NCT06806098已完成不适用
Cessation Clinical Trial
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,555
- 试验地点
- 2
- 主要终点
- 30-day point prevalent abstinence
研究概览
简要总结
The Cessation Clinical Trial will investigate the effectiveness of a digital quit tobacco program in promoting abstinence from tobacco product use compared to usual care.
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 (Participant)
盲法说明
Data collection staff will be blinded to study condition.
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
- •Current tobacco use (past 30-day use of one or more of the following: cigarettes, cigars, little cigars, cigarillos, e-cigarettes, or oral nicotine products)
- •US residence
- •Active text message plan (phase 2 only)
排除标准
- •Age 25 or above (phase 2 only)
研究组 & 干预措施
Sponsored cessation intervention
Experimental
Intervention arm receiving sponsored version only available for enterprise client users.
干预措施: Truth Initiative Digital Cessation Program (Behavioral)
Usual Care
Active Comparator
Usual care control arm receiving referral to a free digital cessation program
干预措施: Usual Care (Behavioral)
结局指标
主要结局
30-day point prevalent abstinence
时间窗: 7-months post randomization
30-day point prevalent abstinence from user's primary product to quit indicated at enrollment
次要结局
- Abstinence from all tobacco products(7 months post randomization)
研究者
Amanda L. Graham, PhD
Chief Health Officer
Truth Initiative
研究点 (2)
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