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社会经济地位处于劣势的成年人使用戒烟热线再治疗干预措施:一项析因随机临床试验。

Tobacco Quitline Retreatment Interventions Among Adults With Socioeconomic Disadvantage: A Factorial Randomized Clinical Trial.

机构信息

Center for Tobacco Research and Intervention, University of Wisconsin School of Medicine and Public Health, Madison.

Division of General Internal Medicine, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison.

出版信息

JAMA Netw Open. 2024 Nov 4;7(11):e2443044. doi: 10.1001/jamanetworkopen.2024.43044.

Abstract

IMPORTANCE

A single round of standard tobacco quitline treatment may not be sufficient to sustain abstinence, particularly among people experiencing socioeconomic disadvantage. Adaptive retreatment may help more individuals with socioeconomic disadvantage achieve abstinence and reduce disparities in smoking cessation outcomes.

OBJECTIVE

To evaluate 4 evidence-based strategies for adults with limited education, no insurance, or Medicaid eligibility who continued smoking after quitline treatment.

DESIGN, SETTING, AND PARTICIPANTS: A factorial randomized clinical trial with 4 factors adapting quitline strategies was conducted for participants enrolled from June 7, 2018, to January 25, 2023, with 6-month follow-up. Adults using the Wisconsin Tobacco Quit Line who were smoking cigarettes 3 to 6 months after prior quitline treatment who were uninsured, Medicaid insured, or had no more than a high school education were included.

INTERVENTIONS

Quitline retreatment strategies were (1) increased counseling intensity (4 calls vs 1 call), (2) increased nicotine replacement therapy intensity (4 weeks of combination nicotine patch plus nicotine lozenge vs 2 weeks of nicotine patch), (3) text-message support (National Cancer Institute SmokefreeTXT program vs none), and (4) financial incentives for engagement in counseling and SmokefreeTXT ($30/call and/or 6-week SmokefreeTXT retention vs no incentives).

MAIN OUTCOMES AND MEASURES

Primary outcome was 7-day point-prevalence biochemically confirmed abstinence 26 weeks after the target quit day. Intention-to-treat analysis was performed.

RESULTS

Of 6019 people assessed for eligibility, 1316 (21.9%) participants were randomized (mean [SD] age, 53.1 [11.9] years; 760 [57.8%] women), and 919 (69.8%) provided final follow-up. Intention-to-treat analyses showed 162 participants (12.3%) had biochemically confirmed abstinence at 26 weeks (368 [28.0% self-reported abstinence]). There were no significant main effects for the primary outcome: 1 call (11.6% [77 of 662]) vs 4 calls (13.0% [85 of 654]) (odds ratio [OR], 1.04; 95% CI, 0.88-1.24), 2-week patch (11.2% [73 of 654]) vs 4-week combination nicotine replacement therapy (13.4% [89 of 662]) (OR, 1.12; 95% CI, 0.94-1.34), no SmokefreeTXT (13.4% [88 of 657]) vs SmokefreeTXT (11.2% [74 of 659]) (OR, 0.88; 95% CI, 0.74-1.05), and no financial incentives (12.8% [85 of 662]) vs financial incentives (11.8% [77 of 654]) (OR, 0.94; 95% CI, 0.78-1.11).

CONCLUSIONS AND RELEVANCE

In this randomized clinical trial evaluating enhancements to tobacco quitlines for adults with socioeconomic disadvantage who were smoking after quitline treatment, none of the adaptive treatment strategies robustly improved long-term abstinence. Strategies are needed to enhance quitline retreatment effectiveness for adults with socioeconomic disadvantage.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT03538938.

摘要

重要性

单次标准戒烟热线治疗可能不足以维持戒烟,尤其是在社会经济处于不利地位的人群中。适应性再治疗可能有助于更多社会经济处于不利地位的人实现戒烟,并减少戒烟结果的差异。

目的

评估 4 种针对接受过戒烟热线治疗后继续吸烟且受教育程度有限、没有保险或符合医疗补助资格的成年人的循证策略。

设计、设置和参与者:这是一项采用 4 个因素的析因随机临床试验,针对 2018 年 6 月 7 日至 2023 年 1 月 25 日期间参加威斯康星州戒烟热线的参与者进行,随访时间为 6 个月。包括使用威斯康星州戒烟热线且在之前戒烟热线治疗后 3 至 6 个月吸烟、没有保险、医疗补助保险或受教育程度不超过高中的成年人。

干预措施

戒烟热线再治疗策略为(1)增加咨询强度(4 次通话与 1 次通话),(2)增加尼古丁替代疗法强度(4 周联合尼古丁贴片加尼古丁含片与 2 周尼古丁贴片),(3)使用国家癌症研究所无烟短信支持计划(NCI SmokefreeTXT)与不使用(4)对参与咨询和无烟短信的激励(每次通话 30 美元和/或 6 周无烟短信保留与无激励)。

主要结果和措施

主要结局为目标戒烟日 26 周时通过生物化学方法确认的 7 天点前戒烟率。采用意向治疗分析。

结果

在符合条件的 6019 人中,有 1316 人(21.9%)被随机分配(平均[标准差]年龄,53.1[11.9]岁;760[57.8%]为女性),919 人(69.8%)提供了最终随访。意向治疗分析显示,26 周时有 162 名参与者(12.3%)通过生物化学方法确认戒烟(368 名[28.0%]自我报告戒烟)。主要结局无显著主要效应:1 次通话(11.6%[77/662])与 4 次通话(13.0%[85/654])(比值比[OR],1.04;95%CI,0.88-1.24),2 周贴片(11.2%[73/654])与 4 周联合尼古丁替代疗法(13.4%[89/662])(OR,1.12;95%CI,0.94-1.34),无无烟短信(13.4%[88/657])与无烟短信(11.2%[74/659])(OR,0.88;95%CI,0.74-1.05),无财务激励(12.8%[85/662])与财务激励(11.8%[77/654])(OR,0.94;95%CI,0.78-1.11)。

结论和相关性

在这项针对接受过戒烟热线治疗后继续吸烟且社会经济处于不利地位的成年人的适应性戒烟热线治疗增强策略的随机临床试验中,没有一种适应性治疗策略能显著提高长期戒烟率。需要制定策略来增强社会经济处于不利地位的成年人的戒烟热线再治疗效果。

试验注册

ClinicalTrials.gov 标识符:NCT03538938。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de52/11541633/c2a9b876a589/jamanetwopen-e2443044-g001.jpg

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