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Non-Inferiority Trial of TrIGR for PTSD (TrIGR/CPT)

Primary Purpose

PTSD

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Trauma Informed Guilt Reduction Therapy
Cognitive Processing Therapy
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 PTSD focused on measuring PTSD, trauma, moral injury, intervention, guilt, shame

Eligibility Criteria

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

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.

Sites / Locations

  • VA San Diego Healthcare System, San Diego, CARecruiting
  • James A. Haley Veterans' Hospital, Tampa, FLRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Trauma Informed Guilt Reduction Therapy (TrIGR)

Cognitive Processing Therapy (CPT)

Arm Description

behavioral intervention aimed to reduce trauma-related guilt and shame

behavioral intervention aimed at reducing PTSD symptoms

Outcomes

Primary Outcome Measures

change in Clinician Administered PTSD Scale - 5 (CAPS-5)
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

change in Patient Health Questionnaire - 9 (PHQ-9)
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.
Trauma Related Guilt Inventory (TRGI)
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.
Trauma Related Shame Inventory (TRSI)
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.

Full Information

First Posted
March 15, 2023
Last Updated
July 13, 2023
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT05789329
Brief Title
Non-Inferiority Trial of TrIGR for PTSD
Acronym
TrIGR/CPT
Official Title
Non-Inferiority Trial of Trauma Informed Guilt Reduction Therapy (TrIGR) for PTSD
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2023 (Actual)
Primary Completion Date
March 31, 2027 (Anticipated)
Study Completion Date
September 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
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PTSD
Keywords
PTSD, trauma, moral injury, intervention, guilt, shame

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly assigned to Trauma Informed Guilt Reduction Therapy (TrIGR) or Cognitive Processing Therapy (CPT).
Masking
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.
Allocation
Randomized
Enrollment
158 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Trauma Informed Guilt Reduction Therapy (TrIGR)
Arm Type
Experimental
Arm Description
behavioral intervention aimed to reduce trauma-related guilt and shame
Arm Title
Cognitive Processing Therapy (CPT)
Arm Type
Active Comparator
Arm Description
behavioral intervention aimed at reducing PTSD symptoms
Intervention Type
Behavioral
Intervention Name(s)
Trauma Informed Guilt Reduction Therapy
Other Intervention Name(s)
TrIGR
Intervention Description
behavioral intervention aimed to reduce trauma-related guilt and shame
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Processing Therapy
Other Intervention Name(s)
CPT
Intervention Description
behavioral intervention aimed at reducing PTSD symptoms
Primary Outcome Measure Information:
Title
change in Clinician Administered PTSD Scale - 5 (CAPS-5)
Description
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.
Time Frame
baseline to 28 weeks later
Secondary Outcome Measure Information:
Title
change in Patient Health Questionnaire - 9 (PHQ-9)
Description
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.
Time Frame
baseline to 28 weeks later
Title
Trauma Related Guilt Inventory (TRGI)
Description
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.
Time Frame
baseline to 28 weeks later
Title
Trauma Related Shame Inventory (TRSI)
Description
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.
Time Frame
baseline to 28 weeks later

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sonya B Norman, PhD
Phone
(858) 552-8585
Ext
5198
Email
Sonya.Norman@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Kaitlyn Panza, PhD
Phone
(858) 552-8585
Email
kaitlyn.panza@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sonya B. Norman, PhD
Organizational Affiliation
VA San Diego Healthcare System, San Diego, CA
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA San Diego Healthcare System, San Diego, CA
City
San Diego
State/Province
California
ZIP/Postal Code
92161-0002
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sonya B Norman, PhD
Phone
858-552-8585
Ext
5198
Email
Sonya.Norman@va.gov
First Name & Middle Initial & Last Name & Degree
Sonya B. Norman, PhD
Facility Name
James A. Haley Veterans' Hospital, Tampa, FL
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brittany Davis, PhD
Phone
813-972-2000
Email
brittany.davis@va.gov
First Name & Middle Initial & Last Name & Degree
Risa Nakase-Richardson, PhD
Phone
8139722000
Email
risa.Nakase-Richardson@va.gov

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
A de-identified, anonymized dataset without personal identifiers will be generated and shared with those who request and are granted access (see access criteria). Any HIPAA identifiers, or combinations of variables that could be used for re-identification, will be excluded, as will any proprietary information. The plan does not include any access to individually identifiable or proprietary data. Therefore, this plan will ensure the protection of personal privacy, the confidentiality of individually identifiable private information, and the security of proprietary data and information.
IPD Sharing Time Frame
After publication of the primary outcome paper.
IPD Sharing Access Criteria
Requests for access must be made in writing signed by a requester from the United States and include an email address for delivery and an assurance that the recipient will not attempt to identify or re-identify any individual. The request should reference the publication underlying the request.

Learn more about this trial

Non-Inferiority Trial of TrIGR for PTSD

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