MedPath

Developing a measurement protocol for upper extremity function in boys with Duchenne muscular dystrophy

Completed
Conditions
Duchenne muscular Dystrophy (DMD)
muscular dystrophy
10028302
Registration Number
NL-OMON34431
Lead Sponsor
niversitair Medisch Centrum Sint Radboud
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
7
Inclusion Criteria

DNA established diagnosis of DMD
Boys who are at the end of their ambulation or are recently wheelchair confined
Boys that are able to sit for 20 minutes without arm and with back support
Boys who have Brooke scale one or two (able to raise hands above the head)

Exclusion Criteria

Other disabling diseases influencing upper extremity mobility
Boys <= ten years old
Surgical scoliosis correction

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary outcome measures of this study are the kinematics of the elbow and<br /><br>shoulder, the active range of motion (ROM) of the elbow and shoulder and the<br /><br>normalized EMG signal. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secundary outcome measures are kinematics of the head and the thorso.</p><br>
© Copyright 2025. All Rights Reserved by MedPath