Actively Recruiting

Phase 4
Age: 18Years - 55Years
All Genders
NCT05649059

Investigating the Effects of Cannabidiol on Social Anxiety Disorder

Led by Massachusetts Institute of Technology · Updated on 2025-12-03

50

Participants Needed

1

Research Sites

59 weeks

Total Duration

On this page

Sponsors

M

Massachusetts Institute of Technology

Lead Sponsor

M

Massachusetts General Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

Investigating the Effects of Cannabidiol on Social Anxiety Disorder

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability and willingness to provide written informed consent
  • Sufficiently fluent in English to participate in the trial
  • Between 18 and 55 years of age (inclusive)
  • Right-hand dominant
  • Current medications are stable for past 30 days with no changes to dose or frequency
  • Negative result on pregnancy test (if female)
  • Negative result on urine drug screening
  • Liebowitz Social Anxiety Scale (LSAS) score of 60 or higher
Not Eligible

You will not qualify if you...

  • History of bipolar disorder, schizophrenia, psychosis, or 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 preventing study completion
  • Significant neurological illness or cognitive dysfunction such as seizures or dementia
  • History of substance use disorder within past 6 months except nicotine and caffeine
  • Use of any cannabis-containing products in past 30 days
  • Use of benzodiazepines in past 2 weeks
  • Use of alpha- or beta-blockers in past week
  • History of claustrophobia
  • Contraindications for MRI such as shrapnel
  • Any other medical condition that may interfere with study procedures
  • Use of medications strongly interacting with cannabidiol
  • History of liver disease
  • History of hypersensitivity to cannabinoids
  • History of hypersensitivity to sesame seed oil
  • Currently breastfeeding (if female)

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Massachusetts Institute of Technology

Cambridge, Massachusetts, United States, 02139

Actively Recruiting

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Research Team

O

Omar Rutledge, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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