Walking-related digital biomarkers for childhood-onset neuromuscular conditions

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

NIH-funded research Columbia University Health Sciences · NIH-11312657

This project uses wearable sensors to track walking and identify digital signs of change for children, teens, and young adults with inherited neuromuscular disorders such as Duchenne.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionColumbia University Health Sciences NIH-funded
Lab location1 site (New York, United States)
Project IDNIH-11312657 on NIH RePORTER

What this research studies

If I join, researchers will ask me to wear sensors (like accelerometers or foot-worn monitors) during my normal daily activities so my real-world walking is recorded. They will compare consumer activity trackers with research-grade devices and analyze stride-by-stride walking patterns to develop sensitive digital markers of mobility. The study focuses on children, adolescents, and young adults with genetically confirmed childhood-onset neuromuscular disorders and may include occasional clinic visits for device calibration or checks. The goal is to detect changes in walking that routine clinic tests miss and create measures that could be used in future treatment trials.

Who could benefit from this research

Good fit: Children, adolescents, and young adults with genetically confirmed childhood-onset neuromuscular disorders who can walk and are willing to wear activity sensors during daily life would be ideal candidates.

Not a fit: People who are non-ambulatory, have conditions that prevent safe use of wearable devices, or do not want continuous activity monitoring are unlikely to benefit from participation.

Why it matters

Potential benefit: If successful, these digital measures could detect early or subtle declines in walking and help track treatment effects more precisely than standard clinic tests.

How similar studies have performed: Previous work using wearable trackers in Duchenne and spinal muscular atrophy has shown promise for monitoring mobility but has been limited by device accuracy and few stride-level measures, so this project builds on earlier but still-developing approaches.

Where this research is happening

New York, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Conditions Aran-Duchenne disease
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.