Actively Recruiting

Early Phase 1
Age: 18Years - 50Years
All Genders
Healthy Volunteers
ID05283382

Cannabidiol Effects on Learning and Anxiety

Led by University of Connecticut · Updated on 2026-04-29

160

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the effects of Cannabidiol (CBD) on fear learning and anxiety in college students who have high levels of social anxiety. This early phase 1 trial recruits undergraduates at the University of Connecticut who show elevated social anxiety on standard tests. The study aims to see if CBD can help reduce fear responses during a controlled fear conditioning experiment. Participants will undergo a fear conditioning test where they learn to associate one face with a mild wrist shock and another face with no shock. After learning, half of the participants will receive a single 600 mg dose of CBD isolate gel capsules, while the other half will receive placebo capsules. Following this, participants will be exposed to the faces again without shocks to measure how quickly and effectively their fear responses diminish. Throughout the study, researchers will monitor participants' electrodermal responses and subjective fear ratings using a visual scale to assess fear extinction. The primary outcome is the electrodermal activity measured over 20 minutes. The trial is randomized and double-blind, with all participants completing the study within a single session. Safety and response data will be collected during this time to evaluate how CBD affects anxiety and learning.

CONDITIONS

Brief Title

Cannabidiol Effects on Learning and Anxiety

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18-50 years of age
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - One day

Participants receive a one-time dose of either 600 mg Cannabidiol Isolate Gel Capsules or placebo capsules.

1 visit (in-person)

Follow-up

Duration - 20 minutes

Participants are observed for effects on learning and anxiety including electrodermal activity for 20 minutes after dosing.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

University of Connecticut

Storrs, Connecticut, United States, 06269-1020

Actively Recruiting

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Research Team

R

Robert Astur, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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