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APPROVED AS MODIFIED Apr 14, 2016 WIRE Mind Share For Research Purposes TITLE:Mind Share: A Research Study Measuring the Relationship Between Lifestyle, Health, and Alzheimer's DiseasePROTOCOL NO.:03102016 WIRE
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01
Begin by clearly explaining the purpose of the study or medical procedure to the individual who will be giving their consent.
02
Provide all necessary information about the study or procedure, including the potential risks and benefits involved.
03
Make sure that the individual understands the information provided by using clear and easily understandable language.
04
Allow the individual ample time to ask questions and seek clarification.
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Ensure that the individual is capable of making an informed decision by assessing their competency to understand the information.
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If the individual agrees to participate or undergo the procedure, have them sign the informed consent form.
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Provide a copy of the signed form to the individual for their records.

Who needs informed consent in human?

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Informed consent in humans is required for any medical research study or experimental procedure that involves human subjects.
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It is also necessary for any medical treatment or intervention that carries potential risks or requires the individual's voluntary participation.
03
Informed consent is an ethical and legal requirement to protect the rights and autonomy of individuals participating in any human-related activities.
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Informed consent in human research refers to the process by which individuals are fully informed about the research study before deciding whether or not to participate.
Researchers conducting human research studies are required to obtain and file informed consent from participants.
Informed consent in human research should be filled out by providing all necessary information about the study, risks, benefits, confidentiality, and the rights of participants.
The purpose of informed consent in human research is to protect the rights and well-being of research participants by ensuring they have all necessary information to make an informed decision about participating.
Informed consent in human research must include details about the study purpose, procedures, risks, benefits, confidentiality, compensation, and participant rights.
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