Actively Recruiting
Wearable Focal Vibration Therapy on Upper Extremity Function of People With Multiple Sclerosis: A Pilot Study
Led by University of Florida · Updated on 2026-03-06
15
Participants Needed
2
Research Sites
16 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This pilot mixed-method study will evaluate the feasibility, preliminary efficacy, and user experience of a home-based wearable Focal Vibration Therapy (FVT) intervention for improving upper extremity (UEx) function in people with multiple sclerosis (MS). Fifteen adults with relapsing-remitting MS (PRMS) and self-reported UEx impairments will participate in a 4-week FVT program using MyovoltTM wearable FVT devices applied to arm muscles.
CONDITIONS
Official Title
Wearable Focal Vibration Therapy on Upper Extremity Function of People With Multiple Sclerosis: A Pilot Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged over 18 years
- Confirmed diagnosis of relapsing-remitting multiple sclerosis according to the McDonald criteria
- No MS relapse or worsening symptoms within the past 6 months
- Self-report of upper extremity impairment such as reduced arm/hand function, muscle weakness, spasticity, or pain
- Stable on current MS treatment for at least 4 weeks with no plans to start new treatments
- Able and agree to use the Focal Vibration Therapy device after training
- Sufficient English proficiency to participate in interviews and follow instructions
- Able to visit the laboratory for assessments
- Able to provide written informed consent
You will not qualify if you...
- Cognitive impairment interfering with following instructions (Mini-MoCA score less than 12)
- Other neurological or psychiatric conditions affecting upper extremity function (e.g., stroke, severe carpal tunnel syndrome)
- Unstable heart disease or major medical illnesses preventing participation
- Known contraindications to vibration therapy such as pregnancy, acute deep vein thrombosis, severe osteoporosis, chronic migraines, epilepsy, active cancer in the target area, unstable heart disease, or implanted pacemaker without clearance
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Norman Fixel Institute for Neurological Diseases
Gainesville, Florida, United States, 32608
Actively Recruiting
2
University of Florida
Gainesville, Florida, United States, 32610
Actively Recruiting
Research Team
H
Hongwu Wang, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DEVICE_FEASIBILITY
Number of Arms
1
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