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Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial

BACKGROUND: Hospitalized older patients spend most of the waking hours in bed, even if they can walk independently. Excessive bedrest contributes to the development of frailty and worse hospital outcomes. We describe the study protocol for the Breaking Bad Rest Study, a randomized clinical trial aim...

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Autores principales: Theou, Olga, O’Brien, Myles W., Godin, Judith, Blanchard, Chris, Cahill, Leah, Hajizadeh, Mohammad, Hartley, Peter, Jarrett, Pamala, Kehler, Dustin Scott, Romero-Ortuno, Roman, Visvanathan, Renuka, Rockwood, Kenneth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416381/
https://www.ncbi.nlm.nih.gov/pubmed/37563553
http://dx.doi.org/10.1186/s12877-023-04172-x
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author Theou, Olga
O’Brien, Myles W.
Godin, Judith
Blanchard, Chris
Cahill, Leah
Hajizadeh, Mohammad
Hartley, Peter
Jarrett, Pamala
Kehler, Dustin Scott
Romero-Ortuno, Roman
Visvanathan, Renuka
Rockwood, Kenneth
author_facet Theou, Olga
O’Brien, Myles W.
Godin, Judith
Blanchard, Chris
Cahill, Leah
Hajizadeh, Mohammad
Hartley, Peter
Jarrett, Pamala
Kehler, Dustin Scott
Romero-Ortuno, Roman
Visvanathan, Renuka
Rockwood, Kenneth
author_sort Theou, Olga
collection PubMed
description BACKGROUND: Hospitalized older patients spend most of the waking hours in bed, even if they can walk independently. Excessive bedrest contributes to the development of frailty and worse hospital outcomes. We describe the study protocol for the Breaking Bad Rest Study, a randomized clinical trial aimed to promoting more movement in acute care using a novel device-based approach that could mitigate the impact of too much bedrest on frailty. METHODS: Fifty patients in a geriatric unit will be randomized into an intervention or usual care control group. Both groups will be equipped with an activPAL (a measure of posture) and StepWatch (a measure of step counts) to wear throughout their entire hospital stay to capture their physical activity levels and posture. Frailty will be assessed via a multi-item questionnaire assessing health deficits at admission, weekly for the first month, then monthly thereafter, and at 1-month post-discharge. Secondary measures including geriatric assessments, cognitive function, falls, and hospital re-admissions will be assessed. Mixed models for repeated measures will determine whether daily activity differed between groups, changed over the course of their hospital stay, and impacted frailty levels. DISCUSSION: This randomized clinical trial will add to the evidence base on addressing frailty in older adults in acute care settings through a devices-based movement intervention. The findings of this trial may inform guidelines for limiting time spent sedentary or in bed during a patient’s stay in geriatric units, with the intention of scaling up this study model to other acute care sites if successful. TRIAL REGISTRATION: The protocol has been registered at clinicaltrials.gov (identifier: NCT03682523). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-023-04172-x.
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spelling pubmed-104163812023-08-12 Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial Theou, Olga O’Brien, Myles W. Godin, Judith Blanchard, Chris Cahill, Leah Hajizadeh, Mohammad Hartley, Peter Jarrett, Pamala Kehler, Dustin Scott Romero-Ortuno, Roman Visvanathan, Renuka Rockwood, Kenneth BMC Geriatr Study Protocol BACKGROUND: Hospitalized older patients spend most of the waking hours in bed, even if they can walk independently. Excessive bedrest contributes to the development of frailty and worse hospital outcomes. We describe the study protocol for the Breaking Bad Rest Study, a randomized clinical trial aimed to promoting more movement in acute care using a novel device-based approach that could mitigate the impact of too much bedrest on frailty. METHODS: Fifty patients in a geriatric unit will be randomized into an intervention or usual care control group. Both groups will be equipped with an activPAL (a measure of posture) and StepWatch (a measure of step counts) to wear throughout their entire hospital stay to capture their physical activity levels and posture. Frailty will be assessed via a multi-item questionnaire assessing health deficits at admission, weekly for the first month, then monthly thereafter, and at 1-month post-discharge. Secondary measures including geriatric assessments, cognitive function, falls, and hospital re-admissions will be assessed. Mixed models for repeated measures will determine whether daily activity differed between groups, changed over the course of their hospital stay, and impacted frailty levels. DISCUSSION: This randomized clinical trial will add to the evidence base on addressing frailty in older adults in acute care settings through a devices-based movement intervention. The findings of this trial may inform guidelines for limiting time spent sedentary or in bed during a patient’s stay in geriatric units, with the intention of scaling up this study model to other acute care sites if successful. TRIAL REGISTRATION: The protocol has been registered at clinicaltrials.gov (identifier: NCT03682523). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-023-04172-x. BioMed Central 2023-08-10 /pmc/articles/PMC10416381/ /pubmed/37563553 http://dx.doi.org/10.1186/s12877-023-04172-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Theou, Olga
O’Brien, Myles W.
Godin, Judith
Blanchard, Chris
Cahill, Leah
Hajizadeh, Mohammad
Hartley, Peter
Jarrett, Pamala
Kehler, Dustin Scott
Romero-Ortuno, Roman
Visvanathan, Renuka
Rockwood, Kenneth
Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial
title Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial
title_full Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial
title_fullStr Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial
title_full_unstemmed Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial
title_short Interrupting bedtime to reverse frailty levels in acute care: a study protocol for the Breaking Bad Rest randomized controlled trial
title_sort interrupting bedtime to reverse frailty levels in acute care: a study protocol for the breaking bad rest randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416381/
https://www.ncbi.nlm.nih.gov/pubmed/37563553
http://dx.doi.org/10.1186/s12877-023-04172-x
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