← Back to Clinical Trials
Recruiting NCT07427199

NCT07427199 Effect of Digitally Supported Medical Nutrition Therapy on Left Ventricular Ejection Fraction in Patients With ST-Elevation Myocardial Infarction

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07427199
Status Recruiting
Phase
Sponsor Saglik Bilimleri Universitesi
Condition ST-elevation Myocardial Infarction (STEMI)
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2025-12-30
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 19 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Digital Content-Supported Medical Nutrition Therapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 200 participants in total. It began in 2025-12-30 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

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

Contact & Investigator

Central Contact

Sena Yücel

✉ senayucel633@gmail.com

📞 +90 530 118 8468

Frequently Asked Questions

Who can join the NCT07427199 clinical trial?

This trial is open to participants of all sexes, aged 19 Years or older, up to 65 Years, studying ST-elevation Myocardial Infarction (STEMI). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07427199 currently recruiting?

Yes, NCT07427199 is actively recruiting participants. Contact the research team at senayucel633@gmail.com for enrollment information.

Where is the NCT07427199 trial being conducted?

This trial is being conducted at Samsun, Turkey (Türkiye).

Who is sponsoring the NCT07427199 clinical trial?

NCT07427199 is sponsored by Saglik Bilimleri Universitesi. The trial plans to enroll 200 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology