Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/81190
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dc.contributorDepartment of Rehabilitation Sciences-
dc.creatorPin, TW-
dc.creatorButler, PB-
dc.creatorPurves, S-
dc.date.accessioned2019-08-23T08:29:40Z-
dc.date.available2019-08-23T08:29:40Z-
dc.identifier.urihttp://hdl.handle.net/10397/81190-
dc.language.isoenen_US
dc.publisherBioMed Central Ltd.en_US
dc.rights© The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiveren_US
dc.rightsThe following publication Pin, T. W., Butler, P. B., & Purves, S. (2019). Use of whole body vibration therapy in individuals with moderate severity of cerebral palsy-a feasibility study. BMC neurology, 19(1), 80 is available at https://doi.org/10.1186/s12883-019-1307-5en_US
dc.subjectBalanceen_US
dc.subjectCerebral palsyen_US
dc.subjectFunctional abilitiesen_US
dc.subjectStatic standingen_US
dc.subjectWhole body vibrationen_US
dc.titleUse of whole body vibration therapy in individuals with moderate severity of cerebral palsy- a feasibility studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume19-
dc.identifier.issue1-
dc.identifier.doi10.1186/s12883-019-1307-5-
dcterms.abstractBackground: This pilot study was to examine the feasibility and tolerance of whole body vibration therapy (WBVT) for children and adults with moderate severity of cerebral palsy (CP) being graded as levels III or IV on the Gross Motor Function Classification Scale (GMFCS). Methods: Study participants received the additional WBVT when standing still on the vibration platform for three 3-min bouts of vibration (20 Hz, 2 mm amplitude), 4 days per week for 4 weeks. In addition to questions relating to feasibility and participants' opinions, assessment at baseline and completion of the intervention included the Gross Motor Function Measure-66 Item Set (GMFM-66 IS), 2-min walk test (2MWT), Timed Up and Go test (TUG) and Pediatric Evaluation of Disability Inventory (PEDI). Wilcoxon Signed Ranks test was used to compare the results. Results: Fourteen participants (mean age = 25.25 years SD 3.71; 9 males, 64%; GMFCS level III n = 13, 92%) were recruited and completed the study. The attendance rate was over 90% with no adverse events. All participants tolerated the protocol which was satisfactorily delivered in a clinical setting. Conclusions: The present WBVT protocol was feasible, safe and well-tolerated by the participants with moderate severity of CP, justifying future studies with larger samples and more rigorous study design. Trial registration: The present study has been registered under the ClinicalTrials.gov (NCT03375736) and the date of registration commenced on 18 December 2017.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBMC Neurology, 2019, v. 19, no. 1, 80-
dcterms.isPartOfBMC Neurology-
dcterms.issued2019-
dc.identifier.scopus2-s2.0-85065254682-
dc.identifier.pmid31043157-
dc.identifier.eissn1471-2377-
dc.identifier.artn80-
dc.description.validate201908 bcma-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.pubStatusPublisheden_US
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