ArticleFrontiers in neuroscience2019
Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain-Computer Interface.
Article in Frontiers in neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Closed-loop error damping in human BCI using pre-error motor cortex activity.bioRxiv : the preprint server for biology · 2026Article
- NEuroMOrphic Neural-Response Decoding System for Adaptive and Personalized Neuro-Prosthetics' Control.Biomimetics (Basel, Switzerland) · 2025Article
- Unsupervised adaptation of an ECoG based brain-computer interface using neural correlates of task performance.Scientific reports · 2022Article
- AJILE12: Long-term naturalistic human intracranial neural recordings and pose.Scientific data · 2022Article
- Single-Trial Classification of Error-Related Potentials in People with Motor Disabilities: A Study in Cerebral Palsy, Stroke, and Amputees.Sensors (Basel, Switzerland) · 2022Article
- What to Believe? Impact of Knowledge and Message Length on Neural Activity in Message Credibility Evaluation.Frontiers in human neuroscience · 2021Article
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6 authors.
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Abstract
Brain-computer interfaces (BCIs) benefit greatly from performance feedback, but current systems lack automatic, task-independent feedback. Cortical responses elicited from user error have the potential to serve as state-based feedback to BCI decoders. To gain a better understanding of local error potentials, we investigate responsive cortical power underlying error-related potentials (ErrPs) from the human cortex during a one-dimensional center-out BCI task, tracking the topography of high-gamma (70-100 Hz) band power (HBP) specific to BCI error. We measured electrocorticography (ECoG) in three human subjects during dynamic, continuous control over BCI cursor velocity. Subjects used motor imagery and rest to move the cursor toward and subsequently dwell within a target region. We then identified and labeled epochs where the BCI decoder incorrectly moved the cursor in the direction opposite of the subject's expectations (i.e., BCI error). We found increased HBP in various cortical areas 100-500 ms following BCI error with respect to epochs of correct, intended control. Significant responses were noted in primary somatosensory, motor, premotor, and parietal areas and generally regardless of whether the subject was using motor imagery or rest to move the cursor toward the target. Parts of somatosensory, temporal, and parietal areas exclusively had increased HBP when subjects were using motor imagery. In contrast, only part of the parietal cortex near the angular gyrus exclusively had an increase in HBP during rest. This investigation is, to our knowledge, the first to explore cortical fields changes in the context of continuous control in ECoG BCI. We present topographical changes in HBP characteristic specific to the generation of error. By focusing on continuous control, instead of on discrete control for simple selection, we investigate a more naturalistic setting and provide high ecological validity for characterizing error potentials. Such potentials could be considered as design elements for co-adaptive BCIs in the future as task-independent feedback to the decoder, allowing for more robust and individualized BCIs.
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