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This document invites students from the University of Greenwich to participate in a research study on digital literacy through a short questionnaire. It outlines the study's purpose, voluntary nature,
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How to fill out participant information sheet

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How to fill out Participant Information Sheet

01
Start with your personal details: Name, Age, Gender.
02
Provide contact information: Phone number, Email address.
03
Indicate your study identification number if applicable.
04
Fill out the section regarding your background: Education, Occupation.
05
Provide any relevant health information if required by the study.
06
Review and confirm your consent to participate in the study.
07
Sign and date the form at the bottom.

Who needs Participant Information Sheet?

01
Research participants in clinical trials or studies.
02
Ethics committees for approval and oversight.
03
Researchers conducting the study for data collection.
04
Institutions or organizations sponsoring the research.
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It should be a concise document; the length and design should encourage a potential participant to read it in full. A brief introduction; for example: Before you decide to take part in this study it is important for you to understand why the research is being done and what it will involve.
The purpose of a Participant Information Sheet (PIS) is to set out in writing what taking part in your study will involve for the participant. Including how participation may impact on their treatment and/or their lives and the lives of others close to them. You must consider the potential participants' perspective.

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A Participant Information Sheet is a document that provides key details about a research study, including its purpose, procedures, risks, and benefits, meant to inform participants before they decide whether to take part.
Researchers and organizations conducting studies involving human participants are required to file a Participant Information Sheet to ensure ethical compliance and participant awareness.
The Participant Information Sheet should be filled out by including clear and concise information about the study's objectives, procedures, duration, potential risks, benefits, confidentiality measures, and who to contact for more information.
The purpose of the Participant Information Sheet is to provide participants with sufficient information to make an informed decision about their involvement in the study, thereby ensuring informed consent.
The Participant Information Sheet must report information such as the study's purpose, procedures, expected duration, risks and benefits, alternatives to participation, confidentiality of data, and contact details for questions or concerns.
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