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Light-Therapy in the Treatment of the Acute Phase of the Bipolar Type II Depression (BPII-DEP-LT)

Primary Purpose

Bipolar Type II Disorder, Depression, Bipolar

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Northern Light Technology (SADelite lamp) bright light-therapy
Northern Light Technology (SADelite lamp) Dim light-therapy
Sponsored by
Douglas Mental Health University Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Type II Disorder focused on measuring bipolar type II disorder, depression, remission, light-therapy, efficacy, safety

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Douglas Mental Health University Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Outcomes

Primary Outcome Measures

the response rate as defined by a 50% improvement of the depressive symptoms score on the MADRS scale

Secondary Outcome Measures

the remission rate (MADRS scale ≤ 8 )
the relapse rate into depression or hypomania
the sleep quality as per PSQI scale
the quality of life as per SF-36 and Q-LES-Q SF scales
the incidence of side-effects as per the UKU scale

Full Information

First Posted
December 26, 2007
Last Updated
February 17, 2023
Sponsor
Douglas Mental Health University Institute
Collaborators
National Alliance for Research on Schizophrenia and Depression
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1. Study Identification

Unique Protocol Identification Number
NCT00590265
Brief Title
Light-Therapy in the Treatment of the Acute Phase of the Bipolar Type II Depression
Acronym
BPII-DEP-LT
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2008 (undefined)
Primary Completion Date
June 2025 (Anticipated)
Study Completion Date
June 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Douglas Mental Health University Institute
Collaborators
National Alliance for Research on Schizophrenia and Depression

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
Bipolar type II depression is a very frequent condition for which we still have a significant lack of acute treatments. There is now consistent evidence that light-therapy treatment produced a significant decrease of depressive symptoms for seasonal and non-seasonal unipolar depression. But there are no long-term studies of light therapy for the treatment of non-seasonal unipolar depression. It is also important to note that many of these studies involved co-therapy with antidepressant drugs or sleep-deprivation, making the interpretation of the results even more difficult. Therefore, we propose to study the efficacy and safety of light therapy for the treatment of bipolar type II patients relapsing into a depressive phase during the period of September to mid-March. This will be a double-blind randomized placebo-controlled study. Bipolar II out-patients will be recruited from our bipolar disorders program and from our 5 general psychiatry out-patient clinics. We will recruit bipolar type II patients facing a depressive phase and after they give their informed consent and we had verified they meet all inclusion and exclusion criteria, they will be randomized blindly to Bright-light (10 000 lux) vs Dim-light placebo (100 lux) therapies. Both, patient and investigator/rater will be blind to the type of light treatment assigned to the patient. The light therapy will take place during 30 minutes daily in the morning AFTER the usual awakening time of the patient in order to avoid even partial sleep deprivation which would confound the results if we were to observe a greater switch rate into mania or hypomania. Reasons for study termination can be serious side-effects, development of suicidal ideations or hypomanic/manic symptoms, patient's own decision, or any other of the exclusion criteria being fulfilled during the course of the study. Depressive and manic/hypomanic symptoms, quality of life, sleep quality and side-effects will be assessed at baseline and during the study. Biological parameters will also be measured along the study. We think that this study will allow us to determine the efficacy and safety of a 5 weeks bright light therapy for Bipolar type II depression and provide open label data as to the long term benefits of this treatment if prolonged over 5 weeks during the "dark" months of the year.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Type II Disorder, Depression, Bipolar
Keywords
bipolar type II disorder, depression, remission, light-therapy, efficacy, safety

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Device
Intervention Name(s)
Northern Light Technology (SADelite lamp) bright light-therapy
Other Intervention Name(s)
Northern Light Technology (SADelite lamp) with two 36W bulbs
Intervention Description
10 000 lux for 30 minutes
Intervention Type
Device
Intervention Name(s)
Northern Light Technology (SADelite lamp) Dim light-therapy
Other Intervention Name(s)
Northern Light Technology (SADelite lamp) with two 18W bulbs + red filter (Medium Red 27 High Temperature treated, LEE Filters, Y = 3.64%)
Intervention Description
<100 lux for 30 minutes
Primary Outcome Measure Information:
Title
the response rate as defined by a 50% improvement of the depressive symptoms score on the MADRS scale
Time Frame
5 and 45 weeks
Secondary Outcome Measure Information:
Title
the remission rate (MADRS scale ≤ 8 )
Time Frame
5 and 45 weeks
Title
the relapse rate into depression or hypomania
Time Frame
5 and 45 weeks
Title
the sleep quality as per PSQI scale
Time Frame
5 and 45 weeks
Title
the quality of life as per SF-36 and Q-LES-Q SF scales
Time Frame
5 and 45 weeks
Title
the incidence of side-effects as per the UKU scale
Time Frame
5 and 45 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Serge Beaulieu, Ph.D.
Organizational Affiliation
McGill University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Douglas Mental Health University Institute
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4H 1R3
Country
Canada

12. IPD Sharing Statement

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Light-Therapy in the Treatment of the Acute Phase of the Bipolar Type II Depression

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