Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30967
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dc.contributor.authorCox, Narelle S-
dc.contributor.authorEldridge, Beverley-
dc.contributor.authorRawlings, Sarah-
dc.contributor.authorDreger, Julianna-
dc.contributor.authorCorda, Jennifer-
dc.contributor.authorHauser, Jennifer-
dc.contributor.authorButton, Brenda M-
dc.contributor.authorBishop, Jennifer R-
dc.contributor.authorNichols, Amanda-
dc.contributor.authorMiddleton, Anna-
dc.contributor.authorWard, Nathan-
dc.contributor.authorDwyer, Tiffany-
dc.contributor.authorDentice, Ruth-
dc.contributor.authorLazarus, Raynuka-
dc.contributor.authorO'Halloran, Paul-
dc.contributor.authorLee, Joanna Y T-
dc.contributor.authorMellerick, Christie-
dc.contributor.authorMackintosh, Kelly-
dc.contributor.authorMcNarry, Melitta-
dc.contributor.authorWilliams, Craig Anthony-
dc.contributor.authorHolland, Anne E-
dc.date2022-
dc.date.accessioned2022-10-07T05:29:48Z-
dc.date.available2022-10-07T05:29:48Z-
dc.date.issued2023-01-
dc.identifier.citationThorax 2023; 78(1)en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30967-
dc.description.abstractPhysical activity levels are known to decline following hospitalisation for people with cystic fibrosis (pwCF). However, optimal physical activity promotion strategies are unclear. This study investigated the effect of a web-based application (ActivOnline) in promoting physical activity in young pwCF. Multicentre randomised controlled trial with assessor blinding and qualitative evaluation. People with CF (12-35 years) admitted to hospital for a respiratory cause were eligible and randomised to the 12-week ActivOnline intervention (AO) or usual care (UC). The primary outcome was change in device-based time spent in moderate-to-vigorous physical activity (MVPA) from baseline to post-intervention. Follow-up was at 6 months from hospital discharge when qualitative evaluation was undertaken. 107 participants were randomised to AO (n=52) or UC (n=55). Sixty-three participants (59%) contributed to the intention-to-treat analysis. Mean (SD) age was 21 (6) years (n=46, <18 years). At baseline, physical activity levels were high in both groups (AO 102 (52) vs UC 127 (73) min/day). There was no statistically significant difference in MVPA between groups at either timepoint (post-intervention mean difference (95% CI) -14 mins (-45 to 16)). Uptake of the intervention was low with only 40% (n=21) of participants accessing the web application. A web-based application, including individualised goal setting, real-time feedback and motivation for behavioural change, was no better than usual care at promoting physical activity in young pwCF following hospital discharge. High levels of baseline physical activity levels in both groups, and limited engagement with the intervention, suggest alternative strategies may be necessary to identify and support young pwCF who would benefit from enhanced physical activity. ACTRN12617001009303, 13 July 13 2017.en_US
dc.language.isoeng-
dc.subjectCystic Fibrosisen_US
dc.subjectExerciseen_US
dc.subjectPulmonary Rehabilitationen_US
dc.titleWeb-based physical activity promotion in young people with CF: a randomised controlled trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThoraxen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationPhysiotherapy, Sydney Children's Hospital Network Westmead, Sydney, New South Wales, Australiaen_US
dc.identifier.affiliationPhysiotherapy, Royal Adelaide Hospital, Adelaide, South Australia, Australiaen_US
dc.identifier.affiliationDiscipline of Physiotherapy, Sydney School of Health Sciences, University of Sydney, Sydney, New South Wales, Australiaen_US
dc.identifier.affiliationRespiratory Medicine, Royal Prince Alfred Hospital, Sydney, New South Wales, Australiaen_US
dc.identifier.affiliationPhysiotherapy, Royal Prince Alfred Hospital, Sydney, New South Wales, Australiaen_US
dc.identifier.affiliationRespiratory Research@Alfred, Department of Immunology and Pathology, Monash University, Melbourne, Victoria, Australia narelle.cox@monash.edu.. Institute for Breathing and Sleep, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationCollege of Science, Health and Engineering, La Trobe University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationChildren's Medical Research Institute, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationMonash Health, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationPhysiotherapy, The Royal Children's Hospital Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationTasmanian Adult CF Service, Royal Hobart Hospital, Hobart, Tasmania, Australiaen_US
dc.identifier.affiliationPhysiotherapy, Alfred Health, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationAllergy, Immunology and Respiratory Medicine, Alfred Health, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationFaculty of Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationRespiratory Medicine, Westmead Hospital, Sydney, New South Wales, Australiaen_US
dc.identifier.affiliationCollege of Engineering, Swansea University, Swansea, UK..en_US
dc.identifier.affiliationChildren's Health and Exercise Research Centre, University of Exeter, Exeter, UK..en_US
dc.identifier.doi10.1136/thorax-2022-218702en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-6403-2894en_US
dc.identifier.orcid0000-0002-6977-1028en_US
dc.identifier.orcid0000-0003-2061-845Xen_US
dc.identifier.pubmedid36180067-
local.name.researcherCox, Narelle S
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
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