Abstract
Purpose
The Questionnaire – Children with Difficulties (QCD) has been developed and used to evaluate daily-life problems in children during specified periods of the day. The objective of this study was to evaluate the reliability and validity of the QCD for Chinese children or adolescents with attention-deficit/hyperactivity disorder (ADHD).
Patients and methods
Outpatients with ADHD aged 6–18 years who visited psychiatry clinics were enrolled at four study centers in China. Patients with severe psychiatric disorders were excluded. Parents of all enrolled patients were given the QCD, the Swanson, Nolan and Pelham IV (SNAP-IV), and the Weiss Functional Impairment Scale-Parent (WFIRS-P) questionnaires and were asked to complete all three questionnaires. The reliability of the QCD was examined by Cronbach’s alpha, which assessed the internal consistency of the questionnaire. Concurrent criterion validity of QCD scores was examined by Spearman’s correlation of QCD with SNAP-IV and WFIRS-P scores.
Results
A total of 200 Chinese patients were analyzed (average age, 10.4±2.66 years). The majority of patients were male (77.5%), and 49.0% had the combined ADHD subtype. Cronbach’s alpha for QCD was 0.88. Correlation coefficients of the QCD total score with SNAP-IV total score and WFIRS-P average score were −0.47 and −0.57, respectively. Correlations for the QCD with SNAP-IV and WFIRS-P were statistically significant (P<0.01). The area under the curve for sensitivity and specificity of the QCD compared with the SNAP-IV and WFIRS-P was 0.70 and 0.71, respectively. The ADHD severity discrimination threshold range of the QCD total score was 30–35.
Conclusion
Our study results found the QCD to be a reliable and valid instrument and recommend its use in clinical practice to identify and evaluate daily-life problems of ADHD patients during specified periods of the day in China.
Acknowledgments
This study was funded and supported by Eli Lilly and Company. The authors would like to thank Rakesh Ojha, PhD, from Syneos Health for medical writing, and Antonia Baldo from Syneos Health for editorial support in the preparation of this manuscript. The authors would also like to thank Wan Qi Zhao from Eli Lilly and Company for project management, and Wendong Chen and Yi Chen from Changsha Normin Medical Technology Ltd., for assistance in the project operational processes, data cleanup, and project management.
Author contributions
Yi Zheng, Yasong Du, Lin Yan Su, and Xiao Yan Ke contributed to the study design, data collection and analysis, and critical revision of the manuscript. Yanlei Zhang, Zheng Yuan, and Yun Chen contributed to the study design, data management, analysis, interpretation, and critical revision of the manuscript. Qing Liu contributed to the data management, analysis, interpretation, and critical revision of the manuscript. All authors contributed toward data analysis, drafting and revising the paper and agree to be accountable for all aspects of the work.
Disclosure
Yanlei Zhang, Zheng Yuan, Yun Chen, and Qing Liu are employees of Eli Lilly and Company. The other authors report no conflicts of interest in this work.