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Reducing the Unnecessary Use of Heavily Marketed Medications: A Randomized Controlled Trial

V

Veterans Affairs (VA) Boston Healthcare System

Status

Completed

Conditions

Use of Sleep Medications

Treatments

Behavioral: Alerts Plus Detailing
Behavioral: Computerized alerts

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT00788346
5.12.05

Details and patient eligibility

About

Prescribing decisions by clinicians are often thought to be simple: a patient's clinical problem leads a prescriber to choose the optimal treatment. However, many factors other than the patient's condition affect prescribing decisions, including the marketing of pharmaceuticals. Clinicians are subjected to direct "detailing" by representatives of the pharmaceutical industry, advertisements in medical journals and requests for specific treatments from patients, who are increasingly exposed to direct-to-consumer (DTC) advertising. These influences, often based on biased or inaccurate information, contribute to a variety of problems in prescribing, including the unnecessary use of expensive, heavily marketed medications.

Overcoming these influences requires innovative approaches. The movement toward widespread adoption of electronic health records (EHRs) and electronic prescribing presents new opportunities to educate both clinicians and patients at the time of medication prescribing. This project, endorsed by the AHRQ-supported Centers for Education and Research on Therapeutics (CERTs; www.certs.hhs.gov) and the U.S. Food and Drug Administration (FDA), aims to test the effectiveness of computerized prescribing alerts and state-of-the-art educational outreach to reduce the unnecessary use of heavily marketed medications. A second goal is to improve clinicians' knowledge of industry marketing practices, so that they can more effectively assess information provided by drug companies. Thus, the study has two specific aims:

Specific Aim 1: To assess whether computerized prescribing alerts linked electronically to patient educational material can reduce prescribing of heavily marketed medications.

Specific Aim 2: To assess whether group academic detailing increases clinicians' knowledge about industry marketing practices and increases the effect of prescribing alerts.

Enrollment

257 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Internal medicine clinicians

Exclusion criteria

  • none

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

257 participants in 3 patient groups

Computerized Alerts
Experimental group
Description:
Computerized Clinical Decision Support to clinician at the time of prescribing
Treatment:
Behavioral: Computerized alerts
Alerts PLUS Detailing
Experimental group
Description:
Computerized Clinical Decision Support to clinician at the time of prescribing PLUS one group academic detailing session
Treatment:
Behavioral: Alerts Plus Detailing
Usual Care
No Intervention group
Description:
Usual Care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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