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The use of a sequence of experiments, where the design of each may depend on the results of previous experiments, including the possible decision to stop experimenting, is within the scope of sequential analysis, a field that was pioneered [12] by Abraham Wald in the context of sequential tests of statistical hypotheses. [13]
The choice of how to group participants depends on the research hypothesis and on how the participants are sampled.In a typical experimental study, there will be at least one "experimental" condition (e.g., "treatment") and one "control" condition ("no treatment"), but the appropriate method of grouping may depend on factors such as the duration of measurement phase and participant ...
The Design of Experiments is a 1935 book by the English statistician Ronald Fisher about the design of experiments and is considered a foundational work in experimental design. [2] [3] [4] Among other contributions, the book introduced the concept of the null hypothesis in the context of the lady tasting tea experiment. [5]
A way to design psychological experiments using both designs exists and is sometimes known as "mixed factorial design". [3] In this design setup, there are multiple variables, some classified as within-subject variables, and some classified as between-group variables. [3] One example study combined both variables.
The researcher attempts to describe accurately the interaction between the instrument (or the human senses) and the entity being observed.If instrumentation is involved, the researcher is expected to calibrate his/her instrument by applying it to known standard objects and documenting the results before applying it to unknown objects.
When a manipulation creates significant differences between experimental conditions in both (1) the dependent variable and (2) the measured manipulation check variable, the interpretation is that (1) the manipulation "causes" variation in the dependent variable (the "effect") and (2) the manipulation also explains variation in some other, more ...
There are several methods of finding an optimal design, given an a priori restriction on the number of experimental runs or replications. Some of these methods are discussed by Atkinson, Donev and Tobias and in the paper by Hardin and Sloane. Of course, fixing the number of experimental runs a priori would be impractical. Prudent statisticians ...
A clinical control group can be a placebo arm or it can involve an old method used to address a clinical outcome when testing a new idea. For example in a study released by the British Medical Journal, in 1995 studying the effects of strict blood pressure control versus more relaxed blood pressure control in diabetic patients, the clinical control group was the diabetic patients that did not ...