Comparative Effectiveness and Feasibility of SBIRT in a General Dental Clinic

SBIRT 在普通牙科诊所中的有效性和可行性比较

• 批准号: 7826393
• 负责人: THOMAS F BABOR
• 金额: $ 48.5万
• 依托单位: UNIVERSITY OF CONNECTICUT SCH OF MED/DNT
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-21 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7826393
• 关键词: Address; Alcohol consumption; Alcohol or Other Drugs use; Alcohols; Area; Attention; Attitude; Behavior; Behavioral; Chronic; Clinic; Clinical Sciences; Clinical Trials; Clinical Trials Design; Communities; Conduct Clinical Trials; Connecticut; Counseling; Data; Dental; Dental Care; Dental Clinics; Dental caries; Dentistry; Disadvantaged; Drug Addiction; Drug usage; Early identification; Education; Effectiveness; Gingival Recession; Goals; Growth; Health; Health Services Accessibility; Hour; Impaired wound healing; Individual; Interview; Knowledge; Leukoplakia; Link; Low income; Malignant neoplasm of pharynx; Measures; Medicaid; Medical; Methods; Mouth Diseases; Oral cavity; Oral health; Oropharyngeal; Outcome; Participant; Pathology; Patients; Periodontal Diseases; Prevention; Primary Health Care; Procedures; Process Measure; Protocols documentation; Public Health Dentistry; Randomized; Randomized Controlled Trials; Recruitment Activity; Research; Residencies; Resources; Risk; Risk Factors; Screening procedure; Secondary Prevention; Services; Smoke; Smoker; Smoking; Substance Use Disorder; Technology; Testing; Time; Tobacco; Tobacco use; Tooth Loss; Training; Translational Research; Trauma; Uninsured; Universities; Waiting Lists; World Health Organization; abstracting; active method; alcohol risk; base; brief intervention; clinical practice; cohort; comparative effectiveness; drinking; effectiveness research; evidence base; follow-up; improved; primary care setting; programs; screening and brief intervention; success; willingness; working group

DESCRIPTION (provided by applicant): (Abstract) "Comparative Effectiveness and Feasibility of SBIRT in a General Dental Clinic" addresses the broad Challenge Area, (05) Comparative Effectiveness Research and specific Challenge Topic, 05-DE-102: Treatment of tobacco and drug dependence in dental settings. This protocol describes a 2-year, randomized controlled trial designed to achieve two primary aims: 1) to evaluate the short-term effectiveness of screening, brief intervention and referral services (SBIRT) for tobacco and other psychoactive substance use when delivered separately and in combined forms and 2) to evaluate the feasibility of implementing SBIRT for patients with at-risk substance use in a community general dental setting. This research will provide the basis for a more ambitious clinical trial that would be conducted in multiple dental settings and include a longer follow-up period. To achieve Aim 1, 175 patients who are smokers and at-risk substance users (including at-risk alcohol users) will be recruited from the general dentistry clinic at the University of Connecticut Health Center. Research staff will use the Alcohol, Smoking and Substance Involvement Screening Test (ASSIST), developed by the World Health Organization, to identify eligible patients. Participants will be randomized to one of three experimental conditions: 1) a smoking-only brief intervention group; 2) a smoking + other substance use brief intervention group; or 3) a wait-list control condition that includes general dental health counseling. Those assigned to the "active" treatment conditions will be given a brief intervention that will link the patient's screening assessment data with dental risk factors associated with tobacco only or tobacco + other substance use. Participants will be re- interviewed at 12-weeks post randomization to assess outcome and process measures using a combination of quantitative and qualitative interviewing methods. Regarding Aim 2, the timing of this opportunity and implementation of this clinical trial provides a unique opportunity to follow two cohorts of dental residents to examine the impact of SBIRT residency training on subsequent clinical practice. The first cohort will already be on staff when the study begins and will not have received SBIRT training as part of the residency requirements. The second cohort of residents will be exposed to a three-hour SBIRT training session that will supplement the residency requirements for July, 2010. Although residents will not be asked to provide the brief interventions for the randomized study, they will be encouraged to reinforce the information delivered by research staff. Differences between the two cohorts with regard to attitudes, knowledge and willingness to engage in SBIRT program activities will be measured. There has been a remarkable growth in translational research organized around the SBIRT concept, with numerous clinical trials conducted, new screening tests developed, and implementation programs evaluated to determine the feasibility of SBIRT in primary care and other medical settings. Despite the obvious relevance of SBIRT to the prevention of dental pathology, there has been little attention to the determination of its feasibility, effectiveness and implementation in dental settings. We believe there is now a real research opportunity to not only evaluate the effectiveness of SBIRT with dental patients, but also to improve the technology so that oral health practitioners can feel confident conducting screening, brief intervention and referrals for at-risk users of tobacco, alcohol and other substances. The research described in this application could have significant implications on both clinical science and public health dentistry.

描述（由申请人提供）：（摘要）“SBIRT在普通牙科诊所的比较有效性和可行性”涉及广泛的挑战领域，（05）比较有效性研究和特定挑战主题，05-DE-102：牙科环境中烟草和药物依赖的治疗。本方案描述了一项为期2年的随机对照试验，旨在实现两个主要目的：1）评价烟草和其他精神活性物质使用的筛查、简短干预和转诊服务（SBIRT）在单独和联合使用时的短期有效性; 2）评价在社区普通牙科环境中对高危物质使用患者实施SBIRT的可行性。这项研究将为一项更雄心勃勃的临床试验提供基础，该试验将在多个牙科环境中进行，并包括更长的随访期。为了实现目标1，将从康涅狄格大学健康中心的普通牙科诊所招募175名吸烟者和高危物质使用者（包括高危酒精使用者）。研究人员将使用世界卫生组织开发的酒精，吸烟和物质参与筛选测试（ASSIST）来识别合格的患者。参与者将被随机分配到三个实验条件之一：1）仅吸烟的短暂干预组; 2）吸烟+其他物质使用的短暂干预组;或3）包括一般牙齿健康咨询的等待列表控制条件。那些被分配到“积极”治疗条件的人将得到一个简短的干预，将患者的筛选评估数据与仅与烟草或烟草+其他物质使用相关的牙科风险因素联系起来。将在随机化后12周再次对参与者进行访谈，以使用定量和定性访谈方法相结合的方式评估结果和过程措施。关于目标2，这个机会的时机和实施这项临床试验提供了一个独特的机会，跟随两个队列的牙科住院医师，以检查SBIRT住院医师培训对后续临床实践的影响。第一个队列在研究开始时已经在职，并且没有接受过作为住院医师要求的一部分的SBIRT培训。第二批住院医师将接受为期三小时的SBIRT培训，以补充2010年7月的住院医师要求。虽然住院医师不会被要求为随机研究提供简短的干预措施，但他们将被鼓励加强研究人员提供的信息。将测量两个组群在态度、知识和参与SBIRT方案活动的意愿方面的差异。围绕SBIRT概念组织的转化研究有了显着的增长，进行了许多临床试验，开发了新的筛查测试，并评估了实施方案，以确定SBIRT在初级保健和其他医疗环境中的可行性。尽管SBIRT与预防牙科病理学有明显的相关性，但很少有人关注其在牙科环境中的可行性，有效性和实施的确定。我们相信，现在有一个真实的研究机会，不仅可以评估SBIRT对牙科患者的有效性，而且可以改进技术，使口腔健康从业者能够有信心为烟草，酒精和其他物质的高危使用者进行筛查，简短干预和转介。本申请中描述的研究可能对临床科学和公共卫生牙科学具有重要意义。