Actively Recruiting

Phase Not Applicable
Age: 17Years - 75Years
All Genders
NCT06385834

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

221 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the study was to intervene in the Aerobic exercise time of patients with STEMI and to explore the optimal exercise time for STEMI patients

CONDITIONS

Official 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 6531mm 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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Trial Site Locations

Total: 1 location

1

Renji Hospital

Shanghai, China

Actively Recruiting

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Research Team

J

Jun PU, MD

CONTACT

Y

YiHong Du, Master

CONTACT

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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