Treating Major Depression With Yoga: A Prospective, Randomized Controlled Pilot Trial
Completed · Not applicable
Conditions studied: Depression, Unipolar
In brief
This was a randomized controlled pilot trial to evaluate clinical efficacy and feasibility of hatha yoga as a mono-therapy for major depression. Investigators recruited 38 adults in San Francisco meeting criteria for major depression of mild-to-moderate severity, per structured psychiatric interview and scores of 14-28 on Beck Depression Inventory-II (BDI). At screening, individuals engaged in psychotherapy, antidepressant pharmacotherapy, herbal/nutraceutical mood therapies, or mind-body practices were excluded. Twenty participants were randomized to 90-minute hatha yoga practice groups twice weekly for 8 weeks. Eighteen participants were randomized to 90-minute attention control education groups twice weekly for 8 weeks. Certified yoga instructors delivered both interventions at a university clinic. Primary outcome was depression severity, measured by BDI scores every 2 weeks from intervention start at 0 weeks until finish at 8 weeks. Secondary outcomes were self-efficacy and self-esteem, measured by scores on the General Self-Efficacy Scale (GSES) and Rosenberg Self-Esteem Scale (RSES) at 0 weeks and 8 weeks. Blinded assessors analyzed whether change in outcome measures would be statistically comparable between the two intervention groups.
Key facts
- Study ID
- NCT01210651
- Run by
- University of California, San Francisco
- People needed
- 38
- Starts
- 2010-05-01
- Expected to finish
- 2011-01-01
- Last updated by the study team
- 2017-01-11
Who can join
Age: 14 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Individuals 14 years of age and older
- English proficiency sufficient for study participation
- Diagnosis of Axis I unipolar major depression, per screening Mini International Neuro-Psychiatric Interview (MINI)
- Depressive symptoms of mild to moderate intensity, per score of 14-28 on screening Beck Depression Inventory-II (BDI)
- Able to attend all required study sessions
You may not qualify if…
- Cognitive Impairment, as per Folstein Mini-mental Status Exam Score < 24
- Use of any antidepressant medication or herbal/nutraceutical mood therapy within the 2 months prior to screening, or during study period
- Use of psychotherapy during study period
- Use of any yoga or other mind-body practices during study period, other than study intervention
- Per screening MINI, diagnosis of any Axis I disorder other than unipolar major depression, such as bipolar disorder, dysthymia or anxiety disorders
- Per screening MINI, diagnosis of substance use disorders within prior 3 months
- Per screening MINI, current suicidal ideation or past suicide attempts
- Severe depressive symptoms, as per screening BDI score > 28
Where it is running
- University of California San Francisco — San Francisco, California, United States
Full record on ClinicalTrials.gov
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