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This document is an invitation to participate in a research study examining the use of continuous glucose monitoring (CGM) devices in pregnant women to potentially replace the oral glucose tolerance test (OGTT) for diagnosing gestational diabetes mellitus (GDM). It outlines the study\'s purpose, procedures, participant responsibilities, potential risks, benefits, and details on confidentiality and participant rights.
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How to fill out participant information sheet and

01
Start by providing the title of the study at the top of the sheet.
02
Include the name and contact information of the principal investigator.
03
Explain the purpose of the study in clear, concise language.
04
Detail what participation entails, including duration and activities involved.
05
Describe any risks or discomforts that may be experienced.
06
Highlight any potential benefits to participants or to society.
07
Explain the confidentiality measures in place to protect personal information.
08
Provide information about compensation or reimbursement for expenses, if applicable.
09
Include a section on voluntary participation and the right to withdraw at any time.
10
Finish with a section for participants to ask questions or express concerns.

Who needs participant information sheet and?

01
Researchers conducting studies requiring participant involvement.
02
Institutional Review Boards (IRBs) that oversee ethical considerations.
03
Participants in research studies to understand their rights and obligations.
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A participant information sheet is a document that outlines the details of a participant in a research study or project, including personal and demographic information, and provides the necessary information regarding the study's purpose, procedures, risks, and benefits.
Researchers, project administrators, and organizations conducting studies that involve human participants are typically required to file a participant information sheet to ensure compliance with ethical standards and regulations.
To fill out a participant information sheet, provide accurate personal and demographic details, follow the formatting guidelines provided, and ensure all necessary sections regarding consent, study information, and participant rights are completed.
The purpose of a participant information sheet is to inform participants about the study they are involved in, ensuring they understand the nature of the research, their role, any potential risks, and their rights, facilitating informed consent.
The information that must be reported on a participant information sheet includes participant demographics, study objectives, procedures, risks, benefits, contact information for questions, and consent details.
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