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Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial
Poor intervertebral disc (IVD) health is associated with low back pain (LBP). This 12-week parallel randomised controlled trial will evaluate the efficacy of a progressive interval running programme on IVD health and other clinical outcomes in adults with chronic LBP. Participants will be randomised...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853241/ https://www.ncbi.nlm.nih.gov/pubmed/36684712 http://dx.doi.org/10.1136/bmjsem-2022-001524 |
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author | Tagliaferri, Scott D Belavy, Daniel L Bowe, Steven J Clarkson, Matthew J Connell, David Craige, Emma A Gollan, Romina Main, Luana C Miller, Clint T Mitchell, Ulrike H Mundell, Niamh L Neason, Christopher Samanna, Claire L Scott, David Tait, Jamie L Vincent, Grace E Owen, Patrick J |
author_facet | Tagliaferri, Scott D Belavy, Daniel L Bowe, Steven J Clarkson, Matthew J Connell, David Craige, Emma A Gollan, Romina Main, Luana C Miller, Clint T Mitchell, Ulrike H Mundell, Niamh L Neason, Christopher Samanna, Claire L Scott, David Tait, Jamie L Vincent, Grace E Owen, Patrick J |
author_sort | Tagliaferri, Scott D |
collection | PubMed |
description | Poor intervertebral disc (IVD) health is associated with low back pain (LBP). This 12-week parallel randomised controlled trial will evaluate the efficacy of a progressive interval running programme on IVD health and other clinical outcomes in adults with chronic LBP. Participants will be randomised to either a digitally delivered progressive interval running programme or waitlist control. Participants randomised to the running programme will receive three individually tailored 30 min community-based sessions per week over 12 weeks. The waitlist control will undergo no formal intervention. All participants will be assessed at baseline, 6 and 12 weeks. Primary outcomes are IVD health (lumbar IVD T2 via MRI), average LBP intensity over the prior week (100-point visual analogue scale) and disability (Oswestry Disability Index). Secondary outcomes include a range of clinical measures. All outcomes will be analysed using linear mixed models. This study has received ethical approval from the Deakin University Human Research Ethics Committee (ID: 2022-162). All participants will provide informed written consent before participation. Regardless of the results, the findings of this study will be disseminated, and anonymised data will be shared via an online repository. This will be the first study to evaluate whether a progressive interval running programme can improve IVD health in adults with chronic LBP. Identifying conservative options to improve IVD health in this susceptible population group has the potential to markedly reduce the burden of disease. This study was registered via the Australian New Zealand Clinical Trials Registry on 29 September 2022 (ACTRN12622001276741). |
format | Online Article Text |
id | pubmed-9853241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-98532412023-01-21 Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial Tagliaferri, Scott D Belavy, Daniel L Bowe, Steven J Clarkson, Matthew J Connell, David Craige, Emma A Gollan, Romina Main, Luana C Miller, Clint T Mitchell, Ulrike H Mundell, Niamh L Neason, Christopher Samanna, Claire L Scott, David Tait, Jamie L Vincent, Grace E Owen, Patrick J BMJ Open Sport Exerc Med Protocol Poor intervertebral disc (IVD) health is associated with low back pain (LBP). This 12-week parallel randomised controlled trial will evaluate the efficacy of a progressive interval running programme on IVD health and other clinical outcomes in adults with chronic LBP. Participants will be randomised to either a digitally delivered progressive interval running programme or waitlist control. Participants randomised to the running programme will receive three individually tailored 30 min community-based sessions per week over 12 weeks. The waitlist control will undergo no formal intervention. All participants will be assessed at baseline, 6 and 12 weeks. Primary outcomes are IVD health (lumbar IVD T2 via MRI), average LBP intensity over the prior week (100-point visual analogue scale) and disability (Oswestry Disability Index). Secondary outcomes include a range of clinical measures. All outcomes will be analysed using linear mixed models. This study has received ethical approval from the Deakin University Human Research Ethics Committee (ID: 2022-162). All participants will provide informed written consent before participation. Regardless of the results, the findings of this study will be disseminated, and anonymised data will be shared via an online repository. This will be the first study to evaluate whether a progressive interval running programme can improve IVD health in adults with chronic LBP. Identifying conservative options to improve IVD health in this susceptible population group has the potential to markedly reduce the burden of disease. This study was registered via the Australian New Zealand Clinical Trials Registry on 29 September 2022 (ACTRN12622001276741). BMJ Publishing Group 2023-01-17 /pmc/articles/PMC9853241/ /pubmed/36684712 http://dx.doi.org/10.1136/bmjsem-2022-001524 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Protocol Tagliaferri, Scott D Belavy, Daniel L Bowe, Steven J Clarkson, Matthew J Connell, David Craige, Emma A Gollan, Romina Main, Luana C Miller, Clint T Mitchell, Ulrike H Mundell, Niamh L Neason, Christopher Samanna, Claire L Scott, David Tait, Jamie L Vincent, Grace E Owen, Patrick J Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial |
title | Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial |
title_full | Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial |
title_fullStr | Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial |
title_full_unstemmed | Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial |
title_short | Assessing safety and treatment efficacy of running on intervertebral discs (ASTEROID) in adults with chronic low back pain: protocol for a randomised controlled trial |
title_sort | assessing safety and treatment efficacy of running on intervertebral discs (asteroid) in adults with chronic low back pain: protocol for a randomised controlled trial |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853241/ https://www.ncbi.nlm.nih.gov/pubmed/36684712 http://dx.doi.org/10.1136/bmjsem-2022-001524 |
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