Reablement in community-dwelling adults: study protocol for a randomised controlled trial

被引:18
|
作者
Tuntland, Hanne [1 ,2 ]
Espehaug, Birgitte [3 ]
Forland, Oddvar [1 ,4 ]
Hole, Astri Drange [5 ]
Kjerstad, Egil [6 ]
Kjeken, Ingvild [7 ,8 ]
机构
[1] Bergen Univ Coll, Ctr Care Res Western Norway, N-5020 Bergen, Norway
[2] Bergen Univ Coll, Dept Occupat Therapy Physiotherapy & Radiog, N-5020 Bergen, Norway
[3] Bergen Univ Coll, Ctr Evidence Based Practice, N-5020 Bergen, Norway
[4] Haraldsplass Deaconess Univ Coll, N-5009 Bergen, Norway
[5] Bergen Univ Coll, N-5020 Bergen, Norway
[6] Uni Res Rokkan Ctr, N-5020 Bergen, Norway
[7] Diakonhjemmet Hosp, Natl Advisory Unit Rehabil Rheumatol, N-0319 Oslo, Norway
[8] Oslo & Akershus Univ Coll Appl Sci, Program Occupat Therapy Prosthet & Orthot, N-0130 Oslo, Norway
关键词
Activities of daily living; Rehabilitation; Aged; Randomised controlled trial; Home-care services; Health care costs; OCCUPATIONAL-PERFORMANCE-MEASURE; RESTORATIVE HOME-CARE; OLDER-PEOPLE; VALIDITY; GO; RELIABILITY; PROGRAM; SERVICE; MODEL;
D O I
10.1186/1471-2318-14-139
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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.
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页数:9
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