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Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial

Background: The therapeutic approach to chronic aspecific low back pain (CALBP) has to consider the multifactorial aetiology of the disorder. International guidelines do not agree on unequivocal treatment indications. Recommendations for fascial therapy are few and of low level evidence but several...

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Autores principales: Branchini, Mirco, Lopopolo, Francesca, Andreoli, Ernesto, Loreti, Ivano, Marchand, Aurélie M, Stecco, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706049/
https://www.ncbi.nlm.nih.gov/pubmed/26834998
http://dx.doi.org/10.12688/f1000research.6890.2
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author Branchini, Mirco
Lopopolo, Francesca
Andreoli, Ernesto
Loreti, Ivano
Marchand, Aurélie M
Stecco, Antonio
author_facet Branchini, Mirco
Lopopolo, Francesca
Andreoli, Ernesto
Loreti, Ivano
Marchand, Aurélie M
Stecco, Antonio
author_sort Branchini, Mirco
collection PubMed
description Background: The therapeutic approach to chronic aspecific low back pain (CALBP) has to consider the multifactorial aetiology of the disorder. International guidelines do not agree on unequivocal treatment indications. Recommendations for fascial therapy are few and of low level evidence but several studies indicate strong correlations between fascial thickness and low back pain. This study aims at comparing the effectiveness of Fascial Manipulation® associated with a physiotherapy program following guidelines for CALBP compared to a physiotherapy program alone. Methods: 24 subjects were randomized into two groups, both received eight treatments over 4 weeks. Outcomes were measured at baseline, at the end of therapy and at a 1 month and a 3 months follow-up. Pain was measured with the visual analogue scale (VAS) and the brief pain inventory (BPI), function with the Rolland-Morris disability questionnaire (RMDQ), state of well-being with the short-form 36 health-survey (SF-36). The mean clinical important difference (MCID) was also measured. Results: Patients receiving Fascial Manipulation® showed statistically and clinically significant improvements at the end of care for all outcomes, in the short (RMDQ, VAS, BPI) and medium term for VAS and BPI compared to manual therapy. The MCID show significant improvements in the means and percentage of subjects in groups in all outcomes post-treatment, in the short and medium term. Conclusion: Fascial tissues were implicated in the aetiology of CALBP and treatment led to decreased symptomatic, improved functional and perceived well-being outcomes that were of greater amplitude compared to manual therapy alone.
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spelling pubmed-47060492016-01-29 Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial Branchini, Mirco Lopopolo, Francesca Andreoli, Ernesto Loreti, Ivano Marchand, Aurélie M Stecco, Antonio F1000Res Research Article Background: The therapeutic approach to chronic aspecific low back pain (CALBP) has to consider the multifactorial aetiology of the disorder. International guidelines do not agree on unequivocal treatment indications. Recommendations for fascial therapy are few and of low level evidence but several studies indicate strong correlations between fascial thickness and low back pain. This study aims at comparing the effectiveness of Fascial Manipulation® associated with a physiotherapy program following guidelines for CALBP compared to a physiotherapy program alone. Methods: 24 subjects were randomized into two groups, both received eight treatments over 4 weeks. Outcomes were measured at baseline, at the end of therapy and at a 1 month and a 3 months follow-up. Pain was measured with the visual analogue scale (VAS) and the brief pain inventory (BPI), function with the Rolland-Morris disability questionnaire (RMDQ), state of well-being with the short-form 36 health-survey (SF-36). The mean clinical important difference (MCID) was also measured. Results: Patients receiving Fascial Manipulation® showed statistically and clinically significant improvements at the end of care for all outcomes, in the short (RMDQ, VAS, BPI) and medium term for VAS and BPI compared to manual therapy. The MCID show significant improvements in the means and percentage of subjects in groups in all outcomes post-treatment, in the short and medium term. Conclusion: Fascial tissues were implicated in the aetiology of CALBP and treatment led to decreased symptomatic, improved functional and perceived well-being outcomes that were of greater amplitude compared to manual therapy alone. F1000Research 2016-01-08 /pmc/articles/PMC4706049/ /pubmed/26834998 http://dx.doi.org/10.12688/f1000research.6890.2 Text en Copyright: © 2016 Branchini M et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Branchini, Mirco
Lopopolo, Francesca
Andreoli, Ernesto
Loreti, Ivano
Marchand, Aurélie M
Stecco, Antonio
Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial
title Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial
title_full Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial
title_fullStr Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial
title_full_unstemmed Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial
title_short Fascial Manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial
title_sort fascial manipulation® for chronic aspecific low back pain: a single blinded randomized controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706049/
https://www.ncbi.nlm.nih.gov/pubmed/26834998
http://dx.doi.org/10.12688/f1000research.6890.2
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