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Reablement in community-dwelling adults: study protocol for a randomised controlled trial
BACKGROUND: As a result of the ageing population, there is an urgent need for innovation in community health-care in order to achieve sustainability. Reablement is implemented in primary care in some Western countries to help meet these challenges. However, evidence to support the use of such home-b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320541/ https://www.ncbi.nlm.nih.gov/pubmed/25519828 http://dx.doi.org/10.1186/1471-2318-14-139 |
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author | Tuntland, Hanne Espehaug, Birgitte Forland, Oddvar Hole, Astri Drange Kjerstad, Egil Kjeken, Ingvild |
author_facet | Tuntland, Hanne Espehaug, Birgitte Forland, Oddvar Hole, Astri Drange Kjerstad, Egil Kjeken, Ingvild |
author_sort | Tuntland, Hanne |
collection | PubMed |
description | BACKGROUND: As a result of the ageing population, there is an urgent need for innovation in community health-care in order to achieve sustainability. Reablement is implemented in primary care in some Western countries to help meet these challenges. However, evidence to support the use of such home-based rehabilitation is limited. Reablement focuses on early, time-intensive, multidisciplinary, multi-component and individualised home-based rehabilitation for older adults with functional decline. The aim of this study is to investigate the effectiveness of reablement in home-dwelling adults compared with standard treatment in relation to daily activities, physical functioning, health-related quality of life, use of health-care services, and costs. METHODS/DESIGN: The study will be a 1:1 parallel-group randomised controlled superiority trial conducted in a rural municipality in Norway. The experimental group will be offered reablement and the control group offered standard treatment. A computer-generated permuted block randomisation sequence, with randomly selected block sizes, will be used for allocation. Neither participants nor health-care providers will be blinded, however all research assistants and researchers will be blinded. The sample size will consist of 60 participants. People will be eligible if they are home-dwelling, over 18 years of age, understand Norwegian and have functional decline. The exclusion criteria will be people in need of institution-based rehabilitation or nursing home placement, and people who are terminally ill or cognitively reduced. The primary outcome will be self-perceived performance, and satisfaction with performance of daily activities, assessed with the Canadian Occupational Performance Measure. In addition, physical capacity, health-related quality of life, use of health-care services, and cost data will be collected at baseline, and after 3 and 9 months in both groups, and again after 15 months in the intervention group. Data will be analysed on an intention-to-treat basis using a linear mixed model for repeated measures. DISCUSSION: The findings will make an important contribution to evaluating cost-effective and evidence-based rehabilitation approaches for community-dwelling adults. TRIAL REGISTRATION: The trial was registered in ClinicalTrials.gov November 20, 2012, identifier: NCT02043262. |
format | Online Article Text |
id | pubmed-4320541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43205412015-02-08 Reablement in community-dwelling adults: study protocol for a randomised controlled trial Tuntland, Hanne Espehaug, Birgitte Forland, Oddvar Hole, Astri Drange Kjerstad, Egil Kjeken, Ingvild BMC Geriatr Study Protocol BACKGROUND: As a result of the ageing population, there is an urgent need for innovation in community health-care in order to achieve sustainability. Reablement is implemented in primary care in some Western countries to help meet these challenges. However, evidence to support the use of such home-based rehabilitation is limited. Reablement focuses on early, time-intensive, multidisciplinary, multi-component and individualised home-based rehabilitation for older adults with functional decline. The aim of this study is to investigate the effectiveness of reablement in home-dwelling adults compared with standard treatment in relation to daily activities, physical functioning, health-related quality of life, use of health-care services, and costs. METHODS/DESIGN: The study will be a 1:1 parallel-group randomised controlled superiority trial conducted in a rural municipality in Norway. The experimental group will be offered reablement and the control group offered standard treatment. A computer-generated permuted block randomisation sequence, with randomly selected block sizes, will be used for allocation. Neither participants nor health-care providers will be blinded, however all research assistants and researchers will be blinded. The sample size will consist of 60 participants. People will be eligible if they are home-dwelling, over 18 years of age, understand Norwegian and have functional decline. The exclusion criteria will be people in need of institution-based rehabilitation or nursing home placement, and people who are terminally ill or cognitively reduced. The primary outcome will be self-perceived performance, and satisfaction with performance of daily activities, assessed with the Canadian Occupational Performance Measure. In addition, physical capacity, health-related quality of life, use of health-care services, and cost data will be collected at baseline, and after 3 and 9 months in both groups, and again after 15 months in the intervention group. Data will be analysed on an intention-to-treat basis using a linear mixed model for repeated measures. DISCUSSION: The findings will make an important contribution to evaluating cost-effective and evidence-based rehabilitation approaches for community-dwelling adults. TRIAL REGISTRATION: The trial was registered in ClinicalTrials.gov November 20, 2012, identifier: NCT02043262. BioMed Central 2014-12-18 /pmc/articles/PMC4320541/ /pubmed/25519828 http://dx.doi.org/10.1186/1471-2318-14-139 Text en © Tuntland et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Tuntland, Hanne Espehaug, Birgitte Forland, Oddvar Hole, Astri Drange Kjerstad, Egil Kjeken, Ingvild Reablement in community-dwelling adults: study protocol for a randomised controlled trial |
title | Reablement in community-dwelling adults: study protocol for a randomised controlled trial |
title_full | Reablement in community-dwelling adults: study protocol for a randomised controlled trial |
title_fullStr | Reablement in community-dwelling adults: study protocol for a randomised controlled trial |
title_full_unstemmed | Reablement in community-dwelling adults: study protocol for a randomised controlled trial |
title_short | Reablement in community-dwelling adults: study protocol for a randomised controlled trial |
title_sort | reablement in community-dwelling adults: study protocol for a randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320541/ https://www.ncbi.nlm.nih.gov/pubmed/25519828 http://dx.doi.org/10.1186/1471-2318-14-139 |
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