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NCI CIRB Protocol: ALLIANCE A031701 Consent Version Number: Update 2 Consent Version Date: 041619 Consent Implementation Date: 061419-Page 1 of 18Research Study Informed Consent Document Study Title
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How to fill out research study informed consent

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How to fill out research study informed consent

01
Provide participants with a clear explanation of the purpose of the research study.
02
Clearly outline the procedures involved in the study and what participants can expect.
03
Inform participants of any potential risks or benefits associated with the study.
04
Make sure participants understand that their participation is voluntary and they can withdraw at any time.
05
Have participants sign the informed consent form to indicate their understanding and agreement to participate.

Who needs research study informed consent?

01
Any individual who is participating in a research study as a participant needs to provide informed consent.
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Research study informed consent is a process in which participants are provided with information about the research study, including the risks and benefits, and are given the opportunity to decide whether or not to participate.
The researchers conducting the study are required to obtain and file research study informed consent from all participants.
Research study informed consent forms are typically filled out by the participant or their legally authorized representative, with guidance from the researcher.
The purpose of research study informed consent is to ensure that participants are fully informed about the research study and voluntarily agree to participate.
Research study informed consent must include information about the study purpose, procedures, risks, benefits, confidentiality, and contact information for questions or concerns.
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