Solutions for Complex Trials: How ePRO Can Improve Gastrointestinal Trial Success

Clinical Trials, Life Sciences,
  • Wednesday, June 12, 2019 | 10am EDT (NA) / 3pm BST (UK) / 4pm CEST (EU-Central)
  • 60 min

With the cascade of new technologies and precision treatments hitting the market today, gastrointestinal (GI) clinical trials present a particularly unique set of challenges for patients, study sites and study sponsors. Now, researchers are looking for a way to manage the burdens that come with innovation.

Using onsite, electronic patient reported outcome (ePRO) technology, for example, is one way to help GI study team personnel eliminate the need for data transcription while simplifying complex protocol workflows and improving data monitoring results. When this approach is used in conjunction with an agile distribution model, it can be deployed faster and will benefit all groups equally. A tech transferable ePRO solution not only enables nimble, efficient clinical data management, but it also provides the site team with the reporting they need in real time.

Sponsors see early benefits when leveraging an ePRO solution as well: Prototyping can begin on day one using the configurable technology and libraries of stored information. GI questionnaires, for example, can be licensed and quickly deployed for use in any study. Rather than wasting time and money prior to beginning a study defining each outcome that needs to be achieved, agile methodology allows users to focus on the patient to create a low burden, functional solution. 

Finally, patients appreciate the ease-of-use that at-home ePRO devices afford over more cumbersome paper-based options, especially considering the demanding reporting requirements of GI trials. 

In this webinar, the featured speaker will discuss how ePRO solutions built specifically for gastrointestinal clinical trials can provide a better avenue for compliance and engagement by:

  • Easing patient and site burden
  • Shortening development timelines
  • Simplifying library build time

Speaker

http://Kyle%20Hogan,%20Clinical%20Ink

Kyle Hogan, Director, eClinical Solutions, Clinical Ink

Kyle Hogan is responsible for the strategic alignment of the company’s native mobile application for ePRO/eCOA and patient engagement in clinical trials. He has delivered technical solutions for complex business challenges since the 1990s and has 15 years of experience in clinical trials. Kyle has managed numerous, global ePRO trial deployments and has been instrumental in the development of Clinical Ink’s mobile solutions for patient-centric ePRO/eCOA. A recognized industry expert in this area, he regularly helps sponsors realize BYOD-capable solutions for clinical trial data collection.

Message Presenter

Who Should Attend?

This webinar will appeal to individuals with the following, or related, job titles:

  • ePRO/ePRO Category/Data Managers
  • Clinical Trial/Clinical Study Leads
  • Therapeutic Strategy Leads
  • Biometrics/Bio Stats Managers
  • Clinical Operations Specialists
  • Clinical Operations Directors/VPs

What You Will Learn

Participants will learn about the advantages of agile ePRO solutions including:

  • Easing patient and site burden
  • Shortening development timelines
  • Simplifying library build time

Xtalks Partner

Clinical Ink

Clinical Ink is a global clinical trial technology company that is transforming the clinical trial experience. Founded in 2007, the company’s proven and future-built eSource platform includes solutions for EDC replacement, eCOA, ePRO, and more. These technology solutions deliver real-time scientific data and smooth user experiences that increase efficiency. With offices in Winston-Salem, NC, and Philadelphia, Clinical Ink is advancing the business model responsible for bringing new treatments to market. Visit clinicalink.com.

You Must Login To Register for this Free Webinar

Already have an account? LOGIN HERE. If you don’t have an account you need to create a free account.

Create Account