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This document seeks consent from participants or their guardians regarding the storage of blood and urine samples for future health studies associated with the National Health and Nutrition Examination
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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
Begin by reading the Consent/Assent document carefully to understand the purpose of the study.
02
Ensure that all sections are completed accurately, including participant information and study details.
03
For Consent, the adult participant must sign and date the document.
04
For Assent, if the participant is a minor, they must sign the assent section to indicate their willingness to participate.
05
Obtain a signature from a parent or legal guardian in the Parental Permission section.
06
Provide the participant and guardian with a copy of the signed documents.
07
Ensure that all necessary forms are securely stored for future reference.

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

01
Adult participants who are directly involved in the study.
02
Minors who are participating and require Assent.
03
Parents or legal guardians of minor participants who must provide Parental Permission.
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Consent refers to the agreement obtained from an adult participant, while assent is the agreement obtained from a minor participant. Parental permission is the agreement obtained from a parent or guardian for a minor to participate in a study and for the storage of their specimens.
Researchers conducting studies involving human participants, especially those involving minors or vulnerable populations, are required to file Consent/Assent and Parental Permission forms for specimen storage and continuing studies.
The forms should be filled out by providing clear information about the study, including its purpose, procedures, risks, benefits, and rights of participants. Participants or parents/guardians must indicate their agreement by signing the form.
The purpose is to ensure that participants understand the nature of the study, the use of their specimens, and their rights, ensuring ethical standards are maintained in research.
The forms must report the study title, researcher contact information, details of the research procedures, risks and benefits, confidentiality measures, and the rights of participants including the option to withdraw consent at any time.
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