Home-based exercise program for stroke recovery
Scale-out of a Home-based Arm and Hand Exercise Program for Stroke: A Multisite Implementation-efficacy Trial
This study tests whether a home-based exercise program can help stroke patients recover better than regular therapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 143 (estimated) |
| Ages | 20 Years and up |
| Sex | All |
| Sponsor | Chang Gung Memorial Hospital Academic / other |
| Locations | 1 site (Chiayi City) |
| Trial ID | NCT06204744 on ClinicalTrials.gov |
What this trial studies
This multisite clinical trial evaluates the effectiveness of a home-based Graded Repetitive Arm Supplementary Program (GRASP) compared to conventional occupational therapy for stroke patients. Participants will be randomly assigned to either the GRASP program or a standard therapy program, with interventions lasting 4 to 6 weeks, involving three sessions per week. The study will assess improvements in upper extremity motor function, daily activities, quality of life, and motor control strategies through clinical evaluations and patient feedback at multiple time points. The trial aims to provide insights into the feasibility and impact of home-based rehabilitation for stroke recovery.
Who should consider this trial
Good fit: Ideal candidates are adults aged 20 years or older who have upper extremity hemiparesis from a first-ever stroke and can follow simple instructions.
Not a fit: Patients with orthopedic conditions affecting the arm or hand, other neurological disorders, or severe pain that limits movement may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly enhance recovery outcomes for stroke patients by providing effective home-based rehabilitation options.
How similar studies have performed: Other studies have shown promising results with home-based rehabilitation programs for stroke recovery, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * are aged 20 years or older * have upper extremity hemiparesis due to the first-ever stroke * have some voluntary movement in the affected UE * are able to follow 2-step instructions Exclusion criteria: * orthopedic conditions affecting the arm/hand or other neurological conditions * severe pain that prevents movement in the affected arm and hand * unstable medical status
Where this trial is running
Chiayi City
- Chiayi Chang Gung Memorial Hospital — Chiayi City, Taiwan (Recruiting)
Study contacts
- Principal investigator: Chieh-ling Yang — Chang Gung University
- Study coordinator: Chieh-ling Yang
- Email: chieh-ling.yang@cgu.edu.tw
- Phone: 03-2118800
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.