Improving Adherence to Pharmacological Treatment
Completed · Not applicable
Conditions studied: Medication Adherence
In brief
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.
Key facts
- Study ID
- NCT00848224
- Run by
- University of Massachusetts, Worcester
- People needed
- 689
- Starts
- 2000-09-01
- Expected to finish
- 2005-05-01
- Last updated by the study team
- 2009-02-20
Who can join
Age: 30 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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%.
You may not qualify if…
- 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.
Where it is running
- UMass Memorial Medical Center — Worcester, Massachusetts, United States
Full record on ClinicalTrials.gov
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