Psilocybin Microdosing on Cognition, Mood and Quality of Life
Part of paid clinical trials in Hartford, Connecticut.
- Sponsor
- Yale University
- Study ID
- NCT07449351
- Phase
- EARLY_PHASE1
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Psychedelic Microdosing Effects on Mood, Cognition, Subjective Well-being and MRI
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - 40 Years
- Healthy Volunteers
- Accepted
Interventions
- Psliocybin — DRUG2.0mg powdered psilocybin derived from Psilocybe cubensis mushrooms, in capsules, provided three times weekly for four weeks
- Placebo — DRUG0mg matching capsules, provided three times weekly for four weeks
Study Details
This study is being conducted to evaluate how of 30 days of intermittently microdosed psilocybin affects mood, cognition, subjective well-being and structural/functional MRI results compared to a placebo. Investigators hypothesize that compared to placebo, 30 days of intermittently microdosed psilocybin will produce observable changes in mood, cognition, subjective well-being and MRI, in the absence of psychedelic experiences.
Key Dates
- Start date
- Apr 1, 2026
- Status verified
- Feb 2026
- Primary completion
- Apr 1, 2028
- Completion
- Apr 1, 2028
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Active Comparator: Psychedelic groupAn imperceptible dose of psilocybin in capsules will be administered to subjects three times weekly for four weeks. Assessments will be conducted once weekly. After 30 days of a steady dose of psilocybin, subjects will be re-assessed with baseline measures.
- Placebo Comparator: Placebo groupAn dose of placebo in capsules, identical to the active, will be administered to subjects three times weekly for four weeks. Assessments will be conducted once weekly. After 30 days of a steady dose of psilocybin, subjects will be re-assessed with baseline measures.
Primary Outcome Measure
The Complex Working Memory Span (CWMS) Task- fMRI measure [ Time Frame: From enrollment to end of treatment at 8 weeks. ]
Central Contacts
- Godfrey Pearlson, MD860-545-7757
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Olin Neuropsychiatry Research Center | Hartford | Connecticut | 06106 |