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dc.contributor.authorLópez-Royo, María Pilar-
dc.contributor.authorGómez-Trullén, Eva María-
dc.contributor.authorOrtiz Lucas, María-
dc.contributor.authorGalán-Díaz, Rita María-
dc.contributor.authorBataller-Cervero, Ana Vanessa-
dc.contributor.authorAl-Boloushi, Zaid-
dc.contributor.authorHamam Alcober, Yasmina-
dc.contributor.authorHerrero Gállego, Pablo-
dc.date.accessioned2021-03-17T10:43:17Z-
dc.date.available2021-03-17T10:43:17Z-
dc.date.issued2020-01-23-
dc.identifier.citationLópez-Royo MP, Gómez-Trullén EM, Ortiz-Lucas M,et al. Comparative study of treatment interventions for patellar tendinopathy: a protocol for a randomised controlled trial. BMJ Open2020;10:e034304. doi:10.1136/bmjopen-2019-034304es_ES
dc.identifier.issn2044-6055es_ES
dc.identifier.urihttps://repositorio.usj.es/handle/123456789/524-
dc.description.abstractIntroductionPatellar tendinopathy is a degenerative disease of the patellar tendon, which affects athletes from a variety of sports, and is especially predominant in sports involving high-impact jumping. The aim of this study is to determine the additional effect of two interventions combined with eccentric exercise and compare which one is the most effective at short-term and long-term follow-up for patients with patellar tendinopathy.Methods and analysisThis study is a randomised controlled trial with blinded participants. Measurements will be carried out by a specially trained blinded assessor. A sample of 57 patients with a medical diagnosis of patellar tendinopathy will participate in this study and will be divided into three treatment groups. Eligible participants will be randomly allocated to receive either: (a) treatment group with percutaneous needle electrolysis, (b) treatment group with dry needling or (c) treatment group with placebo needling. In addition, all groups will perform eccentric exercise. Functionality and muscle strength parameters, pain, ultrasound appearances and patient perceived quality of life shall be evaluated using the Victorian Institute of Sports Assessment for patellar (VISA-P), jump tests, Visual Analogue Scale, ultrasound images and Short Form-36 (SF-36), respectively. Participants will be assessed at baseline, at 10 weeks and at 22 weeks after baseline. The expected findings will allow us to advance in the treatment of this injury, as they will help determine whether a needling intervention has additional effects on an eccentric exercise programme and whether any of the needling modalities is more effective than the otheres_ES
dc.format.extent8 p.es_ES
dc.format.mimetypeapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherBMJ PUBLISHING GROUPes_ES
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectPlatelet-rich plasmaes_ES
dc.subjectJumpers kneees_ES
dc.subjectEccentric exercisees_ES
dc.subjectDifferent sportses_ES
dc.subjectTendónes_ES
dc.subjectReliabilityes_ES
dc.subjectPrevalencees_ES
dc.subjectValidityes_ES
dc.subjectSquates_ES
dc.titleComparative study of treatment interventions for patellar tendinopathy: a protocol for a randomised controlled triales_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1136/bmjopen-2019-034304es_ES
dc.rights.accessrightsinfo:eu-repo/semantics/openAccesses_ES
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