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The present study investigates the efficacy of a mobile application in facilitating home cardiac rehabilitation for patients who have undergone percutaneous coronary intervention (PCI)

The present study investigates the efficacy of a mobile application in facilitating home cardiac rehabilitation for patients who have undergone percutaneous coronary intervention (PCI)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101547
Enrollment
Unknown
Registered
2025-04-25
Start date
2022-02-23
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Coronary Heart Disease

Interventions

Control Group:Cardiac rehabilitation program
Intervention Group:Cardiac rehabilitation program + portable ECG monitoring and smartphone app

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Age 18-65 years old, gender is not limited; 2) PCI surgery patients, at least 4 weeks postoperatively at the time of enrollment; 3) post-PCI angiography showed no untreated stenosis >70% of blood vessels; 4) normal blood troponin value (0.02 ~ 0.13 µg/L) in biochemical examination; 5) Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) The results of the cardiopulmonary exercise test include any of the following: the presence of angina pectoris symptoms or typical ischemic ECG changes, the appearance of angina pectoris symptoms/signs during low-intensity exercise (<5METs = or convalescence), and the presence of complex arrhythmias at rest or exercise; 2) Cardiogenic shock or heart failure after PCI surgery; 3) Survivors of sudden death or cardiac arrest; 4) Patients with severe psychological disorders; 5) LVEF < 40% on cardiac ultrasound before enrollment; 6) Those who are unable to perform aerobic exercise and cardiopulmonary exercise test due to neuromuscular or skeletal diseases; 7) Patients with intermittent claudication of lower limb arterial lesions; 8) Other cardiac lesions treated at the same time as PCI surgery, such as valvular lesions, macrovascular lesions, ventricular aneurysms, etc.; 9) pregnant or lactating women; 10) have rapidly developing neurological diseases; 11) Patients with acute and chronic lung impairment, liver failure, and renal failure.

Design outcomes

Primary

MeasureTime frame
Peak Oxygen uptake;

Secondary

MeasureTime frame
Anaerobic threshold;Weight;Body mass index, BMI;Blood Pressure;Blood lipid;Body fitness;Quality of life;Compliance;Physical ability;

Countries

China

Contacts

Public ContactYue Wu

Fuwai Hospital, Chinese Academy of Medical Sciences

wuyue1201@fuwaihospital.org+86 178 0101 3905

Outcome results

None listed

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