A Case Management Algorithm for Women Victims of Violence

Recruiting N/A Interventional Study
Post-Traumatic Stress Disorder Violence-Related Symptom
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
756 (estimated)
Sponsor
University Hospital, Lille · Other
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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 fut…
Trial Locations
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Eligibility Criteria
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…
Contacts

Arnaud Leroy, MD

+33 320444460

arnaud.leroy@chru-lille.fr

CONTACT

Anne-Laure Demarty

+33 320444145

anne-laure.demarty@chru-lille.fr

CONTACT