RecruitingNot ApplicableNCT04953273

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


Sponsor

University Hospital, Lille

Enrollment

756 participants

Start Date

Jul 6, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Sex: FEMALEMin Age: 18 Years

Inclusion Criteria6

  • Women
  • 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 Criteria3

  • Do no consent to participate to the study
  • Intrafamilial or intimate partner violence
  • Do not speak french

Interventions

OTHERVigitrauma

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

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NCT04953273


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