Status:
COMPLETED
Enhancing Sleep Slow Waves Using External Stimuli
Lead Sponsor:
University of Wisconsin, Madison
Collaborating Sponsors:
Philips Healthcare
Conditions:
Sleep, Slow-wave Sleep, Sleep Enhancement, Sleep Optimization
Eligibility:
All Genders
18-75 years
Brief Summary
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
Detailed Description
This is a single-site,unblinded study at the University of Wisconsin to determine the effectiveness of various stimulation modalities and parameters to maximize effectiveness for increasing slow waves...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
August 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 13 2019
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT03323814
Start Date
August 1 2009
End Date
June 13 2019
Last Update
October 14 2020
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