Automated Identification and Quantification of Sleep Disordered Breathing Using Non-Invasive Cardiopulmonary Signals
This study aims to develop a method for automatically identifying and quantifying sleep disordered breathing using non-invasive cardiopulmonary signals, potentially improving the diagnosis of sleep disorders.
Non-invasive technique to diagnose and quantitate sleep-disordered breathing
Apnea+5
+ Nervous System Diseases
+ Respiration Disorders
Diagnostic Study
Summary
Sleep disordered breathing, including sleep apnea, is a common condition with significant impacts on quality of life and societal costs. The NYU Sleep Research Laboratory is focusing on improving the diagnosis of mild sleep disordered breathing, also known as upper airway resistance syndrome. They've developed a non-invasive method to detect increased airway resistance from the airflow signal, which shows a characteristic change in the inspiratory flow contour, indicating flow limitation. This research aims to enhance the diagnosis and treatment of this condition, potentially improving care and addressing current challenges. Currently, all respiratory events are manually identified and counted, which is time-consuming and prone to variability. This project aims to improve this process by creating an artificially intelligent system to identify and quantify sleep disordered breathing using non-invasive cardiopulmonary signals collected during a routine sleep study. The system will also evaluate the usefulness of other reported indices of sleep disordered breathing. The successful development of this automated system could simplify, standardize, and improve the diagnosis of sleep disordered breathing, while also aiding research and clinical work in this area.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Diagnostic Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location