Electronic Clinical Outcome Assessment refers to the use of electronic devices, such as smartphones, tablets, or computers, to collect patient-reported outcome measures, clinical assessments, and other relevant data directly from study participants.
Set-up your eCOA solution fast with our validatet scale libary, collect high quality clinical data and monitor the process in a single or multi-centre trial.
Your Research offers the most innovative modules (eCRF, ClinRO, ePRO, PerfO, ObsRo) to collect data, with role based access and notifications on key decisions and monitoring.
Replace traditional paper-based methods and enable efficient and accurate data collection, enhancing the quality and reliability of clinical trial outcomes.
eCOA allows for the electronic capture of validated patient-reported outcome measures, clinical assessments, and other relevant data directly from study participants, replacing traditional paper-based methods.
Data can be collected in real-time, providing immediate access to patient-reported information.
This enables researchers to monitor patient progress, assess treatment efficacy, and make timely decisions based on up-to-date data.
The Your Research eCOA module provides standardised assessments and data collection processes, ensuring consistency and minimising variability in data entry and reporting.
This helps maintain data quality and enhances the reliability of clinical trial results.
Accelerate data entry, reduce administrative burden, and have real-time access to collected data.
eCOA eliminates the errors and inconsistencies associated with manual data entry, ensuring accurate and reliable collection of patient-reported outcomes and clinical assessments.
This leads to higher data quality and improves the overall validity of trial results.
The Your Research eCOA module offers a user-friendly interfaces with interactive features that engage participants in the data collection process.
This can lead to higher patient compliance, as it simplifies and streamlines the reporting of symptoms, adherence to treatment protocols, and overall participation in the study.
eCOA enables efficient data collection, as it automates the process of capturing and managing patient-reported data.
This accelerates data entry, reduces administrative burden, and allows for real-time access to collected data, facilitating quicker analysis and decision-making by researchers and sponsors.
Discover how the Your Research eCOA module optimises clinical trials and academic research, enhancing data collection and participant comprehension.
With Your Research, you have the flexibility to utilize stand-alone modules, integrate them with your existing software vendors, or connect them to other modules within Your Research to enhance the participant journey.