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Clinical Trial Summary

The purpose of this study is to evaluate the use of a voice activated prosthesis interface controller for functional outcomes as compared to standard prosthesis control.


Clinical Trial Description

The study will take place over two separate visits spaced about 1 week apart. During the first visit participants will undergo informed consent. They will then be randomly assigned one of two test conditions, (a) standard control, or (b) voice recognition control. For both conditions participants will be allowed to train on the control scheme until they are comfortable with it's usage. Subjects will then be asked to manipulate common objects as a test of improved control and utility. Functional outcome measures will be utilized to standardize the tasks performed and evaluate the advantages of voice control. On the second visit participants will be assigned the alternate condition, allowed to train with the control scheme, and run through the same set of functional outcomes measures. Upon completion of the second visit participants will be asked to fill out a questionnaire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04595071
Study type Interventional
Source Liberating Technologies, Inc.
Contact
Status Completed
Phase N/A
Start date November 13, 2019
Completion date June 30, 2020

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