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This consent form outlines the participant\'s agreement to partake in the HAE IMPACT PRO tool study, assessing hereditary angioedema in Australian adults.
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How to fill out participant consent form

01
Provide the participant with the consent form and explain the purpose of the form.
02
Ensure that the participant reads the form carefully and understands all the information provided.
03
Have the participant sign and date the form to indicate their agreement to participate.
04
Make a copy of the completed form for both the participant and the research team's records.

Who needs participant consent form?

01
Researchers conducting studies that involve human subjects require participant consent forms.
02
Healthcare professionals may also need participant consent forms for certain medical procedures or treatments.
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A participant consent form is a document that provides information about a study or research project and obtains the permission from participants to partake in it, typically outlining the nature, purpose, risks, and benefits of the participation.
Researchers or organizations conducting studies involving human participants are required to file a participant consent form.
To fill out a participant consent form, individuals should read the information provided carefully, complete any required personal information, and sign the form to indicate their consent.
The purpose of a participant consent form is to ensure that individuals are informed about the study and voluntarily agree to participate, safeguarding their rights and well-being.
The participant consent form must report information such as study purpose, procedures, risks, benefits, confidentiality assurances, and the participant's right to withdraw.
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