NCT07753915

Brief 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. 1.Can a social-ecological model-based cardiac rehabilitation intervention improve adherence to cardiac rehabilitation among patients with myocardial infarction following PCI?\]
  2. 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 \[group differences in cardiac rehabilitation adherence, cardiac function, and quality of life levels\].

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 14, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 20, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 20, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

August 3, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 10, 2026

Completed
Last Updated

August 10, 2026

Status Verified

August 1, 2026

Enrollment Period

3 months

First QC Date

August 3, 2026

Last Update Submit

August 6, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Left Ventricular Ejection Fraction

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

Study Arms (2)

Control Group

NO INTERVENTION

Intervention Group

EXPERIMENTAL
Other: A Cardiac Rehabilitation Nursing Intervention Program Based on the Social-Ecological Theory Model

Interventions

Building on routine cardiac nursing care, implement a cardiac rehabilitation nursing intervention based on the socio-ecological model, with an intervention period of 1 month. Interventions were carried out at the individual, interpersonal, organizational, community, and policy levels: at the individual level, guidance was provided on exercise, diet, medication, and emotional management; at the organizational level, a multidisciplinary rehabilitation team was established; at the interpersonal level, family members were mobilized to participate in collaborative care; at the community level, a system of continuous follow-up management was established, with monthly online and in-person rehabilitation guidance and assessments; and at the policy level, policy interpretation and guidance were provided to different population groups.

Intervention Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The First Affiliated Hospital of Jinzhou Medical University

Jinzhou, Liaoning, 121001, China

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Nurse

Study Record Dates

First Submitted

August 3, 2026

First Posted

August 10, 2026

Study Start

March 14, 2026

Primary Completion

June 20, 2026

Study Completion

June 20, 2026

Last Updated

August 10, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

To protect patient privacy, all raw data will be uploaded to the ResMan Clinical Trial Management Platform (https://www.myresman.com/) six months after the study is completed.

Locations