Down Syndrome Clinical Trials

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Dysautonomia InVestigation in Individuals With Down SyndromE: DIVE Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Down syndrome (DS), the most common genetic cause of intellectual disability, is associated with widespread organ dysfunction, including abnormalities in the autonomic nervous system (ANS). The ANS regulates critical functions such as heart rate (HR) and blood pressure (BP), both essential for maintaining homeostasis and supporting physical activity. Individuals with DS often exhibit blunted HR responses to exercise-typically \ 30 beats per minute below expected levels-suggesting reduced sympathetic nervous system (SNS) activity. The SNS governs rapid changes in HR and BP during stress by releasing catecholamines: epinephrine (from the adrenal medulla) and norepinephrine (from sympathetic nerve endings). Despite its importance, SNS function has not been comprehensively assessed among individuals with DS. This study addresses a critical knowledge gap by evaluating SNS responses to physiological stressors in individuals with DS. The investigators will measure beat-to-beat HR and BP, along with plasma catecholamine levels, in response to sympathetic activation, comparing individuals with DS to age- and sex-matched controls. Understanding the mechanisms of SNS dysfunction in DS is vital, as it likely underlies reduced exercise capacity and contributes to broader clinical challenges. These insights may guide targeted interventions to improve cardiovascular function, physical capacity, and overall quality of life in this understudied population.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 50
Healthy Volunteers: t
View:

• 18-50 yrs old and apparently healthy individuals

• Ability to understand the study and give assent to participate

• Has a study partner who can attend all visits for the individuals with DS, and answer questionnaires, provide consent when necessary

• Corrected or non-existent congenital heart disease

• Euthyroid or on stable thyroid medication dose for at least 6 months

• Free from cardiovascular, pulmonary, inflammatory, or metabolic disease in the past 6 months that would prevent participation in study procedures

• BMI \<45kg/m2

• Ability to tolerate repeated blood draws / catheter placement

Locations
United States
Colorado
Linda Crnic Institute for Down Syndrome, University of Colorado Anschutz Medical Campus
RECRUITING
Aurora
Contact Information
Primary
Sara R Sherman, PhD
sara.r.sherman@cuanschutz.edu
303-724-0598
Backup
Constance Brecl
constance.brecl@cuanschutz.edu
Time Frame
Start Date: 2026-04-06
Estimated Completion Date: 2029-12
Participants
Target number of participants: 200
Treatments
Experimental: Individuals with Down syndrome
The investigators will be recruiting participants between the ages of 18-50 for the study investigating responses to six sympathetic stressors compared to age and sex matched individuals without Down syndrome.
Experimental: Individuals without Down syndrome
The investigators will be recruiting individuals without Down syndrome between the ages of 18-50 to serve as the comparisons for individuals with Down syndrome across the six sympathetic stressors.
Sponsors
Collaborators: GLOBAL Down Syndrome Foundation, Linda Crnic Institute for Down Syndrome, National Institute on Aging (NIA), University of Colorado Colorado Clinical and Translational Sciences Institute
Leads: University of Colorado, Denver

This content was sourced from clinicaltrials.gov