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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03298243
Other study ID # HR-3303
Secondary ID 1R15HD093086
Status Recruiting
Phase N/A
First received
Last updated
Start date July 17, 2023
Est. completion date May 31, 2025

Study information

Verified date May 2024
Source Marquette University
Contact Robert A Scheidt, PhD
Phone (414)288-6124
Email robert.scheidt@marquette.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Supplementing or augmenting sensory information to those who have lost proprioception after stroke could help improve functional control of the arm. Thirty subjects will be recruited to a single site to evaluate the ability of supplemental kinesthetic feedback (a form of vibrotactile stimulation) to improve motor function. Participants will be tested in performing reaching movements as well as more functional tasks such as simulated drinking from a glass


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Vibrotactile stimulation
Non-invasive, computer-controlled miniature tendon vibrators, similar to those used in off-the-shelf activity monitors.

Locations

Country Name City State
United States Marquette University Milwaukee Wisconsin

Sponsors (3)

Lead Sponsor Collaborator
Marquette University Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Medical College of Wisconsin

Country where clinical trial is conducted

United States, 

References & Publications (10)

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Outcome

Type Measure Description Time frame Safety issue
Primary Root Mean Square Kinematic Error orthogonal distance between target and hand position during reaching and stabilizing across experimental sessions spanning a typical time frame of 4 to 6 weeks
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