印度哈里亚纳邦卫生机构在戒烟方面共同决策的有效性——一项双盲、平行组随机对照试验方案

IF 2.2 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Pranav Kshtriya , Sonu Goel , Abhishek Ghosh
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引用次数: 0

摘要

背景:共享决策(SDM)将证据、患者价值观和偏好纳入医疗决策。SDM和决策辅助工具可以促进卫生专业人员的参与和患者对戒烟疗法的了解,从而改善使用和效果。与个人决策不同,SDM促进了与患者优先事项相一致的更明智的判断的对话。因此,本研究将试图确定共同决策在烟草依赖治疗中的功效。方法:1)设计:双组平行随机对照试验(RCT); 2)设置:选定印度哈里亚纳邦3个政府卫生中心;3)参与者:选定卫生中心门诊部/戒烟中心(TCC)就诊的596名年龄≥18岁的吸烟者。4)干预与比较:干预组采用专门设计的基于三语戒烟模型的决策辅助工具,共享药物治疗(尼古丁替代疗法、安非他酮)的处方决策过程,对照组采用标准治疗。5)测量:主要结果包括尿可替宁分析,用于评估7天点流行性戒断。次要结局包括患者满意度问卷PSQ-18评分、累计戒烟天数、自我报告的戒烟尝试次数和戒断率。将比较干预组和比较组之间的结果,如行为状态的改变,即戒烟。两组比较时,比例差异采用卡方检验,均数差异采用t检验。在比较两组的结果时,将进行意向治疗分析。讨论:SDM在医疗机构戒烟治疗中的研究不足,因此本研究着眼于不同环境下的可比干预措施,以增加证据。这表明,这项关于SDM在戒烟治疗中的研究,包括医疗保健专业人员,旨在帮助患者做出基于证据和价值的医疗决策。试验注册:本方案已在印度临床试验注册中心注册,注册号为CTRI/2022/10/046793。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of shared decision making in tobacco cessation among health facilities of Haryana, India – A double blinded, parallel group Randomized Controlled trial Protocol

Background

Shared decision-making (SDM) incorporates evidence, patient values, and preferences into medical decision-making. SDM and decision aids might promote health professional engagement and patient knowledge of tobacco cessation therapy, improving usage and results. The SDM facilitates talks that lead to better-informed judgements that align with patients' priorities, unlike individual decision-making. Thus, the study will attempt to identify the efficacy of shared decision making in tobacco dependence treatment.

Methods

1) Design: a two-arm parallel group randomized controlled trial (RCT) 2) Setting: Three selected government health centers of Haryana, India. 3) Participants: 596 tobacco users aged ≥18 visiting the outpatient department/Tobacco cessation centers (TCC) of selected health centers. 4) Intervention and Comparator: The intervention group will receive shared decision process for prescribing pharmacotherapy (Nicotine replacement therapy, Bupropion) using specially designed decision aid based on three-talk model for tobacco cessation, while the control group will get standard care. 5) Measurements: Primary outcomes include urinary cotinine analysis for evaluating 7-day point prevalence abstinence. Secondary outcomes include patient satisfaction questionnaire PSQ-18 score, cumulative days of tobacco abstinence, self-reported number of quit attempts, and the rate of withdrawal. The outcomes such as change in behavior status i.e. tobacco cessation will be compared between the intervention and the comparator groups. When comparing the two groups, differences between proportions will be assessed by chi-square test, differences between means with t-test. An intention to treat analysis will be done when comparing outcomes in both arms.

Discussion

SDM in tobacco cessation therapies in healthcare settings is understudied, thereby this study looks at comparable interventions in different settings to add to the evidence. This suggests that this study on SDM in tobacco cessation therapy, which includes healthcare professionals, aims to assist patients in making evidence- and value-based medical decisions.

Trial registration

This protocol has been registered under the registration number CTRI/2022/10/046793 with the Clinical Trials Registry in India.
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来源期刊
Public Health in Practice
Public Health in Practice Medicine-Health Policy
CiteScore
2.80
自引率
0.00%
发文量
117
审稿时长
71 days
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