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Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention

Interventions developed to improve disability outcomes for low back pain (LBP) often show only small effects. Mediation analysis was used to investigate what led to the effectiveness of the Stratified Targeted Treatment (STarT) Back trial, a large primary care-based trial that treated patients consu...

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Autores principales: Mansell, Gemma, Hill, Jonathan C., Main, Chris, Vowles, Kevin E., van der Windt, Daniëlle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Churchill Livingstone 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123895/
https://www.ncbi.nlm.nih.gov/pubmed/27565304
http://dx.doi.org/10.1016/j.jpain.2016.08.005
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author Mansell, Gemma
Hill, Jonathan C.
Main, Chris
Vowles, Kevin E.
van der Windt, Daniëlle
author_facet Mansell, Gemma
Hill, Jonathan C.
Main, Chris
Vowles, Kevin E.
van der Windt, Daniëlle
author_sort Mansell, Gemma
collection PubMed
description Interventions developed to improve disability outcomes for low back pain (LBP) often show only small effects. Mediation analysis was used to investigate what led to the effectiveness of the Stratified Targeted Treatment (STarT) Back trial, a large primary care-based trial that treated patients consulting with LBP according to their risk of a poor outcome. The high-risk subgroup, randomized to receive either psychologically-informed physiotherapy (n = 93) or current best care (n = 45), was investigated to explore pain-related distress and pain intensity as potential mediators of the relationship between treatment allocation and change in disability. Structural equation modeling was used to generate latent variables of pain-related distress and pain intensity from measures used to identify patients at high risk (fear-avoidance beliefs, depression, anxiety, and catastrophizing thoughts). Outcome was measured using the Roland–Morris Disability Questionnaire. Change in pain-related distress and pain intensity were found to have a significant mediating effect of .25 (standardized estimate, bootstrapped 95% confidence interval, .09–.39) on the relationship between treatment group allocation and change in disability outcome. This study adds to the evidence base of treatment mediation studies in pain research and the role of distress in influencing disability outcome in those with complex LBP. PERSPECTIVE: Mediation analysis using structural equation modeling found that change in pain-related distress and pain intensity mediated treatment effect in the STarT Back trial. This type of analysis can be used to gain further insight into how interventions work, and lead to the design of more effective interventions in future.
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spelling pubmed-51238952016-11-29 Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention Mansell, Gemma Hill, Jonathan C. Main, Chris Vowles, Kevin E. van der Windt, Daniëlle J Pain Original Report Interventions developed to improve disability outcomes for low back pain (LBP) often show only small effects. Mediation analysis was used to investigate what led to the effectiveness of the Stratified Targeted Treatment (STarT) Back trial, a large primary care-based trial that treated patients consulting with LBP according to their risk of a poor outcome. The high-risk subgroup, randomized to receive either psychologically-informed physiotherapy (n = 93) or current best care (n = 45), was investigated to explore pain-related distress and pain intensity as potential mediators of the relationship between treatment allocation and change in disability. Structural equation modeling was used to generate latent variables of pain-related distress and pain intensity from measures used to identify patients at high risk (fear-avoidance beliefs, depression, anxiety, and catastrophizing thoughts). Outcome was measured using the Roland–Morris Disability Questionnaire. Change in pain-related distress and pain intensity were found to have a significant mediating effect of .25 (standardized estimate, bootstrapped 95% confidence interval, .09–.39) on the relationship between treatment group allocation and change in disability outcome. This study adds to the evidence base of treatment mediation studies in pain research and the role of distress in influencing disability outcome in those with complex LBP. PERSPECTIVE: Mediation analysis using structural equation modeling found that change in pain-related distress and pain intensity mediated treatment effect in the STarT Back trial. This type of analysis can be used to gain further insight into how interventions work, and lead to the design of more effective interventions in future. Churchill Livingstone 2016-11 /pmc/articles/PMC5123895/ /pubmed/27565304 http://dx.doi.org/10.1016/j.jpain.2016.08.005 Text en © The American Pain Society. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Report
Mansell, Gemma
Hill, Jonathan C.
Main, Chris
Vowles, Kevin E.
van der Windt, Daniëlle
Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention
title Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention
title_full Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention
title_fullStr Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention
title_full_unstemmed Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention
title_short Exploring What Factors Mediate Treatment Effect: Example of the STarT Back Study High-Risk Intervention
title_sort exploring what factors mediate treatment effect: example of the start back study high-risk intervention
topic Original Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123895/
https://www.ncbi.nlm.nih.gov/pubmed/27565304
http://dx.doi.org/10.1016/j.jpain.2016.08.005
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