Conroy 2011
Methods | Prospective, single‐blinded RCT Method of randomisation: choosing a sealed envelope | |
Participants | Country: USA Sample size: 62 participants (41 in the treatment group and 21 in the control group) Inclusion criteria: diagnosis of clinically defined, unilateral hemiparetic stroke with radiologic exclusion of other possible diagnoses; onset of stroke 6 months before randomisation for ischaemic stroke, 12 months for haemorrhagic stroke; manual muscle testing of grade 3 or lower for at least 1 muscle of the affected arm; > 18 years of age Exclusion criteria: serious complicating medical illness or stroke occurring within the previous 6 months (or both); contractures or orthopaedic problems limiting the range of joint movement in the potential study arm; visual loss limiting the ability to see the test patterns on the robot monitor; Botox injection of the affected arm 3 months before study onset or during the study |
|
Interventions | 3 groups:
|
|
Outcomes | Outcomes were recorded 3 times at baseline and after 6 weeks and 3 months later (follow‐up)
|
|
Notes | We combined the results of both the planar group and the planar and vertical group in 1 (collapsed) group and compared this collapsed group with the results of the control group | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Stratified randomisation by a computer scheme |
Allocation concealment (selection bias) | Unclear risk | Insufficient information about the sequence generation process |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Assessment was performed by a single experienced evaluator blinded to group assignment |
Selective reporting (reporting bias) | Unclear risk | Insufficient information to permit judgement |