The Neuro-Flux Band is designed to achieve the long-standing goal in neurotechnology of creating a brain monitoring system as accessible and familiar as a smartwatch: a device that can be worn throughout the day to track cognitive states, mental wellness, and overall brain performance. This design emphasizes the need for affordability, comfortable all-day wearability, and battery life sufficient for 24-hour operation.
Neuro-Flux Band: The Wearable Brain Monitor
Introduction
Design and Technology
To balance these goals, the Neuro-Flux Band uses a hybrid multimodal optical-electrical sensing approach that combines the speed of electrical signals with the depth-sensitivity and physiological specificity of modern optical techniques. It integrates Time-Resolved fNIRS, Diffuse Correlation Spectroscopy, Event-Related Optical Signal, and dry-electrode EEG, each chosen for complementary strengths. TR-fNIRS and DCS provide depth-discriminated measurements of blood oxygenation and cerebral blood flow, solving the common problem of scalp contamination and allowing the device to reliably measure cortical metabolic activity in real-world settings. EROS contributes the millisecond-scale temporal resolution needed for real-time cognitive metrics by detecting rapid structural changes associated with neuronal firing. Meanwhile, dry EEG electrodes track electrical oscillations across alpha, beta, and gamma bands. Together, these modalities offer a complete picture of both fast neural dynamics and slower hemodynamic processes, enabling high-quality interpretations using fewer sensors than lab-grade systems. A moderate sensor layout of 24–36 channels spanning the frontal, temporal, and parietal areas is ideal for reducing cost, while still capturing cognitive data.
Data Processing and User Experience
Using this multimodal dataset, the Neuro-Flux Band computes user-facing metrics through machine learning models that fuse fast (EEG/EROS) and slow (TR-fNIRS/DCS) signals. Cognitive load and focus are estimated from frontal beta/gamma EEG activity and EROS changes, supported by local increases in oxygenation and blood flow. Mental resilience and fatigue are predicted through continuous metabolic patterns, allowing the system to warn users before performance drops. Sleep quality is assessed by tracking brainwave stages alongside changes in deep-tissue oxygenation. These metrics are grounded in established neuroscientific evidence: EEG frequency bands have decades of validation in attention and workload research, EROS captures fast optical responses tied to neuronal membrane changes, and TR-fNIRS/DCS has a strong empirical foundation in metabolic coupling and blood-flow regulation.
Device Design
The Neuro-Flux Band is a lightweight, flexible fabric headband, chosen over rigid eyeglasses or earbuds because it offers the best surface area for multimodal sensor contact while remaining comfortable for prolonged wear. The device weighs under 100 grams, uses a breathable performance fabric, and is adjustable for different head shapes. To withstand daily use, the headband is designed to be sweat-resistant, splash-proof, and built with sealed optical/electrical components, ensuring durability during exercise, sleep, and normal wear. The optical components rely on VCSEL light sources and SiPM detectors, which are significantly smaller, cheaper, and more power-efficient than traditional lab-grade elements. The band’s flexible electronics, embedded within a textile base that lightly adheres to the skin, dramatically reduce motion artifacts, one of the major challenges in real-world optical monitoring. The battery is engineered for 24-hour operation, supported by an adaptive energy-harvesting array combining small photovoltaic and photoluminescent elements to recharge from ambient light. Bluetooth Low Energy handles wireless data transmission, while AI processing offloads to the user’s smartphone to save device power. This design prioritizes convenience, comfort, and reliability while ensuring that signal quality is not compromised by hair, sweat, or head movement. The trade-off is a slightly lower sensor density than high-end research caps, but this is balanced by the deeper, more accurate readings provided by the time-domain optical system.
User Interface and Application
The user experience is centered around the Flux App, which converts complex neurophysiological data into simple, actionable information. Instead of raw waveforms, the user sees intuitive visualizations: real-time color-changing gauges, numerical focus scores, fatigue warnings, and nightly sleep summaries. The app provides real-time neurofeedback during structured sessions like meditation or productivity sprints, while also generating daily and weekly reports that reveal long-term cognitive trends. Its recommendation system uses personalized AI models to identify patterns in the user’s brain activity. For example, suggesting breaks when metabolic reserves fall or proposing breathing exercises when stress biomarkers rise. The primary “killer feature” of the Neuro-Flux Band is its ability to quantify both instantaneous neural performance and underlying metabolic reserve, something current consumer devices cannot offer. This helps users understand why they feel mentally drained and how to structure their day for improved productivity and well-being.
Validation and Market Position
Scientific credibility is ensured through a multi-phase validation strategy. The Neuro-Flux Band’s temporal accuracy must be benchmarked against high-density EEG and laboratory EROS systems using standard rapid-stimulus paradigms. Its depth-sensitive measurements (TR-fNIRS/DCS) require spatial validation against fMRI and functional ultrasound to confirm that the device correctly identifies cortical activation patterns. Behavioral studies must demonstrate strong correlations between Neuro-Flux metrics and objective performance outcomes, such as sustained attention accuracy or driving simulator performance. To avoid the pitfalls of pseudoscience common in consumer neurotech, the system communicates its confidence levels directly to users and avoids making unvalidated medical claims. Initially, the Neuro-Flux Band is marketed strictly as a wellness and performance optimization device, delaying regulatory approval processes until further clinical evidence is collected. Transparency about limitations helps build trust and mitigates misuse.
Business Model and Ethical Considerations
Finally, the business model must support widespread adoption while keeping the device affordable for mass-market consumers. At scale, the estimated manufacturing cost of the Neuro-Flux Band is projected to fall in the $120–$150 range, allowing a sustainable retail price of $250–$300 initially, with a long-term goal of approaching the smartwatch benchmark of less than $200. Achieving this price tier requires several cost-reduction strategies: high-volume manufacturing runs, component economies of scale, and the sharply declining costs of VCSEL emitters, SiPM detectors, and flexible-PCB fabrication once production exceeds several hundred thousand units. These efficiencies shrink the bill of materials far below traditional neuroimaging devices, making the product viable for everyday consumers rather than niche laboratory use. Key competitors include devices like the Muse S Athena and the Neurosity Crown, but the Neuro-Flux Band differentiates itself by allowing it to measure not only electrical patterns but also deep-tissue oxygenation, blood flow, and fast optical responses linked to neuronal firing. This results in metrics that are more accurate because they come from real brain signals like oxygen use and blood flow that traditional EEG systems cannot provide. Because brain data is highly sensitive, privacy is a core ethical priority. Data is stored locally on the user’s phone by default, encrypted, and never shared without explicit permission. This data is encrypted end-to-end, meaning the company itself cannot view raw neural signals, derived metrics, or historical cognitive trends unless the user explicitly chooses to upload them for research participation. Access is restricted to the user alone, and sharing can only occur through granular, opt-in permissions that specify exactly what data is shared, for what purpose, and for how long. The company’s policies explicitly forbid selling or providing brain data to employers, insurers, or third parties, preventing coercive uses of continuous neural monitoring. Continuous brain monitoring raises several ethical concerns that go beyond ordinary wearable technology. The first major concern is mental privacy, because brain signals can reveal patterns related to attention, stress, emotional state, fatigue, and potentially early signs of neurological conditions. Unlike heart rate or step count, these signals represent aspects of a person’s inner life, which creates the risk of unwanted psychological profiling. A second concern is data misuse, particularly by employers, insurers, or institutions that might attempt to use neural information to judge productivity, mental stability, or cognitive performance. Without strict protections, continuous monitoring could enable behavioral surveillance, discrimination, or subtle coercion. A third concern is loss of autonomy, where individuals may feel pressured, directly or indirectly, to share neural data to maintain employment, access insurance benefits, or participate in academic or athletic programs. Continuous brain monitoring also raises broader societal concerns about the normalization of tracking cognitive states, which could gradually erode expectations of privacy and mental freedom. Recognizing these risks, the Neuro-Flux Band adopts a user-sovereignty model to ensure that neural data remains private, controlled, and free from external pressure or exploitation.
References
- Gratton, G., & Fabiani, M. (2001). The event-related optical signal: a new tool for studying brain function. International journal of psychophysiology: official journal of the International Organization of Psychophysiology, 42(2), 109–121. https://doi.org/10.1016/s0167-8760(01)00161-1
- Shoemaker, L. N., Milej, D., Mistry, J., & St Lawrence, K. (2023). Using depth-enhanced diffuse correlation spectroscopy and near-infrared spectroscopy to isolate cerebral hemodynamics during transient hypotension. Neurophotonics, 10(2), 025013. https://doi.org/10.1117/1.NPh.10.2.025013
- Gao, Y., Chao, H., Cavuoto, L., Yan, P., Kruger, U., Norfleet, J. E., Makled, B. A., Schwaitzberg, S., De, S., & Intes, X. (2022). Deep learning-based motion artifact removal in functional near-infrared spectroscopy. Neurophotonics, 9(4), 041406. https://doi.org/10.1117/1.NPh.9.4.041406
- Kam, J. W. Y., Griffin, S., Shen, A., Patel, S., Hinrichs, H., Heinze, H. J., Deouell, L. Y., & Knight, R. T. (2019). Systematic comparison between a wireless EEG system with dry electrodes and a wired EEG system with wet electrodes. NeuroImage, 184, 119–129. https://doi.org/10.1016/j.neuroimage.2018.09.012
- Richer, N., Bradford, J. C., & Ferris, D. P. (2024). Mobile neuroimaging: What we have learned about the neural control of human walking, with an emphasis on EEG-based research. Neuroscience & Biobehavioral Reviews, 162, 105718. https://doi.org/10.1016/j.neubiorev.2024.105718
- Xing, C., Feng, J., Yao, J., Xu, X. M., Wu, Y., Yin, X., Salvi, R., Chen, Y. C., & Fang, X. (2024). Neurovascular coupling dysfunction associated with cognitive impairment in presbycusis. Brain communications, 6(4), fcae215. https://doi.org/10.1093/braincomms/fcae21
- Fantini, S., & Sassaroli, A. (2020). Frequency-Domain Techniques for Cerebral and Functional Near-Infrared Spectroscopy. Frontiers in neuroscience, 14, 300. https://doi.org/10.3389/fnins.2020.00300
- Yuste, R., Goering, S., Arcas, B. A. Y., Bi, G., Carmena, J. M., Carter, A., Fins, J. J., Friesen, P., Gallant, J., Huggins, J. E., Illes, J., Kellmeyer, P., Klein, E., Marblestone, A., Mitchell, C., Parens, E., Pham, M., Rubel, A., Sadato, N., Sullivan, L. S., … Wolpaw, J. (2017). Four ethical priorities for neurotechnologies and AI. Nature, 551(7679), 159–163. https://doi.org/10.1038/551159a
Other Course Work
📊 Assignment 1: EEG Analysis
Screenshot 2025-09-22 at 11.52.57 AM - Hannah Cooper.png
🎨 Assignment 2: BrainImation
📄 Code Comparisons - Hannah Cooper.pdf
View Original PDFOriginal Code:
// Neural mandala
let angle = 0 ;
function setup() {
colorMode( HSB , 360 , 100 , 100 );
}
function draw() {
background( 0 , 0 , 0 , 0.05 );
translate(width/ 2 , height/ 2 );
let layers = 5 ;
for ( let layer = 0 ; layer < layers; layer++) {
let radius = 50 + layer * 40 ;
let points = 6 + layer * 2 ;
for ( let i = 0 ; i < points; i++) {
let a = angle + ( TWO_PI / points) * i;
let x = cos(a) * radius;
let y = sin(a) * radius;
let hue = (angle * 57.3 + layer * 60 ) % 360 ;
let brightness = 50 + eegData.attention * 40 ;
let size = 5 + eegData.alpha * layer * 2 ;
fill(hue, 80 , brightness, 0.7 );
noStroke();
ellipse(x, y, size);
}
}
angle += eegData.meditation * 0.02 + 0.005 ;
}
New Code
// Neural mandala
// Neural mandala — EEG-reactive visualization by Hannah Cooper
// This animation transforms EEG brainwave data into a colorful, pulsating mandala.
// The piece visualizes focus (attention), relaxation (alpha), and calmness
(meditation)
// through color, brightness, size, and rotational speed.
let angle = 0 ;
function setup() {
// Use HSB color mode for dynamic hue control (easier to shift colors smoothly)
colorMode( HSB , 360 , 100 , 100 );
noStroke(); // Clean, glowing look with no outlines
}
// Simulated EEG data for testing (BrainImation will replace these values in
real-time)
let eegData = {
attention: 0.6 , // Represents mental focus or engagement (0–1)
alpha: 0.5 , // Represents relaxation or calm wakefulness (0–1)
meditation: 0.4 // Represents deep calm and reduced stress (0–1)
};
function draw() {
// Create a faint trail effect for smooth animation persistence
background( 0 , 0 , 0 , 0.05 );
// Center the mandala on the screen
translate(width / 2 , height / 2 );
let layers = 6 ; // Number of concentric circular layers (rings of petals)
// Loop through each layer to build the mandala structure
for ( let layer = 0 ; layer < layers; layer++) {
// Radius grows with each layer and expands with meditation (flower “blooming”)
let radius = 30 + layer * 40 * ( 1 + eegData.meditation);
// Each layer has more points (petals) as it expands outward
let points = 6 + layer * 2 ;
// Draw each point (petal) in the circular layer
for ( let i = 0 ; i < points; i++) {
// Determine angular position around the circle
let a = angle + ( TWO_PI / points) * i;
// Add gentle pulsing motion using sine waves for organic breathing effect
let pulse = sin(angle * 3 + i * 0.5 + layer) * 10 ;
// Convert polar coordinates to (x, y) with pulse offset
let x = cos(a) * (radius + pulse);
let y = sin(a) * (radius + pulse);
// Visual characteristics based on EEG data and motion
let hue = (angle * 40 + layer * 60 + i * 15 ) % 360 ; // Color rotation by angle +
layer depth
let brightness = 40 + eegData.attention * 60 ; // More attention = brighter
colors
let size = 5 + eegData.alpha * layer * 2 ; // More alpha = larger petal
size (relaxed flow)
// Conceptual variables for extended design ideas (petal stretching)
let petalWidth = 10 + eegData.alpha * 20 ;
let petalHeight = 30 + eegData.alpha * 50 + pulse;
// Draw each petal point with its hue, saturation, and brightness
fill(hue, 80 , brightness, 0.9 );
ellipse(x, y, size);
}
}
// Draw the mandala’s center — its size pulses with meditation level (calmness)
fill( 50 , 80 , 90 , 0.9 );
let centerSize = 50 + eegData.meditation * 100 * sin(angle * 2 );
ellipse( 0 , 0 , centerSize);
// Rotation speed adjusts with the center’s size (more calmness = smoother movement)
// constrain() prevents extreme speed changes
let clampedCenter = constrain(centerSize, 30 , 170 );
let speed = map(clampedCenter, 30 , 170 , 0.003 , 0.035 );
angle += speed; // Update global rotation angle
}
// Automatically resize canvas when window changes size
function windowResized() {
resizeCanvas(windowWidth, windowHeight);
📄 Hannah_Cooper_Assignment2_BrainImation_APA_Format - Hannah Cooper.pdf
View Original PDFHannah Cooper
1771074
Psych 403 A1: Neuroimaging and Neurostimulation
October 20, 2025
Word count: 1,188
BrainImation : Neural Mandala
My project, Neural Mandala , visualizes the relationship between focus, calmness, and
mental balance through brainwave data. I wanted to show how the mind is always in motion
even in states of meditation and how moments of focus and calm coexist. The animation takes
the form of a mandala, a traditional symbol of harmony and self - awareness, but it reacts
dynamically to EEG signals. The center orb expands and contracts based on meditation levels,
symbolizing rhythmic breathing and inner stillness. The surrounding petals rotate in response to
these changes, speeding up as the center grows and slowing down as it contracts. The result is a
visual balance between stillness and motion, where the speed and flow of the pattern reflect
mental state. Overall, the animation captures the idea that calmness is not the absence of activity,
but a state where everything flows in sync. By linking human cognitive states to visual motion,
this piece explores how data from the mind can become a dynamic form of digital expression.
Ultimately, the visualization bridges neuroscience and art, turning invisible cognitive data into
visible, expressive motion.
I began with the original Neural Mandala template provided in BrainImation but made
substantial modifications to create a more responsive and expressive visualization. I first defined
a simulated EEG data object to represent three core cognitive variables: attention, alpha
(relaxation), and meditation. I then integrated these values into the mandala’s structure so that
attention now controls color brightness, alpha affects the size and pulsing of the petals, and
meditation influences the rotational speed and overall expansion of the form. I also introduced
sinusoidal motion to create a breathing - like effect, making the mandala feel alive and organic.
Additionally, I added a dynamic center pulse that grows and contracts with meditation levels to
visually emphasize changes in pace. The rotation speed was remapped to this pulse rather than
being linearly tied to EEG values, allowing for smoother, more natural transitions. Finally, I
improved usability by adding automatic canvas resizing and moving noStroke() to setup() for
efficiency and cleaner visuals. I also included detailed comments throughout the code to explain
what each section does and how it connects to EEG data.
The biggest challenge was balancing the visual motion to look smooth and meaningful
rather than chaotic. At first, the petals all rotated at a constant speed, which made the animation
feel mechanical and disconnected from the intended meditative tone. Linking the rotation tempo
to the meditation - driven center size solved this, creating a natural breathing rhythm. I also had to
experiment with the range mapping for speed and brightness so the visual changes were neither
too subtle nor too extreme. Finding the right map() values for angle and color transitions required
several rounds of testing to achieve a visually coherent result.
This project helped me understand how brain - computer interfaces can be used creatively
to visualize mental states. I discovered that attention, alpha, and meditation each represent
measurable aspects of cognition and emotion that can be artistically expressed through
parameters like color, size, and speed. I developed stronger technical skills in P5.js animation,
particularly in using mapping functions, sinusoidal motion, and responsive rendering.
Conceptually, I learned how art and technology can work toge ther to communicate inner
experiences that are often invisible. Through this project, I realized that neuroart is not just about
displaying data; it is about translating brain activity into something emotionally resonant and
deeply human.
🎯 Midterm Project
📄 Written (1) - Hannah Cooper.pdf
View Original PDFHannah Cooper
1771074
Part 1: EG Snake: Target and Adaptive Neurofeedback Game
My project, EG Snake , is a closed-loop neurofeedback game that merges two advanced
BCI principles: target brain-state training and adaptive difficulty control. The system begins with
a brief calibration phase that establishes my personal alpha baseline and defines a target
threshold ( targetAlpha ). During gameplay, the animation continuously measures how closely my
live alpha activity matches this target. As my brain approaches the ideal range, the visuals
become more harmonious. The background glow intensifies, and a status badge progresses
from NEAR to CLOSE to IN ZONE. When the “IN ZONE” state is maintained, the score
multiplier accelerates and a streak counter builds, rewarding sustained self-regulation and
reinforcing calm, stable alpha production.
Simultaneously, beta activity (associated with attention and arousal) drives an adaptive
difficulty loop. Higher beta reduces challenge by slowing the snake’s speed, enlarging the food,
and smoothing turning, while lower beta increases the difficulty to keep engagement high. This
dual-feedback system ensures the player’s brain not only influences the environment but also
learns from it, creating a dynamic balance between challenge and relaxation rather than a
one-way visual response.
Developing this as a non-coder was challenging but highly educational. I learned to
debug real-time loops, tune thresholds, and manage smooth visual feedback without disrupting
logic flow. Implementing the calibration and adaptive loops revealed several key insights: EEG
signals drift and require recalibration; tiered, gradual feedback is more effective than simple
binary cues; and integrating two adaptive systems demands careful balancing of timing and
reward. Even when I did not reach the exact target state, watching the system respond
dynamically felt rewarding and motivating, illustrating the power of neurofeedback to sustain
engagement and promote self-awareness.
Hannah Cooper
1771074
Part 2: ERP Experiment (P300 Oddball with Circle→Annulus)
This experiment measures the P300 (P3) component, a positive ERP deflection
occurring approximately 300–600 ms after an unexpected or task-relevant event. According to
classic oddball literature (e.g., Polich, 2007), rare or significant stimuli evoke larger P300
amplitudes than frequent ones, reflecting attention allocation and working-memory updating.
Each 1000 ms trial begins from baseline. At 0 ms, a filled black circle (~100 px diameter)
appears for 30 ms, followed by a 60 ms blank gap, then a black annulus for 30 ms (outer radius
≈ 2× inner). The entire sequence lasts 120 ms, maintaining a 1 s inter-trial interval. Trials are
pseudorandomly assigned as STANDARD (80%) or RARE (20%). The physical stimuli are
identical, only the condition label differs, ensuring that ERP differences reflect cognitive rather
than visual factors.
For each trial, an epoch from −200 to +800 ms around circle onset is extracted across
channels TP9, AF7, AF8, and TP10 (256 Hz sampling). Baseline correction uses the
pre-stimulus −200 to 0 ms mean. Separate online averages are maintained for STANDARD and
RARE trials using incremental updating capped at roughly 20 epochs per condition to keep the
display responsive. The visualization shows two colored traces aligned to stimulus onset with
100 ms tick marks, vertical zero-line, condition counters, and a live stimulus monitor that
indicates phase and trial number.
If tested with real EEG, the RARE condition should display a larger parietal positivity
between 300 and 600 ms compared with the STANDARD trace, most pronounced at TP9 and
TP10. Both conditions would baseline near 0 μV before stimulus onset, and their divergence
would represent the classic P300 effect. This design fulfills all ERP-analysis criteria: clearly
Hannah Cooper
1771074
defined component, controlled stimulus manipulation, proper epoching and averaging, labeled
dual-trace visualization, and expected differential amplitude consistent with empirical literature.
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🎥 fin 4 - Hannah Cooper.mov
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📝 cooper_midterm_part1 (3) - Hannah Cooper.txt
💡 Code is embedded in this portfolio - opens instantly in the live BrainImation editor (no internet required!)
📝 cooper_midterm_part2_code - Hannah Cooper.txt
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