Coordinated Treatment of Addiction to Prescription Pain Medications
Coordinated Treatment of Addiction to Prescription Pain Medications
批准号:
8453666
负责人:
Mary P Metcalf
金额:
$26.53万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-09-15 至 2014-08-31
关键词:
AddressAgreementAlcohol or Other Drugs useAnalgesicsArchivesAttentionAttitudeAwarenessBehaviorBehavior ControlBuprenorphineClinicClinicalCommunicationCommunication ToolsCompetenceComplexDataData CollectionDevelopmentDrug AddictionDrug PrescriptionsDrug usageEducationElectronic Health RecordEvaluationEvaluation ReportsFeedbackGenetic Crossing OverGoalsHealthHealth Insurance Portability and Accountability ActHealth PersonnelHealth ProfessionalHousingIllicit DrugsInterviewKnowledgeLeadLocationMeasuresMethodologyMonitorMorbidity - disease rateOnline SystemsOpiate AddictionOpioidOutcomeOutcome AssessmentOutcome MeasureOutpatientsOverdoseOxycodonePainParticipantPatient CarePatientsPharmaceutical PreparationsPhasePhysiciansPilot ProjectsPrimary Health CarePrivacyProceduresProcessProductionProviderPublishingRandomizedRecruitment ActivityReportingResearch DesignRoleSelf EfficacyServicesSiteSpeedStagingStructureSurveysTestingTimeTrainingTraining SupportUrineVisitWaiting ListsWorkaddictionbasedata sharingdesigndrug seeking behaviordrug testingevaluation/testingexpectationexperiencehealth care service organizationheuristicsimprovedinstrumentmembermortalitynovelpatient orientedphase 2 studypreferenceprescription opioidprototypepublic health relevancesatisfactionskillsskills trainingtoolusability
中文摘要
描述(由申请人提供):2010年,超过1200万人报告非医学(无处方)使用处方止痛药(阿片类药物)[1],200万人报告首次非医学使用处方止痛药[1]。2009年,1/3的12岁以上的人通过非医疗使用处方药开始使用非法药物[2]。每个
每年,这个问题导致更多的发病率和死亡率(通常是由于意外过量)。使用丁丙诺啡的阿片类药物治疗(OBOT)可以打破阿片类药物成瘾的循环。不幸的是,处方阿片类药物成瘾治疗的质量和可用性
变化,并涉及新的协议和测试(例如,尿液药物检测)。患者还必须应对复杂的治疗过程,其中包括特殊问题和独特的挑战,包括固定和频繁的门诊就诊,并遵循标准程序以限制丁丙诺啡的转移和滥用。我们现有的和成功的PC/移动的基于网络的供应商教育产品已经为数千名医生提供了关于丁丙诺啡正确处方的培训。在这个项目中,我们寻求为阿片类处方药成瘾治疗患者增加一个新的支持框架,称为BupPractice.com:患者支持中心。组件包括:1.患者和提供者匹配的数据收集和通信功能,以促进开放和准确的通信,并允许患者和提供者协同工作以治疗阿片类药物成瘾。通过该功能,他们可以收集和交流患者数据,请求信息和交流计划。我们将研究将我们的服务整合到EMR中; 2.患者支持扩展,为患者提供知识,技能,鼓励和意识,以充分参与OBOT; 3.额外的提供者培训,以帮助提供者实施更以患者为中心的方法。第一阶段的重点是产品设计工作,开发原型工具,衡量产品的可接受性和可用性,第二阶段的规划包括最后确定评估测试地点。第一阶段完成产品,并使用随机、交叉等待列表对照设计评估其影响,包括对患者结局的影响。我们将具体评估:1。对患者知识、自我效能、态度和满意度的短期影响。提供者的可接受性和满意度的经验,和3。使用标准化工具(如简明成瘾监测仪(BAM))和由提供者完成的所需患者行为清单)对患者进行治疗。最终的第二阶段产品将被整合到我们的一个评估站点的电子健康记录中。
英文摘要
DESCRIPTION (provided by applicant): In 2010, more than 12 million people reported using prescription pain medications (opioids) non-medically (without a prescription) [1], and 2 million people reported using prescription painkillers non-medically for the first time [1]. In 2009, 1/3 o people older than 12 initiated illicit drug use via non-medical use of prescription drugs [2]. Each
year the problem results in more morbidity and mortality (often due to accidental overdose). Office-based opioid treatment (OBOT) with buprenorphine can break the cycle of addiction to opioids. Unfortunately, the quality and availability of treatment for prescription opioid addiction
varies, and involves novel agreements and testing (e.g., urine drug testing). Patients must also navigate a complex treatment process with special concerns and unique challenges including fixed and frequent outpatient visits, and following standard procedures to limit diversion and misuse of buprenorphine. Our existing and successful PC/mobile web-based provider education product has provided training to thousands of physicians on the proper prescribing of buprenorphine. In this project, we seek to add a novel supporting framework for patients in treatment for opioid prescription drug addiction called The BupPractice.com: Patient Support Center. Components include: 1. Patient and provider matched data collection and communication functionality to facilitate open and accurate communication and allow the patient and provider to work in tandem to treat opioid addiction. Via the functionality they can collect and communicate patient data, request information, and communicate plans. We will investigate integrating our service into an EMR; 2. A patient support extension that provides patients with the knowledge, skills, encouragement, and awareness to fully participate in OBOT; 3. Additional provider training to assist providers in implementing a more patient-centered approach. Phase I focuses on product design work, developing prototype tools, measuring acceptability and usability of the product, and Phase II planning including finalizing evaluation test sites. Phase I completes the product and evaluates its impact using a randomized, cross-over wait-list control design to assess impact, including effect on patient outcomes. We will specifically assess: 1. Short term impact on patient's knowledge, self-efficacy, attitude, and satisfaction, 2. Providers' acceptability and satisfaction with the experience, and 3. Patient outcomes using standardized instruments such as the Brief Addiction Monitor (BAM), and a checklist of required patient behaviors to be completed by the providers. The finalized Phase II product will be integrated it into an electronic health record in one of our evaluation sites.
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