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Gastrointestinal Virtual Clinical Trials

Progressing GI health through better data

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If you are a participant looking to join a clinical trial, please click here.

For Participants

ObvioHealth’s decentralized study design and user-friendly app break down barriers to traditional GI research.

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ObvioHealth and GI Alliance Partner to Bring Better GI Care to Patients

ObvioHealth has partnered with GI Alliance, one of the nation's largest independent gastroenterology services organization to facilitate more efficient hybrid clinical trials. This collaboration will make research easier and safer for patients and provide better efficacy data for trial sponsors.

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Image Collection of Infant/ Toddler Stools for Software Development and GI Assessment

A fully virtual observational study using the ObvioHeath app to collect and classify images of infant stool samples and gather data representative of GI function.

• 2,366 evaluable images collected
• 95% retention

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Evaluating Efficacy and GI Tolerance of Inulin Fiber Bars

A fortune 500 multinational food company wanted to understand clinical efficacy, GI tolerance, and consumer perception of four iterations of its inulin fiber bar. ObvioHealth virtually recruited, randomized, shipped and captured data across 4 samples in record time.

• 85% questionnaire compliance
• 92% retention

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Studying the Impact of Infant GI Disorders on Parents in Asia

Parents of 1000 healthy infants and toddlers completed a six-part, logic-based questionnaire to assess the prevalence and management of FGIDs, impacts on QoL, and efficacy of treatments.

• 1000 patients enrolled in less than 1 month

Our Client Roster

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Anatara logo.
Bayer logo.
Danoone Logo.
DSM logo.
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Janssen logo.
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mithra logo.
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Curious if Your GI Study Can Go Virtual?

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Delivering Better Data for Your GI Study

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Recruitment & Onboarding

Recruitment is often a huge barrier to trial success, particularly for GI studies. ObvioHealth uses digital targeting methods to find untapped populations. We identify the online behaviors that point to people with a positive pre-disposition for a specific trial and, because our studies are virtual, we are not geographically tied to a site location.  Data is collected through our proprietary app, giving participants more privacy in their responses.

Once recruited, we enroll participants through virtual prescreening/screening and e-consent. This eliminates the burdensome cost of site retention and staffing requirements, and often shortens the recruitment period.

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Outcomes Measurement

The ObvioHealth platform and app incorporates multiple data capture technologies to adapt to the needs of any given trial.  These include simple survey-type completion of questionnaires and diaries, image, video and audio capture and use of wearables. Complementary data collection methods ensure more robust data based on real world outcomes.  

Symptoms of GI disorders can be physically uncomfortable, but also quite awkward to discuss with a doctor, leading to fear of embarrassment in face to face interactions. GI study subjects are generally more willing to contribute to research, knowing they can participate from the comfort and discretion of their homes without the burden of traveling to site visits.  

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Logistics Management 

Our platform makes it easy to trigger, track and manage products and payment of incentives. ObvioHealth can reimburse participants with the stipend program that is fully virtual. We ship any needed study supplies or devices directly to the participant’s home.

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Medication Adherence & Adverse Events

An important advantage of ObvioHealth’s app is the real time remote monitoring of medication adherence and potential adverse events. Our escalating system of reminders and immediate AE/SAE detection make our studies safer, while also improving medication adherence.

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Higher compliance, higher retention, more accurate data

Our easy-to-use, convenient app makes it easier for participants to remain compliant. There is little to no time wasted travelling to clinical sites, so there are fewer drop-outs. All of this means that studies end on time or ahead of schedule. And because participants are able to report more real world and real time experiences, the resulting data is more accurate and reliable.