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. 2010 Mar-Apr;33(3):193-200.
doi: 10.1016/j.jmpt.2010.01.010.

Mechanical vs manual manipulation for low back pain: an observational cohort study

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Mechanical vs manual manipulation for low back pain: an observational cohort study

Michael J Schneider et al. J Manipulative Physiol Ther. 2010 Mar-Apr.

Abstract

Objective: This is an observational prospective cohort study to explore the treatment effect of mechanical vs manual manipulation for acute low back pain.

Methods: Ninety-two patients with a history of acute low back pain were recruited from 3 private chiropractic offices, 2 of which used manual lumbar manipulation and 1 used mechanical instrument manipulation (Activator) as their primary modes of treatment. The chiropractors used their "treatment-as-usual" protocols for a maximum of 8 visits or 4 weeks, whichever occurred first. Primary outcome measures were changes in Numeric Pain Rating Scale (NPRS) and Oswestry Disability Index (ODI) scores from baseline to 4 weeks. The linear regression models were adjusted for baseline NPRS and ODI scores, age, and treatment expectancy.

Results: Comparison of baseline characteristics did not show any significant differences between the groups except for age (38.4 vs 49.7 years, P < .001) and treatment expectancy (5.7 vs 6.3, P = .003). Linear regression revealed significantly lower NPRS scores in the manual manipulation group at 4 weeks (beta = -1.2; 95% confidence interval, -2.1 to -.28) but no significant difference in ODI scores between the 2 groups at 4 weeks (beta = 1.5; 95% confidence interval, -8.3 to 2.4). Treatment expectancy, but not age, was found to have a significant main effect on both NPRS and ODI scores at 4 weeks. Exploratory analysis of the clinical patterns of care between the clinicians revealed significant differences in treatment frequency, duration, modality, and radiograph use between the 2 cohorts.

Conclusions: This study highlights the challenges inherent with conducting research that allows for "treatment as usual." The data and experience derived from this investigational study will be used to design a future randomized clinical trial in which tighter controls will be imposed on the treatment protocol.

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Conflict of interest statement

FUNDING SOURCES AND CONFLICTS OF INTEREST

Dr. Schneider completed this study while receiving salary support under a grant from the National Institutes of Health (NIH) National Center for Complementary and Alternative Medicine (NCCAM) NIH/NCCAM Grant #: K99 A T004196-01. No conflicts of interest were reported for this study.

Figures

Figure 1
Figure 1
Baseline and 4-week unadjusted mean Numeric Pain Rating Scores (NPRS) by cohort. Regression analysis revealed that a significant difference in the mean adjusted 4-week pain scores remained after controlling for baseline pain, cohort, and expectation.
Figure 2
Figure 2
Baseline and four-week unadjusted mean Oswestry Disability Index (ODI) scores by cohort. Regression analysis did not reveal any significant difference in mean four-week ODI scores after controlling for baseline ODI.

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