The purpose of this study is to test the ability of a brainwave measurement device (SLEEPSCOPE) in identifying and assisting in the diagnosis of depression. The brainwave data from individuals with untreated depression and healthy participants will be collected and analyzed. The ability to obtain brainwave data from individuals in their homes while they're sleeping would represent a significant advance in depression research.
The purpose of study is to collect and analyze human sleeping brainwave data, to better understand depression in humans. First visit: * Informed consent procedures, including explanation of research background, purpose, details of implementation, and study benefits and risks * Interview with questionnaires (MINI International Psychiatric Interview, Hamilton Rating Scale for Depression, Beck Depression Inventory, Patient Health Questionnaire for Depression \[PHQ-9\]), physical examination. * Urine drug sample for screening of controlled substances. * Inform participants that those qualifying will be informed whether or not to proceed with second visit Second visit: * Explanation of EEG measurement (placement of two electrodes, one on the forehead and one behind the ear) * Sleep diary provided for participant to complete at home for each night until third visit * Distribution of EEG devices for home use * EEG measurement conducted at participant's residence for three nights of stable sleep-wake cycles Third visit: \- Collect EEG devices and check completeness of downloaded data
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
24
Brainwave measurement device which is connected to the participant by an electrode attached to the forehead and another electrode behind one ear
Stanford Sleep Medicine Center
Redwood City, California, United States
Assist in the diagnosis of depression
The SLEEPSCOPE data will be analyzed to determine if it can help to identify individuals with depression
Time frame: 1 month
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