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Assessment of Safety and Acute Effects of a Lower-limb Powered Dermoskeleton in Patients With Neuromuscular Disorders
Sponsor: Institut de Myologie, France
Summary
The aims of the current study are as follow: i) Evaluate the safety, usability, and acute efficiency of a programmable ambulation exoskeleton (KeeogoTM Dermoskeleton System, B-Temia Inc., Quebec, Canada) in patients with neuromuscular disorders, ii) Elaborate recommendations regarding usability criteria for safe and efficient use the device in patients with neuromuscular disorders (e.g. type and severity of patient's functional deficits), iii) generate necessary data to foresee a future study involving a home use of the device and assessment of long-term benefits.
Key Details
Gender
All
Age Range
18 Years - 70 Years
Study Type
INTERVENTIONAL
Enrollment
50
Start Date
2021-12-01
Completion Date
2025-04-22
Last Updated
2026-04-16
Healthy Volunteers
Yes
Conditions
Interventions
Lower-limb powered dermoskeleton
Patients and healthy subjects will wear the movement assistance device to perform different standardised physical evaluations.
Locations (1)
Institute of Myology
Paris, France