Ethics Education Modules

The Research Ethics Educational Modules are interactive learning resources designed to support the ethical conduct and review of child health research.

Developed through the CHEER project and now hosted by the Maternal, Infant, Child and Youth Research Network (MICYRN), the modules provide practical guidance for researchers, Research Ethics Board members, administrators, and patient and family partners.

Through real-world scenarios and expert insights, the modules address key ethical considerations in pediatric research and support consistent, high-quality research ethics practices across Canada.

Module 1: Participant Recruitment

In this module, you will spend some time considering how (participant) recruitment in child health research differs from recruitment in adult research.

Module 2: Patient and Public Engagement

In this module, you will learn about patient and public engagement in child health research.

Module 3: Participant Consent and Assent

In this module, you will learn about participant assent and consent.

Module 4: Research Data

In this module, you will explore the different types of research data and how it can be collected, used, stored, and accessed in child health research in an ethical and equitable way.

Module 5: Study Design

In this module, you will learn about different types of study designs that are commonly used in child health research and the numerous scientific, practical, and ethical factors considered in designing child health studies.

This project was made possible thanks to funding from the CIHR Institute of Human Development, Child and Youth Health and the CIHR Institute of Genetics.

MICYRN offers consultation with the MICYRN leadership team to discuss pre- and post-award ARO services. Click on the button to learn more and access the form.