Effects of Different Colors of Light on Human Physiology

August 8, 2014 updated by: Steven W. Lockley, Brigham and Women's Hospital

Mechanism Underlying the Effects of Blue Light in Humans

This study will determine which color of light is most effective in stimulating a range of biological functions in humans including activation of sleep-wake regulatory system (alertness, performance, microsleeps, brain activity), activation of the nervous system (heart rate, temperature, blood pressure, breathing rate), and shifting the timing of the internal 24-hour (circadian) pacemaker.

Study Overview

Status

Completed

Detailed Description

Light has long been proposed to have a stimulatory effect on a range of biological functions in humans including increased feelings of activation, such as improved alertness or ability to perform. The mechanisms underlying how light stimulates these neurobiological systems remain to be elucidated. We propose to investigate the effects of different colors of light on human physiology, and in particular, test the claims that specific colors of light preferentially stimulate neurobiological, physiological and hormonal systems. Using classical photobiological techniques, we will construct action spectra for the effects of different colors of light on a range of non-image forming responses in humans.

We will test the hypotheses that: 1) light-induced activation of the neurobiological sleep-wake regulatory system, as indicated by increased alertness, faster reaction time, suppression of EEG alpha activity, microsleeps and slow rolling eye movements, and suppression of pineal melatonin, is most sensitive to retinal exposure to short wavelength blue light (460 nm) compared to equal photons of other colors of visible light; 2) light-induced activation of autonomic and hypothalamic-pituitary-adrenal axis measures of arousal, as indicated by increased heart rate variability, core body temperature, blood pressure, respiration rate, plasma cortisol levels and urinary catecholamines, is most sensitive to exposure to short wavelength blue light (460 nm) compared to equal photons of other colors; 3) phase shifts of the human circadian pacemaker, as assessed by changes in temperature, melatonin and cortisol rhythms, are most sensitive to exposure to short wavelength blue light (460 nm) compared to equal photons of other colors. The resultant action spectra will help to identify the photoreceptor mechanism(s) by which light activates arousal and circadian resetting, these non-image-forming physiological responses and enable us to distinguish between major candidate photoreceptive mechanisms, including potential novel photoreceptor systems, that might mediate such responses.

Study Type

Interventional

Enrollment (Actual)

47

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Boston, Massachusetts, United States, 02115
        • Division of Sleep Medicine, Brigham and Women's Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Free from any acute, chronic or debilitating medical, psychological, or ophthalmological conditions
  • Drug-free (including caffeine, nicotine, and alcohol) for entire study duration

Exclusion Criteria:

  • History of drug or alcohol dependency
  • History of psychiatric illnesses or evidence of psychopathology according to standardized questionnaires, or in a structured clinical interview
  • Night shift work during the past 3 years
  • Transmeridian travel in the last 3 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 1
420 nm light
Monochromatic light in the visible range from 420-620 nm up to 60uW/cm2 for 6.5 hours
Experimental: 2
480 nm
Monochromatic light in the visible range from 420-620 nm up to 60uW/cm2 for 6.5 hours
Experimental: 3
507 nm
Monochromatic light in the visible range from 420-620 nm up to 60uW/cm2 for 6.5 hours
Experimental: 4
555 nm
Monochromatic light in the visible range from 420-620 nm up to 60uW/cm2 for 6.5 hours
Experimental: 5
620 nm
Monochromatic light in the visible range from 420-620 nm up to 60uW/cm2 for 6.5 hours
Experimental: 6
460 nm
Monochromatic light in the visible range from 420-620 nm up to 60uW/cm2 for 6.5 hours

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Subjective alertness prior to, during and after light exposure
Time Frame: 9.5 hours
9.5 hours
Auditory psychomotor performance prior to, during and after light exposure
Time Frame: 9.5 hours
9.5 hours
EEG power frequency prior to, during and after light exposure
Time Frame: 9.5 hours
9.5 hours
Plasma melatonin and cortisol prior to, during and after light exposure
Time Frame: 60 hours
60 hours
Heart rate, blood pressure, respiration rate and temperature prior to, during and after light exposure
Time Frame: 9.5 hours
9.5 hours
Urinary catecholamines prior to, during and after light exposure
Time Frame: 32 hours
32 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Steven W Lockley, Ph.D., Brigham and Women's Hospital, Harvard Medical School

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2005

Primary Completion (Actual)

February 1, 2007

Study Completion (Actual)

February 1, 2007

Study Registration Dates

First Submitted

September 12, 2005

First Submitted That Met QC Criteria

September 13, 2005

First Posted (Estimate)

September 20, 2005

Study Record Updates

Last Update Posted (Estimate)

August 12, 2014

Last Update Submitted That Met QC Criteria

August 8, 2014

Last Verified

August 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • R01AT002129-01 (U.S. NIH Grant/Contract)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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