All Stories

  1. Engendering trustworthiness in the community: Strategies for researchers
  2. Improving diversity in research: Successes and limitations of research team education in fostering inclusive recruitment practices and community voice
  3. Co-Designing Effective Pediatric Vaccine Promotion Strategies: Insights From Rural Wisconsin Parents
  4. “We Don’t Always Know What we are Missing.” Research Teams’ Perspectives on the Recruitment of Adults with Intellectual and Developmental Disabilities in General Population Research
  5. Increasing confidence for pediatric COVID-19 and influenza vaccines using messages affirming parental autonomy: A randomized online experiment
  6. Fostering Trust in Public Health Messaging: Tailoring Communication for Rural Parents
  7. “My Blood, You Know, My Biology Being out There…”: Consent and Participant Control of Biological Samples
  8. Just Research: Evaluation findings of an educational program to promote inclusive research among investigators and research staff
  9. Designing and testing social media campaign messages to promote COVID-19 vaccine confidence among rural adults: A community-engaged approach featuring rural community leader and clinician testimonials
  10. The importance of transparency in the conduct of biomarker research
  11. Applying the Hornik & Woolf Approach to Identify Messaging Themes and Improve COVID-19 Vaccine Confidence Among Federally Qualified Health Centers’ Workforce in Wisconsin
  12. “There’s not much we can do…” researcher-level barriers to the inclusion of underrepresented participants in translational research
  13. Patient perceptions, opinions and satisfaction of telehealth with remote blood pressure monitoring postpartum
  14. Building Sustainable Organizational and Community Capacity for Research Partnerships: A Decade of Experience
  15. Co-designing to advance community health and health equity in Wisconsin: Building the Neighborhood Health Partnerships Program
  16. Use of a Qualitative Story Deck to Create Scenarios and Uncover Factors Associated with African American Participation in Genomics Research
  17. Training needs of investigators and research team members to improve inclusivity in clinical and translational research participation
  18. Setting and motivation in the decision to participate: An approach to the engagement of diverse samples in mobile research
  19. “I’m a Little More Trusting”: Components of Trustworthiness in the Decision to Participate in Genomics Research for African Americans
  20. Mission of Mercy emergency dental clinics: an opportunity to promote general and oral health
  21. The 2014 Mid-Maryland Mission of Mercy Dental Clinic: Building Community Capacity and Complementing Public Policy
  22. Message Received: African American Women and Breast Cancer Screening
  23. Defining Family: Anthropological Contributions to Practice and Policy in Child Welfare
  24. Building a “Deep Fund of Good Will”: Reframing Research Engagement
  25. The Symbolic Value and Limitations of Racial Concordance in Minority Research Engagement
  26. African Americans With a Family History of Colorectal Cancer: Barriers and Facilitators to Screening
  27. Evidence-based care for breast cancer survivors: Communicating the Institute of Medicine Guidelines in medical practice
  28. Exploring Patient-Physician Communication in Breast Cancer Care for African American Women Following Primary Treatment
  29. Knowledge, Attitudes, and Beliefs about Dilated Eye Examinations among African-Americans
  30. Putting On Airs