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A Web-Based Platform for Educating Researchers About Bioethics and Biobanking
Ivana Sehovic1, Clement K Gwede1,2, Cathy D Meade1,2
1Department of Health Outcomes & Behavior, Moffitt Cancer Center, Tampa, FL, USA.
A new web-based curriculum effectively educates researchers on ethical considerations for biobanking involving individuals with familial risk for hereditary cancer (IFRs) and underserved populations.
Area of Science:
- Bioethics
- Public Health
- Genomics
Background:
- Biobanking is crucial for understanding hereditary cancer and minority health.
- Gaps exist in researcher knowledge regarding ethical concerns of vulnerable populations in biobanking.
Purpose of the Study:
- To develop and evaluate a web-based curriculum addressing ethical concerns in biobanking for individuals with familial risk for hereditary cancer (IFRs) and underserved/minority populations.
Main Methods:
- Formative research and expert panel assessments informed curriculum development.
- Researchers evaluated curriculum clarity and content; public health graduate students pilot-tested its effectiveness.
- A systematic, integrative approach was used for curriculum and website creation.
Main Results:
- All 14 researchers found the curriculum easy to understand, relevant, and well-assessed.
- 77% of 22 pilot-testing graduate students demonstrated improved test scores after curriculum completion.
- Dialogue animations were rated as interesting and valuable by most participants.
Conclusions:
- A web-based curriculum is an acceptable and effective method for educating researchers on biobanking ethics for vulnerable groups.
- Future work will focus on integrating the curriculum with larger organizations to broaden its reach.
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