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Study identifier: NCT04953273 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Case Management Algorithm for Women Victims of Violence

Condition: Post-Traumatic Stress Disorder · Violence-Related Symptom  ·  Sponsor: University Hospital, Lille

PhaseNA
Planned participants756
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Arnaud Leroy, MD  ·  +33 320444460  ·  arnaud.leroy@chru-lille.fr

Anne-Laure Demarty  ·  +33 320444145  ·  anne-laure.demarty@chru-lille.fr

Always discuss trial participation with your own doctor first.

Locations (8)

University Hospital, AmiensAmiens, FranceNot Yet Recruiting
General Hospital, Boulogne sur MerBoulogne-sur-Mer, FranceNot Yet Recruiting
University Hospital, CaenCaen, FranceNot Yet Recruiting
General Hospital, CreilCreil, FranceNot Yet Recruiting
University Hospital, LilleLille, FranceRecruiting
University Hospital, RouenRouen, FranceNot Yet Recruiting
General Hospital, Saint-QuentinSaint-Quentin, FranceNot Yet Recruiting
General Hospital, ValenciennesValenciennes, FranceNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT04953273