Chronic obstructive pulmonary disease
Conditions
Interventions
Comparison:Usual care
Intervention:intelligent intervention
Observation group:None
Sponsors
Peking University First Hospital
Eligibility
Sex/Gender
All
Age
40 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Permanent residents under institution management who have the opportunity to receive influenza vaccine advocacy and vaccination services during the study observation period; 2.Patients with a confirmed diagnosis of COPD based on past medical records, health records, or a physician’s diagnosis; 3.Age >= 40 years; 4.Able to obtain influenza vaccination outcomes through health records, follow-up records, or the vaccination information system; 5.The participant has provided informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: 1.Expected to move away during the study period, making follow-up impossible; 2.Existing, clear contraindications to influenza vaccination; 3.Already vaccinated with the influenza vaccine for the current influenza season prior to the start of the study; 4.Cognitive impairment, severe mental illness, or other reasons preventing participation in follow-up, and no representative available to assist; 5.Already participating in other intervention studies that may influence influenza vaccination behavior.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Influenza vaccination rate among patients with COPD; | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction;Percentage of patients who received advocacy for influenza vaccine;Influenza vaccination advocacy rate among primary care providers;Influenza vaccination interval; | — |
Countries
China
Contacts
Public ContactChi Chunhua
Peking University First Hospital
Outcome results
None listed