Authors
Tekampe, D. L., Santangelo, P. S., Sulaj, A., Tekampe, P., Schwartze, M., Hausfeld, L.
Abstract
Immersive virtual reality (VR) can preserve the logic of laboratory attention tasks while altering the perceptual-action context in which attentional control is expressed. In this study, we examined the neural underpinnings of location-response compatibility in a VR adaptation of the Attention Network Test-Revised (ANT-VR), using a restricted preprocessing multiverse to account for uncertainty arising from defensible EEG analysis choices. Forty-four young adults contributed complete ANT-VR behavioural data. Target-locked EEG analyses were conducted across 192 preprocessing branches, with branch-level participant contributions varying after quality check and trial-count filtering. The contrast compared location-response incompatible with compatible trials and was balanced within participants across cue-target interval, cue condition, flanker congruency, and, for spatial-cue trials, conditions in which spatial cues were valid or invalid for subsequent targets. Across the multiverse, the N2pc-window posterior-lateralisation contrast could be defined in all branches and showed high directional stability: the median incompatible-minus-compatible effect was 0.30 uV [IQR: 0.22 to 0.41], with positive effects in 192/192 branches, nominal evidence in 79/192 branches, and Holm-corrected evidence in 42/192 branches. Comparison across ERP measures indicated that this pattern was more consistent for N2pc-window posterior lateralisation than for P1, posterior N1, frontocentral N2, P3, or response-referenced C3/C4 measures. Comparison across C3/C4 reference frames further constrained the interpretation: target-location-referenced C3/C4 showed the strongest effect, whereas response-referenced C3/C4 was weaker. Behavioural analyses showed no reliable compatibility differences. These findings suggest that location-response compatibility in immersive ANT-VR modulates target-locked lateralised neural activity associated with spatial selection and target-location coding, rather than producing broad sensory, conflict-related, P3-related, or specifically response-referenced modulation.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 26 Aug 2026.
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