Clin2
NCT07630389Likely a fitRecruiting

Remote monitoring for childhood myotonic dystrophy

Myotonic Dystrophy Type 1Congenital DM1Juvenile DM1Childhood DM1

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

This study uses video calls and online assessments to track how myotonic dystrophy (a muscle-weakening condition) affects children over time. Researchers will also look at genetic factors to better understand the disease and improve care.

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

Phase
N/A
Enrollment
100 people
Ages
birth to 17 years
Study type
Observational

Who can take part

  • Child is between newborn and 17 years old
  • Child has been diagnosed with congenital, childhood, or juvenile myotonic dystrophy type 1 (DM1)
  • Family speaks English at home
  • Parent or guardian can help with study visits and give permission
  • Reliable wifi internet access at home for remote video assessments
  • No other serious brain or nerve conditions (like cerebral palsy) that could affect muscle testing

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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