Characteristics of Genealogical Representations of Perpetrators of Sexual Violence. (CARG-AVS)

Apparent Characteristics of Genealogical Representations of Perpetrators of Sexual Violence.

Two French studies report that 25% of sexual abuse occurs in intrafamily sphere. To be victim of sexual abuse leads to cognitive troubles and redesign of psychological processes. Lot of studies report that offenders had been victims (30-97%). How psychological redesign is destroying genealogical representation and hinders the proper construction of family ties.

This study to study characteristics data about family, and how the patients see it, from medical records of a specific department for sexual offenders in University Hospital of Saint Etienne. Study is realized blind from criminal categories. Data are gathered with a standardized grid, to guarantee reproducibility of data collection.

Study Overview

Status

Completed

Conditions

Detailed Description

The CARG-AVS study does not involve any additional examinations or consultations compared to usual practice. It consists of collecting information from patients' medical records.

Study Type

Observational

Enrollment (Actual)

56

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Saint-Étienne, France
        • CHU Saint-Etienne

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients followed up in the sexual offender's department of University Hospital of Saint Etienne will be included.

Description

Inclusion Criteria:

  • Patients followed up in the sexual offender's department of University Hospital of Saint Etienne.
  • Patients who did the nursing assessment at time of analysis.

Exclusion Criteria:

  • Patients in the preliminary follow up in the department
  • Refusal to participate at this study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Sexual offender
Patients followed up in the sexual offender's department of University Hospital of Saint Etienne will be included.

Collect data of medical record:

  • Genealogy characteristics
  • Family characteristics: Number of members in the sibling, rank in the sibling / incestuous relationships or not
  • Graphic representation: age / gender / age at time of sexual assault / whether or not a victim of sexual violence / education / family dynamics / living environment during childhood / Criminal category

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Characteristic of family
Time Frame: the day of the medical file review
Structural characteristic of family tree according to the penal category Collected in medical record.
the day of the medical file review

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Family members
Time Frame: the day of the medical file review
Number of members in the sibling, rank in the sibling collected in medical record.
the day of the medical file review
Incestuous relationships
Time Frame: the day of the medical file review
Number of incestuous relationships in the family collected in medical record.
the day of the medical file review
Psychological traumatisms: sexual abuse
Time Frame: the day of the medical file review
Existence of psychological traumatisms: sexual abuse collected in medical record.
the day of the medical file review
Psychological traumatisms: brutal deat
Time Frame: the day of the medical file review
Existence of psychological traumatisms: brutal deat collected in medical record.
the day of the medical file review
Psychological traumatisms: severe illness
Time Frame: the day of the medical file review
Existence of psychological traumatisms: severe illness collected in medical record.
the day of the medical file review
Psychological traumatisms: suicide
Time Frame: the day of the medical file review
Existence of psychological traumatisms: suicide collected in medical record.
the day of the medical file review
Criminal category
Time Frame: the day of the medical file review
Criminal category collected in medical record.
the day of the medical file review

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Tristan GABRIEL, MD, CHU Saint-Etienne

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 5, 2022

Primary Completion (Actual)

April 28, 2022

Study Completion (Actual)

April 28, 2022

Study Registration Dates

First Submitted

December 10, 2021

First Submitted That Met QC Criteria

December 10, 2021

First Posted (Actual)

December 23, 2021

Study Record Updates

Last Update Posted (Estimate)

February 28, 2023

Last Update Submitted That Met QC Criteria

February 27, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • IRBN1052021/CHUSTE

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Sexual Offence

Clinical Trials on Collect data of medical record

Subscribe