Porovnat metody
Prohlédněte si vybrané metody vedle sebe; řádky, které se liší, jsou zvýrazněny.
| Cluster Randomized Factorial Experiment× | Klastrově randomizovaná kontrolovaná studie× | |
|---|---|---|
| Obor | Plánování experimentů | Plánování experimentů |
| Rodina | Process / pipeline | Process / pipeline |
| Rok vzniku≠ | 1990s (formalized in group-randomized trial literature) | 1978–1980s |
| Tvůrce≠ | David M. Murray and colleagues; Allan Donner & Neil Klar | Cornfield (1978); systematised by Donner and colleagues (1980s) |
| Typ | Experimental design | Experimental design |
| Původní zdroj≠ | Murray, D. M. (1998). Design and Analysis of Group-Randomized Trials. Oxford University Press. ISBN: 978-0195120912 | Donner, A., & Klar, N. (2000). Design and Analysis of Cluster Randomization Trials in Health Research. Arnold. ISBN: 978-0340652978 |
| Další názvy | cluster-randomized factorial design, group-randomized factorial trial, CRT factorial, clustered factorial experiment | cluster RCT, group-randomized trial, community randomized trial, cluster-randomized experiment |
| Příbuzné≠ | 5 | 4 |
| Shrnutí≠ | A cluster randomized factorial experiment assigns intact groups (clusters such as schools, clinics, or communities) at random to all combinations of two or more treatment factors, enabling simultaneous evaluation of multiple interventions and their interactions while respecting the natural grouping of participants. It merges the logistical and ethical advantages of cluster randomization with the efficiency of factorial design. | A cluster randomized controlled trial (cluster RCT) is an experimental design in which intact social or organisational groups — such as schools, clinics, villages, or workplaces — are randomly assigned to treatment conditions rather than individual participants. Outcomes are still measured at the individual level, but the unit of randomization is the cluster. This design is essential when an intervention is delivered to whole groups, when there is a risk of contamination between participants in the same setting, or when individual randomization is logistically or ethically impractical. |
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