Self-Help Cognitive Processing Therapy (CPT)/Women Veterans Network (WoVeN) Study

NCT ID: NCT07250061

Last Updated: 2026-01-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-03-31

Study Completion Date

2028-03-31

Brief Summary

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Posttraumatic stress disorder (PTSD) can have significant impairment on aspects of mental well-being (MWB) including functioning, loneliness, physical health, and quality of life. There are several evidence-based treatments (EBPs) effective in treating PTSD such as Cognitive Processing Therapy (CPT) which is a specific type of cognitive behavioral therapy that has been proven effective in reducing symptoms of PTSD. However, there are several barriers (e.g., lack of providers, waitlists, costs, stigma, disabilities that complicate travel) that can prevent someone from engaging with these treatments. Recently, a self-help version of CPT was created to help address these barriers; but little research has been conducted to test its efficacy. Further, less is know about how a peer support program may augment improvements from participating in an EBP. The Women Veteran Network (WoVeN), a peer support program designed for women veterans, has a manualized 8-week program that directly targets MWB. It has been found to help foster belongingness and connectedness, particularly in those suffering from PTSD and depression.

The present study aims to establish the feasibility, acceptability and tolerability of a scalable, sustainable, and effective treatment option for trauma survivors with subthreshold or full PTSD. The overarching goal is to understand the effectiveness of a self-help version of an EBP (either alone or in combination with a peer support program) in reducing PTSD symptoms while also helping improve mental well-being, reduce barriers, and increase access to quality care within health disparity populations.

Detailed Description

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The design for this study is a three-arm, randomized, controlled clinical trial (RCT) with a national sample of women veterans who suffer from PTSD. Participants will be recruited from WoVeN and from the women veteran population. Treatment conditions will be 1.) self-help CPT only (shCPT), 2.) concurrent WoVeN + self-help CPT (BOTH), or 3.) referral + treatment as usual (TAU). All treatments must be completed within 10 weeks. Ninety women will be randomized in a 1:1:1 ratio across the three treatment conditions. Patient participants will be asked to complete three major assessments (baseline, post-treatment, three month follow up) that consist of a structured interview and questionnaire. These major assessment will take \~2.5 hours to complete. Participants will also be asked to complete weekly surveys that will help monitor ongoing progress engagement with the intervention. Before the RCT launches, an open trial involving 6 women will pilot the BOTH condition. Information gathered from this will be used to refine the study before recruiting more women.

Conditions

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Posttraumatic Stress Disorder Depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

A three-arm, randomized, controlled clinical trial will be conducted with a national sample of women veterans who suffer from PTSD.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Self-Help Cognitive Processing Therapy (shCPT)

Participants randomized to this arm will receive Cognitive Processing Therapy (CPT) and a self- help book.

Group Type EXPERIMENTAL

Self-Help Cognitive Processing Therapy

Intervention Type BEHAVIORAL

Participants will be given a copy of the CPT self-help book that guides the trauma survivor through the same CPT protocol that is typically delivered by a therapist but supplemented with significant additional guidance and suggestions to aid the survivor in their journey toward recovery. This 10-week program also provides links to educational videos, fillable worksheets, and resources for the individual if they would like to seek additional care

Women Veterans Network (WoVeN) + self-help CPT (BOTH)

Participants randomized to this arm will receive Cognitive Processing Therapy by trained peer leaders from the Women Veterans Network (WoVeN).

Group Type EXPERIMENTAL

Self-Help Cognitive Processing Therapy

Intervention Type BEHAVIORAL

Participants will be given a copy of the CPT self-help book that guides the trauma survivor through the same CPT protocol that is typically delivered by a therapist but supplemented with significant additional guidance and suggestions to aid the survivor in their journey toward recovery. This 10-week program also provides links to educational videos, fillable worksheets, and resources for the individual if they would like to seek additional care

Women Veterans Network (WoVeN)

Intervention Type BEHAVIORAL

Participants will complete the CPT self-help book while also enrolled in a WoVeN group. WoVeN is a national, peer support network with groups led by women veterans, for women veterans. During this 8-week program, Peer Leaders who are trained by national experts in the WoVeN curriculum conduct weekly groups. Groups consist of approximately 4-8 women veterans, each lasting about 90 minutes, and focus on relevant themes such as life transitions, balance, hope, connections, trust, and esteem.

Treatment as Usual (TAU)

Participants randomized to this arm will receive TAU.

Group Type ACTIVE_COMPARATOR

Treatment as Usual

Intervention Type OTHER

Participants will receive psychoeducation about PTSD and different treatment options using the materials developed by the VA National Center for PTSD. They will also be provided with a referral list with guidance and suggestions and assistance in navigating the list and the referral process. All interventions must be completed within 10 weeks.

Interventions

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Self-Help Cognitive Processing Therapy

Participants will be given a copy of the CPT self-help book that guides the trauma survivor through the same CPT protocol that is typically delivered by a therapist but supplemented with significant additional guidance and suggestions to aid the survivor in their journey toward recovery. This 10-week program also provides links to educational videos, fillable worksheets, and resources for the individual if they would like to seek additional care

Intervention Type BEHAVIORAL

Women Veterans Network (WoVeN)

Participants will complete the CPT self-help book while also enrolled in a WoVeN group. WoVeN is a national, peer support network with groups led by women veterans, for women veterans. During this 8-week program, Peer Leaders who are trained by national experts in the WoVeN curriculum conduct weekly groups. Groups consist of approximately 4-8 women veterans, each lasting about 90 minutes, and focus on relevant themes such as life transitions, balance, hope, connections, trust, and esteem.

Intervention Type BEHAVIORAL

Treatment as Usual

Participants will receive psychoeducation about PTSD and different treatment options using the materials developed by the VA National Center for PTSD. They will also be provided with a referral list with guidance and suggestions and assistance in navigating the list and the referral process. All interventions must be completed within 10 weeks.

Intervention Type OTHER

Other Intervention Names

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shCPT BOTH TAU

Eligibility Criteria

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Inclusion Criteria

* Identifies as a woman
* Has served in the United States military
* A full or subthreshold (meets criteria for 2 out of 4 of the symptom clusters for PTSD) Post Traumatic Stress Disorder (PTSD) diagnosis
* Able to read English well enough to complete study questionnaires

Exclusion Criteria

* Clinician judgment that the participant is not appropriate for self-help level of care for PTSD (i.e., recent psychiatric hospitalization, requires detox, volatile, active suicidality)
* Current psychosis or unstable bipolar disorder (determined during baseline interview as described in screening and enrollment procedures)
* Must not have participated in a WoVeN group within the last year
* Must not be receiving an evidenced-based therapy for PTSD at the time of the screening
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

Boston University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tara E Galovski, PhD

Role: PRINCIPAL_INVESTIGATOR

BUCA School of Medicine, Psychiatry and VA Medical Center

Central Contacts

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Tara E Galovski, PhD

Role: CONTACT

(857) 364-4129

Lauren Mcsweeney, PhD

Role: CONTACT

(617) 480-0429

Other Identifiers

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1R34MH138605-01A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

H-46292

Identifier Type: -

Identifier Source: org_study_id

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