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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...

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Autores principales: Andersen, Tonny Elmose, Ellegaard, Hanne, Schiøttz-Christensen, Berit, Mejldal, Anna, Manniche, Claus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
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.
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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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