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Supplementary File 1Participant Information PackContentParticipant Information Sheet Informed Consent declaration. PARTICIPANT INFORMATION SHEET What drives inappropriate antibiotic use? A mix methodology
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Who needs informed consent declaration?

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Anyone who is participating in a research study or clinical trial that requires informed consent.
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Patients undergoing medical procedures or treatments that involve potential risks or side effects.
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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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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.
Researchers and institutions conducting studies that involve human participants are required to file informed consent declarations.
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.
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.
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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