Low Back Pain Clinical Trial
Official title:
Short-term Effects of Thoracic Spine Thrust Manipulation for Individuals With Low Back Pain: A Randomized Control Trial
The purpose of this study is to determine the short-term effects of thoracic spine thrust manipulation on participants with low back pain. Participants in this study will be randomized to receive either the lower thoracic spinal manipulation and a standard set of exercises, or a sham manipulation and the same standard set of exercises. It is hypothesized that thoracic manipulation when combined with core strengthening exercises will have positive short term improvements in pain and function for patients with LBP as compared to a sham manipulation combined with core strengthening exercises.
This study aims to use a randomized controlled trial design to investigate the effects of
thoracic spinal manipulation in conjunction with core strengthening exercises when compared
to a sham manipulation and core strengthening exercises on patients with low back pain. Core
strengthening exercises have been shown to improve pain and functional status in patients
with non-specific low back pain when compared to conventional exercise. However, there is
strong evidence to suggest that exercise alone is not adequate for the management of low back
pain. Spinal manipulation has demonstrated promising results for the management of low back
pain, but it is unclear whether the targeted location of manipulation is important. It is
hypothesized that thoracic manipulation when combined with core strengthening exercises will
have positive short term improvements in pain and function for patients with LBP as compared
to a sham manipulation combined with core strengthening exercises based on the theory of
regional interdependence. The specific aims of the study are as follows:
1. To determine the effects of thoracic spine manipulation and core strengthening exercise
on function in individuals with low back pain, specifically measured by changes in
Modified Oswestry Low Back Pain Disability Questionnaire (MODQ).
2. To determine the participant's perception of improvement following thoracic spine
manipulation and core exercises, measured by global rating of change (GROC), when
compared to a sham manipulation.
3. To determine the effects of thoracic spine manipulation and core exercises on fear
avoidance, measured by fear-avoidance belief questionnaire (FABQ), on individuals with
low back pain.
4. To determine the effects of thoracic spine manipulation and core exercises on pain using
numeric pain rating scale (NPRS).
The ability to demonstrate the effectiveness of a manipulation targeted at the thoracic spine
in conjunction with core exercises could provide clinicians a simple, effective treatment
strategy for low back pain that not only has minimal injury risk, but has the potential to
improve pain and function, ultimately decreasing the healthcare costs associated with low
back pain.
The effects of treatment on disability, fear-avoidance, and pain will be analyzed using a 2x2
repeated measures multivariate analysis of variance (MANCOVA), with pre/post-test measures
and time as the two factors and duration of symptoms serving as a covariate. An independent t
test will be used to determine differences for the Global Rating of Change between groups at
follow up, and the number needed to treat (NNT) will be calculated. Spinal manipulation has
some potentially serious risks including, fracture, numbness, tingling, or injury to the
spinal cord. However, these risks are very low in the thoracic spine where manipulation is
targeted during this study. In a recent systematic review which evaluated the safety of
thoracic spine manipulation, the authors found only seven cases of serious trauma which have
resulted from thoracic spine manipulation. The majority of these cases were performed by a
chiropractor and it is unsure whether participants had contraindications to manipulation. In
order to mitigate these risks, participants will be thoroughly screened for contraindications
to spinal manipulation. If an adverse event does occur, the participant will be referred to
the appropriate provider and their participation in the study will be discontinued.
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