Actively Recruiting

Phase Not Applicable
Age: 16Years - 20Years
All Genders
ID06433401

The Effect of Structured Transition Care Model Applied to Adolescents With Congenital Heart Disease on Transition Readiness, Self-Management Skills and Care Satisfaction

Led by Ankara Yildirim Beyazıt University · Updated on 2025-01-31

70

Participants Needed

2

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Congenital heart disease is a common birth defect with significant health risks, especially as affected children transition from pediatric to adult care. This research evaluates a structured transition care model aimed at adolescents with congenital heart disease to improve their readiness for adult care, self-management skills, and satisfaction with care during this change. The study addresses the need for professional support and education to help adolescents and their families adapt to adult health systems and reduce complications. Participants are randomly assigned to one of two groups: the transition care group receives individualized training through three educational modules delivered face-to-face monthly, each lasting about 35-40 minutes. The control group continues with routine care and may receive the training after the study concludes. The intervention includes brochures, posters, and slide materials, with education sessions occurring at one and two months after the first interview. During the one-year study, participants will complete assessments at specific intervals including the Transition Readiness Assessment Scale, Chronic Disease Self-Management Scale, and Transitional Care Satisfaction Rating Scale. Researchers will also collect sociodemographic and medical data. The study monitors how well adolescents prepare for adult care, manage their condition, and their satisfaction with the care received, aiming to guide nursing practices for this population.

CONDITIONS

Brief Title

The Effect of Structured Transition Care Model Applied to Adolescents With Congenital Heart Disease

Who Can Participate

Age: 16Years - 20Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Voluntarily agree to participate in the research
  • Be between 16 and 20 years old
  • Have a diagnosis of congenital heart disease
  • Have been followed for congenital heart disease for at least one year at the study clinic
  • Be able to communicate in Turkish
  • Have no mental deficiency that prevents communication
Not Eligible

You will not qualify if you...

  • Refuse to participate in the research
  • Unable to communicate in Turkish
  • Do not attend follow-ups regularly
  • Have any mental disability that prevents communication

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Approximately 2 months

Participants in the transition care group receive individualized transitional care training consisting of three modules delivered face-to-face. Education sessions occur at 1 and 2 months after the first interview to support transition readiness, self-management skills, and care satisfaction.

3 visits (in-person)

Long-term Monitoring

Duration - Up to 1 year

Participants are followed for up to 1 year after the initial training to assess transition readiness, self-management, and care satisfaction.

Follow-up assessments at certain intervals during 1 year

Trial Site Locations

Total: 2 locations

1

Republic of Turkey Ministry of Health Ankara Etlik City Hospital

Ankara, Ankara Yenimahalle, Turkey (Türkiye), 06170

Not Yet Recruiting

2

Republic of Turkey Ministry of Health Ankara Etlik City Hospital

Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

T

Tutku KIRÇI TEMİZ, PhD s.

U

Utku ARMAN ÖRÜN, Prof.Dr.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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