Impact of a Structured Clinical Assessment MIDSA, Its Feedback and Support for Change on Commitment to Care of Perpetrators of Sexual Offenses

NCT ID: NCT05013996

Last Updated: 2025-11-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-20

Study Completion Date

2025-01-14

Brief Summary

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Evaluate the effectiveness of an intervention including the clinical assessment carried out with the (Multidimensional Inventory of Development, Sex, and Aggression) MIDSA and the review of the results with the professional in charge of the subject on the adherence and commitment to the care of the sexual offenders.

Detailed Description

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The intervention of MIDSA (Multidimensional Inventory of Development, Sex, and Aggression), a multidimensional investigation tool for issues related to sexuality and violence, could be prove very useful by providing AICS patients as well as the professionals who take care of them with a complete clinical assessment which enlightens the patient on his psychopathological functioning and / or his disorders, and which guides the care through the axes of intervention to be implemented in response to the criminological and non-criminological needs of the patient. This should allow the latter a better awareness (awareness) of his difficulties in the relationship with the other, facilitate his adherence to care, obtain a better commitment on his part in the process of change and consequently, bring him change their lifestyle and gradually adopt proactive attitudes and behavior that ultimately reduce the risk of recidivism of sexual and general violence. However, recourse to MIDSA as a "change operator" in a patient's trajectory is only possible if it is accompanied by a resumption of his clinical assessment by a professional who supports the change process by strengthening his motivation to change their criminal behavior.

Conditions

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Offense, Sex

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

open label multicenter randomized controlled trial
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Intervention

Patients randomized to the experimental (MIDSA groupe) will be treated according to the usual methods of each of the centers (CMP / CRIAVS / private practitioners, etc.) completed with the Multidimensional Inventory of Development, Sex, and Aggression-MIDSA groupe Multidimensional Inventory of Development, Sex, and Aggression-inventory tool.

Group Type EXPERIMENTAL

MIDSA

Intervention Type BEHAVIORAL

Multidimensional Inventory of Development, Sex, and Aggression

Control

Patients randomized to the control group will be treated according to the usual methods of each of the participating centers (CMP / CRIAVS / private practitioners, etc.).

Group Type ACTIVE_COMPARATOR

Usual methods of evaluation

Intervention Type BEHAVIORAL

Usual methods of evaluation of each of the participating centers (CMP / CRIAVS / private practitioners, etc.).

Interventions

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MIDSA

Multidimensional Inventory of Development, Sex, and Aggression

Intervention Type BEHAVIORAL

Usual methods of evaluation

Usual methods of evaluation of each of the participating centers (CMP / CRIAVS / private practitioners, etc.).

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Adult male patients
* Express written consent of the participant after receiving the study information
* Subject making contact or being taken in charge by a psychiatric service (even an addictology service or by liberal practitioners in connection with psychiatry), a CRIAVS or a care unit dedicated to the care of perpetrators of a sexual offense (AICS) ;
* For a problem of sexual violence such as sexual harassment, assault and rape of adult women (including marital rape), incest, pedophilic or hebephilic acts, sexual sadism, exhibition, voyeurism, frotteurism, use and possession of child pornography or addiction sexual.

* Affiliated to a social security scheme

Exclusion Criteria

* Maximum stage (maintenance phase) listed on the URICA scale
* Poor understanding of the French language;
* Patient imprisoned, under legal protection, under guardianship or curatorship
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Tours

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Robert COURTOIS, MD-PhD

Role: STUDY_DIRECTOR

University Hospital of TOURS

Locations

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CHRU Lille - URSAVS Lille

Lille, , France

Site Status

CH LE Vinatier - Service de Psychiatrie Légale

Lyon, , France

Site Status

CHU Montpellier Lapeyronie - CRIAVS Languedoc-Roussillon

Montpellier, , France

Site Status

CHU Poitiers Henri Laborit - CRIAVS - CMP Espace Vienne - SMPR

Poitiers, , France

Site Status

CHRU Tours - UC3P

Tours, , France

Site Status

Countries

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France

Other Identifiers

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2020-A02628-31

Identifier Type: REGISTRY

Identifier Source: secondary_id

DR190059

Identifier Type: OTHER

Identifier Source: secondary_id

EV-AICS (DR190059)

Identifier Type: -

Identifier Source: org_study_id

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