This survey database consists of people living with HIV receiving care at the University of Miami/Jackson Health System HIV Clinic. Questions included in the survey cover demographics, general HIV risk group, substance use, sexual risk behaviors, psychological distress, trauma, homelessness, stigma, HIV care adherence, and co-occurring health conditions. Consent for inclusion in the database includes permission to be contacted for future studies and to extract relevant data from medical records related to study inclusion criteria (e.g., mental health comorbidities, HIV viral load, CD4, medications, visit attendance). Submit a request via the Research Navigation Portal to request additional information on this database or to access the data for recruitment purposes, for a grant, or develop a manuscript.
This survey database consists mainly of individuals at high risk for HIV (people living with HIV are not excluded, but the survey is not conducted in HIV clinics). Serving as a general cross-study screener for center investigators, the brief (3-5 minute) survey documents demographic information (e.g., race/ethnicity, country of origin, years in the US, language, sexual orientation, socio-economic information); general HIV risk group /behaviors/ status (e.g., MSM, heterosexual, sexual risk, substance and needle use, PTSD, depression); and contact information/contact preferences. Completion of the brief survey constitutes consent to be included in the database and contacted for future studies, and includes community members. Submit a request via the Research Navigation Portal to request additional information on this database or to access the data for recruitment purposes, for a grant, or develop a manuscript. Contact charm@miami.edu or 305-243-0987 if your research team or community agency is interested in collaborating on this research activity.
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