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A Self-Management Program for Completers of Trauma-Focused Therapy for PTSD (EMPOwER)

Primary Purpose

Posttraumatic Stress Disorder

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Self-Management Program
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 Posttraumatic Stress Disorder focused on measuring Stress Disorders, Posttraumatic, Self-Management

Eligibility Criteria

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

Inclusion Criteria:

Patients will be eligible to participate if they:

  • completed a course of individually-delivered trauma-focused therapy (TFT) with a provider trained to deliver the self-management intervention at the Minneapolis VAMC
  • experienced a clinically meaningful reduction in PTSD symptomology (PCL decrease of at least 10 points) from pre-TFT to the time of the enrollment
  • at the time of enrollment are not planning to initiate another active course of psychotherapy for PTSD in the following three months
  • are willing to participate in a self-management intervention, and
  • can provide informed consent

Exclusion Criteria:

  • Veterans will be excluded if they have suicidal or homicidal ideation that in the opinion of their TFT therapist needs to be the focus of treatment.

Sites / Locations

  • Minneapolis VA Health Care System, Minneapolis, MN

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Self-Management Program

Arm Description

Patients in this arm will receive the therapist assisted self-management intervention following completion of trauma-focused therapy for PTSD.

Outcomes

Primary Outcome Measures

Credibility-Expectancy Scale (Credibility Subscale)
Measures treatment rationale credibility in clinical outcome studies (range 1-9; higher scores = higher credibility).
Client Satisfaction Scale
Measures client satisfaction with mental health services (range = 8-32; higher scores = higher satisfaction)

Secondary Outcome Measures

Change From Baseline in Illness Perception Questionnaire - Revised (Personal Control Subscale)
Measures patients' self-efficacy for managing PTSD symptoms; range = 1-5 (higher scores = greater perceived control; change from pre- to post-intervention reported.
Change From Baseline on PTSD Checklist - 5
Measures DSM-5 PTSD symptoms; Range = 0-80; higher scores = more severe symptoms; change score from pre- to post-treatment reported
Change From Baseline on Patient Health Questionnaire - 9
Measures symptoms of depression; range = 0-27; higher scores = more severe symptoms; pre- to post-treatment change score reported
Change From Baseline on Recovery Orientation Scale (Current Mental Health Subscale)
Measures patients' perceived mental health; range 1-5; lower scores = better perceived mental health
Change From Baseline on World Health Organization Quality of Life - BREF
Measures patients' current quality of life; higher score = better quality of life; range = 0-100. Change score from pre- to post-treatment reported
Change From Baseline on Military to Civilian Questionnaire
Measures patients' community engagement; range: 0-4; higher scores = more difficulty; change score from pre- to post-intervention reported
Change From Baseline on Brief Inventory of Psychosocial Functioning
Measure of PTSD-related psychosocial functional impairment; higher scores = more severe; range = 0-49; change from pre- to post-treatment reported

Full Information

First Posted
July 19, 2017
Last Updated
February 4, 2021
Sponsor
VA Office of Research and Development
Collaborators
VA Boston Healthcare System, Syracuse VA Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03225859
Brief Title
A Self-Management Program for Completers of Trauma-Focused Therapy for PTSD
Acronym
EMPOwER
Official Title
Pilot Test of a Self-Management Program for Completers of Trauma-Focused Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
November 5, 2018 (Actual)
Primary Completion Date
February 17, 2020 (Actual)
Study Completion Date
February 28, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
VA Boston Healthcare System, Syracuse VA Medical Center

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
No

5. Study Description

Brief Summary
Veterans who complete trauma-focused therapies (TFTs) report improvements in posttraumatic stress disorder symptoms, quality of life, and social and role functioning. However, many also report uncertainty regarding their ability to maintain and build upon progress made during TFTs following the end of treatment. Veterans who recently completed a course of TFT believe the likelihood of their ongoing success would be bolstered by mental health services that support additional practice and reinforcement of skills learned in TFT. Currently no evidence-based approach for post-TFT care exists; however, Veterans' reported treatment needs are well-suited to a therapist-assisted self-management approach. The objective of this project is to complete Stage 1 (intervention refinement and piloting) of the Stage Model of Treatment Development for a post-TFT therapist-assisted self-management program designed to help Veterans maintain or build upon gains made in TFT, increase self-efficacy for managing their PTSD symptoms, and enhance community engagement. The aims of the project are to: 1) Refine a self-management treatment protocol through eliciting feedback from experienced TFT providers on a draft of the self-management program, 2) Conduct a pilot open trial to assess the acceptability and feasibility of the self-management program, and 3) Explore the effects of the program on Veterans' confidence in managing their PTSD and Veterans' functioning, quality of life, community engagement, and mental health symptoms.
Detailed Description
Impact: Findings from this project will improve the mental health and well-being of Veterans with posttraumatic stress disorder (PTSD) by refining and evaluating the first post-trauma focused therapy (TFT) intervention designed to help Veterans increase self-efficacy for managing their PTSD symptoms, maintain or build upon gains made in TFT, and increase community engagement. The current VA / Department of Defense PTSD clinical practice guidelines recommend decreasing the frequency and intensity of care (e.g. stepping-down) following successful TFT completion; this project is the initial step in developing the first evidence-based intervention for this important process. The project will advance RR&D's missions of evaluating interventions designed to maximize psychological recovery and prioritizing functional outcomes and societal engagement. Finally, the project will advance the scientific literature by being the first examination of a self-management intervention designed to be used to step down from an intensive course of therapy for PTSD. Background: TFTs reduce the suffering associated with PTSD; a majority of Veterans who complete prolonged exposure or cognitive processing therapy report improvements in PTSD symptomology, quality of life, and functioning. Despite their effectiveness, emerging data suggest that Veterans who complete TFTs continue to perceive a need for mental health treatment; the investigators' pilot data demonstrated that the primary post-TFT mental health treatment need among completers who experienced at least a partial improvement in PTSD symptoms is support for additional practice and reinforcement of skills learned in TFT. Veterans expressed low self-efficacy for maintaining or building upon their existing gains and believed continued contact with their TFT therapist would increase their likelihood of success. These treatment needs are particularly well-suited to a therapist-assisted self-management approach. Self-management protocols teach patients to be responsible for the day-to-day management of their symptoms, thereby emphasizing patients' roles in wellness. The existing literature on self-management interventions for PTSD has demonstrated that such approaches are acceptable, safe, and effective; however, they have exclusively been used as stand-alone treatments or as the first step up in a stepped-care model. Therefore, the investigators are proposing the first examination of a self-management intervention designed to be used to step down from an intensive course of TFT for PTSD. Objectives: The objective of this study is to complete stages 1A and 1B of the Stage Model of Treatment Development for the self-management program for Veterans who have recently completed a course of TFT for PTSD. Specifically, the investigators will: (1) Refine a self-management treatment protocol through eliciting feedback from experienced TFT providers, (2) Conduct a pilot open trial to assess the (a) acceptability of the self-management program components, structure, and materials and (b) feasibility of the self-management program (retention and intervention fidelity) and study approach (screening, recruitment, assessment process), and (3) Explore the effects of the program on Veterans' confidence in managing their PTSD (self-efficacy), functioning, quality of life, community engagement, and mental health symptoms. Methods: To achieve Aim 1, the investigators will conduct semi-structured individual interviews with a sample of TFT providers (n = 10-12), during which participants will be asked to provide feedback on the planned components and structure of the self-management program. To achieve Aims 2 and 3, the investigators will enroll twelve Veterans in a non-randomized, open-trial pilot test of the intervention at the Minneapolis VA Healthcare Systems (VAHCS). Enrolled Veterans will complete survey batteries immediately post-TFT, and survey batteries and qualitative interviews two weeks after the final self-management program therapist contact. Findings from this project will strongly position us to apply for Merit funding to conduct a randomized clinical trial (Stage 2 of the Stage Model of Treatment Development) of this innovative self-management program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorder
Keywords
Stress Disorders, Posttraumatic, Self-Management

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The study non-randomized, open-trial pilot test of the intervention with twelve Veterans who will all receive the study intervention.
Masking
None (Open Label)
Masking Description
As everyone in the study will receive the same intervention, no masking is being employed
Allocation
N/A
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Self-Management Program
Arm Type
Experimental
Arm Description
Patients in this arm will receive the therapist assisted self-management intervention following completion of trauma-focused therapy for PTSD.
Intervention Type
Behavioral
Intervention Name(s)
Self-Management Program
Intervention Description
This therapist-assisted self-management program will increase Veterans' self-efficacy for managing their PTSD, enable the maintenance or building upon gains made in trauma-focused therapy, and encourage engagement in meaningful activities. Patients will have four contacts with their providers over the ten weeks following trauma-focused therapy completion. The intervention will help patients: 1)self-monitor symptoms, 2) continue to practice skills learned in trauma-focused therapy, 3) acquire and apply additional coping skills, 4) engage in meaningful activities, and 5) set goals
Primary Outcome Measure Information:
Title
Credibility-Expectancy Scale (Credibility Subscale)
Description
Measures treatment rationale credibility in clinical outcome studies (range 1-9; higher scores = higher credibility).
Time Frame
Prior to first self-management session (baseline)
Title
Client Satisfaction Scale
Description
Measures client satisfaction with mental health services (range = 8-32; higher scores = higher satisfaction)
Time Frame
Three months after first self-management session (follow-up)
Secondary Outcome Measure Information:
Title
Change From Baseline in Illness Perception Questionnaire - Revised (Personal Control Subscale)
Description
Measures patients' self-efficacy for managing PTSD symptoms; range = 1-5 (higher scores = greater perceived control; change from pre- to post-intervention reported.
Time Frame
Prior to first self-management session (baseline) and three months after first self-management session (follow-up)
Title
Change From Baseline on PTSD Checklist - 5
Description
Measures DSM-5 PTSD symptoms; Range = 0-80; higher scores = more severe symptoms; change score from pre- to post-treatment reported
Time Frame
Prior to first self-management session (baseline) and three months after first self-management session (follow-up)
Title
Change From Baseline on Patient Health Questionnaire - 9
Description
Measures symptoms of depression; range = 0-27; higher scores = more severe symptoms; pre- to post-treatment change score reported
Time Frame
Prior to first self-management session (baseline) and three months after first self-management session (follow-up)
Title
Change From Baseline on Recovery Orientation Scale (Current Mental Health Subscale)
Description
Measures patients' perceived mental health; range 1-5; lower scores = better perceived mental health
Time Frame
Prior to first self-management session (baseline) and three months after first self-management session (follow-up)
Title
Change From Baseline on World Health Organization Quality of Life - BREF
Description
Measures patients' current quality of life; higher score = better quality of life; range = 0-100. Change score from pre- to post-treatment reported
Time Frame
Prior to first self-management session (baseline) and three months after first self-management session (follow-up)
Title
Change From Baseline on Military to Civilian Questionnaire
Description
Measures patients' community engagement; range: 0-4; higher scores = more difficulty; change score from pre- to post-intervention reported
Time Frame
Prior to first self-management session (baseline) and three months after first self-management session (follow-up)
Title
Change From Baseline on Brief Inventory of Psychosocial Functioning
Description
Measure of PTSD-related psychosocial functional impairment; higher scores = more severe; range = 0-49; change from pre- to post-treatment reported
Time Frame
Prior to first self-management session (baseline) and three months after first self-management session (follow-up)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients will be eligible to participate if they: completed a course of individually-delivered trauma-focused therapy (TFT) with a provider trained to deliver the self-management intervention at the Minneapolis VAMC experienced a clinically meaningful reduction in PTSD symptomology (PCL decrease of at least 10 points) from pre-TFT to the time of the enrollment at the time of enrollment are not planning to initiate another active course of psychotherapy for PTSD in the following three months are willing to participate in a self-management intervention, and can provide informed consent Exclusion Criteria: Veterans will be excluded if they have suicidal or homicidal ideation that in the opinion of their TFT therapist needs to be the focus of treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shannon M. Kehle-Forbes, PhD
Organizational Affiliation
Minneapolis VA Health Care System, Minneapolis, MN
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
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Research datasets included in primary publications resulting from this proposed research will involve large amounts of individual PHI data and cannot reasonably or efficiently be fully deidentified. Investigators will create analytic datasets that can be requested by outside investigators. These data however will remain within the VA firewall and be housed on VINCI data servers. Outside investigators can follow VA procedures and receive training and approval for access within VA firewalls.

Learn more about this trial

A Self-Management Program for Completers of Trauma-Focused Therapy for PTSD

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