Digital Monitoring for Patients Post Coronary Interventions to Reduce Risk for Recurrent Adverse Cardiovascular Events

Part of paid clinical trials in Sacramento, California.

Sponsor
University of California, Davis
Study ID
NCT06114615
Status
Recruiting
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Conditions

  • Coronary Artery Disease

Eligibility Criteria

Sex
ALL
Age
N/A - N/A
Healthy Volunteers
Not accepted

Interventions

  • LiveCare — DEVICE
    Patient use LiveCare device to monitor their blood pressure and data is transmitted to dashboard.
  • Text Messages — BEHAVIORAL
    Patients also receive text messages after their PCI procedure for follow up appointment reminders, enrollment in cardiac rehab, and diet and exercise counseling.
  • Conventional Care — OTHER
    No digital monitoring with LiveCare device and no text messages.

Study Details

The study aims to support patients immediately after percutaneous coronary intervention (PCI) by implementing a telemonitoring program. Eligible patients have coronary heart disease and undergo PCI. The intervention group receives remote monitoring and text-based follow-up, with established health goals and education on using the telemonitoring application, along with necessary devices. The control group gets standard care. Outcomes measured include blood pressure, LDL levels, patient satisfaction, revascularization, and mortality. The study findings will enhance patient care after PCI and contribute evidence for widespread telemonitoring implementation in healthcare systems, aiding medical therapy and lifestyle modifications.

Key Dates

Start date
Jan 1, 2024
Status verified
Feb 2026
Primary completion
Jan 1, 2027
Completion
Jan 1, 2027

Study Design

Enrollment
200 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Active Comparator: Discharged with LiveCare and Text Message Intervention
    Patients receive blood pressure monitoring and text messages reminders for enrollment in cardiac rehab, follow up appointment, diet and exercise counseling.
  • Sham Comparator: Discharged with Conventional Care
    Patients do not receive blood pressure monitoring and text messages reminders for enrollment in cardiac rehab, follow up appointment, diet and exercise counseling.

Primary Outcome Measure

blood pressure, systolic and diastolic [ Time Frame: 1 month, 6 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of California, Davis Medical Center Division of Cardiovascular MedicineSacramentoCalifornia95817
Surabhi Atreja, MD
[email protected]
916-734-6082

Find similar trials in Sacramento, CA

By research site
University of California, Davis Medical Center Division of Cardiovascular Medicine· Sacramento, CA

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