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Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial

INTRODUCTION: Frailty in Older people: Rehabilitation, Treatment, Research Examining Separate Settings (the FORTRESS study) is a multisite, hybrid type II, stepped wedge, cluster, randomised trial examining the uptake and outcomes of a frailty intervention. The intervention is based on the 2017 Asia...

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Autores principales: Manuel, Kisani, Block, Heather, Crotty, Maria, Harvey, Gillian, Kurrle, Susan E, Cameron, Ian, Lockwood, Keri, Sherrington, Catherine, Pond, Dimity, Nguyen, Tuan A, Laver, Kate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277088/
https://www.ncbi.nlm.nih.gov/pubmed/37295839
http://dx.doi.org/10.1136/bmjopen-2022-070267
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author Manuel, Kisani
Block, Heather
Crotty, Maria
Harvey, Gillian
Kurrle, Susan E
Cameron, Ian
Lockwood, Keri
Sherrington, Catherine
Pond, Dimity
Nguyen, Tuan A
Laver, Kate
author_facet Manuel, Kisani
Block, Heather
Crotty, Maria
Harvey, Gillian
Kurrle, Susan E
Cameron, Ian
Lockwood, Keri
Sherrington, Catherine
Pond, Dimity
Nguyen, Tuan A
Laver, Kate
author_sort Manuel, Kisani
collection PubMed
description INTRODUCTION: Frailty in Older people: Rehabilitation, Treatment, Research Examining Separate Settings (the FORTRESS study) is a multisite, hybrid type II, stepped wedge, cluster, randomised trial examining the uptake and outcomes of a frailty intervention. The intervention is based on the 2017 Asia Pacific Clinical Practice Guidelines for the Management of Frailty and begins in the acute hospital setting and transitions to the community. The success of the intervention will require individual and organisational behaviour change within a dynamic health system. This process evaluation will examine the multiple variables at play in the context and mechanism of the frailty intervention to enhance understanding of the outcomes of the FORTRESS study and how the outcomes can be translated from the trial into broader practice. METHODS AND ANALYSIS: The FORTRESS intervention will recruit participants from six wards in New South Wales and South Australia, Australia. Participants of the process evaluation will include trial investigators, ward-based clinicians, FORTRESS implementation clinicians, general practitioners and FORTRESS participants. The process evaluation has been designed using realist methodology and will occur in parallel to the FORTRESS trial. A mixed-method approach will be used with qualitative and quantitative data collected from interviews, questionnaires, checklists and outcome assessments. Qualitative and quantitative data will be examined for CMOCs (Context, Mechanism, Outcome Configurations) and programme theories will be developed, tested and refined. This will facilitate development of more generalisable theories to inform translation of frailty intervention within complex healthcare systems. ETHICS AND DISSEMINATION: Ethical approval for the FORTRESS trial, inclusive of the process evaluation, has been obtained from the Northern Sydney Local Health District Human Research Ethics Committees reference number 2020/ETH01057. Recruitment for the FORTRESS trial uses opt-out consent. Dissemination will be via publications, conferences and social media. TRIAL REGISTRATION NUMBER: ACTRN12620000760976p (FORTRESS trial).
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spelling pubmed-102770882023-06-19 Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial Manuel, Kisani Block, Heather Crotty, Maria Harvey, Gillian Kurrle, Susan E Cameron, Ian Lockwood, Keri Sherrington, Catherine Pond, Dimity Nguyen, Tuan A Laver, Kate BMJ Open Geriatric Medicine INTRODUCTION: Frailty in Older people: Rehabilitation, Treatment, Research Examining Separate Settings (the FORTRESS study) is a multisite, hybrid type II, stepped wedge, cluster, randomised trial examining the uptake and outcomes of a frailty intervention. The intervention is based on the 2017 Asia Pacific Clinical Practice Guidelines for the Management of Frailty and begins in the acute hospital setting and transitions to the community. The success of the intervention will require individual and organisational behaviour change within a dynamic health system. This process evaluation will examine the multiple variables at play in the context and mechanism of the frailty intervention to enhance understanding of the outcomes of the FORTRESS study and how the outcomes can be translated from the trial into broader practice. METHODS AND ANALYSIS: The FORTRESS intervention will recruit participants from six wards in New South Wales and South Australia, Australia. Participants of the process evaluation will include trial investigators, ward-based clinicians, FORTRESS implementation clinicians, general practitioners and FORTRESS participants. The process evaluation has been designed using realist methodology and will occur in parallel to the FORTRESS trial. A mixed-method approach will be used with qualitative and quantitative data collected from interviews, questionnaires, checklists and outcome assessments. Qualitative and quantitative data will be examined for CMOCs (Context, Mechanism, Outcome Configurations) and programme theories will be developed, tested and refined. This will facilitate development of more generalisable theories to inform translation of frailty intervention within complex healthcare systems. ETHICS AND DISSEMINATION: Ethical approval for the FORTRESS trial, inclusive of the process evaluation, has been obtained from the Northern Sydney Local Health District Human Research Ethics Committees reference number 2020/ETH01057. Recruitment for the FORTRESS trial uses opt-out consent. Dissemination will be via publications, conferences and social media. TRIAL REGISTRATION NUMBER: ACTRN12620000760976p (FORTRESS trial). BMJ Publishing Group 2023-06-09 /pmc/articles/PMC10277088/ /pubmed/37295839 http://dx.doi.org/10.1136/bmjopen-2022-070267 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Geriatric Medicine
Manuel, Kisani
Block, Heather
Crotty, Maria
Harvey, Gillian
Kurrle, Susan E
Cameron, Ian
Lockwood, Keri
Sherrington, Catherine
Pond, Dimity
Nguyen, Tuan A
Laver, Kate
Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial
title Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial
title_full Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial
title_fullStr Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial
title_full_unstemmed Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial
title_short Implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the FORTRESS trial
title_sort implementation of a frailty intervention in the transition from hospital to home: a realist process evaluation protocol for the fortress trial
topic Geriatric Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277088/
https://www.ncbi.nlm.nih.gov/pubmed/37295839
http://dx.doi.org/10.1136/bmjopen-2022-070267
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