NCT03259646.

Study name	The IPV provider network: engaging the healthcare provider response to interpersonal violence against women
Methods	Design: cluster‐RCT Unit of randomisation: unclear
Participants	Healthcare provider: unclear Other: women aged 18 ‐ 59 years old seeking health care at a partner clinic Location/Setting: USA Sample size: 6272 Number of withdrawals/dropouts: N/A Sex: N/A Mean age: N/A Inclusion criteria: seeking healthcare at one of the partner clinics, able to complete an online survey on a safe device (e.g. tablet) in English or Spanish, has a safe email address or phone number and is not acutely ill Exclusion criteria: male, not seeking health care at partner clinics, < 18 years, > 59 years, cannot read or speak English or Spanish, no access to safe devices for completing online survey, no safe email or phone number, is acutely ill
Interventions	Intervention (n = not available): integration into the clinic setting IPV/sexual assault screening, universal education, trauma informed counselling, warm referrals (e.g. provider/staff contact advocacy programme with survivor) to local IPV/Sexual assault advocacy agencies, and access to the evidence‐based myPlan safety decision aid application Control (n = not available): standard clinical practice
Outcomes	Primary outcomes Women’s use of safety behaviours Readiness to take action Decisional conflict Self‐efficacy to use harm reduction strategies Provider's adherence to universal education intervention (i.e. discussing healthy and unhealthy relationships during the visit, and referring to resources) Secondary outcomes Decisional conflict Readiness to take action Timing of outcome assessment: unclear
Starting date	26 May 2017
Contact information	Email:nglass1@jhu.edu
Notes	Registered at:clinicaltrials.gov/ct2/show/NCT03259646