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J Empir Res Hum Res Ethics ; 8(3): 53-7, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23933776

ABSTRACT

Critical illness clinical trials that entail genomic data collection pose unique challenges. In this qualitative study, we found that surrogate decision makers (SDMs) for critically ill individuals, such as those who would be approached for study participation, appeared to have a limited grasp of genomic principles. We argue that low levels of genomic literacy should neither preclude nor be in conflict with the conduct of ethically rigorous clinical trials.


Subject(s)
Biomedical Research/ethics , Critical Illness , Decision Making , Genetic Privacy , Genome , Health Literacy/ethics , Proxy , Third-Party Consent/ethics , Humans
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