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Development and Application of an Intervention Program for Return-to-Work in Young and Middle-Aged Patients with Coronary Heart Disease after Percutaneous Coronary Intervention

Development and Application of an Intervention Program for Return-to-Work in Young and Middle-Aged Patients with Coronary Heart Disease after Percutaneous Coronary Intervention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117380
Enrollment
Unknown
Registered
2026-01-23
Start date
2025-08-25
Completion date
Unknown
Last updated
2026-01-27

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 :The intervention consisted of usual care plus a return-to-work program developed based on the Behavior Change Wheel (BCW) theory. The program comprised exercise training, psycholog
Control group:Usual care

Sponsors

The Second Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1.Patients with a diagnosis of coronary heart disease who had undergone PCI; 2.Aged 18 to 59 years for males and 18 to 54 years for females 3.Classified as low or intermediate risk according to the "Risk Stratification for Cardiac Rehabilitation in CHD Patients (Trial Version)"; 4.Being employed (including self-employed entrepreneurs and migrant workers) prior to hospital admission; 5.Possessing basic literacy and comprehension skills to enable effective communication; 6.Owning a smartphone and being capable of using the WeChat application; 7.Voluntarily agreeing to participate in the study and providing informed consent.

Exclusion criteria

Exclusion criteria: 1.Contract expiration or planned retirement within 6 months after discharge; 2.Presentation with acute phase of Acute Coronary Syndrome (within 3-5 days), left main disease, or equivalent conditions without complete revascularization; 3.Unstable angina not adequately controlled by medication; 4.Severe structural or functional cardiac abnormalities (e.g., severe valvular disease, left ventricular outflow tract obstruction, mural thrombus, left ventricular ejection fraction [LVEF] 160 mmHg or diastolic blood pressure [DBP] > 100 mmHg); 8.Comorbid severe respiratory or musculoskeletal diseases, or other acute/chronic conditions such as malignant tumors, severe infection, anemia, renal failure, hyperthyroidism, etc; 9.Inability to adhere to the study protocol or to cooperate with data collection.

Design outcomes

Primary

MeasureTime frame
Proportion of patients who return to work;

Secondary

MeasureTime frame
Readiness for return-to-work;Fear of disease progression;Return-to-work self-efficacy;Depression;Anxiety;Quality of life;

Countries

China

Contacts

Public ContactGuo Xiaolan

The Second Affiliated Hospital of Air Force Medical University

610814723@qq.com+86 139 9188 7205

Outcome results

None listed

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