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Long-term improvements following a residential combined physical and psychological programme for chronic low back pain
OBJECTIVES: Evaluate the outcomes and explore experiences of patients undergoing a residential combined physical and psychological programme (CPPP) for chronic low back pain. DESIGN: A longitudinal observational cohort design, with a parallel qualitative design using semistructured interviews. SETTI...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112434/ https://www.ncbi.nlm.nih.gov/pubmed/33972364 http://dx.doi.org/10.1136/bmjoq-2020-001068 |
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author | Wellburn, Shaun Ryan, Cormac G Coxon, Andrew Dickson, Alastair J Dickson, D John Fatoye, Francis Ferguson, Diarmaid Green, Paul W Greenhough, Charles Hamilton, Sharon Jess, Mary-Anne Jones, Andrea Peat, Glynis Martin, Denis J |
author_facet | Wellburn, Shaun Ryan, Cormac G Coxon, Andrew Dickson, Alastair J Dickson, D John Fatoye, Francis Ferguson, Diarmaid Green, Paul W Greenhough, Charles Hamilton, Sharon Jess, Mary-Anne Jones, Andrea Peat, Glynis Martin, Denis J |
author_sort | Wellburn, Shaun |
collection | PubMed |
description | OBJECTIVES: Evaluate the outcomes and explore experiences of patients undergoing a residential combined physical and psychological programme (CPPP) for chronic low back pain. DESIGN: A longitudinal observational cohort design, with a parallel qualitative design using semistructured interviews. SETTING: Residential, multimodal rehabilitation. PARTICIPANTS: 136 adults (62 male/74 female) referred to the CPPP, 100 (44 male/56 female) of whom completed the programme, during the term of the study. Ten (2 male/8 female) participated in the qualitative evaluation. INTERVENTION: A 3-week residential CPPP. OUTCOME MEASURES: Primary outcome measures were the STarT Back screening tool score; pain intensity—11-point Numerical Rating Scale; function—Oswestry Disability Index (ODI); health status/quality of life—EQ-5D-5L EuroQol five-Dimension-five level; anxiety—Generalised Anxiety Disorder-7; depression—Patient Health Questionnaire-9. Secondary outcome measures were the Global Subjective Outcome Scale; National Health Service Friends and Family Test;. RESULTS: At discharge, 6 and 12 months follow ups, there were improvements from baseline that were greater than minimum clinically important differences in each of the outcomes (with the sole exception of ODI at discharge). At 12 months, the majority of people considered themselves a lot better (57%) and were extremely likely (86%) to recommend the programme to a friend. The qualitative data showed praise for the residential nature of the intervention and the opportunities for interaction with peers and peer support. There were testimonies of improvements in understanding of pain and how to manage it better. Some participants said they had reduced, or stopped, medication they had been taking to manage their pain. CONCLUSIONS: Participants improved, and maintained long term, beyond minimum clinically important differences on a wide range of outcomes. Participants reported an enhanced ability to self-manage their back pain and support for the residential setting. |
format | Online Article Text |
id | pubmed-8112434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-81124342021-05-25 Long-term improvements following a residential combined physical and psychological programme for chronic low back pain Wellburn, Shaun Ryan, Cormac G Coxon, Andrew Dickson, Alastair J Dickson, D John Fatoye, Francis Ferguson, Diarmaid Green, Paul W Greenhough, Charles Hamilton, Sharon Jess, Mary-Anne Jones, Andrea Peat, Glynis Martin, Denis J BMJ Open Qual Original Research OBJECTIVES: Evaluate the outcomes and explore experiences of patients undergoing a residential combined physical and psychological programme (CPPP) for chronic low back pain. DESIGN: A longitudinal observational cohort design, with a parallel qualitative design using semistructured interviews. SETTING: Residential, multimodal rehabilitation. PARTICIPANTS: 136 adults (62 male/74 female) referred to the CPPP, 100 (44 male/56 female) of whom completed the programme, during the term of the study. Ten (2 male/8 female) participated in the qualitative evaluation. INTERVENTION: A 3-week residential CPPP. OUTCOME MEASURES: Primary outcome measures were the STarT Back screening tool score; pain intensity—11-point Numerical Rating Scale; function—Oswestry Disability Index (ODI); health status/quality of life—EQ-5D-5L EuroQol five-Dimension-five level; anxiety—Generalised Anxiety Disorder-7; depression—Patient Health Questionnaire-9. Secondary outcome measures were the Global Subjective Outcome Scale; National Health Service Friends and Family Test;. RESULTS: At discharge, 6 and 12 months follow ups, there were improvements from baseline that were greater than minimum clinically important differences in each of the outcomes (with the sole exception of ODI at discharge). At 12 months, the majority of people considered themselves a lot better (57%) and were extremely likely (86%) to recommend the programme to a friend. The qualitative data showed praise for the residential nature of the intervention and the opportunities for interaction with peers and peer support. There were testimonies of improvements in understanding of pain and how to manage it better. Some participants said they had reduced, or stopped, medication they had been taking to manage their pain. CONCLUSIONS: Participants improved, and maintained long term, beyond minimum clinically important differences on a wide range of outcomes. Participants reported an enhanced ability to self-manage their back pain and support for the residential setting. BMJ Publishing Group 2021-05-10 /pmc/articles/PMC8112434/ /pubmed/33972364 http://dx.doi.org/10.1136/bmjoq-2020-001068 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Wellburn, Shaun Ryan, Cormac G Coxon, Andrew Dickson, Alastair J Dickson, D John Fatoye, Francis Ferguson, Diarmaid Green, Paul W Greenhough, Charles Hamilton, Sharon Jess, Mary-Anne Jones, Andrea Peat, Glynis Martin, Denis J Long-term improvements following a residential combined physical and psychological programme for chronic low back pain |
title | Long-term improvements following a residential combined physical and psychological programme for chronic low back pain |
title_full | Long-term improvements following a residential combined physical and psychological programme for chronic low back pain |
title_fullStr | Long-term improvements following a residential combined physical and psychological programme for chronic low back pain |
title_full_unstemmed | Long-term improvements following a residential combined physical and psychological programme for chronic low back pain |
title_short | Long-term improvements following a residential combined physical and psychological programme for chronic low back pain |
title_sort | long-term improvements following a residential combined physical and psychological programme for chronic low back pain |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112434/ https://www.ncbi.nlm.nih.gov/pubmed/33972364 http://dx.doi.org/10.1136/bmjoq-2020-001068 |
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