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Recruiting NCT06499051

NCT06499051 Epidemiology of French Sexual Offenders. A Cross-sectional Study

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Clinical Trial Summary
NCT ID NCT06499051
Status Recruiting
Phase
Sponsor Hôpital le Vinatier
Condition Psychiatric Disorder
Study Type OBSERVATIONAL
Enrollment 400 participants
Start Date 2024-05-10
Primary Completion 2027-06-01

Trial Parameters

Condition Psychiatric Disorder
Sponsor Hôpital le Vinatier
Study Type OBSERVATIONAL
Phase N/A
Enrollment 400
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-05-10
Completion 2027-06-01
Interventions
cognition, impulsivity, emotional regulation, sexuality, diagnosis, sexual violence, motivation, self-esteem, social desirability, and defense mechanisms

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Brief Summary

The epidemiology of sexual offenders has been poorly studied in the literature. A retrospective and prospective study will allow for the examination of the clinical profile of sexual offense perpetrators, risk and recurrence factors, as well as psychiatric or medical treatment. Since 2015, the Auvergne-Rhône-Alpes region has 8 reference platforms for sexual offense perpetrators, offering personalized assessment according to criteria defined by the Regional Health Agency (ARS). After this assessment, a multidisciplinary meeting is organized to define a tailored care plan. This study, called ARAVS (Auvergne Rhone-Alpes Sexual Offenders), aims to conduct an epidemiological, clinical, and socio-demographic study of patients in these platforms.

Eligibility Criteria

All sexual offenders who are part of the PFR and meet the inclusion criteria will be invited to participate in this study. Inclusion criteria: * Adults (age ≥ 18 years). * Under injunction of care for a sexual offense. * Or Awaiting sentencing for a sexual offense. * Or Currently under legal proceedings for a sexual offense. * Or Under a legal obligation for care related to a sexual offense. * Or Falling within the scope of an alternative to incarceration for a sexual offense. Exclusion criteria: * Patient refusal to participate in the study. * Patients with physical or mental incapacity to complete the questionnaires.

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