跳至主要内容
临床试验/NCT06318026
NCT06318026招募中不适用

Systematic Implementation of Patient-centered Care for Alcohol Use Trial: Beyond Referral to Treatment

Kaiser Permanente2 个研究点 分布在 1 个国家目标入组 1,500 人开始时间: 2025年3月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,500
试验地点
2
主要终点
Documentation of alcohol or substance use disorder treatment in the electronic health record (including insurance claims).

研究概览

简要总结

The Systematic Implementation of Patient-centered Care for Alcohol Use Trial is a pragmatic, cluster-randomized, effectiveness-implementation trial testing two interventions in Kaiser Permanente Washington to systematically implement shared decision-making with primary care patients with symptoms due to alcohol use: a primary care intervention and a centralized intervention. An anticipated 25 primary care clinics will be randomized to one of three conditions: usual care or the primary care or centralized interventions.

研究设计

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

盲法说明

EHR and survey (latter masked)

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

  • Adult primary care patients ≥18 years old on the day of a primary care appointment; and
  • ≥4 symptoms on the Alcohol Symptom Checklist, or 2-3 symptoms on the Alcohol Symptom Checklist with at least one symptom associated with high risk of progression to severe symptoms, documented in the electronic health record associated with the primary care appointment; and
  • high-risk drinking on the alcohol screening questionnaire (AUDIT-C ≥7) on the day of the Alcohol Symptom Checklist or in the prior 30 days documented in the electronic health record.

排除标准

  • Documented request to not participate in research, or
  • Patient was eligible for the Vanguard pilot study.

结局指标

主要结局

Documentation of alcohol or substance use disorder treatment in the electronic health record (including insurance claims).

时间窗: Treatment initiated up to 12 months.

Continuous measure of change in alcohol use as documented on the AUDIT-C screening questionnaire.

时间窗: Up to 24 months.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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