NIH-funded research R01 grant

Noninvasive breathing imaging to guide care for people with muscular dystrophy

Official title: Noninvasive Phenotyping of Respiratory Function in People with Muscular Dystrophies Using Electrical Impedance Tomography

Funded at Colorado State University · NIH-11415735 · Data updated 2026-11-12

A noninvasive imaging tool called electrical impedance tomography (EIT) will be studied to help decide when to start noninvasive ventilation for people with muscular dystrophy.

More Muscular Dystrophies research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionColorado State University
NIH-funded
Lab location1 site (Fort Collins, United States)
Project startSeptember 15, 2025
Project endJune 30, 2030
Funding year2026
Award (this year)$581,202
NIH project number5R01HL175869-02
Project IDNIH-11415735 on NIH RePORTER

Who could benefit from this research

Could help

Individuals with muscular dystrophy who experience respiratory muscle weakness and may require or soon require noninvasive ventilation.

Less likely to help

Patients without muscular dystrophy or without respiratory involvement are unlikely to benefit from this study.

What this research studies

People with muscular dystrophy often develop breathing problems as their muscles weaken. This project tests a real-time, air-timing imaging method (EIT) that does not require masks or sleep settings to see how well the lungs are working at rest and during breathing. By comparing EIT data with traditional tests, doctors may get clearer, earlier signals to start ventilator support when needed. The goal is to make monitoring easier and more comfortable, especially for kids and adults who cannot complete standard tests. If successful, this approach could become a bedside tool to personalize respiratory care.

Why it matters

Potential benefit: If successful, patients with muscular dystrophy could receive more timely and personalized guidance on when to begin breathing support.

How similar studies have gone: Previous small studies support the potential of EIT as a noninvasive monitoring method, but broader validation in muscular dystrophy is needed.

Where this research is happening

  • Colorado State University
    Fort Collins, United States
    Active

Researchers

  • Principal investigator: Mueller, Jennifer Lynn — Colorado State University
  • Study coordinator: Mueller, Jennifer Lynn

Related research

Other NIH-funded projects on the same topics.

  • Bicistronic gene therapy for limb girdle muscular dystrophy type R9

    A patient-facing overview of a first-in-class gene therapy approach using two genes delivered by AAV to help people with LGMDR9.

    NIH research Research Inst Nationwide Children's Hosp · Columbus, United States · NIH-11397452

  • Understanding why scarring happens in muscular dystrophy muscles

    Researchers are studying why scar tissue forms in muscles affected by muscular dystrophy and how to slow or reverse it in patients.

    NIH research University of Florida · Gainesville, United States · NIH-11370556

  • Addressing Shortcomings of AAV Gene Therapies for Muscular Dystrophy

    A national research center is working to improve AAV-based gene therapies for Duchenne and related muscular dystrophies so that patients may get safer, more effective treatments.

    NIH research University of Florida · Gainesville, United States · NIH-11310128

  • Two-gene AAV therapy for Limb-Girdle Muscular Dystrophy R9

    Developing a two-gene AAV gene therapy to replace the faulty gene and rebuild muscle for people with LGMDR9 (Limb Girdle Muscular Dystrophy Type R9).

    NIH research Research Inst Nationwide Children's Hosp · Columbus, United States · NIH-11169982

  • Improving Gene Therapies for Muscular Dystrophies

    This center is working to improve gene therapies for Duchenne and Limb Girdle Muscular Dystrophy, aiming to make them safer and more effective for patients.

    NIH research University of Florida · Gainesville, United States · NIH-11130228

  • Stopping Muscle Scarring in Muscular Dystrophies

    This project explores how muscle scarring, called fibrosis, develops in muscular dystrophies like Duchenne MD, hoping to find new ways to help muscles heal better.

    NIH research University of Florida · Gainesville, United States · NIH-11092236

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.
Last reviewed 2026-11-14 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.