题目
单项选择题
Question49 Informed consent is one of the pillars of ethical human participant health based research, which if the following elements relates to good practice when it comes to informed consent. Select one alternative: A fair explanation of the procedures to be followed, including identification of those that are ‘experimental’ In order to increase sample size participants should only be told of serious risks of a research project as discomforts are expcted and might scare of particiaptnd unnecessarily. In order to keep a study blinded and the participant anonymous the participant should be clearly informed to keep their participation secret especially from their medical team. Participants recruitment participants should be informed that once they have entered a clinical trial they cannot leave until the trial is complete. Reset
选项
A.A fair explanation of the procedures to be followed, including identification of those that are ‘experimental’
B.In order to increase sample size participants should only be told of serious risks of a research project as discomforts are expcted and might scare of particiaptnd unnecessarily.
C.In order to keep a study blinded and the participant anonymous the participant should be clearly informed to keep their participation secret especially from their medical team.
D.Participants recruitment participants should be informed that once they have entered a clinical trial they cannot leave until the trial is complete.
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思路分析
The question centers on what constitutes good practice in informed consent within ethical human participant research. Each option should be assessed for alignment with ethical norms and regulatory standards for consent.
Option 1: 'A fair explanation of the procedures to be followed, including identification of those that are ‘experimental’' — This option aligns with core consent principles. It requires a clear, comprehensible description of what the study involves, including which procedures are experimental, potential risks, benefits, and alternatives. It emphasiz......Login to view full explanation登录即可查看完整答案
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Question at position 9 Q9 Hall (consent)YesNo
Informed consent is when a patient is provided with all the risks, benefits, and alternatives for a procedure, intervention, or medication and discussion is facilitated as needed in order to make a decision.
Failing to obtain informed consent before treatment can lead to:
"We've reviewed your treatment plan and discussed options. Together, we've determined that your goal is to stop the progression of your periodontal disease. Erin has presented the fianancial information. I appreciate your questions, do you have any other concerns?" This is an example of what thype of consent?
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