Clin2
NCT06847282Possibly a fitRecruiting

Motor skills study for children with FSHD

Muscular Dystrophy, Facioscapulohumeral

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This study looks at how children with FSHD move and function over time. It uses walking tests and optional MRI scans to understand muscle changes. Your child's participation could help researchers learn more about FSHD progression in kids.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
80 people
Ages
5 years to 17 years
Study type
Observational

Who can take part

  • Your child must be between 5 and 17 years old.
  • They must have a genetic diagnosis of FSHD (type 1 or 2).
  • They should have muscle weakness in the face, shoulders, belly, or legs.
  • They must be able to walk 10 meters (about the length of a school bus) in under 12 seconds, with or without a cane or brace.
  • Up to 8 kids who walk slower than 12 seconds or use a wheelchair may also join.
  • Your child must be willing to try an MRI scan at least once.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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