Healthy adults meeting the inclusion criteria
Conditions
Interventions
This study will conduct a randomized crossover trial comparing face-to-face spirometry and telespirometry to evaluate the advantage of testing skills.
Sponsors
Juntendo University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy adults aged 18 years or older who have never undergone spirometry.
Exclusion criteria
Exclusion criteria: 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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Secondary
| Measure | Time frame |
|---|---|
| Conducting a questionnaire survey with participants to evaluate the testing time and the number of test attempts. | — |
Countries
Japan
Contacts
Public ContactMiki Matsuki
Juntendo University Graduate School of Health Care and Nursing Clinical Research Unit of Respiratory Pathophysiology
Outcome results
None listed