跳至主要内容
临床试验/NCT05487807
NCT05487807招募中1 期

Quit4Life+: Adapting and Evaluating a Phone-Based Tobacco Use Cessation Program for People Living With HIV in Uganda and Zambia (Quit4Life+ )

University of Southern California2 个研究点 分布在 2 个国家目标入组 800 人开始时间: 2023年9月13日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
800
试验地点
2
主要终点
Prolonged tobacco abstinence

研究概览

简要总结

This proposal tests the efficacy of a phone-based tobacco cessation intervention for people living with HIV (PLWH) in comparison to the standard of care (brief advice to quit) and nicotine replacement therapy (nicotine patches) in Uganda and Zambia. This study will provide insight into the efficacy, feasibility, applicability, and affordability of delivering tobacco cessation interventions through health care professionals at HIV treatment centers in two countries with different tobacco use patterns, policy environments, and health care resources. The previously tested SMS-platform to be used in this study is uniquely positioned to be scaled in low- and middle-income countries worldwide, in which case rigorous research showing even modest success in reducing the prevalence of tobacco consumption among PLWH could confer substantial health and economic benefits.

详细描述

While there is substantial evidence supporting interventions to help tobacco users in the general population quit, little is available relevant to the challenges facing HIV+ tobacco users, especially those living in low-income African countries. This study approaches this gap with the first randomized control trial (RCT) to test the efficacy of a tailored short message service (SMS) based tobacco use cessation intervention on prolonged tobacco use abstinence at 6 months post program initiation in comparison to the standard of care (brief advice to quit) and nicotine replacement therapy (nicotine patches) among PLWH in Uganda and Zambia. This study will provide insight into the efficacy, feasibility, applicability, and affordability of delivering tobacco cessation interventions through health care professionals at HIV treatment centers in two countries with different tobacco use patterns, policy environments, and health care resources and provide needed information to providers and policymakers looking for cost-effective tobacco cessation interventions.

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
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

入选标准

  • 未提供

排除标准

  • Females who are pregnant, planning to get pregnant, or breastfeeding
  • <18 years (underage of consent)
  • Visitor, not receiving continuous care at study site
  • Not a current daily tobacco user
  • Any physical, cognitive, or psychological disabilities that would prevent them from participating in the study
  • Illiterate in English and/or local languages
  • Does not consent

研究组 & 干预措施

Nicotine Replacement

Active Comparator

This group will receive the standard of care and be prescribed nicotine replacement therapy

干预措施: Nicotine patch (Drug)

Text Messaging

Active Comparator

This group will receive the standard of care and receive text message support

干预措施: text messaging (Behavioral)

Nicotine replacement and text messaging

Active Comparator

This group will receive the standard of care, be prescribed nicotine replacement therapy, and receive text message support

干预措施: Nicotine patch (Drug)

Nicotine replacement and text messaging

Active Comparator

This group will receive the standard of care, be prescribed nicotine replacement therapy, and receive text message support

干预措施: text messaging (Behavioral)

结局指标

主要结局

Prolonged tobacco abstinence

时间窗: 6 months post enrollment

The primary outcome for this efficacy trial is the proportion of study participants that have prolonged abstinence (i.e., no tobacco use from the target quit date through follow-up) at 3 and 6 months post enrollment measured by self-report and biochemically-verified as recommended by the Society for Research on Nicotine and Tobacco, the biomarker being assessed is urinary cotinine (\<12 ng/mL) at 6 months post enrollment

次要结局

  • Point Prevalence(4 weeks, 8 weeks, and 3 months post enrollment)

研究者

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

Heather Wipfli

Associate Professor

University of Southern California

研究点 (2)

Loading locations...

相似试验