Retrospective Study on Myoelectric Elbow-Wrist-Hand Orthosis User Outcomes
Completed
Conditions studied: Stroke, Brachial Plexus Injury, Spinal Cord Injuries, Neurological Disease
In brief
The objective of this study is to retrospectively evaluate the outcomes and clinical benefits provided by this brace to adult patients with upper limb impairment or paralysis due to brachial plexus, stroke (CVA), spinal cord injury, or other neurological disease or injury.
Key facts
- Study ID
- NCT05575674
- Run by
- Myomo
- People needed
- 21
- Starts
- 2022-10-05
- Expected to finish
- 2023-04-11
- Last updated by the study team
- 2023-10-10
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults, 65 years and older at the time of MyoPro delivery
- Completed the DASH questionnaire at evaluation before receiving the MyoPro
- Completed the DASH questionnaire at least six months after receiving the MyoPro
- Has intact cognition
- Able to clearly and verbally communicate in the English language
You may not qualify if…
- Life-changing event(s) or change(s) in medical status that affected ability to use the MyoPro
- Did not complete the DASH after receiving the MyoPro
- Other conditions (e.g., cognitive issues) or circumstances that would preclude safe and/or effective participation
Where it is running
- Myomo, Inc. — Boston, Massachusetts, United States
- Geauga Rehabilitation Engineering, Inc. — Chardon, Ohio, United States
- Orthocare Innovations, LLC — Edmonds, Washington, United States
Full record on ClinicalTrials.gov
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