Actively Recruiting

Age: 18Years +
All Genders
NCT06499051

Epidemiology of French Sexual Offenders. A Cross-sectional Study

Led by Hôpital le Vinatier · Updated on 2025-07-17

400

Participants Needed

1

Research Sites

172 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Epidemiology of French Sexual Offenders. A Cross-sectional Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Under injunction of care for a sexual offense
  • Awaiting sentencing for a sexual offense
  • Currently under legal proceedings for a sexual offense
  • Under a legal obligation for care related to a sexual offense
  • Falling within the scope of an alternative to incarceration for a sexual offense
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study
  • Physical or mental incapacity to complete the questionnaires

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CRIAVS - Centre Hospitalier Le Vinatier

Bron, France, 69678

Actively Recruiting

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Research Team

S

Sabine Mouchet, Dr

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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