- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04820998
Living in a Precarious Situation With an Autistic Child: What Are the Issues at Stake for Support in Care (HaSPrEA)
Living in a Precarious Situation With an Autistic Child: What Are the Issues at Stake for Support in Care: Qualitative Study - Monocentric Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Identify the living conditions related to the housing of children with autism spectrum disorders (ASD) treated at the Léo Kanner Center (CLK), psychopathology department of the Saint-Étienne University Hospital. The aim is to describe through the trajectories of children with ASD and their families, their living conditions, and through interviews with professionals who support them, how the specificities related to precarious situations are identified and taken into account.
A qualitative survey, carried out by sociological interviews with families whose children are followed at the Léo Kanner Center (CLK) and the professionals who care for them, would make it possible to collect data on the development of a young child with autism in his home and more generally in his habitat.
The purpose of this study is to study the specificities of families in a precarious situation with a child with autism spectrum disorders (ASD) in terms of housing, in order to better support them in different social spaces and improve collaboration between professionals and parents. The project aims to bring children with autism spectrum disorders (ASD) into a dynamic of access to human rights. He suggests three levers to achieve this: rely on a precise inventory of needs; work towards a transformation of representations; streamline access to healthcare and common law services.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Saint-Étienne, France, 42055
- CHU St Etienne
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Families having their child followed in the child psychiatry service of the Léo Kanner Center (CLK),
- Children followed for Autism Spectrum Disorders (ASD),
- Families who received informed information about the study and who co-signed a consent to participate in the study with the investigator.
Exclusion Criteria:
- Opinion of the child's referring physician contraindicating inclusion
- Refusal of one of the legal guardians to participate in the study
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
living conditions of children with Autism Spectrum Disorders (ASD)
Time Frame: hours 2
|
To identify the living conditions related to the housing of children with Autism Spectrum Disorders (ASD) who are cared for at the Léo Kanner Center (CLK), psychopathology department of the University Hospital of Saint-Etienne.
|
hours 2
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Precarity
Time Frame: hours 2
|
Families's interviews about their precarious situation of living and the consequences on their autistic child care
|
hours 2
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Professionals
Time Frame: hours 2
|
Interviews so as to know how the specifics of precarious situations are identified and taken into account by the professionals
|
hours 2
|
Collaborators and Investigators
Investigators
- Principal Investigator: VALERIE ROUSSELON-CHARLES, MD, CHU ST ETIENNE FRANCE
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20CH029
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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