Recruiting soon

EMPOWERTrauma-Informed Care, CBT-SM and Women's MOVE for Improved Health and Well-being of Women Veterans

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

EBQI Booster (EBQI/B)

+ EBQI Booster + External Facilitation (EBQI/B+EF)

Behavioral
Who is being recruted

Trauma and Stressor Related Disorders+24

+ Treatment Adherence and Compliance

+ Behavior

See all eligibility criteria
How is the trial designed

Services Research Study

Interventional
Study Start: October 2026
See protocol details

Summary

Principal SponsorVA Office of Research and Development
Study ContactAlison B Hamilton, PhD MPHMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 2026

Actual date on which the first participant was enrolled.

The EMPOWER 3.0 study focuses on improving the mental and physical health of women veterans, specifically those in midlife. This group often faces unique health challenges such as menopause, obesity, and an increased risk of chronic diseases. The study also aims to address the high burden of trauma and physical and mental health issues that women veterans often experience, which can negatively impact their trust in healthcare providers. The ultimate goal is to enhance the quality of care, trust, well-being, and engagement of women veterans in VA care by offering trauma-informed, evidence-based interventions that meet their high-priority health needs in midlife. The study will implement three evidence-based practices (EBPs): Trauma-Informed Care (TIC), Cognitive Behavioral Therapy for Symptoms of Menopause (CBT-SM), and Women's MOVE!. TIC aims to support trust and safety in primary care interactions. CBT-SM provides group-based therapy, education, and personalized referrals for women across the menopausal transition. Women's MOVE! offers lifestyle and weight management support to enhance women veterans' health and well-being. The study will evaluate the effectiveness of these EBPs in terms of improved access to trauma-informed care for women veterans, implementation strategy fidelity, speed of implementation, and sustainment, recipient perspectives on and experiences of EBP implementation, and costs of implementation and business case analysis to support sustained EBP use.

Official TitleEnhancing Mental and Physical Health of Women Through Engagement and Retention (EMPOWER) 3.0 (QUE 25-015)
NCT07356479
Principal SponsorVA Office of Research and Development
Study ContactAlison B Hamilton, PhD MPHMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

18 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Services Research Study

These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Trauma and Stressor Related DisordersTreatment Adherence and ComplianceBehaviorMental DisordersBody WeightCardiovascular DiseasesDiabetes MellitusEndocrine System DiseasesHypertensionMetabolic DiseasesNutrition DisordersNutritional and Metabolic DiseasesObesityPatient Acceptance of Health CarePatient ParticipationPrediabetic StateSigns and SymptomsStress Disorders, Post-TraumaticPathological Conditions, Signs and SymptomsVascular DiseasesHealth BehaviorPatient SatisfactionStress Disorders, TraumaticOvernutritionGlucose Metabolism DisordersOverweightPatient Preference

Criteria

Inclusion Criteria: * This study is recruiting VA sites - not individual patients. * Prior to randomization, the study team will work with sites to ensure they have met the preconditions necessary to enroll in the study, which includes VISN, regional and/or facility level leadership support for participation. Exclusion Criteria: * N/A

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator
A two-hour EBQI Booster delivered virtually to site-identified QI champions and local implementation teams for each EBP reviewing key EBQI components and providing examples grounded in the EBPs.

Group II

Experimental
A two-hour EBQI Booster delivered virtually to site-identified QI champions and local implementation teams for each EBP reviewing key EBQI components and providing examples grounded in the EBPs, plus 12 months of external facilitation.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

VA Greater Los Angeles Healthcare System, West Los Angeles, CA

West Los Angeles, United StatesOpen VA Greater Los Angeles Healthcare System, West Los Angeles, CA in Google Maps
Recruiting soonOne Study Center