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Parental perspectives on consent for participation in large-scale, non-biological data repositories.

Kiran Pohar ManhasStacey PageShawn X DoddNicole LetourneauAleta AmbroseXinjie CuiSuzanne C Tough
Published in: Life sciences, society and policy (2016)
Though parent participants agree that their research data should be made available for secondary use, they believe their consent is still required. Given their understanding that obtaining and informed consent can be challenging in the case of secondary use, parents agreed that a broad, one-time consent model was acceptable, reducing the logistical burden while maintaining respect for their contribution. This broad model also maintained participant trust in the research and secondary use of their data. The broad, one-time model also reflected parents' perspectives surrounding child involvement in the consent process. The majority of parents felt decision made during childhood were the parents responsibility and should remain in parental purview until the child reaches the age of majority.
Keyphrases
  • electronic health record
  • big data
  • mental health
  • physical activity
  • healthcare
  • data analysis
  • deep learning