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Can a Community-Based rehab program boost heart recovery after a first attack?

NCT ID NCT07753915

Disease control Sponsor: Jinzhou Medical University Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time

Summary

This trial tests whether a cardiac rehabilitation program based on a socio-ecological model can improve recovery in adults who have had a first heart attack and undergone a stent procedure. The program goes beyond standard care by providing guidance on exercise, diet, medication, and emotions, and by building a support network that includes healthcare teams and community resources. Researchers will compare this group to patients receiving routine care, measuring heart function, rehabilitation adherence, and quality of life over six months.

What this could mean

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

Active substance
A cardiac rehabilitation nursing intervention based on the socio-ecological model, including exercise, diet, medication, and emotional guidance, plus multidisciplinary team support and follow-up.
What this could lead to
If effective, this program could become a standard approach to help heart attack patients stick with rehabilitation, improve heart function, and enhance quality of life after stent placement.
What could go wrong
This is a small, early-stage study, so results may not apply to all patients. The intervention's success depends on patient adherence and support systems, which can vary widely.

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

66 people

The number who actually took part.

Started

Mar 2026

Finished

Jun 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: * 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.

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Conditions

The condition(s) this trial relates to.

acute myocardial infarction

As listed by the trial registrant

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

Acute myocardial infarction (AMI) Percutaneous coronary intervention (PCI)

Contacts and locations

Locations

  • The First Affiliated Hospital of Jinzhou Medical University

    Jinzhou, Liaoning, 121001, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.