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NCT00164567 · ClinicalTrials.gov registry record · Phase 2
Intimate Partner Violence (IPV)Screening in Health Care Clinics in Rural South Carolina
A Phase 2 study, sponsored by Centers for Disease Control and Prevention.
- Completed
- Registry status
- Phase 2
- Development phase
- 1,200
- Enrollment target
NCT00164567 is a Phase 2 study that has completed, run by Centers for Disease Control and Prevention. The registered enrollment target is 1,200 participants.
The verdict
NCT00164567, a Phase 2 study, has completed, sponsored by Centers for Disease Control and Prevention.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 1,200 participants
- Enrollment target
Study 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 women's 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 intervention(s) 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) women's help-seeking behaviors, risk of poor mental and physical health, and (d) women's risk of subsequent IPV victimization. To evaluate these outcomes, we will survey clinicians and prospectively follow a group of consenting IPV+ women (N=300 in each int
Interventions
- BEHAVIORAL Onsite IPV specialist
- BEHAVIORAL Empowerment focused intervention
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,200 participants |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00164567
The ClinicalTrials.gov registry entry for NCT00164567 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 1,200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Centers for Disease Control and Prevention, which has 139 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Onsite IPV specialist is the first listed.
NCT00164567 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00164567 about?
NCT00164567 is a clinical study titled "Intimate Partner Violence (IPV)Screening in Health Care Clinics in Rural South Carolina". 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 inc...
What is the current status of trial NCT00164567?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 1,200 participants.
What interventions are being tested in trial NCT00164567?
The interventions under investigation include: Onsite IPV specialist (BEHAVIORAL), Empowerment focused intervention (BEHAVIORAL).
Who is sponsoring clinical trial NCT00164567?
This trial is sponsored by Centers for Disease Control and Prevention, which has 139 total clinical trials registered on ClinicalTrials.gov.
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