Actively Recruiting

Phase Not Applicable
Age: 12Years - 19Years
All Genders
ID06973759

Bright Light Therapy for Adolescents With Depression and Eveningness A Randomized, Placebo-Controlled, Assessor-Blinded Study

Led by Chinese University of Hong Kong · Updated on 2026-03-19

90

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effectiveness of bright light therapy as a treatment for adolescents aged 12 to 19 who have unipolar non-seasonal depression and an evening chronotype. This study is a randomized, placebo-controlled, and assessor-blinded trial conducted by the Chinese University of Hong Kong. It aims to compare the effects of bright light therapy against dim red light (placebo) on depression severity, sleep patterns, and circadian rhythms. Participants are randomly assigned to one of two groups: the experimental group receives blue-enriched white light therapy, while the placebo group receives dim red light. Both treatments are administered daily for 15 to 30 minutes over an 8-week period. The study includes several assessment points at baseline, during treatment, after treatment, and at follow-up visits to monitor changes in clinical symptoms and sleep-related measures. During the study, participants will undergo evaluations with depression rating scales, sleep assessments, and measurement of circadian markers. Researchers will track adherence to the light therapy and monitor participants for any changes in depressive symptoms and other clinical signs. The primary outcome is the change in depressive symptoms shortly after the intervention, with additional secondary outcomes assessing other clinical symptom changes. The total study duration includes treatment and follow-up phases extending through the study timeline.

CONDITIONS

Brief Title

Adjunctive Bright Light Therapy in Adolescents With Depression and Eveningness

Who Can Participate

Age: 12Years - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Chinese individuals aged 12 to 19 years old
  • Written informed assent/consent provided by participant and parent/guardian if under 18
  • Diagnosis of unipolar non-seasonal depression confirmed by psychiatric interview
  • Children's Depression Rating Scale score of at least 40
  • Classified as evening chronotype with a score less than 12 on the reduced Horne-Östberg Morning-Eveningness Questionnaire
Not Eligible

You will not qualify if you...

  • Current diagnosis of substance abuse or dependence
  • History or current manic or hypomanic episode, schizophrenia spectrum disorders, organic mental disorders, or intellectual disabilities
  • Clinically significant suicidality with plan or attempt
  • Participation in other clinical trials within one month before study entry
  • Antidepressant medication started or changed within past 4 weeks
  • Receiving any structured psychotherapy currently or previously
  • Hearing or speech deficits
  • Working night shifts
  • Trans-meridian flight across at least two time zones in past 3 months or during the study
  • Presence of eye diseases such as retinal blindness, severe cataract, or glaucoma

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 8 weeks

Participants receive daily bright light therapy or dim red light for 15-30 minutes a day as an intervention for depression and eveningness.

Weekly visits for 8 weeks

Follow-up

Duration - Approximately 1 to 2 weeks after treatment

Participants are assessed after completing the light therapy to evaluate changes in depressive symptoms and other clinical outcomes.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

The Chinese University of Hong Kong

Hong Kong, Hong Kong, Hong Kong, 999077

Actively Recruiting

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Research Team

J

Joey WY Chan

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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