伦敦运动与孕期吸烟女性(LEAP)试验:一项关于孕期戒烟身体活动的随机对照试验及经济评估

The London Exercise And Pregnant smokers (LEAP) trial: a randomised controlled trial of physical activity for smoking cessation in pregnancy with an economic evaluation.

作者信息

Ussher Michael, Lewis Sarah, Aveyard Paul, Manyonda Isaac, West Robert, Lewis Beth, Marcus Bess, Riaz Muhammad, Taylor Adrian H, Barton Pelham, Daley Amanda, Essex Holly, Esliger Dale, Coleman Tim

机构信息

Population Health Research Institute, St George's, University of London, London, UK.

Division of Epidemiology and Public Health and UK Centre for Tobacco and Alcohol Studies, University of Nottingham, Nottingham, UK.

出版信息

Health Technol Assess. 2015 Oct;19(84):vii-xxiv, 1-135. doi: 10.3310/hta19840.

Abstract

BACKGROUND

Smoking during pregnancy is the main preventable cause of poor birth outcomes. Improved methods are needed to help women to stop smoking during pregnancy. Pregnancy provides a compelling rationale for physical activity (PA) interventions as cessation medication is contraindicated or ineffective, and an effective PA intervention could be highly cost-effective.

OBJECTIVE

To examine the effectiveness and cost-effectiveness of a PA intervention plus standard behavioural support for smoking cessation relative to behavioural support alone for achieving smoking cessation at the end of pregnancy.

DESIGN

Multicentre, two-group, pragmatic randomised controlled trial and economic evaluation with follow-up at the end of pregnancy and 6 months postnatally. Randomisation was stratified by centre and a computer-generated sequence was used to allocate participants using a 1 : 1 ratio.

SETTING

13 hospitals offering antenatal care in the UK.

PARTICIPANTS

Women between 10 and 24 weeks' gestation smoking five or more cigarettes a day before pregnancy and one or more during pregnancy.

INTERVENTIONS

Participants were randomised to behavioural support for smoking cessation (control) or behavioural support plus a PA intervention consisting of supervised treadmill exercise plus PA consultations. Neither participants nor researchers were blinded to treatment allocation.

MAIN OUTCOME MEASURES

The primary outcome was self-reported, continuous smoking abstinence between a quit date and end of pregnancy, validated by expired carbon monoxide and/or salivary cotinine. Secondary outcomes were maternal weight, depression, birth outcomes, withdrawal symptoms and urges to smoke. The economic evaluation investigated the costs of the PA intervention compared with the control intervention.

RESULTS

In total, 789 women were randomised (n = 394 PA, n = 395 control). Four were excluded post randomisation (two had been enrolled twice in sequential pregnancies and two were ineligible and randomised erroneously). The intention-to-treat analysis comprised 785 participants (n = 392 PA, n = 393 control). There was no significant difference in the rate of abstinence at the end of pregnancy between the PA group (7.7%) and the control group (6.4%) [odds ratio for PA group abstinence 1.21, 95% confidence interval (CI) 0.70 to 2.10]. For the PA group compared with the control group, there was a 33% (95% CI 14% to 56%), 28% (95% CI 7% to 52%) and 36% (95% CI 12% to 65%) significantly greater increase in self-reported minutes of moderate- and vigorous-intensity PA from baseline to 1 week, 4 weeks and 6 weeks respectively. Accelerometer data showed that there was no significant difference in PA levels between the groups. There were no significant differences between the groups for change in maternal weight, depression, withdrawal symptoms or urges to smoke. Adverse events and birth outcomes were similar between the groups except for there being significantly more caesarean births in the control group than in the PA group (28.7% vs. 21.3%; p < 0.023). The PA intervention was less costly than the control intervention by £35 per participant. This was mainly attributable to increased health-care usage in the control group. However, there was considerable statistical uncertainty around this estimate.

CONCLUSIONS

During pregnancy, offering an intervention combining supervised exercise and PA counselling does not add to the effectiveness of behavioural support for smoking cessation. Only 10% of participants had PA levels accessed by accelerometer and it is, therefore, unclear whether or not the lack of an effect on the primary outcome is the result of insufficient increases in PA. Research is needed to identify the smoking populations most suitable for PA interventions and methods for increasing PA adherence.

TRIAL REGISTRATION

Current Controlled Trials ISRCTN48600346.

FUNDING

This project was funded by the NIHR Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 19, No. 84. See the NIHR Journals Library website for further project information.

摘要

背景

孕期吸烟是导致不良出生结局的主要可预防因素。需要改进方法来帮助孕妇戒烟。孕期进行体育活动(PA)干预具有充分的理由,因为戒烟药物存在禁忌或无效,而有效的PA干预可能具有很高的成本效益。

目的

研究PA干预加标准行为支持戒烟相对于单纯行为支持在孕期结束时实现戒烟的有效性和成本效益。

设计

多中心、两组、实用随机对照试验及经济评估,在孕期结束时和产后6个月进行随访。随机分组按中心分层,使用计算机生成的序列以1∶1的比例分配参与者。

地点

英国13家提供产前护理的医院。

参与者

妊娠10至24周、孕前每天吸烟5支或更多且孕期每天吸烟1支或更多的女性。

干预措施

参与者被随机分为接受戒烟行为支持(对照组)或行为支持加PA干预,PA干预包括有监督的跑步机锻炼和PA咨询。参与者和研究人员均未对治疗分配设盲。

主要结局指标

主要结局为自我报告的从戒烟日到孕期结束持续戒烟情况,通过呼出一氧化碳和/或唾液可替宁验证。次要结局包括孕妇体重、抑郁、出生结局、戒断症状和吸烟冲动。经济评估调查了PA干预与对照干预的成本。

结果

总共789名女性被随机分组(PA组394名,对照组395名)。随机分组后排除4名(2名在连续妊娠中被重复纳入,2名不符合条件且随机分组错误)。意向性分析包括785名参与者(PA组392名,对照组393名)。PA组(7.7%)和对照组(6.4%)在孕期结束时的戒烟率无显著差异[PA组戒烟的优势比为1.21,95%置信区间(CI)0.70至2.10]。与对照组相比,PA组自我报告的中度和剧烈强度PA从基线到第1周、第4周和第6周的分钟数分别显著增加33%(95%CI 14%至56%)、28%(95%CI 7%至52%)和36%(95%CI 12%至65%)。加速度计数据显示两组的PA水平无显著差异。两组在孕妇体重、抑郁、戒断症状或吸烟冲动的变化方面无显著差异。除对照组剖宫产率显著高于PA组(28.7%对21.3%;p<0.023)外,两组的不良事件和出生结局相似。PA干预比对照干预每名参与者成本低35英镑。这主要归因于对照组医疗保健使用增加。然而,该估计存在相当大的统计不确定性。

结论

孕期提供结合有监督锻炼和PA咨询的干预并不能增加戒烟行为支持的有效性。只有10%的参与者的PA水平通过加速度计测量,因此尚不清楚对主要结局缺乏影响是否是由于PA增加不足所致。需要开展研究以确定最适合PA干预的吸烟人群以及提高PA依从性的方法。

试验注册号

Current Controlled Trials ISRCTN48600346。

资助

本项目由英国国家卫生研究院卫生技术评估项目资助,将全文发表于《卫生技术评估》;第19卷,第84期。有关更多项目信息,请见英国国家卫生研究院期刊图书馆网站。

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