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临床试验/NCT07419425
NCT07419425招募中4 期

Comparing Three Multicomponent Interventions to Help Adults Quit Smoking

University of Wisconsin, Madison5 个研究点 分布在 1 个国家目标入组 1,550 人开始时间: 2026年7月6日最近更新:
干预措施

试验速览

阶段
4 期
状态
招募中
入组人数
1,550
试验地点
5
主要终点
Biochemically confirmed abstinence from combusted tobacco at 26-weeks post-target quit day

研究概览

简要总结

The overarching goal of this program of research is to reduce smoking-related health disparities by increasing smoking cessation among Black adults. The goal of this research proposal is to determine whether more intensive, culturally specific, evidence-based interventions are more effective at promoting long-term cessation and other key patient-centered outcomes compared to the usual evidence-based standard of care: services provided by a state-run quitline. This study compares the relative effectiveness of three different treatments (Standard, Intensive, and Intensive Incentivized) on long-term smoking cessation (biochemically confirmed abstinence from combusted tobacco at 26-weeks post-target quit day) among Black adults who smoke and want to quit.

详细描述

Primary Objective: Identify the most effective treatment for increasing long-term smoking abstinence among Black adults who smoke.

Secondary Objectives:

  • Compare the 3 interventions on key patient-relevant outcomes (e.g., treatment satisfaction, smoke fewer cigarettes per day, quality of life) using validated measures collected at 8 and 26 weeks post-target quit day (TQD)
  • Identify subgroups for whom these treatments are especially effective or ineffective with respect to the primary and secondary outcomes.
  • Compare indices of treatment engagement (e.g., percentage of counseling sessions attended, percentage of days used nicotine patch) among Black people who smoke and are randomly assigned to the 3 different treatment conditions.

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 (Outcomes Assessor)

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • self-identify as Black
  • smoke cigarettes (greater than or equal to 1 cigarette on greater than or equal to 4 days/week)
  • motivated to quit smoking
  • willing to discontinue any non-study smoking cessation pharmacotherapy use during study treatment.

排除标准

  • currently taking bupropion for non-smoking cessation reasons

研究组 & 干预措施

Intensive Incentivized Intervention

Experimental

The Intensive Incentivized Intervention will include all components provided in the Intensive intervention (8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content) and up to $50 for completing counseling sessions ($5 for completing sessions 1-6 and $10 for completing sessions 7 and 8)

干预措施: Counseling Sessions (Other)

Standard Intervention

Active Comparator

The Standard Intervention will include 2 weeks of nicotine patches + 4 quitline-style counseling phone calls.

干预措施: Quitline Counseling Phone Calls (Other)

Intensive Intervention

Experimental

The Intensive Intervention will include 8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content.

干预措施: Nicotine patch (Drug)

Standard Intervention

Active Comparator

The Standard Intervention will include 2 weeks of nicotine patches + 4 quitline-style counseling phone calls.

干预措施: Nicotine patch (Drug)

Intensive Intervention

Experimental

The Intensive Intervention will include 8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content.

干预措施: Counseling Sessions (Other)

Intensive Intervention

Experimental

The Intensive Intervention will include 8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content.

干预措施: Pathways to Freedom (Other)

Intensive Incentivized Intervention

Experimental

The Intensive Incentivized Intervention will include all components provided in the Intensive intervention (8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content) and up to $50 for completing counseling sessions ($5 for completing sessions 1-6 and $10 for completing sessions 7 and 8)

干预措施: Monetary Incentive (Other)

Intensive Incentivized Intervention

Experimental

The Intensive Incentivized Intervention will include all components provided in the Intensive intervention (8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content) and up to $50 for completing counseling sessions ($5 for completing sessions 1-6 and $10 for completing sessions 7 and 8)

干预措施: Pathways to Freedom (Other)

Intensive Incentivized Intervention

Experimental

The Intensive Incentivized Intervention will include all components provided in the Intensive intervention (8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content) and up to $50 for completing counseling sessions ($5 for completing sessions 1-6 and $10 for completing sessions 7 and 8)

干预措施: Nicotine patch (Drug)

结局指标

主要结局

Biochemically confirmed abstinence from combusted tobacco at 26-weeks post-target quit day

时间窗: 26 weeks post-TQD

The primary outcome for this study will be biochemically confirmed (anabasine less than 2 ng/ml) 7-day point-prevalence smoking abstinence at 26- weeks post-TQD

次要结局

  • Biochemically confirmed abstinence from any nicotine product at 26-weeks post-target quit day(26 weeks post-TQD)
  • Treatment Satisfaction(8 weeks post-TQD)
  • Cigarettes per day(baseline, 8 and 26 weeks post-TQD)
  • Quality of Life measured by the Medical Outcomes Study's 12-item Short Form Survey Instrument (SF-12)(baseline, 8 and 26 weeks post-TQD)
  • Money spent on cigarettes per week(baseline, 8 and 26 weeks post-TQD)
  • Smoking Cessation Self-efficacy using a single 10-point Likert scale(baseline, 8 and 26 weeks post-TQD)
  • Psychological Distress measured by the 6-item Kessler screener (K6)(baseline, 8 and 26 weeks post-TQD)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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