Evaluation of an Outpatient Modified Prescription Form

This study has been completed.
Sponsor:
Collaborator:
Health Resources and Services Administration (HRSA)
Information provided by (Responsible Party):
Amanda Kennedy, University of Vermont
ClinicalTrials.gov Identifier:
NCT00256594
First received: November 17, 2005
Last updated: December 14, 2011
Last verified: December 2011

November 17, 2005
December 14, 2011
August 2005
February 2010   (final data collection date for primary outcome measure)
error rates of standard versus modified prescriptions per prescriber [ Time Frame: 200 prescriptions each ] [ Designated as safety issue: No ]
error rates of standard versus modified prescriptions per prescriber
Complete list of historical versions of study NCT00256594 on ClinicalTrials.gov Archive Site
 
differences in omissions, commissions, legibility, use of prohibited abbreviations, and satisfaction between standard and modified prescriptions per prescriber
 
 
 
Evaluation of an Outpatient Modified Prescription Form
Evaluation of an Outpatient Modified Paper Prescription Form in 4 Rural States to Address the Public Health Problem of Prescribing Error

The purpose of this study is to determine if a modified paper prescribing form decreases prescribing errors compared to a traditional or standard paper prescribing form.

The broad goal of this proposal is to reduce outpatient prescribing errors in rural primary care practices. Although computerized technology is available for prescribing, it has not yet been implemented in most settings. Additionally, rural prescribers will likely be the last to have the means to adopt this technology. Due to the substantial morbidity and mortality in the United States caused by outpatient medication errors, there is an urgent need for low-cost solutions. This research plan will evaluate a modified paper prescription form that may be implemented in rural primary care settings cheaply and quickly with the goal of outpatient prescription error reduction.

The specific aims of this project are:

  1. To determine if a modified paper prescription form decreases overall prescribing errors compared to a standard paper prescription form
  2. To determine if a modified paper prescription form decreases omission errors compared to a standard paper prescription form
  3. To determine prescriber satisfaction with the modified prescription form

Rural prescribers from four states will be randomly recruited to write prescriptions on standard and modified forms. Prescription duplicates of both types will be analyzed for errors. Prescriber satisfaction with the modified form will be evaluated using surveys and focus groups.

Medication errors are a public health problem. Low-cost technology that is shown to reduce medication errors would benefit all rural patients who receive prescriptions.

Interventional
 
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Prevention
Medication Errors
Device: prescription form
Two prescription pads contained modified forms and two prescription pads were similar to the prescription pads the prescriber had been using. Providers completed 100 standard and 100 modified prescriptions
 

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
84
January 2011
February 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Must be a physician, nurse practitioner, or physician assistant with a current license to write outpatient prescriptions
  • Must practice in Family Practice, Internal Medicine, or Pediatrics
  • Must practice in rural Vermont, West Virginia, South Dakota, or Montana
  • Must write outpatient paper prescriptions
  • Must write prescriptions in English

Exclusion Criteria:

  • Not licensed to write prescriptions
  • Practice in a specialty, inpatient, or long term care setting
  • Do not write paper prescriptions
  • Do not write prescriptions in English
Both
21 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00256594
1 R04RH05814-01-00
No
Amanda Kennedy, University of Vermont
University of Vermont
Health Resources and Services Administration (HRSA)
Principal Investigator: Amanda G Kennedy, PharmD University of Vermont
University of Vermont
December 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP