Objective Evaluation of Depression Using Sleep EEG

Depression Clinical Trial

Official title:

A Study on Realization of Objective Evaluation Method of Depression Using Sleep EEG

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03133013
• Other study ID #: 41103
• Status: Completed
• Phase: N/A
• Start date: May 1, 2017
• Est. completion date: May 31, 2019

Study information

• Verified date: December 2019
• Source: Stanford University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: May 31, 2019
• Est. primary completion date: May 31, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 30 Years to 59 Years

Eligibility

Inclusion Criteria:

Individuals with Untreated Depression:

• 16 men and 16 women aged from 30 to 59 years, with an approximate ethnic balance of 10 Asian, 3 White and 3 other ethnicity for each gender, whom are diagnosed with Major Depressive Disorder by a psychiatric specialist of this research according to MINI screening and DSM-5 criteria, and defined as a score of 15 or higher on the clinician-administered Hamilton Rating Scale for Depression, Beck Depression Inventory, and Patient Health Questionnaire for Depression (PHQ-9).

Healthy Participants:

• 16 men and 16 women age-, ethnic-, and gender-matched healthy participants to the cohort with untreated depression, with absence of mental disorders, including but not limited to depression and sleep disorders, by a psychiatric specialist according to MINI screening and DSM-5 criteria, and negative Hamilton Rating Scale for Depression, Beck Depression Inventory, and Patient Health Questionnaire for Depression (PHQ-9).

Exclusion Criteria:

Participants corresponding to any of the following conditions are considered ineligible for the trial.

• Diagnosed with epilepsy or other organic brain disorder.

• Medical conditions resulting in depressive symptoms such as hypothyroidism, Cushing's disease, systemic lupus erythematosus; neurological conditions resulting in depressive symptoms such as Parkinson's disease, Huntington's disease, multiple sclerosis

• Patients with suspected sleep apnea, based on symptoms and a BMI of 30 or greater

• Prescribed interferon regularly with stimulants, opioid drugs (Ritalin, Opioid, etc.) and steroids

• Repetitive thoughts of death, current thoughts about suicide, suicide attempts, or a suicide plan

• Tested positive to controlled substance use by a urine drug screening before commencement of testing

• Current or past drug or alcohol dependence

• Shift work or rotating work schedule

• Nursing, pregnant or planning to become pregnant

• Participating in other clinical trials

Related Conditions & MeSH terms

• Depression
• Depressive Disorder

Intervention

Device:
• SLEEPSCOPE
Brainwave measurement device which is connected to the participant by an electrode attached to the forehead and another electrode behind one ear

Locations

Country	Name	City	State
United States	Stanford Sleep Medicine Center	Redwood City	California

Sponsors (1)

Lead Sponsor	Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assist in the diagnosis of depression	The SLEEPSCOPE data will be analyzed to determine if it can help to identify individuals with depression	1 month