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Open design of a reproducible videogame controller for MRI and MEG.

Harel, Y ; Cyr, A ; et al.
In: PloS one, Jg. 18 (2023-11-01), Heft 11, S. e0290158
Online academicJournal

Open design of a reproducible videogame controller for MRI and MEG  Introduction

Videogames are emerging as a promising experimental paradigm in neuroimaging. Acquiring gameplay in a scanner remains challenging due to the lack of a scanner-compatible videogame controller that provides a similar experience to standard, commercial devices. In this paper, we introduce a videogame controller designed for use in the functional magnetic resonance imaging as well as magnetoencephalography. The controller is made exclusively of 3D-printed and commercially available parts. We evaluated the quality of our controller by comparing it to a non-MRI compatible controller that was kept outside the scanner. The comparison of response latencies showed reliable button press accuracies of adequate precision. Comparison of the subjects' motion during fMRI recordings of various tasks showed that the use of our controller did not increase the amount of motion produced compared to a regular MR compatible button press box. Motion levels during an ecological videogame task were of moderate amplitude. In addition, we found that the controller only had marginal effect on temporal SNR in fMRI, as well as on covariance between sensors in MEG, as expected due to the use of non-magnetic building materials. Finally, the reproducibility of the controller was demonstrated by having team members who were not involved in the design build a reproduction using only the documentation. This new videogame controller opens new avenues for ecological tasks in fMRI, including challenging videogames and more generally tasks with complex responses. The detailed controller documentation and build instructions are released under an Open Source Hardware license to increase accessibility, and reproducibility and enable the neuroimaging research community to improve or modify the controller for future experiments.

Videogames offer a wide range of rich and dynamic environments which open exciting avenues for research in cognitive neuroscience [[1]]. Major neuroimaging techniques such as functional magnetic resonance imaging (fMRI) and magnetoencephalography (MEG) adversely interact with any electronic equipment, which precludes the use of traditional videogame controllers during neuroimaging sessions. This paper reports on a videogame controller compatible with fMRI and MEG systems, developed by the team of the Courtois project on neuronal modeling (CNeuroMod). We evaluated the performance of this new device by comparing it to a regular, commercially available, videogame controller. We also assessed possible interactions between the controller and the quality of fMRI and MEG data acquisitions. In the spirit of open science, we released publicly the plans and documentation for building this controller, and confirmed that an independent team was able to build a reproduction based on the plans and documentation.

Neuroimaging videogames studies have examined how brain networks interact to produce a variety of complex behaviors such as aggression [[2]–[5]], learning [[6]], expertise [[8]] and flow [[10]]. Videogames often recruit many complementary abilities at once, e.g. spatial navigation and decision making in first-person shooters, thus probing the integration of diverse cognitive domains within a single environment [[11]]. Brain activity during videogame play is actively being studied with EEG (e.g. [[12]]) and fNIRS (e.g. [[13]]), two neuroimaging techniques that can be used with a traditional videogame setup, but only a handful of studies have attempted to use fMRI or MEG (e.g. [[14]]) to acquire high-quality functional brain data. Experiments conducted in MRI and MEG scanners need compatible response devices that do not create major acquisition artifacts or safety concerns [[15]]. These requirements prevent the use of commercially available controllers in research conducted using fMRI and MEG. Although possible to shield electronics [[16]], such a procedure only partially alleviates concerns on signal quality and possible safety concerns in an MRI environment. Videogames collected during fMRI sessions have relied on non-ecological MRI-compatible response devices such as button pads [[2], [4]–[6], [17]], joysticks [[19]], trackwheel mouse [[18]], and data gloves [[6], [8]]. These devices do not necessarily match those normally used to play the corresponding videogames, for example a button pad instead of a gamepad [[17]], or a trackball [[18]] instead of a mouse. Atypical devices may negatively impact the experience and performance of players in a brain scanner, and severely limit the type of games which can effectively be played within a scanning environment.

A commercial, fully MRI-compatible handheld videogame controller was recently proposed by Current Designs Inc., Philadelphia, PA, USA, requiring the separate acquisition of an electronics interface and a fiber optics cord extension, resulting in significant costs. An alternative approach to commercial solutions for research has however emerged: Open Source Hardware (OSH), made possible by the increasing accessibility of 3D printing, engineering parts, and modular micro-electronics [[21]]. Inspired by the Free and Open Source Software philosophy, OSH refers to technological artifacts for which the design files, documentation, and required software are freely available under an open-source license specifically dedicated to sharing hardware products. This approach provides many benefits, in line with the principles of open science: promoting accessibility and reproducibility, significantly reducing construction costs, and allowing for iterative design and customization.

The aim of this study was to develop and validate a videogame controller that is both MRI- and MEG-compatible and can be reproduced by other neuroimaging research teams. This was achieved by making detailed documentation and design files accessible to allow for 3D printing and assembly. The controller was evaluated by comparing its responsiveness to a reference controller used in a mock scanner, in terms of button press and release latencies in a cued-response experiment. We also checked the impact of the CNeuroMod controller usage on subject motion, using frame displacement metrics derived from fMRI acquisitions. Finally, we acquired phantom MRI scans as well as MEG empty room data to determine if any change in background noise could be attributed to the controller's presence in the scanning environment.

Methods

Controller

The documentation for building the controller is provided in the Appendix of this article and can also be found at https://controller-doc.readthedocs.io/en/latest/. It contains a Bill of Materials (BOM) of the commercial parts necessary to build the controller, detailed assembly instructions, source code for the microcontroller, and a download section for the 3D models and Gerber files. The 3D model files are available either as.STL files, which can be readily sent to a 3D printer, or as. STEP files for manipulation and modification using Computer-Aided Design (CAD) software. Gerber files describe the different layers of the Printed Circuit Board (PCB) that need to be sent to a manufacturer for production. The buttons layout of the controller is presented in Fig 1.

Graph: Fig 1 Models and pictures of the different controller parts.A Split view of the various 3D-printed parts B 3D models of the assembled switch part. C 3D model of the PCB. D 3D model of the assembled controller. E-H Real pictures of the corresponding elements as assembled at our facility.

Design choices

The design of handheld videogame controllers has been heavily influenced by the early model of the Super Nintendo Entertainment System (SNES, Nintendo). This controller features two sets of buttons: one for the left hand which consists of four arrow-like keys intended for spatial navigation, and another set of four buttons for the right hand offering various types of game-specific actions. The combination of these eight buttons is sufficient for players to explore rich action spaces and covers the basic requirements of a vast array of videogame titles, especially retro videogames (that is, games released on consoles of the generations preceding the PlayStation and XBox systems).

The controller was designed with the six following specific criteria in mind. Accordingly, the handheld part of the controller must:

  • be built using a 3D printer and commercially available parts in order for it to be easily reproducible,
  • be entirely void of electronics and ferro-magnetic components to ensure MRI- and MEG-compatibility,
  • reliably register all button presses with a temporal precision comparable to that of the reference controller,
  • mimic the feeling and comfort of a reference commercial videogame controller, the Super NES controller, a device held with both hands each manipulating a set of 4 buttons using the thumbs,
  • allow users to comfortably play while lying down (position as imposed by MRI scanner and possible in some MEG scanners),
  • be comfortable to use for individuals with different hand sizes.
Controller system

The device is made up of two parts linked by a bundle of fiber optics (Fig 2): the first is the actual handheld controller, and the second is a printed circuit board (PCB) that allows communication between the controller and a stimulation computer. The handheld controller and fiber optics bundle are MRI and MEG-compatible, and as such can be used in the MRI room or MEG chamber while the PCB contains unshielded electronics and must remain in the control room. Our pilot controller featured a 10m long fiber optics cable, which was sufficient to connect the controller in the MRI room with the PCB in the control room.

Graph: Fig 2 Schematics of the two main parts of the controller.The PCB is installed in the control room, while the handheld part is MRI-compatible and can be used in the MRI scanning room.

Software

A Teensy 3.5 (Teensy®) microcontroller board was programmed to parse the optical signals and manage communication between the PCB and a stimulation computer. Programming was done in the Arduino Integrated Development Environment (IDE; Arduino) using the Teensyduino add-on (https://www.pjrc.com/teensy/teensyduino.html), which allows programming Teensy family boards using most of the Arduino libraries. This software must be uploaded to the Teensy board located atop the PCB.

Task design

The datasets used in this study come from the Courtois NeuroMod databank (https://www.cneuromod.ca/gallery/datasets/). For the purpose of this project, we only utilized data from 4 subjects of 6 participants available in the databank, specifically the 4 subjects that performed the gamepad task. The code used for data analysis is available at https://doi.org/10.5281/zenodo.7847577 (or on GitHub https://github.com/courtois-neuromod/controller_validation).

Subjects

Four participants (2 female) were scanned while they performed a variety of tasks in the MEG and MRI scanners. All four subjects were right-handed and had normal hearing for their age, ages ranged between 31 and 47 at first data set acquisitions in 2018 (i.e. hcptrt dataset), and the timespan between first and last dataset acquisition (i.e. gamepad dataset, see Control datasets section) was approximately 2 years and 7 months. Subjects were recruited as part of the Courtois NeuroMod project (CNeuroMod), a dense fMRI database that is being collected on 6 subjects using both naturalistic and controlled stimuli from a broad range of cognitive domains and the main motivator for building the controller. Although the participants of the gamepad task do not properly reflect the population of videogame players, we expected their behavior to be illustrative of the controllers capability as the task didn't include videogame components per se.

Ethics statement

The study was approved by the "Comité d'éthique de la recherche vieillissement neuroimagerie" of the CIUSSS du Centre-Sud-de-l'île-de-Montréal (CIUSSS-CSMTL) under the number CER VN 18-19-22 and all participants provided written consent.

Utility ratings

A subjective evaluation of the controller in accordance with ISO-9241 on device comfort was assessed via a questionnaire of 8 items answered on a 5-points Likert scale, adapted from [[22]]. For the items smoothness during operation, general comfort and overall useability, higher scores indicate better fitness. For the items finger and wrist fatigue, lower scores indicate better fitness. For all other items, better fitness is indicated by scores around 3. All subjects of the CNeuroMod sample answered the questionnaire after having completed the totality of the validation task.

MRI acquisition

fMRI data used in this paper were collected as part of the CNeuroMod project using a 3T Siemens Prima Fit MR scanner, a 64-channel head coil, and an accelerated simultaneous multi-slice imaging sequence [[23]]. The spatial resolution was 2mm isotropic, and the TR was 1.49s. All subjects wore custom CaseForge [[24]] head cases to minimize motion. Visual stimuli were projected onto a screen via a waveguide and presented to participants on a mirror mounted on the head coil, and sound was delivered using S15 Sensimetrics headphone inserts. Additionally an anatomical scan was collected using a T1-weighted MPRAGE 3D sagittal sequence, (TR = 2.4 s, TE = 2.2 ms, flip angle = 8 deg, voxel size = 0.8 mm). fMRI and anatomical data were preprocessed using the fMRIprep pipeline [[25]], using the "long term support" version 20.2.3. For a more detailed description of the MRI or fMRI sequences and set up visit the CNeuroMod'st documentation page: (http://www.docs.cneuromod.ca/en).

Gamepad task

We set out to evaluate the reliability of button responses of our custom controller by comparing it to that of a commercially available, non-MRI-compatible controller. Thus, this experiment consisted of a basic cued-response task implemented in PsychoPy [[21]] that was administered in two setups in a pseudo-randomized fashion: either in the MRI scanner using our homemade MRI-compatible controller, or in a mock scanner (i.e. a replica of a MRI scanner that does not contain a magnet) equipped with a generic commercial controller modeled after the classic SNES controller.

In the MRI setup our MRI-compatible controller was installed in the MRI scanner and connected through a waveguide to the controller interface, located in the control room. The controller interface was in turn connected to the stimulation computer via USB to register and log key presses during the task. The remaining set up was exactly as described above in the section on fMRI acquisition (Fig 3).

Graph: Fig 3 Schematics of the MRI and Mock setups.The mock setup closely replicated the MRI setup while allowing the use of a commercial controller instead of our MRI-compatible controller. Icons obtained under CC license at https://thenounproject.com/.

In the mock setup we used an MRI simulator made by Psychology Software Tools (https://pstnet.com/products/mri-simulator/), and used an in-house 3D printed replica of the Siemens 64 channel head coil used in the MRI. An in-house built mirror mount replicating the Siemen's mirror attached to the head coil was used to present images to the participants. Instead of a projection, visual stimuli were presented using a small monitor placed within the mock bore, closely replicating the manner in which visual stimuli are presented in the MR scanner. A replica of the SNES controller (iNNEXT Retro USB Super Classic Controller, iNNEXT) was installed inside the mock scanner, and directly connected to the stimulation computer via USB (Fig 3).

Participants were instructed they would have to perform a cued-response task, in which, using visual cues, they would have to press one of the 8 buttons present on either the MRI or SNES controllers, for a short or long period of time. Short presses were indicated by the presence of a yellow dot prior during a trial and long presses were indicated by a green bar during a trial (Fig 4). In short trials, a yellow dot preceding the cue instructed the participants to press and release the cued button as fast as possible (cue displayed for 300ms), while in long trials participants were instructed to hold the cued button as long as the green bar was present on the screen (cue was displayed for a duration between 1 and 3 seconds with a gaussian jitter). Participants performed the tasks in 4 sessions, and during each session performed the task in both the MRI and mock setups (2 runs each). In a run, the subject performed 5 repetitions of each of the 8 buttons in the two conditions (short and long) for a total of 80 trials per run (5*8*2). Each participant performed 8 runs per setup (Mock and MRI) split in 4 sessions, for a total of 1 280 trials (80*8*2).

Graph: Fig 4 Illustration of the unfolding of the simple cued-response task.

Control datasets

To illustrate the values of keypress durations that naturally occur when playing action platformer videogames, and use them as reference to interpret the results of our gamepad task, we computed the durations observed in the training phase of the shinobi dataset. The data for the shinobi_training dataset were obtained using the commercial controller (i.e non-MRI controller that was also part of our Mock scan condition of the gamepad task). This dataset comprised the same 4 subjects that performed the gamepad and shinobi tasks, and totals 1 165 trials across the 3 selected levels of Shinobi III: Return of the Ninja Master [[26]]. The game was played and recorded at 60 frames per second, allowing us to compute keypress durations with a precision of 16ms.

In order to estimate the amount of motion induced by our controller both in controlled and naturalistic conditions, we compared the motion (quantified by Framewise Displacement, FD) observed during the fMRI acquisitions of the gamepad and the shinobi datasets respectively with other datasets obtained on the same 4 subjects, chosen as a reference because they did not involve the controller. One exception is the shinobi dataset as sub-03 did not participate, and thus we only included data from 3 of the 4 subjects. The control datasets (friends, hcptrt-gamble, hcptrt-motor and hcptrt-rest) were selected to reflect the variety of motion amounts one can expect during conventional active and passive tasks. We used around 38h of fMRI data from the friends dataset during which the subjects were watching seasons 1 up to 4 of the Friends TV show [[27]]. Given the engaging nature of the stimuli and the passive nature of the task, we expected the associated FD values for this dataset to indicate relatively low motion [[28]].

We also used data from the hcptrt dataset, namely the resting state, gambling and motor tasks. All tasks in the hcptrt dataset were designed by the team at the Human Connectome Project [[29]] and each task was repeated up to 15 times. The resting state task was repeated 4 or 5 times per subject and consisted of staring at a cross (no response). The gambling task was repeated between 15 and 17 times per subject; using a standard MRI response box subjects were instructed to guess if they thought a hidden number (represented by a "?") was above or below 5.

The motor task was repeated between 15 and 18 times per subject. In this task, participants were presented a visual cue and were asked move a body part (ie. tongue, fingers, toes, hand, feet) in response to that cue. We expected these three datasets to reflect relatively low, moderate and high levels of motion for the resting, gambling and motor tasks respectively.

Lastly we used fMRI data from 3 of the participants in the shinobi dataset, which consists of about 10h (approximately 56 runs) of fMRI data per subject. During the shinobi task, subjects played three selected levels of Shinobi III: Return Of The Ninja Master [[26]], a retro videogame released on Sega Genesis, using our custom videogame controller. We expected this last dataset to reflect the amount of motion typically observed during fMRI acquisitions involving videogame play with the CNeuroMod controller.

For more information on each of the control datasets, see the Courtois NeuroMod's Project documentation page: (https://docs.cneuromod.ca/en/latest/).

fMRI phantom recordings

Thirty runs of 60 volumes were acquired using a fBIRN gel phantom with the custom controller in the scanner, and 30 more without the controller, all following the imaging sequence described in the MRI acquisition section. Each run lasted about 2 minutes, and a total of 60 runs were acquired on a single day.

MEG empty room recordings

Empty room noise recordings were acquired as part of the routine procedure for MEG acquisitions. The data was collected on separate days with a MEG CTF-275 (with 270 functioning channels) while no participant was inside the MEG shielded room. In each recording, 35 seconds of signal were acquired at a sampling frequency of 1200Hz. No offset removal nor filters were used during these acquisitions. We used the empty room recordings acquired between 02/04/2019 and 09/06/2021 (N = 80), and split them into 4 subsets of 20 consecutive recordings. These subsets, named T1, T2, T3 and T4 include data acquired before the installation of our custom controller (T1, T2 and T3), and data acquired after the installation of our controller at the MEG facility (T4). Each of these subsets contained recordings spanning over between 1 and 3 and a half months.

Analyses

Response latencies (custom controller VS SNES controller)

In order to verify that our controller had the same performance capacity as the commercial controller, we tested the hypothesis of a greater response latency in the MRI (using our controller) than in the mock scanner (using the commercial reference controller). We removed: (a) trials for which no button press of the instructed key was recorded; (b) trials with negative reaction times and durations, which correspond to trials that were anticipated by the subject due to the task's pseudo-random sequence; and (c) trials for which the press timing was recorded but no timing for the release was recorded due to an overlap with the subsequent trial. Additionally, we removed (d) trials from the "long-press" condition for which the press duration was below 1s, as these trials might have been mistakenly performed as "short-press" trials. In total, we removed 71 trials of the mock condition and 50 trials of the MRI condition (Table 1). Statistical analyses were conducted on pooled reaction times, and on press duration for long and short trials separately. One-tailed Kolmogorov-Smirnov tests for independent samples with FDR (Benjamini-Hochberg) correction for multiple comparisons were conducted between the two setups. Effects size were estimated using Cohen's D.

Graph

Table 1 Number of removed trials at each step of the preprocessing pipeline.

ABXYUpDownLeftRightTotal
MistakesMock3384976747
MRI6303633226
Negative RTsMock021000003
MRI010001002
Negative durationsMock000000000
MRI000010001
Delayed trialsMock012021017
MRI0000730111
Missed trialsMock3212320114
MRI1311301010
Retained trialsMock2342322282342262302342311849
MRI2132132192162032132162171710
Total removedMock6812614106971
MRI77141774350

Motion assessment (custom controller VS control tasks)

Framewise Displacement (FD) values were obtained from the confounds file generated by the fMRIprep preprocessing pipeline [[25]] applied to each of the the datasets listed above. For each run of every dataset, the median of FD values were computed, then compared across datasets separately for each subject using two-tailed Kolmogorov-Smirnov tests for independent samples with FDR (Benjamini-Hochberg) correction for multiple comparisons. Specifically, we tested the differences between the gamepad dataset and the friends, hcp-rest, hcp-gamble and hcp-motor datasets for all 4 subjects, and the differences between the shinobi dataset and all others datasets for the 3 subjects that performed the shinobi task.

fMRI temporal SNR (with versus without controller). Temporal Signal-to-Noise Ratio (SNR) maps were computed on each run then averaged per condition (data from the tasks was divided into one of two conditions; with or without the controller present in the scanner) using Nipype [[30]]. For each voxel, the mean and standard deviation across the distribution of runs were computed and displayed separately for the two conditions. Additionally, we extracted the voxels located within an EPI mask (i.e. voxels located in the gel phantom) and compared the distributions of mean and standard deviation using independent T-Tests.

MEG noise covariance (with versus without controller)

Noise covariance matrices were computed on each empty room acquisition run using the MNE-python toolbox [[31]]. Because covariance matrices are symmetric, only the upper part of the matrices were used for subsequent analysis. The covariance matrices of the 20 recordings of each subset (T1, T2, T3 and T4) were averaged separately and then Z-scored. The difference between these two distributions of covariances was assessed using a Wilcoxon signed-rank test. The Pearson correlation between the two distributions of values was computed to estimate the effect size of that difference. Finally, pairwise Pearson correlations were computed between individual recordings of each pair of subsets to compare the distributions of correlation coefficients across subsets.

Results

Utility ratings

The answers (N = 4) to each question of the utility ratings survey were averaged and inspected separately. All scales ranged from 1 to 5, although the interpretation of each score varies as summarized below and detailed in the methods section. For smoothness during operation, the average rating was 4.75 (±0.5 std, higher is better). For the force required for actuation and the operation speed, the average rating was 3.25 (±0.5 std, a score of 3 is best). The mental effort required for operation was rated at 3 (±0 std, a score of 3 is best). Both finger and wrist fatigue were rated below 2 (2±1.15 std and 1.25±0.5 std respectively, lower is better). Finally, both general comfort and overall useability were rated above 4 (4.25±0.5 std and 4.75±0.5 std respectively, higher is better).

Response latencies (custom controller versus reference controller)

Analysis of reaction times (Fig 5) showed no differences (all p > 0.05, see Table 2) between our MRI-compatible controller (MRI condition) and the commercial controller (Mock condition) when comparing each key separately. Analysis of release reaction times in long trials revealed significant (p < 0.05) differences for 6 of the 8 keys, showing that the MRI-compatible controller led to longer release reaction times (-0.417 < Cohen's D < -0.040 for all significant comparisons) than the reference controller. Analysis of press durations in short trials also showed significant differences (p < 0.05) for all keys, showing that the duration of short presses was longer using our MRI-compatible controller (-1.332 < Cohen's D < -0.300 for all comparisons).

Graph: Fig 5 Distributions of response latencies (pooled across subjects) in the MRI and Mock conditions.ns: p < = 1.00e+00; *: 1.00e-02 < p < = 5.00e-02; **: 1.00e-03 < p < = 1.00e-02; ***: 1.00e-04 < p < = 1.00e-03; ****: p < = 1.00e-04. A Comparison of reaction times (ms). B Comparison of release reaction times (ms) for long trials only. C Comparison of total key press durations (ms) for short trials only.

Graph

Table 2 Statistics table showing the comparisons between the MRI and Mock conditions.

MockMRIDifference
NMeanSTDNMeanSTDKSDMean
Press reaction times—All trials (ms)A23446083213466920.071 (ns)-0.0716.251
B23244496213436950.022 (ns)0.0848.012
Down2305011552134611210.000 (ns)0.29340.675
Left2345141702164571080.000 (ns)0.39756.612
Right2314881322174551130.026 (ns)0.26632.773
Up2265081412034771560.015 (ns)0.20730.625
X2284731422194521090.020 (ns)0.16420.772
Y234472104216449940.001 (ns)0.23323.132
Release reaction times—Long trials (ms)A1163291621043381530.100 (ns)-0.0589.118
B1173251011063441820.283***-0.12919.089
Down1133301131063601580.312****-0.21529.518
Left114307117107357870.449****-0.4950.538
Right1122951521073251270.284***-0.2230.775
Up109309107973311540.266***-0.1722.609
X110338971103431280.136 (ns)-0.0475.318
Y11632793107357980.185*-0.31430.006
Press durations—Short trials (ms)A11819240109211490.245***-0.43919.633
B11519536107222740.198*-0.45726.578
Down11718946107213570.293****-0.4724.418
Left12018041109208610.287****-0.53627.904
Right11917648110236620.580****-1.07859.652
Up11718641106231720.321****-0.76244.517
X11820157109209520.149 (ns)-0.1528.34
Y11820250109222450.341****-0.41219.595

1 One-tailed (MRI > Mock) Kolmogorov-Smirnov tests for independent samples, with FDR (Benjamini-Hocheberg) correction. KS: Kolmogorov-Smirnov statistics. D: Cohen's D. ns: p < = 1.00e+00;

  • 2 *: 1.00e-02 < p < = 5.00e-02;
  • 3 **: 1.00e-03 < p < = 1.00e-02;
  • 4 ***: 1.00e-04 < p < = 1.00e-03;
  • 5 ****: p < = 1.00e-04.

For reference, the naturalistic key durations observed during play in the shinobi_training dataset (Table 3) ranged from from an average of 164ms (for phasic actions that aren't impacted by keypress duration, such as hitting an enemy) to 1153ms for tonic actions that can be maintained over time, such as moving to the right.

Graph

Table 3 Descriptive statistics of keypress durations observed in the training phase of the shinobi dataset. These values reflect typical keypress durations when playing an action platformer videogame on a regular controller.

Duration (ms)
CountMeanSTDMin25%50%75%Max
SubjectKey
sub-01B (Hit)2793913445161161331501400
Y (Jump)29645350187162003174671484
Down24710469423162333505679367
Left106836696701620045088315134
Right290141320212316133567160038650
Up6478428105516336625016217
sub-02B (Hit)49597235169161171833163800
Y (Jump)41653426263162503665332800
Down176977917301631663410008967
Left115596166131620043478413950
Right482031228160616100750176656317
Up15443490511161503675847316
sub-03B (Hit)2155180214161331501834834
Y (Jump)904508384172173847044700
Down74782485816250667107513533
Left398575517162334348174617
Right16271159166616300666135822384
Up32844653316833166216317
sub-06B (Hit)259616153165050675516
Y (Jump)1478626626016661504331483
Down6461473423162004165847833
Left4699369370161172505083883
Right171006568971611633488820017
Up705236142716962504836600
TotalB (Hit)10565216414416831331835516
Y (Jump)86988374248162003335004700
Down496155895811623443376613533
Left273395936101618340076615134
Right959441153170416117567155056317
Up29301445658166728353416217

Motion assessment (custom controller versus control tasks)

Analysis of run-median FD values (Fig 6 and Table 4) showed no significant differences of motion between the gamepad dataset and the other datasets that didn't use our MRI-compatible controller, namely the hcp-rest, hcp-motor and hcp-gamble datasets and the friends dataset (all p > 0.05), with the exception of 2 subjects that showed significant differences between the gamepad and friends datasets (p < 0.01). For all 3 subjects, the shinobi dataset had significantly higher run-median FD values than all the other datasets (all p < 0.05), except for one subject that showed no significant difference between the shinobi dataset and the hcptrt resting-state dataset.

Graph: Fig 6 Distributions of the median of FD values across runs in the datasets included in this study.Data were analyzed separately for each subject, which showed similar effects (A-D). E shows the pooled data of all subjects. ns: p < = 1.00e+00; *: 1.00e-02 < p < = 5.00e-02; **: 1.00e-03 < p < = 1.00e-02; ***: 1.00e-04 < p < = 1.00e-03; ****: p < = 1.00e-04.

Graph

Table 4 Descriptive statistics of the run-median Framewise Displacement (FD) values for the different datasets used in the motion analysis.

sub-01sub-02sub-03sub-06Total
NMeanSTDDur. (hours)NMeanSTDDur. (hours)NMeanSTDDur. (hours)NMeanSTDDur. (hours)NMeanSTDDur. (hours)
friends1940.0980.02737.891940.1390.04337.891960.0390.02238.3081940.1430.03337.897780.1050.031151.978
gamepad80.0630.0280.68580.0990.0220.68580.0250.0140.68580.130.0220.685320.0790.0222.74
hcp-gamble150.0550.0210.801150.0970.050.801150.010.0050.801170.1030.0350.908620.0660.0283.311
hcp-motor150.0530.0190.901150.1380.0410.894150.0270.0290.894180.1560.0511.073630.0940.0353.762
hcp-rest50.1020.0241.24250.1410.0411.24250.0250.0091.24260.1480.0351.49210.1040.0275.216
shinobi570.120.01810.572560.1580.02910.7350NaNNaN0560.2060.03111.3431690.1610.02632.65

fMRI temporal SNR

The temporal SNR maps showed similar distributions of means and standard deviations across the runs acquired with and without the presence of our controller in the MRI scanner (Fig 7). Comparing the average of voxels located within the EPI mask, the two distributions showed significant differences (both p < = 1.00e-04; Mcontroller = 80.88; STDcontroller = 0.88; Mnocontroller = 78.11; STDnocontroller = 0.72) suggesting a slight decrease in noise levels after the controller was introduced in the MRI scanning room.

Graph: Fig 7 Temporal SNR maps on runs acquired with and without the controller present in the scanner.A and B show the mean SNR across runs recorded with and without the controller respectively. C shows the distributions of the averaged SNR values for voxels within the EPI mask. D, E, and F show the same visualizations but for STD values instead. ****: p < = 1.00e-04.

MEG noise covariance

Analysis of the difference between averaged covariance matrices acquired before (T3) and after (T4) the controller installation (Fig 8) showed no significant difference (Wilcoxon signed-rank test, p = 0.139). In contrast, although the controller wasn't present in the scanner during recordings of both T1 and T2, the comparison between these two subsets led to a significant difference (Wilcoxon signed-rank test, p = 0.004), showing that the impact of environmental fluctuations on noise levels could be detected by this method, while the controller's effect could not. In both cases (T1 vs T2 and T3 vs T4), the Pearson correlation between the two averaged matrices was fairly high (r = 0.901 and r = 0.953, respectively). Finally, the similarity of the distributions of pairwise correlations between individual recordings in the different subsets further suggests that the noise patterns observed after the addition of our custom controller weren't altered more than expected by normal environmental fluctuations.

Graph: Fig 8 Comparison of MEG sensors noise covariance over time.A—D Normalized average covariance across T1 and T2 subsets, and correlation between these two distributions. T1 and T2 both were acquired without the CNeuroMod controller present in the MEG scanner. E—H Normalized average covariance across T3 and T4 subsets, and correlation between these two distributions. T3 was acquired without the controller present in the scanner, while T4 was acquired with the controller. I—L Distributions of the pairwise correlations between each pair of individual recordings, for each pair of subsets.

Reproduction

A reproduction of the CNeuroMod controller was built by the engineering team at Neurospin and members of the MIND team at Inria (Paris-Saclay, France; Fig 9). The MIND team was not involved in the design process. The reproduced controller was built according to the design plans and documentation made available online and was fitted to their local MRI system. Minor modifications were implemented by the MIND team, for example the shutter and the cap were printed together instead of assembled after printing and the fiber optic cable was 12m long instead of 10m. Other minor assembly issues (buttons getting stuck) were reported and troubleshooted directly with AC, although other teams will also be able to obtain support via GitHub. The controller was tested by 9 different players during gameplay on Super Mario Bros [[32]] within the MRI scanner and player reported satisfying device useability as measured by the utility ratings. More specifically, the players reported a value of 3 (±0.70 std, a score of 3 is best) for the force required for button activation, 2.55 (±0.88 std, higher is better) for the smoothness during operation, 2.66 (±0.71 std, a score of 3 is best) for the amount of mental effort, 2.88 (±0.33 std, a score of 3 is best) for operation speed, 1.88 (±0.78 std, lower is better) for finger fatigue, 1.33 (±0.71 std, lower is better) for wrist fatigue, 3.33 (±1.22 std, higher is better) for general comfort, and 2.44 (±1.01 std, higher is better) for overall useability.

Graph: Fig 9 Pictures of the reproduced controller by team members at Inria/NeuroSpin.A shows the assembled PCB. B shows the bottom part of the controller, with the switch mechanism in the process of being assembled. C shows the optics fibers installed in the handheld part. D shows the fully assembled controller.

Discussion

We built the CNeuroMod videogame controller to be compatible with both fMRI and MEG. We wrote the documentation, plans needed by other teams to reproduce the controller and its software and made it publically available under an Open Source Hardware license. A feasibility study showed that our controller consistently registers button presses and releases with only small differences in timing compared with a commercial controller. We showed that the CNeuroMod controller can be used without inducing abnormal motion levels. The presence of the CNeuroMod controller in the scanning environment had small effects on tSNR maps and noise covariance matrices with fMRI and MEG, respectively.

Open design and reusability

The design files, software and documentation required to build the controller are all released under a CERN-OHL-P license, an Open Hardware License that allows users to reproduce, modify and redistribute the covered material. This license has been chosen as it is the most permissive version of the CERN-OHL flavors, with the goal of allowing maximal freedom of reuse to anyone. The presented device requires moderate engineering and technical resources to be built, and the materials used were chosen on the basis of their availability and low costs. All the necessary parts can be obtained for an estimated price around 1000 CAD (Table 5). In comparison, the device proposed by Current Design Inc. (including cables and interface) are sold for a total price of 8390 USD at the time of writing. The provided documentation covers all the steps involved in the preparation, assembly and use of the controller. Through the release of this hardware under a permissive OHL, we anticipate that other research teams or commercial entities will be able to easily reuse and/or modify the controller design beyond purely financial considerations.

Graph

Table 5 Bill of material with estimated prices at the time of writing of this manuscript. More details about the suppliers and item numbers can be found in the documentation.

PartSupplierQtyPrice (CAD)
Fiber optic cable duplex 100mDigikey1279.71
Fiber optic transmitterDigikey8163.2
Fiber optic receiverDigikey8198.72
Teensy 3.5 microcontroller boardDigikey137.76
Gate driverDigikey57
Hose 13mm ID, black PE 1Digikey1111.55
Hose 19.48mm ID, black PE 1Digikey1160.38
Voltage regulatorDigikey12.93
Resistor 330 ΩDigikey83.67
Resistor 65 ΩDigikey82.39
Capacitor ceramic 0.1 μFDigikey82.49
Capacitor ceramic 10 μFDigikey22.3
Connector header pin breakaway 24 posDigikey414.28
Connector receptacle 24 posDigikey29.18
Polycarbonate Pan Head Philips Screw 8–32 x 1" 2McMaster-Carr22
Polycarbonate Pan Head Philips Screw 8–32 x 1/2" 2McMaster-Carr33
Polycarbonate Pan Head Philips Screw 4–40 x 3/16" 3McMaster-Carr83.49
Nylon 6/6 Female Threaded Round Standoff 8–32 x 1/4" 2McMaster-Carr58.35
Nylon 6/6 Female Threaded Round Standoff 4–40 x 1/8" 3McMaster-Carr813.12
Total1025.52

Reactivity of the CNeuroMod videogame controller

The study showed that the CNeuroMod controller consistently registers button presses as well as releases with a temporal precision comparable to a commercial controller. Although no differences were observed in button press reaction times, small significant differences were detected in release reaction times (for long presses) and in press duration (for short presses), showing longer release times with the prototype than with the reference controller. This result might indicate the presence of mechanical friction during the button release, an aspect that could be improved in further design iterations.

This difference in release reaction time could impact game play performance, particularly in games that require dense repetitions of button presses, but is likely negligible when playing most other games, as suggested by the successful collection of the shinobi dataset as well as the pilot implemented by the MIND team with Super Mario Bros [[32]]. As a point of reference, the difference in short button press duration observed during the gamepad task (about 30ms on average) is relatively small compared to the duration of button presses observed while participants played Shinobi using the commercial controller (164ms in average), with very few button presses lasting less than 50ms. In most cases, players can adapt to the controller and learn to release the buttons slightly earlier than they would on another controller. This interpretation of our results was confirmed qualitatively by the participants who all reported that it was necessary to adapt to the controller, but then reported they could play comfortably following this adaptation phase. This effect could also contribute to the utility ratings observed across both instances of the prototype (CNeuroMod and MIND teams). Users from both groups reported great to acceptable usability for all items, although a slightly high finger fatigue (2 for the CNeuroMod sample, 1.88 for the Inria/Neurospin sample) was detected. If the delay at release observed during the cued-response task is caused by mechanical friction, attempts from the subjects at compensating this effect might induce unnecessary finger fatigue, which could be improved in further iterations by adjusting the button and shutter mechanism.

Motion comparison across various data sets

The analyses conducted on fMRI runs collected on a wide range of tasks showed similar amounts of motion during our gamepad task compared to control tasks that did not involve the use of a videogame controller. This suggests that the CNeuroMod controller does not increase the amount of motion in the scanner. Conversely, the comparison between the motion measured during the shinobi dataset to that of other control datasets indicated significantly higher levels of motion for the gaming task (shinobi), likely to be attributable to the videogame content and not to the controller itself. Even in the case of the shinobi dataset, many runs had a fairly low level of motion, with median FD levels below 0.2 or even 0.1. Overall, the usage of the Courtois NeuroMod controller seems compatible with the collection of usable fMRI data, and in some instances even high-quality low-motion data.

fMRI and MEG compatibility

Analyses performed on fMRI data acquired on a gel phantom head showed a small impact of the CNeuroMod controller on temporal SNR. These differences are statistically significant but are relatively small compared to the amount of noise typically observed during such recordings. Because fMRI recordings are known to be sensitive to thermal noise [[33]], which can fluctuate across the time of the day, the observed differences might be attributable to the fact that these two series of recordings were acquired within the same day but at different time and thus, at slightly different room temperatures. Replicating these results with other datasets would further confirm that the amount of noise induced by the controller stays well within acceptable range.

The MEG noise covariance matrices showed no significant impact of the CNeuroMod controller. Further analysis of empty room recordings collected at various periods (from April 2019 to June 2021) showed that the variation of noise levels induced by the controller stayed well within the range of changes that could be expected from normal environmental fluctuations.

Implications and future work

The CNeuroMod MRI- and MEG-compatible videogame controller provides a versatile device to play most videogames. This versatility extends to any experimental task that requires the use of 8 or less buttons, representing a very large action space. For example, one can use this controller to answer complex questionnaires, e.g. featuring Likert scale, or perform neuropsychological tasks where users navigate many questions. The CNeuroMod controller is specifically geared towards retro gaming from the generation of the Super Nintendo Entertainment System (SNES, Nintendo). Although some modern titles require basic input sets that can be covered by our controller, most console games published after the release of the XBox (Microsoft) and PlayStation (Sony) use joysticks and trigger buttons under the index.

Future design iterations could reduce the latency of button releases, and enable the inclusion of additional buttons and analog joysticks that would expand the scope of playable videogames to modern titles.

Conclusions

The CNeuroMod controller is designed to be built using commonly accessible tools and materials, and released under an Open Hardware License for maximal reusability. A feasibility study showed response latencies comparable to a standard commercial controller. MRI and MEG experiments showed that the controller does not increase subject motion and has marginal effects on acquisition noise, if any. We hope that the CNeuroMod controller will assist researchers in leveraging the richness of videogame tasks in cognitive neuroscience. Our open design can also contribute to a growing ecosystem of open hardware for reproducible neuroimaging research.

Supporting information

S1 Appendix. Build instructions and documentation.

(PDF)

S1 Dataset. Cued-response task results.

(CSV)

S2 Dataset. Shinobi training behavioral data.

(GZ)

S3 Dataset. FD values of CNeuroMod datasets.

(CSV)

S4 Dataset. fMRI phantom data.

(CSV)

S5 Dataset. Noise covariances of MEG empty room data.

(GZ)

S6 Dataset. Utility ratings of the controller in both sites.

(ODS)

S1 Graphical abstract.

(TIF)

Decision Letter 0

King Bradley R. Academic Editor

19 Jun 2023

PONE-D-23-14328Open design and validation of a reproducible videogame controller for MRI and MEGPLOS ONE

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"The Courtois project on neural modeling was made possible by a generous donation from the Courtois foundation, administered by the Fondation Institut Gériatrie Montréal at CIUSSS du Centre-Sud-de-l'île-de-Montréal and University of Montreal. The Courtois NeuroMod team is based at "Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal", with several other institutions involved. See the CNeuromod documentation for an up-to-date list of contributors (https://docs.cneuromod.ca). The replication of the controller by the MIND team, Inria, France has received funding from the European Union's Horizon 2020 Framework Programme for Research and Innovation under the Specific Grant Agreement No. 945539 (Human Brain Project SGA3) and through the joint Inria "NeuroMind" team grant to PB, KJ, BT and Alexandre Gramfort. PB is a senior fellow ("chercheur boursier senior") of the "Fonds de recherche du Québec - Santé". KJ is supported by funding from the Canada Research Chairs program and a Discovery Grant from the Natural Sciences and Engineering Research Council of Canada.

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Reviewer #2: Yes

***

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Reviewer #2: Yes

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5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The manuscript reports results from a project to build and test a prototype handheld videogame controller that is designed for full compatibility with the key technical limitations of brain imaging equipment. The report includes conceptual drawings, programming support and analysis of the prototype's response characteristics collected from a small sample of participants in the targeted neuroimaging environments.

The motivation, execution and testing analysis of the scanner-compatible controller are explained. The authors' interpretation of the success of the project is sound and supported by their data, and a confirming example from another research group is reported as well.

The report will interest some neuroimaging research teams that have the skills and mindset to build their own hardware rather than adopt commercially available products. A few concerns are described below, which could be addressed in a revision to make a stronger version of the manuscript.

1. The motivation to build a scanner-compatible videogame controller in-house and publish a thorough engineering analysis of the project is apparent in the Introduction, but it can be stated in more complete fashion.

Based on the prototype, the in-house device costs approximately CAD$1,000 in parts and an undefined amount of experienced labor to build. A bit of investigation reveals that the industry standard Current Designs scanner-compatible videogame controller costs approximately US$4,600, plus fees. The authors appear to justify their project by offering a less costly solution, but a detailed calculation is not presented to support this justification.

A further concern about the relative cost as a justification to build a controller in-house is that the comparability of the haptics and user satisfaction between the device alternatives is not addressed. The participant sample in the results is small and from a narrow age range. Although a larger cohort from a much broader age range would be desirable, some sort of utility rating (as collected from the MIND Team confirmation study) is really needed to fully support the conclusion that the CNeuroMod controller is a suitable substitute for the commercially proven and available alternative.

2. Release reaction times on long trials were significantly longer with the prototype than the mock condition commercial controller (non-scanner compatible). No explanation is offered in the Results or Discussion.

Why is there an apparent difference in the responsiveness of the prototype, depending upon duration of the button presses? How does this responsiveness relate to the poor rating from the MIND Team confirmation study participants (i.e., "a value of 2 for the following items: smoothness during operation and general comfort.")?

3. The title and text refer to a validation of the original test results, which had showed the comparability of the functional values from the prototype with a non-scanner compatible mock-up device. No true validation study is reported. In other words, there are no results from two or more cohorts performing the same tests as sequential experiments, and there is no analysis of validating results (i.e., an independent samples t-test, for example).

The MIND Team "study" is relevant, but not well described. The measures in the main results do not appear in the MIND Team section (3.4), and the Mind Team user ratings do not appear in the main results. This is not a replication, and referring to the MIND Team information as a replication needs to corrected throughout.

  • 4. The manuscript reads clearly enough, although the voice or writing style changes noticeably between sections of the text. Conforming the entire report to one writing style would improve its readability.
  • 5. Figure 8 includes panels A through L. The legend for Figure 8 only explains panels A through J.

Panels K and L should either be explained in the legend and text, or eliminated from the figure.

Reviewer #2: Overall the paper was quite straightforward and clearly addresses the core question the team started out with. I have one methodological question with regard to how the number of participants and their demographics was chosen. 4 participants isn't very many obviously and the age range of the participants isn't necessarily a good match for what I'd expect of most future work on gaming/neuroimaging. So it'd be useful for the authors to speak to how they determined the sample size and what types of criteria for participants were considered. I'd note though that because I would call this a "feasibility" illustration, the small sample size & potential non-representativeness of the participants aren't "fatal flaws"; but it would be valuable for readers to know how these factors were chosen.

The other issue that I think would improve the paper is a deeper dive into what I would call the exceptionally dated configuration of the controller. The authors indicate that, "Key features of the SNESTM controller can still be found in modern systems such as the XBoxTM (Microsoft) and PlayStationTM (Sony)" which is true, but still reasonably misleading. For instance, it's a bit like if the team created a new car that was basically a Model T Ford, but said that it "still contains many features of modern cars such as the 2023 Honda Accord." It might be true (e.g., it would have 4 wheels, a steering wheel, a windshield), it would still be super dated. Video game controllers have used a dual stick setup since the late 1990s. There are essentially no modern games that I can think of that someone would be able to play with the controller developed here - certainly none of the games used in the research that the authors reference in the introduction (i.e., most of that work on video games/neuroscience has been after the year 2000). So the authors should spend some time on that particular limitation (or else on why it isn't a limitation).

***

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Author response to Decision Letter 0

29 Jul 2023

Response to reviewers

We thank the editor for providing us the opportunity to revise our work, and the reviewers for the insightful comments which have helped improve our study. A point-by-point response to reviewers can be found below.

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    "The Courtois project on neural modeling was made possible by a generous donation from the Courtois foundation, administered by the Fondation Institut Gériatrie Montréal at CIUSSS du Centre-Sud-de-l'île-de-Montréal and University of Montreal. The Courtois NeuroMod team is based at "Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal", with several other institutions involved. See the CNeuromod documentation for an up-to-date list of contributors (https://docs.cneuromod.ca). The replication of the controller by the MIND team, Inria, France has received funding from the European Union's Horizon 2020 Framework Programme for Research and Innovation under the Specific Grant Agreement No. 945539 (Human Brain Project SGA3) and through the joint Inria "NeuroMind" team grant to PB, KJ, BT and Alexandre Gramfort. PB is a senior fellow ("chercheur boursier senior") of the "Fonds de recherche du Québec - Santé". KJ is supported by funding from the Canada Research Chairs program and a Discovery Grant from the Natural Sciences and Engineering Research Council of Canada.

    The authors would like to thank the MEG Imaging Center and Courtois-Neuromod scanning crews for acquiring the validation data. "

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    "The Courtois project on neural modeling was made possible by a generous donation from the Courtois foundation, administered by the Fondation Institut Gériatrie Montréal at CIUSSS du Centre-Sud-de-l'île-de-Montréal and University of Montreal. The Courtois NeuroMod team is based at "Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal", with several other institutions involved. See the CNeuromod documentation for an up-to-date list of contributors (https://docs.cneuromod.ca). The replication of the controller by the MIND team, Inria, France has received funding from the European Union's Horizon 2020 Framework Programme for Research and Innovation (https://research-and-innovation.ec.europa.eu/funding/funding-opportunities/funding-programmes-and-open-calls/horizon-2020%5fen) under the Specific Grant Agreement No. 945539 (Human Brain Project SGA3) and through the joint Inria "NeuroMind" team grant to PB, KJ, BT and Alexandre Gramfort. PB is a senior fellow ("chercheur boursier senior") of the "Fonds de recherche du Québec - Santé". KJ is supported by funding from the Canada Research Chairs (https://www.chairs-chaires.gc.ca/home-accueil-eng.aspx) program and a Discovery Grant from the Natural Sciences and Engineering Research Council of Canada (https://www.nserc-crsng.gc.ca/index%5feng.asp). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript."

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    Authors answer : We removed the paragraph related to funding information in the "Acknowledgement" section. The information ("Financial Disclosure") provided in the submission form were verified and are correct.

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    Authors answer : We saved the cleaned versions of the datasets used to generate the figures as.csv files (and a.pkl file for MEG covariance matrices) and added them to Supporting Information.

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    Authors answer : We added a section named Supporting Information that mentions the documentation and dataset files.

    Content :

    1a. The motivation to build a scanner-compatible videogame controller in-house and publish a thorough engineering analysis of the project is apparent in the Introduction, but it can be stated in more complete fashion.

    Based on the prototype, the in-house device costs approximately CAD$1,000 in parts and an undefined amount of experienced labor to build. A bit of investigation reveals that the industry standard Current Designs scanner-compatible videogame controller costs approximately US$4,600, plus fees. The authors appear to justify their project by offering a less costly solution, but a detailed calculation is not presented to support this justification.

    Authors answer : We thank the reviewer for pointing out the need for a more thorough price comparison. We modified the paragraph named "Open design and reusability" to add a table (Table 5) that breaks down the prices of the bill of materials. The Discussion has been modified to also discuss the price of a commercial vs open solution.

    1b. A further concern about the relative cost as a justification to build a controller in-house is that the comparability of the haptics and user satisfaction between the device alternatives is not addressed. The participant sample in the results is small and from a narrow age range. Although a larger cohort from a much broader age range would be desirable, some sort of utility rating (as collected from the MIND Team confirmation study) is really needed to fully support the conclusion that the CNeuroMod controller is a suitable substitute for the commercially proven and available alternative.

    Authors answer : The utility ratings of the CNeuroMod sample (i.e. the subjects who performed the cued-response task) were added to the paper as well as the answers of the Inria/Neurospin participants. These additional data are now presented in the Utility ratings sections of the Methods and Results. The Discussion has been modified to relate utility ratings to other behavioral results, and the ratings dataset has been added to Supporting Information.

    2. Release reaction times on long trials were significantly longer with the prototype than the mock condition commercial controller (non-scanner compatible). No explanation is offered in the Results or Discussion.

    Why is there an apparent difference in the responsiveness of the prototype, depending upon duration of the button presses? How does this responsiveness relate to the poor rating from the MIND Team confirmation study participants (i.e., "a value of 2 for the following items: smoothness during operation and general comfort.")?

    Authors answer : We discuss this effect under the section named "Reactivity of the CNeuroMod videogame controller". We agree that the wording did not make clear that we were addressing specifically the longer release times of our prototype, so we modified the text to make it more explicit. We also added a sentence stating that this effect would likely contribute to the poor utility ratings.

    3. The title and text refer to a validation of the original test results, which had showed the comparability of the functional values from the prototype with a non-scanner compatible mock-up device. No true validation study is reported. In other words, there are no results from two or more cohorts performing the same tests as sequential experiments, and there is no analysis of validating results (i.e., an independent samples t-test, for example).

    The MIND Team "study" is relevant, but not well described. The measures in the main results do not appear in the MIND Team section (3.4), and the Mind Team user ratings do not appear in the main results. This is not a replication, and referring to the MIND Team information as a replication needs to corrected throughout.

    Authors answer : We agree with the reviewer that the terms "replication" and "validation" were used improperly. We removed the term validation from the title. We also replaced references to this study as "validation" for other terms, such as "feasibility study". We replaced references to "replication" by "reproduction" of the controller device, because the study wasn't replicated by the MIND team, but they produced a second controller unit.

    4. The manuscript reads clearly enough, although the voice or writing style changes noticeably between sections of the text. Conforming the entire report to one writing style would improve its readability.

    Authors answer : The style and voice of the manuscript have been reviewed and corrected by one of the authors who is a native English speaker.

    5. Figure 8 includes panels A through L. The legend for Figure 8 only explains panels A through J.

    Panels K and L should either be explained in the legend and text, or eliminated from the figure.

    Authors answer : The legend was corrected to cover panels A through L.

    6. Overall the paper was quite straightforward and clearly addresses the core question the team started out with. I have one methodological question with regard to how the number of participants and their demographics was chosen. 4 participants isn't very many obviously and the age range of the participants isn't necessarily a good match for what I'd expect of most future work on gaming/neuroimaging. So it'd be useful for the authors to speak to how they determined the sample size and what types of criteria for participants were considered. I'd note though that because I would call this a "feasibility" illustration, the small sample size & potential non-representativeness of the participants aren't "fatal flaws"; but it would be valuable for readers to know how these factors were chosen.

    Authors answer : We modified the "Participants" section to explain that the subjects were recruited as part of a larger, longitudinal dataset acquisition for which the controller has been developed. We also included a sentence to state that we expected the task to reflect the controllers capability irrespective of videogame experience.

    7. The other issue that I think would improve the paper is a deeper dive into what I would call the exceptionally dated configuration of the controller. The authors indicate that, "Key features of the SNESTM controller can still be found in modern systems such as the XBoxTM (Microsoft) and PlayStationTM (Sony)" which is true, but still reasonably misleading. For instance, it's a bit like if the team created a new car that was basically a Model T Ford, but said that it "still contains many features of modern cars such as the 2023 Honda Accord." It might be true (e.g., it would have 4 wheels, a steering wheel, a windshield), it would still be super dated. Video game controllers have used a dual stick setup since the late 1990s. There are essentially no modern games that I can think of that someone would be able to play with the controller developed here - certainly none of the games used in the research that the authors reference in the introduction (i.e., most of that work on video games/neuroscience has been after the year 2000). So the authors should spend some time on that particular limitation (or else on why it isn't a limitation).

    Authors answer : We agree that our description of the controllers main features could be misleading. To clarify, we adjusted paragraph 2.1.1. to remove the reference to modern titles and state that the goal behind the design of this controller was to enable retro videogame play, and not necessarily modern titles. We additionally modified the discussion section called "Implications and future work" to explicitly state that future improvements of the design are going to be required to play modern titles.

    Attachment.

    Submitted filename: response_letter.docx

    Decision Letter 1

    King Bradley R. Academic Editor

    3 Aug 2023

    Open design of a reproducible videogame controller for MRI and MEG

    PONE-D-23-14328R1

    Dear Dr. Harel,

    We're pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

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    Acceptance letter

    King Bradley R. Academic Editor

    15 Aug 2023

    PONE-D-23-14328R1

    Open design of a reproducible videogame controller for MRI and MEG

    Dear Dr. Harel:

    I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

    If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

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    on behalf of

    Dr. Bradley R. King

    Academic Editor

    PLOS ONE

    The authors would like to thank the MEG Imaging Center, the Functional Neuroimaging Unit at CRIUGM and the Courtois NeuroMod scanning crews for acquiring the data.

    Footnotes 1 The authors have declared that no competing interests exist. References Dale G, Joessel A, Bavelier D, Green CS. A new look at the cognitive neuroscience of video game play. Ann N Y Acad Sci. 2020 Mar; 1464(1):192–203. doi: 10.1111/nyas.14295, 31943260 2 Klasen M, Wolf D, Eisner PD, Eggermann T, Zerres K, Zepf FD, et al. Serotonergic Contributions to Human Brain Aggression Networks. Front Neurosci. 2019 Feb 22; 13:42. doi: 10.3389/fnins.2019.00042, 30853880 3 Klasen M, Mathiak KA, Zvyagintsev M, Sarkheil P, Weber R, Mathiak K. Selective reward responses to violent success events during video games. Brain Struct Funct. 2020 Jan; 225(1):57–69. doi: 10.1007/s00429-019-01986-7, 31754792 4 Wolf D, Klasen M, Eisner P, Zepf FD, Zvyagintsev M, Palomero-Gallagher N, et al. Central serotonin modulates neural responses to virtual violent actions in emotion regulation networks. Brain Struct Funct. 2018 Sep; 223(7):3327–45. doi: 10.1007/s00429-018-1693-2, 29948188 5 Zvyagintsev M, Klasen M, Weber R, Sarkheil P, Esposito F, Mathiak KA, et al. Violence-related content in video game may lead to functional connectivity changes in brain networks as revealed by fMRI-ICA in young men. Neuroscience. 2016 Apr; 320:247–58. doi: 10.1016/j.neuroscience.2016.01.056, 26855192 6 Lim SJ, Fiez JA, Holt LL. Role of the striatum in incidental learning of sound categories. Proc Natl Acad Sci. 2019 Mar 5; 116(10):4671–80. doi: 10.1073/pnas.1811992116, 30782817 7 Takeuchi N, Mori T, Suzukamo Y, Izumi SI. Integration of Teaching Processes and Learning Assessment in the Prefrontal Cortex during a Video Game Teaching–learning Task. Front Psychol [Internet]. 2017 Jan 9 [cited 2021 Jul 20]; 7. Available from: http://journal.frontiersin.org/article/10.3389/fpsyg.2016.02052/full, 28119650 8 Anderson JR, Bothell D, Fincham JM, Moon J. The sequential structure of brain activation predicts skill. Neuropsychologia. 2016 Jan; 81:94–106. doi: 10.1016/j.neuropsychologia.2015.12.014, 26707716 9 Wang M, Dong G, Wang L, Zheng H, Potenza MN. Brain responses during strategic online gaming of varying proficiencies: Implications for better gaming. Brain Behav. 2018 Aug; 8(8):e01076. doi: 10.1002/brb3.1076, 30020566 Huskey R, Craighead B, Miller MB, Weber R. Does intrinsic reward motivate cognitive control? a naturalistic-fMRI study based on the synchronization theory of flow. Cogn Affect Behav Neurosci. 2018 Oct; 18(5):902–24. doi: 10.3758/s13415-018-0612-6, 29923098 Gray WD. Game‐XP: Action Games as Experimental Paradigms for Cognitive Science. Top Cogn Sci. 2017 Apr; 9(2):289–307. doi: 10.1111/tops.12260, 28296290 Sheikholeslami C, Yuan H, He EJ, Bai X, Yang L, He B. A High Resolution EEG Study of Dynamic Brain Activity during Video Game Play. In: 2007 29th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. 2007. p. 2489–91. Klarkowski M, Causse M, Duprès A, del Campo N, Vella K, Johnson D. Using fNIRS to Assess Cognitive Activity During Gameplay. Proc ACM Hum-Comput Interact. 2022 Oct 31; 6(CHI PLAY):256:1–256:23. Cheyne D, Jobst C, Tesan G, Crain S, Johnson B. Movement-related neuromagnetic fields in preschool age children: Movement-Related Brain Activity in Preschool Children. Hum Brain Mapp. 2014 Sep; 35(9):4858–75. Gross-Weege N, Dey T, Gebhardt P, Schug D, Weissler B, Schulz V. Characterization methods for comprehensive evaluations of shielding materials used in an MRI. Med Phys. 2018; 45(4):1415–24. doi: 10.1002/mp.12762, 29363769 Trees J, Snider J, Falahpour M, Guo N, Lu K, Johnson DC, et al. Game controller modification for fMRI hyperscanning experiments in a cooperative virtual reality environment. MethodsX. 2014; 1:292–9. doi: 10.1016/j.mex.2014.10.009, 26150964 Cross L, Cockburn J, Yue Y, O'Doherty JP. Using deep reinforcement learning to reveal how the brain encodes abstract state-space representations in high-dimensional environments. Neuron. 2021 Feb; 109(4):724–738.e7. doi: 10.1016/j.neuron.2020.11.021, 33326755 Zhang T, Gao JS, Çukur T, Gallant JL. Voxel-Based State Space Modeling Recovers Task-Related Cognitive States in Naturalistic fMRI Experiments. Front Neurosci. 2021 May 6; 14:565976. doi: 10.3389/fnins.2020.565976, 34045937 Kätsyri J, Hari R, Ravaja N, Nummenmaa L. The Opponent Matters: Elevated fMRI Reward Responses to Winning Against a Human Versus a Computer Opponent During Interactive Video Game Playing. Cereb Cortex. 2013 Dec; 23(12):2829–39. doi: 10.1093/cercor/bhs259, 22952277 Gentile DA, Swing EL, Anderson CA, Rinker D, Thomas KM. Differential neural recruitment during violent video game play in violent- and nonviolent-game players. Psychol Pop Media Cult. 2016 Jan; 5(1):39–51. Peirce J, Gray JR, Simpson S, MacAskill M, Höchenberger R, Sogo H, et al. PsychoPy2: Experiments in behavior made easy. Behav Res Methods. 2019 Feb 1; 51(1):195–203. doi: 10.3758/s13428-018-01193-y, 30734206 Natapov D, Castellucci SJ, MacKenzie IS. ISO 9241–9 Evaluation of Video Game Controllers. Setsompop K, Gagoski BA, Polimeni JR, Witzel T, Wedeen VJ, Wald LL. Blipped-controlled aliasing in parallel imaging for simultaneous multislice echo planar imaging with reduced g-factor penalty. Magn Reson Med. 2012; 67(5):1210–24. doi: 10.1002/mrm.23097, 21858868 Power JD, Silver BM, Silverman MR, Ajodan EL, Bos DJ, Jones RM. Customized head molds reduce motion during resting state fMRI scans. NeuroImage. 2019 Apr; 189:141–9. doi: 10.1016/j.neuroimage.2019.01.016, 30639840 Esteban O, Ciric R, Finc K, Blair RW, Markiewicz CJ, Moodie CA, et al. Analysis of task-based functional MRI data preprocessed with fMRIPrep. Nat Protoc. 2020 Jul; 15(7):2186–202. doi: 10.1038/s41596-020-0327-3, 32514178 Sega. Shinobi III: Return of the Ninja Master. Sega; 1993. Friends [TV series]. 1994. Crane, D & Kauffman, M (Executive Producers). National Broadcasting Company Vanderwal T, Kelly C, Eilbott J, Mayes LC, Castellanos FX. Inscapes: A movie paradigm to improve compliance in functional magnetic resonance imaging. NeuroImage. 2015 Nov 15; 122:222–32. doi: 10.1016/j.neuroimage.2015.07.069, 26241683 Van Essen DC, Smith SM, Barch DM, Behrens TEJ, Yacoub E, Ugurbil K. The WU-Minn Human Connectome Project: An overview. NeuroImage. 2013 Oct 15; 80:62–79. doi: 10.1016/j.neuroimage.2013.05.041, 23684880 Gorgolewski K, Burns C, Madison C, Clark D, Halchenko Y, Waskom M, et al. Nipype: A Flexible, Lightweight and Extensible Neuroimaging Data Processing Framework in Python. Front Neuroinformatics [Internet]. 2011 [cited 2023 May 9]; 5. Available from: https://www.frontiersin.org/articles/10.3389/fninf.2011.00013, 21897815 Gramfort A, Luessi M, Larson E, Engemann D, Strohmeier D, Brodbeck C, et al. MEG and EEG data analysis with MNE-Python. Front Neurosci [Internet]. 2013 [cited 2023 May 9]; 7. Available from: https://www.frontiersin.org/articles/10.3389/fnins.2013.00267, 24431986 Nintendo. Super Mario Bros. Nintendo; 1983. Krüger G, Glover GH. Physiological noise in oxygenation-sensitive magnetic resonance imaging. Magn Reson Med. 2001; 46(4):631–7. doi: 10.1002/mrm.1240, 11590638

    By Yann Harel; André Cyr; Julie Boyle; Basile Pinsard; Jeremy Bernard; Marie-France Fourcade; Himanshu Aggarwal; Ana Fernanda Ponce; Bertrand Thirion; Karim Jerbi and Pierre Bellec

    Reported by Author; Author; Author; Author; Author; Author; Author; Author; Author; Author; Author

    Titel:
    Open design of a reproducible videogame controller for MRI and MEG.
    Autor/in / Beteiligte Person: Harel, Y ; Cyr, A ; Boyle, J ; Pinsard, B ; Bernard, J ; Fourcade, MF ; Aggarwal, H ; Ponce, AF ; Thirion, B ; Jerbi, K ; Bellec, P
    Link:
    Zeitschrift: PloS one, Jg. 18 (2023-11-01), Heft 11, S. e0290158
    Veröffentlichung: San Francisco, CA : Public Library of Science, 2023
    Medientyp: academicJournal
    ISSN: 1932-6203 (electronic)
    DOI: 10.1371/journal.pone.0290158
    Schlagwort:
    • Humans
    • Reproducibility of Results
    • Magnetic Resonance Imaging methods
    • Neuroimaging
    • Magnetoencephalography
    • Video Games
    Sonstiges:
    • Nachgewiesen in: MEDLINE
    • Sprachen: English
    • Publication Type: Journal Article; Research Support, Non-U.S. Gov't
    • Language: English
    • [PLoS One] 2023 Nov 01; Vol. 18 (11), pp. e0290158. <i>Date of Electronic Publication: </i>2023 Nov 01 (<i>Print Publication: </i>2023).
    • MeSH Terms: Magnetoencephalography* ; Video Games* ; Humans ; Reproducibility of Results ; Magnetic Resonance Imaging / methods ; Neuroimaging
    • References: Front Neuroinform. 2011 Aug 22;5:13. (PMID: 21897815) ; Front Neurosci. 2021 May 06;14:565976. (PMID: 34045937) ; Brain Struct Funct. 2018 Sep;223(7):3327-3345. (PMID: 29948188) ; Neuroimage. 2013 Oct 15;80:62-79. (PMID: 23684880) ; Neuroscience. 2016 Apr 21;320:247-58. (PMID: 26855192) ; Neuron. 2021 Feb 17;109(4):724-738.e7. (PMID: 33326755) ; Cereb Cortex. 2013 Dec;23(12):2829-39. (PMID: 22952277) ; Annu Int Conf IEEE Eng Med Biol Soc. 2007;2007:2489-91. (PMID: 18002499) ; Neuroimage. 2019 Apr 1;189:141-149. (PMID: 30639840) ; Top Cogn Sci. 2017 Apr;9(2):289-307. (PMID: 28296290) ; Front Neurosci. 2019 Feb 22;13:42. (PMID: 30853880) ; Front Neurosci. 2013 Dec 26;7:267. (PMID: 24431986) ; Hum Brain Mapp. 2014 Sep;35(9):4858-75. (PMID: 24700413) ; Neuroimage. 2015 Nov 15;122:222-32. (PMID: 26241683) ; Behav Res Methods. 2019 Feb;51(1):195-203. (PMID: 30734206) ; Proc Natl Acad Sci U S A. 2019 Mar 5;116(10):4671-4680. (PMID: 30782817) ; Nat Protoc. 2020 Jul;15(7):2186-2202. (PMID: 32514178) ; Brain Struct Funct. 2020 Jan;225(1):57-69. (PMID: 31754792) ; Ann N Y Acad Sci. 2020 Mar;1464(1):192-203. (PMID: 31943260) ; Magn Reson Med. 2012 May;67(5):1210-24. (PMID: 21858868) ; Med Phys. 2018 Apr;45(4):1415-1424. (PMID: 29363769) ; Neuropsychologia. 2016 Jan 29;81:94-106. (PMID: 26707716) ; MethodsX. 2014 Nov 04;1:292-9. (PMID: 26150964) ; Front Psychol. 2017 Jan 09;7:2052. (PMID: 28119650) ; Magn Reson Med. 2001 Oct;46(4):631-7. (PMID: 11590638) ; Cogn Affect Behav Neurosci. 2018 Oct;18(5):902-924. (PMID: 29923098) ; Brain Behav. 2018 Aug;8(8):e01076. (PMID: 30020566)
    • Entry Date(s): Date Created: 20231101 Date Completed: 20231103 Latest Revision: 20231103
    • Update Code: 20240514
    • PubMed Central ID: PMC10619825

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