Abstract

African Americans are more likely than non-Hispanic whites to be diagnosed with and die from diabetes. A contributing factor to these health disparities is African Americans’ poor diabetes medication adherence that is due in part to sociocultural barriers (e.g., medicine and illness misperceptions), which negatively affect diabetes management. In our prior work, we engaged with community stakeholders to develop and test a brief version of a culturally adapted intervention to address these barriers to medication adherence. The objective of this study was to elicit feedback to inform the refinement of the full 8-week intervention. We utilized a community-engaged study design to conduct a series of meetings with two cohorts of patient advisory boards of African Americans with type 2 diabetes who were adherent to their diabetes medicines (i.e., peer ambassadors). In total, 15 peer ambassadors were paired with 21 African American participants (i.e., peer buddies) to provide specific intervention support as peers and serve in an advisory role as a board member. Data were collected during nine board meetings with the patient stakeholders. A qualitative thematic analysis of the data was conducted to synthesize the findings. Feedback from the patient advisory board contributed to refining the intervention in the immediate-term, short-term, and long-term. The inclusion of African American community members living with type 2 diabetes on the advisory board contributed to further tailoring the intervention to the specific needs of African Americans with type 2 diabetes in the community.

Highlights

  • Engaging patients and community members as stakeholders in research heightens the importance of the study for the target population and strengthens the quality of the research [1]

  • The objective of this paper is to describe our approach to engaging with the African American community to implement, elicit feedback about, and refine the full 8-week peer-led medication adherence intervention

  • 15 African American peer ambassadors (PAs) were paired with 21 PBs to provide specific intervention support as peers and serve in an advisory role as a board member

Read more

Summary

Introduction

Engaging patients and community members as stakeholders in research heightens the importance of the study for the target population and strengthens the quality of the research [1]. This type of engagement in the research process has the potential to: uncover new research questions; contribute a community perspective to inform the design of recruitment, retention, and research protocols, tailor interventions to the population of interest, and improve the dissemination of study findings to the community [1,2]. Using a community-engaged approach is important for research focused on addressing health disparities experienced by underserved/marginalized populations because it facilitates building trust by creating an equal partnership between the academic researchers and the community and emphasizing a two-way exchange of knowledge [3–5]. An important strategy for self-managing type 2 diabetes is taking medications to reduce blood glucose levels; African Americans have a 25% lower adherence to diabetes medicines than non-Hispanic whites [7,8]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call