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临床试验/NCT02301351
NCT02301351已完成不适用

Effects of Implicit Messaging by Cigarette Pack Color on Smoking Behaviors

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 316 人开始时间: 2014年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
316
试验地点
2
主要终点
Daily Cigarette Rate (smoking behavior)

研究概览

简要总结

The purpose of this study is to examine the effect of changes in cigarette package color and warning label features on smoking behaviors and beliefs about cigarette risks.

详细描述

This project will recruit 360, current daily Marlboro, non-menthol, red (n=180) or gold (n=180) cigarette smokers to a 50-day protocol using a randomized factorial design with two factors: (1) cigarette pack color manipulation (within subject: red, gold, plain packaging) and (2) warning label manipulation (between subject: graphic vs. standard text). The randomization will be stratified by own brand cigarette. To evaluate effects of changes in cigarette package coloring, participants will smoke commercially available cigarettes that may or may not be similar to their preferred brand of cigarettes throughout the study, but in different colored packages during three 15-day study periods (i.e., one period will be Marlboro plain (tan-olive) packs, one will be Marlboro gold packs and one will be Marlboro red packs; order counterbalanced). Participants will visit the Center every 5 days to complete assessments (11 total sessions).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Other
盲法
Single (Participant)

入排标准

年龄范围
21 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female smokers who are between 21 and 60 years of age and self-report smoking at least 5 cigarettes per day for at least the past 12 months.
  • Smokers of primarily non-menthol, Marlboro red or gold type cigarettes.
  • Not using any forms of nicotine other than cigarettes.
  • Not currently undergoing smoking cessation treatment or tying to quit.
  • Able to communicate fluently in English (speaking, writing, and reading).
  • Plan to remain in the area over the duration of the trial.
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the combined consent and HIPAA form.

排除标准

  • Smoking Behavior.
  • Use of any nicotine products other than cigarettes.
  • Enrollment or plans to enroll in a smoking cessation program over the duration of the trial.
  • Provide a Carbon Monoxide (CO) reading less than 5 parts per million (ppm) at Day
  • Alcohol/Drugs.
  • History of substance abuse (other than nicotine) in the past 12 months and/or currently receiving medical treatment for substance abuse.
  • Current alcohol consumption that exceeds 25 standard drinks/week.
  • Provide a breath alcohol concentration (BrAC) reading greater than .000 at Day
  • Women who are pregnant, planning a pregnancy, and/or lactating.
  • Any impairment including, but not limited to, visual, physical, and/or neurological impairments preventing the completion of procedures included within this protocol. Notable impairments will be evaluated by the Principal Investigator and eligibility will be determined on a case-by-case basis.
  • Color blindness.
  • Serious or unstable disease within the past 12 months (e.g. heart disease, cancer). Applicable conditions will be evaluated by the Principal Investigator and eligibility will be determined on a case-by-case basis.
  • Psychiatric.
  • Lifetime history or current diagnosis of psychosis, bipolar disorder, and/or schizophrenia.
  • Current diagnosis of major depression. Subjects with a history of major depression, in remission for 6 months or longer, are considered eligible.
  • Any medical condition, extenuating circumstance, illness, disorder, adverse event (AE), and/or concomitant medication that could compromise participant safety and/or completion of the study procedures, as determined by the Principal Investigator. Subjects may be deemed ineligible or withdrawn for any of the aforementioned reasons at any point throughout the study.
  • Non-compliance with the protocol and/or study design as determined by the Principal Investigator.

结局指标

主要结局

Daily Cigarette Rate (smoking behavior)

时间窗: Days 0-50

Daily cigarette consumption will be determined by the difference of unused cigarettes and used cigarette filters returned to the Center every Session after Day 0.The number of used cigarette filters and self-reported daily smoking rate will be recorded on a Smoking Rate Data Collection Form. We will examine changes in daily cigarette consumption averaged over each of the three 15-day pack periods.

次要结局

  • Smoking Topography(Days 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, & 50)
  • Subjective Cigarette Ratings(Days 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, & 50)
  • Cigarette Risk Beliefs(Days 0, 5, 20, 35, & 50)
  • Carbon Monoxide (CO)(Days 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, & 50)
  • Attitudes and Intentions (to use product)(Days 0, 5, 20, 35, & 50)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Andrew Strasser

Research Associate Professor

University of Pennsylvania

研究点 (2)

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