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UnknownNCT01985048

Cardiometabolic Risk in Cardiac Rehab

Cardiometabolic Risk in the Setting of Cardiac Rehabilitation

Status
Unknown
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Health Diagnostic Laboratory, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

1. Primary Objectives: * To characterize cardiometabolic risk factor profiles of patients entering cardiac rehab using traditional approaches (eg LDL-C) as well as a more comprehensive panel of cardiovascular and metabolic biomarkers. It is hypothesized that the comprehensive panel will identify further increased risk that would not have been detected using only traditional approaches. Specifically, it is hypothesized that a greater percentage of the cohort will be identified with "high risk" levels of LDL-P (\>1100 nmol/L) and/or apoB (\>80 mg/dL) than of LDL-C (\>100 mg/dL). It is further hypothesized that the prevalence of elevated Lp(a) and elevated levels of inflammatory and insulin resistance markers will be higher in this cohort when compared to population norms (HDL, inc reference data). * To assess improvements in laboratory and lifestyle risk factors and rate of goal attainment at completion of rehab (eg 3 months). This objective is primarily descriptive, and improvements in traditional risk factors (eg LDL-C) will be compared to existing published data. Improvements in non-traditional risk factors (eg LDL-P, insulin resistance markers) in a cardiac rehab population have not been extensively investigated. * To determine which attributes at baseline best predicted recurrent events and re-hospitalizations assessed one year later. 2. Secondary/Developmental Objective: * To inform and guide development of a subsequent study protocol designed to compare outcomes associated with biomarker-guided personalized treatment plans vs. standard of care in the cardiac rehab setting.

Detailed description

This pilot study will characterize risk factors of patients as they enter cardiac rehab, track how comprehensive biomarker profiles change during the normal course of rehab, and associate biomarkers at baseline with MACE outcomes assessed one year later. Blood draws, vitals, and patient medical histories will be collected as subjects enter rehab and at the end of the rehab program. Major adverse cardiac events will be assessed via phone interview at 12 months.

Conditions

Timeline

Start date
2013-10-01
Primary completion
2015-03-01
Completion
2015-03-01
First posted
2013-11-15
Last updated
2015-02-13

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01985048. Inclusion in this directory is not an endorsement.