Outcome Measures Study on an Adult Myoelectric Elbow-Wrist-Hand Orthosis

Status Active, not recruiting

Clinical Trial Summary

Clinical Trial Description

The objective of this study is to evaluate the therapeutic and functional gains of a myoelectric elbow-wrist-hand orthosis for adult individuals with upper limb impairments using repeated measures studies that combines both gross motion and quantitative function outcome measures. The primary outcomes of this study will collect data on the participants' therapeutic and functional outcome measures when using the MyoPro over time in their home. Baseline data without the device will be collected prior to receiving the MyoPro. Data with and without the device will then be collected at 2-weeks post fitting and then at 1-month intervals thereafter for 12 months. These outcome measures will enable an understanding of the participants' functional gains with and without the MyoPro and over time with the MyoPro. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04900896
Study type	Observational
Source	Myomo
Contact
Status	Active, not recruiting
Phase
Start date	May 11, 2021
Completion date	December 2023

View Details

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