Literature DB >> 33275082

Assessment of the All of Us research program's informed consent process.

Megan Doerr1, Sarah Moore1, Vanessa Barone1, Scott Sutherland2,3, Brian M Bot1, Christine Suver1, John Wilbanks1.   

Abstract

Informed consent is the gateway to research participation. We report on the results of the formative evaluation that follows the electronic informed consent process for the All of Us Research Program. Of the nearly 250,000 participants included in this analysis, more than 95% could correctly answer questions distinguishing the program from medical care, the voluntary nature of participation, and the right to withdraw; comparatively, participants were less sure of privacy risk of the program. We also report on a small mixed-methods study of the experience of persons of very low health literacy with All of Us informed consent materials. Of note, many of the words commonly employed in the consent process were unfamiliar to or differently defined by informants. In combination, these analyses may inform participant-centered development and highlight areas for refinement of informed consent materials for the All of Us Research Program and similar studies.

Entities:  

Keywords:  Informed consent; biomedical research; confidentiality and privacy; genetic research; human subjects research; research ethics

Year:  2020        PMID: 33275082     DOI: 10.1080/23294515.2020.1847214

Source DB:  PubMed          Journal:  AJOB Empir Bioeth        ISSN: 2329-4515


  5 in total

Review 1.  The Ethics of Consent in a Shifting Genomic Ecosystem.

Authors:  Sandra Soo-Jin Lee
Journal:  Annu Rev Biomed Data Sci       Date:  2021-07-20

2.  Education and Consent for Population-Based DNA Screening: A Mixed-Methods Evaluation of the Early Check Newborn Screening Pilot Study.

Authors:  Holly L Peay; Angela You Gwaltney; Rebecca Moultrie; Heidi Cope; Beth Lincoln- Boyea; Katherine Ackerman Porter; Martin Duparc; Amir A Alexander; Barbara B Biesecker; Aminah Isiaq; Jennifer Check; Lisa Gehtland; Donald B Bailey; Nancy M P King
Journal:  Front Genet       Date:  2022-05-12       Impact factor: 4.772

3.  From paper to screen: regulatory and operational considerations for modernizing the informed consent process.

Authors:  Nichelle L Cobb; Dorothy F Edwards; Erin M Chin; James J Lah; Felicia C Goldstein; Cecilia M Manzanares; Christine M Suver
Journal:  J Clin Transl Sci       Date:  2022-03-28

4.  An Idealized Clinicogenomic Registry to Engage Underrepresented Populations Using Innovative Technology.

Authors:  Patrick Silva; Deborah Vollmer Dahlke; Matthew Lee Smith; Wendy Charles; Jorge Gomez; Marcia G Ory; Kenneth S Ramos
Journal:  J Pers Med       Date:  2022-04-29

5.  Newborn Screening by Genomic Sequencing: Opportunities and Challenges.

Authors:  David Bick; Arzoo Ahmed; Dasha Deen; Alessandra Ferlini; Nicolas Garnier; Dalia Kasperaviciute; Mathilde Leblond; Amanda Pichini; Augusto Rendon; Aditi Satija; Alice Tuff-Lacey; Richard H Scott
Journal:  Int J Neonatal Screen       Date:  2022-07-15
  5 in total

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