Actively Recruiting

Phase Not Applicable
Age: 21Years - 100Years
All Genders
NCT05946174

Tackling Disruptions to Frailty Interventions: Developing Personalized Interventions Targeted for Older Persons With Cardiac Frailty

Led by National Heart Centre Singapore · Updated on 2025-06-05

500

Participants Needed

6

Research Sites

258 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Background: Muscle mass loss and metabolic dysfunction, exacerbated by inactivity and nutritional inadequacies, underpin both cardiovascular disease and frailty in ageing. The investigators' proposal seeks to develop interventions in exercise and diet that are targeted for older adults with cardiac frailty. Methods: The investigators' proposal is a five-year study comprising of first phase (first 2-2.5 years) and second phase (next 2-2.5 years). In the first phase cardiac frail participants (up to N=500) from each healthcare transition (inpatient hospital, step-down community hospital, outpatient clinic/community) will be randomized to receive Intervention Sets or usual care. The second phase will scale up these programs. Three Intervention Sets A, B, and C will be implemented in the outpatient, step-down community hospital, and acute hospital settings. Diet intervention comprises meal sets prepared with nutrients involved in energy metabolism. Exercise training is facilitated by hospital gyms and hospital physiotherapists. Diet and exercise behavior will be monitored using questionnaires, video conferencing and meal photos. Significance: Clinical studies are urgently needed using consistent frailty tools to evaluate the efficacy and promise of frailty interventions, targeted to achieve reversal/retardation of frailty. When scaled up, these approaches will provide high-quality science needed to manage cardiac frailty towards healthier population ageing.

CONDITIONS

Official Title

Tackling Disruptions to Frailty Interventions: Developing Personalized Interventions Targeted for Older Persons With Cardiac Frailty

Who Can Participate

Age: 21Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 21 years or older
  • Able to walk outdoors
Not Eligible

You will not qualify if you...

  • Bed-bound status
  • Dementia stage 6 or higher
  • Living in sheltered or nursing homes
  • Having cancer
  • Participating in ongoing clinical trials involving drugs or devices
  • Uncontrolled hypertension (systolic 4160 mmHg or diastolic 490 mmHg) despite treatment
  • Low blood pressure (systolic <90 mmHg or diastolic <40 mmHg)
  • Uncontrolled atrial fibrillation (controlled allowed)
  • Ventricular arrhythmias such as ventricular tachycardia
  • Renal failure requiring dialysis
  • Chronic kidney disease stage 4 or above
  • Nephrotic syndrome
  • Liver cirrhosis Child's B or higher
  • Inflammatory bowel disease
  • Severe uncontrolled gout
  • Poorly controlled diabetes with Hba1c 49%
  • Taking warfarin
  • Having food allergies such as shellfish or prawn
  • Life expectancy less than one year as assessed by investigator
  • Receiving nasogastric or parenteral nutrition
  • Hypertrophic cardiomyopathy
  • Cardiac amyloidosis
  • Cardiac sarcoidosis

AI-Screening

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Trial Site Locations

Total: 6 locations

1

Alexandra Hospital

Singapore, Singapore, 159964

Actively Recruiting

2

National Heart Centre Singapore

Singapore, Singapore, 169609

Actively Recruiting

3

Changi General Hospital

Singapore, Singapore, 529889

Actively Recruiting

4

Sengkang General Hospital

Singapore, Singapore, 544886

Actively Recruiting

5

Jurong Community Hospital

Singapore, Singapore, 609606

Actively Recruiting

6

NHG Polyclinics

Singapore, Singapore

Actively Recruiting

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Research Team

A

Angela Su-Mei Koh

CONTACT

G

Gina Sihui Lee

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

6

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