Pilot Study to Test the Effectiveness of Combining Conventional and Complementary Medicine to Treat Low Back Pain

NCT ID: NCT00118859

Last Updated: 2009-12-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-07-31
• Study Completion Date: 2006-04-30

Brief Summary

This pilot study will determine the feasibility of enrolling participants from different populations for a larger study of low back pain (LBP) treatment. In addition, this study will assess the effectiveness of data collection instruments and procedures as well as utilize feedback from participants to refine a future study.

Detailed Description

Back pain is one of the most common health problems in the United States, afflicting up to 50% of adults each year. Back pain is the leading cause of visits to orthopedic surgeons and the second leading cause of visits to general practitioners. In the United States, the estimated annual cost of back pain, including medical costs and lost productivity, is between $50 and $100 billion. Unfortunately, conventional medical care has been largely ineffective in treating back pain of most people. An increasing number of people with back pain, particularly with LBP, are seeking relief from unconventional sources such as chiropractors and massage therapies. Although complementary and alternative medicine (CAM) therapies are being used to treat LBP, their effectiveness has not been thoroughly examined. Even less is known about the effectiveness of combining conventional medical care with CAM therapies to provide "integrative care." This pilot study will recruit participants from three different patient populations to determine the effectiveness of integrative care in treating LBP symptoms.

This study will last 26 weeks and will comprise three participant populations: patients at an occupational health clinic, primary care patients at a medical clinic, and workers' compensation patients at the same medical clinic. At study start, participants will be interviewed about the care they have already received for LBP, any activities limited by their LBP, their attitudes toward CAM back pain treatments, job satisfaction, social support in the workplace, and medical history. Participants will also complete a self-report pain scale and a disability questionnaire. Participants will then be randomly assigned to either receive treatment for their LBP at an Integrative Care Center or continue to receive usual care provided by their medical or occupational health clinic.

Participants assigned to receive integrative care will be evaluated by both a medical doctor and a CAM clinician immediately after being interviewed. Following the evaluation, the two clinicians will meet and develop a treatment plan, which will include conventional medical care and some form of CAM such as acupuncture, chiropractic, exercise, massage, mind-body therapy, or nutritional counseling. Treatments will occur either once or twice weekly for the 12-week duration of treatment; clinicians may revise treatment plans during the study. LBP symptoms will be assessed through phone interviews at Weeks 2, 5, 12, and 26.

Conditions

Low Back Pain

Keywords

Back Pain; Integrative Care; Acupuncture; Chiropractic; Exercise; Massage Therapy; Mind-Body Therapy; Nutritional Counseling; Complementary Therapies; Complementary and Alternative Medicine

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

Integrative care for low back pain

Intervention Type: BEHAVIORAL

Conventional treatment for low back pain

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Low back pain beginning 3 to 6 weeks prior to study entry
• Patient of Partners Occupational Health Center or Harvard Vanguard Medical Associates (HVMA)
• Able to speak and understand English
• Willing and able to comply with all study requirements

Exclusion Criteria

• History of back surgery within 3 years prior to study entry
• History of vertebral fracture or dislocation
• Progressive or severe neurological symptoms such as loss of bowel or bladder control, numbness in groin or rectal area, or extreme leg weakness
• Severe inflammation of the vertebrae, stiffening of the joints and ligaments, or scoliosis
• Pacemaker or implanted defibrillator
• Underlying systemic or visceral disease which might be causing back pain
• Osteoporosis
• Cancer within 5 years prior to study entry. Participants with non-melanoma skin cancer are not excluded.
• Unexplained weight loss or recent unexplained fever
• Bleeding disorder or current use of anticoagulant medication
• Any disabling medical condition
• Major organ transplantation
• Current use of systemic corticosteroids
• Current use of immunosuppressive medications
• Current use of intravenous drugs
• Pregnancy

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Center for Complementary and Integrative Health (NCCIH)

NIH

Sponsor Role: lead

Principal Investigators

David Eisenberg, PhD

Role: PRINCIPAL_INVESTIGATOR

Harvard Medical School (HMS and HSDM)

Countries

United States

Other Identifiers

ICC

Identifier Type: -

Identifier Source: secondary_id

R01AT000905

Identifier Type: NIH

Identifier Source: org_study_id

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