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Authordc.contributor.authorSacomori, Cinara
Authordc.contributor.authorLorca, Luz Alejandra
Authordc.contributor.authorMartínez Mardones, Mónica
Authordc.contributor.authorSalas Ocaranza, Roberto
Authordc.contributor.authorReyes Reyes, Guillermo Patricio
Authordc.contributor.authorPizarro Hinojosa, Marta Natalia
Authordc.contributor.authorPlasser Troncoso, Jorge Isaías
Admission datedc.date.accessioned2021-11-05T13:33:52Z
Available datedc.date.available2021-11-05T13:33:52Z
Publication datedc.date.issued2021
Cita de ítemdc.identifier.citationTrials (2021) 22:448es_ES
Identifierdc.identifier.other10.1186/s13063-021-05396-1
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/182602
Abstractdc.description.abstractBackgroundThere is scarcity of trials about preventative strategies for low anterior resection syndrome (LARS) in rectal cancer patients. The aim of this study is to evaluate the effectiveness of a pre- and post-surgical pelvic floor rehabilitation program on the bowel symptoms, pelvic floor function, and quality of life of rectal cancer patients.MethodsA randomized controlled trial with parallel groups (pelvic floor rehabilitation versus control group), with a blinded evaluator. Participants and setting: 56 stage I to III rectal cancer patients aged from 18 to 80years old undergoing sphincter preservation surgery at Hospital del Salvador and who have a sufficient knowledge of Spanish. Main outcome measures: ICIQ-B questionnaire for intestinal symptoms, high-resolution anorectal manometry (Alacer Multiplex 24-channel manometry equipment) for anorectal function, pelvic floor muscle strength test with Oxford Modified Scale, and a quality of life test with the EORTC QLQ C30 questionnaire. The evaluations will be carried out at five stages: before surgery, before and after the pelvic floor rehabilitation, and during a 3-month and 1-year follow-up. Interventions: one pre-rehabilitation session and 9 to 12 sessions of pelvic floor rehabilitation, including patient education, pelvic floor muscle exercises, pelvic floor electromyography biofeedback, and capacitive and sensory rectal training with a balloon probe. Rehabilitation will begin 3-5weeks before the ileostomy is removed (four sessions) and around 3 weeks after stoma removal (5-8 sessions).DiscussionWe expect the program to improve the bowel symptoms, pelvic floor function, and quality of life of rectal cancer patients.Trial registrationAustralian New Zealand Clinical Trials Register ACTRN12620000040965. Registered on 21 January 2020es_ES
Patrocinadordc.description.sponsorshipCONICYT/ANID [National Research and Development Agency] FONDECYT INICIACION PROGRAM Award [National Fund for Scientific and Technological Development Research Initiation Program], Government of Chile 11191016es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherBMCes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceTrialses_ES
Keywordsdc.subjectRectal canceres_ES
Keywordsdc.subjectPelvic floores_ES
Keywordsdc.subjectLow anterior resection syndromees_ES
Keywordsdc.subjectRehabilitationes_ES
Keywordsdc.subjectPreventiones_ES
Keywordsdc.subjectPhysiotherapyes_ES
Keywordsdc.subjectBowel symptomses_ES
Keywordsdc.subjectQuality of lifees_ES
Títulodc.titleA randomized clinical trial to assess the effectiveness of pre- and post-surgical pelvic floor physiotherapy for bowel symptoms, pelvic floor function, and quality of life of patients with rectal cancer: CARRET protocoles_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States