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临床试验/NCT05029362
NCT05029362已完成不适用

SmokefreeSGM, A Text-based Smoking Cessation Intervention for Sexual and Gender Minority Groups

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2022年1月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
2
主要终点
Perceived Usability as Assessed by the System Usability Scale (SUS)

研究概览

简要总结

The purpose of this study is to pretest the design of a text-based smoking cessation program tailored to sexual minority individuals.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Smoke five or more cigarettes per day, has smoked at least 100 cigarettes in their lifetime and smokes everyday
  • Have an interest in quitting smoking in the next 15 days
  • Have a cellphone number with an unlimited short messaging service (SMS) plan
  • Have US mailing and email addresses
  • Positive cotinine saliva test results

排除标准

  • Individuals who are found to have a prepaid cell phone
  • Individuals who are found to have a cellphone number that does not work or is registered to someone else
  • Pregnant or breastfeeding women
  • Contraindication for nicotine patch
  • Regular use of tobacco products other than cigarettes
  • Current use of tobacco cessation medications
  • Enrolled in another smoking cessation study
  • Non-English speakers
  • Having inadequate equipment/device (webcam, speakers, mic) for participating in telehealth sessions

结局指标

主要结局

Perceived Usability as Assessed by the System Usability Scale (SUS)

时间窗: 1 month after quit date

The 10-item System Usability Scale (SUS) was used to assess the usability of the SmokefreeSGM text messaging program. Total score ranges from 0 to 100, with a higher score indicating greater acceptability and a score above 75 indicating that the program is perceived as acceptable.

次要结局

  • Engagement as Assessed by the Number of Text Messages Sent and Received by Study Participants After Enrollment.(1 month after enrollment)

研究者

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

Irene Tami-Maury

Assistant Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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