A Case Management Algorithm for Women Victims of Violence
Recruiting now · Not applicable
Conditions studied: Post-Traumatic Stress Disorder, Violence-Related Symptom
In brief
A considerable body of research has demonstrated that women who are victims of interpersonal violence are at substantially elevated risk for the development of post-traumatic stress disorder (PTSD). In France, victims can request a medico-legal examination in a clinical forensic medicine unit. Although these units are also a place for initial psychological examination, women often don't attend future scheduled appointments. Decision-making algorithm using phone contact are effective in suicide prevention. Our aim is to assess the effectiveness of case management algorithm using early phone contact compared to a control group treated as usual on clinical outcome after consultation requested in a clinical forensic medicine unit by female victims of violence. Method: Prospective, multicenter, open-label, randomized controlled clinical trial, for women victims of violence. Victims randomized in VIGITRAUMA group will be contacted by phone at 3 weeks after the consultation in a clinical forensic medicine unit, and a second phone call can be done. If the subject is not contacted after the second phone call, he will receive a postcard. Control group will benefit from usual follow-up. All the subjects included will be then evaluated at 3 months, 6 months and 1 year during a phone call.
Key facts
- Study ID
- NCT04953273
- Run by
- University Hospital, Lille
- People needed
- 756
- Starts
- 2021-07-06
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2026-05-14
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women
- 18 years and older
- Consultation requested in a clinical forensic medicine unit after being victim of violence
- The person was exposed to: death, threatened death, actual or threatened serious injury, or actual or threatened sexual violence (PTSD criterion A - DSM -5)
- With social insurance
- Consent to participate to the study
You may not qualify if…
- Do no consent to participate to the study
- Intrafamilial or intimate partner violence
- Do not speak french
Where it is running
- University Hospital, Lille — Lille, France (enrolling)
- General Hospital, Boulogne sur Mer — Boulogne-sur-Mer, France
- University Hospital, Caen — Caen, France
- General Hospital, Creil — Creil, France
- University Hospital, Rouen — Rouen, France
- General Hospital, Saint-Quentin — Saint-Quentin, France
- University Hospital, Amiens — Amiens, France
- General Hospital, Valenciennes — Valenciennes, France
Full record on ClinicalTrials.gov
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