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Version date: 01/17/2020Northeastern University, Department of Electrical and Computer Engineering
Protocol Title: TICS to Improve Motivation and Memory in Elderly (TIME)
Principal Investigator: Sumatra
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The informed consent form v20200117docx is typically required by individuals who are participating in research studies, medical treatments, surgical procedures, or other situations that involve potential risks or legal implications. It is necessary to ensure that the person giving consent fully understands the nature of the decision they are making and the potential consequences.
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What is informed consent form v20200117docx?
The informed consent form v20200117docx is a document that outlines the risks and benefits of participating in a research study or medical procedure.
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The individuals participating in the research study or undergoing the medical procedure are required to file the informed consent form v20200117docx.
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To fill out the informed consent form v20200117docx, individuals must read the document carefully, sign it if they agree to the terms, and provide any requested information or details.
What is the purpose of informed consent form v20200117docx?
The purpose of the informed consent form v20200117docx is to ensure that individuals are fully informed about the risks and benefits of the research study or medical procedure, and to obtain their voluntary agreement to participate.
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The informed consent form v20200117docx must include information about the study or procedure, the risks involved, the benefits, alternative options, confidentiality, and the right to withdraw consent.
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