Registry-Based Research
Registry-based research uses systematically collected clinical data from patient registries—organized databases of patients with a specific disease or condition—to conduct observational studies. Registries began in the mid-20th century but have proliferated since the 2000s as electronic health records expanded and funding agencies recognized their value for real-world evidence generation. Registry studies provide large, diverse, representative populations without the cost of recruiting and following prospectively, enabling rapid generation of clinical evidence.
Catatan sumber
Kutipan disalin apa adanya dari catatan sumber metode. Tidak ada verifikasi tingkat klaim yang disimpulkan darinya.
- Gini, R., Francesconi, P., Mazzaglia, G., Brignoli, G., Cricelli, C., Lapi, F., & Cricelli, A. (2020). Chronic disease prevalence from Italian administrative databases: the PREVALENTIST study. BMC Public Health, 13, 191. · URL
- Hoque, D. M. E., Ruseckaite, R., Braithwaite, J., & Ting, H. P. (2017). Quality of life measurement in patients with Parkinson's disease: a systematic review of generic and disease-specific instruments and their clinimetric properties. Quality of Life Research, 26(8), 2117–2130. · URL
- Ikehara, S., Iso, H., Yamagishi, K., Yamagishi, K., Maruyama, K., & Inoue, M. (2016). Healthy lifestyle and life expectancy among Japanese adults: findings from the JPHC study. Journal of Epidemiology, 26(2), 88–97. · URL
Klaim yang dikurasi
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Metode terkait
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