方法对比
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| PedsQL 镰状细胞病模块× | 儿童哮喘生活质量问卷 (PAQLQ)× | |
|---|---|---|
| 领域 | 儿科学 | 儿科学 |
| 方法族 | Process / pipeline | Process / pipeline |
| 起源年份≠ | 2012 | 1996 |
| 提出者≠ | James W. Varni | E. F. Juniper |
| 类型≠ | Child self-report and parent proxy | Child self-report; parent version available |
| 开创性文献≠ | Varni, J. W., Limbers, C. A., Bryant, W. P., & Wilson, D. P. (2012). The PedsQL in pediatric sickle cell disease: Measurement model, factor structure, and reliability and validity of the pediatric quality of life inventory sickle cell disease module. Journal of Health Psychology, 17(7), 1012-1024. link ↗ | Juniper, E. F., Guyatt, G. H., Feeny, D. H., Ferrie, P. J., Griffith, L. E., & Townsend, M. (1996). Measuring quality of life in children with asthma. Quality of Life Research, 5(1), 35-46. DOI ↗ |
| 别名 | PedsQL 3.0 Sickle Cell | PAQLQ-S |
| 相关 | 4 | 4 |
| 摘要≠ | The PedsQL Sickle Cell Disease Module is a disease-specific instrument developed by Varni et al. in 2012 to measure quality of life in children and adolescents with sickle cell disease aged 2–18 years. Measuring across domains including pain and symptoms, functional limitations, school impact, and disease-related worry, it captures how sickle cell disease and its complications affect daily life and well-being. Used alongside the PedsQL Generic Core Scales, it provides comprehensive assessment of sickle cell disease-specific and general health-related quality of life. | The PAQLQ is a 23-item self-report instrument developed by Juniper et al. in 1996 to measure quality of life in children aged 7–17 years with asthma. It assesses how asthma and its treatment affect daily functioning, emotions, and activity levels. The instrument has become the gold standard for evaluating asthma-specific health-related quality of life in pediatric populations. |
| ScholarGate数据集 ↗ |
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