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The General Consent for Treatment and Release of Information form is used to obtain authorization from and provide information to the patient or their representative.
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.
Follow these steps to write an effective consent form. Step 1: Title and introduction. Step 2: Description of the activity. Step 3: Risks and benefits. Step 4: Confidentiality and data handling. Step 5: Voluntary participation and withdrawal. Step 6: Consent statement. Step 7: Signature and date. Step 8: Contact information.
If you prefer to write your own consent document, you may do so, but be sure to include all required elements of informed consent.
Language - Consent forms should be written in the 2nd person (i.e., you are) and in a language that is clear, concise, and understandable to the subject population. This includes both reading level and language (e.g, English, Spanish, French).

People also ask

What is a Consent Form? Consent forms, sometimes called release forms, are legal documents that serve as written permission to send or receive information among participating parties. They often inform them of associated use risks and release the provider from associated claims.
A consent form gives written permission to another party to perform an activity or host an event, indicating that the signatory understands the associated terms and cannot hold the other party liable for any injury or harm.
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.

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