Who is eligible for clinical trial NCT07360301?

Participants must meet the protocol's inclusion criteria for Well-Being, Psychological. The stated age range is 18 Years to 45 Years. Confirm all requirements with the study coordinator.

Does clinical trial NCT07360301 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2026-06-30

Consciousness and Psilocybin Effects on Well-Being: The CoPEWell Study (NCT07360301)

🟡 Not Yet Recruiting Phase1 💊 Investigational Drug / Biologic Sponsor: University of Wisconsin, Madison

🩺 Plain-English Summary (8th-Grade Level)

This study is exploring how psilocybin (a psychedelic drug) may improve mood and wellbeing. Many people report feeling better after taking psilocybin, but it is not clear why. The CoPEWell study will test whether these improvements come from the psychedelic experience itself (the "trip") or from direct effects on the brain. To study this, up to 120 participants will be enrolled to receive psilocybin either while awake or asleep and can expect to be on study for up to 4 months.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (5 items) and avoid the listed exclusions (7 items).

Location: University of Wisconsin — Madison, Wisconsin

Age range: 18 Years to 45 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Age 18 to 45 years (inclusive) at screening, of any identified gender and racial/ethnic group
Physically healthy; does not meet criteria for an exclusionary medical condition
No exclusionary sleep condition
English-speaking (able to provide consent and complete questionnaires)
Sub-optimal self-reported wellbeing

Usually NOT eligible if any of the following apply:

Exclusion Criteria:
Exclusionary DSM-5 psychiatric diagnosis and/or active suicidal ideation
Exclusionary medical conditions or sleep conditions
Clinically significant safety lab abnormalities (i.e., Complete Blood Count with Differential, Comprehensive Metabolic Panel, and urinalysis)
Clinically significant electrocardiogram (ECG)
Use of psychotropic or CNS-altering medications within 3 months of screening
Hypertension or tachycardia

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

University of Wisconsin — Madison, Wisconsin

📞 Contact the Study Coordinator

Phone: (608) 263-4852

Email: copewell@psychiatry.wisc.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

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💡 How to Participate

Check the checklist above to see if you may qualify.
Contact the study coordinator using the phone/email above.
Ask about the visit schedule, what is covered at no cost, and any travel support.
Confirm with your own doctor before making a decision.

🏛️ View Official NIH Record ↗