NCT06499051

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
16mo left

Started May 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress60%
May 2024Sep 2027

Study Start

First participant enrolled

May 10, 2024

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 10, 2024

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 12, 2024

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2027

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

July 17, 2025

Status Verified

July 1, 2025

Enrollment Period

3.1 years

First QC Date

June 10, 2024

Last Update Submit

July 16, 2025

Conditions

Keywords

sexual offensesepidemiology

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

Mental Disorders

Interventions

Sex

Intervention Hierarchy (Ancestors)

Reproductive Physiological PhenomenaReproductive and Urinary Physiological Phenomena

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

Locations