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Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial

BACKGROUND: Sensorimotor training (SMT) is popularly applied as a preventive or rehabilitative exercise method in various sports and rehabilitation settings. Yet, there is only low-quality evidence on its effect on pain and function. This randomised controlled trial will investigate the effects of a...

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Autores principales: McCaskey, Michael A., Schuster-Amft, Corina, Wirth, Brigitte, de Bruin, Eling D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678691/
https://www.ncbi.nlm.nih.gov/pubmed/26666457
http://dx.doi.org/10.1186/s13063-015-1104-4
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author McCaskey, Michael A.
Schuster-Amft, Corina
Wirth, Brigitte
de Bruin, Eling D.
author_facet McCaskey, Michael A.
Schuster-Amft, Corina
Wirth, Brigitte
de Bruin, Eling D.
author_sort McCaskey, Michael A.
collection PubMed
description BACKGROUND: Sensorimotor training (SMT) is popularly applied as a preventive or rehabilitative exercise method in various sports and rehabilitation settings. Yet, there is only low-quality evidence on its effect on pain and function. This randomised controlled trial will investigate the effects of a theory-based SMT in rehabilitation of chronic (>3 months) non-specific low back pain (CNLBP) patients. METHODS/DESIGN: A pilot study with a parallel, single-blinded, randomised controlled design. Twenty adult patients referred to the clinic for CNLBP treatment will be included, randomised, and allocated to one of two groups. Each group will receive 9 x 30 minutes of standard physiotherapy (PT) treatment. The experimental group will receive an added 15 minutes of SMT. For SMT, proprioceptive postural exercises are performed on a labile platform with adjustable oscillation to provoke training effects on different entry levels. The active comparator group will perform 15 minutes of added sub-effective low-intensity endurance training. Outcomes are assessed on 4 time-points by a treatment blinded tester: eligibility assessment at baseline (BL) 2–4 days prior to intervention, pre-intervention assessment (T0), post-intervention assessment (T1), and at 4 weeks follow-up (FU). At BL, an additional healthy control group (n = 20) will be assessed to allow cross-sectional comparison with symptom-free participants. The main outcomes are self-reported pain (Visual Analogue Scale) and functional status (Oswestry Disability Index). For secondary analysis, postural control variables after an externally perturbed stance on a labile platform are analysed using a video-based marker tracking system and a pressure plate (sagittal joint-angle variability and centre of pressure confidence ellipse). Proprioception is measured as relative cervical joint repositioning error during a head-rotation task. Effect sizes and mixed-model MANOVA (2 groups × 4 measurements for 5 dependent variables) will be calculated. DISCUSSION: This is the first attempt to systematically investigate effects of a theory-based sensorimotor training in patients with CNLBP. It will provide analysis of several postural segments during a dynamic task for quantitative analysis of quality and change of the task performance in relation to changes in pain and functional status. TRIAL REGISTRATION: Trial registry number on cliniclatrials.gov is NCT02304120, first registered on 17 November 2014.
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spelling pubmed-46786912015-12-16 Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial McCaskey, Michael A. Schuster-Amft, Corina Wirth, Brigitte de Bruin, Eling D. Trials Study Protocol BACKGROUND: Sensorimotor training (SMT) is popularly applied as a preventive or rehabilitative exercise method in various sports and rehabilitation settings. Yet, there is only low-quality evidence on its effect on pain and function. This randomised controlled trial will investigate the effects of a theory-based SMT in rehabilitation of chronic (>3 months) non-specific low back pain (CNLBP) patients. METHODS/DESIGN: A pilot study with a parallel, single-blinded, randomised controlled design. Twenty adult patients referred to the clinic for CNLBP treatment will be included, randomised, and allocated to one of two groups. Each group will receive 9 x 30 minutes of standard physiotherapy (PT) treatment. The experimental group will receive an added 15 minutes of SMT. For SMT, proprioceptive postural exercises are performed on a labile platform with adjustable oscillation to provoke training effects on different entry levels. The active comparator group will perform 15 minutes of added sub-effective low-intensity endurance training. Outcomes are assessed on 4 time-points by a treatment blinded tester: eligibility assessment at baseline (BL) 2–4 days prior to intervention, pre-intervention assessment (T0), post-intervention assessment (T1), and at 4 weeks follow-up (FU). At BL, an additional healthy control group (n = 20) will be assessed to allow cross-sectional comparison with symptom-free participants. The main outcomes are self-reported pain (Visual Analogue Scale) and functional status (Oswestry Disability Index). For secondary analysis, postural control variables after an externally perturbed stance on a labile platform are analysed using a video-based marker tracking system and a pressure plate (sagittal joint-angle variability and centre of pressure confidence ellipse). Proprioception is measured as relative cervical joint repositioning error during a head-rotation task. Effect sizes and mixed-model MANOVA (2 groups × 4 measurements for 5 dependent variables) will be calculated. DISCUSSION: This is the first attempt to systematically investigate effects of a theory-based sensorimotor training in patients with CNLBP. It will provide analysis of several postural segments during a dynamic task for quantitative analysis of quality and change of the task performance in relation to changes in pain and functional status. TRIAL REGISTRATION: Trial registry number on cliniclatrials.gov is NCT02304120, first registered on 17 November 2014. BioMed Central 2015-12-15 /pmc/articles/PMC4678691/ /pubmed/26666457 http://dx.doi.org/10.1186/s13063-015-1104-4 Text en © McCaskey et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
McCaskey, Michael A.
Schuster-Amft, Corina
Wirth, Brigitte
de Bruin, Eling D.
Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial
title Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial
title_full Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial
title_fullStr Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial
title_full_unstemmed Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial
title_short Effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial
title_sort effects of postural specific sensorimotor training in patients with chronic low back pain: study protocol for randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678691/
https://www.ncbi.nlm.nih.gov/pubmed/26666457
http://dx.doi.org/10.1186/s13063-015-1104-4
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