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The Informed Consent is described in ethical codes and regulations for human subjects research. The goal of the informed consent process is to provide sufficient information so that a participant can make an informed decision about whether or not to enroll in a study or to continue participation.
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Informed consent is one of the founding principles of research ethics. Its intent is that human participants can enter research freely (voluntarily) with full information about what it means for them to take part, and that they give consent before they enter the research. Consent should be obtained before the participant enters the research (prospectively).
According to (Taylor, 2008), “informed consent is a formal authorization by the child’s parents or guardian allowing an invasive procedure to be performed or for participation in research.” Usually before a heath care profession can even touch a patient a consent form must be signed. Informed consent is required in all heath care agencies.
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Guidance on Writing an Outline Research Proposal. In order to assess your application, it is helpful to see an outline of the research area in which you would like to do your doctoral study. This information helps your application in two ways.