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This document provides consent for the storage of blood and urine samples for future health studies related to the National Health and Nutrition Examination Survey (NHANES).
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How to fill out consentassent and parental permission

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How to fill out Consent/Assent and Parental Permission for Specimen Storage and Continuing Studies

01
Read the information sheet provided about the study carefully.
02
Understand the purpose of specimen storage and how it relates to the continuing studies.
03
Gather all necessary personal information required for the form.
04
Fill out the consent/assent section, clearly indicating your agreement or disagreement.
05
If applicable, provide signatures where required, including the date.
06
For parental permission, make sure the parent or guardian reviews the information and fills out their section.
07
Ensure all sections of the form are completed accurately before submission.
08
Submit the completed form as directed in the provided instructions.

Who needs Consent/Assent and Parental Permission for Specimen Storage and Continuing Studies?

01
Participants in research studies involving specimen storage.
02
Minors participating in studies who require parental permission.
03
Parents or guardians of minors who intend to participate in such studies.
04
Individuals who are involved in ongoing studies that necessitate continued specimen storage.
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Consent/Assent refers to the agreement obtained from participants to allow their specimens to be stored and used for research purposes. Parental Permission is the consent obtained from a parent or guardian for minors to participate in such studies.
Researchers conducting studies involving human subjects, especially when data includes specimens from minors, are required to obtain and file Consent/Assent and Parental Permission.
To fill out the forms, researchers must ensure all sections are completed, including participant details, the purpose of the study, the nature of specimen storage, and any potential risks and benefits. Participants and parents/guardians must sign and date the forms.
The purpose is to ensure ethical standards are met by obtaining permission from participants and their guardians before collecting specimens for research, safeguarding their rights and autonomy.
The forms must report the study purpose, procedures, risks, benefits, confidentiality assurances, and the rights of participants, including the right to withdraw at any time without penalty.
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