Home › NCT07735403

Dozee Validation for Contactless Heart Rate and Respiration Monitoring in Clinical Settings

Dozee System Validation for Contactless Heart Rate and Respiration Monitoring in Clinical Settings

Who can join

Ages 22 to 100 · All sexes · Healthy volunteers welcome

Inclusion Criteria:

* Adults Male or female. (≥ 22 years of age)
* Provide written informed consent.
* Weight over 40kg/88.18lbs

Exclusion Criteria:

* Are connected to a device that may interfere with the device monitoring in this study.
* Are receiving any bedside care which may be incompatible with the study procedures.
* A likely need to receive or undergo a procedure during the testing period.
* Cannot accept a nasal cannula, or have an ECG leads placed on the chest.
* Have a significant medical condition in the judgement of the investigator, which may compromise the study testing procedures.
* Prisoners

About the study

The Dozee VS system (K221555) is a contactless device that tracks heart rate and breathing rate using a sensor sheet placed under the mattress. It captures body vibrations and converts them into vital signs, which can be monitored remotely in real time. The system also supports add-ons like a blood pressure cuff, pulse oximeter, and thermometer, offering a complete monitoring solution. This study aims to validate the updated AI-powered heart rate and improved breathing rate algorithms across different sensor sheet types to confirm clinical accuracy

What is being tested

• Telemetry monitoring (device)

Sponsor: Turtle Shell Technologies Pvt. Ltd. · Participants: 20 · Started: Jul 15, 2026

Contact the study team

• Lindsay Darthard, LVN LNFA · Phone: 979-297-0425

Official record on ClinicalTrials.gov — NCT07735403

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.