RecruitingNANCT05397951

Evaluation of Wearable Multi-modality Sensors for Monitoring Vital Signs

Sponsor: University of North Carolina, Chapel Hill

Trial Details

ConditionHealthy, Health Behavior
InterventionMulti-modality Noninvasive Biosensor; Oximeter; Portable Blood Pressure Monitor; Vicorder Pulse Wave Velocity Monitor
PhaseNA
StatusRecruiting
Participants22
Est. Completion1 Nov 2026
Last Updated17 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

United States
View Registry Entry

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