Focal Vibration Therapy for Upper Extremity Dysfunction

Wearable Focal Vibration Therapy on Upper Extremity Function of People With Multiple Sclerosis: A Pilot Study

Recruiting N/A Interventional Study
Multiple Sclerosis (MS) - Relapsing-remitting Upper Extremity Dysfunction
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 100
Sex
Any
Study type
Interventional
Purpose
Device Feasibility
Participants needed
15 (estimated)
Sponsor
University of Florida · Other
Who this trial is looking for

This trial is looking for adults with relapsing-remitting multiple sclerosis (MS) who have difficulty using their arms or hands. Participants will try a wearable device for 4 weeks to see if it helps improve their arm function.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am over 18 years old.
  • I have been diagnosed with relapsing-remitting MS.
  • I have not had any MS relapses in the last 6 months.
  • I have reported problems with my arm or hand function.
  • I have been on my current MS treatment for at least 4 weeks.
  • I can use the FVT device after training.
  • I can speak English well enough to follow instructions.
  • I can visit the lab for assessments.

You may not be able to join if

  • I have cognitive impairment affecting my ability to follow instructions.
  • I have other neurological or psychiatric conditions affecting my arms.
  • I have unstable heart disease or a major medical issue.
  • I am pregnant or have conditions that make vibration therapy unsafe.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial
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 wea…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Aged over 18 years * Confirmed diagnosis of RRMS according to the McDonald criteria (33) * No MS relapse or exacerbation within the past 6 months (ensuring stability of symptoms) * Self-report on clinical evidence of UEx impairment (including reduced arm/hand function, muscle …
Contacts

Hongwu Wang, PhD

352-273-9934

hongwu.wang@ufl.edu

CONTACT