3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Impact of a transition education program on health-related quality of life in pediatric patients with congenital heart disease: study design for a randomised controlled trial

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Recent advances in the field of congenital heart disease (CHD) led to an improved prognosis of the patients and in consequence the growth of a new population: the grown up with congenital heart disease. Until recently, more than 50% of these patients were lost to follow up because of the lack of specialized structures. The critical moment is the transition between paediatric and adult unit. Therapeutic education is crucial to solve this issue by helping patients to become independent and responsible. The TRANSITION-CHD randomized trial aims to assess the impact of a transition education program on health-related quality of life (HRQoL) of adolescents and young adults with CHD.

          Methods

          Multicentre, randomised, controlled, parallel arm study in CHD patients aged from 13 to 25 years old. Patients will be randomised into 2 groups (education program vs. no intervention). The primary outcome is the change in self-reported HRQoL between baseline and 12-month follow-up. A total of 100 patients in each group is required to observe a significant increase of the overall HRQoL score of 7 ± 13.5 points (on 100) with a power of 80% and an alpha risk of 5%. The secondary outcomes are: clinical outcomes, cardiopulmonary exercise test parameters (peak VO2, VAT, VE/VCO2 slope), level of knowledge of the disease using the Leuven knowledge questionnaire for CHD, physical and psychological status.

          Discussion

          As the current research is opening on patient related outcomes, and as the level of proof in therapeutic education is still low, we sought to assess the efficacy of a therapeutic education program on HRQoL of CHD patients with a randomized trial.

          Trial registration

          This study was approved by the National Ethics Committee (South-Mediterranean IV 2016-A01681-50) and was registered on Clinicaltrials.gov (NCT03005626).

          Related collections

          Most cited references39

          • Record: found
          • Abstract: not found
          • Article: not found

          The levels of evidence and their role in evidence-based medicine.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            PedsQL 4.0: reliability and validity of the Pediatric Quality of Life Inventory version 4.0 generic core scales in healthy and patient populations.

            The PedsQL (Pediatric Quality of Life Inventory) (Children's Hospital and Health Center, San Diego, California) is a modular instrument for measuring health-related quality of life (HRQOL) in children and adolescents ages 2 to 18. The PedsQL 4.0 Generic Core Scales are multidimensional child self-report and parent proxy-report scales developed as the generic core measure to be integrated with the PedsQL Disease-Specific Modules. The PedsQL 4.0 Generic Core Scales consist of 23 items applicable for healthy school and community populations, as well as pediatric populations with acute and chronic health conditions. The 4 PedsQL 4.0 Generic Core Scales (Physical, Emotional, Social, School) were administered to 963 children and 1,629 parents (1,677 subjects accrued overall) recruited from pediatric health care settings. Item-level and scale-level measurement properties were computed. Internal consistency reliability for the Total Scale Score (alpha = 0.88 child, 0.90 parent report), Physical Health Summary Score (alpha = 0.80 child, 0.88 parent), and Psychosocial Health Summary Score (alpha = 0.83 child, 0.86 parent) were acceptable for group comparisons. Validity was demonstrated using the known-groups method, correlations with indicators of morbidity and illness burden, and factor analysis. The PedsQL distinguished between healthy children and pediatric patients with acute or chronic health conditions, was related to indicators of morbidity and illness burden, and displayed a factor-derived solution largely consistent with the a priori conceptually-derived scales. The results demonstrate the reliability and validity of the PedsQL 4.0 Generic Core Scales. The PedsQL 4.0 Generic Core Scales may be applicable in clinical trials, research, clinical practice, school health settings, and community populations.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Congenital heart disease in the general population: changing prevalence and age distribution.

              Empirical data on the changing epidemiology of congenital heart disease (CHD) are scant. We determined the prevalence, age distribution, and proportion of adults and children with severe and other forms of CHD in the general population from 1985 to 2000. Where healthcare access is universal, we used administrative databases that systematically recorded all diagnoses and claims. Diagnostic codes conformed to the International Classification of Disease, ninth revision. Severe CHD was defined as tetralogy of Fallot, truncus arteriosus, transposition complexes, endocardial cushion defects, and univentricular heart. Prevalence of severe and other CHD lesions was determined in 1985, 1990, 1995, and 2000 using population numbers in Quebec. Children were subjects <18 years of age. The prevalence was 4.09 per 1000 adults in the year 2000 for all CHD and 0.38 per 1000 (9%) for those with severe lesions. Female subjects accounted for 57% of the adult CHD population. The median age of all patients with severe CHD was 11 years (interquartile range, 4 to 22 years) in 1985 and 17 years (interquartile range, 10 to 28 years) in 2000 (P<0.0001). The prevalence of severe CHD increased from 1985 to 2000, but the increase in adults was significantly higher than that observed in children. In the year 2000, 49% of those alive with severe CHD were adults. The prevalence in adults and median age of patients with severe CHD increased in the general population from 1985 to 2000. In 2000, there were nearly equal numbers of adults and children with severe CHD.
                Bookmark

                Author and article information

                Contributors
                pascal.amedro@gmail.com
                Journal
                Health Qual Life Outcomes
                Health Qual Life Outcomes
                Health and Quality of Life Outcomes
                BioMed Central (London )
                1477-7525
                19 January 2021
                19 January 2021
                2021
                : 19
                : 23
                Affiliations
                [1 ]GRID grid.157868.5, ISNI 0000 0000 9961 060X, Pediatric and Congenital Cardiology Department, M3C Regional Reference CHD Centre, , University Hospital, ; 371 Avenue du Doyen Giraud, 34295 Montpellier, France
                [2 ]Pediatric Cardiology and Rehabilitation Unit, St-Pierre Institute, Palavas-Les-Flots, France
                [3 ]GRID grid.411175.7, ISNI 0000 0001 1457 2980, Pediatric and Congenital Cardiology Department, , M3C Regional Reference CHD Centre, Toulouse University Hospital, ; Toulouse, France
                [4 ]GRID grid.157868.5, ISNI 0000 0000 9961 060X, Epidemiology and Clinical Research Department, , University Hospital, ; Montpellier, France
                [5 ]GRID grid.121334.6, ISNI 0000 0001 2097 0141, Clinical Investigation Centre, INSERM–CIC 1411, , University of Montpellier, ; Montpellier, France
                [6 ]GRID grid.121334.6, ISNI 0000 0001 2097 0141, Department of General Medicine, , University of Montpellier, ; Montpellier, France
                [7 ]GRID grid.121334.6, ISNI 0000 0001 2097 0141, PhyMedExp, INSERM, CNRS, , University of Montpellier, ; Montpellier, France
                Author information
                http://orcid.org/0000-0003-3649-0294
                Article
                1668
                10.1186/s12955-021-01668-1
                7814637
                61ee0dda-7082-4ed7-98f8-4e1c1fd34ea6
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 31 July 2020
                : 4 January 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100005630, Société Française de Cardiologie;
                Award ID: Bourse Hélène de Marsan
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100009242, Direction de l’hospitalisation et de l’offre de Soins;
                Award ID: GIRCI-SOHO-APIRES-2017
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100005261, Centre Hospitalier Régional Universitaire de Montpellier;
                Award ID: AOI-2016
                Award Recipient :
                Categories
                Study Protocol
                Custom metadata
                © The Author(s) 2021

                Health & Social care
                transition,therapeutic education,congenital heart disease,quality of life,adolescent

                Comments

                Comment on this article