Evaluation of a Computerized Opioid Overdose Prevention Program
Development and Validation of a Computerized Opioid Overdose Intervention.
研究概览
地位
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Maryland
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Baltimore、Maryland、美国、21224
- Johns Hopkins University Bayview Medical Campus
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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:
- Age (>18yrs old)
- Past yr diagnosis of opioid dependence
- Recent completion of opioid detoxification
Exclusion Criteria:
- Completion of local overdose prevention programs and/or beta-testing of the computerized intervention
- Physical limitations that will prevent adequate seeing/hearing of the intervention, or from using computer
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:Computer + Fluency
Will receive computerized intervention and will be required to periodically demonstrate mastery of information before proceeding to the next module in the computerized intervention.
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有源比较器:Computer Only
Will receive computerized intervention but will not be required to demonstrate mastery of information as part of the intervention.
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有源比较器:Treatment as Usual
Will receive publicly available pamphlets that contain same information as the computerized intervention.
Will not have access to computerized intervention and will not be required to demonstrate mastery of information as part of the intervention.
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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 |
---|---|---|
Knowledge Gain
大体时间:Before the intervention (pre-test) and immediately after the intervention (post-test), an average of 10 minutes.
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The primary outcome is based on performance in the randomized, controlled trial and is change from baseline on a knowledge test that is administered immediately before and after the intervention. At the time of the study, no validated scales to assess general information regarding overdose in a true/false manner were available. Therefore the study developed a scale for the purpose of measuring knowledge increase. The scale included 51 items, rated as "true", "false", or "I don't know" (to discourage random guessing from resulting in accurate responses accidentally). The answers to all items were included as part of the intervention content so it was possible for every answer to be learned. The scale was summed together as a single measure of number correct responses (range 0-51) with no subscales. Higher values indicated more correct responses. |
Before the intervention (pre-test) and immediately after the intervention (post-test), an average of 10 minutes.
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Percent Participants Who Would Recommend the Intervention to a Family Member or Friend.
大体时间:Immediately after the intervention (an average of 10 minutes).
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Participant willingness (yes or no) to recommend the intervention to a family member or friend.
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Immediately after the intervention (an average of 10 minutes).
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合作者和调查者
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
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 (实际的)
上次提交的符合 QC 标准的更新
最后验证
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.
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