Summary

for people ages 18 years and up (full criteria)
at San Diego, California
study started
estimated completion:
Mallory J. Loflin

Description

Summary

The trial will include a randomized control trial to evaluate the efficacy of using Cannabidiol (CBD), a non-intoxicating cannabinoid, as an adjunctive to Prolonged Exposure therapy (PE). The trial will compare PE + CBD to PE + placebo in a sample of 136 military Veterans with PTSD at the VA San Diego Medical Center. The study represents the logical and innovative next step for augmenting existing treatments and developing novel pharmacotherapy for PTSD. Findings from the proposed RCT will inform clinical practice and policy by investigating whether administration of CBD in the context of PE therapy will improve treatment outcomes for military Veterans with PTSD.

Official Title

Cannabidiol as an Adjunctive to Prolonged Exposure for the Treatment of PTSD

Details

Prolonged exposure therapy (PE) is among the most efficacious treatments for PTSD and is designated as a VA/DoD frontline treatment. However, PE does not always lead to clinically meaningful symptom reductions in Veterans with PTSD. Successful PE treatment relies on extinction learning, which is often impaired in patients with PTSD. Cannabidiol (CBD) is a non-intoxicating phytocannabinoid. Administration of specific phytocannabinoids, like CBD, increase extinction learning in patients with PTSD, and could increase the speed and effectiveness of PE therapy. CBD also modulates 5-HT1A, which may directly improve hyperarousal/insomnia symptoms, and improve engagement and retention in treatment. Given these findings, adjunctive administration of CBD+PE could improve response rates to PE and reduce the number of sessions of PE needed to reach clinically meaningful change. The proposed study is designed to test the efficacy of using CBD in conjunction with PE for the treatment of PTSD in US Military Veterans. A randomized, controlled, double-blind study will compare Veterans who receive PE+CBD to PE+placebo. Participants will include 136 male and female Veterans from all service eras with PTSD. The primary hypothesis is that PE+CBD will reduce PTSD symptoms to a greater degree than PE+placebo.

Keywords

PTSD cannabidiol CBD Veterans Prolonged Exposure Prolonged Exposure + Cannabidiol

Eligibility

You can join if…

Open to people ages 18 years and up

  • Over the age of 18 at the time of screening.
  • Judged by the study physician to be in generally good health.
  • Meet clinical criteria for Posttraumatic Stress Disorder (PTSD) on the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5).
  • Body mass index between 18-35 kg/m2.
  • Negative urine pregnancy test.

You CAN'T join if...

  • History of significant allergic condition, significant drug-related hypersensitivity,or allergic reaction to cannabinoids.
  • Used cannabis, synthetic cannabinoid, cannabinoid analogue, or any CBD or THC-containing product within 30 days of eligibility screening.
  • Patient has had a change in psychopharmacotherapy regimen in the last 4 weeks, or has any plans to change regimen over the course of the study.
  • Patient is engaged in trauma-related psychotherapy for PTSD.
  • Current or past DSM-5 diagnosis of dissociative identity disorder, eating disorder with active purging, personality disorders, primary psychotic disorder, or bipolar affective disorder type 1.
  • Patient is currently prescribed medications with possible CBD-drug interactions.
  • History of actual suicide attempt in the last 5 years.
  • Obstructive sleep apnea.
  • Positive drug screen for THC, barbiturates, amphetamines, benzodiazepines, and/or opiates.
  • History of treatment for, or evidence of, alcohol or drug abuse within the past year or regular alcohol consumption exceeding recommended limits.
  • Lifetime history of Cannabis Use Disorder.

Location

  • VA San Diego Healthcare System, San Diego, CA not yet accepting patients
    San Diego California 92161 United States

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
VA Office of Research and Development
ID
NCT03518801
Phase
Phase 2
Lead Scientist
Mallory J. Loflin
Study Type
Interventional
Last Updated
April 25, 2018