De-Implementing Opioid Use and Implementing Optimal Pain Management Following Dental Extractions
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 5,722
- 试验地点
- 2
- 主要终点
- Opioid Prescribing at the Extraction Encounter
研究概览
简要总结
The overarching goal of this project is to de-implement the reliance on opioid analgesics and to implement reliance on non-opioid analgesics to manage postoperative pain following dental extractions. Using a prospective, provider-level, 3-arm cluster randomized trial design, the investigators will compare different strategies to reduce the reliance on opioids and increase the use of alternative pain management approaches utilizing information support tools aimed at both providers and their patients.
详细描述
The primary objective of this project is to de-implement the use of opioid analgesics for the management of postoperative pain following dental extractions and to implement effective alternative pain management. The investigators propose a cluster-randomized trial design in which dental practitioners will be randomly assigned to 1 of 3 conditions involving different implementation strategies. The first condition, Standard Practice, will serve as a control condition. The second condition will implement a clinical decision support (CDS) tool that will extract patient history and interface with the state prescription drug monitoring program to provide personalized recommendations for analgesic prescribing and offer language for discussing optimal, evidence-based non-opioid pain management with dental extraction patients. The third condition will involve an enhanced version of the CDS (CDS-E) that will also include information regarding optimal, evidence-based, non-opioid pain management delivered directly to the patient both before and following the dental extraction visit. The investigators will examine opioid and non-opioid prescribing data from the electronic health record across study arms as well as other provider- and patient-focused outcomes using mixed methods.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 16 Years 至 —(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Have a dental extraction of a permanent teeth performed by an eligible HealthPartners provider during the intervention period
排除标准
- •Patients who have opted out of research at HealthPartners
- •Meet above age criteria
结局指标
主要结局
Opioid Prescribing at the Extraction Encounter
时间窗: At the extraction encounter
Number of participants prescribed an opioid.
次要结局
- Compare the Study Arm Differences in Patient Experiences of Post-extraction Pain(3-6 days after the extraction encounter)
- Compare the Study Arm Differences in Shared Decision-making(3-6 days after the extraction encounter)
- Exclusive Non-opioid Prescribing or Recommendations at the Extraction Encounter(At the extraction encounter)
