Engagement practices that join scientific methods with community wisdom: designing a patient-centered, randomized control trial with a Pacific Islander community.

ACTION research; ASIANS; COMMUNITIES; CONSENSUS (Social sciences); CULTURE; DECISION making; LANGUAGE & languages; RESEARCH methodology; EVALUATION of medical care; MINORITIES; RESEARCH funding; STATISTICAL sampling; SURVEYS; HEALTH equity; RANDOMIZED controlled trials; CONTROL groups; RESEARCH personnel; PATIENT-centered care; MEDICALLY underserved persons

OCEANIA; ARKANSAS

This article illustrates how a collaborative research process can successfully engage an underserved minority community to address health disparities. Pacific Islanders, including the Marshallese, are one of the fastest growing US populations. They face significant health disparities, including extremely high rates of type 2 diabetes. This article describes the engagement process of designing patient-centered outcomes research with Marshallese stakeholders, highlighting the specific influences of their input on a randomized control trial to address diabetes. Over 18 months, an interdisciplinary research team used community-based participatory principles to conduct patient-engaged outcomes research that involved 31 stakeholders in all aspects of research design, from defining the research question to making decisions about budgets and staffing. This required academic researcher flexibility, but yielded a design linking scientific methodology with community wisdom. [ABSTRACT FROM AUTHOR]