EMPOWERTrauma-Informed Care, CBT-SM and Women's MOVE for Improved Health and Well-being of Women Veterans
EBQI Booster (EBQI/B)
+ EBQI Booster + External Facilitation (EBQI/B+EF)
Trauma and Stressor Related Disorders+24
+ Treatment Adherence and Compliance
+ Behavior
Services Research Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.18 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
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.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
ExperimentalStudy 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
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