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临床试验/NCT07102082
NCT07102082招募中不适用

Ifluence of Authorized Smokeless Tobacco Product Modified Risk Claims II: Laboratory Assessment of Sensory and Subjective Effect

Roswell Park Cancer Institute2 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2025年9月25日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
160
试验地点
2
主要终点
Demand for cigarettes

研究概览

简要总结

To explore consumer responses to the announcement and implementation of new modified risk claims for Copenhagen and General Snus (brands of smokeless tobacco (ST) products) using a series of complementary and innovative research activities and methods.

详细描述

Primary Objectives:

To assess the influence of smokeless tobacco products' modified risk claims on:

  1. Product demand (measured as willingness to pay in USD) using an experimental auction approach; and
  2. Perceived risk of tobacco-associated diseases as assessed using questionnaire-based measures.

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
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Residing in one of the 8 counties of Western New York (Erie, Niagara, Cattaraugus, Chautauqua, Allegheny, Livingston, Genesee, Orleans, Wyoming).
  • Smoke cigarettes every day, at least 5 cigarettes per day, for at least 1 year.
  • Open to trying a non-combusted oral tobacco product.
  • Have access to a device (ie: computer/tablet/smartphone) with internet capabilities to participate in an online survey study.
  • Have the ability to read, write, and communicate in English.
  • Participant must understand the investigational nature of this study and an Independent Ethics Committee/Institutional Review Board approved information sheet prior to receiving any study related procedure

排除标准

  • Plan to quit smoking in the next 30 days.
  • Use of smokeless tobacco at least weekly in the last 6 months.
  • Lifetime use (that is, ever used at any time prior to the study) of Copenhagen or General Snus.
  • Unwilling or unable to follow protocol requirements.
  • Pregnant or planning to become pregnant (by self report)

研究组 & 干预措施

Group A - no claim

Sham Comparator

Participants view smokeless tobacco ads with no claims

干预措施: Modified Risk - None (Behavioral)

Group B - Modified Risk Tobacco Product Claim

Active Comparator

Participants view ads with a modified risk claim

干预措施: Modified Risk Claim (Behavioral)

结局指标

主要结局

Demand for cigarettes

时间窗: After one session - 1 hour

After watching a series of advertisements for oral smokeless tobacco products, participants will provide opinions of them, including likelihood of buying product.

Increase in knowlege of tobacco-associated diseases

时间窗: After one session - I hour

multi item assessment questionnaires of perceived harm/risks from products

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 (2)

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