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RECRUITINGINTERVENTIONAL

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

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - Individuals aged 19-65 who have fully completed the voluntary consent form - Being of normal weight (BMI 18.5-24.9 kg/m²) or obese (30-34.99 kg/m²) - Having suffered a heart attack with ST elevation (STEMI) - To be enrolled in the study within the first 72 hours after hospital admission - To be willing to participate in a follow-up period of at least 3 months Who Should NOT Join This Trial: - Those who did not sign the voluntary consent form - Individuals aged over 65 - Weight loss exceeding 5% in the last 3 months - Those with malignancy, chronic renal failure or severe systemic disease - Patients unable to complete the questionnaires due to severe cognitive impairment - Those who have previously received nutrition education or eating awareness training Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Individuals aged 19-65 who have fully completed the voluntary consent form * Being of normal weight (BMI 18.5-24.9 kg/m²) or obese (30-34.99 kg/m²) * Having suffered a heart attack with ST elevation (STEMI) * To be enrolled in the study within the first 72 hours after hospital admission * To be willing to participate in a follow-up period of at least 3 months Exclusion Criteria: * Those who did not sign the voluntary consent form * Individuals aged over 65 * Weight loss exceeding 5% in the last 3 months * Those with malignancy, chronic renal failure or severe systemic disease * Patients unable to complete the questionnaires due to severe cognitive impairment * Those who have previously received nutrition education or eating awareness training

Treatments Being Tested

BEHAVIORAL

Digital Content-Supported Medical Nutrition Therapy

Participants receive a personalized medical nutrition therapy program supported by digital content. The program includes educational materials, meal planning guides, and remote support. The intervention lasts 3 months, with follow-up visits at baseline, 1 month, and 3 months. Heart function (LVEF) will be measured at each time point.

Locations (1)

Ondokuz Mayıs Üniversitesi Tıp Fakültesi Hastanesi
Samsun, Atakum, Turkey (Türkiye)