Literature DB >> 12626956

Enrolling the uninsured in clinical trials: an ethical perspective.

Christine Pace1, Franklin G Miller, Marion Danis.   

Abstract

Research participation by individuals who lack health insurance raises significant but seldom-discussed ethical issues for clinical investigators. Of particular concern are the possibility that their lack of options for getting care at the time of enrollment makes the uninsured susceptible to undue inducement to join trials and the possibility that their inability to access research products after trials leads to their exploitation. In tension with these concerns, however, is the right of the uninsured to fair consideration for research participation. We discuss these competing issues and make recommendations for how investigators can both protect uninsured research participants and provide the uninsured with fair access to research in their recruitment and enrollment strategies.

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Year:  2003        PMID: 12626956     DOI: 10.1097/01.CCM.0000054907.33928.48

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  26 in total

1.  Clinical trial participation and time to treatment among adolescents and young adults with cancer: does age at diagnosis or insurance make a difference?

Authors:  Helen M Parsons; Linda C Harlan; Nita L Seibel; Jennifer L Stevens; Theresa H M Keegan
Journal:  J Clin Oncol       Date:  2011-09-19       Impact factor: 44.544

2.  Justice and fairness in the Kennedy Krieger Institute lead paint study: the ethics of public health research on less expensive, less effective interventions.

Authors:  David R Buchanan; Franklin G Miller
Journal:  Am J Public Health       Date:  2006-03-29       Impact factor: 9.308

3.  Barriers to and strategies for recruiting Korean Americans for community-partnered health promotion research.

Authors:  Hae-Ra Han; Jeonghee Kang; Kim B Kim; Jai P Ryu; Miyong T Kim
Journal:  J Immigr Minor Health       Date:  2007-04

4.  Exploring the ethics of clinical research in an urban community.

Authors:  Christine Grady; Lindsay A Hampson; Gwenyth R Wallen; Migdalia V Rivera-Goba; Kelli L Carrington; Barbara B Mittleman
Journal:  Am J Public Health       Date:  2006-10-03       Impact factor: 9.308

Review 5.  Clinical research with economically disadvantaged populations.

Authors:  Colleen C Denny; Christine Grady
Journal:  J Med Ethics       Date:  2007-07       Impact factor: 2.903

6.  Coming Soon to a Physician Near You: Medical Neoliberalism and Pharmaceutical Clinical Trials.

Authors:  Jill A Fisher
Journal:  Harvard Health Policy Rev       Date:  2007

7.  Sharing the benefits of research fairly: two approaches.

Authors:  Joseph Millum
Journal:  J Med Ethics       Date:  2011-09-24       Impact factor: 2.903

Review 8.  The ethics of uninsured participants accessing healthcare in biomedical research: A literature review.

Authors:  Hae Lin Cho; Marion Danis; Christine Grady
Journal:  Clin Trials       Date:  2018-08-02       Impact factor: 2.486

9.  Worth the risk? Relationship of incentives to risk and benefit perceptions and willingness to participate in schizophrenia research.

Authors:  Laura B Dunn; Daniel S Kim; Ian E Fellows; Barton W Palmer
Journal:  Schizophr Bull       Date:  2008-02-14       Impact factor: 9.306

Review 10.  The potential exploitation of research participants in high income countries who lack access to health care.

Authors:  Rafael Dal-Ré; Annette Rid; Ezekiel Emanuel; David Wendler
Journal:  Br J Clin Pharmacol       Date:  2016-02-29       Impact factor: 4.335

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