Department of Health Promotion, School for Public Health and Primary Care (Caphri), Maastricht University, PO Box 616, 6200 MD Maastricht, The Netherlands.
Contemp Clin Trials. 2010 May;31(3):251-8. doi: 10.1016/j.cct.2010.03.001. Epub 2010 Mar 6.
PAS (Personal Advice in Stopping smoking) combines two of the most effective smoking cessation interventions: multiple computer tailoring and tailored counselling by a practice nurse in the general practice.
METHODS/DESIGN: Since May 2009, practice nurses are recruiting smoking patients. Each practice nurse is asked to recruit 15 adult smokers who are willing to quit within 6months and have access to the Internet. Smokers can sign up for PAS through the PAS website and are then randomized into one of three groups receiving multiple tailoring and counselling (MTC), multiple tailoring (MT) or usual care (UC), respectively. All groups receive questionnaires at baseline, 2days after a set quit date and at 6weeks, 6months and 12months follow-up. The MT group receives tailored, iterative feedback letters at the first four measurements points. At 12months follow-up biochemical validation will take place amongst respondents reporting to have quit. The three groups will be compared with regard to quit attempt rate, point prevalence abstinence and continued abstinence by means of logistic multilevel regression analyses. Linear multilevel regression analyses will be used to compare the three groups regarding smoking related beliefs.
The present paper provides an extensive description of the development of PAS and of the design of the study towards its effectiveness. This might provide insight into PAS' potentially effective working mechanisms. The results concerning effectiveness may contribute to knowledge about the effectiveness of smoking cessation interventions aimed at smoking adults.
Dutch Trial Register NTR1351.
PAS(个人戒烟建议)结合了两种最有效的戒烟干预措施:多次计算机定制和由全科医生的实践护士进行定制咨询。
方法/设计:自 2009 年 5 月以来,执业护士一直在招募吸烟患者。要求每位执业护士招募 15 名愿意在 6 个月内戒烟且能上网的成年吸烟者。吸烟者可以通过 PAS 网站注册 PAS,并随机分为三组,分别接受多次定制和咨询(MTC)、多次定制(MT)或常规护理(UC)。所有组在基线、设定戒烟日期后 2 天以及 6 周、6 个月和 12 个月随访时接受问卷调查。MT 组在头四个测量点收到定制、迭代反馈信。在 12 个月的随访中,对报告已戒烟的受访者进行生物化学验证。将通过逻辑多元回归分析比较三组的戒烟尝试率、点患病率和持续戒烟率。线性多元回归分析将用于比较三组关于吸烟相关信念的情况。
本论文提供了 PAS 的开发和研究设计的广泛描述,以评估其有效性。这可能提供了对 PAS 潜在有效工作机制的深入了解。关于有效性的结果可能有助于了解针对成年吸烟者的戒烟干预措施的有效性。
荷兰试验注册 NTR1351。