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Can diet coaching boost heart attack recovery?

NCT ID NCT07624240

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether giving heart attack patients personalized diet advice during early cardiac rehab helps them eat better. Fifty adults who recently had a heart attack took part. Some got standard rehab, while others also received one-on-one counseling from a dietitian. The goal was to see if the extra support improves diet quality and knowledge.

What this could mean

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

Active substance
dietary education
What this could lead to
If it works, this could show that adding personalized diet advice to standard rehab helps heart attack patients eat healthier.
What could go wrong
This is a small, completed study with only 50 people, so results may not apply to everyone. It's about improving diet, not treating the heart attack itself.

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

50 people

The number who actually took part.

Started

Jun 2024

Finished

Mar 2026

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

18 years and older

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: * age ≥18 years, * recent myocardial infarction treated according to standard clinical practice, * qualification for early cardiac rehabilitation after myocardial infarction, * clinically stable status at enrollment, * ability to participate in standard rehabilitation and additional nutritional education, * ability to complete dietary and nutritional knowledge questionnaires, * ability to undergo anthropometric measurements and bioelectrical impedance analysis, * provision of written informed consent. Exclusion Criteria: * refusal or inability to provide informed consent, * contraindications to cardiac rehabilitation, * severe clinical instability, including unstable hemodynamic status, recurrent ischemia, uncontrolled arrhythmia, or decompensated heart failure, preventing participation in rehabilitation; * severe cognitive, psychiatric, or communication limitations preventing participation in educational sessions or reliable questionnaire completion, * conditions preventing valid body composition assessment (according to device producer e.g. large metal implants).

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Medical University of Lublin

    Lublin, 20-093, Poland

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