Heart Failure Precision Medicine Study

Part of paid clinical trials in Sacramento, California.

Sponsor
University of California, Davis
Study ID
NCT04196842
Status
Recruiting

Conditions

Eligibility Criteria

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

Interventions

  • Telemonitoring devices — DEVICE
    Set of telemonitoring devices: heart rate and blood pressure monitor, scale and activity tracker.

Study Details

The study aims to test the hypothesis that multi-omics studies can identify Heart Failure profiles at risk of adverse outcomes and evaluate a telemonitoring intervention in the optimization of guideline-directed medical therapy.

Key Dates

Start date
Oct 16, 2019
Status verified
Feb 2026
Primary completion
Oct 16, 2026
Completion
Oct 16, 2026

Study Design

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

Arms

  • Experimental: Telemonitoring
    Blood pressure and heart rate monitoring, scale, activity tracker.
  • No Intervention: No intervention
    No intervention.

Primary Outcome Measure

Rate of adverse outcomes in heart failure [ Time Frame: Five years from enrollment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
UC Davis Medical CenterSacramentoCalifornia95817
Pablo Acevedo, BS
916-703-2071

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