Clin2
NCT06708468Possibly a fitRecruiting

Personalized training for rare neuromuscular disorders

Neuromuscular Diseases (NMD)Charcot Marie Tooth Disease (CMT)Facioscapulohumeral Muscular DystrophyMyotonic Dystrophy Type 1 (DM1)

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

This study tests a personalized exercise program for people with rare neuromuscular diseases like FSHD, DM1, or CMT to see if it improves their physical function and quality of life.

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

Phase
N/A
Enrollment
120 people
Ages
18 years to 70 years
Study type
Interventional

Who can take part

  • You have a confirmed diagnosis of one of these: FSHD, DM1, or CMT.
  • You are between 18 and 70 years old.
  • You can stand, get up from a chair, and walk at least 10 meters, with or without a walker, cane, or other assistance.
  • Your doctor or physical therapist agrees that you need rehabilitation.
  • You can understand and follow instructions in Norwegian.
  • You are not pregnant or planning pregnancy.
  • You do not have other serious health problems like severe arthritis, heart failure, active cancer treatment, or past alcohol/drug abuse.

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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