Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05283382

Cannabidiol Effects on Learning and Anxiety

Status
Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
160 (estimated)
Sponsor
University of Connecticut · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

To examine the extent to which Cannabidiol (CBD) enhances fear conditioning extinction in college undergraduates who show elevated social anxiety. Undergraduates who display elevated social anxiety on standard assessments will be recruited at the University of Connecticut. All participants will be put in a standard fear conditioning paradigm where they are conditioned to fear a face that occasionally is followed by a shock to their wrist. The other face never is paired with a shock. After everybody learns this, half of the participants will receive 600 mg CBD Isolate Gel Capsules one time, and the other half will receive a placebo dose. Participants will then be presented with the faces with no shocks, and the rate and duration of extinction as measured by electrodermal response as well as subjective fear ratings via a visual analogue scale will be examined. It is hypothesized that participants that receive CBD will display enhanced extinction compared to the placebo group, as evidenced by reduced electrodermal response and reduced visual analogue fear ratings.

Conditions

Interventions

TypeNameDescription
DRUGCannabidiol Oral ProductParticipants will receive a one-time dose of 600 mg Cannabidiol Isolate Gel Capsules in the form of six 100mg capsules.
OTHERPlaceboParticipants will receive a one-time dose of placebo capsules in the form of six capsules.

Timeline

Start date
2024-10-30
Primary completion
2025-12-30
Completion
2026-02-01
First posted
2022-03-17
Last updated
2025-04-18

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05283382. Inclusion in this directory is not an endorsement.