BMJ 2001;322:866 ( 7 April )

Letters

Trial experience and recollection of consent

The first 100% of the full text of this article appears below.

EDITOR---Elbourne et al in their article discuss a common, and entirely avoidable, problem.1 People asked to sign consent forms, for both research and treatment, often do not recollect the exact details later. This is perfectly understandable. The courteous and common sense thing to do is surely to give all trial participants, parents of children in trials, and ordinary patients not in trials, a copy of the consent form they have just signed. The form should be accompanied by an information sheet giving all relevant details (including randomisation if any).

This should not replace verbal explanation but supplement it. This strategy would avoid much confusion, unhappiness, and even perhaps litigation. It is amazing to us that such a simple procedure, which is routine in business transactions, is still not observed routinely in clinical practice in the United Kingdom.

Heather Goodare, Chair
Breast UK (Breast-cancer Research Ethics and Advocacy), Horsham, West Sussex RH13 6DF hm.goodare@virgin.net

Charlotte Williamson, chair
CERES (Consumers for Ethics in Research), London N16 0BW



1. Elbourne E, Snowdon C, Garcia J, Field D. Trial experience and problems of parental recollection of consent. BMJ 2001; 322: 49-50[Free Full Text]. (6 January.)


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Relevant Article

Trial experience and problems of parental recollection of consent
Diana Elbourne, Claire Snowdon, Jo Garcia, and David Field
BMJ 2001 322: 49. [Extract] [Full Text]

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Rapid Responses:

Read all Rapid Responses

Consent/patient information copies
Craig Leaper
bmj.com, 7 Apr 2001 [Full text]



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