RECRUITING

AeviceMD for Pediatric Asthma Management

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

A wearable remote patient monitor (AeviceMD) is to be used to monitor the respiratory health of pediatric asthma patients in this pilot study. Patients prescribed with AeviceMD should be able to gain better control over their disease during home management. Physicians should be able to optimize treatment for these patients using objective data collected from and of these patients outside of the clinic. The AeviceMD should also be used as a remote auscultation device for teleconsultations.

Official Title

AeviceMD for Pediatric Asthma Management

Quick Facts

Study Start:2024-11-05
Study Completion:2026-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06321471

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 to 18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Provision of signed and dated informed consent form
  2. * Stated willingness to comply with all study procedures and availability for the duration of the study
  3. * Aged 3 to 18 as of first recruitment
  4. * Diagnosed with poorly controlled asthma
  5. * Asthma control test score below
  6. * Caregiver able operate a mobile application
  7. * Has access high-speed wireless internet (WiFi) at home
  8. * Able to read English
  9. * Agreement to adhere to medical device use regimen throughout the study duration
  1. * Known allergy to silicone, gold, or zinc
  2. * Abnormal skin conditions on chest
  3. * Sleep apnea diagnosis

Contacts and Locations

Study Contact

Irina Dralyuk, MD
CONTACT
310-423-4433
Irina.Dralyuk@cshs.org
Bobby Marker
CONTACT
310-423-0901
Robert.Marker@cshs.org

Principal Investigator

Irina Dralyuk, MD
PRINCIPAL_INVESTIGATOR
Cedars-Sinai Medical Center

Study Locations (Sites)

Cedars-Sinai Medical Center
Los Angeles, California, 90048
United States

Collaborators and Investigators

Sponsor: Irina Dralyuk

  • Irina Dralyuk, MD, PRINCIPAL_INVESTIGATOR, Cedars-Sinai Medical Center

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 Date2024-11-05
Study Completion Date2026-02

Study Record Updates

Study Start Date2024-11-05
Study Completion Date2026-02

Terms related to this study

Keywords Provided by Researchers

  • Wearable Medical Device

Additional Relevant MeSH Terms

  • Asthma
  • Asthma in Children
  • Pediatric Asthma
  • Chronic Respiratory Disease