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Yoga Dosing Study for Chronic Low Back Pain

Not Applicable
Completed
Conditions
Back Pain Lower Back Chronic
Interventions
Behavioral: Yoga class once per week
Behavioral: Yoga class twice per week
Registration Number
NCT01761617
Lead Sponsor
Boston Medical Center
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
96
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Yoga Class Once per WeekYoga class once per weekParticipants attend one hatha yoga class each week for 12 weeks.
Yoga Class Twice Per WeekYoga class twice per weekParticipants attend two hatha yoga classes each week for 12 weeks.
Primary Outcome Measures
NameTimeMethod
Average pain intensityup to 12 weeks

Measured on 0-10 scale; asked at baseline, 6 weeks and 12 weeks

Modified Roland Morris Disability Questionnaire for back pain-specific disabilityup to 12 weeks

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
NameTimeMethod
Pain medication useup to 12 weeks

Asked at baseline, 6 weeks and 12 weeks

Number of Participants with Adverse Eventsup to 12 weeks

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.

Trial Locations

Locations (6)

Dorchester House Multi-service Center

🇺🇸

Dorchester, Massachusetts, United States

South Boston Community Health Center

🇺🇸

Boston, Massachusetts, United States

Codman Square Health Center

🇺🇸

Dorchester, Massachusetts, United States

Upham's Corner Health Center

🇺🇸

Dorchester, Massachusetts, United States

Roslindale Greater Medical and Dental Center

🇺🇸

Roslindale, Massachusetts, United States

Boston Medical Center

🇺🇸

Boston, Massachusetts, United States

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