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This form is to be completed by children aged 12 and under, along with their parent or guardian, to provide assent for participation in a project regarding the CF Registry. It includes questions to ensure understanding of the project and consent requirements.
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How to fill out assent form for children

01
Start by reviewing the document to understand its purpose and requirements.
02
Prepare a clear and child-friendly explanation of the study or treatment, tailored to the child's understanding.
03
Include information about what participation involves, potential risks, and benefits.
04
Ensure the child understands that their participation is voluntary and they can withdraw at any time.
05
Use simple language and check for understanding by asking the child questions.
06
Provide spaces for the child's name, signature, and date on the form.
07
Include a section for the parent or guardian's signature to provide consent alongside the child's assent.

Who needs assent form for children?

01
Children participating in clinical trials or research studies.
02
Young participants in educational or psychological studies.
03
Minors involved in any form of medical treatment where assent is ethically required.
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An assent form is a document used to obtain agreement from children participating in research or clinical studies. It ensures that children understand the nature of the study and agree to participate voluntarily.
Researchers are typically required to file assent forms for children involved in studies where informed consent is also obtained from a parent or legal guardian.
To fill out an assent form, researchers should present the information in child-friendly language, explain the study's purpose, risks, and benefits, and provide space for the child to sign or mark their agreement.
The purpose of the assent form is to ensure that children provide informed agreement to participate in research, respecting their rights and autonomy while acknowledging their developmental capacity to understand the information.
The assent form must report information such as the study's purpose, procedures, risks, benefits, the voluntary nature of participation, and contact information for questions or concerns.
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