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临床试验/NCT04383457
NCT04383457已完成不适用

Covid-19 Triage Using Camera-based AI

Vastra Gotaland Region1 个研究点 分布在 1 个国家目标入组 214 人开始时间: 2020年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
214
试验地点
1
主要终点
Agreement between the new camera based method and reference standard to estimate heart rate

研究概览

简要总结

The vital signs are critical in assessing the severity and prognosis of infections, such as Covid-19. The devices used today for measuring the vital signs have to be in physical contact with the patients. There is an apparent risk of transferring infections from one patient to the next (or to healthcare professionals).

This project aims to evaluate a new camera-based system for contactless measurement of vital signs as well as an artificial intelligence (AI) predicting hospitalization or death within 30 days. This particular study will evaluate the new system's ability without interfering with standard care of the patient.

详细描述

Background and aim:

The vital signs are critical in assessing the severity and prognosis of infections, i.e., Covid-19, influenza, sepsis and pneumonia. Quick and accurate triage is critical when facing a pandemic with an overwhelming number of cases (confirmed and suspected). This study aims a) to evaluate a new method for rapid camera-based non-contact measurement of five vital signs; body temperature, heart rate, blood oxygen saturation, respiratory rate, and blood pressure, and b) if an AI can predict hospitalization or death within 30 days.

Methods:

A method-comparison study design is used comparing each vital sign measured with the new method to the corresponding standard reference method. Furthermore, a cohort design is used to follow up any hospitalization or death within 30 days. The investigated new system consists of a high-speed digital video camera, a digital radiometric infrared camera, LED lights and a computer for data recording. This system faces the subject at a distance of approximately one meter, capturing a 30 second recording of the subject's face. First, all vital signs will be measured using one set of reference devices. Secondly the investigated device will record a 30 second video of the patient's face. Thirdly, and last, all vital signs will be measured using the same set of reference devices. A copy of the vital sign readings (using the standard reference methods) will be handed over by an investigator to the clinical professionals responsible for the subsequent medical care for each subject. Afterwards, the collected 30-second recordings will be run through specific software algorithms to extract the vital signs. The results from the new camera-based contactless measurement of vital signs and the outcome of the AIs prediction of risk for hospitalization or death will not be presented in the care situation of the patient.

Expected Findings:

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The patient is attending for triage presenting with symptoms of an infection.
  • Subject has provided informed consent
  • Age ≥18 years
  • Fluent in Swedish (reading, writing, conversational)
  • Mental state is such that he or she is able to understand and give informed consent to participation in the study by signing the Information and Consent Form
  • The investigator determines that the new method, and the reference methods, can be used as intended with adequate reliability and safety
  • The time for investigations in this study is estimated to approximately 15-20 minutes. Vital signs will be handed over to the care provider responsible for the further management of the patient saving approximately 5-10 minutes of their time. Hence, the delay in the management of each patient introduced by this study is approximately 10 minutes. Patients deemed being in such a severe medical condition on arrival, that 10 minutes of delay is deemed detrimental will not be included.

排除标准

  • Depressed level of consciousness from inclusion up until all investigations are completed (during approximately 15-20 minutes).
  • Patient request to be withdrawn from the study.

结局指标

主要结局

Agreement between the new camera based method and reference standard to estimate heart rate

时间窗: Two minutes between measurements

Heart rate will be measured with the new camera based method as well as with a conventional apparatus for measuring pulse rate. Both measurements will estimate the heart rate in beats per minute. The agreement between body temperature estimated with the new method and the reference method will be made using the statistical methods Bland-Altman plots and limits of agreement as the outcome.

Agreement between the new camera based method and reference standard to estimate body temperature

时间窗: Two minutes between measurements

Body temperature will be measured with the new camera based method as well as with a conventional ear thermometer. Both measurements will estimate the body temperature in degrees Celsius. The agreement between body temperature estimated with the new method and the reference method will be made using the statistical methods Bland-Altman plots and limits of agreement as the outcome.

Agreement between the new camera based method and reference standard to estimate blood oxygen saturation

时间窗: Two minutes between measurements

Blood oxygen saturation will be measured with the new camera based method as well as with a conventional apparatus for measuring blood oxygen saturation. Both measurements will estimate the blood oxygen saturation in percent (ranging from 0-100%). The agreement between blood oxygen saturation estimated with the new method and the reference method will be made using the statistical methods Bland-Altman plots and limits of agreement as the outcome.

Agreement between the new camera based method and reference standard to estimate systolic blood pressure

时间窗: Two minutes between measurements

Systolic blood pressure will be measured with the new camera based method as well as with a conventional apparatus for measuring systolic blood pressure. Both measurements will estimate the systolic blood pressure in mm Hg. The agreement between systolic blood pressure estimated with the new method and the reference method will be made using the statistical methods Bland-Altman plots and limits of agreement as the outcome.

Agreement between the new camera based method and reference standard to estimate diastolic blood pressure

时间窗: Two minutes between measurements

Diastolic blood pressure will be measured with the new camera based method as well as with a conventional apparatus for measuring diastolic blood pressure. Both measurements will estimate the diastolic blood pressure in mm Hg. The agreement between diastolic blood pressure estimated with the new method and the reference method will be made using the statistical methods Bland-Altman plots and limits of agreement as the outcome.

Agreement between the new camera based method and reference standard to estimate respiratory rate

时间窗: Two minutes between measurements

Respiratory rate will be measured with the new camera based method as well as manually using a stethoscope. Both measurements will estimate the respiratory rate in breath per minute. The agreement between respiratory rate estimated with the new method and the reference method will be made using the statistical methods Bland-Altman plots and limits of agreement as the outcome.

次要结局

  • Prediction of hospital admission using vital signs estimated using the new camera based method(Hospital admission for any cause up until 30 days after inclusion)
  • Prediction of hospital admission using vital signs estimated using reference standard methods(Hospital admission for any cause up until 30 days after inclusion)
  • Prediction of death using vital signs estimated using reference standard methods(Death for any cause up until 30 days after inclusion)
  • Prediction of death using vital signs estimated using the new camera based method(Death for any cause up until 30 days after inclusion)
  • Prediction of hospital admission using raw camera data(Hospital admission for any cause up until 30 days after inclusion)
  • Prediction of death using raw camera data(Death for any cause up until 30 days after inclusion)

研究者

发起方
Vastra Gotaland Region
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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