Dias 2006
Methods | RCT Method of randomisation: permuted block randomisation Blinding of outcome assessors: stated as blinded Adverse events: none stated Deaths: none Drop‐outs: none ITT: not stated but probably done because there were no drop‐outs | |
Participants | Country: Portugal 40 participants (20 in treatment group, 20 in control group) Ambulatory at start of study Mean age: 69 years Inclusion criteria: first‐ever stroke patients > 12 months after stroke; age > 18 and < 80 years; cognitive (Mini Mental State Examination > 19) and communication capacities of understanding the treatment; absence of cardiac, psychological and orthopaedic contraindications Exclusion criteria: not stated | |
Interventions | 2 arms:
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Outcomes | Outcomes were recorded at baseline and after 4 weeks and 3 months later
After study end and at follow‐up, participants rated satisfaction with and efficiency of treatment in a self‐questionnaire (Likert scale) |
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Notes | Published and unpublished data provided by the authors | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Unclear |
Allocation concealment (selection bias) | Low risk | Central allocation |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Not done |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No missing outcome data |