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For an ethically valid consent, information provided to a research subject should include, but not be limited to: information about the health condition for which the research is proposed; details of the nature and purpose of the research; the expected duration of the subject's participation; a detailed description of ...
A consent form should normally be used to record the consent process and a participant's agreement to take part in your study. A signature on a consent form alone does not constitute legal or ethical consent, for more guidance please visit our section on 'Principles'.
Consent is often wrongly equated with a patient's signature on a consent form. A signature on a form is evidence that the patient has given consent, but is not proof of valid consent. If a patient is rushed into signing a form, on the basis of too little information, the consent may not be valid, despite the signature.
In limited cases, implied consent may be allowed. The identities of subjects will be completely anonymous if the consent form is not signed, and there is minimal risk involved in the study.
Legal Rights and Signatures: I (fill in your name here), consent to participate in (insert study name here) conducted by (insert investigator name here). I have understood the nature of this project and wish to participate. I am not waiving any of my legal rights by signing this form.