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Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial

BACKGROUND: Low back pain (LBP) is a recognized public health problem, impacting up to 80% of US adults at some point in their lives. Patients with LBP are utilizing integrative health care such as spinal manipulation (SM). SM is the therapeutic application of a load to specific body tissues or stru...

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Autores principales: Wilder, David G, Vining, Robert D, Pohlman, Katherine A, Meeker, William C, Xia, Ting, DeVocht, James W, Gudavalli, R Maruti, Long, Cynthia R, Owens, Edward F, Goertz, Christine M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148990/
https://www.ncbi.nlm.nih.gov/pubmed/21708042
http://dx.doi.org/10.1186/1745-6215-12-161
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author Wilder, David G
Vining, Robert D
Pohlman, Katherine A
Meeker, William C
Xia, Ting
DeVocht, James W
Gudavalli, R Maruti
Long, Cynthia R
Owens, Edward F
Goertz, Christine M
author_facet Wilder, David G
Vining, Robert D
Pohlman, Katherine A
Meeker, William C
Xia, Ting
DeVocht, James W
Gudavalli, R Maruti
Long, Cynthia R
Owens, Edward F
Goertz, Christine M
author_sort Wilder, David G
collection PubMed
description BACKGROUND: Low back pain (LBP) is a recognized public health problem, impacting up to 80% of US adults at some point in their lives. Patients with LBP are utilizing integrative health care such as spinal manipulation (SM). SM is the therapeutic application of a load to specific body tissues or structures and can be divided into two broad categories: SM with a high-velocity low-amplitude load, or an impulse "thrust", (HVLA-SM) and SM with a low-velocity variable-amplitude load (LVVA-SM). There is evidence that sensorimotor function in people with LBP is altered. This study evaluates the sensorimotor function in the lumbopelvic region, as measured by postural sway, response to sudden load and repositioning accuracy, following SM to the lumbar and pelvic region when compared to a sham treatment. METHODS/DESIGN: A total of 219 participants with acute, subacute or chronic low back pain are being recruited from the Quad Cities area located in Iowa and Illinois. They are allocated through a minimization algorithm in a 1:1:1 ratio to receive either 13 HVLA-SM treatments over 6 weeks, 13 LVVA-SM treatments over 6 weeks or 2 weeks of a sham treatment followed by 4 weeks of full spine "doctor's choice" SM. Sensorimotor function tests are performed before and immediately after treatment at baseline, week 2 and week 6. Self-report outcome assessments are also collected. The primary aims of this study are to 1) determine immediate pre to post changes in sensorimotor function as measured by postural sway following delivery of a single HVLA-SM or LVVA-SM treatment when compared to a sham treatment and 2) to determine changes from baseline to 2 weeks (4 treatments) of HVLA-SM or LVVA-SM compared to a sham treatment. Secondary aims include changes in response to sudden loads and lumbar repositioning accuracy at these endpoints, estimating sensorimotor function in the SM groups after 6 weeks of treatment, and exploring if changes in sensorimotor function are associated with changes in self-report outcome assessments. DISCUSSION: This study may provide clues to the sensorimotor mechanisms that explain observed functional deficits associated with LBP, as well as the mechanism of action of SM. TRIAL REGISTRATION: This trial is registered in ClinicalTrials.gov, with the ID number of NCT00830596, registered on January 27, 2009. The first participant was allocated on 30 January 2009 and the final participant was allocated on 17 March 2011.
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spelling pubmed-31489902011-08-03 Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial Wilder, David G Vining, Robert D Pohlman, Katherine A Meeker, William C Xia, Ting DeVocht, James W Gudavalli, R Maruti Long, Cynthia R Owens, Edward F Goertz, Christine M Trials Study Protocol BACKGROUND: Low back pain (LBP) is a recognized public health problem, impacting up to 80% of US adults at some point in their lives. Patients with LBP are utilizing integrative health care such as spinal manipulation (SM). SM is the therapeutic application of a load to specific body tissues or structures and can be divided into two broad categories: SM with a high-velocity low-amplitude load, or an impulse "thrust", (HVLA-SM) and SM with a low-velocity variable-amplitude load (LVVA-SM). There is evidence that sensorimotor function in people with LBP is altered. This study evaluates the sensorimotor function in the lumbopelvic region, as measured by postural sway, response to sudden load and repositioning accuracy, following SM to the lumbar and pelvic region when compared to a sham treatment. METHODS/DESIGN: A total of 219 participants with acute, subacute or chronic low back pain are being recruited from the Quad Cities area located in Iowa and Illinois. They are allocated through a minimization algorithm in a 1:1:1 ratio to receive either 13 HVLA-SM treatments over 6 weeks, 13 LVVA-SM treatments over 6 weeks or 2 weeks of a sham treatment followed by 4 weeks of full spine "doctor's choice" SM. Sensorimotor function tests are performed before and immediately after treatment at baseline, week 2 and week 6. Self-report outcome assessments are also collected. The primary aims of this study are to 1) determine immediate pre to post changes in sensorimotor function as measured by postural sway following delivery of a single HVLA-SM or LVVA-SM treatment when compared to a sham treatment and 2) to determine changes from baseline to 2 weeks (4 treatments) of HVLA-SM or LVVA-SM compared to a sham treatment. Secondary aims include changes in response to sudden loads and lumbar repositioning accuracy at these endpoints, estimating sensorimotor function in the SM groups after 6 weeks of treatment, and exploring if changes in sensorimotor function are associated with changes in self-report outcome assessments. DISCUSSION: This study may provide clues to the sensorimotor mechanisms that explain observed functional deficits associated with LBP, as well as the mechanism of action of SM. TRIAL REGISTRATION: This trial is registered in ClinicalTrials.gov, with the ID number of NCT00830596, registered on January 27, 2009. The first participant was allocated on 30 January 2009 and the final participant was allocated on 17 March 2011. BioMed Central 2011-06-28 /pmc/articles/PMC3148990/ /pubmed/21708042 http://dx.doi.org/10.1186/1745-6215-12-161 Text en Copyright ©2011 Wilder et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Wilder, David G
Vining, Robert D
Pohlman, Katherine A
Meeker, William C
Xia, Ting
DeVocht, James W
Gudavalli, R Maruti
Long, Cynthia R
Owens, Edward F
Goertz, Christine M
Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial
title Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial
title_full Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial
title_fullStr Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial
title_full_unstemmed Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial
title_short Effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial
title_sort effect of spinal manipulation on sensorimotor functions in back pain patients: study protocol for a randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148990/
https://www.ncbi.nlm.nih.gov/pubmed/21708042
http://dx.doi.org/10.1186/1745-6215-12-161
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