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Clinical Trial Summary

The purpose of this study is to evaluate the effects of myo-electric training tools on prosthesis functional outcomes.


Clinical Trial Description

Participants will undergo informed consent and schedule an initial site visit. A logging device will be used to track activity of prosthetic arm usage while in everyday use at home. After a baseline period, participants will schedule a second visit to be introduced to the training technology. The study will span up to 7 months with participants training at home for 15-60 minutes, 3-5 times a day. Every 3-6 weeks, investigators will schedule a study event and sit visit to conduct functional outcome tasks and measurements. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04354493
Study type Interventional
Source Liberating Technologies, Inc.
Contact
Status Completed
Phase N/A
Start date April 4, 2019
Completion date September 18, 2022

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