- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04628754
A Randomized Control Trial of an Intervention to Reverse Frailty and Enhance Resilience Through Exercise and Education (REFEREE)
A Randomized Control Trial of a Primary Care Intervention to Reverse Frailty and Enhance Resilience Through Resistance Exercise and Dietary Protein Education (REFEREE) Among Community Dwelling Adults Aged 65 and Over
Resistance training done at home and protein supplementation may be the most effective and easiest to implement interventions to reverse frailty and build resilience. However, it is not common practice to offer and support such interventions in primary care.
This study provides an opportunity to assess the effectiveness of an optimised intervention with community-dwelling adults aged 65 and over, whose baseline clinical frailty score is not worse than mild (i.e. 5 or less), evaluate improvements in health outcomes and demonstrate how the intervention may be incorporated efficiently in clinical practice. The results are intended to encourage mainstream adoption of practical interventions to reverse clinical frailty and build resilience in primary care.
An intervention with ten recommended resistance exercises and dietary guidance on protein consumption has been derived from findings of our systematic review and meta-analysis and optimised through a patient and public involvement (PPI) process and feasibility study.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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-
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Dublin, Irland
- Beechlawn Medical Centre
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Aged 65 or older at baseline
- Rockwood clinical frailty scale score 4 or 5 (vulnerable or mildly frail)
- Able and willing to provide informed consent and to comply with the requirements of this study protocol
Exclusion Criteria:
- Rockwood clinical frailty scale score > 5
- End of life care
- Persons in residential care home
- Concurrent malignancy CKD stage 3 or 4
- Coded diagnosis of severe dementia as per GP or consultant geriatrician diagnosis or baseline Montreal Cognitive assessment (MoCA) score <= 10
- Persons unable to engage in discussion on frailty due to acute care needs or determined to be inappropriate by GP (e.g., needing transfer to ED or acutely unwell or disorders resulting in intolerance of the intervention)
- Subjects unable to provide written informed consent
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Ingen indgriben: Styring
Sædvanlig pleje
|
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Eksperimentel: Intervention
Resistance exercise and dietary protein guidance
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Home based exercise regime and dietary protein guidance
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Frailty status
Tidsramme: 3 months
|
Frailty status as measured by SHARE-frailty instrument measurement
|
3 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Clinical frailty status
Tidsramme: 3 months
|
Clinical frailty status measured by Clinical Frailty Scale 1 to 9, 9 is worse
|
3 months
|
Sarcopenia/ muscle mass
Tidsramme: 3 months
|
Sarcopenia/ muscle mass measured by bioelectrical impedance
|
3 months
|
Ease of the intervention
Tidsramme: 3 months
|
Ease of the intervention measured on a five-point scale: 'very easy', 'somewhat easy', 'neither easy nor hard', 'somewhat hard', or 'very hard'
|
3 months
|
Subjective difference to general health
Tidsramme: 3 months
|
Difference to general health as a result of the exercises measured on a five-point scale: 'much better', 'slightly better', 'about the same', 'slightly worse' or 'much worse'
|
3 months
|
Bone mass
Tidsramme: 3 months
|
Bone mass measured by bioelectrical impedance
|
3 months
|
Body fat
Tidsramme: 3 months
|
measured by bioelectrical impedance
|
3 months
|
Biological age
Tidsramme: 3 months
|
measured by bioelectrical impedance
|
3 months
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studieleder: Marie Therese Cooney, PhD, University College Dublin
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- REFEREE
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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Kliniske forsøg med Exercise and protein
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Anglia Ruskin UniversityDanone Nutricia ResearchRekrutteringGastrointestinal dysfunktion | AminosyreændringDet Forenede Kongerige
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USDA Grand Forks Human Nutrition Research CenterAktiv, ikke rekrutterendeFedmeForenede Stater
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University of AarhusArla Foods; Mejeribrugets ForskningsFond; Innovation foundationAfsluttetProteinmetabolismeDanmark
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Pennington Biomedical Research CenterAfsluttet
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USDA Grand Forks Human Nutrition Research CenterNorth Dakota Beef CommissionAfsluttet
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Arne AstrupAfsluttetUndersøgelsesfokus: AppetitDanmark
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University of CincinnatiNational Institute of Nursing Research (NINR)RekrutteringSlag | FamilieplejereForenede Stater
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Purdue UniversityAfsluttet
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University of KielAfsluttet
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University of UtahAfsluttet