Literature DB >> 12587135

Goodness-of-fit ethic for informed consent to research involving adults with mental retardation and developmental disabilities.

Celia B Fisher1.   

Abstract

This article reviews current theory and research on informed consent policies for adults with mental retardation within a relational ethics framework that re-conceptualizes consent vulnerability in terms of the goodness-of-fit between participant decisional capacities and the specific consent context. Conceptualizing informed consent competence as a product of the relationship between person and consent context shifts assessment of decisional capacity away from an exclusive focus on a research participant's cognitive deficiencies to (a) an examination of those aspects of the consent setting that are creating or exacerbating consent vulnerability and (b) consideration of how the setting can be modified to produce a consent process that best reflects and protects the hopes, values, concerns, and welfare of adults with developmental disabilities. Copyright 2003 Wiley-Liss, Inc. MRDD Research Reviews 2003;9:27-31.

Entities:  

Keywords:  Biomedical and Behavioral Research

Mesh:

Year:  2003        PMID: 12587135     DOI: 10.1002/mrdd.10052

Source DB:  PubMed          Journal:  Ment Retard Dev Disabil Res Rev        ISSN: 1080-4013


  9 in total

1.  The ethics and regulatory landscape of including vulnerable populations in pragmatic clinical trials.

Authors:  Mary Jane Welch; Rachel Lally; Jennifer E Miller; Stephanie Pittman; Lynda Brodsky; Arthur L Caplan; Gina Uhlenbrauck; Darcy M Louzao; James H Fischer; Benjamin Wilfond
Journal:  Clin Trials       Date:  2015-09-15       Impact factor: 2.486

2.  Enhancing HIV vaccine trial consent preparedness among street drug users.

Authors:  Celia B Fisher
Journal:  J Empir Res Hum Res Ethics       Date:  2010-06       Impact factor: 1.742

3.  Parent ratings of ability to consent for clinical trials in fragile X syndrome.

Authors:  Donald B Bailey; Melissa Raspa; Anne Wheeler; Anne Edwards; Ellen Bishop; Carla Bann; David Borasky; Paul S Appelbaum
Journal:  J Empir Res Hum Res Ethics       Date:  2014-07       Impact factor: 1.742

4.  Relationship of external influence to parental distress in decision making regarding children with a life-threatening illness.

Authors:  Victoria A Miller; Mary Frances Luce; Robert M Nelson
Journal:  J Pediatr Psychol       Date:  2011-06-21

5.  "You can't be cold and scientific": community views on ethical issues in intellectual disability research.

Authors:  Katherine E McDonald; Nicole M Schwartz; Colleen M Gibbons; Robert S Olick
Journal:  J Empir Res Hum Res Ethics       Date:  2015-03-13       Impact factor: 1.742

6.  Assessing Understanding and Obtaining Consent from Adults with Intellectual Disabilities for a Health Promotion Study.

Authors:  Willi Horner-Johnson; Danielle Bailey
Journal:  J Policy Pract Intellect Disabil       Date:  2013-09

7.  Paradigm shifts in disability and health: toward more ethical public health research.

Authors:  Katherine E McDonald; Dora M Raymaker
Journal:  Am J Public Health       Date:  2013-10-17       Impact factor: 9.308

8.  Enhancing the Responsible Conduct of Sexual Health Prevention Research Across Global and Local Contexts: Training for Evidence-Based Research Ethics.

Authors:  Celia B Fisher
Journal:  Ethics Behav       Date:  2014-12-01

9.  Research ethics and intellectual disability: broadening the debates.

Authors:  Licia Carlson
Journal:  Yale J Biol Med       Date:  2013-09-20
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.