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Genet Med. 2008 Jan;10(1):46-53. doi: 10.1097/GIM.0b013e31815f1e00.

DNA data sharing: research participants' perspectives.

Author information

1
Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas 77030, USA. amcguire@bcm.edu

Abstract

PURPOSE:

Current genomic research policy calls for public data release with specific consent for data sharing. Because most clinical investigators are not responsible for and do not anticipate data broadcast few include information about data sharing in their informed consent process. Model language is therefore urgently needed and should be responsive to research participants' attitudes and judgments. The purpose of this study was to describe research participants' attitudes and judgments about data release and their preferences for varying levels of control over decision-making.

METHODS:

Focus group sessions with patients and controls from a genetic study of epilepsy.

RESULTS:

Despite wide variation in judgments, there was general interest in receiving information and making decisions about data sharing. Participants preferred multiple data sharing options, but were more likely to consent to public data release when given fewer options. For existing samples most participants felt that genomic information should not be publicly released without explicit consent from research participants.

CONCLUSIONS:

Specific information about data sharing ought to be included in the consent process for all genetic research. These participants desire multiple data release options, but the effect, if any, on consent to public release deserves further investigation.

PMID:
18197056
PMCID:
PMC2767246
DOI:
10.1097/GIM.0b013e31815f1e00
[Indexed for MEDLINE]
Free PMC Article

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