跳至主要内容
临床试验/NCT00957424
NCT00957424已完成不适用

International Study of the Acceptability of Less Harmful Alternatives to Cigarettes (ISALHAC) - A Pilot Study

Roswell Park Cancer Institute1 个研究点 分布在 1 个国家目标入组 67 人开始时间: 2009年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
67
试验地点
1
主要终点
Number of Participants That Completed 1-week Trial

研究概览

简要总结

RATIONALE: A study that evaluates participants' beliefs about smokeless tobacco products and nicotine replacement therapy may be useful in helping smokers stop smoking.

PURPOSE: This clinical trial is studying the acceptability of less harmful alternatives to cigarettes.

详细描述

OBJECTIVES:

Primary

  • To assess the impact of factual information (a fact sheet) about the relative harms of smokeless (SL)/nicotine replacement (NR) products on participants' beliefs about relative harmfulness.
  • To assess the impact of trying samples of NR and/or SL products on intentions to use such products as alternatives to cigarettes.

Secondary

  • To explore the effects of factual information in regard to smoked tobacco on smokers' intentions to use such products as alternatives to cigarettes.
  • To assess potential barriers to use of both NR and SL products as substitutes for cigarettes.
  • To obtain estimates of possible effect sizes for powering a proposed comprehensive test of the likely outcomes of using these products in preference to cigarettes (and other smoked products).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
None

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Overall

Other

Single-armed study

干预措施: telephone-based intervention (Behavioral)

Overall

Other

Single-armed study

干预措施: nicotine replacement therapy (Drug)

Overall

Other

Single-armed study

干预措施: informational intervention (Other)

Overall

Other

Single-armed study

干预措施: internet-based intervention (Other)

Overall

Other

Single-armed study

干预措施: questionnaire administration (Other)

结局指标

主要结局

Number of Participants That Completed 1-week Trial

时间窗: One week

Number of Participants Willing to Try HRPs

时间窗: Baseline

Number of Participants Willing to Continue With Preferred HRP

时间窗: 1 week follow up

Number of Participants With no Interest in Trial of Harm-reduction Products (HRPs)

时间窗: Baseline

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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