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This document serves as an informed consent form for participants considering joining a clinical trial that investigates the safety and effectiveness of cabozantinib when used in combination with radiation therapy for treating high-risk soft tissue sarcomas of the extremities. It outlines the study\'s purpose, procedures, risks, benefits, and participant rights and responsibilities.
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How to fill out informed consent form
How to fill out informed consent form
01
Read the informed consent form carefully.
02
Ensure you understand all the information provided.
03
Check if the purpose, risks, and benefits of the study or procedure are clearly described.
04
Ask questions about anything that is unclear or concerning.
05
Fill out your personal information as required (name, date of birth, etc.).
06
Indicate your willingness to participate by signing and dating the form.
07
Keep a copy of the signed form for your records.
Who needs informed consent form?
01
Patients participating in medical research or clinical trials.
02
Participants in psychological studies or behavioral research.
03
Individuals involved in experimental procedures or treatments.
04
Legal guardians signing for minors in any sensitive research.
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What is informed consent form?
An informed consent form is a document that provides potential participants in a study or medical procedure with detailed information about the purpose, risks, benefits, and procedures involved, ensuring that they understand and voluntarily agree to participate.
Who is required to file informed consent form?
Researchers conducting studies involving human participants, as well as healthcare providers performing medical procedures that require participant agreement, are required to file informed consent forms.
How to fill out informed consent form?
To fill out an informed consent form, the researcher or healthcare provider should clearly outline the study or procedure details, provide risk and benefit information, ensure the participant understands, and obtain the participant's signature to confirm consent.
What is the purpose of informed consent form?
The purpose of an informed consent form is to protect the rights and autonomy of participants by ensuring they are fully informed about the nature of the study or procedure and voluntarily agree to participate.
What information must be reported on informed consent form?
The informed consent form must include information about the study's objectives, procedures, potential risks and benefits, confidentiality assurances, the right to withdraw, and contact information for inquiries.
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