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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04882280
Other study ID # Reverse DRC
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 2022
Est. completion date July 2024

Study information

Verified date March 2022
Source VA Palo Alto Health Care System
Contact Jamie Zeitzer, PhD
Phone 6504935000
Email jzeitzer@stanford.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to systematically examine the impact of different intensities of daytime light and the subsequent impact that such exposure has on non-image forming responses to light in the evening.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 48
Est. completion date July 2024
Est. primary completion date June 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. Aged 18-65 2. Good health 3. Male or female 4. Normal color vision Exclusion Criteria: 1. Sleep disorders 2. Extreme chronotypes 3. Routine smoker 4. Significant hearing loss 5. Depressed 6. Alcohol use disorder 7. Use of illegal drugs

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Light
10 hours of light exposure during the daytime, starting 2 hours after habitual wake time

Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Palo Alto Veterans Institute for Research

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Suppression of melatonin production Difference in salivary melatonin concentrations between active arm and 3 lux control condition 4 hours
Primary Phase shift in the timing of melatonin onset Change in the onset of melatonin secretion after experimental stimulus 2 days
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