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Families Becoming Healthy TogetherConsent for Research Participation Research Study Title: Families Becoming Healthy Together Researcher(s): Hollie Ray nor, PhD, RD, LIN, University of Tennessee Knoxville Leonard
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Read the consent form carefully to understand the purpose of the research, the procedures involved, and any potential risks or benefits.
02
Fill in your personal information such as name, age, contact details, etc.
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Make sure to clearly indicate your voluntary participation by signing and dating the consent form.
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If there are any sections where you do not want to give consent or have concerns, communicate it to the research team.
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Return the completed consent form to the research team or designated personnel.

Who needs consent for research participation?

01
Anyone who wishes to participate in a research study or experiment needs to provide consent. This includes individuals of legal age who are capable of giving informed consent.
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In certain cases, consent may be required from legal guardians or parents for minors or individuals who are not capable of giving informed consent.
03
Consent is also necessary for vulnerable populations, such as individuals with cognitive impairments or those who may have difficulty understanding the research process.
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Consent for research participation is a process through which individuals voluntarily agree to participate in a research study after being informed of all relevant aspects of the study, including its purpose, procedures, risks, and benefits.
Researchers and institutions conducting the study are required to file consent for research participation, ensuring that participants are fully informed and their rights are protected.
Filling out consent for research participation typically involves completing a consent form that includes information about the study, an explanation of the participant's rights, and a signature from the participant or their legal representative.
The purpose of consent for research participation is to ensure that individuals make informed decisions about their involvement in a study and to protect their autonomy, rights, and welfare.
Consent forms must report information including the study's purpose, procedures, risks, benefits, confidentiality, voluntary participation, and the right to withdraw at any time without penalty.
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