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Este documento informa a los participantes sobre un estudio de investigación en el Centro Médico Nacional Infantil relacionado con la planificación del cuidado al final de la vida para adolescentes con cáncer. Se explican los propósitos del estudio, los procedimientos involucrados, los riesgos potenciales, los beneficios y los derechos de los participantes.
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What is informed consent form?
An informed consent form is a document that outlines the information patients or participants need to understand regarding a medical procedure, research study, or treatment, allowing them to make an informed decision about their participation.
Who is required to file informed consent form?
Researchers, healthcare providers, or institutions conducting studies or medical treatments that involve human participants are required to file informed consent forms.
How to fill out informed consent form?
To fill out an informed consent form, read the document carefully, ensure that all necessary information is provided, including the purpose of the study or treatment, risks, benefits, and contact information, and then sign and date it to indicate understanding and agreement.
What is the purpose of informed consent form?
The purpose of an informed consent form is to ensure that individuals are fully informed about the nature of a procedure or study, including potential risks and benefits, thus allowing them to voluntarily decide whether to participate.
What information must be reported on informed consent form?
An informed consent form must report information such as the purpose of the research or treatment, procedures involved, potential risks and benefits, confidentiality assurances, and the participant's rights.
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