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February 2019Survey Approval Consent Conversion 1.3MSTF Student Approval Resurvey NEW FOR 2019: If this survey is about gathering initial information, that is not private information and is a maximum
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How to fill out participants informed consent form

01
Step 1: Read and understand the informed consent form yourself.
02
Step 2: Provide a clear and concise explanation of the study to the participant.
03
Step 3: Answer any questions or concerns the participant may have.
04
Step 4: Inform the participant that their participation is voluntary and they have the right to withdraw at any time.
05
Step 5: Have the participant carefully read the informed consent form.
06
Step 6: Ensure the participant understands the content of the form and address any additional questions.
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Step 7: Ask the participant to sign and date the informed consent form.
08
Step 8: Make a copy of the signed form for the participant and keep the original for your records.

Who needs participants informed consent form?

01
Researchers conducting medical, psychological, or social science studies that involve human subjects.
02
Clinical trial organizers.
03
Academic researchers and students.
04
Healthcare professionals.
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The participants informed consent form is a document that provides potential research participants with detailed information about a study, including its purpose, procedures, risks, and benefits, to ensure that they can make an informed decision about their participation.
Researchers and institutions conducting studies involving human participants are required to file the participants informed consent form.
To fill out the participants informed consent form, researchers should clearly specify the study's details, including objectives, procedures, potential risks, benefits, and the voluntary nature of participation. The form should be written in clear, understandable language and signed by the participant.
The purpose of the participants informed consent form is to protect the rights of participants by ensuring they are fully informed about the study and voluntarily agree to participate.
The information reported on the participants informed consent form must include the study's purpose, procedures, potential risks and benefits, confidentiality measures, contact information for questions, and a statement indicating that participation is voluntary.
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