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STUDY ID: _ _ _ _ _ _ PARTICIPANT INFORMED CONSENT FORM IRAS reference number: 325272REC number: 23SS0087Initial boxes to indicate your agreement with the compulsory parts of the study: 1. I have

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How to fill out participant informed consent form

01

Begin by reading the title of the study and the investigator's information.

02

Review the purpose of the study and what participation entails.

03

Read through the eligibility criteria to determine if you qualify.

04

Understand the risks and benefits associated with participation.

05

Indicate whether you have had the opportunity to ask questions.

06

Provide clear information about data handling and confidentiality measures.

07

Confirm your voluntary participation and understanding of the consent.

08

Sign and date the form where indicated.

Who needs participant informed consent form?

01

Participants in clinical trials or research studies.

02

Researchers conducting studies involving human subjects.

03

Ethics boards reviewing studies to ensure compliance.

04

Organizations funding or overseeing research studies.

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What is participant informed consent form?

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

Who is required to file participant informed consent form?

Researchers conducting studies involving human participants are required to file a participant informed consent form in order to ensure ethical standards and participant rights are upheld.

How to fill out participant informed consent form?

To fill out a participant informed consent form, provide clear and concise information about the study, including title, purpose, procedures, risks, benefits, confidentiality measures, contact details for questions, and an area for the participant's consent signature.

What is the purpose of participant informed consent form?

The purpose of the participant informed consent form is to ensure that participants are fully informed about the study, understand their involvement, and voluntarily consent to participate, protecting their rights and welfare.

What information must be reported on participant informed consent form?

The participant informed consent form must report information such as the study's purpose, procedures, potential risks and benefits, confidentiality measures, and the right to withdraw consent at any time.

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