Effects of Powered Hip Flexion Device in Persons With Multiple Sclerosis
Starting soon · Not applicable
Conditions studied: Multiple Sclerosis (MS) Relapsing Remitting
In brief
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 facts
- Study ID
- NCT07724093
- Run by
- University of Dayton
- People needed
- 10
- Starts
- 2026-07-15
- Expected to finish
- 2028-05-01
- Last updated by the study team
- 2026-07-23
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18-80
- Diagnosis of relapsing remitting, primary progressive or secondary progressive MS
- Unilateral or bilateral hip flexion weakness (Manual muscle testing score of 3 or less)
- Ability to walk at least 30 meters without requiring rest and without physical support or assistance from another person.
- Waist circumference 26-48", Height 5 '- 6'2", Weight 100-230lbs
You may not qualify if…
- Prior regular use of a hip flexion orthosis within the past 6 months.
- Cognitive or communication deficits that would limit ability to participate safely.
- Significant pain or deformity of the lower extremities that could impact walking ability.
- Severe spasticity (Modified Ashworth Score of 3 or 4) of the hips or lower extremities that could impact walking ability.
- Any other neurological conditions that may affect gait.
Where it is running
- University of Dayton — Dayton, Ohio, United States
Full record on ClinicalTrials.gov
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