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NCT04964245 Clinical Trial

Respiratory Measurement of Volume Change Using Accelerometer, Thermographic Camera Electrical Impedance Tomography and Motion Correlation Analysis Using Mattress Sensor in Healthy Individuals

Healthy Adult Clinical Trial

Official title:
Respiratory Measurement of Volume Change Using Accelerometer, Thermographic Camera Electrical Impedance Tomography and Motion Correlation Analysis Using Mattress Sensor in Healthy Individuals

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04964245
Other study ID # 4-2020-1320
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 2021
Est. completion date August 2021

Study information
Verified date July 2021
Source Yonsei University
Contact Jeongmin Kim
Phone +82 10-8926-2684
Email ANESJEONGMIN@yuhs.ac
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Tidal volume can be the most important technical indicator for ventilation. Measuring the volume of breathing can be used as an indicator of how effective a patient's gas exchange is, and as a predictive indicator of the statue of respiratory disease indirectly. These Tidal volumes can be measured using spirometry and pneumotachograph, and the breathing volume and the rate of airflow can directly or indirectly evaluate the lung function of the patient. However, spirometry has limitations that patients who are difficult to measure, and that it is difficult to measure in bed. In this work, the movement of the thorax due to breathing is measured in a non-invasive manner (accelerometer, thermographic camera) and the accuracy is compared through changes in thoracic impedance obtained through Pulmovista 500. Furthermore, we would like to correlate the motion of the measured object through a mattress sensor.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 10
Est. completion date August 2021
Est. primary completion date August 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 19 Years to 50 Years
Eligibility Inclusion Criteria: 1. over 19, under 50 years old and common BMI 2. non-smoking, person without cardiopulmonary disease. Exclusion Criteria: 1. smoking, cardiopulmonary, infectious diseases.

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• accelometer
the respiration parameters are measured using an accelometer.
• thermographic camera
the respiration parameters are measured using an thermographic camera.
• Electrical Impedance Tomography
the respiration parameters are measured using an electrical impedance tomograhy.
• Mattress Sensor
the respiration parameters are measured using an Mattress pressure

Locations
Country Name City State
Korea, Republic of Severance Hospital, Yonsei University Health System Seoul

Sponsors (1)
Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary The accuracy of respiration measurements The accuracy respiration measurements between thermographic camera, accelerometer, electrical impedance tomography, and mattress sensor. about 20 min
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