ACTIVE_NOT_RECRUITING

Efficacy of Virtual Warrior Renew Therapy for Veterans Who Experienced Military Sexual Trauma

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Conditions

Military Sexual Trauma (MST)Post Traumatic Stress Disordergroup therapymilitary sexual traumarandomized clinical trialPTSDMST

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Group treatments may be helpful for Veterans who have experienced military sexual trauma (MST). By doing this study, the investigators hope to learn if two different groups: Warrior Renew and Health \& Wellness are effective in reducing mental health symptoms in Veterans who have experienced MST and if either is more effective than the other. Participation in this research will last about 16 weeks.

Official Title

Efficacy of Virtual Warrior Renew Therapy for Veterans Who Experienced Military Sexual Trauma

Quick Facts

Study Start:2023-07-17
Study Completion:2026-10-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05776719

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Has established care with VA medical or mental health provider.
  2. 2. Reports having experienced military sexual trauma.
  3. 3. Between the ages of 18 and 75.
  4. 4. Is an outpatient and is able to comply with all study procedures, including the eight weeks of group treatment and the assessment measures.
  5. 5. Positive screen on the Primary Care PTSD Screen for DSM-5 (PC-PTSD-5).
  6. 6. Able to participate in virtual group therapy via telehealth.
  1. 1. Impaired decision-making capacity that in the clinical judgment of their provider would affect their ability to provide informed consent.
  2. 2. Current/active suicidal ideation as evidenced by a positive screen on the Columbia Suicide Severity Rating Scale (C-SSRS), or a suicide attempt or psychiatric hospitalization within the past year.
  3. 3. Dissociative, delusional or psychotic symptoms due to medical conditions or mental health disorders that in the clinical judgement of the PI or LSI would impede the participant's ability to participate actively in the study.
  4. 4. Current/active diagnosis of a substance use disorder or an alcohol use disorder as measured by the Alcohol Use Disorders Identification Test-Concise (AUDIT-C).
  5. 5. Unable to read English.
  6. 6. Currently receiving trauma-focused group or individual psychotherapy treatment. (Previous psychotherapy, current pharmacotherapy, peer support groups, or maintenance therapy groups or individual therapy, defined as therapeutic services that have been ongoing for at least three months and are not trauma-focused, is acceptable).
  7. 7. Concurrently enrolled in another research protocol involving a mental health intervention during this study.
  8. 8. Has had previous Warrior Renew treatment.

Contacts and Locations

Principal Investigator

Amanda E Wood, PhD
PRINCIPAL_INVESTIGATOR
VA Puget Sound Health Care System

Study Locations (Sites)

VA Portland Health Care System
Portland, Oregon, 97239
United States
VA Puget Sound Health Care System
Seattle, Washington, 98105
United States

Collaborators and Investigators

Sponsor: Seattle Institute for Biomedical and Clinical Research

  • Amanda E Wood, PhD, PRINCIPAL_INVESTIGATOR, VA Puget Sound Health Care System

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-07-17
Study Completion Date2026-10-30

Study Record Updates

Study Start Date2023-07-17
Study Completion Date2026-10-30

Terms related to this study

Keywords Provided by Researchers

  • group therapy
  • military sexual trauma
  • randomized clinical trial
  • PTSD
  • MST

Additional Relevant MeSH Terms

  • Military Sexual Trauma (MST)
  • Post Traumatic Stress Disorder