Actively Recruiting
Prospective Evaluation of Multidisciplinary Follow-up After Transitional Consultation for Esophageal Atresia in Young Adults
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-03-06
50
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on young adults aged 18 to 30 with esophageal atresia, a condition studied through a multidisciplinary follow-up after a transitional consultation. The initiative aims to start adult medical, psychological, and social care, empower these individuals in managing their future health, and create personalized follow-up plans. This project is unique in addressing post-traumatic stress disorder (PTSD) in this population, with a 3-year analysis planned to evaluate its impact on quality of life. Participants will undergo a 3-year follow-up involving assessments of PTSD prevalence, anxiety and depression levels, quality of life, nutritional, gastrointestinal, and respiratory health. Evaluations include clinical history correlation with PTSD and thorough monitoring of somatic and psychosocial variables. The study is observational and does not involve experimental treatments, focusing on careful data collection and analysis. During the study, participants will complete questionnaires and undergo tests such as thoracic CT scans and respiratory function tests at the start and after 3 years. Researchers will track changes in weight, height, body mass index, and eating habits, alongside psychological assessments. The primary outcome is PTSD prevalence at the beginning, with secondary outcomes including anxiety, depression, quality of life, and physical health measures monitored over the study period.
CONDITIONS
Brief Title
Prospective Evaluation of the Results of Multidisciplinary Follow-up After a Transitional Consultation for Esophageal Atresia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with esophageal atresia
- Aged 18 to 30 years
- Followed at Hôpital Saint Louis
- Informed about the study and not opposed to participation
- Affiliated with a social security scheme
You will not qualify if you...
- Unable to answer questionnaires
- Under legal guardianship
- Under Aide Médicale d'Etat (AME) in France
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 years
Participants are followed for 3 years to evaluate post traumatic stress disorder prevalence, anxiety and depression, quality of life, nutritional, gastrointestinal, and respiratory status.
Assessments at day 0 and at 3 years
Trial Site Locations
Total: 1 location
1
Hopital Saint Louis
Paris, France
Actively Recruiting
Research Team
P
Pierre Cattan, MD PhD
J
Jérôme Lambert, MD PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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