The effect of a six-week osteopathic visceral manipulation in patients with non-specific chronic low back pain and functional constipation: study protocol for a randomized controlled trial

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dc.creatorWalkyria Vilas Boas Fernandes
dc.creatorCleofás Rodríguez Blanco
dc.creatorFabiano Politti
dc.creatorFernanda de Córdoba Lanza
dc.creatorPaulo Roberto Garcia Lucareli
dc.creatorJoão Carlos Ferrari Corrêa
dc.date.accessioned2023-01-19T12:00:11Z
dc.date.accessioned2025-09-08T23:29:12Z
dc.date.available2023-01-19T12:00:11Z
dc.date.issued2018
dc.description.sponsorshipCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
dc.description.sponsorshipOutra Agência
dc.format.mimetypepdf
dc.identifier.doihttps://doi.org/10.1186/s13063-018-2532-8
dc.identifier.issn1745-6215
dc.identifier.urihttps://hdl.handle.net/1843/48982
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofTrials
dc.rightsAcesso Aberto
dc.subjectDor lombar
dc.subjectConstipação
dc.subjectTécnicas de relaxamento
dc.subjectEletromiografia
dc.subjectMedicina osteopática
dc.subject.otherVisceral manipulation
dc.subject.otherLow back pain
dc.subject.otherConstipation
dc.subject.otherFlexion-relaxation
dc.subject.otherElectromyography
dc.titleThe effect of a six-week osteopathic visceral manipulation in patients with non-specific chronic low back pain and functional constipation: study protocol for a randomized controlled trial
dc.typeArtigo de periódico
local.citation.epage8
local.citation.issue151
local.citation.spage1
local.citation.volume19
local.description.resumoBackground: The aim of the proposed study is to analyze the effect of a six-week osteopathic visceral manipulation (OVM) program on the flexion-relaxation phenomenon in individuals with non-specific chronic low back pain (LBP) and functional constipation. Methods/Design: An assessor-blinded, two-arm, randomized, placebo-controlled trial will be conducted. The sample will comprise 76 individuals with non-specific chronic LBP who have functional intestinal constipation, aged 18–65 years. The participants will be randomly allocated to two groups: (1) OVM and (2) sham OVM (SOVM). Evaluations will involve an interview, the Oswestry Disability Index, Fear-Avoidance Beliefs Questionnaire, functional constipation according to Rome III criteria, Biering-Sorensen test to normalize electromyographic (EMG) data, T12–L1 paraspinal level of the EMG signal during the flexion-relaxation phenomenon, 11-point numeric pain rating scale and fingertip-to-floor test. OVM and SOVM will be performed once per week for six weeks. Group 1 will receive OVM for 15 min and Group 2 will receive a sham visceral technique. Evaluations will be performed before and after the first session, after six weeks of treatment, and three months after randomization (follow-up). The findings will be analyzed statistically considering a 5% significance level (p ≤ 0.05). The limitation of the study is that the therapist will not be blinded. Discussion: This will be the first trial to analyze the clinical response and electromyographic signals during the flexion-relaxation phenomenon after OVM.
local.identifier.orcidhttps://orcid.org/0000-0002-8674-9180
local.identifier.orcidhttps://orcid.org/0000-0001-6383-0034
local.identifier.orcidhttps://orcid.org/0000-0002-4748-6947
local.identifier.orcidhttps://orcid.org/0000-0002-7148-575X
local.identifier.orcidhttps://orcid.org/0000-0002-8642-9814
local.publisher.countryBrasil
local.publisher.departmentEEF - DEPARTAMENTO DE FISIOTERAPIA
local.publisher.initialsUFMG
local.url.externahttps://trialsjournal.biomedcentral.com/articles/10.1186/s13063-018-2532-8

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