Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06906302

RISE Versus Advocacy-based Enhanced Care as Usual for Patients Experiencing IPV

Led by Boston University · Updated on 2025-10-14

172

Participants Needed

3

Research Sites

224 weeks

Total Duration

On this page

Sponsors

B

Boston University

Lead Sponsor

V

VA Boston Healthcare System

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to improve treatment for Veterans Health Administration (VHA) patients who experience intimate partner violence (IPV). This study will evaluate two brief counseling interventions for VHA patients who have experienced IPV in the past 12 months: Recovering from IPV through Strength and Empowerment (RISE) and advocacy-based Enhanced Care as Usual (ECAU). The RISE intervention includes up to 8 sessions and includes specific topic areas (e.g., social support, health effects, resources). The other intervention, ECAU, includes a single session that includes supportive education about IPV and health effects, discussion of ways to increase safety, and information about resources. This study will test which approach is better for improving self-efficacy and other aspects of health. Participants will answer surveys about their self-efficacy and other health and safety indicators (e.g., mental health symptoms) right before receiving treatment, approximately 12 weeks later, and then every three months after that for one year. Participation in this research will last about 15 months.

CONDITIONS

Official Title

RISE Versus Advocacy-based Enhanced Care as Usual for Patients Experiencing IPV

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients receiving care at an enrolled Veterans Health Administration site or affiliated Community-Based Outpatient Clinic (CBOC)
  • Experienced physical, psychological, and/or sexual intimate partner violence in the past year as reported on an established IPV screening tool used in VHA
  • Able to provide informed consent and permission for intervention sessions to be recorded
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment
  • Suicide or homicide intent with a specific plan
  • Untreated or unstable symptoms of mania or psychosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 3 locations

1

VA Boston Healthcare System

Boston, Massachusetts, United States, 02130

Actively Recruiting

2

VA Minneapolis Healthcare System

Minneapolis, Minnesota, United States, 55417

Actively Recruiting

3

VA Philadelphia Healthcare System

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

Loading map...

Research Team

K

Katherine M Iverson, PhD

CONTACT

J

Julianne Brady

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

RISE Versus Advocacy-based Enhanced Care as Usual for Patients Experiencing IPV | DecenTrialz