Comparer des méthodes

	Expérience factorielle fractionnaire croisée	Expérience factorielle complète par croisement
Domaine	Plans d'expériences	Plans d'expériences
Famille	Process / pipeline	Process / pipeline
Année d'origine	1950s–1970s (fractional factorial from 1940s; crossover integration from 1960s–1970s)	Mid-to-late 20th century (crossover trials formalised ~1960s–1980s; full factorial DoE from Fisher ~1935)
Auteur d'origine	Box, Hunter & Hunter (fractional factorial); Senn & Williams (crossover integration)	Developed within the design-of-experiments tradition (R. A. Fisher and successors); crossover adaptation formalised by B. Jones and M. G. Kenward
Type	Within-subject multi-factor experimental design	Within-subject full factorial experimental design
Source fondatrice	Senn, S. (2002). Cross-over Trials in Clinical Research (2nd ed.). Wiley. ISBN: 978-0471496533	Jones, B., & Kenward, M. G. (2003). Design and Analysis of Cross-Over Trials (2nd ed.). Chapman and Hall/CRC. ISBN: 978-1584883429
Alias	crossover FF design, within-subject fractional factorial, repeated-measures fractional factorial, crossover FFE	within-subject full factorial design, repeated-measures full factorial experiment, crossover factorial trial, full factorial crossover design
Apparentées	5	6
Résumé	A crossover fractional factorial experiment is a within-subject design in which each participant receives a strategically chosen subset of all possible factor-level combinations in a defined sequence, with washout periods between treatment periods. By combining the run-economy of fractional factorial designs with the within-subject efficiency of crossover designs, it allows estimation of main effects and selected interactions while controlling for between-subject variability using far fewer participants and experimental runs than a full factorial crossover.	A crossover full factorial experiment combines the efficiency of a crossover (within-subject) design with the comprehensiveness of a full factorial design. Every participant receives all combinations of the factor levels across successive treatment periods, separated by washout intervals, allowing complete estimation of all main effects and interactions while using each participant as their own control.