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INFORMED CONSENT TO TAKE PART IN THE HISPANIC HEALTH RESEARCH CENTER HEALTH IMPROVEMENT EFFORTS DIABETES IMPACT STUDY HOUSEHOLD SURVEY Slowing the Epidemic of Obesity and Type 2 Diabetes and their
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01
Clearly explain the purpose of the informed consent form to the participant.
02
Provide all necessary information about the study, including potential risks and benefits.
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Allow the participant enough time to review the form and ask any questions.
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Keep a copy of the signed informed consent form for your records.

Who needs effects of informed consent?

01
Researchers conducting studies that involve human participants.
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Medical professionals obtaining consent for treatment or procedures.
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Legal entities requiring informed consent for certain activities or services.
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Informed consent is the process by which a person agrees to participate in a study after being provided with relevant information about the study.
Researchers conducting studies involving human subjects are required to file effects of informed consent.
Effects of informed consent should be filled out by providing details about the study, the information provided to participants, and the participants' decision to participate.
The purpose of effects of informed consent is to ensure that participants are fully informed about the study and voluntarily agree to participate.
Information reported on effects of informed consent includes details about the study, risks and benefits, confidentiality, and participants' rights.
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