Efficacy and Neural Mediators of Response to Trauma Management Therapy for PTSD

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT03449576
Collaborator
(none)
69
1
2
42
1.6

Study Details

Study Description

Brief Summary

Social difficulties are serious and frequent complicating factors in the treatment of post-traumatic stress disorder (PTSD). To better understand how treatment of post-traumatic stress disorder impacts neural mechanisms of social cognition, the investigators are examining behavior and brain processes associated with response to Trauma Management Therapy. Understanding the behavioral and neural impact of psychotherapy may contribute to development of more effective treatments for PTSD.

Condition or Disease Intervention/Treatment Phase
  • Other: Trauma Management Therapy
  • Other: Exposure Therapy with Psychotherapy group
N/A

Detailed Description

PTSD is associated with significant interpersonal difficulties that interfere with functioning. As such, this work is intended to evaluate the empirical support for a novel treatment that fills a significant gap in the treatment options available to Veterans with PTSD who suffer with interpersonal difficulties. In this study the investigators will (i) evaluate the efficacy of Trauma Management Therapy (TMT) for treating PTSD-related interpersonal dysfunction, as well as PTSD-related fear and anxiety, and (ii) evaluate neural mediators of clinical improvements associated with TMT.

This work will provide insights into the mechanisms by which treatments may lead to improvements in social functioning, informing both the biological basis of psychotherapy and the development and refinement of alternative therapeutic interventions targeting social impairments.

Treatment seeking Veterans with PTSD will be randomized to one of two treatments: (i) Trauma Management Therapy, consisting of 12 sessions of individualized exposure therapy followed by 24 sessions of group-based social and emotional rehabilitation, or (ii) Exposure + Comparison Treatment Group consisting of 12 sessions of individualized exposure therapy followed by 24 sessions of group-based psychotherapy. Veterans enrolled in both the TMT and EXP+GRP arms will undergo functional neuroimaging as they engage in an emotional image viewing task, as well as two social interaction tasks. Neurobehavioral assessments will be made prior to and following completion of treatment.

Study Design

Study Type:
Interventional
Actual Enrollment :
69 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Efficacy and Neural Mediators of Response to Trauma Management Therapy for PTSD
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Jul 1, 2022
Actual Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Trauma Management Therapy

Trauma Management Therapy (TMT) consists of a combination of 12 sessions of individualized exposure therapy and 24 sessions of group-based social and emotion rehabilitation.

Other: Trauma Management Therapy
Trauma Management Therapy (TMT) consists of a combination of 12 sessions of individualized exposure therapy and 24 sessions of group-based social and emotion rehabilitation.
Other Names:
  • TMT
  • Active Comparator: Exposure Therapy with Psychoeducation

    Exposure Therapy with Psychoeducation (EXP+EDU) consists of a combination of 12 sessions of individualized exposure therapy and 24 session of group-based psychoeducation.

    Other: Exposure Therapy with Psychotherapy group
    Exposure Therapy with Psychoeducation (EXP+EDU) consists of a combination of 12 sessions of individualized exposure therapy and 24 session of group-based psychoeducation.
    Other Names:
  • EXP+GRP
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Clinician-Administered PTSD Scale for DSM-5 [CAPS-5 will be assessed at two time-points per participant: pre-treatment (week 0) and at completion of treatment (week 8).]

      The Clinician-Administered PTSD Scale for DSM-5 (CAPS-5; Weathers et al. 2013; 2017) is a 30 item semi-structured instrument for the diagnosis and assessment of severity of posttraumatic stress disorder (PTSD). Each DSM-5 item is rated on a 0 (absent) to 4 (extreme/incapacitating) scale, and total score is calculated by summing severity scores across items. Total CAPS-5 severity can range from 0 to 80.

    2. Change in Social Adjustment Scale - Self-Report [SAS will be assessed at two time-points: pre-treatment to treatment (week 0) and at completion of treatment (week 8).]

      The Social Adjustment Scale (SAS; Weissman & Bothwell, 1976) is a 54 item self-report measure that assesses social adjustment in six social areas of functioning including work, social and leisure activities, extended family, marital, parental, and family. Each item is rated on a five point scale, and within each of domain items are averaged. Thus, scores in each domain can range between 1 (high social adjustment) and 5 (low social adjustment).

    Secondary Outcome Measures

    1. Change in PTSD Checklist for DSM-5 [The PCL-5 will be assessed at two time-points: pre-treatment to treatment (week 0) and at completion of treatment (week 8).]

      The PTSD Checklist for DSM-5 (PCL-5; Weathers et al., 2013; Bovin et al., 2016) is a 20 item self-report measure assessing DSM-5 PTSD symptom severity. Each DSM-5 item is rated on a 0 (absent) to 4 (extreme/incapacitating) scale, and total score is calculated by summing severity scores across items. Total CAPS-5 severity can range from 0 to 80.

    2. Change in Aggression Questionnaire [AQ will be assessed at two time-points: pre-treatment to treatment (week 0) and at completion of treatment (week 8).]

      Change in Aggression Questionnaire (AQ; Buss & Warren, 2000) is a 34 item self-report measure that assesses severity of self-perceived aggression and anger. Each item is rated on a 1 (Not at all like me) to 5 (Completely like me) scale, and total scores can range from 34 to 170.

    3. Change in Interpersonal Trust Scale [ITS will be assessed at two time-points: pre-treatment to treatment (week 0) and at completion of treatment (week 8).]

      Change in Interpersonal Trust Scale (ITS; Rotter, 1967) is a 25 item self-report measure that assesses trust within relationships. Each item is rated on a 1 (low trust) to 5 (high trust) scale, and total scores can range from 25 to 125.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male and female veterans of all ethnicities

    • Meet diagnostic criteria for post-traumatic stress disorder (assessed by study staff)

    • Fluent in English

    • Able to see computer display clearly

    • Able to provide informed consent

    • Able to follow written or verbal instructions

    Exclusion Criteria:
    • history of seizures

    • history of stroke

    • Cushing's syndrome

    • history of moderate to severe traumatic brain injury

    • electroconvulsive therapy within 5 years

    • history of chemotherapy for cancer

    • contraindications to fMRI

    • pregnancy

    • diagnosis of schizophrenia, schizoaffective disorder, delusional disorder and/or organic psychosis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Salem VA Medical Center, Salem, VA Salem Virginia United States 24153

    Sponsors and Collaborators

    • VA Office of Research and Development

    Investigators

    • Principal Investigator: Brooks King-Casas, PhD, Salem VA Medical Center, Salem, VA

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    VA Office of Research and Development
    ClinicalTrials.gov Identifier:
    NCT03449576
    Other Study ID Numbers:
    • D2354-R
    First Posted:
    Feb 28, 2018
    Last Update Posted:
    Jul 6, 2022
    Last Verified:
    Jul 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 Jul 6, 2022