Clinical study of non-contact monitoring of Respiratory rate and Heart rate in non-acuity settings
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 158
- Locations
- 1
- Primary Endpoint
- The primary objective is to collect non-contact monitoring data in a non-acuity setting for developing algorithms to extract respiratory rate and heart rate.
Study Overview
Brief Summary
This study is a observational Prospective study focusing on measuring respiratory rate and heart rate in a non – contact manner. The cases where the non-contact monitor will be used are in areas where the patient is recovering from a procedure or intervention. E.g. immediately post a hemodialysis session, burns case and patients in a medical ward. Our study aims at studying and identifying the appropriateness of using a non-contact monitoring system in a relatively low-acuity setting with the intention of improving surveillance and patient safety.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18.00 Year(s) to 90.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients in the recovery room post hemodialysis, Patients in the general ward in non-acuity settings Burns patients who are recovering in non-acuity settings.
Exclusion Criteria
- •Patients requiring acute care Patients in high-acuity hospital settings.
Outcomes
Primary Outcomes
The primary objective is to collect non-contact monitoring data in a non-acuity setting for developing algorithms to extract respiratory rate and heart rate.
Time Frame: 45 minutes
Secondary Outcomes
No secondary outcomes reported