The Data You Need Starts Here
Innovative digital therapeutic and diagnostic companies deserve better than antiquated trial methods that deliver slow, suboptimal results at high costs. You need a partner with expertise in decentralized clinical trial methods that integrate with your tech and accelerate your timelines. Meet ObvioHealth and our digital trial solution.
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ObvioHealth is the world’s first virtual research organization. We combine the clinical excellence of the best CROs with pioneering technology to optimize trials at every stage and touchpoint. Our virtual site and end-to-enddecentralized clinical trial solution gets you the results you need, faster.
ObvioHealth streamlines the clinical trial process, conducting decentralized clinical trials from start to finish. Eliminate the need for site visits (or drastically reduce them) and go virtual for better, faster data.
Accelerated Recruitment
We use digital advertising best practices to reach any demographic, allowing us to fill enrollment funnels faster. Because our prescreening is fully digital, onboarding is fast and easy.
Seamless Device Integration
Our software integrates seamlessly with yours—whether it’s an app-to-app or an EDC integration. This makes data collection easy and fast for sponsors and participants.
Data Collection the Digital Way
Our clinical trial data collection is easier for participants. The combination of user-friendly ePRO and device integration means less data loss, greater accuracy, and fewer participant drop-outs than with other systems.
Automated Data Analysis
Our system is built to process data as it comes in. With automatic data cleaning, auto-edit checks, and advanced query resolutions as the data enters the platform, there’s less need for data cleaning at the end of the study. Our average time between LPO and database lock is 7 to 10 business days.
We conduct usability testing to ensure our app is easy for participants. An easy user experience lowers the burden on participants’ time and maintains their engagement, resulting in better data that helps you reach your trial goals.
Easy eConsent
Easy-to-read eConsent documents with e-signature capabilities are combined with live support if participants have questions.
On-Demand Training
Explainer videos and pamphlets can be accessed by participants at any time during the trial.
Intuitive ePRO
Participants can report symptoms in real time with the click of a button. Our ePRO modules are also designed to be adaptive to screen size, preserving the integrity of questionnaires no matter the device.
Push Notifications
Automatic reminders notify participants when there’s a study task they need to accomplish.
Participant engagement is key to the success of any study. When participants are confused or feel burdened with administrative tasks, their engagement suffers—and so does your data.
The Clinical Oversight and Coordination Hub (COACH) team leverages their deep clinical knowledge and our intuitive platform to actively engage study participants throughout the duration of a trial. The result is a patient-centric clinical trial with higher retention, compliance, and adherence rates versus a traditional CRO.
At ObvioHealth, we believe experience is key. We've developed and validated 250 ePRO/PRO solutions across various therapeutic areas, leading to successful outcomes and endpoints.
Since the start, 7 of our 21 clients have given us repeat business—the greatest proof of satisfaction.
ObvioHealth is truly a global organization. We have conducted trials in 28 countries across 5 continents.
Over the past 5 years, we have worked across 17 therapeutic areas, enabling us to gain powerful insights into how to adapt decentralized trials to specific protocols.
Participants in 14 weeks
Lower Costs
$67/Participant
Retention
ePRO Compliance
Renovia is a digital therapeutics company that develops devices for women with pelvic floor disorders.
The Problem
Renovia Inc.'s plans for a 15-site traditional study of their device for urinary incontinence were derailed when COVID-19 hit. Renovia turned to ObvioHealth to design and manage a fully virtual, decentralized, randomized controlled clinical trial.
The Solution
The Results
The study delivered statistically significant results for participants who used Renovia’s device. The fully virtual study design was effective, even for a population of older adults. Read more on digital clinical trials.
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545 West 25th Street, 20th Floor
New York, NY, USA 10001
(888) 880-1664
