Experiences Accessing and Engaging in Early Psychosis Care Among Hispanic Families.

Abstract

This qualitative study examines the experiences of Hispanic individuals and their families navigating early psychosis care in Washington State. In-depth interviews were conducted with 13 participants recruited from a network of coordinated specialty care (CSC) programs, including three service users and ten family members of those enrolled in services. Data were analyzed using a content analysis approach, and qualitative data coding was facilitated with Atlas.ti software. The findings identified three themes: Limited guidance navigating services leading to diminished trust in early care pathways, the Importance of understanding cultural and linguistic needs in early care pathways and during CSC, and the Restoring trust and building belonging through CSC. Implications for coordinated specialty care include implementing culturally responsive care models that integrate the diverse backgrounds and experiences of individuals affected by psychosis, specifically Hispanic individuals. By building trust, cultural understanding, and strong support networks, coordinated specialty care can create inclusive environments that empower Hispanic individual's experiencing psychosis and their families throughout the recovery journey.