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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02874898
Other study ID # STUDY00001289
Secondary ID 1R34DA040034-01A
Status Completed
Phase N/A
First received
Last updated
Start date June 2016
Est. completion date August 15, 2022

Study information

Verified date August 2022
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date August 15, 2022
Est. primary completion date August 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
United States University of Washington Seattle Washington

Sponsors (2)

Lead Sponsor Collaborator
University of Washington National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Posttraumatic Stress Disorder Symptom Scale- Interview Version (PSS-I) 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 12 Weeks
Primary Treatment drop-out Defined as completion of less than 5 of 6 sessions of IE treatment 2 Weeks
Secondary Change in Quick Inventory of Depressive Symptomatology (QIDS-SR16) 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. baseline, 4 week, and 12 Weeks
Secondary Change in Marijuana Problems Scale (MPS) 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. baseline, 4 week, and 12 Weeks
Secondary Change in Marijuana Frequency and Quantity 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. baseline, 4 week, and 12 Weeks
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