Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT07016815

Telemonitoring to Optimize Medication Titration for Heart Failure: a Feasibility Study

Led by Chinese University of Hong Kong · Updated on 2025-07-30

80

Participants Needed

2

Research Sites

195 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Problem: Aggressive titration of guideline-directed medical therapy is the cornerstone of heart failure management to reduce heart failure related hospitalization and mortality. A major hurdle to uptitration of medical therapy is the safety concerns of these medications namely hypotension and bradycardia. Early and frequent clinic visits will be required to ensure the safe uptitration of these treatments, but this is difficult to implement in daily practice due to resources constrain. Advancement in wearable and wireless technologies enables remote and continuous monitoring of patients in ambulatory setting and potentially achieving safe and effective uptitration of medical therapy while minimizing the demand on the current healthcare system. However, access to these wearable and wireless technologies is not universal and patients in low socio-economic tiers might be deprived of the opportunity to realize the benefits from these technologies. Solution: This project therefore aims to develop a mobile platform and to provide wearable devices to patients with acute heart failure to improve and optimize the use of guideline-directed medical therapy in these patients. Impacts: The finding from this project will inform future heart failure management and help to implement and integrate telemedicine in the vulnerable stage of heart failure care. It will help to maximize healthcare resources utilization and help to bridge the gap between those who have limited access to healthcare services. The model of heart failure care generated from this project can be propagate and replicated in general patients care.

CONDITIONS

Official Title

Telemonitoring to Optimize Medication Titration for Heart Failure: a Feasibility Study

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical symptoms of dyspnoea (exertional or at rest) plus at least one of the following signs: congestion on chest X-ray, rales on chest auscultation, clinically relevant oedema (1+ or greater), or elevated jugular venous pressure
  • NT-proBNP level greater than 300 ng/L (or greater than 600 ng/L if atrial fibrillation/flutter) measured during the same hospitalization
  • Left ventricular ejection fraction less than 40% by any imaging method
  • Age 19 years or older
Not Eligible

You will not qualify if you...

  • Previous hospitalization for heart failure
  • Current hospitalization for acute heart failure caused primarily by pulmonary embolism, stroke, or acute myocardial infarction
  • Cardiac interventions within 30 days before or planned during the study, including major cardiac surgery, transaortic valve implantation, percutaneous coronary intervention, or MitraClip
  • Current or expected heart transplant, left ventricular assist device (LVAD), intra-aortic balloon pump (IABP), or planned outpatient inotropic support
  • Severe uncorrected primary cardiac valvular disease causing hemodynamic instability
  • Estimated glomerular filtration rate (eGFR) less than 30 mL/min/1.73m2 or need for dialysis
  • Allergy or intolerance to beta-blockers, renin-angiotensin-aldosterone system inhibitors, mineralocorticoid receptor antagonists, or angiotensin receptor/neprilysin inhibitors
  • Pregnant or nursing women
  • Psychiatric or severe neurological disorders, cirrhosis, or active cancer with life expectancy under 6 months
  • Non-ambulatory patients
  • Unable to operate simple electronic devices or access mobile network at home
  • Unable to provide written informed consent

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Prince of Wales Hospital

Hong Kong, Hong Kong, Hong Kong, 0000

Actively Recruiting

2

Prince of Wales Hospital

Hong Kong, Shatin, Hong Kong, 0000

Actively Recruiting

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Research Team

D

Daniel Xu

CONTACT

K

Kimmy Ho

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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