Morning Light Exposure for Mood Improvement
(BLM Trial)
Trial Summary
What is the purpose of this trial?
Mood dysregulation and suicidal ideation are closely associated with disruption of sleep and circadian rhythms. Moreover, sleep problems and circadian disruption are commonplace features of military life. Critically, specifically timed light exposure plays a powerful role in regulating mood, circadian rhythms, and sleep-wake patterns. Therefore, we propose to conduct a large-scale clinical trial on the effectiveness of morning light exposure treatment for improving sleep-wake patterns, emotional and mental health, and suicidal thoughts in military personnel.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What data supports the effectiveness of the treatment for mood improvement?
Is morning light exposure generally safe for humans?
Morning light exposure, often used in light therapy, is generally considered safe for humans. Some studies report minor side effects like blurring, but serious issues are rare. Safety measures, such as using lamps without harmful emissions and monitoring eye health, are recommended to minimize risks.12678
How does morning light exposure treatment differ from other treatments for mood improvement?
Morning light exposure is unique because it uses bright light to influence mood by stabilizing circadian rhythms (the body's internal clock), which can improve sleep and mood. Unlike medications, it involves sitting near a light box for a set time each morning, making it a non-invasive option without the side effects associated with drugs.145910
Eligibility Criteria
This trial is for English-speaking military personnel aged 18-60 with at least an 8th grade reading level and mild depression or greater, as indicated by a score of β₯5 on the PHQ-9. It aims to help those struggling with mood regulation and suicidal thoughts.Inclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo a double-blind, placebo-controlled, counterbalanced, crossover design study with 2 weeks of active light therapy and 2 weeks of placebo light therapy, separated by a 2-week washout period.
Follow-up
Participants are monitored for safety and effectiveness after treatment, including assessments of sleep and mental health outcomes.
Treatment Details
Interventions
- Amber light exposure
- Blue light exposure
Blue light exposure is already approved in United States, European Union, Canada for the following indications:
- Seasonal Affective Disorder (SAD)
- Circadian Rhythm Disorders
- Mood Dysregulation
- Seasonal Affective Disorder (SAD)
- Non-seasonal Depressive Episodes
- Circadian Rhythm Disorders
- Seasonal Affective Disorder (SAD)
- Circadian Rhythm Disorders
- Sleep Disorders
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Arizona
Lead Sponsor
U.S. Army Medical Research Acquisition Activity
Collaborator