- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05116527
THC Memory & Reward Learning Pilot
Pilot FMRI Studies of THC Effects on Memory and Reward Learning
Study Overview
Status
Intervention / Treatment
Detailed Description
The protocol below is designed to begin dissecting acute impairment of various forms of memory and learning by THC in cannabis compared to placebo, in a 2-session per subject double-blind, random assignment, placebo-controlled counterbalanced design in young to middle-aged adults. The purpose of these experiments is to gather important pilot data to demonstrate proof of principle for a planned NIDA submission of a P50 center application that will examine cannabis's differential effects on the neural circuit underpinnings these various cognitive domains across the lifespan in much more detail. In other words, these pilot data will show NIDA that the investigators' methods and approaches work and are suitable for use in their proposed center grant application. Unlike in the planned P50, in these small-scale pilot studies the investigators are only concerned with comparing these disrupting effects using a single dose of THC versus placebo, without exploration of age, sleep, or sex-related differential effects or of different dose-related effects.
Tasks tapping each of the major cognitive memory-related domains will be performed in the MRI scanner, to reveal the relevant underlying circuitry and its disruption by drug using functional MRI. Although each of the fMRI tasks is already implemented in the investigators' lab in other contexts, the investigators have never studied alteration of the fMRI tasks by THC. Neither have other investigators elsewhere used this approach. It is also important to point out that the dose of active THC to be administered is the same as that already used safely in the investigators' IRB-approved driving studies, one which subjects state subjectively (a blind to actual dose information) makes them feel moderately intoxicated, and similar to the amount that they would consume themselves recreationally.
The study will consist of 3 days (screening visit and 2 dose days). In a randomized, counterbalanced, double-blind study, investigators will administer high THC marijuana or placebo marijuana using paced inhalation through a vaporizer. Following administration, subjects will provide subjectively-rated CNB intoxication using a verbal analog scale, a short cognitive test battery, then complete 4 fMRI paradigms within ~1.5 hours: a) MSDM task, b) MID task, c) RISE task, and d) Treadway Effort/Reward task. These tests will be counterbalanced across subjects and sessions to minimize order and fatigue effects.
Study Type
Enrollment (Estimated)
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Locations
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Connecticut
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Hartford, Connecticut, United States, 06102
- Hartford Hospital
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 18-55 years old
- Right handed
- CNB use within past 2 years and felt "high" when used
- Able to read, speak, and understand English
- Able and willing to provide written informed consent, and willing to commit to study protocol.
Exclusion Criteria:
- Current marijuana tolerance, desire to cut down, or cravings to sue during periods of abstinence.
- Strongly left-handed
- Positive screen for drug or alcohol (except CNB) on test day will result in rescheduling the appointment
- History of adverse effects with CNB
- CNB users who are abstaining
- Report of any psychotic disorder in a first degree relative
- IQ < 80 on the Wechsler Abbreviated Scale of Intelligence
- Inability to comprehend written instructions using the WRAT-4 reading achievement test
- Pregnant, breastfeeding, and ineffective birth control methods.
- Unable or unsafe to have an MRI
- Serious medical, neuro-ophthalmological, or neurological illness (e.g. cancer, seizure disorders, encephalopathy
- History of head trauma with loss of consciousness > 30 minutes or concussion lasting 30 days.
- Focal brain lesion seen on structural MRI
- Any medical/neurological condition that could compromise neurocognitive performance (e.g. epilepsy, multiple sclerosis, fetal alcohol syndrome).
- Anyone deemed unsafe to study personnel for any reason
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High Dose THC
Participants will receive high dose THC.
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Marijuana flower with a high THC content
Other Names:
|
|
Experimental: Placebo THC
Participants will receive placebo THC.
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Placebo THC - marijuana flower with no THC content
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Marijuana induced performance changes on fMRI Multi-Stage Decision Making (MSDM) Task.
Time Frame: Baseline and post drug administration at 10 minutes.
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The MSDM is a reinforcement learning paradigm that quantifies the degree to which subjects can integrate recent trial-to-trial information about a stimulus' likelihood of reward with acquired knowledge about whether some choices generally lead to disadvantageous outcomes vs. others that more often lead to reward.
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Baseline and post drug administration at 10 minutes.
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Marijuana induced performance changes on Relational and Item Specific Coding (RISE) fMRI Task.
Time Frame: Baseline and post drug administration at 10 minutes.
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The RISE task is a hippocampal-dependent learning paradigm that assesses declarative memory.
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Baseline and post drug administration at 10 minutes.
|
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Marijuana induced performance changes on fMRI Treadway/Effort Reward Task.
Time Frame: Baseline and post drug administration at 10 minutes.
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The Treadway Effort/Reward Task independently measures the neural responses to two dimensions of a cost/benefit decision: the effort required and the magnitude of reward.
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Baseline and post drug administration at 10 minutes.
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Marijuana induced performance changes on fMRI Monetary Incentive Delay (MID) Task.
Time Frame: Baseline and post drug administration at 10 minutes.
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The MID task probes the brain's reward system to assess the anticipation and receipt of rewards or punishment.
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Baseline and post drug administration at 10 minutes.
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Godfrey Pearlson, M.D, Yale University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HHC-2021-0195 (Hartford Healthcare)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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