Chronic Obstructive Pulmonary Disease (COPD)
Conditions
Interventions
Intervention Group:Physicians issued standardized vaccine education prescriptions and integrated vaccination recommendations into routine clinical practice, thereby standardizing and routinizing vacci
Control Group:Routine clinical practice model
Sponsors
Peking University
Eligibility
Sex/Gender
All
Age
35 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Previously diagnosed with COPD; 2. Aged 35 years or above at the time of signing informed consent; 3. Not vaccinated against influenza in the current year; 4. The patient with COPD agrees to participate in the project; 5. Has continuously resided in the study area for at least 6 months and has no plan for long-term absence or relocation within the next 6 months, to ensure completion of follow-up; 6. Able to participate in the study according to the study protocol; 7. Willing and able to sign the electronic informed consent form to participate in the trial.
Exclusion criteria
Exclusion criteria: 1. Has cognitive impairment and is unable to correctly understand the health education materials or complete the surveys required for the study; 2. Is currently participating in another intervention that may affect the outcomes of this study; 3. Has contraindications to influenza vaccination; 4. Has a severe illness or is at the end stage of life; 5. Is considered unsuitable for participation in this study for other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Influenza vaccination rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Healthcare service utilization;Outcomes related to acute exacerbations;All-cause and disease-specific outcomes;Cardiovascular composite outcomes;Vaccine hesitancy; | — |
Countries
China
Contacts
Public ContactHe Ping
Peking University
Outcome results
None listed