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Active IQ Level 3 Diploma in Personal Training (sample manual)

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Manual<br />

<strong>Level</strong> 3 <strong>Diploma</strong> <strong>in</strong><br />

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

Version A<strong>IQ</strong>004228


Unit 1<br />

Section 1: The cardiovascular system<br />

Heart valves<br />

Heart valves are formed from tough connective tissue and are made up of cusps, or flaps, that cover the entrance<br />

or exit to a vessel or chamber. They open and close passively, either sucked <strong>in</strong>to place or blown open depend<strong>in</strong>g on<br />

the differential pressure <strong>in</strong> each chamber or vessel.<br />

• Semilunar valves lie between the ventricles and arteries and prevent backflow of blood from the chamber<br />

to the vessel. The aortic semilunar valve separates the left ventricle and the aorta, and the pulmonary<br />

semilunar valve separates the right ventricle and pulmonary artery.<br />

• Atrioventricular (AV) valves lie between the atria and ventricles and prevent backflow of blood from the<br />

upper to lower chambers. The left AV valve is also known as the bicuspid valve (two cusps) or the mitral valve.<br />

The right AV valve is also known as the tricuspid valve (three cusps).<br />

Figure 1.1 The valves of the heart<br />

Contraction of the heart<br />

SA node<br />

The stimulation starts <strong>in</strong> the s<strong>in</strong>oatrial<br />

(SA) node.<br />

The heart is stimulated to contract by a complex series of <strong>in</strong>tegrated<br />

systems. The heart’s pacemaker – the s<strong>in</strong>oatrial (SA) node – <strong>in</strong>itiates the<br />

cardiac muscle contraction. The SA node is located <strong>in</strong> the wall of the right<br />

atrium (see Figure 1.2). The heart muscle is stimulated to contract about<br />

72 times per m<strong>in</strong>ute.<br />

Atria contract<br />

The <strong>in</strong>terconnected cardiac muscle<br />

fibres pass the impulse across the atria.<br />

AV node<br />

The atrioventricular (AV) node<br />

is stimulated and allows the full<br />

contraction of the atria before<br />

stimulat<strong>in</strong>g the ventricular muscle to<br />

contract.<br />

Ventricles contract<br />

The AV node stimulates the ventricular<br />

muscles to contract.<br />

Figure 1.2 The contraction of the heart<br />

8<br />

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Section 1: The cardiovascular system<br />

Unit 1<br />

Circulation<br />

Pulmonary<br />

arteries<br />

Lungs<br />

Pulmonary<br />

ve<strong>in</strong>s<br />

Right<br />

ventricle<br />

Right<br />

atrium<br />

Venae<br />

cavae<br />

Atherosclerosis<br />

The right side of the heart receives blood from the upper and lower body<br />

via the superior vena cava and <strong>in</strong>ferior vena cava. The blood is saturated <strong>in</strong><br />

carbon dioxide (CO 2<br />

) and is referred to as deoxygenated. The deoxygenated<br />

blood is ejected to the lungs by the right ventricle via the pulmonary artery.<br />

In the pulmonary capillaries, CO 2<br />

diffuses <strong>in</strong>to the lungs to be expired, while<br />

oxygen (O 2<br />

) enters the blood (gaseous exchange). The oxygenated blood<br />

travels to the left atrium of the heart via the merg<strong>in</strong>g venules and ve<strong>in</strong>s that<br />

f<strong>in</strong>ally become the pulmonary ve<strong>in</strong>. The left ventricle then ejects the blood<br />

and O 2<br />

via the aorta to the tissues of the body. Once the oxygenated blood<br />

reaches the capillaries, gaseous exchange occurs – the oxygen diffuses <strong>in</strong>to<br />

the tissues and CO 2<br />

diffuses <strong>in</strong>to the bloodstream.<br />

Body<br />

Aorta<br />

Left<br />

atrium<br />

Left<br />

ventricle<br />

In a healthy blood vessel, blood flows smoothly to reach its target tissue or organ and supply it with the nutrients<br />

and oxygen it requires for optimal function. Vascular disease is the narrow<strong>in</strong>g of the blood vessels, and it is one<br />

of the ma<strong>in</strong> causes of death <strong>in</strong> the developed world. It is triggered by <strong>in</strong>flammation with<strong>in</strong> blood vessels and<br />

the subsequent accumulation of m<strong>in</strong>eral, prote<strong>in</strong> and fat deposits. This creates a build-up of plaques on vessel<br />

walls which can ultimately lead to a blockage that can severely restrict, or completely prevent, blood flow. As a<br />

consequence of this, tissues and organs can be starved of vital nutrients and oxygen.<br />

Vascular disease is most commonly caused by the harden<strong>in</strong>g of arteries – a condition called atherosclerosis (see<br />

Figure 1.3). Atherosclerosis is <strong>in</strong>itiated by the <strong>in</strong>flammatory response to vessel damage that creates plaques us<strong>in</strong>g<br />

cholesterol, prote<strong>in</strong> and m<strong>in</strong>eral deposits <strong>in</strong> an attempt to heal the area.<br />

As plaques build up, the artery wall becomes thicker, harder and less elastic. The artery narrows as a consequence<br />

of the build-up and cannot effectively stretch to accommodate blood.<br />

A lack of blood flow as a result of atherosclerosis can cause target tissue death unless those tissues are supplied<br />

by blood from alternative arteries.<br />

1 – Inflammation<br />

Known as the ‘fatty streak’ stage because this is how<br />

the condition first becomes visible.<br />

Damage (e.g. caused by smok<strong>in</strong>g or hypertension)<br />

<strong>in</strong>itiates an <strong>in</strong>flammatory response.<br />

Applied anatomy and physiology for exercise, health and fitness<br />

2 – Narrow<strong>in</strong>g<br />

The body tries to repair the damaged area us<strong>in</strong>g<br />

cholesterol, prote<strong>in</strong>s and m<strong>in</strong>erals.<br />

These substances build up, creat<strong>in</strong>g a ‘plaque’ that<br />

thickens and hardens the artery walls.<br />

The artery is narrowed by the plaque build-up.<br />

Figure 1.3 Atherosclerosis<br />

3 – Blockage<br />

The plaques build up so much that they rupture and<br />

release cholesterol and connective tissue <strong>in</strong>to the<br />

artery.<br />

The body’s protective mechanism creates a blood<br />

clot around the rupture which further scars, hardens<br />

and can block the entire artery. These are called<br />

‘complicated lesions’.<br />

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Section 2: The musculoskeletal system<br />

Unit 1<br />

Sarcoplasmic reticulum<br />

Myofibril<br />

Endomysium<br />

surround<strong>in</strong>g the<br />

muscle fibre<br />

Myos<strong>in</strong><br />

Epimysium<br />

Act<strong>in</strong><br />

KEY<br />

POINTS<br />

• Each muscle is covered <strong>in</strong> a connective<br />

tissue called the epimysium.<br />

• Bundles of muscle fibres called fasciculi<br />

are covered by the perimysium.<br />

• Each muscle fibre is surrounded by the<br />

endomysium.<br />

• Muscle fibres are made up of myofibrils.<br />

• Myofibrils are segmented <strong>in</strong>to<br />

compartments called sarcomeres.<br />

• Each sarcomere conta<strong>in</strong>s myofilaments<br />

(act<strong>in</strong> and myos<strong>in</strong>).<br />

The slid<strong>in</strong>g filament theory and muscle contractions<br />

Perimysium<br />

surround<strong>in</strong>g<br />

the fascicle<br />

Figure 2.2 The structure of a muscle<br />

Muscular contraction beg<strong>in</strong>s with the two contractile prote<strong>in</strong>s (or myofilaments): act<strong>in</strong> and myos<strong>in</strong>. Act<strong>in</strong> (the th<strong>in</strong><br />

filament) is anchored to the ends of the sarcomere and myos<strong>in</strong> (the thick filament) is located <strong>in</strong> the middle of the<br />

sarcomere.<br />

Spirall<strong>in</strong>g from the myos<strong>in</strong> filament is a series of ‘hook-like’ projections referred to as the myos<strong>in</strong> heads. Dur<strong>in</strong>g<br />

muscular contraction, these heads attach themselves to the act<strong>in</strong> and rotate, pull<strong>in</strong>g on the filaments. This causes<br />

the act<strong>in</strong> to be drawn <strong>in</strong>wards, dragg<strong>in</strong>g the ends of the sarcomere together. This shorten<strong>in</strong>g process is referred<br />

to as the slid<strong>in</strong>g filament mechanism. The characteristic contraction of muscles is caused by the simultaneous<br />

shorten<strong>in</strong>g of multiple sarcomeres.<br />

Applied anatomy and physiology for exercise, health and fitness<br />

Figure 2.3 The slid<strong>in</strong>g filament theory<br />

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Section 2: The musculoskeletal system<br />

Unit 1<br />

Common postural distortions<br />

Kyphosis refers to the outward curve of the thoracic sp<strong>in</strong>e.<br />

Lordosis refers to the <strong>in</strong>ward curve of the lumbar sp<strong>in</strong>e.<br />

These terms are often used to describe excessive curvature,<br />

but normal curvature of the thoracic region is kyphotic <strong>in</strong><br />

nature and normal curvature of the lumbar region is lordotic.<br />

For this reason, the follow<strong>in</strong>g terms can be used to dist<strong>in</strong>guish<br />

dysfunction:<br />

POINT OF<br />

INTEREST<br />

ROOT<br />

WORDS<br />

• Hypo = ‘under’ or ‘less’<br />

• Hyper = ‘over’, ‘above’ or<br />

‘too much’<br />

• Hyperkyphosis – an excessive curve of the thoracic sp<strong>in</strong>e.<br />

• Hypokyphosis – a flattened curve of the thoracic sp<strong>in</strong>e.<br />

• Hyperlordosis – an excessive curve of the lumbar sp<strong>in</strong>e, also known as a ‘hollow back’.<br />

• Hypolordosis – a flattened curve of the lumbar sp<strong>in</strong>e.<br />

The term scoliosis is of Greek orig<strong>in</strong> and means ‘crooked’ or ‘bent’. A scoliotic sp<strong>in</strong>e has an excessive lateral<br />

curvature.<br />

Upper crossed syndrome<br />

Upper crossed syndrome refers to a hyperkyphotic sp<strong>in</strong>al position comb<strong>in</strong>ed with protracted shoulders and a<br />

forward-pok<strong>in</strong>g head. The shortened and lengthened areas caused by this syndrome can be divided by a cross<br />

shape (see Figure 2.6), which is where this condition gets its name.<br />

Shortened/dom<strong>in</strong>ant/<br />

overactive muscles<br />

• Scalenes<br />

• Sternocleidomastoid<br />

• Upper trapezius<br />

• Levator scapula<br />

• Pectoralis major<br />

• Anterior deltoids<br />

• Latissimus dorsi<br />

• Teres major<br />

• Subscapularis<br />

• Pectoralis m<strong>in</strong>or<br />

Lower crossed syndrome<br />

Shortened<br />

Lengthened<br />

Lengthened<br />

Shortened<br />

Lengthened/<strong>in</strong>hibited/<br />

underactive muscles<br />

• Deep neck flexors<br />

(longus capitis and colli)<br />

• Serratus anterior<br />

• Lower trapezius<br />

• Middle trapezius<br />

• Teres m<strong>in</strong>or<br />

• Infrasp<strong>in</strong>atus<br />

• Suprasp<strong>in</strong>atus<br />

• Thoracic erector sp<strong>in</strong>ae<br />

Figure 2.6 Upper crossed syndrome<br />

The shortened and lengthened regions caused by lower crossed syndrome can aga<strong>in</strong> be divided by a cross shape.<br />

This condition is characterised by an anterior pelvic tilt and hyperlordosis (see Figure 2.7).<br />

Applied anatomy and physiology for exercise, health and fitness<br />

Shortened/dom<strong>in</strong>ant/<br />

overactive muscles<br />

• Iliopsoas<br />

• Lumbar erector sp<strong>in</strong>ae<br />

• Rectus femoris<br />

• Adductors<br />

• Tensor fasciae latae<br />

• Quadratus lumborum<br />

• Lumbar multifidus<br />

Shortened<br />

Lengthened<br />

Lengthened<br />

Shortened<br />

Lengthened/<strong>in</strong>hibited/<br />

underactive muscles<br />

• Rectus abdom<strong>in</strong>is<br />

• Obliques<br />

• Transversus abdom<strong>in</strong>is<br />

• Gluteus maximus<br />

• Gluteus medius<br />

• Gluteus m<strong>in</strong>imus<br />

Figure 2.7 Lower crossed syndrome<br />

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Section 4: The endocr<strong>in</strong>e system<br />

Unit 1<br />

Section 4: The endocr<strong>in</strong>e<br />

system<br />

The role of the endocr<strong>in</strong>e system<br />

Along with the nervous system, the endocr<strong>in</strong>e system helps to ma<strong>in</strong>ta<strong>in</strong> homeostasis. Instead of us<strong>in</strong>g action<br />

potentials, however, the endocr<strong>in</strong>e system exerts its <strong>in</strong>fluence via hormones (chemical messengers).<br />

Hormones are chemicals released <strong>in</strong>to the bloodstream to help control and manage the <strong>in</strong>ternal environment of the<br />

body. Hormones are derived from am<strong>in</strong>o acids, steroids or occasionally fatty acids and are released from various<br />

glands around the body, known as the endocr<strong>in</strong>e glands. Different hormones have different chemical shapes which<br />

determ<strong>in</strong>e the effects they will have.<br />

The chemical messages from hormones are slower than the electrical messages (action potentials) of the nervous<br />

system. Cell response times to a specific hormone can range from a few seconds to 30 m<strong>in</strong>utes, depend<strong>in</strong>g on<br />

concentration levels. However, although neural stimulus is very rapid, it does not last; endocr<strong>in</strong>e stimulus can last<br />

for hours, days or even longer.<br />

How hormones work<br />

KEY<br />

POINT<br />

Hormones are chemical messengers (the<br />

key) that affect specific target cells (the lock).<br />

To fully understand how the endocr<strong>in</strong>e system works,<br />

the way hormones function around the body must first<br />

be appreciated. The process beg<strong>in</strong>s when an endocr<strong>in</strong>e<br />

gland receives a stimulus that requires a response. The<br />

response is <strong>in</strong>itiated by releas<strong>in</strong>g a hormone <strong>in</strong>to the<br />

surround<strong>in</strong>g bloodstream. Hormones are transported<br />

around the body, seek<strong>in</strong>g out specific target cells. Each<br />

type of hormone is attracted to particular receptors<br />

with<strong>in</strong> the target cells which, <strong>in</strong> turn, will only be<br />

triggered by the ‘right’ hormone (<strong>in</strong> the same way that<br />

a lock can only be opened with the right key). Once the<br />

released hormone reaches a target cell, it docks at the<br />

cell’s receptor site; this <strong>in</strong>itiates the desired response <strong>in</strong><br />

the cell or group of cells.<br />

F<strong>in</strong>ally, when the hormone response has had the desired<br />

effect, there is usually a feedback loop between the<br />

targeted tissue and the <strong>in</strong>itiat<strong>in</strong>g endocr<strong>in</strong>e gland which<br />

reduces or stops the hormone production.<br />

Applied anatomy and physiology for exercise, health and fitness<br />

Figure 4.1 How hormones work<br />

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Unit 1<br />

Section 6: The digestive system<br />

Mouth and<br />

pharynx<br />

• Chew<strong>in</strong>g (mastication) – mechanical breakdown.<br />

• Produces saliva – conta<strong>in</strong>s enzyme salivary amylase – beg<strong>in</strong>s breakdown<br />

of carbohydrate. Also moistens food and protects teeth aga<strong>in</strong>st decay.<br />

• Food is swallowed and passes from the mouth <strong>in</strong>to the pharynx.<br />

• Rhythmical <strong>in</strong>voluntary muscular contractions (peristalsis) push food <strong>in</strong>to<br />

the stomach.<br />

Oesophagus<br />

Stomach<br />

• Produces gastric juices conta<strong>in</strong><strong>in</strong>g hydrochloric acid (kills bacteria) and the<br />

enzyme peps<strong>in</strong> to break down prote<strong>in</strong>.<br />

Pancreas<br />

• Secretes pancreatic juice conta<strong>in</strong><strong>in</strong>g digestive enzymes<br />

that help further the digestion and absorption of nutrients:<br />

• LIPASE – breaks down fat.<br />

• AMYLASE – breaks down carbohydrate <strong>in</strong>to<br />

glucose.<br />

• TRYPSIN – breaks down prote<strong>in</strong> <strong>in</strong>to am<strong>in</strong>o acids.<br />

• Liver produces bile acids which enable fats to mix with<br />

water (emulsification).<br />

• Gallbladder acts as storage for bile which is released <strong>in</strong>to<br />

the small <strong>in</strong>test<strong>in</strong>e.<br />

Liver and<br />

gallbladder<br />

Small <strong>in</strong>test<strong>in</strong>e<br />

• Receives bile juice from gallbladder and pancreatic juice.<br />

• Primary site for digestion and absorption.<br />

• A comb<strong>in</strong>ation of <strong>in</strong>ner surface folds and f<strong>in</strong>ger-like projections (villi and<br />

microvilli) provide large surface area for absorption.<br />

• Digested food is able to pass <strong>in</strong>to the blood vessels <strong>in</strong> the wall of the<br />

<strong>in</strong>test<strong>in</strong>e through the process of diffusion.<br />

Large <strong>in</strong>test<strong>in</strong>e<br />

(colon)<br />

• Absorbs water, vitam<strong>in</strong>s and m<strong>in</strong>erals.<br />

• Conta<strong>in</strong>s bacteria, which produce vitam<strong>in</strong>s<br />

and help prevent <strong>in</strong>fection <strong>in</strong> the <strong>in</strong>test<strong>in</strong>e.<br />

• Stores faeces.<br />

Rectum<br />

• Open<strong>in</strong>g for elim<strong>in</strong>ation of<br />

waste.<br />

Anus<br />

Figure 6.1 The digestive process<br />

60<br />

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Section 4: Us<strong>in</strong>g nutrients to fuel activity<br />

Unit 2<br />

POINT OF<br />

INTEREST<br />

Aerobic activities <strong>in</strong>clude:<br />

• Jogg<strong>in</strong>g.<br />

• Distance runn<strong>in</strong>g.<br />

• Distance cycl<strong>in</strong>g.<br />

• Distance swimm<strong>in</strong>g.<br />

• Exercise to music.<br />

• Distance row<strong>in</strong>g.<br />

• Brisk walk<strong>in</strong>g.<br />

• Ski<strong>in</strong>g.<br />

Aerobic activities<br />

Dur<strong>in</strong>g aerobic activities (low-<strong>in</strong>tensity, longer-duration) the<br />

demand for energy is slower. ATP is produced us<strong>in</strong>g oxygen,<br />

so this type of exercise can be kept up for longer. Fats can<br />

also be used to produce energy for aerobic activities as<br />

they can only be broken down with oxygen present. The<br />

body has a larger store of fat than carbohydrate.<br />

Most sports and activities <strong>in</strong>volve a mixture of both<br />

anaerobic and aerobic exercise, e.g. football, hockey and<br />

rugby conta<strong>in</strong> short bursts of strenuous activity (spr<strong>in</strong>ts,<br />

kicks, throws) <strong>in</strong>terspersed with longer periods of less<br />

strenuous activity (jogg<strong>in</strong>g, walk<strong>in</strong>g).<br />

Fuel<br />

Creat<strong>in</strong>e<br />

phosphate<br />

Muscle<br />

glycogen<br />

Liver glycogen +<br />

blood glucose<br />

Maximal<br />

short bursts<br />

High<br />

<strong>in</strong>tensity<br />

<strong>in</strong>termittent<br />

Intensity of exercise<br />

High<br />

<strong>in</strong>tensity<br />

150 m<strong>in</strong><br />

Low <strong>in</strong>tensity<br />

Great. Very great. Moderate. Moderate. Moderate. Negligible.<br />

Slight. Moderate. Moderate. Very great. Very great. Negligible.<br />

Negligible. Slight. Slight. Moderategreat.<br />

Great-very<br />

great.<br />

Slight.<br />

Fat Negligible. Slight. Negligible. Negligible. Slight. Slight.<br />

Energy to start exercise<br />

Table 4.2 Depletion of fuel for different types of exercise<br />

At the start of exercise, energy is produced without oxygen. As the heart and lungs work harder, carbohydrates and<br />

fats can be broken down. If the exercise becomes aerobic <strong>in</strong> nature, more oxygen is delivered around the body and<br />

fats start to be broken down <strong>in</strong>to fatty acids, taken to muscle cells and used as energy. For the first 5-15 m<strong>in</strong>utes<br />

(depend<strong>in</strong>g on fitness level) carbohydrate (glycogen) is used for fuel. As time goes on, the use of carbohydrate<br />

lessens and more fat is utilised for energy.<br />

Fatigue<br />

The fitter the <strong>in</strong>dividual is, the longer it takes to fatigue or run out of glycogen. After three or more hours of exercise,<br />

fatigue is caused by the depletion of glycogen <strong>in</strong> the muscles and liver, as well as low blood glucose levels.<br />

The pr<strong>in</strong>ciples of nutrition and their application to exercise and health<br />

No matter what type of exercise is completed, or how fit the<br />

<strong>in</strong>dividual is, the body will always need glycogen. The amount<br />

of glycogen <strong>in</strong> the muscles (and liver) before exercise is<br />

crucial, as the size of a person’s store dictates how long they<br />

will be able to exercise for before fatigu<strong>in</strong>g. The message is<br />

‘always start with a full glycogen store’.<br />

A diet rich <strong>in</strong> carbohydrates ensures high glycogen stores.<br />

The amount of glycogen <strong>in</strong> the muscles dictates how hard<br />

and for how long an athlete can exercise. If the <strong>in</strong>dividual eats<br />

a high-carbohydrate diet prior to tra<strong>in</strong><strong>in</strong>g and competitions,<br />

their stores will be full.<br />

• Low glycogen levels would only allow for low-<strong>in</strong>tensity<br />

exercise and cause early fatigue.<br />

• High glycogen levels mean an athlete can tra<strong>in</strong> harder<br />

and longer.<br />

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