Literature DB >> 12691694

Voluntariness in clinical research at the end of life.

Manish Agrawal1.   

Abstract

Voluntariness is a requirement that is frequently voiced in research ethics but is poorly understood. This article seeks to clarify voluntariness and assess its significance in clinical research at the end of life. First, what voluntariness is and why we consider it important is considered. Next, where voluntariness fits in the overall context of making clinical research ethical is clarified. Finally, the murky terms "vulnerability," "exploitation," and "coercion" are clarified and their relationship to voluntariness examined. The danger of using some of these terms is that they carry a lot of moral weight and labeling patients as "vulnerable" or "coerced" can close off conversation because they are reflexively associated with unethical research. Finally, correctly characterized threats to voluntariness are examined and ways to ameliorate them are presented.

Entities:  

Keywords:  Biomedical and Behavioral Research

Mesh:

Year:  2003        PMID: 12691694     DOI: 10.1016/s0885-3924(03)00057-5

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  11 in total

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2.  Compassion and vigilance: investigators' strategies to manage ethical concerns in palliative and end-of-life research.

Authors:  Susan E Hickman; Juliana C Cartwright; Christine A Nelson; Kathleen Knafl
Journal:  J Palliat Med       Date:  2012-06-25       Impact factor: 2.947

3.  A pragmatic analysis of vulnerability in clinical research.

Authors:  David Wendler
Journal:  Bioethics       Date:  2017-09       Impact factor: 1.898

4.  Research participation by older adults at end of life: barriers and solutions.

Authors:  Melissa Lehan Mackin; Keela Herr; Kimberly Bergen-Jackson; Perry Fine; Chris Forcucci; Sara Sanders
Journal:  Res Gerontol Nurs       Date:  2009-04-30       Impact factor: 1.571

Review 5.  Phase 0 clinical trials: conceptions and misconceptions.

Authors:  Shivaani Kummar; Larry Rubinstein; Robert Kinders; Ralph E Parchment; Martin E Gutierrez; Anthony J Murgo; Jay Ji; Barbara Mroczkowski; Oxana K Pickeral; Mel Simpson; Melinda Hollingshead; Sherry X Yang; Lee Helman; Robert Wiltrout; Jerry Collins; Joseph E Tomaszewski; James H Doroshow
Journal:  Cancer J       Date:  2008 May-Jun       Impact factor: 3.360

6.  Ethical conduct of palliative care research: enhancing communication between investigators and institutional review boards.

Authors:  Amy P Abernethy; Warren H Capell; Noreen M Aziz; Christine Ritchie; Maryjo Prince-Paul; Rachael E Bennett; Jean S Kutner
Journal:  J Pain Symptom Manage       Date:  2014-05-28       Impact factor: 3.612

7.  The ethics of withdrawal from study participation.

Authors:  Elisa J Gordon; Thomas R Prohaska
Journal:  Account Res       Date:  2006 Oct-Dec       Impact factor: 3.057

8.  Desperation May Affect Autonomy but Not Informed Consent.

Authors:  Teresa Swift
Journal:  AJOB Neurosci       Date:  2011-01-13

9.  Ethical aspects of vulnerability in research.

Authors:  Elisabeth Weisser-Lohmann
Journal:  Poiesis Prax       Date:  2012-10-17

10.  Willingness to participate in HIV research at the end of life (EOL).

Authors:  Katya Prakash; Sara Gianella; Karine Dubé; Jeff Taylor; GaYoung Lee; Davey M Smith
Journal:  PLoS One       Date:  2018-07-23       Impact factor: 3.240

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