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Ruth Whitley PhD, NCC, LPC PO Box 377; Greenville, TX 75403 5604 Wesley Street, Suite 101; Greenville, TX 75402 Phone: 9032744140 Fax: 8773109115Page 1 of 4INFORMED CONSENT I would like to congratulate
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To fill out an informed consent, follow these steps:
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Read the consent form carefully before filling it out.
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Provide all the necessary personal information, such as your name, age, and contact details.
04
Understand the purpose and nature of the research or procedure for which you are giving consent.
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Ask any questions you may have to clarify any doubts regarding the research or procedure.
06
Make sure you understand the potential risks and benefits involved.
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Consider the alternatives or other options available.
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If you are satisfied and willing to give your informed consent, sign and date the form.
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Keep a copy of the consent form for your records.
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If applicable, inform the researcher or healthcare professional if you change your mind or want to withdraw your consent.
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Seek legal advice if you have any concerns or doubts about the informed consent process.

Who needs informed consent i would?

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Anyone who is going to participate in a research study or undergo a medical procedure that involves risks or potential benefits needs informed consent. Informed consent is necessary to ensure that individuals are fully aware of what they are agreeing to and have the ability to make an informed decision. This includes participants in clinical trials, patients undergoing surgeries or medical treatments, individuals participating in psychological or social science research, and any other scenario where consent is required for ethical and legal reasons.
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Informed consent is a process where a person is given information about a medical procedure or treatment, and they voluntarily agree to it after understanding the risks and benefits.
Healthcare providers and researchers are required to obtain and file informed consent from patients or participants before conducting any medical procedures or research studies.
Informed consent forms typically include information about the procedure or study, risks and benefits, alternatives, confidentiality, and the right to withdraw consent. Patients or participants need to read and sign the form.
The purpose of informed consent is to ensure that patients or participants are fully informed about the medical procedure or research study, so they can make an educated decision about their participation.
The informed consent form must include details about the procedure or study, risks, benefits, alternatives, confidentiality, rights of participants, and contact information for questions or concerns.
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