Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18066
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dc.contributor.authorEdbrooke, Lara-
dc.contributor.authorAranda, Sanchia-
dc.contributor.authorGranger, Catherine L-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorKrishnasamy, Mei-
dc.contributor.authorMileshkin, Linda-
dc.contributor.authorIrving, Louis-
dc.contributor.authorBraat, Sabine-
dc.contributor.authorClark, Ross A-
dc.contributor.authorGordon, Ian-
dc.contributor.authorDenehy, Linda-
dc.date2017-09-29-
dc.date.accessioned2018-07-10T06:34:25Z-
dc.date.available2018-07-10T06:34:25Z-
dc.date.issued2017-09-29-
dc.identifier.citationBMC Cancer 2017; 17(1): 663en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18066-
dc.description.abstractLung cancer is one of the most commonly diagnosed cancers, and is a leading cause of cancer mortality world-wide. Due to lack of early specific symptoms, the majority of patients present with advanced, inoperable disease and five-year relative survival across all stages of non-small cell lung cancer (NSCLC) is 14%. People with lung cancer also report higher levels of symptom distress than those with other forms of cancer. Several benefits for survival and patient reported outcomes are reported from physical activity and exercise in other tumour groups. We report the protocol for a study investigating the benefits of exercise, behaviour change and symptom self-management for patients with recently diagnosed, inoperable, NSCLC. This multi-site, parallel-group, assessor-blinded randomised controlled trial, powered for superiority, aims to assess functional and patient-reported outcomes of a multi-disciplinary, home-based exercise and supportive care program for people commencing treatment. Ninety-two participants are being recruited from three tertiary-care hospitals in Melbourne, Australia. Following baseline testing, participants are randomised using concealed allocation, to receive either: a) 8 weeks of home-based exercise (comprising an individualised endurance and resistance exercise program and behaviour change coaching) and nurse-delivered symptom self-management intervention or b) usual care. The primary outcome is the between-group difference in the change in functional exercise capacity (six-minute walk distance) from baseline to post-program assessment. Secondary outcomes include: objective and self-reported physical activity levels, physical activity self-efficacy, behavioural regulation of motivation to exercise and resilience, muscle strength (quadriceps and grip), health-related quality of life, anxiety and depression and symptom interference. There is a lack of evidence regarding the benefit of exercise intervention for people with NSCLC, particularly in those with inoperable disease receiving treatment. This trial will contribute to evidence currently being generated in national and international trials by implementing and evaluating a home-based program including three components not yet combined in previous research, for people with inoperable NSCLC receiving active treatment and involving longer-term follow-up of outcomes. This trial is ongoing and currently recruiting. This trial was prospectively registered on the Australian New Zealand Clinical Trials Registry ( ACTRN12614001268639 : (4/12/14).en_US
dc.language.isoeng-
dc.subjectHome-based exerciseen_US
dc.subjectNon-small cell lung canceren_US
dc.subjectPhysical functionen_US
dc.subjectSupportive careen_US
dc.subjectSymptom controlen_US
dc.titleBenefits of home-based multidisciplinary exercise and supportive care in inoperable non-small cell lung cancer - protocol for a phase II randomised controlled trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBMC Canceren_US
dc.identifier.affiliationDepartment of Physiotherapy, The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationCancer Council Australia, Sydney, NSW, Australiaen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationDepartment of Nursing, The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationThe University of Melbourne Centre for Cancer Research, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationThe Peter MacCallum Cancer Centre, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Melbourne Health, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationMelbourne School of Population and Global Health, The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationUniversity of the Sunshine Coast, Sunshine Coast, QLD, Australiaen_US
dc.identifier.affiliationStatistical Consulting Centre, The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.doi10.1186/s12885-017-3651-4en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-4149-5578en_US
dc.identifier.orcid0000-0001-6169-370Xen_US
dc.identifier.orcid0000-0001-6481-3391en_US
dc.identifier.pubmedid28962608-
dc.type.austinClinical Trial, Phase II-
dc.type.austinJournal Article-
dc.type.austinRandomized Controlled Trial-
local.name.researcherGranger, Catherine L
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
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