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INDIANA UNIVERSITY INFORMED CONSENT STATEMENT FOR Insomnia in HIV: Study I are being asked to take part in this research study because you are infected with the Human Immunodeficiency Virus (HIV),
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01
Start by reading the informed consent form thoroughly. Make sure you understand all the information provided.
02
Provide all the necessary personal information requested in the informed consent form.
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Carefully review and understand the purpose and procedures of the study or research project.
04
Read and acknowledge any risks or benefits associated with participating in the study.
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If you have any questions or concerns, don't hesitate to ask the researchers or study coordinators for clarification.
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Once you feel confident and fully informed, sign and date the informed consent form to indicate your voluntary participation in the study.
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Keep a copy of the signed informed consent form for your records.

Who needs indiana university informed consent?

01
Anyone who is participating in a research study or project conducted by Indiana University would need to fill out the informed consent form. This includes students, faculty, staff, and any other individuals who are involved in the study as subjects or participants.
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Indiana University informed consent refers to the process of informing research participants about the purpose, risks, benefits, and procedures of a research study before they decide whether or not to participate.
Researchers conducting studies at Indiana University are required to obtain informed consent from participants.
To fill out Indiana University informed consent, researchers must provide participants with all necessary information about the study, obtain their signature on the consent form, and ensure they understand their rights and responsibilities as participants.
The purpose of Indiana University informed consent is to protect the rights and well-being of research participants by providing them with information to make an informed decision about their participation in a study.
Indiana University informed consent forms must include details about the study purpose, procedures, risks and benefits, confidentiality, voluntariness of participation, contact information for questions and concerns, and participant rights.
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