Mudie 2001: Acute
Methods | Random assignment to 1 of 2 groups Method of randomisation not stated | |
Participants | 36 participants Inclusion criteria: dense hemiplegia (less than or equal to 2 on Motor Assessment Scale items 6 and 7), able to understand instructions, produce a response with non‐hemiplegic arm during bilateral trials, no other strokes or confounding co‐morbidities | |
Interventions | Group 1 (18 participants): unilateral Group 2 (18 participants): bilateral Each group completed 5 trials, including 5 repetitions of 5 seconds each (of isometric contractions for 2 tasks (shoulder abduction and wrist extension)) 15 seconds rest between each of the 5 trials, and 5 minutes rest between the 2 tasks There was no training period: movement and outcome measurement occurred simultaneously Profession of individual(s) providing training unclear (assume occupational therapist) For Group 1, trials 1, 2, 3 and 5 were performed unilaterally and trial 4 bilaterally For Group 2, trials 1, 3 and 5 were performed unilaterally and trials 2 and 4 bilaterally Therefore, data from trial 2 only was extracted for this review | |
Outcomes | Secondary outcomes: motor impairment ‐ strength outcomes: muscle activity (EMG) for shoulder abduction and wrist extension were reported (data from wrist extension activity only was extracted for analysis) | |
Notes | Results for acute and chronic patients presented separately, therefore 2 subgroups of this trial are included in the relevant analysis | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Unclear risk | Method of randomisation and allocation concealment not stated |
Blinding of outcome assessor? | Unclear risk | Assessment completed at the same time as the training |
Intention to treat analysis? | Unclear risk | Not stated |
Baseline similarity | Low risk | No significant differences between groups |