Stopped: Recruitment halted due to recruitment difficulties.
Specific Aim 1: Complete pilot testing of study protocol in individuals with chronic stroke for feasibility evaluation and protocol refinement. Specific Aim 2: Estimate the preliminary effect of CO-OP+tDCS on activity performance in individuals with chronic stroke.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Willingness to be randomized
Timeframe: After study completion, an average of 5 weeks
Recruitment
Timeframe: After study completion, an average of 5 weeks
Retention
Timeframe: After study completion, an average of 5 weeks
Adherence
Timeframe: After study completion, an average of 5 weeks