Primary Care Physicians' Use of Stop-Smoking Plans to Help Patients Who Are Smokers

Sponsor
Kaiser Permanente (Other)
Overall Status
Completed
CT.gov ID
NCT00227786
Collaborator
(none)
344
5
40
68.8
1.7

Study Details

Study Description

Brief Summary

RATIONALE: Stop-smoking plans suggested by physicians may help patients quit smoking. Studying how physicians give stop-smoking treatment as family doctors may increase the chance of smokers receiving such treatment.

PURPOSE: This randomized clinical trial is studying physicians' practice patterns to see if regular feedback to the physician increases the chance of adult smokers receiving stop-smoking treatment.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: smoking cessation intervention
  • Other: counseling intervention
N/A

Detailed Description

OBJECTIVES:
  • Develop an automated coding system using existing electronic medical records (EMRs) to assess adherence to national tobacco-cessation treatment guidelines by individual physicians in the primary care setting at 4 health maintenance organizations.

  • Compare the validity of the automated coding system with that of coding performed by medical record abstractors.

  • Determine the effect of performance feedback on tobacco treatment practice patterns over 2 years among primary care physicians.

  • Provide recommendations for recording tobacco-cessation treatment services in EMR systems and evaluating adherence to treatment guidelines.

  • Produce a set of computer programs that can be easily adopted in diverse health care settings for assessing adherence to the national tobacco-cessation treatment guidelines using data from EMRs.

OUTLINE: This is a randomized, controlled, multicenter study. Physicians from each participating center are sorted into pairs according to their rate of providing advice to quit smoking to identified adult smokers and the number of identified adult smokers seen in the 3-month baseline observation period. Each physician in the pair is then randomized to 1 of 2 arms.

  • Arm I (automated coding system feedback): Physicians receive reports from an automated coding system regarding their performance in administering tobacco-cessation services in each of the five A's (Ask, Advise, Assess, Assist, and Arrange) to identified smokers in comparison with their past performance and in comparison with their anonymous colleagues once every 3 months. One year after randomization, these physicians are further randomized, using the same paired-group approach, to either continue receiving automated coding system feedback for 1 additional year OR to stop receiving feedback.

Physicians receive a survey at the end of 2-year period regarding the usefulness of each aspect of the feedback reports and the feedback program in general.

  • Arm II (control): Physicians do not receive any information regarding their performance in administering tobacco-cessation services in each of the five A's to identified smokers.

A questionnaire about tobacco-cessation services in primary care is sent to patients of all physicians within two weeks of each patient's primary care visit and then at the end of the first year of providing feedback to physicians to compare patient report of tobacco-cessation services with what is documented in the electronic medical record for that primary care visit.

PROJECTED ACCRUAL: At least 40 primary care physicians per participating center and 1,000 patients (250 per participating center) will be accrued for this study.

Study Design

Study Type:
Interventional
Actual Enrollment :
344 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Using Electronic Medical Records to Measure and Improve Adherence to Tobacco Treatment Guidelines in Primary Care
Study Start Date :
Jan 1, 2003
Actual Primary Completion Date :
May 1, 2006
Actual Study Completion Date :
May 1, 2006

Outcome Measures

Primary Outcome Measures

  1. Change in tobacco cessation care delivery of the 5 A's (Ask, Advise, Assess, Assist, and Arrange) and in the percentage of smokers receiving assistance as measured by MediClass classification at 18 months []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
DISEASE CHARACTERISTICS:
  • Primary care physician, meeting all of the following criteria:

  • Practicing medicine in a family practice or internal medicine clinic

  • Scheduled to see adult primary care patients for ≥ 2½ days (or 5 half days or equivalent combination of full and half days) per week

  • Planning to continue full-time practice in their participating organization for at least the next 2 years

  • At least 1 year of experience working with the local electronic medical record system

  • Patient

  • Adult smoker who visited a study physician within the past month

PATIENT CHARACTERISTICS:

Age

  • Adult

Performance status

  • Not specified

Life expectancy

  • Not specified

Hematopoietic

  • Not specified

Hepatic

  • Not specified

Renal

  • Not specified
PRIOR CONCURRENT THERAPY:

Biologic therapy

  • Not specified

Chemotherapy

  • Not specified

Endocrine therapy

  • Not specified

Radiotherapy

  • Not specified

Surgery

  • Not specified

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kaiser Permanente - Aurora Aurora Colorado United States 80014
2 Kaiser Permanente Center for Health Research - Hawaii Honolulu Hawaii United States 96817
3 Massachusetts General Hospital Cancer Center Boston Massachusetts United States 02114
4 Harvard Pilgrim Health Care Boston Massachusetts United States 02215
5 Kaiser Permanente Center for Health Research Portland Oregon United States 97227

Sponsors and Collaborators

  • Kaiser Permanente

Investigators

  • Study Chair: Victor J. Stevens, PhD, Kaiser Permanente

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kaiser Permanente
ClinicalTrials.gov Identifier:
NCT00227786
Other Study ID Numbers:
  • CDR0000448865
  • KAISER-U19-CA099193
First Posted:
Sep 28, 2005
Last Update Posted:
Aug 16, 2013
Last Verified:
Nov 1, 2005
Keywords provided by Kaiser Permanente
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 16, 2013