Comparing two robotic therapy methods with exergaming for stroke rehabilitation
Proximal- Versus Distal-Prioritized Robotic Practice Plus Kinetic Exergaming in Stroke Rehabilitation
NA · Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation · NCT05492175
This study is testing two different robotic therapy methods combined with fun video game exercises to see which one helps stroke patients recover better and improve their daily activities.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 72 (estimated) |
| Ages | 20 Years to 80 Years |
| Sex | All |
| Sponsor | Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation (other) |
| Locations | 4 sites (Taichung and 3 other locations) |
| Trial ID | NCT05492175 on ClinicalTrials.gov |
What this trial studies
This research program investigates the effects of upper-limb robotic therapy combined with interactive exergaming in stroke rehabilitation. It aims to compare proximal versus distal priority robotic priming techniques to assess their impact on sensorimotor function, daily living activities, self-efficacy, quality of life, and motor control strategies in stroke patients. The study will also evaluate the retention effects of these approaches over three months and identify predictors of functional improvements after therapy.
Who should consider this trial
Good fit: Ideal candidates are adults aged 20 to 80 who have experienced their first stroke at least three months prior and meet specific functional criteria.
Not a fit: Patients with acute inflammation, pain, or other neurological conditions that may hinder participation will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could enhance recovery outcomes for stroke patients by improving motor function and quality of life.
How similar studies have performed: Other studies have shown promise in using robotic therapy and exergaming for rehabilitation, suggesting potential success for this innovative approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. a first ever-stroke≧3 months 2. age range between 20 to 80 years 3. baseline Fugl-Meyer assessment of upper extremity scale (FMA-UE) between 18 to 56 4. no excessive muscle spasticity of the affected extremities (Modified Ashworth Scale \< 3 at any joints) 5. able to follow examiners' commands and study instructions (Mini-Mental State Examination score≧22) 6. can maintain a step-standing position for at least 30 seconds 7. can walk for at least 10 meters with or without device 8. no participation in further experimental rehabilitation or drug studies during the duration of the project Exclusion Criteria: 1. acute inflammation and pain 2. concomitant neurologic, neuromuscular or orthopedic conditions that may impede participation in this research.
Where this trial is running
Taichung and 3 other locations
- Feng Yuan Hospital, Ministry of Health and Welfare — Taichung, Taiwan (RECRUITING)
- National Taiwan University Hospital — Taipei, Taiwan (RECRUITING)
- Taipei Municipal Wan Fang Hospital — Taipei, Taiwan (RECRUITING)
- Taipei Tzu Chi Hospital — Taipei, Taiwan (RECRUITING)
Study contacts
- Principal investigator: Keh-Chung Lin, Sc.D — National Taiwan University
- Study coordinator: Keh-Chung Lin, Sc.D
- Email: kehchunglin@ntu.edu.tw
- Phone: +886-3366-8180
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.
Conditions: Stroke Rehabilitation