TrIGR/CPT: Non-Inferiority Trial of TrIGR for PTSD

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Not yet recruiting
CT.gov ID
NCT05789329
Collaborator
(none)
158
2
2
52
79
1.5

Study Details

Study Description

Brief Summary

Trauma-related guilt is common and impairing among trauma survivors, particularly among Veterans with posttraumatic stress disorder (PTSD). The investigators' work shows that a brief treatment targeting trauma-related guilt, Trauma Informed Guilt Reduction Therapy (TrIGR), can reduce guilt and PTSD and depression symptoms. Whether TrIGR is no less effective than longer, more resource heavy PTSD treatments disseminated by by VA, like cognitive processing therapy (CPT), is the next critical question that this study will seek to answer. 158 Veterans across two VA sites will be randomized to TrIGR or CPT to evaluate changes in PTSD, depression, guilt and shame symptoms across the two treatments.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Trauma Informed Guilt Reduction Therapy
  • Behavioral: Cognitive Processing Therapy
N/A

Detailed Description

Trauma-related guilt is common and impairing among trauma survivors, particularly among treatment seeking Veterans with posttraumatic stress disorder (PTSD). Although evidence-based trauma-focused PTSD treatments such as Cognitive Processing Therapy (CPT) are effective to treat PTSD and trauma-related guilt, many still experience symptoms or maintain their diagnosis after treatment, and dropout from these generally 12+ session protocols is high. Veterans show lower response and higher dropout than others with PTSD. Delivering protocols that are generally 12 or more sessions challenges the Veterans Affairs (VA) healthcare system given high demand for mental health care. For these reasons, additional and less burdensome approaches are needed. Brief treatment that targets mechanisms that are distressing and associated with multiple problems and disorders may be an understudied but promising way to treat PTSD and other posttraumatic psychopathology. The investigators' work shows that a brief treatment targeting trauma-related guilt and shame, Trauma Informed Guilt Reduction Therapy (TrIGR), can reduce guilt, PTSD, depression, and distress among Veterans and help them reengage with activities they find meaningful. Whether TrIGR is no less effective than longer, more resource heavy evidence-based PTSD treatments disseminated across by VA, like CPT, is the next critical question.

The proposed randomized clinical trial (RCT) will be the first non-inferiority trial of TrIGR and the first to compare TrIGR to a first tier PTSD treatment, specifically CPT. It will also be the first to evaluate TrIGR with Veterans from all eras with guilt from any type of traumas, as the investigators previous work was exclusively with Veterans of the conflicts in Iraq and Afghanistan with deployment-related traumas. 158 Veterans across two VA sites will be randomized to TrIGR or CPT. Exclusion criteria will be minimal so that generalizability will be high. Treatment will be delivered in VA mental health clinics. The primary aim is to evaluate if TrIGR is non-inferior to CPT in reducing PTSD symptom severity among Veterans with PTSD who endorse trauma-related guilt. Secondary aims are to evaluate TrIGR's non-inferiority relative to CPT regarding depression severity. The investigators will explore potential mechanisms of treatment, such as the relationship between change in guilt and shame change in PTSD symptoms. The study is critical to establish whether TrIGR is effective for a much larger group of Veterans and whether it is as effective as longer treatments already available in VA to inform if TrIGR warrants further study and dissemination in VA.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
158 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be randomly assigned to Trauma Informed Guilt Reduction Therapy (TrIGR) or Cognitive Processing Therapy (CPT).Participants will be randomly assigned to Trauma Informed Guilt Reduction Therapy (TrIGR) or Cognitive Processing Therapy (CPT).
Masking:
Single (Outcomes Assessor)
Masking Description:
A computer-generated masked randomization sequence will be provided and held by a statistician not otherwise involved in the study. Randomization will be stratified by site and gender.
Primary Purpose:
Treatment
Official Title:
Non-Inferiority Trial of Trauma Informed Guilt Reduction Therapy (TrIGR) for PTSD
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Mar 31, 2027
Anticipated Study Completion Date :
Sep 30, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Trauma Informed Guilt Reduction Therapy (TrIGR)

behavioral intervention aimed to reduce trauma-related guilt and shame

Behavioral: Trauma Informed Guilt Reduction Therapy
behavioral intervention aimed to reduce trauma-related guilt and shame
Other Names:
  • TrIGR
  • Active Comparator: Cognitive Processing Therapy (CPT)

    behavioral intervention aimed at reducing PTSD symptoms

    Behavioral: Cognitive Processing Therapy
    behavioral intervention aimed at reducing PTSD symptoms
    Other Names:
  • CPT
  • Outcome Measures

    Primary Outcome Measures

    1. change in Clinician Administered PTSD Scale - 5 (CAPS-5) [baseline to 28 weeks later]

      Clinician Administered PTSD Scale - 5 (CAPS-5) - score range 0 - 80; higher scores are indicative of more severe PTSD symptoms. Reduction in scores is considered a positive outcome.

    Secondary Outcome Measures

    1. change in Patient Health Questionnaire - 9 (PHQ-9) [baseline to 28 weeks later]

      change in Patient Health Questionnaire - 9 (PHQ-9) - score ranges 0-27. higher scores are indicative of more severe depressive symptoms. Reduction in scores is considered a positive outcome.

    2. Trauma Related Guilt Inventory (TRGI) [baseline to 28 weeks later]

      Trauma Related Guilt Inventory (TRGI) - score ranges 0-4. higher scores are indicative of more severe trauma-related guilt. Reduction in scores is considered a positive outcome.

    3. Trauma Related Shame Inventory (TRSI) [baseline to 28 weeks later]

      Trauma Related Shame Inventory (S) - score ranges 0-72. higher scores are indicative of more severe trauma-related shame. Reduction in scores is considered a positive outcome.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • U.S. Veterans age 18 or older;

    • meets diagnostic criteria for PTSD or subthreshold PTSD;

    • a score of 2 or higher ("true" to "extremely true") on feeling trauma-related guilt much or all of the time or scoring 3 or higher ("very true" or "extremely true") on at least one guilt cognition factor (hindsight bias/responsibility, wrongdoing, or lack of justification) on the Trauma Related Guilt Inventor.

    • not currently receiving trauma-focused treatment such as CPT or PE; and

    • willingness to attend psychotherapy and assessment sessions.

    Exclusion Criteria:
    • Impaired mental status as measured by the Montreal Cognitive Assessment (MoCA) (score < 21) and confirmed by a neuropsychologist,

    • Veterans with significant current risk of suicidal/homicidal behavior will be referred to more appropriate treatment;

    • Current severe substance use disorder (in the past two months) based on DSM-5 criteria;

    • Current unmanaged psychosis or mania;

    • life threatening or unstable medical illness; or

    • inability to read.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 VA San Diego Healthcare System, San Diego, CA San Diego California United States 92161-0002
    2 James A. Haley Veterans' Hospital, Tampa, FL Tampa Florida United States 33612

    Sponsors and Collaborators

    • VA Office of Research and Development

    Investigators

    • Principal Investigator: Sonya B. Norman, PhD, VA San Diego Healthcare System, San Diego, CA

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    VA Office of Research and Development
    ClinicalTrials.gov Identifier:
    NCT05789329
    Other Study ID Numbers:
    • MHBP-003-22S
    • MHBP-003-22S
    First Posted:
    Mar 29, 2023
    Last Update Posted:
    Mar 29, 2023
    Last Verified:
    Mar 1, 2023
    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 29, 2023