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psy400ch2p41-46

psy400ch2:THE INSTITUTIONAL REVIEW BOARD

TermDefinition
institutional review boards (IRBs) protecting the health and well-being of research participants, liable for the research they approve.
IRBs ensure that researchers treat participants with respect, consider potential risks and benefits, and secure the confidentiality of participants and their data.
IRB reviews proposals submitted by researchers prior to the start of a research project, evaluating the proposals in light of the ethical principles outlined by the APA
two aspects of the IRB organization the committee itself and the staff that supports the committee
The Committee at least five members, one with research focus is in the sciences, one nonscicntific, and another with no institution ties
The science person is usually an active researcher in the behavioral or biomedical sciences
the nonscientist researcher is often from the humanities
"non-affiliated” individual is generally someone from the local community, often connected to local churches, medical facilities, or community organizations
standards can vary widely between social-behavioral and biomedical IRB panels, even at the same institution
Staff Members do an initial review of the proposal to ensure that it has been fully completed, that all the proper forms (e.g., consent forms, copies of surveys or questionnaires) have been included, the information within the proposal is consistent
Of all IRB committee members, staff members are the people you should get to know
Collaborative Research conducted by researchers at different institutions; all affiliated institutions will need to grant approval
planning and working with de-identified data (data in which the identifying information about participants has been removed) not be interacting with human subjects, their institutional IRB may not require them to obtain approval
Cross-cultural Research involves different ethical rules and regulations, often with few or no standing institutional review board committees.
mission creep: the expansion of IRB oversight to include areas unrelated to the protection of human subjects such as evaluating questions researchers want to ask in qualitative research.
definitions of risk used by many boards have expanded such that they require researchers to proactively manage any problematic outcome that might occur, however unlikely.
well-intentioned informed consent policies have made certain types of research entirely unworkable (e.g., participant observation), while creating substantial barriers to research that employs deception as part of its protocol
With more rigid and expansive IRB oversight, entire areas of scientific inquiry on high-profile, controversial issues may fall outside of the realm of permissibility
time spent by researchers responding to tangential IRB requests could actually take time away from real measures to ensure participant safety
researchers must take the basic responsibility for ethical conduct and that IRBs should be used as a resource, rather than the ultimate source of ethical judgments.
DEFINING RESEARCH: systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge
Generalizable knowledge conclusions drawn from data, underlying principles or laws of nature, explanations, predictions
Northwestern University’s IRB excludes journalism activities patient Case reports, instructor classroom data, death records, autopsy records, or cadaver specimens, oral history
activities that are not intended to produce generalizable knowledge and test particular hypotheses via a systematic investigation tend not to be counted as research
systematic attempts to evaluate a particular hypothesis or hypotheses and to apply findings to a broader context are considered research
investigations intended to be published in an academic journal or presented at an academic meeting likely qualify as research
Created by: james22222222
 

 



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