方法对比
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| 受阻实验室实验× | 随机对照试验 (RCT)× | |
|---|---|---|
| 领域 | 实验设计 | 实验设计 |
| 方法族≠ | Process / pipeline | Hypothesis test |
| 起源年份≠ | 1926–1935 | 1948 |
| 提出者≠ | Ronald A. Fisher | James Lind (early precursor, 1747); modern formulation: Austin Bradford Hill & Medical Research Council (1948) |
| 类型≠ | Controlled experimental design with blocking | Interventional comparative study |
| 开创性文献≠ | Fisher, R. A. (1935). The Design of Experiments. Oliver and Boyd. link ↗ | 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 ↗ |
| 别名 | blocked lab experiment, laboratory randomized block design, RBD laboratory study, blocked within-lab experiment | RCT, randomised controlled trial, clinical trial, Randomize Kontrollü Çalışma (RCT) Tasarımı |
| 相关≠ | 5 | 7 |
| 摘要≠ | A blocked laboratory experiment is a controlled laboratory study in which experimental units are grouped into homogeneous blocks before treatment assignment, and treatments are then randomly assigned within each block. Blocking removes the influence of a known nuisance variable — such as participant batch, equipment run, or testing day — from the error term, increasing the precision of treatment comparisons without expanding sample size. | 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). |
| ScholarGate数据集 ↗ |
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