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A Randomized Trial to Implement the AHCPR Smoking Cessation Guideline

This study has been completed.

Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00013013
  Purpose

Among veterans, smoking is the single most important risk factor for preventable mortality and morbidity, and studies suggest a higher prevalence of smoking among veterans than the general population. The VHA has encouraged adoption of the AHCPR Guideline for Smoking Cessation, yet most hospitals have poorly developed smoking cessation programs.


Condition Intervention Phase
Smoking
Smoking Cessation
Procedure: Systems Support
Phase IV

MedlinePlus related topics:   Smoking    Smoking Cessation    Smoking and Youth   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Official Title:   A Randomized Trial to Implement the AHCPR Smoking Cessation Guideline

Further study details as provided by Department of Veterans Affairs:

Estimated Enrollment:   4000
Study Completion Date:   August 2001

Arms Assigned Interventions
1 Procedure: Systems Support

Detailed Description:

Background:

Among veterans, smoking is the single most important risk factor for preventable mortality and morbidity, and studies suggest a higher prevalence of smoking among veterans than the general population. The VHA has encouraged adoption of the AHCPR Guideline for Smoking Cessation, yet most hospitals have poorly developed smoking cessation programs.

Objectives:

The present study is designed to investigate the effectiveness of an organizational strategy to increase compliance with the AHCPR guideline. Short term goals of the study include increasing the rate of identification of smokers and increasing the delivery of brief smoking cessation interventions. Long term goals include reducing tobacco consumption among veterans.

Methods:

Twenty VAMC�s with active primary care clinics have been randomly assigned to either control (usual practice; UP) or intervention (organizational support; OS) groups. The intervention hospitals receive staff training and site consultation; all hospitals will receive the AHCPR guideline. Rate of identification of smokers in the medical record, smoking cessation rates, provision of smoking cessation services (e.g., NRT, counseling), and costs of NRT will be determined via telephone interviews with patients, chart review, and electronic records.

Status:

Baseline data collection is nearly complete, and the intervention period will be complete in September, 2000. We have completed telephone surveys with approximately 4500 veterans. Analysis of study data is ongoing, and manuscript preparation will begin within the next few months.

  Eligibility
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

Subjects must be smokers.

Exclusion Criteria:

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00013013

Locations
United States, Minnesota
VA Medical Center    
      Minneapolis, Minnesota, United States, 55417

Sponsors and Collaborators

Investigators
Principal Investigator:     Anne M. Joseph, MD MPH     Department of Veterans Affairs    
  More Information


Publications of Results:

Responsible Party:   Department of Veterans Affairs ( Joseph, Anne - Principal Investigator )
Study ID Numbers:   CPG 97-039
First Received:   March 14, 2001
Last Updated:   August 14, 2008
ClinicalTrials.gov Identifier:   NCT00013013
Health Authority:   United States: Federal Government

Study placed in the following topic categories:
Smoking

Additional relevant MeSH terms:
Habits

ClinicalTrials.gov processed this record on October 10, 2008




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