Smoking Cessation
Conditions
Keywords
Motivational Interviewing, Smoking Cessation
Brief summary
The purpose of this study is to determine whether or not motivational interviewing is effective in smoking cessation at general practice setting in China.
Detailed description
OBJECTIVES: • To compare the effectiveness of motivational interviewing versus brief advice by conducting a randomized controlled trial in General Practice Setting in China. OUTLINE: This is a randomized controlled study. Patients are randomized to either the intervention arm or the control arm. • Arm I (intervention): Patients will be given a 20 minutes personal talk in the family physician's office during the visit. The family physicians will determine the stage of change in smoking cessation (precontemplative, contemplative, action, maintenance and relapse) and use the motivational interviewing skills during the talk. The motivational interviewing skills include expressing empathy, developing discrepancy, rolling with resistance, supporting self efficacy. Up to six phone calls will be given to the patients during the follow-up, using the motivational interviewing skill. • Arm II (control): Patients will receive brief advice for smoking cessation, lasting approximately 5 minutes. The risks of smoking and the advantages of quitting will be explained. The information provided during the talk will be standardized. No phone call will be given during the follow-up.
Interventions
1\. Structural motivational interviewing for one section (about 20 mins),provided by family physician;2. Follow-up telephone call,provided by family physician.
Sponsors
Study design
Eligibility
Inclusion criteria
1. Between the ages of 18 and 80 years. 2. Any person who replies Yes when asked Do you smoke?. 3. Agree to participate the trial and be followed for at least one year.
Exclusion criteria
1. With severe mental illness, serious drug dependent patients. 2. Cannot understand conversation or cannot communicate, such as deafness or dementia. 3. Cannot be followed up for one year, such as not likely survive for more than one year.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 1 week point prevalence abstinence (PPA) | Self-reported PPA at 1 week follow-up | Validation: exhaled carbon monoxide (CO) (\< 10 ppm) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 1 month PPA | Self-reported 7-day PPA at 1 month follow-up | Validation: exhaled CO (\< 10 ppm) |
| 3 month PPA | Self-reported 7-day PPA at 3 month follow-up | Validation: exhaled CO (\< 10 ppm) |
| 6 month PPA | Self-reported 7-day PPA at 6 month follow-up | Validation: exhaled CO (\< 10 ppm) |