Copy ESign Professional Medical Consent For Free - Professional Medical Consent Edit

Electronic consent (e-consent) is a method of obtaining informed consent through the use of an electronic system instead of a paper consent form, e.g. in REDCap or .

Writing tips Use the second (you) or third person (he/she) to present the study details. Avoid use of the first person (I). Include a statement of agreement at the conclusion of the informed consent document. The consent doucment must be consistent with what is described in the IRB application.

Drafting tips for preparing consent forms: Use words familiar to the non-medical reader. If possible, keep words to 3 syllables or fewer. Write short, simple, and direct sentences. ... Keep paragraphs short and limited to one idea. Use active verbs.

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.

Write directly to the reader, as though you are explaining the facts in person. Informed consent language should be written in the second person (?you?), not in the first person (?I?). Minimize passive voice to the extent possible.

As with the standard consent process for written consent, the electronic consent process has two parts: Consent Discussion: Informing a participant using electronic means. Consent Documentation: The individual indicates agreement to participate in the study by documenting consent using an electronic signature.

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. Learn more examples of situations where consent forms are used in psychology.