Digital monitoring for patients after heart procedures
Digital Monitoring for Patients Post Coronary Interventions to Reduce Risk for Recurrent Adverse Cardiovascular Events
NA · University of California, Davis · NCT06114615
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
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Sex | All |
| Sponsor | University of California, Davis (other) |
| Locations | 1 site (Sacramento, California) |
| Trial ID | NCT06114615 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates are patients diagnosed with coronary artery disease who are undergoing percutaneous coronary intervention at the University of California, Davis Health.
Not a fit: Patients who do not have coronary artery disease or are not undergoing PCI may not receive any benefit from this study.
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 performed: Other studies have shown success with telemonitoring approaches in managing cardiovascular conditions, indicating potential for this method.
Eligibility criteria
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 this trial is running
Sacramento, California
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Coronary Artery Disease, post-PCI, digital monitoring, cardiac rehabilitation