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临床试验/NCT07210567
NCT07210567招募中不适用

Mindfulness-based Ecological Momentary Intervention for Smoking Cessation Among Cancer Survivors

Rutgers, The State University of New Jersey1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年1月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1
主要终点
System Usablity Scale

研究概览

简要总结

The purpose of the study is to develop a new quit-smoking treatment among individuals with a cancer diagnosis using a smartphone app.

详细描述

The study aims to test the feasibility and acceptability of the smartphone app we developed in conjunction with face-to-face brief cessation counseling and nicotine replacement therapy in a two-arm randomized controlled trial.

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
否

入选标准

  • •≥18 years old
  • •smoked ≥1 cigarette per day (even one or two puffs) within the past 30 days
  • •having been diagnosed with cancer
  • •being motivated to quit in the next 30 days
  • •having a valid home address and functioning phone number
  • •being able to read, write, and speak English
  • •having a smartphone that allows installation of the app
  • •willingness to download the app

排除标准

  • •being enrolled in a smoking cessation program
  • •current use of smoking cessation medications
  • •evidence of current psychosis
  • •current/planning pregnancy or lactation

研究组 & 干预措施

Mindfulness

Experimental

Participants will receive brief counseling, nicotine replacement therapy, and intervention content delivered via the app.

干预措施: Mindfulness (Behavioral)

Quitline

Active Comparator

Participants will be referred to Quitline to receive standard care for smoking cessation.

干预措施: Quitline (Behavioral)

结局指标

主要结局

System Usablity Scale

时间窗: End of Treatment at 4 Weeks

Perceived usability and learnability of the app will be measured on a 5-point scale (1=strongly disagree; 5=strongly agree).

Client Satisfaction Questionnaire

时间窗: End of Treatment at 4 Weeks

Perceived satisfaction with the treatment will be assessed on a 4-point scale (1=very dissatisfied; 4=very satisfied).

Percentage of Participants That Completed Questionnaires

时间窗: 3-month follow-up

Completion of follow-up assessment will be calculated.

次要结局

未报告次要终点

研究者

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

Min-Jeong Yang, Ph.D.

Assistant Professor

Rutgers, The State University of New Jersey

研究点 (1)

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