Epidemiology of French Sexual Offenders. A Cross-sectional Study
ARAVS
Epidemiology of Sexual Offenders. A Cross-sectional Study of Auvergne-Rhône-Alpes Referral Platforms
1 other identifier
observational
400
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2024
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 10, 2024
CompletedFirst Submitted
Initial submission to the registry
June 10, 2024
CompletedFirst Posted
Study publicly available on registry
July 12, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2027
July 17, 2025
July 1, 2025
3.1 years
June 10, 2024
July 16, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Risk of re-offending and associated factors of the participant
Sexual offender recidivism risk will be assessed using Static99 scale. The Static-99 (Hanson \& Thornton, 2000) is the most commonly used actuarial risk tool for estimating sexual offender recidivism risk.The risk assessment instrument Static-99R consists of ten items, where all but items 1 and 5 are dichotomous, resulting in 0 or 1 point being added to the total score. The total score, between -3 and 12, results in one out of five recommended risk levels: level I - very low risk (scores of -3 to -2), level II - below average risk (scores of -1 to 0), level III - average risk (scores of 1 to 3), level IVa - above average risk (scores of 4 to 5), and level IVb - well above average risk (scores of 6+).
From May 2024 to May 2027
Secondary Outcomes (8)
Impulsivity of the participant
From May 2024 to May 2027 (cross-sectional study)
Cognition of the participant
From May 2024 to May 2027 (cross-sectional study)
Emotional status of the participant
From May 2024 to May 2027 (cross-sectional study)
Diagnosis of the participant
From May 2024 to May 2027 (cross-sectional study)
Cognitive distorsions of the participant
From May 2024 to May 2027 ((cross-sectional study)
- +3 more secondary outcomes
Interventions
Eligibility Criteria
All sexual offenders who are part of the PFR and meet the inclusion criteria will be invited to participate in this study.
You may qualify if:
- 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.
You may not qualify if:
- Patient refusal to participate in the study.
- Patients with physical or mental incapacity to complete the questionnaires.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CRIAVS - Centre Hospitalier Le Vinatier
Bron, 69678, France
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 10, 2024
First Posted
July 12, 2024
Study Start
May 10, 2024
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
September 1, 2027
Last Updated
July 17, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share