Exploring the Non-Invasive Methods of Brain- Computer Interface: A Comprehensive Review of their Advances and Applications


Authors : Harsha S. Krishna; Salama Pulikkal

Volume/Issue : Volume 9 - 2024, Issue 8 - August


Google Scholar : https://tinyurl.com/2vmz78km

Scribd : https://tinyurl.com/y6d976uw

DOI : https://doi.org/10.38124/ijisrt/IJISRT24AUG1536

Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.


Abstract : The brain-computer interface technology allows the human brain to control external devices directly without using the brain’s output channels or peripheral nerves. It helps individuals with motor impairments to use mechanical and external devices to communicate with the outside world. Non-invasive BCIs allow communication between the human brain and external devices without the need for surgeries or invasive procedures. Methods like EEG, MEG, fMRI, and fNIRS are used. EEG enables the acquisition of electrical activity along the scalp by measuring voltage fluctuations and neurotransmission activity in the brain. The electrodes are attached to a cap-like device and are placed on the scalp to record the electrical current generated by the brain. Unlike MEG, which necessitates specially constructed rooms, EEG is portable. Lab-grade EEG is expensive but cheaper than other forms of BCI. MEG uses magnetometers to measure magnetic fields produced by electric currents occurring naturally in the brain. MEG is better than EEG at measuring high-frequency activity. MEG signals are less distorted by the skull layer. FMRI records blood oxygen level-dependent (BOLD) signals with high spatial resolution across the entire brain. It does this by tracking the hemodynamic response, which is the increase in blood flow to active brain areas. It does this using the principle of nuclear magnetic resonance, where hydrogen atoms in water molecules in the blood emit signals when subjected to a strong magnetic field. It has an advantage over EEG due to its superior spatial specificity and resolution. FNIRS measures the blood flow and oxygenation in the blood associated with neural activity. It gains insight into the brain's hemodynamic response, which is essential for understanding neural functioning during BCI tasks.

Keywords : Brain-Computer Interface; Non-Inasive; EEG; MEG; Fmri; Fnirs;

References :

  1. Abdulkader SN, Atia A, Mostafa MSM. Brain computer interfacing: Applications and challenges. Egyptian Informatics Journal. 2015 Jul;16(2):213–30.
  2. A. Caria, R. Veit, T. Gaber, R. Sitaram, A. Kuebler, and N. Birbaumer, “Can we learn to increase our emotional involvement?real-timefMRIofanteriorcingulatecortexduringemotional processing,” in Human Brain Mapping, Florence, Italy, June 2006.
  3. Alhudhaif, A. A novel multi-class imbalanced EEG signals classification based on the adaptive synthetic sampling (ADASYN) approach. PeerJ Comput. Sci. 2021, 7, e523.
  4. Allison BZ, Krusienski D. Noninvasive Brain-Computer Interfaces. Encyclopedia of Computational Neuroscience [Internet]. 2014;1–13. Available from:
  5. Al-Nafjan A. Feature selection of EEG signals in neuromarketing. PeerJ Comput Sci. 2022 Apr 26;8:e944. doi: 10.7717/peerj-cs.944. PMID: 35634118; PMCID: PMC9138093.
  6. Ayaz, H.; Onaral, B.; Izzetoglu, K.; Shewokis, P.A.; McKendrick, R.; Parasuraman, R. Continuous monitoring of brain dynamics with functional near infrared spectroscopy as a tool for neuroergonomic research: empirical examples and a technological development. Front. Hum. Neurosci. 2013, 7, 871.
  7. Belluscio, V.; Casti, G.; Ferrari, M.; Quaresima, V.; Sappia, M.S.; Horschig, J.M.; Vannozzi, G. Modifications in Prefrontal Cortex Oxygenation in Linear and Curvilinear Dual Task Walking: A CombinedfNIRSandIMUsStudy. Sensors2021, 21, 6159.
  8. Besserve M, Jerbi K, Laurent F, Baillet S, Martinerie J, Garnero L. Classification methods for ongoing EEG and MEG signals. Biol Res. 2007;40(4):415-37. Epub 2008 May 28. PMID: 18575676.
  9. Brain–computer interfaces for communication and control Jonathan R. Wolpawa,b,*, Niels Birbaumerc,d, Dennis J. McFarlanda , Gert Pfurtschellere , Theresa M. Vaughana a Laboratory of Nervous System Disorders, Wadsworth Center, New York State Department of Health, P.O. Box 509, Empire State Plaza, Albany, NY 12201-0509, USA b State University of New York, Albany, NY, USA
  10. Brain–computer interfaces JONATHAN R. WOLPAW* Wadsworth Center, Laboratory of Neural Injury and Repair, New York State Department of Health and State University of New York, Albany, NY, USA, Handbook of Clinical Neurology, Vol. 110 (3rd series) Neurological Rehabilitation
  11. Buccino, A.P.; Keles, H.; Omurtag, A. Hybrid EEG-fNIRS Asynchronous Brain-Computer Interface for Multiple Motor Tasks. PLoS ONE2016, 11, e0146610
  12. Cooper RJ, Selb J, Gagnon L, Phillip D, Schytz HW, Iversen HK, Ashina M, Boas DA. A systematic comparison of motion artifact correction techniques for functional near-infrared spectroscopy. Front Neurosci. 2012 Oct 11;6:147. doi: 10.3389/fnins.2012.00147. PMID: 23087603; PMCID: PMC3468891.
  13. Chaddad A, Wu Y, Reem Kateb, Bouridane A. Electroencephalography Signal Processing: A Comprehensive Review and Analysis of Methods and Techniques. Sensors. 2023 Jul 16;23(14):6434–4
  14. Daly JJ, Wolpaw JR. Brain–computer interfaces in neurological rehabilitation. The Lancet Neurology. 2008 Nov;7(11):1032–43.
  15. Derosiere, G.; Dalhoumi, S.; Perrey, S.; Dray, G.; Ward, T. Towards a Near Infrared Spectroscopy-Based Estimation of Operator Attentional State. PLoS ONE 2014, 9, e92045.
  16. Di Flumeri G, Aricò P, Borghini G, Sciaraffa N, Di Florio A, Babiloni F. The Dry Revolution: Evaluation of Three Different EEG Dry Electrode Types in Terms of Signal Spectral Features, Mental States Classification and Usability. Sensors (Basel). 2019 Mar 19;19(6):1365. doi: 10.3390/s19061365. PMID: 30893791; PMCID: PMC6470960.
  17. fMRI Brain-Computer Interface: A Tool for Neuroscientific Research and Treatment Ranganatha Sitaram,1 Andrea Caria,1 Ralf Veit,1, 2 Tilman Gaber,1, 2 Giuseppina Rota,1, 3 Andrea Kuebler,1 and Niels Birbaumer1, 4 Hindawi Publishing Corporation Computational Intelligence and Neuroscience Volume 2007, Article ID 25487, 10 pages doi:10.1155/2007/25487
  18. Fred AL, Kumar SN, Kumar Haridhas A, Ghosh S, Purushothaman Bhuvana H, Sim WKJ, Vimalan V, Givo FAS, Jousmäki V, Padmanabhan P, Gulyás B. A Brief Introduction to Magnetoencephalography (MEG) and Its Clinical Applications. Brain Sci. 2022 Jun 15;12(6):788. doi: 10.3390/brainsci12060788. PMID: 35741673; PMCID: PMC9221302.
  19.  F. Tong, K. Nakayama, J. T. Vaughan, and N. Kanwisher, “Binocular rivalry and visual awareness in human extrastriate cortex,” Neuron, vol. 21, no. 4, pp. 753–759, 1998.
  20. G. Rota, R. Sitaram, R. Veit, N. Weiskopf, N. Birbaumer, and G. Dogil, “ fMRI-neurofeedback for operant conditioning and neural plasticity investigation: a study on the physiological self-induced regulation of the BA 45,” in Proceedings of the Cognitive Neuroscience Conference, San Francisco, Calif, USA, 2006.
  21. Goyal I, Mehta A. Acquisition, Pre-Processing, and Feature Extraction of EEG Signals to Convert it into an Image Classification Problem [Internet]. International Research Journal of Engineering and Technology. [cited 2024 Aug 27]. Available from: https://www.irjet.net/archives/V8/i2/IRJET-V8I237.pdf
  22. Halme HL. Development of an MEG-based brain-computer interface [Internet]. [cited 2024 Aug 27]. Available from: https://aaltodoc.aalto.fi/server/api/core/bitstreams/bd2c0df1-ec92-4e9e-b26a-38a4e732f653/content
  23. Huppert, T. J., Hoge, R. D., Diamond, S. G., Franceschini, M. A., and Boas, D. A. (2006). A temporal comparison of BOLD, ASL, and NIRS hemodynamic responses to motor stimuli in adult humans. Neuroimage 29, 368–382. doi: 10.1016/j.neuroimage.2005.08.065
  24. Khan, M.J.; Hong, K.-S. Passive BCI based on drowsiness detection: an fNIRS study. Biomed. Opt. Express 2015, 6, 4063–4078.
  25. Kober SE, Wood G, Kurzmann J, Friedrich EV, Stangl M, Wippel T, Väljamäe A, Neuper C. Near-infrared spectroscopy based neurofeedback training increases specific motor imagery related cortical activation compared to sham feedback. Biol Psychol. 2014 Jan;95:21-30. doi: 10.1016/j.biopsycho.2013.05.005. Epub 2013 May 25. PMID: 23714227.
  26. Li B, Cheng T, Guo Z. A review of EEG acquisition, processing and application. Journal of Physics: Conference Series. 2021 May 1;1907(1):012045.
  27. Mihara, M., Hattori, N., Hatakenaka, M., Yagura, H., and Kawano, T. (2013). Near infrared spectroscopy-mediated neurofeedback enhances efficacy of motor imagery-basedtraining inpoststroke victims apilotstudy. Stroke 44, 1091–1098. doi: 10.1161/STROKEAHA.111.674507
  28. Mihara,M.;Miyai, I.; Hattori, N.; Hatakenaka, M.; Yagura, H.; Kawano, T.; Okibayashi, M.; Danjo, N.; Ishikawa, A.; Inoue, Y.; et al. Neurofeedback Using Real-Time Near-Infrared Spectroscopy Enhances Motor Imagery Related Cortical Activation. PLoS ONE 2012, 7, e32234.
  29. Naseer, N., and Hong, K.-S. (2013). Classification of functional near-infrared spectroscopy signals corresponding to the right- and left-wrist motor imagery for development of a brain-computer interface. Neurosci. Lett. 553, 84–49. doi: 10.1016/j.neulet.2013.08.021
  30. Neuroelectrics. Guide to Electroencephalography: From EEG Data to Classification [Internet]. Neuroelectrics Blog - Latest news about EEG & Brain Stimulation. 2023. Available from: https://www.neuroelectrics.com/blog/2023/09/04/guide-to-electroencephalography-from-eeg-data-to-classification/
  31. Noninvasive Brain–Computer Interfaces. Neuromodulation [Internet]. 2018 Jan 1 [cited 2021 May 1];357–77. Available from: https://www.sciencedirect.com/science/article/pii/B9780128053539000267
  32. Paulmurugan K, Vijayaragavan V, Ghosh S, Padmanabhan P, Gulyás B. Brain–Computer Interfacing Using Functional Near-Infrared Spectroscopy (fNIRS). Biosensors. 2021 Oct 13;11(10):389.
  33. Pinti, P.; Siddiqui, M.F.; Levy, A.D.; Jones, E.J.H.; Tachtsidis, I. An analysis framework for the integration of broadband NIRS and EEGto assess neurovascular and neurometabolic coupling. Sci. Rep. 2021, 11, 1–20
  34. P. van Gelderen, J.A. de Zwart, P. Starewicz, R.S. Hinks, and J.H. Duyn, “Real time shimming to compensate for respiration-induced B0 fluctuations,” Magn. Reson. Med., vol. 57, no. 2, pp. 362–368, 2007.
  35. R. C. DeCharms, F. Maeda, G. H. Glover, et al., “Control over brain activation and pain learned by using real-time functional MRI,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 51, pp. 18626–18631, 2005.
  36. Rieke, J.D.; Matarasso, A.K.; Yusufali, M.M.; Ravindran, A.; Alcantara, J.; White, K.D.; Daly, J.J. Development of a combined, sequential real-time fMRI and fNIRS neurofeedback system to enhance motor learning after stroke. J. Neurosci. Methods 2020, 341, 108719.
  37. R. Sitaram, A. Caria, R. Veit, T. Gaber, A. Kuebler, and N. Bir baumer, “Real-time fMRI based brain-computer interface enhanced by interactive virtual worlds,” in Proceedings of the 45th Annual Meeting Society for Psychophysiological Research, Lis bon, Portugal, 2005.
  38. Shih JJ, Krusienski DJ, Wolpaw JR. Brain-Computer Interfaces in Medicine. Mayo Clinic Proceedings [Internet]. 2012 Mar;87(3):268–79.
  39. Sitaram R, Weiskopf N, Caria A, Veit R, Erb M, Birbaumer N. [ IEEE SIGNAL PROCESSING MAGAZINE [95]. 2008 [cited 2019 May 18]; Available from: https://www.bme.ufl.edu/labs/sitaram/files/2013/10/4.-IEEE-Signal-Processing-Sitaram-2008.pdf
  40. Sorger B, Goebel R. Real-time fMRI for brain-computer interfacing. Handbook of Clinical Neurology [Internet]. 2020 [cited 2021 Aug 27];168:289–302. Available from: https://pubmed.ncbi.nlm.nih.gov/32164860/
  41. Torres EP, Torres EA, Hernández-Álvarez M, Yoo SG. EEG-Based BCI Emotion Recognition: A Survey. Sensors. 2020 Sep 7;20(18):5083.
  42. Värbu K, Muhammad N, Muhammad Y. Past, Present, and Future of EEG-Based BCI Applications. Sensors. 2022 Apr 26;22(9):3331.
  43. Venkata Phanikrishna B, Pławiak P, Jaya Prakash A. A Brief Review on EEG Signal Pre-processing Techniques for Real-Time Brain-Computer Interface Applications [Internet]. www.techrxiv.org. 2021 [cited 2023 Jun 2]. Available from: https://www.techrxiv.org/articles/preprint/A_Brief_Review_on_EEG_Signal_Pre-processing_Techniques_for_Real-Time_Brain-Computer_Interface_Applications/16691605
  44. Weiskopf N, Mathiak K, Bock SW, Scharnowski F, Veit R, Grodd W, et al. Principles of a Brain-Computer Interface (BCI) Based on Real-Time Functional Magnetic Resonance Imaging (fMRI). IEEE Transactions on Biomedical Engineering. 2004 Jun;51(6):966–70.
  45. Weiskopf N, Sitaram R, Josephs O, Veit R, Scharnowski F, Goebel R, et al. Real-time functional magnetic resonance imaging: methods and applications. Magnetic Resonance Imaging. 2007 Jul;25(6):989–1003.
  46. Wet, dry, active and passive electrodes. What are they, and what to choose? [Internet]. BuscaEU. 2023. Available from: https://brainlatam.com/blog/wet-dry-active-and-passive-electrodes.-what-are-they-and-what-to-choose-413
  47. Wolpaw JR, Elizabeth Winter Wolpaw. Brain-computer interfaces : principles and practice. New York: Oxford University Press; 2012.
  48. Yeom, H.G., Kim, J.S. & Chung, C.K. A magnetoencephalography dataset during three-dimensional reaching movements for brain-computer interfaces. Sci Data 10, 552 (2023). https://doi.org/10.1038/s41597-023-02454-y
  49. Yoo SS, Fairneny T, Chen NK, Choo SE, Panych LP, Park H, et al. Brain–computer interface using fMRI: spatial navigation by thoughts. NeuroReport. 2004 Jul;15(10):1591–5.
  50. Yuan H, Li Y, Yang J, Li H, Yang Q, Guo C, Zhu S, Shu X. State of the Art of Non-Invasive Electrode Materials for Brain-Computer Interface. Micromachines (Basel). 2021 Dec 8;12(12):1521. doi: 10.3390/mi12121521. PMID: 34945371; PMCID: PMC8705666.

The brain-computer interface technology allows the human brain to control external devices directly without using the brain’s output channels or peripheral nerves. It helps individuals with motor impairments to use mechanical and external devices to communicate with the outside world. Non-invasive BCIs allow communication between the human brain and external devices without the need for surgeries or invasive procedures. Methods like EEG, MEG, fMRI, and fNIRS are used. EEG enables the acquisition of electrical activity along the scalp by measuring voltage fluctuations and neurotransmission activity in the brain. The electrodes are attached to a cap-like device and are placed on the scalp to record the electrical current generated by the brain. Unlike MEG, which necessitates specially constructed rooms, EEG is portable. Lab-grade EEG is expensive but cheaper than other forms of BCI. MEG uses magnetometers to measure magnetic fields produced by electric currents occurring naturally in the brain. MEG is better than EEG at measuring high-frequency activity. MEG signals are less distorted by the skull layer. FMRI records blood oxygen level-dependent (BOLD) signals with high spatial resolution across the entire brain. It does this by tracking the hemodynamic response, which is the increase in blood flow to active brain areas. It does this using the principle of nuclear magnetic resonance, where hydrogen atoms in water molecules in the blood emit signals when subjected to a strong magnetic field. It has an advantage over EEG due to its superior spatial specificity and resolution. FNIRS measures the blood flow and oxygenation in the blood associated with neural activity. It gains insight into the brain's hemodynamic response, which is essential for understanding neural functioning during BCI tasks.

Keywords : Brain-Computer Interface; Non-Inasive; EEG; MEG; Fmri; Fnirs;

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