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Supplementary File 1Participant
Information
PackContentParticipant Information Sheet
Informed Consent declaration. PARTICIPANT INFORMATION SHEET
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How to fill out informed consent declaration

How to fill out informed consent declaration
01
Read the informed consent declaration carefully to understand its contents.
02
Fill out your personal information, such as name, age, address, and contact details.
03
Provide clear and specific responses to any questions or statements in the declaration.
04
Review the declaration to ensure that all areas are properly filled out.
05
Sign and date the declaration to acknowledge your understanding and agreement.
06
If applicable, have a witness or guardian sign the declaration as well.
07
Keep a copy of the filled out declaration for your records.
08
Submit the completed informed consent declaration to the relevant party or organization.
Who needs informed consent declaration?
01
Anyone who is participating in a research study or clinical trial that requires informed consent.
02
Patients undergoing medical procedures or treatments that involve potential risks or side effects.
03
Individuals participating in activities or events that involve potential physical or psychological risks.
04
Participants in studies or experiments that require their voluntary agreement to participate.
05
Minors or individuals who are unable to give consent on their own, requiring a legal guardian or representative to sign on their behalf.
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What is informed consent declaration?
An informed consent declaration is a formal statement that signifies a participant's voluntary agreement to participate in a study or clinical trial, having been informed of all relevant aspects of the research, including its purpose, procedures, risks, and benefits.
Who is required to file informed consent declaration?
Researchers and institutions conducting studies that involve human participants are required to file informed consent declarations.
How to fill out informed consent declaration?
To fill out an informed consent declaration, the researcher must provide clear information about the study, including the purpose, procedures, potential risks, benefits, confidentiality measures, and the participant's right to withdraw. The participant must then sign to indicate their consent.
What is the purpose of informed consent declaration?
The purpose of an informed consent declaration is to protect the rights and welfare of participants by ensuring that they are fully aware of what their participation entails and that they voluntarily agree to participate.
What information must be reported on informed consent declaration?
The informed consent declaration must include information on the study's purpose, expected duration, procedures, risk factors, benefits, confidentiality assurances, and the voluntary nature of participation.
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