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Випадкове контрольоване дослідження (ВКД)×Адаптивний дизайн клінічних випробувань×
ГалузьПланування експериментуПланування експерименту
РодинаHypothesis testHypothesis test
Рік появи19481994
Автор методуJames Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948)Bauer & Köhne
ТипInterventional comparative studyAdaptive hypothesis test with interim analyses
Основоположне джерелоSchulz, K.F., Altman, D.G., Moher, D., for the CONSORT Group (2010). CONSORT 2010 Statement: Updated Guidelines for Reporting Parallel Group Randomised Trials. BMJ, 340, c332. DOI ↗Bauer, P. & Köhne, K. (1994). Evaluation of Experiments with Adaptive Interim Analyses. Biometrics, 50(4), 1029–1041. DOI ↗
Інші назвиRCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımıadaptive design, group sequential design, sample size re-estimation, platform trial
Пов'язані73
ПідсумокA randomized controlled trial (RCT) is the gold standard experimental design in clinical and health research, in which participants are randomly allocated to a treatment group or a control group so that the effect of an intervention can be measured with the highest possible degree of internal validity. The modern parallel-group RCT was formalized by Austin Bradford Hill and the Medical Research Council in their landmark streptomycin trial of 1948, and its reporting is governed today by the CONSORT 2010 guidelines (Schulz et al., 2010).Adaptive clinical trial design is a flexible experimental framework, formalised by Bauer and Köhne in 1994, in which pre-specified rules allow the trial to be modified mid-course — adjusting sample size, treatment arms, or randomisation ratios — based on accumulating interim data while rigorously controlling the Type I error rate.
ScholarGateНабір даних
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  3. PUBLISHED
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ScholarGateПорівняння методів: Randomized Controlled Trial · Adaptive Clinical Trial Design. Отримано 2026-06-17 з https://scholargate.app/uk/compare