Get Canada Calgary Youth Science Fair Informed Consent Form 2c 2022-2025

There are certain instances in which the IRB cannot apply the waiver for the requirement to document consent for research taking place online. Researchers asking students for access to educational records or are collecting identifiable, sensitive information that must be protected, must document consent.

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 . Not all e-consent systems contain the ability to document legally effective signatures.

Introduction. Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention. The patient must be competent to make a voluntary decision about whether to undergo the procedure or intervention.

The informed consent form consists of two parts: the information sheet and the consent certificate.

Obtaining Written or Verbal Informed Consent. Obtaining consent involves explaining the research and assessing participant comprehension using a consent document, usually a written consent form or information sheet, as a guide for the verbal explanation of the study.

An easier way to get patient consent online is to create a consent form through a provider like JotForm. With online forms, your patients can fill out their information, electronically sign the form, and send it back to you securely, even from their mobile devices.

To get informed consent you'll need to send the participant an information sheet and a consent form in an accessible format at least a few days before the research session date. If they do not return it before the session, you'll still be able to complete it with them before you start.