About this trial
This study aims to evaluate the effect of a personalized technology-based rehabilitative intervention on Upper Limb (UL) motor function and capacity recovery in People with Stroke (PwS). The study is single-cohort study in which eligible participants will undergo baseline and follow-up clinical and instrumental assessments over a 4-5 week period.
The intervention consists of a personalized and specific upper limb technology-based rehabilitation programme delivered three times per week for a total of 12-15 sessions. Each session lasts approximately one hour and is integrated with conventional rehabilitation treatments.
Primary outcomes include Fugl-Meyer Assessment for Upper Extremity (FMA-UE) and Action Research Arm Test (ARAT). Secondary outcomes include instrumental assessment of active range of motion and grip strength.
Eligibility criteria
Qualifiers
Age ≥ 18 years;
First-ever unilateral ischemic or hemorrhagic stroke;
Presence of upper limb motor impairment;
Modified Ashworth Scale (MAS) < 3;
Disqualifiers
Diagnosis of severe aphasia, based on medical records, preventing participation;
Bilateral hemisphere lesions;
Severe and unstable medical conditions (e.g. untreated seizure, heart failure) that preclude participation in rehabilitation;
Other neurological and/or psychiatric diseases;
Trial design
Treatments tested in this trial
- Technology-based UL rehabilitation