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Recruiting NCT06226818

NCT06226818 Evaluation of the Impact on Mental and Physical Health of Caring for Women Who Are Victims of Sexual and Gender-based Violence, Using a Coordinated Multidisciplinary Approach in Women's Centres or Traditional Health Centres.

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Clinical Trial Summary
NCT ID NCT06226818
Status Recruiting
Phase
Sponsor Centre Hospitalier Universitaire Dijon
Condition Domestic and/or Sexual Violence
Study Type OBSERVATIONAL
Enrollment 360 participants
Start Date 2024-08-08
Primary Completion 2027-02

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
completion of scales and questionnaires

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 360 participants in total. It began in 2024-08-08 with a primary completion date of 2027-02.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Gender-based or sexual violence, or violence against women (VAW), is a global public health problem affecting around 30% of women over the age of 15, with significant consequences for physical and mental health, including depression and post-traumatic stress disorder (PTSD). In 2019, the French National Authority for Health (HAS) published recommendations in two parts, one for identifying women who are victims of domestic violence, and the other for dealing with a woman who has been exposed to such violence. But violence against women is not limited to the marital sphere. VAW can simply be detected in a consultation using a translated version of the Abuse Assessment Screen (AAS) questionnaire. Women who are victims of VAW have specific needs linked to the often repeated nature of the violence they experience, and the complex trauma that can ensue. They also tend to combine other risk factors for poor mental health, such as economic insecurity and social isolation. In France, dealing with the specific medical, psychosocial and legal needs of victims-survivors of VAW has come up against a number of obstacles, including a lack of dedicated care facilities, a lack of trained professionals and a lack of coordination between the various parties. Health professionals rarely receive the training they need to deal with VAW-related issues with confidence and professionalism, and often lack the resources to refer female victims to appropriate care. "La Maison des Femmes" (MdF) was set up in 2016 in Saint-Denis, located in a department where a quarter of the women who consult a family planning centre (FPC) has suffered from VAW. It is a hospital service specifically dedicated to the individualised, multidisciplinary care of victims-survivors of VAW, offering health, social and legal support within the same facility. The MdF comprises 4 units: a FPC, a violence management unit (involving doctors, midwives, psychologists, social workers, lawyers, police officers and support groups), a female genital mutilation management unit (surgeons and sexologists) and a 24/7 reception unit for victims of sexual violence. Several MdF-inspired care structures have been set up in France. The service provided by these facilities needs to be evaluated, particularly in terms of their ability to improve the physical and mental health, including post-traumatic stress, of women who have been victims of VAW.

Eligibility Criteria

Inclusion Criteria: * Women who have not objected to taking part in the trial * Adult women (≥18 years), * Victim of domestic and/or sexual violence, consulting at one of our study centres. Exposure to violence, whatever the initial reason for consultation, will be determined by a positive response to at least one question on the French version of the Abuse Assessment Screen, a standardised screening tool which has the advantage of not being limited to domestic violence. * Ability to understand the objectives of the study and to answer the questionnaires Exclusion Criteria: * Not affiliated to the national health insurance system * Person under legal protection (curatorship, guardianship) * Person under court order * Adult who is unable to express his/her non-opposition * Minor

Contact & Investigator

Central Contact

Marc DOMMERGUES

✉ marc.dommergues@gmail.com

📞 01 42 17 77 01

Frequently Asked Questions

Who can join the NCT06226818 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Domestic and/or Sexual Violence. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06226818 currently recruiting?

Yes, NCT06226818 is actively recruiting participants. Contact the research team at marc.dommergues@gmail.com for enrollment information.

Where is the NCT06226818 trial being conducted?

This trial is being conducted at Dijon, France.

Who is sponsoring the NCT06226818 clinical trial?

NCT06226818 is sponsored by Centre Hospitalier Universitaire Dijon. The trial plans to enroll 360 participants.

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