The COVID-19 pandemic led to a rapid shift towards remote electronic informed consent (eConsent). We encourage researchers to use evidence-informed practices when designing their eConsent processes.

What is eConsent?

eConsent involves using electronic devices (e.g., computer, tablet, phone) to obtain consent from a potential participant or legally authorized representative.

The benefits of eConsent include:

• Enabling consent when face-to-face consent is not possible
• More convenient for researchers and participants
• Increased enrollment potential, including recruitment and enrollment of under-represented populations

Different Types of eConsent

Generally, there are two types of eConsent:

1) Researcher-assisted eConsent

• Involves a live discussion between the potential research participant and a member of the study team
• Discussion may occur remotely (not face-to-face)
• Example: research team members use video conferencing to share their screen and walk participants through an electronic consent form

2) Self-administered eConsent without research personnel

• Conducted entirely by the participant without study personnel present
• Can be completed by participants on their own time
• Example: participants use a mobile phone consent app

Evidence-Informed Practices for eConsent

Whichever type of eConsent you use, there are several evidence-informed practices that can help ensure your participants understand the study information. These practices include:

• • Using plain language
  • Using appropriate formatting and web design
  • Assessing for understanding

Click here to learn more about the different types of eConsent and how to apply these practices: