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Vasileios Stavropoulos Department of Psychology, Applied Health, School of Health and Biomedical Sciences, RMIT University, Australia

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Maria Prokofieva Victoria University, Australia

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Daniel Zarate Department of Psychology, Applied Health, School of Health and Biomedical Sciences, RMIT University, Australia

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Michelle Colder Carras Bloomberg School of Public Health, John Hopkins University, Baltimore, USA

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Rabindra Ratan Michigan State University, USA

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Rachel Kowert Psychology Research Institute, Faculty of Social Studies, Masaryk University, Brno, Czech Republic
Department of Communication, University of Münster, Münster, Germany

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Bruno Schivinski School of Media and Communication, RMIT University, Australia

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Tyrone L. Burleigh Department of Psychology, Applied Health, School of Health and Biomedical Sciences, RMIT University, Australia

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Dylan Poulus Physical Activity, Sport and Exercise Research Theme, Faculty of Health, Southern Cross University, Gold Coast, Australia
Manna Institute, Southern Cross University, Gold Coast, Australia

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Leila Karimi Department of Psychology, Applied Health, School of Health and Biomedical Sciences, RMIT University, Australia

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Angela Gorman-Alesi Catholic Care Victoria, Australia

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Taylor Brown Department of Psychology, Applied Health, School of Health and Biomedical Sciences, RMIT University, Australia

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Rapson Gomez Department of Psychology, Applied Health, School of Health and Biomedical Sciences, RMIT University, Australia

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Kaiden Hein Department of Psychology, Applied Health, School of Health and Biomedical Sciences, RMIT University, Australia

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Nalin Arachchilage School of Computing, RMIT University, Australia

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Mark D. Griffiths International Gaming Research Unit, Psychology Dept, Nottingham Trent University, UK

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Open access

Abstract

In response to our study, the commentary by Infanti et al. (2024) raised critical points regarding (i) the conceptualization and utility of the user-avatar bond in addressing gaming disorder (GD) risk, and (ii) the optimization of supervised machine learning techniques applied to assess GD risk. To advance the scientific dialogue and progress in these areas, the present paper aims to: (i) enhance the clarity and understanding of the concepts of the avatar, the user-avatar bond, and the digital phenotype concerning gaming disorder (GD) within the broader field of behavioral addictions, and (ii) comparatively assess how the user-avatar bond (UAB) may predict GD risk, by both removing data augmentation before the data split and by implementing alternative data imbalance treatment approaches in programming.

Abstract

In response to our study, the commentary by Infanti et al. (2024) raised critical points regarding (i) the conceptualization and utility of the user-avatar bond in addressing gaming disorder (GD) risk, and (ii) the optimization of supervised machine learning techniques applied to assess GD risk. To advance the scientific dialogue and progress in these areas, the present paper aims to: (i) enhance the clarity and understanding of the concepts of the avatar, the user-avatar bond, and the digital phenotype concerning gaming disorder (GD) within the broader field of behavioral addictions, and (ii) comparatively assess how the user-avatar bond (UAB) may predict GD risk, by both removing data augmentation before the data split and by implementing alternative data imbalance treatment approaches in programming.

Introduction

In response to our paper (Stavropoulos et al., 2023), the recent commentary by Infanti et al. (2024) highlighted areas requiring further clarification regarding (i) the conceptualization and utility of the user-avatar bond (UAB) as a gaming disorder (GD) risk indicator, and (ii) the optimal application of supervised Machine Learning (ML) techniques in addressing prediction challenges related to imbalanced data, particularly within the context of the UAB-GD association.

Infanti et al. noted that: (i) the UAB may not apply to all game genres and differs across individuals, and (ii) digital phenotyping should involve superior objective data (e.g., screen/application monitoring). They also had concerns regarding methodology, including the (iii) use of synthetic minority oversampling technique (SMOTE) in algorithm development, (iv) the non-use of ML regression methods, (v) how the Gaming Disorder Test (GDT-4) was used, and (vi) the lack of access to the original data.

Such considerations are valuable to promote and foster dialogue and advance clarity in the field. To contribute to this discourse, the present commentary aims to: (i) further clarify the concepts of avatar, UAB, and digital phenotype in relation to GD within the broader context of behavioral addictions, and (ii) provide evidence regarding the UAB-GD-risk association by reproducing our original analysis without augmenting data before the data split, as well as indicatively using a combination of alternative data-balancing techniques.

Conceptual clarity

Infanti et al. (2024) suggest that data used in digital phenotypes should be “superior to self-report,” citing a GD digital phenotyping study by Montag and Rumpf (2021). However, in their study, Montag and Rumpf (2021) argued that “the most accurate picture” of internet use disorders can be found by “asking participants about symptom load related to IUD [internet use disorder]” (i.e., self-report data) in combination with objective recording. Because mental health conditions (including GD) involve disturbances in behaviors, cognitions, and emotions (American Psychiatric Association [APA], 2022), self-reports of thoughts and feelings, including those related to avatars, have always held an important role in diagnosis, with clinical interviews as the gold standard. As stated throughout our original paper, the intent of our study was to improve the ability to identify possible GD risk, not to substitute a comprehensive diagnostic procedure. Using ML to classify individuals as having GD risk (as in the use of ML for determining risk for any condition) based on the intensity of their GD symptoms and the UAB does not imply diagnosis, but rather assigning them to a high-risk category. From an epidemiological perspective, screening for the risk of mental health disorders is important for identifying those who may need treatment or prevention interventions based on their self-reported symptom levels (Eaton et al., 2012).

In that context, revisiting the origins and evolution of the digital phenotype concept can further support its relevance to UAB. Traditionally, a phenotype includes behaviors shaped by a person's predispositions and life experiences, offering essential insights into their physical and mental health (Zarate, Stavropoulos, Ball, De Sena Collier, & Jacobson, 2022). The extended phenotype of an organism refers to all the environmental changes it generates, affecting its Darwinian fitness, or the possibility of its genes being passed to the next generation (i.e., surviving, reproducing; Dawkins, 1982). The digital phenotype, derived from the extended phenotype, refers to the transformations and traces that users leave in their online environment, captured by various detectors to achieve their species-specific aims (e.g., cultural recognition and acceptance; Loi, 2019).

As with other extended phenotypes, the interaction between users and their digital environment introduces a co-evolutionary bond (i.e., users change/affect their digital environment, which later changes/affects them in a perpetual spiral; Loi, 2019). Such observations prompted Haraway (2008) to metaphorically describe digital data as a companion species. Indeed, several studies have explored the phenotypical potential embedded within the use of online/digital media through passive ways (i.e., digital sensors) and/or active ways (e.g., self-report questionnaires in the context of digitally facilitated ecological momentary assessment [EMA]) under the digital phenotype umbrella term (Zarate et al., 2022). To enhance clarity, Zarate et al. (2022) proposed features of objectivity and granularity as key aspects of the digital phenotype, encompassing passive physiological sensing, digital biomarkers, mobile sensing, and cyber-phenotype (i.e., exclusively cyber-behavior) subtypes.

To acknowledge the species-specific functions (e.g., acceptance) and the dynamically co-evolving nature of the user-UAB association, the term 'digital phenotype' was introduced in quotation marks in our study (Stavropoulos et al., 2023). The choice of using digital phenotype as a conceptual proxy was reinforced by: (i) empirical evidence underscoring the significance of the phenotypical information conveyed by the way excessive users experience their connection with their avatar (e.g., Casale, Musicò, Gualtieri, & Fioravanti, 2023; Servidio, Griffiths, Boca, & Demetrovics, 2023; Szolin, 2022), and (ii) clinical evidence leveraging the insights included in the UAB to address disordered gaming use (e.g., Tisseron, 2009).

Infanti et al. (2024) additionally advocated that the UAB may not be operative as a GD risk indicator because avatars are not universally present across all game genres, and even when they are, the customization options and user experiences can vary significantly. This concern is understandable, as what an avatar constitutes is not consistently described in the literature, with more rigid definitions assuming a visual, often anthropomorphic depiction, whereas broader and more flexible conceptualizations include any type of representation (e.g., sounds, usernames, text-descriptions; “any representation of any controller” [Nowak & Fox, 2018; p. 34]). However, despite such discrepancies, there is a consensus that an avatar represents the user digitally, even if not visualized, allowing them to interact with their digital environment and others within it (Nowak & Fox, 2018). In the end, representation and agency are the two necessary and distinctive avatar components (Nowak & Fox, 2018). Therefore, avatars and the bonds that users form with them, are present in every videogame in which the user's actions (agency) are reflected in some perceivable change within the game, and where a form of user portrayal is required (representation). Therefore, avatars can provide valuable insights for the user through projective processes, even if they are not anthropomorphic or embodied (Nowak & Fox, 2018; Tisseron, 2009). For instance, in a real-time strategy game, the player aims to expand their territory and influence using their in-game army, while in their offline life, they may experience a lack of space and control.

Additionally, Infanti et al. (2024) suggested that due to the variability in users' experience with their avatars, a fused relationship between the two may not always be present, complicating the inference of GD risk. We argue that it is exactly this variability of the UAB intensity, assumed to be normally distributed among the gamer population, irrespective of how this may be conceptualized (e.g., Banks & Bowman, 2021; Ratan & Dawson, 2016; Stavropoulos, Motti-Stefanidi, & Griffiths, 2022) that constitutes a source of information itself when dimensionally assessed. For example, users not at risk for GD may report lower levels of UAB, as observed in our study (Stavropoulos et al., 2023). Nevertheless, in our study, role-playing games were emphasized due to their inherent role-playing-avatar features and their higher association with GD risk (Mancini, Imperato, & Sibilla, 2019; Stavropoulos, Motti-Stefanidi, & Griffiths, 2022).

Methodological clarity

From a methodological perspective, Infanti et al. (2024) noted that supervised ML in our study may be affected by using the Synthetic Minority Oversampling Technique (SMOTE) before splitting the data into training and testing sets, and likely inflating an otherwise non-significant relationship. Although this approach has been applied by other ML health studies (e.g., Ishaq et al., 2021), to address this concern, while concurrently expanding on programming capabilities we (i) repeated the initial ML, R-based, analysis involving Naive Bayes, Random Forests, LASSO regression, logistic regression, k Nearest Neighbor (kNN), Support Vector Machine (SVM), and XG Boost without SMOTE before the data split, and (ii) employed, alongside SMOTE, three alternative data-imbalance remedies while training the MLs. These involved the Adaptive Synthetic Sampling Approach for Imbalanced Learning (ADASYN), the Random Over-Sampling Examples (ROSE), and the Tomek-Links approach (Khairy, Mahmoud, & Abd-El-Hafeez, 2024). ADASYN builds on SMOTE by creating synthetic samples while adapting their final number for each minority class instance based on the local density of the majority class (He, Bai, Garcia, & Li, 2008). The ROSE algorithm performs over-sampling combined with smoothing in a multivariate way, and the Tomek-Links approach identifies case pairs from the majority and minority classes that are closest to each other representing borderline/noisy points, which are then used to undersample (Dar & Farooq, 2024; Haixiang et al., 2017). See Appendix for more information.

The random forests model using SMOTE post-split demonstrated acceptable performance (and superior to other MLs examined) considering all evaluated fit criteria across the three alternative data balancing approaches tested in predicting concurrent GD Risk. The findings achieved a Receiver Operating Characteristic (ROC) of 0.707, a Positive Predictive Value (PPV) of 0.808 (i.e., precision, how many of those classified as positive are truly positive), a Negative Predictive Value of 0.500 (NPV; i.e. how likely a person with a not at risk result truly is not at risk), a True Negative Rate of 0.934 (TNR; i.e. specificity or selectivity; how well a model identifies negative cases), a sensitivity of 0.877 (i.e. how well a test can identify true cases), an F-measure of 0.884 (F-meas; i.e., the ratio of the multiplication of recall and precision, multiplied by two, and then divided by the accumulation of recall and precision), a recall of 0.977 (i.e., true positive classified cases divided by the number of true positive cases), and an accuracy of 0.796 (i.e., the ratio of correctly predicted cases, across the total number of cases) (see Appendix). Considering predictions of prospective GD risk (i.e., six months later), the Random Forest model with ADASYN had collectively more balanced performance, comparatively to all other combinations of models and data-balancing modalities assessed across the different fit indices (ROC = 0.631, PPV = 0.808, NPV = 0.286, TNR = 0.167, F-meas = 0.848, Sensitivity = 0.894, recall = 0.894, and accuracy = 0.746). At this point, we wish to note that no other advanced combination of remedies (e.g., concurrent use of SMOTE and Tomek Links in conjunction with ensemble ML modeling, where a sequence of varying models are assembled to inform predictions) has been employed, as is beyond the scope of this commentary.

Infanti et al. (2024) criticized the non-use of ML regression methods, suggesting that more variable-focused approaches would better suit the assessment of GD risk. The classification approach employed was chosen deliberately based on the research aim. Rather than taking a variable-focused approach that identifies risk along a continuous spectrum, the goal was person-focused. It was to specifically highlight those individuals at GD risk. This approach is more practically meaningful, as it directs attention to those who may need intervention, rather than solely analyzing the overall severity of symptoms across a population.

Infanti et al. (2024) additionally highlighted that the four-item GDT-4 is intended to assess GD behavior severity, while the GDT-4 “functional impairment criterion” was not considered (WHO, 2022). It is important to reiterate that our use of the GDT-4 focused on identifying individuals at risk rather than diagnosing (and thus requiring functional impairment), consistent with our person-centered methodology. An individual's level of symptoms, and therefore their risk, can fluctuate over time due to the interplay of personal factors (e.g., predispositions), contextual factors, and virtual contextual factors (e.g., precipitating, perpetuating, and protective factors; Stavropoulos, Motti-Stefanidi, & Griffiths, 2022). Consequently, functional impairment is not always necessary to assess level of risk. Instead, focusing on the subclinical risk thresholds of the GDT-4 as a self-report instrument is more appropriate as it reflects a targeted, prevention-oriented approach rather than a diagnostic claim. As prevention of mental disorders is both efficacious and cost-effective, this is an important goal (Mendelson & Eaton, 2018).

Conclusion

Thanks to Infanti et al. (2024), we had the opportunity to further elaborate on the theoretical aspects of the UAB definition and its GD risk predictive capacity. Although AI and ML techniques are still novel and promising analytical methods in the field of behavioral addictions, including by our team, we believe that the critical and inquisitive stance of Infanti et al. (2024) helps the field progress. On the contrary, the UAB's capacity to reveal information about the user, particularly their GD risk, has been well established over the past decade (e.g., Burleigh, Stavropoulos, Liew, Adams, & Griffiths, 2018; Stavropoulos, Gomez, Mueller, Yucel, & Griffiths, 2020), with ML methods adding a new layer of automation in decoding this information. In this context, we hope that our commentary response constructively promotes dialogue among scholars, while also equipping researchers with more knowledge regarding both the conceptual and methodological points raised. In this line, a corrigendum to the original article has been issued addressing the aforementioned concerns.

Funding sources

Vasileios Stavropoulos has received the Australian Research Council, Discovery Early Career Researcher Aw, Grant/Award Number: DE210101107.

Authors' contribution

Vasileios Stavropoulos wrote the first draft of this commentary response. Vasileios Stavropoulos, Mark D. Griffiths, Michelle Colder Carras, Daniel Zarate, Tyrone L. Burleigh, Bruno Schivinski, Leila Karimi, Angela Gorman-Alesi, Dylan Poulus, Taylor Brown, Rapson Gomez, Kaiden Hein, Rabindra Ratan, and Rachel Kowert contributed to the conceptual clarity around the UAB and around risk assessment in gaming disorder. Maria Prokofieva, Daniel Zarate, Vasileios Stavropoulos, and Nalin Arachchilage contributed to the methodological clarity part. All authors contributed to the writing and editing of the manuscript.

Conflicts of interest

MCC conducts scientific consulting on video games and has received grant support to conduct research on crisis prevention in online gaming communities. MDG has received research funding from Norsk Tipping (the gambling operator owned by the Norwegian government). MDG has received funding for a number of research projects in the area of gambling education for young people, social responsibility in gambling and gambling treatment from Gamble Aware (formerly the Responsibility in Gambling Trust), a charitable body which funds its research program based on donations from the gambling industry. MDG undertakes consultancy for various gambling companies in the area of player protection and social responsibility in gambling.

Acknowledgment

The year 10 student Zakarij MCNAMARA contributed to initially identifying the points raised in the Infanti et al. (2024) commentary and shaping the form of the response politely and graciously during his work-experience week in the Associate Dean for HDR students office of the School of Health and Biomedical Sciences of RMIT University.

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Appendix

Results no SMOTE wave 1

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.5130.8020.5000.8550.0450.9880.9880.796
R Forest0.6660.796NaN0.8870.0001.0001.0000.796
LASSO0.6920.6190.6170.8870.0001.0001.0000.796
Log reg0.6900.6480.6450.8870.0001.0001.0000.796
KNN0.9380.9760.8060.8870.0001.0001.0000.796
SVM0.9820.9900.9550.8870.0001.0001.0000.796
XGB0.9470.8720.8930.8870.0001.0001.0000.796

Results with SMOTE post splitting wave 1

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.5730.8060.3000.8590.8020.6890.9190.759
R Forests0.7070.8080.5000.8840.9340.8770.9770.796
LASSO0.6650.796NaN0.8870.8960.8111.0000.796
Log reg0.6450.796NaN0.8870.5660.6131.0000.590
KNN0.6610.8000.3330.8800.9810.7550.9770.787
SVM0.5240.796NaN0.8870.9530.9151.0000.796
XG Boost0.6370.8160.4000.8700.8960.8110.9300.778

Results with ADASYN post splitting wave 1

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.5830.8120.2310.7230.8020.6890.6510.602
R Forests0.6970.8400.5000.8780.9340.8770.9190.796
LASSO0.6330.8360.2550.6940.5850.6420.5930.583
Log reg0.6290.8310.2450.6760.5660.6130.5700.590
KNN0.5440.7950.2000.7300.9810.7550.6740.602
SVM0.5200.8260.3750.8540.9530.9150.8840.759
XG Boost0.5000.796NaN0.8870.8960.8111.0000.796

Results with ROSE post splitting wave 1

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.6590.8330.2500.6850.5450.5810.5810.574
R Forests0.6310.8640.2860.7030.6360.5930.5930.602
LASSO0.7200.9130.2900.6360.5850.6420.4880.556
Log reg0.7200.9130.2900.6360.8180.4880.4880.590
KNN0.5860.8630.2630.6420.6820.5120.5120.546
SVM0.6290.8960.2830.6420.7730.5000.5000.556
XG Boost0.5000.796NaN0.8870.0001.0001.0000.796

Results with Tomek links post splitting wave 1

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.6770.8000.3330.8800.04550.9770.9770.787
R Forests0.6490.796NaN0.8870.00001.0001.0000.796
LASSO0.6610.796NaN0.8870.00001.0001.0000.796
Log reg0.6800.796NaN0.8870.00001.0001.0000.590
KNN0.6480.796NaN0.8870.00001.0001.0000.796
SVM0.5650.796NaN0.8870.00001.0001.0000.796
XG Boost0.6720.796NaN0.8870.00001.0001.0000.796

Results no SMOTE wave 2

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.6120.7920.1670.8400.0830.8940.8940.729
R Forests0.6100.797NaN0.8870.0001.0001.0000.797
LASSO0.7100.797NaN0.8870.0001.0001.0000.797
Log reg0.6930.797NaN0.8870.0001.0001.0000.797
KNN0.5300.797NaN0.8870.0001.0001.0000.797
SVM0.4450.797NaN0.8870.0001.0001.0000.797
XG Boost0.5000.797NaN0.8870.0001.0001.0000.797

Results with SMOTE post splitting wave 2

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.6240.8290.2780.7730.4170.7230.7230.661
R Forests0.6130.7860.0000.8540.0000.9360.9360.746
LASSO0.5000.797N/A0.8870.0001.0001.0000.797
Log reg0.7040.797N/A0.8870.0001.0001.0000.590
KNN0.5870.797N/A0.8870.0001.0001.0000.797
SVM0.5600.797N/A0.8870.0001.0001.0000.797
XG Boost0.5000.797N/A0.8870.0001.0001.0000.797

Results with ADASYN post splitting wave 2

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.6580.8480.2690.7000.5830.5960.5960.593
R Forests0.6310.8080.2860.8480.1670.8940.8940.746
LASSO0.5000.797NaN0.8870.0001.0001.0000.797
Log reg0.6950.9140.3750.780.7500.6810.6810.695
KNN0.4910.8000.2110.7360.3330.6810.6810.610
SVM0.4860.7920.1820.8000.1670.8090.8090.678
XG Boost0.5000.797NaN0.8871.0000.7970.5000.797

Results with ROSE post splitting wave 2

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.6130.8850.2730.6300.7500.4890.4890.542
R Forests0.6490.8480.2690.7000.5830.5960.5960.593
LASSO0.6810.8290.2500.7070.5000.6170.6170.593
Log reg0.6810.8290.2500.7070.5000.6170.6170.590
KNN0.5500.8120.2220.6580.5000.5530.5530.542
SVM0.6700.8570.2920.7320.5830.6380.6380.627
XG Boost0.5000.797NaN0.8870.0001.0001.0000.797

Results with Tomek links post splitting wave 2

Modelroc_aucppvnpvf_measspecsensrecallaccuracy
NBayes0.5340.8040.2000.8740.08330.9150.9150.780
R Forests0.6560.797NaN0.8870.00001.0001.0000.797
LASSO0.7160.797NaN0.8870.00001.0001.0000.797
Log reg0.6700.797NaN0.8870.00001.0001.0000.651
KNN0.5710.797NaN0.8870.00001.0001.0000.797
SVM0.3010.797NaN0.8870.00001.0001.0000.797
XG Boost0.5000.797NaN0.8870.00001.0001.0000.797

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Dr. Zsolt Demetrovics
Institute of Psychology, ELTE Eötvös Loránd University
Address: Izabella u. 46. H-1064 Budapest, Hungary
Phone: +36-1-461-2681
E-mail: jba@ppk.elte.hu

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2023  
Web of Science  
Journal Impact Factor 6.6
Rank by Impact Factor Q1 (Psychiatry)
Journal Citation Indicator 1.59
Scopus  
CiteScore 12.3
CiteScore rank Q1 (Clinical Psychology)
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SJR Q rank Q1

Journal of Behavioral Addictions
Publication Model Gold Open Access
Submission Fee none
Article Processing Charge 990 EUR/article for articles submitted after 30 April 2023 (850 EUR for articles submitted prior to this date)
Regional discounts on country of the funding agency World Bank Lower-middle-income economies: 50%
World Bank Low-income economies: 100%
Further Discounts Corresponding authors, affiliated to an EISZ member institution subscribing to the journal package of Akadémiai Kiadó: 100%.
Subscription Information Gold Open Access

Journal of Behavioral Addictions
Language English
Size A4
Year of
Foundation
2011
Volumes
per Year
1
Issues
per Year
4
Founder Eötvös Loránd Tudományegyetem
Founder's
Address
H-1053 Budapest, Hungary Egyetem tér 1-3.
Publisher Akadémiai Kiadó
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 2062-5871 (Print)
ISSN 2063-5303 (Online)

Senior editors

Editor(s)-in-Chief: Zsolt DEMETROVICS

Assistant Editor(s): Csilla ÁGOSTON

Associate Editors

  • Stephanie ANTONS (Universitat Duisburg-Essen, Germany)
  • Joel BILLIEUX (University of Lausanne, Switzerland)
  • Beáta BŐTHE (University of Montreal, Canada)
  • Matthias BRAND (University of Duisburg-Essen, Germany)
  • Ruth J. van HOLST (Amsterdam UMC, The Netherlands)
  • Daniel KING (Flinders University, Australia)
  • Gyöngyi KÖKÖNYEI (ELTE Eötvös Loránd University, Hungary)
  • Ludwig KRAUS (IFT Institute for Therapy Research, Germany)
  • Marc N. POTENZA (Yale University, USA)
  • Hans-Jurgen RUMPF (University of Lübeck, Germany)

Editorial Board

  • Sophia ACHAB (Faculty of Medicine, University of Geneva, Switzerland)
  • Alex BALDACCHINO (St Andrews University, United Kingdom)
  • Judit BALÁZS (ELTE Eötvös Loránd University, Hungary)
  • Maria BELLRINGER (Auckland University of Technology, Auckland, New Zealand)
  • Henrietta BOWDEN-JONES (Imperial College, United Kingdom)
  • Damien BREVERS (University of Luxembourg, Luxembourg)
  • Wim VAN DEN BRINK (University of Amsterdam, The Netherlands)
  • Julius BURKAUSKAS (Lithuanian University of Health Sciences, Lithuania)
  • Gerhard BÜHRINGER (Technische Universität Dresden, Germany)
  • Silvia CASALE (University of Florence, Florence, Italy)
  • Luke CLARK (University of British Columbia, Vancouver, B.C., Canada)
  • Jeffrey L. DEREVENSKY (McGill University, Canada)
  • Geert DOM (University of Antwerp, Belgium)
  • Nicki DOWLING (Deakin University, Geelong, Australia)
  • Hamed EKHTIARI (University of Minnesota, United States)
  • Jon ELHAI (University of Toledo, Toledo, Ohio, USA)
  • Ana ESTEVEZ (University of Deusto, Spain)
  • Fernando FERNANDEZ-ARANDA (Bellvitge University Hospital, Barcelona, Spain)
  • Naomi FINEBERG (University of Hertfordshire, United Kingdom)
  • Sally GAINSBURY (The University of Sydney, Camperdown, NSW, Australia)
  • Belle GAVRIEL-FRIED (The Bob Shapell School of Social Work, Tel Aviv University, Israel)
  • Biljana GJONESKA (Macedonian Academy of Sciences and Arts, Republic of North Macedonia)
  • Marie GRALL-BRONNEC (University Hospital of Nantes, France)
  • Jon E. GRANT (University of Minnesota, USA)
  • Mark GRIFFITHS (Nottingham Trent University, United Kingdom)
  • Joshua GRUBBS (University of New Mexico, Albuquerque, NM, USA)
  • Anneke GOUDRIAAN (University of Amsterdam, The Netherlands)
  • Susumu HIGUCHI (National Hospital Organization Kurihama Medical and Addiction Center, Japan)
  • David HODGINS (University of Calgary, Canada)
  • Eric HOLLANDER (Albert Einstein College of Medicine, USA)
  • Zsolt HORVÁTH (Eötvös Loránd University, Hungary)
  • Susana JIMÉNEZ-MURCIA (Clinical Psychology Unit, Bellvitge University Hospital, Barcelona, Spain)
  • Yasser KHAZAAL (Geneva University Hospital, Switzerland)
  • Orsolya KIRÁLY (Eötvös Loránd University, Hungary)
  • Chih-Hung KO (Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Taiwan)
  • Shane KRAUS (University of Nevada, Las Vegas, NV, USA)
  • Hae Kook LEE (The Catholic University of Korea, Republic of Korea)
  • Bernadette KUN (Eötvös Loránd University, Hungary)
  • Katerina LUKAVSKA (Charles University, Prague, Czech Republic)
  • Giovanni MARTINOTTI (‘Gabriele d’Annunzio’ University of Chieti-Pescara, Italy)
  • Gemma MESTRE-BACH (Universidad Internacional de la Rioja, La Rioja, Spain)
  • Astrid MÜLLER (Hannover Medical School, Germany)
  • Daniel Thor OLASON (University of Iceland, Iceland)
  • Ståle PALLESEN (University of Bergen, Norway)
  • Afarin RAHIMI-MOVAGHAR (Teheran University of Medical Sciences, Iran)
  • József RÁCZ (Hungarian Academy of Sciences, Hungary)
  • Michael SCHAUB (University of Zurich, Switzerland)
  • Marcantanio M. SPADA (London South Bank University, United Kingdom)
  • Daniel SPRITZER (Study Group on Technological Addictions, Brazil)
  • Dan J. STEIN (University of Cape Town, South Africa)
  • Sherry H. STEWART (Dalhousie University, Canada)
  • Attila SZABÓ (Eötvös Loránd University, Hungary)
  • Hermano TAVARES (Instituto de Psiquiatria do Hospital das Clínicas da Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil)
  • Alexander E. VOISKOUNSKY (Moscow State University, Russia)
  • Aviv M. WEINSTEIN (Ariel University, Israel)
  • Anise WU (University of Macau, Macao, China)

 

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