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Participant Information Sheet/Consent Form Study 1 Monash UniversityTitle Short Title Project Number Project Sponsor Principal Investigators Associate InvestigatorsSchool of Public Health and Preventive
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How to fill out participant information sheetconsent form

01
Start by downloading the participant information sheet and consent form.
02
Read the instructions carefully to understand the purpose and requirements of the form.
03
Fill in the participant's personal information such as name, age, address, and contact details.
04
Provide relevant medical history and disclose any known health conditions that might impact the study.
05
Clearly state the purpose of the study, the procedures involved, and any potential risks or benefits.
06
Request the participant's signature and date to indicate their informed consent to participate.
07
Make a copy of the completed form for your records and give a signed copy to the participant.
08
Ensure confidentiality and assure the participant that their personal information will be protected.
09
If any additional information or documentation is required, attach it to the participant information sheet consent form.
10
Submit the completed form as per the instructions provided.

Who needs participant information sheetconsent form?

01
Research studies, clinical trials, or any participants in a study or experiment that involves collecting data or undergoing any procedures need to fill out the participant information sheet consent form. It ensures they have a clear understanding of the study's purpose, risks, and benefits, and gives their informed consent to participate.
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Participant information sheet/consent form is a document that includes all necessary information about the study and the individual's consent to participate.
Researchers conducting a study are required to have participants fill out and sign the participant information sheet/consent form.
Participants are typically required to read the information provided on the form, ask any questions they may have, and then sign the form if they agree to participate.
The purpose of the participant information sheet/consent form is to ensure that participants are fully informed about the study they are participating in and to document their agreement to participate.
The participant information sheet/consent form must include details about the study, potential risks and benefits, confidentiality, and the participants' rights.
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