form<strong>in</strong>g the public of potential hazards <strong>in</strong> order that they<br />

can make <strong>in</strong>formed decisions about their safety. Safety signs may conta<strong>in</strong><br />

prohibition notices (such as surf<strong>in</strong>g only or no swimm<strong>in</strong>g), warn<strong>in</strong>g<br />

signs (such as strong currents or deep water) or m<strong>and</strong>atory signs (such<br />

as wear a lifejacket) (Sims, 2006). Flags are often used to show areas patrolled<br />

by lifeguards (such as red <strong>and</strong> yellow flags), restricted areas (such<br />

as black <strong>and</strong> white quartered flags for surf<strong>in</strong>g only), or flags <strong>in</strong>dicat<strong>in</strong>g<br />

weather <strong>and</strong> water conditions (such as red flags for dangerous conditions<br />

or closed beaches).<br />

The use of lifejackets (PFD’s), traditionally associated with boat<strong>in</strong>g<br />

<strong>and</strong> l<strong>and</strong>-based fish<strong>in</strong>g safety, ranked fifth <strong>in</strong> both categories <strong>and</strong> was<br />

deemed important <strong>in</strong> open water swimm<strong>in</strong>g activity especially where<br />

immersion was likely to lead to <strong>in</strong>voluntary submersion (Brooks et al.,<br />

2006). It was especially noted that lifejackets provided safety <strong>in</strong> the water<br />

especially for children, weak, tired or <strong>in</strong>jured swimmers.<br />

In the Care of others category, the Task Force strongly supported<br />

messages related to supervision skills, notably the sett<strong>in</strong>g of water safety<br />

rules (ranked third), the provision of close <strong>and</strong> constant attention of<br />

children (ranked fourth), as well as the lifesav<strong>in</strong>g skills of learn<strong>in</strong>g first<br />

aid <strong>and</strong> CPR (ranked sixth) <strong>and</strong> safe rescue techniques (ranked seventh).<br />

In the latter, because would-be rescuers sometimes become victims <strong>in</strong><br />

multiple drown<strong>in</strong>g tragedies, caution about personal risk was a focal<br />

po<strong>in</strong>t <strong>in</strong> discussion <strong>and</strong> advice for <strong>in</strong>tervention focused on the acquisition<br />

of non-immersion, non-contact rescue techniques.<br />

Results of this project should be treated with some caution <strong>in</strong> light<br />

of several methodological limitations. Firstly, the self-appo<strong>in</strong>ted Task<br />

Force may not have been wholly representative of the drown<strong>in</strong>g prevention<br />

community. High <strong>in</strong>come level countries whose <strong>in</strong>cidence of<br />

drown<strong>in</strong>g are highly related with frequent recreational water use were<br />

over-represented compared to low <strong>in</strong>come level <strong>and</strong> regions whose<br />

drown<strong>in</strong>g rates may not be l<strong>in</strong>ked to aquatic recreation. Secondly, members<br />

were more likely to be <strong>in</strong>volved <strong>in</strong> surf <strong>and</strong> ocean sett<strong>in</strong>gs than lakes<br />

<strong>and</strong> river recreational activities. Fourthly, lack of universally agreed term<strong>in</strong>ology<br />

<strong>and</strong> language constra<strong>in</strong>ts placed limitations on the mean<strong>in</strong>g of<br />

messages. We anticipate that various cultures <strong>and</strong> languages will need to<br />

<strong>in</strong>terpret the recommendations with caution so as to reduce the risk of<br />

loss of mean<strong>in</strong>g <strong>in</strong> translation. F<strong>in</strong>ally, the group was not sanctioned nor<br />

funded by any global organization so participation was voluntary <strong>and</strong><br />

constra<strong>in</strong>ed by other professional commitments <strong>and</strong> personal resources.<br />

These limitations notwithst<strong>and</strong><strong>in</strong>g, the generic water safety messages<br />

provide a comprehensive, concise <strong>and</strong> universal framework for communicat<strong>in</strong>g<br />

open water drown<strong>in</strong>g prevention messages at an <strong>in</strong>ternational,<br />

national, regional, <strong>and</strong> community level.<br />

conclusIon<br />

The recommendations have established <strong>in</strong>formed, consistent, <strong>and</strong> concise<br />

messages that promote safe recreational use of open water. It is<br />

hoped that they will improve the clarity of communication between<br />

drown<strong>in</strong>g prevention organizations <strong>and</strong> the public they serve as well as<br />

provide a framework for safety messag<strong>in</strong>g that is applicable to a range of<br />

communities <strong>and</strong> sett<strong>in</strong>gs with the ultimate goal of sav<strong>in</strong>g lives.<br />

373


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

reFerences<br />

Branche, C.M. & Stewart, S. (Eds.) (2001). Lifeguard Effectiveness: A<br />

Report of<br />

the Work<strong>in</strong>g Group. Atlanta: Centers for Disease Control <strong>and</strong> Prevention,<br />

National Center for Injury Prevention <strong>and</strong> Control.<br />

Brooks, C., Cornelissen, G. & Popp, R. (2006). Lifejackets <strong>and</strong> other<br />

lifesav<strong>in</strong>g appliances. In J.J.L.M. Bierens (Ed.), H<strong>and</strong>book on drown<strong>in</strong>g-<br />

prevention, rescue, <strong>and</strong> treatment (pp. 226-232). Heidelberg:<br />

Spr<strong>in</strong>ger.<br />

Brown, B. (1968). Delphi process: A methodology used for the elicitation of<br />

op<strong>in</strong>ions of experts. Santa Monica, CA: The R<strong>and</strong> Corporation.<br />

Golden, F. & Tipton, M. (2002). Essentials of sea survival. Champaign,<br />

IL: Human K<strong>in</strong>etics<br />

Michalsen, A. (2006). Risk assessment <strong>and</strong> perception. In J.J.L.M. Bierens<br />

(Ed.), H<strong>and</strong>book on drown<strong>in</strong>g- prevention, rescue, <strong>and</strong> treatment<br />

(pp. 93-98). Heidelberg: Spr<strong>in</strong>ger.<br />

Sims, B. (2006). Water safety signs <strong>and</strong> beach safety flags. In J.J.L.M.<br />

Bierens (Ed.), H<strong>and</strong>book on drown<strong>in</strong>g- prevention, rescue, <strong>and</strong> treatment<br />

(pp. 204-214). Heidelberg: Spr<strong>in</strong>ger.<br />

AcKnoWledGeMents<br />

The Task Force wishes to acknowledge the work of the participants <strong>and</strong><br />

their member organizations, the contribut<strong>in</strong>g organizations who reviewed<br />

the f<strong>in</strong>d<strong>in</strong>gs <strong>and</strong> especially Martha Tansik for her patience <strong>and</strong><br />

persistence, her attention to detail <strong>and</strong> her meticulous record<strong>in</strong>g of due<br />

process.<br />

374<br />

Immune Status Changes <strong>and</strong> URTI Incidence <strong>in</strong><br />

the Initial 7 Weeks of a W<strong>in</strong>ter Tra<strong>in</strong><strong>in</strong>g Season <strong>in</strong><br />

Portuguese Swimmers<br />

rama, l. 1 , Alves, F.B. 2 , rosado, F. 1 , Azevedo, s. 3 , Matos, A. 3 ,<br />

henriques, A. 3 , Paiva, A. 3 , teixeira, AM. 1<br />

1Research Centre for Sport <strong>and</strong> Physical Activity, University of Coimbra,<br />

Portugal,<br />

2Faculty of Human K<strong>in</strong>etics, Technical University of Lisbon, Portugal,<br />

3Histocompatibility Centre, Coimbra, Portugal<br />

In swimm<strong>in</strong>g the tra<strong>in</strong><strong>in</strong>g plann<strong>in</strong>g process usually leads to a sudden<br />

<strong>in</strong>crease of tra<strong>in</strong><strong>in</strong>g load <strong>in</strong> the first mesocycle of the season. Swimmers<br />

often come back from off tra<strong>in</strong><strong>in</strong>g periods unfit, so this option could result<br />

<strong>in</strong> a maladaptation condition with impact on the work capacity <strong>and</strong><br />

health of the athletes. This study focused on the variation of hormonal<br />

<strong>and</strong> immune markers, <strong>and</strong> <strong>in</strong> the occurrence of upper respiratory tract<br />

<strong>in</strong>fection symptoms (URTIS) registered dur<strong>in</strong>g the first mesocyce of<br />

preparation, of a w<strong>in</strong>ter season, <strong>in</strong> a group of male swimmers. Results<br />

show that the higher rate of URTIS of the tra<strong>in</strong><strong>in</strong>g season occurred<br />

<strong>in</strong> this period. At rest, an <strong>in</strong>crease <strong>in</strong> leukocyte counts <strong>and</strong> a decrease<br />

<strong>in</strong> CD4+, CD8+ <strong>and</strong> NK cell counts were found. The <strong>in</strong>creased serum<br />

cortisol levels <strong>and</strong> the decrease <strong>in</strong> the testosterone/cortisol ratio, could<br />

lead to a dim<strong>in</strong>ished immune competence observed.<br />

Key words: upper respiratory symptoms, tra<strong>in</strong><strong>in</strong>g load, lymphocyte<br />

sub populations, cortisol, testosterone<br />

IntroductIon<br />

Despite different periodization strategies, there is a known trend for a<br />

substantial <strong>in</strong>crease <strong>in</strong> tra<strong>in</strong><strong>in</strong>g volume <strong>in</strong> the <strong>in</strong>itial mesocycle of the<br />

tra<strong>in</strong><strong>in</strong>g season (Costill et al. 1992). Few studies specifically address<br />

this <strong>in</strong>itial adaptation period of tra<strong>in</strong><strong>in</strong>g. The remarkable impact of this<br />

phase is generally overlooked by coaches, given the low <strong>in</strong>tensity <strong>and</strong><br />

gradual <strong>in</strong>crement of tra<strong>in</strong><strong>in</strong>g load. However, swimmers frequently come<br />

from off tra<strong>in</strong><strong>in</strong>g periods <strong>in</strong> unfit condition, so this tra<strong>in</strong><strong>in</strong>g phase could<br />

produce an important impact as a stress factor.<br />

Coaches admit that swimmers often become ill dur<strong>in</strong>g hard tra<strong>in</strong><strong>in</strong>g<br />

periods, especially dur<strong>in</strong>g <strong>and</strong> after cycles of preparation <strong>in</strong> which they<br />

are submitted to large volumes of tra<strong>in</strong><strong>in</strong>g. It is also reported by coaches<br />

that athletes often show a higher occurrence of upper respiratory tract<br />

<strong>in</strong>fection symptoms (URTIS) dur<strong>in</strong>g this period (Spence et al. 2007).<br />

Among several markers, hormonal responses have been used o monitor<br />

how swimmers adapt to acute exercise, tra<strong>in</strong><strong>in</strong>g sessions <strong>and</strong> even<br />

larger periods of tra<strong>in</strong><strong>in</strong>g (Urhausen et al. 1995). In spite of some controversies<br />

related to the hormonal <strong>and</strong> immunological alterations <strong>in</strong> response<br />

to tra<strong>in</strong><strong>in</strong>g, these parameters may reflect the adaptation process.<br />

It is usually assumed that cortisol <strong>in</strong>creases (Bonifazi et al. 2000) while<br />

testosterone decreases (Tyndall, et al. 1996) dur<strong>in</strong>g <strong>and</strong> after important<br />

aerobic tra<strong>in</strong><strong>in</strong>g cycles.<br />

Due to the well-established <strong>in</strong>terdependence between hormonal<br />

<strong>and</strong> immune function, namely the <strong>in</strong>fluence of cortisol on lymphocytes<br />

counts it is not surpris<strong>in</strong>g that the immune response to hard tra<strong>in</strong><strong>in</strong>g<br />

periods occurs <strong>in</strong> the form of a depression state (Gleeson, 2007).<br />

There are few studies that address the chronic tra<strong>in</strong><strong>in</strong>g effects on immune<br />

parameters, however the ma<strong>in</strong> ones reported are those that show<br />

alterations that occur with T cells, <strong>and</strong> <strong>in</strong>clude lower cells count values<br />

<strong>and</strong> dim<strong>in</strong>ished proliferative capacity (Gleeson, 2006).<br />

In a longitud<strong>in</strong>al study over a competitive season with high level<br />

Australian swimmers, no alterations were found for B or T cells, but<br />

significant decreases on count <strong>and</strong> percentages of NK cells were noted<br />

(Gleeson et al. 1995). NK cells were considered based on their prevalence<br />

<strong>and</strong> function. The majority of NK cells (¾ 90%) are NK dim with


more cytotoxic capacity, <strong>and</strong> NK bright ( 10%) with a higher aff<strong>in</strong>ity to<br />

IL-2 <strong>and</strong> a large capacity to produce cytok<strong>in</strong>es: IFN-γ, TNF-β, GM-<br />

CSF, IL-10, IL-13 after monok<strong>in</strong>e stimulation (Cooper et al. 2001). The<br />

strik<strong>in</strong>g sensivity of NK cells to exercise stress provides strong support<br />

that these cells may be implicated as a potential l<strong>in</strong>k between regular<br />

physical activity <strong>and</strong> overall health status (Timmons & Cieslaak, 2008).<br />

However the results are not without some controversy, as a large<br />

number of studies are conducted us<strong>in</strong>g <strong>in</strong>-vitro assays, <strong>and</strong> when peripheral<br />

blood samples were used, it was not possible to determ<strong>in</strong>e the true<br />

nature of the alterations observed <strong>in</strong> the immune parameters: whether<br />

it is a decrease <strong>in</strong> immune function or an adaptive mechanism such as<br />

changes <strong>in</strong> the cells redistribution patterns.<br />

The aim of this study was to analyze the variation of hormonal <strong>and</strong><br />

immunological parameters <strong>and</strong> the <strong>in</strong>cidence of URTIS, dur<strong>in</strong>g the first<br />

7 weeks of a w<strong>in</strong>ter tra<strong>in</strong><strong>in</strong>g season <strong>in</strong> a group of national level Portuguese<br />

male swimmers.<br />

Methods<br />

This study sample consisted of 13 male swimmers of Portuguese national<br />

level (17.2± 1.3 years old, 174.9 ±5.8 cm, 65.8±6.8 kg of height <strong>and</strong><br />

weight respectively). All subjects gave their written <strong>in</strong>formed consent.<br />

Tra<strong>in</strong><strong>in</strong>g volume <strong>and</strong> <strong>in</strong>tensity were controlled as well as the time<br />

spent <strong>in</strong> dry l<strong>and</strong> activities. Blood samples were collected: 1) <strong>in</strong> the beg<strong>in</strong>n<strong>in</strong>g<br />

of the w<strong>in</strong>ter season, after an off tra<strong>in</strong><strong>in</strong>g period of 6 weeks (t0),<br />

2) after 7 weeks of tra<strong>in</strong><strong>in</strong>g (t1), by venopuncture, always at the same<br />

time of the day (between 15 <strong>and</strong> 17h. At (t1) a time lapse of 48 hours of<br />

rest after the last tra<strong>in</strong><strong>in</strong>g session was respected.<br />

Total leukocyte counts <strong>and</strong> percentage were measured on a Coulter<br />

counter diff TM Analyser. The lymphocyte populations <strong>and</strong> subsets<br />

(CD3+, CD4+, CD8+, CD19+ <strong>and</strong> CD56+) were accessed by flow cytometry<br />

(FACSCalibur; BD, San Jose, C.A., USA).<br />

The serum concentration of cortisol <strong>and</strong> free testosterone were determ<strong>in</strong>ed<br />

by electrochemilum<strong>in</strong>escence (Immulite 2000) at the same time<br />

po<strong>in</strong>ts. The URTIS were assessed by self-report <strong>in</strong> daily log books. Statistical<br />

analysis us<strong>in</strong>g the non-parametric Wilcoxon test was conducted<br />

(p


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

ered the most responsive of the <strong>in</strong>ate immune system, be<strong>in</strong>g cytotoxic<br />

<strong>and</strong> produc<strong>in</strong>g cytok<strong>in</strong>es aga<strong>in</strong>st target cells. Our data shows that the<br />

count <strong>and</strong> the percentage of NK cells tend to exhibit a decrease <strong>in</strong> the<br />

total NK population In addition the significant alterations observed <strong>in</strong><br />

NK cell subsets, with the NKCD56dim subpopulation show<strong>in</strong>g reduced<br />

cell numbers, could represent an impairment of cytotoxic activity with<br />

consequences <strong>in</strong> immune function. The elevation of the NKCD56bright<br />

/NKCD56dim ratio has been associated with a fall <strong>in</strong> cytotoxicity activity<br />

(Susui et al. 2004).<br />

In this study no significant alterations <strong>in</strong> B lymphocyte (CD19+)<br />

cell counts <strong>and</strong> percentage were observed which is <strong>in</strong> accordance to previous<br />

published papers (Gleesson et al. 1995).<br />

conclusIon<br />

The presented data confirm that alterations <strong>in</strong> the immune system may<br />

occur dur<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g periods. The real mean<strong>in</strong>g of this response behaviour,<br />

immune depression or adaptation process is still <strong>in</strong>conclusive.<br />

The ma<strong>in</strong> f<strong>in</strong>d<strong>in</strong>gs of this study po<strong>in</strong>t to an impact on immune<br />

function of progressive <strong>and</strong> light tra<strong>in</strong><strong>in</strong>g loads at the <strong>in</strong>itial phase of<br />

preparation, after long periods of rest, which should be taken <strong>in</strong>to account<br />

by the coaches when adopt<strong>in</strong>g recovery strategies aimed at reduc<strong>in</strong>g<br />

the negative impact of tra<strong>in</strong><strong>in</strong>g. The results also stress the importance<br />

of the use of daily logs or other strategies to monitor how<br />

athletes are adapt<strong>in</strong>g to workload, which could be useful <strong>in</strong> detect<strong>in</strong>g<br />

early signs of difficulties <strong>in</strong> this process. For example, preventive measures<br />

like nutritional supplementation or tra<strong>in</strong><strong>in</strong>g load adjustment could<br />

be implemented. Also important is the medical care support at times of<br />

<strong>in</strong>tensified tra<strong>in</strong><strong>in</strong>g load, allow<strong>in</strong>g for a rapid diagnosis <strong>and</strong> treatment of<br />

the episodes of illness recorded.<br />

In his study we did not look at the immune cells function, so there<br />

is always the possibility that the alterations observed could be related<br />

to blood redistribution factors. However the prevalence of URTIS observed<br />

seems to reflect a real negative impact on immune function <strong>and</strong><br />

to the importance of monitor<strong>in</strong>g the effects of tra<strong>in</strong><strong>in</strong>g load <strong>in</strong> athletes.<br />

reFerences<br />

Bonifazi, M., Sardella, F. & Lupo, C. (2000). Preparatory versus ma<strong>in</strong><br />

competitions: differences <strong>in</strong> performances lactate responses <strong>and</strong> precompetition<br />

plasma cortisol concentrations <strong>in</strong> elite male swimmers.<br />

European Journal of Applied Physiology, 82(5-6), 368-373.<br />

Cooper, M. A., Fehniger, T. A. & Caligiuri, M. A. (2001). The biology<br />

of human natural killer-cell subsets. Trends Immunol, 22(11), 633-640.<br />

Costill, D., Maglischo, E. & Richardson, A. (1992). Swimm<strong>in</strong>g. H<strong>and</strong>book<br />

of Sports Medec<strong>in</strong>e <strong>and</strong> Science: Blackwell Scientific Publications.<br />

Cox, A. J., Gleeson, M., Pyne, D. B., Saunders, P. U., Clancy, R. L. &<br />

Fricker, P. A. (2004). ValtrexTM Therapy for Epste<strong>in</strong>-Barr Virus Reactivation<br />

<strong>and</strong> Upper Respiratory Symptoms <strong>in</strong> Elite Runners. Med.<br />

Sci. Sports Exerc., 36(7), 1104-1110.<br />

Gleeson, M. (2006). Imune Function <strong>in</strong> Sport <strong>and</strong> Exercise (1ª ed.).<br />

Churchill Liv<strong>in</strong>gstone Elsevier.<br />

Gleeson, M. (2007). Immune function <strong>in</strong> sport <strong>and</strong> exercise. J Appl Physiol,<br />

103(2), 693-699.<br />

Gleeson, M., McDonald, W., Cripps, A., Pyne, D., Clancy, R. & Fricker,<br />

P. (1995). The effect on immunity of long-term <strong>in</strong>tensive tra<strong>in</strong><strong>in</strong>g <strong>in</strong><br />

elite swimmers. Cl<strong>in</strong> Exp Immunol, 102(1), 210-216.<br />

Heath, G. W., Macera, C. A. & Nieman, D. C. (1992). Exercise <strong>and</strong> upper<br />

respiratory tract <strong>in</strong>fection: is there a relationship? Sports medic<strong>in</strong>e,<br />

14(6), 353-365.<br />

Mack<strong>in</strong>non, L. (2000). Chronic Exercise Tra<strong>in</strong><strong>in</strong>g Effects on Immune<br />

Function. Med Sci Sports Exerc., 32(7), S369-S376.<br />

Maglischo, E. (2003). Swimm<strong>in</strong>g Fastest. The essential reference on technique,<br />

tra<strong>in</strong><strong>in</strong>g, <strong>and</strong> program design. Human K<strong>in</strong>etics, Champaign.<br />

Nagatomi, R. (2006). The implication of alterations <strong>in</strong> leukocyte subset<br />

counts on immune function. Exerc Immunol Rev, 12, 54-71.<br />

Sh<strong>in</strong>kai, S., Watanabe, S., Asai, H. & Shek, P. N. (1996). Cortisol re-<br />

376<br />

sponse to exercise <strong>and</strong> post-exercise suppression of blood lymphocyte<br />

subset counts. Int J Sports Med, 17(8), 597-603.<br />

Spence, L., Brown, W. J., Pyne, D. B., Nissen, M. D., Sloots, T. P. & Mc-<br />

Cormack, J. G., et al. (2007). Incidence, Etiology, <strong>and</strong> Symptomatology<br />

of Upper Respiratory Illness <strong>in</strong> Elite Athletes. <strong>Medic<strong>in</strong>e</strong> & Science<br />

<strong>in</strong> Sports & Exercise, 39(4), 577-586<br />

Suzui, M., Kawai, T., Kimura, H., Takeda, K., Yagita, H. & Okumura,<br />

K., et al. (2004). Natural killer cell lytic activity <strong>and</strong> CD56dim <strong>and</strong><br />

CD56bright cell distributions dur<strong>in</strong>g <strong>and</strong> after <strong>in</strong>tensive tra<strong>in</strong><strong>in</strong>g. J<br />

Appl Physiol, 96(6), 2167-2173.<br />

Timmons, B. W. & Cieslak, T. (2008). Human natural killer cell subsets<br />

<strong>and</strong> acute exercise: a brief review. Exerc Immunol Rev, 14, 8-23.<br />

Tyndall, G. L., Kobe, R. W. & Houmard, J. A. (1996). Cortisol, testosterone,<br />

<strong>and</strong> <strong>in</strong>sul<strong>in</strong> action dur<strong>in</strong>g <strong>in</strong>tense swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g <strong>in</strong><br />

humans. Eur J Appl Physiol Occup Physiol, 73(1-2), 61-65.<br />

Urhausen, A., Gabriel, H. & K<strong>in</strong>dermann, W. (1995). Blood hormones<br />

as markers of tra<strong>in</strong><strong>in</strong>g stress <strong>and</strong> overtra<strong>in</strong><strong>in</strong>g. Sports <strong>Medic<strong>in</strong>e</strong>, 20,<br />

251-276.<br />

AcKnoWledGeMents<br />

This project was f<strong>in</strong>anced by the Portuguese foundation for Science <strong>and</strong><br />

Technology (FCT PTDC/ DES/ 68647/ 2006)


Swimm<strong>in</strong>g Ability, Perceived Competence <strong>and</strong><br />

Perceived Risk among Young Adults<br />

stallman, r.K. 1,2 , dahl d. 1 , Moran, K. 3 , Kjendlie, P.l. 1,4<br />

1 Norwegian School of Sport Science,<br />

2 Norwegian Life Sav<strong>in</strong>g Association,<br />

3 Univ. of Auckl<strong>and</strong>,<br />

4 Vestfold University College<br />

Why do swimmers get <strong>in</strong>to trouble? Do they over estimate their ability,<br />

underestimate the risk, both? Eighty one (n = 81) university physical education<br />

students completed a questionnaire <strong>and</strong> performed seven practical<br />

swimm<strong>in</strong>g tests. The questionnaire covered a) perception of ability, b)<br />

perception of difficulty <strong>in</strong> open water <strong>and</strong> c) perception of risk. Gender<br />

differences were tested by the Mann-Whitney U test. The women out<br />

performed the men on 4 of 7 practical tests. There were few gender differences<br />

<strong>in</strong> perceived competence. The women were highly confident<br />

about float<strong>in</strong>g <strong>in</strong> open water while the men were certa<strong>in</strong> they could not<br />

do the same. The men predicted 100% success on surface div<strong>in</strong>g to the<br />

bottom of the pool (4m) while the women were less certa<strong>in</strong> (88%). On 5<br />

scenarios depict<strong>in</strong>g risk, there were no gender differences.<br />

Key words: swimm<strong>in</strong>g ability, perceived competence, perceived risk<br />

IntroductIon<br />

This study presents the results of an attempt to compare young adult’s<br />

perception of their ability <strong>in</strong> the water to their real ability. These are the<br />

Norwegian f<strong>in</strong>d<strong>in</strong>gs <strong>in</strong> a larger <strong>in</strong>ternational project, Can You Swim?<br />

Water Safety experts generally believe that water safety education must<br />

<strong>in</strong>clude knowledge, attitude, judgment <strong>and</strong> skill. One of the most important<br />

elements of knowledge is to know your own limits. The ’deadly<br />

duo’ of over estimat<strong>in</strong>g ones ability <strong>and</strong> under estimat<strong>in</strong>g the risk (<strong>in</strong><br />

any given specific situation) can have fatal consequences. McCool et<br />

al. (2009) exam<strong>in</strong>ed exactly this <strong>in</strong> New Zeal<strong>and</strong>; to what degree do<br />

beach goers perceive risk? New Zeal<strong>and</strong> is well known for it’s aquatic<br />

recreational opportunities <strong>and</strong> it is normally considered a sign of an active<br />

healthy life style that young people participate as much as they do.<br />

In New Zeal<strong>and</strong> swimm<strong>in</strong>g is the activity most often engaged <strong>in</strong> prior<br />

to a drown<strong>in</strong>g episode (2005). In Norway, a considerable majority of<br />

drown<strong>in</strong>gs are related to small boat use <strong>and</strong> alcohol is often <strong>in</strong>volved<br />

(Norwegian Peoples Aid, 2007).<br />

It has been speculated however, that <strong>in</strong>creas<strong>in</strong>g the swimm<strong>in</strong>g competency<br />

of any society may <strong>in</strong> fact <strong>in</strong>crease exposure to risk (Baker et<br />

al, 1992). It is thus doubly important <strong>in</strong> any water safety – drown<strong>in</strong>g<br />

prevention effort, to <strong>in</strong>sist that the teach<strong>in</strong>g of swimm<strong>in</strong>g <strong>in</strong>clude more<br />

than only skills. Risk assessment needs to be a rout<strong>in</strong>e affair for persons<br />

frequently engag<strong>in</strong>g <strong>in</strong> aquatic recreation. This cannot be a general k<strong>in</strong>d<br />

of orientation but must address real local conditions.<br />

It is also well known that <strong>in</strong> other daily pursuits, men frequently<br />

are greater risk takers than women. An excellent example of this is the<br />

dramatic over representation of men among traffic <strong>in</strong>juries <strong>and</strong> among<br />

those penalized for reckless driv<strong>in</strong>g <strong>and</strong> driv<strong>in</strong>g while <strong>in</strong>toxicated<br />

(Trygg Trafikk, 2008). Studies <strong>in</strong> New Zeal<strong>and</strong> have identified men as<br />

greater risk takers <strong>in</strong> aquatic activity than women (McCool et al, 2008,<br />

2009, Moran, 2008). There appears to be little available <strong>in</strong>formation on<br />

the relationship between real aquatic competency <strong>and</strong> perceived competency.<br />

The goals of this study were to a) assess the swimm<strong>in</strong>g ability<br />

of university students, b) to assess perceptions of swimm<strong>in</strong>g ability <strong>and</strong><br />

risk, <strong>and</strong> c) to compare real <strong>and</strong> perceived competency.<br />

Method<br />

Eighty one (n = 81) university physical education students participated<br />

<strong>in</strong> the study. The subjects were first year students <strong>and</strong> all test<strong>in</strong>g was<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

conducted <strong>in</strong> the first days of the school year, before they were exposed<br />

to swimm<strong>in</strong>g <strong>in</strong>struction. They first answered a questionnaire which required<br />

less than 30 m<strong>in</strong>. The questionnaire (20 questions) covered a)<br />

perception of swimm<strong>in</strong>g ability (can you swim > 50, 100, 200, 300m?,<br />

etc), b) perception of whether or not the same skills could be accomplished<br />

<strong>in</strong> open water, <strong>and</strong> c) perception of risk <strong>in</strong> five specific scenarios.<br />

The practical tests consisted of seven skills considered essential (Table<br />

1). Table 2 lists the questions used to elicit perceived competence as well<br />

as the perception of difficulty on the same skills <strong>in</strong> open water.<br />

Table 1 Practical Tests <strong>and</strong> Criteria for Success<br />

Test Criteria<br />

Distance swim (25m pool) >2, >4, >8, >12, >16, lengths, non-stop<br />

Float<strong>in</strong>g <strong>in</strong> deep water<br />

cannot float, 2, >4, >8, >12, >16 lengths<br />

3. How do you feel about do<strong>in</strong>g this <strong>in</strong> open water? very difficult, difficult, easy, very easy<br />

4. Can you stay afloat <strong>in</strong> deep water without support? No!


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

Table 4 Results of practical tests by gender<br />

Practical Test Score Male Female Total p<br />

Distance swim<br />

Float<br />

Swim on back<br />

Dive <strong>in</strong>to deep<br />

Under water<br />

Surface dive<br />

Rescue tow<br />

378<br />

n % n % n %<br />

10m 7 15.2 6 18.2 13 16.5 0.48<br />

>15m 8 17.4 6 18.2 14 17.7<br />

>20m 7 15.2 7 21.2 14 17.7<br />

25m 24 52.2 14 42.4 38 48.1<br />

Poor 2 4.3 1 2.9 3 3.7 0.001<br />

Satisfactory 31 66.0 10 9.4 41 50.6<br />

Good 13 27.7 18 52.9 31 38.3<br />

Excellent 1 2.1 5 14.7 6 7.4<br />

Did not f<strong>in</strong>ish 1 2.1 1 2.9 2 2.5 0.0001<br />

Poor 6 12.8 0 0.0 6 7.4<br />

Satisfactory 27 57.4 10 29.4 37 45.7<br />

Good 11 23.4 11 32.4 22 27.2<br />

Excellent 2 4.3 12 35.3 14 17.3<br />

Regard<strong>in</strong>g perceived competence, both the men (87.2%) <strong>and</strong> the women<br />

(76.5%) rated themselves as average to good swimmers. Although<br />

the difference was not significant, the practical tests (item 2, can swim<br />

>400m) showed that the women (100%) were, <strong>in</strong> fact, slightly better<br />

than the men (97.9%).<br />

On the next 14 questions, only two showed a significant gender difference.<br />

The women were highly confident about float<strong>in</strong>g <strong>in</strong> deep water<br />

(83.7%) while the men (only 6.3%) were conv<strong>in</strong>ced that they could not<br />

do this. This was <strong>in</strong> accordance with reality as 91.5% of the men failed to<br />

float at all, while only 73.5% of the women failed. The second question<br />

show<strong>in</strong>g gender difference was regard<strong>in</strong>g surface div<strong>in</strong>g to the bottom of<br />

the pool. One hundred percent (100%) of the men predicted they would<br />

do this while 88.2% of the women predicted success. The practical test<br />

did not confirm the prediction. Among the men, 95.7% managed the<br />

surface dive but 97.1% of the women managed it. Although the difference<br />

appears to be small, it was never the less, statistically significant.<br />

The perceived risk of drown<strong>in</strong>g as <strong>in</strong>dicated by rank<strong>in</strong>g risk from 1-4<br />

on five water related scenarios, showed no differences between the men<br />

<strong>and</strong> the women. In general, only one of the five scenarios elicited reports<br />

of high perceived risk.<br />

dIscussIon<br />

That the women would so clearly out perform the men was not expected.<br />

Of educational significance is the fact that despite significant<br />

gender differences on real competence, both the men <strong>and</strong> the women<br />

performed relatively poorly on a) float<strong>in</strong>g <strong>in</strong> deep water, b) swimm<strong>in</strong>g on<br />

the back <strong>and</strong> c) both surface div<strong>in</strong>g <strong>and</strong> swimm<strong>in</strong>g under water <strong>and</strong> d)<br />

the rescue tow. All of these skills have a real survival value <strong>and</strong> need to be<br />

addressed. Regard<strong>in</strong>g float<strong>in</strong>g, Stallman (1999) showed that with a full<br />

<strong>in</strong>spiration, all women (100%) <strong>and</strong> >90% of all men, have the capacity<br />

to float. Those who failed to live up to their anatomical capacity, clearly<br />

lacked only confidence. When discuss<strong>in</strong>g confidence skills, it has often<br />

been stated that there are no objective measures of confidence <strong>in</strong> the water.<br />

When an <strong>in</strong>dividual has the proven (measured) anatomical capacity<br />

to float <strong>and</strong> fails to do so, there can be no better ’objective’ test of confidence.<br />

Among these subjects (men <strong>and</strong> women), a full 84% failed to float<br />

<strong>in</strong> deep water. A total of 42%, nearly half of the subjects, swam poorly<br />

on the back <strong>in</strong> spite of rank<strong>in</strong>g themselves as average to good swimmers.<br />

Over half of the total surface dived with only satisfactory or poor form<br />

<strong>and</strong> one third (34.2%) could not swim > 15m under water. This should<br />

be a cause for alarm when deal<strong>in</strong>g with university students who have<br />

been through compulsory swimm<strong>in</strong>g <strong>in</strong>struction <strong>in</strong> primary school.<br />

In much of the world, swimm<strong>in</strong>g <strong>in</strong>struction can be held outdoors<br />

for only a small part of the year. Even where this would be practical,<br />

outdoor pools are often used. The consequences of this are that an <strong>in</strong>creas<strong>in</strong>g<br />

number of people have learned to swim <strong>in</strong> a pool. In some parts<br />

of the world, swimm<strong>in</strong>g <strong>in</strong> open water is simply too dangerous because<br />

of the threat of predators <strong>and</strong>/or microbes. However it is well known<br />

that drown<strong>in</strong>g occurs primarily <strong>in</strong> open water. Those who do not survive<br />

an aquatic episode have usually failed to make the transition from the<br />

learn<strong>in</strong>g atmosphere to the recreational or work<strong>in</strong>g atmosphere. Seven<br />

of the questions about perceived ability were followed by the question,<br />

’How do you feel about do<strong>in</strong>g this?’ or ’how do you feel about do<strong>in</strong>g<br />

this <strong>in</strong> open water?’ Us<strong>in</strong>g only one of the open water questions as an<br />

example; 43.2% of the total rated themselves as good to excellent swimmers<br />

<strong>and</strong> 65% said they were able to swim > 400m. However, 64.2%<br />

answered that they could do the same <strong>in</strong> open water as <strong>in</strong> the pool only<br />

with difficulty or with great difficulty.<br />

The subjects <strong>in</strong> this study had previously demonstrated that they<br />

could swim, <strong>in</strong> a physical entrance test which all applicants to the school<br />

must perform. This would suggest that they are above average compared<br />

to their age mates. This can only mean that the general public would<br />

have performed more poorly.<br />

conclusIons<br />

The women performed significantly better than the men on 4 (5) of<br />

seven skills but both performed poorly on several critical skills. This is of<br />

concern. Also, it would appear that on two of the seven skills the subjects<br />

were not able to accurately predict their level of competence. Contrary<br />

to expectations, there were no gender differences <strong>in</strong> perception of risk.<br />

Lastly, while 43% (men <strong>and</strong> women) reported that they were good<br />

to very good swimmers, they performed only from mediocre to poor on<br />

5 of seven tests. And while perform<strong>in</strong>g at only a moderate to poor level,<br />

they reported high risk on only one of the five risk scenarios. It would<br />

appear that they were reasonably good at predict<strong>in</strong>g their competence<br />

on specific skills but were unable to assess their general level of competence<br />

or to relate it to their level of performance on specific skills. Their<br />

perception of what is a good swimmer was skewed.<br />

reFerences<br />

Baker, S.P., O’Neil B., G<strong>in</strong>sburg M.J. & Li, G. (1992). The <strong>in</strong>jury fact<br />

book. N.Y. Oxford University Press.<br />

Brenner, R.A., Moran K., Stallman R.K., Gilchrist J. & McVan J.T.<br />

(2005). Swimm<strong>in</strong>g ability, water safety education <strong>and</strong> drown<strong>in</strong>g<br />

prevention. In: Bierens J. (ed). H<strong>and</strong>book of drown<strong>in</strong>g. Heidelberg:<br />

Spr<strong>in</strong>ger, 112-116<br />

McCool, J.P., Ameratunga S., Moran K. & Rob<strong>in</strong>sen E. (2009). Tak<strong>in</strong>g<br />

a risk perception approach to beach swimm<strong>in</strong>g safety. Int J Beh Med,<br />

16(4), 360-366<br />

McCool, J.P., Moran K., Ameratunga S. & Rob<strong>in</strong>sen E. (2008). New<br />

Zeal<strong>and</strong> beach goers’ swimm<strong>in</strong>g behaviors, swimm<strong>in</strong>g abilities <strong>and</strong><br />

perception of drown<strong>in</strong>g risk. Int J of Aquatic Research <strong>and</strong> Educ, 2(1),<br />

7-15<br />

Moran, K. (2008). Will they s<strong>in</strong>k or swim? New Zeal<strong>and</strong> youth water<br />

safety knowledge <strong>and</strong> skills. Int J of Aquatic Research <strong>and</strong> Educ. 2(2),<br />

114-127


Norwegian Peoples Aid (2007). Annual drown<strong>in</strong>g statistics for Norway<br />

Quan L., Cumm<strong>in</strong>gs P., (2003). Characteristics of drown<strong>in</strong>g by different<br />

age groups. Inj Prevention, 9(2), 163-166<br />

Stallman, R.K. (1998). A comparison of functional buoyancy among<br />

African <strong>and</strong> European children <strong>and</strong> youth. Proceed<strong>in</strong>gs of Nairobi<br />

Congress <strong>in</strong> 1996; The African Assoc. of Health, Physical Education,<br />

Dance <strong>and</strong> Recreation.<br />

Safe Traffic (2008). Traffic statistics for Norway<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

Movement Economy <strong>in</strong> Breaststroke Swimm<strong>in</strong>g: A<br />

Survival Perspective<br />

stallman r.K., Major J., hemmer s., haavaag G.<br />

The Norwegian School of Sport Science<br />

When adopt<strong>in</strong>g a head up position <strong>in</strong> breaststroke the center of gravity<br />

is displaced backward, farther from the center of buoyancy. This causes<br />

a tendency for the legs to s<strong>in</strong>k, <strong>in</strong>creas<strong>in</strong>g the angle of the body with<br />

the horizontal plane <strong>and</strong> concurrently, resistance. Increased resistance<br />

theoretically reduces survival possibilities. The purpose of this study was<br />

to quantify the difference <strong>in</strong> energy expenditure for breaststroke with<br />

the head held constantly above the surface <strong>and</strong> for breaststroke performed<br />

with normal breath<strong>in</strong>g. Classic Douglas bag respirometry was<br />

used. Dur<strong>in</strong>g submaximal swimm<strong>in</strong>g, the volume of oxygen uptake was<br />

significantly higher when swimm<strong>in</strong>g with the face constantly above the<br />

surface than with normal breath<strong>in</strong>g. Both pulse rate <strong>and</strong> blood lactate<br />

levels were also significantly higher when swimm<strong>in</strong>g ”head up”.<br />

Key words: breaststroke, movement economy, survival<br />

IntroductIon<br />

The goals of swimm<strong>in</strong>g <strong>in</strong>struction are numerous but the preservation of<br />

life should be common to all programs. Historically, attempts have been<br />

made to justify one swimm<strong>in</strong>g technique above others, both as the first<br />

to be learned <strong>and</strong> as the most important one. It is well known that North<br />

America has a long tradition of teach<strong>in</strong>g crawl early if not first, <strong>and</strong> that<br />

Europeans generally favor breaststroke. It has been argued that breaststroke<br />

is the easiest stroke to swim with the head up for those who prefer<br />

not to place the face <strong>in</strong> the water. While this may <strong>in</strong> some ways be true,<br />

it is irrelevant <strong>and</strong> <strong>in</strong> many ways contradicts the goals of water safety.<br />

Swimm<strong>in</strong>g educators have long focused on the necessity of breath<br />

hold<strong>in</strong>g/breath control, buoyancy control, orientation, balance <strong>and</strong> rotation<br />

<strong>in</strong> the teach<strong>in</strong>g of swimm<strong>in</strong>g. The 19th century produced the<br />

concept of ”watermanship” often described as the all around aquatic<br />

movement development needed for survival (S<strong>in</strong>clair & Henry, 1893,<br />

Thomas,1904). These same authors also used the expressions ”fancy<br />

swimm<strong>in</strong>g” <strong>and</strong> ”scientific swimm<strong>in</strong>g” referr<strong>in</strong>g to the ability to move<br />

<strong>in</strong> the water <strong>in</strong> harmony with the powers of nature rather than try<strong>in</strong>g to<br />

overcome them. Lanoe (1963) <strong>and</strong> Whit<strong>in</strong>g, (1971) def<strong>in</strong>e a swimmer as<br />

one who can cope with an unexpected submersion. Modern aquatic professionals<br />

emphasize a thorough aquatic experience relat<strong>in</strong>g the characteristics<br />

of the water to our bodies (Skullberg, 1985, Wilke, 2007,),<br />

<strong>and</strong> a movement reperatoir which permits almost any movement <strong>in</strong> any<br />

direction at any time. This rem<strong>in</strong>ds us of the unlimited dem<strong>and</strong>s <strong>and</strong><br />

solutions of the synchronized swimmer or water polo player. Cureton<br />

(1943) <strong>and</strong> the USA Navy (1944) emphasized that an unlimited number<br />

of dangers requires an unlimited number of solutions. Recently the<br />

expression watermanship has been modernized to ”aquatic competence”<br />

(Langendorfer & Bruya , 1995).<br />

To advocate swimm<strong>in</strong>g breaststroke with the head up or to choose<br />

breaststroke as the easiest way to swim with the head up for those who<br />

do not like the water, is to negate virtually all of the goals of aquatic<br />

professionals with regard to water safety – drown<strong>in</strong>g prevention. It is<br />

beyond discussion that such persons are more poorly equipped to cope<br />

with an <strong>in</strong>voluntary submersion (Stallman, et al, 2008). While this is<br />

common sense, there rema<strong>in</strong>s a tendency to argue for breaststroke first<br />

for the very reasons cited above.<br />

Before go<strong>in</strong>g on, the po<strong>in</strong>t must be made that this discussion is not<br />

about choos<strong>in</strong>g between front crawl <strong>and</strong> breaststroke. Both are poorly<br />

suited as a first swimm<strong>in</strong>g technique. And neither is it a matter of<br />

choos<strong>in</strong>g from among the four competitive techniques when so many<br />

others are available. However, <strong>in</strong> the context of this study, the purpose<br />

379


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

was i) to emphasize the importance of effective breath<strong>in</strong>g <strong>and</strong> breath<br />

control (<strong>in</strong> any stroke), <strong>and</strong> ii) to quantify the burden of added resistance<br />

when swimm<strong>in</strong>g breaststroke with the head cont<strong>in</strong>ually above the surface,<br />

considered <strong>in</strong> a survival context.<br />

Lastly the po<strong>in</strong>t must be made that survival is often a matter of<br />

efficiency of movement (or good technique). It has noth<strong>in</strong>g to do with<br />

swimm<strong>in</strong>g fast, although efficient movement is also faster. At any given<br />

velocity, the more efficient the movements, the less energy they will require.<br />

The less energy required per unit time or distance, the longer one<br />

will be able to cont<strong>in</strong>ue <strong>in</strong> any necessary pursuit of survival whether it be<br />

to swim or to rema<strong>in</strong> <strong>in</strong> the same place. This is a po<strong>in</strong>t sadly overlooked<br />

by many swimm<strong>in</strong>g <strong>in</strong>structors, who often express the idea that good<br />

technique is only important for the competitive swimmer. Most aquatic<br />

experts (e.g. Cureton, 1943, The USA Navy, 1944, Lanoe, 1963, Wilke,<br />

2007, Stallman, 2008 ) consider breath<strong>in</strong>g <strong>in</strong> an optimal way, the most<br />

important aspect of efficient technique.<br />

Methods<br />

While quantify<strong>in</strong>g energy expenditure under the two conditions named<br />

above was the primary goal of the study, it was recognized that several<br />

factors might <strong>in</strong>fluence it. Factors considered possible confounders<br />

were: skill level, buoyancy, endurance, drag characteristics <strong>and</strong> motivation.<br />

From 40 volunteers, 20 were selected (12male, 8 female) to give a<br />

broad, representative sample with relation to buoyancy <strong>and</strong> ankle drag.<br />

This would reduce any bias because of these two factors. The subjects<br />

were university physical education students, average age 26.1 (range<br />

19.5-35.0).<br />

Buoyancy was determ<strong>in</strong>ed by hydrostatic weigh<strong>in</strong>g as described by<br />

Katch et al. (1967). As function was of greatest <strong>in</strong>terest, weight at both<br />

full <strong>in</strong>spiration <strong>and</strong> full expiration was recorded uncorrected for trapped<br />

air spaces <strong>and</strong> residual volume. Body density as determ<strong>in</strong>ed by Brozek et<br />

al. (1963) was calculated but not <strong>in</strong>cluded <strong>in</strong> the study. The term functional<br />

buoyancy (Stallman, 1971) is used for the uncorrected values.<br />

Ankle drag was measured as described by Cureton (1943). The subject<br />

adopted a stretched prone position, arms forward <strong>and</strong> together, with full<br />

<strong>in</strong>spiration. A Salter spr<strong>in</strong>g scale registered the weight of the ankles rest<strong>in</strong>g<br />

on a horizontal rod just below the surface, heels under water. Skill<br />

level was def<strong>in</strong>ed by a composite of two values: the number of strokes<br />

required to swim 25m (as few as possible) <strong>and</strong> the fastest time possible<br />

for 25m. Twenty five meters was chosen to m<strong>in</strong>imize the <strong>in</strong>fluence of<br />

endurance <strong>and</strong> to maximize the <strong>in</strong>fluence of technical skill. All trials<br />

were repeated 3 times <strong>and</strong> the best performance was used <strong>in</strong> the analysis.<br />

Energy cost was measured by classical Douglas Bag respirometry<br />

while swimm<strong>in</strong>g <strong>in</strong> a flume. The sub-maximal velocity of 0.5 m·s -1 was<br />

used for all subjects. If this velocity resulted <strong>in</strong> unusually high levels of<br />

plasma lactate, the subject was elim<strong>in</strong>ated. Given that these were physical<br />

education students, few were elim<strong>in</strong>ated for this reason. The subjects<br />

swam approximately 10 m<strong>in</strong>. unh<strong>in</strong>dered to reach a steady state. They<br />

then immediately entered the flume where they swam for approximately<br />

3 m<strong>in</strong>. with gas collection dur<strong>in</strong>g the last m<strong>in</strong>. This same operation was<br />

repeated twice for each subject. Half of the group was r<strong>and</strong>omly selected<br />

to swim first with the head up while the other half swam first with normal<br />

breath<strong>in</strong>g. A blood sample to determ<strong>in</strong>e plasma lactate levels (La)<br />

was taken after each trial.<br />

Lastly, the ability to swim for a longer period of time (simulat<strong>in</strong>g a<br />

survival situation) was measured by swimm<strong>in</strong>g to exhaustion. It was hypothesized<br />

that when swimm<strong>in</strong>g with the head up, the swimm<strong>in</strong>g time<br />

to exhaustion would be shorter. Each subject swam to exhaustion on<br />

two different occasions. Aga<strong>in</strong>, half r<strong>and</strong>omly with head up first <strong>and</strong> half<br />

with normal breath<strong>in</strong>g first. The subject swam easily first for 5 m<strong>in</strong>. Then<br />

five m<strong>in</strong>. at 0.5 m·s -1 . If the subject was able to cont<strong>in</strong>ue, the velocity was<br />

<strong>in</strong>creased by 10% <strong>and</strong> they swam for an additional two m<strong>in</strong>. If after these<br />

two m<strong>in</strong>. the subject was still swimm<strong>in</strong>g, the velocity was aga<strong>in</strong> <strong>in</strong>creased<br />

by 10%. They swam <strong>in</strong> military trousers <strong>and</strong> shirts.<br />

380<br />

results<br />

When swimm<strong>in</strong>g with the face constantly above the surface, the oxygen<br />

uptake (VO 2 ) expressed <strong>in</strong> ml/meter was significantly higher than with<br />

normal breath<strong>in</strong>g (p=


not related to VO 2 , HR or La, thus the differences observed are most<br />

likely caused by a real <strong>in</strong>crease <strong>in</strong> swimm<strong>in</strong>g body angle <strong>and</strong> <strong>in</strong>creased<br />

resistance.<br />

conclusIon<br />

Significantly less energy is used when swimm<strong>in</strong>g breaststroke with the<br />

normal breath<strong>in</strong>g pattern than with the head always up. This seems to<br />

justify the emphasis on master<strong>in</strong>g breath<strong>in</strong>g techniques which most<br />

aquatic professionals would support. This is one example of how improved<br />

technique can have a real effect on potential survival <strong>in</strong> a life<br />

threaten<strong>in</strong>g situation.<br />

reFerences<br />

Brozek, J., Gr<strong>and</strong>e, F., Anderson, J. & Keys A. (1963). Densiometric<br />

analysis of body composition: Revision of some quantitative assumptions.<br />

Annals of the New York Academy of Science 110:96-108, sept.<br />

Cureton, T.K. (1943). Warfare Aquatics. Champaign, IL, Stipes Publish<strong>in</strong>g<br />

Katch, F., Michael, E. & Horvath, S. (1967). Estimation of body volume<br />

<strong>in</strong> assessment of body composition by under water weigh<strong>in</strong>g: description<br />

of a simple method. J Appl Physiol, 23:811-813, Nov<br />

Langendorfer, S.J. & Bruya, L.D. (1995). Aquatic Read<strong>in</strong>ess. Champaign,<br />

IL, Human K<strong>in</strong>etics<br />

Lanoe, F. (1963). Drownproof<strong>in</strong>g. Englewood Cliffs, NJ. Prentiss – Hall<br />

S<strong>in</strong>clair, A. & Henry H. (1893). Swimm<strong>in</strong>g. London, Longmans<br />

Skullberg, A. (1985). Mennesker og vann (Man & water). Norwegian<br />

Maritime Directory.<br />

Stallman, R.K. (1971). The relationship of body density <strong>and</strong> selected anthropometric<br />

measures to the acquisition of beg<strong>in</strong>n<strong>in</strong>g swimm<strong>in</strong>g skills.<br />

Unpublished PhD thesis, Univ. Of Ill<strong>in</strong>ois, Champaign, IL<br />

Stallman, R.K., Junge M. & Blixt T. (2008). The teach<strong>in</strong>g of swimm<strong>in</strong>g<br />

based on a model derived from the causes of drown<strong>in</strong>g. Int J of Aquatic<br />

Research <strong>and</strong> Educ. 2(4), 372-382.<br />

Thomas, R. (1904). Swimm<strong>in</strong>g. London, UK: Sampson, Low, Marston<br />

Whit<strong>in</strong>g, H.T.A. (1971). The persistant non-swimmer. London, Museum<br />

Press<br />

Wilke, K. (2007). Schwimmen Lernen. Aachen, Germany, Meyer &<br />

Meyer Verlag<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

Post-exercise Hypotension <strong>and</strong> Blood Lipoprote<strong>in</strong><br />

Changes follow<strong>in</strong>g Swimm<strong>in</strong>g Exercise<br />

tanaka, h., sommerlad, s.M., renzi, c.P., Barnes, J.n., <strong>and</strong><br />

nualnim, n.<br />

The University of Texas at Aust<strong>in</strong>, USA<br />

It is not known whether an acute bout of swimm<strong>in</strong>g exercise results <strong>in</strong><br />

similar changes <strong>in</strong> risk factors for coronary heart disease. To address this<br />

question, a total of 20 apparently healthy subjects were studied. Each<br />

subject performed 3 experimental sessions (time control, runn<strong>in</strong>g exercise,<br />

<strong>and</strong> swimm<strong>in</strong>g exercise) separated by at least one week. Brachial<br />

blood pressure did not change after the 3 sessions. However, both runn<strong>in</strong>g<br />

<strong>and</strong> swimm<strong>in</strong>g produced significant decreases <strong>in</strong> ankle blood pressure<br />

compared with the time control (P


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

swim were excluded from the study. All subjects were non-smokers,<br />

non-obese, <strong>and</strong> free of overt cardiovascular or other chronic diseases<br />

as assessed by medical history. None of the subjects were tak<strong>in</strong>g cardiovascular-act<strong>in</strong>g<br />

medications. The Human Research Committee reviewed<br />

<strong>and</strong> approved all procedures, <strong>and</strong> written <strong>in</strong>formed consent was<br />

obta<strong>in</strong>ed from all subjects.<br />

Procedures. Subjects came <strong>in</strong>to the laboratory after 12 hours fast<strong>in</strong>g.<br />

Each subject performed all 3 experimental sessions (time control,<br />

runn<strong>in</strong>g exercise, <strong>and</strong> swimm<strong>in</strong>g exercise) r<strong>and</strong>omized <strong>and</strong> separated by<br />

at least one week. Dur<strong>in</strong>g the time control sessions, subjects sat <strong>in</strong> a<br />

temperature-controlled laboratory room. The exercise protocol for the<br />

swimm<strong>in</strong>g <strong>and</strong> runn<strong>in</strong>g sessions consisted of <strong>in</strong>terval tra<strong>in</strong><strong>in</strong>g exercises<br />

at an <strong>in</strong>tensity of ~75% of heart rate reserve determ<strong>in</strong>ed from the graded<br />

exercise test. The target heart rate dur<strong>in</strong>g swimm<strong>in</strong>g was adjusted on<br />

the basis of the observation that maximal heart rate dur<strong>in</strong>g swimm<strong>in</strong>g<br />

is ~10-13 bpm lower than that dur<strong>in</strong>g runn<strong>in</strong>g (Magel et al., 1975). The<br />

<strong>in</strong>tervals were five 10-m<strong>in</strong>ute bouts of exercise with 1 m<strong>in</strong>ute of rest between<br />

each bout (for a total for 54 m<strong>in</strong>utes). Dur<strong>in</strong>g pilot studies, many<br />

subjects expressed difficulty <strong>in</strong> swimm<strong>in</strong>g cont<strong>in</strong>uously for a prolonged<br />

period of time. This necessitated the implementation of the <strong>in</strong>terval<br />

exercise format for the present study. All subjects wore a waterproof<br />

heart rate monitor to ma<strong>in</strong>ta<strong>in</strong> the desired <strong>in</strong>tensity of exercise as well<br />

as to document exercise heart rate. Subjects used the freestyle technique<br />

<strong>in</strong> an <strong>in</strong>door swimm<strong>in</strong>g pool. Dur<strong>in</strong>g the runn<strong>in</strong>g session, subjects ran<br />

on a treadmill <strong>in</strong> a temperature-controlled room. Dur<strong>in</strong>g both exercise<br />

sessions, subjects consumed a st<strong>and</strong>ard amount of water. We made an<br />

attempt to <strong>in</strong>clude a sham control session, <strong>in</strong> which subjects floated <strong>in</strong><br />

the <strong>in</strong>door swimm<strong>in</strong>g pool us<strong>in</strong>g a floatation device. But this session<br />

was ab<strong>and</strong>oned due to excessive heat loss <strong>and</strong> the resultant reduction <strong>in</strong><br />

body temperature.<br />

Blood pressure was measured before each session non<strong>in</strong>vasively<br />

three times <strong>in</strong> the laboratory by the arm <strong>and</strong> ankle cuff techniques (Omron<br />

VP-2000, Bannockburn, IL) after the subject had been quietly ly<strong>in</strong>g<br />

<strong>in</strong> a sup<strong>in</strong>e position for at least 10-15 m<strong>in</strong>utes. In order to elim<strong>in</strong>ate<br />

<strong>in</strong>vestigator bias, arterial blood pressure was measured automatically<br />

with modified oscillometric pressure sensors <strong>in</strong>corporated <strong>in</strong> extremity<br />

cuffs. The validity <strong>and</strong> reliability of measur<strong>in</strong>g ankle blood pressure<br />

us<strong>in</strong>g this automated device have previously been reported by our laboratory<br />

(Cortez-Cooper et al., 2003). The blood pressure measurements<br />

were repeated after exercise at 15-m<strong>in</strong>ute <strong>in</strong>tervals to 60 m<strong>in</strong>utes with<br />

the subject ly<strong>in</strong>g <strong>in</strong> the sup<strong>in</strong>e position. Brachial-ankle pulse wave velocity,<br />

a measure of arterial stiffness, was measured us<strong>in</strong>g the automatic<br />

device (Omron VP-2000). A blood sample was taken before <strong>and</strong> after<br />

the exercise protocols for later enzymatic analyses of plasma lipid <strong>and</strong><br />

lipoprote<strong>in</strong> concentrations.<br />

In order to provide <strong>in</strong>sight <strong>in</strong>to the physiological mechanisms underly<strong>in</strong>g<br />

the hypothesized reductions <strong>in</strong> blood pressure, an echocardiogram<br />

us<strong>in</strong>g the ultrasound mach<strong>in</strong>e (Philips iE33, Bothel, WA) was<br />

performed to assess stroke volume <strong>and</strong> cardiac output. Stroke volume<br />

was calculated from the product of the cross-sectional area of the aortic<br />

orifice (π*(aortic diameter/2)²) <strong>and</strong> the mean velocity time <strong>in</strong>tegral. Cardiac<br />

output was calculated from the product of stroke volume <strong>and</strong> heart<br />

rate recorded dur<strong>in</strong>g the echocardiogram.<br />

Based on the previous f<strong>in</strong>d<strong>in</strong>g that the attenuation of heat loss was<br />

associated with the magnitude of postexercise hypotension (Frankl<strong>in</strong><br />

et al., 1993), core body temperature was measured dur<strong>in</strong>g exercise<br />

through the use of the CorTemp disposable temperature sensor <strong>and</strong> the<br />

data recorder (HQ, Palmeto, FL). Body fat percentage was measured<br />

non-<strong>in</strong>vasively by dual energy X-ray absorptiometry (DEXA). Maximal<br />

oxygen consumption was measured us<strong>in</strong>g a metabolic cart dur<strong>in</strong>g a<br />

modified-Bruce protocol.<br />

Statistical Analyses. ANOVA <strong>and</strong> MANOVA with repeated measures<br />

were used for statistical analyses, <strong>and</strong> Newman-Keuls post-hoc<br />

tests were used to identify significant differences. All data are expressed<br />

as mean±SEM.<br />

382<br />

results<br />

Basel<strong>in</strong>e blood pressure values were not different between the time control,<br />

runn<strong>in</strong>g <strong>and</strong> swimm<strong>in</strong>g sessions. Brachial blood pressure did not<br />

change significantly after all 3 sessions. Both runn<strong>in</strong>g <strong>and</strong> swimm<strong>in</strong>g<br />

produced significant decreases <strong>in</strong> ankle mean blood pressure compared<br />

with the time control (P


Table 2. Plasma lipid <strong>and</strong> lipoprote<strong>in</strong> concentrations<br />

Control Runn<strong>in</strong>g Swimm<strong>in</strong>g<br />

Pre Post Pre Post Pre Post<br />

Total C (mg/dl) 161±8 163±6 166±13 163±12 158±10 160±10<br />

HDL-C (mg/dl) 58±5 58±7 59±6 66±8 58±7 64±8<br />

LDL-C (mg/dl) 85±7 88±6 90±12 80±12 82±8 80±10<br />

VLDL-C (mg/dl) 20±4 18±4 14±2 18±1 18±3 17±3<br />

Triglyceride (mg/dl) 93±13 87±16 81±10 88±8 87±13 83 ±12<br />

C=cholesterol<br />

dIscussIon<br />

A number of studies have documented the changes <strong>in</strong> blood pressure <strong>and</strong><br />

lipoprote<strong>in</strong>s follow<strong>in</strong>g acute bouts of l<strong>and</strong>-based exercise, <strong>in</strong>clud<strong>in</strong>g walk<strong>in</strong>g,<br />

runn<strong>in</strong>g, <strong>and</strong> cycl<strong>in</strong>g (Kenny & Seals, 1993; Durst<strong>in</strong>e et al., 2002;<br />

Williams et al., 2005). However, little or no <strong>in</strong>formation is available regard<strong>in</strong>g<br />

whether an acute bout of swimm<strong>in</strong>g would evoke changes <strong>in</strong> risk<br />

factors for cardiovascular disease. In order to properly address this question,<br />

we provided a l<strong>and</strong>-based exercise control session <strong>in</strong> addition to the<br />

time control session. This allowed us to compare a water-based exercise<br />

with a l<strong>and</strong>-based exercise. The results of the present study <strong>in</strong>dicate that<br />

overall post-exercise responses were not different between runn<strong>in</strong>g <strong>and</strong><br />

swimm<strong>in</strong>g.<br />

Swimm<strong>in</strong>g is an attractive form of exercise as it is easily accessible,<br />

<strong>in</strong>expensive, <strong>and</strong> isotonic (Tanaka, 2009). Because it is a non-weightbear<strong>in</strong>g<br />

activity due to the buoyancy provided by water, adverse effects on<br />

the musculo-skeletal system are rare (Becker & Cole, 1998). In marked<br />

contrast to the widespread popularity of swimm<strong>in</strong>g exercise, research focus<strong>in</strong>g<br />

on swimm<strong>in</strong>g <strong>in</strong> general, <strong>and</strong> on swimm<strong>in</strong>g <strong>and</strong> risk factors for cardiovascular<br />

disease <strong>in</strong> particular, is rare (Tanaka, 2009). To the best of our<br />

knowledge, this is the first study to evaluate the post-exercise responses<br />

<strong>in</strong> blood pressure <strong>and</strong> lipoprote<strong>in</strong>s follow<strong>in</strong>g an acute bout of swimm<strong>in</strong>g.<br />

An <strong>in</strong>terest<strong>in</strong>g <strong>and</strong> rather surpris<strong>in</strong>g f<strong>in</strong>d<strong>in</strong>g of the present study was<br />

that post exercise hypotension was observed only <strong>in</strong> the leg (posterior<br />

tibialis artery) <strong>and</strong> no such changes were seen <strong>in</strong> the arm (brachial artery).<br />

It has been well established that mean arterial blood pressure is<br />

similar <strong>in</strong> all conduit arteries <strong>in</strong> the rest<strong>in</strong>g or basal condition (Kroeker<br />

& Wood, 1955). But it is plausible that local vasodilation may be more<br />

pronounced <strong>in</strong> the lower limbs after exercise contribut<strong>in</strong>g to a reduction<br />

<strong>in</strong> ankle blood pressure. Indeed, the reduction <strong>in</strong> ankle MAP appears<br />

to be mediated by reductions <strong>in</strong> total peripheral resistance as cardiac<br />

output did not decrease <strong>and</strong> arterial stiffness, as assessed by pulse wave<br />

velocity, did not change.<br />

On the other h<strong>and</strong>, it is not clear why a reduction <strong>in</strong> blood pressure<br />

was not observed <strong>in</strong> the brachial artery, especially <strong>in</strong> the runn<strong>in</strong>g session.<br />

A lack of change <strong>in</strong> brachial blood pressure may be related to the exercise<br />

protocol (e.g., <strong>in</strong>terval exercise mode, exercise <strong>in</strong>tensity) <strong>and</strong>/or subject<br />

characteristics (e.g., young, normo-tensive). However, post exercise hypotension<br />

has been observed <strong>in</strong> young healthy normo-tensive populations<br />

(Kenny & Seals, 1993; Williams et al., 2005) similar to our subjects. Additionally,<br />

post-exercise hypotension does not seem dependent upon exercise<br />

<strong>in</strong>tensity or exercise duration (Kenny & Seals, 1993), <strong>and</strong> <strong>in</strong>terval<br />

exercise appears to be as effective as cont<strong>in</strong>uous exercise <strong>in</strong> elicit<strong>in</strong>g post<br />

exercise hypotension (Wilcox et al., 1982). Further <strong>in</strong>vestigations <strong>in</strong>volv<strong>in</strong>g<br />

hypertensive populations are warranted.<br />

No changes <strong>in</strong> serum cholesterol concentrations were observed after<br />

either exercise mode though there was a tendency for HDL-cholesterol to<br />

<strong>in</strong>crease. The results are generally consistent with the only other study <strong>in</strong><br />

the literature that exam<strong>in</strong>ed the effect of an acute bout of swimm<strong>in</strong>g exercise<br />

on blood lipids <strong>and</strong> lipoprote<strong>in</strong>s (Ohkuwa & Itoh, 1993). Ohkuwa<br />

& Itoh, (1993) reported that HDL-cholesterol was significantly <strong>in</strong>creased<br />

follow<strong>in</strong>g an acute bout of swimm<strong>in</strong>g that <strong>in</strong>cluded 30 m<strong>in</strong>utes of warmup<br />

swimm<strong>in</strong>g <strong>and</strong> a 100m swim time trial, whereas total cholesterol <strong>and</strong><br />

LDL-cholesterol did not change <strong>in</strong> 10 male adolescent tra<strong>in</strong>ed swimmers.<br />

It should be noted that <strong>in</strong> the present study, because a blood sample was<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

obta<strong>in</strong>ed at only one po<strong>in</strong>t (60 m<strong>in</strong>utes after exercise), there is a possibility<br />

that we may have missed significant changes that may have occurred<br />

before or after the blood sampl<strong>in</strong>g.<br />

conclusIons<br />

In summary, the results of the present study suggest that post exercise responses<br />

<strong>in</strong> blood pressure <strong>and</strong> blood cholesterol are not different between<br />

runn<strong>in</strong>g <strong>and</strong> swimm<strong>in</strong>g <strong>and</strong> that both exercises <strong>in</strong>duced significant post<br />

exercise hypotension <strong>in</strong> the leg but not <strong>in</strong> the arm.<br />

reFerences<br />

Becker, B.E. & Cole A.J. (1998). Aquatic Rehabilitation. In Rehabilitation<br />

<strong>Medic<strong>in</strong>e</strong>: Pr<strong>in</strong>ciples <strong>and</strong> Practice, Third Edition, ed. DeLisa JA & Gans<br />

BM, pp. 887-901. Lipp<strong>in</strong>cott-Raven, Philadelphia, PA.<br />

Chen, J., Gu, D., Jaquish, C.E., Chen, C.S., Rao, D.C., Liu, D., Hixson,<br />

J.E., Hamm, L.L., Gu, C.C., Whelton, P.K. & He, J. (2008). Association<br />

between blood pressure responses to the cold pressor test <strong>and</strong><br />

dietary sodium <strong>in</strong>tervention <strong>in</strong> a Ch<strong>in</strong>ese population. Arch Intern Med<br />

168, 1740-1746.<br />

Cortez-Cooper, MY., Supak, J.A. & Tanaka, H. (2003). A new device for<br />

automatic measurements of arterial stiffness <strong>and</strong> ankle-brachial <strong>in</strong>dex.<br />

Am J Cardiol 91, 1519-1522, A1519.<br />

Durst<strong>in</strong>e, J.L., Gr<strong>and</strong>jean, P.W., Cox, C.A. & Thompson, P.D. (2002).<br />

Lipids, lipoprote<strong>in</strong>s, <strong>and</strong> exercise. J Cardiopulm Rehabil 22, 385-398.<br />

Frankl<strong>in</strong>, P.J., Green, D.J. & Cable, N.T. (1993). The <strong>in</strong>fluence of thermoregulatory<br />

mechanisms on post-exercise hypotension <strong>in</strong> humans. J<br />

Physiol 470, 231-241.<br />

Henriksen, E.J. (2002). Effects of acute exercise <strong>and</strong> exercise tra<strong>in</strong><strong>in</strong>g on<br />

<strong>in</strong>sul<strong>in</strong> resistance. J Appl Physiol 93, 788-796.<br />

Holmer, I., Ste<strong>in</strong>, E.M., Salt<strong>in</strong>, B., Ekblom, B. & Astr<strong>and</strong>, P.O. (1974).<br />

Hemodynamic <strong>and</strong> respiratory responses compared <strong>in</strong> swimm<strong>in</strong>g <strong>and</strong><br />

runn<strong>in</strong>g. J Appl Physiol 37, 49-54.<br />

Kenny, M.J. & Seals, D.R. (1993). Postexercise hypotension: key features,<br />

mechanisms, <strong>and</strong> cl<strong>in</strong>ical significance. Hypertension 22, 653-664.<br />

Kroeker, E.J. & Wood, E.I. (1955). Comparison of simultaneously recorded<br />

central <strong>and</strong> peripheral arterial pressure pulses dur<strong>in</strong>g rest, exercise<br />

<strong>and</strong> tilted position <strong>in</strong> man. Circ Res 3, 623-632.<br />

Magel, J.R., Foglia, G.F., McArdle, W.D., Gut<strong>in</strong>, B., Pechar, G.S. &<br />

Katch, F.I. (1975). Specificity of swim tra<strong>in</strong><strong>in</strong>g on maximum oxygen<br />

uptake. J Appl Physiol 38, 151-155.<br />

Ohkuwa, T. & Itoh, H. (1993). High density lipoprote<strong>in</strong> cholesterol follow<strong>in</strong>g<br />

anaerobic swimm<strong>in</strong>g <strong>in</strong> tra<strong>in</strong>ed swimmers. J Sports Med Phys<br />

Fitness 33, 200-202.<br />

Parker Jones, P., Davy, K.P., Desouza, C.A. & Tanaka, H. (1999). Total<br />

blood volume <strong>in</strong> endurance-tra<strong>in</strong>ed postmenopausal females: relation<br />

to exercise mode <strong>and</strong> maximal aerobic capacity. Acta Physiol Sc<strong>and</strong> 166,<br />

327-333.<br />

Tanaka, H. (2009). Swimm<strong>in</strong>g exercise: impact of aquatic exercise on cardiovascular<br />

health. Sports Med 39, 377-387.<br />

Tanaka, H. Bassett, D.R., Howley, E.T., Thompson, D.L., Ashraf, M.<br />

& Rawson, F.L. (1997). Swimm<strong>in</strong>g tra<strong>in</strong><strong>in</strong>g lowers the rest<strong>in</strong>g blood<br />

pressure <strong>in</strong> <strong>in</strong>dividuals with hypertension. J Hypertens 15, 651-657.<br />

Thompson, P.D., Crouse, S.F., Goodpaster, B., Kelleu, D., Moyna, N. &<br />

Pescatello, L. (2001). The acute versus the chronic response to exercise.<br />

<strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Science <strong>in</strong> Sports <strong>and</strong> Exercise 33, S438-S445.<br />

Wilcox, R.G., Bennett, T., Brown, A.M. & Macdonald I.A. (1982). Is<br />

exercise good for high blood pressure? Br Med J 285, 767-769.<br />

Williams, J.T., Pricher, M.P. & Halliwill, J.R. (2005). Is postexercise hypotension<br />

related to excess postexercise oxygen consumption through<br />

changes <strong>in</strong> leg blood flow? J Appl Physiol 98, 1463-1468.<br />

AcKnoWledGeMent<br />

This study is <strong>in</strong> part supported by the American Heart Association<br />

grant.<br />

383


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

A Conceptual Paper on the Benefits of a Non-<br />

Governmental Search <strong>and</strong> Rescue Organization<br />

Wengel<strong>in</strong>, M. 1 , de Wet, t. 2<br />

1Lund University, Department of Service Management, Hels<strong>in</strong>gborg, Sweden<br />

2National Lake Rescue Institute, Kampala, Ug<strong>and</strong>a<br />

This conceptual paper aims at discuss<strong>in</strong>g the characteristics of <strong>and</strong> differences<br />

between modern Western <strong>in</strong>dependent SAR <strong>in</strong>stitutions <strong>and</strong><br />

the <strong>in</strong>itiatives that have been taken <strong>in</strong> develop<strong>in</strong>g countries. It highlights<br />

the benefits of the non-governmental SAR organization, not only to<br />

provide search <strong>and</strong> rescue capacity, but also to be a vehicle of progress<br />

<strong>and</strong> change.<br />

Key words: search <strong>and</strong> rescue, safety at sea, poverty reduction<br />

IntroductIon<br />

Maritime Search <strong>and</strong> Rescue (SAR) is a state responsibility covered <strong>in</strong><br />

<strong>in</strong>ternational regulations such as the United Nations Convention on<br />

Law of the Sea (UNCLOS), the Safety of Life at Sea Convention (SO-<br />

LAS) <strong>and</strong> the 1979 SAR Convention. UNCLOS for example, says that<br />

every State must require the master of a ship fly<strong>in</strong>g its flag to render<br />

assistance to any person found at sea <strong>in</strong> danger of be<strong>in</strong>g lost <strong>and</strong> to proceed<br />

to the rescue of persons <strong>in</strong> distress. Furthermore, it requires every<br />

coastal State to promote the establishment, operation <strong>and</strong> ma<strong>in</strong>tenance<br />

of an adequate <strong>and</strong> effective search <strong>and</strong> rescue service regard<strong>in</strong>g safety<br />

on <strong>and</strong> over the sea <strong>and</strong>, where circumstances require, by way of mutual<br />

regional arrangements, to co-operate with neighbour<strong>in</strong>g States for this<br />

purpose. In this way, UNCLOS provides the legal framework for action.<br />

However, the details of search <strong>and</strong> rescue obligations are to be found<br />

<strong>in</strong> various International Maritime Organization (IMO) Conventions.<br />

The Search <strong>and</strong> Rescue (SAR) Convention of 1979 gives a clear<br />

def<strong>in</strong>ition of the term “rescue”. It <strong>in</strong>volves not only “an operation to retrieve<br />

persons <strong>in</strong> distress, provide for their <strong>in</strong>itial medical or other needs” but<br />

also to “deliver them to a place of safety”. This obligation to <strong>in</strong>itiate action<br />

is activated once the responsible authorities of a State Party receive <strong>in</strong>formation<br />

that any person is, or appears to be, <strong>in</strong> distress at sea. It further<br />

states that, once a State Party has accepted responsibility to provide<br />

search <strong>and</strong> rescue services for a specified area, it is obliged to use search<br />

<strong>and</strong> rescue units <strong>and</strong> other available facilities for provid<strong>in</strong>g assistance<br />

to anyone <strong>in</strong> distress at sea, <strong>and</strong> that such assistance is to be provided<br />

“regardless of the nationality or status of such a person or the circumstances <strong>in</strong><br />

which that person is found”.<br />

The Safety of Life at Sea Convention (SOLAS) spells out the obligation<br />

on ships’ masters to render assistance. It says:<br />

384<br />

“The master of a ship at sea which is <strong>in</strong> a position to be able to<br />

provide assistance, on receiv<strong>in</strong>g a signal from any source that<br />

persons are <strong>in</strong> distress at sea is bound to proceed with all speed<br />

to their assistance, if possible <strong>in</strong>form<strong>in</strong>g them or the search <strong>and</strong><br />

rescue service that the ship is do<strong>in</strong>g so.”<br />

Elsewhere, it stipulates that contract<strong>in</strong>g Governments should undertake<br />

measures “to ensure that necessary arrangements are made for the rescue of<br />

persons <strong>in</strong> distress at sea around its coasts.”<br />

In most of the developed world, with a high level of commercial traffic<br />

<strong>and</strong> leisure boat<strong>in</strong>g, this responsibility is h<strong>and</strong>led by a comb<strong>in</strong>ation of<br />

governmental organizations (Coast Guard, Naval units, Mar<strong>in</strong>e Police,<br />

Pilots etc) <strong>and</strong> non-governmental SAR specialists like the Royal National<br />

Lifeboat Institute (RNLI) of the Netherl<strong>and</strong>s, The German Sea<br />

Rescue Society (DGzRS) <strong>and</strong> the Swedish Sea Rescue Society (SSRS).<br />

In the develop<strong>in</strong>g world this is not usually the case. The SAR is <strong>in</strong> many<br />

cases covered by a small <strong>and</strong> not always operative navy <strong>in</strong> comb<strong>in</strong>ation<br />

with Coast Guard <strong>in</strong> areas with commercial traffic or areas with national<br />

strategic importance. In areas with a high density of tourism there might<br />

be found occasional SAR units specialized <strong>in</strong> tak<strong>in</strong>g care of tourism<br />

related accidents like scuba div<strong>in</strong>g cases (Egypt, Red Sea) with a focus<br />

on medical evacuation. With the ma<strong>in</strong> part of the commercial traffic <strong>and</strong><br />

tourism areas basically taken care of, there is one large group of seafarers<br />

left. Who is look<strong>in</strong>g out for the <strong>in</strong>dividual, local, artisanal small-scale<br />

fisherman <strong>in</strong> the small boat, outrigger or canoe?<br />

“In some countries little consideration is given to SAR services for<br />

small scale or artisanal fishermen due to <strong>in</strong>sufficient awareness,<br />

lack of resources, lack of personnel knowledgeable about mar<strong>in</strong>e<br />

safety problems, lack of suitable craft, geographical considerations<br />

(e.g. numerous remote isl<strong>and</strong>s), <strong>in</strong>adequate technical l<strong>and</strong> <strong>in</strong>stitutional<br />

<strong>in</strong>frastructure <strong>and</strong> other reasons. Because many fishermen<br />

are not politically powerful, <strong>and</strong> because there are no compell<strong>in</strong>g<br />

statistics on losses, this issue is often overlooked though,<br />

more recently, fishermen have become more active <strong>in</strong> push<strong>in</strong>g such<br />

services or organiz<strong>in</strong>g them on their own.” The International Labor<br />

Organization (ILO 1999)<br />

Compet<strong>in</strong>g with urgent issues such as combat<strong>in</strong>g diseases like AIDS<br />

<strong>and</strong> malaria, environmental problems, <strong>in</strong>sufficient <strong>in</strong>frastructure <strong>and</strong><br />

<strong>in</strong>vestments <strong>in</strong> the military due to <strong>in</strong>ternal or regional <strong>in</strong>stability, the<br />

<strong>in</strong>vestments <strong>in</strong> a functional SAR network that reaches the outback fish<strong>in</strong>g<br />

village is not high on the priority list. It is also not unusual that a<br />

most urgent need for <strong>and</strong> responsibility for SAR is a borderl<strong>in</strong>e problem<br />

somehow situated between different m<strong>in</strong>istries, as is even the case <strong>in</strong> the<br />

<strong>in</strong>ternational arena, a Department of Shipp<strong>in</strong>g (or the IMO) on the one<br />

h<strong>and</strong> <strong>and</strong> a Department of Fish<strong>in</strong>g or Fish<strong>in</strong>g Authority Organization<br />

on the other. It is furthermore common to categorize maritime search<br />

<strong>and</strong> rescue as be<strong>in</strong>g the most expensive method of sav<strong>in</strong>g lives at sea.<br />

This is, however, a very limited view on SAR <strong>and</strong> is usually put forward<br />

by non SAR professionals. SAR as an operation is the last resort; that<br />

is, carry<strong>in</strong>g out search <strong>and</strong> rescue; to f<strong>in</strong>d <strong>and</strong> save a person <strong>in</strong> distress.<br />

Isolated, this can be seen as a costly exercise, <strong>and</strong> if focus<strong>in</strong>g on high<br />

tech operations with helicopters <strong>and</strong> rescue cruisers it is certa<strong>in</strong>ly rather<br />

expensive. But there is another side of the co<strong>in</strong>. A SAR organization<br />

<strong>and</strong> especially non-governmental ones, works actively to avoid SAR<br />

operations through activities like education, <strong>in</strong>formation, tra<strong>in</strong><strong>in</strong>g, <strong>and</strong><br />

awareness campaigns. These are activities acknowledged as important<br />

for safety at sea (ibid), <strong>and</strong> should be an <strong>in</strong>tegrated part of a SAR system.<br />

A governmental SAR organization, where SAR usually is one of<br />

many tasks, can use the power of regulations when such are <strong>in</strong> place. A<br />

non-governmental organization works more closely with the community,<br />

often actively supported by the community where it is based. From<br />

this perspective SAR is more broadly def<strong>in</strong>ed; sav<strong>in</strong>g lives starts with<br />

knowledge <strong>and</strong> tra<strong>in</strong><strong>in</strong>g, <strong>and</strong> the costs of a SAR organization are thus<br />

seen <strong>in</strong> another light. The specialized competence embedded <strong>in</strong> a SAR<br />

organization is beneficial through the entire cha<strong>in</strong> of “sav<strong>in</strong>g lives”, from<br />

promot<strong>in</strong>g life jackets to actually search<strong>in</strong>g <strong>and</strong> rescu<strong>in</strong>g.<br />

The purposes of this paper are thus i) to highlight the role of the<br />

SAR organization (especially non-governmental) with<strong>in</strong> the broader<br />

perspective of life sav<strong>in</strong>g <strong>and</strong> poverty reduction, ii) to describe the function<br />

of the typical non-governmental SAR organization, <strong>and</strong> iii) to describe<br />

the case study of the National Lake Rescue Institute (NLRI, the<br />

non-governmental SAR organization <strong>in</strong> Ug<strong>and</strong>a).<br />

Methods<br />

This paper is based on qualitative evaluation of an exist<strong>in</strong>g system<br />

of SAR organized by the National Lake Rescue Institute of Ug<strong>and</strong>a<br />

(NLRI). It is also an evaluation of the operation of this organization as a<br />

Non-Governmental Organization as compared to SAR organizations <strong>in</strong><br />

developed countries as well as governmental agencies. The material used


for this paper is a comb<strong>in</strong>ation of operational experience from the East<br />

Africa region <strong>and</strong> field material derived from a safety at sea project <strong>in</strong>itiated<br />

by the Lake Victoria Bas<strong>in</strong> Commission. It is therefore based upon<br />

participatory observations, <strong>in</strong>terviews, <strong>and</strong> <strong>in</strong> regard to the legislative<br />

background, a review of relevant rules <strong>and</strong> regulations. Case studies are<br />

presented of a SAR non-governmental organization from the developed<br />

world <strong>and</strong> one from the develop<strong>in</strong>g world.<br />

descrIPtIon oF sAr orGAnIZAtIons: FroM A<br />

deVeloPed countrY And FroM A deVeloPInG<br />

countrY<br />

SAR operations are dependent on an equation based on survivability<br />

<strong>and</strong> time. Survivability is a function of local conditions like water temperature,<br />

ability to swim, <strong>and</strong> the use of life sav<strong>in</strong>g equipment. This part<br />

of the equation thus provides us with an idea of how long a person <strong>in</strong><br />

distress can survive. Time is a function of distance <strong>and</strong> speed of the<br />

rescuer. Put very simply the two are l<strong>in</strong>ked together; the longer the<br />

survivability the longer the time the rescue mission can take, either to<br />

cover longer distances or perform<strong>in</strong>g with lesser speed. On Lake Victoria,<br />

for example, with an average water temperature of 24-26 degrees<br />

centigrade, the problem of hypothermia is not an immediate concern.<br />

However, with limited swimm<strong>in</strong>g ability <strong>and</strong> experience, <strong>and</strong> the lack of<br />

personal flotation devices (life jackets) or other life sav<strong>in</strong>g devices, survivability<br />

is still low. Paired with an almost total lack of rescue capacity<br />

the situation becomes very serious.<br />

A recent example from a ferry accident on Lake Victoria shows a<br />

less than 50% survivability even though many local fishermen came to<br />

the rescue - 26 of 50 passengers drowned. Here the SAR organization<br />

has a task to fill, decreas<strong>in</strong>g the number of accidents <strong>and</strong> <strong>in</strong>creas<strong>in</strong>g the<br />

survivability when an accident does occur. Be<strong>in</strong>g <strong>in</strong> place with dedicated<br />

resources for search <strong>and</strong> rescue, it can also save lives when all the other<br />

<strong>in</strong>itiatives have been fruitless.<br />

SAR organisations are <strong>in</strong> many countries run as voluntary organisations,<br />

or as Non-Governmental Organizations (NGO’s). A nongovernmental<br />

SAR association can assume full responsibility for all<br />

SAR operations <strong>in</strong> coastal waters, with special emphasis on sav<strong>in</strong>g lives<br />

among the fish<strong>in</strong>g population or leisure boaters (the non IMO fleet).<br />

Operat<strong>in</strong>g models for this are available <strong>in</strong> several countries around the<br />

world. The normal setup is a national association with a small coord<strong>in</strong>at<strong>in</strong>g<br />

head office, also responsible for fundrais<strong>in</strong>g. The SAR stations<br />

are locally adm<strong>in</strong>istered units supported by the mother organization.<br />

There exist different examples of levels of governmental support <strong>and</strong><br />

the share of voluntary <strong>in</strong>volvement. In Norway the government supports<br />

the Norwegian Sea Rescue Society enabl<strong>in</strong>g it to run 24 permanently<br />

manned rescue stations. Another 14 rescue stations are manned<br />

with tra<strong>in</strong>ed voluntary crews funded by memberships <strong>and</strong> donations.<br />

In Sweden, the Swedish Sea Rescue Society (SSRS), founded <strong>in</strong> 1907,<br />

<strong>and</strong> hence hav<strong>in</strong>g celebrated it’s 100 th anniversary <strong>in</strong> 2007, is one of the<br />

world’s lead<strong>in</strong>g <strong>in</strong>dependent SAR organizations. The SSRS operates<br />

approximately 64 rescue stations with about 140 rescue craft manned<br />

by some 1800 volunteers. All boats have been f<strong>in</strong>anced through private<br />

donations from <strong>in</strong>dividuals <strong>and</strong> organisations or through local fundrais<strong>in</strong>g.<br />

This model is extremely successful; tak<strong>in</strong>g care of more than 70%<br />

of all emergencies relayed through the Maritime Rescue Coord<strong>in</strong>ation<br />

Center (MRCC) <strong>in</strong> Gothenburg. The Swedish Sea Rescue Society<br />

receives no contributions at all from taxes or public funds, but is exempted<br />

from value added tax <strong>in</strong> regard to costs directly related to SAR<br />

operations. The examples above have one th<strong>in</strong>g <strong>in</strong> common; the volunteer<br />

part of the work is performed by <strong>in</strong>dividuals with basically a stable<br />

<strong>in</strong>come <strong>and</strong> a permanent liv<strong>in</strong>g place. Their engagement replaces other<br />

leisure activities; <strong>in</strong>stead of play<strong>in</strong>g tennis you spend a couple of hours a<br />

week ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the rescue boat <strong>and</strong> tra<strong>in</strong><strong>in</strong>g with the rest of the crew.<br />

Your professional life allows you to be on st<strong>and</strong>-by <strong>and</strong> to man the rescue<br />

boat with<strong>in</strong> 15 m<strong>in</strong>utes from a call-out. This can be compared to a<br />

“Volunteer Fire Brigade”. Furthermore, the potential “clients” have the<br />

chaPter6.medic<strong>in</strong>e<strong>and</strong>watersafety<br />

f<strong>in</strong>ancial strength to contribute to the organization through donations,<br />

gifts <strong>and</strong>/or membership.<br />

In develop<strong>in</strong>g countries the liv<strong>in</strong>g conditions are different, someth<strong>in</strong>g<br />

that has to have an impact on how a rescue service is set up. A<br />

permanent <strong>and</strong> paid professional crew is required to ensure that there<br />

is a guaranteed core of competence. This will enable the SAR service<br />

to build competence, to ma<strong>in</strong>ta<strong>in</strong> a high level of tra<strong>in</strong><strong>in</strong>g <strong>and</strong> over time<br />

ga<strong>in</strong> necessary experience. Complemented with a group of volunteers <strong>in</strong><br />

tra<strong>in</strong><strong>in</strong>g, to be used for activities <strong>in</strong> addition to the core SAR operations;<br />

this comb<strong>in</strong>ation will create flexibility, redundancy, <strong>and</strong> a high state of<br />

preparedness.<br />

In December 2006 the first volunteer rescue station <strong>in</strong> East Africa<br />

was launched as a part of the National Lake Rescue Institute (NLRI)<br />

<strong>in</strong> Ug<strong>and</strong>a. As a true development station it went <strong>in</strong>to operation on the<br />

border lake between Ug<strong>and</strong>a <strong>and</strong> the Democratic Republic of Congo,<br />

Lake Albert. The station itself was built upon two 40 ft steel conta<strong>in</strong>ers<br />

<strong>and</strong> the rescue craft a locally built wooden boat with a 25 hp outboard<br />

eng<strong>in</strong>e. The crew was <strong>in</strong>itially all volunteer local fishermen tra<strong>in</strong>ed by<br />

an <strong>in</strong>ternational SAR volunteer from the Swedish Sea Rescue Society.<br />

S<strong>in</strong>ce its establishment the Lake Albert rescue station <strong>in</strong> Kaiso alone<br />

has saved more than 255 people <strong>in</strong> distress (no data exist however, for<br />

people saved by wear<strong>in</strong>g an NLRI lifejacket). For the NLRI this establishment<br />

was a milestone. After nearly five years of struggle the first<br />

station outside its headquarters was at last <strong>in</strong> operation. Soon to follow<br />

was a partnership station with the Ug<strong>and</strong>an Wildlife Authority (UWA)<br />

<strong>in</strong> Queen Elisabeth National Park, where the equipment <strong>and</strong> tra<strong>in</strong><strong>in</strong>g<br />

were provided by NLRI <strong>and</strong> the crew consisted of UWA park rangers.<br />

S<strong>in</strong>ce then more stations have followed, partnership stations as well as<br />

<strong>in</strong>dependent stations, <strong>and</strong> today more than 50 crew members have been<br />

tra<strong>in</strong>ed towards an <strong>in</strong>ternationally accepted st<strong>and</strong>ard.<br />

Putt<strong>in</strong>g the NLRI <strong>in</strong>itiative <strong>in</strong> perspective it <strong>in</strong>itially focused on<br />

Lake Victoria, where the number of casualties ranges up to an estimated<br />

5000 per year. A tra<strong>in</strong>ed crew, based on NLRI headquarter employed<br />

personnel, manned a small boat with a 25 hp outboard eng<strong>in</strong>e based just<br />

outside the Ug<strong>and</strong>an capital, Kampala. When a corporate social responsibility<br />

project, f<strong>in</strong>anced by a mult<strong>in</strong>ational oil company, was negotiated,<br />

the focus turned temporarily to Lake Albert. In this area oil prospect<strong>in</strong>g<br />

was tak<strong>in</strong>g place <strong>and</strong> the oil company wanted to manifest its presence<br />

by contribut<strong>in</strong>g to the local community. Support<strong>in</strong>g the NLRI exist<strong>in</strong>g<br />

community based <strong>in</strong>itiatives to establish a rescue service on that lake<br />

was one of the chosen projects. F<strong>in</strong>anc<strong>in</strong>g the rescue station as such was<br />

the first step, recruit<strong>in</strong>g <strong>and</strong> tra<strong>in</strong><strong>in</strong>g a crew towards an <strong>in</strong>ternational<br />

st<strong>and</strong>ard as first responders to maritime <strong>and</strong> environmental emergencies<br />

was the second, <strong>and</strong> f<strong>in</strong>ally sea safety awareness tra<strong>in</strong><strong>in</strong>g <strong>and</strong> <strong>in</strong>formation,<br />

the third. The latter was performed with the station <strong>and</strong> the crew<br />

as a platform. In addition to the emergency response capability the local<br />

sp<strong>in</strong>-off has s<strong>in</strong>ce become obvious; life vest production <strong>and</strong> promotion,<br />

fishermen’s clubs, football tournaments, kids’ sea safety tra<strong>in</strong><strong>in</strong>g <strong>and</strong> <strong>in</strong>formation<br />

etc. Without a susta<strong>in</strong>able f<strong>in</strong>ancial solution it is unlikely that<br />

the development will cont<strong>in</strong>ue <strong>and</strong> the death rate on the great lakes<br />

will cont<strong>in</strong>ue to be appall<strong>in</strong>gly high. Currently a project funded by the<br />

African Development Bank is attempt<strong>in</strong>g to f<strong>in</strong>d a private-public partnership<br />

solution to this very problem, but eventually it will depend on<br />

political will <strong>and</strong> <strong>in</strong>volvement.<br />

dIscussIon<br />

The case study above shows that local <strong>in</strong>itiatives can make a difference.<br />

For commercial traffic, operat<strong>in</strong>g with<strong>in</strong> the framework of IMO regulations,<br />

governmental organizations can enforce <strong>in</strong>ternational safety regulations<br />

thus decreas<strong>in</strong>g the accident rate <strong>and</strong> the need of SAR operations.<br />

Operat<strong>in</strong>g offshore furthermore <strong>in</strong>creases the need of equipment<br />

suitable for the specific environment of the high seas, <strong>and</strong> this activity<br />

is more suitable for a governmental body. However, <strong>in</strong> other waters <strong>and</strong><br />

for other categories of maritime activities, the non-governmental SAR<br />

organization is a vital complement; cooperat<strong>in</strong>g with (<strong>and</strong> with<strong>in</strong>) the<br />

385


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

local communities; provid<strong>in</strong>g education, tra<strong>in</strong><strong>in</strong>g, <strong>and</strong> promot<strong>in</strong>g the use<br />

of life sav<strong>in</strong>g equipment. It is also a cost effective solution to have efficient<br />

<strong>and</strong> dedicated local rescue units h<strong>and</strong>l<strong>in</strong>g smaller operations <strong>in</strong><br />

coastal areas or <strong>in</strong>l<strong>and</strong> lakes, rather than large navy units or coast guard<br />

ships. A non-governmental organization also has the possibility to access<br />

external funds not available for nation states.<br />

The establishment of local, community based, SAR units has been<br />

advocated before <strong>in</strong> different forums. A report for ILO (Ben-Yami<br />

2000) po<strong>in</strong>ts out that:<br />

386<br />

“The way to go, therefore, is by identification of local (<strong>in</strong>clud<strong>in</strong>g<br />

traditional) <strong>in</strong>stitutions <strong>and</strong> local leadership that can, with some<br />

outside support, organize their own SAR <strong>and</strong> storm-safety services<br />

as well as other related projects. In this respect, NGOs can<br />

play a very useful role.”<br />

Furthermore, a report of the risks <strong>and</strong> dangers <strong>in</strong> the small scale fishery<br />

by Tamil Nadu, look<strong>in</strong>g <strong>in</strong>to more than 2000 maritime <strong>in</strong>cidents, concludes<br />

that:<br />

“Exist<strong>in</strong>g community based search <strong>and</strong> rescue (SAR) efforts to be<br />

reviewed <strong>and</strong> to explore possibilities of capacity build<strong>in</strong>g <strong>and</strong> sett<strong>in</strong>g<br />

up of community based SAR units <strong>in</strong> village clusters. The<br />

Coast Guard cannot respond to every call for help from small boat<br />

fishermen” (Swamy 2009).<br />

This however requires a basic organizational <strong>in</strong>frastructure <strong>and</strong> basic<br />

funds to create stability <strong>and</strong> susta<strong>in</strong>ability. This is of national <strong>in</strong>terest<br />

<strong>and</strong> thus <strong>in</strong> the <strong>in</strong>terest of governments <strong>and</strong> should therefore be actively<br />

supported. It would be reasonable to assume that every dollar spent on a<br />

private, non-governmental SAR service would have at least a threefold<br />

multiplier effect on the <strong>in</strong>itial spend<strong>in</strong>g due to the ability of an NGO<br />

to mobilize volunteers <strong>and</strong> raise other funds when properly established.<br />

Furthermore, <strong>in</strong> comparison with spend<strong>in</strong>g on governmental SAR capacity<br />

the NGO will not only provide SAR capacity but will also engage<br />

local communities, advocate safe practise, <strong>and</strong> work actively to decrease<br />

the number of SAR operations as such, someth<strong>in</strong>g that a navy or a coast<br />

guard unit would have problems to achieve. SAR organization <strong>in</strong>itiatives<br />

can arise from anywhere, through cooperatives, fishermen’s organizations,<br />

maritime tra<strong>in</strong><strong>in</strong>g centres or any source imag<strong>in</strong>able. Where it<br />

happens is not important, it is the engagement that matters <strong>and</strong> that<br />

should be supported when the idea <strong>and</strong> model is proven.<br />

Even though there is little statistical <strong>in</strong>formation to be obta<strong>in</strong>ed on<br />

the matter, what there is <strong>in</strong>dicates that the ma<strong>in</strong> category of fatalities<br />

on the seas around the world is related to artisanal fish<strong>in</strong>g <strong>and</strong> small<br />

scale transports/ferries, ma<strong>in</strong>ly <strong>in</strong> coastal waters with<strong>in</strong> 20 nautical<br />

miles (NM) from the shore. An estimated 24 000 lives are lost globally<br />

with<strong>in</strong> this category accord<strong>in</strong>g to an estimate by ILO (1999). This further<br />

strengthens the argument; that non-governmental SAR service is<br />

a good complement to governmental maritime units where the NGO<br />

shares the responsibility <strong>and</strong> caters for the safety of coastal activities<br />

such as fish<strong>in</strong>g, <strong>and</strong> the governmental units operate on the high seas<br />

with large commercial traffic. Such a solution is beneficial for all parties;<br />

for the fish<strong>in</strong>g communities engag<strong>in</strong>g <strong>in</strong> their own safety, br<strong>in</strong>g<strong>in</strong>g<br />

down the rate of accidents <strong>and</strong> <strong>in</strong>creas<strong>in</strong>g the survivability of persons <strong>in</strong><br />

distress, <strong>and</strong> for the governments solv<strong>in</strong>g a problem at a limited cost <strong>and</strong><br />

be<strong>in</strong>g able to focus on other press<strong>in</strong>g issues.<br />

The social impact of a SAR organization should not be underestimated.<br />

Around Lake Victoria it is estimated that every fisherman has<br />

up to seven (7) dependants. If 5000 lives are lost, theoretically another<br />

35000 will lose their primary means of liv<strong>in</strong>g. This will first of all affect<br />

women <strong>and</strong> children. Thus a SAR organization also has an impact<br />

on gender issues. Furthermore, the Lake Albert rescue station example<br />

has also shown that with<strong>in</strong> the community, the rescue station as such<br />

has become a vehicle of progress. When provid<strong>in</strong>g a rural fish<strong>in</strong>g com-<br />

munity with a focal po<strong>in</strong>t, with some k<strong>in</strong>d of reliable organization <strong>and</strong><br />

<strong>in</strong>frastructure, other activities can utilize the facilities. The rescue station<br />

has, for example, become an arena for not only the promotion of safety<br />

awareness but also for HIV/AIDS <strong>in</strong>formation campaigns <strong>and</strong> women’s<br />

clubs - promot<strong>in</strong>g cultivation <strong>and</strong> craftsmanship (life jacket production)<br />

<strong>and</strong> thus <strong>in</strong>creas<strong>in</strong>g womens’ f<strong>in</strong>ancial <strong>in</strong>dependence. Last but not least,<br />

if a region has an ambition to establish itself as a tourist dest<strong>in</strong>ation a<br />

certa<strong>in</strong> level of safety <strong>and</strong> security is important.<br />

conclusIon<br />

A non-governmental SAR organization is a multifaceted tool to h<strong>and</strong>le<br />

several different problems. The primary contribution might be to facilitate<br />

a change of attitude vis-à-vis safety at sea issues, but the total effect<br />

will be broader than that. The social benefits, the community engagement,<br />

<strong>and</strong> the impact of less scattered families will be considerable. For<br />

a government it is a cost effective route to fulfill<strong>in</strong>g the <strong>in</strong>ternational<br />

obligations of the sea.<br />

reFerences<br />

Yami, B. (2000). Risks <strong>and</strong> dangers <strong>in</strong> small scale fisheries: an overview.<br />

ILO Work<strong>in</strong>g paper SAP3.6WP147, Geneva, Switzerl<strong>and</strong><br />

ILO (1999). Safety <strong>and</strong> health <strong>in</strong> the fish<strong>in</strong>g <strong>in</strong>dustry. Report for discussion<br />

at the Tripartite meet<strong>in</strong>g on safety <strong>and</strong> health <strong>in</strong> the fish<strong>in</strong>g <strong>in</strong>dustry.<br />

ILO, Geneva. Can be obta<strong>in</strong>ed at http://www.ilo.org/public/<br />

english/dialogue/sector/techmeet/tmfi99/tmfir.htm<br />

Swamy, J (2009). Risks <strong>and</strong> dangers <strong>in</strong> the small scale fisheries of Tamil<br />

Nadu. SIFFS. Can be obta<strong>in</strong>ed at http://seasafetysouthasia.org<br />

AcKnoWledGeMents:<br />

The authors would like to thank Joanna McDonald <strong>and</strong> Sip Wiebenga<br />

for their important <strong>in</strong>put <strong>and</strong> support, <strong>and</strong> mak<strong>in</strong>g this paper possible<br />

to present.


Author Index<br />

author<strong>in</strong>deX<br />

387


<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />

A<br />

Abraldes, J.A. 42, 67, 77<br />

Aggeloussis, N. 89<br />

Alberty, M. 115, 204<br />

Alcaraz, P.E. 77<br />

Aleixo, I. 291<br />

Allen, J. S. III. 154<br />

Alves, F.B. 194, 215, 217, 220, 374<br />

Andrée F. 97<br />

Andries Júnior O. 47<br />

Arellano, R. 45, 127, 130, 249<br />

Avramidis, S. 354<br />

Azevedo, S. 374<br />

Azizi, M.H. 357<br />

B<br />

Baba,Y. 288<br />

Bagheri, A.B. 357<br />

Baik, W. 213<br />

Baly, L. 50<br />

Barbosa A.C. 47<br />

Barbosa, T.M. 122, 137, 272, 312<br />

Barla, C. 50<br />

Barnes, J.N. 381<br />

Becker, T.J. 314<br />

Bednarik, J. 228<br />

Beidaris, N. 242<br />

Belvis, W.C. 317<br />

Benavent, J. 119, 359<br />

Bennett, E. 371<br />

Berton, E. 50<br />

Bideau, B. 52, 180<br />

Bideau, N. 52<br />

Blanksby, B.A. 105<br />

Blixt, T. 329, 331<br />

Böhnle<strong>in</strong>, S. 278<br />

Boli, A. 89<br />

Bonifazi, M. 84<br />

Botonis, P. 242, 281<br />

Bragada, J.A. 272<br />

Brammer, C.L. 294<br />

Bratusa, F.Z. 245<br />

Bratusa, Z. 276<br />

Brito, C.A.F. 317<br />

Buss, W. 283<br />

Butterly, R. 354<br />

C<br />

Cala, A. 182<br />

Cappozzo, A. 178<br />

Carl, D.L. 247<br />

Castro, F.A.S. 165, 307<br />

Chavallard, F. 55, 206<br />

Chaya, J.A. 333<br />

Cheng, L. 105<br />

Chollet, D. 55, 74, 115, 117, 155, 157, 180,<br />

204, 206, 286<br />

Cid, M. 155<br />

Colado, J.C. 119, 173, 359<br />

Conway, P.P. 59<br />

Corredeira, R. 157<br />

Cortesi, M. 57, 84<br />

Cossor, J.M. 59<br />

Costa, L. 62<br />

Costa, M.J. 137, 272, 312<br />

Cruz, A.M. 312<br />

D<br />

388<br />

Da Boit, M. 57<br />

Dahl D. 377<br />

Daly, D.J. 140, 157<br />

De Aymerich, J. 359<br />

De Jesus, K. 64<br />

Dekerle, J. 196, 259<br />

de la Fuente, B. 249<br />

Denadai, B.S. 215<br />

de Souza Castro, F.A. 257<br />

de Wet, T. 384<br />

Dickerson, T. 247<br />

Diefenthaeler, F. 257<br />

Dietrich, G. 72<br />

Diogo, V. 67<br />

Domínguez-Castells R. 45<br />

Donati, M. 178<br />

Dopsaj, J.M. 245<br />

Dopsaj, M. 69, 192, 222, 276<br />

Douda, H. 252, 254, 299<br />

Drosou, E. 254<br />

E<br />

Elipot M. 97<br />

Elipot, M. 72<br />

Espada, M.A. 194<br />

F<br />

Falco, S. 187<br />

Falenchuk, O. 233<br />

Fantozzi, S. 84<br />

Femia, P. 127, 130<br />

Fern<strong>and</strong>es, R.J. 42, 62, 64, 67, 74, 148, 157,<br />

180, 204, 291<br />

Ferragut, C. 67, 77<br />

Figueiredo, P. 62, 64, 67, 157<br />

Formosa, D.P. 124<br />

Franken, M. 257<br />

Fuj<strong>in</strong>awa, O. 362<br />

G<br />

García Massó, X. 119, 173, 359<br />

Gatta, G. 57, 84, 178<br />

Georgiou, Ch. 252<br />

Gomes, L.E. 86<br />

Gonçalves, P. 64, 148<br />

González Frutos, P. 182<br />

González, L.M. 119, 173, 359<br />

Gourgoulis, V. 89, 252, 254, 296, 299<br />

Gouvernet, G. 50<br />

Grélot, L. 50<br />

Griff<strong>in</strong>, B. 247<br />

H<br />

Halj<strong>and</strong> R. 127<br />

Hanai, A. 364<br />

Hara, H. 213, 319<br />

Hata, H. 226<br />

Hausswirth, C. 196, 259<br />

Havriluk, R. 314, 321<br />

Hellard H. 97<br />

Hellard, P. 72, 155, 196, 204, 259<br />

Henrich, T.W. 199<br />

Henriques, A. 374<br />

H<strong>in</strong>man, M.G. 305<br />

Hirao, M. 213<br />

Hirose, K. 362<br />

Hohmann, A. 262, 278<br />

Homma, M. 91<br />

Houel N. 97<br />

Houel, N. 72, 196, 259<br />

Huang, Z. 201<br />

I<br />

Ichikawa, H. 341<br />

Ide, T. 270<br />

Invernizzi, P.L. 324, 326, 336, 339<br />

Isaka, T. 185<br />

Izumi, T. 185<br />

J<br />

James, R. 142<br />

Jarm, T. 168<br />

Jigami, H. 362<br />

Junge, M. 329, 331<br />

Justham, L.M. 59<br />

K<br />

Kamiya, S. 132<br />

Kaneda, K. 366<br />

Kanefuku, J.Y. 165<br />

Kapus, J. 228<br />

Kapus, V. 168<br />

Kasimatis, P. 89<br />

Kawakami, T. 270<br />

Kawamoto, K. 270<br />

Kawano, H. 208<br />

Kesk<strong>in</strong>en, K.L. 74, 264<br />

Kesk<strong>in</strong>en, O.P. 264<br />

Keys, M. 105<br />

Kishimoto, T. 108<br />

Kiuchi, H. 132<br />

Kjendlie, P.L. 377<br />

Klauck, J 175<br />

Kocherg<strong>in</strong>, A.B. 110<br />

Kojima, K. 267<br />

Kolmogorov, S.V. 110<br />

Komar, J. 204<br />

Kondo, Y. 362<br />

Kurobe, K. 201<br />

L<br />

Langendorfer, S.J. 20, 333<br />

La Torre, M. 86<br />

Leko, G. 238<br />

Lemaître, F. 55, 206<br />

Lemyre, P.-N. 22<br />

Leprêtre, P.M. 204<br />

Leslie, N. 247<br />

Lex, H. 346<br />

Lima, A.B. 42<br />

Llewellyn, J.D. 354<br />

Long, J. 354<br />

Longo, S. 324, 326, 336, 339<br />

Loss, J.F. 86<br />

Lyttle, A. 105<br />

M<br />

Machado, L. 62, 148, 291<br />

Madera, J. 119, 173, 359<br />

Maeda, S. 132<br />

Mahiou, B. 52<br />

Maia, J. 291<br />

Mantha, V.R. 122<br />

Mantripragada, N. 122<br />

Mar<strong>in</strong>ho, D.A. 62, 122, 137, 272, 312<br />

Markste<strong>in</strong>er, A. 247<br />

Marques-Aleixo, I. 157<br />

Mason, B.R. 25, 124


Mateu, J. 173<br />

Matos, A. 374<br />

Matsumoto, N. 213, 319<br />

Matsumoto, T. 185<br />

Matsunaga, H. 362<br />

Mavridis, G. 89<br />

Mavrommatis, G. 89<br />

McKenna, J. 354<br />

Melo, M.O. 86<br />

Mercade, J. 127, 130<br />

Michailidou, D. 299<br />

Michielon, G. 324, 336, 339<br />

Milivoj Dopsaj M. 47<br />

Mohebbi,00 H.D. 357<br />

Monier, L. 52<br />

Morais, P. 74<br />

Morales, E. 127, 130<br />

Moran, K. 368, 371, 377<br />

Moré, F.C. 165<br />

Morlier, J. 155<br />

Morouço, P. 67<br />

Murakawa, T. 213<br />

Murata, N.M. 154<br />

N<br />

Nabekura, Y. 224<br />

Nakajima, K. 132<br />

Nakamura, K. 224<br />

Nakashima, M. 132<br />

Navarro, E. 182<br />

Nesi, X. 196, 259<br />

Nicolas, G. 52, 180<br />

Nishimura, K. 208, 213<br />

Nishiwaki, M. 201<br />

Nomura, T. 135<br />

Nose, Y. 208, 213, 319<br />

Nualnim, N. 381<br />

O<br />

Ogita, F. 201<br />

Ohba, M. 274<br />

Ohgi, Y. 366<br />

Ohishi, K. 185<br />

Okicic T. 47<br />

Okita, K. 288<br />

Oliveira, C. 137<br />

Oliveira, M. 317<br />

Onodera, S. 208, 213, 319<br />

Osborough, C.D. 140<br />

Oxford, S. 142<br />

Ozawa, G. 201<br />

Özkol, Z. 276<br />

P<br />

Paiva, A. 374<br />

Pankey, R.B. 199<br />

Patti, F. 84<br />

Payton, C.J. 140, 142<br />

Pease, D.L. 145<br />

Pereira, S.M. 64, 148<br />

Perez-Infantes E. 45<br />

Perisic, S.M. 245<br />

Pessôa Filho, D.M. 215<br />

Pfeiffer, M. 278<br />

P<strong>in</strong>to, E. 312<br />

Platanou, T. 230, 242, 281<br />

Pöyhönen, T. 264<br />

Price, M. 142<br />

Pr<strong>in</strong>s, J.H. 28, 154<br />

Puel, F. 155<br />

Q<br />

Quan, L. 371<br />

Queirós ,T.M. 312<br />

Querido, A. 157<br />

R<br />

Rakotomanana, L. 52<br />

Rama, L. 217, 374<br />

Rao, G. 50<br />

Razafimahery, F. 52<br />

Reis, J.F. 215, 220<br />

Reis, V.M. 272, 312<br />

Rejman, M. 160<br />

Renzi, C.P. 381<br />

Ribeiro, J. 62<br />

Rodríguez, F.A. 30<br />

Rodriguez, N. 77<br />

Roesler, H. 148<br />

Roig, A. 163<br />

Rosado, F. 374<br />

Rouard, A.H. 33, 122<br />

Rouboa, A. 62, 122<br />

Rozi, G. 222, 230<br />

Rumyantseva, O.A. 110<br />

S<br />

Saiiari, A.R. 357<br />

Sánchez E. 45<br />

Sato, D. 274, 288<br />

Sato, S. 274<br />

Sato, T. 185<br />

Schack, T. 283, 346<br />

Schmidt, A.C. 283<br />

Schnitzler, C. 115, 286<br />

Scurati, R. 324, 326, 336, 339<br />

Seidel, I. 262<br />

Seifert, L. 35, 55, 74, 115, 117, 157, 180, 204,<br />

286<br />

Seki, K. 213<br />

Sengoku, Y. 224<br />

Shibata, Y. 319<br />

Shimojo, H. 341<br />

Shimoyama, Y. 185, 274, 288<br />

Shiraki, T. 226<br />

Siegel, A. 278<br />

Silva, A.J. 62, 122, 137, 272, 312<br />

Silva, R. 291<br />

Silveira, R.P. 165<br />

Slawson, S.E. 59<br />

Soares, S. 42, 67, 291<br />

Sommerlad, S.M. 381<br />

Soukup, G.J. 199<br />

Stager, J.M. 267, 294, 305<br />

Stallman, R.K. 329, 331, 377, 379<br />

Staszkiewicz, A. 160<br />

Steffen, R. 302<br />

Stirn, I. 168<br />

Strojnik, V. 168<br />

Strumbelj, B. 228<br />

Sugimoto, S. 108<br />

T<br />

Tachikawa, K. 362<br />

Tad<strong>in</strong>i, F. 326<br />

Tago, T. 185<br />

Taguchi, N. 201<br />

Takagi, H. 100, 108, 132, 135, 170, 341<br />

Takahara, T. 213<br />

Takamoto, N. 208<br />

Takeda, T. 108, 135, 170, 224<br />

Takise, S. 270<br />

Tam, E. 57<br />

Tanaka, C. 366<br />

Tanaka, H. 381<br />

Tanaka, T. 201<br />

Tanner, D.A. 294<br />

Teixeira, A. 217, 374<br />

Teixeira, G. 137<br />

Tella, V. 119, 173, 359<br />

Thanopoulos, V. 222, 230, 276<br />

Thomaidis, S. 254<br />

Tokmakidis, S.P. 252, 254, 296, 299<br />

Tomikawa, M. 226<br />

Toubekis, A.G. 89, 252, 254, 296, 299<br />

Tour<strong>in</strong>o, C. 67<br />

Toussa<strong>in</strong>t, H.M. 115, 124, 346<br />

Toussa<strong>in</strong>t, J.F. 196, 259<br />

Tsalis, G. 299<br />

Tsubakimoto, S. 108, 170, 224, 341<br />

U<br />

Ungerechts, B.E. 175, 283, 302, 346<br />

Usaj, A. 228<br />

author<strong>in</strong>deX<br />

V<br />

Vannozzi, G. 178<br />

Vantorre, J. 180, 204<br />

Veiga, S. 182<br />

Vennell, R. 145<br />

Vescovi, J.D. 233<br />

Vezos, N. 89<br />

Vieluf, S. 346<br />

Vila, H. 77<br />

Vilas-Boas, J.P. 12, 42, 62, 64, 67, 74, 122,<br />

148, 157, 180, 291<br />

Vogel, K. 302<br />

Vorontsov, A.R. 110<br />

W<br />

Wada, T. 185<br />

Wakayoshi, K. 226<br />

Watanabe, R. 319<br />

Wells G.D. 233<br />

Wengel<strong>in</strong>, M. 384<br />

Wertheimer, V. 238<br />

West, A.A. 59<br />

Wright, B.V. 305<br />

Y<br />

Yamamoto, N. 185<br />

Yamamoto, T. 226<br />

Yamatsu, K. 364<br />

Yoshimura, Y. 270<br />

Yoshioka, A. 208, 213, 319<br />

Z<br />

Zacca, R. 307<br />

Zamparo, P. 57, 187<br />

Zatoń, K. 349<br />

Zoretić, D. 238<br />

389


Pahlen Norge AS<br />

Pahlen Norge AS<br />

Chapter 1. Invited Lectures<br />

Chapter 2. <strong>Biomechanics</strong><br />

Chapter 3. Physiology <strong>and</strong> Bioenergetics<br />

Chapter 4. Tra<strong>in</strong><strong>in</strong>g <strong>and</strong> Performance<br />

Chapter 5. Education, Advice <strong>and</strong> Biofeedback<br />

Chapter 6. <strong>Medic<strong>in</strong>e</strong> <strong>and</strong> Water Safety<br />

ISBN 978-82-502-0438-6<br />

www.pahlennorge.no<br />

www.pahlennorge.no<br />

c o a c h e s i n f o . c o m<br />

i n f o r m a t i o n a n d e d u c a t i o n f o r c o a c h e s

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