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Somatic Experiencing® for patients with low back pain and comorbid posttraumatic stress symptoms – a randomised controlled trial
BACKGROUND: Low back pain (LBP) and comorbid post-traumatic stress symptoms (PTSS) are common after traumatic injuries, and a high level of PTSS is associated with more severe pain and pain-related disability. Few randomised controlled trials (RCT) exist targeting comorbid PTSS and chronic pain, and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473216/ https://www.ncbi.nlm.nih.gov/pubmed/33029333 http://dx.doi.org/10.1080/20008198.2020.1797306 |
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author | Andersen, Tonny Elmose Ellegaard, Hanne Schiøttz-Christensen, Berit Mejldal, Anna Manniche, Claus |
author_facet | Andersen, Tonny Elmose Ellegaard, Hanne Schiøttz-Christensen, Berit Mejldal, Anna Manniche, Claus |
author_sort | Andersen, Tonny Elmose |
collection | PubMed |
description | BACKGROUND: Low back pain (LBP) and comorbid post-traumatic stress symptoms (PTSS) are common after traumatic injuries, and a high level of PTSS is associated with more severe pain and pain-related disability. Few randomised controlled trials (RCT) exist targeting comorbid PTSS and chronic pain, and only one has assessed the effect of Somatic Experiencing®. OBJECTIVE: The aim of this study was to assess the effect of Somatic Experiencing® (up to 12 sessions) + physiotherapeutic intervention (4–8 sessions) (SE+PT) compared with the physiotherapeutic intervention alone (4–8 sessions) (PT) for pain-related disability in LBP with comorbid PTSS. METHODS: The study was a two-group RCT in which participants (n = 114) were recruited consecutively from a large Danish Spine Centre. Patients were randomly allocated to either SE+PT or PT alone. Outcomes were collected at baseline before randomisation, 6 and 12-month post-randomisation. The primary outcome was pain-related disability as measured with the modified version of the Roland Morris Disability Questionnaire at 6-month post-randomisation. Secondary outcomes were PTSS, pain intensity, pain-catastrophising, kinesiophobia, anxiety and depression. RESULTS: No significant group differences were found on any of the outcomes at any timepoints. Both groups achieved a significant reduction in pain-related disability (20–27%) as measured by the Roland Morris Disability Questionnaire at 6 and 12-month follow up. Also, both groups achieved a small reduction in PTSS. CONCLUSIONS: Although significant effects were achieved for both groups, the additional SE intervention did not result in any additional benefits in any of the outcomes. |
format | Online Article Text |
id | pubmed-7473216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74732162020-10-06 Somatic Experiencing® for patients with low back pain and comorbid posttraumatic stress symptoms – a randomised controlled trial Andersen, Tonny Elmose Ellegaard, Hanne Schiøttz-Christensen, Berit Mejldal, Anna Manniche, Claus Eur J Psychotraumatol Clinical Research Article BACKGROUND: Low back pain (LBP) and comorbid post-traumatic stress symptoms (PTSS) are common after traumatic injuries, and a high level of PTSS is associated with more severe pain and pain-related disability. Few randomised controlled trials (RCT) exist targeting comorbid PTSS and chronic pain, and only one has assessed the effect of Somatic Experiencing®. OBJECTIVE: The aim of this study was to assess the effect of Somatic Experiencing® (up to 12 sessions) + physiotherapeutic intervention (4–8 sessions) (SE+PT) compared with the physiotherapeutic intervention alone (4–8 sessions) (PT) for pain-related disability in LBP with comorbid PTSS. METHODS: The study was a two-group RCT in which participants (n = 114) were recruited consecutively from a large Danish Spine Centre. Patients were randomly allocated to either SE+PT or PT alone. Outcomes were collected at baseline before randomisation, 6 and 12-month post-randomisation. The primary outcome was pain-related disability as measured with the modified version of the Roland Morris Disability Questionnaire at 6-month post-randomisation. Secondary outcomes were PTSS, pain intensity, pain-catastrophising, kinesiophobia, anxiety and depression. RESULTS: No significant group differences were found on any of the outcomes at any timepoints. Both groups achieved a significant reduction in pain-related disability (20–27%) as measured by the Roland Morris Disability Questionnaire at 6 and 12-month follow up. Also, both groups achieved a small reduction in PTSS. CONCLUSIONS: Although significant effects were achieved for both groups, the additional SE intervention did not result in any additional benefits in any of the outcomes. Taylor & Francis 2020-08-18 /pmc/articles/PMC7473216/ /pubmed/33029333 http://dx.doi.org/10.1080/20008198.2020.1797306 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Research Article Andersen, Tonny Elmose Ellegaard, Hanne Schiøttz-Christensen, Berit Mejldal, Anna Manniche, Claus Somatic Experiencing® for patients with low back pain and comorbid posttraumatic stress symptoms – a randomised controlled trial |
title | Somatic Experiencing® for patients with low back pain and comorbid
posttraumatic stress symptoms – a randomised controlled trial |
title_full | Somatic Experiencing® for patients with low back pain and comorbid
posttraumatic stress symptoms – a randomised controlled trial |
title_fullStr | Somatic Experiencing® for patients with low back pain and comorbid
posttraumatic stress symptoms – a randomised controlled trial |
title_full_unstemmed | Somatic Experiencing® for patients with low back pain and comorbid
posttraumatic stress symptoms – a randomised controlled trial |
title_short | Somatic Experiencing® for patients with low back pain and comorbid
posttraumatic stress symptoms – a randomised controlled trial |
title_sort | somatic experiencing® for patients with low back pain and comorbid
posttraumatic stress symptoms – a randomised controlled trial |
topic | Clinical Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473216/ https://www.ncbi.nlm.nih.gov/pubmed/33029333 http://dx.doi.org/10.1080/20008198.2020.1797306 |
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