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CONSTRUCTING AN INFORMED CONSENT DOCUMENT UPDATED 5/26/2020 Informed consent embodies the ethical principle of Respect for Persons as described in the Belmont Report. All research conducted at CSU
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Who needs informed consent or assent?

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Informed consent or assent is needed in various situations such as:
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- Medical procedures or treatments
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- Clinical research or experiments
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- Participation in studies or trials
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- Provision of personal information for confidential purposes
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- Participation in activities involving potential risks or legal implications
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- Sharing data or information with third parties
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- Consent for minors or individuals lacking decision-making capacity
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- Any situation where the protection of individual rights and autonomy is paramount.
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Informed consent or assent is a process whereby individuals are given information about a study or procedure in order to make an informed decision about participating.
Researchers conducting studies involving human subjects are required to obtain informed consent or assent.
Informed consent or assent forms should include information about the study, risks and benefits, confidentiality, and how to contact the researcher.
The purpose of informed consent or assent is to ensure that participants understand the study and voluntarily agree to participate.
Informed consent or assent forms must include details about the study, risks and benefits, confidentiality, and contact information for the researcher.
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