Chronic hepatitis B
Conditions
Interventions
Intervention group:The intervention group will receive both the crowdsourced materials and the standard hepatitis health education materials during the study period.
Control group:Receiving routine hepatitis health education materials only
Sponsors
Nanjing Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Medical students (including students of various nationalities/cultural backgrounds) currently enrolled at participating research centers, with their academic year/training stage meeting the definition of the target population as defined by each research center. 2. Majored in clinical medicine; 3. Belonging to a cluster that has been included in the study and undergone randomization; 4. Aged >=18 years; 5. Currently in the third, fourth, or fifth year of undergraduate education; 6. Able to understand the study content and provide electronic or written informed consent; 7. Possessing stable internet access or access to a data collection terminal, and able to complete the baseline survey and at least one follow-up survey during the study period;
Exclusion criteria
Exclusion criteria: 1. Failure to provide valid informed consent; 2. Not belonging to the target population (not a medical student, or not within the specified major/year/training stage); 3. Presence of severe cognitive/language barriers or other circumstances that prevent comprehension of questionnaire content or completion of follow-up measurements; 4. Severe missingness of key variables in the baseline survey or evidently unreliable information (e.g., repeated submissions from the same account, severe logical inconsistencies, abnormal response times, etc., deemed invalid by data quality control); 5. Having participated in the development or pilot testing of intervention materials related to this study, or having a potential conflict of interest with the research team that may significantly affect the results (e.g., serving as an intervention content creator/research assistant and having been exposed to all intervention materials). Such individuals may be excluded or handled separately to avoid bias;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Level of viral hepatitis stigma; | — |
Secondary
| Measure | Time frame |
|---|---|
| HBV/HCV testing behavior;Exposure to external hepatitis-related information;Intervention exposure and acceptability;Knowledge of HBV/HCV and prior exposure; | — |
Countries
China
Contacts
Public ContactDan Wu
Nanjing Medical University
Outcome results
None listed