Study of Messaging to Providers for Chronic Kidney Disease Treatment
This study is testing a new way to help doctors treat Chronic Kidney Disease (CKD) more effectively. It involves a "best practice alert" and "order set" that pops up on a doctor's computer screen when they open a patient's medical record. This alert reminds them about your CKD, shows your lab results, and suggests specific guideline-directed medical therapies (GDMT) that might be helpful. The goal is to see if this tool encourages doctors to prescribe these recommended treatments more often within 90 days. You might be eligible if you are 18 or older and have CKD, defined by specific eGFR (a measure of kidney function) and uACR (a measure of protein in urine) levels. The study aims to enroll 1000 participants.
- Study design
- This is a cluster-randomized clinical trial. Providers will be assigned to either receive the best practice alert or continue with usual care.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your medical records will be reviewed for new GDMT prescriptions within 90 days.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Pragmatic Trial of Messaging to Providers About Treatment of Chronic Kidney Disease
At a glance
Conditions
NCT07430930
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Yale New Haven Health
New Haven, Connecticutno site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Francis P Wilson, MD MSCE · PRINCIPAL_INVESTIGATOR · Yale University
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- New GDMT prescription within 90 daysUp to 90 days of randomization
Proportion of patient subjects with one or more new eligible GDMT prescriptions within 90 days of randomization.