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Webinar: (2022-01) Health Literacy and Human Research Protections: How the IRB Can Make Research More Understandable

Description

Patients, participants, and their caregivers should be provided with understandable research information. IRBs can play an important role in ensuring participant-facing documents include health literacy concepts. The Multi-Regional Clinical Trials Center (MRCT Center) of Brigham and Women’s Hospital and Harvard has developed several resources to raise awareness of, and build competency in, the use of health literacy best practices. In this session the speaker will provide an overview of health literacy and provide practical examples of how health literacy can be championed by IRBs.

Agenda

  • Introduction to health literacy concepts, and what is included under the larger umbrella of health literacy, including numeracy and design/visualization
  • The relationship between clear communications and participant empowerment
  • Ways in which the IRB can review materials through a health literacy lens (including the MRCT Center Health Literacy Checklist for IRBs)
  • Other improvements that can be made to IRB processes(e.g. consent templates and boilerplate)
  • Resources that can further clarify research (e.g. MRCT Center Clinical Research Glossary)
  • Takeaways on health literacy and the IRB
What will I learn?
  • Describe different health literacy concepts and best practices
  • Explain how IRBs can help to promote clear communications and research understanding
  • Apply health literacy concepts to specific situations
Who should attend?
This program is geared toward HRPP/IRB personnel and those working in research programs more broadly including HRPP/IRB directors, members, chairs; researchers and research staff; and more.

New discounts available for groups of various sizes from a single location!

Buy 4 get 1 free
Buy 12 get 6 free

For groups of 40 or more, please contact onlinelearning@primr.org to discuss special discount options.

To receive complimentary registrations, first register the paid registrants (e.g. if you’re using the buy 4 get 1 free discount, register the 4 paid individuals first) and then email onlinelearning@primr.org with a list of those paid individuals, as well as the name(s) and emails of those to receive complimentary registration.

Group discount requests must be received at least 24 hours before the event broadcast begins. Refunds or retroactive discounts are not available.

If you prefer, you can find a paper registration form here. Please send the completed form to registration@primr.org.

Thank you to our sponsor! 

WCG IRB provides the highest quality ethical reviews of clinical research protocols and studies. 

Contributors

  • Sylvia Baedorf Kassis, MPH, CYT

    Sylvia Baedorf Kassis is a Program Manager at the Multi-Regional Clinical Trials Center.  With 20 years of clinical research-related experience in Canada and the United States of America, her expertise includes ethical/regulatory review of research, clinical trial workforce training and capacity building, and study coordination, management and oversight. In her current role, Sylvia is focused predominantly on efforts to make clinical research more understandable and accessible to patients and participants through her work on Health Literacy in Clinical Research.

January 13, 2022
Thu 1:00 PM EST

Duration 1H 15M

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