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A consent form should be a short document (normally one page but may need to be longer depending on the complexity of the study) containing explicit statements of what taking part in the research project involves and what will become of the data collected.
A consent form is a document signed by persons of interest to confirm that they agree with an activity that will happen and that they are aware of the risks or costs that may come with it.
Why do I have to sign a consent form? The main purpose of the informed consent process is to protect the patient. A consent form is a legal document that ensures an ongoing communication process between you and your health care provider.
Types of consent include implied consent, express consent, informed consent and unanimous consent.
I understand that my participation is voluntary and that I am free to withdraw at any time, without giving a reason and without cost. I understand that I will be given a copy of this consent form. I voluntarily agree to take part in this study.
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