Understanding how adolescents with repaired diaphragmatic hernia engage in sports and activities
Official title: Identification of Obstacles and Facilitators to the Engagement in Physical and Sports Activities in a Population of Adolescents Operated on for a Diaphragmatic Hernia
Run by University Hospital, Lille · NCT05666986 · Data updated 2026-11-12
This study looks at how teens who had CDH surgery as babies try sports and physical activities, and what helps or hinders them.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 12 Years to 18 Years |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | University Hospital, Lille Academic / other |
| Locations | 1 site (Lille) |
| Status | Recruiting |
| Started | May 19, 2022 |
| Main results expected | March 2027 |
| Study ends | March 2027 |
| Registry record updated | May 22, 2026 |
| Trial ID | NCT05666986 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adolescents aged 12–18 years who had CDH surgery within the first month of life and are followed at the Lille reference center, with both parents able to consent and French language comprehension.
✕Probably not a fit
Patients who do not engage in questionnaires or interviews or who are not followed at the Lille center may not benefit from the study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational, qualitative study explores the physical activity and sports participation of adolescents who were treated for congenital diaphragmatic hernia in infancy. It uses self-questionnaires and semi-structured interviews to understand experiences, barriers, and facilitators, alongside a clinical and para-clinical medical evaluation. The goal is to report on the disease experience for children and parents while examining real physical capacities. Data will be analyzed from verbatim responses to identify patterns in activity levels, motivation, and environmental influences.
Why it matters
Potential benefit: Findings could guide ways to support CDH patients in participating in age-appropriate physical activities.
How similar studies have gone: Similar qualitative studies in chronic pediatric conditions have successfully identified barriers and facilitators to activity; this study addresses CDH specifically.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
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chu de Lille
Lille, France Recruiting
Study contacts
- Principal investigator: Sébastien MUR, MD — University Hospital, Lille
- Study coordinator: Sébastien MUR, MD
- Email: sebastien.mur@chu-lille.fr
- Phone: 0320445962
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Melatonin plus inhaled nitric oxide for pulmonary hypertension in full-term newborns
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FETO with a Goldballoon device for fetuses with diaphragmatic hernia
This study tests whether performing Fetoscopic Endoluminal Tracheal Occlusion on pregnancies with fetal diaphragmatic hernia improves baby survival and reduces long-term problems.
-
Fetal tracheal occlusion (FETO) for severe congenital diaphragmatic hernia
This trial will test whether fetal endoluminal tracheal occlusion (FETO) helps fetuses with severe congenital diaphragmatic hernia and intrathoracic liver herniation survive to hospital discharge.
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Long-term outcomes after FETO for severe left or right congenital diaphragmatic hernia
This trial will test whether performing FETO in fetuses with isolated severe left or right CDH helps more babies survive to hospital discharge and have fewer long-term problems than standard care.
-
Fetal treatment for congenital diaphragmatic hernia
This study is testing a new way to treat congenital diaphragmatic hernia in unborn babies by placing a balloon in their airway to help their lungs grow before they are born.
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Fetoscopic balloon (FETO) for severe left and right congenital diaphragmatic hernia — long-term outcomes
This trial will try placing and later removing a tiny balloon in the fetal windpipe around 27–29 weeks to help babies with severe congenital diaphragmatic hernia and liver herniation survive the newborn period.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.