Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study
IntroductionA relevant subsample of patients with chronic low back pain (CLBP) have manifested augmented central pain processing, central sensitisation (CS). Patients with CLBP have limited functioning and participation. Theoretically, physical functioning in patients with CLBP can plausibly be link...
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doaj-35d4b713c8a144c39bb64598821856c42021-06-02T11:30:59ZengBMJ Publishing GroupBMJ Open2044-60552020-03-0110310.1136/bmjopen-2019-031592Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort studyMichiel F Reneman0Jone Ansuategui Echeita1Henrica R Schiphorst Preuper2Rienk Dekker3Ilse Stuive4Hans Timmerman5Andre P Wolff63 Department of Rehabilitation Medicine, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands Department of Rehabilitation Medicine, University of Groningen, University Medical Center Groningen, Groningen, The NetherlandsDepartment of Rehabilitation Medicine, University of Groningen, University Medical Center Groningen, Groningen, The NetherlandsDepartment of Rehabilitation Medicine, University of Groningen, University Medical Center Groningen, Groningen, The NetherlandsDepartment of Rehabilitation Medicine, University of Groningen, University Medical Center Groningen, Groningen, The NetherlandsDepartment of Anesthesiology, Pain and Palliative Medicine, Radboud University Medical Center, Nijmegen, The NetherlandsDepartment of Anesthesiology Pain Center, University of Groningen, University Medical Center Groningen, Groningen, The NetherlandsIntroductionA relevant subsample of patients with chronic low back pain (CLBP) have manifested augmented central pain processing, central sensitisation (CS). Patients with CLBP have limited functioning and participation. Theoretically, physical functioning in patients with CLBP can plausibly be linked to CS; however, evidence to explain such association is scarce. Moreover, there is no gold standard for CS diagnosis. The objectives of the study are: (1) to analyse the association between instruments assessing reference symptoms and signs attributed to CS; (2) to analyse whether reference symptoms and signs attributed to CS are associated with functioning measurement outcomes; and (3) to analyse whether changes (between baseline and discharge) in reference symptoms and signs attributed to CS are related to changes in each of the functioning measurement outcomes.Methods and analysisA cross-sectional and longitudinal observational study is performed with measurements taken at baseline and discharge of an interdisciplinary rehabilitation programme. A sample size of 110 adult patients with CLBP has been calculated for the study. CS measurements are: Central Sensitisation Inventory, quantitative sensory testing and heart rate variability. Functioning measurements are: lifting capacity, maximal aerobic capacity, accelerometry and reported functioning. Statistical analyses to be performed are: (1) correlation between CS measurements, (2) multiple regression between functioning (dependent variable) and CS measurements (independent variable), and (3) multiple regression between changes in scores of functioning (dependent variable) and CS measurements (independent variable), and corrected for sex and age.Ethics and disseminationThe study obtained the clearance to its implementation from the Medical Research Ethics Committee of the University Medical Center Groningen in July 2017. The results will be disseminated through scientific publications in peer-reviewed journals, presentations at relevant conferences, and reports to stakeholders.Trial registration numberNTR7167/NL6980.https://bmjopen.bmj.com/content/10/3/e031592.full |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Michiel F Reneman Jone Ansuategui Echeita Henrica R Schiphorst Preuper Rienk Dekker Ilse Stuive Hans Timmerman Andre P Wolff |
spellingShingle |
Michiel F Reneman Jone Ansuategui Echeita Henrica R Schiphorst Preuper Rienk Dekker Ilse Stuive Hans Timmerman Andre P Wolff Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study BMJ Open |
author_facet |
Michiel F Reneman Jone Ansuategui Echeita Henrica R Schiphorst Preuper Rienk Dekker Ilse Stuive Hans Timmerman Andre P Wolff |
author_sort |
Michiel F Reneman |
title |
Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study |
title_short |
Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study |
title_full |
Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study |
title_fullStr |
Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study |
title_full_unstemmed |
Central Sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study |
title_sort |
central sensitisation and functioning in patients with chronic low back pain: protocol for a cross-sectional and cohort study |
publisher |
BMJ Publishing Group |
series |
BMJ Open |
issn |
2044-6055 |
publishDate |
2020-03-01 |
description |
IntroductionA relevant subsample of patients with chronic low back pain (CLBP) have manifested augmented central pain processing, central sensitisation (CS). Patients with CLBP have limited functioning and participation. Theoretically, physical functioning in patients with CLBP can plausibly be linked to CS; however, evidence to explain such association is scarce. Moreover, there is no gold standard for CS diagnosis. The objectives of the study are: (1) to analyse the association between instruments assessing reference symptoms and signs attributed to CS; (2) to analyse whether reference symptoms and signs attributed to CS are associated with functioning measurement outcomes; and (3) to analyse whether changes (between baseline and discharge) in reference symptoms and signs attributed to CS are related to changes in each of the functioning measurement outcomes.Methods and analysisA cross-sectional and longitudinal observational study is performed with measurements taken at baseline and discharge of an interdisciplinary rehabilitation programme. A sample size of 110 adult patients with CLBP has been calculated for the study. CS measurements are: Central Sensitisation Inventory, quantitative sensory testing and heart rate variability. Functioning measurements are: lifting capacity, maximal aerobic capacity, accelerometry and reported functioning. Statistical analyses to be performed are: (1) correlation between CS measurements, (2) multiple regression between functioning (dependent variable) and CS measurements (independent variable), and (3) multiple regression between changes in scores of functioning (dependent variable) and CS measurements (independent variable), and corrected for sex and age.Ethics and disseminationThe study obtained the clearance to its implementation from the Medical Research Ethics Committee of the University Medical Center Groningen in July 2017. The results will be disseminated through scientific publications in peer-reviewed journals, presentations at relevant conferences, and reports to stakeholders.Trial registration numberNTR7167/NL6980. |
url |
https://bmjopen.bmj.com/content/10/3/e031592.full |
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