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RESEARCH CONSENT FORM Use Plate or Print:This section only to be edited by IRB office.MAN#: DOB: Subjects Name:Protocol Title: Improving Neurodevelopmental Outcomes in Children with Congenital Heart
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How to fill out research consent form

01
To fill out a research consent form, follow these steps:
02
Read the form carefully to understand the purpose and procedures of the research.
03
Provide your personal information as requested, such as your name, contact details, and demographic data.
04
Carefully review the terms and conditions, risks, and benefits outlined in the form.
05
If there are any questions or concerns, consult with the researcher or research team.
06
Sign and date the form to indicate your informed consent for participating in the research.
07
Return the completed form to the researcher or designated authority.
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Note: Make sure to keep a copy of the filled-out consent form for your records.

Who needs research consent form?

01
Research consent forms are needed by individuals who are participating in research studies or experiments. This includes individuals who are voluntarily taking part in academic research, medical trials, psychological studies, social science experiments, or any other type of research that involves human subjects. Research consent forms ensure that participants are knowledgeable about the research aims, potential risks, benefits, confidentiality, and rights before agreeing to participate. It is essential to obtain informed consent from participants to prioritize their safety and ethical considerations.
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A research consent form is a document that provides potential participants with detailed information about a research study, including its purpose, procedures, risks, benefits, and their rights, allowing them to make an informed decision about their participation.
Researchers or institutions conducting studies that involve human participants are required to file a research consent form, ensuring that participants are properly informed.
To fill out a research consent form, participants should read the document carefully, understand all sections, and provide their signature and date to indicate their agreement to participate.
The purpose of a research consent form is to protect participants' rights and welfare by ensuring they are fully informed about the study and voluntarily agreeing to participate.
The research consent form must report information such as the study's purpose, procedures, potential risks and benefits, confidentiality measures, and contact information for queries.
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