NCT00257296.

Study name	Evaluation of an intimate partner violence screening‐intervention
Methods	Design: RCT Unit of randomisation: not reported
Participants	Healthcare provider: not reported Other: women aged 18 ‐ 45 years, seen at study sites for primary care Location/Setting: obstetrics‐gynaecology clinics or general medical care in internal medicine clinics in USA Sample size: n = 471 Number of withdrawals/dropouts: N/A Sex: N/A Mean age: N/A Inclusion criteria: women aged 18 ‐ 45 years attending primary care study sites during study periods, English‐speaking, able to separate from accompanying person(s) and willing to participate Exclusion criteria: too ill, unable to separate from accompanying person(s), unable to speak English, refuses to participate
Interventions	Intervention (n = not available): a computer‐based screening tool for IPV and provision of a multi‐faceted intervention based on the needs of the woman and the services she would like to use Control (n = not available): service as usual, including screening for IPV and providing enhanced usual care
Outcomes	Primary outcomes: not reported Secondary outcomes: not reported Timing of outcome assessment: baseline, 1 week, 1, 3, 6, 9 months postintervention
Starting date	22 November 2005
Contact information	Principal investigator: Louise‐Anne McNutt Address: University at Albany
Notes	Registered at:clinicaltrials.gov/ct2/show/NCT00257296 Comment: potentially suspended