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dc.creatorGarcía-Muñoz, Cristinaes
dc.creatorCasuso-Holgado, María Jesúses
dc.creatorHernández Rodríguez, Juan Carloses
dc.creatorPiñero Pinto, Elenaes
dc.creatorPalomo-Carrión, Rocíoes
dc.creatorCortés Vega, María Doloreses
dc.date.accessioned2022-11-17T17:28:59Z
dc.date.available2022-11-17T17:28:59Z
dc.date.issued2021-10
dc.identifier.citationGarcía-Muñoz, C., Casuso-Holgado, M.J., Hernández Rodríguez, J.C., Piñero Pinto, E., Palomo-Carrión, R. y Cortés Vega, M.D. (2021). Feasibility and safety of an immersive virtual reality-based vestibular rehabilitation programme in people with multiple sclerosis experiencing vestibular impairment: a protocol for a pilot randomised controlled trial. BMJ Open, 11 (11), e051478. https://doi.org/10.1136/bmjopen-2021-051478.
dc.identifier.issn2044-6055es
dc.identifier.urihttps://hdl.handle.net/11441/139575
dc.description.abstractIntroduction: Vestibular system damage in patients with multiple sclerosis (MS) may have a central and/or peripheral origin. Subsequent vestibular impairments may contribute to dizziness, balance disorders and fatigue in this population. Vestibular rehabilitation targeting vestibular impairments may improve these symptoms. Furthermore, as a successful tool in neurological rehabilitation, immersive virtual reality (VRi) could also be implemented within a vestibular rehabilitation intervention. Methods and analysis: This protocol describes a parallel-arm, pilot randomised controlled trial, with blinded assessments, in 30 patients with MS with vestibular impairment (Dizziness Handicap Inventory ≥16). The experimental group will receive a VRi vestibular rehabilitation intervention based on the conventional Cawthorne-Cooksey protocol; the control group will perform the conventional protocol. The duration of the intervention in both groups will be 7 weeks (20 sessions, 3 sessions/week). The primary outcomes are the feasibility and safety of the vestibular VRi intervention in patients with MS. Secondary outcome measures are dizziness symptoms, balance performance, fatigue and quality of life. Quantitative assessment will be carried out at baseline (T0), immediately after intervention (T1), and after a follow-up period of 3 and 6 months (T2 and T3). Additionally, in order to further examine the feasibility of the intervention, a qualitative assessment will be performed at T1. Ethics and dissemination: The study was approved by the Andalusian Review Board and Ethics Committee, Virgen Macarena-Virgen del Rocio Hospitals (ID 2148-N-19, 25 March 2020). Informed consent will be collected from participants who wish to participate in the research. The results of this research will be disseminated by publication in peer-reviewed scientific journals.es
dc.formatapplication/pdfes
dc.format.extent12 p.es
dc.language.isoenges
dc.publisherBMJ Publishing Groupes
dc.relation.ispartofBMJ Open, 11 (11), e051478.
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.titleFeasibility and safety of an immersive virtual reality-based vestibular rehabilitation programme in people with multiple sclerosis experiencing vestibular impairment: a protocol for a pilot randomised controlled triales
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Fisioterapiaes
dc.relation.publisherversionhttps://bmjopen.bmj.com/content/11/11/e051478es
dc.identifier.doi10.1136/bmjopen-2021-051478es
dc.journaltitleBMJ Openes
dc.publication.volumen11es
dc.publication.issue11es
dc.publication.initialPagee051478es

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