Loading clinical trials...
Loading clinical trials...
Effectiveness of a Case Management Algorithm on Clinical Outcome After Consultations Requested in a Clinical Forensic Medicine Unit by Female Victims of Violence
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.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
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
Start Date
July 6, 2021
Primary Completion Date
July 1, 2026
Completion Date
July 1, 2026
Last Updated
April 12, 2022
756
ESTIMATED participants
Vigitrauma
OTHER
Lead Sponsor
University Hospital, Lille
Collaborators
NCT07447089
NCT06516874
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions