Wearable Technology to Evaluate Hyperglycemia and HRV in DMD - Longitudinal Aim

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age10+
SponsorVanderbilt University Medical Center

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

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

Trial population

10 adolescent and young adult males with DMD. DMD affects about 1/3500-6000 males and 1/50million females, therefore only male participants will be enrolled.

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

  • wearable technology

    Device

    Three wearable devices

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Rate of hyperglycemia

number of glucose measurements ≥140mg/dL over total number of glucoses

Time frame
5 time points, each over 10 days
2

Standard deviation of the mean R-to-R segment (SDANN)

correlation of rate of hyperglycemia and SDANN, which reflects heart rate variability

Time frame
5 time points, each over 7 days

Secondary outcomes

1

Coefficient of variation on CGM

variability of glucose levels on CGM measured by coefficient of variation (COV)

Time frame
5 time points, each over 10 days
2

Rate of significant hyperglycemia

number of glucose measurements ≥200mg/dL over total number of glucoses

Time frame
5 time points, each over 10 days
3

Activity level

Time spent in sedentary, low intensity, and moderate to vigorous physical activity

Time frame
5 time points, each over 7 days
4

Standard deviation of normal R to R intervals (SDNN)

correlation of rate of hyperglycemia and SDNN

Time frame
5 time points, each over 7 days

Other outcomes

Sponsors and contacts

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