Using a wearable device to detect wheeze in children and adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study evaluates the effectiveness of the AeviceMD wearable device in detecting wheeze in pediatric and adult populations. The device captures and processes lung sounds to assist healthcare professionals in diagnosing respiratory conditions. The primary goal is to compare the accuracy of AeviceMD in detecting wheeze against traditional physician auscultation methods. Additionally, the study aims to explore the feasibility of remote auscultation using the device.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* The subject is willing and/or parents/guardians are able to give informed consent for participation in the study.
* Male or Female, aged ≥ 3 years.
* Diagnosed with acute asthma exacerbation by an ED provider.

Exclusion Criteria:

* Any other significant disease or disorder which, in the opinion of the Investigator, may either put the subjects at risk because of participation in the study, or may influence the result of the study, or the subject's ability to participate in the study.

Where it's running

• Montefiore Medical Center
  The Bronx, New York, United States Recruiting

Study contacts

• Study coordinator: Sunit P. Jariwala, Professor, M.D.
• Email: sjariwal@montefiore.org
• Phone: 718-920-6089

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.