None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults aged 19 years or older at the time of screening. 2. Individuals who have been diagnosed with Chronic Obstructive Pulmonary Disease (COPD) at the time of screening, or who have been receiving treatment for respiratory disease for more than 6 months at the Division of Pulmonology and Allergy, Chungnam National University Hospital. 3. Individuals who are ambulatory and capable of self-care, with an ECOG Performance Status score of 2 or less, as assessed using the ECOG Performance Status Scale questionnaire. 4. Individuals who have received a detailed explanation of this clinical trial, fully understood the information, voluntarily decided to participate, and provided written informed consent agreeing to follow the study instructions.
Exclusion criteria
Exclusion criteria: 1. Individuals who are unable to correctly use the portable pulmonary function testing device provided in this study. 2. Individuals who are scheduled to undergo procedures or treatments that may affect pulmonary function testing from the screening date to the anticipated end of the study. 3. Individuals who have been diagnosed with an acute exacerbation of chronic obstructive pulmonary disease (COPD) or show signs of worsening of an existing respiratory disease within one month prior to the screening date. 4. Individuals who are unable to complete the scheduled visits and procedures according to the study timeline. 5. Individuals deemed unsuitable for participation in this study by the principal investigator or a designated sub-investigator for any other reason.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The results of the portable spirometer test;Adherence to portable spirometer use;Survey score on research participation experience | — |
Secondary
| Measure | Time frame |
|---|---|
| Demographic data | — |
Countries
Korea, Republic of
Contacts
Chungnam National University Hospital