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INFORMED CONSENT FORM(For Control Group)This study is carried out as a master\'s thesis under the supervision of Assistant professor
Serra EVE by Scrap YARDMAN from Gaziantep University Faculty of
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How to fill out informed consent form for
01
Read the informed consent form carefully and understand its contents.
02
Provide all necessary personal information, such as your name, address, and contact details.
03
Make sure to mention any medical conditions, allergies, or medications you are currently taking.
04
Clearly understand the purpose of the research or study for which the informed consent is required.
05
Seek clarification or ask questions if any part of the form is unclear to you.
06
Sign and date the form to indicate your willingness to participate and understand the risks involved.
07
Keep a copy of the informed consent form for your records.
Who needs informed consent form for?
01
Informed consent forms are typically required for any individuals who are going to participate in research studies, clinical trials, medical procedures, or any activity that involves potential risks.
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What is informed consent form for?
The informed consent form is used to ensure that individuals have been provided with all necessary information before they make a decision to participate in a research study.
Who is required to file informed consent form for?
Researchers conducting a study are required to obtain informed consent from participants and file the consent form.
How to fill out informed consent form for?
The informed consent form is typically filled out by the researcher with all relevant study information and then signed by the participant.
What is the purpose of informed consent form for?
The purpose of the informed consent form is to protect the rights and well-being of research participants by ensuring they have been adequately informed before agreeing to participate.
What information must be reported on informed consent form for?
The informed consent form must include information about the research study, its purpose, risks and benefits, confidentiality, and the rights of the participants.
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