Measure of Sickle Cell Stigma (MoSCS) African-Americans Request inclusion into NCIT below "Research or Clinical Assessment Tool". Patient Reported Outcome Adults 18 years and older Bediako, Shawn M et al. “The Measure of Sickle Cell Stigma: Initial Findings from the Improving Patient Outcomes through Respect and Trust Study.” Journal of health psychology (2014): 1359105314539530. PMC. Web. 13 Mar. 2016. PMCID: PMC4627860 Measure of disease specific stigma based on patient reported outcome measurements that assesses 4 MoSCS factors: Social exclusion, Internalized Stigma, Expected Discrimination and Disclosure concerns. Measure includes stigma scores; perceived disease severity, acute care service utilization, hospital admission levels. N=262. J Health Psychol. 2016 May; 21(5): 808–820. Measure of Sickle Cell Stigma None Adults with Sickle Cell Disease MoSCS Quality of Life and Care Measure