Brief Web-Based Alcohol Reduction Intervention for Undergraduates
2014年6月12日 更新者:Robert Leeman、Yale University
Randomized, Controlled Trial of a Brief, Web-Based Alcohol Reduction Intervention for Undergraduates
Tertiary Health Research Intervention Via Email (THRIVE; Kypri et al., 2009), originally utilized with Australian students, is unique in that it contains efficacious components derived from motivational interviewing (e.g., personalized feedback) and cognitive behavioral therapy (protective behavioral strategies), yet is very brief and has established efficacy.
This study aims to test versions of THRIVE tailored to American college students.
In addition to replicating original results with THRIVE, we will also test versions containing unique subsets of protective behavioral strategies to reduce alcohol consumption.
The primary hypothesis is that versions of THRIVE will be associated with lower overall alcohol consumption than an assessment and brief brochure control condition.
研究概览
地位
完全的
研究类型
介入性
注册 (实际的)
207
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
Connecticut
-
New Haven、Connecticut、美国、06519
- Yale University School Of Medicine
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 24年 (成人)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Must be a current student at Albertus Magnus College in New Haven, CT
Exclusion Criteria:
- Under 18 years of age
- 25 years of age or older
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
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 |
|---|---|
|
实验性的:THRIVE replication
Participants in this condition receive THRIVE with a full list of direct and indirect protective behavioral strategies to reduce alcohol consumption.
|
THRIVE stands for (Tertiary Health Research Intervention Via Email).
Participants complete questions related to demographics and their alcohol use and receive brief personalized feedback based on this information, in addition to protective behavioral strategies, facts about alcohol and information about available resources to reduce their alcohol use.
其他名称:
|
|
实验性的:THRIVE direct strategies
Participants in this condition receive THRIVE including a subset of protective behavioral strategies that are directly related to alcohol drinking.
|
THRIVE stands for (Tertiary Health Research Intervention Via Email).
Participants complete questions related to demographics and their alcohol use and receive brief personalized feedback based on this information, in addition to protective behavioral strategies, facts about alcohol and information about available resources to reduce their alcohol use.
其他名称:
|
|
实验性的:THRIVE indirect strategies
Participants in this condition receive THRIVE including a subset of protective behavioral strategies that are indirectly related to alcohol drinking.
|
THRIVE stands for (Tertiary Health Research Intervention Via Email).
Participants complete questions related to demographics and their alcohol use and receive brief personalized feedback based on this information, in addition to protective behavioral strategies, facts about alcohol and information about available resources to reduce their alcohol use.
其他名称:
|
|
假比较器:Brief brochure and assessment control
Participants will answer the same survey questions as participants in the THRIVE conditions, but will receive a brief alcohol-related brochure with only didactic content rather than the intervention components received by participants randomized to THRIVE conditions.
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Frequency of alcohol use
大体时间:1-month post-intervention
|
1-month post-intervention
|
|
Protective behavioral strategy use
大体时间:1-month post-intervention
|
1-month post-intervention
|
|
Overall Weekly Alcohol Consumption
大体时间:1-month post-intervention
|
1-month post-intervention
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Frequency of heavy drinking days
大体时间:1-month post-intervention
|
1-month post-intervention
|
|
Frequency of alcohol use
大体时间:6-months post-intervention
|
6-months post-intervention
|
|
Overall weekly alcohol consumption
大体时间:6-months post-intervention
|
6-months post-intervention
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
合作者
调查人员
- 首席研究员:Robert F Leeman, Ph.D.、Yale University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2012年10月1日
初级完成 (实际的)
2013年11月1日
研究完成 (实际的)
2014年6月1日
研究注册日期
首次提交
2012年9月20日
首先提交符合 QC 标准的
2012年9月24日
首次发布 (估计)
2012年9月26日
研究记录更新
最后更新发布 (估计)
2014年6月16日
上次提交的符合 QC 标准的更新
2014年6月12日
最后验证
2014年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.