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The Validation Study of Bioelectronics

Evaluation of Wearable Multi-modality Sensors for Monitoring Vital Signs

Who can join

Ages 18 to 99 · All sexes · Healthy volunteers welcome

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.

About the study

The purpose of this study is to investigate the safe wearability and basic functions of the multi-modality sensors fabricated in the PI lab.

What is being tested

• Multi-modality Noninvasive Biosensor (device)
• Oximeter (device)
• Portable Blood Pressure Monitor (device)
• Vicorder Pulse Wave Velocity Monitor (device)

Sponsor: University of North Carolina, Chapel Hill · Participants: 22 · Started: Jan 9, 2024

Contact the study team

• Hannah L Weisbecker, BS · Phone: 6786417484
• Wubin Bai, PhD · Phone: 9198439334

Official record on ClinicalTrials.gov — NCT05397951

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.