Methoden vergelijken
Bekijk de geselecteerde methoden naast elkaar; rijen die verschillen zijn gemarkeerd.
| Adaptief Veldexperiment× | Gerandomiseerde gecontroleerde studie (RCT)× | |
|---|---|---|
| Vakgebied | Experimenteel ontwerp | Experimenteel ontwerp |
| Familie≠ | Process / pipeline | Hypothesis test |
| Jaar van ontstaan≠ | 1990s–2000s (formalized in field economics and development research contexts) | 1948 |
| Grondlegger≠ | 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) |
| Type≠ | Adaptive experimental design conducted in naturalistic settings | Interventional comparative study |
| Oorspronkelijke bron≠ | 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 ↗ |
| Aliassen | 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 |
| Verwant≠ | 6 | 7 |
| Samenvatting≠ | 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). |
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