MedPath

Heart Failure Precision Medicine Study

Not Applicable
Recruiting
Conditions
Heart Failure
Interventions
Device: Telemonitoring devices
Registration Number
NCT04196842
Lead Sponsor
University of California, Davis
Brief Summary

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.

Detailed Description

In the US, the estimated prevalence of Heart Failure (HF) is 6.2 million and increasing. The mortality approaches 50% within 5 years of diagnosis and HF is the main cause of hospitalization among patients over 65 years of age. Information on molecular states may enhance understanding of causes and pathophysiological processes, improve risk prediction, identify new therapeutic targets, and improve subclassification for targeted therapy. Time-dependent phenomapping has been used to identify clinical and genomic differences in a longitudinal fashion, which provides a mechanistic link underlying pathophysiology of the disease and associated outcomes. Studies including high-throughput molecular approaches (multi-omics) along with time-dependent phenomapping would likely be even more powerful. The overarching hypothesis of the study is that the integration of Multi-Omics studies with clinical variables can be implemented to identify patients at risk of adverse outcomes. To test this hypothesis we propose: (1) Longitudinal profiling based on clinical data; (2) Longitudinal Multi-Omics Profiling; and (3) randomized of a telemonitoring intervention (Sensor Profiling) and the effectiveness in the optimization of guideline-directed medical therapy. To achieve these aims we propose to: (1) recruit a cohort of 1000 participants; (2) perform cardiovascular clinical characterization from electronic medical records; (3) perform multi-omics studies and (4) randomization of a telemonitoring intervention in the optimization of guideline-directed medical therapy. Proving these hypotheses would identify different meaningful clinical groups of patients within a cohort of patients with similar clinical conditions, health care providers would have a better understanding of the heterogeneity of the disease and the need for different preventive and therapeutic approaches in the context of precision medicine.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Diagnosis of Heart failure
  • Objective evidence of cardiac abnormality of structure or function (abnormal ECHO) or elevated levels of B-type natriuretic peptide (>100 pg/ml)
  • HF stage B-D and class I-IV
Exclusion Criteria
  • Patients unable to consent
  • Inability to comply with the protocol and follow-up requirements
  • Patients unable to use a smartphone
  • Patients assessed irregularly (less than two visits in one year)
  • History of HTx
  • Use of Mechanical circulatory support device (MCSD)
  • Comorbidities that, according to the PI, have the potential to interfere with the interpretation of the results

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
TelemonitoringTelemonitoring devicesBlood pressure and heart rate monitoring, scale, activity tracker.
Primary Outcome Measures
NameTimeMethod
Rate of adverse outcomes in heart failureFive years from enrollment

Rate of Mortality (all cause), hospitalization, Mechanical circulatory support device (MCSD) or heart transplant (HTx)

Secondary Outcome Measures
NameTimeMethod
Disease progressionFive years from enrollment

Disease severity (ACC/AHA Heart Failure classification system)

Trial Locations

Locations (1)

UC Davis Medical Center

🇺🇸

Sacramento, California, United States

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