Methods: This study analyzed qualitative data from four focus groups involving informal kinship caregivers (N=37) from rural and urban counties, and one focus group with kinship navigators (N=8) in Washington State. The data was collected from a university-service agency partnership using a community-engaged research (CEnR) approach. Semi-structured interviews were conducted, with one focus group involving kinship navigators to collect their lived expertise on service delivery, program implementation, fidelity monitoring, and perspectives on service utilization of kinship caregivers attending the KNP. Additionally, four focus groups were conducted to gather informal kinship caregivers' lived experiences of service utilization through the KNP. First, using the RE-AIM framework (Glasgow et al., 2019) as an analytic framework, direct content analysis (Hsieh & Shannon, 2005) was performed through deductive coding and focused coding techniques (i.e., strength of codes). Second, an inductive qualitative thematic approach (Braun & Clarke, 2006) was applied to identify emerging themes from the coded data.
Results: The findings primarily addressed the reach, effectiveness, and implementation aspects of the RE-AIM framework. Rural caregivers faced challenges including limited access, transportation barriers, awareness gaps regarding available resources, and a scarcity of tailored programs and financial aid for non-foster caregivers. Navigators focused on outreach strategies, expanding program reach, comprehensive collaboration, eligibility criteria, serving diverse populations, and securing sustainable funding. Informal kinship caregivers, drawing from lived expertise, voiced multifaceted challenges encompassing legal processes, financial constraints, accessing support services, and managing intergenerational family dynamics. They encountered difficulties with paperwork, healthcare systems, and obtaining financial aid. Navigators played a crucial role by offering information, facilitating support groups , and making referrals (e.g., legal assistance, educational support, childcare, respite care). Nevertheless, informal caregivers encountered accessibility and awareness issues, necessitating enhanced outreach, communication, and expanded coverage. Financial constraints, legal issues, eligibility criteria, and income limitations impeded access to support, highlighting the need for addressing these barriers. Despite challenges, community connection, shared lived experiences, self-care opportunities, respite care, parenting knowledge, and vicarious resilience through support groups were pivotal for caregiver well-being and enhanced informal kinship care.
Conclusions: Service utilization behaviors of informal kinship caregivers and the service utilization-delivery gap should be addressed.