NCT07818096

Brief Summary

AP-HP has recently opened five hospital-based care units dedicated to supporting women who are victims of violence. Referrals of women to these units rely mainly on healthcare professionals. Despite the recommendations of the French National Authority for Health (HAS), screening for Intimate Partner Violence (IPV) is not systematically performed. Moreover, although women tend to disclose experiences of violence preferentially to healthcare professionals, these professionals report feeling insufficiently trained to address this issue. In France, only one national survey assessing knowledge and screening capacities regarding domestic violence has been conducted, and it was limited to midwives. No study has evaluated screening practices and the ability to manage women experiencing IPV. One questionnaire is available: the PREMIS questionnaire (Physician Readiness to Manage Intimate Partner Violence Survey). This self-administered questionnaire includes 67 items and was developed and validated in a population of healthcare professionals in the United States. It demonstrated good internal consistency, with a Cronbach's alpha coefficient greater than 0.65 for all validated subscales. Its external validity was also tested by comparing questionnaire responses with a field-based observational survey of professional practices, showing good correlation. Stability of responses over time (12 months) was also demonstrated. The questionnaire is able to discriminate between respondents who have received training and those who have not, with a positive correlation between knowledge acquired through experience and the number of hours of personal training. To our knowledge, it is the only validated tool to assess healthcare professionals' preparedness to screen for and manage intimate partner violence. Its French transcultural adaptation was scientifically validated in 2021.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
11mo left

Started Sep 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress9%
Sep 2026Sep 2027

First Submitted

Initial submission to the registry

February 26, 2026

Completed
6 months until next milestone

Study Start

First participant enrolled

September 1, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

September 14, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

September 14, 2026

Status Verified

August 1, 2026

Enrollment Period

6 months

First QC Date

February 26, 2026

Last Update Submit

September 7, 2026

Conditions

Keywords

Intimate Partner ViolencePerinatal PeriodHealthcare ProfessionalsPREMIS Questionnaire

Outcome Measures

Primary Outcomes (1)

  • Conducting routine screening by healthcare professionals.

    Based on the responses to the questionnaires, determine the number of healthcare professionals at the APHP who screen pregnant women for domestic violence and the potential impact on this practice of having a specialized care unit for women who are victims of domestic violence.

    Day 1

Secondary Outcomes (3)

  • Ability of Healthcare Professionals to provide care to women who Are victims of domestic violence during the perinatal period

    Day 1

  • Analysis of Healthcare Professionals' Capacity to Care for Women Who Are Victims of Domestic Violence During the Perinatal Period

    Day 1

  • Identification of professional practices that could be improved through targeted training.

    Day 1

Study Arms (1)

Healthcare professionals

Healthcare professionals involved in perinatal care at AP-HP, including midwives, obstetricians, nurses, and other staff who may screen for and manage women experiencing intimate partner violence. Participants complete the PREMIS questionnaire to assess their readiness to identify and respond to IPV during the perinatal period.

Other: PREMIS Questionnaire

Interventions

Participants, consisting of perinatal healthcare professionals (midwives, obstetricians, nurses, and related staff) at AP-HP, will complete the PREMIS (Physician Readiness to Manage Intimate Partner Violence Survey) self-administered questionnaire. The questionnaire evaluates their preparedness to screen for, identify, and manage women experiencing intimate partner violence during the perinatal period.

Healthcare professionals

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Licensed perinatal healthcare professionals (midwives, nurses, psychologists, physicians, and residents in obstetrics/gynecology, pediatrics, general practice, or psychiatry) currently working in a maternity unit within AP-HP.

You may qualify if:

  • Licensed perinatal healthcare professionals, including midwives, physicians and residents in obstetrics/gynecology, pediatrics, general practice, psychiatry, psychologists, nurses, and pediatric nurses.
  • Currently working in a maternity unit at AP-HP.
  • Actively involved in clinical care.
  • Willing to participate in the online questionnaire.

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Maison des femmes - Hôtel Dieu

Paris, Île-de-France Region, 75004, France

Location

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 26, 2026

First Posted

September 14, 2026

Study Start

September 1, 2026

Primary Completion (Estimated)

March 1, 2027

Study Completion (Estimated)

September 1, 2027

Last Updated

September 14, 2026

Record last verified: 2026-08

Locations