授权安全管理人员支持在建筑行业实施戒烟服务:顺序多任务随机试验方案。

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-06-09 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0324717
Taghrid Asfar, David J Lee, Ramzi G Salloum, Jennifer H LeLaurin, Erin Kobetz, Nipesh Pradhananga, Roxana A De Dios Despaux, Kathryn E McCollister, Olusanya Oluwole, Laura Corbin, Jennifer Laine, Zoran Bursac
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引用次数: 0

摘要

在所有职业中,美国建筑工人(CWs)的吸烟率最高(27.2%对15%),但工作场所戒烟服务的覆盖率最低(14%对29%)。本研究旨在授权安全管理人员在建造业推行戒烟服务。采用参与式研究方法,本研究旨在:1)制定多层次策略(MLIs),以实施建筑工地安全管理人员提供的适应性戒烟计划;2)进行集群随机,混合类型1的有效性实施,两期顺序多任务随机试验(SMART)来测试该计划(ClinicalTrials.gov: NCT06098144)。mli包括:1)创建外部环境(研究调查员,利益相关者)和内部环境促进(公司咨询委员会,研究倡导者),2)对工作流程进行实地观察评估,3)培训安全管理人员提供干预措施,4)进行实施过程评估。在SMART项目中,将有8家公司的32个建筑工地和608名员工参加。在第一阶段,试验点将被随机分配到A1(转介到烟草戒烟热线-TQL)或B1(转介到TQL +尼古丁替代治疗(NRT) + 1组行为咨询会议)。在第二阶段,在3个月戒烟的应答者仅继续进行评估,而无应答者将被重新随机分配到C组(4次咨询+ NRT;A1 + C, B1 + C)或额外的1期治疗剂量(A2, B2)。参与者将在3、6、9和12个月接受4次随访评估。主要结局是A1 + A2 vs. B1 + B2和A1 + C vs. B1 + C的有效性(12个月生物标志物证实的延长戒断)和成本-效果(成本/戒烟,成本/质量调整生命年)。第二个结果是项目实施的可行性。我们假设B1 + B2将优于A1 + A2, B1 + C将优于A1 + C。该项目将为建筑业戒烟项目的有效性、成本效益和实施可行性提供新的科学证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Empowering safety managers to champion the implementation of smoking cessation services in the construction industry: Protocol for a sequential multiple assignment randomized trial.

Empowering safety managers to champion the implementation of smoking cessation services in the construction industry: Protocol for a sequential multiple assignment randomized trial.

Empowering safety managers to champion the implementation of smoking cessation services in the construction industry: Protocol for a sequential multiple assignment randomized trial.

Empowering safety managers to champion the implementation of smoking cessation services in the construction industry: Protocol for a sequential multiple assignment randomized trial.

US construction workers (CWs) have the highest cigarette smoking rate among all occupations (27.2% vs. 15%), yet the lowest coverage of workplace smoking cessation services (14% vs. 29%). This study aims to empower safety managers to implement smoking cessation services in the construction industry. Using participatory research methods, this study aims to: 1) Develop multilevel strategies (MLIs) to implement adaptive smoking cessation programs delivered by the safety manager on construction sites, and 2) conduct a cluster-randomized, hybrid type 1 effectiveness-implementation, 2-phase sequential multiple assignment randomized trial (SMART) to test the programs (ClinicalTrials.gov: NCT06098144). The MLIs include: 1) creating the outer setting (research investigators, stakeholders) and inner setting facilitation (companies' advisory committee, study champion), 2) conducting observational field assessments of workflows, 3) training safety managers to deliver the intervention, and 4) conducting implementation process evaluations. In SMART, 32 construction sites within 8 companies with 608 CWs will be enrolled. In Phase 1, sites will be randomized to A1 (referral to Tobacco Quitline -TQL) or B1 (referral to TQL + nicotine replacement treatment (NRT) + 1 group behavioral counseling session). In Phase 2, responders who quit smoking at 3 months continue with the assessment only, while non-responders will be re-randomized to C (4 counseling sessions + NRT; A1 + C, B1 + C) or an extra dose of Phase 1 treatment (A2, B2). Participants will receive 4 follow-up assessments at 3, 6, 9, and 12 months. Primary outcomes are the effectiveness (12-month biomarker-confirmed prolonged abstinence) and cost-effectiveness (cost/quit, cost/quality-adjusted life-year) of A1 + A2 vs. B1 + B2 and A1 + C vs. B1 + C. The secondary outcome is the feasibility of the program's implementation. We hypothesize that B1 + B2 will outperform A1 + A2, and B1 + C will outperform A1 + C. This project will generate novel scientific evidence on the effectiveness, cost-effectiveness, and implementation feasibility of smoking cessation programs in the construction industry.

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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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