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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 WeGuide?

WeGuide is a platform for running clinical studies, registries and care programs through an app on participants' own phones (iOS and Android). Researchers and clinicians screen and consent participants with eConsent, send ePRO and PROM surveys with reminders, and track results in analytics. Wearable data comes in through a native Garmin integration, including raw accelerometer and gyroscope data on supported models, and through Apple Health and Health Connect. Data flows to REDCap by API, and to Castor and Medidata Rave. WeGuide is Class I medical device software on the ARTG (355337) and ISO 27001 certified. It supports 21 CFR Part 11, HIPAA and GDPR requirements, and participant data stays in Australian data centres. The BRACE trial, led by Murdoch Children's Research Institute, ran on it in five countries. Pricing is project based, with all modules in the core licence. WeGuide Pty Ltd is based in Melbourne and is a product from Curve Tomorrow.

Media

Media

Integrations Supported

Integrations Supported

Castor EDC
REDCap

API Availability

API Availability

Pricing Information

Pricing not provided

Pricing Information

Project based, all modules included in the core licence. Pricing on request.

Supported Platforms

SaaS

Supported Platforms

SaaS
Android
iPhone
On-Prem

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Not specified

Training Options

Documentation Hub
Online Training
On-Site Training

Training Options

Not specified

Company Facts

Organization Name

uMotif

Date Founded

2012

Company Location

United Kingdom

Company Website

umotif.com

Company Facts

Organization Name

WeGuide Pty Ltd

Company Location

The Royal Children's Hospital, Ground Floor, 50 Flemington Road, Parkville VIC 3052, Australia

Company Website

www.weguide.health

Categories and Features

Categories and Features

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