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The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial
BACKGROUND: Low back pain (LBP) is costly to society and improving patient outcomes is a priority. Stratifying LBP patients into more homogenous groups is advocated to improve patient outcome. The STarT Back tool, a prognostic screening tool has demonstrated efficacy and greater cost effectiveness i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029484/ https://www.ncbi.nlm.nih.gov/pubmed/24308746 http://dx.doi.org/10.1186/1471-2474-14-342 |
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author | Murphy, Susan E Blake, Catherine Power, Camillus K Fullen, Brona M |
author_facet | Murphy, Susan E Blake, Catherine Power, Camillus K Fullen, Brona M |
author_sort | Murphy, Susan E |
collection | PubMed |
description | BACKGROUND: Low back pain (LBP) is costly to society and improving patient outcomes is a priority. Stratifying LBP patients into more homogenous groups is advocated to improve patient outcome. The STarT Back tool, a prognostic screening tool has demonstrated efficacy and greater cost effectiveness in physiotherapy settings. The management of LBP patients in groups is common but to date the utility of the STarT Back tool in group settings has not been explored. The aim of this study is to determine if the implementation of ‘stratified care’ when delivered in a group setting will lead to significantly better physical and psychological outcomes and greater cost effectiveness in LBP patients compared to a bestcare historical control group. METHODS/DESIGN: This study is a non randomised controlled trial. Low back pain patients recruited from the Waterford Primary Care area (population = 47,000) will be stratified into low, medium or high risk of persisting symptoms using the STarT Back Tool. Low risk patients will be offered a single one off education/exercise class offering positive messages on LBP management in line with recommended guidelines. Medium risk patients will be offered a 12 week group exercise/education intervention addressing their dominant physical obstacles to recovery. A 12 week group cognitive behavioural approach will be delivered to the high risk patients, characterised by the presence of high levels of psychosocial prognostic factors. These patients will be compared with a historical control group where therapists were blinded as to the risk stratification of patients and a generic group intervention was delivered to all patients, irrespective of their initial risk stratification. The primary outcome measure will be disability (Roland Morris Disability Questionnaire). Secondary outcomes will include back pain intensity (Visual Analogue Scale), distress (Distress and Risk Assessment Method), back beliefs (Back Beliefs Questionnaire), health status (Euroqol), global benefit (7 point likert scale), satisfaction (7 point likert scale), cost effectiveness and functional status. Outcome will be measured at baseline, 12 weeks and 6 months. DISCUSSION: This paper details the rationale, design, methods, planned analysis and operational aspects of a study examining the utility of the STarT Back Tool as a ‘stratification tool for targeted treatment’ in a group intervention. TRIAL REGISTRATION: Current controlled trials: ACTRN12613000431729. |
format | Online Article Text |
id | pubmed-4029484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40294842014-05-22 The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial Murphy, Susan E Blake, Catherine Power, Camillus K Fullen, Brona M BMC Musculoskelet Disord Study Protocol BACKGROUND: Low back pain (LBP) is costly to society and improving patient outcomes is a priority. Stratifying LBP patients into more homogenous groups is advocated to improve patient outcome. The STarT Back tool, a prognostic screening tool has demonstrated efficacy and greater cost effectiveness in physiotherapy settings. The management of LBP patients in groups is common but to date the utility of the STarT Back tool in group settings has not been explored. The aim of this study is to determine if the implementation of ‘stratified care’ when delivered in a group setting will lead to significantly better physical and psychological outcomes and greater cost effectiveness in LBP patients compared to a bestcare historical control group. METHODS/DESIGN: This study is a non randomised controlled trial. Low back pain patients recruited from the Waterford Primary Care area (population = 47,000) will be stratified into low, medium or high risk of persisting symptoms using the STarT Back Tool. Low risk patients will be offered a single one off education/exercise class offering positive messages on LBP management in line with recommended guidelines. Medium risk patients will be offered a 12 week group exercise/education intervention addressing their dominant physical obstacles to recovery. A 12 week group cognitive behavioural approach will be delivered to the high risk patients, characterised by the presence of high levels of psychosocial prognostic factors. These patients will be compared with a historical control group where therapists were blinded as to the risk stratification of patients and a generic group intervention was delivered to all patients, irrespective of their initial risk stratification. The primary outcome measure will be disability (Roland Morris Disability Questionnaire). Secondary outcomes will include back pain intensity (Visual Analogue Scale), distress (Distress and Risk Assessment Method), back beliefs (Back Beliefs Questionnaire), health status (Euroqol), global benefit (7 point likert scale), satisfaction (7 point likert scale), cost effectiveness and functional status. Outcome will be measured at baseline, 12 weeks and 6 months. DISCUSSION: This paper details the rationale, design, methods, planned analysis and operational aspects of a study examining the utility of the STarT Back Tool as a ‘stratification tool for targeted treatment’ in a group intervention. TRIAL REGISTRATION: Current controlled trials: ACTRN12613000431729. BioMed Central 2013-12-05 /pmc/articles/PMC4029484/ /pubmed/24308746 http://dx.doi.org/10.1186/1471-2474-14-342 Text en Copyright © 2013 Murphy 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 Murphy, Susan E Blake, Catherine Power, Camillus K Fullen, Brona M The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial |
title | The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial |
title_full | The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial |
title_fullStr | The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial |
title_full_unstemmed | The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial |
title_short | The effectiveness of a stratified group intervention using the STarTBack screening tool in patients with LBP - a non randomised controlled trial |
title_sort | effectiveness of a stratified group intervention using the startback screening tool in patients with lbp - a non randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029484/ https://www.ncbi.nlm.nih.gov/pubmed/24308746 http://dx.doi.org/10.1186/1471-2474-14-342 |
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