Study to Investigate Vagus Nerve Stimulation Paired With Motor Task for Remyelination and Functional Recovery
Part of paid clinical trials in Aurora, Colorado.
- Sponsor
- University of Colorado, Denver
- Study ID
- NCT06641271
- Status
- Recruiting
Conditions
- Multiple Sclerosis
- Multiple Sclerosis (MS) - Relapsing-remitting
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Closed Loop Trans-Auricular Vagus Nerve Stimulation System — DEVICEA closed loop system that delivers stimulation to the vagus nerve via the ear non-invasively following a trigger event.
- Placebo — DEVICEA closed-loop vagus nerve stimulation device that can deliver sham stimulation to the ear to simulate stimulation of the vagus nerve.
Study Details
The goal of this clinical trial is to learn if stimulating the vagus nerve in combination with a motor task in people with multiple sclerosis can improve motor function. The main questions it aims to answer are: * Is stimulating the vagus nerve safe and feasible after demyelinating episodes? * Does a paired motor task with vagus nerve stimulation improve motor function with someone who has multiple sclerosis? Researchers will compare active vagus nerve stimulation to a sham stimulation to see if the paired vagus nerve stimulation can improve motor control. Participants will: * Come in for study visits over a six month period. Study visits are three times weekly for the first month, then single follow up visits at two, three, and six months. * During study visits, participants will complete 30 minutes of the paired vagus nerve stimulation with a motor task, specifically the grooved peg test. * At various timepoints in the study, motor and disability tests will be administered to see if there are any changes in motor control for that participants. These tests include the timed 25 foot walk test, expanded disability scale, the upper extremity portion of the Fugl-Meyer Assessment, and the Multiple Sclerosis Impact Scale - 29.
Key Dates
- Start date
- Jan 21, 2025
- Status verified
- Mar 2025
- Primary completion
- Nov 30, 2027
- Completion
- Nov 30, 2027
Study Design
- Enrollment
- 70 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: Experimental - Active StimulationParticipants in this arm will receive active stimulation during the paired motor task.
- Sham Comparator: Control - Sham StimulationParticipants in this arm will receive sham stimulation during the paired motor task to create a control to the experimental group.
Primary Outcome Measure
Change from baseline in time to complete the grooved peg test [ Time Frame: End of Study (6 months) ]
Central Contacts
- Adrienne Ellett, MS7204280944
- Pamela David Gerecht(303)724-4134
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Clinical Translational Research Center at CU Anschutz | Aurora | Colorado | 80010 | Jeffrey Bennett, MD (PRINCIPAL_INVESTIGATOR) |
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