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Name: Fillable Online Consent to Participate in a Research Study Fax Email Print - pdfFiller
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This document outlines the consent form for adult participants in a research study conducted by the University of North Carolina at Chapel Hill, focusing on the impact of the immune system on responses to social experiences. Participants will engage in surveys, tasks, and conversations as part of the study, which includes receiving an influenza vaccine or a sham vaccine, with all procedures explained in detail.

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What is informed consent?

Informed consent is the process by which a person is educated about and understands the risks, benefits, and alternatives of a treatment or procedure, and voluntarily agrees to it without coercion.

Who is required to file informed consent?

Typically, healthcare providers, researchers, and institutions conducting medical treatments or clinical trials are required to obtain and file informed consent from participants.

How to fill out informed consent?

To fill out informed consent, the provider must present the relevant information to the participant, ensure they understand it, answer any questions, and then have the participant sign the consent form to indicate their agreement.

What is the purpose of informed consent?

The purpose of informed consent is to ensure that individuals have the autonomy to make informed decisions about their medical care or participation in research, while also protecting their rights and safety.

What information must be reported on informed consent?

Informed consent must include information about the nature of the procedure or research, potential risks and benefits, alternatives to the proposed treatment, confidentiality assurances, and the individual's right to withdraw consent at any time.

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