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The impact of digital health management on clinical outcomes of patients with acute coronary syndrome after PCI--a multicenter, randomized, controlled study

The impact of digital health management on clinical outcomes of patients with acute coronary syndrome after PCI--a multicenter, randomized, controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086452
Enrollment
Unknown
Registered
2024-07-02
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

acute coronary syndrome

Interventions

Experimental group:Within one year after discharge, in addition to receiving current routine postoperative follow-up management, they also received digital platform management.
control group:Received current routine postoperative follow-up management within 1 year after discharge

Sponsors

The First Affiliated Hospital of Xi 'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: a. 18 years = Age<70 years; b. Newly diagnosed patients who meet the clinical diagnosis of ACS; c. Patients who meet the discharge criteria after PCI surgery; d. Patients with an expected survival period of more than 1 year; e. Patients who have certain learning, understanding and communication skills, can correctly understand the content related to the experiment, and can actively cooperate with research needs; f. Patients who can use smartphones, operate specialized software for Jiuyi, and are interested in research; g. The clinical data is complete and the patient voluntarily participates. The family members agrees to sign an informed consent form.

Exclusion criteria

Exclusion criteria: a. accompanied by severe heart, liver and kidney dysfunction, immune dysfunction, and other serious acute and chronic systemic diseases; b. Patients with severe complications such as dissection, shock, and massive hematoma after PCI surgery; c. Patients with hemorrhagic diseases and malignant tumors; d. Untreated ventricular tachycardia, severe heart failure, uncontrolled hypertension or hypotension; e. have a history of cardiac surgery; f. Patients with mental illness, severe cognitive impairment or lack of autonomous behavior ability; g. Patients who are unable to operate smartphones for experimental purposes (such as vision, hearing, or flexibility disorders); h. Lack of Internet access in residence; i. Patients who refuse to sign informed consent forms.

Design outcomes

Primary

MeasureTime frame
The incidence of major adverse cardiovascular and cerebrovascular events (MACCE) in the first year after discharge;

Secondary

MeasureTime frame
The incidence of all-cause mortality;The incidence of cardiogenic death;The incidence of non fatal myocardial infarction;The incidence of revascularization;Cardiac function indicators;quality of life score;Psychological health score;Biochemical indicators;The incidence of non fatal stroke;

Countries

China

Contacts

Public ContactLei Xinjun

The First Affiliated Hospital of Xi 'an Jiaotong University

xinjunlei@xjtu.edu.cn+86 137 0029 8310

Outcome results

None listed

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