Pagan, JoanPaikai, Kawailehua2021-06-082021-06-082021-06-08http://hdl.handle.net/10790/6154Native Hawaiian data collection and dissemination continue to be underrepresented and often inaccurate. While there is progress in how the government collects data on Native Hawaiian Pacific Islander (NHPI) populations, there is still a lack of accurate and reliable health data to assess access to care and healthcare utilization in the Native Hawaiian community. The COVID-19 pandemic exposed the need for data disaggregation and appropriate funding for Native Hawaiians and the organizations that serve them. Native Hawaiian health outcomes have been highly affected by the pandemic, and there is limited data to address access to care and health inequities. This project's scope is to pilot a screening tool to collect and analyze data from the Native Hawaiian population regarding their perception and experiences to access care during the COVID-19 pandemic.74en-USsocial determinants of healthHawaiiansaccess to caredata collectiondata disaggregationperception+experienceCOVID-19 (Disease)Medical careDoctoral Project