Compara mètodes
Revisa els mètodes seleccionats l'un al costat de l'altre; les files que difereixen es ressalten.
| Experiment de camp amb disseny crossover× | Experiment de laboratori amb disseny creuat× | |
|---|---|---|
| Camp | Disseny experimental | Disseny experimental |
| Família | Process / pipeline | Process / pipeline |
| Any d'origen≠ | 1960s–1970s (field experiment framework); crossover application in non-clinical fields from 1980s onward | Mid-20th century; consolidated 1980s–2000s |
| Autor original≠ | Crossover design principles attributed to R. A. Fisher (1930s); field experiment tradition developed by Donald T. Campbell and Julian Stanley (1960s) | Established in pharmacological and behavioral research; Jones & Kenward formalized the framework |
| Tipus≠ | Within-subject experimental design conducted in naturalistic settings | Within-subjects experimental design |
| Font seminal≠ | Senn, S. (2002). Cross-over Trials in Clinical Research (2nd ed.). John Wiley & Sons. ISBN: 978-0471496533 | Jones, B., & Kenward, M. G. (2014). Design and Analysis of Cross-Over Trials (3rd ed.). CRC Press. ISBN: 978-1439861424 |
| Àlies | within-subject field experiment, crossover field trial, repeated-measures field experiment, field crossover design | within-subjects crossover lab study, repeated-measures crossover experiment, crossover controlled lab experiment, within-person laboratory crossover trial |
| Relacionats | 5 | 5 |
| Resum≠ | A crossover field experiment is a within-subject experimental design conducted outside the laboratory in naturalistic, real-world settings. Each participant or unit receives multiple treatments in a randomized sequence, separated by washout periods, allowing researchers to observe causal effects while each unit serves as its own control. This approach combines the internal validity of crossover designs with the ecological validity characteristic of field experimentation. | A crossover laboratory experiment is a within-subjects experimental design conducted in a controlled lab environment in which each participant receives two or more treatments sequentially, serving as their own control. By eliminating between-person variability from the error term, it yields high statistical power with relatively small samples. Treatment order is randomized or counterbalanced across participants to guard against order and carryover effects. |
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