Clinical Research Directory

Inclusion Criteria: * Provision of signed and dated informed consent form * Declaration of willingness to comply with all study procedures and availability during the study * Age 18 years old or older * Male sex designated at birth * Identify as trans woman, woman or another gender identity not associated with being a man * Desire to use or re-start PrEP * HIV uninfected * Speaks English or Spanish * Live in the New Orleans metropolitan statistical area (which includes 8 parishes) Exclusion Criteria: * Confirmed HIV infection by rapid algorithm testing and/or laboratory testing (described above) * Prior or current participation in the active arm of an HIV vaccine trial with evidence of vaccine-induced seropositivity * Concurrent or planned enrollment in a research study that provides PrEP * Unwilling to attend quarterly follow-up visits, which will include survey participation * Has any other condition which, based on the opinion of the investigator, would preclude provision of informed consent; make participation in the project unsafe; complicate interpretation of outcome data; or otherwise interfere with achieving the project objectives