Adult Consent Documents

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Commonly Asked Questions about Adult Consent Documents

What 3 things are needed for consent?

Valid informed consent for research must include three major elements: (1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision.

Can I make my own consent form?

To create a consent form, you need to list the consenting parties and specify the activities or data covered by the consent. It should also state the parties rights and responsibilities and include dates, contact information, and other necessary details.

How do I write a consent form?

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.

Can you write your own consent form?

If you prefer to write your own consent document, you may do so, but be sure to include all required elements of informed consent.

How should consent forms be written?

The consent form should be written in plain language, free from jargon, and should allow the participant to clearly respond to points such as: The participant has read and understood information about the project. The participant has been given the opportunity to ask questions.

What is the documentation of consent?

Documenting informed consent occurs after explaining the research and assessing participant comprehension. At minimum, it involves obtaining the signature of the participant (or the legally-authorized representative or parent(s), when approved) as well as the person obtaining consent.

What is informed consent for adults?

You have the right to help decide what medical care you want to receive. By law, your health care providers must explain your health condition and treatment choices to you.