eConsent

The eConsent platform is designed to streamline the consenting process for patients and caregivers involved in clinical studies. It aims to improve patient understanding and reduce dropout rates by providing study information through various formats such as text, videos, and quizzes. This approach ensures participants and their legally authorized representatives (LARs) fully comprehend the information presented, leading to a better overall experience.

High dropout rates are a significant challenge in clinical studies, often exacerbated by complex legal jargon and time constraints during onsite visits. The eConsent system addresses these issues by allowing participants and caregivers ample time to absorb and engage with the consent materials, ultimately increasing retention and engagement.

Key Features

• Dynamic content delivery to enhance participant understanding.
• Insights Dashboard for tracking consent form distribution and completion.
• Facilitates follow-up with participants who are delayed in providing consent.

The Insights Dashboard is an integral part of the platform, offering an easy way to monitor who has received and completed consent forms. It also identifies participants who are at risk of falling behind, enabling study teams to take timely action to address potential issues.