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A randomized controlled trial to assess feasibility of aerobic exercise-based cardiac rehabilitation on patients with coronary heart disease

A randomized controlled trial to assess feasibility of aerobic exercise-based cardiac rehabilitation on patients with coronary heart disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17010556
Enrollment
Unknown
Registered
2017-02-06
Start date
2016-06-01
Completion date
Unknown
Last updated
2018-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coronary heart disease

Interventions

Intervention group:aerobic exercise training with target intensity
Control group:Leisure walk

Sponsors

Shanghai Xuhui Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Coronary heart disease patients; 2. aged 45 to 80 years old; 3. stratified into low, moderate risk; 4. signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) cognitive impairment or mental disorder assessed by MMSE 160 mmHg or resting diastolic blood pressure > 100 mmHg); (5) cardiac function class IV; (6) coronary heart disease accompanied by acute complications (coronary artery dissection, ventricular aneurysm, large area of myocardial infarction associated with shock, acute vascular occlusion including stent thrombosis) and high cardiac risk for rehabilitation; (7) active pericarditis or myocarditis, serious infection, chronic obstructive pulmonary disease, moderate to serious aortic stenosis, resting heart rate after drug control > 100 times/min; (8) new deep vein thrombosis, thrombophlebitis, aortic dissection or aneurysm in other parts of the body, lower limb occlusive atherosclerosis; (9) cannot tolerate exercise with fracture, arthritis or muscle pain; (10) abnormal electrolyte such as potassium, sodium or calcium; (11) uncontrolled hyperthyroidism or hypothyroidism at the time of recruitment; (12) COPD with signs of infection such as fever, sore throat, coughing.

Design outcomes

Primary

MeasureTime frame
retention rate;recruitment rate;

Secondary

MeasureTime frame
hypertension;dyslipidemia;diabetes;obesity;smoking status;anaerobic threshold;

Countries

China

Contacts

Public ContactJIAN YANG

Shanghai Xuhui Central Hospital

jyang@scrc.ac.cn+86 13361801366

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026