Long-term Follow-up Study of Substance Abuse Screening and Intervention in Multi Primary Care Centers
2020年3月19日 更新者：DU, Jiang、Shanghai Mental Health Center
The purpose of this research is to improve the ability of primary medical staffs in screening and intervention for alcohol, benzodiazepines, and other illicit drug use.
研究概览
详细说明
In order to reduce the social and personal harm caused by drugs, it is urgent to strengthen the ability of the primary health institutions in screening and intervention the addictive substances use.
Firstly, the investigators will invite 10 primary medical staffs and 10 experts in addition to revise the manual of Alcohol, Smoking, and Substance Use Involvement Screening Test (ASSIST) and Brief Intervention (BI).
Then, the investigators will recruit related medical staffs in five provinces to participate the training of ASSIST and BI.
Secondly, the researcher will investigate the effects of BI technology in reducing the use of addictive substances, improve the addiction related knowledge of patients through randomized controlled study.
Finally, the investigators will collect the research information, revise the manual, and promote the training.
研究类型
介入性
注册 (实际的)
480
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
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Henan、中国
- Henan Provincical Peoples Hospital
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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 75年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- aged 18-75 years;
- the patient to the community medical institutions;
- ASSIST score is in 12-27, in a moderate risk;
- voluntary to participate;
- to agree to complete baseline interviews and follow-up studies
Exclusion Criteria:
- unable to complete the questionnaire;
- serious physical illness, action inconvenience.
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：放映
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：Intervention Group
The medical staffs who received the training will use the manual of brief intervention to deliver it and other materials about the harm of substance use.
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The medical staffs who received the training will use the manual of brief intervention to deliver BI and other materials about the harm of substance use.BI refers to a standard 15-30 minute intervention that includes a series of standard models that stimulate knowledge, motivation and behavior that reduce substance abuse.the
harm of substance use is a dedicated paper publicity handbook, written by the SHMC, detailing the hazards of substance abuse.
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其他：Control Group
The participants only receive the materials about the harm of substance use
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The participants only receive the materials about the harm of substance use.the harm of substance use is a dedicated paper publicity handbook, written by the SHMC, detailing the hazards of substance abuse.
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实验性的：Intervention Group 1
The medical staffs who received the training will use the manual of brief intervention twice to deliver it and other materials about the harm of substance use.
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The medical staffs who received the training will use the manual of brief intervention to deliver BI and other materials about the harm of substance use.BI refers to a standard 15-30 minute intervention that includes a series of standard models that stimulate knowledge, motivation and behavior that reduce substance abuse.the
harm of substance use is a dedicated paper publicity handbook, written by the SHMC, detailing the hazards of substance abuse.
|
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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Change from baseline in risk behaviors at 1 and 3 month
大体时间：baseline, 1 and 3 month
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Risk Behaviors will be measured by ASSIST questionnaire.
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baseline, 1 and 3 month
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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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Knowledge related to Substance Use measured by Knowledge related to Addiction questionnaire
大体时间：baseline, 1 and 3 month
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Knowledge related to substance use will be measured by Knowledge related to Addiction questionnaire
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baseline, 1 and 3 month
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Motivation measured by Pre-treatment Readiness Scale
大体时间：baseline, 1 and 3 month
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PRSS is a 5-point scale and the highest score at any stage represents the patient at this stage.
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baseline, 1 and 3 month
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Depression measured by Self-Rating Depression Scale (SDS)
大体时间：baseline, 1 and 3 month
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SDS contains 20 items and the standard total score is 53, 53-62: mild to mild depression; 63-72: moderate to severe;> 72: severe depression
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baseline, 1 and 3 month
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Anxiety measured by Self-Rating Anxiety Scale (SAS).
大体时间：baseline, 1 and 3 month
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SDS contains 20 items.
According to the Chinese norm results, the standard points of the cut-off value is 50 points, of which 50-59 is divided into mild anxiety, 60-69 is divided into moderate anxiety, 70 points for severe anxiety
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baseline, 1 and 3 month
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Self-esteem measured by Self-esteem questionnaire
大体时间：baseline, 1 and 3 month
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the change of self-esteem will be measured by Self-esteem questionnaire.
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baseline, 1 and 3 month
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Positive and Negative Affect measured by Positive and Negative Affect Scale (PANAS)
大体时间：baseline, 1 and 3 month
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It contains 20 entries.
A high positive emotional score indicates an individual's energy, concentration, and emotional well-being while a low score indicates indifference.
Negative emotional high points that the individual subjective feeling puzzled, painful emotional state, while the score is low that calm.
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baseline, 1 and 3 month
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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。
调查人员
- 首席研究员：Jiang Du, M.D、Study Principal Investigator Shanghai Mental Health Center
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
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 (实际的)
2018年4月14日
初级完成 (实际的)
2018年7月10日
研究完成 (实际的)
2020年3月10日
研究注册日期
首次提交
2018年1月19日
首先提交符合 QC 标准的
2018年2月28日
首次发布 (实际的)
2018年3月2日
研究记录更新
最后更新发布 (实际的)
2020年3月23日
上次提交的符合 QC 标准的更新
2020年3月19日
最后验证
2020年3月1日
更多信息
与本研究相关的术语
其他研究编号
- JDu-004
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.
Intervention Group的临床试验
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Ege Miray Topcu完全的
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University of North Carolina, Chapel HillEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)尚未招聘
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University of Wisconsin, MadisonNational Cancer Institute (NCI); Northwestern University完全的