跳至主要内容
临床试验/NCT05577026
NCT05577026
进行中(未招募)
不适用

Safe and Appropriate Prescribing of Opioids in Primary Care: a Randomized Control Trial

Region Stockholm1 个研究点 分布在 1 个国家目标入组 52 人2023年2月9日

概览

阶段
不适用
干预措施
Educational intervention and prescription feedback
疾病 / 适应症
Opioid-Related Disorders
发起方
Region Stockholm
入组人数
52
试验地点
1
主要终点
Change in opioid prescriptions
状态
进行中(未招募)
最后更新
2个月前

概览

简要总结

Opioid analgesics are commonly prescribed addictive narcotics intended for the treatment of pain. Inappropriate prescription of opioids in quantities and for conditions which lack clinical evidence contributes to the risk of misuse and addiction. The majority of opioid prescriptions are written by physicians (general practitioners) in primary health care (PHC). PHC is thus an important setting for efforts to encourage the safe and appropriate prescription of opioids. Increasing knowledge of pain treatment recommendations, risks of opioids, and guidelines for the prescription of opioids may decrease inappropriate prescription, and thereby risk of tolerance, dependence, and addiction.

详细描述

Opioids are a class of addictive narcotic drugs which can be obtained by prescription for the treatment of pain. There is clinical evidence for the use of opioids for acute, post-operative, and cancer related pain, although guidelines recommend the lowest effective dose and duration be prescribed. There is less evidence for the long-term benefits of opioid therapy for chronic non-cancer pain and the risk for harm and addiction is increased with prolonged use. Patients with long-term treatment may experience only marginal pain reduction and a risk of long-term consequences including tolerance, dependence, and adverse effects such as cognitive disturbance and decline, behavioral problems, emergency visits, accidents, suicide, and drug-related mortality. As the majority of opioids are prescribed by physicians in primary health care, this is an important setting for promoting the safe and appropriate use of prescription opioids. This trial evaluates whether a brief educational intervention in primary health care (PHC) followed by 12 months of feedback on prescription data changes the prescription of opioids in primary care. PHC centers in Stockholm County will be invited to participate in the study. Centers that express interest in participating, meet the inclusion criteria, and do not meet the exclusion criteria will be randomized to the intervention or control group. Personnel at the intervention centers will participate in a brief educational intervention followed by 12 months of regular feedback on opioid prescriptions, with benchmarking to other local PHC centers. Centers randomized to the active control group will receive written information on treatment guidelines but will not receive the onsite educational intervention or prescription feedback. The primary outcome, change in opioid prescription, will be measured at 12 months after intervention start. Data on outcomes and characteristics of participating primary health care centers including prescription before, during and after the intervention will be extracted from regional health care registers and databases and analyzed statistically.

注册库
clinicaltrials.gov
开始日期
2023年2月9日
结束日期
2027年3月1日
最后更新
2个月前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Eligibility criteria apply to primary health care centers.
  • Inclusion Criteria:
  • Employs at least two full-time physicians
  • Has at least 3000 listed patients
  • Has a regional care agreement (contract)
  • Connected to the regional quality register (Stockholm County)

排除标准

  • In operation for less than 12 months

研究组 & 干预措施

Educational intervention with prescription feedback

Healthcare personnel will participate in a brief educational intervention with information regarding treatment guidelines, recommendations, and risks of prescribing opioids. The presentation will include benchmarking on clinic opioid prescription patterns compared to other primary health centers, followed by targeted feedback on prescription patterns over the subsequent 12 months. Standardized materials will be provided, including a patient-provider agreement, outline of a patient treatment plan, and recommendations of how shared routines at the center can be improved.

干预措施: Educational intervention and prescription feedback

Written information on guidelines

The manager at each PHC center in the active control group will receive written information on treatment guidelines for pain management. These centers will not receive the intervention, consisting of the onsite educational visit and targeted prescription feedback.

干预措施: General information on treatment guidelines

Standard care

The passive control group will consist of PHC centers that met the eligibility criteria for the study but did not actively participate in the study. Care as usual will proceed at the centers. Prescription data will be gathered directly from regional registers and databases; thus there will be no need to communicate directly with the centers. This arm will be used only if the General Data Protection Regulation continues to allow access to regional registers and databases in primary health care.

结局指标

主要结局

Change in opioid prescriptions

时间窗: 12 months

Change in prescription of opioids as measured by defined daily dose (DDD) and morphine milligram equivalents (MME)

次要结局

  • Change in opioid types(12 months)
  • Change in opioid prescriptions(24 months)

研究点 (1)

Loading locations...

相似试验