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Jill R. Stevens, MA, CPC
INFORMED CONSENT
I realize that starting counseling is a major decision, and you may have many questions.
This document is intended to inform you of my policies, state and
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How to fill out informed consent forms
How to fill out informed consent forms
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Step 1: Read the entire informed consent form carefully.
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Step 2: Make sure you understand all the information provided in the form.
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Step 3: If you have any questions or concerns, ask the person providing the form for clarification.
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Step 4: Provide all the requested information accurately and honestly.
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Step 5: Sign and date the informed consent form in the designated areas.
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Step 6: Retain a copy of the signed consent form for your records.
Who needs informed consent forms?
01
Informed consent forms are needed by individuals who are participating in a research study, clinical trial, medical procedure, or any other activity that involves their voluntary participation and requires them to be fully informed about the purpose, risks, benefits, and alternatives involved.
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What is informed consent forms?
Informed consent forms are documents that ensure a participant's voluntary agreement to partake in a study or procedure after being fully informed of the risks, benefits, and nature of the participation.
Who is required to file informed consent forms?
Researchers and organizations conducting studies that involve human participants are required to file informed consent forms.
How to fill out informed consent forms?
Informed consent forms should be filled out by providing clear information about the study, its purpose, procedures, potential risks, benefits, and the participant's right to withdraw at any time without penalty.
What is the purpose of informed consent forms?
The purpose of informed consent forms is to protect participants’ autonomy by ensuring they understand what their participation entails and to provide legal protection for researchers.
What information must be reported on informed consent forms?
Informed consent forms must report information regarding the study's purpose, procedures, potential risks and benefits, confidentiality, and the participant's rights.
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