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Preapproved Parental Consent Form for Lunchtime Meal Feeding Study for Preschool Children ClinicalTrials.gov Protocol ID: ChildFood402 ClinicalTrials.gov ID Number: NCT03926065 Principal Investigator:
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How to fill out irb-approved parental consent form

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How to fill out irb-approved parental consent form

01
Step 1: Begin by obtaining the IRB-approved parental consent form from your institution or research organization.
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Step 2: Read the instructions on the form carefully to understand the requirements and necessary information to be filled out.
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Step 3: Provide the personal details of the parent or legal guardian, such as their full name, contact information, and relationship to the child being enrolled in the research study.
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Step 4: Clearly state the purpose of the research study and explain any potential risks or benefits to the child involved.
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Step 5: Outline the procedures and methods used in the research study, ensuring that they are explained in a manner that is easily understandable by the parent or legal guardian.
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Step 6: Include a section where the parent or legal guardian can provide their consent by signing and dating the form.
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Step 7: Provide a space for any additional comments or questions from the parent or legal guardian.
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Step 8: Review the completed form to ensure all required information is provided and the consent is properly documented.
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Step 9: Submit the IRB-approved parental consent form according to the guidelines provided by your institution or research organization.
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Step 10: Keep a copy of the completed parental consent form for your records.

Who needs irb-approved parental consent form?

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Any research study that involves the participation of minors or individuals under the age of 18 requires an IRB-approved parental consent form.
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This includes studies conducted in educational institutions, hospitals, universities, and other research settings.
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The form is necessary to ensure that the parent or legal guardian fully understands the nature of the research study and gives their informed consent for their child's participation.
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An IRB-approved parental consent form is a document that has been reviewed and authorized by an Institutional Review Board (IRB) that allows parents or guardians to give permission for their children to participate in research studies.
Researchers conducting studies involving minors or individuals who cannot provide informed consent on their own are required to file an IRB-approved parental consent form.
To fill out an IRB-approved parental consent form, provide the necessary information about the study, including its purpose, procedures, risks, and benefits, and ensure that signatures from parents or guardians are obtained.
The purpose of the IRB-approved parental consent form is to ensure that parents or guardians are informed about the research study and willingly consent to their child’s participation, protecting the rights and welfare of participants.
The information that must be reported includes the study's purpose, procedures, potential risks, benefits, confidentiality provisions, contact information, and acknowledgment of voluntary participation.
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