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Randomized controlled trial to evaluate a prevention program for frail community-dwelling older adults

Authors :
Birgitte Schoenmakers
Eva Dierckx
Sebastiaan Engelborghs
Ellen Elisa De Roeck
Anne van der Vorst
Jan De Lepeleire
Martinus Josephus Maria Kardol
Deborah Lambotte
Nico De Witte
Sarah Dury
Dominique Verté
Gertrudis I. J. M. Kempen
G. A. Rixt Zijlstra
Bram Fret
Daan Duppen
Michaël Van der Elst
Liesbeth De Donder
Jos M. G. A. Schols
Lieve Hoeyberghs
An Sofie Smetcoren
Peter Paul De Deyn
RS: CAPHRI - R1 - Ageing and Long-Term Care
Promovendi PHPC
Health Services Research
Family Medicine
RS: Academische Werkplaats Ouderenzorg
Educational Science
Belgian Ageing Studies
Brussels research center for Innovation in Learning and Diversity
Clinical sciences
Neurology
Gerontology
Psychology
Brain, Body and Cognition
Personality and Psychopathology
Psychopathology and Information Processing in Older Adults
Source :
BMC Geriatrics, BMC geriatrics, BMC Geriatrics, Vol 18, Iss 1, Pp 1-12 (2018), BMC Geriatrics, 18:194. BioMed Central Ltd
Publication Year :
2018
Publisher :
BioMed Central Ltd, 2018.

Abstract

BACKGROUND: Frail community-dwelling older adults, whom might experience problems regarding physical, cognitive, psychological, social and environmental factors, are at risk for adverse outcomes such as disability, institutionalization and mortality. People in need of help do not always find their way to care and support services and are left undetected. The aim of the D-SCOPE project is to detect frail community-dwelling older adults who previously went unnoticed and to improve their access to care and support. Goal is to increase their frailty-balance, quality of life, meaning in life, life satisfaction, mastery, community inclusion and ageing well in place. METHODS/DESIGN: The study is a prospective, longitudinal randomized four-armed controlled trial with follow-up at 6 months. The study group aims to include 900 community-dwelling older adults aged 60 years and over from 3 municipalities in Flanders (Belgium). While selecting the study group, risk profiles for frailty will be taken into account. Participants will be randomly selected from the census records in each municipality. Data will be collected prospectively at baseline (T0) and at follow-up, 6 months after baseline (T1). At baseline, participants who are at least mild frail on one of the 5 domains of frailty (CFAI-plus) or feel frail based on the subjective assessment of frailty will be randomly assigned to (1) the study group or (2) the control group. A mixed method design with the inclusion of quantitative and qualitative data analyses will be used to evaluate the efficacy and experiences of the detection and prevention program on frailty. DISCUSSION: The study will contribute to an innovative vision concerning the organization of care and support, and a timely and accurate detection and support of community-dwelling older adults at risk for frailty. TRIAL REGISTRATION: This trial was registered at ClinicalTrials.gov, on May 26, 2017, identifier: NCT03168204 . ispartof: BMC GERIATRICS vol:18 issue:1 ispartof: location:England status: published

Details

Language :
English
ISSN :
14712318 and 03168204
Volume :
18
Database :
OpenAIRE
Journal :
BMC Geriatrics
Accession number :
edsair.doi.dedup.....28b6d483a2df56fb19d1dbd528c938d4
Full Text :
https://doi.org/10.1186/s12877-018-0875-3