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Implementation of a Pharmacy-Intervention to Enhance Prescription and Use of Lipid-Lowering Drugs

R

Radboud University Medical Center

Status

Completed

Conditions

Cardiovascular Diseases

Treatments

Other: control
Other: intensive implementation programme

Study type

Interventional

Funder types

Other

Identifiers

NCT00509717
WOK/WINAp/CZ-02

Details and patient eligibility

About

The purpose of this study is to determine the effectiveness of maximal support of community pharmacies to implement a pharmaceutical care model for improving underprescription and treatment persistence regarding lipid-lowering medication in patients with cardiovascular disease.

Full description

Cardiovascular disease is the main cause of death in large parts of the world. Next to life style changes, pharmaceutical treatment is a keystone in the treatment of cardiovascular disease. Despite the strong evidence for the effectiveness of lipid-lowering therapy, less than half of the people eligible are treated. With specific medication searches in the community pharmacy database, an easy tool for detecting patients who are undertreated is available. Based on this tool, a pharmaceutical care model for improving underprescription and treatment persistence regarding lipid-lowering medication in patients with cardiovascular disease was constructed.

Moreover, it is not known yet how to implement this pharmaceutical care model in community pharmacies effectively. With multifaceted interventions the behaviour of health professionals can be changed. In this study the effectiveness of a maximal support strategy, including interactive educational meetings, reminders, audit and feedback, is compared to a minimal implementation strategy.

Enrollment

70 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • pharmacies: resident in the south of the Netherlands
  • patients: with antiplatelet therapy and without lipid-lowering medication

Exclusion Criteria:for patients:

  • terminal disease
  • severe mental disorder

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

experimental
Experimental group
Treatment:
Other: intensive implementation programme
control
Active Comparator group
Treatment:
Other: control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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