Yoga Dosing Study for Chronic Low Back Pain (YLBP2)
Primary Purpose
Back Pain Lower Back Chronic
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Yoga class once per week
Yoga class twice per week
Sponsored by

About this trial
This is an interventional treatment trial for Back Pain Lower Back Chronic focused on measuring Yoga, Chronic Low Back Pain, CAM, Complementary and Alternative Medicine, Minorities
Eligibility Criteria
Inclusion Criteria:
- 18-64 years old
- Current non-specific low back pain persisting >12 weeks. Mean low back pain intensity for the previous week 4 or greater on a 0 to 10 numerical rating scale (0=no pain to 10=worst possible pain).
- English fluency sufficient to follow treatment instructions and answer survey questions
- Willingness to list comprehensive contact information for at least one (preferably two) friend, family member, or work colleague who will always know how to contact the participant.
Exclusion Criteria:
- Use of yoga in the previous 6 months
- New CLBP treatments started within the previous month or anticipated to begin in the next 12 months
- Pregnancy
- Back surgery in the previous three years
- Specific CLBP pathologies
- Severe or progressive neurological deficits
- Sciatica pain equal to or greater than back pain
- Active substance or alcohol abuse
- Active or planned worker's compensation, disability, or personal injury claims
Sites / Locations
- Boston Medical Center
- South Boston Community Health Center
- Dorchester House Multi-service Center
- Codman Square Health Center
- Upham's Corner Health Center
- Roslindale Greater Medical and Dental Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Yoga Class Twice Per Week
Yoga Class Once per Week
Arm Description
Participants attend two hatha yoga classes each week for 12 weeks.
Participants attend one hatha yoga class each week for 12 weeks.
Outcomes
Primary Outcome Measures
Average pain intensity
Measured on 0-10 scale; asked at baseline, 6 weeks and 12 weeks
Modified Roland Morris Disability Questionnaire for back pain-specific disability
Roland Morris Disability Questionnaire is a widely used health status measure for low back pain; asked at baseline, 6 weeks and 12 weeks
Secondary Outcome Measures
Pain medication use
Asked at baseline, 6 weeks and 12 weeks
Number of Participants with Adverse Events
Participants encouraged to contact study staff immediately if they have experienced an adverse event that may or definitely be a result of their involvement in the study. All data collections will include questions on whether the participant believes he/she incurred any possible intervention-related adverse events.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01761617
Brief Title
Yoga Dosing Study for Chronic Low Back Pain
Acronym
YLBP2
Official Title
Yoga Dosing Study for Chronic Low Back Pain in a Predominantly Low-Income Minority Population
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
December 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Boston Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A 12-week randomized controlled trial (RCT) for chronic low back pain in predominantly minority populations comparing yoga classes once/week vs. twice/week. Primary outcomes are pain intensity and measure of disability; secondary outcomes are pain medication use, treatment adherence, and health-related quality of life.
Detailed Description
Chronic low back pain (CLBP) affects 5-10% of U.S. adults annually and costs over $50 billion per year in direct health care expenditures. Individuals from low-income minority backgrounds are disproportionately impacted by CLBP due to disparities in access and treatment. Several recent studies suggest yoga is effective for CLBP. Yoga may also have other relevant benefits for CLBP patients, such as improved mood, stress reduction, and lower cost. However, there are no studies which directly compare different doses of yoga for CLBP. It is unknown if there is a meaningful dose- response effect of yoga for CLBP. If there is a dose/response effect, the magnitude of the effect is unknown. The total dose of a yoga intervention depends upon the duration of total intervention, frequency of yoga classes, duration of each yoga class, and home practice (amount, duration and frequency).
To assess the impact of yoga dose, we propose conducting a Pilot Yoga Dosing Study for 96 adults from Boston Medical Center. The Dosing Study will be a 12-week randomized controlled trial where participants are assigned to either once per week 75-minute yoga classes or twice per week 75 minute yoga classes.
During this 12-week study, there will be three points of data collection (baseline, 6 weeks, 12 weeks). In addition, little is known about the reliability of different forms of survey administration in low back pain trials. For example, it is unknown if telephone administered questionnaires or web-based data collection are reliable compared to the traditional paper- administered questionnaire.Therefore we will compare different methods of survey administration at each time point. The results of this Pilot will inform the design of a larger future comparative effectiveness RCT of yoga, physical therapy, and education for chronic low back pain.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Back Pain Lower Back Chronic
Keywords
Yoga, Chronic Low Back Pain, CAM, Complementary and Alternative Medicine, Minorities
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
96 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Yoga Class Twice Per Week
Arm Type
Active Comparator
Arm Description
Participants attend two hatha yoga classes each week for 12 weeks.
Arm Title
Yoga Class Once per Week
Arm Type
Active Comparator
Arm Description
Participants attend one hatha yoga class each week for 12 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Yoga class once per week
Intervention Description
The protocol consists of one 75-minute yoga class per week for 12 weeks. The 12 weeks are divided into four 3-week segments, each with a theme (e.g., "Listening to the Wisdom of the Body," "Engaging your Power"). The number of postures learned and degree of difficulty increases with each segment. The protocol provides variations and uses various aids (e.g., chair, yoga strap, yoga block) to accommodate a range of physical abilities. Classes are taught by a team of yoga instructors to ensure a low participant-to-teacher ratio.
Intervention Type
Behavioral
Intervention Name(s)
Yoga class twice per week
Intervention Description
The protocol consists of two 75-minute yoga classes per week for 12 weeks. The 12 weeks are divided into four 3-week segments, each with a theme (e.g., "Listening to the Wisdom of the Body," "Engaging your Power"). The number of postures learned and degree of difficulty increases with each segment. The protocol provides variations and uses various aids (e.g., chair, yoga strap, yoga block) to accommodate a range of physical abilities. Classes will have eight participants at a time and are taught by a team of two yoga instructors to ensure a low yoga participant-to-teacher ratio.
Primary Outcome Measure Information:
Title
Average pain intensity
Description
Measured on 0-10 scale; asked at baseline, 6 weeks and 12 weeks
Time Frame
up to 12 weeks
Title
Modified Roland Morris Disability Questionnaire for back pain-specific disability
Description
Roland Morris Disability Questionnaire is a widely used health status measure for low back pain; asked at baseline, 6 weeks and 12 weeks
Time Frame
up to 12 weeks
Secondary Outcome Measure Information:
Title
Pain medication use
Description
Asked at baseline, 6 weeks and 12 weeks
Time Frame
up to 12 weeks
Title
Number of Participants with Adverse Events
Description
Participants encouraged to contact study staff immediately if they have experienced an adverse event that may or definitely be a result of their involvement in the study. All data collections will include questions on whether the participant believes he/she incurred any possible intervention-related adverse events.
Time Frame
up to 12 weeks
Other Pre-specified Outcome Measures:
Title
Improvement in low back pain
Description
Participants asked to rate how their low back feels compared to when they began treatment on scale 0-6 where 0 is "extremely worsened" and 6 is "extremely improved." Asked at 6 weeks and 12 weeks.
Time Frame
up to 12 weeks
Title
Patient satisfaction
Description
Satisfaction with treatment of low back pain
Time Frame
up to 12 weeks
Title
Health-related Quality of Life (SF-36)
Description
The SF-36 is a multi-purpose, generalized health survey that assesses the health benefits produced by a wide range of different treatments.
Time Frame
up to 12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18-64 years old
Current non-specific low back pain persisting >12 weeks. Mean low back pain intensity for the previous week 4 or greater on a 0 to 10 numerical rating scale (0=no pain to 10=worst possible pain).
English fluency sufficient to follow treatment instructions and answer survey questions
Willingness to list comprehensive contact information for at least one (preferably two) friend, family member, or work colleague who will always know how to contact the participant.
Exclusion Criteria:
Use of yoga in the previous 6 months
New CLBP treatments started within the previous month or anticipated to begin in the next 12 months
Pregnancy
Back surgery in the previous three years
Specific CLBP pathologies
Severe or progressive neurological deficits
Sciatica pain equal to or greater than back pain
Active substance or alcohol abuse
Active or planned worker's compensation, disability, or personal injury claims
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert B Saper, MD, MPH
Organizational Affiliation
Boston Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Boston Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Facility Name
South Boston Community Health Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Facility Name
Dorchester House Multi-service Center
City
Dorchester
State/Province
Massachusetts
ZIP/Postal Code
02122
Country
United States
Facility Name
Codman Square Health Center
City
Dorchester
State/Province
Massachusetts
ZIP/Postal Code
02124
Country
United States
Facility Name
Upham's Corner Health Center
City
Dorchester
State/Province
Massachusetts
ZIP/Postal Code
02125
Country
United States
Facility Name
Roslindale Greater Medical and Dental Center
City
Roslindale
State/Province
Massachusetts
ZIP/Postal Code
02131
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
24716775
Citation
Cerrada CJ, Weinberg J, Sherman KJ, Saper RB. Inter-method reliability of paper surveys and computer assisted telephone interviews in a randomized controlled trial of yoga for low back pain. BMC Res Notes. 2014 Apr 9;7:227. doi: 10.1186/1756-0500-7-227.
Results Reference
derived
PubMed Identifier
23878604
Citation
Saper RB, Boah AR, Keosaian J, Cerrada C, Weinberg J, Sherman KJ. Comparing Once- versus Twice-Weekly Yoga Classes for Chronic Low Back Pain in Predominantly Low Income Minorities: A Randomized Dosing Trial. Evid Based Complement Alternat Med. 2013;2013:658030. doi: 10.1155/2013/658030. Epub 2013 Jun 26.
Results Reference
derived
Learn more about this trial
Yoga Dosing Study for Chronic Low Back Pain
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