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Multimodal Magnetoencephalography and Electroencephalography Exploration of the Acute Effects of THC Exposure on Neural Noise and Information Transmission Within Working Memory Networks

Multimodal Magnetoencephalography and Electroencephalography Exploration of the Acute Effects of THC Exposure on Neural Noise and Information Transmission Within Working Memory Networks

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05641766
Acronym
THC-MEG
Enrollment
50
Registered
2022-12-08
Start date
2025-08-31
Completion date
2025-12-01
Last updated
2025-06-10

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

Conditions

THC

Keywords

MEG, EEG, THC, Placebo, Working Memory, Neural Noise, Cognitive Process

Brief summary

The purpose of this study is to use non-invasive brain imaging methods (MEG and EEG) to characterize the effects of THC on brain activity during learning.

Detailed description

The goal of this study is to use multimodal MEG/EEG to gain novel insight into the acute effects of THC on neural noise and its interaction with the fast information processing dynamics of the brain's cognition-related functional neural networks.

Interventions

DRUGTHC

Participants will receive THC into a rapidly flowing IV infusion.

OTHERPlacebo

Participants will receive an equivalent amount (about 1-2 ml) of placebo (sterile 190 proof USP ethanol). The placebo does not produce any measurable blood alcohol levels or subjective/behavioral effects.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Intervention model description

This proof-of-concept study will use a double-blind, randomized, cross-over (within-subject), placebo-controlled, counterbalanced study design in which participants will receive 0 (placebo) or 0.03 mg/kg intravenous THC over 20 minutes while undergoing simultaneous MEG/EEG data collection.

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Cannabis use at least once in the past 12 months * No cannabis use during the course of the study confirmed with negative urine toxicology at screening and on each test day * Good physical and mental health

Exclusion criteria

* Cannabis naïve individuals * Lifetime or current medical, psychiatric or psychosocial disorders or history that is deemed unsuitable for participation in the study per PI discretion. * Positive pregnancy test, lactation, or refusal to practice birth control for the duration of the study and for two weeks following completion * Major current or recent stressors * Positive urine drug test * Contraindication for Magnetic Resonance Imaging * Treatment with psychotropic medication as per discretion of the PI * IQ less than 80 * Weight exceeding 166kg * Diagnosis of major psychotic or manic disorder in first-degree relatives.

Design outcomes

Primary

MeasureTime frameDescription
Changes in brain dynamics during the Sternberg Working Memory TaskBaseline and starting at +15 minutes after start of IV THC or placebo administrationChanges in brain dynamics will be characterized during the Sternberg Working Memory Task where participants are presented with a list of items to memorize, followed by a memory maintenance period during which the subject must maintain the list of items in memory.

Secondary

MeasureTime frameDescription
Visual Analog Scale (VAS)Baseline and starting at +15 minutes after start of IV THC or placebo administrationTo confirm the acute effects of THC, feeling states associated with cannabis intoxication will be measured using a self-reported visual analogue scale of four feeling states (high,anxious,calm and relaxed, and tired) associated with cannabis effects. Subjects will be asked to score the perceived intensity of these feeling states at that moment on a 11mm line from 0=not at all to 100=extremely.
Clinician Administered Dissociative Symptoms Scale (CADSS)Baseline and starting at +15 minutes after start of IV THC or placebo administrationTo confirm the acute effects of cannabis, perceptual alterations will be measured using the CADSS. This is a scale consisting of 19 self-report items and 8 clinician-rated items scored 0=not at all to 4=extremely. The scale captures alterations in environmental/time/body perception, feelings of unreality, and memory impairment.

Countries

United States

Contacts

Primary ContactJose Cortes-Briones, PhD
jose.briones@yale.edu203-903-5711

Outcome results

None listed

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