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Participant Information Sheet/Consent Form Interventional Study Adult providing own consentMonash Medical Center ClaytonTitlePrednisolone vs Dexamethasone to treat COVID-19 in pregnancy Short Title PROVED
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How to fill out participants informed consent in

01
Begin by explaining the purpose of the study to the participant.
02
Provide information about what will be asked of the participant during the study.
03
Clearly outline any risks or benefits associated with participation.
04
Ensure the participant understands that participation is voluntary and they can withdraw at any time.
05
Have the participant sign the consent form to indicate their understanding and agreement to participate.

Who needs participants informed consent in?

01
Participants informed consent is needed in any study or research involving human subjects.
02
This includes clinical trials, surveys, experiments, or any other form of data collection that involves human participants.

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Participants informed consent is a process in research where participants are provided with all relevant information about a study and give their voluntary agreement to participate.
Researchers conducting a study are required to file participants informed consent.
Participants informed consent forms are typically filled out by researchers or study coordinators with input from participants.
The purpose of participants informed consent is to ensure that participants are fully informed about a study, its potential risks and benefits, and to ensure that participation is voluntary.
Participants informed consent forms must include details about the study, its purpose, process, risks, benefits, confidentiality, and participant rights.
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