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Digital diet plan aims to boost heart pumping power after heart attack

NCT ID NCT07427199

Disease control Sponsor: Saglik Bilimleri Universitesi Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a personalized nutrition program, supported by digital tools like meal plans and remote guidance, can improve heart function in people who recently had a severe heart attack (STEMI). Two hundred participants will follow the program for three months, and doctors will measure their heart's pumping ability at the start, one month, and three months. The goal is to see if better nutrition can help the heart recover more effectively.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
digital content-supported medical nutrition therapy
What this could lead to
If it works, this could point toward a simple, low-cost way to help heart attack patients recover better heart function through diet.
What could go wrong
This is a small, early-stage trial with only 200 people. The nutrition program is short (3 months), so any benefits may be modest or not last long. Diet changes can be hard to stick with.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Dec 2025

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

19 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

ST-elevation myocardial infarction

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

ST elevation myocardial infarction (stemi)

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Ondokuz Mayıs Üniversitesi Tıp Fakültesi Hastanesi

    RECRUITING

    Samsun, Atakum, Turkey (Türkiye)

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