Study Results
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View full resultsBasic Information
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COMPLETED
NA
192 participants
INTERVENTIONAL
2004-07-31
2007-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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HVLA-SM
HVLA-SM, Experimental, high-velocity low amplitude spinal manipulation
HVLA-SM
HVLA-SM, Experimental, high-velocity low amplitude spinal manipulation
LVVA-SM
LVVA-SM, Experimental, low velocity variable amplitude spinal manipulation
LVVA-SM
LVVA-SM, Experimental, low velocity variable amplitude spinal manipulation
Usual Medical Care
Usual Medical Care, Active Comparator, advice, exercises and medications
Usual Medical Care
Arm: Active Comparator: Usual Medical Care Usual Medical Care, Active Comparator, advice, exercises and medications (Celebrex, Aleve, Bextra, Naptoxen)
Interventions
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HVLA-SM
HVLA-SM, Experimental, high-velocity low amplitude spinal manipulation
LVVA-SM
LVVA-SM, Experimental, low velocity variable amplitude spinal manipulation
Usual Medical Care
Arm: Active Comparator: Usual Medical Care Usual Medical Care, Active Comparator, advice, exercises and medications (Celebrex, Aleve, Bextra, Naptoxen)
Eligibility Criteria
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Inclusion Criteria
* Idiopathic mechanical low back pain (LBP) matching classification 1-4 of the Quebec Task Force.
* LBP classified as subacute (onset 4-12 weeks previous) or chronic (onset more than 12 weeks previous), with the current episode occurring at least four weeks prior to the date of contact with the clinic: In order to exclude the greatest proportion of LBP patients that have a favorable natural history of improvement.
* Written Informed Consent
* A minimum baseline score on the Roland Morris Disability Questionnaire (RMQ) of 6 points.
Exclusion Criteria
* LBP diagnosis not meeting Classifications 1 through 4 of the Quebec Task Force, especially the following: low back pain associated with frank radiculopathy defined as typical shooting leg pain; positive straight leg-raising test; an altered lower extremity reflex; a dermatomal sensory deficit; at least one of the following: progressive unilateral muscle weakness or motor loss, or symptoms of cauda equina compression; and CT or MRI evidence of related anatomical pathology (e.g. abnormal disc, stenosis).
* Co-morbid pathology or poor health conditions in patients; Co-morbid conditions and general poor health significantly complicate the prognosis of LBP, and inject a variety of uncontrollable factors in case-management, not to mention experimental analysis and interpretation. Patients who have case histories and physical examination findings indicating other that average good health will be excluded from the study.
* Bone and joint pathology contraindicating patient for SM of the lumbar spine and pelvis: Patients with spinal fractures, tumors, infections, arthropathies, and significant osteoporosis will be referred to appropriate health care.
* Other contraindications for SM of the lumbar spine and pelvis (e.g. bleeding disorders or anticoagulant therapy, extreme obesity).
* Retention of legal advice related to this or a previous LBP episode: Patients with occupational or personal injuries will not be automatically excluded from the study unless they answer yes to a specific question about the retention of legal advice with respect to their LBP episode at the baseline interview.
* Pregnancy: Pregnancy is a contraindication for exposing a patient to ionizing radiation and is a confounding factor in the usual course of LBP.
* Inability to read or verbally comprehend English.
* Clear evidence of narcotic or other drug abuse as determined by history and examination: injects significant confounding factors with respect to internal validity and feasibility.
* Major clinical depression: Patients with scores greater than 17 on the Beck Depression Inventory will be excluded from the study. Patients with evidence of other psychiatric disorders as determined by history and exam will also be excluded.
* Use of manipulative care for any reason within the past 3 months as determined by history: to exclude the possibility of carryover effects.
* Unwillingness to postpone use of all other types of manual treatment for LBP except those provided in the study (including chiropractic and osteopathic SM, physical therapy, and massage) for the duration of the study period: to eliminate confounding effects.
21 Years
55 Years
ALL
Yes
Sponsors
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Department of Health and Human Services
FED
Palmer College of Chiropractic
OTHER
Responsible Party
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Principal Investigators
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William C Meeker, DC, M.P.H.
Role: PRINCIPAL_INVESTIGATOR
Palmer Chiropractic College
David Wilder, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Iowa
Locations
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Palmer Center for Chiropractic Research
Davenport, Iowa, United States
Countries
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References
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Xia T, Long CR, Gudavalli MR, Wilder DG, Vining RD, Rowell RM, Reed WR, DeVocht JW, Goertz CM, Owens EF Jr, Meeker WC. Similar Effects of Thrust and Nonthrust Spinal Manipulation Found in Adults With Subacute and Chronic Low Back Pain: A Controlled Trial With Adaptive Allocation. Spine (Phila Pa 1976). 2016 Jun;41(12):E702-E709. doi: 10.1097/BRS.0000000000001373.
Hondras MA, Long CR, Haan AG, Spencer LB, Meeker WC. Recruitment and enrollment for the simultaneous conduct of 2 randomized controlled trials for patients with subacute and chronic low back pain at a CAM research center. J Altern Complement Med. 2008 Oct;14(8):983-92. doi: 10.1089/acm.2008.0066.
Related Links
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Similar Effects of Thrust and Nonthrust Spinal Manipulation Found in Adults With Subacute and Chronic Low Back Pain: A Controlled Trial With Adaptive Allocation.
Other Identifiers
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U19P3
Identifier Type: -
Identifier Source: org_study_id
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