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| Pilot fraktioneret faktorielt eksperiment× | Pilot Randomiseret Kontrolleret Forsøg× | |
|---|---|---|
| Fagområde | Forsøgsdesign | Forsøgsdesign |
| Familie | Process / pipeline | Process / pipeline |
| Oprindelsesår≠ | 1950s–1960s (fractional factorial foundation); pilot study integration formalized in 20th century DOE practice | 1990s–2000s (methodological formalization) |
| Ophavsperson≠ | Box, Hunter & Hunter (fractional factorial); pilot study concept developed broadly in industrial and clinical experimentation | Formalized through clinical trials methodology community |
| Type≠ | Experimental screening design (pilot phase) | Experimental feasibility design |
| Oprindelig kilde≠ | Montgomery, D. C. (2017). Design and Analysis of Experiments (9th ed.). Wiley. ISBN: 978-1119492443 | Thabane, L., Ma, J., Chu, R., Cheng, J., Ismaila, A., Rios, L. P., ... & Goldsmith, C. H. (2010). A tutorial on pilot studies: the what, why and how. BMC Medical Research Methodology, 10(1), 1. DOI ↗ |
| Aliasser | pilot FFE, screening pilot design, pilot fractional factorial, pilot FF screening study | pilot RCT, feasibility RCT, pilot trial, preliminary RCT |
| Relaterede | 5 | 5 |
| Resumé≠ | A pilot fractional factorial experiment is a small-scale preliminary study that uses a fractional factorial design — testing only a subset of all possible factor combinations — to screen multiple factors simultaneously before committing to a full-scale investigation. It provides early estimates of effect sizes, variance, and feasibility at substantially reduced cost and participant burden compared to a full factorial pilot or a full-scale trial. | A pilot randomized controlled trial (pilot RCT) is a small-scale, fully randomized experiment conducted before a definitive RCT to test the feasibility of study procedures, estimate key parameters such as recruitment rates and effect-size variability, and identify practical barriers. It uses the same randomization, intervention, and measurement protocol as the planned full trial but on a fraction of the target sample. The goal is not to confirm efficacy but to refine and justify the main trial design. |
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