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临床试验/NCT03337009
NCT03337009进行中(未招募)不适用

The Impact of a Web-Based Naloxone Intervention Under Standing Orders to Patients Prescribed Chronic Opioid Therapy

Kaiser Permanente1 个研究点 分布在 1 个国家目标入组 1,004 人开始时间: 2017年12月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,004
试验地点
1
主要终点
Change in Opioid-Related Risk Behavior

研究概览

简要总结

In the setting of naloxone standing orders, this study will assess the impact of a targeted, web-based overdose prevention and naloxone intervention for patients prescribed chronic opioid therapy. Outcomes are changes in opioid risk behaviors, naloxone uptake, and knowledge about overdose and naloxone.

详细描述

This is a patient level randomized study of a targeted, web-based overdose prevention and naloxone intervention for patients prescribed chronic opioid therapy. This study will be conducted in a health system which has implemented naloxone standing orders. Adults prescribed chronic opioid therapy will be identified in the electronic health record, outreached, and recruited for participation. Once enrolled, participants will be randomized to usual care or the intervention. The web-based intervention is an animated video which provides education on what is an opioid overdose, how to prevent and recognize an opioid overdose, and how to respond with naloxone. This video also encourages patients to pick up naloxone from a pharmacy under standing orders. Participants will be given knowledge and risk surveys over the follow-up. The primary outcome is opioid risk behavior. Secondary outcomes include knowledge about overdose and naloxone, substance use, and pain intensity. Patients will also be followed in the electronic health record for naloxone dispensings, changes in opioid dose, aberrant urine toxicology results, and overdose events.

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
Single (Investigator)

入排标准

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

入选标准

  • •18 years of age or greater
  • •Prescribed chronic opioid therapy
  • •Have a health plan which covers the formulation of naloxone available at the pharmacy they received their opioid prescriptions from.

排除标准

  • •Non-English speaking, hospice enrollment, do-not-resuscitate order, no internet access

研究组 & 干预措施

Naloxone Navigator

Experimental

Targeted, web-based animated video (Naloxone Navigator [NN]):

This arm is a web-based intervention targeted to patients receiving chronic opioid therapy identified in the electronic health record. Participants in this arm have access to naloxone under standing orders from the pharmacy or with a prescription from their providers.

干预措施: Naloxone Navigator (NN) (Behavioral)

Usual Care

No Intervention

Participants in the usual care arm will receive usual care from their health plan, pharmacy and clinicians. As part of usual care, participants can access naloxone through physician prescription or standing orders.

结局指标

主要结局

Change in Opioid-Related Risk Behavior

时间窗: Change from baseline to 4-6 months, and 8-12 months

Risk behavior will be assessed using the Opioid-Related Behaviors in Treatment (ORBIT) scale. The ORBIT is a scale used to identify recent risk behavior among patients receiving chronic opioid therapy. Scores on the single scale range from 0-40, with lower values representing less risk behavior.

次要结局

  • Patient reported naloxone pick-up(Baseline to 12 months)
  • Overdose and Naloxone Knowledge(Baseline post-intervention and sustained effects at 4-6 and 8-12 months)
  • Change in Hazardous Drinking and Alcohol Use Disorders(Change from baseline to 4-6 months, and 8-12 months)
  • Rate of Naloxone Dispensings(Baseline to 12 months)
  • Change in opioid dose(Baseline to 12 months)
  • Change in Drug Use Risk Behavior(Change from baseline to 4-6 months, and 8-12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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