Aurora, CONCT07238465Now EnrollingIRB Ready

Down Syndrome Clinical Trial in Aurora, CO

Access cutting-edge down syndrome treatment through this clinical trial at a research site in Aurora. Study-provided care at no cost to qualified participants.

Sponsored by University of Colorado, Denver

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Expert Care in Aurora

Access down syndrome specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related down syndrome treatment provided free

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Check if you qualify for this down syndrome clinical trial in Aurora, CO

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Aurora

    Convenient for CO residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Aurora site if eligible
  4. 4Begin participation

About This Down Syndrome Study in Aurora

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.

Sponsor: University of Colorado, Denver

Who Can Participate

Inclusion Criteria

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

Exclusion Criteria

Hypertension (resting systolic blood pressure \[SBP\] ≥140 and/or diastolic blood pressure \[DBP\] ≥90 mmHg) this includes those on medications to treat hypertension
Hypotension (resting BP of \<90/60 mmHg)
Cancer in the last six months
Any heart-rate-altering medications or any other medication that may modify metabolic responses
Self-reported diabetes or use of glucose-lowering medication
Tobacco products, including vaping, or marijuana use
Currently pregnant
Post-menopausal women Specific Exclusion Criteria for Certain Stressors:
Orthopedic limitations that would prohibit exercise or movement for exercise
Fracture of limb to be immersed for CPT
Open cut or sore on hand to be immersed for CPT
Raynaud's syndrome for CPT
Chronic caffeine drinkers for caffeine stressor (consumption of caffeine in the last 7 days)

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Aurora?

Yes, this clinical trial (NCT07238465) has an active research site in Aurora, CO that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Down Syndrome Treatment Options in Aurora, CO

If you're searching for down syndrome treatment options in Aurora, CO, this clinical trial (NCT07238465) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Aurora research site is actively enrolling participants for this clinical trial. You'll receive care from experienced down syndrome specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all down syndrome clinical trials near you to find additional studies recruiting in your area.

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