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Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial
BACKGROUND: Bariatric surgery is an effective approach to weight loss and long-term comorbidity resolution. Although recommended in several guidelines, supervised exercise has not been systematically prescribed after bariatric surgery. The aim of this study is to determine the effects of two types o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849097/ https://www.ncbi.nlm.nih.gov/pubmed/33522950 http://dx.doi.org/10.1186/s13063-021-05056-4 |
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author | Herrera-Santelices, Andrea Tabach-Apraiz, Andrea Andaur-Cáceres, Karen Zamunér, Antonio Roberto |
author_facet | Herrera-Santelices, Andrea Tabach-Apraiz, Andrea Andaur-Cáceres, Karen Zamunér, Antonio Roberto |
author_sort | Herrera-Santelices, Andrea |
collection | PubMed |
description | BACKGROUND: Bariatric surgery is an effective approach to weight loss and long-term comorbidity resolution. Although recommended in several guidelines, supervised exercise has not been systematically prescribed after bariatric surgery. The aim of this study is to determine the effects of two types of exercise, moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT), on body composition, cardiopulmonary function, and perceived quality of life in bariatric surgery patients. METHODS: This randomized controlled exploratory pilot trial will include 75 adults of both sexes scheduled for bariatric surgery. They will be randomly assigned to one of three groups: (1) MICT, (2) HIIT, or (3) a control group. The intervention will occur 2 days a week for 4 months. Outcomes will be assessed at four points: (1) 1 week before surgery, (2) 21 days after surgery (baseline before the exercise program), (3) 8 weeks after beginning the exercise program, and (4) 1 week after the end of intervention. Primary outcomes will include body composition, heart rate variability, and 6-min walk test and quality of life scores. Secondary outcomes will be maximal respiratory pressure, flowmeter, hand dynamometry, and 30-s sit-to-stand test results. DISCUSSION: Both exercise protocols in this study were developed according to evidence-based practice. It is expected that, after 16 weeks of intervention, body composition (measured by electrical bioimpedance), cardiopulmonary function (measured by heart rate variability, maximal inspiratory pressure, maximal expiratory pressure, peak expiratory flow, handgrip strength, and the 6-min walk test), and perceived quality of life (measured by the Moorehead-Ardelt quality of life questionnaire II and bariatric analysis and reporting outcome system scores) will improve, especially in the HIIT group. TRIAL REGISTRATION: ClinicalTrials.gov NCT04235842. Registered on 22 January 2020. |
format | Online Article Text |
id | pubmed-7849097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78490972021-02-03 Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial Herrera-Santelices, Andrea Tabach-Apraiz, Andrea Andaur-Cáceres, Karen Zamunér, Antonio Roberto Trials Study Protocol BACKGROUND: Bariatric surgery is an effective approach to weight loss and long-term comorbidity resolution. Although recommended in several guidelines, supervised exercise has not been systematically prescribed after bariatric surgery. The aim of this study is to determine the effects of two types of exercise, moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT), on body composition, cardiopulmonary function, and perceived quality of life in bariatric surgery patients. METHODS: This randomized controlled exploratory pilot trial will include 75 adults of both sexes scheduled for bariatric surgery. They will be randomly assigned to one of three groups: (1) MICT, (2) HIIT, or (3) a control group. The intervention will occur 2 days a week for 4 months. Outcomes will be assessed at four points: (1) 1 week before surgery, (2) 21 days after surgery (baseline before the exercise program), (3) 8 weeks after beginning the exercise program, and (4) 1 week after the end of intervention. Primary outcomes will include body composition, heart rate variability, and 6-min walk test and quality of life scores. Secondary outcomes will be maximal respiratory pressure, flowmeter, hand dynamometry, and 30-s sit-to-stand test results. DISCUSSION: Both exercise protocols in this study were developed according to evidence-based practice. It is expected that, after 16 weeks of intervention, body composition (measured by electrical bioimpedance), cardiopulmonary function (measured by heart rate variability, maximal inspiratory pressure, maximal expiratory pressure, peak expiratory flow, handgrip strength, and the 6-min walk test), and perceived quality of life (measured by the Moorehead-Ardelt quality of life questionnaire II and bariatric analysis and reporting outcome system scores) will improve, especially in the HIIT group. TRIAL REGISTRATION: ClinicalTrials.gov NCT04235842. Registered on 22 January 2020. BioMed Central 2021-02-01 /pmc/articles/PMC7849097/ /pubmed/33522950 http://dx.doi.org/10.1186/s13063-021-05056-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Study Protocol Herrera-Santelices, Andrea Tabach-Apraiz, Andrea Andaur-Cáceres, Karen Zamunér, Antonio Roberto Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial |
title | Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial |
title_full | Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial |
title_fullStr | Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial |
title_full_unstemmed | Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial |
title_short | Effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial |
title_sort | effect of physical exercise in bariatric surgery patients: protocol of a randomized controlled clinical trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849097/ https://www.ncbi.nlm.nih.gov/pubmed/33522950 http://dx.doi.org/10.1186/s13063-021-05056-4 |
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