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Evaluation of an Outpatient Modified Prescription Form

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: University of Vermont
HRSA/Maternal and Child Health Bureau
Information provided by: University of Vermont
ClinicalTrials.gov Identifier: NCT00256594
  Purpose

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.


Condition Intervention
Medication Errors
Device: prescription form

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Randomized, Open Label, Placebo Control, Crossover Assignment, Safety/Efficacy Study
Official Title:   Evaluation of an Outpatient Modified Paper Prescription Form in 4 Rural States to Address the Public Health Problem of Prescribing Error

Further study details as provided by University of Vermont:

Primary Outcome Measures:
  • error rates of standard versus modified prescriptions per prescriber

Secondary Outcome Measures:
  • differences in omissions, commissions, legibility, use of prohibited abbreviations, and satisfaction between standard and modified prescriptions per prescriber

Estimated Enrollment:   100
Study Start Date:   August 2005
Estimated Study Completion Date:   August 2007

Detailed Description:

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.

  Eligibility
Ages Eligible for Study:   21 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

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
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00256594

Locations
United States, Vermont
University of Vermont, Division of General Internal Medicine    
      Burlington, Vermont, United States, 05401

Sponsors and Collaborators
University of Vermont
HRSA/Maternal and Child Health Bureau

Investigators
Principal Investigator:     Amanda G Kennedy, PharmD     University of Vermont    
  More Information


Publications:

Study ID Numbers:   1 R04RH05814-01-00
First Received:   November 17, 2005
Last Updated:   September 6, 2006
ClinicalTrials.gov Identifier:   NCT00256594
Health Authority:   United States: Institutional Review Board

Keywords provided by University of Vermont:
Medical Errors  
Medication Errors  
Prescriptions, Drug  

ClinicalTrials.gov processed this record on September 19, 2008




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