Moderating Role of Presence in EEG Responses to Visuo-haptic Prediction Error in Virtual Reality
Lukas Gehrke, Leonie Terfurth, Klaus Gramann
TL;DR
The paper addresses how to continuously quantify presence in VR by linking moment-to-moment sensorimotor prediction errors to neural activity. Using a within-subject design that contrasts visual-only and visuo-haptic immersion with occasional glitches, the study combines EEG with presence questionnaires to identify ERP and oscillatory signatures of prediction error, localized to ACC and PCC. Findings show robust PEN-like fronto-central ERP components and parietal negativities to mismatches, with PCC alpha suppression selectively enhanced under high-immersion mismatches, supporting a hierarchical predictive-coding account where frontal monitoring is immersion-invariant while posterior multisensory integration scales with sensory precision. These results advance understanding of presence in VR and point to neural markers that could enable neuroadaptive VR systems, though inter-individual presence effects did not reliably moderate neural responses in this setup.
Abstract
Virtual reality (VR) can create compelling experiences that evoke presence, the sense of ``being there.'' However, problems in rendering can create sensorimotor disruptions that undermine presence and task performance. Presence is typically assessed with post-hoc questionnaires, but their coarse temporal resolution limits insight into how sensorimotor disruptions shape user experience. Here, we combined questionnaires with electroencephalography (EEG) to identify neural markers of presence-affecting prediction error in immersive VR. Twenty-five participants performed a grasp-and-place task under two levels of immersion (visual-only vs.~visuo-haptic). Occasional oddball-like sensorimotor disruptions introduced premature feedback to elicit prediction errors. Overall, higher immersion enhanced self-presence but not physical presence, while accuracy and speed improved over time irrespective of immersion. At the neural level, sensorimotor disruptions elicited robust event-related potential effects at FCz and Pz, accompanied by increases in frontal midline $θ$ and posterior $α$ suppression. Through source analyses localized to anterior- and posterior cingulate cortex (ACC/PCC) we found that PCC $α$ activity showed heightened sensitivity to disruptions exclusively in visuo-haptic immersion. Exploratory moderation analyses by presence scores revealed no consistent patterns. Together, these results suggest that higher immersion amplifies both the benefits and costs of sensorimotor coherence.
