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Cognitive Behavioral Smoking Cessation Intervention for Adults With Chronic Pain

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ClinicalTrials.gov Identifier: NCT01091090
Recruitment Status : Completed
First Posted : March 23, 2010
Last Update Posted : May 25, 2012
Information provided by:
Mayo Clinic

March 10, 2010
March 23, 2010
May 25, 2012
November 2009
September 2011   (Final data collection date for primary outcome measure)
The key measurement to be used to assess the effect of the experimental intervention will be the status of cigarette smoking at 6-month follow-up. [ Time Frame: 6 months ]
The smoking status will be determined by assessing the 7-day point prevalence use of cigarettes which is defined as the use of any cigarettes within the preceding 7 days of the follow-up date at 6-months.
Same as current
Complete list of historical versions of study NCT01091090 on ClinicalTrials.gov Archive Site
A key secondary outcome measure will be self-report pain severity at 6-months following completion of the experimental intervention. [ Time Frame: 6 month ]
Same as current
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Cognitive Behavioral Smoking Cessation Intervention for Adults With Chronic Pain
Cognitive Behavioral Smoking Cessation Intervention for Adults With Chronic Pain
Millions of individuals with chronic pain smoke and our preliminary research suggests that currently available strategies to help people quit smoking may not be effective for individuals with chronic pain. This is important in that smokers with chronic pain have worse pain-related health outcomes compared to nonsmokers with chronic pain. The primary aim of this research project is to develop a smoking cessation intervention for specific use in an outpatient clinical setting for smokers with chronic pain.
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Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Smoking Cessation
  • Behavioral: Cognitive behavioral
    Cognitive behavioral intervention for smoking cessation
    Other Names:
    • Cognitive
    • Behavioral
    • Smoking Cessation
  • Behavioral: Control
    Treatment as usual
  • Experimental: Cognitive behavioral
    Subjects with receive a cognitive behavioral intervention for smoking cessation
    Intervention: Behavioral: Cognitive behavioral
  • Active Comparator: Control
    Treatment as usual
    Intervention: Behavioral: Control

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
September 2011
September 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Chronic pain
  • Age > 18 years
  • Cigarette smoker > 10 per day

Exclusion Criteria:

  • Concurrent substance use disorder other than nicotine dependence
  • Concurrent major psychiatric disorder
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
United States
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W. Michael Hooten, MD, Mayo Clinic Foundation
Mayo Clinic
Not Provided
Not Provided
Mayo Clinic
May 2012

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