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Physical fitness training for stroke patients (Review) - Update Software

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Cooke 2010<br />

Methods Design: phase I multicenter trial; 4 centres; mixed <strong>training</strong> plus usual care versus usual care -<br />

during usual care - i.e. functional strength <strong>training</strong> (FST) plus conventional physiotherapy<br />

(CPT) versus conventional physiotherapy alone and versus conventional physiotherapy<br />

plus conventional physiotherapy (CPT + CPT)<br />

Randomisation: computer-generated random allocation in blocks of 9 per trial centre (stratified<br />

allocation by baseline scores <strong>for</strong> visual spatial neglect)<br />

Allocation concealment: sequentially numbered sealed opaque envelopes<br />

Blinding: assessor blinded to group allocation<br />

Intention-to-treat: attempt to measure participants at outcome and follow-up even if they<br />

withdraw but analyses were not per<strong>for</strong>med according to intention-to-treat principle<br />

Measurements: at the end of intervention (6 weeks) and 12 weeks later (follow-up)<br />

Withdrawals: at outcome 10 (9%) had withdrawn. 7 participants were lost at outcome<br />

in the control CPT group (3 unwell, 3 withdrew, 1 moved abroad) and 3 in the CPT +<br />

CPT group (2 unwell, 1 sectioned). At follow-up, a further 18 participants had withdrawn<br />

(26%). 14 participants were lost in the CPT group (5 unwell, 4 withdrew, 1 moved abroad,<br />

2 housebound, 2 died); 7 in the CPT + CPT group (5 unwell, 1 sectioned, 1 withdrew);<br />

and 7 in the CPT + FST group (5 unwell, 2 withdrew)<br />

Participants Randomised: total 109 participants. 38 participants were randomised to CPT, 35 to CPT<br />

+ CPT, and 36 to FST + CPT (only the results from the CPT and the CPT + FST groups<br />

were included in this review)<br />

Intervention: FST + CPT = 36 participants: 22 males (61%) and 14 females (39%); mean<br />

age: 71.17 (SD 10.6); 33.86 (SD 16.50) days after <strong>stroke</strong><br />

Control: CPT = 38 participants: 21 males (55%) and 17 females (45%); mean age: 66.37<br />

(SD 13.7); 36.76 (SD 22.41) days after <strong>stroke</strong><br />

Inclusion criteria: in<strong>patients</strong> between 1 and 13 weeks after anterior circulation <strong>stroke</strong> (ischaemic<br />

and haemorrhagic); independently mobile; some voluntary contraction in the<br />

lower affected limb; no orthopaedic surgery or trauma affecting the lower limb in the last<br />

8 weeks; no previous history of neurological diseases; able to follow a 1-stage command<br />

Exclusion criteria: not reported<br />

Interventions Intervention: FST/mixed <strong>training</strong> plus CPT. FST consisted of increasing the amount<br />

of bodyweight the <strong>patients</strong> needed to move; increasing movements resistance; reducing<br />

amount of bodyweight support during treadmill <strong>training</strong>. Frequency of intervention: 1<br />

hour <strong>for</strong> 4 days/week <strong>for</strong> 6 weeks<br />

Control: CPT included soft issue mobilisation, facilitation of muscle activity, facilitation<br />

of co-ordinated multi-joint movement; tactile and proprioceptive input, resistive exercise,<br />

and functional re<strong>training</strong>. Frequency of intervention: 1 hour <strong>for</strong> 4 days/week <strong>for</strong> 6 weeks<br />

Setting: hospital<br />

Outcomes Included outcomes: walking speed; health related quality of life measures (e.g. EuroQuol)<br />

Other outcomes: gait parameters; paretic knee torque <strong>for</strong>ce analysis; modified RMI<br />

Notes Trial authors stated ’strength <strong>training</strong>’ but intervention was actually mixed <strong>training</strong><br />

Risk of bias<br />

Bias Authors’ judgement Support <strong>for</strong> judgement<br />

<strong>Physical</strong> <strong>fitness</strong> <strong>training</strong> <strong>for</strong> <strong>stroke</strong> <strong>patients</strong> (<strong>Review</strong>)<br />

Copyright © 2011 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.<br />

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