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Search / Trial NCT04225507

Technology-Supported Treatment of Sleep Apnea in Prediabetes

Launched by UNIVERSITY OF CHICAGO · Jan 8, 2020

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying the impact of a treatment called CPAP (continuous positive air pressure) on people who have sleep apnea and are at risk for diabetes due to prediabetes and being overweight or obese. The goal is to see if using CPAP, in addition to making lifestyle changes like eating healthier and exercising, can help improve heart health and reduce the risk of diabetes more effectively than lifestyle changes alone.

To be eligible for this study, participants need to be overweight or obese, have prediabetes, and also have sleep apnea. Unfortunately, those who already have diabetes, are in a formal weight loss program, or have other serious health conditions may not qualify. If you decide to participate, you can expect to receive support for both the lifestyle changes and the CPAP treatment, helping to improve your overall health. This trial is currently recruiting participants of all genders aged 18 and older, so it’s a great opportunity for individuals looking to manage their health proactively.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Overweight or obese
  • Prediabetes
  • Sleep apnea
  • Exclusion Criteria:
  • Diabetic
  • enrolled in a formal weight loss program
  • Any underlying disease likely to limit life span and/or increase risk of interventions

About University Of Chicago

The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

Esra Tasali, MD

Principal Investigator

University of Chicago

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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