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Clinical Trial Summary

To evaluate the usefulness of an upper extremity (UE) assistive device, called (MyoPro) in improving upper extremity activities in people with incomplete spinal cord injury (iSCI)

Clinical Trial Description

The study will take me approximately 10 weeks from the time of consent. This includes initial screening visit, a baseline assessment, and a follow-up visit (after 6 weeks of therapy). The baseline and follow up visit will include 2 separate testing sessions, each session will last approximately 2 hours. I will also participate in approximately 3 training sessions per week for 6 weeks. Each training session will last approximately 60 minutes. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT04855812
Study type Interventional
Source Kessler Foundation
Status Recruiting
Phase N/A
Start date October 27, 2019
Completion date September 30, 2021

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