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...
Saved in:
Published in | Ethics & human research Vol. 41; no. 5; pp. 35 - 40 |
---|---|
Main Author | |
Format | Journal Article |
Language | English |
Published |
United States
Hastings Center
01.09.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
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. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2578-2355 2578-2363 2578-2363 |
DOI: | 10.1002/eahr.500031 |