The Effects of Low-volume High-intensity Interval Training Combined with Virtual Reality Technology on Cardiac Autonomic Nervous Function and Quality of Life in Patients with Coronary Heart Disease

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500107281

Enrollment

Unknown

Registered

2025-08-07

Start date

2025-03-04

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

Coronary Heart Disease

Interventions

REST group:Conduct regular rehabilitation training in the rehabilitation hall according to the specific conditions of the patient, 3 times a week, 30 minutes each time.

LV-HIIT group:Power bike training is carried out using the LV-HIIT exercise protocol, and exercise is carried out under the monitoring of electrocardiogram, blood pressure and pulse oximetry to ensure

LV-HIIT+VR group:Combine VR training on the basis of the LV-HIIT exercise prescription.

Eligibility

Sex/Gender

All

Age

40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meeting the diagnostic criteria for coronary heart disease, including chronic stable exertional angina pectoris, stable phase after acute coronary syndrome, asymptomatic ischemic heart disease, vasospastic angina pectoris, and microvascular angina pectoris; (2) Aged 40-80 years; (3) New York Heart Association (NYHA) functional class < III, and stable condition; (4) Low-risk or intermediate-risk in coronary heart disease exercise risk stratification; (5) Informed consent obtained from patients and their families, and voluntary signing of the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with coronary heart disease who have coronary artery stenosis =50% in the left main coronary artery or =70% in other coronary arteries as indicated by coronary angiography or coronary CTA, and who have not undergone revascularization therapy; (2) Patients with a cardiac pacemaker implanted; (3) Patients with malignant arrhythmia, grade ? atrioventricular block, acute pericarditis, severe valvular heart disease, myocardial disease, or other comorbid medical conditions that make them unable to tolerate exercise training; (4) Patients with unstable cerebrovascular disease; (5) Patients with mental disorders.

Design outcomes

Primary

Measure	Time frame
cardiopulmonary function ;indexes of cardiac autonomic nervous function ;cardiac structure parameters ;	—

Secondary

Measure	Time frame
Quality of Life Questionnaire Assessment ;serious cardiovascular adverse events ;hematological examination ;	—

Countries

China

Contacts

Public ContactLi Jia

Dean Hospital of Changzhou

609234006@qq.com+86 159 5057 8729

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026