Electronic Patient Reported Outcome (ePRO)

Stay on top of the latest trend, best practices, and enabling technology in clinical research space through our latest blogs, webinars, white-papers and more about this topic.

Strategies to Minimize Participant and Healthcare Provider Burden in Clinical Trials

This article examines strategies to reduce participant and provider burden in clinical trials while ensuring high-quality data collection....

30 December 2024

What do we measure with PROs in head and neck cancer? Pain, QoL, adverse events and more

Patient-Reported Outcomes (PROs) are essential in head and neck cancer research, offering insights into symptoms, quality of life,...

24 September 2024

Unlocking FDA’s Vision for PRO Collection in RWE: Timing, Methods, and Insights

Discover FDA's guidance on collecting PROs for Real-World Evidence (RWE), focusing on timing, methods, and improving data quality.

eCOA: Afterthought or Essential Strategy? An Expert’s View on Choosing and Developing an eCOA Strategy

The Evolving Landscape of eCOA in Clinical Trials Clinical trials have long grappled with the complexities of data...

Evaluating “Bother” as a Component of Patient-Reported Outcomes in Clinical Studies

Patient-reported outcome (PRO) instruments refer to multiple scales and questionnaires designed to collect patients’ personal feedback on their...

Revolutionizing Blood Pressure Monitoring: Insights from Aktiia and Castor’s Collaboration

How Aktiia brought their continuous BP device to market by integrating vast amounts of blood pressure data with...

5 Best Practices for Getting Started with ePRO

Electronic Patient Reported Outcomes (ePRO) can become a powerhouse for gathering high-quality data directly from patients. To help...

Can BYOD help us end an era of waste and burden in eCOA?

Bring Your Own Device (BYOD) represents the future of eCOA, and prioritizes flexibility & convenience for trial participants....

Measuring the true patient experience in Cancer Trials with ePRO

Shedding light on the complexities and advancements in measuring PROs, drug tolerability, and quality of life in cancer...

The Place of PROs in the Future of Healthcare

Learn how integrating Patient-Reported Outcomes (PROs) into clinical trials can drive success in Value-Based Care (VBC).

Unlocking the power of Real-World Evidence in FDA submissions

An avalanche of data from so many real-world sources is available today, with the promise of more data...

21 November 2022

AKRN optimizes patient assessment collection with Castor ePRO

Castor's ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own,...

22 September 2022

AKRN handles mid-study changes in medical device clinical trials with Castor EDC

AKRN Scientific Consulting, a medical device CRO, used Castor's flexible EDC solution to handle constant mid-study changes for...

Electronic Case Report Forms (eCRFs) in Clinical Trials: Shifting to a Modern Research Paradigm

Castor is shifting the research paradigm for eCRF in clinical trials, transitioning from old, inefficient processes to a...

PMCF & RWE: Roles of Medical Device Registry Studies & ePROs

Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes...

10 November 2020

Electronic Patient Reported Outcome (ePRO) Measures: Questionnaires & More

Patient reported outcome measures in clinical trials have traditionally been done on paper. Surveys are a common way...

Mitigating the impact of COVID-19 on clinical research

Clinical trials are experiencing significant disruption worldwide due to the COVID-19 pandemic. Medical research is not immune to...

Forecasting the impact of COVID-19 on medical device trials

As of early April 2020, over 1,000,000 people have been confirmed infected with the SARS-CoV-2 coronavirus, and governments...

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