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Este documento es un formulario de consentimiento informado para participar en el estudio de investigación \'Dulce Digital-COVID Aware\', que se centra en integrar la educación sobre COVID-19 con
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Provide personal information such as your name, contact details, and any other required identifiers.
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Review the information about the study or procedure, including its purpose, duration, and any potential risks involved.
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An informed consent form is a legal document that outlines the details and risks of a proposed medical treatment or research study, ensuring that participants are fully aware of what they are agreeing to before giving their consent.
Researchers and medical professionals conducting clinical trials or medical procedures involving patients or subjects are required to file an informed consent form.
To fill out an informed consent form, participants should read the document thoroughly, ask questions for clarification, and provide their signature to indicate their willingness to participate after fully understanding the information provided.
The purpose of an informed consent form is to protect the rights and welfare of participants by ensuring they are adequately informed about the study or treatment, including potential risks and benefits, before consenting to participate.
The informed consent form must report information such as the purpose of the study, procedures involved, risks and benefits, confidentiality measures, and the right to withdraw from the study at any time.
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