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Clinical Trials in France / NCT06499051
Recruiting Observational

Epidemiology of French Sexual Offenders. A Cross-sectional Study

NCT06499051 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-05-10
Last updated
2025-07-17

Condition(s) studied

Psychiatric Disorder

Investigational drug(s) / intervention(s)

cognition, impulsivity, emotional regulation, sexuality, diagnosis, sexual violence, motivation, self-esteem, social desirability, and defense mechanisms

cognition, impulsivity, emotional regulation, sexuality, diagnosis, sexual violence, motivation, self-esteem, social desirability, and defense mechanisms: self-administered questionnaires

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CRIAVS - Centre Hospitalier Le Vinatier Bron France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06499051 on ClinicalTrials.gov ↗ ← All trials in France