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Clinical Trials/NCT00127751
NCT00127751
Completed
Phase 2

A Cardiovascular Disease Multifactor Risk Reduction Program for Medically Underserved High-Risk Patients

Stanford University1 site in 1 country150 target enrollmentMay 2000

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Coronary Heart Disease
Sponsor
Stanford University
Enrollment
150
Locations
1
Primary Endpoint
Cardiovascular disease risk score
Status
Completed
Last Updated
20 years ago

Overview

Brief Summary

The primary objective of this study was to evaluate the effectiveness of a multifactor cardiovascular disease (CVD) risk reduction program using team case management in high risk patients who have low family incomes and limited access to medical care. Patients were randomized to case management (99) or usual care (49) with baseline, 6-month and 12-month evaluations of CVD risk factors, clinical status and quality of life.

Detailed Description

The primary objective of this study was to evaluate the effectiveness of a multifactor cardiovascular disease (CVD) risk reduction program using team case management in high risk patients who have low family incomes and limited access to medical care. Patients were randomized to case management (99) or usual care (49) with baseline, 6-month and 12-month evaluations of CVD risk factors, clinical status and quality of life. Subjects were primarily recruited from patients being seen in free medical clinics in Santa Clara County California. Primary eligibility was ≥ 35 years of age, one or more CVD risk factors (with or without clinical CVD), low family income, and residing in Santa Clara County. Patients in the case management group were provided counseling services by specially trained registered nurses (RNs) and registered dieticians (RDs) and assisted in obtaining medications and medical services from programs provided in the county or indigent drug programs provided by selected pharmaceutical companies. Protocol driven treatment algorithms based on national practice guidelines were used and use of existing programs and resources were maximized. On average patients in case management were seen by staff 6-9 in the 12 months.

Registry
clinicaltrials.gov
Start Date
May 2000
End Date
May 2003
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Men and women ≥ 35 years
  • One or more major risk factors
  • Live in Santa Clara County
  • Low family income that limits access to medical care

Exclusion Criteria

  • Under active medical treatment for cancer, CVD or other major medical disorder
  • Reasonable access to health care
  • Under 35 years of age
  • Not a resident of Santa Clara County

Outcomes

Primary Outcomes

Cardiovascular disease risk score

Low-density lipoprotein (LDL)-cholesterol

Systolic blood pressure

Secondary Outcomes

  • Body mass index (BMI)
  • Physical activity score
  • Nutrition score

Study Sites (1)

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