Trial-level sequence modeling reveals hidden dynamics of dual-task interference

Publication date

2026-05-20

Authors

den Otter, Rick
Dame, Anna
Stuit, S.M.ORCID 0000-0003-3891-2171ISNI 0000000419434423
van Maanen, LeendertORCID 0000-0001-9120-1075ISNI 0000000388786943

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Advisors

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Document Type

Article
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License

cc_by

Abstract

Theories of dual-task interference assume that the same cognitive operations underlie multitasking regardless of stimulus timing, yet this core assumption has remained untested due to methodological limitations of behavioral averaging. Here, we combine hidden multivariate pattern (HMP) analysis with deep spatiotemporal sequence modeling of single-trial EEG to uncover the neural dynamics of multitasking in the psychological refractory period (PRP) paradigm. Using a deep spatiotemporal sequence model trained on Long stimulus-onset asynchrony (SOA) trials, we identify Encoding, Central, and Response operations and show that these same operations occur in the Short SOA condition, demonstrating shared cognitive processes across interference conditions. Additionally, trial-level decoding reveals multiple distinct sequences of cognitive operations across both tasks during interference, varying both within and across individuals. These sequences predict behavioral differences in reaction time and accuracy, revealing how interference timing within the cognitive operation sequence influences performance. In other words, we found trial-by-trial variability related to individual strategies directly affecting accuracy and reaction time (RT). Our findings challenge static bottleneck accounts and establish trial-level sequence modeling as a powerful tool to investigate the hidden dynamics of multitasking.

Keywords

Ecology, Evolution, Behavior and Systematics, Ecology, Modelling and Simulation, Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Computational Theory and Mathematics

Citation

den Otter, R, Dame, A, Stuit, S & van Maanen, L 2026, 'Trial-level sequence modeling reveals hidden dynamics of dual-task interference', PLoS Computational Biology, vol. 22, no. 5, e1014302. https://doi.org/10.1371/journal.pcbi.1014302