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Researcher Knowledge, Attitudes, and Communication Practices for Genomic Data Sharing.

Heather P NickKelsey KehoeAmanda GammonJorge L ContrerasKimberly A Kaphingst
Published in: Journal of empirical research on human research ethics : JERHRE (2020)
This study examines knowledge, attitudes, and communication practices toward genomic data sharing among principal investigators and research coordinators engaged in cancer and non-cancer studies. We conducted 25 individual semi-structured interviews and conducted a qualitative thematic analysis. Most interviewees had basic knowledge of data sharing requirements, but lacked specific details of recent changes to NIH policy. Principal investigators perceived more risks to participants for data sharing than the research coordinators who generally obtained consent. Interviewees perceived a trend toward providing fewer data sharing options to participants in the consent process, and had observed that parents of pediatric patients asked more questions than adult patients. Our findings highlight potential areas for improvement related to data sharing during consent processes.
Keyphrases
  • healthcare
  • electronic health record
  • health information
  • social media
  • big data
  • mental health
  • public health
  • depressive symptoms
  • social support
  • gene expression
  • data analysis
  • young adults
  • copy number
  • childhood cancer