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What is uMotif?

uMotif presents a groundbreaking platform for electronic Clinical Outcome Assessment (eCOA), electronic Patient-Reported Outcomes (ePRO), and electronic consent (eConsent), designed to bolster both clinical and real-world research initiatives. Developed with direct feedback from patients, this platform ensures exceptional engagement, leading to significant enhancements in the efficiency, quality, and accuracy of data gathering. By merging uMotif's eCOA/ePRO system with real-time glucose monitoring, the platform demonstrated impressive compliance rates during an extensive diabetes research project throughout Europe. In a separate case, an immunology trial reaped the benefits of the patient-centric eCOA/ePRO solution, allowing the sponsor to meet data collection targets a remarkable six months earlier than planned. Furthermore, during a CNS study required by the FDA, participants leveraged their own devices to submit ePRO data that was ready for review, illustrating the platform's adaptability. Committed to a patient-first design philosophy, uMotif places a strong emphasis on comprehending the patient experience and the variables that affect their actions. This deep-rooted understanding not only drives the creation of software tailored to patient needs but also achieves exceptionally high levels of engagement for study sponsors, creating a mutually beneficial scenario for all involved. With such innovative features, uMotif is poised to set new standards in the realm of patient-reported outcomes and clinical research methodologies.

What is Clinical StudyPal?

Our strategy for aiding your team starts with our groundbreaking, multi-dimensional platform. Clinical StudyPal serves as a complete, customizable, and patient-centered technology designed to optimize your research processes, rendering them faster, simpler, and more cost-effective. Functioning as a mobile application, it promotes collaboration and boosts interaction between sites and patients, while its web interface facilitates efficient study management backed by comprehensive analytics. Furthermore, it operates as a notification system, ensuring that both patients and the study team are kept well-informed at all times. What advantages might Clinical StudyPal provide for your organization? A more critical question could be, what constraints does it present? With our advanced technology and dedication to patient-focused solutions, our committed team is enthusiastic about supporting yours in establishing a smooth and successful trial experience tailored to your specific requirements. Ultimately, our aim is to empower your research initiatives in every conceivable manner, enhancing the overall effectiveness of your studies. By integrating Clinical StudyPal into your workflow, you can harness the full potential of modern technology to advance your clinical research.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

uMotif

Date Founded

2012

Company Location

United Kingdom

Company Website

umotif.com

Company Facts

Organization Name

Delve Health

Date Founded

2018

Company Location

United States

Company Website

delvehealth.com/services/

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

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