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Formulation and Efficacy of Exercise Prescription for Patients With Coronary Heart Disease

J

Jing Ma

Status

Unknown

Conditions

Coronary Heart Disease

Treatments

Behavioral: High intensity exercise prescription
Behavioral: Moderate intensity exercise prescription

Study type

Interventional

Funder types

Other

Identifiers

NCT04923711
2021-249

Details and patient eligibility

About

The purposes of this study is to standardize the process of formulating exercise prescriptions for coronary heart disease(CHD), verify the safety and effectiveness of exercise prescriptions, and establish a database of exercise prescriptions for CHD, with a view to providing new solutions for cardiac rehabilitation.

Full description

This study conducted a comparative study on the therapeutic effect and safety of exercise prescriptions for patients with coronary heart disease with different risk stratifications. The purposes of this study is to standardize the process of formulating exercise prescriptions for coronary heart disease(CHD), verify the safety and effectiveness of exercise prescriptions, and establish a database of exercise prescriptions for CHD, with a view to providing new solutions for cardiac rehabilitation.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18-80 years old with a diagnosis of coronary heart disease,NYHA class I-III HF patients.

Exclusion criteria

  • acute myocardial infarction within 2 weeks
  • Uncontrolled tachycardia (heart rate at rest >120bpm
  • Uncontrolled polypnea(breath rate at rest >30 breath per minute
  • Uncontrolled respiratory failure (SPO2 ≤90%)
  • Uncontrolled hyperglycemia (Random blood glucose>18mmol/L)
  • Uncontrolled malignant arrhythmia with hemodynamic instability
  • Uncontrolled septic shock and septicopyemia
  • Uncooperation of the patients

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

200 participants in 2 patient groups

Moderate Intensity Group
Experimental group
Description:
Group received a moderate exercise prescription of moderate intensity
Treatment:
Behavioral: Moderate intensity exercise prescription
High Intensity Group
Experimental group
Description:
Group received a moderate exercise prescription of high intensity
Treatment:
Behavioral: High intensity exercise prescription

Trial contacts and locations

1

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Central trial contact

Jing Ma

Data sourced from clinicaltrials.gov

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