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Usefulness of Monitoring Using Breath Sound Analysis and Visualization System in Bronchial Asthma Patients

Usefulness of Monitoring Using Breath Sound Analysis and Visualization System in Bronchial Asthma Patients - Usefulness of Monitoring Using Breath Sound Analysis and Visualization System in Bronchial Asthma Patients (Utility of Remote Auscultatory Monitoring in Asthma)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs032230488
Enrollment
30
Registered
2023-12-04
Start date
2024-11-07
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Asthma or suspected asthma Respiratory sounds, wheezes, peak flow value, asthma control test

Interventions

(1) Prescribe asthma medications (controller and reliever) on day 0 and instruct patients to use them as prescribed. (2) On day 0, instruct patients on the auscultation procedure as follows. a. Measur
Breath sound analysis and visualization system, electronic stethoscope, breath sounds, peak flow values, asthma control test

Sponsors

Soejima Kenzo
Lead Sponsor
Soejima Kenzo
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria will be included in this study (1) Patients who have given written consent to participate in this study (2) Patients who are at least 18 years of age at the time consent is obtained (3) Patients diagnosed with bronchial asthma (BA) or clinically suspected BA with wheezing or rhonchi on auscultation (4) Have no acute illness other than asthma attack within 2 weeks prior to the date of consent (5) Who understand and can actually use the Respiratory Sound Analysis and Visualization System's electronic stethoscope and respiratory sound analysis and recording application.

Exclusion criteria

Exclusion criteria: Patients who meet any of the following criteria will not be included in the study. (1) Those who are unable to cooperate during the 15-day study period (i. Suffering from an active fatal acute disease requiring immediate therapeutic intervention such as myocardial infarction, cerebral infarction, or pulmonary embolus, ii. Has a pre-planned and difficult-to-modify examination or treatment such as surgery or chemotherapy; iii. Other unchangeable plans such as travel, weddings, funerals, etc.) (2) Pregnant or lactating, or possibly pregnant (3) Any other person whom the principal investigator (or subinvestigator) judges to be inappropriate.

Design outcomes

Primary

MeasureTime frame
Coefficient of determination for single regression of peak flow value to percentage of own best value by quantitative value of breath sound analysis and visualization system on day0, day3, and day14

Secondary

MeasureTime frame
(1)Correlation between quantitative value in breath sound analysis and visualization systems and ACT score on day0 and day14 (2)Correlation between quantitative value in breath sound analysis and visualization systems and exhaled NO on day0 and day14 (3)Correlation between quantitative value in breath sound analysis and visualization systems and FEV1 on day0 and day14 (4)Correlation between quantitative value in breath sound analysis and visualization systems and transcutaneous arterial blood oxygen saturation on day0 and day14

Contacts

Public ContactYoshinori Uchida

University of Yamanashi Hospital

youchida@yamanashi.ac.jp+81-55-273-9591

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026