Сравнение методов

	Экспериментальный дизайн с пилотной контрольной группой	Пилотное рандомизированное контролируемое исследование
Область	Планирование эксперимента	Планирование эксперимента
Семейство	Process / pipeline	Process / pipeline
Год появления	Mid-20th century; widely formalized by 1980s–2000s	1990s–2000s (methodological formalization)
Автор метода	Established through clinical and behavioral research traditions; formalized by Bradford Hill and colleagues in mid-20th century trial methodology	Formalized through clinical trials methodology community
Тип	Experimental design (pilot/feasibility variant)	Experimental feasibility design
Основополагающий источник	Thabane, L., Ma, J., Chu, R., Cheng, J., Ismaila, A., Rios, L. P., Robson, R., Thabane, M., Giangregorio, L., & Goldsmith, C. H. (2010). A tutorial on pilot studies: the what, why and how. BMC Medical Research Methodology, 10, 1.	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.
Другие названия	pilot controlled experiment, pilot RCT feasibility study, small-scale controlled trial, pilot control group study	pilot RCT, feasibility RCT, pilot trial, preliminary RCT
Связанные	4	5
Сводка	A pilot control group experimental design is a small-scale, preliminary experiment that includes both a treatment group and a control group, conducted before the main study to test whether the full trial is feasible. It produces early effect-size estimates, identifies protocol problems, and confirms that random (or systematic) assignment to conditions is workable — all while generating a genuine comparison between treated and untreated participants.	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.