Morning Bright Light Therapy and Daytime Functioning in University Students
BLIGHT
Effects of Morning Bright Light Therapy on Sleep, Alertness, Mood, and Cognition in Healthy University Students: A Randomized Crossover Trial
2 other identifiers
interventional
153
1 country
1
Brief Summary
This study tests whether a week of morning bright light therapy changes how well healthy young adults sleep and how alert, positive, and mentally sharp they feel during the day. Morning light is the body's main signal for keeping its internal clock and sleep-wake timing on track. Many university students keep irregular hours and spend most of the day indoors, where light is far dimmer than daylight. This study asks whether adding a short, bright morning light session can help. Each participant takes part for two weeks. For one week they use a bright light box for 30 minutes each morning, shortly after waking; for the other week they keep their usual lighting. The order of the two weeks is decided at random, and each person serves as their own comparison. Throughout both weeks, sleep is tracked with a wrist-worn Fitbit and a short daily diary. Participants also rate their sleepiness and mood, complete brief computer-based attention and memory tasks, and take part in a short interview at the end about their experience. The study compares the bright-light week with the usual-light week to see whether morning bright light improves sleep regularity and efficiency, reduces daytime sleepiness, lifts mood, or affects thinking performance. The trial is being conducted in waves; a first wave has completed and a second wave is planned, pending additional funding.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2024
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2024
CompletedFirst Submitted
Initial submission to the registry
June 29, 2026
CompletedFirst Posted
Study publicly available on registry
July 6, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2028
July 6, 2026
June 1, 2026
4.2 years
June 29, 2026
June 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Sleep regularity
Regularity of sleep timing derived from wrist-worn Fitbit actigraphy and a daily sleep diary (e.g., day-to-day variability in sleep onset and offset). Condition-week values are compared between the bright-light week and the usual-light week.
Recorded continuously across each 1-week condition (bright-light week and usual-light week).
Daytime sleepiness (Karolinska Sleepiness Scale)
Subjective daytime sleepiness rated on the 9-point Karolinska Sleepiness Scale (KSS) at fixed times of day. Condition-week values are compared between the bright-light week and the usual-light week.
Assessed daily at fixed times across each 1-week condition (bright-light week and usual-light week).
Positive affect (PANAS Positive Affect subscale)
Positive affect measured with the Positive and Negative Affect Schedule (PANAS) positive-affect subscale. Condition-week scores are compared between the bright-light week and the usual-light week.
End of each 1-week condition (bright-light week and usual-light week).
Cognitive performance (computer-based battery)
Objective cognitive performance on a computer-based battery (Stroop, Flanker, Corsi block-tapping, and verbal span tasks). Condition-week performance is compared between the bright-light week and the usual-light week.
End of each 1-week condition (bright-light week and usual-light week).
Study Arms (2)
Morning Bright Light Therapy
EXPERIMENTALDuring this one-week condition, participants self-administer a 30-minute session of 10,000 lux bright light (melanopic equivalent daylight illuminance ≈ 8,989 lux) each morning, approximately 30 minutes after waking, using a standard light therapy lamp positioned per manufacturer guidance.
Usual Light (Control)
NO INTERVENTIONDuring this one-week condition, participants maintain their usual indoor lighting and morning routine without the light therapy lamp.
Interventions
Self-administered 30-minute session of 10,000 lux (photopic) bright light each morning, approximately 30 minutes after waking, for one week, using a standard 10,000-lux light therapy lamp positioned per manufacturer guidance. Stimulus characterized in melanopic units (melanopic equivalent daylight illuminance ≈ 8,989 lux).
Eligibility Criteria
You may qualify if:
- Enrolled university student
- Aged 18 years or older
- Generally healthy, with no diagnosed sleep disorder (sleep quality screened using the Pittsburgh Sleep Quality Index)
- Residing in shared student housing
You may not qualify if:
- Diagnosed insomnia or other diagnosed sleep disorder
- Other medical, psychiatric, or neurological condition that could affect sleep, mood, or cognition
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The Hong Kong Polytechnic Universitylead
- Northumbria Universitycollaborator
Study Sites (1)
The Hong Kong Polytechnic University
Hung Hom, Hong Kong
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research assistant professor
Study Record Dates
First Submitted
June 29, 2026
First Posted
July 6, 2026
Study Start
May 1, 2024
Primary Completion (Estimated)
June 30, 2028
Study Completion (Estimated)
June 30, 2028
Last Updated
July 6, 2026
Record last verified: 2026-06