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The Effectiveness of Smoking Cessation Guidelines in the Emergency Department

2011年11月2日 更新者:University of Iowa
Although 78% of smokers report that a health professional has previously advised them to quit smoking, most smokers are not advised to stop smoking or offered assistance with smoking cessation during a given ED visit. There are multiple barriers to routine implementation of smoking cessation guidelines by emergency clinicians, however, and rigorously performed clinical trials are needed to demonstrate that routine screening and counseling of ED patients results in increased quit rates. To determine the feasibility of implementing the Agency for Healthcare Research and Quality (AHRQ) Smoking Cessation Guideline in the ED, we will conduct a clinical trial in 974 ambulatory adult smokers who present to 2 emergency departments, using a pre-post design. During the 3-month baseline period, clinicians will perform their usual duties but will not receive training in use of the AHRQ Guideline. Based on the Chronic Care Model, the 3-month intervention period will include: 1) a tutorial on brief cessation counseling for ED nurses and physicians, 2) use of an ED algorithm that includes recommended tobacco counseling items, 3) fax referral of motivated smokers to Quitline Iowa for proactive telephone counseling plus free nicotine replacement therapy, and 4) group and individual feedback to ED staff. We will conduct exit interviews of ED patients to assess performance of guideline-recommended actions by ED staff and 3- and 6-month telephone follow-up to determine 7-day point-prevalence abstinence (with biochemical confirmation of self-reported quitters at 6 months). Our main analyses will examine the contrast between the intervention and control periods in the performance of guideline-recommended actions and in 6-month quit rates, using hierarchical logistic regression to adjust for baseline differences in potentially confounding patient variables. In secondary analyses, we will assess the change in attitudes of ED nurses and physicians toward smoking cessation counseling. This feasibility study will determine the receptivity of patients and ED staff to the guideline-based intervention and will provide estimates of effect size in planning a full scale multi-site clinical trial of the study intervention in community hospital EDs.

研究概览

研究类型

介入性

注册 (实际的)

789

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Iowa
      • Des Moines、Iowa、美国、50316
        • Iowa Methodist Medical Center
      • Iowa City、Iowa、美国、52242
        • The University of Iowa Hospitals and Clinics Emergency Treatment Center

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

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Presentation to the Emergency Department by private vehicle or on a walk-in basis
  • Current cigarette smoker (5 or more cigarettes per day)

Exclusion Criteria:

  • Acute medical decompensation (e.g., acute respiratory failure requiring intubation, cardiac arrest, cardiogenic or septic shock)
  • Life-threatening trauma
  • Altered mental status
  • Dementia
  • Language barrier
  • Incarceration
  • Transfer to another ED
  • Departure from the ED prior to evaluation
  • Inability to be contacted by telephone
  • ED presentation for sexual assault
  • ED presentation for acute psychiatric crisis (e.g., suicidal ideation)
  • Participation in a smoking cessation program in the past 3 months

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:卫生服务研究
  • 分配:非随机化
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
无干预:Baseline Period
实验性的:Intervention Period
  1. a tutorial on brief cessation counseling for ED nurses and physicians
  2. use of an ED algorithm that includes recommended tobacco counseling items
  3. fax referral of motivated smokers to Quitline Iowa for proactive telephone counseling plus free nicotine replacement therapy
  4. group feedback to ED staff

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Performance of smoking cessation guideline-recommended actions by ED staff
大体时间:Assessed within two weeks after discharge from ED
Assessed within two weeks after discharge from ED

次要结果测量

结果测量
大体时间
7-day point-prevalence smoking abstinence
大体时间:3 and 6 months post enrollment
3 and 6 months post enrollment

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:David A Katz, MD, MSc、The Univesity of Iowa College of Medicine

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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

2008年9月1日

初级完成 (实际的)

2011年6月1日

研究完成 (实际的)

2011年6月1日

研究注册日期

首次提交

2008年9月19日

首先提交符合 QC 标准的

2008年9月19日

首次发布 (估计)

2008年9月22日

研究记录更新

最后更新发布 (估计)

2011年11月4日

上次提交的符合 QC 标准的更新

2011年11月2日

最后验证

2011年11月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • R21DA021607 (美国 NIH 拨款/合同)

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.

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