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Exhibit 69_TMP_447ICF_Template_SurveyInterviewIntervention_Minors_Assent_713447 ICF Template: Assent Form Interview/Survey/Intervention Research Involving Minors (ages 713) Model Consent Language

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How to fill out irb consent and assent

01

Start by reading through the IRB consent and assent form thoroughly.

02

Make sure all participants understand the purpose of the study, the procedures involved, and any potential risks or benefits.

03

Provide participants with ample time to ask questions and seek clarification on any aspects of the form.

04

Have participants sign and date the form to indicate their informed consent or assent to participate in the study.

05

Keep copies of the signed consent and assent forms for your records.

Who needs irb consent and assent?

01

Anyone participating in a research study that involves human subjects needs to provide IRB consent or assent. This includes both adult participants who can provide informed consent and minors who are required to provide assent along with parental consent.

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What is irb consent and assent?

IRB consent is obtaining permission from participants in a research study while IRB assent is obtaining agreement from children or individuals who may have trouble understanding the full scope of the research.

Who is required to file irb consent and assent?

Researchers conducting studies involving humans are required to file IRB consent and assent.

How to fill out irb consent and assent?

IRB consent and assent forms are typically filled out by detailing the study procedures, risks, benefits, confidentiality, and participant rights.

What is the purpose of irb consent and assent?

The purpose of IRB consent and assent is to protect the rights and welfare of research participants by ensuring they are fully informed about the study and voluntarily agree to participate.

What information must be reported on irb consent and assent?

Information such as study procedures, risks, benefits, confidentiality, participant rights, contact information for questions, and withdrawal procedures must be reported on IRB consent and assent forms.

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