Effects of Powered Hip Flexion Device in Persons With Multiple Sclerosis (NCT07724093) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effects of Powered Hip Flexion Device in Persons With Multiple Sclerosis
United States10 participantsStarted 2026-07-15
Plain-language summary
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?
Who can participate
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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
Exclusion Criteria:
* 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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.