Pilot Randomised Controlled Trial of ToQuit, A Technology Delivered Tobacco Cessation Intervention in India: Study Protocol
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
- 试验地点
- 2
- 主要终点
- Self-reported abstinence from tobacco in past 7 days preceding the outcome assessment
研究概览
简要总结
Tobacco use is associated with high mortality, and a range of morbidities including cancer, and lung and cardiovascular diseases. Furthermore, tobacco users who die prematurely deprive their families of income, raise the cost of health care and hinder economic development. India is the second-largest consumer (current use-48% males, 20% females; 275 million adults) and third largest producer of tobacco in the world5; and has one of the highest mortality related to tobacco. The treatment gap for tobacco use in India is as high as 92%. Opportunistic screening and brief interventions in primary care, although recommended by the World Health Organization (WHO), is largely missing in current practice in India.
The existing tobacco cessation strategy in India has shown limited success due to poor availability and accessibility of tobacco cessation services, and non-availability of interventions that are culturally relevant and contextual to the target population.
Preliminary formative research as a part of the larger ToQuit study has informed the development of the first version of the treatment package. This first version of the package was tested through a case series, by refining the intervention content and delivery mechanisms through an iterative process, to develop the final intervention. This pilot Randomised Control Trial (RCT) will aim to empirically evaluate the feasibility and acceptability of the mobile-based brief intervention (BI) for tobacco use, generate preliminary estimates of the impact of the BI, and fine-tune the procedures for a definitive RCT.
详细描述
ToQuit study aims to overcome the accessibility and feasibility hurdles by developing and evaluating a tobacco-cessation intervention that can be delivered using low cost and easily available mobile text messaging. India has 1.2 billion mobile phone subscriptions (tele-density 92%) and this provides a unique opportunity to significantly increase the penetration and coverage of tobacco cessation interventions in a low health-resource setting.
This pilot Randomised Control Trial (RCT) will aim to empirically evaluate the feasibility and acceptability of the mobile-based brief intervention (BI) for tobacco use, generate preliminary estimates of the impact of the BI, and fine-tune the procedures for a definitive RCT.
This protocol will serve as a research framework for the implementation of the proposed pilot RCT.
Objectives:
- To test and refine procedures for a definitive RCT.
- To assess the feasibility and acceptability of delivering the mobile-based BI for tobacco use.
- To refine the mobile-based BI package for a definitive RCT.
- To assess the impact of the mobile-based BI on tobacco use.
- To inform sample size calculations for the definitive RCT.
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 (Investigator, Outcomes Assessor)
盲法说明
The PI and outcomes assessor will be masked. The screeners will recruit participants into the study, who will then be randomized to one of the two study arms. The data team will assign a masked outcome assessor to collect outcome data.
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
- •Adult (>18 years) current users of tobacco in any form. Current user will be defined as individuals who have used tobacco at least once in the past 28 days.
- •Willing to quit tobacco in next 2 months,
- •Having a personal mobile phone, and
- •Able to read and reply to short message service (SMS) text in English or Hindi
排除标准
- •Participants having a shared/family phone
- •Age <18 years
- •Owns a mobile phone, but cannot read and reply to English or Hindi messages
结局指标
主要结局
Self-reported abstinence from tobacco in past 7 days preceding the outcome assessment
时间窗: At 3 months post-randomisation in all participants regardless of treatment completion.
After 3 months post-randomisation, all the participants will be asked if they used tobacco at least once in past 7 days.
次要结局
- Change in mean ASSIST score, from baseline to 3 months post-randomisation(At baseline and at 3 months post-randomisation in all participants regardless of treatment completion.)
- Self-reported abstinence from tobacco in past 28 days preceding the outcome assessment(At 3 months post-randomisation in all participants regardless of treatment completion.)
研究者
Abhijit Nadkarni
Associate Professor
London School of Hygiene and Tropical Medicine
