Autonom-e for Research

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A complete and customisable digital solution for the design, delivery, and management of research studies

  • Customisable eCOA tools and eConsent forms
  • Automatic anonymisation of data at the point of collection before sharing with authorised research teams
  • Scalable research platform deployable across multiple clinical sites, public environments, and international territories worldwide
  • A proven platform used to deliver NIHR, Innovate UK, ESRC, MRC funded projects, and national service evaluations for NHS England, NHS Scotland, and Universities globally.
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The system has been developed to support scalable research studies at local, regional, national and international level.

Research teams of varying size are able to configure the platform’s features based on a study’s protocol, desired duration and participant information.

The Portal

About the Web Portal

Digital autonom-e offers an online web portal for research organisations to manage their study cohort across one or more localities.

From here, staff can set up new participants, configure different PROMs, view results, and access powerful reporting tools for the individual participant, the overall cohort, or a pre-defined group of users.

Reports are automatically generated which can be exported for external storage.

The system is hosted in the cloud, meaning no installation is required.

Pseudonymised data can also be viewed by staff with lower access rights.

The App

About the App

Participants have access to their own dedicated profile on mobile or online via our web app, meaning even those without personal devices can access autonom-e online; independently, with a carer, or family member as part of a telephone appointment.

Participants can use the app to complete assessments, track progress and follow study protocols.

Key Features and Benefits

  • Access to clinically validated PROMs.
  • Access to other common PROMs and PREMs prescribed by clinics, including the EQ-5D-5L, PHQ9, GAD7, FFT and more le (aAP) Diary for dysautonomia
  • Access to relevant support resources related to study or clinical practice if running concurrent to the study.
  • Dedicated profiles for participants.
  • Unique, secure login.
  • Available on mobile.
  • Available online via a web app on tablet or desktop for those without access to a mobile.
  • Accessible by staff to complete with participants via telephone.
  • Complete assessments independently, with a carer, or with staff in a telephone appointment.
  • View assessment history and track progress over time.
  • Simple, insightful graphs to understand changes in symptom severity.
  • Goal setting and e-diaries.
  • Configurable automatic reminders.

Research Tools

  • Configure scalable multi-site research projects to run separate or concurrently to clinical practice
  • Customisable eCOAs / PROMs according to protocol
  • Automatic reminders for completion
  • Configurable e-consenting process
  • Automatic pseudonymisation of data based on participant consent
  • Access to PIS and study material within the app
  • Direct anonymous communication with participants
  • Interactive reporting tools to analyse different demographic groups and compare cohorts

Benefits for Researchers

  • Research staff-time reduced by up to 90%
  • Improved compliance and adherence to study protocol
  • C19-YRS heavily cited in literature for comparison
  • Numerous configuration options
  • Automatic filtering of participants that give consent
  • Time saving in recording consent manually
  • Compliance with necessary data protection and ethical requirements
  • Continous, enhanced, accelerated data analysis, auditing and evaluation
  • Automatically generate reports for individual participants or study cohort

The Web Portal: for Research

  • Secure and compliant research tool to collect data anonymously for use in research.
  • Customisable e-consent forms.
  • Oversee study participants across multiple research sites.
  • Customisable assessments and tasks as per study protocol.

Custom assessments and support resources for multiple conditions.

Easy to use, secure, and scalable platform to oversee patients.

User friendly with visual aids for patients to monitor progress.

Reduce paper, save time and money.

Research Projects

LOCOMOTION Long COVID Study

The University of Leeds led a £3.4 million multi-national research study on Long Covid funded by the NIHR. It includes 8 UK Universities and 10 NHS sites, with ELAROS named as its technology partner. The digital C19-YRS system is central to the project and will accelerate the remote collection of patient data collection from 3 British nations.

National Service Evaluations for NHS England and NHS Scotland

In 2023, NHS England commissioned University of Leeds to evaluate clinical outcomes collected across 14 NHS Long COVID Services using ELAROS' digital platform to support commissioning guidelines for Post Covid services.

In 2024, a similar study was commissioned by NHS Scotland for national outcomes collected across 11 Scottish Health Boards using ELAROS' platform as part of a nationally commissioned clinical rollout of our system.

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