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The study protocol was reviewed and approved by the Institutional Review Board of Hallym University Sacred Heart Hospital (approval number: HALLYM 2023-07-015-001). All participants provided written informed consent before participation.
1. Instruments
NOTE: During testing, the background noise level inside the booth was maintained below approximately 35 dBA, ensuring that external noise did not interfere with sound localization performance.
A soundproof booth (internal dimensions of approximately 3,800 × 2,200 × 2,100 mm) provided a controlled free-field listening environment with minimal ambient noise. A semicircular loudspeaker rack with a radius of 3,000 mm was installed inside the booth. Seven loudspeakers were mounted at 30° intervals spanning from −90° to +90° azimuth, and all loudspeakers were positioned at the same height (head level when seated; approximately 1,050 mm) and at an equal distance from the participant's head (Figure 1). The loudspeakers were connected to a multichannel audio interface using balanced, shielded XLR audio cables.
NOTE: When connecting multiple loudspeakers to a personal computer located outside the soundproof booth, a wall-mounted cable panel or feedthrough was installed on the booth wall. This facilitated stable cable routing between the interior and exterior of the booth while maintaining acoustic isolation and minimizing cable clutter.
Stimulus presentation and data acquisition were controlled using a Windows-based personal computer running custom-developed software (Figure 2; see Table of Materials). A height-adjustable chair equipped with a headrest was prepared to stabilize the participant's head position during stimulus presentation. A custom-made chair with adjustable seat height and headrest position was used to accommodate individual participant anthropometry. The headrest provided tactile feedback to help participants maintain a consistent forward-facing head orientation during stimulus presentation.
NOTE: The custom software was developed in-house to support automated sound localization testing. Once the test was initiated, the software controlled stimulus presentation and trial sequencing, collected participant responses via a touchscreen interface, and automatically computed localization performance metrics, including root mean square error (RMSE), mean absolute error (MAE), and localization bias at the completion of the test.

Figure 1. Loudspeaker array for the horizontal sound localization test Please click here to view a larger version of this figure.

Figure 2. Schematic of the experimental system. The system comprised a personal computer connected to an audio interface, which delivered signals to a power amplifier and subsequently to the loudspeaker array. A sound level meter was used for calibration to ensure consistent output levels across all the loudspeakers. Please click here to view a larger version of this figure.
2. Setup01
Before starting the test, a calibration procedure was performed to ensure consistent sound presentation levels across all test loudspeakers. A broadband noise stimulus that was root mean square (RMS) matched to the test stimuli was presented sequentially from each loudspeaker. A Class 1 precision sound level meter equipped with a free-field microphone was placed on a tripod at head level (approximately 1,050 mm) at the participant position. The equivalent continuous sound level (LZeq; Z-weighted, time-averaged sound pressure level) from each loudspeaker was measured, and output levels were adjusted so that the measured LZeq was approximately 60 dB SPL (±0.5 dB) across all loudspeakers.
NOTE: Adjustment of loudspeaker output levels was performed at the audio interface level to ensure consistent calibration across loudspeakers. The custom software did not include level-control functions and was used solely for stimulus presentation, trial control, response collection, and computation of localization metrics.
3. Experiment
The participant was seated on the custom-made chair so that the head was aligned with the frontal loudspeaker (0° azimuth, the central position of the semicircular array) and was positioned at the center of the semicircular loudspeaker array. The headrest was adjusted to fit firmly against the occipital protuberance, and the participant was instructed to maintain contact with the headrest throughout the test. A touchpad was placed directly in front of the participant to record responses, and instructions on its use were provided.
NOTE: Improper positioning at the beginning of the test may affect the effective loudspeaker angles and compromise measurement accuracy. The headrest provided tactile feedback, enabling participants to monitor whether the head remains correctly positioned. The response device must not act as a visual or audio barrier and the touchpad should not obstruct the direct line of sight between the participant and the central loudspeaker.
The participant identification code and trial number were entered, and the hearing-device status (cochlear implant, hearing aid, or no hearing aid) was selected using the graphical user interface (GUI). The familiarization sequence was started. On the GUI, the Familiarization button was selected to initiate the familiarization sequence. The participant was instructed to maintain gaze toward the central loudspeaker throughout the sequence. During the familiarization sequence, the system automatically presented auditory stimuli sequentially from each loudspeaker.
NOTE: The participant was instructed to keep the head directed forward and avoided turning toward the sound source during this step. The sound localization test employed broadband noise stimuli (20-20,000 Hz) generated in two spectral shapes and were presented at three intensity levels (55, 60, and 65 dB HL). All stimuli had a duration of 500 ms with 5 ms onset and offset ramps, consistent with established localization protocols1,2. In total, six unique stimuli were presented once from each of the seven loudspeakers in randomized order, resulting in 42 trials per participant.

Figure 3. Speaker-map interface used for participant responses. Please click here to view a larger version of this figure.
On the GUI, the Pre-test button was selected to activate the pre-test mode. The participant was instructed to face the frontal loudspeaker and to press the Start button on the touchpad when ready, while maintaining a forward head orientation. Upon pressing the Start button, the system presented the first test sound from one of the loudspeakers. After the sound presentation, the touchpad display switched to a loudspeaker map, on which the participant selected the perceived sound-source location (Figure 3).
After each response, the system provided immediate feedback. For correct responses, a confirmation message was displayed before progression to the next trial was allowed. For incorrect responses, the correct loudspeaker location was highlighted on the map, and the sound was replayed three times from that loudspeaker. The pre-test consisted of three trials and was automatically terminated by the system upon completion of the third trial.
NOTE: The participant was monitored to ensure that the head remained directed toward the frontal loudspeaker during the feedback sequence, as turning the head interfered with accurate perception of spatial cues. Because individual trials could not be repeated within the automated sequence, any instance in which the participant clearly failed to maintain the required forward head position triggered a session restart rather than trial-level repetition. These restarted sessions were not included in the final analysis. The number of pre-test trials was predefined in the system (limited to three trials) and could not be modified by the examiner8,9.
After completion of the pre-test, the main test button was clicked to start the main test sequence. The participant pressed the Start button on the touchpad to trigger the presentation of a sound from one of the loudspeakers. After the sound presentation, the touchpad display switched to a loudspeaker map, on which the participant selected the perceived sound location. Following each response, the system displayed the Next button. The participant was allowed to take additional time before pressing the Next button to rest and verify proper head orientation prior to initiating the subsequent trial. The system automatically advanced through the predefined number of trials, repeated the trial sequence, and continued until the main test was completed.
NOTE: It was emphasized that the head remained directed toward the frontal loudspeaker throughout the test. This position ensured a consistent perception of spatial cues and prevented bias due to unintended head movements. After the stimulus ended, participants were allowed to turn their heads to identify and select the perceived loudspeaker visually. Before the next trial began, however, they returned to the initial frontal position to ensure that all subsequent stimuli were perceived under the same standardized condition. Although the system did not include integrated head-tracking, the examiner visually monitored head orientation throughout the test to ensure that participants maintained the required forward position before each stimulus.
At the end of the test, the system automatically terminated the session and generated a log file. The log contained records of each trial, including the stimulus presented, the direction of the sound source, and the participant's response. On the basis of these responses, the system calculated the RMSE, MAE, and response bias, which were saved together with the trial log for subsequent analysis.
NOTE: The log file was properly stored after the session, as it contained both the raw response data and the calculated performance metrics required for further analysis.
4. Data Processing and Analysis
After completion of the sound localization test, the system automatically calculated the RMSE, MAE, and response bias for each participant based on the recorded trial responses. For visualization and figure preparation, the exported data were subsequently processed using custom-developed scripts.
To facilitate a clinically meaningful interpretation of sound localization performance, localization error metrics were additionally categorized using an International Classification of Functioning, Disability and Health (ICF)-based framework. This approach was adopted based on a previously proposed consensus classification system for horizontal sound localization, which mapped quantitative localization errors onto graded levels of functional impairment1. In this framework, localization performance was classified into five categories-no, mild, moderate, severe, and complete impairment-based on the distribution of localization error in a normal-hearing (NH) reference group and the chance level associated with the specific test setup. Importantly, this classification did not replace conventional error metrics (e.g., RMSE or MAE) but served as an interpretive layer that translated numerical performance measures into functionally relevant categories. The ICF-based classification was applied post hoc to the localization results obtained in the present study to support standardized interpretation and to facilitate comparison across participants and listener groups.