So sánh phương pháp

	Thiết kế thử nghiệm Tiền kiểm-Hậu kiểm Thích ứng	Thử nghiệm đối chứng ngẫu nhiên thích ứng
Lĩnh vực	Thiết kế thí nghiệm	Thiết kế thí nghiệm
Họ	Process / pipeline	Process / pipeline
Năm ra đời	2000s (integration of adaptive principles with classic pre-post structure)	1980s–2000s (formalized; earlier sequential testing roots from Wald, 1947)
Người khởi xướng	Synthesizes Campbell & Stanley (1963) pretest-posttest framework with adaptive design methodology formalized by Chow & Chang (2000s)	Donald Berry and others; foundational adaptive trial methods developed through 1980s–2000s biostatistics literature
Loại	Experimental design	Experimental design — adaptive variant of RCT
Công trình gốc	Campbell, D. T., & Stanley, J. C. (1963). Experimental and Quasi-Experimental Designs for Research. Rand McNally.	Chow, S.-C., & Chang, M. (2008). Adaptive Design Methods in Clinical Trials. Chapman & Hall/CRC. ISBN: 978-1584887690
Tên gọi khác	adaptive pre-post design, adaptive pretest-posttest trial, adaptive two-period design, pre-post adaptive experiment	Adaptive RCT, Response-adaptive RCT, Adaptive clinical trial, Platform trial
Liên quan	6	6
Tóm tắt	An adaptive pretest-posttest experimental design measures all participants before and after an intervention while allowing pre-specified modifications to the trial — such as sample size re-estimation, treatment arm dropping, or randomization ratio adjustment — based on accumulated interim data. It combines the interpretive power of change-score analysis with the efficiency gains and ethical safeguards of adaptive methodology, making it particularly valuable in clinical, educational, and behavioral research where early data can inform better resource allocation.	An adaptive randomized controlled trial (adaptive RCT) is an experimental design in which pre-specified rules allow modifications to the trial while it is ongoing — such as changing allocation ratios, dropping underperforming arms, or stopping early for efficacy or futility — based on accumulating interim data. These adaptations are planned before the trial starts and governed by statistical rules to preserve Type I error control and validity.