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Smokers' Health Project: Self-Determination and Maintaining Tobacco Abstinence (SHP)
This study is currently recruiting participants.
Verified by University of Rochester, March 2008
Sponsors and Collaborators: University of Rochester
National Cancer Institute (NCI)
New York State Department of Health
Greater Rochester Area Tobacco Cessation Center
Health Maintenance Consortium
National Institutes of Health (NIH)
Information provided by: University of Rochester
ClinicalTrials.gov Identifier: NCT00178685
  Purpose

These two studies will examine the role of autonomous motivation in maintained adherence. The first study will determine whether smokers are still abstinent from tobacco 32 months after starting in a previous project (Smoker's Health Study). The purpose of the second study is to determine which of three treatments for tobacco dependence provides the greatest amount of protection from relapsing to smoking after quitting. Specifically, the investigators will determine if extending the length of treatment time focusing on relapse prevention and arranging for support from important others prevents relapse compared to community care. Also, the investigators will determine if providing extended treatment time and support from important others plus providing medications to those that don't want to quit prevents long term relapse compared to just extending the length of treatment time and support from others. Additionally, a sub set of the population will be randomized to using hand held palm devices to recover real-time data assessment during the last 10 months of the project.


Condition Intervention Phase
Tobacco Use Disorder
Behavioral: Self-determination Intervention for Tobacco Dependence
Phase IV

MedlinePlus related topics: Smoking
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Efficacy Study
Official Title: Self-Determination and Maintaining Tobacco Abstinence

Further study details as provided by University of Rochester:

Primary Outcome Measures:
  • 12 month prolonged abstinence from tobacco measured at 24 months from randomization [ Time Frame: 12 months after subject enters trial ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Tobacco abstinence measured as a latent variable with the following three indicators: longest number of days not smoking, the number of days since last cigarette, and the 12 month prolonged abstinence [ Time Frame: 12 months and 24 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 950
Study Start Date: August 2004
Estimated Study Completion Date: June 2009
Estimated Primary Completion Date: June 2008 (Final data collection date for primary outcome measure)
Intervention Details:
    Behavioral: Self-determination Intervention for Tobacco Dependence
    autonomy supported behavioral intervention for tobacco dependent individuals
Detailed Description:

These two studies will extend our examination of self-determination theory (SDT) based counseling interventions to the issue of maintained abstinence from tobacco use. Two projects are proposed, both of which build on the results of our current trial. The first is a 32-month follow-up of the smoking status of patients in the preceding trial called the Smoker's Health Study (self-determination, smoking, diet, and health). That SDT intervention (4 counselor visits over 6 months) increased cessation at 6 months relative to community care, and was also effective in increasing 12 month prolonged abstinence, and the results have been reported in two manuscripts (Williams, McGregor, Sharp, Levesque, Kouides, Ryan, and Deci, In press; Williams, McGregor, Sharp, Levesque, Kouides, Ryan, and Deci, 2005). The part of this first project that will be conducted as part of this grant will be to complete 32 month follow-up of smokers in the Smoker's Health Study. The second project is a 3-cell clinical trial called the Smoker's Health Project that will examine two extensions of the current intervention, both of which place greater emphasis on use of, and adherence to, cessation medications. The two arms will be compared to community care. Both arms involve two visits with a physician to discuss medications and side effects. In both interventions, counselors will address medication adherence. The two arms differ in that patients not ready to quit in one arm will receive a smoking reduction approach (with medications) in which they first try to reduce their smoking to half and then attempt cessation. In addition, to place greater emphasis on medications and to examine medication adherence as a mediator of maintained cessation.

There will be two major changes in the intervention intended to facilitate long-term maintenance. First, the intervention will extend over 12 months (whereas the current one lasts only 6 months) with meetings during the additional 6 months focusing on maintenance and relapse prevention. Second, at least one family member or best friend of each patient will be encouraged to meet with a counselor to learn how to be more autonomy supportive with the patient around issues related to tobacco. Cessation and maintained abstinence will be examined with logistic regression. The SDT process model of maintained cessation will be tested using structural equation modeling, and cost-effectiveness analyses will be done for the interventions.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Smoking 5 or more cigarettes per day.
  • 18 years of age or older.
  • Speak and read English.
  • Eligible regardless of desire to quit smoking

Exclusion Criteria:

  • Pregnancy
  • History of psychotic illness other than depression
  • Life expectancy of less than 24 months
  • Dementia, or incompetence for medical decision making
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00178685

Contacts
Contact: Laurie S Passalacqua, BS, MS 585-530-3368 Laurie_Passalacqua@urmc.rochester.edu

Locations
United States, New York
Smokers' Health Project Recruiting
Rochester, New York, United States, 14607
Contact: Laurie S Pulver, BS, MS     585-530-3368     Laurie_Pulver@urmc.rochester.edu    
Principal Investigator: Geoffrey C Williams, MD, Ph.D.            
Sponsors and Collaborators
University of Rochester
New York State Department of Health
Greater Rochester Area Tobacco Cessation Center
Health Maintenance Consortium
Investigators
Principal Investigator: Geoffrey C Williams, MD, Ph.D. University of Rochester
  More Information

Related Info  This link exits the ClinicalTrials.gov site
Related Info  This link exits the ClinicalTrials.gov site

Publications:
Responsible Party: University of Rochester, Smokers' Health Project ( Geoffrey C Williams )
Study ID Numbers: 10085, R01 CA10666, 1R21CA119112-01A2
Study First Received: September 13, 2005
Last Updated: March 21, 2008
ClinicalTrials.gov Identifier: NCT00178685  
Health Authority: United States: Food and Drug Administration

Keywords provided by University of Rochester:
Self-determination
motivation
adherence
competence
autonomy
tobacco dependence
Tobacco use and dependence
Behavior change

Study placed in the following topic categories:
Mental Disorders
Tobacco Use Disorder
Substance-Related Disorders
Disorders of Environmental Origin

ClinicalTrials.gov processed this record on January 14, 2009