Cognitive Behavioral Smoking Cessation Intervention for Adults With Chronic Pain
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Smoking Cessation
- Sponsor
- Mayo Clinic
- Enrollment
- 26
- Locations
- 1
- Primary Endpoint
- 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.
- Status
- Completed
- Last Updated
- 13 years ago
Overview
Brief Summary
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.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
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.
Secondary Outcomes
- A key secondary outcome measure will be self-report pain severity at 6-months following completion of the experimental intervention.(6 month)