Design, methods, and participant characteristics of the Impact of Personal Genomics (PGen) Study, a prospective cohort study of direct-to-consumer personal genomic testing customers

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作者
Deanna Alexis Carere
Mick P Couper
Scott D Crawford
Sarah S Kalia
Jake R Duggan
Tanya A Moreno
Joanna L Mountain
J Scott Roberts
Robert C Green
机构
[1] Harvard School of Public Health,Department of Epidemiology, Program in Genetic Epidemiology and Statistical Genetics
[2] Brigham and Women’s Hospital,Department of Medicine, Division of Genetics
[3] University of Michigan Institute for Social Research,Survey Research Center
[4] Survey Sciences Group,Department of Health Behavior and Health Education
[5] LLC,Harvard Medical School
[6] Pathway Genomics,undefined
[7] 23andMe Inc,undefined
[8] University of Michigan School of Public Health,undefined
[9] EC Alumnae Building,undefined
[10] Partners Personalized Medicine,undefined
来源
关键词
Clinical Genetic Testing; Personal Genomic Testing; Participant Confidentiality; Warning Letter; Navigation Button;
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摘要
Designed in collaboration with 23andMe and Pathway Genomics, the Impact of Personal Genomics (PGen) Study serves as a model for academic-industry partnership and provides a longitudinal dataset for studying psychosocial, behavioral, and health outcomes related to direct-to-consumer personal genomic testing (PGT). Web-based surveys administered at three time points, and linked to individual-level PGT results, provide data on 1,464 PGT customers, of which 71% completed each follow-up survey and 64% completed all three surveys. The cohort includes 15.7% individuals of non-white ethnicity, and encompasses a range of income, education, and health levels. Over 90% of participants agreed to re-contact for future research.
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