Cognitive Behavioral Smoking Cessation Intervention for Adults With Chronic Pain

Not Applicable

Completed

• Conditions: Smoking Cessation
• Interventions: Behavioral: Cognitive behavioral; Behavioral: Control

• Registration Number: NCT01091090
• Lead Sponsor: Mayo Clinic

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-11
• Study First Submitted: 2010-03-10
• Study First Submitted QC: 2010-03-19
• Study First Posted: 2010-03-23
• Primary Completion: 2011-09
• Study Completion: 2011-09
• Status Verified: 2012-05
• Last Update Submitted: 2012-05-23
• Last Update Posted: 2012-05-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

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

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Exclusion Criteria

• Concurrent substance use disorder other than nicotine dependence
• Concurrent major psychiatric disorder

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Cognitive behavioral	Cognitive behavioral	Subjects with receive a cognitive behavioral intervention for smoking cessation
Control	Control	Treatment as usual

Primary Outcome Measures

Name	Time	Method
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.	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 Outcome Measures

Name	Time	Method
A key secondary outcome measure will be self-report pain severity at 6-months following completion of the experimental intervention.	6 month

Trial Locations

Locations (1)

Mayo Pain Rehabilitation Center; 🇺🇸 Rochester, Minnesota, United States