2.1. Participants
To determine the sample size, we calculated the power (1-β) needed to detect a two-way interaction using PANGEA (https://jakewestfall.shinyapps.io/pangea/). Assuming that we recruited 16 participants and obtained at least 20 epochs of EFRPs, the power was found to be 0.81 (effect size (d) = 0.45, variance of error = 0.33, variance of two-way interaction = 0.08, repetitions = 20). To meet this criterion, we recruited 19 individuals between the ages of 19 and 24 (Mage = 20.6, SDage = 1.1). Three participants were excluded from the analysis (see 2.4. Recording and analyses). All participants were right-handed with corrected vision, and they received an honorarium of 4,000 Japanese yen in the form of an Amazon gift card. This experiment was approved by the ethics board of Bunkyo Gakuin University and was carried out in accordance with The Code of Ethics of the World Medical Association (Declaration of Helsinki). Written informed consent was obtained from all participants.
2.2. Stimuli
Twenty color photographs of people were used as a stimulus set. Each photograph showed a different person. The persons were Asian, and their face, eyes, and body were facing forward. Their visual angle was approximately 8º (w) × 8º (h). A set of five photographs, randomly selected from the set of 20, was used in each of the conditions described below. The set used in one condition was not used in the other condition. A black circle figure was also used as a target, with the visual angle of approximately 2º (w) × 2º (h).
2.3. Procedure
The participants sat in a chair, in front of a computer display, keyboard, and mouse. Before an EEG was recorded, the participants did a story creation task, where they were presented with file names of photographs in the set. Each file name was assigned a random number between 1 and 5. Each participants selected and opened only one photograph on their own. Following the selection, the participants were asked to create a fictional story of a crime they committed with person in the photo as an accomplice, including details such as the accomplice's name and the specifics of the crime, all within a five-minute time limit. For this procedure, two conditions were set: a no-secret condition and a concealed condition. In the no-secret condition, the participants disclosed the number of the selected photograph, and information about the accomplice and crime to the experimenter. In the concealed condition, they did not disclose any information to the experimenter. The computer operation during this task was monitored in a separate room, without the participants' knowledge, allowing the experimenter to record the number of the selected photograph in both conditions.
Following the story creation task, participants performed a modified CIT task while their EEG was being recorded (Figure. 1). The selected (or an unselected) photograph and a target were presented continuously on alternating sides of the display. The photograph was randomly selected from the set used in the story creation task, and this photograph and target were presented 16 and 2 times, respectively, in random order. Each stimulus was presented for 1,200 ms, and no inter-stimulus-interval was set. The participants were instructed to follow the stimuli with their eyes and press a button for the target. After 18 presentations, participants were asked whether the presented person was the accomplice and were told to always answer "No." The same procedure was repeated for the other photographs in the set, and the procedure from stimulus presentation to question and answer was performed twice for each photograph. In the concealed condition, participants were instructed to conceal their accomplices successfully so that their brain potentials would not indicate their guilt. After completing one condition, a five-minute break was taken, and the other condition was performed.
2.4. Recording and analyses
EEG was recorded using an actiCHamp amplifier (Brain Products, Germany) and Ag/AgCl electrodes from six sites (Fp1, Fp2, Fz, Cz, Pz, and Oz) with an electrode cap (Easy-cap (Asian cut), Brain Products, Germany). A ground and a reference electrode were placed on the nose tip and AFz, respectively. EOG was recorded from electrodes placed on the outer canthus of both eyes. Electrode impedances were kept below 10 kΩ. The sampling rate was 1,000 Hz with 0.01 - 100 Hz bandpass filter.
To select the participants who looked at the photographs appropriately, individuals whose rate of the response to target (pressing the button within 1,000 ms after eye fixation to it) was 90% or higher in each condition were included in the analysis. Two participants who did not meet this criterion and one participant who fell asleep during the experiment were excluded from the following analyses.
The EEGLAB toolbox [12], ERPLAB toolbox [13], and EYE-EEG extension [14-15] in MATLAB (The MathWorks, Inc., USA) were used for the EFRPs analyses. The saccade offsets were detected from right EOG and Fp2 signals using the EYE-EEG extension. Missed detections were corrected manually. All physiological responses were filtered using a noncausal Butterworth filter (half-amplitude cutoff at 30 Hz, 12 dB/oct roll-off). Based on the detected events, epochs of 700 ms, including 200 ms before the eye-fixations, were extracted. Baseline correction was performed in reference to before the eye-fixation. Epochs in which the EEG signal exceeded ± 100 μV were excluded. The average number of remaining epochs for selected and unselected photographs were 28 and 104 in the concealed condition and 28 and 107 in the no-secret one. No subject had fewer than 24 epochs, and we determined from previous reports [10,16] that all data could be analyzed for P1 and P300.
A positive wave at the occipital site predominance was observed around 100 ms after the eye fixation. This feature indicated that this response was P1 [5,17]. Although a distinct P300 was not confirmed from the EFRP waveforms at parietal site, late positive component (LPC) differed between photographs. Based on previous reports [5-6,17] and obtained waveforms, the amplitudes of P1 at Oz (80 – 100 ms) and LPC at Pz (250 – 450 ms) were analyzed.
In addition, it was possible that each EFRP amplitude was affected by EOG because EFRPs were calculated using this. To check this influence, mean EOG amplitudes were calculated from the same latency window of the P1 and LPC amplitudes. Then, the EOG waveforms caused by saccades from right to left (EOGRtoL) and vice versa (EOGLtoR) were separately calculated because the responses would cancel each other out if they were averaged. Two-way repeated measures ANOVAs were conducted for each amplitude: Condition (no-secret and concealed conditions) × Item (selected and unselected photographs). When significant interaction was obtained, a simple main effect test was conducted. We reported ηp2 as an effect size and the significance level was set at .05.