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临床试验/NCT00799279
NCT00799279已完成不适用

Comparative Evaluation of the Efficacy and Cost-effectiveness of Two Interventions for Integrating Smoking Cessation Into Routine Primary Care Practice: A Cluster-randomized Trial

University of Waterloo0 个研究点目标入组 835 人开始时间: 2009年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
835
主要终点
smoking abstinence

研究概览

简要总结

The aim of this study is to determine if providing smokers identified in family doctors offices with follow-up counselling enhances their success with quitting and the number of health professionals helping patients with quitting. Six to eight family medicine clinics will be involved in the study. We will compare the frequency of addressing smoking with patients and the proportion of smokers who are successful with quitting 16-weeks following the clinic appointment between practices. It is hypothesized that the addition of follow-up counseling to a multi-component smoking cessation intervention will improve smoking outcomes.

详细描述

A family doctor's advice to quit has been shown to increase a smoker's motivation to quit. Despite the evidence supporting the importance of smoking cessation, there is a well-documented practice gap in the rates at which smoking cessation is being addressed by practitioners. The primary objectives of this research study are to determine whether adjunct telephone-based smoking cessation follow-up counselling when delivered as part of a multi-component intervention:

  1. Increases the rate at which evidence-based smoking cessation interventions are delivered to smokers identified in family doctors offices, compared to providing only practice supports.
  2. Increases smoking abstinence as measured three months after the estimated target quit date (i.e.16 weeks) compared to providing only practice supports.
  3. Is more cost-effective (cost/quit) than providing only practice supports to family doctors offices.

A two-arm before-after matched-pair cluster randomized trial, will test the effectiveness of two strategies for integrating smoking cessation treatments into primary care practice routines and enhancing cessation. Six to eight family doctors offices will be randomized to either a practice support (PS) group, or a follow-up counseling (FC) group. From each of the intervention practices a cross-sectional sample of 50 eligible smokers will be recruited pre- and post-intervention to assess 5A's delivery and smoking abstinence.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • •Practices will be eligible for participation in the present study if they meet the following criteria:
  • •Practice is a family health team (FHT), family health group (FHG); or family health network (FHN);
  • •All physicians within the practice are willing to participate in the study;
  • •Practice will see an average of 50 patients per day and 10% of patients are smokers;
  • •Practice is willing to provide consent to contact patients in waiting rooms and survey patients during office hours and by telephone.
  • •Patients will be eligible to participate in the study if they meet the following criteria:
  • •Patient is seen in clinic for annual exam or non-urgent visit;
  • •Patient is a current smoker (>1 cigarette per day on most days of the week);
  • •Patient is 18 years of age or older;
  • •Patient is able to read and understand English or French;
  • •Patient has a home or mobile telephone which can be used to receive follow-up telephone counselling calls

排除标准

  • •Patients who do not have the mental capacity to provide informed consent and complete study protocols will be excluded.

研究组 & 干预措施

Follow-up Counseling Arm

Experimental

smoking cessation training for providers,practice tools for providers, patient quit plan, and follow-up telephone counselling for smokers

干预措施: Smoking cessation training, support, and telephone follow-up (Behavioral)

Practice Support Arm

Active Comparator

smoking cessation training for providers,practice tools for providers, patient quit plan for smokers.

干预措施: smoking cessation intervention (Behavioral)

结局指标

主要结局

smoking abstinence

时间窗: 16-weeks

Self-report and biochemically validated point prevelence smoking abstinence

次要结局

  • cost-effectiveness(16-weeks)
  • Rate of provider delivery of evidence-based smoking treatments(exit survey on day of clinic visits)

研究者

申办方类型
Other

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