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STAND Community College Tobacco Cessation Trial

2017年3月29日 更新者:University of California, Davis

Sacramento Taking Action Against Nicotine Dependence (STAND) at Sacramento City College

Community colleges have 45% of the nation's undergraduates and have a higher smoking prevalence rate than 4-year colleges. California's community colleges comprise the nation's largest higher education system, and Sacramento has the second largest community college district. As more colleges are encouraged to become smoke and tobacco-free campuses, smokers enrolled at community college campuses need greater support. However, community colleges may lack the student health clinic resources that 4-year colleges have for students who live on campus. Little evidence to date demonstrates effective interventions for smokers on community college campuses.

This pilot study seeks to demonstrate the feasibility and promising outcomes of two cessation interventions, compared with usual care on a community college campus. The first intervention was based on a promising model of brief motivational interviewing delivered by peer educators, developed by the community lead Breathe California of Sacramento-Emigrant Trails (BCSET) through the Sacramento Taking Action Against Tobacco Dependence (STAND) project. The second intervention was based on direct enrollment into the California Smokers' Helpline, which has demonstrated utility for promoting smoking cessation among young adults with low socioeconomic status. Usual care consisted of students going to the student health center for smoking cessation assistance.

研究概览

研究类型

介入性

注册 (实际的)

113

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • adult 18 years or older
  • current smoker in the past 30 days
  • smoker wants to quit
  • smoker not currently participating in other smoking cessation activities, and
  • smoker must be willing to accept randomization into any of the 3 study arms

Exclusion Criteria:

  • students not proficient in communicating in English
  • adults unable to consent

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:Usual Care
Students referred to student health for tobacco cessation resources including campus "Quit Kits"
Participant provided "Quit Kit" water bottle with small cessation aids (eg. sunflower seeds) and educated about student health as a cessation resource
有源比较器:Brief Motivational Interviewing
Students received brief motivational interviewing by a student peer educator about tobacco cessation
Participant provided "Quit Kit" water bottle with small cessation aids (eg. sunflower seeds) and educated about student health as a cessation resource
Peer educator conducts brief motivational interviewing about smoking cessation and participant goals
有源比较器:Direct referral to quitline
Students were directly referred to the state quitline for follow-up counseling
Participant provided "Quit Kit" water bottle with small cessation aids (eg. sunflower seeds) and educated about student health as a cessation resource
Peer educator educates about state quitline services and gets verbal consent to use quitline's direct referral web portal for quitline to contact participant in 1-2 business days about free counseling services to make a quit plan

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Biochemically validated smoking cessation
大体时间:6 months
Point prevalence abstinence validated by saliva cotinine level
6 months

次要结果测量

结果测量
措施说明
大体时间
Self-reported smoking cessation
大体时间:6 months
Point prevalence abstinence by self-report on survey
6 months
Self-reported smoking cessation
大体时间:3 months
Point prevalence abstinence by self-report on survey
3 months
Self-reported smoking cessation
大体时间:1 month
Point prevalence abstinence by self-report on survey
1 month

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Elisa Tong, MD、University of California, Davis

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2014年9月1日

初级完成 (实际的)

2016年6月1日

研究完成 (实际的)

2016年6月1日

研究注册日期

首次提交

2016年12月19日

首先提交符合 QC 标准的

2016年12月21日

首次发布 (估计)

2016年12月26日

研究记录更新

最后更新发布 (实际的)

2017年3月30日

上次提交的符合 QC 标准的更新

2017年3月29日

最后验证

2017年3月1日

更多信息

与本研究相关的术语

其他研究编号

  • 491744
  • 22BT-0057 (其他标识符:Other)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

Usual Care的临床试验

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