Please use this identifier to cite or link to this item: https://erepository.fmesinstitute.org/handle/123456789/1714
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dc.contributor.authorGittner, L. S.-
dc.contributor.authorRoach, M. J.-
dc.contributor.authorKikano, G.-
dc.contributor.authorGrey, S.-
dc.contributor.authorDawson, N. V. N. V.-
dc.date.accessioned2019-11-29T16:02:57Z-
dc.date.available2019-11-29T16:02:57Z-
dc.date.issued2011-
dc.identifier.citationGittner, L. S., Roach, M. J., Kikano, G., Grey, S., & Dawson, N. V. (2011). Health service research: The square peg in human subjects protection regulations. Journal of Medical Ethics, 37(2), 118–122.en_US
dc.identifier.urihttps://doi.org/10.1136/jme.2010.037226-
dc.identifier.urihttps://erepository.fmesinstitute.org/handle/123456789/1714-
dc.description.abstractProtection of human participants is a fundamental facet of biomedical research. We report the activities of a health service research study in which there were three institutional review boards (IRBs), three legal departments and one research administration department providing recommendations and mandating changes in the study methods. Complying with IRB requirements can be challenging, but can also adversely affect study outcomes. Multiple protocol changes mandated from multiple IRBs created a research method that was not reflective of how substance use screening would be performed in a clinical setting. There was direct conflict between the IRBs' perceptions of participants' protection with the researchers' need to use research methodology that assures the clinical relevancy of results.en_US
dc.language.isoenen_US
dc.publisherJournal of Medical Ethicsen_US
dc.titleHealth service research: The square peg in human subjects protection regulations.en_US
dc.typeJournal Articleen_US
fmes.numPages118–122en_US
Appears in Collections:Ethics

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