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首页> 外文期刊>BMJ Open >A randomised controlled trial to prevent smoking relapse among recently quit smokers enrolled in employer and health plan sponsored quitlines
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A randomised controlled trial to prevent smoking relapse among recently quit smokers enrolled in employer and health plan sponsored quitlines

机译:一项随机对照试验,以防止雇主和健康计划赞助的戒烟热线中最近戒烟的吸烟者复发

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摘要

Objective To test adding an interactive voice response (IVR)-supported protocol to standard quitline treatment to prevent relapse among recently quit smokers. Design Parallel randomised controlled trial with three arms: standard quitline, standard plus technology enhanced quitline with 10 risk assessments (TEQ-10), standard plus 20 TEQ assessments (TEQ-20). Setting Quit For Life (QFL) programme. Participants 1785 QFL enrolees through 19 employers or health plans who were 24+ h quit. Interventions QFL is a 5-call telephone-based cessation programme including medications and web-based support. TEQ interventions included 10 or 20 IVR-delivered relapse risk assessments over 8?weeks with automated transfer to counselling for those at risk. Main outcome measures Self-reported 7-day and 30-day abstinence assessed at 6-month and 12-month post-enrolment (response rates: 61% and 59%, respectively). Missing data were imputed. Results 1785 were randomised (standard n=592, TEQ-10 n=602, TEQ-20 n=591). Multiple imputation-derived, intent-to-treat 30-day quit rates (95% CI) at 6?months were 59.4% (53.7% to 63.8%) for standard, 62.3% (57.7% to 66.9%) for TEQ-10, 59.4% (53.7% to 65.1%) for TEQ-20 and 30-day quit rates at 12?months were 61.2% (55.6% to 66.8%) for standard, 60.6% (56.0% to 65.2%) for TEQ-10, 54.9% (49.0% to 60.9%) for TEQ-20. There were no significant differences in quit rates. 73.3% of TEQ participants were identified as at-risk by IVR assessments; on average, participants completed 0.41 IVR-transferred counselling calls. Positive risk assessments identified participants less likely (OR=0.56, 95% CI 0.42 to 0.76) to be abstinent at 6?months. Conclusions Standard treatment was highly effective, with 61% remaining abstinent at 12?months using multiple imputation intent-to-treat (intent-to-treat missing=smoking quit rate: 38%). TEQ assessments identified quitters at risk for relapse. However, adding IVR-transferred counselling did not yield higher quit rates. Research is needed to determine if alternative designs can improve outcomes. Trial registration number NCT00888992.
机译:目的测试将交互式语音应答(IVR)支持的协议添加到标准戒烟热线治疗中,以防止最近戒烟的吸烟者复发。设计平行,随机对照试验,分为三组:标准戒烟热线,标准加技术增强的戒烟热线,具有10个风险评估(TEQ-10),标准加20个TEQ评估(TEQ-20)。设置退出生命(QFL)程序。参与者通过24小时以上退出的19位雇主或健康计划参加了1785名QFL参与者。干预QFL是一个基于5个电话的戒烟计划,其中包括药物和基于Web的支持。 TEQ干预包括在8周内进行10或20次IVR进行的复发风险评估,并自动转移至有风险者的咨询处。主要结局指标入学后6个月和12个月评估的自我报告的7天和30天戒断(应答率分别为61%和59%)。缺少的数据被估算。结果1785被随机化(标准n = 592,TEQ-10 n = 602,TEQ-20 n = 591)。 6个月时多次插补衍生的意向性治疗30天退出率(95%CI)为59.4%(53.7%至63.8%),TEQ-10为62.3%(57.7%至66.9%) ,TEQ-20的59.4%(53.7%至65.1%)和12个月的30天退出率是标准的61.2%(55.6%至66.8%),TEQ-10的60.6%(56.0%至65.2%) ,TEQ-20为54.9%(49.0%至60.9%)。退出率没有显着差异。 IVR评估将73.3%的TEQ参与者确定为高危人群;平均而言,参与者完成了0.41个IVR转接的咨询电话。积极的风险评估表明参与者在6个月时戒断的可能性较小(OR = 0.56,95%CI 0.42至0.76)。结论标准治疗是高度有效的,使用多次插补治疗意向治疗(12个月时仍能戒断61%)(缺失治疗意向=戒烟率:38%)。 TEQ评估确定了退出者有复发风险。但是,增加IVR转移的咨询并不能提高戒烟率。需要进行研究以确定替代设计是否可以改善结果。试用注册号NCT00888992。

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