Multisensory-Rhythmic Intervention for Elderly Rehabilitation
Linking From an Artificial-Intelligence Driven Assessment of Upper Extremity Motor Adaptation to a Novel Multisensory-Rhythmic Intervention in Geriatric Rehabilitation
This study is testing a new way to help older adults improve their movement and stay independent by using virtual reality and rhythmic activities.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 108 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | National Cheng-Kung University Hospital Academic / other |
| Locations | 1 site (Tainan) |
| Trial ID | NCT06151626 on ClinicalTrials.gov |
What this trial studies
This intervention focuses on enhancing motor control in elderly individuals through a novel multisensory-rhythmic approach. It utilizes virtual reality and rhythmic skill training to provide sensory stimulation and improve motor planning. Participants will engage in various activities, including visual feedback training and relaxation exercises, aimed at preserving their independence in daily activities. The study targets both healthy older adults and those with mild cognitive impairment, assessing their motor responses in a supportive environment.
Who should consider this trial
Good fit: Ideal candidates include healthy older adults and those with mild cognitive impairment aged 65-85, as well as healthy young participants aged 20-39.
Not a fit: Patients with significant mental illness, central nervous system disorders, or recent skeletal, muscular, or neurological problems may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this intervention could significantly improve motor function and quality of life for elderly patients, helping them maintain independence.
How similar studies have performed: While the specific approach of multisensory-rhythmic intervention is novel, similar studies in motor rehabilitation have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Montreal Cognitive Assessment (MoCA) score of 23 or higher, 2. Clinical Dementia Rating (CDR) of 0 (for normal subjects) or 1 (for mild cognitive impairment subjects), 3. Healthy young participants aged between 20-39 years, healthy older adults and mild cognitive impairment participants aged between 65-85 years, 4. No skeletal, muscular, or neurological problems in the upper limbs in the past year, and 5. Sufficient visual acuity to complete the tasks. Exclusion Criteria: * Any subjects with significant mental illness, central nervous system disorders, or medical history
Where this trial is running
Tainan
- National Cheng-Kung University Hospital — Tainan, Taiwan (Recruiting)
Study contacts
- Study coordinator: Hsiu-Yun Hsu, Ph.D
- Email: hyhsu@mail.ncku.edu.tw
- Phone: 886-6-2353535
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.