Compara mètodes
Revisa els mètodes seleccionats l'un al costat de l'altre; les files que difereixen es ressalten.
| Assaig controlat aleatori amb blocs (blocked RCT)× | Assaig controlat aleatori (RCT) adaptatiu× | |
|---|---|---|
| Camp | Disseny experimental | Disseny experimental |
| Família | Process / pipeline | Process / pipeline |
| Any d'origen≠ | 1920s (Fisher's blocking principle); applied to RCTs from the 1940s onward | 1980s–2000s (formalized; earlier sequential testing roots from Wald, 1947) |
| Autor original≠ | R. A. Fisher (blocking principle); systematic RCT application by Bradford Hill and later Pocock, Friedman et al. | Donald Berry and others; foundational adaptive trial methods developed through 1980s–2000s biostatistics literature |
| Tipus≠ | Experimental design | Experimental design — adaptive variant of RCT |
| Font seminal≠ | Friedman, L. M., Furberg, C. D., DeMets, D. L., Reboussin, D. M., & Granger, C. B. (2010). Fundamentals of Clinical Trials (4th ed.). Springer. ISBN: 978-1441915856 | Chow, S.-C., & Chang, M. (2008). Adaptive Design Methods in Clinical Trials. Chapman & Hall/CRC. ISBN: 978-1584887690 |
| Àlies | blocked RCT, block-randomized trial, stratified block randomization trial, permuted block randomization | Adaptive RCT, Response-adaptive RCT, Adaptive clinical trial, Platform trial |
| Relacionats≠ | 5 | 6 |
| Resum≠ | A blocked randomized controlled trial (blocked RCT) uses permuted-block randomization to ensure that treatment groups remain balanced in size — and optionally in key characteristics — throughout recruitment. Within each block of fixed or randomly varied size, all treatment allocations are present in equal numbers, so imbalance cannot accumulate even if the trial is stopped early. This makes blocked RCTs the standard randomization approach in clinical and behavioral intervention research. | 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. |
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