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RECRUITINGINTERVENTIONAL

A Case Management Algorithm for Women Victims of Violence

Effectiveness of a Case Management Algorithm on Clinical Outcome After Consultations Requested in a Clinical Forensic Medicine Unit by Female Victims of Violence

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 Who Should NOT Join This Trial: - Do no consent to participate to the study - Intrafamilial or intimate partner violence - Do not speak french Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 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 Exclusion Criteria: * Do no consent to participate to the study * Intrafamilial or intimate partner violence * Do not speak french

Treatments Being Tested

OTHER

Vigitrauma

Case management algorithm using early phone contact

Locations (8)

University Hospital, Amiens
Amiens, France
General Hospital, Boulogne sur Mer
Boulogne-sur-Mer, France
University Hospital, Caen
Caen, France
General Hospital, Creil
Creil, France
University Hospital, Lille
Lille, France
University Hospital, Rouen
Rouen, France
General Hospital, Saint-Quentin
Saint-Quentin, France
General Hospital, Valenciennes
Valenciennes, France