“…First, they are less likely to be invited to screen by providers, clinical settings, and clinical trials sites. Then, when asked, they may be more likely to decline to screen or enroll than their White peers, or, if they do screen, they are more likely to face serious social, structural, and individual barriers to completing screening and enrolling into trials compared to their White peers, as this is a complex and lengthy process [8,57]. Thus, clinic and clinical trials sites have the potential to greatly reduce racial/ethnic disparities in ACTs by offering all patients regular and repeated access ACT screening, regardless of their potential eligibility or perceived interest [13], implementing interventions such as the ACT2 PDI to build patients’ motivation and capabilities to screen for and join ACTs, and ameliorating the socio-demographic and other factors identified in the present paper during the screening and enrollment process in order to further increase access to ACTs for PLHA of color.…”