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NCT06656715Active, not recruiting

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

Source: ClinicalTrials.gov · Last updated 14 Jul 2026

Brief summary (registry, in English)

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

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
102 (actual)
First submitted
11 Oct 2024
Start date
16 Dec 2024
Primary completion date
1 Sept 2026
Lead sponsor
M.D. Anderson Cancer Center
NCT number
NCT06656715

What you commit to

  • Study type: Observational
  • Participants enrolled: 102
  • From 16 Dec 2024 to the primary completion date, 1 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Participants undergoing active cancer treatment.

Other

  • Inability to provide consent in the medical record, such as cognitively impaired individuals.

Who the study is looking for

  • Age 18 years and older
  • Individuals with a concurrent solid tumor cancer diagnosis
  • Not receiving active cancer treatment except for those on maintenance (i.e., Selective ER modulators (SERMs)\[Tamoxifen\], Aromatase inhibitors (Anastrozole, Letrozole, Exemestane), Ovarian suppression therapy (GnRH Agonists \[Leuprolide\], Androgen deprivation therapy for prostate cancer
  • Completed cancer treatment at least 3 months and up to 3 years before study enrollment.
    • Therapy
  • Able to read, speak and consent in English
  • Ability to understand and the willingness to sign a written informed consent document
  • Diagnosis of heart failure, confirmed by echocardiogram, MUGA, or cardiac catheterization
  • Internet access via smart phone, tablet, a computer, or another device with the capacity to 1) download the Fitbit App and 2) complete electronic study assessments via REDCap.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University of Texas of MD Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.