Brown Richard A, Niaura Raymond, Lloyd-Richardson Elizabeth E, Strong David R, Kahler Christopher W, Abrantes Ana M, Abrams David, Miller Ivan W
Brown Medical School, Department of Psychiatry and Human Behavior and Butler Hospital, Providence, RI 02906, USA.
Nicotine Tob Res. 2007 Jul;9(7):721-30. doi: 10.1080/14622200701416955.
This study is a randomized, double-blind, placebo-controlled clinical trial examining the effects of an intensive cognitive-behavioral mood management treatment (CBTD) and of bupropion, both singularly and in combination, on smoking cessation in adult smokers. As an extension of our previous work, we planned to examine the synergistic effects of CBTD and bupropion on smoking cessation outcomes in general and among smokers with depression vulnerability factors. Participants were 524 smokers (47.5% female, M (age) = 44.27 years) who were randomized to one of four 12-week treatments: (a) standard, cognitive-behavioral smoking cessation treatment (ST) plus bupropion (BUP), (b) ST plus placebo (PLAC), (c) standard cessation treatment combined with cognitive-behavioral treatment for depression (CBTD) plus BUP, and (d) CBTD plus PLAC. Follow-up assessments were conducted 2, 6, and 12 months after treatment, and self-reported abstinence was verified biochemically. Consistent with previous studies, bupropion, in comparison with placebo, resulted in better smoking outcomes in both intensive group treatments. Adding CBTD to standard intensive group treatment did not result in improved smoking cessation outcomes. In addition, neither CBTD nor bupropion, either alone or in combination, was differentially effective for smokers with single-past-episode major depressive disorder (MDD), recurrent MDD, or elevated depressive symptoms. However, findings with regard to recurrent MDD and elevated depressive symptoms should be interpreted with caution given the low rate of recurrent MDD and the low level of depressive symptoms in our sample. An a priori test of treatment effects in smokers with these depression vulnerability factors is warranted in future clinical trials.
本研究是一项随机、双盲、安慰剂对照临床试验,旨在考察强化认知行为情绪管理治疗(CBTD)和安非他酮分别及联合使用对成年吸烟者戒烟的影响。作为我们先前工作的延伸,我们计划考察CBTD和安非他酮对总体戒烟结果以及对有抑郁易感性因素吸烟者戒烟结果的协同作用。参与者为524名吸烟者(47.5%为女性,平均年龄 = 44.27岁),他们被随机分配到四种为期12周的治疗方案之一:(a)标准认知行为戒烟治疗(ST)加安非他酮(BUP),(b)ST加安慰剂(PLAC),(c)标准戒烟治疗联合抑郁症认知行为治疗(CBTD)加BUP,以及(d)CBTD加PLAC。在治疗后2个月、6个月和12个月进行随访评估,并通过生化方法验证自我报告的戒烟情况。与先前研究一致,与安慰剂相比,安非他酮在两种强化组治疗中均产生了更好的戒烟效果。在标准强化组治疗中加入CBTD并未改善戒烟效果。此外,单独或联合使用时,CBTD和安非他酮对单次发作的重度抑郁症(MDD)、复发性MDD或抑郁症状加重的吸烟者均无差异疗效。然而,鉴于我们样本中复发性MDD的发生率较低以及抑郁症状水平较低,关于复发性MDD和抑郁症状加重的研究结果应谨慎解释。未来的临床试验有必要对有这些抑郁易感性因素的吸烟者进行治疗效果的预先检验。