SHOW NOTES

S1.E1. Leading Nursing Science: Closing the Health Equity Gap Holistically

In this episode, Dr. Shannon Zenk discussed NINR’s 2022-2026 Strategic Plan, which involves advancing health equity, diversity, and inclusion, and tackling today’s pressing health challenges. She also referenced some things NIH is doing to promote equity and inclusion which include: the UNITE Initiative and the Faculty Institutional Recruitment for Sustainable Transformation (FIRST) program, which aims to enhance cultures of inclusive excellence in the biomedical research community.

Lastly, she responded to the Nature op-ed piece.


S1.E2. Not GQ, It’s CQ: What’s Cultural Intelligence?

In this episode, Dr. Richard-Eaglin shares her expertise as a Certified Professional Cultural Intelligence and Unconscious Bias Facilitator to define cultural intelligence. Drs. Richard-Eaglin and Ibemere discuss cultural intelligence in the context of clinical practice, education, and leadership. Dr. Richard-Eaglin guides the audience through cultural intelligence approaches which allow us to address racial justice and equity in research. She also responded to the Nature op-ed piece.


S1.E3. Systemic Racism in Research: Addressing Colorblind Racism and White Hegemony

In this episode, we sit down with Prof. Eduardo Bonilla-Silva, the J.B. Duke Distinguished Professor of Sociology in the Department of Sociology at the Duke University Trinity College of Arts and Sciences. In this exciting interview, Prof. Bonilla-Silva discusses Race, Racial Theory, and Racial Grammar. In the aftermath of the murder of George Floyd, Prof. Bonilla-Silva was a pioneer in developing the conceptual basis, underpinnings, and nomenclature for researching and combating systematic racism. He discusses how systematic racism leads to advantages for some, which is not random and leads to serious consequences. He discusses his theories on the Myth of Objectivity and Unconscious Bias.  


S1.E4. “The Algorithm is Not a Sentient Being:” Health Equity in Data Science

In this episode, we sit down with Heather Krause, the founder of the We All Count project aimed to increase data equity in research; as well as DataAssist which aims to help non-profits, communities, and governments tell better stories through data. She discusses how we, as clinical researchers, can use advanced statistical techniques to advance the social world not only in shiny boardrooms but primarily on the ground involving the participants we hope to serve. Krause calls us to action to harness data, as a privilege, to make meaningful changes in the world. She references Nigerian-American artist and researcher, Mimi Ọnụọha’s groundbreaking art piece, The Library of Missing Data Sets. Further in the interview, she discusses her theory of Onus of Change, which involves moving the onus from individuals to systems, by leveraging disaggregated data, thus allowing us to translate words into actions. Ultimately, she reiterates that we are storytellers and must include the human side of statistics. To accomplish this goal, she provides listeners with concrete tools to tell better stories using statistics.


S1.E5. Uprooting the Causes of Health Inequities: A Syndemic Orientation

Rosa González-Guarda, PhD, MPH, RN, CPH, FAAN is an Associate Professor at Duke School of Nursing and Co-Director of the Community Engaged Research Initiative at the Duke Clinical Translational Science Institute. Dr. González-Guarda explains how researchers can work in partnership with community members based through community engaged approaches. Dr. González-Guarda defines how researchers can apply a syndemic orientation and framework to the description of health disparities and the development of interventions. She briefly mentions her work supporting the RADx Initiative at NIH as well as her experience on an NIH review panel. Dr. González-Guarda discusses her research progression from addressing the individual to the study of systems-level drivers of inequity in pursuit of using an antiracist frame in research.  


S1.E6. Clinical Trials, Data Repositories, Health Services Research, and More!

In this interview, we discussed several topics and resources. Dr. Adrian Hernandez leads the Duke Clinical Research Institute and has a leadership role at the Duke University School of Medicine. Dr. Hernandez has conducted large clinical trials and mentioned the ADAPTABLE study. We discussed the importance of implementation science, patient and community engagement, open science, and data repositories in research. The Chronic Care Model is mentioned in one interlude. At the end of the interview, Dr. Hernandez discusses implicit bias and clinical care checklists; take an implicit bias test yourself!  


S1.E7. Leveraging Clinical and Research Nurse Experience: Improving Health in the LGBTQIA+ Community

Dr. Flores is an Assistant Professor of Nursing at the University of Pennsylvania School of Nursing and also does work with the Center for Interdisciplinary Research on AIDS at Yale University, Asian Pacific American Nursing Student Association, and the Program on Sexuality, Technology, and Action Research. Much of his research, teaching, and clinical focus addresses the Social Determinants of Health in Sexual and Gender Minority Youth. We discussed our time as predoctoral colleagues at the Duke University School of Nursing, thinking of oneself as a nurse scientist, nurse researcher, and funding for nurse scientists. Dr. Flores describes participating in Philadelphia PRIDE as a member of the local community.  


S1.E8. Decide With . . . Not For: Partnering with Stakeholders to Address Health Disparities

In this interview, Dr. Bettger described leadership and involvement in the Duke University Roybal Center, Bass Connections, Margolis Center for Health Policy, and Clinical and Translational Science Institute at Duke University. We discussed the importance of integrated care, implementation science, and specific implementation strategies. Dr. Bettger discussed projects that use North Carolina 360, claims data, and telehealth. She mentioned gaining insight from the Patient-Centered Outcomes Research Institute and the National Academy of Medicine Catalyst Award Competition. Dr. Better mentioned the John’s Hopkins University Diversity Wheel and the concept of community-engaged research 


S1.E9. Is Our Picture of Health Disparities Incomplete?: Importance of Inclusion in Research

Bei Wu, PhD, FGSA, FAGHE is an inaugural co-director of the Aging Incubator at New York University (NYU). She holds the position of Vice Dean for Research, dean’s professor in global health and director of global health and aging research at NYU Rory Meyers College of Nursing. In this episode, Dr. Wu describes how she applies the principles of the Social Determinants of Health and the Life Course Perspective to studies on health disparities among rural populations in West Virginia, older adults, and Asian immigrants in the U.S.  She discusses the bias researchers should be mindful of when using existing data sources.  Dr. Wu also outlines how a newly funded research center at Rutgers and NYU for Asian health promotion and equity can advance research on cardiometabolic disease and mental health of Asian adults and foster the next generation of health disparities scholars.  


S1.E10. Creating a Safe Place: LATIN-19 Working Together for the Community

Dr. Viviana Martinez-Bianchi, MD, FAAFP, a Family Medicine and Primary Care Physician at Duke Family Medicine Center and an associate professor in Family Medicine and Community Health at Duke University. She is also a co-founder of the LatinX Advocacy Team & Interdisciplinary Network for COVID-19 (LATIN-19), a group founded to advance health equity for the LatinX community. At the beginning of the interview, Dr. Martinez-Bianchi describes how this group was created and how the aims of the group are rooted in health promotion, reduction in health disparities, and social justice. Dr. Martinez-Bianchi describes the use of a health equity lens to consider the ways policy, systems, interventions, etc. affect certain groups of people. Dr. Martinez-Bianchi also discusses the importance of medical education rooted in health equity, activating communities to be involved in transforming healthcare and health systems, and the development of multilevel relationships to address health inequity.


S1.E11. Remarkable Research: The Community as Partners in Research

In this interview, we discussed Dr. Schenita Randolph’s research with, not in, the black community. Dr. Randolph co-leads the Community Engagement and Dissemination Core at the Duke REACH Equity Center. In this interview, she stresses the importance of the role of nurse leaders and the critical need to better understand racial inequities in health. She notes a major gap in the current science behind HIV prevention in women of color. The CDC provides evidence-based PrEP Best Practices but as Dr. Randolph point out, none exist for women or women of color. She is working to change that and currently leads a study entitled, A Salon-Based, Multi-level Intervention to Improve PrEP Uptake among Black Women living in the United States South, funded by Gilead Sciences, Inc. The CDC has called out racism as a public health emergency and priority but Dr. Randolph says more training on racial equity and lived experiences of scientists of color is needed among decision makers at funding agencies. She also reflects on Academia and the need to reexamine how scientists are evaluated. In conclusion, Dr. Randolph wants listeners to remember that diversity, equity and inclusion are linked to real people.