Light at the end of the tunnel? new trial tests bright light for bipolar depression
NCT ID NCT05357313
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether sitting under a bright light for 30 minutes each day for six weeks can improve mood in people with bipolar depression who also tend to be evening types. Seventy adults will be randomly assigned to either the bright light or a placebo device. The goal is to see if this simple, drug-free approach can reduce depressive symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- bright light therapy
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease depression in people with bipolar disorder who tend to be night owls.
- What could go wrong
- This is a small, early-stage trial with only 70 people. The placebo effect is strong in depression studies, and results may not apply to everyone with bipolar disorder.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2022
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Aged 18-65 years. 2. Is capable to give informed consent. 3. Meeting the diagnostic criteria of bipolar depression (including both bipolar I and II disorders) by the Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-V), Disorders (SCID-V). 4. a score 20 or above representing current moderate or severe episode of major depression and a score of at least 1 on items H1 or H2 on the Structured Interview Guide for the Hamilton Depression Rating Scale with Atypical Depression Supplement (SIGH-ADS), corresponding to at least moderate severity. 5. A score of 41 or less by the Morningness-Eveningness Questionnaire which represents eveningness. 6. On a stable dose of antimanic treatment for bipolar disorder for at least four weeks. Exclusion Criteria: 1. Major Depressive Disorder fulfilling the Seasonal Pattern Specifier of the DSM-V (Seasonal Affective Disorder). 2. A past history of rapid-cycling within the past twelve months or a Young Mania Rating Scale more than 12 at screening 3. A current or past history of schizophrenia, mental retardation, organic mental disorder; or current substance use disorder. 4. Presence of psychotic symptoms or substantial suicidal risk as judged by the clinician and/or screening instruments. 5. Presence of contraindications to bright light therapy: for example, history of light induced migraine/ epilepsy; current use of photosensitizing medications such as St. John's wart; presence of eye disease: e.g. retinal blindness, severe cataract, glaucoma, and photosensitive skin condition e.g. systemic lupus erythematosus 6. Significant medical condition/ hearing impairment/ speech deficit leading to incapability of completing clinical interview. 7. Regular shift-workers or trans-meridian flight in the past 3 months or during study 8. Enrolment in another clinical trial of an investigational medicinal product or device. 9. Receiving regular psychotherapy.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The Chinese University of Hong Kong
Hong Kong, Hong Kong
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Other studies related to the condition(s) this trial covers.
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