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Clinical Trials/NCT05165381
NCT05165381
Completed
N/A

Video Plethysmography for Contactless Vital Signs Measurement: A Pilot Study

University Health Network, Toronto2 sites in 1 country216 target enrollmentFebruary 11, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Blood Pressure, Heart Rate, Respiratory Rate, Heart Rate Variability, Stress Index, Vital Signs Monitoring
Sponsor
University Health Network, Toronto
Enrollment
216
Locations
2
Primary Endpoint
HRV and stress index pressure
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This pilot study will determine the feasibility and effectiveness of implementing video plethysmography (PPG) for contactless vital signs and str5ess index measurements from surgical patients in preoperative care. Our primary objective is to determine the feasibility and validity of using video PPG to collect contactless BP, HR and RR measurements when compared medical-grade instruments. Our secondary objective is to validate the use of video PPG in measuring HRV and stress index when compared to a validated stress questionnaire.

Detailed Description

The huge impact of the COVID-19 pandemic on global healthcare systems has given rise to an increased need for virtual care. This pilot study will determine the feasibility and effectiveness of implementing video plethysmography (PPG)for contactless vital signs measurements such as blood pressure (BP), heartrate (HR), respiratory rate (RR) and heart rate variability (HRV) from surgical patients in preoperative care. We also aim to validate the use of video PPG in measuring HRV and stress index when compared to a validated stress questionnaire. This study aims to assess how video PPG technology can be implemented in a clinical and telemedicine. If proven to be effective, this technology can be integrated into any smartphone or tablet and will allow users to monitor their vital signs with just a 1.5-minute video.

Registry
clinicaltrials.gov
Start Date
February 11, 2022
End Date
December 15, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients undergoing elective ambulatory surgery with general and/or regional anesthesia;
  • 18 years or older;
  • able to comprehend study instructions in English

Exclusion Criteria

  • refusal to consent for the study

Outcomes

Primary Outcomes

HRV and stress index pressure

Time Frame: 24 hours

4. HRV and stress index pressure will be measured by video PPG, stress index will be measured with a validated questionnaire

Vital signs measurement

Time Frame: 24 hours

Breathing rate will be measured by using both video PPG and standard medical grade blood pressure machine preoperatively

Study Sites (2)

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