Randomized Trial of An Innovative Smartphone Intervention for Smoking Cessation
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,503
- 试验地点
- 1
- 主要终点
- 30-day Point Prevalence Abstinence, Complete-case
研究概览
简要总结
The goal of this study is to determine whether the novel smartphone app (SmartQuit) provides higher quit rates than the current standard smoking cessation app.
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
- Single (Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •age 18 or older
- •smokes at least five cigarettes daily for at least past 12 months
- •wants to quit cigarette smoking in the next 30 days
- •if concurrently using any other nicotine or tobacco products, wants to quit using them within the next 30 days
- •interested in learning skills to quit smoking
- •willing to be randomly assigned to either condition
- •resides in US
- •has at least daily access to their own personal Apple iPhone, Android, or Windows Phone
- •knows how to login and download a smartphone application
- •willing and able to read in English
- •not using other smoking cessation interventions (including apps or our other intervention studies).
- •willing to complete all three follow-up surveys
- •provide email, phone, and mailing address.
排除标准
- •The exclusion criteria are opposite of the inclusion criteria listed above.
研究组 & 干预措施
Experimental
This is the experimental arm of the study. This includes receiving the novel/experimental smartphone smoking cessation app. Therapy description withheld to protect the integrity of the study.
干预措施: Smartphone-delivered Intervention (SmartQuit) (Behavioral)
Control
This is the control arm of the study. This includes receiving the standard of care smartphone smoking cessation app. Therapy description withheld to protect the integrity of the study.
干预措施: : Smartphone-delivered Intervention (Standard of care app) (Behavioral)
结局指标
主要结局
30-day Point Prevalence Abstinence, Complete-case
时间窗: 12 months post randomization
Percentage of participants reporting no smoking in the past 30 days, 12 months post-treatment. Participants missing follow-up data are excluded for the complete-case analysis. Exact 2-sided CI was based on the observed proportion of participants.
次要结局
- 30-day Point Prevalence Abstinence, Missing=Smoking Imputation(12 months post randomization)