No travel needed: new study uses video calls to uncover genetic secrets of childhood muscle disease

NCT ID NCT07630389

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aims to learn why myotonic dystrophy type 1 affects children differently than adults, and why symptoms vary even within the same family. Researchers will observe 100 children (ages 0-17) through video calls and simple at-home activities, and analyze their genes from a blood sample. No travel is required—families get an iPad and tools shipped to them.

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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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Conditions

The condition(s) this trial relates to.

childhood-onset Steinert myotonic dystrophy congenital myotonic dystrophy juvenile dermatomyositis juvenile-onset Steinert myotonic dystrophy myotonic dystrophy myotonic dystrophy type 1

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • University of Rochester

    RECRUITING

    Rochester, New York, 14642, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact