ACT-SS: Acceptance and Commitment Therapy to Improve Social Support for Veterans With PTSD

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Recruiting
CT.gov ID
NCT04567680
Collaborator
(none)
150
2
2
43
75
1.7

Study Details

Study Description

Brief Summary

Veterans with PTSD often have impaired social relationships and poor social support. The negative outcomes associated with poor social support are of particular concern for Veterans with PTSD, who often perceive the world to be dangerous, view their social support network as a threat to their safety, and avoid members of their support network in order to increase their perceived safety. The goal of this project is to evaluate the efficacy of Acceptance and Commitment Therapy to Improve Social Support for Veterans with PTSD (ACT-SS), a treatment focused on helping Veterans with PTSD to increase social support with family relationships, partners, and peers by targeting maladaptive patterns of interpersonal difficulties, feelings of detachment from others, irritability, and avoidance of social situations. The primary aim of this study is to conduct a two-site randomized controlled trial of ACT-SS (n=75) vs. PCT (n=75), a common treatment for social support difficulties. If positive, this study will provide a critically-needed treatment for Veterans with PTSD to improve their social functioning and social reintegration in the community.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Acceptance and Commitment Therapy to Improve Social Support for Veterans with PTSD
  • Behavioral: Present-Centered Therapy
N/A

Detailed Description

Veterans with PTSD often have substantial interpersonal problems and low perceived social support from family, partners, and peers. Interpersonal problems result in poor social reintegration, which in turn permeates all aspects of their functioning and is associated with greater suicidal ideation. The problems emerge rapidly, with one study showing a fourfold increase in rates of self-reported interpersonal conflict within six months of returning from deployment. Veterans with PTSD report considerable avoidance in relationships, marital stress, intimacy difficulties, and parenting problems. Low social support is a key factor related to poor physical health, emotional functioning, and increased mortality risk. Given the importance of social relationships in buffering against negative outcomes and suicidal ideation for persons with PTSD, there is a strong need for more research and treatment development to improve the social functioning of these Veterans. The proposed project will focus on evaluating an innovative treatment for improving the social relationships and social support among Veterans with PTSD.

The goal of this project is to evaluate the efficacy of Acceptance and Commitment Therapy to Improve Social Support for Veterans with PTSD (ACT-SS), a treatment focused on helping Veterans with PTSD to increase social support with family relationships, partners, and peers by targeting maladaptive patterns of interpersonal difficulties, feelings of detachment from others, irritability, and avoidance of social situations. ACT-SS provides Veterans with PTSD with more adaptive coping skills (i.e., acceptance and mindfulness, focus on values-based living) to improve social relationships, social support, and help manage PTSD-related distress. The investigators' pilot data of ACT-SS indicates that ACT-SS results in improved social relationships and reduced PTSD symptoms, with preliminary data showing that ACT-SS results in significantly better improvement in social functioning outcomes compared to Present-Centered Therapy (PCT).

The primary aim of this study is to conduct a two-site randomized controlled trial of ACT-SS (n=75) vs. PCT (n=75), a common treatment for social support difficulties. Study outcomes will include measures of social support, social relationships, quality of life, and PTSD symptoms. This proposal, supported by the promising pilot data, represents an important step in examining the potential efficacy of ACT-SS, including social functioning and quality of life in Veterans with PTSD. If positive, results from this study may provide a new treatment approach for improving the social reintegration of Veterans with PTSD.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
An independent evaluator will assess outcomes for each study participant.
Primary Purpose:
Treatment
Official Title:
Acceptance and Commitment Therapy to Improve Social Support for Veterans With PTSD
Actual Study Start Date :
Mar 1, 2021
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Sep 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Acceptance and Commitment Therapy to Improve Social Support

This treatment is designed to help Veterans with PTSD increase social support in family, partner, and peer relationships by reducing experiential avoidance. ACT-SS is specifically designed to address deficits in the entire social support network for Veterans with PTSD.

Behavioral: Acceptance and Commitment Therapy to Improve Social Support for Veterans with PTSD
This treatment is designed to help Veterans with PTSD increase social support in family, partner, and peer relationships by reducing experiential avoidance. ACT-SS is specifically designed to address deficits in the entire social support network for Veterans with PTSD.
Other Names:
  • ACT-SS
  • Active Comparator: Present-Centered Therapy

    PCT is designed to provide the emotional support for individuals with PTSD that will assist with recovery. The focus of PCT is on the "here and now," including current life difficulties that are directly or indirectly related to the experience of trauma. PCT aims to help the patient consider ways to react to these difficulties.

    Behavioral: Present-Centered Therapy
    PCT is designed to provide the emotional support for individuals with PTSD that will assist with recovery. The focus of PCT is on the "here and now," including current life difficulties that are directly or indirectly related to the experience of trauma. PCT aims to help the patient consider ways to react to these difficulties.
    Other Names:
  • PCT
  • Outcome Measures

    Primary Outcome Measures

    1. Change in the Social Adjustment Scale-Self Report [Baseline, End of Treatment (12 weeks), 3-month follow-up, and 6-month follow-up]

      The Social Adjustment Scale-Self Report (SAS-SR) is a 54-item measure of current social functioning in 6 domains: Work; Social and Leisure; Extended Family; Primary Relationship; Parental; and Family Unit. It is the primary measure of change in social functioning for the study. An Overall Adjustment scale provides a total score (alpha = .74-.85; test-retest r's = .78-.80). The SAS-SR is sensitive to change and has good convergent and discriminant validity. Higher scores indicate better functioning. Scores for each role area are calculated by averaging the scores for all answered items within that area. The total score is calculated by averaging all applicable items.

    2. Change in the MOS Social Support Survey [Baseline, End of Treatment (12 weeks), 3-month follow-up, and 6-month follow-up]

      Social Support: The MOS Social Support Survey is a 19-item multidimensional, self-administered survey of social support for individuals with chronic conditions. It includes four functional support scales, including emotional/informational, tangible, affectionate, and positive social interaction. Scores range from 0-100. A higher score for an individual scale or for the overall support index indicates more support.

    Secondary Outcome Measures

    1. Change in the Quality of Life, Enjoyment, and Satisfaction Questionnaire [Baseline, End of Treatment (12 weeks), 3-month follow-up, and 6-month follow-up]

      Quality of Life: The Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q) is a commonly used self-report measure to assess quality of life in several domains: general activities, physical health, subjective feelings, leisure time activities, social relationships, work, and household duties. The minimum raw score on the Q-LES-Q-SF is 14, and the maximum score is 70. Percent maximum scores range from 0-100. Higher scores indicating greater life satisfaction and enjoyment.

    2. Change in the Clinician Administered PTSD Scale (CAPS-5) [Baseline, End of Treatment (12 weeks), 3-month follow-up, and 6-month follow-up]

      The Clinician Administered PTSD Scale (CAPS-5) is a structured interview that will be used to diagnose PTSD and to obtain data (pre and post treatment, follow-up) on the frequency and severity of PTSD symptoms. The CAPS-5 is the gold standard for assessing PTSD. CAPS-5 scores range from 0 to 80 with higher scores indicating greater PTSD symptom severity.

    3. Change in the PTSD Checklist (PCL-5) [Baseline, End of Treatment (12 weeks), 3-month follow-up, and 6-month follow-up]

      The PCL-5 is a 20-item self-report measure of PTSD symptoms, selected for its dimensional sensitivity, with higher scores reflecting greater PTSD severity. A total symptom severity score (range - 0-80) can be obtained by summing the scores for each of the 20 items.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Current DSM-5 PTSD diagnosis

    • Minimum score of 31 on the PCL-5

    • Clinically significant difficulties in interpersonal relationships

    • Competent to provide written informed consent

    • Ages 18 and older

    • If being treated with psychoactive medication, no change in drugs or dose for the past 2 months

    • Willingness to be audio-taped

    Exclusion Criteria:
    • Any current or lifetime DSM-5 psychotic disorder

    • Current or recent (within 1 month of study entry) DSM-5 substance use disorder

    • Cognitive impairment that would interfere with study participation

    • Current manic episode

    • Recent clinically significant suicidality (past 3 months)

    • Moderate to severe domestic violence (measured by the Conflict Tactics Scale-2)

    • Current PTSD psychotherapy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Rocky Mountain Regional VA Medical Center, Aurora, CO Aurora Colorado United States 80045
    2 VA Bedford HealthCare System, Bedford, MA Bedford Massachusetts United States 01730

    Sponsors and Collaborators

    • VA Office of Research and Development

    Investigators

    • Principal Investigator: Megan Marie Kelly, PhD MS, VA Bedford HealthCare System, Bedford, MA

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    VA Office of Research and Development
    ClinicalTrials.gov Identifier:
    NCT04567680
    Other Study ID Numbers:
    • D3382-R
    • 1I01RX003382-01A1
    First Posted:
    Sep 28, 2020
    Last Update Posted:
    Mar 24, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    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 Mar 24, 2022