Yoga in Unipolar and Bipolar Disorders
Primary Purpose
Bipolar Disorder, Major Depression, Dysthymia
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
psychoeducation
Yoga
Sponsored by
About this trial
This is an interventional treatment trial for Bipolar Disorder focused on measuring Yoga, Bipolar disorder, Major depression, Dysthymia, Randomized
Eligibility Criteria
Inclusion Criteria:
- Male or female patients meeting DSM-IV-TR diagnostic criteria for either Major Depression, Dysthymia, Bipolar I or Bipolar II disorder
- MADRS score of ≥10 and ≤24 and a YMRS score of ≤8
- Age 18 to 75 years
- Free of significant physical illness as evidenced by medical history, physical exam, routine clinical investigations and as clinically judged to be able to tolerate physical activities
- Participants taking prophylactic pharmacotherapy for unipolar or bipolar disorders at a stable dose for a minimum of two weeks prior to enrollment
Exclusion Criteria:
- Participants currently in a Manic, Hypomanic, or Mixed Phase
- Participants meeting DSM-IV-TR diagnostic criteria for Rapid Cycling specifier
- History of psychosis not due to Major Depression or Bipolar Disorder, e.g. schizophrenia, schizoaffective disorder, etc.
- Alcohol or Substance Abuse or Dependence within past 3 months
- Participants currently receiving any systematic structured psychotherapy. Supportive therapy is allowed.
- Those with major medical illness, or physical impairment that impact ones ability to participate in the study as evidenced by medical history, physical exam, and clinical investigations
Sites / Locations
- Centre for Addition and Mental Health
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Yoga
Psychoeducation
Arm Description
Yoga was offered twice a week for 8 weeks, 1.5 hours per session
Psychoeducation was offered twice a week for 8 weeks, 1.5 hours per session
Outcomes
Primary Outcome Measures
Montgomery-Asberg Depression Rating Scale (MADRS)
Secondary Outcome Measures
Salivary cortisol levels
Clinical Global Impression Scale
Quality of Life Enjoyment and Satisfaction Scale
Perceived Stress Scale
Coping Strategies Scale
Beck Depression Inventory
Full Information
NCT ID
NCT00482482
First Posted
June 1, 2007
Last Updated
December 4, 2012
Sponsor
Centre for Addiction and Mental Health
1. Study Identification
Unique Protocol Identification Number
NCT00482482
Brief Title
Yoga in Unipolar and Bipolar Disorders
Official Title
The Safety and Effectiveness of Yoga as Augmentation in Improving Residual Depressive Symptoms in Unipolar and Bipolar Disorders.
Study Type
Interventional
2. Study Status
Record Verification Date
December 2012
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
March 2011 (Actual)
Study Completion Date
March 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre for Addiction and Mental Health
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Major depression, chronic depression and bipolar depression are complex and difficult disorders to treat. They are often associated with residual symptoms with significant functional impairment. Yoga has been shown to be beneficial in treating depressive symptoms but without the added risks associated with medication use and has the advantage of high consumer appeal (with likelihood of good compliance). However, it has only been tested in unipolar depression, thus far. Yoga if shown to be effective (as an adjunctive to pharmacotherapy) in improving residual symptoms and decreasing risk of relapse, would be of significant long-term benefit to patients not only with major and chronic depression, but also for those with bipolar disorder.
The aim of the study is to determine the safety and effectiveness of Yoga as an augmentation treatment to pharmacotherapy and in comparison to psychoeducation, in improving residual symptoms of depression over 16 weeks and in prevention of relapse/recurrence of mood episodes over 1 year, in subjects with unipolar and bipolar disorders.
Detailed Description
Major depression (particularly recurrent and chronic depression) and bipolar depression remain complex and vexing problems for the clinician. They can be difficult to treat with pharmacotherapy alone and the persistence of residual symptoms (with consequent impact on function) and sub-syndromal symptoms increase the risk of relapse. Psychotherapy and alternative therapies have been explored as adjunctive treatments to pharmacotherapy and have shown efficacy in symptom relief. Complementary therapies, like herbal remedies and yoga, have also shown efficacy, but primarily in unipolar depression.
Yoga is a widely accepted practice that is very accessible and adaptable to different age ranges and levels of physical ability. Yoga, has been shown to be effective in the treatment of major depression and dysthymia in randomized, controlled trials. To date,Yoga has not been investigated in subjects with bipolar disorder.
We would like to replicate current investigative results on yoga and depression in a Canadian sample with unipolar and chronic depression, and would like to extend the literature by investigating its efficacy in bipolar disorder. Could adjunctive Yoga treat sub-syndromal depressive symptoms and thus reduce the risk of relapse in patients with unipolar and bipolar depression? With high consumer desirability, there is general agreement on the need for well-designed, randomized controlled trials examining the efficacy and safety of these interventions in clinical populations.
This is a prospective, assessor-blind, crossover, randomized controlled study, and will be carried out in three phases: 1) 16-week treatment phase, 2) 1 year follow-up phase. Forty patients meeting DSM-IV-TR diagnostic criteria for either Major Depression, Dysthymia, Bipolar I or Bipolar II will be recruited. Patients who have provided written consent, have met study criteria, and are stabilized on pharmacotherapy (i.e. receiving either one or two mood stabilizer(s) alone, or in combination with an oral atypical antipsychotic or an antidepressant or lamotrigine) will be enrolled into the study.
All patients will receive treatment with Yoga and psychoeducation in addition to their standard pharmacotherapy and will be randomized to one of two treatment groups groups 1) 8 weeks of yoga followed by 8 weeks of psychoeducation; or 2) 8 weeks of psychoeducation followed by 8 weeks of Yoga. After completion of the treatment phase, there will be a 12-month follow-up phase.
The specific hypotheses are:
At week 8 (the end of the first part of the treatment phase), those who are treated with Yoga plus pharmacotherapy would show a decrease in residual depressive symptoms indicated by greater reduction in MADRS scores relative to baseline and an increase in quality of life measures, as compared to those treated with psychoeducation plus pharmacotherapy.
At week 16 (the end of the second part of the treatment phase), those who are treated with yoga plus pharmacotherapy would show a decrease in residual depressive symptoms indicated by greater reduction in MADRS scores relative to baseline and an increase in quality of life measures, as compared to those treated with psychoeducation plus pharmacotherapy..
Improvement in depressive symptoms will correlate with neuroendocrine changes in salivary cortisol.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder, Major Depression, Dysthymia
Keywords
Yoga, Bipolar disorder, Major depression, Dysthymia, Randomized
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Yoga
Arm Type
Experimental
Arm Description
Yoga was offered twice a week for 8 weeks, 1.5 hours per session
Arm Title
Psychoeducation
Arm Type
Active Comparator
Arm Description
Psychoeducation was offered twice a week for 8 weeks, 1.5 hours per session
Intervention Type
Behavioral
Intervention Name(s)
psychoeducation
Intervention Description
on weekly basis for 8 weeks
Intervention Type
Behavioral
Intervention Name(s)
Yoga
Intervention Description
on weekly basis for 8 weeks
Primary Outcome Measure Information:
Title
Montgomery-Asberg Depression Rating Scale (MADRS)
Time Frame
Start of study, 8 weeks and 16 weeks
Secondary Outcome Measure Information:
Title
Salivary cortisol levels
Time Frame
Start of study, 8 weeks, 16 weeks
Title
Clinical Global Impression Scale
Time Frame
Start of study, 8 weeks and 16 weeks
Title
Quality of Life Enjoyment and Satisfaction Scale
Time Frame
Start of study, 8 weeks and 16 weeks
Title
Perceived Stress Scale
Time Frame
Start of study, 8 weeks and 16 weeks
Title
Coping Strategies Scale
Time Frame
Start of study, 8 weeks and 16 weeks
Title
Beck Depression Inventory
Time Frame
Start of study, 8 weeks and 16 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female patients meeting DSM-IV-TR diagnostic criteria for either Major Depression, Dysthymia, Bipolar I or Bipolar II disorder
MADRS score of ≥10 and ≤24 and a YMRS score of ≤8
Age 18 to 75 years
Free of significant physical illness as evidenced by medical history, physical exam, routine clinical investigations and as clinically judged to be able to tolerate physical activities
Participants taking prophylactic pharmacotherapy for unipolar or bipolar disorders at a stable dose for a minimum of two weeks prior to enrollment
Exclusion Criteria:
Participants currently in a Manic, Hypomanic, or Mixed Phase
Participants meeting DSM-IV-TR diagnostic criteria for Rapid Cycling specifier
History of psychosis not due to Major Depression or Bipolar Disorder, e.g. schizophrenia, schizoaffective disorder, etc.
Alcohol or Substance Abuse or Dependence within past 3 months
Participants currently receiving any systematic structured psychotherapy. Supportive therapy is allowed.
Those with major medical illness, or physical impairment that impact ones ability to participate in the study as evidenced by medical history, physical exam, and clinical investigations
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arun Ravindran, MD, PhD
Organizational Affiliation
Centre for Addiction and Mental Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre for Addition and Mental Health
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5T 1R8
Country
Canada
12. IPD Sharing Statement
Links:
URL
http://www.camh.net/research
Description
Information about research at the Centre for Addiction and Mental Health
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Yoga in Unipolar and Bipolar Disorders
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