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Neuroscience Research AustraliaPARTICIPANT INFORMATION SHEET AND CONSENT FORM Exploring the effectiveness of product information on child restraint useable Chief Investigators Investigator/research
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How to fill out participant consent information sheet

01
Start by providing basic information about the participant, such as their full name, date of birth, and contact details.
02
Include any relevant demographic information, such as gender, race, or ethnicity, if necessary for the study.
03
Clearly explain the purpose of the study and what participation entails, ensuring that the participant understands the potential risks and benefits.
04
Outline the procedures involved in the study, including any interventions or data collection methods that will be used.
05
Clearly state the participant's rights, including the right to withdraw from the study at any time without penalty.
06
Include a statement about confidentiality and how the participant's personal information will be protected.
07
Provide contact information for the study investigator or a designated contact person in case the participant has any questions or concerns.
08
Leave space for the participant to sign and date the consent form, indicating their voluntary agreement to participate.
09
Make copies of the signed consent form for both the participant and the study investigator's records.

Who needs participant consent information sheet?

01
Anyone conducting a research study or clinical trial involving human participants needs a participant consent information sheet.
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The participant consent information sheet is a document that explains to participants the purpose of a study, their rights, risks and benefits, and what information will be collected from them.
Researchers conducting a study involving human subjects are required to provide participants with a participant consent information sheet.
The participant consent information sheet should be filled out by the researcher with all relevant information about the study, risks, benefits, and participant rights.
The purpose of the participant consent information sheet is to inform participants about the study they are participating in, their rights, and what information will be collected from them.
The participant consent information sheet must include the purpose of the study, risks and benefits, participant rights, information to be collected, and contact information for researchers.
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