Objective: (1) Is an increase in blue light exposure during daytime office hours effective in increasing subjective alertness and performance levels? (2) Is the timing of light exposure important for this effect and is it different for different…
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
daytime functioning and night time sleep
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Subjective sleepiness and mood by rating scales. Rest-activity rhythms by
activity meters and sleep characteristics with ZEO.
Secondary outcome
Evaluation of well being and subjective ratings of performance over two weeks,
Eye strain and headache complaints. 24h- light intensity. Chronotype
measurements with rating scale.
Background summary
Light is not only necessary for vision, but it also has non-image forming
effects on mood, alertness and performance. Most studies tested these effects
during the night or the early-morning/late-evening hours. Recently studies
showed that also daytime light is able to increase alertness and improve
performance. The goal of the current study is to test the importance of timing
of light exposure during office hours, investigate individual variation in
responses, and increase knowledge on the mechanism through which light is
effective in improving daytime performance.
Study objective
Objective: (1) Is an increase in blue light exposure during daytime office
hours effective in increasing subjective alertness and performance levels? (2)
Is the timing of light exposure important for this effect and is it different
for different chronotypes? (3) Is this increase of alertness only an acute
effect during exposure or is there also a long-term effect through a better
quality of sleep.
Study design
In a cross-over design 45 subjects will participate in a control condition and
three experiment light conditions. Each condition will last 2 weeks. In the
three experimental conditions light intensity of, mainly blue, light will be
increased during 3 hours each day, spread over the day, during at least 4
working days per week.
Intervention
Each condition lasts 2 weeks: (1) normal office lighting (full spectrum light
vertical intensity ~ max 200 lux; (2) extra blue light during first 3 hours ..;
(3) extra blue light during middle 3 hours ..; (4) extra blue light during last
3 hours of daytime working period.
Study burden and risks
There are no risks involved when participating in this project. Light intensity
is much lower compared to the regular exposure to natural light or light of
light therapy devices. The light intensity is only increased relative to
regular office lighting. The burden for the subjects is relatively low.
Subjects perform the measurements mainly at home or during office hours. Due to
this, employers have to agree with participations. Wearing an activity meter at
the wrist is not prohibiting normal behaviour, the light meter is worn at a
necklace and does not induce any disturbance either. At night subjects will be
asked to wear an elastic, comfortable band around the head to measure sleep.
Rating scales and tests are distributed over time. Daily burden is low (2 min
raing scales in the morning). Only during one day each week, subjects are asked
to invest more time in rating scales and tests: they will perform the tests at
4 timepoints during the day and each testpoint will last approximately 15 min.
In addition at 4 timepoints one rating of sleepiness is collected. Subject
receive a PDA for this research purpose and this will not restrict them in
performing their normal daily life. Filling in evaluation questionnaires takes
place 4 times and last 5 min each.
Oliemolenstraat 5
Drachten 9203 ZN
NL
Oliemolenstraat 5
Drachten 9203 ZN
NL
Listed location countries
Age
Inclusion criteria
• Healthy men and women, ages between 25 and 45 years
• Indoor office workers with a 4-5 days working week
• Habitual working days of 8-9h with at least 3 hours of computer work
• In general the subjective energy profile over the day shows either a morning, a lunch, or an afternoon dip, characterized by increased sleepiness and lowered performance
Exclusion criteria
• Psychiatric diagnose, e.g. mood disorder
• Sleep disorder (PSQI>10, mild sleep complaints are allowed)
• Alcohol or drug problems
• Depressive mood (BDI-II NL > 8)
• Regular use of photosensitizing medication, sleep medication or stimulant drugs
• Colour blindness or other visual impairment that is not solved with contact lenses or glasses
• On average more than 2 naps a week
• High levels of caffeine intake during a day (> 8 cups)
• Shift work schedule in the 3 months prior to participation
• Travel over 2 or more time zones in 1 month prior to participation
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL42066.042.12 |