CompletedNot Applicable

A Study on the Development and Application of a Cardiac Rehabilitation Nursing Intervention Protocol for Patients With First-Episode Acute Myocardial Infarction Following PCI, Based on a Socio-Ecological Theory Model

China66 participantsStarted 2026-03-14

Plain-language summary

The purpose of this \[Study Type: Clinical Trial\] is to investigate whether a cardiac rehabilitation nursing intervention based on the socio-ecological model can improve rehabilitation-related outcomes in patients. The study population consists of \[adult patients with acute myocardial infarction who have undergone percutaneous coronary intervention (PCI)\]. The primary research questions addressed in this study are: 1. Can a social-ecological model-based cardiac rehabilitation intervention improve adherence to cardiac rehabilitation among patients with myocardial infarction following PCI?\] 2. Can a social-ecological model-based cardiac rehabilitation intervention improve cardiac function and quality of life among patients with myocardial infarction following PCI?\] The researchers will compare the \[intervention group and the control group\] to observe whether there are \[group differences in cardiac rehabilitation adherence, cardiac function, and quality of life levels\]. Intervention group: Receives routine cardiology care combined with a social-ecological model-based cardiac rehabilitation intervention (1. In-hospital guidance; 2. Multidimensional, continuous rehabilitation support at home and in the community; 3. Regular follow-up assessments, etc.); Control Group: Received routine care from the cardiology department and standard discharge cardiac rehabilitation education; All participants completed questionnaire surveys and had cardiac function-related indicators collected at baseline, 3 months into the intervention, and 6 months into the intervention.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients with a first-time diagnosis of acute myocardial infarction who underwent PCI for the first time; * Age ≥ 18 years; * Alert and able to communicate effectively; ④ Willing to participate and sign an informed consent form. Exclusion Criteria: * Presence of absolute contraindications to exercise (e.g., unstable angina, severe heart failure, malignant arrhythmias, etc.); * Concurrent severe comorbidities (e.g., end-stage renal disease, malignant tumors, severe cognitive impairment); * Participation in other rehabilitation clinical trials.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Left Ventricular Ejection Fraction

Timeframe: From enrollment through the end of the three-month follow-up

Trial details

NCT IDNCT07753915

SponsorJinzhou Medical University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-06-20

View on ClinicalTrials.gov More Acute Myocardial Infarction (AMI) trials