Literature DB >> 25359560

Testing an online, dynamic consent portal for large population biobank research.

Daniel B Thiel1, Jodyn Platt, Tevah Platt, Susan B King, Nicole Fisher, Robert Shelton, Sharon L R Kardia.   

Abstract

BACKGROUND: Michigan's BioTrust for Health, a public health research biobank comprised of residual dried bloodspot (DBS) cards from newborn screening contains over 4 million samples collected without written consent. Participant-centric initiatives are IT tools that hold great promise to address the consent challenges in biobank research.
METHODS: Working with Private Access Inc., a pioneer in patient-centric web solutions, we created and pilot tested a dynamic informed consent simulation, paired with an educational website, focusing on consent for research utilizing DBSs in Michigan's BioTrust for Health.
RESULTS: Out of 187 pilot testers recruited in 2 groups, 137 completed the consent simulation and exit survey. Over 50% indicated their willingness to set up an account if the simulation went live and to recommend it to others. Participants raised concerns about the process of identity verification and appeared to have little experience with sharing health information online.
CONCLUSIONS: Applying online, dynamic approaches to address the consent challenges raised by biobanks with legacy sample collections should be explored, given the positive reaction to our pilot test and the strong preference for active consent. Balancing security and privacy with accessibility and ease of use will continue to be a challenge.
© 2014 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2014        PMID: 25359560      PMCID: PMC4289420          DOI: 10.1159/000366128

Source DB:  PubMed          Journal:  Public Health Genomics        ISSN: 1662-4246            Impact factor:   2.000


  36 in total

1.  Policy issues and stakeholder concerns regarding the storage and use of residual newborn dried blood samples for research.

Authors:  Erin Rothwell; Rebecca Anderson; Jeffrey Botkin
Journal:  Policy Polit Nurs Pract       Date:  2010-05-10

2.  Informed consent and biobanks.

Authors:  Ellen Wright Clayton
Journal:  J Law Med Ethics       Date:  2005       Impact factor: 1.718

3.  From newborn screening to population health research: implementation of the Michigan BioTrust for health.

Authors:  Carrie Langbo; Janice Bach; Mary Kleyn; Frances Pouch Downes
Journal:  Public Health Rep       Date:  2013 Sep-Oct       Impact factor: 2.792

Review 4.  Reforming biobank consent policy: a necessary move away from broad consent toward dynamic consent.

Authors:  Dorit T Stein; Sharon F Terry
Journal:  Genet Test Mol Biomarkers       Date:  2013-12

5.  "Broad" consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose.

Authors:  Carlo Petrini
Journal:  Soc Sci Med       Date:  2009-10-21       Impact factor: 4.634

6.  Newborn screening: a spot of trouble.

Authors:  Mary Carmichael
Journal:  Nature       Date:  2011-07-13       Impact factor: 49.962

7.  From consent to institutions: designing adaptive governance for genomic biobanks.

Authors:  Kieran C O'Doherty; Michael M Burgess; Kelly Edwards; Richard P Gallagher; Alice K Hawkins; Jane Kaye; Veronica McCaffrey; David E Winickoff
Journal:  Soc Sci Med       Date:  2011-07-02       Impact factor: 4.634

8.  Assessing public attitudes on the retention and use of residual newborn screening blood samples: a focus group study.

Authors:  Erin Rothwell; Rebecca Anderson; Aaron Goldenberg; Michelle H Lewis; Louisa Stark; Matthew Burbank; Bob Wong; Jeffrey R Botkin
Journal:  Soc Sci Med       Date:  2012-02-18       Impact factor: 4.634

9.  Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health.

Authors:  Daniel B Thiel; Tevah Platt; Jodyn Platt; Susan B King; Sharon L R Kardia
Journal:  J Community Genet       Date:  2013-07-27

10.  A dynamic model of patient consent to sharing of medical record data.

Authors:  William G Dixon; Karen Spencer; Hawys Williams; Caroline Sanders; David Lund; Edgar A Whitley; Jane Kaye
Journal:  BMJ       Date:  2014-02-05
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  20 in total

1.  Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples.

Authors:  Kurt D Christensen; Sarah K Savage; Noelle L Huntington; Elissa R Weitzman; Sonja I Ziniel; Phoebe L Bacon; Cara N Cacioppo; Robert C Green; Ingrid A Holm
Journal:  J Empir Res Hum Res Ethics       Date:  2017-04       Impact factor: 1.742

2.  Did I Tell You That? Ethical Issues Related to Using Computational Methods to Discover Non-Disclosed Patient Characteristics.

Authors:  Kenrick D Cato; Walter Bockting; Elaine Larson
Journal:  J Empir Res Hum Res Ethics       Date:  2016-07       Impact factor: 1.742

3.  Engaging a state: Facebook comments on a large population biobank.

Authors:  Tevah Platt; Jodyn Platt; Daniel Thiel; Sharon L R Kardia
Journal:  J Community Genet       Date:  2017-04-05

4.  A/B design testing of a clinical trial recruitment website: A pilot study to enhance the enrollment of older adults.

Authors:  Hailey N Miller; Timothy B Plante; Kelly T Gleason; Jeanne Charleston; Christine M Mitchell; Edgar R Miller; Lawrence J Appel; Stephen P Juraschek
Journal:  Contemp Clin Trials       Date:  2021-10-12       Impact factor: 2.261

5.  Broad Consent for Research on Biospecimens: The Views of Actual Donors at Four U.S. Medical Centers.

Authors:  Teddy D Warner; Carol J Weil; Christopher Andry; Howard B Degenholtz; Lisa Parker; Latarsha J Carithers; Michelle Feige; David Wendler; Rebecca D Pentz
Journal:  J Empir Res Hum Res Ethics       Date:  2018-02-01       Impact factor: 1.742

Review 6.  Brain tumor biobanking in the precision medicine era: building a high-quality resource for translational research in neuro-oncology.

Authors:  Quinn T Ostrom; Karen Devine; Jordonna Fulop; Yingli Wolinsky; Peter Liao; Lindsay Stetson; Marta Couce; Andrew E Sloan; Jill S Barnholtz-Sloan
Journal:  Neurooncol Pract       Date:  2016-12-30

7.  "I'm a Little More Trusting": Components of Trustworthiness in the Decision to Participate in Genomics Research for African Americans.

Authors:  Susan Racine Passmore; Amelia M Jamison; Gregory R Hancock; Moaz Abdelwadoud; C Daniel Mullins; Taylor B Rogers; Stephen B Thomas
Journal:  Public Health Genomics       Date:  2020-01-17       Impact factor: 2.000

8.  Interactive multimedia consent for biobanking: a randomized trial.

Authors:  Christian M Simon; David W Klein; Helen A Schartz
Journal:  Genet Med       Date:  2015-04-02       Impact factor: 8.822

9.  Demonstrating 'respect for persons' in clinical research: findings from qualitative interviews with diverse genomics research participants.

Authors:  Stephanie A Kraft; Erin Rothwell; Seema K Shah; Devan M Duenas; Hannah Lewis; Kristin Muessig; Douglas J Opel; Katrina A B Goddard; Benjamin S Wilfond
Journal:  J Med Ethics       Date:  2020-10-06       Impact factor: 2.903

10.  Preferences for Updates on General Research Results: A Survey of Participants in Genomic Research from Two Institutions.

Authors:  Casey Overby Taylor; Natalie Flaks Manov; Katherine D Crew; Chunhua Weng; John J Connolly; Christopher G Chute; Daniel E Ford; Harold Lehmann; Alanna Kulchak Rahm; Iftikhar J Kullo; Pedro J Caraballo; Ingrid A Holm; Debra Mathews
Journal:  J Pers Med       Date:  2021-05-11
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