Data Collection For Adventitious Lung Sounds Algorithm Using Eko Digital Devices in a Clinical Setting
1 other identifier
observational
750
1 country
1
Brief Summary
The purpose of this research is to collect patient lung sounds in order to develop an artificial machine learning algorithm that can potentially tell a doctor if a patient is at risk of certain lung conditions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 23, 2024
CompletedFirst Submitted
Initial submission to the registry
February 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 21, 2025
CompletedFirst Posted
Study publicly available on registry
January 22, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 15, 2026
CompletedJanuary 22, 2026
February 1, 2025
11 months
February 24, 2025
January 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Lung Sounds Collected from Number of Patients
The primary objective of this study is to collect normal and abnormal lung sounds of up to 750 patients per study site, by having clinicians use the Eko CORE and/or Eko CORE 500 device(s) in real clinical settings, as part of standard of care clinical practice which will then be used to explore an ML algorithm for classifiers for wheeze, coarse crackle, fine crackle, rhonchus, stridor, rales, and cough, as well as determine any correspondences between the type and/or location of adventitious lung sounds and the type of pulmonary conditions as reported by clinicians.
Through study completion, an average of 8 months
Interventions
Use of the Eko CORE 500 digital stethoscope and 3M Littmann CORE Digital Stethoscope to listen for and record lung sounds.
Eligibility Criteria
Potential research subjects with complaints of shortness of breath or relevant diagnoses like COPD/heart failure/asthma will be screened for eligibility from the upcoming clinic schedule and then recruited during their clinical appointment. Inpatients may also be identified from the EHR and recruited from inpatient units. In order to achieve the harder-to-fill buckets, it may be necessary to directly target existing registries or patient databases, and/or bring patients in for a research-specific visit. Additionally, patients seen in clinic or in hospital with no known respiratory condition will be recruited and evaluated.
You may qualify if:
- Suspected or diagnosed lower respiratory condition OR Presence of wheeze, coarse crackle, fine crackle, rhonchus, stridor, rales, and cough discovered during routine auscultation
- Normal patients with no adventitious lung sounds
- Adults patients (18 years or older)
You may not qualify if:
- Unable to have multiple recordings taken on chest and back (e.g. compromised mobility)
- On mechanical ventilation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Care United Research
Forney, Texas, 75126, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 24, 2025
First Posted
January 22, 2026
Study Start
August 23, 2024
Primary Completion
July 21, 2025
Study Completion
March 15, 2026
Last Updated
January 22, 2026
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will not share