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| Børnesundhedsspørgeskema (CHQ)× | Livskvalitet ved barndomsepilepsi (QOLCE)× | |
|---|---|---|
| Fagområde | Pædiatri | Pædiatri |
| Familie | Process / pipeline | Process / pipeline |
| Oprindelsesår≠ | 1996 | 2000 |
| Ophavsperson≠ | John M. Landgraf | Mark Sabaz |
| Type≠ | Parent report (primary) and child self-report versions available | Parent report; child self-report version available |
| Oprindelig kilde≠ | Landgraf, J. M., Abetz, L., & Ware, J. E. (1996). The CHQ User's Manual. HealthAct. ISBN: 978-0965475303 | Sabaz, M., Cairns, D. R., Lah, S., Williams, B., Gurrin, L., Connelly, A., & Berkovic, S. F. (2000). Validation of the Quality of Life in Childhood Epilepsy Questionnaire in Australian children with newly diagnosed and chronic epilepsy. Neurology, 55(9), 1646-1652. DOI ↗ |
| Aliasser≠ | CHQ-50, CHQ-28, CHQ-PF28, CHQ-CF87 | QOL in Childhood Epilepsy Questionnaire |
| Relaterede | 4 | 4 |
| Resumé≠ | The Child Health Questionnaire is a generic, parent-reported instrument developed by Landgraf et al. in 1996 to measure health-related quality of life in children aged 5–18 years. Unlike disease-specific measures, the CHQ captures broad domains of physical, emotional, social, and school functioning, making it suitable for diverse pediatric populations with or without chronic conditions. The CHQ-50 is the most widely used parent-report form; shorter (CHQ-28) and comprehensive (CHQ-CF87 child + family) versions are also available. | The QOLCE is a comprehensive 76-item disease-specific instrument developed by Sabaz et al. in 2000 to assess quality of life in children with epilepsy aged 4–16 years. Measuring across 16 distinct domains including seizure worry, cognitive concerns, medication effects, school/peer functioning, and family impact, the QOLCE provides a nuanced profile of how epilepsy and its treatment affect daily life. It exists in parent-report (QOLCE-P) and child self-report (QOLCE-C) versions. |
| ScholarGateDatasæt ↗ |
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