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Yoga for Chronic Low Back Pain and Its Mechanism of Action (YoMA)

Yoga for Chronic Low Back Pain and Its Mechanism of Action (YoMA)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01739140
Acronym
YoMA
Enrollment
24
Registered
2012-12-03
Start date
2012-12-31
Completion date
2015-12-31
Last updated
2019-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low Back Pain

Brief summary

This is a study to better understand how a yoga intervention helps improve symptoms in people with chronic low back pain. This study will be a 12-week intervention of about 24 participants with chronic low back pain where all individuals will receive weekly yoga classes and instructions for home practice. The purpose of this study is to collect feasibility data and to conduct preliminary analyses in preparation for a larger planned NIH study.

Interventions

BEHAVIORALYoga

Sponsors

Bowes Fund for Innovative Research
CollaboratorUNKNOWN
University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Chronic low back pain lasting \> 3 months * Back pain that is rated at least 3 on a numeric pain rating scale that ranges from 0 to 10 (0-no pain, 10 worst pain imaginable). * English language fluency

Exclusion criteria

* BMI \> 40 * Inability to provide informed consent * Recent diagnosis of abdominal aneurism * Recent diagnosis of metastatic cancer * Recent diagnosis of discitis * Recent diagnosis of disk disease * Recent diagnosis of spinal stenosis * Recent diagnosis of spondylolisthesis * Recent diagnosis of infectious cause of back pain * Recent diagnosis of fracture of vertebra * Recent diagnosis of Fibromyalgia * Recent diagnosis of rheumatoid arthritis * Recent diagnosis of ankylosing spondylitis * Recent diagnosis of paralysis * Pregnancy * Prior or planned back surgery * Blindness or severe vision problems * Deafness or severe hearing problems * Bipolar or manic depression and not taking medication * Major depression * Psychoses (major) * a substance abuse condition * Dementia * Unable to get up and down from the floor * Involvement in a lawsuit related to back pain * Lack of transportation * Other disabling chronic conditions (e.g., disabling heart or lung disease, diabetic neuropathy, receiving treatment for hepatitis) * Currently (within the past 3 months) using yoga classes for more than 15 minutes per week * Inability to be contacted by phone or email * no computer access * schedule does not allow for participation in classes/home practice * planning to move out of town or take a long vacation during the period of the study

Design outcomes

Primary

MeasureTime frame
Roland Morris Disability QuestionnaireBaseline to 3 months post-intervention.

Secondary

MeasureTime frame
Numeric Rating Scale for PainBaseline to 3 months post-intervention.
Pain Medication Usage SurveyBaseline to 3 months post-intervention.

Other

MeasureTime frame
Pain Catastrophizing ScaleBaseline to 3 months post-intervention.
Five Facet Mindfulness QuestionnaireBaseline to 3 months post-intervention.
Multidimensional Assessment of Interoceptive AwarenessBaseline to 3 months post-intervention.
Patient Reported Outcomes Measurement Information System: Pain - BehaviorBaseline to 3 months post-intervention.
Inflammatory pain related cytokinesBaseline to 3 months post-intervention.
Patient Reported Outcomes Measurement Information System: Emotional Distress - DepressionBaseline to 3 months post-intervention.
Patient Reported Outcomes Measurement Information System: Emotional Distress - AnxietyBaseline to 3 months post-intervention.
Patient Reported Outcomes Measurement Information System: Physical FunctionBaseline to 3 months post-intervention.
Patient Reported Outcomes Measurement Information System: Pain - InterferenceBaseline to 3 months post-intervention.
Heart rate variabilityBaseline to 3 months post-intervention.
International Physical Activity QuestionnaireBaseline to 3 months post-intervention.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026