Salīdzināt metodes

	Vienkāršots A/B testēšanas kontrolēts eksperiments ar dalībnieku aklumu	Eksperiments ar vairākām grupām
Nozare	Eksperimentu plānošana	Eksperimentu plānošana
Saime	Process / pipeline	Process / pipeline
Izcelsmes gads	mid-20th century (blinded RCT framework); A/B test nomenclature ~1990s–2000s	1990s–2000s (clinical formalization); multi-arm concept implicit in ANOVA-era factorial designs
Autors	Fisher, R. A. (randomisation basis); blinding practice formalised in clinical trials mid-20th century	Developed within clinical trials methodology; formalized by Parmar, Royston and colleagues (UK MRC CTU, early 2000s)
Tips	Controlled experiment with partial blinding	Experimental design
Pirmavots	Kohavi, R., Tang, D., & Xu, Y. (2020). Trustworthy Online Controlled Experiments: A Practical Guide to A/B Testing. Cambridge University Press. ISBN: 978-1108724265	Royston, P., Parmar, M. K. B., & Qian, W. (2003). Novel designs for multi-arm clinical trials with survival outcomes with an application in ovarian cancer. Statistics in Medicine, 22(14), 2239–2256.
Citi nosaukumi	single-masked A/B test, single-blind split test, blinded two-condition experiment, participant-blind A/B test	multi-arm trial, multiple-arm experiment, multi-group experiment, many-arm design
Saistītās	6	5
Kopsavilkums	A single-blind A/B test is a controlled two-condition experiment in which participants are randomised to condition A (control) or condition B (treatment) but are kept unaware of which condition they have received, while researchers and analysts remain aware. The blind prevents participants from changing their behaviour in response to knowledge of their assignment, reducing demand characteristics and response bias while still allowing the investigator to monitor the trial.	A multi-arm experiment simultaneously compares three or more treatment or intervention conditions — each called an arm — against a shared control or against one another. By testing multiple alternatives in a single study, it yields more information per participant than running separate two-group experiments sequentially, while controlling the overall Type I error rate through pre-specified comparison strategies.