Literature DB >> 21495516

Viewing research participation as a moral obligation: in whose interests?

Stuart Rennie1.   

Abstract

A moral paradigm shift has been proposed for participation in health-related research. It's not just a praiseworthy option, some say; it's a social obligation. Recasting research participation in this way would have global ramifications, however. Who ultimately stands to gain the most from it, and who has the most to lose?

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Mesh：

Year:  2011        PMID： 21495516      PMCID： PMC4681491          DOI： 10.1353/hcr.2011.0025

Source DB:  PubMed          Journal:  Hastings Cent Rep        ISSN： 0093-0334            Impact factor:   2.683


  12 in total

1.  A piece of my mind. Beyond folklore.

Authors:  Daniel W Fitzgerald; Frieda M T F Behets
Journal:  JAMA       Date:  2002-12-11       Impact factor: 56.272

2.  Ethics. Fair benefits for research in developing countries.

Authors: 
Journal:  Science       Date:  2002-12-13       Impact factor: 47.728

Review 3.  Scope and impact of financial conflicts of interest in biomedical research: a systematic review.

Authors:  Justin E Bekelman; Yan Li; Cary P Gross
Journal:  JAMA       Date:  2003 Jan 22-29       Impact factor: 56.272

4.  Scientific research is a moral duty.

Authors:  John Harris
Journal:  J Med Ethics       Date:  2005-04       Impact factor: 2.903

5.  Correcting social ills through mandatory research participation.

Authors:  Anita Ho
Journal:  Am J Bioeth       Date:  2008-10       Impact factor: 11.229

6.  In defense of the duty to participate in biomedical research.

Authors:  Rosamond Rhodes
Journal:  Am J Bioeth       Date:  2008-10       Impact factor: 11.229

7.  The obligation to participate in biomedical research.

Authors:  G Owen Schaefer; Ezekiel J Emanuel; Alan Wertheimer
Journal:  JAMA       Date:  2009-07-01       Impact factor: 56.272

8.  John Harris' argument for a duty to research.

Authors:  Iain Brassington
Journal:  Bioethics       Date:  2007-03       Impact factor: 1.898

9.  Participation in biomedical research is an imperfect moral duty: a response to John Harris.

Authors:  Sandra Shapshay; Kenneth D Pimple
Journal:  J Med Ethics       Date:  2007-07       Impact factor: 2.903

10.  Moral imagination: the missing component in global health.

Authors:  Solomon R Benatar
Journal:  PLoS Med       Date:  2005-12-27       Impact factor: 11.069
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  6 in total

1.  An empirical assessment of the short-term impacts of a reading of Deborah Zoe Laufer's drama Informed Consent on attitudes and intentions to participate in genetic research.

Authors:  Erin Rothwell; Jeffrey R Botkin; Sydney Cheek-O'Donnell; Bob Wong; Gretchen A Case; Erin Johnson; Trent Matheson; Alena Wilson; Nicole R Robinson; Jared Rawlings; Brooke Horejsi; Ana Maria Lopez; Carrie L Byington
Journal:  AJOB Empir Bioeth       Date:  2018-04-06

2.  Harms, benefits, and the nature of interventions in pragmatic clinical trials.

Authors:  Joseph Ali; Joseph E Andrews; Carol P Somkin; C Egla Rabinovich
Journal:  Clin Trials       Date:  2015-09-15       Impact factor: 2.486

3.  Secondary consent to biospecimen use in a prostate cancer biorepository.

Authors:  Bettina F Drake; Katherine Brown; Lucy D'Agostino McGowan; Jennifer Haslag-Minoff; Kimberly Kaphingst
Journal:  BMC Res Notes       Date:  2016-07-18

Review 4.  Consent, ethics and genetic biobanks: the case of the Athlome project.

Authors:  Rachel Thompson; Michael J McNamee
Journal:  BMC Genomics       Date:  2017-11-14       Impact factor: 3.969

5.  Willingness to Participate in Health Information Networks with Diverse Data Use: Evaluating Public Perspectives.

Authors:  Jodyn Platt; Minakshi Raj; Ayşe G Büyüktür; M Grace Trinidad; Olufunmilayo Olopade; Mark S Ackerman; Sharon Kardia
Journal:  EGEMS (Wash DC)       Date:  2019-07-25

6.  Child's objection to non-beneficial research: capacity and distress based models.

Authors:  Marcin Waligora; Joanna Różyńska; Jan Piasecki
Journal:  Med Health Care Philos       Date:  2016-03
  6 in total

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