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OpenTrials
Completed

NCT Number: NCT07827534

Feasibility of Systematic Domestic Violence Screening Using WAST in the Villefranche/Saône Emergency Department.

This single-center observational study aims to assess the feasibility of systematically screening for intimate partner violence (IPV) against women in the emergency department of Hôpital Nord-Ouest de Villefranche-sur-Saône. The study utilizes the Woman Abuse Screening Tool (WAST), a self-administered questionnaire, to identify cases of IPV. The primary objective is to evaluate the feasibility and acceptability of implementing this systematic screening within an emergency setting. The study will measure feasibility through factors such as the implementation rate and adherence by healthcare staff, while acceptability will be assessed based on patient participation and response rates. By analyzing these criteria, the study seeks to determine whether IPV screening can be effectively integrated into routine emergency care. The findings are expected to provide insights into potential barriers and facilitators for screening implementation, contributing to improved detection and support strategies for women experiencing domestic violence.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Hopitaux Nord-Ouest

Gleizé, France, 69400

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female
  • Aged 18 years or older
  • Able to read and write French

Exclusion criteria

  • Refusal to participate in the study
  • Neurocognitive disorders, confusion, or psychotic disorders that preclude study participation
  • Severe uncorrected sensory impairment
  • Life-threatening emergency requiring immediate management in the resuscitation area

Treatment and study plan

Self-questionnaire

Other

Self-questionnaire completed in the waiting room of the emergency department, either on paper or online by scanning a QR-code

Primary outcomes

  1. Feasibility of systematic screening using WAST

    Time frame: At the time of outpatient consultation (Day 0)

    Assessed by the proportion of eligible women screened with WAST.

  2. Acceptability of WAST

    Time frame: At the time of outpatient consultation (Day 0)

    Assessed using an acceptability questionnaire completed by healthcare patient

Sponsors and collaborators

Lead sponsor

L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône

Other

Registry information

Official study title

Etude de faisabilité d'un dépistage systématique Des Violences Conjugales Envers Les Femmes Par l'Utilisation de l'Auto-questionnaire WAST (Woman Abuse Screening Tool) Dans le Service Des Urgences de l'hôpital Nord-Ouest de Villefranche/Saône.

Acronym: FdsVC-WAST-u

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Sep 18, 2026
Registry last updated
Sep 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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