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Clinical Trials/NCT02370147
NCT02370147
Unknown
Not Applicable

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

Chinese PLA General Hospital0 sites500 target enrollmentMarch 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Smoking Cessation
Sponsor
Chinese PLA General Hospital
Enrollment
500
Primary Endpoint
self-reported 7-day point prevalence quit rate
Last Updated
11 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
June 2017
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Chinese PLA General Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yao He

Institute of Geriatrics

Chinese PLA General Hospital

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

self-reported 7-day point prevalence quit rate

Time Frame: at 12 months follow-up

prolonged abstinence quit rate

Time Frame: at 12 months follow-up

Secondary Outcomes

  • smoking reduction rates(baseline and at 12 months follow-up)

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