跳至主要内容
临床试验/NCT03521466
NCT03521466已完成不适用

A Randomized Control Trial Evaluating the Effectiveness of a Medical Student Guided Smoking Cessation Program for Hospitalized Smokers in India

University Hospitals Cleveland Medical Center2 个研究点 分布在 1 个国家目标入组 700 人开始时间: 2018年12月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
700
试验地点
2
主要终点
Biochemically verified 7 day quit rate measured 6 months after enrolment.

研究概览

简要总结

The purpose of this randomized control trial is two- fold. The primary hypothesis of the study is that smoking cessation counseling delivered through trained medical students will lead to higher rates of abstinence amongst patients in the intervention group, as compared to a control group, when measured by self-reported and biochemical testing at 6 months after enrolment .

The secondary hypothesis is that medical students engaging in a structured curriculum that includes counseling hospitalized smokers will show demonstrable increases in knowledge, confidence in their abilities, and use of smoking cessation techniques in regular practice.

详细描述

India is the 2nd largest consumer of tobacco in the world, with 275 million Indians using tobacco. Each hospitalization is an opportunity for providers to motivate their patients to quit. However, the Indian medical curriculum typically offers little training in the skills required to successfully counsel a patient to quit smoking. The investigators hypothesize that trained medical students can increase subsequent quit rates among hospitalized smokers, while acquiring skills in tobacco cessation counseling.

The investigators propose a 2-armed multicenter randomized controlled trial (RCT) that will compare the effectiveness of standard hospital practice versus a medical student-guided smoking cessation program initiated inpatient and continued for three months after discharge. The target study population includes current smokers admitted to the general medicine, pulmonary and cardiology wards. These patients will be randomized to receive either usual care or the intervention. The intervention group will receive both inpatient and longitudinal post-discharge telephone counseling by medical students who have successfully completed a training workshop in tobacco cessation counseling and pharmacotherapy. The students can also recommend nicotine replacement therapy (NRT) to the patient if indicated. The control group will receive counseling and/or NRT at the discretion of the treating physician. They will not receive phone based counseling after discharge.

Patients from both groups will be asked to report their quit status 6 months after enrolment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

盲法说明

Coordinators calling the patient to assess quit status are blinded to group assignment.

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients age 18-70 years old, who are admitted to the medical, and if required surgical wards.
  • Patients must be current smokers (cigarettes and/or bidis) at the time of admission or report having smoked at all in the last 4 weeks prior to admission (to account for changes in behaviour during illness).
  • Patients living within 10 Km radius of the hospital.

排除标准

  • Unwilling to participate
  • Patients who use only non-smoked tobacco will be excluded.
  • Patients who are are daily alcohol users, daily cannabis or psychotropic drug users.
  • Patients who do not have a telephone/ unable to follow up
  • Patients unable to understand the local/common language
  • Patients with psychiatric conditions rendering them incapable of interacting with the providers
  • Medically unstable patients
  • Patients with expected hospital stay <24 hours
  • Patients with life expectancy < 12 months
  • Pregnant patients
  • Patients currently participating in a tobacco cessation program
  • Prior participation in this trial during another hospitalisation

结局指标

主要结局

Biochemically verified 7 day quit rate measured 6 months after enrolment.

时间窗: 6 months from enrolment

At 6 months from enrolment, patients will be asked to report abstinence from smoking over the last 7 days (No more than 5 cigarettes in total since quit date); those who claim to have quit will be asked to provide biochemical confirmation by exhaled carbon monoxide breath testing (\<10 Parts Per Million will be considered a verified quit attempt).

次要结局

  • Correlation between verified quit rates at 6 months and FTND scores at enrolment(6 months from enrolment)
  • Agreement between self reported quit 7 day quit rate and biochemically verified 7 day quit rate, measured at 6 months from enrolment(6 months from enrolment)
  • Biochemically verified 90 day quit rate, measured 6 months after enrolment(6 months from enrolment)
  • Qualitative analysis of student attitudes towards smoking cessation counseling(12 months after training)
  • Number of patients achieving a 50% reduction in the number of cigarettes /bidis smoked in a week, measured at 2 and 6 months after enrolment(2 and 6 months from enrolment)
  • Number of patients who report having quit smoking in the last 7 days (irrespective of biochemical verification)(2 and 6 months from enrolment)
  • Pre-post analysis of medical student knowledge about counseling techniques and pharmacotherapy(6 weeks and 12 months after training)
  • Qualitative analysis of the feasibility and acceptability of the intervention(12 months after training)
  • No of patients who have refrained from using smokeless tobacco in the last 7 days, measured at 6 months.(6 months from enrolment)

研究者

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

Richard Josephson, MS MD

Director CVP Rehabilitation, Harrington Heart and Vascular Institute

University Hospitals Cleveland Medical Center

研究点 (2)

Loading locations...

相似试验