Actively Recruiting
Wearable Technology to Evaluate Hyperglycemia and HRV in DMD - Longitudinal Aim
Led by Vanderbilt University Medical Center · Updated on 2025-11-06
10
Participants Needed
1
Research Sites
333 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Wearable Technology to Evaluate Hyperglycemia and HRV in DMD - Longitudinal Aim
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male aged 10 years or older
- Clinical diagnosis of Duchenne Muscular Dystrophy confirmed by muscle biopsy or genetic testing
- Informed consent provided by participants 18 years or older
- Parent or guardian consent and child assent for participants under 18 years
- Able to undergo cardiac MRI without sedation
You will not qualify if you...
- Refusal to participate in the study
- Diabetes diagnosis before the study or use of insulin/anti-diabetic drugs within 4 weeks prior to treatment
- Unable to fast for 10 hours
- Presence of pacemaker, implantable cardioverter-defibrillator, or other implanted devices
- Unable to comply with study procedures as judged by the investigator
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37232
Actively Recruiting
Research Team
J
Jaclyn Tamaroff, MD
CONTACT
A
Andrea Lee, MA, MLS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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