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dc.contributor.authorRodríguez-Molinero, Alejandroes_ES
dc.contributor.authorHernández-Vara, Jorgees_ES
dc.contributor.authorMiñarro, Antonioes_ES
dc.contributor.authorPérez-López, Carloses_ES
dc.contributor.authorBayes-Rusiñol, Àngelses_ES
dc.contributor.authorMartínez-Castrillo, Juan Carloses_ES
dc.contributor.authorPérez-Martínez, David Aes_ES
dc.contributor.authorInfante Ceberio, Jon es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-02-23T15:39:41Z
dc.date.available2022-02-23T15:39:41Z
dc.date.issued2021-07-19es_ES
dc.identifier.issn2044-6055es_ES
dc.identifier.urihttp://hdl.handle.net/10902/24035
dc.description.abstractIntroduction In recent years, multiple studies have aimed to develop and validate portable technological devices capable of monitoring the motor complications of Parkinson's disease patients (Parkinson's Holter). The effectiveness of these monitoring devices for improving clinical control is not known. Methods and analysis This is a single-blind, cluster-randomised controlled clinical trial. Neurologists from Spanish health centres will be randomly assigned to one of three study arms (1:1:1): (a) therapeutic adjustment using information from a Parkinson?s Holter that will be worn by their patients for 7 days, (b) therapeutic adjustment using information from a diary of motor fluctuations that will be completed by their patients for 7 days and (c) therapeutic adjustment using clinical information collected during consultation. It is expected that 162 consecutive patients will be included over a period of 6 months. The primary outcome is the efficiency of the Parkinson?s Holter compared with traditional clinical practice in terms of Off time reduction with respect to the baseline (recorded through a diary of motor fluctuations, which will be completed by all patients). As secondary outcomes, changes in variables related to other motor complications (dyskinesia and freezing of gait), quality of life, autonomy in activities of daily living, adherence to the monitoring system and number of doctor?patient contacts will be analysed. The noninferiority of the Parkinson's Holter against the diary of motor fluctuations in terms of Off time reduction will be studied as the exploratory objective. Ethics and dissemination approval for this study has been obtained from the Hospital Universitari de Bellvitge Ethics Committee. The results of this study will inform the practical utility of the objective information provided by a Parkinson's Holter and, therefore, the convenience of adopting this technology in clinical practice and in future clinical trials. We expect public dissemination of the results in 2022.es_ES
dc.description.sponsorshipFunding This work is supported by AbbVie S.L.U, the Instituto de Salud Carlos III [DTS17/00195] and the European Fund for Regional Development, 'A way to make Europe'.es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherBMJ Publishing Group Ltdes_ES
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceBMJ open 2021; 11(7): e045272.es_ES
dc.titleMulticentre, randomised, single-blind, parallel group trial to compare the effectiveness of a Holter for Parkinson's symptoms against other clinical monitoring methods: study protocoles_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1136/bmjopen-2020-045272es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International