Cancer Prevention and Control Program, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA.
Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, DC, USA.
Nicotine Tob Res. 2021 Nov 5;23(12):2037-2046. doi: 10.1093/ntr/ntab110.
Increased rates of smoking cessation will be essential to maximize the population benefit of low-dose CT screening for lung cancer. The NCI's Smoking Cessation at Lung Examination (SCALE) Collaboration includes eight randomized trials, each assessing evidence-based interventions among smokers undergoing lung cancer screening (LCS). We examined predictors of trial enrollment to improve future outreach efforts for cessation interventions offered to older smokers in this and other clinical settings.
We included the six SCALE trials that randomized individual participants. We assessed demographics, intervention modalities, LCS site and trial administration characteristics, and reasons for declining.
Of 6285 trial- and LCS-eligible individuals, 3897 (62%) declined and 2388 (38%) enrolled. In multivariable logistic regression analyses, Blacks had higher enrollment rates (OR 1.5, 95% CI 1.2,1.8) compared to Whites. Compared to "NRT Only" trials, those approached for "NRT + prescription medication" trials had higher odds of enrollment (OR 6.1, 95% CI 4.7,7.9). Regarding enrollment methods, trials using "Phone + In Person" methods had higher odds of enrollment (OR 1.6, 95% CI 1.2,1.9) compared to trials using "Phone Only" methods. Some of the reasons for declining enrollment included "too busy" (36.6%), "not ready to quit" (8.2%), "not interested in research" (7.7%), and "not interested in the intervention offered" (6.2%).
Enrolling smokers in cessation interventions in the LCS setting is a major priority that requires multiple enrollment and intervention modalities. Barriers to enrollment provide insights that can be addressed and applied to future cessation interventions to improve implementation in LCS and other clinical settings with older smokers.
We explored enrollment rates and reasons for declining across six smoking cessation trials in the lung cancer screening setting. Offering multiple accrual methods and pharmacotherapy options predicted increased enrollment across trials. Enrollment rates were also greater among Blacks compared to Whites. The findings offer practical information for the implementation of cessation trials and interventions in the lung cancer screening context and other clinical settings, regarding intervention modalities that may be most appealing to older, long-term smokers.
增加戒烟率对于最大限度地提高低剂量 CT 筛查肺癌的人群效益至关重要。NCI 的肺癌筛查中的戒烟(SCALE)合作包括八项随机试验,每项试验都评估了在接受肺癌筛查(LCS)的吸烟者中进行的基于证据的干预措施。我们研究了试验参与的预测因素,以改善为该和其他临床环境中的老年吸烟者提供的戒烟干预措施的未来外展工作。
我们纳入了随机个体参与者的六项 SCALE 试验。我们评估了人口统计学、干预方式、LCS 地点和试验管理特征以及拒绝的原因。
在 6285 名符合试验和 LCS 条件的个体中,3897 人(62%)拒绝,2388 人(38%)入组。在多变量逻辑回归分析中,黑人的入组率更高(OR 1.5,95%CI 1.2,1.8)与白人相比。与“NRT 仅”试验相比,那些参与“NRT + 处方药物”试验的人入组的可能性更高(OR 6.1,95%CI 4.7,7.9)。关于入组方法,使用“电话+亲自”方法的试验入组的可能性更高(OR 1.6,95%CI 1.2,1.9)与仅使用“电话”方法的试验相比。拒绝入组的一些原因包括“太忙”(36.6%)、“还没准备好戒烟”(8.2%)、“对研究不感兴趣”(7.7%)和“对提供的干预措施不感兴趣”(6.2%)。
在 LCS 环境中招募吸烟者参与戒烟干预是一项主要任务,需要多种入组和干预方式。入组障碍提供了可以解决的见解,并可应用于未来的戒烟干预措施,以改善在 LCS 和其他有老年吸烟者的临床环境中的实施。
我们探讨了肺癌筛查环境中六项戒烟试验的入组率和拒绝原因。提供多种入组方法和药物治疗选择可预测试验中入组率的增加。与白人相比,黑人的入组率也更高。这些发现为在肺癌筛查背景下和其他临床环境中实施戒烟试验和干预措施提供了实用信息,涉及可能对长期吸烟的老年吸烟者最有吸引力的干预措施模式。