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Reach Out and RELATE: Communicating and Understanding Scientific Research


About this course
Everyone - non-scientists and scientists alike - has some form of expertise, but communicating across a gap in knowledge or experience is challenging. In this Teach-Out, we address this challenge by helping participants to develop core communication skills and more effectively communicate with one another. For more information or to enroll, click here.

What you'll learn

  •     Understand why science communication is both important and challenging
  •     Develop strategies to effectively bridge communications between public audiences and scientific researchers
  •     Understand expert perspectives on different areas of public engagement with science
  •     Shape a compelling, message-focused STEM narrative for a specific audience
  •     Discuss important issues in science communication with others


Meet the instructors

Elyse L. Aurbach PhD
Co-Founder and Co-Director of RELATE

Brian J. Zikmund-Fisher PhD
Associate Professor of Health Behavior and Health Education

Brandon Patterson MS
Co-Director of RELATE

Katherine E. Prater PhD
Co-Founder and Co-Director of RELATE

Click here for more information.

CBSSM Seminar: Julie Wright Nunes, MD, MPH

Wed, May 17, 2017, 3:00pm
Location: 
NCRC, Building 16, Room 266C

Julie Wright Nunes, MD, MPH
Assistant Professor, Internal Medicine

Title: Patient Education and Care: Challenges and Opportunities in Chronic Kidney Disease

Abstract: Twenty million people, or 20% of U.S. adults ages 60 and older, have chronic kidney disease (CKD). CKD is a significant public health threat carrying high risk of morbidity, mortality, and renal failure. Health behavior theory suggests that patient motivation and healthy behavior change require patients to have knowledge of their chronic condition, as well as the self-efficacy and skills to do what is needed to stay healthy. The chronic care model promotes early patient engagement in care. Yet, less than 20% of  patients with CKD are aware of their diagnosis. Even patients who are aware often do not understand the implications of their CKD diagnosis or what they need to do to optimize their health. Dr. Wright Nunes will discuss her research aimed to develop, test, and disseminate sustainable patient-centric education and coaching support interventions to improve quality of care and outcomes in patients who have CKD.

Bioethics Grand Rounds -Anna Kirkland, JD, PhD

Wed, June 28, 2017, 12:00pm
Location: 
UH Ford Auditorium

Anna Kirkland, JD, PhD Title –  "The Vaccine Injury Compensation Court and Its Critics"

Presenter –  Anna Kirkland, JD, PhD, Arthur F. Thurnau Professor of Women's Studies and Political Science, University of Michigan

Abstract: The so-called vaccine court is a small special court in the United States Court of Federal Claims that handles controversial claims that a vaccine has harmed someone. The government steps in as the defendant and vaccine manufacturers are protected from liability. In this court, lawyers, activists, judges, doctors, and scientists come together, sometimes arguing bitterly, trying to figure out whether a vaccine really caused a person’s medical problem. Drawing on her recently published book, Vaccine Court: The Law and Politics of Injury (NYU Press, 2016), Prof. Anna Kirkland will discuss the ethical controversies surrounding the vaccine court, from the perspective of anti-vaccine movement activists as well as from the mainstream.

Fri, July 14, 2017

A study by current and former CBSSM faculty and staff was recently highlighted in Horsetalk (NZ). Angela Fagerlin, Thomas Valley, Aaron Scherer, Megan Knaus, Enny Das, and Brian J. Zikmund-Fisher were co-authors on an international study looking at the impact of flu labels (including "Horse Flu" and "Yarramin Flu") and graphics on risk perceptions and behavioral intentions.

 

Jodyn Platt, MPH, PhD, Assistant Professor of Learning Health Sciences, has been named a University of Chicago MacLean Fellow.

As part of the one year Cancer Genomics and Ethics Big Data Science Fellowship she will receive clinical training in the Medical Ethics Summer Intensive Program and conduct a research project with Olufunmilayo Olopade, MD, FACP, Director of the Center for Clinical Cancer Genetics at University of Chicago Medicine.

Platt explains how her work as a fellow will begin: "I would like to systematically observe and interview individuals involved in shaping how data evolves and moves from the patient encounter to the big data enterprise and back to clinical care." Looking forward to expanding her network over the course of the year, she plans "to engage in, and lead, interdisciplinary scholarship that will ensure the revolution in healthcare delivery brought on by big data and cancer genomics is an ethical one." 

Platt is also the organizer of the upcoming ELSI-LHS symposium on November 15th at U-M which explores the “Ethical, Legal and Social Implications of Learning Health Systems”.

Jeffrey DeWitt, PhD

Fellow

Jeff DeWitt completed a PhD in Social Psychology in 2017 while working in Dr. Gretchen Chapman's Medical Decision Making Lab at Rutgers University. Broadly, Jeff's research is focused on the interplay between social cognition and behavioral decision making with an emphasis on healthcare applications. In particular, he has investigated how our representations and predictions of others' beliefs and goals can influence our own in altruistic medical contexts such as whether to donate blood or receive a flu shot. 

Last Name: 
DeWitt

Jennifer Skillicorn, DrPH, MPH

Research Associate

Jennifer joined CBSSM in August 2017. She works with Dr. Susan Goold and community partners on grant funded research projects related to evaluating Medicaid expansion and its impact on beneficiaries through the Healthy Michigan Plan and ways in which to engage minority and underserved communities in setting priorities for community health.

Last Name: 
Skillicorn

CBSSM Seminar: Peter Jacobson, J.D., M.P.H.

Tue, October 10, 2017, 3:00pm
Location: 
NCRC, Building 16, Room 266C

Peter Jacobson, J.D., M.P.H.
Professor of Health Law and Policy
Director, Center for Law, Ethics, and Health

Title:  Addressing Health Equity Through Health in All Policies Initiatives.

Scholars and public health advocates have expressed optimism about the potential for Health in All Policies (HiAP) initiatives to improve both health equity and population health. HiAP is a collaborative approach across multiple sectors. In a qualitative study to assess these concepts, we found considerable variation across the sites on: how HiAP and equity initiatives are defined and governed; the integration of equity as a core goal; institutional capacity; and the determination of actual policy changes. We found a general migration from a HiAP-centered strategy to one based more on health equity. Regardless of the specific nomenclature, the implementation focus was directed more toward changing practices than policies.

 

CBSSM was well-represented at the annual American Society for Bioethics & Humanities (ASBH) in Kansas City, MO (Oct 19-22) and the Society for Medical Decision Making (SMDM) in Pittsburgh, PA (Oct 22-25).

At ASBH, Andrew Shuman, Susan Goold, Kayte Spector-Bagdady, Janice Firn, Kerry Ryan, Michele Gornick, Stephanie Kukora, Naomi Laventhal, and Christian Vercler presented.

At SMDM, Michele Gornick, Sarah Hawley, and Dean Shumway presented. Several CBSSM alumni also presented.
 

CBSSM Seminar: Roi Livne, PhD

Wed, November 08, 2017, 3:00pm
Location: 
NCRC, Building 16, Room 266C

Roi Livne, PhD
Assistant Professor, Sociology

Title: “The New Economy of Dying: Palliative Care, Morality, and Finance in the Age of Excess”

Abstract: This talk argues that over the past 40 years, a new economy has emerged around end-of-life care: one seeking to control, cap, and limit both spending and treatment near the end of life. Built around the expertise of Hospice and Palliative Care, this economy draws on the moral conviction that near the end of life, less treatment (and consequently, less spending) is better. Based on a historical analysis and ethnographic fieldwork in three California hospitals, Livne examines the interactive work that palliative care clinicians do with severely ill patients and their families, trying to facilitate their voluntary consent to pursue less life-sustaining and life-prolonging treatments.

 

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