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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05666986
Other study ID # 2021_0342
Secondary ID 2021-A02518-33
Status Not yet recruiting
Phase
First received
Last updated
Start date March 2023
Est. completion date March 2024

Study information

Verified date December 2022
Source University Hospital, Lille
Contact Sébastien MUR, MD
Phone 0320445962
Email sebastien.mur@chu-lille.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective is to understand how a population of adolescents - who have undergone diaphragm surgery within their first month of life (i.e. subjects who have been carriers of a rare impacting disease such as congenital diaphragmatic hernia (CDH)) - engages in physical and sports activities and what can be the hindering factors as well as the factors facilitating these practices. Based on self-questionnaires and semi-structured interviews, this research is a qualitative research in the field of human and social sciences. The qualitative survey will make it possible to report on the experience of the disease of children and parents; in parallel, a complete medical evaluation of the subjects (clinical and para-clinical) will be carried out. The analysis of the verbatim of the self-questionnaires and interviews with regard to the real physical capacities of the subjects, will be discussed.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date March 2024
Est. primary completion date March 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria: - Child/adolescent having undergone surgery for CDH in the first month of life, aged 12 to 18 years; absence of polypathology (i.e. diaphragmatic hernia not associated with another pathology); follow-up at the CDH reference centre, Lille site - Written consent from both parents allowing the collection of data from the child/adolescent - Written consent from the parent(s) agreeing to participate in the study by answering the questionnaires and the individual interview, for themselves and for their child - Possibility of accessing equipment to conduct a video-conference interview if necessary. Exclusion Criteria: - Parents or child/adolescent not understanding French - Parents under guardianship or child under legal protection

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Lille APEHDia, a french CDH patient association, Rare Disease Foundation, France

Outcome

Type Measure Description Time frame Safety issue
Primary Self-questionnaire (for the subjects) to collect the level of investment of the subject in their sport participation (from the subject's point of view) At the time of inclusion
Primary Self-questionnaire (for the subject's parents) to collect the subject's level of involvement in their sport (from the subject's parents' point of view At the time of inclusion
Primary semi-directive interview of the subject allowing the identification of the dynamics of involvement in physical activities and sports practices, from the point of view of the subject (the adolescent) At the time of inclusion
Primary semi-directive interview of the subject's parents allowing the identification of the dynamics of involvement in physical activities and sports practices, from the point of view of the subject's parents At the time of inclusion
Secondary study of the diaphragmatic kinetics by cardiac MRI Complete clinical examination of the subjects and detailed paraclinical evaluation according to the recommendations of the PNDS with the addition of a sequence during the cardiac MRI allowing the study of the diaphragmatic kinetics. At the time of inclusion
Secondary Self-questionnaire and interviews (for the subjects) Analysis of the verbatim of the self-questionnaires and the interviews, with regard to the real physical capacities of the subjects. At the time of inclusion
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