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This example models time to first entry into a
source/evidence AOI. Repeated trials occur under
standard and evidence_prompt conditions.
Complete usable trials that never inspect the evidence AOI remain in the
risk set until the observation window ends and are right censored.
raw <- simulate_gaze_survival_inputs(
"verification",
seed = 20260918,
n_participants = 36,
trials_per_participant = 3
)The synthetic input is deliberately not pre-censored. The survival state is constructed from the event definition and the explicit trial observation window.
verification <- prepare_gaze_survival_data(
raw$trials,
raw$events,
target_aoi = "source_evidence",
event_type = "first_aoi_entry",
condition_col = "condition_id",
min_valid_fraction = .90,
time_origin = "trial_start",
event_detector = "synthetic_truth",
aoi_specification = "fixed synthetic source/evidence AOI"
)
validate_gaze_survival_data(verification, raise_on_error = FALSE)## [1] severity code n message
## <0 rows> (or 0-length row.names)
## condition n_trials n_analyzable n_observed_events n_censored
## 1 evidence_prompt 54 54 53 1
## 2 standard 54 54 49 5
## n_review_required censoring_fraction
## 1 0 0.01851852
## 2 0 0.09259259
A missing target event becomes ordinary right censoring only when the observation window is complete and usable. Unresolved or poor-quality trials remain review cases.
Lower survival at a given time means a larger proportion of trials has already inspected the evidence AOI.
This is the complement of the Kaplan-Meier survival curve for one target event. Do not interpret it as a competing-risks cumulative-incidence function when multiple mutually exclusive events compete.
This plot is most useful as a diagnostic view of when event increments occur relative to the risk set; it should not be oversold as a smooth underlying hazard function.
cox <- fit_gaze_mixed_cox_model(
verification,
"condition",
participant_col = "participant_id",
structure = "cluster_robust"
)
tidy_gaze_survival_model(cox)## term estimate_log_scale std_error hazard_ratio conf_low
## 1 conditionstandard -1.087844 0.2157481 0.3369423 0.2207549
## conf_high statistic p_value effect_measure
## 1 0.5142812 -5.042194 4.602255e-07 hazard_ratio
## term rho chisq p_value alpha ph_flag
## 1 condition NA 6.369666 0.01160874 0.05 TRUE
## 2 GLOBAL NA 6.369666 0.01160874 0.05 TRUE
The hazard ratio is an instantaneous evidence-inspection-rate contrast among trials still at risk. It is not a ratio of mean latencies.
weibull <- fit_gaze_aft_model(
verification,
"condition",
distribution = "weibull"
)
lognormal <- fit_gaze_aft_model(
verification,
"condition",
distribution = "lognormal"
)
compare_gaze_survival_models(cox, weibull, lognormal)## Warning: Information criteria are not directly comparable across Cox partial
## likelihood, coxme penalized frailty likelihood, and AFT full likelihood, or
## across different analysis-row counts. Use diagnostics and estimand-specific
## interpretation instead of ranking by AIC/BIC.
## model family backend logLik AIC BIC n
## 1 model_1 cox_repeated survival::coxph -381.0763 764.1526 766.7776 102
## 2 model_2 aft_weibull survival::survreg -138.6049 283.2098 291.2562 108
## 3 model_3 aft_lognormal survival::survreg -140.0168 286.0335 294.0799 108
## likelihood_basis information_criteria_comparable
## 1 cox_partial_likelihood FALSE
## 2 full_likelihood FALSE
## 3 full_likelihood FALSE
Interpret the AFT effects as time ratios under the named distribution. Do not select Weibull versus log-normal because one gives a more favorable p-value.
Stop and resolve the scientific/data contract rather than silently modifying rows when:
For coxme frailty fits, report a corresponding marginal
Cox PH diagnostic separately rather than pretending
cox.zph() applies to the frailty object.
Evidence-inspection latency was analysed as a right-censored time-to-event outcome. The target event was first entry into the source/evidence AOI from trial onset. Complete usable trials without an evidence entry were retained as right-censored observations; unresolved gaze-quality trials were not recoded as censoring. We fitted a participant-clustered Cox model and reported hazard ratios with 95% confidence intervals. Proportional-hazards diagnostics and pre-specified Weibull/log-normal AFT sensitivity models were examined.
Report participants, trials, events, censored trials and percentage, review-required rows, event/AOI/time-origin definitions, gaze-quality rule, repeated-participant structure, effect estimate with 95% CI, diagnostics, sensitivity analyses, and package/backend versions.
Preparation and validation:
prepare_gaze_survival_data(),
validate_gaze_survival_data(),
summarise_gaze_censoring().
Models and diagnostics: fit_gaze_mixed_cox_model(),
fit_gaze_aft_model(),
check_gaze_proportional_hazards(),
compare_gaze_survival_models().
Reporting and visualization: tidy_gaze_survival_model(),
report_gaze_survival_model(),
plot_gaze_survival_curve().
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.