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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06027944
Other study ID # IRB-71791
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2023
Est. completion date September 30, 2024

Study information

Verified date September 2023
Source VA Palo Alto Health Care System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators are examining whether the content of a visual scene impacts the antidepressant effects of light or if this impact is solely mediated by the intensity of the light.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date September 30, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Aged 18-60 - Mild depressive symptomatology Exclusion Criteria: - No depressive symptomatology - Severe depressive symptomatology - Active or unstable medical condition - Diabetes

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Light exposure
Participants will be exposed to 15 minutes of each arm. They will be exposed twice and a randomized order (1/2/1/2 or 2/1/2/1)

Locations

Country Name City State
United States VA Palo Alto Health Care System Palo Alto California

Sponsors (2)

Lead Sponsor Collaborator
VA Palo Alto Health Care System Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in mood Change in subjective mood as recored by the Positive and Negative Affect Schedule (PANAS). The PANAS ranges 10-50 on a positive mood scale (higher = more positive) and 10-50 on a negative mood scale (higher = more negative) 15 minutes
Secondary Change in fast brain electrical activity Change in the beta power spectrum (12.5-30 Hz) of the electroencephalogram (brain waves, measured in microvolts) 15 minutes
Secondary Change in systolic blood pressure (SBP) Change in SBP (mm Hg) as measured by finger plethysmography 15 minutes
Secondary Change in heart rate variability (HRV) Shift in the ratio of the power of low frequency to high frequency components in heart rate variability 15 minutes
Secondary Change in sympathetic activity Sympathetic activity will be imputed through the galvanic skin response (GSR). Change in skin conductance (the electrical activity on the skin) will be measured in microsiemens 15 minutes
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