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Motivational Interviewing for Smoking Cessation

Motivational Interviewing Versus Brief Advice for Smoking Cessation in General Practice

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02645838
Enrollment
210
Registered
2016-01-05
Start date
2016-04-30
Completion date
2018-04-30
Last updated
2016-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking Cessation

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

BEHAVIORALMotivational interviewing

1\. Structural motivational interviewing for one section (about 20 mins),provided by family physician;2. Follow-up telephone call,provided by family physician.

Sponsors

Capital Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

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

MeasureTime frameDescription
1 week point prevalence abstinence (PPA)Self-reported PPA at 1 week follow-upValidation: exhaled carbon monoxide (CO) (\< 10 ppm)

Secondary

MeasureTime frameDescription
1 month PPASelf-reported 7-day PPA at 1 month follow-upValidation: exhaled CO (\< 10 ppm)
3 month PPASelf-reported 7-day PPA at 3 month follow-upValidation: exhaled CO (\< 10 ppm)
6 month PPASelf-reported 7-day PPA at 6 month follow-upValidation: exhaled CO (\< 10 ppm)

Contacts

Primary ContactYafang Huang, PHD
huangyafang85@163.com+86-10-83911726

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026