NCT07685262

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
153

participants targeted

Target at P75+ for not_applicable

Timeline
24mo left

Started May 2024

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress54%
May 2024Jun 2028

Study Start

First participant enrolled

May 1, 2024

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

June 29, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 6, 2026

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2028

Last Updated

July 6, 2026

Status Verified

June 1, 2026

Enrollment Period

4.2 years

First QC Date

June 29, 2026

Last Update Submit

June 29, 2026

Conditions

Keywords

Bright light therapyMelanopic illuminanceMorning light exposureSleep regularitySleep efficiencyDaytime alertnessCrossover trialUniversity studentsWearable sleep trackingKarolinska Sleepiness Scale

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

EXPERIMENTAL

During 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.

Device: Bright light therapy (10,000 lux light box)

Usual Light (Control)

NO INTERVENTION

During 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).

Morning Bright Light Therapy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

The Hong Kong Polytechnic University

Hung Hom, Hong Kong

RECRUITING

MeSH Terms

Conditions

Disorders of Excessive Somnolence

Interventions

Ultraviolet Therapy

Condition Hierarchy (Ancestors)

Sleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesMental Disorders

Intervention Hierarchy (Ancestors)

PhototherapyTherapeutics

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Model Details: Randomized within-subject crossover trial. Each participant completes two consecutive 1-week conditions - morning bright light therapy and usual-light control - in counterbalanced (randomized) order with no washout period. Each participant serves as their own control; mixed-effects analyses include condition, period, and sequence terms.
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

Locations