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Step 1:

Study Design

Design Your Trial With Precision

ObvioGo’s Study Designer gives you full control over trial setup—without coding delays or IT bottlenecks. Configure protocols, workflows, and data capture directly in the platform, so your team can move faster with confidence. Whether you need a simple design or a complex global study, ObvioGo gives you the tools to build smarter trials—on your terms.

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Collaboration with Industry Experts

ObvioGo is built to put trial design and execution in your hands—but when deeper scientific and regulatory expertise is needed, we’ve got you covered.

Through our expanded partnership with sister company SPRIM PRO, we bring world-class clinical and scientific capabilities into the ObvioGo ecosystem. This collaboration enhances our ability to support complex studies with services like protocol optimization, endpoint strategy, instrument validation, and regulatory guidance.

By combining ObvioHealth’s digital innovation with SPRIM PRO’s clinical depth, sponsors benefit from an agile, tech-powered platform backed by expert support—ensuring faster, more confident trial execution across global markets.

Our Scientific Support Services Include:

Instrument Selection

Endpoint Identification

Participant Training

Participant Journey Optimization

Evidence Strategy

Regulatory Guidance

Instrument Selection and Validation

Ensure your study uses the right tools, devices, and wearables for accurate, participant-friendly data capture.

Reduce Participant Burden

We select instruments, devices, and wearables that are most appropriate for your study’s population and condition to minimize participant burden while maintaining clinical relevance and promoting compliance.

Enhance Data Validity

We arbitrate between the reduction of patient burden and the delivery of outcomes quality, taking into consideration fatigue, usability, and granularity of data to ensure high-integrity data collection.

Endpoint Identification

Define endpoints that are clinically meaningful, measurable, and aligned with your protocol goals.

Enhance Data Accuracy

We apply analytical tools and scientific expertise to refine endpoint selection, ensuring clinical relevance and precision. By aligning endpoints with study objectives and protocol intent, we drive stronger, more actionable outcomes.

Optimizing Endpoint Collection

We tailor platform workflows and study strategies to ensure endpoints are captured efficiently and accurately. Our approach integrates the right technologies and workflows to maximize precision while minimizing participant and site burden.

Participant Training

Equip participants with the knowledge and tools they need to engage confidently and follow study protocols reliably.

Improve Data Quality

Tailored training improves participant understanding of study requirements, promoting consistent reporting and tool usage. It reduces errors, improves protocol adherence, and strengthens the reliability of collected data.

Adapt for Participant Diversity

We tailor training materials to meet the needs of diverse populations—adapting for language, literacy levels, cultural context, and digital comfort to ensure clear understanding and confident participation.

Patient Journey Optimization

Design participant-centered trials that foster trust, minimize burden, and improve study reliability.

Simplifying the Patient Experience

We identify potential roadblocks in the participant journey and address them early—streamlining interactions, clarifying instructions, and building participant confidence. The result is improved engagement, stronger retention, and higher-quality data throughout the trial.

Promote Protocol Adherence

We design engagement and support strategies that guide participants through complex protocols—reducing the risk of deviations and increasing consistency across study arms, visit schedules, and diverse geographies.

Evidence Strategy

Design studies that produce both regulatory and market-access data for long-term success.

Build a Value-Centric Evidence Plan

We design trials that go beyond traditional efficacy endpoints—strategically integrating economic, quality-of-life, and real-world data to support reimbursement, value-based care, and stakeholder alignment.

Extend Impact Beyond Approval

We help sponsors plan for post-market success by identifying endpoints and data strategies that enable early access, pricing justification, and global expansion—turning study outputs into long-term value.

Regulatory Guidance

Align your protocols, technologies, and strategies with global regulatory standards.

Navigate Global Requirements

We guide sponsors through region-specific regulatory landscapes—advising on decentralized design, data privacy, informed consent, and remote oversight. This helps reduce friction, resolve local compliance challenges, and enable cross-border approvals.

Strengthen Protocol Readiness

We review and refine protocols to align with global regulatory expectations—ensuring your study design meets standards for safety, data quality, and participant protection across digital and hybrid trial models.
Next Step:
Recruitment & Prescreening