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首页> 外文期刊>Clinical trials: journal of the Society for Clinical Trials >Designing a smoking cessation intervention for the unique needs of homeless persons: A community-based randomized clinical trial
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Designing a smoking cessation intervention for the unique needs of homeless persons: A community-based randomized clinical trial

机译:设计针对无家可归者独特需求的戒烟干预措施:一项基于社区的随机临床试验

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Background Although smoking prevalence remains strikingly high in homeless populations (~70% and three times the US national average), smoking cessation studies usually exclude homeless persons. Novel evidence-based interventions are needed for this high-risk subpopulation of smokers.Purpose To describe the aims and design of a first-ever smoking cessation clinical trial in the homeless population. The study was a two-group randomized community-based trial that enrolled participants (n = 430) residing across eight homeless shelters and transitional housing units in Minnesota. The study objective was to test the efficacy of motivational interviewing (MI) for enhancing adherence to nicotine replacement therapy (NRT; nicotine patch) and smoking cessation outcomes.Methods Participants were randomized to one of the two groups: active (8 weeks of NRT + 6 sessions of MI) or control (NRT + standard care). Participants attended six in-person assessment sessions and eight retention visits at a location of their choice over 6 months. Nicotine patch in 2-week doses was administered at four visits over the first 8 weeks of the 26-week trial. The primary outcome was cotinine-verified 7-day point-prevalence abstinence at 6 months. Secondary outcomes included adherence to nicotine patch assessed through direct observation and patch counts. Other outcomes included the mediating and/or moderating effects of comorbid psychiatric and substance abuse disorders.Results Lessons learned from the community-based cessation randomized trial for improving recruitment and retention in a mobile and vulnerable population included: (1) the importance of engaging the perspectives of shelter leadership by forming and convening a Community Advisory Board; (2) locating the study at the shelters for more visibility and easier access for participants; (3) minimizing exclusion criteria to allow enrollment of participants with stable psychiatric comorbid conditions; (4) delaying the baseline visit from the eligibility visit by a week to protect against attrition; and (5) regular and persistent calls to remind participants of upcoming appointments using cell phones and shelter-specific channels of communication.Limitations The study's limitations include generalizability due to the sample drawn from a single Midwestern city in the United States. Since inclusion criteria encompassed willingness to use NRT patch, all participants were motivated and were ready to quit smoking at the time of enrollment in the study. Findings from the self-select group will be generalizable only to those motivated and ready to quit smoking. High incentives may limit the degree to which the intervention is replicable.Conclusions Lessons learned reflect the need to engage communities in the design and implementation of community-based clinical trials with vulnerable populations.
机译:背景资料尽管无家可归者的吸烟率仍然很高(约为70%,是美国全国平均水平的三倍),但戒烟研究通常将无家可归者排除在外。对于这种高风险的吸烟人群,需要采取新颖的循证干预措施。目的描述无家可归人群中首次戒烟临床试验的目的和设计。该研究是一项两组基于社区的随机试验,纳入了明尼苏达州八个无家可归者收容所和过渡性住房单元中的参与者(n = 430)。研究目的是检验动机访谈(MI)增强对尼古丁替代疗法(NRT;尼古丁贴片)的依从性和戒烟效果的功效。方法将参与者随机分为两组之一:活跃(NRT + 8周+ 6个疗程的MI)或对照(NRT +标准护理)。在6个月内,参加者在他们选择的地点参加了6次面对面的评估会议和8次保留访问。在为期26周的试验的前8周中,在4次就诊时给予了2周剂量的尼古丁贴剂。主要结局是在6个月时通过可替宁验证的7天戒断率。次要结果包括通过直接观察和贴剂计数评估对尼古丁贴剂的依从性。其他结果包括合并症和/或调节性精神病和药物滥用合并症的影响。结果从社区戒烟随机试验中获得的经验教训对改善流动人口和弱势人群的招募和留住率有以下启示:(1)通过组建和召集社区咨询委员会来了解住房领导的观点; (2)将研究放置在庇护所,以增加参与者的视野并使其更容易进入; (3)最小化排除标准,以允许患有稳定的精神病合并症的受试者入组; (4)将基准访问时间从资格访问时间推迟一周,以防止人员流失; (5)定期和不间断的通话,以提醒参与者使用手机和庇护所特定的沟通渠道来进行约会。局限性该研究的局限性包括由于来自美国中西部一个城市的样本而具有普遍性。由于纳入标准包括愿意使用NRT贴剂的意愿,因此所有参与者都受到了激励,并准备在参加研究时戒烟。自我选择小组的调查结果将仅适用于那些有动机并准备戒烟的人。较高的激励措施可能会限制干预措施的可复制程度。结论所吸取的教训反映出需要让社区参与设计和实施针对弱势人群的社区临床试验的需求。

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