RECRUITING

Wearable Electronic Breath Sound Sensing Device

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

This study will assess the ability of a wearable stethoscope to monitor wheezing in high-risk asthma patients admitted at Children's Healthcare of Atlanta. This study is important to assist in the health management of patients with chronic lung diseases that can experience exacerbations leading to their health worsening and requiring hospitalization. The population that will be approached for this study will include 10 pediatric subjects hospitalized at Children's Healthcare of Atlanta for an asthma-related exacerbation. Participants will wear the patches for up to 8 hours on their chest and back wall from their date of consent until their hospital discharge. This may range from the participant taking part in 1 to 14 visits that could last up to 8 hours.

Official Title

Pilot Study of Wearable Electronic Breath Sound Sensing Device for Monitoring of Breath Sounds in Pediatric Patients with Asthma

Quick Facts

Study Start:2025-01
Study Completion:2026-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06734793

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:6 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Age 6-17 years
  2. * Diagnosis of persistent asthma
  3. * Being treated for an acute asthma exacerbation
  4. * Parent can speak and understand English
  1. * Unable to provide consent for the study
  2. * History of prematurity
  3. * History of other chronic lung conditions - cystic fibrosis, bronchiectasis, or primary ciliary dyskinesia
  4. * History of latex allergy or allergy to medical tape adhesive
  5. * Patients currently using another medical device - implanted pacemaker or vagal nerve stimulator or diaphragm pacing device

Contacts and Locations

Study Contact

Lokesh Guglani, MD
CONTACT
404-712-2324
lokesh.guglani@emory.edu

Principal Investigator

Lokesh Guglani, MD
PRINCIPAL_INVESTIGATOR
Emory University

Study Locations (Sites)

Arthur M. Blank Hospital | Children's Healthcare of Atlanta
Atlanta, Georgia, 30329
United States

Collaborators and Investigators

Sponsor: Emory University

  • Lokesh Guglani, MD, PRINCIPAL_INVESTIGATOR, Emory University

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 Date2025-01
Study Completion Date2026-03-01

Study Record Updates

Study Start Date2025-01
Study Completion Date2026-03-01

Terms related to this study

Keywords Provided by Researchers

  • Hospital admission
  • Wearable stethoscope
  • Asthma Exacerbations

Additional Relevant MeSH Terms

  • Asthma in Children
  • Asthma Attack