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Get the free Interactive Prototype Consent Form - vis berkeley

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This document serves as a consent form for participants in the CS160 project to observe and record their interactions with a prototype, ensuring no identifying information will be used without consent.
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How to fill out interactive prototype consent form

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How to fill out Interactive Prototype Consent Form

01
Read the instructions carefully provided at the top of the form.
02
Enter your personal information in the designated fields, including your name and contact details.
03
Review the purpose of the prototype and how your feedback will be used.
04
Check the consent section to ensure you understand what you are agreeing to.
05
Sign and date the form at the bottom to indicate your consent.
06
Submit the completed form as instructed, either digitally or in person.

Who needs Interactive Prototype Consent Form?

01
Participants who will engage in testing the interactive prototype.
02
Researchers or developers conducting user testing sessions.
03
Organizations requiring ethical approval for user participation.
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The Interactive Prototype Consent Form is a document that seeks the approval of participants involved in a prototype testing process, ensuring they understand the nature of their participation and any associated risks.
Individuals or organizations that are conducting research or testing using interactive prototypes with human participants are required to file the Interactive Prototype Consent Form.
To fill out the Interactive Prototype Consent Form, you should provide identifying information about the study, describe the purpose and procedures, outline potential risks and benefits, and include a section for participants to indicate their consent.
The purpose of the Interactive Prototype Consent Form is to inform participants about the study they are involved in, ensure their voluntary participation, and protect their rights and welfare during the research process.
The Interactive Prototype Consent Form must report information such as the title of the research, purpose of the study, procedures involved, potential risks, benefits, confidentiality measures, and any compensation details for participants.
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