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Research Consent and Authorization Form Rhode Island Hospital, The Miriam Hospital, EP Bradley Hospital, Newport Hospital, and Gateway Healthcare of Study Participant:___Principal Investigator:Kirsten

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How to fill out research consent form and

01

Read the entire consent form carefully to understand all the relevant information.

02

Fill out your personal details such as name, age, contact information, and any other required information accurately.

03

Ask any questions you may have about the research study or the consent form before signing.

04

Sign and date the consent form to indicate your agreement to participate in the research study.

05

Keep a copy of the signed consent form for your records.

Who needs research consent form and?

01

Any individual who is being asked to participate in a research study needs to fill out a research consent form.

02

This includes participants of all ages, from children to adults, who are part of the research study.

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What is research consent form?

A research consent form is a document that provides potential participants with information about a study, including its purpose, procedures, risks, benefits, and their rights, allowing them to make an informed decision about participation.

Who is required to file research consent form?

Researchers and institutions conducting studies that involve human participants are required to file a research consent form to ensure ethical compliance and participant understanding.

How to fill out research consent form?

To fill out a research consent form, the researcher should provide clear information about the study, outline the risks and benefits, ensure the form is understandable, and allow participants to ask questions before signing.

What is the purpose of research consent form?

The purpose of a research consent form is to ensure that participants are fully informed about the study and voluntarily agree to participate, thereby protecting their rights and welfare.

What information must be reported on research consent form?

A research consent form must report information such as the study's purpose, procedures, duration, potential risks, benefits, confidentiality assurances, and the right to withdraw at any time.

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