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Construction and application research of smoking cessation intervention program for middle-aged and young myocardial infarction patients from the perspective of social ecological theory

Construction and application research of smoking cessation intervention program for middle-aged and young myocardial infarction patients from the perspective of social ecological theory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123848
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

acute myocardial infarction

Interventions

Experimental group:Implementing an evidence-based smoking cessation intervention plan
Control group:Implement routine cardiology nursing

Sponsors

Nantong University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1. Meet the AMI diagnostic criteria established by the "Guidelines for the Diagnosis and Treatment of Acute Myocardial Infarction," and must satisfy at least two of the following three criteria: (1) Clinical history of ischemic chest pain; (2) Dynamic changes in electrocardiogram (ECG); (3) Dynamic changes in serum cardiac biomarkers indicating myocardial necrosis. 2. Confirmed diagnosis of acute myocardial infarction by a cardiovascular specialist; 3. Age 18-59 years; 4. Smoker: According to the WHO definition of smoking, someone who smokes daily or almost daily (averaging 5 or more days per week) with a smoking history of more than 1 year, and is currently still smoking; 5. Voluntarily participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Individuals with severe complications or comorbidities of other systems, such as severe sequelae of stroke or severe liver and kidney diseases; 2.Individuals with mental illness or cognitive impairment; 3.Those who are unable to use electronic devices such as smartphones and tablets.

Design outcomes

Primary

MeasureTime frame
Long term sustained smoking cessation rate;

Secondary

MeasureTime frame
Reabsorption rate;Patient's quality of life;Patient's smoking cessation cognition and motivation at different time points;Patient's tobacco dependence level;

Countries

China

Contacts

Public ContactWang Yueyuan

Nantong University Affiliated Hospital

wyy880925@126.com+86 151 6277 0920

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026