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Evaluating Treatments for Suicidal Veterans With PTSD

Primary Purpose

Self-directed Violence, Post-traumatic Stress Disorder (PTSD)

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dialectical Behavior Therapy
Dialectical Behavior Therapy Prolonged Exposure protocol
Prolonged Exposure therapy
Suicide risk management
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Self-directed Violence focused on measuring Stress Disorders, Post-Traumatic, Suicide, Self-Injurious Behavior

Eligibility Criteria

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

Inclusion Criteria: PTSD Recent and repeated self-directed violence Current suicidal ideation Emotion dysregulation Veteran eligible for VHA mental health care at participating site (Seattle, Minneapolis, and Durham VAs) Age 18+ Willing to participate in all study activities Exclusion Criteria: Unable to maintain safety independently Currently engaged in and/or recent (past year) history of receiving a sufficient dose of DBT or PE Plan to move away or be unavailable for >4 weeks in the next 18 months Unable to sufficiently comprehend study procedures due to lack of English proficiency or moderate to severe cognitive impairment

Sites / Locations

  • Minneapolis VA Health Care System, Minneapolis, MN
  • Durham VA Medical Center, Durham, NC
  • VA Puget Sound Health Care System Seattle Division, Seattle, WA

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

DBT + DBT PE

PE + SRM

Arm Description

This condition combines one year of standard Dialectical Behavior Therapy (DBT) with the DBT Prolonged Exposure (DBT PE) protocol for PTSD.

This condition provides up to 18 sessions of Prolonged Exposure therapy (PE) for PTSD augmented with suicide risk management (SRM).

Outcomes

Primary Outcome Measures

Self-Injurious Thoughts and Behaviors Interview - Revised Short Form (SITBI-R-SF)
Number of self-directed violence episodes
Clinician-Administered PTSD Scale for DSM-5 Revised (CAPS-5-R)
Total Severity Score (range = 0 - 200, higher is worse)

Secondary Outcome Measures

Beck Scale for Suicide Ideation (BSSI)
Total Score (range = 0 - 38, higher is worse)
Brief Symptom Inventory (BSI)
Global Severity Index (range = 0 to 4, higher is worse)
Difficulties in Emotion Regulation Scale-16 (DERS-16)
Total Score (range = 16 - 80, higher is worse)
World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0)
General Disability Score (range = 12 - 60, higher is worse)
Self-Injurious Thoughts and Behaviors Interview Revised Short Form (SITBI-R-SF)
Non-suicidal self-injury frequency and remission; Suicide attempt frequency and remission
Clinician-Administered PTSD Scale for DSM-5 Revised (CAPS-5-R)
PTSD diagnostic status

Full Information

First Posted
July 5, 2023
Last Updated
July 25, 2023
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT05974631
Brief Title
Evaluating Treatments for Suicidal Veterans With PTSD
Official Title
A Hybrid Effectiveness-Implementation Trial of Treatments for Veterans With PTSD at Elevated Acute Risk for Suicide
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
February 1, 2024 (Anticipated)
Primary Completion Date
April 30, 2027 (Anticipated)
Study Completion Date
July 30, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

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
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Posttraumatic Stress Disorder (PTSD) is a significant driver of suicide risk among Veterans, but there is a critical knowledge gap about how to treat PTSD among people at elevated risk for suicide. Although evidence-based treatments for PTSD reduce suicide risk, Veterans at high risk for suicidal behavior rarely receive these potentially life-saving treatments. Prior research suggests that a treatment that combines Dialectical Behavior Therapy (DBT) with the DBT Prolonged Exposure protocol (DBT PE) for PTSD improves both PTSD and suicide-related outcomes. This study will evaluate whether DBT + DBT PE improves these outcomes more than Prolonged Exposure plus suicide risk management, the gold standard VA care for this population. The proposed study will also examine factors that make it easier and harder to implement these treatments in VA settings. The results will help to inform treatment guidelines for this high-priority Veteran population.
Detailed Description
Background: Posttraumatic stress disorder (PTSD) is a significant risk factor for suicide among Veterans. Evidence-based psychotherapies (EBPs) for PTSD reduce suicide risk, but Veterans at elevated acute risk for suicide, such as those who have engaged in self-directed violence (SDV), rarely receive these treatments. This is largely due to the historical exclusion of high-risk individuals from PTSD treatment trials, which has resulted in a lack of evidence-based guidance about indicated treatments for this population. Without such guidance, clinicians are often reluctant to use EBPs for PTSD with suicidal individuals. A treatment that combines Dialectical Behavior Therapy (DBT), a suicide-focused EBP, with the DBT Prolonged Exposure (DBT PE) protocol for PTSD has been developed for this high-risk population and shows promise in reducing both SDV and PTSD while being feasible, acceptable, and safe to deliver. However, a large-scale randomized controlled trial (RCT) is needed. This study will compare the effectiveness of DBT + DBT PE to the current VHA gold standard of care for this population, Prolonged Exposure therapy augmented with suicide risk management (PE + SRM), while also examining the potential for implementation of both interventions in VHA. Significance: There is a critical gap in knowledge about how to treat PTSD among individuals at high risk for suicidal behavior. As a result, VA/DoD Clinical Practice Guidelines do not specify indicated treatment strategies for this population. Experts have recommended two approaches to facilitate the safe and effective use of EBPs for PTSD with individuals at elevated acute suicide risk, including combining these treatments with suicide-focused EBPs or augmenting them with suicide risk management strategies. This project will help to fill this critical gap by rigorously evaluating these two approaches among Veterans with SDV. The results will provide important information to inform guidelines about indicated treatments for this high-risk population. Innovativeness: This will be the first large-scale RCT to evaluate treatments for PTSD among Veterans who have engaged in SDV, an HSR&D high priority group. The DBT + DBT PE intervention is the first treatment designed to address both SDV and PTSD, and results will indicate if this novel treatment improves outcomes compared to the current VHA gold standard of care. To facilitate more rapid implementation of these findings into clinical practice, implementation barriers and facilitators for both treatments will also be evaluated. Specific Aims: This study will randomize 200 Veterans with PTSD, recent and repeated SDV, current suicidal ideation, and emotion dysregulation to DBT + DBT PE (intervention) or PE + SRM (control). Aim 1 will test the hypothesis that DBT + DBT PE will be superior to PE + SRM in improving clinical outcomes and engagement in trauma-focused treatment. Exploratory analyses will examine Veteran characteristics that may predict better engagement and outcomes in DBT + DBT PE versus PE + SRM. Aim 2 will examine barriers and facilitators to implementation of both treatments. Methods: This is a multi-site hybrid type 1 effectiveness-implementation trial. Veterans will be treated in outpatient settings at three VA sites and assessed at 5 points over 18 months. A mixed-methods approach will be used to evaluate barriers and facilitators to implementation, including conducting interviews with 45 key stakeholders (Veterans, providers, and leadership). Primary Outcomes/Endpoints: Primary outcomes will be reductions in SDV episodes at 18-month follow-up and reductions in PTSD severity at post-treatment. Implementation/Next Steps: This project will provide much-needed information about how to safely and effectively treat PTSD among Veterans at elevated acute risk for suicide. If one or both treatments are found effective, Aim 2 will provide vital information about how to maximize future implementation success. Future implementation activities would be coordinated with the investigators' national operational partners.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Self-directed Violence, Post-traumatic Stress Disorder (PTSD)
Keywords
Stress Disorders, Post-Traumatic, Suicide, Self-Injurious Behavior

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
2-arm randomized clinical trial
Masking
Outcomes Assessor
Masking Description
Outcome assessors will be masked to participants' treatment condition
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
DBT + DBT PE
Arm Type
Experimental
Arm Description
This condition combines one year of standard Dialectical Behavior Therapy (DBT) with the DBT Prolonged Exposure (DBT PE) protocol for PTSD.
Arm Title
PE + SRM
Arm Type
Active Comparator
Arm Description
This condition provides up to 18 sessions of Prolonged Exposure therapy (PE) for PTSD augmented with suicide risk management (SRM).
Intervention Type
Behavioral
Intervention Name(s)
Dialectical Behavior Therapy
Other Intervention Name(s)
DBT
Intervention Description
Standard Dialectical Behavior Therapy (DBT), including DBT individual therapy (1 hour/week), DBT group skills training (2 hours/week), between-session coaching (as needed during business hours), and therapist consultation team (1-1.5 hours/week).
Intervention Type
Behavioral
Intervention Name(s)
Dialectical Behavior Therapy Prolonged Exposure protocol
Other Intervention Name(s)
DBT PE
Intervention Description
DBT PE is designed to be integrated into DBT to formally treat PTSD once patients meet standardized readiness criteria. The core procedures are in vivo and imaginal exposure with processing that are delivered in individual therapy sessions (1.5 hours/week).
Intervention Type
Behavioral
Intervention Name(s)
Prolonged Exposure therapy
Other Intervention Name(s)
PE
Intervention Description
Standard PE is delivered in individual therapy sessions (1.5 hours/week) and uses the core procedures of in vivo and imaginal exposure with processing.
Intervention Type
Behavioral
Intervention Name(s)
Suicide risk management
Other Intervention Name(s)
SRM
Intervention Description
Standard VA suicide risk management procedures, including comprehensive suicide risk assessment and safety planning.
Primary Outcome Measure Information:
Title
Self-Injurious Thoughts and Behaviors Interview - Revised Short Form (SITBI-R-SF)
Description
Number of self-directed violence episodes
Time Frame
Baseline to 18 months
Title
Clinician-Administered PTSD Scale for DSM-5 Revised (CAPS-5-R)
Description
Total Severity Score (range = 0 - 200, higher is worse)
Time Frame
Baseline to 18 months
Secondary Outcome Measure Information:
Title
Beck Scale for Suicide Ideation (BSSI)
Description
Total Score (range = 0 - 38, higher is worse)
Time Frame
Baseline to 18 months
Title
Brief Symptom Inventory (BSI)
Description
Global Severity Index (range = 0 to 4, higher is worse)
Time Frame
Baseline to 18 months
Title
Difficulties in Emotion Regulation Scale-16 (DERS-16)
Description
Total Score (range = 16 - 80, higher is worse)
Time Frame
Baseline to 18 months
Title
World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0)
Description
General Disability Score (range = 12 - 60, higher is worse)
Time Frame
Baseline to 18 months
Title
Self-Injurious Thoughts and Behaviors Interview Revised Short Form (SITBI-R-SF)
Description
Non-suicidal self-injury frequency and remission; Suicide attempt frequency and remission
Time Frame
Baseline to 18 months
Title
Clinician-Administered PTSD Scale for DSM-5 Revised (CAPS-5-R)
Description
PTSD diagnostic status
Time Frame
Baseline to 18 months
Other Pre-specified Outcome Measures:
Title
Treatment History Interview (THI)
Description
Non-VA psychotherapy, psychiatric crisis services, and psychotropic medications
Time Frame
Baseline to 18 months
Title
VA Service Use Form
Description
VA mental health service use and psychotropic medications
Time Frame
Baseline to 18 months
Title
Credibility Expectancy Questionnaire (CEQ)
Description
Total score (range = 1 - 7, higher is better)
Time Frame
Baseline to 18 months
Title
Client Satisfaction Questionnaire (CSQ)
Description
Total score (range = 8 - 32, higher is better)
Time Frame
Post-treatment (4 months in PE + SRM, 12 months in DBT + DBT PE)
Title
Dissociative Experiences Scale - Taxon (DES-T)
Description
Total score (range = 0 - 80, higher is worse)
Time Frame
Baseline to 18 months
Title
Trauma-Related Shame Inventory (TRSI)
Description
Total score (range = 0 - 72, higher is worse)
Time Frame
Baseline to 18 months
Title
Self-Compassion Scale (SCS)
Description
Total score (range = 1 - 5, higher is better)
Time Frame
Baseline to 18 months
Title
Borderline Symptom List - Behavioral Supplement (BSL-BS)
Description
Total score (range = 0 - 44, higher is worse)
Time Frame
Baseline to 18 months
Title
PTSD Checklist for DSM-5 (PCL-5)
Description
Total severity score (range = 0 - 80, higher is worse)
Time Frame
Every other week during PE or DBT PE, an average of 12 weeks
Title
Post-Traumatic Cognitions Inventory-9 (PTCI-9)
Description
Total score (range = 9 to 63, higher is worse)
Time Frame
Baseline to 18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PTSD Recent and repeated self-directed violence Current suicidal ideation Emotion dysregulation Veteran eligible for VHA mental health care at participating site (Seattle, Minneapolis, and Durham VAs) Age 18+ Willing to participate in all study activities Exclusion Criteria: Unable to maintain safety independently Currently engaged in and/or recent (past year) history of receiving a sufficient dose of DBT or PE Plan to move away or be unavailable for >4 weeks in the next 18 months Unable to sufficiently comprehend study procedures due to lack of English proficiency or moderate to severe cognitive impairment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Melanie S Harned, PhD
Phone
(206) 277-3650
Email
melanie.harned@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
John C Fortney, PhD
Phone
(206) 764-2821
Email
John.Fortney@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Melanie S Harned, PhD
Organizational Affiliation
VA Puget Sound Health Care System Seattle Division, Seattle, WA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Minneapolis VA Health Care System, Minneapolis, MN
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55417-2309
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lindsay Andrews-Wiebusch, PhD
Phone
612-629-7656
Email
Lindsay.Andrews-Wiebusch@va.gov
First Name & Middle Initial & Last Name & Degree
Laura Meis, PhD
Phone
6124674516
Email
Laura.Meis@va.gov
Facility Name
Durham VA Medical Center, Durham, NC
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705-3875
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elizabeth Van Voorhees, PhD
Phone
919-824-5529
Email
Elizabeth.Vanvoorhees@va.gov
First Name & Middle Initial & Last Name & Degree
Charlotte Ready, PhD
Phone
9192860411
Ext
177062
Email
Charlotte.Ready@va.gov
Facility Name
VA Puget Sound Health Care System Seattle Division, Seattle, WA
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108-1532
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melanie S Harned, PhD
Phone
206-277-3650
Email
melanie.harned@va.gov
First Name & Middle Initial & Last Name & Degree
John C Fortney, PhD
Phone
(206) 764-2821
Email
John.Fortney@va.gov
First Name & Middle Initial & Last Name & Degree
Melanie S Harned, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified, anonymized data that underlie results in a publication may be shared.
IPD Sharing Time Frame
Starting after publication of relevant data
IPD Sharing Access Criteria
Data may be shared in response to written requests submitted to the PI by other researchers. Such data sharing will take place under a written agreement that prohibits the recipient from identifying or re-identifying (or taking steps to identify or re-identify) any individual whose data are in the dataset.

Learn more about this trial

Evaluating Treatments for Suicidal Veterans With PTSD

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