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Insert Header with institutions name or institutions letterheadParticipant Information Sheet/Consent Form Adult providing own consent Title Australasian COVID-19 Trial (ASCOT) Adaptive Platform Trial
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01
Begin by providing the participant with the participant information sheet and consent form.
02
Clearly explain each section of the form to the participant and answer any questions they may have.
03
Ask the participant to read through the form carefully and fill out all required information accurately.
04
Have the participant sign and date the consent form as evidence of their agreement to participate.
05
Collect the completed form and provide a copy to the participant for their records.

Who needs participant information sheetconsent form?

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Anyone conducting research or gathering data from participants needs to provide them with a participant information sheet and consent form.
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The participant information sheet/consent form is a document that provides information to participants about a research study and obtains their informed consent to participate.
Researchers conducting a study involving human participants are required to provide a participant information sheet/consent form.
The participant information sheet/consent form should be filled out by including all relevant information about the study, risks and benefits, confidentiality, and procedures for obtaining consent.
The purpose of the participant information sheet/consent form is to ensure that participants are fully informed about the study and voluntarily consent to participate.
The participant information sheet/consent form should include details about the study objectives, procedures, risks, benefits, confidentiality measures, and contact information for the researchers.
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