Table 4.

Data collection for each specific research objective

	Specific research objectives
Data collection	SO1 Access to care, retention, and healthcare pathways	SO2 Clinical, behavioral, and social evolution	SO3 Initiation, practices, and compliance with PrEP	SO4 Comparison of HIV care (PRINCESSE vs. current)	SO5 Prevention and care of hepatitis B	SO6 Unintended consequences of the PRINCESSE intervention	SO7 Vaginal microbiota, HPV infection types, and antimicrobial STI resistance
PRINCESSE cohort
P1. Clinical and safety data	X	X	X	X	X		X
P2. Socio-behavioral questionnaires	X	X	X		X	X
P3. Biological data		X	X	X	X		X
P4. In-depth interviews with participants	X		X			X
Additional data collection
A1. Medical and activity records of Aprosam (PRINCESSE participants)	X
A2. Medical records of HIV+ FSW patients (not participating in the PRINCESSE cohort)				X
A3. In-depth interviews with members and key informants of the FSW community			X			X
A4. In-depth interviews with PRINCESSE follow-up actors	X		X			X