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This document provides information regarding a research study at the Royal Hospital for Women focusing on the evaluation of fetal heart function using ultrasound techniques in both normal pregnancies and those complicated by congenital heart disease. It outlines the study\'s purpose, eligibility criteria for participants, details about procedures involved, risks, confidentiality provisions, and contacts for further inquiries.
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What is participant consent information sheet?
A participant consent information sheet is a document that provides potential research participants with details about the study, including its purpose, procedures, risks, benefits, and their rights, to ensure they can make an informed decision about their participation.
Who is required to file participant consent information sheet?
Researchers or institutions conducting studies involving human participants are required to file a participant consent information sheet to ensure ethical standards are upheld and participants are adequately informed.
How to fill out participant consent information sheet?
To fill out a participant consent information sheet, provide clear and concise information about the study's objectives, procedures, risks, benefits, confidentiality measures, and contact information, ensuring that the language is understandable to the target audience.
What is the purpose of participant consent information sheet?
The purpose of a participant consent information sheet is to inform potential participants about the study in order to obtain their informed consent, ensuring they understand what participation involves and their rights.
What information must be reported on participant consent information sheet?
The participant consent information sheet must report information about the study's purpose, procedures, potential risks and benefits, how confidentiality will be maintained, the right to withdraw, and contact information for questions or concerns.
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