跳至主要内容
临床试验/NCT07525258
NCT07525258招募中不适用

Feasibility and Acceptability of a Novel Implementation Intervention to Promote Alcohol Use Disorder Treatment in Hepatology Clinics

Yale University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年4月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
Recruitment success to assess Feasibility

研究概览

简要总结

The goal of this project is to improve provision of integrated medications for alcohol use disorder (MAUD) with brief counseling for patients with alcohol use disorder (AUD) and alcohol-associated liver disease (ALD) in hepatology clinics. There are many benefits of AUD treatment among patients with AUD and ALD such as reduction in liver-related complications and hepatology clinicians providing this care in an integrated fashion can improve access and uptake.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Must provide care for patients with liver disease at a hepatology clinical location within the Yale School of Medicine and YNHH medical system.

排除标准

  • Providers who do not treat patients with chronic liver disease and alcohol-associated liver disease.

研究组 & 干预措施

Hepatology Clinicians

Experimental

Clinician participants will participate in a multipronged intervention including hepatology clinician education, patient education, clinical decision support, and clinician audit and feedback which will be adapted and tested. Participants will attend two approximately 60-minute-long educational sessions in which key points related to AUD treatment based on the HPCR resource and implementation facilitation intervention will be reviewed.

干预措施: Implementation Intervention (Behavioral)

结局指标

主要结局

Recruitment success to assess Feasibility

时间窗: 3, 6 and 12 months

Percentage of clinicians enrolled out of all recruited

Educational Workshop Attendance to assess Feasibility

时间窗: 3, 6 and 12 months

Percentage of clinicians that attend the educational workshops

Clinician Decision Support Tool Use to assess Feasibility

时间窗: 3, 6 and 12 months

Percentage of visits involving patients with AUD and ALD in which the clinical decision support tool is used

Acceptability of Intervention Measure (AIM) to assess Acceptability

时间窗: 3, 6 and 12 months

4-item measure of perceived intervention acceptability. Total score 1-5 with higher scores indicating greater acceptability

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 (1)

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