Impact of an internet safety decision aid on health and safety of IPV survivors: Findings from the IRIS randomized controlled trial

Glass, Nancy

Friday, March 20, 2015: 1:50 PM-3:10 PM

Room 8/9 (Renaissance Washington, DC Downtown Hotel)

Speaker:
Nancy Glass, PhD, MPH, RN, FAAN, Johns Hopkins University

Authors:
Karen Eden, Phd, Oregon Health & Science University
Nancy A. Perrin, PhD, Kaiser Permanente
Jill Messing, PhD, MSW, Arizona State University
Tina L. Bloom, PhD, MPH, RN, University of Missouri
Jacquelyn Campbell, PhD, RN, FAAN, Johns Hopkins University
Andrea Gielen, ScD, Johns Hopkins Center for Injury Research and Policy
Amber Clough, MSW, Johns Hopkins University

Presentation Format:
Scientific Program Report

Learning Objectives:

Describe the health and safety outcomes of IPV survivors enrolled in the IRIS study.
Discuss the implications of the IRIS study findings on practice and research with IPV survivors.

Description:
The overall purpose of the IRIS study was to test the effectiveness of a safety decision aid compared with usual safety planning (control) delivered through a secure website, using a multi-state randomized controlled trial design. The study outcomes include reduced decisional conflict about safety, increased safety behaviors, reduced repeat IPV and improved mental health for survivors.