Dozee Validation for Contactless Heart Rate and Respiration Monitoring in Clinical Settings (NCT07735403) | Clinical Trial Compass
RecruitingNot Applicable
Dozee Validation for Contactless Heart Rate and Respiration Monitoring in Clinical Settings
United States20 participantsStarted 2026-07-15
Plain-language summary
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
Who can participate
Age range
22 Years – 100 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Mean Absolute Error (MAE) of Dozee's Heart Rate a from the Gold Standard ECG
Timeframe: 6 months
2
Mean Absolute Error (MAE) of Dozee's Respiratory Rate from the Gold Standard Capnography