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Appendix G Informed Consent This study is being conducted by STUDENT who is a student at the Illinois School of Professional Psychology at National Louis University working on a Clinical Research

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Who needs informed consent - sampledoc?

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Anyone who is participating in a research study or medical procedure that requires consent from the individual.

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What is informed consent - sampledoc?

Informed consent is a process through which individuals voluntarily confirm their willingness to participate in a specific activity or research after being informed of all relevant facts, risks, and implications associated with their decision.

Who is required to file informed consent - sampledoc?

Researchers, healthcare providers, and institutions that are conducting studies or treatments involving human participants are required to file informed consent documentation.

How to fill out informed consent - sampledoc?

To fill out informed consent, one must provide clear information about the study or intervention, outline any potential risks or benefits, obtain the participant's signature, and ensure that they have understood the information provided.

What is the purpose of informed consent - sampledoc?

The purpose of informed consent is to ensure that individuals make informed decisions about their participation, safeguarding their autonomy and rights while minimizing potential harm.

What information must be reported on informed consent - sampledoc?

Informed consent must include information about the purpose of the study, procedures involved, risks and benefits, confidentiality assurances, and the right to withdraw from the study at any time.

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