About this trial
The NeuroFinance Human Stress Trial (NFHST-2026-001) is a decentralized observational clinical study designed to evaluate how financial market volatility, economic uncertainty, digital media exposure, and information-driven stress environments affect human physiologic and behavioral health. Participants will undergo remote monitoring using wearable biosensors, cardiovascular telemetry devices, sleep tracking systems, heart rate variability monitoring, and behavioral analytics platforms. The study will use artificial intelligence and machine learning systems to analyze relationships between external financial and informational events and biologic stress responses, including autonomic nervous system activity, sleep disruption, cardiovascular strain, emotional resilience, and inflammatory signaling. The goal of the study is to develop predictive digital biomarkers and AI-assisted forecasting systems capable of identifying stress-related physiologic deterioration before clinical manifestation.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Adults age 18 years and older.
Ability to provide informed consent.
Willingness and ability to comply with study procedures and remote monitoring requirements.
Access to a compatible smartphone, tablet, or internet-connected device for decentralized study participation.
Disqualifiers
Individuals unable or unwilling to provide informed consent.
Individuals unable to comply with remote monitoring procedures or wearable device usage requirements.
Active medical or psychiatric instability that, in the opinion of study investigators, may interfere with study participation or data integrity.
Current incarceration or institutionalization limiting voluntary participation.
Trial population
The study population will consist of adult participants exposed to varying levels of financial market activity, economic stress environments, occupational stress, and digital media exposure. Participants may include retail investors, financial professionals, active traders, technology workers, digitally connected individuals, and members of the general population. The study is designed to evaluate physiologic, behavioral, cardiovascular, autonomic nervous system, and sleep-related responses to financial and informational stress environments using wearable biosensors, digital health technologies, and artificial intelligence-assisted analytics platforms.
Trial design
Cohort
Prospective
Treatments tested in this trial
Wearable Physiologic Monitoring Platform
DeviceCommercially available wearable physiologic monitoring devices and digital health technologies will be used to collect continuous or intermittent biometric, cardiovascular, autonomic nervous system, behavioral, and sleep-related data during exposure to financial market volatility, economic uncertainty, and information-driven stress environments. Monitoring technologies may include: wearable ECG devices, heart rate variability (HRV) monitors, blood pressure monitoring systems, sleep tracking devices, galvanic skin response sensors, activity monitoring wearables, voice analysis systems, and optional EEG-enabled wearable technologies. Data generated from these systems will be integrated with artificial intelligence and machine learning-based analytics platforms for evaluation of physiologic stress responses and digital biomarker forecasting.
Treatment groups
Trial outcomes
Primary outcomes
Change in Heart Rate Variability (HRV) During Financial Stress Exposure
Heart rate variability will be measured using wearable electrocardiographic or photoplethysmographic monitoring devices. HRV will be quantified as the root mean square of successive differences (RMSSD) in milliseconds. Higher RMSSD values generally indicate improved autonomic nervous system flexibility and lower physiologic stress burden.
Change in Sleep Duration
Sleep duration will be measured in hours per night using wearable sleep monitoring devices.
Change in Resting Heart Rate
Resting heart rate will be measured in beats per minute using wearable biosensor devices.
Change in Perceived Stress Scale-10 (PSS-10) Total Score
Perceived stress will be assessed using the validated 10-item Perceived Stress Scale-10 questionnaire. Scores range from 0 to 40, with higher scores indicating greater perceived psychological stress and worse stress-related outcomes.
Secondary outcomes
Change in Sleep Efficiency
Sleep efficiency percentage measured using wearable sleep tracking systems.
Change in Galvanic Skin Response (GSR) Measurements
Electrodermal activity will be measured in microsiemens using wearable biosensor devices to assess sympathetic nervous system activation and physiologic stress responsiveness. Higher values may reflect increased autonomic arousal during stress exposure conditions.
Change in Generalized Anxiety Disorder-7 (GAD-7) Total Score
Anxiety symptoms will be assessed using the validated Generalized Anxiety Disorder-7 questionnaire. Scores range from 0 to 21, with higher scores indicating greater anxiety symptom severity and worse psychological outcomes.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: