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临床试验/NCT06456294
NCT06456294进行中(未招募)不适用

Evaluation of a Medication Health Center to Promote Opioid Safety

Kaiser Permanente2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2022年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
14
试验地点
2
主要终点
Number of participants with a Medication Health Center visit

研究概览

简要总结

This study will assess the impact of an opioid safety clinic intervention for patients prescribed chronic opioid therapy. Outcomes are visits to the clinic, naloxone dispensings, Prescription Drug Monitoring reviews, and Urine Drug Screens conducted

详细描述

Given ongoing concerns about the risk of opioid overdose among people taking chronic opioid therapy for pain, Kaiser Permanente Colorado (KPCO) sought to develop a standardized approach to promote opioid safety. Operational stakeholders adapted an existing Opioid Safety Clinic model, tailored it for KPCO's context, and implemented it in three geographically dispersed KPCO clinics with leadership support. The approach was a multidisciplinary "Medication Health Center" to assess patients, educate them about overdose risk, provide naloxone, and ensure adherence to standard monitoring. Operations and the research team then collaborated to assess the effectiveness of the program to inform decisions to scale the program to other regions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Number of participants with a Medication Health Center visit

时间窗: Outcomes are assessed in a two-month post-intervention period.

Medication Health Center (MHC) Visits will be assessed using data from the electronic medical record.

次要结局

  • Number of participants with a Urine Drug Screens completed(Outcomes are assessed in a two-month post-intervention period.)
  • Number of participants with a Naloxone dispensing(Outcomes are assessed in a two-month post-intervention period.)
  • Number of participants with a Prescription Drug Monitoring Program (PDMP) review(Outcomes are assessed in a two-month post-intervention period.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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