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Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial

BACKGROUND: In people with cystic fibrosis (CF), higher exercise capacity is associated with better health-related quality of life (HRQoL), reduced risk of hospitalisation for a respiratory infection and survival. Therefore, optimisation of exercise capacity is an important treatment goal. The Austr...

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Autores principales: Sawyer, Abbey, Cavalheri, Vinicius, Jenkins, Sue, Wood, Jamie, Cecins, Nola, Singh, Bhajan, Hill, Kylie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219072/
https://www.ncbi.nlm.nih.gov/pubmed/30450213
http://dx.doi.org/10.1186/s13102-018-0108-2
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author Sawyer, Abbey
Cavalheri, Vinicius
Jenkins, Sue
Wood, Jamie
Cecins, Nola
Singh, Bhajan
Hill, Kylie
author_facet Sawyer, Abbey
Cavalheri, Vinicius
Jenkins, Sue
Wood, Jamie
Cecins, Nola
Singh, Bhajan
Hill, Kylie
author_sort Sawyer, Abbey
collection PubMed
description BACKGROUND: In people with cystic fibrosis (CF), higher exercise capacity is associated with better health-related quality of life (HRQoL), reduced risk of hospitalisation for a respiratory infection and survival. Therefore, optimisation of exercise capacity is an important treatment goal. The Australian and New Zealand clinical practice guidelines recommend that people with CF complete 30 to 60 min of moderate intensity aerobic exercise on most days of the week. This recommendation can be difficult to achieve by people with CF because of time constraints, and intolerable breathlessness and muscle fatigue during continuous exercise. In contrast, a low-volume, high intensity interval training (HIIT) program may be a more achievable and efficient training method to improve exercise capacity in people with CF. METHODS: A randomised controlled trial will be undertaken. Forty people with CF (aged ≥15 years) will be randomly allocated, on a 1:1 ratio, to either the experimental or control group. Regardless of their group allocation, all participants will be asked to continue with their usual daily treatment for the study duration. Those in the experimental group will complete 8 weeks of thrice weekly HIIT on a cycle ergometer. Those in the control group will receive weekly contact with the investigators. The primary outcome of this study is exercise capacity. Secondary outcomes are HRQoL, exercise self-efficacy, feelings of anxiety, depression and enjoyment. These outcomes will be recorded at baseline (i.e. prior to randomisation) and following the 8-week intervention period. The study will also report other outcomes of the HIIT program (cardiovascular responses, symptom response, post-exercise muscle soreness and tolerance) and behaviour change techniques such as reinforcement, feedback and goal setting, used during the HIIT program. DISCUSSION: This study will determine the effects of 8-weeks of supervised, low-volume HIIT, completed on a cycle ergometer on measures of exercise capacity, HRQoL, exercise self-efficacy, feelings of anxiety, depression and enjoyment. If effective, this type of training could be an attractive alternative to traditional continuous training because it may be more achievable and time efficient. TRIAL REGISTRATION: Australian and New Zealand Clinical Trials Registry (ANZCTR):12617001271392 (04/09/2017).
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spelling pubmed-62190722018-11-16 Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial Sawyer, Abbey Cavalheri, Vinicius Jenkins, Sue Wood, Jamie Cecins, Nola Singh, Bhajan Hill, Kylie BMC Sports Sci Med Rehabil Study Protocol BACKGROUND: In people with cystic fibrosis (CF), higher exercise capacity is associated with better health-related quality of life (HRQoL), reduced risk of hospitalisation for a respiratory infection and survival. Therefore, optimisation of exercise capacity is an important treatment goal. The Australian and New Zealand clinical practice guidelines recommend that people with CF complete 30 to 60 min of moderate intensity aerobic exercise on most days of the week. This recommendation can be difficult to achieve by people with CF because of time constraints, and intolerable breathlessness and muscle fatigue during continuous exercise. In contrast, a low-volume, high intensity interval training (HIIT) program may be a more achievable and efficient training method to improve exercise capacity in people with CF. METHODS: A randomised controlled trial will be undertaken. Forty people with CF (aged ≥15 years) will be randomly allocated, on a 1:1 ratio, to either the experimental or control group. Regardless of their group allocation, all participants will be asked to continue with their usual daily treatment for the study duration. Those in the experimental group will complete 8 weeks of thrice weekly HIIT on a cycle ergometer. Those in the control group will receive weekly contact with the investigators. The primary outcome of this study is exercise capacity. Secondary outcomes are HRQoL, exercise self-efficacy, feelings of anxiety, depression and enjoyment. These outcomes will be recorded at baseline (i.e. prior to randomisation) and following the 8-week intervention period. The study will also report other outcomes of the HIIT program (cardiovascular responses, symptom response, post-exercise muscle soreness and tolerance) and behaviour change techniques such as reinforcement, feedback and goal setting, used during the HIIT program. DISCUSSION: This study will determine the effects of 8-weeks of supervised, low-volume HIIT, completed on a cycle ergometer on measures of exercise capacity, HRQoL, exercise self-efficacy, feelings of anxiety, depression and enjoyment. If effective, this type of training could be an attractive alternative to traditional continuous training because it may be more achievable and time efficient. TRIAL REGISTRATION: Australian and New Zealand Clinical Trials Registry (ANZCTR):12617001271392 (04/09/2017). BioMed Central 2018-11-06 /pmc/articles/PMC6219072/ /pubmed/30450213 http://dx.doi.org/10.1186/s13102-018-0108-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Sawyer, Abbey
Cavalheri, Vinicius
Jenkins, Sue
Wood, Jamie
Cecins, Nola
Singh, Bhajan
Hill, Kylie
Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial
title Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial
title_full Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial
title_fullStr Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial
title_full_unstemmed Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial
title_short Effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial
title_sort effects of high intensity interval training on exercise capacity in people with cystic fibrosis: study protocol for a randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219072/
https://www.ncbi.nlm.nih.gov/pubmed/30450213
http://dx.doi.org/10.1186/s13102-018-0108-2
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