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THC + CBD and Memory Study

Primary Purpose

Marijuana Use, Cannabis Use, Cannabis Intoxication

Status
Not yet recruiting
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
High THC/No CBD Marihuana
High THC/High CBD Marihuana
No THC/No CBD Marihuana
Sponsored by
Hartford Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Marijuana Use focused on measuring marijuana, cannabidiol, memory, THC, cannabis, intoxication, MRI, glutamate, MRS

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Right-handed
  • Prior MJ users (has used MJ at least once in the past year, but no more than 1x/month in the past 12 months)
  • Medically healthy (as determined by medical history and treatment)
  • Adequate comprehension of English in order to complete study materials
  • Acceptable birth control method for women (i.e., no copper IUD or any device that is not MRI safe)

Exclusion Criteria:

  • Participant currently uses psychoactive medications or substances
  • Psychiatric diagnoses (determined by DSM-V)
  • Participant heavily or regularly uses MJ (more than 1x/month in the past year)
  • Current or past substance dependence (including MJ)
  • Positive urine toxicology screens
  • Positive pregnancy screens
  • MRI contraindications (e.g., heart pacemaker)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Experimental

    Arm Label

    Occasional Users - High THC and High CBD Dose

    Occasional Users - High THC and No CBD Dose

    Occasional Users - No THC and No CBD Dose

    Arm Description

    People who smoke marijuana occasionally will be given a dose of high THC high CBD marijuana at the study visit

    People who smoke marijuana occasionally will be given a dose of high THC and no CBD marijuana at the study visit

    People who smoke marijuana occasionally will be given a dose of marijuana that contains no THC or CBD

    Outcomes

    Primary Outcome Measures

    fMRI response
    Blood oxygen level dependent functional magnetic resonance imaging (fMRI) response during the relational and item specific encoding task. fMRI response will be evaluated during the encoding phase (relational vs. item encoding), item recognition phase (hits vs. misses for item-specific encoding, and hits vs. misses for relational encoding), and associative recognition phase (hits vs. misses).
    Glutamate
    Magnetic resonance spectroscopy (MRS)-acquired glutamate containing compounds (Glx).

    Secondary Outcome Measures

    HVLT-R performance
    The Hopkins Verbal Learning Test-Revised will ascertain verbal list learning and immediate and delayed recall (~15min); alternate forms have been validated, and the order of versions participants receive will be randomized
    Performance on CHARLIE cognitive task
    This is a computer-based cognitive battery that administers the Digit Span and Letter/Number Sequencing Test (working memory) and the Digit Symbol Coding test (processing speed). It should take about 10 minutes to complete.
    Blood THC and CBD concentration testing
    A blood sample will be taken once per dose visit to assess the concentration of the following metabolites in ng/mL: delta-9-tetrahydrocannabinol, 11-hydroxy-tetrahydrocannabinol, 11-Nor-9-Carboxy-tetrahydrocannabinol (THCCOOH), tetrahydrocannabinol-Glucuronide, THCCOOH-Glucuronide, cannabinol (CBN), and cannabidiol (CBD).
    Subjective effects on drug effects questionnaire
    This self-report will be used to assess subjective reports every 60 minutes throughout the dose visit days. These subjective ratings will be obtained using rapidly completed Visual Analog Scales (VASs) scored on a 0-100 scale. Items include: Do you feel a drug effect right now?, Are you high right now?, Do you dislike any of the effects you are feeling right now?, Do you like any of the effects you are feeling right now? and Would you like more of the drug you took, right now?

    Full Information

    First Posted
    April 19, 2021
    Last Updated
    January 4, 2022
    Sponsor
    Hartford Hospital
    Collaborators
    Yale University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04855526
    Brief Title
    THC + CBD and Memory Study
    Official Title
    Effects of Marijuana on Memory-Related Neurochemistry and Neural Response
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 1, 2022 (Anticipated)
    Primary Completion Date
    June 30, 2022 (Anticipated)
    Study Completion Date
    June 30, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Hartford Hospital
    Collaborators
    Yale University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Memory deficits are one of the most consistently observed cognitive effects of marijuana use. There is evidence that some decrements attributable to the primary psychoactive ingredient, delta-9-tetrahydrocannabinol (THC), may be attenuated by cannabidiol (CBD). This study will help us learn more about the relationship between THC and CBD consumption with memory processes. A combination of MRI and neuropsychological tests (which are computer and paper/pencil tasks) will be used to measure the neurocognitive and behavioral impacts of THC and CBD use.
    Detailed Description
    With increased legalization and medicalization of marijuana (MJ), there is an urgent need to understand the acute effects of use. One of the most consistently observed cognitive outcomes associated with MJ use is memory dysfunction, which may have a substantial impact on daily life in individuals using MJ for recreational or medicinal purposes. Notably, there are numerous preparations of MJ with varying proportions of cannabinoids, which may differ in behavioral and cognitive effects. For instance, there is emerging evidence that acute administration of delta-9-tetrahydrocannabinol (THC), the main psychoactive constituent of MJ, hinders memory and reduces prefrontal and hippocampal functional magnetic resonance imaging (fMRI) activation, but cannabidiol (CBD) may mitigate some of these impairments. Given the role of glutamate in learning and memory, the investigators suggest that these effects may be subserved, in part, by glutamatergic mechanisms. The investigators will use magnetic resonance spectroscopy (MRS) to non-invasively measure glutamate in order to explore the neurochemical underpinnings of memory-related fMRI response changes following acute administration of THC and CBD in a randomized, double-blind, placebo-controlled, cross-over design. A total of 9 healthy participants ages 18-40 will be enrolled. Participants will first undergo one screening visit (~4 hours), comprising informed consent, assessment of health history, psychiatric diagnoses, cognitive function, and substance use history, and a structural MRI session. This will be followed by 3 separate MJ dose visits (~4 hours each), at which participants will complete neuroimaging after administration of one of 3 preparations of vaporized MJ in a randomized, counterbalanced, double-blinded fashion: 1) high THC and no CBD (THC), 2) high THC and high CBD (THC+CBD), and 3) no THC and no CBD (placebo MJ). As in the investigator's ongoing studies, bulk MJ plant material will be provided by the National Institute on Drug Abuse. MJ dose visits will comprise MJ administration, blood collection, MRS/fMRI scan, subjective reports, and a brief cognitive assessment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Marijuana Use, Cannabis Use, Cannabis Intoxication
    Keywords
    marijuana, cannabidiol, memory, THC, cannabis, intoxication, MRI, glutamate, MRS

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Early Phase 1
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    9 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Occasional Users - High THC and High CBD Dose
    Arm Type
    Experimental
    Arm Description
    People who smoke marijuana occasionally will be given a dose of high THC high CBD marijuana at the study visit
    Arm Title
    Occasional Users - High THC and No CBD Dose
    Arm Type
    Experimental
    Arm Description
    People who smoke marijuana occasionally will be given a dose of high THC and no CBD marijuana at the study visit
    Arm Title
    Occasional Users - No THC and No CBD Dose
    Arm Type
    Experimental
    Arm Description
    People who smoke marijuana occasionally will be given a dose of marijuana that contains no THC or CBD
    Intervention Type
    Drug
    Intervention Name(s)
    High THC/No CBD Marihuana
    Intervention Description
    high THC (65 mg THC) and no CBD (0 mg CBD)
    Intervention Type
    Drug
    Intervention Name(s)
    High THC/High CBD Marihuana
    Intervention Description
    high THC (65 mg THC) and high CBD (50 mg CBD)
    Intervention Type
    Drug
    Intervention Name(s)
    No THC/No CBD Marihuana
    Intervention Description
    no THC (0 mg THC) and no CBD (0 mg CBD); placebo drug
    Primary Outcome Measure Information:
    Title
    fMRI response
    Description
    Blood oxygen level dependent functional magnetic resonance imaging (fMRI) response during the relational and item specific encoding task. fMRI response will be evaluated during the encoding phase (relational vs. item encoding), item recognition phase (hits vs. misses for item-specific encoding, and hits vs. misses for relational encoding), and associative recognition phase (hits vs. misses).
    Time Frame
    approximately 1 hour following drug administration
    Title
    Glutamate
    Description
    Magnetic resonance spectroscopy (MRS)-acquired glutamate containing compounds (Glx).
    Time Frame
    approximately 1 hour following drug administration
    Secondary Outcome Measure Information:
    Title
    HVLT-R performance
    Description
    The Hopkins Verbal Learning Test-Revised will ascertain verbal list learning and immediate and delayed recall (~15min); alternate forms have been validated, and the order of versions participants receive will be randomized
    Time Frame
    Approximately 2.50 hours after drug administration
    Title
    Performance on CHARLIE cognitive task
    Description
    This is a computer-based cognitive battery that administers the Digit Span and Letter/Number Sequencing Test (working memory) and the Digit Symbol Coding test (processing speed). It should take about 10 minutes to complete.
    Time Frame
    Approximately 3.00 hours after drug administration
    Title
    Blood THC and CBD concentration testing
    Description
    A blood sample will be taken once per dose visit to assess the concentration of the following metabolites in ng/mL: delta-9-tetrahydrocannabinol, 11-hydroxy-tetrahydrocannabinol, 11-Nor-9-Carboxy-tetrahydrocannabinol (THCCOOH), tetrahydrocannabinol-Glucuronide, THCCOOH-Glucuronide, cannabinol (CBN), and cannabidiol (CBD).
    Time Frame
    Immediately after drug administration (~0.25 hours after drug administration)
    Title
    Subjective effects on drug effects questionnaire
    Description
    This self-report will be used to assess subjective reports every 60 minutes throughout the dose visit days. These subjective ratings will be obtained using rapidly completed Visual Analog Scales (VASs) scored on a 0-100 scale. Items include: Do you feel a drug effect right now?, Are you high right now?, Do you dislike any of the effects you are feeling right now?, Do you like any of the effects you are feeling right now? and Would you like more of the drug you took, right now?
    Time Frame
    Post drug administration at: 0.00 hours (immediately after); 1.0 hours; 2.0 hours; 3.0 hours

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Right-handed Prior MJ users (has used MJ at least once in the past year, but no more than 1x/month in the past 12 months) Medically healthy (as determined by medical history and treatment) Adequate comprehension of English in order to complete study materials Acceptable birth control method for women (i.e., no copper IUD or any device that is not MRI safe) Exclusion Criteria: Participant currently uses psychoactive medications or substances Psychiatric diagnoses (determined by DSM-V) Participant heavily or regularly uses MJ (more than 1x/month in the past year) Current or past substance dependence (including MJ) Positive urine toxicology screens Positive pregnancy screens MRI contraindications (e.g., heart pacemaker)
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Chelsea N Meagher, BA
    Phone
    860-545-7106
    Email
    chelsea.meagher@hhchealth.org
    First Name & Middle Initial & Last Name or Official Title & Degree
    Diana G King, BA
    Phone
    860-545-7563
    Email
    diana.king@hhchealth.org
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Godfrey Pearlson, MD
    Organizational Affiliation
    Hartford Hospital - Olin Neuropsychiatry Research Center; Yale University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Alecia Dager, PhD
    Organizational Affiliation
    Hartford Hospital - Olin Neuropsychiatry Research Center; Yale University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Michael Stevens, PhD
    Organizational Affiliation
    Hartford Hospital - Olin Neuropsychiatry Research Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    THC + CBD and Memory Study

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