Evaluation of Wearable Multi-modality Sensors for Monitoring Vital Signs
Sponsor: University of North Carolina, Chapel Hill
Trial Details
| Condition | Healthy, Health Behavior |
| Intervention | Multi-modality Noninvasive Biosensor; Oximeter; Portable Blood Pressure Monitor; Vicorder Pulse Wave Velocity Monitor |
| Phase | NA |
| Status | Recruiting |
| Participants | 22 |
| Est. Completion | 1 Nov 2026 |
| Last Updated | 17 Apr 2026 |
Primary Outcome
Mean Comfort Level of Wearable Sensors; Mean Safety Level of Wearable Sensors; Mean Agreement Over Time of Physiological Parameters between Newly-Fabricated Wearable Sensors and Approved Devices
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Individuals with ages between 18 and 99. * Healthy individuals (not known to suffer any significant illness relevant to the proposed study). Exclusion Criteria: * Pregnant or lactating. * History of active (clinically significant) skin disorders that make skin vulnerable to contact conventional electronic devices. * History of allergic response to silicones or adhesives (such as 3M Tegaderm). * Broken, damaged or irritated skin or rashes near the sensor application sites (finger, wrist, temple, subclavian, arm, neck, and thigh). * Subjects who are physically or cognitively unable to normally perform activities of daily living, assessed at the discretion of the investigator to ensure safe completion of study tasks. * Subjects who are unable to participate in moderate exercise for 6 minutes.
Trial Sites
Countries
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