| Unique ID issued by UMIN | UMIN000056577 |
|---|---|
| Receipt number | R000064648 |
| Scientific Title | An innovative mobile tele-spirometry system: development and validation study:Assessment of Consistency |
| Date of disclosure of the study information | 2025/01/08 |
| Last modified on | 2025/06/10 17:26:51 |
An innovative mobile tele-spirometry system: development and validation study:Assessment of Consistency
An innovative mobile tele-spirometry system: development and validation study
An innovative mobile tele-spirometry system: development and validation study:Assessment of Consistency
An innovative mobile tele-spirometry system: development and validation study
| Japan |
Healthy adults meeting the inclusion criteria
| Adult |
Others
NO
The purpose of this study is to develop a mobile tele-spirometry system by integrating a communication system using widely available information and communication technology (ICT) devices, a laptop computer, and a portable, easy-to-maintain flow meter, and to evaluate its feasibility. Specifically, the study aims to assess the consistency of measurement values between face-to-face spirometry and tele-spirometry and verify whether tele-spirometry demonstrates reliability equivalent to face-to-face spirometry.
Efficacy
The primary outcome is the evaluation of the consistency of measurement values (vital capacity, forced vital capacity, forced expiratory volume in 1 second, peak expiratory flow, and extrapolated volume) between face-to-face spirometry and tele-spirometry. Additionally, the validity and reproducibility of these measurements will be assessed.
1.Conducting a questionnaire survey with participants to evaluate the testing time and the number of test attempts.
2.Measuring noise levels in the testing environment to verify whether tele-spirometry contributes to improvements in the environment of testing and consultation rooms.
Interventional
Single arm
Non-randomized
Open -no one is blinded
Self control
1
Prevention
| Maneuver |
This study aims to conduct a randomized crossover trial comparing face-to-face spirometry and tele-spirometry. The objective is to evaluate the equivalence and consistency of measurement values between tele-spirometry and face-to-face spirometry.
| 20 | years-old | <= |
| Not applicable |
Male and Female
Healthy adults aged 20 years or older who have never undergone spirometry.
1.Individuals receiving treatment for acute cardiac, vascular, or respiratory diseases.
2.Individuals being monitored for chronic respiratory diseases (e.g., COPD, asthma).
3.Individuals receiving treatment or being monitored for active infections.
4.Individuals with a history of forced expiration- or cough-induced syncope.
5.Individuals with hearing impairments.
6.Other individuals deemed ineligible by the researcher.
34
| 1st name | Jun |
| Middle name | |
| Last name | Ueki |
Juntendo University Graduate School of Health Care and Nursing
Clinical Research Unit of Respiratory Pathophysiology
279-0023
2-5-1, Takasu, Urayasu City, Chiba
0473553111
junueki@juntendo.ac.jp
| 1st name | Miki |
| Middle name | |
| Last name | Matsuki |
Juntendo University Graduate School of Health Care and Nursing
Clinical Research Unit of Respiratory Pathophysiology
279-0023
2-5-1, Takasu, Urayasu City, Chiba
0473553111
mmatsuki@bgu.ac.jp
Juntendo University
Juntendo University
Other
Juntendo University
2-1-1 Hongo Bunkyo-ku Tokyo
0338133111
junueki@juntendo.ac.jp
NO
| 2025 | Year | 01 | Month | 08 | Day |
Unpublished
No longer recruiting
| 2022 | Year | 04 | Month | 01 | Day |
| 2022 | Year | 02 | Month | 24 | Day |
| 2022 | Year | 06 | Month | 01 | Day |
| 2027 | Year | 03 | Month | 31 | Day |
| 2024 | Year | 12 | Month | 26 | Day |
| 2025 | Year | 06 | Month | 10 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064648