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Saint Louis University Institutional Review BoardBehavioral & Social Sciences (Nonclinical) Informed Consent TemplateGUIDELINES FOR PREPARING AN INFORMED CONSENT DOCUMENT1. INFORMED CONSENT MODEL
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How to fill out ined consent ampamp assent

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How to fill out informed consent ampamp assent

01
Read the informed consent and assent forms thoroughly.
02
Understand the purpose of the study and the procedures involved.
03
Seek clarification from the researcher or study coordinator if any part of the forms is unclear.
04
Provide honest and accurate information about yourself or the participant, if applicable.
05
Sign and date the informed consent form if you agree to participate.
06
If the participant is a child or lacks capacity to provide consent, obtain assent from the participant and consent from a legally authorized representative.
07
Keep a copy of the signed forms for your records.

Who needs informed consent ampamp assent?

01
Informed consent and assent are required in various research studies involving human participants, especially when there are potential risks or when participants are vulnerable populations such as children, prisoners, mentally impaired individuals, or pregnant women.
02
Medical experiments, clinical trials, behavioral studies, surveys, and any research involving human subjects generally require informed consent and assent to protect the rights and well-being of the participants.

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Informed consent is the process by which a participant agrees to participate in a study after being fully informed about the study's procedures and potential risks. Assent is the agreement of a minor to participate in a study, with the understanding that their parents or guardians have also provided consent.
Researchers conducting studies involving human subjects, especially minors, are required to ensure informed consent and assent are obtained from participants and their guardians.
Informed consent and assent forms should clearly outline the study's purpose, procedures, potential risks, benefits, confidentiality measures, and participants' rights. Participants and guardians should sign these forms to indicate their agreement to participate.
The purpose of informed consent and assent is to ensure that participants fully understand the study they are agreeing to be part of, including any risks involved, and that their consent is voluntary and informed.
Informed consent and assent forms should include detailed information about the study's procedures, risks, benefits, confidentiality measures, contact information for the researchers and institutional review board, and participants' rights.
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