RECRUITING

Validation of Belun Ring Gen3 Deep Learning Algorithms With Subxiphoid Body Sensor

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

Hypothesis: BR's Gen3 DL algorithms, combined with its subxiphoid body sensor, can accurately diagnose OSA, categorize its severity, identify REM OSA and supine OSA, and detect central sleep apnea (CSA). Primary Objective: To rigorously evaluate the overall performance of the BR with Gen3 DL Algorithms and Subxiphoid Body Sensor in assessing SDB in individuals referred to the sleep labs with clinical suspicion of sleep apnea and a STOP-Bang score \> 3, by comparing to the attended in-lab PSG, the gold standard. Secondary Objectives: To determine the accuracy of BR sleep stage parameters using the Gen3 DL algorithms by comparing to the in-lab PSG; To assess the accuracy of the BR arrhythmia detection algorithm; To assess the impact of CPAP on HRV (both time- and frequency-domain), delta HR, hypoxic burden, and PWADI during split night studies; To assess if any of the baseline HRV parameters (both time- and frequency-domain), delta heart rate (referred to as Delta HR), hypoxic burden, and pulse wave amplitude drop index (PWADI) or the change of these parameters may predict CPAP compliance; To evaluate the minimum duration of quality data necessary for BR to achieve OSA diagnosis; To examine the performance of OSA screening tools using OSA predictive AI models formulated by National Taiwan University Hospital (NTUH) and Northeast Ohio Medical University (NEOMED).

Official Title

Belun Ring Gen3 Deep Learning Algorithms With Subxiphoid Body Sensor: Exploring Its Diagnostic Capabilities for Sleep Disordered Breathing With Analysis of Biomarker Dynamics

Quick Facts

Study Start:2024-07-19
Study Completion:2027-09-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06255613

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:18 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Provision of signed informed consent form.
  2. * Clinically assessed and suspicious for OSA with a STOP-Bang score ≥ 3.
  1. * Full night PAP titration study.
  2. * On home O2, noninvasive ventilator, diaphragmatic pacing, or any form of a nerve stimulator.
  3. * Having atrial fibrillation-flutter, pacemaker/defibrillator, left ventricular assist device (LVAD), or status post cardiac transplantation.
  4. * Recent hospitalization or recent surgery in the past 30 days.
  5. * Unstable cardiopulmonary status on the night of the study judged to be unsafe for sleep study by the sleep tech and/or the on-call sleep physician.

Contacts and Locations

Study Contact

Tiffany Tsai
CONTACT
216-844-3201
tiffany.tsai2@va.gov

Principal Investigator

Ambrose A. Chiang, MD
PRINCIPAL_INVESTIGATOR
University Hospitals Cleveland Medical Center
Susheel P. Patil, MD
PRINCIPAL_INVESTIGATOR
University Hospitals Cleveland Medical Center
Kingman P. Strohl, MD
PRINCIPAL_INVESTIGATOR
University Hospitals Cleveland Medical Center

Study Locations (Sites)

UH Geauga Health Center Services
Chardon, Ohio, 44024
United States
University Hospitals Cleveland Medical Center
Cleveland, Ohio, 44106
United States

Collaborators and Investigators

Sponsor: Belun Technology Company Limited

  • Ambrose A. Chiang, MD, PRINCIPAL_INVESTIGATOR, University Hospitals Cleveland Medical Center
  • Susheel P. Patil, MD, PRINCIPAL_INVESTIGATOR, University Hospitals Cleveland Medical Center
  • Kingman P. Strohl, MD, PRINCIPAL_INVESTIGATOR, University Hospitals Cleveland 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 Date2024-07-19
Study Completion Date2027-09-30

Study Record Updates

Study Start Date2024-07-19
Study Completion Date2027-09-30

Terms related to this study

Keywords Provided by Researchers

  • Obstructive Sleep Apnea
  • Wearable
  • Home Sleep Test
  • Photoplethysmography
  • Deep Learning
  • Predictive AI models

Additional Relevant MeSH Terms

  • Sleep-Disordered Breathing
  • Sleep Architecture
  • Arrhythmia