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A pilot study for Validation of the clinical utility of a lung function remote monitoring system with respiratory rehabilitation software in patients with chronic respiratory patients

A pilot study for Validation of the clinical utility of a home IoT based lung function remote monitoring system with respiratory rehabilitation software in patients with chronic respiratory patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0012297
Enrollment
80
Registered
2026-07-20
Start date
2025-12-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

None listed

Interventions

Medical Device : The experimental group performed home-based respiratory rehabilitation for approximately 30 minutes per session, at least three times a week, for four weeks using the portable pulmona

Sponsors

Chungnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The selection criteria are defined as adults aged 19 to under 80 years diagnosed with chronic respiratory disease such as COPD or dyspnea of ??grade 2 or lower according to American Thoracic Society (ATS) standards, and an FEV1/FVC ratio of less than 0.7 in a pulmonary function test performed within 6 months of the selection date. Additionally, individuals are defined as those who do not experience physical or cognitive difficulties in using digital devices such as smartphones or tablets.

Exclusion criteria

Exclusion criteria: Participants are excluded from the study if they have severe pulmonary hypertension, if participation in rehabilitation is inappropriate due to physical or cognitive decline caused by acute heart disease or cerebrovascular disease, if they have experienced an acute exacerbation within the last three months, if they are pregnant, or if it is determined that they cannot perform the study due to other diseases. Additionally, the safety of exercise performance is assessed in advance using the PAR-Q physical activity readiness questionnaire prior to participation; if a risk is identified in one or more items, the decision to enroll or exclude is made based on the medical judgment of the investigator.

Design outcomes

Primary

MeasureTime frame
FVC (Forced vital capacity), FEV1 (Forced expiratory volume in 1 second), and PEF (Peak expiratory flow) in spirometry

Secondary

MeasureTime frame
Subjective questionnaire on respiratory symptoms using the CAT(COPD assessment test) and ATS(American Thoracic Society) dyspnea scales;Subjective survey on quality of life related to respiratory diseases via SGRQ(Saint George's respiratory questionnaire)

Countries

Korea, Republic of

Contacts

Public ContactGreen Hong

Chungnam National University Hospital

ihongreen@naver.com+82-2-280-7147

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Aug 10, 2026