So sánh phương pháp
Xem các phương pháp đã chọn cạnh nhau; những hàng khác biệt được làm nổi bật.
| Thí nghiệm thực địa thích ứng× | Nghiên cứu đối chứng ngẫu nhiên (RCT)× | |
|---|---|---|
| Lĩnh vực | Thiết kế thí nghiệm | Thiết kế thí nghiệm |
| Họ≠ | Process / pipeline | Hypothesis test |
| Năm ra đời≠ | 1990s–2000s (formalized in field economics and development research contexts) | 1948 |
| Người khởi xướng≠ | Developed at the intersection of adaptive trial methodology (Berry, Bauer) and field experimentation (Duflo, Kremer, List) | James Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948) |
| Loại≠ | Adaptive experimental design conducted in naturalistic settings | Interventional comparative study |
| Công trình gốc≠ | Berry, D. A. (2004). Bayesian statistics and the efficiency and ethics of clinical trials. Statistical Science, 19(1), 175–187. DOI ↗ | Schulz, 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 ↗ |
| Tên gọi khác | adaptive field trial, sequentially adaptive field experiment, responsive field experiment, adaptive randomized field study | RCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımı |
| Liên quan≠ | 6 | 7 |
| Tóm tắt≠ | An adaptive field experiment is a randomized study conducted in a real-world environment in which pre-specified decision rules allow the researcher to modify the trial as interim data accumulate — for example, by reallocating participants toward more effective arms, adjusting sample size, or stopping early for efficacy or futility — all while maintaining statistical integrity. | A 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). |
| ScholarGateBộ dữ liệu ↗ |
|
|