Nomad P-KAFO Study
Recruiting now · Not applicable
Conditions studied: Cerebrovascular Accident, Post-polio Syndrome, Spinal Cord Injuries, Multiple Sclerosis, Muscular Dystrophy, Paralysis
In brief
The goal of this clinical trial is to evaluate the impact of using the Nomad powered KAFO in people who have had a musculoskeletal or neurological injury that has affected their ability to walk. The main questions it aims to answer are to quantify the effectiveness of the Nomad in improving mobility, balance, frequency of falls, and quality of life in individuals with lower-extremity impairments compared to their own brace, over three months of daily home and community use. Participants will: * Wear a sensor that records everyday activities and mobility. * Perform measures of mobility and different activities of participation using their own brace. * Perform measures of mobility and different activities of participation using the Nomad powered KAFO
Key facts
- Study ID
- NCT05644522
- Run by
- Shirley Ryan AbilityLab
- People needed
- 36
- Starts
- 2024-03-01
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-05-11
Who can join
Age: 18 and older, up to 89. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Regular and compliant use of a unilateral or bilateral KAFO or SCO or other passive KAFOs for impairment due to neurological or neuromuscular disease, orthopedic disease, or trauma
- Cognitive ability to understand and follow the study protocol; willingness to provide informed consent
- Willing to wear and charge an activity monitor for three-months home trials.
You may not qualify if…
- Flexion contracture in the knee and/or hip joint in excess of 15 degrees
- Non-correctable knee varus/valgus in excess of 15 degrees
- Severe spasticity
- Inability to stabilize the trunk with or without assistive devices (crutches, canes, etc.)
Where it is running
- Shirley Ryan AbilityLab — Chicago, Illinois, United States (enrolling)
Full record on ClinicalTrials.gov
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