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This document provides information about a clinical research study testing an experimental drug, ABI-5366, aimed at preventing recurrent genital herpes caused by HSV-2 infection. It outlines the study\'s
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01
Begin by entering the title of the study at the top of the sheet.
02
Include the name and contact information of the principal investigator.
03
Fill in the purpose of the study in a clear and concise manner.
04
Provide a brief description of the study procedures.
05
List any potential risks and benefits associated with participation.
06
Specify the duration and frequency of participation required from participants.
07
Include information on data confidentiality and how participant information will be protected.
08
Provide contact information for questions or concerns.
09
Include a section for participant consent or signature.

Who needs participant information sheet and?

01
Research participants who are considering joining a study.
02
Institutional review boards (IRBs) that review the research ethics.
03
Researchers and study coordinators responsible for recruiting participants.
04
Ethics committees ensuring compliance with regulations.
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A participant information sheet is a document provided to participants in a study or research project that outlines essential information about the study, including its purpose, procedures, risks, benefits, and the rights of the participants.
Researchers conducting studies that involve human participants are typically required to file a participant information sheet to ensure participants are fully informed.
To fill out a participant information sheet, researchers should include key information such as the study's purpose, what participation involves, potential risks and benefits, confidentiality measures, and contact information for any questions.
The purpose of a participant information sheet is to provide clear and comprehensive information to participants, ensuring informed consent and promoting transparency in the research process.
The information that must be reported on a participant information sheet includes the study's objectives, procedures, duration, risks, benefits, confidentiality assurances, voluntary participation notice, and contact details for the research team.
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Relevant keywords

HSV-2 infection recurrent genital herpes clinical trial ABI-5366 participant consent investigational drug medical research side effects safety monitoring clinical study

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