Digital monitoring for patients after heart procedures
Official title: Digital Monitoring for Patients Post Coronary Interventions to Reduce Risk for Recurrent Adverse Cardiovascular Events
Run by University of California, Davis · NCT06114615 · Data updated 2026-11-12
This study is testing if a new telemonitoring program can help people recovering from heart procedures feel better and manage their health more effectively compared to standard care.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | University of California, Davis Academic / other |
| Locations | 1 site (Sacramento, California) |
| Status | Recruiting |
| Started | January 1, 2024 |
| Main results expected | January 1, 2027 |
| Study ends | January 1, 2027 |
| Registry record updated | February 23, 2026 |
| Trial ID | NCT06114615 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients diagnosed with coronary artery disease who are undergoing percutaneous coronary intervention at the University of California, Davis Health.
✕Probably not a fit
Patients who do not have coronary artery disease or are not undergoing PCI may not receive any benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study supports patients recovering from percutaneous coronary intervention (PCI) by implementing a telemonitoring program. Participants with coronary artery disease will be divided into two groups: one receiving remote monitoring and text-based follow-up, and the other receiving standard care. The intervention group will have established health goals and education on using the telemonitoring application, while outcomes such as blood pressure, LDL levels, and patient satisfaction will be measured. The findings aim to enhance post-PCI patient care and provide evidence for the broader implementation of telemonitoring in healthcare systems.
Why it matters
Potential benefit: If successful, this approach could significantly improve patient outcomes and reduce the risk of recurrent cardiovascular events after PCI.
How similar studies have gone: Other studies have shown success with telemonitoring approaches in managing cardiovascular conditions, indicating potential for this method.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Includes patients with coronary heart disease diagnosis and treatment with PCI who follow up at University of California Davis Health.
Where it's running
-
University of California, Davis Medical Center Division of Cardiovascular Medicine
Sacramento, California, United States Recruiting
Study contacts
- Study coordinator: Surabhi Atreja, MD
- Email: smatreja@ucdavis.edu
- Phone: (916) 734-2011
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.