In diabetes clinical trial studies, patients are often asked to track blood glucose levels, insulin intake, and even record and report meals. With these requests we place significant burden on patients who already face many challenges in managing their own treatment.
Increasing the burden on patients without considering how to better engage them and make the process as seamless as possible often results in lower study compliance and a frustrating lack of information for trial outcomes.
Join Katie Garner, Therapeutic Areas Manager at CRF Health, for an educational webinar on best practices for improving the collection of PRO data in diabetes trials, including:
- Key considerations when using eCOA in diabetes trials.
- How integrated technology supports patients and investigators
- Designing patient-centric eCOA solutions for diabetes studies
About the Author
Therapeutics Area Manager at CRF HealthMore Content by Katie Garner