Evidence map›Paper›PMID 42793493›Full record

ArticleHealthcare (Basel, Switzerland)2026

Feasibility of Home-Based Spirometry Monitoring as a Decentralized Clinical Trial Component in Patients with Chronic Obstructive Pulmonary Disease and Other Respiratory Diseases.

Ye Chan Park, So-Yun Kim, Green Hong, Jang Hee Hong, Dongil Park, Jung Sunwoo

Abstract read
In one paragraph

Article in Healthcare (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ye Chan ParkClinical Trials Center, Chungnam National University Hospital, Daejeon 35015, Republic of Korea.ORCID 0009-0007-2762-7742
So-Yun KimDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, Chungnam National School of Medicine, Chungnam National University Hospital, Daejeon 35015, Republic of Korea.ORCID 0009-0000-7155-3567
Green HongDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, Chungnam National School of Medicine, Chungnam National University Hospital, Daejeon 35015, Republic of Korea.ORCID 0009-0006-9841-2514
Jang Hee HongClinical Trials Center, Chungnam National University Hospital, Daejeon 35015, Republic of Korea.ORCID 0000-0002-0623-5455
Dongil ParkDivision of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, Chungnam National School of Medicine, Chungnam National University Hospital, Daejeon 35015, Republic of Korea.ORCID 0000-0001-7329-1724
Jung SunwooClinical Trials Center, Chungnam National University Hospital, Daejeon 35015, Republic of Korea.ORCID 0000-0001-8801-0323

Funding

Ministry of Health and Welfare RS-2023-KH141354
6 · The paper itself

Abstract

introductionHome-based spirometry has emerged as a potential component of decentralized clinical trials (DCTs) in respiratory medicine, but its real-world feasibility in patients with chronic obstructive pulmonary disease (COPD) and other respiratory diseases remains insufficiently characterized. This study evaluated the feasibility of remote pulmonary function monitoring using a portable spirometer and mobile application in adults with COPD or other respiratory diseases.

methodsThis exploratory single-arm study enrolled adults aged 19 years or older with COPD or other respiratory diseases. Participants were asked to perform home-based spirometry at six prespecified time points (Days 15, 29, 43, 57, 71, and 85). Feasibility was assessed using visit-level and participant-level adherence, spirometry quality grades, and patient-reported usability and satisfaction. Participants completing at least 5 of 6 scheduled measurements were classified as the high-adherence group; this cut-off was an operational, study-specific definition.

resultsA total of 30 participants were enrolled (19 with chronic obstructive pulmonary disease, 5 with asthma, 2 with asthma-COPD overlap, and 4 with other respiratory conditions), and 23 completed the study. Visit-level completion rates declined over time, from 88.5% on Day 15 to 47.8% on Day 71 and 56.5% on Day 85. Nine participants completed all six measurements, while 13 completed at least five. Portable spirometry quality showed variability across visits, with both high-quality and low-quality measurements observed. Compared with the low-adherence group, the high-adherence group reported significantly higher scores for convenience, communication with the research team, overall satisfaction, willingness to participate in future telemedicine-based trials, device training adequacy, ease of device use, and application usability.

conclusionsHome-based spirometry may be a useful decentralized trial component in patients with COPD and other respiratory diseases; however, the decline in adherence over time and the variability in measurement quality indicate that substantial operational refinement is needed before broader implementation. Because no feasibility threshold was prespecified, no concurrent laboratory spirometry comparison was performed, and the study population was diagnostically heterogeneous, these findings are exploratory and address operational feasibility rather than measurement validity.

Indexed as

chronic obstructiveclinical trialmobile applicationspatient compliancepulmonary diseasespirometrytelemedicine

Identifiers

PMID42793493
PMCPMC13606866

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.