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PARTICIPANT INFORMATION STATEMENT AND CONSENT FORM (PIS CF) Positively Women: A research project using art to express what it means to be a woman living with HIV in Australia Dr Allison Carter, Kirby
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01
To fill out a participant information statement:
02
Start by writing your full name and contact information at the top of the form.
03
Include any relevant identification numbers or codes, such as a participant ID or study code.
04
Provide your date of birth and gender.
05
Fill in any medical information that may be required, such as allergies or pre-existing conditions.
06
Include emergency contact details, including the name, relationship, and phone number of someone who can be reached in case of an emergency.
07
Sign and date the statement to indicate your consent and understanding of the information provided.
08
Make sure to review the completed form for accuracy before submitting it to the appropriate party.

Who needs participant information statement and?

01
Participant information statements are typically required for various research studies or clinical trials.
02
They are used to inform and obtain consent from individuals who wish to participate in these studies.
03
Researchers and institutions conducting the study need these statements to ensure that participants are fully informed about the purpose, risks, and benefits of the study before agreeing to participate.
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Participant information statement is a document that contains details about individuals participating in a study, program, or event.
Organizations or individuals responsible for collecting participant data are required to file participant information statement.
Participant information statement can be filled out by providing accurate and complete information about each participant.
The purpose of participant information statement is to ensure the confidentiality and privacy of participant data.
Participant information statement must include personal details, contact information, and any relevant data collected during the study or program.
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