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NCT06811519Recruiting

AI-based Prediction of Cardiac Function Using Echocardiography and Body Composition Data (ECHO-FIT Study)

Source: ClinicalTrials.gov · Last updated 4 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This prospective observational study (ECHO-FIT Study) aims to develop and validate a predictive model for cardiac function, particularly left ventricular ejection fraction (LVEF), by integrating echocardiographic measurements with body composition data obtained from the QCCUNIQ BC 720 device. The study plans to enroll 2,000 adult participants, comprising 1,000 individuals with normal LVEF (≥50%) and 1,000 with heart failure (LVEF \<50%), all of whom will undergo standard-of-care echocardiography and body composition analysis. By analyzing the relationships between key echocardiographic parameters (such as LVEF and diastolic function) and body composition measures (including fat mass, skeletal muscle mass, and total body water), we will develop a non-invasive prediction model capable of identifying individuals at higher risk of cardiac dysfunction. This innovative approach has the potential to enhance early detection and personalized management of heart failure, reduce dependence on resource-intensive diagnostic procedures, and ultimately improve patient outcomes.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2000 (estimated)
First submitted
31 Jan 2025
Start date
24 Feb 2025
Primary completion date
31 Dec 2027
Lead sponsor
Yonsei University
NCT number
NCT06811519

What you commit to

  • Study type: Observational
  • Planned participants: 2000
  • From 24 Feb 2025 to the primary completion date, 31 Dec 2027
  • 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

  • Having a physical or mental condition that makes it impossible to conduct an echocardiogram or perform body composition analysis.

Other

  • Deemed inappropriate for study participation by the researcher (e.g., unable to cooperate).

Who the study is looking for

  • Aged 20 years or older.
  • Undergoing a standard echocardiographic examination.
  • Providing consent to undergo body composition analysis.
  • Signing the informed consent form to voluntarily participate in the study.

Age in the registry: 20 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Yongin Severance Hospital
Coordinator of this site? Confirm its status
YŏnginSouth KoreaRecruiting

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