Actively Recruiting

Phase Not Applicable
Age: 40Years - 85Years
All Genders
Healthy Volunteers
NCT04962711

Risk-guided Disease Management Plan to Prevent Heart Failure in Patients Treated With Previous Chemotherapy (REDEEM)

Led by Baker Heart and Diabetes Institute · Updated on 2025-05-31

685

Participants Needed

1

Research Sites

143 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a prospective study in which a process of identifying and reducing heart failure (HF) risk will be applied to cancer survivors \>55 years old with chemotherapy \>5 years ago. The overall goal of this study to identify the feasibility and value of risk-guided cardiac rehabilitation (exercise, risk factor modification, and behavioural support) as a component of survivorship care.

CONDITIONS

Official Title

Risk-guided Disease Management Plan to Prevent Heart Failure in Patients Treated With Previous Chemotherapy (REDEEM)

Who Can Participate

Age: 40Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • History of cancer more than 10 years ago
  • Have received potentially toxic chemotherapy including Anthracycline (any dose), Trastuzumab (Herceptin) in breast cancer with HER2 mutation, Tyrosine kinase inhibitors (e.g., sunitinib), or left chest radiotherapy
Not Eligible

You will not qualify if you...

  • Ejection fraction less than 50% at baseline echocardiogram
  • Valvular stenosis or regurgitation of more than moderate severity
  • History of previous heart failure with baseline New York Heart Association classification greater than 2
  • Systolic blood pressure less than 110 mmHg
  • Pulse less than 60 per minute if not on beta blockers
  • Inability to obtain interpretable images from baseline echocardiogram
  • Contraindications to beta blockers or angiotensin-converting enzyme inhibitors
  • Life expectancy less than 12 months due to oncologic or other medical conditions, including pregnancy
  • Already taking both angiotensin converting enzyme inhibitors/angiotensin receptor blockers and beta blockers, or intolerance/allergy to both
  • Unable to provide written informed consent to participate in this study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Baker Heart and Diabetes Institute

Melbourne, Victoria, Australia, 3004

Actively Recruiting

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Research Team

J

Joel Smith

CONTACT

T

Thomas H Marwick, MD,PhD,MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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