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REMOVE ALL THE INSTRUCTIONS IN RED BEFORE PRINTING Assent Forms should NOT include section headings, HIPAA language, JHU boilerplate or signature pre-research ASSENT FORMProtocol Title:Application
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How to fill out research assent form

01
Start by reading the research assent form thoroughly to understand its purpose and what you are agreeing to.
02
Fill out your personal information accurately, including your name, age, and contact information.
03
Make sure to understand the study procedures, risks, benefits, and any compensation involved before providing your consent.
04
If you have any questions or concerns, don't hesitate to ask the researcher or study team for clarification.
05
Write your signature and date the form to indicate your agreement and consent to participate in the research.
06
Keep a copy of the filled-out research assent form for your records.

Who needs research assent form?

01
Anyone who is under the legal age of consent for research participation.
02
Individuals who are considered vulnerable due to their age, cognitive abilities, or mental health condition.
03
Participants in research studies involving human subjects.

What is RESEARCH ASSENT - Johns Hopkins Hospital Form?

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A research assent form is a document that is used to obtain permission from participants, typically minors or individuals unable to give full consent, to take part in a research study.
Researchers who involve participants who are minors or individuals unable to provide informed consent on their own are required to file a research assent form.
To fill out a research assent form, a researcher must provide clear information about the study, including its purpose, procedures, risks, and benefits, in an age-appropriate language, and then ask the participant to indicate their willingness to participate.
The purpose of the research assent form is to ensure that participants understand the study they are being invited to join and to gauge their willingness to participate, thereby respecting their autonomy.
The research assent form should include information about the study's purpose, procedures, potential risks and benefits, the right to withdraw, and contact information for questions or concerns.
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