Evaluation of Transition With a Heart, a Transition Program for Adolescents With Congenital Heart Disease and Parents

Not Applicable

Completed

• Conditions: Transitional Care; Congenital Heart Disease in Adolescence
• Interventions: Other: Transition With a Heart (TWAH)

• Registration Number: NCT05479630
• Lead Sponsor: University Hospital, Ghent

Brief Summary

The department of Congenital Heart Disease of the Ghent University Hospital (Belgium) developed a transition program dedicated to adolescents with congenital heart disease (CHD): 'Transition With a Heart´ (TWAH). TWAH was developed based on the Dutch program 'On your own feet´, starting at the age of 12 years and continuing after transfer. The most vital core components include a general and individualized flowchart, adolescent-centred communication, a joined transfer consultation and an appointed transition coordinator. TWAH focuses on promoting disease knowledge, autonomy and skills development of adolescents with CHD. Interventions encompass the use of a communication-paper, autonomously talking to professionals, individualized education and skills development plan. Interventions were selected from the highest sources of scientific evidence currently available including (quasi-) experimental studies, narrative literature reviews and expert opinions.

TWAH is the intervention in the conducted study. Hence, the intervention group are adolescents with CHD and their parents who are participating in TWAH. Adolescents and their parents who are transferred according to standard care (joined transfer consultation only) are identified as the control group and will be examined in the post test phase in order to be able to make comparisons with the intervention group. At baseline (the start of TWAH) participants of the control group already made the transfer to the adult ward.

The investigators consider the following hypothetical scenario:

- TWAH will have a positive influence on disease knowledge and transition experiences of the participants.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-11-05
• Study First Submitted: 2020-10-16
• Primary Completion: 2021-12-01
• Study First Submitted QC: 2022-07-26
• Study First Posted: 2022-07-29
• Study Completion: 2022-12-01
• Status Verified: 2023-01
• Last Update Submitted: 2023-01-27
• Last Update Posted: 2023-01-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 81

Inclusion Criteria

• Clinical diagnosis of a CHD of great or moderate complexity (6)
• From the age of 12 years or older
• Must be able to complete the questionnaires
• Dutch speaking AND/OR
• Parents having children who are meeting the inclusion criteria above

Exclusion Criteria

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Adolescents and their parent of the intervention group	Transition With a Heart (TWAH)	Adolescents and their parent who are participating in TWAH

Primary Outcome Measures

Name	Time	Method
Change in disease-related knowledge of adolescents of the intervention group (paired test)	At baseline (first transition outpatient visit around 14y) and through study completion, an average of 1 year from the transfer consultation	Total knowledge score assesed by the Leuven Knowledge Questionnaire for Congenital Heart Disease (LKQCHD): and consists of 27 multiple choice questions for girls and 25 items for boys (Philip Moons et al., 2001). The total knowledge score consists of a ratio of the sum of correct answers to the total number of questions resulting in a 0-100 scale, where a higher score reflects a better disease-related knowledge.
Comparison between disease-related knowledge scores of adolescents of the intervention group and adolescents of the control group	Through study completion, an average of 1 year from the transfer consultation	Total knowledge score assesed by the Leuven Knowledge Questionnaire for Congenital Heart Disease (LKQCHD): and consists of 27 multiple choice questions for girls and 25 items for boys (Philip Moons et al., 2001). The total knowledge score consists of a ratio of the sum of correct answers to the total number of questions resulting in a 0-100 scale, where a higher score reflects a better disease-related knowledge.

Secondary Outcome Measures

Name	Time	Method
Comparison between levels of health-related quality of life of adolescents of the intervention group and adolescents of the control group	Through study completion, an average of 1 year from the transfer consultation	Level of health-related quality of life of adolescents assesed by the Pediatric Quality of Life inventory (PEDSQoL) adolescent version: cardiac and general module. Adolescents were asked to indicate the degree to which they experienced problems with these respective items over the past month using a five-point Likert scale (from 0=never to 4=always). For calculating the total score, the answers were reversed and computed to the domain and total scores on a 0-100 scale, where a higher score reflects a higher perceived QoL.
Comparison of transfer experiences between adolescents of the intervention group and the adolescents of the control group	Through study completion, an average of 1 year from the transfer consultation	Assesed with the On Your Own Feet Tranfer Experience Scale and consists of two subscales: 1) perceived alignment and collaboration between pediatric and adult care and 2) experienced preparation for transfer, including readiness. The items could be rated on a five-point Likert scale (from 1= strongly disagree to 5=strongly agree). The theoretical scores range from 11 to 55 for the first subscale and 7 to 35 for the second. A higher score reflects a higher level of satisfaction with the transitional process. In addition, the overall satisfaction of the transfer could be indicated using a using visual analogue scale (from 1 if completely unsatisfied to 10 if completely satisfied), as well as confidence in the pediatric cardiologist and the adult cardiologist (from 1= no confidence to 10=complete confidence)
Change in health-related quality of life of adolescents of the intervention group (paired test)	At baseline (first transition outpatient visit around 14y) and through study completion, an average of 1 year from the transfer consultation	Level of health-related quality of life of adolescents assesed by the Pediatric Quality of Life inventory (PEDSQoL) adolescent version: cardiac and general module. Adolescents were asked to indicate the degree to which they experienced problems with these respective items over the past month using a five-point Likert scale (from 0=never to 4=always). For calculating the total score, the answers were reversed and computed to the domain and total scores on a 0-100 scale, where a higher score reflects a higher perceived QoL.
Comparison of transfer experiences between parents in the intervention group and control group	Through study completion, an average of 1 year from the transfer consultation	Assesed with the On Your Own Feet Tranfer Experience Scale and consists of two subscales: 1) perceived alignment and collaboration between pediatric and adult care and 2) experienced preparation for transfer, including readiness. The items could be rated on a five-point Likert scale (from 1= strongly disagree to 5=strongly agree). The theoretical scores range from 11 to 55 for the first subscale and 7 to 35 for the second. A higher score reflects a higher level of satisfaction with the transitional process. In addition, the overall satisfaction of the transfer could be indicated using a using visual analogue scale (from 1 if completely unsatisfied to 10 if completely satisfied), as well as confidence in the pediatric cardiologist and the adult cardiologist (from 1= no confidence to 10=complete confidence)

Trial Locations

Locations (1)

Ghent University Hospital; 🇧🇪 Ghent, Belgium