Vibration therapy to improve arm and hand function in chronic stroke survivors
Effects of Vibration on Motor Function of Survivors of Chronic Stroke
This study tests if using vibration therapy along with robotic training can help improve arm and hand function in people who have had a stroke for a long time.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Shirley Ryan AbilityLab Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Trial ID | NCT06663501 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effects of vibration on the tendons during arm and hand training for individuals who have survived a chronic stroke. The investigators hypothesize that combining robotic training of the wrist and elbow with body awareness training will enhance motor function. The study aims to address the significant motor disabilities that many stroke survivors face, particularly those who have not fully recovered after six months. By focusing on improving proprioception and motor control, the research seeks to facilitate better rehabilitation outcomes for these patients.
Who should consider this trial
Good fit: Ideal candidates are individuals who have experienced a stroke more than six months prior and are medically stable without current anti-spasticity medications.
Not a fit: Patients with recent changes in medications, unstable medical conditions, or significant musculoskeletal issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance motor function and quality of life for chronic stroke survivors.
How similar studies have performed: Other studies have shown promising results with similar approaches to enhancing motor function in stroke rehabilitation, indicating potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * If stroke, more than 6 months after * Medically stable * Not currently taking any anti-spasticity medications (for at least 2 weeks) * Able to comply with study requirements Exclusion Criteria: * Recent change in the use of any medications * Other physical conditions such as orthopedic injuries or surgeries * Unstable Medical conditions or any other clinical observations that may affect the candidates performance, health, safety, or ability to participate in the study as determined by the treating therapist * Anti-spasticity drug injection in the 3 months prior to participation * Presence of significant cardiorespiratory or metabolic disease * Inability to achieve standard position required for EMG recordings * Intrathecal baclofen pump * Musculoskeletal conditions/surgeries resulting in difficulty participating * Adults unable to consent * Pregnant women, prisoners, and individuals under the age of 18
Where this trial is running
Chicago, Illinois
- Shirley Ryan AbilityLab — Chicago, Illinois, United States (Recruiting)
Study contacts
- Principal investigator: William Z Rymer, PhD — Shirley Ryan AbilityLab
- Study coordinator: Alexander J Barry, MS, CCRC
- Email: alex.barry92@gmail.com
- Phone: 16309817670
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.