Using mirror therapy and augmented reality for stroke rehabilitation
Mirror Therapy Preceding Augmented Reality in Stroke Rehabilitation: A Cross-Setting Study
This study is testing if combining mirror therapy with augmented reality can help stroke patients recover better during a 9-week program at home and in clinics.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 20 Years to 80 Years |
| Sex | All |
| Sponsor | National Taiwan University Hospital Academic / other |
| Locations | 5 sites (New Taipei City and 4 other locations) |
| Trial ID | NCT05467813 on ClinicalTrials.gov |
What this trial studies
This research aims to explore innovative rehabilitation strategies for stroke patients by combining mirror therapy with augmented reality (AR) techniques. The study will assess the effectiveness of these hybrid interventions in both clinic and home settings, utilizing telehealth methods to monitor patient progress. Participants will engage in a 9-week program designed to enhance their rehabilitation experience and outcomes. The approach is based on previous research funded by the National Health Research Institutes, focusing on the complexities of stroke recovery.
Who should consider this trial
Good fit: Ideal candidates include adults aged 20 to 80 who have experienced a first-ever unilateral stroke at least 3 months prior and meet specific functional criteria.
Not a fit: Patients with acute inflammation, serious medical issues, or those unable to participate in the rehabilitation program may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve rehabilitation outcomes for stroke patients, leading to better recovery and quality of life.
How similar studies have performed: While the combination of mirror therapy and augmented reality is innovative, similar approaches in stroke rehabilitation have shown promise, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. a first-ever unilateral stroke ≥3 months 2. age between 20 and 80 years 3. baseline FMA-UE \>10 4. no severe spasticity in any joints of the affected arm MAS \< 3) 5. ability to follow the instructions of the evaluator and therapists (Mini-Mental State Examination Score ≥22) 6. ability to stand in a step-standing position for at least 30 seconds 7. ability to walk a minimum of 10 meters with or without a device 8. no severe vision impairments and other major neurologic diseases 9. ability to take part in a rehabilitation intervention program for 9 weeks 10. not participating in other studies over the study period and willingness to provide informed written consent. Exclusion Criteria: 1. acute inflammation 2. serious medical problems or poor physical conditions that might be detrimental to study participation
Where this trial is running
New Taipei City and 4 other locations
- Taipei Tzu Chi Hospital, Buddhist Tzu Chi Foundation — New Taipei City, Taiwan (Recruiting)
- Feng Yuan Hospital, Ministry of Health and Welfare — Taichung, Taiwan (Recruiting)
- National Taiwan University Hospital — Taipei, Taiwan (Recruiting)
- Taipei Hospital, Ministry of Health and Welfare — Taipei, Taiwan (Recruiting)
- Linkou Chang Gung Memorial Hospital, Chang Gung Medical Foundation — Taoyuan, 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.