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Psychotherapy for PTSD Among Veterans Also Receiving Drug or Alcohol Treatment (COMPASS)

Primary Purpose

Stress Disorders, Post-Traumatic, Substance Use Disorders

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Prolonged Exposure Therapy
Cognitive Processing Therapy
Present Centered Therapy
Sponsored by
Center for Veterans Research and Education
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stress Disorders, Post-Traumatic focused on measuring PTSD, Substance Use Disorders, Psychotherapy, Randomized Clinical Trial, Comparative Effectiveness

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

INCLUSION CRITERIA:

  1. Initiate an episode of outpatient SUD treatment at an enrolled facility.
  2. meet DSM-5 criteria for a current SUD (Tobacco Use Disorder alone is not sufficient for inclusion).
  3. Report substance use in the past 30 days (or in the 30 days prior to entering a controlled environment if exiting said controlled environment at time of enrollment)
  4. meet DSM-5 criteria for PTSD
  5. provide informed consent and be willing to be randomized to PTSD treatment condition
  6. agree to not receive non-study, active psychotherapy for PTSD during study treatment

EXCLUSION CRITERIA:

  1. Severe cognitive impairment
  2. Current suicidal or homicidal intent with a specific plan
  3. Unstable psychotic or manic symptoms not attributable to SUD
  4. More than 30 days between index outpatient SUD intake/treatment planning appointment & consent or more than 90 days between the index outpatient SUD visit and the first PTSD psychotherapy session

Sites / Locations

  • San Diego VA Healthcare System
  • Tampa VA Medical Center
  • Atlanta VA Medical Center
  • Edward Hines, Jr. VA Hospital
  • Southeast Louisiana Veterans Health Care System
  • Minneapolis VA Medical Center
  • Syracuse VA Medical Center
  • Durham VA Medical Center
  • Cincinnati VA Healthcare System
  • Louis Stokes Cleveland VA Medical Center
  • Philadelphia VA Medical Center
  • Salt Lake City VA Healthcare System
  • Puget Sound VA Healthcare System
  • Madison VA Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Trauma-Focused Therapy

Non-Trauma-Focused Therapy

Arm Description

Patients randomized to Trauma Focused Therapy will receive either Prolonged Exposure (PE) or Cognitive Processing Therapy (CPT). According to standard VA practice, assignment will be determined according to which trauma-focused therapy the assigned provider is verified to provide; if the assigned therapist is verified in both PE and CPT, the provider will decide which treatment to deliver. PE and CPT are both recommended as frontline treatments by all published PTSD guidelines. The standard treatment length will be 12 weekly sessions; however, patients and providers can collaboratively agree to early completion or extension as warranted.

Those randomized to non-trauma-focused therapy will receive present centered therapy (PCT). Originally designed as a strong comparator for psychotherapy research that included the components of "good therapy," PCT is now a bona-fide PTSD treatment suggested at the second tier in multiple clinical practice guidelines. The standard treatment length will be 12 weekly sessions; however, patients and providers can collaboratively agree to early completion or extension as warranted.

Outcomes

Primary Outcome Measures

Clinician Administered Scale for PTSD -5 (CAPS-5) Severity Score
PTSD Symptom Severity - Clinician Assessed; range 0-80; higher scores = greater severity.
PTSD Treatment Non-completion
Proportion of veterans who do not complete a full course of assigned PTSD treatment

Secondary Outcome Measures

PTSD Checklist-5 (PCL-5)
PTSD Symptom Severity - Self-Reported; Range = 0-80; higher scores = more severe symptoms
PTSD Checklist-5 (PCL-5)
PTSD Symptom Severity - Self-Reported; Range = 0-80; higher scores = more severe symptoms
PTSD Checklist-5 (PCL-5)
PTSD Symptom Severity - Self-Reported; Range = 0-80; higher scores = more severe symptoms
% Days with drug use or heavy drinking over prior 28 days
Substance use as measured by the Timeline Follow-Back Interview (TLFB)
% Days with drug use or heavy drinking over prior 28 days
Substance use as measured by the Timeline Follow-Back Interview (TLFB)
% Days with drug use or heavy drinking over prior 28 days
Substance use as measured by the Timeline Follow-Back Interview (TLFB)
Clinician Administered Scale for PTSD -5 (CAPS-5) Severity Score
PTSD Symptom Severity - Clinician Assessed; range 0-80; higher scores = greater severity.
Clinician Administered Scale for PTSD -5 (CAPS-5) Severity Score
PTSD Symptom Severity - Clinician Assessed; range 0-80; higher scores = greater severity.
Short Inventory of Problems, Revised (SIP-R)
Problems associated with drug or alcohol use; range = 0-51, higher scores = more severe
Short Inventory of Problems, Revised (SIP-R)
Problems associated with drug or alcohol use; range = 0-51, higher scores = more severe
Short Inventory of Problems, Revised (SIP-R)
Problems associated with drug or alcohol use; range = 0-51, higher scores = more severe
Brief Inventory of Psychosocial Functioning (BIPF)
PTSD-related psychosocial functioning; higher scores = more severe
Brief Inventory of Psychosocial Functioning (BIPF)
PTSD-related psychosocial functioning; higher scores = more severe
Brief Inventory of Psychosocial Functioning (BIPF)
PTSD-related psychosocial functioning; higher scores = more severe
Insomnia Severity Index
Self-reported sleep disturbances; range 0-28; higher scores = more severe
Insomnia Severity Index
Self-reported sleep disturbances; range 0-28; higher scores = more severe
Insomnia Severity Index
Self-reported sleep disturbances; range 0-28; higher scores = more severe
Dimensions of Anger Reactions (DAR)
Self-reporter anger; range = 2-25; higher scores = more severe
Dimensions of Anger Reactions (DAR)
Self-reporter anger; range = 2-25; higher scores = more severe
Dimensions of Anger Reactions (DAR)
Self-reporter anger; range = 2-25; higher scores = more severe
WHO Quality of Life, Brief (WHOQOL-BREF)
Self-reported quality of life; higher score = better quality of life
WHO Quality of Life, Brief (WHOQOL-BREF)
Self-reported quality of life; higher score = better quality of life
WHO Quality of Life, Brief (WHOQOL-BREF)
Self-reported quality of life; higher score = better quality of life
Patient Health Questionnaire-9 (PHQ-9)
Self-reported depression; range = 0-27; higher scores = more severe symptoms
Patient Health Questionnaire-9 (PHQ-9)
Self-reported depression; range = 0-27; higher scores = more severe symptoms
Patient Health Questionnaire-9 (PHQ-9)
Self-reported depression; range = 0-27; higher scores = more severe symptoms
Client Satisfaction Questionnaire - 8 (CSQ-8)
Treatment satisfaction; range = 8-32; higher scores = more severe symptoms

Full Information

First Posted
September 29, 2020
Last Updated
March 31, 2023
Sponsor
Center for Veterans Research and Education
Collaborators
Patient-Centered Outcomes Research Institute, Minneapolis Veterans Affairs Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04581434
Brief Title
Psychotherapy for PTSD Among Veterans Also Receiving Drug or Alcohol Treatment
Acronym
COMPASS
Official Title
Comparative Effectiveness of Trauma-Focused and Non-Trauma-Focused Treatment Strategies for PTSD Among Those With Co-Occurring SUD (COMPASS)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 8, 2020 (Actual)
Primary Completion Date
February 1, 2024 (Anticipated)
Study Completion Date
February 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Center for Veterans Research and Education
Collaborators
Patient-Centered Outcomes Research Institute, Minneapolis Veterans Affairs Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Many people who have posttraumatic stress disorder (PTSD) also struggle with problematic alcohol or drug use (substance use disorders [SUD]). Patients with both conditions prefer PTSD be treated alongside SUD. However, clinicians don't know if treatments that have been found to help those with PTSD work as well for people who also have SUD. This often leads to delaying PTSD treatment or using psychotherapies without research support. Trauma-focused psychotherapy (TFT) is the type of psychotherapy for PTSD that has been studied most often among people with both PTSD and SUD. It reduces symptoms of PTSD and substance use, although it might not work as well in those who have SUD as those who do not. Further, many patients with both PTSD and SUD do not complete TFT. Another strategy for treating PTSD is non-trauma-focused psychotherapy (NTFT). One NTFT, Present Centered Therapy, has been found to reduce symptoms of PTSD and more patients are able to complete NTFT than are able to finish TFT. However, no one has studied how well Present Centered Therapy works among patients who also have SUD. We will test which approach (TFT of NTFT) is better for reducing symptoms of PTSD and which is more likely to be completed by patients with both PTSD and SUD at VA healthcare facilities. We will also test to see whether some participants did better than others, so we can learn how to individualize treatment recommendations to patients. Participants will be assigned by chance to either TFT of NTFT. Patients assigned to TFT will receive either Prolonged Exposure or Cognitive Processing Therapy; both are weekly psychotherapies focused on addressing thoughts and/or memories related to their trauma. Those assigned to NTFT will receive Present Centered Therapy, a weekly psychotherapy in which patients learn about how PTSD relates to their current difficulties and problem solve current life difficulties. All participants will also receive SUD treatment. Participants will answer questions about their symptoms and experience with treatment before, right after they finish, and three and six months after they finish PTSD treatment. At the end of the study we will compare which treatment approach worked better to decrease PTSD symptom severity and which treatment patients were better able to complete. We will also track other outcomes that are important to patients (e.g., how they are doing in their relationships).
Detailed Description
Background and Significance: Posttraumatic stress disorder (PTSD) and substance use disorder (SUD) comorbidity is common. The Veterans Affairs (VA)/Department of Defense Clinical Practice Guideline for PTSD strongly recommends providing guideline-concurrent care for PTSD alongside SUD treatment, but there is insufficient evidence about which guideline-recommended treatments for PTSD work best in this population. Trauma-focused therapy (TFT) is a frontline treatment approach; yet its effectiveness is less well-established among patients with co-occurring SUD, and TFT dropout rates are uniquely high in this population. Multiple guidelines suggest non-trauma-focused treatment (NTFT) as a second-line treatment approach for PTSD; higher completion rates for some NTFT (e.g., Present Centered Therapy) may make this strategy particularly effective for those with comorbid SUD. Despite providers' desire for an NTFT option for patients with PTSD/SUD, no guideline-recommended NTFTs have been evaluated in those with the comorbidity Study Aims: Our long-term objective is to improve the lives of patients with co-occurring PTSD and SUD. To meet this objective, we will conduct a pragmatic randomized clinical trial that will yield decisive data regarding the comparative effectiveness of two evidence-based approaches for the treatment of PTSD in this understudied patient population: trauma-focused and non-trauma-focused psychotherapy. The major aims are: (1) Determine whether TFT differs at a clinically-meaningful magnitude from NTFT in its effects on posttreatment PTSD symptoms among patients with co-occurring PTSD and SUD (2) Determine whether patients with co-occurring PTSD and SUD randomized to TFT drop out of PTSD treatment more often than those randomized to NTFT, and (3) Determine if TFT differs at a clinically-meaningful level from NTFT in PTSD symptom reduction and number of PTSD therapy sessions attended in patients with varying (a) levels of baseline SUD severity, (b) classes of misused substances, and (c) treatment preferences. Study Description: We propose a prospective, pragmatic randomized comparative effectiveness trial at 14 VA Medical Center sites (11 confirmed). Randomization will occur at the patient level and will assign participants to either (1) TFT (Prolonged Exposure or Cognitive Processing Therapy) or 2) NTFT (Present Centered Therapy). All participants will also receive concurrent SUD treatment-as-usual. Participants will complete self-report measures and a clinician-administered interview pretreatment, posttreatment, and six-months posttreatment. 420 participants (210 per arm) will be veterans seeking outpatient SUD treatment in an enrolled clinic who meet DSM-5 criteria for a current SUD and PTSD. The sample will be diverse in sex, race, age, and geography. Main outcomes will be PTSD symptom severity measured by the Clinician Administered PTSD Scale for DSM-5 (CAPS-5), and PTSD treatment dropout (dichotomous indicator of completion of all PTSD treatment sessions). Major Aim 1 will be tested using a linear mixed model using study intervention, assessment point, and their interaction as fixed effects and including random effects for participant, clinician, and study site. Major Aim 2 will be testing using a random effects logistic regression of therapy retention on intervention and baseline CAPS incorporating random effects for clinician and site.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress Disorders, Post-Traumatic, Substance Use Disorders
Keywords
PTSD, Substance Use Disorders, Psychotherapy, Randomized Clinical Trial, Comparative Effectiveness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
420 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Trauma-Focused Therapy
Arm Type
Experimental
Arm Description
Patients randomized to Trauma Focused Therapy will receive either Prolonged Exposure (PE) or Cognitive Processing Therapy (CPT). According to standard VA practice, assignment will be determined according to which trauma-focused therapy the assigned provider is verified to provide; if the assigned therapist is verified in both PE and CPT, the provider will decide which treatment to deliver. PE and CPT are both recommended as frontline treatments by all published PTSD guidelines. The standard treatment length will be 12 weekly sessions; however, patients and providers can collaboratively agree to early completion or extension as warranted.
Arm Title
Non-Trauma-Focused Therapy
Arm Type
Experimental
Arm Description
Those randomized to non-trauma-focused therapy will receive present centered therapy (PCT). Originally designed as a strong comparator for psychotherapy research that included the components of "good therapy," PCT is now a bona-fide PTSD treatment suggested at the second tier in multiple clinical practice guidelines. The standard treatment length will be 12 weekly sessions; however, patients and providers can collaboratively agree to early completion or extension as warranted.
Intervention Type
Behavioral
Intervention Name(s)
Prolonged Exposure Therapy
Intervention Description
Prolonged Exposure Therapy is an individually-delivered treatment for PTSD that includes in vivo exposure to trauma reminders and imaginal exposure to the trauma memory delivered in 90-minute weekly sessions.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Processing Therapy
Intervention Description
Cognitive Processing Therapy is an individually-delivered treatment for PTSD that focuses on challenging and modifying maladaptive beliefs related to the trauma, with an optional written trauma account during weekly 60-minute sessions
Intervention Type
Behavioral
Intervention Name(s)
Present Centered Therapy
Intervention Description
Present Centered Therapy is an individually-delivered treatment for PTSD that focuses on "current life problems as manifestations of PTSD" in weekly 60-minute sessions. It includes psychoeducation and normalization of responses to trauma, problem solving related to current life difficulties and stress identified by patients, and emotional support and validation
Primary Outcome Measure Information:
Title
Clinician Administered Scale for PTSD -5 (CAPS-5) Severity Score
Description
PTSD Symptom Severity - Clinician Assessed; range 0-80; higher scores = greater severity.
Time Frame
Immediately after ending treatment
Title
PTSD Treatment Non-completion
Description
Proportion of veterans who do not complete a full course of assigned PTSD treatment
Time Frame
Immediately after ending treatment
Secondary Outcome Measure Information:
Title
PTSD Checklist-5 (PCL-5)
Description
PTSD Symptom Severity - Self-Reported; Range = 0-80; higher scores = more severe symptoms
Time Frame
Immediately after ending treatment
Title
PTSD Checklist-5 (PCL-5)
Description
PTSD Symptom Severity - Self-Reported; Range = 0-80; higher scores = more severe symptoms
Time Frame
3-months after ending treatment
Title
PTSD Checklist-5 (PCL-5)
Description
PTSD Symptom Severity - Self-Reported; Range = 0-80; higher scores = more severe symptoms
Time Frame
6-months after ending treatment
Title
% Days with drug use or heavy drinking over prior 28 days
Description
Substance use as measured by the Timeline Follow-Back Interview (TLFB)
Time Frame
Immediately after ending treatment
Title
% Days with drug use or heavy drinking over prior 28 days
Description
Substance use as measured by the Timeline Follow-Back Interview (TLFB)
Time Frame
3 months after ending treatment
Title
% Days with drug use or heavy drinking over prior 28 days
Description
Substance use as measured by the Timeline Follow-Back Interview (TLFB)
Time Frame
6 months after ending treatment
Title
Clinician Administered Scale for PTSD -5 (CAPS-5) Severity Score
Description
PTSD Symptom Severity - Clinician Assessed; range 0-80; higher scores = greater severity.
Time Frame
3 months after treatment
Title
Clinician Administered Scale for PTSD -5 (CAPS-5) Severity Score
Description
PTSD Symptom Severity - Clinician Assessed; range 0-80; higher scores = greater severity.
Time Frame
6 months after treatment
Title
Short Inventory of Problems, Revised (SIP-R)
Description
Problems associated with drug or alcohol use; range = 0-51, higher scores = more severe
Time Frame
Immediately after treatment
Title
Short Inventory of Problems, Revised (SIP-R)
Description
Problems associated with drug or alcohol use; range = 0-51, higher scores = more severe
Time Frame
3-months after treatment
Title
Short Inventory of Problems, Revised (SIP-R)
Description
Problems associated with drug or alcohol use; range = 0-51, higher scores = more severe
Time Frame
6-months after treatment
Title
Brief Inventory of Psychosocial Functioning (BIPF)
Description
PTSD-related psychosocial functioning; higher scores = more severe
Time Frame
Immediately after treatment
Title
Brief Inventory of Psychosocial Functioning (BIPF)
Description
PTSD-related psychosocial functioning; higher scores = more severe
Time Frame
3 months after treatment
Title
Brief Inventory of Psychosocial Functioning (BIPF)
Description
PTSD-related psychosocial functioning; higher scores = more severe
Time Frame
6 months after treatment
Title
Insomnia Severity Index
Description
Self-reported sleep disturbances; range 0-28; higher scores = more severe
Time Frame
Immediately after treatment
Title
Insomnia Severity Index
Description
Self-reported sleep disturbances; range 0-28; higher scores = more severe
Time Frame
3 months after treatment
Title
Insomnia Severity Index
Description
Self-reported sleep disturbances; range 0-28; higher scores = more severe
Time Frame
6 months after treatment
Title
Dimensions of Anger Reactions (DAR)
Description
Self-reporter anger; range = 2-25; higher scores = more severe
Time Frame
Immediately after treatment
Title
Dimensions of Anger Reactions (DAR)
Description
Self-reporter anger; range = 2-25; higher scores = more severe
Time Frame
3 months after treatment
Title
Dimensions of Anger Reactions (DAR)
Description
Self-reporter anger; range = 2-25; higher scores = more severe
Time Frame
6 months after treatment
Title
WHO Quality of Life, Brief (WHOQOL-BREF)
Description
Self-reported quality of life; higher score = better quality of life
Time Frame
Immediately after treatment
Title
WHO Quality of Life, Brief (WHOQOL-BREF)
Description
Self-reported quality of life; higher score = better quality of life
Time Frame
3 months after treatment
Title
WHO Quality of Life, Brief (WHOQOL-BREF)
Description
Self-reported quality of life; higher score = better quality of life
Time Frame
6 months after treatment
Title
Patient Health Questionnaire-9 (PHQ-9)
Description
Self-reported depression; range = 0-27; higher scores = more severe symptoms
Time Frame
Immediately after treatment
Title
Patient Health Questionnaire-9 (PHQ-9)
Description
Self-reported depression; range = 0-27; higher scores = more severe symptoms
Time Frame
Three months after treatment
Title
Patient Health Questionnaire-9 (PHQ-9)
Description
Self-reported depression; range = 0-27; higher scores = more severe symptoms
Time Frame
Six months after treatment
Title
Client Satisfaction Questionnaire - 8 (CSQ-8)
Description
Treatment satisfaction; range = 8-32; higher scores = more severe symptoms
Time Frame
Immediately after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA: Initiate an episode of outpatient SUD treatment at an enrolled facility. meet DSM-5 criteria for a current SUD (Tobacco Use Disorder alone is not sufficient for inclusion). Report substance use in the past 30 days (or in the 30 days prior to entering a controlled environment if exiting said controlled environment at time of enrollment) meet DSM-5 criteria for PTSD provide informed consent and be willing to be randomized to PTSD treatment condition agree to not receive non-study, active psychotherapy for PTSD during study treatment EXCLUSION CRITERIA: Severe cognitive impairment Current suicidal or homicidal intent with a specific plan Unstable psychotic or manic symptoms not attributable to SUD More than 30 days between index outpatient SUD intake/treatment planning appointment & consent or more than 90 days between the index outpatient SUD visit and the first PTSD psychotherapy session
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shannon Kehle-Forbes, PhD
Organizational Affiliation
Minneapolis VA Healthcare System
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hildi Hagedorn, PhD
Organizational Affiliation
Minneapolis VA Healthcare System
Official's Role
Principal Investigator
Facility Information:
Facility Name
San Diego VA Healthcare System
City
San Diego
State/Province
California
ZIP/Postal Code
92161
Country
United States
Facility Name
Tampa VA Medical Center
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Name
Atlanta VA Medical Center
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30033
Country
United States
Facility Name
Edward Hines, Jr. VA Hospital
City
Hines
State/Province
Illinois
ZIP/Postal Code
60141
Country
United States
Facility Name
Southeast Louisiana Veterans Health Care System
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70119
Country
United States
Facility Name
Minneapolis VA Medical Center
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55417
Country
United States
Facility Name
Syracuse VA Medical Center
City
Syracuse
State/Province
New York
ZIP/Postal Code
13210
Country
United States
Facility Name
Durham VA Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705
Country
United States
Facility Name
Cincinnati VA Healthcare System
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45220
Country
United States
Facility Name
Louis Stokes Cleveland VA Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Philadelphia VA Medical Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Salt Lake City VA Healthcare System
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84148
Country
United States
Facility Name
Puget Sound VA Healthcare System
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States
Facility Name
Madison VA Medical Center
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53705
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
35987487
Citation
Kehle-Forbes SM, Nelson D, Norman SB, Schnurr PP, Shea MT, Ackland PE, Meis L, Possemato K, Polusny MA, Oslin D, Hamblen JL, Galovski T, Kenny M, Babajide N, Hagedorn H. Comparative effectiveness of trauma-focused and non-trauma-focused psychotherapy for PTSD among veterans with comorbid substance use disorders: Protocol & rationale for a randomized clinical trial. Contemp Clin Trials. 2022 Sep;120:106876. doi: 10.1016/j.cct.2022.106876. Epub 2022 Aug 18.
Results Reference
derived

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Psychotherapy for PTSD Among Veterans Also Receiving Drug or Alcohol Treatment

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