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This form is intended for obtaining assent from adolescents aged 13-17 to participate in research studies. It includes instructions for investigators and necessary language for compliance with RSRB
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How to fill out child rsrb assent 13-17

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How to fill out child rsrb assent 13-17

01
Gather all necessary information about the child participant, including their name and age.
02
Review the purpose and procedures of the research study with the child in a clear and age-appropriate manner.
03
Discuss any potential risks and benefits of participation to ensure the child understands.
04
Provide the child the opportunity to ask questions about the study.
05
Explain the concept of voluntary participation and the right to withdraw at any time without penalty.
06
Ensure the child expresses understanding and willingness to participate by signing the assent form.
07
If applicable, include a witness who can confirm that the child understands and consents to the study.

Who needs child rsrb assent 13-17?

01
Children aged 13 to 17 who are participating in research studies that involve more than minimal risk.
02
Researchers conducting studies that require parental consent but also seek the child's agreement to participate.
03
Institutional Review Boards (IRBs) assessing studies involving minors.

What is Child Rsrb Assent 13-17 Year Old Form?

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Child RSRB assent 13-17 refers to the process of obtaining agreement from children aged 13 to 17 years old to participate in research studies, acknowledging their understanding of the study's nature and their role in it.
Researchers who conduct studies involving children aged 13 to 17 must file Child RSRB assent forms to ensure ethical standards and that participants understand the study.
To fill out the Child RSRB assent 13-17, researchers should provide clear information about the study, including its purpose, procedures, potential risks, and benefits, and ensure the form is understandable to the child.
The purpose of Child RSRB assent 13-17 is to ensure that minors are informed about the research they are participating in and to make sure they willingly agree to participate.
The information that must be reported on Child RSRB assent 13-17 includes the study's purpose, procedures, possible benefits and risks, confidentiality assurances, and the child's right to withdraw at any time.
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