Transition care for adolescents with congenital heart disease

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the impact of a structured transition care model on adolescents with congenital heart disease as they move from pediatric to adult healthcare systems. It aims to enhance their readiness for adult care, improve self-management skills, and raise awareness about the importance of regular medical follow-ups. The intervention includes training materials such as brochures, posters, and slide presentations to support the transition process. The study is designed as a randomized controlled trial to assess the effectiveness of this approach.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Voluntarily agree to participate in the research
* To be between the ages of 16-20,
* Having a diagnosis of congenital heart disease,
* Being followed up with a diagnosis of congenital heart disease for at least one year in the polyclinics where the study was conducted,
* To be able to communicate in Turkish,
* Not having any mental deficiency that may prevent communication

Exclusion Criteria:

* Refusing to participate in the research,
* Not being able to communicate in Turkish,
* Not showing up regularly for follow-ups,
* Having any mental disability that may prevent communication

Where it's running

• Republic of Turkey Ministry of Health Ankara Etlik City Hospital
  Ankara, Turkey (Türkiye) Recruiting
• Republic of Turkey Ministry of Health Ankara Etlik City Hospital
  Ankara, Ankara Yenimahalle, Turkey (Türkiye) Not yet recruiting

Study contacts

• Principal investigator: Tutku KIRÇI TEMİZ, PhD s. — Ankara Yildirim Beyazıt University
• Study coordinator: Tutku KIRÇI TEMİZ, PhD s.
• Email: tutkukrc29095@gmail.com
• Phone: +905064278982

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.