Sleep Apnea Obstructive (OSA)
Conditions
Keywords
sleep, sleep apnea obstructive (OSA)
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.
Interventions
BEHAVIORALWake training + TMR
In this within-participant design, all participants will undergo the same intervention of waking training and TMR. Waking training - waking training will associate an auditory cue with a specific learned behavioral response (a tongue protrusion and inhalation) during daily sessions for approximately one week, with home sleep monitoring. TMR - Targeted memory reactivation (TMR) refers to the process of playing learning-associated audio cues quietly during sleep in order to reactivate memories associated with the cue. After completion of waking training, TMR occurs in a laboratory setting, with PSG recording, during a single night.
Sponsors
Northwestern University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No
Inclusion 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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Apnea-Hypopnea Index (AHI) | Day 1 | AHI indexes the severity of OSA on the night of the study. |
| Respiratory event duration | Day 1 | The duration of a hypopnea or apnea on the night of the study. |
Countries
United States
Contacts
CONTACTKen A Paller, PhD
PRINCIPAL_INVESTIGATORKen A Paller, PhD
Northwestern University
Outcome results
None listed