Published online Feb 19, 2026. doi: 10.5498/wjp.v16.i2.114358
Revised: October 24, 2025
Accepted: November 19, 2025
Published online: February 19, 2026
Processing time: 135 Days and 18.2 Hours
Neurofeedback therapy (NFT) has emerged as a promising noninvasive inter
Core Tip: Neurofeedback therapy (NFT), a non-invasive technique using real-time electroencephalography feedback to self-regulate brain activity, may offer benefits for neural dysregulation in autism spectrum disorder. However, current evidence is limited by small sample sizes and protocol variability. While NFT could potentially enhance neuroplasticity and complement behavioral therapies, its clinical application requires validation through rigorous randomized controlled trials. Future work should focus on personalizing protocols based on biomarkers and improving accessibility via telehealth solutions.
- Citation: Zhang Y, Wang JJ, Xing HY, Yan J. Neurofeedback for autism spectrum disorder: Current evidence, challenges, and future directions. World J Psychiatry 2026; 16(2): 114358
- URL: https://www.wjgnet.com/2220-3206/full/v16/i2/114358.htm
- DOI: https://dx.doi.org/10.5498/wjp.v16.i2.114358
Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by deficits in social communication and restricted behaviors[1]. Conventional interventions such as applied behavior analysis (ABA) often fail to address underlying neural dysregulation. Neurofeedback therapy (NFT), which enables self-regulation of brain activity via real-time electroencephalography (EEG) feedback, has emerged as a potential adjunctive approach. Wang et al[2] reported improvements in social responsiveness following NFT combined with conventional therapy in 2025. This editorial critically evaluates current evidence, mechanistic insights, and future directions for NFT in ASD, emphasizing methodological limitations[1,2].
NFT shows potential as an intervention for ASD, with studies reporting improvements in core symptoms. For instance, NFT combined with conventional therapy has been associated with significant enhancements in social responsiveness, as measured by tools such as the Social Responsiveness Scale (SRS), and in cognitive functions, such as improved performance on executive function tasks such as the Flanker test[2,3]. These behavioral gains are often supported by electrophysiological changes, including reductions in P300 latency, which may indicate accelerated neural processing[4,5]. Mechanistically, NFT is thought to modulate prefrontal gamma-band activity and strengthen connectivity within social brain networks such as the default mode network (DMN), promoting neuroplasticity[6-8].
However, the evidence remains preliminary due to significant methodological limitations. Most studies have small sample sizes (often under 50 participants), which limits statistical power and generalizability[2,3]. Furthermore, protocols vary widely in terms of session duration, frequency, and target EEG frequencies, creating heterogeneity that hinders cross-study comparisons and meta-analytic synthesis[5]. A short-term focus is another constraint, as most trials lack long-term follow-up beyond six months, leaving the durability of effects uncertain[2]. The absence of double-blind designs in many studies also introduces risks of expectation bias as improvements may be influenced by non-specific factors such as placebo effects[5]. Future research must address these gaps through larger, standardized, and long-term trials to defi
| Domain | Key findings | Effect size/Latency change | Limitations |
| Social communication | SRS scores enhance | 15% reduction | Small samples; no active sham |
| Emotion regulation | ABC scores decrease; P300 latency decrease | ∆41.95 ms (P < 0.05) | Short-term follow-up |
| Cognitive function | Executive function (Flanker test) enhance | ∆1.59 (P < 0.001) | High-functioning ASD bias |
NFT operates by enabling patients to voluntarily self-regulate brain activity through visual or auditory feedback derived from real-time EEG signals. The key mechanisms underpinning its efficacy in ASD include the following.
NFT frequently targets the dorsolateral and medial prefrontal regions, which are critically involved in executive function and social cognition. Abnormal gamma-band activity (30-80 Hz) in these areas—often associated with excitatory/inhibitory imbalances in ASD—can be normalized through targeted training. Wang et al’s protocol[2], which incorporated cartoon-based attention tasks to enhance gamma activity, aligns with previous studies demonstrating improved social responsiveness post intervention[8]. For instance, Wang et al[2] reported that beta-band NFT increased functional connectivity within the default mode and salience networks, reducing static network variability and concomitantly improving social behaviors[4] (Table 2).
| Innovation domain | Key technological advance | Clinical application | Evidence strength |
| Hybrid neuromodulation | rTMS priming + NFT reinforcement | Enhanced reduction of repetitive behaviors and hyperactivity in ASD | Controlled trials[6] |
| Artificial intelligence integration | Machine learning-driven real-time parameter adjustment | Personalized training intensity based on moment-to-moment brain states | Platform development[3] |
| Telehealth expansion | Portable EEG devices with cloud connectivity | Home-based treatment for ASD with remote supervision | Market report[2] |
| Biomarker personalization | EEG neuromarkers (e.g., P300, gamma ratios) for prediction | Protocol selection based on individual neurophysiological profiles | Research validation[4] |
NFT promotes experience-dependent synaptic plasticity within social brain networks (e.g., DMN, mirror neuron system) by reinforcing the desired EEG oscillatory patterns. Combining NFT with repetitive transcranial magnetic stimulation (rTMS) enhanced EEG gamma activity and reduced repetitive behaviors, suggesting the strengthening of neural pa
NFT induces measurable changes in event-related potentials (ERPs), reflecting optimized neural resource allocation and processing efficiency. Slow cortical potential training shortened P300 latency (331.41 ms post-training vs 373.36 ms baseline), indicating accelerated emotional stimulus evaluation[5]. Moreover, changes in late positive potential amplitude correlated with improved positive emotion processing (r = 0.53), underscoring enhanced emotional regulation capacity[5].
NFT has demonstrated potential efficacy in addressing core symptoms of ASD, such as social communication deficits and emotional dysregulation. Studies including a retrospective analysis by Wang et al[2] indicate that NFT, particularly when combined with conventional rehabilitation, can lead to significant improvements in standardized metrics such as the SRS and Aberrant Behavior Checklist scores, with some reports suggesting superior outcomes compared to conventional therapy alone[2]. Meta-analytical evidence supports these findings, showing that NFT may have positive effects on social communication and behavior, although effect sizes vary[3].
Therapeutically, NFT is thought to modulate aberrant neural circuits by normalizing electrophysiological imbalances, such as excessive theta/beta ratios, and enhancing gamma-band activity in prefrontal regions. These changes are associated with improved functional connectivity within critical networks such as the DMN, which is involved in social cognition. For example, reductions in P300 latency following NFT correlate with accelerated emotional stimulus eva
However, the evidence base faces significant challenges. A major limitation is the lack of protocol standardization, with substantial variation in session duration, training frequency, and target neural parameters across studies, which hinders comparison and replication[3]. Most research involves small sample sizes (often under 50 participants) and lacks long-term follow-up data beyond six months, leaving questions about the durability of effects and potential need for booster sessions[2,5]. The high cost of clinical NFT systems and need for trained practitioners limit accessibility, while emerging home-based devices raise concerns about data security and treatment fidelity without professional supervision[8]. Furthermore, mechanistic uncertainties persist; it remains unclear whether behavioral improvements are directly due to neural modulation or influenced by non-specific factors such as placebo effects[2,3]. Finally, the generalizability of findings is constrained as most studies focus on high-functioning ASD individuals, with efficacy in low-functioning or non-verbal populations remaining largely unexplored[2,5]. Future research requires large-scale, sham-controlled trials and biomarker validation to establish NFT's role in ASD management.
NFT demonstrates several distinct advantages over conventional treatment approaches, primarily through its capacity to guide self-regulation of neural function via real-time EEG feedback. In contrast to pharmacotherapy (e.g., antipsychotics or stimulants), NFT is non-invasive and medication-free, thereby avoiding drug-related adverse effects such as weight gain, sedation, or cardiovascular risks. Treatment-emergent adverse events (e.g., transient headache or fatigue) are ge
A key strength of NFT lies in its personalized intervention approach. Protocols are tailored to individual EEG patterns—such as elevated theta/beta ratio or excessive gamma activity—enabling precise neuromodulation of dysfunctional neural circuits. This individualized approach contrasts with traditional behavioral therapies (e.g., ABA), which often employ generalized methodologies; additionally, NFT dynamically adapts parameters based on real-time neural activity[3].
Furthermore, NFT exhibits significant complementary effects when integrated with existing interventions. When combined with behavioral therapy, it may enhance neuroplasticity and facilitate skill acquisition by priming neural networks. In comparison, pharmacotherapy often targets symptomatic relief without promoting sustained neural adaptation[2,5].
In terms of treatment durability, NFT-induced neuroplastic changes often yield sustained therapeutic benefits, potentially reducing the need for long-term intervention. This contrasts with behavioral techniques, which typically require continuous implementation, and pharmacotherapies, whose effects commonly diminish following discontinuation[5].
The future advancement of NFT necessitates a multifaceted research agenda to establish efficacy, optimize protocols, and ensure clinical translatability. A primary imperative is the execution of large-scale, multi-site randomized controlled trials (RCTs) employing active sham-control conditions (e.g., placebo EEG feedback) to isolate NFT-specific effects from non-specific factors such as participant expectation. Such studies must enroll demographically and clinically diverse cohorts to enhance generalizability[2].
Concurrently, biomarker-driven personalization is essential, focusing on validating electrophysiological neuromarkers (e.g., P300 latency, gamma power spectral ratios) that predict individual treatment response. Integrating machine learning for real-time EEG analysis can enable closed-loop systems that adapt to neurophysiological states, maximizing outcomes[2,5]. Furthermore, hybrid approaches combining NFT with other neuromodulation techniques such as rTMS or tran
These innovations collectively represent a potential approach toward more precise, accessible, and effective neuromodulation therapies that are increasingly integrated with digital health infrastructures and personalized through computational analytics[5].
The future advancement of NFT for ASD requires a multifaceted research agenda to establish efficacy and ensure clinical translatability. A primary imperative involves conducting large-scale, multi-site RCTs employing active sham-control conditions to isolate NFT-specific effects from non-specific factors while enrolling demographically and clinically diverse cohorts to enhance generalizability[2]. Concurrently, biomarker-driven personalization is essential, focusing on validating electrophysiological neuromarkers such as P300 latency or gamma power spectral ratios to predict individual treatment response. Integrating machine learning for real-time EEG analysis can enable closed-loop systems that adapt to neu
| Research direction | Primary objectives | Key considerations & challenges |
| Large-scale RCTs | Establish causal efficacy, isolate NFT-specific effects from placebo | Requires significant funding, multi-site collaboration, development of credible sham protocols |
| Biomarker personalization | Identify predictive neuromarkers (e.g., P300, gamma), develop adaptive algorithms | High inter-individual variability, need for standardized measurement and analysis |
| Hybrid neuromodulation | Explore synergistic effects of NFT with rTMS/tDCS, prime neural circuits | Protocol optimization, safety of combined modalities, mechanistic understanding |
| Telehealth & home-based NFT | Increase accessibility, reduce costs, enable remote training | Device affordability and reliability, data security, user adherence, signal quality |
| Longitudinal & developmental | Assess durability of effects, identify critical intervention windows | Long-term funding, participant retention, controlling for confounding life factors |
| Multimodal integration | Enhance outcomes by combining NFT with behavioral therapy, OT, exercise, VR | Treatment coordination, cost, measuring specific contribution of each component |
In summary, the future trajectory of NFT research hinges on rigorous efficacy trials, personalized protocol optimization through computational analytics, strategic combination with complementary neuromodulation techniques, and thou
NFT represents a potential approach in ASD intervention, directly targeting the neural circuitry underpinning social-emotional and cognitive deficits. Wang et al’s study[2], alongside recent clinical trials and meta-analyses, underscores its potential to ameliorate core symptoms through mechanisms such as prefrontal gamma modulation, ERP optimization, and enhanced functional connectivity. Emerging innovations—including hybrid neuromodulation, artificial intelligence-driven protocols, and biomarker personalization—hold promise for further enhancing NFT’s efficacy and accessibility. However, addressing challenges related to protocol standardization, costs, and mechanistic clarity through collaborative, rigorous research is essential. As the field advances, NFT may evolve into a viable component of precision psychiatry for ASD, offering renewed hope for millions affected by this complex and heterogeneous disorder.
| 1. | Lord C, Elsabbagh M, Baird G, Veenstra-Vanderweele J. Autism spectrum disorder. Lancet. 2018;392:508-520. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 1136] [Cited by in RCA: 1337] [Article Influence: 167.1] [Reference Citation Analysis (0)] |
| 2. | Wang XN, Luo WW, Li HY, Zhang T. Application of neurobiofeedback therapy technology on social skills and emotion regulation in children with autism spectrum disorder. World J Psychiatry. 2025;15:111522. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in RCA: 1] [Reference Citation Analysis (0)] |
| 3. | Konicar L, Radev S, Prillinger K, Klöbl M, Diehm R, Birbaumer N, Lanzenberger R, Plener PL, Poustka L. Volitional modification of brain activity in adolescents with Autism Spectrum Disorder: A Bayesian analysis of Slow Cortical Potential neurofeedback. Neuroimage Clin. 2021;29:102557. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 11] [Cited by in RCA: 13] [Article Influence: 2.6] [Reference Citation Analysis (0)] |
| 4. | Fietz J, Auer G, Plener P, Poustka L, Konicar L. Empathy and event related potentials before and after EEG based neurofeedback training in autistic adolescents. Sci Rep. 2025;15:30824. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in Crossref: 1] [Cited by in RCA: 1] [Article Influence: 1.0] [Reference Citation Analysis (0)] |
| 5. | Pineda JA, Juavinett A, Datko M. Self-regulation of brain oscillations as a treatment for aberrant brain connections in children with autism. Med Hypotheses. 2012;79:790-798. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 30] [Cited by in RCA: 25] [Article Influence: 1.8] [Reference Citation Analysis (0)] |
| 6. | Sokhadze EM, El-Baz AS, Tasman A, Sears LL, Wang Y, Lamina EV, Casanova MF. Neuromodulation integrating rTMS and neurofeedback for the treatment of autism spectrum disorder: an exploratory study. Appl Psychophysiol Biofeedback. 2014;39:237-257. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 53] [Cited by in RCA: 47] [Article Influence: 3.9] [Reference Citation Analysis (0)] |
| 7. | Christoffersen GRJ, Schachtman TR. Electrophysiological CNS-processes related to associative learning in humans. Behav Brain Res. 2016;296:211-232. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 19] [Cited by in RCA: 16] [Article Influence: 1.5] [Reference Citation Analysis (0)] |
| 8. | Rezaee M, Effatpanah M, Nasehi MM, Ghamkhar L, Barati N. Assessing the Impact of Neurofeedback on Cognitive Function in Individuals with Autism Spectrum Disorder: A Systematic Review. Iran J Child Neurol. 2025;19:27-37. [RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)] [Cited by in RCA: 2] [Reference Citation Analysis (0)] |
| 9. | Dong HY, Wang B, Li HH, Shan L, Jia FY. [Correlation between serum 25-hydroxyvitamin D level and core symptoms of autism spectrum disorder in children]. Zhonghua Er Ke Za Zhi. 2017;55:916-919. [RCA] [PubMed] [DOI] [Full Text] [Cited by in RCA: 9] [Reference Citation Analysis (0)] |
| 10. | Aman MG, Singh NN, Stewart AW, Field CJ. The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects. Am J Ment Defic. 1985;89:485-491. [PubMed] |
| 11. | Constantino JN. Social Responsiveness Scale, Second Edition. Los Angeles: Western Psychological Services, 2012. |
| 12. | Schopler E, Reichler RJ, DeVellis RF, Daly K. Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS). J Autism Dev Disord. 1980;10:91-103. [RCA] [PubMed] [DOI] [Full Text] [Cited by in Crossref: 1395] [Cited by in RCA: 1338] [Article Influence: 29.1] [Reference Citation Analysis (0)] |
| 13. | Rimland B, Edelson SM. Autism Treatment Evaluation Checklist. [cited 16 September 2025]. Available from: https://psycnet.apa.org/doiLanding?doi=10.1037%2Ft03995-000. |
