https://scholars.lib.ntu.edu.tw/handle/123456789/538952
標題: | Measuring knowledge of patients with congenital heart disease and their parents: Validity of the 'Leuven Knowledge Questionnaire for Congenital Heart Disease' | 作者: | HSIAO-LING YANG Chen Y.-C. JOU-KOU WANG BIH-SHYA GAU Chen C.-W. Moons P. |
公開日期: | 2012 | 卷: | 11 | 期: | 1 | 起(迄)頁: | 77-84 | 來源出版物: | European Journal of Cardiovascular Nursing | 摘要: | Background: Patients with congenital heart disease (CHD) and their parents need to have sufficient knowledge on their condition, treatment, medication, and preventive measures. The Leuven Knowledge Questionnaire for Congenital Heart Disease (LKQCHD) was developed to comprehensively measure the level of knowledge in patients with CHD. Aims: This study aimed to translate the LKQCHD into Chinese and to test its validity to be used in patients with CHD and their parents. Method: Questionnaire translation was guided by a three-step linguistic validation method. Evidence based on test content and on relation with other variables was obtained. For test content, we included five experts in CHD and research methods. Furthermore, the instrument was tested in 89 pairs of adolescents with CHD and their parents. Results: We found a high item-level content validity index (>0.78 in all except two items), high scale-level content validity index (>0.90), high free-marginal multirater Kappa (>0.75), and low average proportion of missing values (0.49% in adolescents; 0.51% in parents), showing an excellent content validity. The hypothesized positive correlations between parental knowledge and parental educational level and between patient's knowledge and patient's age, as well as the hypothesis that parents have more knowledge than their children, were confirmed. This provides validity evidence based on relation with other variables. Conclusions: The Chinese version of the LKQCHD is valid to assess the level of knowledge in patients with CHD and their parents. ? The European Society of Cardiology 2012. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84862640540&doi=10.1177%2f1474515111429662&partnerID=40&md5=cf2df4afc9b41c611760ceb83a7ded13 https://scholars.lib.ntu.edu.tw/handle/123456789/538952 |
ISSN: | 1474-5151 | DOI: | 10.1177/1474515111429662 | SDG/關鍵字: | adolescent; adult; article; child; Chinese; congenital heart disease; content validity; educational status; evidence based practice; female; human; knowledge; major clinical study; male; parent; patient assessment; priority journal; questionnaire; school child; validation study; Asian; attitude to health; child psychology; congenital heart malformation; ethnology; language; psychological aspect; questionnaire; reproducibility; standard; Adolescent; Adolescent Psychology; Adult; Asian Continental Ancestry Group; Evidence-Based Practice; Health Knowledge, Attitudes, Practice; Heart Defects, Congenital; Humans; Language; Parents; Questionnaires; Reproducibility of Results |
顯示於: | 醫學系 |
在 IR 系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。