Clinical studies often fail to recruit and retain diverse participants, leading to knowledge gaps in understanding diseases, preventive care, and treatment effectiveness across different demographic groups. Underserved and underrepresented communities face barriers such as geographic limitations, mistrust, poor communication, and prejudice, further exacerbating disparities in healthcare research. The project READI aims is to create a more inclusive and integrated ecosystem around clinical studies by engaging diverse communities, equipping stakeholders with effective tools and training, and developing a sustainable, patient-centered digital platform to enhance access to clinical studies and foster participation.
