Individualized Chiropractic and Integrative Care for Low Back Pain
1 other identifier
interventional
201
1 country
1
Brief Summary
This study proposes to compare two innovative treatment approaches for LBP, both of which focus on delivering individualized care through evidence-based, clinical care pathways. The primary aim of the project is to determine the relative clinical efficacy of 1) chiropractic care and 2) multidisciplinary, integrative care in 200 patients with sub-acute or chronic LBP, in both the short-term (after 12 weeks) and long-term (after 52 weeks). The primary outcome measure in this study is patient-rated back pain. Chiropractic care will include therapies within the professional scope of practice. Integrative, multidisciplinary care will include chiropractic, massage therapy, traditional Chinese medicine (including acupuncture), medication, cognitive behavioral therapy, exercise, and patient education. Secondary aims are to assess between group differences in frequency of symptoms, disability, fear avoidance behavior, self efficacy, general health, improvement, patient satisfaction, work loss, medication use, lumbar dynamic motion, and torso muscle endurance. Patients' and providers' perceptions of treatment will be described using qualitative methods and cost-effectiveness and cost utility will be assessed in the short- and long-term. This innovative study is an exciting collaboration between an experienced and established team of chiropractic, conventional, and CAM professionals dedicated to advancing the care of pervasive and costly LBP conditions. This trial will provide new and important information for all health care providers and LBP patients, informing decision making and improving care delivery systems.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 2007
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2007
CompletedFirst Submitted
Initial submission to the registry
December 3, 2007
CompletedFirst Posted
Study publicly available on registry
December 4, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2013
CompletedMay 12, 2015
May 1, 2015
3.3 years
December 3, 2007
May 9, 2015
Conditions
Outcome Measures
Primary Outcomes (1)
Patient-rated back pain.
Short term: 12 weeks, Long term: 52 weeks
Secondary Outcomes (10)
Frequency of Symptoms
12 and 52 weeks
Low Back Disability
12 and 52 weeks
Fear Avoidance
12 and 52 weeks
Self-Efficacy
12 and 52 weeks
General Health Status
12 and 52 weeks
- +5 more secondary outcomes
Study Arms (2)
1
OTHER2
OTHERInterventions
A combination of professional therapies with the scope of practice, including spinal manipulation therapy, spinal mobilization, stretching and strengthening exercises, and self-care education.
A combination of therapies which may include acupuncture/Oriental medicine, chiropractic, cognitive behavioral therapy, exercise therapy, medicine, self-care information, and massage therapy.
Eligibility Criteria
You may qualify if:
- Mechanical LBP classified as 1, 2, 3, or 4 using Quebec Task Force (QTF) classification.70 (This includes back pain, stiffness or tenderness with or without musculoskeletal and neurological signs).
- LBP localized to posterior aspect of body, below the costal margin and above the inferior gluteal folds.
- Pain level \> 3 on 0 to 10 scale
- Current LBP episode \> 6 weeks duration
- years of age and older
- Stable prescription medication plan (No changes in prescription medications that affect musculoskeletal pain in the previous month.)
You may not qualify if:
- Ongoing treatment for LBP by other non-study providers
- Progressive neurological deficits or cauda equina syndrome
- QTF classifications 5 (spinal instability or fracture) and 11 (other diagnoses including visceral diseases, compression fractures, metastases). These are serious conditions not amenable to the conservative treatments proposed.
- QTF 7 (Spinal stenosis syndrome characterized by pain and/or paresthesias in one or both legs aggravated by walking).
- Uncontrolled hypertension or metabolic disease
- Blood clotting disorders
- Severe osteoporosis
- Inflammatory or destructive tissue changes of the spine
- Patients with surgical lumbar spine fusion or patients with multiple incidents of lumbar surgery. This is a subgroup of LBP patients which generally have a poorer prognosis.
- Pregnant or nursing women
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Northwestern Health Sciences University
Bloomington, Minnesota, 55431, United States
Related Publications (3)
Bronfort G, Maiers M, Schulz C, Leininger B, Westrom K, Angstman G, Evans R. Multidisciplinary integrative care versus chiropractic care for low back pain: a randomized clinical trial. Chiropr Man Therap. 2022 Mar 1;30(1):10. doi: 10.1186/s12998-022-00419-3.
PMID: 35232482DERIVEDMaiers MJ, Westrom KK, Legendre CG, Bronfort G. Integrative care for the management of low back pain: use of a clinical care pathway. BMC Health Serv Res. 2010 Oct 29;10:298. doi: 10.1186/1472-6963-10-298.
PMID: 21034483DERIVEDWestrom KK, Maiers MJ, Evans RL, Bronfort G. Individualized chiropractic and integrative care for low back pain: the design of a randomized clinical trial using a mixed-methods approach. Trials. 2010 Mar 8;11:24. doi: 10.1186/1745-6215-11-24.
PMID: 20210996DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Gert Bronfort, DC, PhD
Northwestern Health Sciences University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 3, 2007
First Posted
December 4, 2007
Study Start
June 1, 2007
Primary Completion
October 1, 2010
Study Completion
December 1, 2013
Last Updated
May 12, 2015
Record last verified: 2015-05