The proposed study is a two-arm randomized clinical trial designed to assess the effects of the StrokeWear system on clinical outcomes over a period of 6-months in subacute stroke survivors. The Intervention group will use StrokeWear system in combination to a motor and behavioral home intervention whereas the Control group will follow usual care which consists of a home-exercise plan (HEP).
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Change in Motor Activity Log-Amount of Use
Timeframe: Change from baseline Motor Activity Log-Amount of Use score at 6 months
Change in Fugl-Meyer Upper-Extremity
Timeframe: Change from baseline Fugl-Meyer Upper-Extremity score at 6 months
Change in Upper-Extremity Activity Counts
Timeframe: Change from baseline Upper-Extremity Activity Counts score at 6 months