“…Perceived risks included side effects, fear of physical pain or uncomfortable procedures, potential ART resistance, permanent harm, and even death [ 22 , 23 , 25 , 29 – 32 , 35 , 38 – 40 , 42 – 44 , 46 – 52 ]. The second barrier was possible social risks , such as concern about transmitting HIV while participating in clinical trials, being treated poorly by the research staff, and privacy concerns [ 22 , 23 , 25 , 30 , 31 , 35 , 41 – 43 , 46 , 48 , 49 , 51 – 56 ]. Lastly, some barriers were rooted in practical considerations such as fear that research participation would interfere with day-to-day life, needing to take time off from work or family, financial risks, and health insurance concerns [ 23 , 29 , 30 , 35 , 39 , 42 , 44 , 46 , 48 – 53 , 55 , 57 , 58 ].…”