Actively Recruiting
Clinical Validation of the Dozee System for Contactless Monitoring of Heart Rate, Respiration Rate, Motion, and Bed-Exits
Led by Turtle Shell Technologies Pvt. Ltd. · Updated on 2025-11-03
60
Participants Needed
1
Research Sites
1 weeks
Total Duration
On this page
Sponsors
T
Turtle Shell Technologies Pvt. Ltd.
Lead Sponsor
E
Eastside Research Associates
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the Dozee VS system, a contactless device designed to monitor heart rate and breathing rate using a sensor sheet placed under the mattress. This system captures body vibrations and converts them into vital signs that can be monitored remotely in real time. The study aims to validate updated AI-powered heart rate and improved breathing rate algorithms across different sensor sheet types to ensure clinical accuracy. Participants in this observational study will be monitored using the Dozee VS device along with standard telemetry monitoring methods such as Electrocardiography and Capnography, which serve as the gold standards. The Dozee system includes hardware upgrades with dual-sensor sheets and uses AI/ML algorithms to improve accuracy in detecting heart rate and respiratory rate. Data from both Dozee and the gold standard devices will be collected simultaneously. During the six-month study, participants' heart rate, respiratory rate, movement, and bed-exits will be closely monitored and recorded. The study will measure the accuracy and mean absolute error of the Dozee system compared to standard monitoring. Data will be displayed on a secure online dashboard for real-time observation. Participants will be assessed on their ability to move and exit the bed safely, and their vital signs will be continuously recorded to evaluate the system's performance.
CONDITIONS
Brief Title
Validating Dozee for Contactless Monitoring of Heart, Breathing, and Movemen
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults male or female, above 18 years of age
- Provide written informed consent
- Weight between 40 kg (88.18 lbs) and 120 kg (264.55 lbs)
- Agree to not eat during the testing period
- Able to move and exit the bed independently and safely
You will not qualify if you...
- Connected to a device that may interfere with study monitoring
- Receiving bedside care incompatible with study procedures
- Likely to need a procedure during the testing period
- Cannot accept nasal cannula or ECG leads placement on the chest
- Have a significant medical condition that may affect study testing in investigator's judgment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 6 months
Participants are monitored using the Dozee contactless device placed under the mattress alongside standard telemetry monitoring (ECG and Capnography) to measure heart rate, respiration rate, movement, and bed-exits simultaneously.
Continuous monitoring with periodic data collection visits
Trial Site Locations
Total: 1 location
1
ERA Health Research
Midland, Texas, United States, 79707
Actively Recruiting
Research Team
H
Hinali Zhaveri
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Frequently Asked Questions
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