Evaluation of Home Based Assessments on Participants With DMD

Status Completed

Clinical Trial Summary

This study is designed to evaluate the feasibility, wearability and participant satisfaction of novel outcome assessment tools in DMD patients which are performed in the home environment.

Clinical Trial Description

This is a low interventional feasibility study to evaluate the use of: 1. An FDA 510(k) cleared Class II wearable medical device designed to collect medical grade, clinical quality biometric, physiological and other electronic clinician outcome assessments data in a clinical trial setting, and; 2. The Duchenne Video Assessment (DVA) tool to evaluate the quality of movement in patients with Duchenne Muscular Dystrophy (DMD) This study will provide data on suitability of these tools in future clinical trials. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05657938
Study type	Observational
Source	Solid Biosciences Inc.
Contact
Status	Completed
Phase
Start date	October 13, 2022
Completion date	April 4, 2023

View Details

See also
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