This is an observational study to determine if the presentation of sensory stimulation during sleep can increase slow-wave activity during non-rapid eye movement sleep
Who can participate
Age range18 Years – 75 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:Able to provide written informed consent prior to admission.
* Able to understand and speak English;
* Left or right-handed subjects may be included.
* Age of ≥18 years and ≤ 75;
* Able to understand and speak English;
* Left or right-handed subjects may be included.
* Age of ≥18 years and ≤ 75;
Exclusion Criteria:
* Subjects taking medications that could affect sleep patterns (based on self-report and review with a study clinician).
* Subjects who have had travel in the last 2 weeks or who intend to travel during the 4 experimental weeks (for at-home subjects) with time zone shifts \>1h;
* The investigator anticipates that the subject will be unable to comply with the protocol.
* Individuals who self-report a current severe or chronic medical condition or sleep disorder that may affect sleep patterns (based on self-report and review with a study clinician).
* Individuals who self-report a history of recurrent seizures or epilepsy or family history of hereditary epilepsy or have a history of medical conditions that could increase the chance of seizures (e.g. stroke, aneurysm, brain surgery, structural brain lesion).
* Subjects who do report not being consistent in their daily use of alcohol, caffeine, or nicotine.