Attention is a core component and an integral player in the human sensation, perception, and cognition organization that hierarchically affects elemental processing and higher-level mental operations (
1). Deficits in attentional capacity profoundly disturb the formation of advanced adaptive behaviors and have repeatedly been evidenced in various neuropsychiatric pathologies such as dementia (
2), psychotic (
3), mood (
4), and personality disorders (
5). Notably, our ability to focus on the ongoing task, selective attention, stems from the coherent suppression of the task-irrelevant attributes that necessitate the recruitment of complicated specialized mechanisms for producing this intricacy throughout the limited channel of attention (
6,
7). A dual-mechanism control (DMC) framework implies that the variations in attentional control could be the immediate consequence of the rivalry between two categories of controlling routes: A proactive process that contributes to the features of the stimulus (e.g., paying attention to color and ignoring the word) and a reactive pathway that plays roles after the stimulus is processed. Both of them trigger some conflicts represented in different segments of neural correlates (
8,
9). Determining these steps and their interaction could provide the field with a valuable tenet. Among the currently existing paradigms, the Stroop task explicitly evaluates the concept of interference and conflict processing (monitoring, detection, and resolution), such that reaction time in a color-naming task would be increased due to the incongruent semantic characteristics in the target stimuli (
10). In the color word Stroop task (
11), the responding process is formed according to the task-related information in the presence of distractors. Through the Stroop task two differential mind representations are competing, and the response should be for relevant stimuli. Specifically, the color is requested to be detected while mentally eliminating the words and vice versa. Naturally, word reading is more automatic, inhibitory control must override the automatic response to the word. Slower responses are recorded when the word competes with the color of the word (incongruent condition, the word blue written in green ink) than when it is not (congruent condition: the word blue written in blue color) (
12).
Since the scalp EEG and event-related potentials (ERPs) allow the real-time demonstration of the neural underpinnings, simultaneous Stroop task and EEG recording might yield further insights (
13). Evidently, the representation of the Stroop effect-related incongruity evokes distinct fluctuations in the EEG signal that could statistically be discriminated from the constituents generated within the congruent trials. The brain pulses of the incongruent stimuli might phenomenally originate from neuronal activities aimed at classifying and inhibiting the irrelevancy throughout the task performance. To date, each individual design has considered one or more sections of the associated signal to elucidate the neural correlates of conflict monitoring. Among them, the temporal interval between 300 - 500 ms has gained much significance as the most supported finding. This period comprises cognitive control domains and mainly negative deflections (called N450) (
14-
19), while other sections have also had roles in mismatch and interference processing (the earlier segments encompassing 150 - 300 ms). Subtraction of the congruent-related epoch signal from equivalent incongruent-associated epochs is assumed to produce a differentiated signal that encompasses the inhibition of task-irrelevant information and irrelevance detection effects. Additionally, within the frequency domain of the EEG signal, the Delta band has also shown some relevance to the task-related inhibition. It has been indicated that midfrontal delta could be a potentially selective marker of motor inhibition (
20).