Informed Consent Form: An Informed Consent Form is a legal document that outlines the rights and responsibilities of a participant in a research study, clinical trial, or other research project. It is a written agreement between the researcher and the participant that describes the purpose of the study, what will be asked of the participant, and any potential risks involved. The form must be signed by the participant before the study starts. Types of Informed Consent Forms: Standard Informed Consent Form, Short Form Informed Consent Form, Electronic Informed Consent Form. Online Consent Form: An Online Consent Form is a web-based form that is used to collect consent from participants in a research study. It is similar to an Informed Consent Form but is administered online rather than in person. The form is usually hosted on a secure website and requires participants to fill out their contact information, agree to the terms and conditions of the study, and provide a signature. Types of Online Consent Forms: Standard Online Consent Form, Short Form Online Consent Form, Electronic Online Consent Form. Informed Consent Explained: Informed Consent Explained is the process of educating research participants about the research study and its potential risks and benefits. It is the researcher’s responsibility to ensure that the participant fully understands the study and any risks associated with it before the participant signs an Informed Consent Form. The process includes providing the participant with written information about the study, and then verbally discussing the information with the participant and answering any questions they may have.