| Literature DB >> 25657634 |
Abstract
Linear mixed-effects models (LMMs) are increasingly being used for data analysis in cognitive neuroscience and experimental psychology, where within-participant designs are common. The current article provides an introductory review of the use of LMMs for within-participant data analysis and describes a free, simple, graphical user interface (LMMgui). LMMgui uses the package lme4 (Bates et al., 2014a,b) in the statistical environment R (R Core Team).Entities:
Keywords: R; experimental psychology; graphical user interface; linear mixed-effects models; within-participant design
Year: 2015 PMID: 25657634 PMCID: PMC4302710 DOI: 10.3389/fpsyg.2015.00002
Source DB: PubMed Journal: Front Psychol ISSN: 1664-1078
Figure 1Reaction times (RT) in ms as a function of telephone sound level in dB SPL during a hypothetical telephone-ringing detection experiment. Each panel represents a different listener (L1–L9) and each line represents a different language of the concurrent speech (see legend in panel of L1). RT decreases with increasing sound level, and the gradient of this function (“slope”) is correlated with the RT at 0 dB (true “intercept” is not shown), which varies between listeners.
Figure 2Example windows of LMMgui. Once a data file has been selected, the user is requested to classify the variables using the top window. In this hypothetical example (see Equation 1), the variables are classified as follows: “RT” is the response variable, “Listener” is the participant variable (random factor) and “Level” (sound level) is a continuous fixed covariate. Any variables which are not classified by radio-button or check box are treated as discrete fixed factors: in this example, “Language.” Once variables have been classified, the next step is model specification (middle window). Users select which terms to include in two models by checking items in the drop down menu. The results of the models fits and comparison are available from the results (bottom) window. The user can inspect a summary of each model, diagnostic plots (fitted vs. residual plot and histogram of normality of residuals), and the result of the model comparison (shown). File format details, prerequisites, and output files are described in the Appendix.