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

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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 — DRUG
    2.0mg powdered psilocybin derived from Psilocybe cubensis mushrooms, in capsules, provided three times weekly for four weeks
  • Placebo — DRUG
    0mg 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 group
    An 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 group
    An 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

Locations (1)

FacilityCityStateZIPSite coordinators
Olin Neuropsychiatry Research CenterHartfordConnecticut06106
Diana King
860-545-7563

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