Depression, Bipolar Clinical Trial
— BPII-DEP-LTOfficial title:
Light-Therapy in the Treatment of the Acute Phase of the Bipolar Type II Depression: Double-Blind, Placebo-Controlled Study to Establish Efficacy and Safety
Verified date | February 2023 |
Source | Douglas Mental Health University Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to evaluate the efficacy and safety of light therapy for the treatment of bipolar type II patients relapsing into a depressive phase during autumn or winter.
Status | Active, not recruiting |
Enrollment | 50 |
Est. completion date | June 2025 |
Est. primary completion date | June 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Bipolar type II disorder, depressive phase meeting DSM-IV criteria as per the SCID interview - Hamilton Depression Rating Scale 21 items (HAMD-21) = 17 and a Montgomery Asberg rating Scale (MADRS) = 15 for at least 2 weeks and the episode has begun during the month of september or a later month - Able to give their consent and willingness to participate to the study Exclusion Criteria: - Other psychiatric condition, organic brain disorder, unstable and/or untreated medical condition such as hypothyroidism, diabetes, cardiac condition, hypertension - Deficit in vitamin B12 or folate - Sub-syndromic hypomania symptoms as per a Young Mania Rating Scale (YMRS) score = 4 - History of manic or hypomanic switch when exposed to bright light or during prolonged exposure to the sun during previous depressive phases - Pregnancy or absence of a contraceptive treatment - History of light-induced migraine or epilepsy - Marked suicidal ideation - Retinal blindness or severe cataract - Glaucoma, retinal diseases of the eye - Alcohol or drug abuse - Known skin sensitivity to sunlight, especially in patients receiving photosensitizing drugs such as lithium or phenothiazines - Past history of light therapy |
Country | Name | City | State |
---|---|---|---|
Canada | Douglas Mental Health University Institute | Montreal | Quebec |
Lead Sponsor | Collaborator |
---|---|
Douglas Mental Health University Institute | National Alliance for Research on Schizophrenia and Depression |
Canada,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | the response rate as defined by a 50% improvement of the depressive symptoms score on the MADRS scale | 5 and 45 weeks | ||
Secondary | the remission rate (MADRS scale = 8 ) | 5 and 45 weeks | ||
Secondary | the relapse rate into depression or hypomania | 5 and 45 weeks | ||
Secondary | the sleep quality as per PSQI scale | 5 and 45 weeks | ||
Secondary | the quality of life as per SF-36 and Q-LES-Q SF scales | 5 and 45 weeks | ||
Secondary | the incidence of side-effects as per the UKU scale | 5 and 45 weeks |
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