Recruiting

Observational Study

Sponsor:

Vanderbilt University Medical Center

Code:

NCT06093100

Conditions

Duchenne Muscular Dystrophy

Eligibility Criteria

Sex: Male

Age: 10+

Healthy Volunteers: Not accepted

Interventions

wearable technology

Study Details

Brief summary:

Duchenne Muscular Dystrophy (DMD) is an X-linked disorder that causes muscle wasting, cardiopulmonary failure, and premature death. Heart failure is a leading cause of death in DMD, but substantial knowledge gaps exist regarding predisposing risk factors. In the general population, hyperglycemia, insulin resistance, and decreased heart rate variability (HRV; reflecting autonomic dysfunction) are associated with cardiomyopathy (CM). It is unclear whether these factors are associated with DMD-CM. Closing this knowledge gap may lead to novel screening and therapeutic strategies to delay progression of DMD related CM. Despite risk factors for hyperglycemia, including the use of glucocorticoids, low muscle mass, obesity, and reduced ambulation, little is known regarding glucose abnormalities in DMD. Some of these same risk factors, along with the distance needed to travel for specialty care, present significant barriers to research participation and clinical care for individuals with DMD. Remote wearable technology may improve research participation in this vulnerable population. Therefore, this study will leverage remote wearable technologies to overcome these barriers and define the relationship between dysglycemia and DMD-CM.

In this Aim of the study, the investigators will assess the utility of remote wearable technology to predict changes in traditional metrics of metabolism and cardiac function. In this pilot study, 10 individuals with DMD will undergo cardiac magnetic resonance imaging (CMR) and oral glucose tolerance tests (OGTTs) at baseline and two years. The investigators will remotely assess glycemia (using continuous glucose monitors), HRV (using extended Holter monitors), and activity (using accelerometers) every 6 months over the 2 years and evaluate if changes in wearable metrics predict changes in CMR and OGTT.

Conditions

Duchenne Muscular Dystrophy

Study ID

NCT06093100

Start date

Jul 10, 2024

Status verified date

Nov, 2025

Completion date

Dec, 2030

Anticipated

Primary completion date

Dec, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 10+

Healthy Volunteers: Not accepted

Inclusion and Exclusion Criteria:

Inclusion criteria

  • Male- ≥10 years
  • Clinical phenotype of DMD confirmed with muscle biopsy or genotype.
  • Informed consent for individuals ≥18 years
  • Parent/guardian informed consent and child assent for individuals < 18 years
  • Able to undergo non-sedated CMR

Exclusion Criteria

  • Refusal to participate
  • Diagnosis of diabetes prior to the study and/or taking insulin or other anti-diabetic drug therapy in < 4 weeks prior to treatment
  • Inability to fast for 10 hours
  • Use of a pacemaker, implantable cardioverter-defibrillator (ICD), or other implanted device
  • Unable to comply with study procedures, in the opinion of the investigator.

Study Design

Enrollment

10 participants

Anticipated

Interventions and Outcome Measures

Interventions

wearable technology

Three wearable devices

Primary outcome measure

  • Rate of hyperglycemia [ Time Frame: 5 time points, each over 10 days ]
  • Standard deviation of the mean R-to-R segment (SDANN) [ Time Frame: 5 time points, each over 7 days ]

Central Contacts and Locations

Central contacts

Locations

Vanderbilt University Medical Center

Recruiting

Nashville, Tennessee, United States, 37232

Contacts

More Information

Sponsor

Vanderbilt University Medical Center

Last update posted

Nov 6, 2025

Last verified

Nov, 2025

Keywords

  • Duchenne Muscular Dystrophy
  • heart failure
  • cardiomyopathy
  • hyperglycemia
  • heart rate variability

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Vanderbilt University Medical Center on 2025-11-06.