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临床试验/NCT05510154
NCT05510154已完成不适用

Impact of E-cigarette Training on Puff Patterns, Cigarette Smoking, and Health Outcomes Among Smokers With COPD

University of Kansas Medical Center1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2022年3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
45
试验地点
1
主要终点
Changes in puff duration in seconds from pre- to post-e-cigarette training

研究概览

简要总结

This study is for people with chronic obstructive pulmonary disease (COPD) and who smoke. Investigators are trying to find out if training on e-cigarette use will help smokers switch to e-cigarettes. If training helps, how much training is needed for people to fully switch from cigarettes to e-cigarettes?

详细描述

Investigators are doing this study with people who smoke and have chronic obstructive pulmonary disease (COPD). Investigators are trying to find out if e-cigarettes can reduce tobacco-related harm among smokers. Investigators want to know if training on e-cigarette use will help smokers switch to e-cigarettes. If training helps, how much training is needed for people to fully switch from cigarettes to e-cigarettes? This study is an in-lab smoking study and randomized trial. The study takes place at the Main University of Kansas Medical Center (KUMC) campus in Kansas City, Kansas (KS). device. Participants will come to the lab on seven separate days. Between visits, participants will use the study e-cigarette at home. Each time participants come in, participants will fill out surveys about participants tobacco use and use the study product. Investigators will ask participants to switch to the study e-cigarette for 12 weeks during the study.

The study product is an e-cigarette device and is available for sale in the US. Participants will do a few different breathing tests where participants blow into a machine, Investigators will measure participants blood pressure and pulse, and Investigators will do a short walking test. Before three of the visits Investigators will ask participants to not smoke or use an e-cigarette for 12 hours leading up to the visit. During three of the visits, Investigators will ask participants to use the e-cigarette for 30 minutes and take two blood samples. Each visit will last about 2-4 hours. There will be a total of seven visits.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
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
是

入选标准

  • •Diagnosed with COPD
  • •≥21 years old
  • •Speak and understand English
  • •Smoke on >25 of the last 30 days for the past 3 months
  • •Willing to switch from cigarettes to the study e-cigarette for the duration of the study
  • •Have tried but failed to quit smoking in the last year
  • •Unwilling to make a pharmacotherapy-assisted quit attempt in the next 30 days
  • •Willing to complete six in-person study visits
  • •Willing to have blood drawn
  • •Have reliable transportation to attend all in-person assessments
  • •Have a working phone number
  • •Plan to remain in the Kansas City area for the full duration of the trial.
  • •Dual users:
  • •Diagnosed with COPD
  • •≥21 years old
  • •speak and understand English
  • •smoke on ≥15 days of the last 30 days for the past 3 months
  • •willing to switch from cigarettes and their own e-cigarette to the study e-cigarette for the duration of the study
  • •use an e-cigarette on >15 days of the last 30 days for the past 3 months
  • •Have tried but failed to quit smoking in the last year
  • •Unwilling to make a pharmacotherapy-assisted quit attempt in the next 30 days
  • •Willing to complete six in-person study visits
  • •Willing to have blood drawn
  • •Have reliable transportation to attend all in-person assessments
  • •Have a working phone number
  • •Plan to remain in the Kansas City area for the full duration of the trial.

排除标准

  • •Use of tobacco products other than cigarettes including e-cigarettes in the past 30 days
  • •current use of cessation medications
  • •pregnant, planning to become pregnant, or breastfeeding
  • •recent history of cardiovascular or pulmonary events in the past 3 months
  • •household member current or previously enrolled in the study
  • •weekly use of an e-cigarette over the last 6 months
  • •Dual Users:
  • •Use of tobacco products other than cigarettes and e-cigarettes in the past 30 days
  • •current use of cessation medications
  • •pregnant, planning to become pregnant, or breastfeeding
  • •recent history of cardiovascular or pulmonary events in the past 3 months
  • •household member current or previously enrolled in the study

研究组 & 干预措施

Brief Advice

Experimental

Brief Advice involves basic e-cigarette education and advice to switch.

干预措施: Brief advice (Behavioral)

Single Training

Experimental

Single Training is the same as Brief Advice but includes one session of real-time training on how to puff on the e-cigarette.

干预措施: Single Training (Behavioral)

Training to Competency

Experimental

Training to Competency is the same as Single Training but includes three real-time training sessions rather than one.

干预措施: Training to Competency (Behavioral)

结局指标

主要结局

Changes in puff duration in seconds from pre- to post-e-cigarette training

时间窗: 12 weeks

Researchers are using a puff topography device to capture real-time electronic cigarette puff and usage patterns. The electronic cigarette is attached to a device during 30-minute sessions where participants use the electronic cigarette as much or as little as they want. Researchers are measuring changes in puff duration in seconds from pre- to post-e-cigarette training/brief advice between smokers who received brief advice versus e-cigarette training (single episode and enhanced e-cigarette training arms combined). Measurements are compared from the first visit to the last visit at week 12.

次要结局

  • Complete switch to e-cigarette(12 weeks)

研究者

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

Eleanor Leavens

Assistant Professor

University of Kansas Medical Center

研究点 (1)

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