Viewing Study NCT00164567



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Study NCT ID: NCT00164567
Status: COMPLETED
Last Update Posted: 2009-10-23
First Post: 2005-09-12

Brief Title: Intimate Partner Violence IPVScreening in Health Care Clinics in Rural South Carolina
Sponsor: Centers for Disease Control and Prevention
Organization: Centers for Disease Control and Prevention

Study Overview

Official Title: IPV Screening in Health Care Clinics in Rural South Carolina
Status: COMPLETED
Status Verified Date: 2009-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to implement universal screening for intimate partner violence IPV and to test two clinic-based interventions for women who screen positive for current or recent IPV The study population will be implemented in Pee Dee region of the state of South Carolina and will include primarily low-income women who seek care at selected primary health care clinics in the region

In this study all women 18 and older receiving care at selected primary care clinics will be offered screening for IPV annually Clinicians will use a structured screening tool to assess physical sexual and psychological IPV in a current relationship IPV or IPV experienced by the woman in the past five years Recent IPV Clinics will be randomly assigned to implement a clinic-based intervention for women who screen positive for current or recent IPV Two interventions will be implemented using a factorial design In the Empowerment-Focused Patient Education Intervention clinicians will conduct a 7-session intervention focusing on the health and well-being of the woman and attempt to link womens IPV experience with their health In the IPV Services Intervention IPV Specialists who are trained advocates from the Pee Dee Coalition Against Domestic and Sexual Assault PDC will be based in the clinic to a counsel women about IPV including safety planning b provide linkages to PDC services and c link women to clinic-based support groups developed specifically for this project

We hypothesize the interventions will change a clinician screening referral and IPV documentation patterns b clinician IPV knowledge and perceived skills in working with women who have experienced IPV and their children c womens help-seeking behaviors risk of poor mental and physical health and d womens risk of subsequent IPV victimization To evaluate these outcomes we will survey clinicians and prospectively follow a group of consenting IPV women N300 in each intervention arm to assess changes in their help-seeking health behavior and status IPV experience over two-years of follow-up
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
US4CCU419014 None None None