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Clinical Trials/NCT07155928
NCT07155928Not yet recruitingNot Applicable

The Effect of Cardiac Rehabilitation on Left Ventricular Remodeling in Patients Undergoing Primary Percutaneous Coronary Intervention for Acute Myocardial Infarction

Assiut University0 sites100 target enrollmentStarted: November 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
100
Primary Endpoint
Change in LV remodeling assessed by LV ejection fraction (LVEF)

Study Overview

Brief Summary

Cardiac rehabilitation has proven to improve the functional capacity of patients who had acute myocardial infarction. However, its effect on Left ventricular remodeling following an MI event treated with Primary PCI is not yet fully understood. So, for this randomized controlled trial our objectives are as follows:

  • Primary: To assess the effect of a structured CR program on LV remodeling parameters (LVEF, LVESV, LVEDV, LVESD, LVEDD + SWMA) in STEMI patients treated with primary PCI.
  • Secondary: To evaluate changes in exercise capacity, heart rate recovery and clinical outcomes such as major adverse cardiovascular events and the effect of CR on the patients' Quality of Life.

These results will be compared to the same parameters in a control group that will not undergo cardiac rehabilitation to properly assess the effect of cardiac rehab.

Participants in the intervention group will be asked to undergo a supervised CR program based on published guidelines (FITT principle). The core will be a moderate-intensity aerobic exercise regimen (e.g. treadmill or cycle ergometer) 2-3 times per week for 12 weeks. Each session will last ~20-60 minutes of exercise followed by cool-down, with intensity gradually increased to High intensity interval training (HIIT) in low-moderate risk individuals, as it has shown better improvement in cardiovascular health while being safe in MI patients. Resistance exercises (e.g. light weights or band exercises) will also be included twice weekly. Exercise dose (frequency, intensity, time) will be tracked. Physical therapists will supervise all sessions in an outpatient CR facility or affiliated gym. Patients' vitals and ECG will be monitored during initial sessions for safety.

Detailed Description

ST-segment elevation myocardial infarction (STEMI) remains a leading cause of morbidity and mortality worldwide. Primary percutaneous coronary intervention (PCI) is the gold standard for reperfusion therapy in STEMI, significantly improving survival rates. However, adverse left ventricular (LV) remodeling post-STEMI can lead to heart failure, poor clinical outcomes and deterioration in patients' quality of life.

Cardiac rehabilitation (CR) is a multidisciplinary intervention designed to optimize cardiovascular recovery. It involves a spectrum of interventions including a structured exercise program, patient education, nutritional counseling, risk factor modification and psychosocial support. CR is divided into 4 stages. Stage I is in-hospital exercise (early mobilization and patient education). Stage II is early outpatient supervised rehabilitation in rehabilitation centers lasting 3 months post-PCI. Stage III starts at 3-12 months and is usually home-based rehabilitation with frequent visits to rehabilitation centers. Stage IV is long term rehab where the patient continues to exercise and commit to a healthy lifestyle to prevent further episodes of cardiovascular disease. Research has shown that stage II is the most crucial of them all, and starting during early in-hospital setting has shown no further improvement in cardiovascular health.

Exercise-based programs, have especially shown beneficial effects on LV function post-AMI, improving exercise capacity and potentially limiting adverse remodeling process. It has been reported that supervised exercise training after STEMI significantly increased LVEF and reduced the rate of unfavorable remodeling at 6 months compared to usual care.

Moreover, there was a significant reduction in post-treatment LV mass, EF, and LV dimensions relative to pretreatment. It has also been suggested that early initiation of CR may reduce systemic inflammation and promote favorable ventricular remodeling.

However, other studies have shown that CR may not have a clinically significant improvement in LV parameters despite the overall improvement in patient's exercise capacity , but these studies were performed with a small sample size. Other trials have shown mixed results, with some showing favorable remodeling after exercise therapy, and some showing no improvement in cardiac dimensions. Another study mentioned that CR may have a positive effect on LV diastolic dysfunction, without any change to LV dimensions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Underwent successful primary PCI within 24 hours of symptom onset.
  • •Hemodynamically stable and able to participate in rehabilitation.

Exclusion Criteria

  • •Stage IV Heart failure, LVEF < 30%
  • •Life-threatening arrhythmias
  • •Unstable Angina
  • •Severe Valvular Diseases
  • •Uncontrolled Hypertension
  • •CKD Stages IV and V
  • •Hypothyroidism
  • •Cardiomyopathy
  • •Inability to ambulate or consent

Arms & Interventions

Intervention Group

Experimental

Standard Treatment + Cardiac Rehabilitation

Intervention: Cardiac Rehabilitation (Behavioral)

Intervention Group

Experimental

Standard Treatment + Cardiac Rehabilitation

Intervention: Primary Percutaneous Coronary Intervention (Procedure)

Control Group

Active Comparator

Standrad Treatment Only

Intervention: Primary Percutaneous Coronary Intervention (Procedure)

Outcomes

Primary Outcomes

Change in LV remodeling assessed by LV ejection fraction (LVEF)

Time Frame: Before and after a 3-month cardiac rehabilitation program

LVEF assessed in "%"

Change in LV remodeling assessed by LV end-systolic Volume (LVESV), LV end-diastolic Volume (LVEDV)

Time Frame: Before and after a 3-month cardiac rehabilitation program

LVESV and LVEDV are both assessed in mL

Change in LV remodeling assessed by LV ejection fraction (LVEF)

Time Frame: Before and after a 3-month cardiac rehabilitation program

LVEF assessed in "%"

Change in LV remodeling assessed by LV end-systolic Volume (LVESV), LV end-diastolic Volume (LVEDV)

Time Frame: Before and after a 3-month cardiac rehabilitation program

LVESV and LVEDV are both assessed in mL

Change in LV remodeling assessed by LV end-systolic Diameter (LVESD) and LV end-diastolic Diameter (LVEDD).

Time Frame: Before and after a 3-month cardiac rehabilitation program

LVESD and LVEDD are both assessed in millimeters

Secondary Outcomes

  • Exercise capacity assessed in METs(Before and after a 3-month cardiac rehabilitation program)
  • Heart rate recovery post-exercise.(Before and after a 3-month cardiac rehabilitation program)
  • Incidence of MACE during follow-up(Throughout the 3 month CR program)
  • Exercise capacity assessed in METs(Before and after a 3-month cardiac rehabilitation program)
  • Heart rate recovery post-exercise.(Before and after a 3-month cardiac rehabilitation program)
  • Incidence of MACE during follow-up(Throughout the 3 month CR program)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Hatem Hassan Mohammed Maghraby

Principal investigator

Assiut University

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