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Related Experiment Video

Updated: May 16, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
09:18

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy

Published on: January 12, 2019

Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients.

L Servais1, N Deconinck, A Moraux

  • 1Institute of Myology, AP-HP, Groupe hospitalier La Pitié Salpétrière, Paris, France. l.servais@institut-myologie.org

Neuromuscular Disorders : NMD
|December 11, 2012
PubMed
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Early diagnosis of Duchenne muscular dystrophy - A Treat-NMD international workshop.

Neuromuscular disorders : NMD·2024

New tools accurately measure upper limb strength and function in non-ambulant individuals, particularly those with Duchenne muscular dystrophy. These reliable assessments aid in tracking disease progression and treatment effectiveness.

Area of Science:

  • Neurology
  • Rehabilitation Medicine
  • Biomedical Engineering

Background:

  • Assessing upper limb function in non-ambulant patients, especially those with Duchenne muscular dystrophy (DMD), presents significant challenges.
  • Existing assessment tools may lack the precision needed to capture functional deficits in this population.

Purpose of the Study:

  • To develop and validate novel tools for precise measurement of upper limb strength and repetitive movement capacity.
  • To evaluate the feasibility and reliability of these new tools in non-ambulant individuals with DMD and healthy controls.

Main Methods:

  • Designed and implemented MyoPinch, MyoGrip, MyoWrist, and MoviPlate for assessing pinch, grip, wrist, and repetitive finger/wrist movements.
  • Assessed feasibility and reliability in 30 non-ambulant DMD patients and 30 age-matched controls.

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Related Experiment Videos

Last Updated: May 16, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
09:18

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy

Published on: January 12, 2019

Home-Based Monitor for Gait and Activity Analysis
07:24

Home-Based Monitor for Gait and Activity Analysis

Published on: August 8, 2019

An Objective and Child-friendly Assessment of Arm Function by Using a 3-D Sensor
07:25

An Objective and Child-friendly Assessment of Arm Function by Using a 3-D Sensor

Published on: February 12, 2018

  • Compared results with established measures like Motor Function Measure, Tapping, and Brooke Upper Extremity Functional Rating Scale.
  • Main Results:

    • MyoGrip, MyoPinch, and MoviPlate demonstrated high feasibility across tested upper limbs.
    • Excellent reliability was observed for all tests in both patient and control groups, though MyoWrist was not feasible in patients with contractures.
    • Motor capacity showed a decline correlated with time spent in a wheelchair and partially correlated with other clinical measures.

    Conclusions:

    • The validated panel of upper limb strength and function measures is suitable for Duchenne Muscular Dystrophy patients across a spectrum of weakness.
    • These tools provide a reliable and feasible method for assessing upper limb function in non-ambulant populations.
    • The findings support the use of these novel tools for monitoring disease progression and potentially evaluating interventions in DMD.