Micromanaging Human Sleep Physiology to Treat Sleep Apnea and Other Disorders

Description

This study will examine whether a combination of breathing training during wake and targeted reactivation of the training during sleep can induce breathing changes during sleep and subsequent cognitive benefits during wake. Participants with obstructive sleep apnea (who have not yet been treated for sleep apnea) will be recruited. Participants will engage in breath training for one week in their own homes and to record their sleep at home using commercially available mobile devices and subsequently have their sleep monitored for one night of polysomnography recordings plus targeted reactivation in a laboratory setting.

Conditions

Sleep Apnea Obstructive (OSA)

Study Overview

Study Details

Study overview

This study will examine whether a combination of breathing training during wake and targeted reactivation of the training during sleep can induce breathing changes during sleep and subsequent cognitive benefits during wake. Participants with obstructive sleep apnea (who have not yet been treated for sleep apnea) will be recruited. Participants will engage in breath training for one week in their own homes and to record their sleep at home using commercially available mobile devices and subsequently have their sleep monitored for one night of polysomnography recordings plus targeted reactivation in a laboratory setting.

Micromanaging Human Sleep Physiology to Treat Sleep Apnea and Other Disorders

Micromanaging Human Sleep Physiology to Treat Sleep Apnea and Other Disorders

Condition
Sleep Apnea Obstructive (OSA)
Intervention / Treatment

-

Contacts and Locations

Chicago

Northwestern University, Chicago, Illinois, United States, 60611

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Right-handed, English-speaking adults, 18-60 years old who report normal hearing during sleep
  • 2. Participants with suspected obstructive sleep apnea (OSA) (including those who have been diagnosed by a physician and those whose self-reported symptoms of OSA on the STOP-BANG questionnaire classify them as being "individuals with intermediate to high risk".
  • 3. No report of any other sleep disorder besides OSA.
  • 4. No report of any neurological or cardiometabolic diseases or disorders.
  • 5. Not currently under active treatment for sleep apnea.
  • 6. BMI ≤ 40.

Ages Eligible for Study

18 Years to 60 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Northwestern University,

Ken A Paller, PhD, PRINCIPAL_INVESTIGATOR, Northwestern University

Study Record Dates

2027-04