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About:
Rationale and protocol of the StayFitLonger study: a multicentre trial to measure efficacy and adherence of a home-based computerised multidomain intervention in healthy older adults
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Rationale and protocol of the StayFitLonger study: a multicentre trial to measure efficacy and adherence of a home-based computerised multidomain intervention in healthy older adults
Creator
Widmer, A
Agrigoroaei, S
Aubertin-Leheudre, M
Belleville, S
Berryman, N
Bherer, L
Bieler-Aeschlimann, M
Bier, N
Boller, B
Cardin, S
Cuesta, M
Demonet, J
Giacomino, K
Hager, A
Perez-Marcos, D
Source
Medline; PMC
abstract
BACKGROUND: In older adults, multidomain training that includes physical and cognitive activities has been associated with improvement of physical and cognitive health. The goal of the multisite StayFitLonger study is to assess a home-based computerised training programme, which combines physical exercises, stimulating cognitive activities and virtual coaching. METHODS: One hundred twenty-eight cognitively healthy older adults will be recruited from the community in Switzerland, Canada and Belgium. The study will comprise (1) a 26-week double-blind randomized controlled efficacy trial and (2) a 22-week pragmatic adherence sub-study. In the efficacy trial, participants will be randomly assigned to an experimental or an active control intervention. In the experimental intervention, participants will use the StayFitLonger programme, which is computerised on a tablet and provides content that combines physical activities with a focus on strength and balance, as well as divided attention, problem solving and memory training. Outcomes will be measured before and after 26 weeks of training. The primary efficacy outcome will be performance on the “Timed-Up & Go” test. Secondary outcomes will include measures of frailty, cognition, mood, fear of falling, quality of life, and activities of daily living. Age, sex, education, baseline cognition, expectation, and adherence will be used as moderators of efficacy. Following the 26-week efficacy trial, all participants will use the experimental programme meaning that participants in the control group will ‘cross over’ to receive the StayFitLonger programme for 22 weeks. Adherence will be measured in both groups based on dose, volume and frequency of use. In addition, participants’ perception of the programme and its functionalities will be characterised through usability, acceptability and user experience. DISCUSSION: This study will determine the efficacy, adherence and participants’ perception of a home-based multidomain intervention programme and its functionalities. This will allow for further development and possible commercialization of a scientifically validated training programme. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04237519 Registered on January 22, 2020 - Retrospectively registered.
has issue date
2020-08-28
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xsd:dateTime
)
bibo:doi
10.1186/s12877-020-01709-2
bibo:pmid
32859156
has license
no-cc
sha1sum (hex)
68d44ce4350f90e4831f1520ae806c9a35f3660d
schema:url
https://doi.org/10.1186/s12877-020-01709-2
resource representing a document's title
Rationale and protocol of the StayFitLonger study: a multicentre trial to measure efficacy and adherence of a home-based computerised multidomain intervention in healthy older adults
has PubMed Central identifier
PMC7453698
has PubMed identifier
32859156
schema:publication
BMC Geriatr
resource representing a document's body
covid:68d44ce4350f90e4831f1520ae806c9a35f3660d#body_text
is
schema:about
of
named entity 'older adults'
named entity 'physical exercises'
named entity 'assess'
named entity 'COACHING'
named entity 'cognitive'
named entity 'cognitive'
named entity 'The goal'
named entity 'Chat room'
named entity 't-test'
named entity 'peer-reviewed'
named entity 'older adults'
named entity 'Research team'
named entity 'IADL'
named entity 'activities'
named entity 'cognitive'
named entity 'arcade game'
named entity 'DSST'
named entity 'physical exercises'
named entity 'problem-solving'
named entity 'phenotype'
named entity 'correlated data'
named entity 'Parkinson's disease'
named entity 'executive functions'
named entity 'usability'
named entity 'physical status'
named entity 'Belgium'
named entity 'sample size'
named entity 'physical exercises'
named entity 'older adults'
named entity 'body position'
named entity 'Assisted Living'
named entity 'physical exercises'
named entity 'Switzerland'
named entity 'general health'
named entity 'sample size'
named entity 'older adults'
named entity 'facial expressions'
named entity 'Switzerland'
named entity 'parallel-group'
named entity 'stress regulation'
named entity 'free recall'
named entity '49, 50'
named entity 'wheelchair'
named entity 'cognition'
named entity 'smartwatch'
named entity 'quality control'
named entity 'accelerometer'
named entity 'WAIS-IV'
named entity 'User experience'
named entity 'Hospital Anxiety and Depression Scale'
named entity 'executive functions'
named entity 'double-blind'
named entity 'Pac-Man'
named entity 'Regression analyses'
named entity 'data integrity'
named entity 'CVLT'
named entity 'significant difference'
named entity 'Quality of Life'
named entity 'usability'
named entity 'fixed effects'
named entity 'HES-SO'
named entity 'Switzerland'
named entity 'RCT'
named entity 'Sedentary'
named entity 'polynomial regression'
named entity 'fatigue'
named entity 'physical exercises'
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