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临床试验/NCT04044521
NCT04044521已完成不适用

Promoting the Implementation of Clinical Guidelines for Opioid Prescribing in Primary Care Using Systems Consultation

University of Wisconsin, Madison4 个研究点 分布在 1 个国家目标入组 268 人开始时间: 2020年1月31日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
268
试验地点
4
主要终点
Average Morphine Milligram Equivalent of Chronic Opioid Prescriptions of Prescribers

研究概览

简要总结

This study aims to understand the optimal sequencing and combination of implementation strategies that specific types of clinics and prescribers need to adopt clinical guidelines for opioid prescribing. The pragmatic goal is to give health systems a tool they can use to predict which clinics and prescribers will benefit most from which sequence and combination of implementation strategies.

详细描述

The proposed study evaluates a sequence and combination of implementation strategies that is tailored to the needs of stakeholders at different levels (health system, clinic, and prescriber). We will deliver an adaptive version of systems consultation that progressively and adaptively drills down to offer more and more personalized levels of implementation support. The intervention starts with academic detailing, a systems-level strategy consisting of an expert-led training session plus distance-based follow up support. This strategy continues for the 21-month intervention for all clinics, but at 3 months, half of the clinics will be randomized to receive practice facilitation. Practice facilitation is a clinic-level strategy in which a highly-skilled external change agent helps clinics improve processes related to opioid prescribing. At 6 months, half of prescribers will be randomized to receive physician peer coaching. Physician peer coaching is a clinic-level strategy in which a physician expert gives one-on-one support to prescribers in managing their patients on long-term opioid therapy. These 3 discrete strategies will be delivered in a sequential, multiple-assignment randomized trial to 38 clinics from 2 Wisconsin health systems. The study has 3 specific aims:

  1. Compare the effect over 21 months of (1). An adaptive systems consultation implementation strategy (intervention group) vs. (2). Academic detailing alone (control group) on average morphine milligram equivalent dose (the primary outcome).
  2. Develop an assessment of contextual factors that influence the effectiveness of different implementation strategies. This aim will test 4 moderators and assess other factors that affect implementation. The goal is to develop a tool that decision-makers can use to predict which implementation strategies will be most effective in different settings.
  3. Estimate the costs of delivering 4 different sequences and combinations of strategies, including the incremental cost effectiveness of adding facilitation and physician peer coaching. Results will help decision-makers weigh the costs and effects of using different implementation strategies.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Health Services Research
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

  • Clinics will be eligible for the study if they:
  • are a primary care clinic (non-pediatric primary care, internal medicine, or family medicine);
  • have not received the systems consultation intervention;
  • do not explicitly prohibit initiating opioid therapy;
  • do not exceed the performance on key measures of guideline concordance (fewer than 80% of long-term opioid patients have treatment agreements and a urine drug screen in the past 12 months)
  • Prescribers will be eligible if they:
  • are a primary care provider at the clinic;
  • are not temporary providers who do not manage stable panels or patients;
  • While patients are not subjects of study, de-identified prescriber panel data will be used to assess outcome measures. To be included in the de-identified prescriber panel data, patients must:
  • have a primary care provider at the clinic;
  • are prescribed opioid therapy for at least 3 consecutive months;
  • do not have a cancer diagnosis or are receiving hospice care.

排除标准

  • Clinics will be excluded if they are not a primary care clinic, have received the systems consultation intervention, prohibit initiating opioid therapy, or exceed the threshold on key measures of guideline concordance.
  • Prescribers will be excluded if they don't have prescribing privileges or are temporary providers who do not manage stable panels or patients.
  • De-identified prescriber panel data will be excluded from outcome measures if they do not have a primary care provider at the clinic, are not prescribed opioid therapy for at least 3 consecutive months, or have a cancer diagnosis or are receiving hospice care.

结局指标

主要结局

Average Morphine Milligram Equivalent of Chronic Opioid Prescriptions of Prescribers

时间窗: up to 30 months

The average morphine milligram equivalent will be reported at the prescriber level. Patients included in this outcome are those who are prescribed at least 3 opioid orders in the last 3 consecutive months.

Average Morphine Milligram Equivalent (MME) Per Day of Chronic Opioid Prescriptions of Clinics

时间窗: up to 30 months

The average morphine milligram equivalent will be reported at the clinic level. Patients included in this outcome are those who are prescribed at least 3 opioid orders in the last 3 consecutive months. For a comparison of opioids doses, a conversion factors were developed to equate the many different opioids into one standard value. This standard value is based on morphine and its potency, referred to as morphine milligram equivalents (MME) or morphine equivalent doses (MED).

次要结局

  • Number of Patients at Clinics(up to 30 months)
  • Average Hours of Intervention Received Per Clinic(up to 30 months)
  • Number of Eligible Clinics That Participated(up to 30 months)
  • Number of Clinicians Who Attended the Intervention Meetings(up to 30 months)
  • Number of Clinicians Who Participated in the Study(up to 30 months)
  • Estimated Cost of Each Study Arm in US Dollars(up to 30 months)
  • Average Hours of Intervention Received Per Prescriber(up to 30 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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