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临床试验/NCT01889771
NCT01889771已完成不适用

A Cost-effectiveness Study of Nicotine Patches Distributed Through a Quitline

University of Colorado, Denver0 个研究点目标入组 1,495 人开始时间: 2010年3月最近更新:
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
1,495
主要终点
7-day smoking abstinence

研究概览

简要总结

The study is to understand whether distribution of two different supplies of nicotine patches through a telephone quitline has an effect on quit rates. The two different supplies are four vs. eight (in two separate four-week mailings) weeks of nicotine patches. The hypothesis is that eight weeks will be slightly more efficacious but four weeks will be more cost-effective.

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
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

入选标准

  • All callers to the Colorado QuitLine who report currently smoking 16-20 cigarettes
  • who enroll in QuitLine services
  • who do not require physician approval to obtain nicotine replacement therapy
  • who are willing to receive the nicotine patch

排除标准

  • Contraindications to receiving the nicotine patch through the QuitLine without physician approval include: history of hearth disease (heart attack, chest pain, or coronary artery disease), high blood pressure, pregnancy, skin conditions such as difficult to manage psoriasis or eczema, or history of a local reaction to the nicotine patch
  • those who do not complete the call in English

研究组 & 干预措施

Nicotine Patch (4 weeks)

Experimental

participants receive one 4-weeks supply of nicotine patches

干预措施: Nicotine Patch (Drug)

Nicotine Patch (8 weeks)

Experimental

participants receive up to 8 weeks of nicotine patches in up to two 4-week supplies

干预措施: Nicotine Patch (Drug)

结局指标

主要结局

7-day smoking abstinence

时间窗: 7 days

cost-effectiveness

时间窗: 6 months

cost per quit of each study arm will be calculated based on the total costs of the intervention from actual utilization data (nicotine patch costs + counseling call costs) and quit rates

6-month smoking abstinence

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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