Actively Recruiting

Phase Not Applicable
Age: 19Years - 65Years
All Genders
NCT07427199

Effect of Digitally Supported Medical Nutrition Therapy on Left Ventricular Ejection Fraction in Patients With ST-Elevation Myocardial Infarction

Led by Saglik Bilimleri Universitesi · Updated on 2026-02-23

200

Participants Needed

1

Research Sites

48 weeks

Total Duration

On this page

Sponsors

S

Saglik Bilimleri Universitesi

Lead Sponsor

O

Ondokuz Mayis University Training and Research Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study is designed to investigate the effect of a nutrition program supported by digital content on heart function in patients who have experienced a heart attack with ST-elevation. Participants will receive personalized dietary guidance and digital support materials for three months. The main goal is to determine whether this digital support materials can improve heart pumping function (measured by left ventricular ejection fraction). Participation involves following the dietary program and undergoing heart function measurements at the beginning, after one months and after three months.

CONDITIONS

Official Title

Effect of Digitally Supported Medical Nutrition Therapy on Left Ventricular Ejection Fraction in Patients With ST-Elevation Myocardial Infarction

Who Can Participate

Age: 19Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 19 to 65 who have fully completed the voluntary consent form
  • Normal weight (BMI 18.5-24.9 kg/m8) or obese (BMI 30-34.99 kg/m8)
  • Experienced a heart attack with ST elevation (STEMI)
  • Enrolled within 72 hours after hospital admission
  • Willing to participate in a follow-up period of at least 3 months
Not Eligible

You will not qualify if you...

  • Did not sign the voluntary consent form
  • Aged over 65
  • Weight loss exceeding 5% in the last 3 months
  • Have malignancy, chronic renal failure, or severe systemic disease
  • Unable to complete questionnaires due to severe cognitive impairment
  • Previously received nutrition education or eating awareness training

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

Ondokuz Mayıs Üniversitesi Tıp Fakültesi Hastanesi

Samsun, Atakum, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

Sena Yücel

CONTACT

Z

Ziya Erokay Metin, Doç.Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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