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临床试验/NCT03659734
NCT03659734已完成不适用

Randomized Controlled Trial to Evaluate the Relative Efficacy of Motivational Interviewing and Guided Opioid Tapering Support vs. Enhanced Usual Care to Promote Opioid Cessation After Orthopedic Surgery

Stanford University2 个研究点 分布在 1 个国家目标入组 179 人开始时间: 2019年7月12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
179
试验地点
2
主要终点
Time to Opioid Cessation

研究概览

简要总结

The purpose of this study is to evaluate the relative efficacy of enhanced usual care versus motivational interviewing and guided opioid tapering support to promote opioid cessation after total hip or knee replacement surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

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

  • Planning to undergo surgery
  • English speaking
  • Ability and willingness to complete questionnaires and assessments
  • Scheduled for total hip, knee, or shoulder replacement
  • Preoperative opioid use and opioid use 14 days after surgery to increase the likelihood of delayed opioid cessation.
  • Not under the care of a current pain management provider

排除标准

  • Any conditions causing inability to complete assessments
  • Known pregnancy
  • Elevated suicidality
  • Enrollment in conflicting perioperative trial

结局指标

主要结局

Time to Opioid Cessation

时间窗: Through study completion, an average of 1 year

Time to opioid cessation between the two groups will be analyzed using survival analysis

次要结局

  • Number of Participants With Opioid Misuse (Postoperative COMM Score Greater Than or Equal to 9)(Through study completion, 1 year after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jennifer Hah

Principal Investigator

Stanford University

研究点 (2)

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