Functional Outcomes of Cannabis Use (FOCUS) in Veterans With Posttraumatic Stress Disorder

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Recruiting
CT.gov ID
NCT04565028
Collaborator
(none)
40
1
1
47.1
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Study Details

Study Description

Brief Summary

Posttraumatic stress disorder (PTSD) is a disabling psychiatric disorder that affects 20%-30% of U.S. Veterans. PTSD is strongly associated with increased risk for substance abuse comorbidity, including cannabis use disorder. Multiple states now include PTSD as a condition for which patients can be legally prescribed medical marijuana, despite the fact that there has not been a single large-scale randomized clinical trial demonstrating the efficacy of cannabis to treat PTSD to date. The overall objective of the current proposal is to study the impact of reduced cannabis use on functioning among Veterans with PTSD. The investigators will evaluate the relationship between cannabis use and daily functioning among cannabis users and heavy cannabis users. The central hypothesis is that reductions in cannabis use will lead to positive changes in the functional outcomes of Veterans. The rationale for this research is that it will provide the first and only real-time data concerning the impact of reduced cannabis use on daily functioning among Veterans with PTSD.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Contingency Management (CM)
N/A

Detailed Description

Posttraumatic stress disorder (PTSD) is a disabling psychiatric disorder that affects 20%-30% of U.S. Veterans. PTSD is strongly associated with increased risk for substance abuse comorbidity, including cannabis use disorder; however, multiple states now include PTSD as a condition for which patients can be legally prescribed medical marijuana, despite the fact that there has not been a single large-scale randomized clinical trial demonstrating the efficacy of cannabis to treat PTSD to date. The overall objective of the current proposal is to prospectively study the impact of reduced cannabis use on psychosocial functioning among Veterans with PTSD. To do so, the investigators will first use ecological momentary assessment (EMA) methods to evaluate the relationship between cannabis use and daily functioning among Veterans with PTSD. Next, the investigators will use mobile contingency management (CM) and EMA to assess the impact of reduced cannabis use on daily functioning among Veterans with PTSD who are heavy cannabis users. The central hypothesis is that reductions in cannabis use will lead to positive changes in the functional outcomes of Veterans. The rationale for this research is that it will provide the first and only real-time data concerning the impact of reduced cannabis use on daily functioning among Veterans with PTSD. As a result, this innovative and timely project has the potential to significantly advance VHA healthcare and will directly inform the ongoing national debate concerning the impact of cannabis use on the long-term functional recovery of Veterans with PTSD.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Functional Outcomes of Cannabis Use (FOCUS) in Veterans With Posttraumatic Stress Disorder
Actual Study Start Date :
Jan 26, 2022
Anticipated Primary Completion Date :
Dec 30, 2025
Anticipated Study Completion Date :
Dec 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Contingency Management (CM)

Mobile contingency management (CM) will be used to promote reductions in cannabis use among Veterans with PTSD who are heavy cannabis users. CM is an intensive behavioral therapy in which participants are paid to reduce substance use.

Behavioral: Contingency Management (CM)
Contingency management is an intensive behavioral therapy in which participants are paid to reduce substance use.
Other Names:
  • Mobile Contingency Management (mCM)
  • Outcome Measures

    Primary Outcome Measures

    1. Change in functional impairment as measured by the World Health Organization Disability Assessment Schedule 2.0 (WHO-DAS) [Baseline and post-treatment (approximately six weeks)]

      Functional impairment will be measured by the simple score on the World Health Organization Disability Assessment Schedule 2.0 (WHO-DAS). This measure has a scoring range of 0 to 144, with lower scores indicating lower functional impairment.

    2. Change in functional impairment as measured by the Inventory of Psychosocial Functioning (IPF) [Baseline and post-treatment (approximately six weeks)]

      Functional impairment will be measured by the Inventory of Psychosocial Functioning (IPF). This measure has a scoring range of 0 to 480, with lower scores indicating higher functional impairment.

    3. Change in psychiatric distress [Baseline and post-treatment (approximately six weeks)]

      Psychiatric distress will be measured by the 90-item Symptom Checklist (SCL-90). This measure has a scoring range of 0 to 360, with lower scores indicating lower distress related to mental health.

    4. Change in quality of life, as measured by the WHOQOL-BREF [Baseline and post-treatment (approximately six weeks)]

      Quality of life will be measured with the World Health Organization Quality of Life Brief (WHOQOL-BREF). The measure has a scoring range of 0 to 100, with higher scores denoting a higher quality of life.

    5. Change in quality of life, as measured by the Quality of Life Scale [Baseline and post-treatment (approximately six weeks)]

      Quality of life will be measured with the 16-item Quality of Life Scale. The measure has a scoring range of 6 to 112, with higher scores denoting a higher quality of life.

    6. Change in number of days of drugged driving as measured by timeline follow-back [Baseline and post-treatment (approximately six weeks)]

      Number of days of drugged driving in the past month will be self-reported by participants using a Timeline Follow-Back Interview.

    7. Change in cannabis use [Baseline and post-treatment (approximately six weeks)]

      Cannabis use, as measured in milligrams, will be measured by taking the product of number of days used and amount used per day in the previous week.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Veteran status

    • Ability to speak and write fluent English

    • Current PTSD diagnosis

    • Use of cannabis on 13+ days in the past month (i.e., use on 3+ days per week)

    Exclusion Criteria:
    Participants will be excluded if they:
    • Have experienced a change in their psychiatric medication regimen during the past month (e.g., a new medication has been prescribed or the dose of an existing medication has been changed), or expect to experience a such a change during the course of the study

    • Are receiving non-study CUD treatment

    • Meet diagnostic criteria for bipolar disorder or schizophrenia (note that the SCID-5 (First et al., 2015) will be used to diagnoses these and other disorders)

    • Become imprisoned

    • Become hospitalized for psychiatric reasons

    • Report imminent risk for suicide or homicide

    • Meet current criteria for a substance use disorder other than cannabis use disorder or tobacco

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Durham VA Medical Center, Durham, NC Durham North Carolina United States 27705

    Sponsors and Collaborators

    • VA Office of Research and Development

    Investigators

    • Principal Investigator: Jean C Beckham, PhD, Durham VA Medical Center, Durham, NC

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    VA Office of Research and Development
    ClinicalTrials.gov Identifier:
    NCT04565028
    Other Study ID Numbers:
    • D3276-R
    First Posted:
    Sep 25, 2020
    Last Update Posted:
    Feb 7, 2022
    Last Verified:
    Feb 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
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by VA Office of Research and Development
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 7, 2022