Actively Recruiting

Phase Not Applicable
Age: 17Years - 75Years
All Genders
ID06385834

The Effect of Morning vs Evening Aerobic Exercise Training on Cardiac Remodeling and Function Improvement in Patients After ST Elevation Myocardial Infarction

Led by RenJi Hospital · Updated on 2024-12-31

201

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cardiovascular disease is a leading cause of death worldwide, with over 30% of related deaths due to ST-segment Elevation Myocardial Infarction (STEMI). Aerobic exercise after STEMI has been shown to improve survival and heart function, but the best time of day for exercise to provide optimal heart benefits is not yet known. This study aims to evaluate whether morning or evening aerobic exercise can better improve heart remodeling and function in patients after STEMI. Participants will be randomly assigned to one of three groups: a morning aerobic exercise group exercising from 8:00 to 9:00 AM, an evening aerobic exercise group exercising from 4:00 to 5:00 PM, or a control group receiving standard care including medication and lifestyle advice. The exercise programs last 12 weeks with sessions three times a week, each including warm-up, aerobic, and relaxation exercises. Exercise intensity will be personalized based on initial testing and monitored using a fatigue scale. During the study, researchers will measure heart function through left ventricle ejection fraction at baseline, six weeks, and after 12 weeks of training or follow-up. Additional assessments include oxygen consumption, endothelial function, muscle and fat mass, cardiac structure, blood glucose and lipids, and heart-related biomarkers. Participants will be monitored for major cardiovascular events up to one year after rehabilitation, with ongoing follow-up to assess the lasting effects of exercise timing on heart health.

CONDITIONS

Brief Title

The Effect of Morning vs Evening Aerobic Exercise Training on Cardiac Remodeling and Function Improvement in Patients After ST Elevation Myocardial Infarction

Who Can Participate

Age: 17Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Between 18 and 75-years-old
  • Typical symptoms of acute myocardial infarction within 24 hours, with ST segment elevation of 61mm in two consecutive leads on electrocardiogram
  • After receiving complete revascularization treatment
  • Cardiac function grading I to II without any other serious complications
  • Left ventricular ejection fraction >30%
  • Compliant with the guidelines of the American College of Cardiology/American Heart Association for participating in cardiac rehabilitation standards
  • Signed written informed consent.
Not Eligible

You will not qualify if you...

  • Patients with unstable angina
  • Severe symptomatic congestive heart failure detectable myocardial ischemia
  • Valvular disease requiring surgery
  • Severe ventricular arrhythmias
  • Severe concomitant life-threatening diseases such as cancer, and rheumatoid disease
  • Osteoarticular diseases that may affect the exercise process

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants undergo a 12-week outpatient aerobic exercise training program three times a week, either in the morning or evening, including warm-up, aerobic, and relaxation exercises. Exercise intensity is personalized and gradually increased based on individual fitness assessments.

Three visits per week for 12 weeks (outpatient sessions)

Follow-up

Duration - 1 year

Participants are followed for one year after completing the exercise program to monitor major adverse cardiovascular events and overall cardiac health.

Regular follow-up visits over one year

Trial Site Locations

Total: 1 location

1

Renji Hospital

Shanghai, China

Actively Recruiting

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Research Team

J

Jun PU, MD

Y

YiHong Du, Master

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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