A Therapeutic Experience Program (TEP) Study for Improvement of Gait in People With Multiple Sclerosis (MS)
NCT ID: NCT05437276
Last Updated: 2025-03-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
43 participants
OBSERVATIONAL
2022-07-01
2024-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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People with mild to moderate Multiple Sclerosis and gait deficit
All enrolled subjects will go through 14 weeks therapy: Phase 1 (2-week in-clinic supervised PoNS therapy) followed by Phase 2 (12-week period of at-home unsupervised - PoNS therapy).
Six-Month Observation: subjects will be asked to return to the clinic six months after the end of the 14-week course of therapy for an observation visit.
Individual subjects could receive, upon investigator's opinion of need, an ad hoc second 12-week course of PoNS therapy.
PoNS®
The PoNS device used in conjunction with rehabilitative physical therapy
Interventions
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PoNS®
The PoNS device used in conjunction with rehabilitative physical therapy
Eligibility Criteria
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Inclusion Criteria
2. EDSS scores \< 6.5 at screening; a demonstrated gait deficit.
3. Can walk at least 10 meters with or without the use of walking aids.
4. Participants must be stable without relapse for at least 60 days and agree to PoNS therapy regimen.
Exclusion Criteria
2. Dementia.
3. Subjects who are currently attending physical rehabilitation and are unwilling to switch to PoNS-specific physical therapy regimen.
4. Subjects who are already functional community ambulators (gait speed\>120cm/s43).
5. Subjects will also be excluded as per the Helius Medical PoNS device indication for usage ("electrical stimulation should not be used: if there is an active or suspected malignant tumor; in areas of recent bleeding or open wounds; in areas that lack normal sensation; in women who are pregnant, or in people with sensitivity to nickel, gold or copper").
22 Years
ALL
No
Sponsors
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Helius Medical Inc
INDUSTRY
Responsible Party
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Principal Investigators
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Antonella Favit-VanPelt
Role: STUDY_DIRECTOR
Helius Medical Inc
Locations
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Shepherd Center
Atlanta, Georgia, United States
MGH Institute of Health Professions
Boston, Massachusetts, United States
Neurology Center of New England, P.C.
Foxborough, Massachusetts, United States
NYU Langone Health, NYU Grossman School of Medicine
New York, New York, United States
Oregon Health and Science university (OHSU)
Portland, Oregon, United States
Countries
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Other Identifiers
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HMI-MS-PoNS-TE001
Identifier Type: -
Identifier Source: org_study_id
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