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Clinical Trials/NCT05889832
NCT05889832
Completed
Not Applicable

Contactless Measurement of Heart Rate, Heart Rate Variability and Breathing Rate Using Face Video Analysis (Remote Photoplethysmography) - Validation of Shen.AI Vitals Software.

MX LABS spółka z ograniczoną odpowiedzialnością oddział w Polsce1 site in 1 country136 target enrollmentApril 26, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Rate
Sponsor
MX LABS spółka z ograniczoną odpowiedzialnością oddział w Polsce
Enrollment
136
Locations
1
Primary Endpoint
Accuracy of heart rate variability index (SDNN) measurement with the software under test compared with the ECG-based measurement
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study it to evaluate the accuracy of heart rate, heart rate variability and breathing rate measurement with the use of Shen.AI Vitals software developed by MX Labs.

Detailed Description

Resting heart rate (HR), heart rate variability (HRV) and breathing rate (BR) will be measured (estimated) with the use of remote photoplethysmography (1-minute face video analysis with Shen.AI Vitals software). The measurements will be taken with various camera-equipped devices (smartphones, tablets, laptops) using either front camera (self-measurement) or rear camera (measurement made by someone else), in two different lighting conditions (artificial light or natural daylight), with various levels of device stability (fully stable or held in hand/s), and in two different body positions (sitting or supine). In total, each participant will have 8 measurements taken. Standard deviation of normal heartbeat intervals (SDNN) will be used as the main HRV index. Apart from the average HR (averaged over the whole 1-minute measurement), instantaneous values of HR (averaged over 10 s) will also be determined and displayed every 1 s by the Shen.AI VItals software. In all cases, reference measurements will be taken simultaneously (chest ECG for the calculation of average and instantaneous HR as well as HRV; impedance pneumography for the determination of BR). The reference measurements will be taken with Finapres Nova with the ECG+Resp module (Finapres Medical Systems B.V.). For each measured parameter, the results from both methods will be compared using the Bland-Altman analysis or non-parametric limits of agreement.

Registry
clinicaltrials.gov
Start Date
April 26, 2023
End Date
June 6, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
MX LABS spółka z ograniczoną odpowiedzialnością oddział w Polsce
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age ≥ 18 years
  • ability to read and write in Polish or English
  • ability to operate a smartphone, tablet and laptop without the need for glasses
  • ability to understand the study procedure
  • ability to communicate and follow the instructions of the study staff
  • written consent to participate in the study and to the processing of personal data by the research team and the sponsor of the study

Exclusion Criteria

  • failure to provide the required information in the participant's information survey
  • failure to comply with the study procedure or the instructions of the study stuff
  • extensive facial skin damage (including abrasions, wounds, burns)
  • a disease process involving a large part of the face that makes the video- based measurement impossible
  • extensive face dressing
  • extensive facial skin tattoo or face painting
  • marked deformation of the face (e.g. a tumor)
  • inability to keep the head stable in the required position during the measurement
  • persistent cough making it impossible to remain still during the measurement
  • respiratory dysfunction in the form of shortness of breath or irregular or shallow breathing

Outcomes

Primary Outcomes

Accuracy of heart rate variability index (SDNN) measurement with the software under test compared with the ECG-based measurement

Time Frame: day 1 (single visit, approximately 30 minutes)

In each participant, the standard deviation of normal heartbeat intervals (SDNN) will be estimated from 1-minute video-based remote photoplethysmography of the facial skin (software under test) and calculated from simultaneously recorded ECG. Measurements will be made in resting conditions (seated position), with artificial lighting and a fully stabilized camera device. The results from both methods will be compared using the Bland-Altman analysis.

Accuracy of breathing rate (BR) measurement with the software under test compared with the impedance pneumography-based measurement

Time Frame: day 1 (single visit, approximately 30 minutes)

In each participant, the breathing rate will be estimated from 1-minute video-based remote photoplethysmography of the facial skin (software under test) and calculated from simultaneously recorded impedance pneumography signal. Measurements will be made in resting conditions (seated position), with artificial lighting and a fully stabilized camera device. The results from both methods will be compared using the Bland-Altman analysis.

Accuracy of instantaneous heart rate measurement with the software under test compared with the ECG-based measurement

Time Frame: day 1 (single visit, approximately 30 minutes)

In each participant, multiple instantaneous heart rate values (averaged over 10 s) will be estimated from the software under test and calculated from simultaneously recorded ECG. Measurements will be made in resting conditions (seated position), with artificial lighting and a fully stabilized camera device. The results from both methods will be compared using non-parametric limits of agreement.

Accuracy of heart rate (HR) measurement with the software under test compared with the ECG-based measurement

Time Frame: day 1 (single visit, approximately 30 minutes)

In each participant, average HR will be estimated from 1-minute video-based remote photoplethysmography of the facial skin (software under test) and calculated from simultaneously recorded ECG. Measurements will be made in resting conditions (seated position), with artificial lighting and a fully stabilized camera device. The results from both methods will be compared using non-parametric limits of agreement.

Secondary Outcomes

  • Accuracy of measurement of heart rate variability index (SDNN - the standard deviation of NN intervals) with the software under test on a smartphone held in hand/s (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of heart rate (HR) with the software under test on a smartphone held in hand/s (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of heart rate (HR) with the software under test in daylight conditions (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of breathing rate (BR) with the software under test on a smartphone held by someone else (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of heart rate variability index (SDNN - the standard deviation of NN intervals) with the software under test in daylight conditions (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of heart rate (HR) with the software under test on a smartphone held by someone else (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of heart rate variability index (SDNN - the standard deviation of NN intervals) with the software under test on a smartphone held by someone else (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of breathing rate (BR) with the software under test on a smartphone held in hand/s (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Utility of the software under test for self-measurement of physiological parameters (assessed with a questionnaire).(day 1 (after a single visit, approximately 30 minutes))
  • Utility of the software under test for the measurement of someone's physiological parameters (assessed with a questionnaire).(day 1 (after a single visit, approximately 30 minutes))
  • Accuracy of measurement of breathing rate (BR) with the software under test in daylight conditions (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement breathing rate (BR) with the software under test in the supine position (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of heart rate (HR) with the software under test in the supine position (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))
  • Accuracy of measurement of heart rate variability index (SDNN - the standard deviation of NN intervals) with the software under test in the supine position (compared with reference measurements).(day 1 (single visit, approximately 30 minutes))

Study Sites (1)

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