跳至主要内容
临床试验/NCT07356297
NCT07356297尚未招募不适用

Comparing Remotely-delivered Interventions to Promote Cessation Among Adults Who Smoke Menthol Cigarettes

University of Michigan0 个研究点目标入组 1,200 人开始时间: 2026年11月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
1,200

研究概览

简要总结

The purpose of this study is to evaluate whether a digital, incentive-based program, used in conjunction with traditional quitline (QL) services, can be beneficial to quitline callers who smoke menthol cigarettes. The services evaluated focus on coaching, support, and/or incentives for individuals who wish to quit smoking.

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
Double (Care Provider, Outcomes Assessor)

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

  • adults (ages 18+) who call partnered quitlines (QL); and
  • currently smoke menthol cigarettes; and
  • are fluent in English; and
  • plan to live in the United States for the full trial duration; and
  • have daily smartphone access (including data access) or are willing to use a study-provided smartphone and data plan
  • ability to provide informed consent

排除标准

  • not ready to set a quit date within 30 days; or
  • have not smoked in the past 7 days
  • Inability to speak/understand English
  • Conditions precluding informed consent or understanding of intervention or assessment content
  • PI discretion

研究组 & 干预措施

Quitline (QL)

Active Comparator

Participants complete QL services

干预措施: Quitline (QL) (Behavioral)

Quitline (QL) + App

Active Comparator

Participants complete QL services and download our incentive-based mobile app

干预措施: Quitline (QL) (Behavioral)

Quitline (QL) + App

Active Comparator

Participants complete QL services and download our incentive-based mobile app

干预措施: Mobile incentive-based intervention (Behavioral)

研究者

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

Lara Coughlin

Principal Investigator

University of Michigan

相似试验

已完成
3 期
Once-A-Day Pregabalin For Partial Seizures
CTRI/2011/08/001976Pfizer Limited264
进行中(未招募)
1 期
A randomized, double-blind, placebo-controlled, adaptive-design study to assess the safety and efficacy of daily 200 mg fluvoxamine as add-on therapy to standard of care in moderate severity COVID-19 patientsSARS-CoV-2 infected patientsMedDRA version: 23.0Level: LLTClassification code 10084270Term: SARS-CoV-2 acute respiratory diseaseSystem Organ Class: 100000004862
EUCTR2020-002299-11-HUSigmaDrugs Research Ltd.100
进行中(未招募)
不适用
A randomized, double-blind, placebo-controlled, parallel group, multicenter twoweek study to evaluate the efficacy and safety of once-daily, intranasaladministration of GW685698X aqueous nasal spray 100 mcg in adult andadolescent subjects with seasonal allergic rhinitis in EuropeSeasonal allergic rhinitis (SAR)
EUCTR2004-004434-14-SEGlaxoSmithKline Research & Development Ltd288
进行中(未招募)
1 期
Efficacy and Safety of Alirocumab Versus Placebo on Top of Maximally Tolerated Lipid Lowering Therapy in Patients with Hypercholesterolemia Who Have Type 1 or Type 2 Diabetes and are Treated with Insulin (ODYSSEY DM - Insulin)Hypercholesterolemia
EUCTR2015-000799-92-ITSANOFI-AVENTIS GROUPE517
进行中(未招募)
不适用
Evaluation of cardiovascular outcomes in patients with type 2 diabetes after acute coronary syndrome during treatment with AVE0010 (lixisenatide)
EUCTR2009-012852-26-LVsanofi-aventis Recherche & Développement6,000