New study aims to decode FSHD muscle patterns with High-Tech scans and gait analysis
NCT ID NCT07164937
First seen Nov 01, 2025 · Last updated May 23, 2026 · Updated 16 times
Summary
This study is for 40 adults with a confirmed genetic diagnosis of FSHD, a muscle disease that causes progressive weakness. Researchers will use MRI scans to see which muscles are most affected and combine that with 3D motion capture to analyze how people walk and move. The goal is to find better ways to design orthopedic supports and tailor rehabilitation to each person's needs.
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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.
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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Contacts and locations
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Locations
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UOC Neurologia
Rome, 00168, Italy
Conditions
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