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InstructionsComment Code The assessment should be administered by the study staff member to the potential participant after the informed consent discussion is completed but before the participant
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Read through the comprehension and informed consent form carefully.
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Who needs comprehension and informed consent?

01
Anyone participating in a research study or clinical trial.
02
Patients receiving medical treatment or procedures.
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Individuals undergoing surgery or other medical interventions.

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Comprehension and informed consent refer to the process by which individuals are given comprehensive information regarding a study or procedure, ensuring they understand the implications and outcomes before agreeing to participate.
Researchers and institutions conducting studies that involve human subjects are required to file comprehension and informed consent.
To fill out comprehension and informed consent, individuals must provide clear information about the study, including its purpose, risks, benefits, and the right to withdraw. Participants then need to acknowledge their understanding and agreement.
The purpose is to ensure participants are fully informed and understand what they are consenting to, thereby protecting their autonomy and rights.
Information must include study details, potential risks and benefits, data handling procedures, participant rights, and contact information for inquiries.
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