search
Back to results

Enhancing Mental and Physical Health of Women Veterans (EMPOWER)

Primary Purpose

Cardiovascular Diseases, Overweight, Obesity

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EBQI
REP
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Cardiovascular Diseases focused on measuring Cardiovascular diseases, Overweight, Obesity, Smoking, Hypertension, Cholesterol, Diabetes Mellitus, Prediabetic State, Pregnancy, Depression, Postpartum, Depression, Women, Veterans, Primary Health Care, Mental Health, Patient Participation, Patient Satisfaction, Patient Preference, Physicians, Primary Care, Physicians, Women, Health Behavior, Quality Improvement, Prevention, Heart Disease Risk Factors

Eligibility Criteria

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

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

Sites / Locations

  • VA Greater Los Angeles Healthcare System, West Los Angeles, CARecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

REP

EBQI

Arm Description

Replicating Effective Practices (REP) is a lower-intensity implementation strategy with explicit process framework for local tailoring

Evidence-Based Quality Improvement (EBQI) is a higher-intensity implementation strategy that entails external facilitation and formal training in quality improvement.

Outcomes

Primary Outcome Measures

Access to virtual care for preventive services
Proportion of eligible women Veterans who enroll in virtual DPP, TLC, or ROSE at each site
Engagement in virtual care for preventive services
Proportion of eligible women Veterans who attend 1 or more virtual DPP, TLC, or ROSE sessions at each site

Secondary Outcome Measures

Participation and engagement: DPP
average # of sessions attended by women Veterans who enrolled in DPP at each site
Participation and engagement: DPP
proportion who completed >9 and >16 sessions among women Veterans who enrolled in DPP at each site
Participation and engagement: DPP
% weight change among women Veterans who enrolled in DPP at each site
Participation and engagement: TLC
average # of TLC sessions completed among women Veterans who enrolled in TLC at each site
Participation and engagement: TLC
% with health behavioral goal among women Veterans who enrolled in TLC at each site
Participation and engagement: TLC
% with behavioral change (physical activity, diet: fruit, vegetable and sugary beverage intake, stress and coping, and weight) at each site
Participation and engagement: ROSE
average # of ROSE sessions completed at each site

Full Information

First Posted
September 9, 2021
Last Updated
August 16, 2023
Sponsor
VA Office of Research and Development
search

1. Study Identification

Unique Protocol Identification Number
NCT05050266
Brief Title
Enhancing Mental and Physical Health of Women Veterans
Acronym
EMPOWER
Official Title
Enhancing Mental and Physical Health of Women Through Engagement and Retention (EMPOWER) QUERI 2.0 (QUE 20-028)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 21, 2021 (Actual)
Primary Completion Date
September 30, 2025 (Anticipated)
Study Completion Date
September 30, 2025 (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
No

5. Study Description

Brief Summary
Women Veterans are the fastest growing segment of VA users. This dramatic growth has created challenges for VA to ensure that appropriate services are available to meet women Veterans' needs, and that they will want and be able to use those services. The EMPOWER QUERI 2.0 Program is a cluster randomized type 3 hybrid implementation-effectiveness trial testing two strategies designed to support implementation and sustainment of evidence-based practices for women Veterans in up to 20 VA facilities from 4 regions.
Detailed Description
Women Veterans are the fastest-growing segment of users in the Veterans Health Administration (VA). Their numbers are projected to increase by 73%, from 9.3% to 16.4%, between 2015 and 2043. Despite VA investment in improving care for women Veterans, gender disparities persist in cardiovascular (CV) and diabetes risk factor control. Also, the rate of perinatal depression among women Veterans is higher than that among civilian women, which is of particular concern given the association between perinatal depression and suicidality. Barriers to care for women Veterans include distance to VA care, rurality, competing work and caregiving responsibilities, comorbid mental health issues, and harassment on VA grounds. Improvements are still needed to increase women Veterans' access to and engagement in convenient, safe, evidence-based, patient-centered care that achieves the VA "lane of effort" of Veterans' "lifelong health, well-being, and resilience." Since its inception in 2015, the Enhancing Mental and Physical health of Women through Engagement and Retention (EMPOWER) QUERI 1.0 team has focused on implementing gender-tailored care models for women Veteran patients. In EMPOWER 1.0 studies, women expressed preferences for gender-specific (women only) care and for virtual care options. Therefore, the EMPOWER 2.0 Impact Goal is to expand access to virtual, evidence-based, preventive lifestyle and mental health services for women Veterans with high-priority health conditions in rural and urban-isolation areas. This cluster randomized type 3 hybrid implementation-effectiveness trial will randomize up to 20 VA sites to one of two implementation strategies, the Replicating Effective Practices (REP) or Evidence-Based Quality Improvement (EBQI), to support implementation and sustainment of evidence-based practices (EBPs). The EBPs focus on preventive lifestyle and mental health care for women Veterans across VA facilities, several of which are rural, low-performing in women's health care, and/or lead sites for high reliability organization. The study team will conduct a mixed methods implementation evaluation to compare the effectiveness of REP and EBQI in terms of: (a) improved access to and rates of engagement in virtual preventive lifestyle and mental health services and improved VA performance metrics for virtual and telehealth care delivery and related clinical outcomes for women Veterans; (b) progression along the Stages of Implementation Completion; (c) adaptation, sense-making, and experiences of EBP implementation among multilevel stakeholders; and (d) cost and return on investment. On 8/15/23, as part of our 12 month registration update we are correcting the primary outcomes to accurately reflect the randomized trial and analyses design. The cluster randomized trial will evaluate the effectiveness of two implementation strategies (REP and EBQI) in implementing evidence-based practices (EBPs) for preventive services. Although we are implementing three evidence-based practices (DPP, TLC and ROSE), the EBPs are combined for each of the trial's two primary outcomes (access and engagement).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Overweight, Obesity, Smoking, Hypertension, Cholesterol, Diabetes Mellitus, Prediabetic State, Pregnancy, Depression, Postpartum, Prevention, Implementation Science, Quality Improvement, Virtual Care
Keywords
Cardiovascular diseases, Overweight, Obesity, Smoking, Hypertension, Cholesterol, Diabetes Mellitus, Prediabetic State, Pregnancy, Depression, Postpartum, Depression, Women, Veterans, Primary Health Care, Mental Health, Patient Participation, Patient Satisfaction, Patient Preference, Physicians, Primary Care, Physicians, Women, Health Behavior, Quality Improvement, Prevention, Heart Disease Risk Factors

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster randomized type 3 hybrid implementation-effectiveness trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
REP
Arm Type
Active Comparator
Arm Description
Replicating Effective Practices (REP) is a lower-intensity implementation strategy with explicit process framework for local tailoring
Arm Title
EBQI
Arm Type
Experimental
Arm Description
Evidence-Based Quality Improvement (EBQI) is a higher-intensity implementation strategy that entails external facilitation and formal training in quality improvement.
Intervention Type
Behavioral
Intervention Name(s)
EBQI
Intervention Description
EBQI is a systematic quality improvement method for engaging frontline practices in improvement that introduces "best science" and evidence in the service of operational goals. EBQI has been tested in several VA implementation trials. Sites randomized to EBQI will meet monthly with the implementation support team (i.e., high-intensity).
Intervention Type
Behavioral
Intervention Name(s)
REP
Intervention Description
The REP framework consists of 4 phases: pre-conditions, pre-implementation, implementation and maintenance/evolution. REP has a strong evidence-base and application in VHA health services research in promoting uptake of EBPs. Sites randomized to REP will meet quarterly with the implementation support team (i.e., low-intensity).
Primary Outcome Measure Information:
Title
Access to virtual care for preventive services
Description
Proportion of eligible women Veterans who enroll in virtual DPP, TLC, or ROSE at each site
Time Frame
12 months
Title
Engagement in virtual care for preventive services
Description
Proportion of eligible women Veterans who attend 1 or more virtual DPP, TLC, or ROSE sessions at each site
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Participation and engagement: DPP
Description
average # of sessions attended by women Veterans who enrolled in DPP at each site
Time Frame
6 and 12 months
Title
Participation and engagement: DPP
Description
proportion who completed >9 and >16 sessions among women Veterans who enrolled in DPP at each site
Time Frame
6 and 12 months
Title
Participation and engagement: DPP
Description
% weight change among women Veterans who enrolled in DPP at each site
Time Frame
6 and 12 months
Title
Participation and engagement: TLC
Description
average # of TLC sessions completed among women Veterans who enrolled in TLC at each site
Time Frame
6 months
Title
Participation and engagement: TLC
Description
% with health behavioral goal among women Veterans who enrolled in TLC at each site
Time Frame
6 months
Title
Participation and engagement: TLC
Description
% with behavioral change (physical activity, diet: fruit, vegetable and sugary beverage intake, stress and coping, and weight) at each site
Time Frame
6 months
Title
Participation and engagement: ROSE
Description
average # of ROSE sessions completed at each site
Time Frame
6 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alison B Hamilton, PhD MPH
Phone
(310) 478-3711
Ext
44157
Email
Alison.Hamilton@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Bevanne A Bean-Mayberry, MD MHS
Phone
(818) 891-7711
Ext
36009
Email
bevanne.bean-mayberry@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alison B Hamilton, PhD MPH
Organizational Affiliation
VA Greater Los Angeles Healthcare System, West Los Angeles, CA
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Greater Los Angeles Healthcare System, West Los Angeles, CA
City
West Los Angeles
State/Province
California
ZIP/Postal Code
90073-1003
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alison B Hamilton, PhD MPH
Phone
310-478-3711
Ext
44157
Email
Alison.Hamilton@va.gov
First Name & Middle Initial & Last Name & Degree
Ismelda A Canelo, MPA
Phone
(818) 891-7711
Ext
36069
Email
Ismelda.Canelo@va.gov
First Name & Middle Initial & Last Name & Degree
Alison B Hamilton, PhD MPH
First Name & Middle Initial & Last Name & Degree
Bevanne A Bean-Mayberry, MD MHS
First Name & Middle Initial & Last Name & Degree
Erin P Finley, PhD MPH
First Name & Middle Initial & Last Name & Degree
Tannaz Moin, MD MBA MSHS

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data sets underlying all publications resulting from the proposed research will not be shared outside VA, except as required under the Freedom of Information Act (FOIA), because VHA policy would prohibit re-disclosure.
Links:
URL
https://www.queri.research.va.gov/centers/EMPOWER.pdf
Description
project executive summary

Learn more about this trial

Enhancing Mental and Physical Health of Women Veterans

We'll reach out to this number within 24 hrs