跳至主要内容
临床试验/NCT02370147
NCT02370147Unknown不适用

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 个研究点目标入组 500 人开始时间: 2015年3月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
500
主要终点
self-reported 7-day point prevalence quit rate

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

结局指标

主要结局

self-reported 7-day point prevalence quit rate

时间窗: at 12 months follow-up

prolonged abstinence quit rate

时间窗: at 12 months follow-up

次要结局

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

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yao He

Institute of Geriatrics

Chinese PLA General Hospital

相似试验