RECRUITING

Investigating the Effects of Cannabidiol on Social Anxiety Disorder

Description

The purpose of this study is to test whether a single-dose of Epidiolex (cannabidiol) is associated with reduced psychological, physiological, and neuroimaging measures of anxiety in people diagnosed with social anxiety disorder (SAD).

Conditions

Study Overview

Study Details

Study overview

The purpose of this study is to test whether a single-dose of Epidiolex (cannabidiol) is associated with reduced psychological, physiological, and neuroimaging measures of anxiety in people diagnosed with social anxiety disorder (SAD).

Investigating the Effects of Cannabidiol on Social Anxiety Disorder

Investigating the Effects of Cannabidiol on Social Anxiety Disorder

Condition
Phobia, Social
Intervention / Treatment

-

Contacts and Locations

Cambridge

Massachusetts Institute of Technology, Cambridge, Massachusetts, United States, 02139

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Ability and willingness to provide written informed consent.
  • * Sufficiently fluent in English to participate in the trial.
  • * Between 18-55 years of age (inclusive).
  • * Right-hand dominant.
  • * Current medications are stable for past 30 days (no changes to dose or frequency).
  • * Negative result on pregnancy test (if female).
  • * Negative result on urine drug screening.
  • * Liebowitz Social Anxiety Scale (LSAS ≥ 60).
  • * History of bipolar disorder, schizophrenia, psychosis, delusional disorders.
  • * History of eating disorder within past 6 months.
  • * History of any traumatic brain injury.
  • * Currently diagnosed with diabetes mellitus.
  • * Presence of severe medical illness that would prevent completion of study procedures.
  • * Presence of significant neurological illness or cognitive dysfunction (e.g.; seizures, dementia).
  • * History of substance use disorder within past 6 months (other than nicotine and caffeine).
  • * Use of any cannabis-containing products in past 30 days (CBD or THC).
  • * Use of benzodiazepines in past 2 weeks.
  • * Use of alpha- or beta-blockers in past week.
  • * History of claustrophobia.
  • * Contraindications for MRI (e.g.; shrapnel).
  • * Presence of any other medical condition that, in the investigator's opinion, may interfere with the study procedures.
  • * Use of concomitant medication that has a strong interaction with CBD.
  • * History of liver disease.
  • * History of hypersensitivity to cannabinoids.
  • * History of hypersensitivity to sesame seed oil.
  • * Currently breastfeeding (if female).

Ages Eligible for Study

18 Years to 55 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Massachusetts Institute of Technology,

John Gabrieli, PhD, PRINCIPAL_INVESTIGATOR, Massachusetts Institute of Technology

Study Record Dates

2026-09