- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06100094
Qualitative Study on a Psychoeducation Group for Juvenile Sex Offenders
Qualitative Study on CRIAVS-LR (Resource Centre for Sex Offenders in Languedoc-Roussillon, France) Psychoeducation Group for Juvenile Sex Offenders
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In France, 25% of perpetrators of sexual offenses are minors. Faced with this increasingly present problem in our society, the answer seems to be more on the side of education and care. However, this new problem confronts us with the limits of our care and forces us to reconsider the organization of care. Indeed, to date, there is no specific support for juvenile sex offenders. Little research exists on the subject because of the many difficulties in setting up this type of study: low power, problem of definition, variables that are difficult to compare, few therapists specialized in this field... In fact, studies must continue to demonstrate the effectiveness of psychoeducational treatment. Although there is no consensus on the profiles of juvenile sex offenders in the literature, there are common characteristics among these individuals. Indeed, the lack of social skills, relationship difficulties, empathy, self-esteem, sex education, impulse control and therefore self-control are issues that can be worked on by psychoeducation.
CRIAVS-LR's team have therefore decided to create a specific psychoeducation group for minors and young adults who are perpetrators of sexual violence. The objective is to improve their skills of knowing, knowing how to be and knowing how to do in the areas of affective and sexual interpersonal relationships and thus find alternative solutions to violence, particularly sexual violence. The qualitative aspect of this study would make it possible to provide data in this still little explored field, to try to understand the experience of the young people participating in this group and to improve its structure and content so that it reaches best its goals.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: magali teillard, psychologist
- Phone Number: 33 0467338577
- Email: m-teillard_dirat@chu-montpellier.fr
Study Contact Backup
- Name: celine BAIS, Ph
- Phone Number: 33 0467338677
- Email: c-bais@chu-montpellier.fr
Study Locations
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Montpellier, France, 34295
- Recruiting
- UH MONTPELLIER - La Colombiere CRIAVS
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Contact:
- Celine BAIS, PhD
- Phone Number: 33 0467338577
- Email: c-bais@chu-montpellier.fr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- patient aged 14 to 20
- commit a sexual offense
- takes part to CRIAVS-LR psychoeducation group
Exclusion Criteria:
- severe intellectual disability, decompensated psychiatric disease
- Illiterate or unable to understand the purpose and methodology of the study
- Patient not affiliated to a French social security scheme or not a beneficiary of such a scheme
- Person unable to give consent
- Refusal of consent after information
- Adult protected by law (guardianship, curatorship)
- Person under psychiatric care
- Person participating in another research project with an exclusion period still in progress,
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
juvenile sex offender psychoeducation group
The psychoeducation group consists of 10 sessions of approximately 1.5 hours each, once a week or every two weeks depending on the availability of the therapists.
Among the sessions, 9 correspond to a specific theme: reminder of the law and violence, sexism, consent, control, social pressure, self-control, empathy, seduction and romantic relationships, sex under the influence.
The last session is devoted to a resumption of all the themes previously discussed.
Semi-structured qualitative interviews addressing their feelings regarding the psychoeducation group, what they learned from it, what they had difficulty with.
|
During the interview, a list of semi-open questions will be asked :
Interviews will be carried out until data saturation. Collection of socio-demographic data (age), medical history and criminal history in the patient's file |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The feelings of patients who participated on a psychoeducation group
Time Frame: At the end of the 10 sessions (week 10) of the psychoeducation group
|
One Guided Interview : The analysis of the interviews uses a phenomenological method aimed at bringing out data from the lived experience collected in the verbatims, each representing an aspect of the phenomenon studied. The raw data will be prepared in a word document. After a division into units of meaning and thematization by an inductive coding procedure using classificatory logic, the analysis consists of identifying the relevant elements in relation to the research question and in particular in relation to the chosen indicators. These different indicators will constitute an a priori analysis grid. They will be distributed in the different "boxes" previously established concerning the chosen indicators. Apart from these a priori indicators, concepts not planned in advance will be reported Patient's expectations before the group, description of the lived experience, emotions felt between two sessions, group description, patient's feed back after their participation. |
At the end of the 10 sessions (week 10) of the psychoeducation group
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Socio-demographic data
Time Frame: At the end of the 10 sessions (week 10) of the psychoeducation group
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age and criminal records
|
At the end of the 10 sessions (week 10) of the psychoeducation group
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: celine BAIS, Ph, University Hospital, Montpellier
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB-MTP_2023_09_202301455
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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