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THC + CBD and Memory Study

Effects of Marijuana on Memory-Related Neurochemistry and Neural Response

Status
Not yet recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04855526
Enrollment
9
Registered
2021-04-22
Start date
2025-12-01
Completion date
2026-12-30
Last updated
2025-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis Intoxication, Cannabis Use, Marijuana Use

Keywords

marijuana, cannabidiol, memory, THC, cannabis, intoxication, MRI, glutamate, MRS

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.

Interventions

DRUGHigh THC/No CBD Marihuana

high THC (65 mg THC) and no CBD (0 mg CBD)

DRUGHigh THC/High CBD Marihuana

high THC (65 mg THC) and high CBD (50 mg CBD)

DRUGNo THC/No CBD Marihuana

no THC (0 mg THC) and no CBD (0 mg CBD); placebo drug

Sponsors

Yale University
CollaboratorOTHER
Hartford Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
fMRI responseapproximately 1 hour following drug administrationBlood 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).
Glutamateapproximately 1 hour following drug administrationMagnetic resonance spectroscopy (MRS)-acquired glutamate containing compounds (Glx).

Secondary

MeasureTime frameDescription
HVLT-R performanceApproximately 2.50 hours after drug administrationThe 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 taskApproximately 3.00 hours after drug administrationThis 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 testingImmediately after drug administration (~0.25 hours after drug administration)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 questionnairePost drug administration at: 0.00 hours (immediately after); 1.0 hours; 2.0 hours; 3.0 hoursThis 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?

Contacts

Primary ContactChelsea N Meagher, BA
chelsea.meagher@hhchealth.org860-545-7106
Backup ContactDiana G King, BA
diana.king@hhchealth.org860-545-7563

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026