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Very Brief Smoking Reduction Intervention

The Effect of Very Brief Smoking Reduction Intervention in Smokers Who Having no Intention to Quit: Study Protocol for a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02370147
Enrollment
500
Registered
2015-02-24
Start date
2015-03-31
Completion date
2017-06-30
Last updated
2015-02-24

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

Conditions

Smoking Cessation

Keywords

smoking reduction intervention, no intention to quit, randomized controlled trial, telephone follow-up intervention

Brief summary

A two-arm randomized controlled trial for smokers who are not intent to quit smoking will be proposed in outpatient department clinics of People's Liberation Army General Hospital in Beijing, China. Smoking reduction intervention arm (SRI) consisting of a very brief face-to-face individual smoking reduction intervention lasted about one minute, and five follow-up interventions lasted for about minute each. Control arm (EDA) consisting of a very brief face-to-face individual exercise and dietetic advices lasted for the same intervention time as SRI, and also five follow-up interventions lasted for one minute each with different intervention contents.

Interventions

BEHAVIORALExercise and diet advice control

Smokers will be asked to do regular activities for three or four times per week, and to have a healthy and balanced diet, having more fruit and vegetables which are rich in vitamins, high in nutrition yet low in calories. In the whole process, advises will not refer to smoking cessation or smoking reduction.

BEHAVIORALSmoking reduction intervention

Smokers was informed that many harmful effects were proved to be related with smoking, such as cancer, coronary heart disease, respiratory disease and many other health problems, and one out of two smokers will be killed by smoking. Smokers will be advised to reduce smoking consumption for at least half of their total consumption in the next month. Finally, all smokers were warned to keep in mind that the current attempt to reduce smoking is an intermediate step before the complete cessation.

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Aged ≥18 years old; 2. Smoked more than 10 cigarettes per day in the past month. 3. Have no intent to smoking cessation now. 4. Agreed to participate in the follow-up, offer telephone number and signed an informed consent form.

Exclusion criteria

1. Smoked less than 10 cigarettes per day in the past month. 2. Had some diseases that let the physician think that it would be unethical not to advise him to quit smoking as soon as possible. 3. Cognitively impaired (such as those with deafness or who could not understand and complete the questionnaire reliably). 4. Pregnant females.

Design outcomes

Primary

MeasureTime frame
self-reported 7-day point prevalence quit rateat 12 months follow-up
prolonged abstinence quit rateat 12 months follow-up

Secondary

MeasureTime frameDescription
smoking reduction ratesbaseline and at 12 months follow-upnumber of cigarettes smoked per day reduced at least 50%

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026