A Community Pharmacist-led Intervention to Improve Adherence to Lipid-lowering Treatment

NCT00493337 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 373

Last updated 2010-06-28

No results posted yet for this study

Summary

The objective of the study is to test the effectiveness of a community pharmacist-led intervention to increase adherence to lipid lowering treatment.

Conditions

Interventions

BEHAVIORAL

advanced adherence counseling+reminder

DEVICE

Compliance Card

Sponsors & Collaborators

  • Service Apotheek BV

    collaborator UNKNOWN
  • Harvard University

    collaborator OTHER
  • Department of Clinical Pharmacy, University Medical Centre St Radboud, The Netherlands.

    collaborator OTHER
  • Scientific Institute for Dutch Pharmacists, The Netherlands

    collaborator OTHER
  • Federation of Patients and Consumer Organisations in the Netherlands

    collaborator UNKNOWN
  • Utrecht Institute for Pharmaceutical Sciences

    lead OTHER

Principal Investigators

  • Boris LG Van Wijk, PharmD, PhD · Department of Pharmacoepidemiology & Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences, Utrecht University

  • Anthonius De Boer, MD, PhD · Department of Pharmacoepidemiology & Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences, Utrecht University

  • Olaf H Klungel, PharmD, PhD · Department of Pharmacoepidemiology & Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences, Utrecht University

  • William H Shrank, MD, MSHS · Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston

  • Peter AG De Smet, PharmD, PhD · Scientific Institute of Dutch Pharmacists, The Hague

  • Eibert R Heerdink, PhD · Department of Pharmacoepidemiology & Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences, Utrecht University

  • Emma Giesen, PharmD · Service Apotheek BV

  • Marnix Westein, PharmD · Federation of Patients and Consumer Organisations in the Netherlands, Utrecht, The Netherlands

  • Martina Teichert, PharmD · Scientific Institute of Dutch Pharmacists, The Hague, The Netherlands

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
65 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2010-03-31
Completion
2010-03-31

Countries

  • Netherlands

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00493337 on ClinicalTrials.gov