Onboarding flow and consent module for digital N-of-1 study. This is what users see when they first click on the study to participate -- they go throu... (continued)
Digital N-of-1 study consent form focused on caffeine (Tx) & cognition (outcome) (more resources to follow)
Peer-reviewed reserach protocol outlining the methodology of an app-based contraceptive efficacy study of the Dynamic Optimal Timing (Dot) app. The pr... (continued)
A comprehensive outline of best practices for using consumer wearable devices put together through funding from the Robert Wood Johnson Foundation.
The Department of Health and Human Services Office of Civil Rights (OCR) recently released guidance on HIPAA and cloud computing that clarifies that C... (continued)
IRBs are responsible for protecting the welfare of study participants. This responsibility includes ensuring there are adequate measures in place to p... (continued)
Our research involved subjects engaged in their regular behavior in their natural environments for several days, while a mobile app periodically (for ... (continued)
The guidance provides recommendations on the use of electronic systems and processes that may employ multiple electronic media to obtain informed cons... (continued)
INTRODUCTION The purposes of this form are to provide you (as a prospective research study participant) information that may affect your decision as t... (continued)