RECRUITING

AeviceMD for Detection of Wheeze in Pediatric and Adult Populations

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Respiratory signs and symptoms consisting of wheeze, cough, and breathlessness are obtained in a manual fashion through history taking and physical examination by the healthcare professional. Auscultation of the lung assesses airflow through the trachea-bronchial tree and is helpful in diagnosing various respiratory disorders. AeviceMD is a wearable device that can acquire and process lung sounds, thus assisting in the detection of abnormal lung sounds. The primary objective of this study is to determine if AeviceMD can detect wheeze of pediatrics and adults as accurately as a physician through auscultation. The secondary objective is to investigate if AeviceMD can be used for remote auscultation of breath sounds.

Official Title

A Pilot Study to Assess Aevice Medical Device for Detection of Wheeze in Pediatric and Adult Populations

Quick Facts

Study Start:2023-06-29
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06691971

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:3 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * The subject is willing and/or parents/guardians are able to give informed consent for participation in the study.
  2. * Male or Female, aged ≥ 3 years.
  3. * Diagnosed with acute asthma exacerbation by an ED provider.
  1. * 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.

Contacts and Locations

Study Contact

Sunit P. Jariwala, Professor, M.D.
CONTACT
718-920-6089
sjariwal@montefiore.org
Carlos L. Lutz, Assistant Professor, M.D.
CONTACT
718-920-6626
clutz@montefiore.org

Study Locations (Sites)

Montefiore Medical Center
Bronx, New York, 10467
United States

Collaborators and Investigators

Sponsor: Aevice Health Pte. Ltd.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-29
Study Completion Date2025-06

Study Record Updates

Study Start Date2023-06-29
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • Wheeze
  • Auscultation
  • Wearable Medical Device

Additional Relevant MeSH Terms

  • Subject Presenting Wheeze
  • Asthma
  • Bronchial Disease
  • Respiratory Tract Diseases
  • Pediatric Asthma
  • Chronic Respiratory Disease