Actively Recruiting

Age: 18Years +
All Genders
NCT06656715

Symptom Burden and Health Related Quality of Life of Cancer Patients With Concurrent Heart Failure

Led by M.D. Anderson Cancer Center · Updated on 2025-12-23

100

Participants Needed

1

Research Sites

193 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To describe and compare the symptom burden in cancer patients with concurrent diagnosis of heart failure (HFrEF compared to HFpEF).

CONDITIONS

Official Title

Symptom Burden and Health Related Quality of Life of Cancer Patients With Concurrent Heart Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years and older
  • Individuals with a concurrent solid tumor cancer diagnosis
  • Not receiving active cancer treatment except for maintenance treatments such as Selective ER modulators (Tamoxifen), Aromatase inhibitors (Anastrozole, Letrozole, Exemestane), or Ovarian suppression therapy (GnRH Agonists like Leuprolide), and Androgen deprivation therapy for prostate cancer
  • Completed cancer treatment at least 3 months and up to 3 years before study enrollment
  • Able to read, speak, and consent in English
  • Willing and able to sign a written informed consent document
  • Diagnosis of heart failure confirmed by echocardiogram, MUGA, or cardiac catheterization
  • Access to internet via smartphone, tablet, computer, or another device capable of downloading the Fitbit App and completing electronic study assessments via REDCap
Not Eligible

You will not qualify if you...

  • Participants undergoing active cancer treatment
  • Inability to provide consent as documented in the medical record, such as cognitive impairment

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

The University of Texas of MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

A

Anceita Fadol, MSN,PHD,RN

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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