CITI -Social&Behavioral Research (2024) Questions & Answers Already Graded A+

What procedures must be described in an agreement called an "assurance of compliance" with OHRP? - Answer-Procedures in place that ensure that subjects will be protected in a manner commensurate with the Common Rule, including review by an independent committee comparable to an IRB. A researcher proposes to conduct a study at a foreign site that has been determined to be exempt from the federal regulations by institutional policy. According to federal regulations, is review required at the foreign site? - Answer-If a proposed study qualifies for exemption, federal regulations do not require review at the foreign site where it will be conducted. What are some considerations for a U.S. researcher conducting a study in a non-U.S. setting when obtaining informed consent from subjects? - Answer-In addition to the consent of the research subjects, are there other individuals or groups whose permission must be sought? Nuremberg Code - Answer-Judged human experimentation conducted by Nazis. Voluntary consent by human subject is absolutely essential Declaration of Helsinki - Answer-basis of good clinical practices. Addresses research protocols, informed consent, risks/benefits, et plus Belmont Report - Answer-basic ethical principles for research involving human subjects. -Respect for person's autonomy -Beneficence -Justice Respect for Person - Answer-individuals treated as autonomous agents, and those with diminished autonomy are entitled protection Beneficence - Answer-Make effort to secure well-being.-Do not harm -Maximize possible benefits and minimize possible harm/risk Justice - Answer-Equals be treated equally. -To each person an equal share. -To each person according to individual need. -To each person according to individual effort. -To each person according to societal contribution. -And to each person according to merit. IRB Review - Answer-to protect the rights and welfare of human subjects by ensuring equitable subject selection, assuring adequate informed consent, assessing and minimizing risks, and maintaining privacy and confidentiality. Exempt Review - Answer-research with human subjects that generally involves no more than minimal risk. Does not require ongoing review, unless amended st it no longer fulfills the exempt criteria Expedited Review - Answer-research presents no more than minimal risk. Does not have to be full convened committee. Full Board (convened) Review - Answer-research that involve more than minimal risk require full board review at a convened meeting at which a quorum of IRB members is present. Must receive approval by majority of members. Research - Answer-a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge. To test a hypothesis with conclusions to be drawnHuman subject - Answer-a living individual ABOUT whom an investigator (whether professional or student) conducting research obtains (1) data through intervention or interaction with the individual, or (2) identifiable private information. Which of the following studies need IRB approval? - Answer-Studies collecting data about living individuals. Which type of IRB review does not require an IRB approval but does require a determination by the IRB or an IRB designee? - Answer-Exempt Which of the following on-line research strategies raises the most concerns regarding the ethical principle of respecting the autonomy of research subjects and the corresponding federal regulations requiring informed consent? - Answer-A researcher proposes to join a moderated support group for cancer survivors posing as a survivor. She plans to insert comments to see how the members respond