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Feasibility Study of Remote Monitoring Using Decentralized Clinical Trial Elements

Feasibility Study of Remote Monitoring Using Decentralized Clinical Trial Elements: Remote Monitoring Using a Portable Spirometer in Patients with Chronic Obstructive Pulmonary Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011124
Enrollment
30
Registered
2025-11-10
Start date
2025-08-26
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Chungnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime frame
The results of the portable spirometer test;Adherence to portable spirometer use;Survey score on research participation experience

Secondary

MeasureTime frame
Demographic data

Countries

Korea, Republic of

Contacts

Public ContactPark Yechan

Chungnam National University Hospital

dpcks33@naver.com+82-42-280-6850

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026