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IRB NUMBER: 201910343 IRB APPROVAL DATE: 08/24/2022 IRB EXPIRATION DATE: 08/23/2023ORAL CONSENT SCRIPT The Diabetes Prevention Program consists of sessions that discuss topics such as staying active,

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01

Begin by familiarizing yourself with the content of the oral consent script form.

02

Make sure to have all necessary information readily available before starting to fill out the form.

03

Start by entering the date at the top of the form to indicate when the oral consent was obtained.

04

Follow the prompts on the form to provide clear and concise information about the study or research project.

05

Ensure all parties involved in providing oral consent sign and date the form to acknowledge their agreement.

06

Review the completed form for accuracy and completeness before submitting it for processing.

Who needs oral consent script form?

01

Researchers conducting studies or projects that require oral consent from participants.

02

Institutional review boards or ethics committees overseeing research protocols.

03

Participants who have agreed to take part in a study that requires oral consent.

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What is oral consent script form?

The oral consent script form is a document used to obtain and record verbal consent from participants, typically in research or clinical settings.

Who is required to file oral consent script form?

Researchers or organizations that conduct studies involving human participants where oral consent is obtained are required to file the oral consent script form.

How to fill out oral consent script form?

To fill out the oral consent script form, you need to provide details about the study, the consent process, participant information, and a record of the consent conversation.

What is the purpose of oral consent script form?

The purpose of the oral consent script form is to ensure that participants are adequately informed about the study and have voluntarily agreed to participate, thereby protecting their rights.

What information must be reported on oral consent script form?

The information that must be reported includes the study title, investigator's contact information, a description of the study, risks, benefits, and a statement confirming that the participant understands and agrees to participate.

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