Ucar 2014.
| Methods | RCT
Method of randomisation: random number list Blinding of outcome assessors: yes Adverse events: not described Deaths: not described Dropouts: not described ITT: unknown |
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| Participants | Country: Turkey
22 participants (11 in treatment group, 11 in control group)
Ambulatory at start of study
Mean age: 56 years in experimental group and 62 years in control group Inclusion criteria: adult male (> 18 years), ability to ambulate 10 metres without personal assistance, and not receiving any other physical therapy Exclusion criteria: body weight more than 300 pounds (135 kg), FAC score < 3 and not able to walk consistently or independently within the community, cognitive deficits, cardiac disease, spasticity of the lower limbs preventing robotic walking, traumatic stroke, intracranial space occupying lesion‐induced strokes, and seizures |
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| Interventions | 2 arms:
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| Outcomes | Outcomes were assessed at baseline and after 2 and 8 weeks:
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| Notes | ||
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | Random number list |
| Allocation concealment (selection bias) | Unclear risk | Not described |
| Blinding of outcome assessment (detection bias) All outcomes | Low risk | Stated as blinded |
| Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Unclear |