Jesse T Kaye, Julie A Kirsch, Daniel M Bolt, Kathleen H Kobinsky, Katrina A Vickerman, Kristina Mullis, David L Fraser, Timothy B Baker, Michael C Fiore, Danielle E McCarthy
{"title":"对社会经济状况不佳的成年人进行戒烟热线再治疗干预:一项因子随机临床试验。","authors":"Jesse T Kaye, Julie A Kirsch, Daniel M Bolt, Kathleen H Kobinsky, Katrina A Vickerman, Kristina Mullis, David L Fraser, Timothy B Baker, Michael C Fiore, Danielle E McCarthy","doi":"10.1001/jamanetworkopen.2024.43044","DOIUrl":null,"url":null,"abstract":"<p><strong>Importance: </strong>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.</p><p><strong>Objective: </strong>To evaluate 4 evidence-based strategies for adults with limited education, no insurance, or Medicaid eligibility who continued smoking after quitline treatment.</p><p><strong>Design, setting, and participants: </strong>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.</p><p><strong>Interventions: </strong>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).</p><p><strong>Main outcomes and measures: </strong>Primary outcome was 7-day point-prevalence biochemically confirmed abstinence 26 weeks after the target quit day. Intention-to-treat analysis was performed.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusions and relevance: </strong>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.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov Identifier: NCT03538938.</p>","PeriodicalId":14694,"journal":{"name":"JAMA Network Open","volume":"7 11","pages":"e2443044"},"PeriodicalIF":10.5000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11541633/pdf/","citationCount":"0","resultStr":"{\"title\":\"Tobacco Quitline Retreatment Interventions Among Adults With Socioeconomic Disadvantage: A Factorial Randomized Clinical Trial.\",\"authors\":\"Jesse T Kaye, Julie A Kirsch, Daniel M Bolt, Kathleen H Kobinsky, Katrina A Vickerman, Kristina Mullis, David L Fraser, Timothy B Baker, Michael C Fiore, Danielle E McCarthy\",\"doi\":\"10.1001/jamanetworkopen.2024.43044\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Importance: </strong>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.</p><p><strong>Objective: </strong>To evaluate 4 evidence-based strategies for adults with limited education, no insurance, or Medicaid eligibility who continued smoking after quitline treatment.</p><p><strong>Design, setting, and participants: </strong>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.</p><p><strong>Interventions: </strong>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).</p><p><strong>Main outcomes and measures: </strong>Primary outcome was 7-day point-prevalence biochemically confirmed abstinence 26 weeks after the target quit day. Intention-to-treat analysis was performed.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusions and relevance: </strong>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.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov Identifier: NCT03538938.</p>\",\"PeriodicalId\":14694,\"journal\":{\"name\":\"JAMA Network Open\",\"volume\":\"7 11\",\"pages\":\"e2443044\"},\"PeriodicalIF\":10.5000,\"publicationDate\":\"2024-11-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11541633/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JAMA Network Open\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1001/jamanetworkopen.2024.43044\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAMA Network Open","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1001/jamanetworkopen.2024.43044","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
摘要
重要性:单轮标准戒烟治疗可能不足以维持戒烟,尤其是在社会经济条件较差的人群中。适应性再治疗可以帮助更多社会经济条件较差的人实现戒烟,减少戒烟结果的差异:目的:评估针对教育程度有限、无保险或无医疗补助资格的成年人在接受戒烟治疗后继续吸烟的 4 种循证策略:对 2018 年 6 月 7 日至 2023 年 1 月 25 日期间注册的参与者进行了一项因子随机临床试验,对戒烟热线策略进行了 4 个因子的调整,并进行了 6 个月的随访。研究对象包括使用威斯康星州烟草戒烟热线的成人,他们在接受戒烟热线治疗 3 至 6 个月后仍在吸烟,且无保险、有医疗补助保险或学历不超过高中:戒烟热线再治疗策略包括:(1)增加咨询强度(4次呼叫 vs 1次呼叫);(2)增加尼古丁替代疗法强度(4周尼古丁贴片加尼古丁锭剂组合疗法 vs 2周尼古丁贴片疗法);(3)短信支持(美国国家癌症研究所SmokefreeTXT项目 vs 无);(4)对参与咨询和SmokefreeTXT给予经济奖励(30美元/次呼叫和/或保留6周SmokefreeTXT vs 无奖励):主要结果: 主要结果是目标戒烟日26周后7天的生化证实戒烟率。进行了意向治疗分析:在接受资格评估的 6019 人中,1316 人(21.9%)接受了随机治疗(平均 [SD] 年龄为 53.1 [11.9] 岁;760 [57.8%] 名女性),919 人(69.8%)接受了最终随访。意向治疗分析表明,162 名参与者(12.3%)在 26 周时经生化证实戒毒(368 人 [28.0% 自我报告戒毒])。主要结果没有明显的主效应:34),无SmokefreeTXT(13.4% [657中的88例]) vs SmokefreeTXT(11.2% [659中的74例])(OR,0.88;95% CI,0.74-1.05),以及无经济激励(12.8% [662中的85例]) vs 经济激励(11.8% [654中的77例])(OR,0.94;95% CI,0.78-1.11):在这项随机临床试验中,评估了针对社会经济条件较差、接受戒烟治疗后仍在吸烟的成年人的戒烟热线改进措施,结果发现没有一种适应性治疗策略能有效提高长期戒烟率。我们需要制定一些策略来提高针对社会经济条件较差的成年人的戒烟热线再治疗效果:试验注册:ClinicalTrials.gov Identifier:NCT03538938。
Tobacco Quitline Retreatment Interventions Among Adults With Socioeconomic Disadvantage: A Factorial Randomized Clinical Trial.
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.
期刊介绍:
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