Make Data Central to Your CNS Pain Trials with Data Capture Solutions

Life Sciences, Clinical Trials, Patient Recruitment & Retention,
  • Thursday, September 03, 2020

In pain studies, to overcome the pileup of complicated eligibility criteria, extensive data collection, relentless monitoring requirements, and hefty patient burden, you need a first-rate technology solution. In this webinar, you’ll learn how an integrated eSource platform configured expressly for your CNS clinical trial with eCOA, BYOD ePRO, and eConsent modules helps patients adhere to exacting protocols and improves data quality and integrity. Standard pain questionnaires can be incorporated into the platform as needed to suit the protocol.

Cleaner data and confident decisions are much more accessible when patients are given assistance to stay on track. You’ll learn how timed assessments can incorporate patient-centric, prototype-driven functionality that prompt adherence and allow study teams to monitor compliance, no matter how intricate the protocol is. You’ll also see how event diaries can engage patients with review screens that clarify next steps to ensure the right information is entered.

In pain studies, such as those for migraine, rescue medication workflows are common, and present special challenges because it’s paramount to keep patient responses to the study drug separate from patient responses to the rescue medication. This talk will explain how the right data capture solution can prompt the patient to follow the correct procedures and automatically sort the responses as needed, according to protocol.

In this webinar participants will learn:

  • How to take control of pain data
  • How to keep patients engaged
  • How to make rescue medication workflows work
  • Why BYOD makes sense for pain trials
  • How to implement a solution infour to six weeks

In many pain trials, patients are overwhelmed, sites are overburdened, and sponsors struggle to achieve objectives, but it doesn’t have to be this way. In this talk, you’ll learn about technology solutions that can be up and running to simplify pain trials for sponsors, sites and patients, fast.


Kyle Hogan, Clinical Ink

Kyle Hogan, VP, Outcome Solutions, Clinical Ink

Kyle Hogan, the vice president outcome solutions, is responsible for the company’s ePRO/eCOA and patient engagement solutions in clinical trials. He has had over13 years of experience in clinical trials and has managed numerous global ePRO trial deployments.

Kyle has been instrumental in the development of Clinical Ink’s solutions for patient-centric ePRO/eCOA and patient engagement. A recognized industry expert in this area, he regularly helps sponsors realize various ePRO/eCOA solutions including BYOD, provisioned, hybrid and patient engagement enabled implementations for clinical trial data collection from patients and clinicians.

Message Presenter

Gena Gough, MBA, PMP, Outcome Solutions Director, Clinical Ink

Gena Gough is a Project Management Professional with 20+ years’ experience applied to clinical trials, eCOA, non-profit and academic medical centers. She is also a subject matter expert for ePRO/eCOA, engagement and technology standards in support of sales, product development & project management. She has over 10 years of ePRO/eCOA experience across 90+ Phase II/III trials.

Message Presenter

Who Should Attend?

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

  • Clinical Trial/Clinical Study Leads
  • Therapeutic Strategy Leads
  • Head of Immunology
  • ePRO/ePRO Category/Data Managers
  • Biometrics/Bio Stats Managers
  • Clinical Operations Specialists
  • Clinical Operations Directors/VPs
  • SLE (Lupus) Specialists, Rheumatologists

What You Will Learn

In this webinar participants will learn:

  • How to take control of your pain data
  • How to keep patients engaged
  • How to make rescue medication workflows work
  • Why BYOD makes sense for pain trials
  • How to implement a solution in four-six weeks

Xtalks Partner

Clinical Ink

Clinical Ink, a global clinical technology company, offers data certainty from source to submission. Our Lumenis™ eSource clinical technology and configurable direct data capture, eCOA, ePRO, and eConsent modules — a suite of solutions for capturing and integrating electronic data from sites, clinicians, and patients at its source — naturally enhance your clinical trial workflow by reducing manual labor, providing anytime, anywhere data access, and saving resources as your trials progress. Visit

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