Schulze Muscular Dystrophy Ability Clinical Study

Status Recruiting

Clinical Trial Summary

The primary objective of the Schulze study is to evaluate the function of the upper limbs of subjects diagnosed with neuromuscular disorders, with and without use of the Abilitech Assist device in the clinic and home environments. Functional outcomes will include documenting active range of motion and the ability to perform activities of daily living (ADLs) using the standardized Canadian Occupational Performance Measure (COPM) and the Role Evaluation of Activities of Life (REAL) assessments. Secondary objectives are to assess the safety record and report on adverse events (AEs) and parameters related to device usage, including device usage time and the time required to don/doff the device. Secondary objectives also include characterization of user upper limb performance based on etiology.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05409079
Study type	Interventional
Source	AbiliTech Medical Inc.
Contact	Chief Executive Officer
Phone	833.225.3123
Email	info@abilitechmedical.com
Status	Recruiting
Phase	N/A
Start date	May 26, 2022
Completion date	June 30, 2023

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