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This document serves as a template for researchers, particularly doctoral candidates, to create an informed consent form for research studies. It includes instructions and examples on necessary components such as study purpose, participant criteria, rights, risks, benefits, data collection, and contact information, ensuring compliance with federal regulations.
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A letter of informed consent is a document that provides potential participants in a study or trial with detailed information about the research, including its purpose, procedures, risks, benefits, and the rights of participants.
Researchers and institutions conducting studies involving human subjects are required to file a letter of informed consent to ensure that participants are fully informed before agreeing to take part.
To fill out a letter of informed consent, include information such as the study title, the purpose of the research, a description of the procedures, potential risks and benefits, confidentiality assurances, and a section for participants' signatures to indicate their agreement to participate.
The purpose of a letter of informed consent is to ensure that participants are adequately informed about the study they are involved in and to obtain their voluntary agreement to participate based on that information.
The letter of informed consent must report information such as the study objectives, procedures, risks and benefits, confidentiality measures, the right to withdraw from the study, and contact information for the researchers.
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