New study aims to simplify walking assessments for rare muscle disease
NCT ID NCT06600308
First seen Mar 04, 2026 · Last updated May 16, 2026 · Updated 12 times
Summary
This study looks at whether quick, easy walking tests can effectively measure mobility problems in adults with facioscapulohumeral muscular dystrophy (FSH), a genetic muscle disease that often causes walking difficulties. Researchers will compare these simple tests with the standard, time-consuming assessment method. The goal is to find a faster, more practical way for doctors to monitor how the disease affects walking in everyday life.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Chu Dijon Bourgogne
RECRUITINGDijon, 21000, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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