Drug Effects on Mood and Behavior - Expectancy
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Chicago
- Study ID
- NCT07061886
- Phase
- EARLY_PHASE1
- Status
- Recruiting
Conditions
- LSD
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 40 Years
- Healthy Volunteers
- Accepted
Interventions
- LSD — DRUGThe serotonin 2A receptor agonist LSD
- Placebo — DRUGDistilled water (0.26 mL)
Study Details
This study will examine the effects of a single low dose of the 5HT2A agonist LSD (Lysergic Acid Diethylamide) (13 µg) or placebo in individuals who are or are not explicitly told what drug they will receive. Although it is known that expectancies strongly influence subjective responses to most drugs, no studies have examined expectancies on response to a very low dose of LSD. This is especially important in the context of 'microdosing' of drugs. People who practice microdosing typically do so with strong expectations of positive effects, making it difficult to determine whether there is a pharmacological effect. To minimize expectancies in the laboratory, participants are usually not told exactly what drug they will receive (i.e., double-blind), but given a range of possibilities. In the present study, the study team will test half the subjects under single-blind conditions, where the participants (but not the research assistant) will know exactly what they are receiving. Other subjects will receive the usual instructions. Healthy volunteers will receive either a marginally detectable dose of LSD (13 micrograms) or placebo, under conditions where they i) know for sure what drug they are receiving or ii) where the identity of the drug is uncertain. Four groups of subjects (N=12 each) will attend single 4-hour laboratory session. The study team will examine subjective and behavioral responses to the drug in each of four conditions (Known-Drug; Known-Placebo; Uncertain-Drug; Uncertain-Placebo).
Key Dates
- Start date
- Jun 26, 2025
- Status verified
- Apr 2026
- Primary completion
- Jun 5, 2026
- Completion
- Jun 5, 2026
Study Design
- Enrollment
- 48 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: LSD (13 micrograms), Identity of substance knownLSD tartrate in tasteless solution (0.13 mL). Subjects will receive LSD, and they (but not the research assistant) will be told the identity of the drug.
- Active Comparator: LSD (13 micrograms), Identity uncertainLSD tartrate in tasteless solution (0.13 mL). Subjects will be told they might receive a stimulant, sedative, low dose of hallucinogen, or placebo, and will receive LSD.
- Placebo Comparator: Placebo, Identity of substance knownDistilled water (0.13 mL). Subjects will receive placebo, and they (but not the research assistant) will be told the identity of the drug.
- Placebo Comparator: Placebo, Identity uncertainDistilled water (0.13 mL). Subjects will be told they might receive a stimulant, sedative, low dose of hallucinogen, or placebo, and will receive placebo.
Primary Outcome Measure
Visual Analog Scale (VAS) [ Time Frame: During in-lab session: Pre-drug, and every 60 minutes post-drug from 0-4 hours ]
Central Contacts
- Hanna Molla7737023560
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago | Chicago | Illinois | 60637 | Hanna Molla Harriet de Wit (PRINCIPAL_INVESTIGATOR) |
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