Open & begin
Pick the person and tap begin. The whole capture runs on the phone they already own. No clinic, no wearable, no calibration step.
Cardiology has its troponin. Endocrinology has its A1C. Brain health has, until now, depended on what the patient says or what the observer sees. Chronic Trace turns a single video capture into objective indices, scored against a personal baseline, so recovery and return-to-play or return-to-duty become decisions you can see, not guess.
Software-as-a-Medical-Device in development. Nine U.S. patents pending. Manipulation-resistant by architecture.
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On the ground, today.
Chronic Trace is a research-stage platform, positioned as a decision-support tool only. It is not diagnostic; results require clinical interpretation, and clinical decisions remain with licensed healthcare professionals.
Chronic Trace is invitation-led during pivotal validation. Tell us about your program and we'll respond within one business day.
The same thirty-second capture serves indications across sport, defense, pharmaceutical trials, pre-hospital stroke triage, and outpatient behavioral health. The science is shared. The pathways differ.
Team, league, and fitness-for-duty programs.
Pre-participation baselines, sub-concussive exposure monitoring, return-to-play decision support, and pre-shift readiness for safety-critical work. Captures the slow-accumulation signal that subjective checklists miss.
Cohort names reflect ongoing data-collection programs and research collaborations. No identifiable subject data is shown.
No clinic, no wearable, no training. A health worker, a coach, a parent: anyone runs the full capture and reads one calibrated index at the end. Here is the whole protocol, the way the instrument reads it.
Pick the person and tap begin. The whole capture runs on the phone they already own. No clinic, no wearable, no calibration step.
Standing naturally, arms relaxed at their sides. The camera reads the involuntary postural sway no one can consciously suppress.
Their eyes track a moving target while heart-rate variability is lifted from the same facial video. Two involuntary systems, one clip, nothing fakeable.
A short, timed cognitive trail. Number to number under light time pressure: attention under load. (Operator can swap Trail-Making for Stroop per session.)
A single response area waits gray, then flashes. The subject taps as fast as they can. Millisecond-precision latency per trial under randomized inter-stimulus intervals so the timing can't be paced.
Every signal folds into one Concussion Likelihood Index, measured against this person's own baseline.
A decision-support signal, not a diagnosis. Clinical decisions remain with licensed professionals.
A single short capture, processed on the device the subject already owns, lifts involuntary physiological signal and task-based performance metrics across the platform's eleven biomarker domains. None of the involuntary streams can be consciously modulated.
Five domains are live in production today, two run in research mode while we promote consumer-camera artifacts to clinical-grade, and four are on the engineering pipeline. Our Dispersion-Based Cognitive Intra-Individual Variability (d-CIIV) framework fuses the live signal into a calibrated, longitudinally-comparable family of indices.
Saccadic latency and peak velocity, antisaccade error rate, smooth pursuit gain, fixation stability, nystagmus characterization.
33-point skeletal landmark tracking, sway amplitude and frequency, pronator drift, gait kinematics where ambulation is permitted.
Trail-Making (number-to-number under time pressure) or Stroop interference, operator's choice per session. Path efficiency, error rate, completion latency, per-condition slowing.
Simple reaction time at millisecond precision with randomized inter-stimulus intervals so timing can't be paced. False-start detection and a deliberate-slowing flag at the trial level.
Heart-rate variability extracted from facial skin video — RMSSD, SDNN, HF/LF/LF:HF ratios; atrial-fibrillation detection from RR irregularity.
Baseline diameter, light-reflex amplitude and latency, constriction velocity, pupillary unrest under steady illumination.
Computed across all foregoing domains; in EEG-integrated embodiments, frontal alpha asymmetry as a primary depression biomarker.
The only non-invasive optical window to live CNS microvasculature — arteriovenous color ratio, vessel caliber, pulsation rhythm.
Prosodic flattening, fundamental-frequency contour, articulation rate, jitter, shimmer, dysarthria detection, semantic coherence.
468-point face mesh at 30+ fps, bilateral activation symmetry, central-versus-peripheral discrimination, blink rate and duration.
In wearable-integrated deployments, sleep architecture, fragmentation, REM latency, and circadian phase.
An individual cannot, by force of will, alter the latency of a saccadic eye movement, the constriction velocity of the pupil to a light flash, the diameter of a retinal arteriole, the cardiac rhythm, or the involuntary postural corrections of stance maintenance.
Software-as-a-Medical-Device platform under development. All indices described are research-stage and positioned as decision-support only — not diagnostic. Results require clinical interpretation, and clinical decisions remain with licensed healthcare professionals.
Every domain folded into a continuous score relative to the subject's own baseline. Slide to see how each band is interpreted. The CLI is a decision-support signal, not diagnostic; results require clinical interpretation.
Indices coherent with the subject's own prior captures.
If something here doesn't resolve your question, a real person responds within one business day.
Get in touchOne technology, one capture, one patent moat, pointed at the last major domain of medicine without an objective test. Reserve a non-binding allocation before the offering opens.
A thirty-second video, on the camera in your pocket — a family of calibrated, manipulation-resistant indices for the last major domain of medicine without an objective biomarker.