Status:

NOT_YET_RECRUITING

The Therapeutic Effect of Phase I Cardiac Rehabilitation on Elderly Patients With CHD Complicated by Sarcopenia

Lead Sponsor:

Qilu Hospital of Shandong University

Conditions:

Coronary Disease

Sarcopenia

Eligibility:

All Genders

60-90 years

Phase:

NA

Brief Summary

The purpose of this clinical trial is to explore whether Phase I cardiac rehabilitation can treat elderly patients with coronary heart disease complicated by sarcopenia. It will also investigate the m...

Detailed Description

The main purpose of this study is to explore the clinical efficacy of Phase I cardiac rehabilitation in the treatment of elderly patients with coronary heart disease complicated by sarcopenia and its ...

Eligibility Criteria

Inclusion

  • Age ≥ 60 years;
  • Coronary heart disease confirmed by coronary CTA or coronary angiography, with stable condition within the past 8 hours, including: ① no new or recurrent chest pain; ② no further elevation of troponin level; ③ no new signs of decompensated heart failure (dyspnea at rest accompanied by moist rales); ④ no new malignant arrhythmias or dynamic changes in electrocardiogram. Basic vital signs are normal, including: ① resting heart rate of 50-100 beats per minute; ② resting blood pressure of 90-150/60-100 mmHg (1 mmHg = 0.133 kPa); ③ oxygen saturation \> 95%.
  • Meeting the diagnostic criteria for sarcopenia (2024 Edition of Chinese Guidelines for the Diagnosis and Treatment of Sarcopenia);
  • Having good compliance to ensure the completion of this study;
  • Being able to understand the purpose of the trial, voluntarily participating in the study and signing the informed consent form.

Exclusion

  • Severe arrhythmia, decompensated heart failure, severe respiratory failure, untreated severe aortic stenosis, acute aortic dissection, resting hypertension with systolic and/or diastolic blood pressure \> 200/110 mmHg;
  • Mental disorders with limited cooperation ability; severe cognitive or behavioral disorders; end-stage diseases; acute diseases (e.g., acute infections, injuries) that restrict physical activity;
  • Poor compliance and inability to cooperate with the completion of this study.

Key Trial Info

Start Date :

October 10 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 10 2026

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT07197463

Start Date

October 10 2025

End Date

November 10 2026

Last Update

September 29 2025

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