2012
DOI: 10.1111/j.1748-720x.2012.00726.x
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More Than Cheating: Deception, IRB Shopping, and the Normative Legitimacy of IRBs

Abstract: Deception, cheating, and loopholes within the IRB approval process have received significant attention in the past several years. Surveys of clinical researchers indicate common deception ranging from omitting information to outright lying, and controversy surrounding the FDA's decision not to ban "IRB shopping" (the practice of submitting protocols to multiple IRBs until one is found that will approve the protocol) has raised legitimate concerns about the integrity of the IRB process. While at first blush the… Show more

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Cited by 9 publications
(8 citation statements)
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“…Presently, the few studies dealing with outcome assessment focused mostly on statistical analysis of approval, while investigating compliance and the ‘correctness of decisions’ is unduly ‘neglected’. In the light of the common deception, “ranging from omitting information to outright lying in research”, and information on clinical researchers perspectives on value of ethics review [ 42 ], further studies are necessary to understand to what extent ethical decisions are followed [ 43 ]. The aim is not to point out non-compliance of animal researchers but to contribute to increase legitimacy of AECs by facilitating communication between researchers and AECs [ 44 ].…”
Section: Discussionmentioning
confidence: 99%
“…Presently, the few studies dealing with outcome assessment focused mostly on statistical analysis of approval, while investigating compliance and the ‘correctness of decisions’ is unduly ‘neglected’. In the light of the common deception, “ranging from omitting information to outright lying in research”, and information on clinical researchers perspectives on value of ethics review [ 42 ], further studies are necessary to understand to what extent ethical decisions are followed [ 43 ]. The aim is not to point out non-compliance of animal researchers but to contribute to increase legitimacy of AECs by facilitating communication between researchers and AECs [ 44 ].…”
Section: Discussionmentioning
confidence: 99%
“…This is particularly true in criminology and criminal justice which, oftentimes, involves research designs and issues that IRB committee members do not have experience with and that require a prisoner representative—an individual who is currently or formerly a prisoner or an individual who has a close working knowledge, understanding, and appreciation of prison conditions from the perspective of the prisoner (e.g., prison chaplain, prison social worker, prison health care worker) (Tierney & Corwin, 2007). As a result, researchers may engage in lying or deception to the IRB to gain approval or even resort to “IRB shopping” whereby the researcher, if working collaboratively with other academics at other institutions, may choose which IRB to submit the protocol to be granted the best chance of research approval (Spellecy & May, 2012). At a minimum, the creativity of social science researchers is stifled as they sort out how to conduct their research with the mindset of how to gain IRB approval rather than approaching their research with the best design to answering their pressing questions (Bledsoe et al, 2007).…”
Section: Literature Reviewmentioning
confidence: 99%
“…Participants sometimes sign the consent document without understanding what participation entails (Rowbotham et al 2013). At the same time, investigators point out that IRB reviews sometimes ask that even more information be provided on a consent form, require changes for stylistic purposes, and require changes that do not concern safety or benefits but emphasize study design (Spellecy and May 2012). The exclusive focus on the informed consent document by IRBs undermines the premise that informed consent is a process rather than a checkbox (Emanuel et al 2004).…”
Section: Introductionmentioning
confidence: 99%