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Heart Rate Variability and Nocturnal Blood Oxygen Saturation in Patients With Idiopathic Pulmonary Fibrosis

Differences in Heart Rate Variability and Nocturnal Blood Oxygen Saturation of Patients With Idiopathic Pulmonary Fibrosis Between at Baseline and During Acute Exacerbation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06027372
Enrollment
70
Registered
2023-09-07
Start date
2020-05-21
Completion date
2024-06-30
Last updated
2023-09-07

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

Conditions

Idiopathic Pulmonary Fibrosis

Brief summary

The goal of this observational study is to compare the overnight heart rate variability (HRV) and nocturnal oxygen saturation (SpO2) in patients with idiopathic pulmonary fibrosis (IPF). The main questions it aims to answer are: (1). if there are correlations between pulmonary function test and HRV and overnight SpO2; (2). if HRV and SpO2 can predict the occurrence of acute exacerbation in patients with IPF. Participants will be asked to examine pulmonary function test (including lung volumes and six-minute walk test) and wear pulse oxygenation recorder and LARGAN ECG Holter (LARGAN HEALTH TECHNOLOGY Sleep Apnea And Sleep Quality Examination System) during sleep.

Interventions

DEVICELARGAN ECG Holter

wear LARGAN ECG Holter during sleep once after completion of pulmonary function test

Sponsors

Taipei Veterans General Hospital, Taiwan
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* individuals meet the diagnosis of idiopathic pulmonary fibrosis * individuals agree to participate this study and sign the informed consent * individuals have cognitive and behavioral abilities

Exclusion criteria

* age less than 50 years old * individuals refuse to participate this study and sign the informed consent * individuals of unclear consciousness

Design outcomes

Primary

MeasureTime frame
The correlations between measures of pulmonary function test and heart rate variability1 day test duration

Countries

Taiwan

Contacts

Primary ContactFang-Chi Lin, PhD
fclin3@vghtpe.gov.tw+886-937-021-807

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026