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
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 - 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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