Denver, CONCT06281756Now EnrollingIRB Ready

Insomnia Clinical Trial in Denver, CO

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

Sponsored by Milton S. Hershey Medical Center

Quick Self-Assessment

See if you qualify for this Denver location

Preparing your pre-screening questions…

Expert Care in Denver

Access insomnia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related insomnia treatment provided free

Apply for This Denver Location

Check if you qualify for this insomnia clinical trial in Denver, CO

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Denver

    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 Denver site if eligible
  4. 4Begin participation

About This Insomnia Study in Denver

Individuals who have insomnia with short sleep duration (ISS) differ from individuals who have insomnia with normal sleep duration (INS) in terms of health risks (i.e., hypertension) and treatment response. This study will examine whether patients with ISS and INS demonstrate a differential response to two common insomnia treatments. One is behavioral, Cognitive Behavioral Therapy for Insomnia (CBT-I). The other is a widely prescribed, non-habit-forming medication, trazodone used at a low dose. The investigators' findings could lead to evidence-based treatment guidelines that help clinicians more effectively match treatments to insomnia patients and reduce associated health problems.

Sponsor: Milton S. Hershey Medical Center

Who Can Participate

Inclusion Criteria

Age 18 or older
Able to read and effectively communicate in English at the United States sites or able to read and effectively communicate in English or French at the Canadian site.
Meets criteria for chronic insomnia
Body Mass Index (BMI) 18.5 kg/m2 and higher

Exclusion Criteria

Unable to read and effectively communicate in English at the United States sites or able to read and effectively communicate in English or French at the Canadian site.
Unwilling to share email address/cell phone number to accept survey links.
Life time diagnosis of psychotic or bipolar disorder
History of severe apnea or an Apnea Hypopnea Index (AHI) ≥15 that is not currently treated with Positive Airway Pressure (PAP) therapy, an oral device or an implanted device, or was not treated with surgery or weight loss.
Started new or changed treatment for sleep apnea in the past three months
Does not meet criteria for chronic insomnia
Meets criteria for narcolepsy or hypersomnia disorder
Meets criteria for circadian rhythm disorder (including night shift work)
Unstable medical conditions that would make participation unsafe or unfeasible
Falls resulting in hospitalization, significant injury or fracture within past 12 months
2 hospitalizations or emergency room visits within past 12 months for chronic conditions
Active chemotherapy or radiation therapy for cancer
Lifetime diagnoses/treatment of chronic renal failure, hepatic insufficiency, chronic heart failure
Does not agree to refrain from other treatments for insomnia beyond what is offered in this study
BMI less than 18.5
Substance abuse or dependence in the past 12 months
Current use of prescription or over the counter medications taken for sleep greater than 2 times per week
Current use of systemic corticosteroids or opiate medications
Current pregnancy or breastfeeding; plans to get pregnant or unwillingness to use birth control for the length of the study
Current use of medications contraindicated with trazodone
Sleep apnea or periodic leg movement disorder as determined by sleep study
Blood Pressure levels defined as seated SBP greater than 180 or DBP greater than 110 mmHg
EKG corrected QT interval greater than or equal to 500 ms

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 Denver?

Yes, this clinical trial (NCT06281756) has an active research site in Denver, 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.

Insomnia Treatment Options in Denver, CO

If you're searching for insomnia treatment options in Denver, CO, this clinical trial (NCT06281756) 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 Denver research site is actively enrolling participants for this clinical trial. You'll receive care from experienced insomnia 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 insomnia clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Denver, CO