• Bmc Musculoskel Dis · Jan 2013

    Does a patient's physical activity predict recovery from an episode of acute low back pain? A prospective cohort study.

    • Paul Hendrick, Stephan Milosavljevic, Leigh Hale, Deirdre A Hurley, Suzanne M McDonough, Peter Herbison, and G David Baxter.
    • Division of Physiotherapy Education, University of Nottingham, Hucknall Road, Nottingham NG5 1PB, UK. paul.hendrick@nottingham.ac.uk
    • Bmc Musculoskel Dis. 2013 Jan 1;14:126.

    BackgroundAdvice to remain active and normalisation of activity are commonly prescribed in the management of low back pain (LBP). However, no research has assessed whether objective measurements of physical activity predict outcome and recovery in acute low back pain.MethodThe aims of this study were to assess the predictive relationship between activity and disability at 3 months in a sub-acute LBP population. This prospective cohort study recruited 101 consenting patients with sub-acute LBP (< 6 weeks) who completed the Roland Morris Disability Questionnaire (RMDQ), the Visual Analogue Scale, and resumption of full 'normal' activity question (Y/N), at baseline and 3 months. Physical activity was measured for 7 days at both baseline and at 3 months with an RT3 accelerometer and a recall questionnaire.ResultsObserved and self-reported measures of physical activity at baseline and change in activity from baseline to 3 months were not independent predictors of RMDQ (p > 0.05) or RMDQ change (p > 0.05) over 3 months. A self-report of a return to full 'normal' activities was significantly associated with greater RMDQ change score at 3 months (p < 0.001). Paired t-tests found no significant change in activity levels measured with the RT3 (p = 0.57) or the recall questionnaire (p = 0.38) from baseline to 3 months.ConclusionsThese results question the predictive role of physical activity in LBP recovery, and the assumption that activity levels change as LBP symptoms resolve. The importance of a patient's perception of activity limitation in recovery from acute LBP was also highlighted.Trial RegistrationClinical Trial Registration Number, ACTRN12609000282280.

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