What factor sometimes influences an Institutional Review Board to approve a research study that requires the use of deception? a. The findings of the research would be likely to be beneficial to society. b. The knowledge sought can be acquired in some other way. c. The research participants may be harmed by the deception. d. The IRB is really interested in the topic.

The findings of the research would be likely to be beneficial to society. More test answers on https://studyhippo.com/research-midterm-fall-12/

IRB stands for: A. Institutional Review Board. B. International Research Board. C. Internal Review Board. D. Intelligence Research Board.

A. Institutional Review Board More test answers on https://studyhippo.com/famr-exam-1/

One purpose of an institutional review board is to

Ensure that the rights of research subjects are protected More test answers on https://studyhippo.com/research-final-exam/

Which of the following statements is TRUE? A) The actual rules and regulations for the protection of human research participants were issued by the U.S. Department of Health and Human Services. B) Every institution that receives federal funds must have an Institutional Review Board. C) All research conducted at an institution is reviewed in some way by the IRB. D) all of these

D) all of these More test answers on https://studyhippo.com/psy3213-practice-final-exam/

The basic goal of the Institutional Review Board (IRB) is to ensure: 1. family history data of each patient enrolled in a protocol is protected 2. human subjects are screened 3. study design meets the criteria of the study 4. rights of human subjects are protected

the rights of human subjects are protected More test answers on https://studyhippo.com/ctr-practice-exam-1/

In a study involving false feedback about performance, the reseacher is required to (a) use debriefing after the session is over (b) obtain informed consent from te institutional review board (c) use deceptive research methods (d) conceal the results of the study from participants

(a) use debriefing after the session is over See page 40 More test answers on https://studyhippo.com/py-exam-study-questions/

(IRB) Institutional review board

a committee of at least five members with varying backgrounds that determines the acceptability of proposed human subjects research in accordance with institutional policies, applicable law, and standards of professional practice and conduct More test answers on https://studyhippo.com/chapter-7-and-8-fundamentals-of-law-for-health-informatics-and-information-management-brodnik/

Define Institutional Review Board (IRB)

A committee responsible for interpreting ethical principles and ensuring that research using human participants is conducted ethically. This includes at least 5 people who come from specified backgrounds. At least one member must be a scientist, one has to have academic interests outside the sciences, and one should be a community member who has no ties to the institution. More test answers on https://studyhippo.com/ch-4-psy-350/

What is the Institutional Review Board (IRB) charged with? (There may be more than one correct answer. Please be sure to select all correct answers.)

Protecting the rights and welfare of human subjects. – Assuring that all applicable institutional policies and federal regulations related to research with human subjects are followed. – Reviewing subject recruitment materials and strategies. More test answers on https://studyhippo.com/research-methods-citi-220340/

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Institutional Review Board Flashcards, test questions and answers

Q: Institutional review Board (IRB)

A committee of physicians, staticians, community advocated, and others which ensure that a clinical trial is ethical and that the rights of the study participants are protected. All clinical trials must be approved by an IRB before they begin. More test answers on https://studyhippo.com/napsrcnpr-exam/

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What is Institutional Review Board?

An Institutional Review Board (IRB) is an administrative body established by universities and other research institutions to ensure the ethical conduct of research involving human participants. IRBs are responsible for reviewing proposed research projects, assessing potential risks and benefits to participants, approving consent forms, monitoring ongoing studies, and providing guidance on ethical issues related to human subject protection.The purpose of IRBs is to protect the rights and welfare of individuals who participate in research activities. They do this by ensuring that researchers adhere to established standards for protecting participant privacy, reducing risk of harm or injury during a study, minimizing coercion or undue influence on recruitment practices, ensuring informed consent from participants, providing oversight throughout the duration of a study, and addressing any safety concerns that arise during data collection or analysis. In addition to their role as regulatory bodies overseeing research ethics compliance at institutions conducting human subjects research studies worldwide, IRBs also serve educational roles in promoting awareness about best practices regarding human subjects protection. This includes engaging with researchers both prior to initiating research activities (through review meetings) as well as after completion of a project (through post-review meetings). Through these interactions with investigators across disciplines and methodological approaches coupled with institutional policies governing such activities IRBs play important roles in helping foster strong culture within academic environments around safeguarding the rights and interests of all those involved in scientific inquiry. Ultimately then while each individual institution has its own unique set up when it comes to management structure/processes associated with establishing/maintaining an effective IRB program overall the goals remain consistent: Ensure robust protections for all those participating in any given study activity while simultaneously fostering meaningful scholarly discourse between investigators and reviewers alike so that ethical considerations are taken into account throughout entire project lifecycle.