Literature DB >> 16883621

The therapeutic misconception and our models of competency and informed consent.

Charles W Lidz1.   

Abstract

The doctrine of informed consent rests on empirical claims. This is true particularly of what commentators have characterized as the "strong" model of informed consent. This model assumes that if adequate information is given to a competent individual, understanding will result and, permitted to make a voluntary decision, the individual will make a rational decision. However, the "therapeutic misconception" posits that individuals may confuse the goals of research with those of treatment and may make decisions that do not rest on adequate understanding. This article reviews research suggesting that this may in fact be true, and concludes that, as a result, traditional notions of informed consent may not yield results consistent with the assumptions on which the doctrine of informed consent rests. Copyright (c) 2006 John Wiley & Sons, Ltd.

Mesh:

Year:  2006        PMID: 16883621     DOI: 10.1002/bsl.700

Source DB:  PubMed          Journal:  Behav Sci Law        ISSN: 0735-3936


  13 in total

1.  Audit of the informed consent process as a part of a clinical research quality assurance program.

Authors:  Pramod M Lad; Rebecca Dahl
Journal:  Sci Eng Ethics       Date:  2013-08-24       Impact factor: 3.525

2.  The therapeutic misconception: not just for patients.

Authors:  Dana J Lawrence
Journal:  J Can Chiropr Assoc       Date:  2008-08

Review 3.  Oncofertility and informed consent: addressing beliefs, values, and future decision making.

Authors:  Felicia Cohn
Journal:  Cancer Treat Res       Date:  2010

Review 4.  Therapeutic misconception: hope, trust and misconception in paediatric research.

Authors:  Simon Woods; Lynn E Hagger; Pauline McCormack
Journal:  Health Care Anal       Date:  2014-03

5.  Ethical issues in health research in children.

Authors: 
Journal:  Paediatr Child Health       Date:  2008-10       Impact factor: 2.253

6.  Informed consent, therapeutic misconception, and clinical trials for Alzheimer's disease.

Authors:  James M Wilkins; Brent P Forester
Journal:  Int J Geriatr Psychiatry       Date:  2020-01-26       Impact factor: 3.485

7.  Informed consent: do information pamphlets improve post-operative risk-recall in patients undergoing total thyroidectomy: prospective randomized control study.

Authors:  Hussain Alsaffar; Lindsay Wilson; Dev P Kamdar; Faizullo Sultanov; Danny Enepekides; Kevin M Higgins
Journal:  J Otolaryngol Head Neck Surg       Date:  2016-02-13

8.  Capacity to consent to research participation in adults with metastatic cancer: comparisons of brain metastasis, non-CNS metastasis, and healthy controls.

Authors:  Kyler Mulhauser; Dario A Marotta; Adam Gerstenecker; Gabrielle Wilhelm; Terina Myers; Meredith Gammon; David E Vance; Burt Nabors; John Fiveash; Kristen Triebel
Journal:  Neurooncol Pract       Date:  2020-03-09

9.  An effective multisource informed consent procedure for research and clinical practice: an observational study of patient understanding and awareness of their roles as research stakeholders in a cancer biobank.

Authors:  Silvia Cervo; Jane Rovina; Renato Talamini; Tiziana Perin; Vincenzo Canzonieri; Paolo De Paoli; Agostino Steffan
Journal:  BMC Med Ethics       Date:  2013-07-30       Impact factor: 2.652

Review 10.  Once a clinician, always a clinician: a systematic review to develop a typology of clinician-researcher dual-role experiences in health research with patient-participants.

Authors:  E Jean C Hay-Smith; Melanie Brown; Lynley Anderson; Gareth J Treharne
Journal:  BMC Med Res Methodol       Date:  2016-08-09       Impact factor: 4.615

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.