Actively Recruiting
WIM Exosuit Wearable Soft Robot for Enhancing Walking Activity
Led by Shirley Ryan AbilityLab · Updated on 2025-08-29
20
Participants Needed
1
Research Sites
155 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is to develop, test, and optimize a soft hip wearable robot for individuals who have experience a stroke.
CONDITIONS
Official Title
WIM Exosuit Wearable Soft Robot for Enhancing Walking Activity
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be at least 6 months post-stroke, have a diagnosis of Parkinson's, have a diagnosis of multiple sclerosis, or be an adult older than 65 with no known neurological diagnoses.
- For optimization, healthy individuals with no impairments may also participate.
- Age between 18 and 89 years.
- For stroke, Parkinson's, multiple sclerosis, or older adults, must have adequate cognitive function (MMSE score >17).
- Ability to walk at least 10 meters with maximum one person assist.
- Able to safely fit into the WIM exosuit as confirmed by in-person fitting.
You will not qualify if you...
- Less than 90 days post major orthopedic surgery (hip, knee, or ankle joint replacement).
- Less than 6 months post coronary artery bypass graft (CABG) or cardiac valve procedure.
- Skin irritations or conditions preventing toleration of the exosuit.
- Severe osteoporosis requiring or recommended pharmacologic treatment or history of fractures.
- Serious cardiac conditions such as recent myocardial infarction, heart surgery within 3 months, congestive heart failure, unstable arrhythmias, hypertrophic cardiomyopathy, severe aortic stenosis, or angina/dyspnea at rest or during daily activities.
- Pregnancy.
- Uncontrolled hypertension (resting systolic ≥150 or diastolic ≥90), with re-check after sitting quietly for 5 minutes.
- Lower extremity fracture currently or within past 6 months.
- Modified Ashworth Spasticity scores ≥3 in hip flexors or extensors if post-stroke or multiple sclerosis.
- Pre-existing neurological disorders like ALS or dementia.
- History of major head trauma, lower extremity amputation, non-healing ulcers, active infections, legal blindness, or significant psychiatric illness.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Shirley Ryan AbilityLab
Chicago, Illinois, United States, 60611
Actively Recruiting
Research Team
K
Katelyn Aragon
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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