Порівняння методів
Переглядайте обрані методи поруч; рядки з відмінностями підсвічено.
| Пілотний дизайн ABA× | Пілотне рандомізоване контрольоване дослідження× | |
|---|---|---|
| Галузь | Планування експерименту | Планування експерименту |
| Родина | Process / pipeline | Process / pipeline |
| Рік появи≠ | 1960s (ABA design); pilot adaptation in clinical and behavioral research from 1980s onward | 1990s–2000s (methodological formalization) |
| Автор методу≠ | Murray Sidman (ABA reversal logic); pilot study methodology broadly attributed to clinical trial traditions | Formalized through clinical trials methodology community |
| Тип≠ | Single-subject experimental pilot design | Experimental feasibility design |
| Основоположне джерело≠ | Sidman, M. (1960). Tactics of Scientific Research: Evaluating Experimental Data in Psychology. Basic Books. link ↗ | 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 ↗ |
| Інші назви | Pilot ABA reversal design, Pilot withdrawal design, Pilot single-subject reversal design, Feasibility ABA design | pilot RCT, feasibility RCT, pilot trial, preliminary RCT |
| Пов'язані≠ | 6 | 5 |
| Підсумок≠ | The Pilot ABA Design is a small-scale single-subject experiment that applies the ABA reversal structure — baseline, intervention, withdrawal — to test the feasibility, acceptability, and preliminary effect of an intervention before committing to a full-scale study. It provides early evidence of whether the treatment produces a detectable change and whether the reversal is ethically and practically achievable. | 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. |
| ScholarGateНабір даних ↗ |
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