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Clinical Trials/NCT06926036
NCT06926036RecruitingNot Applicable

Micromanaging Human Sleep Physiology to Treat Sleep Apnea and Other Disorders

Northwestern University1 site in 1 country18 target enrollmentStarted: April 3, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
18
Locations
1
Primary Endpoint
Apnea-Hypopnea Index (AHI)

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Right-handed, English-speaking adults, 18-60 years old who report normal hearing during sleep
  • •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".
  • •No report of any other sleep disorder besides OSA.
  • •No report of any neurological or cardiometabolic diseases or disorders.
  • •Not currently under active treatment for sleep apnea.

Exclusion Criteria

  • Not provided

Arms & Interventions

All participants

Experimental

Intervention: Wake training + TMR (Behavioral)

Outcomes

Primary Outcomes

Apnea-Hypopnea Index (AHI)

Time Frame: Day 1

AHI indexes the severity of OSA on the night of the study.

Respiratory event duration

Time Frame: Day 1

The duration of a hypopnea or apnea on the night of the study.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ken Paller

Professor

Northwestern University

Study Sites (1)

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