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STATEMENT OF INFORMED CONSENT 1. I have read and understood the information sheet about the Primary Progressive Multiple Sclerosis (PPM) Study, or it has been read to me in full. I understand the
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How to fill out a statement of informed consent:

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Begin by reading the statement carefully to understand its purpose and what it entails.
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Write your full name and contact information at the top of the form.
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Include the date when you are signing the statement.
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Read through each section of the statement thoroughly and ensure that you understand the content and implications. If you have any questions or concerns, reach out to the appropriate person or organization for clarification.
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Consider whether you are comfortable with the information provided and if you agree to the terms outlined in the statement. If you have any reservations, discuss them with the relevant parties involved.
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If required, provide additional information such as any medical conditions, allergies, or medications that may be relevant to the situation.
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Sign and date the statement at the designated space to indicate your informed consent.
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Make a copy of the completed statement for your records, if necessary.

Who needs a statement of informed consent?

01
Researchers conducting scientific or medical studies involving human participants typically require signed statements of informed consent. This ensures that participants are aware of the study's purpose, potential risks, benefits, and their rights as participants.
02
Healthcare professionals may ask patients to sign a statement of informed consent before undergoing medical procedures or treatments that carry significant risks or side effects. This ensures that patients are fully informed about the procedure and have willingly agreed to it.
03
Surgeries, particularly those deemed high-risk or experimental, also commonly require patients to sign a statement of informed consent. This ensures that patients understand the potential outcomes, risks, and alternatives to the procedure before making an informed decision.
Overall, the statement of informed consent serves to protect the rights and well-being of individuals by ensuring they have all the necessary information to make informed decisions regarding their participation in various activities.
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A statement of informed consent is a document that explains the risks and benefits of participating in a research study, clinical trial, or medical procedure.
Researchers, medical professionals, or institutions conducting the study or clinical trial are required to file a statement of informed consent.
The statement of informed consent should be filled out by including detailed information about the study, the risks and benefits involved, and obtaining the signature of the participant or legal guardian.
The purpose of the statement of informed consent is to ensure that participants are fully informed about the study or trial before giving their consent to participate.
The statement of informed consent must include detailed information about the study procedures, risks involved, benefits, confidentiality, contact information, and the right to withdraw from the study at any time.
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