Rochester, MNNCT07486882Now EnrollingIRB Ready

Chronic Insomnia Disorder Clinical Trial in Rochester, MN

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

Sponsored by Mayo Clinic

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Expert Care in Rochester

Access chronic insomnia disorder specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related chronic insomnia disorder treatment provided free

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Check if you qualify for this chronic insomnia disorder clinical trial in Rochester, MN

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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 Rochester

    Convenient for MN 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 Rochester site if eligible
  4. 4Begin participation

About This Chronic Insomnia Disorder Study in Rochester

The purpose of this study is to compare changes in sleep quality in patients with moderate to severe insomnia, in participants randomized to Cognitive Behavioral Therapy for Insomnia (CBT-I) arm versus those randomized to the SONU Headband Acoustic Resonance Therapy (ART) arm at end of treatment (6 weeks).

Sponsor: Mayo Clinic

Who Can Participate

Inclusion Criteria

Adult subjects, 22 years of age and older at screening
Moderate-to-severe insomnia disorder, as defined by the International Classification of Sleep Disorders (ICSD-3)\
and the Insomnia Severity Index (ISI) and have been diagnosed for more than three months.
Not pregnant by subject self-report at time of consent.
Have the ability to provide informed consent.
Have the ability to complete all aspects of this trial.
Have access to an iOS mobile device (iPhone X or above).
Have no contraindicating comorbid health condition that would interfere with the proper use of the SONU Headband system, as determined by the clinical investigators.
Participants who are taking sleep-aiding pills must agree to no changes to medication and dosage during the study.
According to the third edition of the International Classification of Sleep Disorders (ICSD-3), insomnia is characterized by difficulty in either initiating sleep, maintaining sleep continuity, or poor sleep quality

Exclusion Criteria

Patients who are unable to commit to avoiding the consumption of alcohol during the study.
Patients who are unable to commit to avoid consumption of caffeine after 12 pm (noon).
Patients who have a clinically significant or unstable medical or surgical condition.
Participants using pacemakers or cardiac monitors.
Participants with severe physical illness or immediately post-surgery
Participants with severe mental disorders, such as schizophrenia, severe major depression, severe anxiety, bipolar disorder, dementia, substance use disorder, or severe neurological diseases such as a seizure, stroke, or Parkinson's disease.
Participants with other serious sleep disorders, such as severe obstructive sleep apnea.
Participants who are unable to attend regular follow-up evaluations.
Any unstable medical or mental health condition as determined by the physician investigator.

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 Rochester?

Yes, this clinical trial (NCT07486882) has an active research site in Rochester, MN 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.

Chronic Insomnia Disorder Treatment Options in Rochester, MN

If you're searching for chronic insomnia disorder treatment options in Rochester, MN, this clinical trial (NCT07486882) 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 Rochester research site is actively enrolling participants for this clinical trial. You'll receive care from experienced chronic insomnia disorder 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 chronic insomnia disorder clinical trials near you to find additional studies recruiting in your area.

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See all insomnia clinical trials recruiting in Rochester — not just this study.

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