- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06378307
A Transferability Study on the Conditions for a Successful Inclusive Education (TIAP)
Study Overview
Status
Conditions
Detailed Description
The TIAP study aims to study the transferability of a local innovation in the field of inclusive education in order to identify the functions that can be transferred. Grounded in a theory based evaluation (called realist evaluation) the TIAP study is a qualitative case study. The study population comprises various participant profiles including students with disabilities, students without disabilities, families, educational professionals, social workers and professionals/volunteers working in recreational activities. Participants will be recruited in two schools from a French department (Eure et Loir). In this department the intervention (also called innovation) is implemented. This intervention implies a complete transformation carried out by the service providers for students with intellectual deficiencies as well as the educational system. Students with disabilities go at school in their geographical area. They attend a standard classroom and have educational and therapeutical support offered by the local service provider (DAME : Dispositif d'Accompagnement Médico-Educatif ). Service providers are seen as ressources for education professionals.
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.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Linda Cambon
- Phone Number: 33 0557571184
- Email: linda.cambon@u-bordeaux.fr
Study Contact Backup
- Name: Eleonore Segard
- Phone Number: 33 0557571184
- Email: eleonore.segard@firah.org
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Children with disabilities
- 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
Exclusion Criteria: None for the different populations
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Students, families, professionals
Students with disabilities, students without disabilities, families, educational professionals, social workers and professionals/volunteers working in recreational activities
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of inclusive education on children with disabilities autonomy and social participation at school
Time Frame: Day 0
|
Perceptions of students with disabilities on : learning practices and support, accessibility, inclusion climate in their school , peer relations at school.
|
Day 0
|
|
Effect of inclusive education on children with disabilities autonomy and social participation in their proximal living environment (leisures participation)
Time Frame: Day 0
|
Perceptions of students with disabilities during leisure participation on : support, accessibility, inclusion climate, peer relations in their living environment
|
Day 0
|
|
Effect of inclusive education on social participation of families with children with disabilities
Time Frame: Day 0
|
Perceptions of families on their social participation in their living environment
|
Day 0
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
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
- CHUBX2022-06
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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