Violence, Domestic Clinical Trial
Official title:
The IPV Provider Network: Engaging the Health Care Provider Response to Interpersonal Violence Against Women
Verified date | January 2020 |
Source | Johns Hopkins University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Violence against women is a major public health threat that carries significant consequences
for women's health. Moreover, women experiencing intimate partner violence (IPV) and sexual
assault (SA) are more likely than non-abused women to seek certain forms of health services,
such as for sexually transmitted infections, chronic pain and illnesses, depression and/or
pregnancy-related concerns. As a result, the health sector is an ideal setting to identify
and support survivors. The U.S. Institute of Medicine has identified the health care system,
including the public health infrastructure, as key for identification of and support for
survivors of violence, as well as for violence prevention. While some evidence-based models
exist, no current national consensus has been reached on scalable best practices in screening
and brief counseling for IPV/SA.
This multi-level intervention includes integrating into the clinic setting IPV/SA screening,
universal education, trauma informed counseling, warm referrals (e.g. provider/staff contact
advocacy program with survivor) to local IPV/SA advocacy agencies, and access to the
evidence-based myPlan safety decision aid app. The evaluation, using a cluster randomized
trial design, will measure longitudinal outcomes (over 6 months) of patient self-efficacy,
health and safety outcomes, as well as participant and provider perceptions of the
intervention and clinic level changes in primary and reproductive health clinics in four
states (Arizona, Massachusetts, Pennsylvania and West Virginia) to achieve the following
aims:
Aim 1. Evaluate the effectiveness of an evidence-based screening, universal education and
trauma-informed counseling with tailored safety action plan and referrals to partner IPV/SA
programs compared to standard practice, on survivor health and safety outcomes over a
cumulative period of six months.
Aim 2. Examine longitudinal changes in clinic-level screening, universal education, trauma
informed counseling, safety action plans and referrals to on-site and/or partner IPV/SA
programs and improved standards for documentation through the electronic health record (EHR)
and continuous quality measurement and reporting.
Status | Completed |
Enrollment | 6272 |
Est. completion date | April 25, 2019 |
Est. primary completion date | April 25, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 59 Years |
Eligibility |
Inclusion Criteria: - Seeking healthcare at one of 14 partner clinics - Ability to complete a survey on a device (computer/tablet/smartphone in English or Spanish) - Access to safe device (as defined above) if doing surveys online - Has a safe email address or safe phone number - Is not acutely ill Exclusion Criteria: - Male - Not seeking healthcare at one of 9 partner clinics - Younger than 18 years of age - Older than 59 years of age - Cannot read/speak English or Spanish - No access to safe device if doing surveys online - Does not have a safe email address or safe phone number - Acutely ill |
Country | Name | City | State |
---|---|---|---|
United States | Partners Health Care Brigham and Women's Hospital | Boston | Massachusetts |
United States | Women's Health Center | Charleston | West Virginia |
United States | North County HealthCare | Kingman | Arizona |
United States | North Country HealthCare | Lake Havasu City | Arizona |
United States | Valley Health | Mill Creek | West Virginia |
United States | Magee-Women's Hospital of UPMC | Pittsburgh | Pennsylvania |
United States | Greenbrier Co. Health Dept | Ronceverte | West Virginia |
United States | FamilyCare Health Center | Scott Depot | West Virginia |
United States | North Country HealthCare | Williams | Arizona |
Lead Sponsor | Collaborator |
---|---|
Johns Hopkins University | Futures Without Violence, Office of Research on Women's Health (ORWH), University of Pittsburgh |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in use of safety behaviors | Measured by percent of safety behaviors the woman has tried and found helpful on the Safety Behaviors Checklist. The checklist was adapted from Sullivan and colleagues and Parker and colleagues. Includes use of community resources and safety steps (e.g. asked for help, hidden emergency money) and use of formal services (e.g., women's shelter, protection order, mental health services). | 6 months | |
Primary | Change in Self-Efficacy to Use Harm Reduction Strategies | Measure adapted from Tancredi et al and Hibbard et al, assesses confidence to seek help for abuse, if needed, from a health care provider. | 6 months | |
Primary | Provider Behavior | Clinic level measure. Provider Behavior at Visit Survey items administered after the provider visit to assess the provider's adherence to universal education intervention, i.e. discussing healthy and unhealthy relationships during the visit, and referring to resources. | Baseline | |
Secondary | Change in decisional conflict | We have adapted questions from validated subscales of the Decisional Conflict Scale as a measure of decision process. Measures whether the intervention helps a woman to understand the advantages and disadvantages of safety planning options and to know her values related to them. The Decisional Conflict Scale discriminates between people who make decisions and those who delay making decisions. | 6 months | |
Secondary | Change in Readiness to Take Action | 0-10 scale of readiness to make changes to relationship for safety | 6 months |
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