Effects of Powered Hip Flexion Device in Persons With Multiple Sclerosis
Part of paid clinical trials in Dayton, Ohio.
- Sponsor
- University of Dayton
- Study ID
- NCT07724093
- Status
- Not Yet Recruiting
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Conditions
- Multiple Sclerosis (MS) Relapsing Remitting
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Powered Hip Flexion Orthosis (Hypershell X) — DEVICEParticipants will perform a series of 10 meters walks while wearing the hip flexion assist device under the following conditions. 1) No assistance (passive mode) 2) 25% power assistance 3) 50% power assistance 4) 75% power assistance During the trial subjects will wear motion sensors that provide the following gait parameters: speed, step and stride length, foot clearance, foot angle at heel strike, circumduction, single and double support time.
Study Details
The purpose of this study is to assess the immediate effects of a commercially available non-FDA regulated powered hip flexion assist device (Hypershell X, Shenzhen, China) on walking ability in persons with MS. The main question it aims to answer is: Does a powered hip flexion device provide immediate improvements in walking ability over short distances for people with MS?
Key Dates
- First listed
- Jul 23, 2026
- Start date
- Jul 15, 2026
- Status verified
- Jul 2026
- Primary completion
- May 1, 2027
- Completion
- May 1, 2028
Study Design
- Enrollment
- 10 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Hip flexion assistParticipants will perform a series of 10 meters walks while wearing the hip flexion assist device under the following conditions. 1. No assistance (passive mode) 2. 25% power assistance 3. 50% power assistance 4. 75% power assistance During the trial subjects will wear motion sensors that provide the following gait parameters: speed, step and stride length, foot clearance, foot angle at heel strike, circumduction, single and double support time.
Primary Outcome Measure
Gait speed [ Time Frame: Day 1 (immediate effect of device use) ]
Central Contacts
- Kurt Jackson, PhD937-229-5605
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Dayton | Dayton | Ohio | 45469 |
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