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Confidential IPV Screening Tool

EHR-based Screening and Intervention for Intimate Partner Violence

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06284148
Enrollment
19655
Registered
2024-02-28
Start date
2010-10-06
Completion date
2023-07-31
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Violence, Domestic

Keywords

Intimate Partner Violence

Brief summary

Intimate partner violence (IPV) against women in the US is a serious public health problem and a human rights issue. Our research team has developed confidential screening tools using exam-room computer for intimate partner violence to be used in primary care.

Detailed description

The objective of this study was to develop and evaluate an integrated suite of electronic health record (EHR) tools that automates best practices from Northern California Kaiser Permanente for screening and intervention for IPV identified within clinical settings. The goal of the intervention goes beyond mere screening of patients for IPV and includes tools for assessment of IPV risk, for documentation of IPV care, and support for a warm hand-off during the primary care visit to a national IPV hotline resource. Importantly, the study includes work to keep notes documenting IPV and billing for IPV care confidential, segmenting this care in a secure segment of the electronic health record.

Interventions

confidential screening using exam computer

OTHERAssessment and referral

confidential assessment and referral of high-risk patients using decision-support templates

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
SCREENING
Masking
NONE

Intervention model description

This is a stepped wedge cluster randomized trial which has 3 sequences starting intervention in randomized order.

Eligibility

Sex/Gender
ALL
Age
18 Years to 49 Years
Healthy volunteers
No

Inclusion criteria

* Being an Medical University of South Carolina patient at primary care clinics (family medicine) * Women 18-49 years of age inclusive * Reported yes to wanting to be contacted for a follow-up research study * English-speaking

Exclusion criteria

* No

Design outcomes

Primary

MeasureTime frameDescription
IPV positive (Yes/No)29 monthsDepending on patient's answers to screening questions, they are flagged as either IPV positive or negative
Screening completed (Yes/No)29 monthsWhether the assigned screening was completed during patient visit

Secondary

MeasureTime frameDescription
Severity of risk29 monthsusing Danger 5 risk assessment, ranging from 0 to 5
Physician compliance with IPV management tools29 monthsMeasured as the rate of completion of follow-up decision templates, and the rate of referrals for post-visit counseling to a national hotline (a share from screened positive patients

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026