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Diet and Exercise for FRAILty: DEFRAIL

The effect of a standardised exercise and nutritional intervention on clinical and biochemical markers of frailty in older adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN46458028
Enrollment
24
Registered
2020-06-18
Start date
2019-01-02
Completion date
Unknown
Last updated
2023-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty Signs and Symptoms Frailty

Interventions

The intervention is an eight-week program of multi-component resistance, aerobic, balance, and flexibility) exercise classes, combined with protein supplementation in the form of commercially availabl

Sponsors

Royal College of Surgeons in Ireland
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged =65 years 2. Clinical Frailty Scale (CFS) score of =5 as assessed by the multidisciplinary team of a geriatric medicine outpatient clinic

Exclusion criteria

Exclusion criteria: 1. Unable to mobilise without the assistance of another person 2. Severe cognitive or sensory impairment that would prevent participation in the intervention, even despite reasonable supports 2. Participation in any research that could impact on the outcome of this study 3. Documented milk-allergy

Design outcomes

Primary

MeasureTime frame
Frailty assessed by Fried frailty criteria comprised of identification of weak grip strength, slow gait speed, excessive weight loss, exhaustion and reduced activity based on pre-determined thresholds at baseline, 8 and 16 weeks

Secondary

MeasureTime frame
1. Falls risk as assessed by the Timed Up & Go (TUG) test at baseline, 8 and 16 weeks 2. Functional leg strength assessed by the 30-second sit-to-stand (30STS) test at baseline, 8 and 16 weeks 3. Frailty assessed by Electronic frailty Index (eFI) at baseline, 8 and 16 weeks 4. Body composition assessed by the Bio-electrical Impedance Analysis (BIA) using BodyStat Quadscan 4000 at baseline, 8 and 16 weeks 5. Arterial stiffness assessed by Carotid-femoral Pulse Wave Velocity (cfPWV) using Complior Analyse device & software at baseline, 8 and 16 weeks 6. Cognitive impairment assessed by Montreal Cognitive Assessment (MoCA) by face-to-face interview at baseline, 8 and 16 weeks 7. Depression assessed by the Geriatric Depression Scale Short Form (GDS-SF) by face-to-face interview at baseline, 8 and 16 weeks 8. Quality of life assessed by the CASP-19 quality of life scale by face-to-face interview at baseline, 8 and 16 weeks 9. Pain as assessed by the Pain Numerical Rating Scale (PNRS) by face-to-face interview at baseline, 8 and 16 weeks 10. Frailty assessed through biochemical markers of frailty in serum samples analysed using MagPix Luminex system (CRP, IL-6, IL-8, IL-10, TNF-alpha and IFN-gamma) and standalone ELISA (Cystatin-C) at baseline, 8 and 16 weeks

Countries

Ireland

Contacts

Public ContactPádraig Bambrick
padraigbambrick@rcsi.ie+35351842390

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 15, 2026