The Effect of a Interdisciplinary Alcohol Cessation Intervention
The Effect of an Interdisciplinary "Booster" Session in Primary Care Following Brief Intervention in Hospitals - a Randomized Clinical Trial
研究概览
详细说明
The study is a randomized clinical trial, and aims to recruit 60 X 2 patients. Patients admitted to Stavanger University Hospital with an alcohol contributed condition, and who has been given a brief alcohol intervention may be recruited. Candidates for secondary healthcare related to alcohol misuse will be excluded. The interdisciplinary "booster" session will be given two weeks after discharge, and will be given in the facility of the primary care physician, facilitated by both the physician and an liaison alcohol nurse from Stavanger University Hospital. The intervention is based on motivational interview technique. The primary outcome will be assessed using the Alcohol Use Disorder Identification Test-C, six months after discharge. The outcome assessor will be blinded for the intervention. All outcomes will be collected by telephone interview.
The study aims to start recruiting candidates in October-November 2010, and will stoop recruiting in December 2012 at the latest.
The study was approved by the national ethical comite in August 2011. The results of the study wil be published in international referee based journals.
研究类型
注册 (预期的)
阶段
- 不适用
联系人和位置
学习地点
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Stavanger、挪威、4011
- 招聘中
- Stavanger University Hospital
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接触:
- Kristian Oppdal, MD
- 电话号码:+47 48124947
- 邮箱:kiop@sus.no
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Admission with an alcohol related disorder
Exclusion Criteria:
- Lack of ability to give informed consent
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:生活方式咨询
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Motivational interview
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无干预:照常治疗
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Alcohol Use Disorder Identification -C (AUDIT-C)
大体时间:6 months
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Alcohol Use Disorder Identification -C.
Dicothomous outcome.
More or less than four points for women and five points for men.
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6 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Timeline followback
大体时间:6 months
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Grams og alcohol pr week.
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6 months
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Readmissions
大体时间:6 months
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Readmission to a hospital for an alcohol related and/or a non-alcohol related condition within six months after discharge.
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6 months
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Readiness to Change Questionaire (RTCQ)
大体时间:6 months
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Continous variable
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6 months
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Quality of Life
大体时间:6 months
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SF 12
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6 months
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合作者和调查者
调查人员
- 学习椅:Kristian Oppedal, MD、Helse Stavanger HF
- 研究主任:Sverre Nesvaag, Dr、Helse Stavanger HF
研究记录日期
研究主要日期
学习开始
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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