- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07476131
Psychiatric Care and Education for Adolescents and Young Adults in the Ile-de-France Region: Expectations and Experiences of Young People and Parents Concerned (Soins-Etude)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Mixed prospective (interviews) and retrospective (letters) multicenter study, qualitative and data mining (excluding Jardé law) Qualitative
The first part of the research will follow a qualitative methodology in accordance with COREQ recommendations. The aim is to gather insights from young people and one or both of their parents on the care they received in the care-study program. Two populations will be included:
- young people currently hospitalized in educational care at the end of their treatment, as well as one or both of their parents,
- those who have been discharged from educational care for more than a year, as well as one or both of their parents.
All will be interviewed about their experience in educational care. The approach will be phenomenological-pragmatic, a comprehensive research paradigm. The interpretative phenomenological approach (IPA) allows for detailed and nuanced analyses of each individual's experiences. The objective of this perspective is to delve deeply into the unique universe of each individual in order to reconstruct a common meaning, a common model. In addition, it allows us to grasp and understand the experiences of a young person and one of their parents.
Data mining In order to identify young people's expectations regarding psychiatric care and education prior to admission, their letters of motivation from the last five years will be used. The analysis of this set of textual data requires the use of appropriate data mining methods. This method does not prejudge the participants' responses and aims to determine patient-centered evaluation criteria for care and education and to generate hypotheses.
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Qualitative study: Young people receiving psychiatric care in the four centers, either currently hospitalized (close to discharge) or discharged for more than one year (between one and two years); and for each of these young people, at least one of their parents will be interviewed during a single interview (two interviews will be conducted if both parents wish to testify but a joint interview is not possible).
Data mining study: Young high school students receiving psychiatric care in the four centers in 2020, 2021,2022,2023,2024 and 2025
Exclusion Criteria:
Qualitative study: Refusal to participate Data mining study: Opposition to the use of data.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Collect feedback
Time Frame: letters of motivation ( data mining) day 1
|
In order to identify young people's expectations regarding psychiatric care and education prior to admission, their letters of motivation from the last five years will be used.
Analysis of this textual data set requires the use of appropriate data mining methods
|
letters of motivation ( data mining) day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
interview
Time Frame: Interview guide (interview) day 1
|
The objective is to gather insights from young people and one of their parents (or both) on the care they received in terms of healthcare and education. Two populations will be included:
|
Interview guide (interview) day 1
|
Collaborators and Investigators
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2026-A00545-46
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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