NCT07624240Completed
Educational Dietary Intervention in Early Cardiac Rehabilitation After Myocardial Infarction
Source: ClinicalTrials.gov · Last updated 5 Jun 2026
Brief summary (registry, in English)
The trial is designed to assess whether individualized nutritional education provides additional benefit beyond standard early cardiac rehabilitation in patients after myocardial infarction. Patients referred for cardiac rehabilitation after myocardial infarction are randomized to a control group receiving standard rehabilitation care or to an intervention group receiving standard care plus structured personalized dietary education. The educational intervention is tailored to baseline dietary habits, nutritional knowledge, and adherence to cardioprotective dietary recommendations. Outcomes include changes in diet quality, adherence to the Mediterranean diet, nutritional knowledge, anthropometric measures, and bioelectrical impedance analysis-derived body composition parameters. The study will evaluate the feasibility and effectiveness of integrating individualized dietary education into early cardiac rehabilitation after myocardial infarction.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 50 (actual)
- First submitted
- 8 May 2026
- Start date
- 1 Jun 2024
- Primary completion date
- 31 Mar 2026
- Lead sponsor
- Medical University of Lublin
- Diseases
- Coronary artery disease
- NCT number
- NCT07624240
What you commit to
- Study type: Interventional
- Participants enrolled: 50
- From 1 Jun 2024 to the primary completion date, 31 Mar 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- 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).
Other
- refusal or inability to provide informed consent,
Who the study is looking for
- 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.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Medical University of Lublin Coordinator of this site? Confirm its status | Lublin | Poland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.