Methods | RCT Methods of randomisation: random‐number table |
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Participants | Country: Taiwan Sample size: 48 Inclusion criteria: at least 6 months after onset of a unilateral stroke, an initial score of the FMA arm assessment of 20 to 50 (SD 25), minimal hand function (i.e. extension of the wrist ≥ 10°, extension of at least 2 fingers > 0° and > 10°, and abduction of thumb ≥ 10°, no excessive spasticity in any of the joints of the affected arm (MAS ≥ 4), no arm fracture within 3 months or painful arthritis of the joints, and able to follow study instructions and perform study tasks (Mini‐Mental State Examination score ≥ 22) Exlusion criteria: none described |
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Interventions | 3 groups:
Participants in each group received 20 training sessions of 90 to 105 min/day, 5 days/week for 4 weeks. In addition to the intervention provided in the clinics, all participants were encouraged to use their affected upper limb during activities in their daily life situations (e.g. at home) |
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Outcomes | Outcomes were recorded at baseline and post‐treatment after 4 weeks
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Notes | We combined the results of both the RT + CIT group and the RT group (collapsed) group and compared this collapsed group with the results of the CT group | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Randomisation assignments were generated from a random‐number table |
Allocation concealment (selection bias) | Low risk | Sequentially numbered, sealed, and opaque envelopes and a blinded investigator assigned each participant to a treatment group |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Blinded assessor |
Selective reporting (reporting bias) | Unclear risk | Insufficient information to permit judgement |