Literature DB >> 31580791

Return of Value in the New Era of Biomedical Research-One Size Will Not Fit All.

Dmitry Khodyakov1, Alexandra Mendoza-Graf1, Sandra Berry1, Camille Nebeker2, Elizabeth Bromley1,3.   

Abstract

Background: There is a growing interest in creating large-scale repositories that store genetic, behavioral, and environmental data for future, unspecified uses. The All of Us Research Program is one example of such a repository. Its participants will get access to their personal data and the results of the studies that used them. However, little is known about what researchers should return to participants and how they should do it in a way that is valuable and meaningful to participants.
Methods: To better understand the concept of "return of value" and the practice of returning valuable study information, we conducted semi-structured telephone interviews with 44 stakeholders with diverse perspectives on this topic. All interviews have been transcribed and coded thematically to identify the most salient themes, to explore differences between returning different types of study results, and to describe differences and similarities in perspectives of different stakeholder groups.
Results: We found that one size does not fit all when it comes to returning value to participants: the decisions about return of results are affected by participant preferences, researchers' concerns about feasibility, the types of data collected, their level of granularity, and available options for supporting result interpretation. Conclusions: Our findings suggest that the key to operationalizing return of value and to identifying ways to return valuable information to study participants may be to find a point of equilibrium between criteria that may affect usefulness and feasibility. The point of equilibrium may vary by study, by participants' backgrounds and preferences, by their health literacy and access to regular healthcare, and by the resources available to professionals controlling the data. Future studies should explore the factors that determine the point of equilibrium between feasibility and usefulness.

Entities:  

Keywords:  All of us research program; data repository; research ethics; research participants; return of results; return of value

Mesh:

Year:  2019        PMID: 31580791      PMCID: PMC6803105          DOI: 10.1080/23294515.2019.1666175

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


  22 in total

Review 1.  Dissemination of results in community-based participatory research.

Authors:  Peggy G Chen; Nitza Diaz; Georgina Lucas; Marjorie S Rosenthal
Journal:  Am J Prev Med       Date:  2010-10       Impact factor: 5.043

2.  Ethical challenges for the "outside" researcher in community-based participatory research.

Authors:  Meredith Minkler
Journal:  Health Educ Behav       Date:  2004-12

Review 3.  Research ethics and the challenge of whole-genome sequencing.

Authors:  Amy L McGuire; Timothy Caulfield; Mildred K Cho
Journal:  Nat Rev Genet       Date:  2008-02       Impact factor: 53.242

4.  Offering individual genetic research results: context matters.

Authors:  Laura M Beskow; Wylie Burke
Journal:  Sci Transl Med       Date:  2010-06-30       Impact factor: 17.956

5.  Sample size in qualitative research.

Authors:  M Sandelowski
Journal:  Res Nurs Health       Date:  1995-04       Impact factor: 2.228

6.  Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.

Authors:  Richard R Fabsitz; Amy McGuire; Richard R Sharp; Mona Puggal; Laura M Beskow; Leslie G Biesecker; Ebony Bookman; Wylie Burke; Esteban Gonzalez Burchard; George Church; Ellen Wright Clayton; John H Eckfeldt; Conrad V Fernandez; Rebecca Fisher; Stephanie M Fullerton; Stacey Gabriel; Francine Gachupin; Cynthia James; Gail P Jarvik; Rick Kittles; Jennifer R Leib; Christopher O'Donnell; P Pearl O'Rourke; Laura Lyman Rodriguez; Sheri D Schully; Alan R Shuldiner; Rebecca K F Sze; Joseph V Thakuria; Susan M Wolf; Gregory L Burke
Journal:  Circ Cardiovasc Genet       Date:  2010-12

Review 7.  Evolving approaches to the ethical management of genomic data.

Authors:  Jean E McEwen; Joy T Boyer; Kathie Y Sun
Journal:  Trends Genet       Date:  2013-02-28       Impact factor: 11.639

8.  Offering aggregate results to participants in genomic research: opportunities and challenges.

Authors:  Laura M Beskow; Wylie Burke; Stephanie M Fullerton; Richard R Sharp
Journal:  Genet Med       Date:  2012-01-26       Impact factor: 8.822

9.  The new era of precision population health: insights for the All of Us Research Program and beyond.

Authors:  Courtney R Lyles; Mitchell R Lunn; Juno Obedin-Maliver; Kirsten Bibbins-Domingo
Journal:  J Transl Med       Date:  2018-07-27       Impact factor: 5.531

Review 10.  Big Data Analytics in Healthcare.

Authors:  Ashwin Belle; Raghuram Thiagarajan; S M Reza Soroushmehr; Fatemeh Navidi; Daniel A Beard; Kayvan Najarian
Journal:  Biomed Res Int       Date:  2015-07-02       Impact factor: 3.411

View more
  5 in total

1.  Predictive Analytics and the Return of "Research" Information to Participants.

Authors:  Shengzhi Wang; Ellen E Lee; Benjamin Zywicki; Ho-Cheol Kim; Dilip Jeste; Camille Nebeker
Journal:  Appl Hum Factors Ergon Conf       Date:  2020-07-10

2.  Return of individual research results from genomic research: A systematic review of stakeholder perspectives.

Authors:  Danya F Vears; Joel T Minion; Stephanie J Roberts; James Cummings; Mavis Machirori; Mwenza Blell; Isabelle Budin-Ljøsne; Lorraine Cowley; Stephanie O M Dyke; Clara Gaff; Robert Green; Alison Hall; Amber L Johns; Bartha M Knoppers; Stephanie Mulrine; Christine Patch; Eva Winkler; Madeleine J Murtagh
Journal:  PLoS One       Date:  2021-11-08       Impact factor: 3.240

3.  Use of machine learning to transform complex standardized nursing care plan data into meaningful research variables: a palliative care exemplar.

Authors:  Tamara G R Macieira; Yingwei Yao; Gail M Keenan
Journal:  J Am Med Inform Assoc       Date:  2021-11-25       Impact factor: 7.942

4.  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

5.  Practical Considerations in Using Online Modified-Delphi Approaches to Engage Patients and Other Stakeholders in Clinical Practice Guideline Development.

Authors:  Dmitry Khodyakov; Sean Grant; Brian Denger; Kathi Kinnett; Ann Martin; Holly Peay; Ian Coulter
Journal:  Patient       Date:  2020-02       Impact factor: 3.883

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.