HIV/AIDS
Conditions
Interventions
Control arm Nutritional information
Sponsors
University of Pennsylvania
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Female Age 18-24 years Self-reported history of sexual activity in the past 12 months Self-reported HIV-negative status or unknown HIV status at enrolment Willing and able to provide written informed consent Able to read and understand English
Exclusion criteria
Exclusion criteria: Unwilling or unable to provide consent for study participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intention to receive the HIV vaccine following exposure to misinformation | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes: (1) intention to receive the HIV vaccine 2-6 weeks following the exposure, believability and persuasiveness of misinformation, interest in sharing misinformation, and motivational threat associated with misinformation; (2) We will explore subgroup effects by relevant sociodemographic and behavioural factors including HIV risk, PrEP history, COVID-19 vaccine history, general vaccine | — |
Countries
South Africa
Contacts
Public ContactCandice Chetty Makkan
Principal Researcher and Indlela Co Director
Outcome results
None listed