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Value of Cardiac Rehabilitation on the Treatment of Cardiovascular Disease

Value of Cardiac Rehabilitation on the Treatment of Cardiovascular Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05320848
Enrollment
100
Registered
2022-04-11
Start date
2021-02-01
Completion date
2025-02-01
Last updated
2022-04-11

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

Conditions

Cardiac Rehabilitation

Brief summary

Cardiac rehabilitation is a valuable treatment for patients with a broad spectrum of cardiac disease. Current guidelines support its use in patients after acute coronary syndrome, coronary artery bypass grafting, coronary stent placement, valve surgery, and stable chronic systolic heart failure. Its use in these conditions is supported by a robust body of research demonstrating improved clinical outcomes. Despite this evidence, cardiac rehabilitation referral and attendance remains low and interventions to increase its use need to be developed.

Detailed description

The trial was conducted in Shenzhen in China. This study will recruit 100 patients with cardiovascular disease with a median and minimum follow-up of 24 and 6 months. Patients will be individually randomized to receive either a cardiac rehabilitation program (n = 50) or enhanced standard care involving educational advice (n = 50). The co-primary outcomes are: 1) first occurrence of major adverse cardiovascular events (MACE) (composite of all-cause mortality, myocardial infarction, stroke, or emergency cardiovascular hospitalization); and 2) self-rated health on the Quality of Life-5 Dimensions-5 Level visual analogue scale.

Interventions

BEHAVIORALcardiac rehabilitation

Cardiac rehabilitation is a valuable treatment for patients with a broad spectrum of cardiac disease.

Sponsors

Shenzhen People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Cardiovascular disease

Exclusion criteria

* Incalculable TFC * Coronary artery spasm or ectasia * LV ejection fraction \< 52% in males or \< 54% in females * Abnormal heart structure (congenital heart disease, cardiomyopathies, or valvular dysfunction) * Pericardial disease (pericardial effusion or constrictive pericarditis) * Previous history of myocardial infarction * Uncontrolled hypertension (systolic blood pressure \> 160 mmHg or diastolic blood pressure \> 105 mmHg) * Hyperthyroidism * Hypothyroidism * Malignancy * Autoimmune disease * Infection * Pulmonary, hepatic, and renal disorders * Haematological disorders (anaemia, bone marrow involved by neoplastic disease, or red blood cell transfusions)

Design outcomes

Primary

MeasureTime frameDescription
first occurrence of major adverse cardiovascular events (MACE)3 yearsfirst occurrence of major adverse cardiovascular events (MACE) (composite of all-cause mortality, myocardial infarction, stroke, or emergency cardiovascular hospitalization)
maximum oxygen uptake3 yearsmaximum oxygen uptake

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026