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RecruitingNCT05666986CHASAMUpdated May 22, 2026

Engagement in Physical Activities and Sports in Adolescents With Diaphragmatic Hernia

An observational study in Congenital Diaphragmatic Hernia, sponsored by University Hospital, Lille. Recruiting at 1 site in France. Open to participants aged 12 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-22.

Sponsored by University Hospital, Lille · Observational

From the registry’s dates

  • Started May 2022; still recruiting 4 years 4 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
20
Ages
12 Years to 18 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Congenital Diaphragmatic Hernia

Keywords

  • CDH
  • physical activity and sports
  • childhood and adolescence
  • environment sociological
  • psychological clinical
03

In context

Hernias, Diaphragmatic, Congenital

93 studies on the registry are indexed under Hernias, Diaphragmatic, Congenital; 39 are open to participants now.

This study's planned enrollment of 20 is below the median of 78 across 25 observational studies indexed under Hernias, Diaphragmatic, Congenital.

Browse Hernias, Diaphragmatic, Congenital studies →

Lead sponsor

University Hospital, Lille is the lead sponsor of 625 studies on the registry; 141 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

All adolescents who had CDH surgery in the first month of life, without any other pathology, now aged 12-18 and followed up at the CDH Lille Reference Center, will be asked to take part in the study.

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

Exclusion Criteria:

  • Parents or child/adolescent not understanding French
  • Parents under guardianship or child under legal protection
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
20 participants (estimated)
Patient registry
No

Groups and cohorts

  • Adolescents who had CDH surgery in the first month of life,

    without any other pathology, now aged 12-18 and followed up at the CDH Lille Reference Center

06

What researchers measure

Primary outcomes

  1. 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)

    Time frame: At the time of inclusion

  2. 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

    Time frame: At the time of inclusion

  3. 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)

    Time frame: At the time of inclusion

  4. 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

    Time frame: At the time of inclusion

Secondary outcomes

  1. 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.

    Time frame: At the time of inclusion

  2. 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.

    Time frame: At the time of inclusion

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05666986
Lead sponsor
University Hospital, Lille
Collaborators
APEHDia, a french CDH patient association, Rare Disease Foundation, France
Responsible party
Sponsor
First posted
Dec 28, 2022
Start date
May 19, 2022
Primary completion
Mar 2027 (estimated)
Completion
Mar 2027 (estimated)
Last update
May 22, 2026

Study contacts

Sébastien MUR, MD
Contact
sebastien.mur@chu-lille.fr
0320445962 ext. +33
Sébastien MUR, MD
principal investigator · University Hospital, Lille

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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