######################################## ## LIBRARIES ######################################## library(TAM) library(doMC) library(parallel) library(pbmcapply) ####################################### ## ANALYSIS FUNCTIONS ####################################### pcm_analysis <- function(df=NULL,treatment='TT',irtmodel='PCM2',method='MML') { nbitems <- sum(sapply(1:20,function(x) paste0('item',x)) %in% colnames(df)) resp <- df[,sapply(seq(1,nbitems),function(x) paste0('item',x))] if (method=='MML') { tam1 <- tam.mml(resp=resp,Y=df[,treatment],irtmodel = irtmodel,est.variance = T,verbose=F) } if (method=='JML') { tam1 <- tam.jml(resp=resp,group=1+df[,treatment]) } if (method!='MML' & method!='JML') { stop('Invalid method. Please choose among MML or JML') } return(tam1) } replicate_pcm_analysis <- function(df=NULL,treatment='TT',irtmodel='PCM2',method='MML',sequence='replication',truebeta=0,eff.size=0,difsize=NA,nbdif=0) { nbitems <- sum(sapply(1:20,function(x) paste0('item',x)) %in% colnames(df)) resp <- df[,sapply(seq(1,nbitems),function(x) paste0('item',x))] if (method=='MML') { n <- max(df[,sequence]) print(n) tam1 <- pbmclapply(seq(1,n), function(x) pcm_analysis(df=df[df[,sequence]==x,],treatment=treatment,irtmodel=irtmodel) ) } listitems <- sapply(seq(1,nbitems),function(x) paste0('item',x)) returndat <- data.frame(matrix(nrow=max(df[,sequence]),ncol=length(listitems))) colnames(returndat) <- listitems for (s in seq(1,max(df[,sequence]))) { for (k in seq(1,nbitems)) { returndat[s,paste0('item',k)] <- tam1[[s]]$xsi$xsi[k] } } returndat$beta <- sapply(seq(1,max(df[,sequence])),function(k) tam1[[k]]$beta[2]) returndat$se.beta <- 1.413612*sapply(seq(1,max(df[,sequence])),function(k) tam.se(tam1[[k]])$beta$se.Dim1[2] ) returndat$low.ci.beta <- returndat$beta-1.96*returndat$se.beta returndat$high.ci.beta <- returndat$beta+1.96*returndat$se.beta returndat$true.value.in.ci <- 1*(truebeta>returndat$low.ci.beta & truebetareturndat$low.ci.beta & 0