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Implementation Strategies for a Simple Intervention to Reduce Longterm Benzodiazepine Use in Dutch Community Pharmacies

R

Radboud University Medical Center

Status

Completed

Conditions

Benzodiazepines Therapeutic Use

Treatments

Behavioral: training and follow-up of pharmacists
Behavioral: patient-directed discontinuation letter

Study type

Interventional

Funder types

Other

Identifiers

NCT00268775
WOK/WINAp/CZ-01

Details and patient eligibility

About

The purpose of this study is to compare the effect of two implementation strategies for a simple patient-directed intervention to reduce long-term benzodiazepine use in Dutch community pharmacies.

Full description

In Dutch community pharmacies many projects have been undertaken in the field of pharmaceutical care, with mixed results. It is not yet clear which elements exactly contribute to the success of these projects and to implementation of pharmaceutical care.

One of the subjects to which attention is paid in community pharmacies, is the undesirable long-term use of benzodiazepines. Treatment methods for discontinuation of long-term benzodiazepine use have been studied rather extensively. A simple patient-directed discontinuation letter proved to be effective in several studies.

Comparison: a minimal intervention group (pharmacists carrying out the intervention guided by a manual only) compared to a maximal intervention group (pharmacists receiving a manual, a training aimed at better cooperation and communication with family practitioners and some support in the management of the project).

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • benzodiazepine use for more than 3 months in the last 12 months AND for more than 60 days in the last 2 months

Exclusion criteria

  • treatment by psychiatrist, treatment of alcohol- or drug misuse, psychotic episodes in history, epilepsy, terminal disease, not mastering the Dutch language, individual criteria used by the family practitioner

Trial contacts and locations

90

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Data sourced from clinicaltrials.gov

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