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July 09, 2009

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There seem to be two variables: !, where the differences might affect the ability of a person to make use of the services of a government agency (NIH) and 2. where the differences might affect the welfare of the person logging on. The ethical problem with the first is that there may be some diminution in the quality or quantity of the service provided by the agency, thereby affecting the duty of the agency to the public. The ethical problem with the second, of course, is that a person might be giving something up or opening himself/herself to some disadvantage in the future (privacy loss, reduction in access to care, etc.) Both are important but only the second requires informed consent of the user.

Given that the information to be obtained from the experiments is useful and any changes excited by the new information is likely to benefit the public, the ethical problems arising from the first variable are minimal. The duty is to the public through the government and the government more likely than not approved of the experiment, taking all that into account.

As to the second, what would count as informed consent that would nevertheless allow the experiment to work? I suppose something like this work: "For the next few weeks we will be making alterations on our web site (or in our e-mail notifications, information leaflets or ...) in order to determine how we might serve you better. The changes may, in a few cases, affect your understanding of our services. If you have any question whatever concerning what the kind and manner of application of our services may affect your wellbeing, please be sure to call ... We need your comments to improve the way in which we provide information."

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