Clin2
NCT07591779Likely a fitNot yet recruiting

Home Activity Tracking in CMT1A Nerve Disease Patients

Charcot-Marie-Tooth Disease, Type IAPeripheral Neuropathy HereditaryMotor ActivityWalking, DifficultyNeuromuscular Diseases

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

This study watches how much you move around at home using a small wearable sensor if you have CMT1A, a genetic nerve condition that affects walking. Researchers want to understand daily activity patterns to better support patients with this condition.

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

Phase
N/A
Enrollment
60 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years or older
  • You have been genetically confirmed to have CMT1A (a specific genetic change called PMP22 duplication)
  • You are able to walk on your own, with or without aids like canes or walkers
  • You can wear a small sensor device on your skin without allergic reactions or discomfort
  • You live in France and are enrolled in the French social security system
  • You are not pregnant, breastfeeding, or under legal guardianship

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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