Evaluating the health impact of caring for women victims of violence
Assessing 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 or Traditional Health Centres: a Prospective, Quasi-experimental, Multicentre, National Study.
This study looks at how caring for women who have experienced domestic and sexual violence affects their mental and physical health.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 360 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Centre Hospitalier Universitaire Dijon Academic / other |
| Locations | 1 site (Dijon) |
| Trial ID | NCT06226818 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the mental and physical health outcomes of women who are victims of domestic and sexual violence. It utilizes a coordinated multidisciplinary approach in women's centers or traditional health centers, focusing on the specific needs of these women. Participants will complete various scales and questionnaires to evaluate their experiences and health status. The study seeks to identify effective strategies for addressing the complex trauma associated with gender-based violence.
Who should consider this trial
Good fit: Ideal candidates for this study are adult women aged 18 and older who have experienced domestic or sexual violence and are consulting at one of the study centers.
Not a fit: Patients who are not affiliated with the national health insurance system or are under legal protection may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved health outcomes and support services for women affected by violence.
How similar studies have performed: Other studies have shown success in addressing the health impacts of gender-based violence using similar multidisciplinary approaches.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Dijon
- Chu Dijon Bourgogne — Dijon, France (Recruiting)
Study contacts
- Study coordinator: Marc DOMMERGUES
- Email: marc.dommergues@gmail.com
- Phone: 01 42 17 77 01
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.