Revolutionizing Clinical Trials: The Future of eCOA Research & Patient-Centered Solutions

In a digital-first world, the future of clinical trials is no longer bound by clinic walls. Thanks to the power of eCOA research (electronic Clinical Outcome Assessments), innovative technologies are transforming how data is collected, how patients participate, and how sponsors manage trials.

At the forefront of this evolution is Delve Health—your partner in building smarter, decentralized, and patient-first clinical trials.

Let’s dive into how eCOA research and ePRO (electronic Patient-Reported Outcomes) are reshaping the landscape of modern medicine.

About Us: Who We Are
Delve Health is a leading digital health company committed to delivering decentralized clinical trial (DCT) solutions. We specialize in eCOA research that bridges the gap between patients and researchers—wherever they are.

With our scalable platform, sponsors, CROs, and sites can empower patients with seamless, secure, and intuitive tools that make participation easier and data collection more accurate.

Our Mission
Our mission is to make clinical trials more human, accessible, and data-driven.

Enable access to all patients, regardless of geography or health condition

Improve data quality with real-time digital tools

Reduce site burdens and administrative delays

Foster diversity by expanding trial reach

Leverage automation for smarter decision-making

With Delve Health, research becomes more inclusive, efficient, and impactful.

What is eCOA Research?
Electronic Clinical Outcome Assessments (eCOA) allow researchers to digitally collect health outcomes from patients, clinicians, and observers. eCOA platforms include:

ePRO (Electronic Patient-Reported Outcomes)

ClinRO (Clinician-Reported Outcomes)

ObsRO (Observer-Reported Outcomes)

eCOA research allows for:

Real-time digital reporting

Remote trial participation

Greater accuracy and security

Patient-friendly engagement through multimedia and mobile devices

Our platform integrates all aspects of eCOA, providing a seamless digital experience from patient input to sponsor analysis.

Understanding ePRO Clinical Trials
ePRO trials empower patients to log symptoms, side effects, and daily well-being directly from their smartphones or tablets—no clinic visit needed.

With ePRO tools, you get:

Improved data accuracy

Real-time patient feedback

Increased patient engagement

Broader demographic inclusion

Our ePRO tools are built for ease of use, with automated reminders, multimedia guides, and analytics dashboards for real-time monitoring.

Key Features of Our eCOA & ePRO Platform

Real-Time Reporting
Patients can log their data anytime, anywhere, improving recall and minimizing missing data.

Multimedia Instructions
Video, images, and audio ensure patients understand their assessments clearly.

Compliance & Security
Delve Health meets all global standards:

HIPAA

GDPR

FDA 21 CFR Part 11

Smart Reminders
Our system keeps participants on track with alerts and automated follow-ups.

Wearable Integration
Seamless connectivity with popular wearables tracks:

Heart rate

Blood pressure

Oxygen levels (SpO2)

Temperature

Sleep & activity

Objective data from these devices complements self-reported outcomes—creating a full 360-degree patient profile.

Boost Study Management with IRT
Beyond ePRO and eCOA research, Delve Health includes Interactive Response Technology (IRT), giving sites and sponsors tools to:

Randomize participants

Track inventory

Access performance dashboards in real-time

This ensures smooth operations from recruitment to trial closeout. To get more information you can pop over to this site https://delvehealth.com/services/epro-ecoa/.

Anywhere Access: Join Trials from Home, Work, or on the Go
With Delve Health’s decentralized trial platform, participation is possible from:

Home

Workplace

While traveling

This flexibility increases retention, widens representation, and removes travel burdens—making trials more inclusive and effective.

Why Digital eCOA Research Works

Fast enrollment through digital pre-screening

Familiar devices = less training needed

Accurate data entry reduces manual errors

Audit-ready logs and time-stamped records

Enhanced patient understanding with media support

Reduced trial costs by minimizing physical site visits

The result? Better data, happier patients, and faster trials.

Why Partner with Delve Health?
When you choose Delve Health, you get more than software—you gain a dedicated partner in innovation.

Decades of experience in decentralized trials

Full integration with CTMS, EDC, and wearable devices

Flexible for small pilot or global Phase III trials

Designed for sponsors, CROs, and site teams

24/7 onboarding & tech support

Whether you're launching your first eCOA research study or scaling globally, we’re here to help you succeed—every step of the way.

Let’s Digitize Your Next Trial
Ready to modernize your research with Delve Health’s eCOA and ePRO solutions?

Address: 8100 Wayzata Blvd, Golden Valley, MN 55426, USA
Phone: +1 952-200-6228

Revolutionizing Clinical Trials with Wearable Vital Sign Monitors & eConsent

Welcome to a new era of clinical trials with Delve Health. We are transforming research by integrating wearable vital sign monitors, eConsent technology, and clinical trial IRT (Interactive Response Technology) to enhance patient engagement and optimize data accuracy.

Our mission is to revolutionize clinical research by ensuring a seamless, transparent, and patient-focused experience. Whether you're a researcher seeking innovative solutions or a patient looking for a hassle-free trial process, Delve Health is here to make participation more accessible and efficient.

About Us
At Delve Health, we are pioneers in digital health solutions. By integrating wearable vital sign monitors with eConsent and clinical trial IRT, we empower both researchers and patients with cutting-edge technology. Our solutions make clinical trials more efficient, data-driven, and patient-friendly.

We are dedicated to bridging the gap between technology and healthcare, ensuring that trials are faster, smarter, and more inclusive. Our focus is to streamline research while maintaining the highest standards of compliance and accuracy. For more information you can pop over to this site https://delvehealth.com/services/wearables/.

Our Mission
Our mission is simple: to enhance clinical trials with innovative, patient-centric technologies. By leveraging wearable vital sign monitors, eConsent, and IRT, we provide solutions that improve trial efficiency, patient engagement, and regulatory compliance.

We believe in making research more inclusive by enabling remote participation and real-time monitoring, ensuring that every patient has equal access to life-changing treatments.

Understanding Wearable Vital Sign Monitors, eConsent & Clinical Trial IRT
Wearable Vital Sign Monitors
Wearable devices track real-time patient health metrics like heart rate, blood pressure, oxygen levels, and temperature. These monitors provide continuous data, reducing the need for frequent hospital visits while improving trial accuracy.

eConsent (Electronic Informed Consent)
eConsent allows patients to digitally review and sign consent forms, using interactive tools like videos and infographics for better understanding. This method enhances transparency and ensures patients are fully informed before participating in a trial.

Clinical Trial IRT (Interactive Response Technology)
IRT automates trial logistics, including patient randomization, inventory management, and data tracking. This technology ensures smooth operations, compliance, and efficient data collection in real time.

How Delve Health Combines These Innovations
Interactive & Transparent eConsent
Patients receive consent forms with videos, infographics, and interactive Q&A sections to ensure clarity before signing. This leads to informed decision-making and greater trust.

Real-Time Monitoring with Wearable Vital Sign Monitors
Patients wear non-invasive devices that continuously track key health metrics, reducing the need for in-person visits and improving data accuracy. These devices send real-time updates directly to researchers.

Seamless Randomization & Data Collection
Using IRT, trial teams can randomize patients, track participation, and manage trial supplies efficiently—ensuring smooth operations and regulatory compliance.

Remote Accessibility for Global Trials
Patients can participate from anywhere using smartphones, tablets, or computers. This removes geographic barriers, making trials more inclusive and diverse.

Enhanced Compliance & Audit Trails
Automated tracking ensures every step is documented for regulatory compliance, minimizing risks while increasing transparency for all stakeholders.

Why Wearable Vital Sign Monitors & eConsent are Game-Changers
Continuous patient monitoring enhances data accuracy and safety
Faster enrollment and improved retention with eConsent
Remote participation eliminates travel barriers
Enhanced data integrity with real-time updates through IRT
Automated documentation and tracking ensure regulatory compliance
By integrating wearable vital sign monitors with eConsent and IRT, Delve Health empowers researchers to conduct faster, more efficient trials while prioritizing patient safety and comfort.

Why Choose Delve Health?
With years of expertise in wearable technology, eConsent, and clinical trial IRT, Delve Health provides unparalleled solutions to modernize research. Our commitment to innovation ensures that trials are conducted with accuracy, transparency, and inclusivity.

Whether you're a patient or a researcher, our technology-driven approach makes the clinical trial experience seamless, reliable, and patient-friendly.

Start Your Wearable-Powered Clinical Trial Journey with Delve Health Today!
Are you ready to experience the future of clinical trials? Let Delve Health transform the way research is conducted with wearable vital sign monitors, eConsent, and IRT.

Address: 8100 Wayzata Blvd, Golden Valley, MN 55426, United States
Phone: +1 952-200-6228