All research studies need to submit documentation around the appropriate policies and procedures implemented to protect the rights and welfare of humans participating as subjects in the research. To accomplish this, IRBs use a group process to review research protocols and related materials (e.g., informed consent documents and investigator brochures) to ensure protection of the rights and welfare of human subjects of research. For research studies using the Way To Health platform, we have prepared a set of documents and templates to accompany the submission.
|Document Name||Intent||Download Link|
|Way to Health Summary of Data Protections||This document outlines how Protected Health Information is stored, secured and accessed on the Way to Health platform.||Word File|
|Sample Documents for Way to Health Studies||Template: This document provides a sample IRB protocol for a study using Way to Health. It includes details such as study design, recruitment strategies and examples of informed consent.||Word File|
|Way to Health Content and Messaging Template||Template: This document provides a framework for clearly defining wording and content that the participant will see for each enrollment step, content of their study dashboard, and the automated feedback messaging. Update with specific study content as appropriate.||Word File|