The purpose of this study is to assess the changes in physiological parameters and clinical scales resulting from treatment with AOT (action observation training) in subjects with subacute stroke. Furthermore, this study assess the perception of applicability and satisfaction degree for this kind of treatments.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change in Fugl-Meyer Assessment Upper Extremity between four time points
Timeframe: Baseline, week 3, week 4, after 6 months
Change in Barthel Index between four time points
Timeframe: Baseline, week 3, week 4,after 6 months
Change in Box and Block Test between four time points
Timeframe: Baseline, week 3, week 4,after 6 months
Change in Modified Ashworth Scale between four time points
Timeframe: Baseline, week 3, week 4,after 6 months
Change in Visual Analogue Scale between four time points
Timeframe: Baseline , week 3, week 4,after 6 months
Electroencephalography power in alpha band
Timeframe: Up to 1 month
Motion Capture (MOCAP) recordings
Timeframe: Up to 1 month
Change in Oxford Cognitive Screen between two time points
Timeframe: Baseline and week 4