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Participant Information Sheet Version 18 Date: 25/10/2018 IRAS Ref: 136118 PROTECT Study: Platform for Research Online to investigate Genetics and Cognition in Aging Invitation to take part in a research
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Start by gathering all the necessary information from the participant.
02
Create a participant information sheet template with fields for personal details such as name, age, contact information, address, etc.
03
Ensure that the form also includes sections for medical history, emergency contact information, and any relevant consent forms.
04
Clearly label each field and provide instructions if necessary.
05
Distribute the participant information sheet to the individuals who need to fill it out.
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Instruct participants to fill out all the required fields accurately and completely.
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Collect the filled out participant information sheets and review them for any missing or incorrect information.
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Make sure to store the completed sheets securely and confidentially, adhering to any data protection regulations.
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If necessary, follow up with participants to clarify any unclear or incomplete information.
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Use the collected participant information for the intended purpose, such as organizing an event or providing personalized services.

Who needs participant information sheet?

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Participant information sheets are needed by organizations, event planners, researchers, healthcare providers, and any other entity that requires detailed information about individuals participating in their activities or programs.
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Participant information sheet is a document that collects important details about an individual participating in a study or program.
Researchers, study coordinators, or program administrators are typically required to file participant information sheets.
Participant information sheet can be filled out by providing accurate and complete information about the participant, including demographics, medical history, and consent forms.
The purpose of participant information sheet is to gather relevant data about participants in a study or program to ensure proper documentation and informed decision-making.
Information such as name, age, contact details, medical history, study protocol details, and consent forms must be reported on participant information sheet.
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