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Clinical Trial Summary

The primary study objective is to compare post-stroke upper extremity (UE) movement while wearing a brace called the MyoPro 2 Motion G versus UE movement while wearing a resting splint and no device in stroke survivors with moderate UE dysfunction. During the study, subjects will undergo general training in the operation of the EMG-controlled orthosis and the comparison orthosis, and then guided through a series of standard clinical outcome measures. These outcome measures will allow the researchers to directly compare the relative benefit of the MyoPro 2 Motion G with a resting hand splint and no device in reducing UE impairment and increasing UE dexterity and functional task performance.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04266158
Study type Interventional
Source Ohio State University
Contact
Status Terminated
Phase N/A
Start date October 1, 2017
Completion date September 18, 2018

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