A Transferability Study on the Conditions for a Successful Inclusive Education
NCT ID: NCT06378307
Last Updated: 2024-04-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
114 participants
OBSERVATIONAL
2024-04-30
2025-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
FCT With Young Children With ID in the UK: A Feasibility Project V.1
NCT02721394
Clinical and Neurophysiological Evolutions Through a Functional Rehabilitation of Social Communication in ASD
NCT02444117
Computer-Mediated Intervention to Enhance Emotional Competence in Children With Autism in Schools
NCT05902832
Engaging Siblings of Adults With Autism in Future Planning
NCT03374072
Investigation the Effect of the Social-Communication Area Developmental Screening Test for Infants and Young Children Training Program Applied in Addition to the DIR/Floortime™ Therapy Program in Children with Developmental Risk
NCT06345170
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Qualitative data will be collected by interviewers through individual or collective interviews, Data collection will be based on the configurational elements Contest, Mechanisms, Outcomes based on a realist evaluation.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Students, families, professionals
Students with disabilities, students without disabilities, families, educational professionals, social workers and professionals/volunteers working in recreational activities
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Under 15 years of age
* With a disability (notified by the Maison Départementale de l'Autonomie - MDA - for support by the local service provider (DAME : Dispositif d'Accompagnement Médico-Educatif)
* Enrolled in either the elementary school or middle school selected for the study
* Whose parents have not objected to their participation in the study
Children who do not have a disability
* Under 15 years of age
* In the same classroom as a student with a disability already participating in the study
* Whose parents did not object to their participation in the study
Families
* Father and/or mother, with parental authority, of a child with a disability participating in the study
* Over 18 years of age
* Not under guardianship or curatorship
* Have signed a study participation consent form
Education professionals:
* Working in one of the 2 schools selected for the study
* Working as (if possible, 1 representative from each of these professional categories):
* a member of the school's management team, the ULIS (Unité Unités Localisées pour l'Inclusion Scolaire) teacher, the teachers of the standard classroom of the disabled children taking part in the study.
* Members of the school life team (lunchtime, recess)
* professionals working towards inclusive education at the level of the school and the department
* Having signed a consent to participate in the study
Professionals of the service provider (DAME : Dispositif d'Accompagnement Médico-Educatif):
* Working in the service provider's sector of the school chosen for the research.
* Supporting a disabled child taking part in the research project
* Working within the DAME management team, i.e. a DAME specialist teacher, the DAME pedagogical coordinator, professionals providing different educational or therapeutic support (if possible, 1 representative from each of these professional categories).
* Having signed a consent form to participate in the study
Professionals who work with children during leisure time, outside school hours (if possible, 1 representative from each of these professional categories):
* Being professionals of associations of leisure centers, sports clubs ... and support a disabled child participating in the study
* Professionals working for the Espace Ressources Handicap, which coordinates these activities, and working in one of the 2 schools chosen for the study.
* Have signed a consent form to participate in the study
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Bordeaux
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CHUBX2022-06
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.