--- title: "Scoring questionnaires" output: rmarkdown::html_vignette vignette: > %\VignetteIndexEntry{Scoring questionnaires} %\VignetteEngine{knitr::rmarkdown} %\VignetteEncoding{UTF-8} --- ```{r, include = FALSE} knitr::opts_chunk$set(collapse = TRUE, comment = "#>") ``` ```{r setup} library(colleyRstats) ``` Turning raw item columns into subscale scores is the most repeated step of a user study, and the one most able to be wrong without anything looking wrong. Every project re-implements the same reverse-coding and averaging by hand, and a single mis-numbered item changes every result downstream without producing a single error. `score_questionnaire()` applies a published instrument's own scoring key. ## What is available ```{r} list_questionnaires()[, c("key", "name", "n_items", "n_subscales", "scale")] ``` ## Scoring Point it at the item columns. A prefix is usually enough: ```{r} set.seed(1) study <- data.frame(participant = factor(1:8)) study[paste0("sus_", 1:10)] <- lapply(1:10, function(i) sample(1:5, 8, TRUE)) score_questionnaire(study, "sus", prefix = "sus_") ``` The SUS score is the sum of the ten recoded items times 2.5, which puts it on 0--100. That is a percentage of the maximum, **not** a percentile: the mean SUS across published studies is about 68, so 68 is average rather than poor. Every instrument's notes say this sort of thing, and `questionnaire_items()` prints them: ```{r} questionnaire_items("ueq_s") ``` ### Declaring the response range Instruments are administered on whatever scale the survey tool offered. Say which one you used and the responses are rescaled onto the instrument's own range before scoring: ```{r} tlx <- data.frame( mental = c(14, 3), physical = c(2, 1), temporal = c(11, 4), performance = c(6, 2), effort = c(13, 5), frustration = c(9, 1) ) # The 21-point NASA-TLX sheet, scored onto the conventional 0-100 score_questionnaire(tlx, "nasa_tlx", scale = c(1, 21)) ``` Responses outside the range you declare are an error rather than a silent rescale, which is what stops a 1--7 export from being scored as if it were the 0--100 TLX. ### Adding scores to the data ```{r} scored <- score_questionnaire(study, "sus", prefix = "sus_", append = TRUE) names(scored)[1:3] scored$SUS ``` ## Verify the mapping before you trust the scores This is the important part. Item numbers, item order and item polarity belong to the sheet a study actually administered, not to the instrument in the abstract. Survey tools renumber items, translations reorder them, short forms drop them from the middle, and semantic differentials get printed with the poles the other way round. This package applies each instrument's *published* key — the right default, and still only a default. `score_questionnaire()` maps your columns onto the instrument's items *positionally*, so a shifted export produces scores that look entirely reasonable and are wrong. Nothing errors when that happens, which is why R says it out loud: the first time each distinct mapping is scored in a session, the mapping and a caution print together. Read them rather than tuning them out, and double-check any number before it reaches a paper. Run this once per instrument, per study, and read what it prints: ```{r} invisible(check_questionnaire(study, "sus", prefix = "sus_")) ``` It shows which column supplies which item, which subscale that item loads on, whether it is reverse-coded, and the observed range of each column -- so a column of all-3s where you expected variation, or a 1--7 export where the instrument expects 1--5, is visible immediately. If your survey stored a pair the other way round, `reverse_items` toggles it. Naming an item that the key already reverses *un*-reverses it: ```{r} # A survey that anchored NASA-TLX performance "Good" at the high end scores <- score_questionnaire(tlx, "nasa_tlx", scale = c(1, 21), reverse_items = "performance" ) scores$Performance ``` A named `items` argument avoids positional mapping altogether, and is the safer choice for an export you did not lay out yourself: ```{r} score_questionnaire( tlx, "nasa_tlx", scale = c(1, 21), items = c( mental = "mental", physical = "physical", temporal = "temporal", performance = "performance", effort = "effort", frustration = "frustration" ) )$RTLX ``` ## Incomplete responses By default a subscale is scored only if every one of its items was answered, and is `NA` otherwise. Nothing is imputed silently. ```{r} gappy <- study gappy$sus_3[1] <- NA score_questionnaire(gappy, "sus", prefix = "sus_")$SUS[1] # Score responses that are at least 80% complete score_questionnaire(gappy, "sus", prefix = "sus_", min_valid = 0.8)$SUS[1] ``` With `min_valid` relaxed, a subscale is the mean of the items present, and a sum-scored instrument such as the SUS is scaled up proportionally so it stays on its published 0--100 range. ## Internal consistency `score_reliability()` computes Cronbach's alpha on the same recoded matrix that is aggregated, so reverse-coded items are already flipped: ```{r} score_reliability(study, "sus", prefix = "sus_") ``` Because the reversal has already happened, a negative alpha means a real problem -- the items of that subscale do not point the same way -- rather than a forgotten flip. It warns when one appears. Do not read the values above as anything: the example responses are random, so `Usability` is near zero as it should be, while the two-item `Learnability` looks respectable purely by chance. Eight participants is far too few to estimate alpha at all, which is itself worth remembering -- `n_complete` is reported next to it for that reason. ## Your own instruments `define_questionnaire()` registers one, after which it behaves exactly like a built-in. Put the call in a project's setup script and every analysis in that project scores it identically: ```{r} define_questionnaire( key = "acceptance", name = "Van der Laan acceptance scale", reference = "Van der Laan, Heino & De Waard (1997), Transp. Res. C 5(1)", scale = c(-2, 2), label = c( "useful - useless", "pleasant - unpleasant", "bad - good", "nice - annoying", "effective - superfluous", "irritating - likeable", "assisting - worthless", "undesirable - desirable", "raising alertness - sleep-inducing" ), subscale = rep(c("Usefulness", "Satisfying"), length.out = 9), reverse = c(1, 2, 4, 5, 7, 9), higher = "better" ) vdl <- as.data.frame(matrix(c(-2, 2, -2, 2, -2, 2, -2, 2, -2), nrow = 1)) names(vdl) <- paste0("item", 1:9) score_questionnaire(vdl, "acceptance") ``` ## Sickness over time FMS and MISC are single items sampled repeatedly during exposure, so the analysis lives in the time course rather than in any one measurement. `summarize_sickness()` produces the per-participant measures those studies report: ```{r} ratings <- data.frame( participant = rep(c("p1", "p2"), each = 5), minute = rep(0:4, 2), fms = c(0, 1, 3, 6, 8, 0, 0, 1, 1, 2) ) summarize_sickness(ratings, value = "fms", id = "participant", time = "minute", threshold = 5 ) ``` `auc` is the trapezoidal area under the rating curve and `auc_rate` is that divided by the observed duration, i.e. the time-weighted mean rating -- which is comparable across participants who were exposed for different lengths of time. Note that MISC is *ordinal* and unevenly spaced: the step from 6 (nausea) to 10 (vomiting) is not four times the step from 0 to 1. Analyse it with an ordinal model rather than by taking means. You have to say so, though. A 0--10 MISC column has more distinct values than `classify_outcome()`'s `ordinal_max_levels` of 7, so left to itself it is taken for a count and `recommend_test()` proposes a Poisson GLMM: ```{r} misc <- data.frame(misc = c(0, 1, 3, 6, 10, 2, 4, 8)) classify_outcome(score_questionnaire(misc, "misc")$MISC) ``` Pass `outcome_type = "ordinal"` to `fit_recommended()`, or raise `ordinal_max_levels` to 11. ## Onward `fit_recommended()` takes the scored data and fits the model each outcome calls for. Here is the whole path, from raw items to a manuscript sentence: ```{r} set.seed(7) trial <- expand.grid( participant = factor(1:12), condition = factor(c("baseline", "ambient", "explicit")) ) effect <- c(baseline = 0, ambient = 0.6, explicit = 1.2)[trial$condition] # Participants differ from one another too, which is what the random intercept # of the mixed model is there to absorb. person <- rnorm(12, 0, 0.6)[as.integer(trial$participant)] for (i in 1:10) { raw <- 3 + effect + person + rnorm(nrow(trial), 0, 0.5) if (i %% 2 == 0) raw <- 6 - raw # the even SUS items are negatively worded trial[[paste0("sus_", i)]] <- pmin(pmax(round(raw), 1), 5) } scored <- score_questionnaire(trial, "sus", prefix = "sus_", append = TRUE) fit <- fit_recommended( scored, outcome = "SUS", predictors = "condition", cluster = "participant", verbose = FALSE ) fit$recommendation$recommendation fit$text ``` The sentence is LaTeX; `expand_latex_macros()` renders it as plain text if you want to read it here rather than paste it into a manuscript. Watch the classification when an outcome stays whole-numbered — a raw NASA-TLX subscale or a MISC rating is taken for a count unless you say `outcome_type = "continuous"` or `"ordinal"`. SUS and RTLX are fractional, so they classify as continuous on their own. `use_study_project()` scaffolds a whole analysis around this -- scoring, models, figures, and the generated LaTeX a manuscript reads -- as a `targets` pipeline, and writes those `outcome_type` declarations for you.