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Informed ConsentInvestigator: Art Grasses (6782364) Department of Psychology University of MemphisTitle: Learning Gains Evaluation of Auto Tutor, hereby agree to participate as a volunteer in the
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Read the informed consent form thoroughly and make sure you understand all the information provided.
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If you have any questions or concerns, reach out to the researcher or an appropriate representative for clarification.
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Carefully consider the risks and benefits involved in participating in the study.
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If you decide to participate, sign and date the informed consent form.
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Keep a copy of the signed consent form for your records.
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Follow any additional instructions provided by the researcher for participating in the study.

Who needs informed consent - facstaffcbuedu?

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Anyone who is being asked to participate in a research study or clinical trial needs to provide informed consent. This includes individuals of all ages, ethnicities, genders, and backgrounds. Informed consent is a fundamental ethical principle that ensures individuals have the necessary information to make an informed decision about their participation in a study.

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Informed consent is a process that ensures individuals are fully aware of and understand the implications, risks, and benefits associated with a particular action, procedure, or research study before agreeing to participate.
Individuals conducting research involving human participants are required to file informed consent, ensuring that all participants are adequately informed before they consent to participate.
To fill out informed consent, researchers should provide detailed information about the study's purpose, procedures, potential risks, benefits, and the rights of participants. Participants must then sign to indicate their understanding and agreement.
The purpose of informed consent is to protect the autonomy of individuals by ensuring they have adequate information to make an educated decision regarding their participation in research or procedures.
The information that must be reported on informed consent includes the study's purpose, duration, procedures, risks, benefits, confidentiality assurances, and the right to withdraw without penalty.
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