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Establishing Walking-related Digital Biomarkers in Rare Childhood Onset Progressive Neuromuscular Disorders

NCT06839469 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 106

Last updated 2026-04-09

No results posted yet for this study

Summary

The purpose of this research is (1) to identify disease specific walking-related digital biomarkers of disease severity, and (2) monitor longitudinal changes in natural environments, for extended periods of time, in DMD and SMA.

Conditions

  • Spinal Muscular Atrophy Type 3
  • Duchenne Muscular Dystrophy (DMD)

Sponsors & Collaborators

  • Stevens Institute of Technology

    collaborator OTHER

  • Stanford University

    collaborator OTHER

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH

  • Boston Children's Hospital, Boston, MA, USA

    collaborator OTHER

  • Columbia University

    lead OTHER

Eligibility

Min Age
5 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-05-01
Primary Completion
2027-12-30
Completion
2028-04-01

Countries

  • United States

Study Locations

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Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06839469 on ClinicalTrials.gov