Randomization Among The Other Randomization

A valid informed consent process for a randomized controlled trial requires the disclosure to potential participants that they will be randomized to receive the study intervention or a control intervention. This is a case of randomization within a trial, a type of randomization that has received sig...

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Bibliographic Details
Published inEthics & human research Vol. 41; no. 5; pp. 35 - 40
Main Author Barnbaum, Deborah R.
Format Journal Article
LanguageEnglish
Published United States Hastings Center 01.09.2019
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Summary:A valid informed consent process for a randomized controlled trial requires the disclosure to potential participants that they will be randomized to receive the study intervention or a control intervention. This is a case of randomization within a trial, a type of randomization that has received significant attention in research ethics. When institutions recruit large numbers of research participants for multisite clinical trials, a different, hidden form of randomization may occur: randomization among clinical trials. If it is essential to disclose to potential participants randomization within a clinical trial, then it may be the case that randomization among clinical trials recruiting individuals from the same cohort of eligible participants should also be disclosed. This article examines how randomization among clinical trials might take place and the ethical issues such randomization raises about informed consent to research participation.
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ISSN:2578-2355
2578-2363
2578-2363
DOI:10.1002/eahr.500031