Methoden vergelijken
Bekijk de geselecteerde methoden naast elkaar; rijen die verschillen zijn gemarkeerd.
| Experimenteel enkelvoudig-geval pilotontwerp× | Pilot Randomized Controlled Trial× | |
|---|---|---|
| Vakgebied | Experimenteel ontwerp | Experimenteel ontwerp |
| Familie | Process / pipeline | Process / pipeline |
| Jaar van ontstaan≠ | 2000s–2010s (as an explicitly named piloting strategy for SSED) | 1990s–2000s (methodological formalization) |
| Grondlegger≠ | Derived from single-subject experimental design traditions (Sidman, 1960; Kazdin) and pilot study methodology (Lancaster, Dodd, Williamson, 2004; Thabane et al., 2010) | Formalized through clinical trials methodology community |
| Type≠ | Pilot experimental design | Experimental feasibility design |
| Oorspronkelijke bron | 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 ↗ | 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 ↗ |
| Aliassen | pilot SSED, pilot N-of-1 experiment, pilot single-case experimental design, pilot SCED | pilot RCT, feasibility RCT, pilot trial, preliminary RCT |
| Verwant≠ | 6 | 5 |
| Samenvatting≠ | A pilot single-subject experimental design (pilot SSED) is a small-scale feasibility trial applied to one or very few individuals, combining the repeated-measurement logic of single-subject experimental design with the explicit preparatory aims of a pilot study. It is used to test an intervention protocol, measurement procedures, and design logistics before committing to a full-scale single-case or group experiment. | 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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