Literature DB >> 33023975

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

Stephanie A Kraft1,2, Erin Rothwell3, Seema K Shah4,5, Devan M Duenas6, Hannah Lewis6, Kristin Muessig7, Douglas J Opel6,2, Katrina A B Goddard7, Benjamin S Wilfond6,2.   

Abstract

The ethical principle of 'respect for persons' in clinical research has traditionally focused on protecting individuals' autonomy rights, but respect for participants also includes broader, although less well understood, ethical obligations to regard individuals' rights, needs, interests and feelings. However, there is little empirical evidence about how to effectively convey respect to potential and current participants. To fill this gap, we conducted exploratory, qualitative interviews with participants in a clinical genomics implementation study. We interviewed 40 participants in English (n=30) or Spanish (n=10) about their experiences with respect in the study and perceptions of how researchers in a hypothetical observational study could convey respect or a lack thereof. Most interviewees were female (93%), identified as Hispanic/Latino(a) (43%) or non-Hispanic white (38%), reported annual household income under US$60 000 (70%) and did not have a Bachelor's degree (65%); 30% had limited health literacy. We identified four key domains for demonstrating respect: (1) personal study team interactions, with an emphasis on empathy, appreciation and non-judgment; (2) study communication processes, including following up and sharing results with participants; (3) inclusion, particularly ensuring materials are understandable and procedures are accessible; and (4) consent and authorisation, including providing a neutral informed consent and keeping promises regarding privacy protections. While the experience of respect is inherently subjective, these findings highlight four key domains that may meaningfully demonstrate respect to potential and current research participants. Further empirical and normative work is needed to substantiate these domains and evaluate how best to incorporate them into the practice of research. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  clinical trials; informed consent; research ethics

Year:  2020        PMID: 33023975      PMCID: PMC8021602          DOI: 10.1136/medethics-2020-106440

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  37 in total

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Authors:  Arlene M Davis; Sara Chandros Hull; Christine Grady; Benjamin S Wilfond; Gail E Henderson
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2.  Understanding respect: learning from patients.

Authors:  N W Dickert; N E Kass
Journal:  J Med Ethics       Date:  2009-07       Impact factor: 2.903

3.  Genomics is failing on diversity.

Authors:  Alice B Popejoy; Stephanie M Fullerton
Journal:  Nature       Date:  2016-10-13       Impact factor: 49.962

4.  Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome.

Authors:  Fay Kastrinos; Hajime Uno; Chinedu Ukaegbu; Carmelita Alvero; Ashley McFarland; Matthew B Yurgelun; Matthew H Kulke; Deborah Schrag; Jeffrey A Meyerhardt; Charles S Fuchs; Robert J Mayer; Kimmie Ng; Ewout W Steyerberg; Sapna Syngal
Journal:  J Clin Oncol       Date:  2017-05-10       Impact factor: 44.544

5.  Partnering With Research Staff Members to Bridge Gaps in Consent.

Authors:  Emily E Anderson
Journal:  Am J Bioeth       Date:  2020-06       Impact factor: 11.229

6.  Diverse patient perspectives on respect in healthcare: A qualitative study.

Authors:  Mary Catherine Beach; Emily Branyon; Somnath Saha
Journal:  Patient Educ Couns       Date:  2017-05-05

7.  Patient and family perspectives on respect and dignity in the intensive care unit.

Authors:  Mary Catherine Beach; Lindsay Forbes; Emily Branyon; Hanan Aboumatar; Joseph Carrese; Jeremy Sugarman; Gail Geller
Journal:  Narrat Inq Bioeth       Date:  2015

8.  Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.

Authors:  Isabelle Budin-Ljøsne; Harriet J A Teare; Jane Kaye; Stephan Beck; Heidi Beate Bentzen; Luciana Caenazzo; Clive Collett; Flavio D'Abramo; Heike Felzmann; Teresa Finlay; Muhammad Kassim Javaid; Erica Jones; Višnja Katić; Amy Simpson; Deborah Mascalzoni
Journal:  BMC Med Ethics       Date:  2017-01-25       Impact factor: 2.652

9.  Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.

Authors:  Stephanie A Kraft; Kathryn M Porter; Devan M Duenas; Claudia Guerra; Galen Joseph; Sandra Soo-Jin Lee; Kelly J Shipman; Jake Allen; Donna Eubanks; Tia L Kauffman; Nangel M Lindberg; Katherine Anderson; Jamilyn M Zepp; Marian J Gilmore; Kathleen F Mittendorf; Elizabeth Shuster; Kristin R Muessig; Briana Arnold; Katrina A B Goddard; Benjamin S Wilfond
Journal:  AJOB Empir Bioeth       Date:  2020-09-26

10.  Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolution.

Authors:  Stephanie A Kraft; Carmit McMullen; Nangel M Lindberg; David Bui; Kelly Shipman; Katherine Anderson; Galen Joseph; Devan M Duenas; Kathryn M Porter; Tia L Kauffman; Alyssa Koomas; Chelese L Ransom; Paige Jackson; Katrina A B Goddard; Benjamin S Wilfond; Sandra Soo-Jin Lee
Journal:  Genet Med       Date:  2020-02-24       Impact factor: 8.822

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  3 in total

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Authors:  Elliott Mark Weiss; Katherine F Guttmann; Aleksandra E Olszewski; Brooke E Magnus; Sijia Li; Scott Y H Kim; Anita R Shah; Sandra E Juul; Yvonne W Wu; Kaashif A Ahmad; Ellen Bendel-Stenzel; Natalia A Isaza; Andrea L Lampland; Amit M Mathur; Rakesh Rao; David Riley; David G Russell; Zeynep N I Salih; Carrie B Torr; Joern-Hendrik Weitkamp; Uchenna E Anani; Taeun Chang; Juanita Dudley; John Flibotte; Erin M Havrilla; Alexandra C O'Kane; Krystle Perez; Brenda J Stanley; Seema K Shah; Benjamin S Wilfond
Journal:  J Pediatr       Date:  2021-08-14       Impact factor: 4.406

2.  Promoting Disclosure and Understanding in Informed Consent: Optimizing the Impact of the Common Rule "Key Information" Requirement.

Authors:  Kathryn M Porter; Elliott M Weiss; Stephanie A Kraft
Journal:  Am J Bioeth       Date:  2021-05       Impact factor: 11.229

3.  Identification and management of pragmatic clinical trial collateral findings: A current understanding and directions for future research.

Authors:  Stephanie R Morain; Debra J H Mathews; Gail Geller; Juli Bollinger; Kevin Weinfurt; Jeffrey G Jarvik; Elizabeth May; Jeremy Sugarman
Journal:  Healthc (Amst)       Date:  2021-09-29
  3 in total

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