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John Anderson and John Davis Answer Your Neurofeedback Questions

Updated: 10 hours ago

John Anderson and John Davis


From Clean Signals to Lasting Skills: A Simple Guide to Filters and Caps Used in Neurofeedback


Neurofeedback combines precise signal measurement with human learning.


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Modern neurofeedback relies on signal fidelity, the precise and consistent recording of the brain’s electrical activity. Since Hans Berger’s first EEG recordings in the 1920s, engineers and clinicians have refined amplification systems, electrode design, placement standards, and digital filtering to measure microvolt-level cortical rhythms with accuracy and minimal noise (Fisch, 1999).


A central part of achieving this fidelity is the use of standardized electrode configurations. Contemporary neurofeedback and quantitative EEG (qEEG) assessments commonly employ 19 or more electrodes, positioned according to the International 10–20 or 10–10 system. These proportional placement systems ensure that electrodes are evenly distributed across the scalp, covering all major cortical regions, frontal, central, temporal, parietal, and occipital, so that activity can be compared meaningfully across sessions and individuals.


When 19-channel EEG systems are used for neurofeedback or qEEG mapping, they provide comprehensive spatial coverage sufficient for most clinical and research applications, while higher-density arrays (32, 64, or 128 channels) allow for advanced source modeling and topographic precision. Proper positioning ensures that training targets, such as specific frequency bands or regional asymmetries, accurately reflect true neural activity rather than placement errors or movement artifacts.


Ultimately, modern neurofeedback integrates this careful spatial mapping with high-quality amplification and optimized digital filtering to deliver real-time, artifact-free feedback. Precision electrode placement, whether with 19 electrodes or high-density caps, is therefore foundational to both the reliability of brain mapping and the effectiveness of training.


This post is part of a series by John S. Anderson and John Davis, designed to explain concepts that beginners find challenging.




Filters


What do filters do?


As Fisch (1999) explains:


Filters are used to exclude waveforms of relatively high or low frequency from the EEG so that waveforms in the most important range (1-30 Hz) can be recorded clearly and without distortion. The filters receive the EEG signal after it has passed from the differential amplifier to a second, single-ended, amplifier. After passing through each filter the signal is amplified again by single-ended amplifiers (p. 46).

Neurofeedback uses several common types of filters. A high-pass filter allows frequencies higher than its cutoff point (such as 1 or 2 Hz) to pass through.


A low-pass filter allows frequencies below its cutoff point (such as 30 Hz or higher) to pass through.


A notch filter blocks frequencies around 60 Hz (or 50 Hz outside North America) to prevent electrical interference from power lines from messing up the EEG signal.


Band-pass filters allow practitioners to select a specific frequency range—for instance, 4 to 8 Hz—to define and measure a particular EEG band, such as theta waves.


filters


When the signal requires more amplification, digital filters convert it from an analog (time-based) to a digital (frequency-based) format. Digital filters are essential for transforming the brain’s raw electrical activity into meaningful information for analysis or feedback. Each major filter type has a distinct way of shaping and interpreting EEG signals. Choosing among them involves balancing accuracy, speed, and phase integrity. Graphic © Fouad A. Saad/Shutterstock.com shows the digital reconstruction of an analog waveform.



A/D conversion


These filters are categorized into three main types: FIR (finite impulse response), IIR (infinite impulse response), and FFT (fast Fourier transform). Most practitioners use IIR or FFT filters because they better preserve timing information.

FIR Filters

FIR filters produce outputs that fade completely after a brief impulse, depending only on current and past input values. They act like weighted moving averages and are always stable because no feedback loop is used. Their main advantage is a linear phase response, where all frequencies are delayed equally, thereby preserving the waveform shape. This makes FIR filters ideal when timing and phase relationships matter, as in event-related potentials or precise EEG analysis. The trade-off is higher computational demand and longer latency, especially at high filter orders.

IIR Filters


IIR filters, in contrast, feed part of their output back into the input, creating a theoretically infinite response. This feedback allows them to achieve sharp cutoffs with far fewer calculations, making them efficient for real-time use. However, their feedback structure introduces nonlinear phase distortion, shifting different frequencies by slightly different amounts in time. For most neurofeedback applications, where the focus is on band amplitude rather than precise waveform alignment, IIR filters are preferred because they minimize delay and maintain feedback as nearly instantaneous as possible.



Three FIR IIR Filter Questions Are FIR “better” than IIR for preserving phase relationships?

For absolute phase: Yes (FIR, linear‑phase). For relative phase/coherence between channels with matched filters: No meaningful difference.



Do IIR filters mess up coherence/phase neurofeedback?

No, provided filters are identical, time-invariant, and well-implemented, time-invariant pipelines offer low latency. Simply, issues mainly stem from transients, mismatches, or unaccounted delays.



Are IIR filters good enough for coherence neurofeedback?

Yes. They are widely used in real‑time pipelines because of low latency; just calibrate and report delays.



Filter Precision is Determined by Their Order


The precision with which IIR and FIR digital filters operate to measure a frequency is determined by their so-called order. The order setting of the filter is simply the number of samples used in the calculation of the output. Samples reflect the sampling rate of the amplifier, which is the number of times the amplifier measures or ‘samples’ the incoming EEG signal. Thus, a higher-order filter uses more samples for calculation, resulting in greater precision.

filter order



The Trade-off Between Precision and Speed


However, this precision comes at the expense of speed. A higher-order filter, using more samples (measurements), is also slower to produce an output. For example, a typical 3rd order IIR filter, often used for neurofeedback training, produces an output to the display in 11 ms when the amplifier is sampling the EEG signal at 256 samples per second (sps).


This is fast enough to provide timely feedback to the client so that the changes in the feedback display closely mirror the actual brain-based behavior being measured (sampled). A third-order filter will also accurately represent EEG activity, providing useful information for the feedback display.


When choosing a filter for offline processing of the EEG, where greater precision is desired, a higher-order filter may be used because real-time feedback is not required. Thus, the increased complexity of the calculation with a higher-order filter gives a more precise measurement.



FFT Filters


FFT filters work differently. The fast Fourier transform isn't a filter design but a mathematical algorithm that decomposes time-domain signals into their frequency components. It allows rapid computation of how much power each frequency contributes over short time windows. In neurofeedback, FFT-based processing is widely used to estimate spectral power (e.g., theta, alpha, or beta) in near real-time.


The window length determines how quickly feedback updates: shorter windows provide faster feedback but coarser frequency resolution. FFT filters can vary in complexity, mainly based on the time window chosen for analysis. A Fourier Transform calculation needs at least 1 second of data to work. Most FFT calculations use 2 seconds or more to be more precise.


More complex FFT calculations utilize a technique known as sliding windows. Think of it like taking overlapping snapshots of data—each new window includes some data from the previous one as it "slides" along the data stream. Some people mistakenly think this sliding window approach can produce output as quickly as digital filters (IIR or FIR filters). But this isn't true. No matter how often the window recalculates the data—that is, how quickly it slides along—the math behind FFT still requires at least 1 second of data to create an output.


This creates a problem for neurofeedback training: the data sent to the feedback display is too slow. For effective training, the maximum delay between when something happens in the brain and when the client sees it on the display should be 250-350 milliseconds (Cooper, Heron, & Howard, 2007; Felsinger & Gladstone, 1947; Grice, 1948; Malott & Trojan-Suarez, 2004; Miller, 2006; Miltenberger, 2008). That's about ¼ of a second.


Because of this delay, FFT is better suited for offline data processing, database comparisons, and other tasks—but it's not considered fast enough for neurofeedback training. The one exception is when training slow frequencies below approximately 10 Hz, where the FFT's slower response might be acceptable, although it's still not ideal.


Remember that all filters only reduce (attenuate, not eliminate) frequencies outside their set boundaries—for example, frequencies outside an 8 to 10 Hz range. While higher-order filters can cut off unwanted frequencies more sharply, they require longer calculation times. Additionally, when using digital filters for multiple frequencies, they must all be of the same type (such as all FFT).


There's one exception to this same-type rule: You can use different calculation types for the same neurofeedback display. For example, you might use 3rd-order IIR filters to provide direct feedback for 4-8 Hz and 15-18 Hz activity in an inhibit/reward display, while also showing the theta/beta power ratio from FFTs for informational purposes.



Filter Comparison


In practice, FIR filters preserve waveform fidelity, IIR filters enable fast and efficient feedback, and FFT filters provide flexible, frequency-based monitoring. Each has its place in neurofeedback: FIR when precision and phase accuracy are critical, IIR when immediacy is crucial, and FFT when spectral tracking is the primary goal. The key principle is consistency—using the same filter type and parameters across sessions ensures that any observed change reflects the brain, not the math.


The accuracy of IIR and FIR digital filters depends on their "order"—basically, how complex their calculations are. Higher numbers mean more complex calculations and more precise measurements. FFT filters also vary in complexity. Remember that filters only reduce (not eliminate) frequencies outside their boundaries—for example, frequencies outside an 8 to 10 Hz range.


While higher-order filters can cut off unwanted frequencies more sharply, they require longer processing times. Additionally, when using digital filters for multiple frequencies, they must all be of the same type (e.g., all FFT).



Phase Distortion and Latency


In neurofeedback, two technical considerations are particularly relevant: phase distortion and latency.


Phase distortion occurs when a filter delays different frequencies by unequal amounts, subtly shifting parts of the EEG waveform in time. This alters the true timing relationship between components of the signal.


Latency refers to the total time delay between when brain activity occurs and when feedback about it is presented to the client.


In neurofeedback, both factors matter because learning depends on the brain recognizing a clear, immediate link between its activity and the feedback it receives. Excessive phase distortion can misrepresent which brain events are being rewarded, and prolonged latency weakens the sense of cause and effect that drives operant learning. Ideally, filters and processing pipelines are designed to minimize both, preserving signal accuracy while keeping total delay short enough (usually <250 ms) for feedback to feel instantaneous and reinforce the intended neural state (Fisch, 1999).


FIR filters are typically linear-phase (phase relationships are preserved), but they may require higher-order filters, which can add computational delay. In contrast, IIR filters achieve sharp transitions with fewer coefficients but introduce frequency-dependent phase shifts (Fisch, 1999).


In feedback learning, contiguity—how immediate the feedback feels relative to neural events—modulates the effectiveness of reinforcement, allowing systems to balance the steepness of attenuation with minimal group delay.


Many platforms compute band activity using short-window FFT power or recursive IIR band envelopes. Either approach is acceptable if applied consistently across sessions, because mixing methods can complicate the interpretation of change over time.


Finally, filters attenuate but do not eliminate artifacts; good technique (e.g., posture, blink strategy, short rest breaks) is still required to maintain high signal quality upstream of the math (Fisch, 1999).



qEEG Cap Placement (precision from landmarks upward)


How should a qEEG cap be put on a client?


Electrode cap graphic © Roman Ziets/Shutterstock.com.


electrode cap



The electrodes in an EEG cap must follow standard 10-20 or 10-10 system placements. 10-20 system graphic adapted from Fisch (1999).

10-20 system




10-10 system graphic adapted from Fisch (1999).

10-10 system




Preparation and Client Setup


Correct qEEG begins long before you press “record.” Start by preparing the client and selecting the right cap: measure head circumference just above the ears, choose a size that is snug without being constrictive, and ensure the hair is clean, dry, and free of heavy product. Remove metal clips or accessories, and seat the client comfortably with head support. Part the dense hair along the anticipated electrode sites to improve scalp contact and reduce movement- and muscle-related artifacts (Fisch, 1999).


Note that when working with clients with dense, curly, or springy hair, the hair will keep the cap electrodes away from the scalp, regardless of the preparation done. In this case, with electrodes using injected gel, a column of gel is created that connects the electrode with the scalp.


Several things facilitate this process. First, make sure the cap is stable and secure by adjusting any stabilizing mechanisms built into the cap, such as chin straps or perimeter tensioners. Chest anchor straps are not recommended due to the respiratory effects creating movement artifacts.


Once the cap is secure, avoid pressing down on the cap or on individual electrodes as they are filled, as this will compress the column of gel, which can then be disrupted when the cap electrode springs back due to variations in hair density. Pressing on the electrode will also increase the probability of creating a bridge with gel from adjacent electrodes. Finally, be especially careful to avoid overfilling the gel column, which can lead to bridging artifacts.


When using a saline net, the saline pads or sponges must be in contact with the scalp and this often requires significant pressure to make this happen when individuals have very dense hair.

saline net
Magstim saline nets


Dry electrode caps generally have small rounded points, either around the perimeter of each sensor or spaced evenly over the entire surface of the electrode. These points are fairly effective at contacting the scalp, even through the most dense hair, however they often suffer from cardioballistic (pulse) artifacts, particularly at F3 and F4 electrode locations.

dry electrode
Dry electrode cap for Mitsar amplifiers


Landmarks and Alignment


Next, establish the cranial landmarks that anchor all proportional placement. With a flexible tape, locate and lightly mark the nasion at the bridge of the nose, the inion at the external occipital protuberance, and the left and right preauricular notches just anterior to the tragus. Measure the nasion–inion arc along the midline and the ear‑to‑ear arc over the vertex; their 50% points intersect at Cz, the keystone of the montage.


Place the cap so that its midline aligns precisely with the nasion–Cz–inion line and its lateral markers align with the preauricular notches; verify that Cz on the cap matches the actual intersection you measured rather than relying on printed cap logos (Jasper, 1958, 1999; Acharya, Hani, Cheek, Thirumala, & Tsuchida, 2016).



Electrode Positioning and Systems


With Cz verified, position the remaining electrodes by proportional distances. In the International 10–20 system, sites fall at 10% or 20% intervals along the nasion–inion and interaural arcs, yielding the canonical 19‑channel set—Fp1/Fp2, F7/F8, F3/F4, Fz, T7/T8 (historically T3/T4), C3/C4, Cz, P7/P8 (historically T5/T6), P3/P4, Pz, and O1/O2. For denser spatial sampling, the 10–10 and 5% systems apply the same proportional logic at finer increments (e.g., AFz, FCz, CPz, POz), thereby improving topographic resolution and supporting source-space workflows while preserving cross-session reproducibility (Jasper, 1958/1999; Acharya et al., 2016).


Throughout, monitor symmetry: left–right distances from the midline should match, and anterior–posterior distances should maintain the intended ratios. Small errors at Cz propagate across the scalp, so re‑measure if the two halves of nasion–Cz–inion or left‑Cz‑right preauricular lengths are unequal (Acharya et al., 2016).



Site Preparation and Impedance Control


Prepare each site for stable contact. For gel caps, gently reduce impedance at the stratum corneum (the upper skin layer) using a mild abrasive through the grommet, then introduce conductive gel until the electrode makes firm contact with the skin, rather than hair. Avoid gel bridges between adjacent sensors, as they can short-circuit channels and distort topography.

gel headcap
TMSi gel electodes


For saline nets, hydrate per manufacturer guidance and guard against over‑wetting that causes salt bridging; for dry electrodes, spend extra time on hair management and seating pressure to limit motion artifact. Aim for low and balanced impedances (commonly ≤5–10 kΩ, amplifier‑dependent) and recheck after a few minutes to catch drift as gel settles (Fisch, 1999).


Note that if a salt and/or gel bridge occurs, the clinician must then remove the cap and the client must wash their hair and dry it completely before applying a fresh, clean, dry cap to continue the process. There is no way to repair a gel bridge once it has occurred. A salt bridge that occurs when using a saline net can be corrected by removing the net, drying the scalp and hair with a hair dryer, having the client brush the hair well to remove loose mineral salts, and then placing the freshly hydrated net on the dry scalp.



Reference, Ground, and Auxiliary Channels


Choose a reference and ground consistent with your amplifier and analysis plan. Linked mastoids, nose, or an average reference are common choices; whichever you adopt, keep the reference quiet (away from muscle hotspots) and use the same scheme across sessions to protect longitudinal comparability, particularly if you plan qEEG database comparisons. Add auxiliary channels when possible—electro‑oculography near the canthi or inferior orbit to track eye movements and optional frontalis or masseter EMG—so you can identify and manage artifacts during review (Fisch, 1999; Acharya et al., 2016).



Functional Checks and Noise Control


Before recording, conduct rapid functional checks. A brief eyes-closed segment should increase occipital alpha at O1/O2 relative to eyes-open; marked asymmetries, unusually low alpha, or isolated band spikes confined to one site often indicate local placement, contact, or cable issues. Inspect and correct drying gel, hair under the cup, cable tension, or cap drift if patterns look implausible. Manage the environment and leads to minimize interference: route the cable bundle down the back with strain relief, keep power supplies and transformers away from the head and leads, and reserve notch filtering (50/60 Hz) for last—placement, cabling, and environmental control are your first-line noise solutions (Fisch, 1999).



Documentation and Reproducibility


Document everything needed for reproducibility: cap size, sampling rate, filter settings, reference/ground scheme, per‑channel impedances, and any deviations (e.g., moving a site to avoid a scar). For longitudinal neurofeedback or qEEG mapping, replicate the same measurement protocol—landmarks, proportional distances, reference, and skin prep—at every session to stabilize spectral features and topography. Whether you use the standard 19 electrodes or higher‑density arrays (32–128+), the combination of careful landmarking, proportional placement, stable impedances, and quiet referencing is what converts a cap full of sensors into reliable, comparable brain data (Acharya et al., 2016; Fisch, 1999).




Key Takeaways


  1. Neurofeedback relies on clean signals and fast, faithful processing; the choice of filter (FIR/IIR/FFT), order, and sampling rate shapes both accuracy and delay.


  1. For real-time training, low overall latency and minimal phase distortion preserve the brain–feedback link that enables learning; consistency across sessions prevents “math, not mind” effects.


  1. Precise 10–20/10–10 placement anchored to cranial landmarks stabilizes topography and supports valid longitudinal/qEEG comparisons.




infographic




Glossary


amygdala: a limbic structure involved in detecting salience and mediating conditioned fear responses.


analog-to-digital conversion (ADC): a process that converts continuous voltages into discrete samples for digital analysis.


artifact: non-cerebral signal (e.g., eye blinks, muscle, movement) that contaminates the EEG.


band-pass filter: a digital/analog filter that passes only a specified frequency band and attenuates others.


beta waves: EEG activity ≈13–30 Hz associated with alert thinking and task engagement.

canthi: the inner and outer corners where the upper and lower eyelids meet; common EOG electrode sites (outer canthi) for tracking horizontal eye movements in the EEG.


cardioballistic artifacts: tiny, pulse-synchronous voltages and baseline shifts in the EEG caused by cardiac-related blood-volume and scalp/lead movements (often time-locked to the QRS complex). They typically appear as low-frequency deflections or broad-spectrum contamination repeating at the heart rate (and harmonics) and can mimic or mask slow EEG rhythms.


coherence: a frequency-specific measure of phase/amplitude coupling between

channels reflecting functional connectivity.


contingency: the reliability with which a feedback event depends on a target neural state.


delta waves: EEG activity ≈0.5–4 Hz common in deep sleep and early development.

dry electrode cap: a headset or cap with electrodes that make direct contact with the scalp without conductive gel or paste, using spring-loaded or textured sensors to achieve contact; offers faster setup and greater comfort but typically higher and more variable impedance and greater sensitivity to motion/artifact than gel-based systems.

electrode montage: a spatial arrangement/reference scheme of recording electrodes.

electro‑oculography (EOG): surface recording of eye activity using electrodes around the eyes to capture corneo‑retinal potential changes from blinks and saccades; used to detect and correct ocular artifacts in the EEG.

event-related potential (ERP): a time-locked average of the EEG to discrete events, used for precise latency/phase analysis.


Fast Fourier Transform (FFT): an algorithm that decomposes time-domain data into

frequency components; often used to estimate spectral power.


filter order: the number of coefficients/samples used to compute a filter; higher order sharpens transitions but increases computation and delay.


finite impulse response (FIR) filter: a non-recursive filter with finite response; linear phase preserves waveform shape.


frequency resolution: the ability to distinguish nearby frequencies; improves with longer analysis windows.

gel bridge: an unwanted conductive path formed when excess gel or saline connects adjacent electrodes, causing channel crosstalk, distorted amplitudes/topography, and compromised data quality. gel cap: a fabric or silicone electrode cap with integrated electrode wells used with conductive gel to create low-impedance, stable scalp contacts for multi-channel EEG/qEEG recordings.

group delay: the effective time shift introduced by a filter; nonuniform delay across frequencies distorts phase relationships.


hippocampus: a medial temporal structure involved in context processing and generalization gradients.


high-pass filter: a filter that passes frequencies above a cutoff while attenuating slower components.


infinite impulse response (IIR) filter: a recursive filter with feedback; efficient but nonlinear phase can distort timing.


inion: the bony bump on the lower rear of the skull (external occipital protuberance) used as a landmark for EEG electrode placement.


International 10–10 system: a higher-density extension of 10–20 using finer proportional spacing. International 10–20 system: a proportional scalp mapping method using nasion, inion, and preauricular landmarks.


low-pass filter: a filter that passes frequencies below a cutoff while attenuating faster components.

mastoids: the bony prominences just behind each ear (mastoid processes of the temporal bones); frequently used as reference electrode sites (M1/M2) in the EEG/qEEG.

notch filter: a narrowband filter that attenuates a specific frequency (e.g., 50/60 hz mains).


phase distortion: an unequal delay of different frequencies by a filter, altering true temporal relationships.


prefrontal cortex (PFC): frontal networks supporting cognitive control, error monitoring, and metacognition.


preauricular notch: the palpable depression anterior to the ear; a 10–20 landmark.


qEEG (quantitative EEG): the statistical/spectral analysis of the EEG with topographic mapping and database comparison.

saline net electrode array: a cap of integrated sponge or felt electrodes hydrated with saline solution to create conductive contact with the scalp; offers rapid, comfortable setup and moderate impedance for multi-channel EEG/qEEG, but requires careful hydration control to avoid salt-bridging and may have higher noise and shorter recording stability than gel-based systems. salt‑bridging: an unintended electrical connection between neighboring electrodes caused by excess conductive gel or saline spreading across the scalp, which can short channels and distort amplitude, coherence, and topography.

sampling rate (sps): the number of measurements per second acquired by the amplifier; sets the Nyquist limit and temporal resolution.


sensorimotor rhythm (SMR): mid-beta activity ≈12–15 Hz over central sites linked to calm, steady attention.


sliding window: overlapping spectral windows that update estimates by stepping through the time series.


spectral leakage: the energy spread across frequency bins due to windowing; reduced by tapering/longer windows.


spectral power: the magnitude of signal energy within a frequency band over time.


stratum corneum: upper skin layer.


theta waves: EEG activity ≈4–8 Hz associated with drowsiness, memory processes, and some training protocols.


topographic map (topography): the spatial distribution of EEG features across the scalp.

tragus: the small cartilaginous flap in front of the ear canal; a nearby landmark is the preauricular notch (just anterior to the tragus), which anchors lateral measurements for the 10–20 placement system.

ventromedial prefrontal cortex (vmPFC): a region implicated in safety learning and extinction recall.


window length: the duration of data used per spectral estimate; longer windows improve frequency resolution but increase delay.




References


Acharya, J. N., Hani, A. J., Cheek, J., Thirumala, P. D., & Tsuchida, T. N. (2016). American Clinical Neurophysiology Society Guideline 2: Guidelines for standard electrode position nomenclature. Journal of Clinical Neurophysiology, 33(4), 308–311. https://doi.org/10.1097/WNP.0000000000000316


Fisch, B. J. (1999). Fisch and Spehlmann’s EEG primer: Basic principles of digital and analog EEG (3rd ed.). Elsevier.


Milad, M. R., & Quirk, G. J. (2012). Fear extinction as a model for translational neuroscience: Ten years of progress. Annual Review of Psychology, 63, 129–151. https://doi.org/10.1146/annurev.psych.121208.131631


Morey, R. A., Dunsmoor, J. E., Haswell, C. C., Brown, V. M., McCarthy, G., & LaBar, K. S. (2015). Fear learning circuitry is biased toward generalization of fear associations in posttraumatic stress disorder. Translational Psychiatry, 5, e700. https://doi.org/10.1038/tp.2015.196

Nicholson, A. A., Rabellino, D., Densmore, M., Frewen, P., Paret, C., Kluetsch, R., … Lanius, R. A. (2017). The neurobiology of emotion regulation in PTSD: Amygdala downregulation via real‑time fMRI neurofeedback. Human Brain Mapping, 38(1), 541–560. https://doi.org/10.1002/hbm.23402


Zhao, Z., Kirlic, N., Cosgrove, K. T., Craske, M. G., Paulus, M. P., & Khalsa, S. S. (2023). Amygdala downregulation training using fMRI neurofeedback in post‑traumatic stress disorder: A randomized, double‑blind trial. Translational Psychiatry, 13, 167. https://doi.org/10.1038/s41398-023-02467-6


Zotev, V., Phillips, R., Misaki, M., Wong, C. K., Wurfel, B. E., Krueger, F., Feldner, M., & Bodurka, J. (2018). Real‑time fMRI neurofeedback training of the amygdala activity with simultaneous EEG in veterans with combat‑related PTSD. NeuroImage: Clinical, 19, 106–121. https://doi.org/10.1016/j.nicl.2018.04.010




About the Authors


John S. Anderson, MA, LADC, BCB, BCN, QEEGD, is a veteran neurofeedback practitioner and educator with over five decades of experience in biofeedback and neurofeedback, beginning his work in 1974. He holds a master's degree in psychology and is certified by the Biofeedback Certification International Alliance (BCIA) and the International QEEG Certification Board. As the founder of the Minnesota Neuro-Training Institute, Anderson provides clinical services, mentorship, and professional training in neurotherapy. His clientele includes individuals with ADHD, learning disorders, chronic pain, and addiction. He is also a recognized instructor, offering BCIA-approved courses and QEEG certification programs, and contributes to educational initiatives such as Biosource Software's "Seminars Without Borders." Anderson integrates holistic healing practices with contemporary neurophysiological research to develop effective neurofeedback protocols.


John S. Anderson



Dr. John Raymond Davis is an adjunct lecturer in the Department of Psychiatry and Behavioural Neurosciences at McMaster University's Faculty of Health Sciences. His scholarly contributions include research on EEG changes in major depression and case studies on neurological conditions. ​


John Davis





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