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Clinical Trials/NCT00848224
NCT00848224
Completed
N/A

Improving Adherence to Pharmacological Treatment

University of Massachusetts, Worcester1 site in 1 country689 target enrollmentSeptember 2000

Overview

Phase
N/A
Intervention
Not specified
Conditions
Medication Adherence
Sponsor
University of Massachusetts, Worcester
Enrollment
689
Locations
1
Primary Endpoint
The primary outcome evaluated is the percentage of patients with a serum low-density lipoprotein cholesterol (LDL-C) level <70 mg/dl.
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The overall goal of this study was to implement and evaluate the effects of a systems-based and pharmacist-mediated program designed to improve adherence for patients with known coronary heart disease (CHD) to lipid-lowering pharmacologic therapy and of their physicians/nurse practitioners to the National Cholesterol Education Program Guidelines.

Detailed Description

Patients were randomly assigned to a usual care condition which consisted of patients provided with usual care only, or to the Special Intervention (SI) condition. The intervention was implemented and coordinated by pharmacists, who utilized for tracking and communication the Lotus Notes®-based system that was developed for the project.

Registry
clinicaltrials.gov
Start Date
September 2000
End Date
May 2005
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Massachusetts, Worcester

Eligibility Criteria

Inclusion Criteria

  • was between 30 and 85 years of age;
  • had known CHD, defined as the presence of at least one coronary lesion at coronary angiography of \>50%.

Exclusion Criteria

  • was unable or unwilling to give informed consent;
  • had a history of intolerance to two or more statin drugs;
  • planned to move out of the area within one year of recruitment;
  • had a poor prognosis such that life expectancy was thought to be \<5 years;
  • had a psychiatric illness which limited ability to participate; or
  • had no telephone.

Outcomes

Primary Outcomes

The primary outcome evaluated is the percentage of patients with a serum low-density lipoprotein cholesterol (LDL-C) level <70 mg/dl.

Time Frame: One year

Secondary Outcomes

  • Proportion of prescribed lipid-lowering medication taken by patients as measured by a continuous multiple-interval (CMA) measure of medication availability based on pharmacy records.(One year)

Study Sites (1)

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