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临床试验/NCT05447156
NCT05447156已完成不适用

QuitGuide for American Indians: Aims 2 & 3

Masonic Cancer Center, University of Minnesota2 个研究点 分布在 1 个国家目标入组 115 人开始时间: 2022年12月14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
115
试验地点
2
主要终点
Frequency of App Use

研究概览

简要总结

Aim 3: To test feasibility, acceptability, and preliminary efficacy of the tailored QuitGuide for smoking cessation among AIs.

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

入选标准

  • American Indian person based on self-report
  • Age ≥ 18 years
  • Interested in quitting smoking
  • Smoke ≥ 3 commercial tobacco cigarette per day (CPD) in the past 30 days
  • o Use of other commercial tobacco products (e.g., e-cigarettes) is permitted if they report cigarettes being their primary product
  • Smartphone ownership with the ability to download applications and sufficient data to complete research procedures

排除标准

  • New or change in pharmacotherapy for smoking cessation (includes: nicotine gum, patch, lozenge, inhaler OR medications Chantix/Wellbtrutin/Zyban/Bupropion) in past month
  • Does not speak or read English

研究组 & 干预措施

Aim 3:Tailored App

Experimental

Randomized subset of participants will use the tailored QuitGuide app, a smoking cessation app, downloaded to their personal phone.

干预措施: Tailored QuitGuide app (Behavioral)

Aim 3: Standard App

Placebo Comparator

Randomized subset of participants will use the standard QuitGuide app, a smoking cessation app available to the public, downloaded to their personal phone.

干预措施: Standard QuitGuide app (Behavioral)

结局指标

主要结局

Frequency of App Use

时间窗: 5 weeks post enrollment and 1 week post randomization

The number of times the app is initiated per day will be measured using data from Smokefree.gov. If a participant does not use the app on a particular day, Smokefree.gov records this as non-use or 0 for that day. The total number of times will be summarized for analysis by totaling the number of times the app is initiated from randomization to 5 weeks post-randomization.

次要结局

  • Study Attrition Measured as Percentage of Randomized Participants That Complete the Final Phone Interview at 5 Weeks(5 weeks post enrollment aim 3)
  • Frequency of Returning Saliva Sample by 2 Weeks Post the Week 5 Interview(5 weeks post enrollment aim 3)
  • Usability of App Design Measured Using System Usability Scale (SUS)(5 weeks post enrollment)
  • Acceptability of Overall App(5 weeks post enrollment)
  • Fit of App With Culture(5 weeks post enrollment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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