influenza
Conditions
Interventions
Intervention group:Conduct a three - month comprehensive intervention based on the Health Belief Model for patients, which includes health education, popular science materials, short videos, and patie
Control group:None
Sponsors
The First Medical Center of the Chinese People's Liberation Army (PLA) General Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Questionnaire Survey (Observational Study) (1).Aged 18 years or older, regardless of gender; (2).Patients who have been diagnosed with cancer through pathophysiological methods and are aware of their own condition; (3). Conscious, without language communication or visual impairments, and with a certain reading ability; (4). With an educational level of primary school or above; (5). Willingly participate in the study and sign the informed consent form. 2. Interventional study (1).Aged 18 years or above, regardless of gender; (2).Patients who have been pathophysiologically confirmed to have cancer and are aware of their own condition; (3).Conscious, without language communication or visual impairments, and with the ability to read; (4).With an educational level of primary school or above; (5).Patients are proficient in using smartphones and have an estimated survival period of more than 6 months; (6).Willing to participate in the study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Questionnaire Survey (Observational Study): (1).Have a history of mental illness or cognitive dysfunction, and are unable to understand the content and requirements of the study. 2. Interventional study: (1).Those who are allergic to any components in the vaccine (including excipients, formaldehyde, adjuvants, and antibiotics) or have a history of severe allergic reactions to any influenza vaccine; (2).Those with a history of Guillain - Barré syndrome; (3) Patients with brain diseases that affect their decision - making ability. (4)Those with a history of mental illness or cognitive impairment who are unable to understand the research content and requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the willingness to receive influenza vaccination before and after the intervention; | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in the knowledge level of influenza vaccine vaccination before and after the intervention;Changes in the actual influenza vaccine vaccination rate; | — |
Countries
China
Contacts
Public ContactHui Ma
Chinese People's Liberation Army (PLA) General Hospital
Outcome results
None listed