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INFORMED CONSENT FORM FOR RESEARCH ON HUMAN SUBJECTS 1. The Rev. Eric Alderman, a student in the Doctor of Ministry program at McCormick Theological Seminary (Chicago, Illinois, USA×, is conducting
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How to fill out an informed consent form:

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Begin by carefully reading through the entire form to understand its contents and requirements.
02
Provide your personal information accurately and completely in the designated spaces. This may include your name, address, contact details, and any other necessary identifying information.
03
Review the purpose of the study, research, or medical procedure for which the consent form is being filled out. Ensure that you understand what you are consenting to and any potential risks or benefits involved.
04
If there are any sections that you are unsure about or have concerns regarding, seek clarification from the research team or healthcare professionals involved. It is essential to have a full understanding before proceeding.
05
Sign and date the form to indicate your consent. It is important to remember that your signature signifies voluntary agreement and understanding of the information provided.
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If you are filling out the informed consent form on behalf of a minor or someone with limited capacity, ensure that you have the legal authority to do so. Follow any additional instructions or requirements provided for representative consent.
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Keep a copy of the signed consent form for your records. This can serve as documentation of your participation or agreement, if needed in the future.

Who needs an informed consent form:

01
Participants in scientific research studies: Informed consent forms are crucial for individuals who voluntarily participate in research studies. These forms ensure that participants are fully informed about the purpose, risks, benefits, and any other relevant information related to the study before choosing to participate.
02
Patients undergoing medical procedures: Informed consent forms are necessary for patients who are about to undergo medical procedures or interventions. These forms provide patients with a detailed understanding of the procedure, potential risks, alternative treatment options, and enable them to make an informed decision about their healthcare.
03
Individuals involved in legal agreements or contracts: Informed consent forms may also be used in legal agreements or contracts when individuals are required to understand and consent to the terms and conditions of a specific arrangement. This ensures that all parties involved have a clear understanding of their rights and responsibilities before entering into the agreement.
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An informed consent form is a document that provides essential information to a person before they agree to participate in a research study or a medical procedure.
Researchers, healthcare providers, and medical professionals are required to file an informed consent form before conducting a research study or performing a medical procedure.
To fill out an informed consent form, one must provide detailed information about the study or procedure, risks and benefits, confidentiality, voluntariness, and contact information for questions or concerns.
The purpose of an informed consent form is to ensure that individuals are fully informed about the study or procedure they are participating in, and to protect their rights and well-being.
The informed consent form must include details about the study or procedure, potential risks and benefits, confidentiality measures, voluntariness of participation, and contact information for questions or concerns.
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