Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Nursing, Family, Community & Health Systems, University of Alabama at Birmingham, Birmingham, AL, USA.
Nicotine Tob Res. 2021 Aug 18;23(9):1575-1583. doi: 10.1093/ntr/ntab029.
Adherence to smoking cessation medications remains suboptimal, particularly among low-income smokers. Guided, experiential sampling of nicotine replacement therapies (NRTs) may increase NRT adherence and smoking cessation over gold standard counseling plus NRT. The present pilot study aimed to examine feasibility, acceptability, and preliminary efficacy of a novel experiential intervention.
This pilot randomized controlled trial (N = 83) compared gold standard smoking cessation treatment (four weekly sessions of behavioral counseling followed by self-selected combination NRT in week 5) to a novel experiential approach (ie, In Vivo; four weekly sessions of sampling each short form of NRT-gum, lozenge, inhaler, nasal spray-in-session while wearing the nicotine patch followed by NRT selection in week 5). Both groups received 8 weeks of nicotine patch plus their selected additional short form NRT for smoking cessation followed by a 1-month assessment.
Screening and enrollment rates supported feasibility. In Vivo was comparable in acceptability with the gold standard of care intervention; however, there was greater attrition in the In Vivo group compared with the gold standard of care group. Results suggested higher medication adherence and improvements in smoking behavior in the In Vivo intervention; with generally small-to-medium effect sizes.
This experiential approach to sampling NRT is feasible and acceptable to low-income people who smoke. This intervention may increase adherence and reduce harmful smoking behavior but needs to be tested on a larger scale.
Medication adherence remains a significant impediment to the successful smoking cessation. The results of this study suggest that guided sampling of NRT products improves adherence among low-income smokers. Additionally, this approach yielded greater improvements in smoking behavior compared with gold standard smoking cessation treatment. This intervention shows promise as a feasible smoking cessation treatment for low-income smokers.
戒烟药物的依从性仍然不理想,尤其是在低收入吸烟者中。引导体验式尼古丁替代疗法(NRT)采样可能会增加 NRT 的依从性并促进戒烟,优于标准咨询加 NRT。本初步研究旨在检验一种新的体验式干预措施的可行性、可接受性和初步疗效。
本试点随机对照试验(N = 83)比较了标准戒烟治疗(每周 4 次行为咨询,第 5 周自行选择组合 NRT)与新的体验式方法(即体内;每周 4 次采样每种 NRT 形式-口香糖、含片、吸入器、鼻喷雾剂-同时佩戴尼古丁贴片,然后在第 5 周选择 NRT)。两组均接受 8 周的尼古丁贴片加他们选择的额外的短期 NRT 以戒烟,然后进行 1 个月的评估。
筛选和入组率支持可行性。体验式方法在可接受性上与标准护理干预相当;然而,体验式方法组的脱落率高于标准护理组。结果表明,体验式方法组的药物依从性更高,吸烟行为改善;且具有从小到中等的效果。
这种体验式 NRT 采样方法对低收入吸烟者是可行且可接受的。这种干预措施可能会提高依从性并减少有害的吸烟行为,但需要在更大规模上进行测试。
药物依从性仍然是成功戒烟的一个重大障碍。这项研究的结果表明,引导式 NRT 产品采样可提高低收入吸烟者的依从性。此外,与标准戒烟治疗相比,这种方法在吸烟行为方面的改善更大。这种干预措施为低收入吸烟者提供了一种可行的戒烟治疗方法。