A randomized controlled trial protocol for engaging distress tolerance and working memory to aid smoking cessation in low socioeconomic status (SES) adults.
A randomized controlled trial protocol for engaging distress tolerance and working memory to aid smoking cessation in low socioeconomic status (SES) adults.
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DOI:
10.1037/hea0000858
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发表时间:
2020-09
期刊:
影响因子:
--
通讯作者:
Smits JAJ
中科院分区:
文献类型:
--
作者:
Otto MW;Zvolensky MJ;Rosenfield D;Hoyt DL;Witkiewitz K;McKee SA;Bickel WK;Smits JAJ
Low income and low educational attainment are among the strongest predictors of both smoking prevalence and lapse (i.e., return) to smoking following cessation attempts. Treatment refinement is limited by inadequate knowledge of the specific lapse/relapse-relevant vulnerabilities characteristic of populations that should be the target of treatment. In the context of a randomized clinical trial design, we describe an experimental medicine approach for evaluating the role of two specific lapse-relevant targets relative to the higher stress characteristic of low-socioeconomic contexts: low distress tolerance and low working memory capacity. Furthermore, we use an innovative approach for understanding risk of smoking lapse in smokers undergoing a quit attempt to examine candidate mechanistic targets assessed not only during nicotine use, but also during the conditions smokers will face upon a cessation attempt – during stressful nicotine-deprivation windows. This study is designed to show the incremental value of assessments during deprivation windows, in part due to the way in which specific vulnerabilities are modified by, and interact with, the heightened stress and withdrawal symptoms inherent to nicotine-deprivation states. Specifically, the study is designed to evaluate whether a novel mindfulness intervention (mindfulness combined with interoceptive exposure) can improve upon existing mindfulness interventions and extend therapeutic gains to the modification of mechanistic targets assessed in high-stress/negative affectivity contexts. The overall goal is to validate mechanistic targets and associated interventions for the purpose of expanding treatment options for at-risk smokers.
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