Porovnať metódy
Prezrite si vybrané metódy vedľa seba; riadky, ktoré sa líšia, sú zvýraznené.
| Klastrový randomizovaný viacramenný experiment× | Cluster Randomized Controlled Trial× | |
|---|---|---|
| Odbor | Plánovanie experimentov | Plánovanie experimentov |
| Rodina | Process / pipeline | Process / pipeline |
| Rok vzniku≠ | 1990s–2000s (systematic formalization) | 1978–1980s |
| Tvorca≠ | Building on cluster randomization (Donner & Klar) and multi-arm trial methods developed in clinical and public health research | Cornfield (1978); systematised by Donner and colleagues (1980s) |
| Typ | Experimental design | Experimental design |
| Pôvodný zdroj | Donner, A., & Klar, N. (2000). Design and Analysis of Cluster Randomization Trials in Health Research. Arnold. ISBN: 978-0340691533 | Donner, A., & Klar, N. (2000). Design and Analysis of Cluster Randomization Trials in Health Research. Arnold. ISBN: 978-0340652978 |
| Ďalšie názvy | multi-arm cluster RCT, cluster-randomized multi-group trial, multi-arm group-randomized trial, CRCT multi-arm | cluster RCT, group-randomized trial, community randomized trial, cluster-randomized experiment |
| Príbuzné≠ | 6 | 4 |
| Zhrnutie≠ | A cluster randomized multi-arm experiment assigns intact groups — such as schools, clinics, or villages — rather than individuals to three or more experimental conditions simultaneously. Randomization occurs at the cluster level to prevent contamination between arms, while the multi-arm structure allows simultaneous evaluation of several interventions against a common control or each other, improving efficiency over a series of two-arm studies. | 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. |
| ScholarGateDátová sada ↗ |
|
|