STEP: Short-Term Exposure for PTSD

Sponsor
University of Washington (Other)
Overall Status
Completed
CT.gov ID
NCT02874898
Collaborator
National Institute on Drug Abuse (NIDA) (NIH)
46
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Study Details

Study Description

Brief Summary

This study examines how marijuana use affects processes related to recovery from chronic posttraumatic stress disorder (PTSD). Half the participants will be individuals with chronic PTSD and heavy marijuana use and half will be individuals with chronic PTSD and no marijuana use. This study will assess how individuals with PTSD with heavy or no marijuana use perform on a discriminative conditioning and extinction paradigm designed to measure fear extinction learning, and how they respond to a brief daily imaginal exposure treatment in regards to PTSD symptom reduction.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Brief Imaginal Exposure
N/A

Detailed Description

In this study, 36 patients with chronic PTSD and heavy marijuana use (heavy) and 36 patients with chronic PTSD and no marijuana use (no use) will be recruited to examine the effects of marijuana use on behavioral (emotional experiencing), physiological (skin conductance, acoustic startle) and biological (cortisol, blood pressure) responding on a well-established discriminative conditioning and extinction paradigm. To examine real world therapeutic implications, we will also examine how individuals with PTSD and heavy or no marijuana use differentially respond to a brief (6 session, 50 min) daily imaginal exposure (IE) treatment. Throughout treatment, we will monitor level of cannabis metabolites in urine samples of marijuana users to correlate effects to outcomes and preliminarily explore how varying levels of cannabis metabolites affect extinction processes. Independent evaluators will assess patients at baseline, 4 weeks, and 12 weeks following study entry.

Study Design

Study Type:
Interventional
Actual Enrollment :
46 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Marijuana Use, Extinction Learning, and Exposure Therapy in Individuals With PTSD
Actual Study Start Date :
Jun 1, 2016
Actual Primary Completion Date :
Aug 15, 2022
Actual Study Completion Date :
Aug 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Heavy marijuana use

Heavy marijuana users with PTSD

Behavioral: Brief Imaginal Exposure
Psychoeducation and imaginal exposure components of full prolonged exposure, in which patients relive the trauma vividly and process thoughts and feelings related to it

Active Comparator: No marijuana use

Non-marijuana users with PTSD

Behavioral: Brief Imaginal Exposure
Psychoeducation and imaginal exposure components of full prolonged exposure, in which patients relive the trauma vividly and process thoughts and feelings related to it

Outcome Measures

Primary Outcome Measures

  1. Change in Posttraumatic Stress Disorder Symptom Scale- Interview Version (PSS-I) [12 Weeks]

    The PSS-I assesses symptoms of PTSD as defined by the Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5) and is administered at baseline, 4 week, and 12 week follow up to assess change in PTSD symptoms

  2. Treatment drop-out [2 Weeks]

    Defined as completion of less than 5 of 6 sessions of IE treatment

Secondary Outcome Measures

  1. Change in Quick Inventory of Depressive Symptomatology (QIDS-SR16) [baseline, 4 week, and 12 Weeks]

    The QIDS-SR16 assesses symptoms of depression as defined by the Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5) and is administered at baseline, 4 week, and 12 week follow up to assess change in depression symptoms.

  2. Change in Marijuana Problems Scale (MPS) [baseline, 4 week, and 12 Weeks]

    The MPS is a self-report that assesses the impacts of marijuana on various areas of life, including motivation and productivity, social relationships, work and finances, self-esteem, memory impairment, legal problems, and physical health. The MPS is administered at baseline, 4 week and 12 week follow up to assess change in marijuana abuse.

  3. Change in Marijuana Frequency and Quantity [baseline, 4 week, and 12 Weeks]

    The Marijuana Frequency and Quantity Scale assesses the frequency and quantity of marijuana use and is administered at baseline, 4 week and 12 week follow up to assess changes in marijuana use.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Current PTSD diagnosis based on DSM-5 criteria, with a minimum duration of 12 weeks since the traumatic event;

  2. Between the age of 18 and 65;

  3. Current heavy marijuana use (5+ days per week for 3+ months) or no marijuana use in the last 3 months

  4. Current diagnosis of a cannabis use disorder based on DSM-5 or no current diagnosis of a substance use disorder

Exclusion Criteria:
  1. Current diagnosis of schizophrenia, delusional disorder, or organic mental disorder as defined by the DSM-5.

  2. Current diagnosis of bipolar disorder, depression with psychotic features, or depression severe enough to require immediate psychiatric treatment (i.e., serious suicide risk with intent and plan).

  3. Unwilling or unable to discontinue current trauma-focused psychotherapy

  4. Any previous experience with prolonged exposure (PE) treatment

  5. No clear trauma memory or trauma before age 3

  6. Unstable dose of psychotropic medications in the prior 3 months

  7. Ongoing intimate relationship with the perpetrator (in assault related PTSD cases).

  8. Current diagnosis of a substance use disorder according to DSM-5, other than marijuana in the last 3 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Washington Seattle Washington United States 98105

Sponsors and Collaborators

  • University of Washington
  • National Institute on Drug Abuse (NIDA)

Investigators

  • Principal Investigator: Michele A Bedard-Gilligan, PhD, University of Washington

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michele Bedard-Gilligan, Assistant Professor, University of Washington
ClinicalTrials.gov Identifier:
NCT02874898
Other Study ID Numbers:
  • STUDY00001289
  • 1R34DA040034-01A1
First Posted:
Aug 22, 2016
Last Update Posted:
Aug 23, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2022