ClinicalTrials.Veeva

Menu

Cannabidiol Effects on Learning and Anxiety

University of Connecticut logo

University of Connecticut

Status and phase

Enrolling
Early Phase 1

Conditions

Anxiety and Fear

Treatments

Drug: Cannabidiol Oral Product
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT05283382
H21-0159

Details and patient eligibility

About

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.

Enrollment

160 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-50 years of age

Exclusion criteria

  1. Difficulties seeing a computer screen
  2. Anyone currently taking CBD within the last 24 hours.
  3. Anyone using any cannabis product within the last 24 hours.
  4. Heart problems or heart disease
  5. A neurological disorder such as epilepsy, stroke, multiple sclerosis, tumor, vascular malformations, aneurysm
  6. Are currently pregnant or breast-feeding

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

160 participants in 2 patient groups, including a placebo group

Cannabidiol
Experimental group
Description:
600 mg Cannabidiol Isolate Gel Capsules / participant. One-time dose.
Treatment:
Drug: Cannabidiol Oral Product
Placebo
Placebo Comparator group
Description:
Same number of placebo capsules / participant. One-time dose.
Treatment:
Other: Placebo

Trial contacts and locations

1

Loading...

Central trial contact

Robert Astur, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems