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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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To fill out the informed consent form v20200117docx, follow these steps:
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Begin by reading the entire form carefully.
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Fill in your personal information such as name, date of birth, and contact details in the designated sections.
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Ensure you understand the purpose of the consent form and the procedures involved. If you have any questions, seek clarification from the relevant authority.
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Review the risks, benefits, and alternatives associated with the decision you are giving consent for.
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If applicable, provide your medical history and any relevant information that could impact the decision-making process.
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Sign and date the form to indicate your informed consent.
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If the form requires a witness signature, make sure a witness is present and they sign accordingly.
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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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The informed consent form v20200117docx is a document that outlines the risks and benefits of participating in a research study or medical procedure.
The individuals participating in the research study or undergoing the medical procedure are required to file the informed consent form v20200117docx.
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.
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.
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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