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

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Mudge 2009 (Continued)<br />

sessions (e.g. provide participants with relevant and useful in<strong>for</strong>mation <strong>for</strong> everyday activities;<br />

provide intellectual stimulation and enjoyment sessions; play a game; cafe’ outing).<br />

Each session lasted 90 minutes. The control group was led by an occupational therapist.<br />

Measurements per<strong>for</strong>med post-intervention and at 3-month follow-up<br />

Setting: rehabilitation clinic<br />

Outcomes Included outcomes: mean number of steps a day measured by the StepWatch Activity<br />

Monitor; walking speed and walking endurance<br />

Other Outcomes: self-reported confidence during activity of daily living and self-reported<br />

mobility assessed by the ABCS, the RMI, and the PADS<br />

Notes Randomisation was revealed to each participant by the principal investigator after the second<br />

baseline assessment. The trial was limited by the small number of participants. Participants<br />

volunteered to participate and were likely to be highly motivated. The sample appeared in<br />

fact to be higher functioning in terms of gait speed. A gait endurance component was not<br />

included in the <strong>training</strong> circuit<br />

Risk of bias<br />

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

Allocation concealment (selection bias) Unclear risk Not reported<br />

Ouellette 2004<br />

Methods Design: randomised trial of resistance <strong>training</strong> versus non-exercise intervention - after usual<br />

care<br />

Randomisation: unknown<br />

Allocation concealment: unknown<br />

Blinding: investigator<br />

Intention-to-treat: yes<br />

Measurements: end of intervention (12 weeks)<br />

Withdrawals: intervention: 1 withdrew (cardiac problem), and 1 was lost at follow-up<br />

(hernia); control: 2 withdrew during intervention, 1 was lost at follow-up (abnormal ECG)<br />

Participants Randomised: 42 participants<br />

Intervention: 21 participants; number of males and females unknown; age 65.8 years (SD<br />

11.5); 968 days post-<strong>stroke</strong> (SD 460)<br />

Control: 21 participants; number of males and females unknown; age 66.1 years (SD 9.62)<br />

; 779 days post-<strong>stroke</strong> (SD 558)<br />

Inclusion criteria: age ≥ 50 years; 6 months to 6 years after single unilateral mild/moderate<br />

<strong>stroke</strong> with residual lower extremity hemiparesis; community dwelling; independently<br />

ambulatory +/- walking aids; report of ?2 limitations on the physical function subscale of<br />

the SF-36; ability to travel to the exercise laboratory; willing to be randomised<br />

Interventions Intervention: progressive resistance <strong>training</strong> of both lower limbs per<strong>for</strong>med 3 days/week<br />

<strong>for</strong> 12 weeks comprising 3 sets of 8 to 10 repetitions at 70% of 1 repetition maximum (1-<br />

RM); exercises were (1) seated bilateral leg press, and (2) unilateral knee extension, both<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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