Making Clinical Trials
More Patient Centric.

Enabling Research Sites to retain
patients through virtual visits

Why VirTrial Now?

%

Of patients want to participate in relevant clinical trials. ⁽¹⁾

%

Of potential patients live more than 2 hours away from the nearest study center. ⁽²⁾

%

Of potential patients would participate in a trial if it had virtual visits. ⁽⁶⁾

%

Of sites fail to enroll a single patient. ⁽³⁾

%

Drop Out Rate in Standard Trial. ⁽⁴⁾

%

Drop Out Rate in Virtual Trial. ⁽⁵⁾

1. CISCRP 2013 Survey. | 2. B. Adams, “Fierce Biotech”, March 2017. | 3. Medidata, “Non-enrolling sites come at a price”, March 2016 | 4. S. Elvidge, “Importance of Patient Retention Strategies,” Life Science Leader, April 2010 | 5. Center Point internal review data, C. Morgan, “Are Clinical Research Sites a Dying Paradigm?” | 6. Pharmpro- “Are Site-Less Trials the Future of Clinical Research?”, May 2018.

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Timeline

2007 -2017

Leadership team at Radiant Research, conducted >10,000 trials; felt site and patient challenges related to trial enrollment and retention.

2011

Stratus Video
remote video interpretation services (allows hospitals/physicians to connect to a medically certified translator via video (American sign language, 20 languages via video, 183 via audio)

2017

Synzi created
Telemedicine to prevent hospital readmission for chronic diseases.

2018

VirTrial formed, acquired Synzi platform and customized specifically for clinical research.

2019

February
Pilot study conducted – Results confirm both site & patient-centric platform.
March
SCRS GIP announced; supporting site sustainability.

VirTrial Features

R

Any device (BYOD)

R

Any site

R

8+ years proven use with award winning platform (1700 hospitals, 100,000 visits per day)

R

Unique audio and video splitting if bandwidth is low

R

Unlimited multi-way calling (based on connectivity strength)

R

Interpretation services (20 video and 183 audio languages)

R

Variety of secure communication modalities (video, email, text, phone)

R

Programmable to automatically manage patient communication and touchpoints (reminders and engagement messaging) at study or site level

R

Dashboard reporting platform to view compliance; allows sites/sponsors to be proactive

VirTrial Site Focus

R

Official Global Impact Partner (GIP) with the Society for Clinical Research Sites (SCRS)

R

VirTrial platform included as SCRS member benefit:
Sites provided with download of platform.
Training is provided.
Sites become certified as virtual capable.
Sponsors can continue to use their preferred sites.
Sponsors will quickly realize the benefits of hybrid virtual studies.

Hybrid Trials

Our vision is to enhance current research studies by replacing 25-40% of the visits with virtual video visits. We want to help sites maximize resources and get you results faster.

How VirTrial Is Different

VirTrial

Vision:
Hybird Virtual Model

  • Supports sites – Improves their ability to conduct trials more efficiently.
  • Patient-centric – Combining technology with the human
    element to ensure patient safety along with patient convenience and satisfaction.
  • Immediate Solution – Can be implemented today on any device at any site.

Team Experience

  • 50 years combined clinical site operations experience.
  • Over 10,000 trials conducted.
  • Easy to use solution developed from a true site and patient
    perspective.

Competitors

Vision:
Site-less Model

  • Replaces sites – vision for a single metasite.
  • Technology-centric – Another device to provision, for sites to store and for patients to learn; removes the physician to patient relationship.
  • Small solution – Very few studies can safely support a site-less model.

Team Experience

  • Minimal to no clinical site experience.
  • Another technology solution developed from a top down approach.

With VirTrial you’re making Clinical Trials more convenient for patients and sites

Testimonials

More trials should be done this way. You could probably increase patient volume.

Rachel, D.

Study Participant at Albuquerque Clinical Trials.

One advantage I could see from remote visits is convenience for patients especially those that can’t drive or live far from the closest site.

Clinical Research Coordinator at CCT Research

Request your free demo now!

Discover How We Can Help You To Improve Enrollment, Compliance and Retention

REQUEST DEMO

 

Increase Retention
and Compliance

Drop out rate

Virtual clinical
trial is 5%

Standard Phase III
clinical trial is 30%

Analytics allow for Preemptive Intervention

Request your free demo now!

Discover How We Can Help You To Improve Enrollment, Compliance and Retention

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Digitally Innovative and Secure Features

Interpretive Services

Cloud access via any commodity device

Secure HIPAA compliant conversations

Client side encryptions

Dynamic side encryptions

Workflow automation

Communication Rules Engine

Push Notifications

Dashboard Reporting Capabilities

Scalable and customizable to any protocol