Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27976
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dc.contributor.authorDowman, Leona M-
dc.contributor.authorMay, Anthony K-
dc.contributor.authorHill, Catherine J-
dc.contributor.authorBondarenko, Janet-
dc.contributor.authorSpencer, Lissa-
dc.contributor.authorMorris, Norman R-
dc.contributor.authorAlison, Jennifer A-
dc.contributor.authorWalsh, James-
dc.contributor.authorGoh, Nicole S L-
dc.contributor.authorCorte, Tamera-
dc.contributor.authorGlaspole, Ian-
dc.contributor.authorChambers, Daniel C-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorHolland, Anne E-
dc.date2021-
dc.date.accessioned2021-11-16T02:50:46Z-
dc.date.available2021-11-16T02:50:46Z-
dc.date.issued2021-11-10-
dc.identifier.citationBMC pulmonary medicine 2021-11-10; 21(1): 361en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27976-
dc.description.abstractInterstitial lung disease is a debilitating condition associated with significant dyspnoea, fatigue, and poor exercise tolerance. Pulmonary rehabilitation is an effective and key intervention in people with interstitial lung disease. However, despite the best efforts of patients and clinicians, many of those who participate are not achieving clinically meaningful benefits. This assessor-blinded, multi-centre, randomised controlled trial aims to compare the clinical benefits of high intensity interval exercise training versus the standard pulmonary rehabilitation method of continuous training at moderate intensity in people with fibrotic interstitial lung disease. Eligible participants will be randomised to either a standard pulmonary rehabilitation group using moderate intensity continuous exercise training or high intensity interval exercise training. Participants in both groups will undertake an 8-week pulmonary rehabilitation program of twice-weekly supervised exercise training including aerobic (cycling) and strengthening exercises. In addition, participants in both groups will be prescribed a home exercise program. Outcomes will be assessed at baseline, upon completion of the intervention and at six months following the intervention by a blinded assessor. The primary outcome is endurance time on a constant work rate test. Secondary outcomes are functional capacity (6-min walk distance), health-related quality of life (Chronic Respiratory Disease Questionnaire (CRQ), St George's Respiratory Questionnaire idiopathic pulmonary fibrosis specific version (SGRQ-I), breathlessness (Dyspnoea 12, Modified Medical Research Council Dyspnoea Scale), fatigue (fatigue severity scale), anxiety (Hospital Anxiety and Depression Scale), physical activity level (GeneActiv), skeletal muscle changes (ultrasonography) and completion and adherence to pulmonary rehabilitation. The standard exercise training strategies used in pulmonary rehabilitation may not provide an optimal exercise training stimulus for people with interstitial lung disease. This study will determine whether high intensity interval training can produce equivalent or even superior changes in exercise performance and symptoms. If high intensity interval training proves effective, it will provide an exercise training strategy that can readily be implemented into clinical practice for people with interstitial lung disease. Trial registration ClinicalTrials.gov Registry (NCT03800914). Registered 11 January 2019, https://clinicaltrials.gov/ct2/show/NCT03800914 Australian New Zealand Clinical Trials Registry ACTRN12619000019101. Registered 9 January 2019, https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=376050&isReview=true.en_US
dc.language.isoeng-
dc.subjectEndurance trainingen_US
dc.subjectExercise,en_US
dc.subjectHigh-Intensity interval trainingen_US
dc.subjectIdiopathic pulmonary fibrosisen_US
dc.subjectInterstitial lung diseasesen_US
dc.subjectPulmonary Fibrosisen_US
dc.subjectRehabilitationen_US
dc.titleHigh intensity interval training versus moderate intensity continuous training for people with interstitial lung disease: protocol for a randomised controlled trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBMC Pulmonary Medicineen_US
dc.identifier.affiliationFaculty of Medicine and Health Science, Sydney School of Health Sciences, University of Sydney, Sydney, NSW, Australiaen_US
dc.identifier.affiliationSchool of Health Sciences and Social Work, The Hopkins Centre, Menzies Health Institute Queensland, Griffith University, Gold Coast, QLD, Australiaen_US
dc.identifier.affiliationMetro North Hospital and Health Service, The Prince Charles Hospital, Allied Health Research Collaborative, Chermside, QLD, Australiaen_US
dc.identifier.affiliationAllied Health Professorial Unit, Sydney Local Health District, Sydney, NSW, Australiaen_US
dc.identifier.affiliationRespiratory Research @ Alfred, Central Clinical School, Monash University, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationPhysiotherapyen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationMelbourne Medical School, University of Melbourne, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationInstitute for Physical Activity and Nutrition (IPAN), School of Exercise and Nutrition Sciences, Deakin University, Geelong, VIC, Australiaen_US
dc.identifier.affiliationDepartment of Physiotherapy, Royal Prince Alfred Hospital, Sydney, NSW, Australiaen_US
dc.identifier.affiliationDepartment of Physiotherapy, Alfred Health, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Royal Prince Alfred Hospital, Sydney, NSW, Australiaen_US
dc.identifier.affiliationCentral Clinical School, University of Sydney, Sydney, NSW, Australiaen_US
dc.identifier.affiliationNHMRC Centre of Research Excellence in Pulmonary Fibrosis, Sydney, NSW, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Alfred Hospital, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationCentral Clinical School, Monash University, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationSchool of Medicine, University of Queensland, Brisbane, QLD, Australiaen_US
dc.identifier.affiliationQueensland Lung Transplant Service, The Prince Charles Hospital, Brisbane, QLD, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/34758808/en_US
dc.identifier.doi10.1186/s12890-021-01704-2en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-8122-8063en_US
dc.identifier.pubmedid34758808-
local.name.researcherDowman, Leona M
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
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