Varenicline on Reward Responses and Cognition in Adolescent Smokers (GRAND)
2014年1月30日 更新者:Yale University
Examining the Effects of Varenicline on Reward Responses,Cognition, and Tobacco Cues in Adolescent Smokers
This is a pilot project using functional magnetic resonance imaging (fMRI) to examine the influence of varenicline on reward processing, cognitive control, and regulation of craving in adolescent smokers.
We hypothesize that adolescent smokers receiving varenicline, when compared with those receiving placebo, will have differential brain responses to anticipation of rewards, during exposure to the Stroop task, and in response to tobacco cues.
研究概览
详细说明
This is a pilot project using functional magnetic resonance imaging (fMRI) to examine the influence of varenicline on reward processing, cognitive control, and regulation of craving in adolescent smokers.
We hypothesize that adolescent smokers receiving varenicline, when compared with those receiving placebo, will have increased activation of the ventral striatum (VS) in response to anticipation of rewards in the Monetary Incentive Delay Task (MIDT), decreased activation of the dorsolateral prefrontal cortex (dlPFC) during exposure to incongruent stimuli in the Stroop task, and reduced activation of the ventral striatum in response to tobacco cues, and increased activation of the dlPFC during regulation of responses to tobacco cues during the Regulation of Craving (ROC) task.
The results of this pilot project will have important implications regarding the use of varenicline for treating tobacco dependence and understanding varenicline's neurobiological effects in adolescent smokers.
研究类型
介入性
注册 (实际的)
16
阶段
- 阶段1
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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Connecticut
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New Haven、Connecticut、美国、06519
- Substance Abuse Center
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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
16年 至 19年 (孩子、成人)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Between 16-19 years of age
- Able to read and write English
- Smoking 5 or more cigarettes on a daily basis, for at least one year
- Not seeking smoking cessation treatment
- Weighing > 55 kg (121 lbs)
Exclusion Criteria:
- Current criteria for abuse or dependence on another psychoactive substance.
- Current diagnosis of any clinical significant psychiatric disease like major depressive disorder, panic or anxiety disorder, psychosis, schizophrenia, bipolar disorder.
- Those with a prior suicide attempt or with active suicidal ideation at baseline
- Any regular use of any psychoactive drugs including anxiolytics and antidepressants
- Pregnant or lactating girls: females of childbearing potential who are unwilling or unable to use an acceptable method of contraception from at least 14 days prior to study medication administration until 30 days after the last dose of study medication. Acceptable methods of contraception are: abstinence; any form of hormonal contraception such as Depo-Provera, daily oral contraceptive, transdermal patch, or Nuva-ring; intra-uterine device, sterilization; or double barrier contraception which is a combination of any two of the following methods: condoms, spermicide, diaphragm.
- Evidence or history of clinically significant neurological, hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, or allergic disease.
- History of prior use of or sensitivity to varenicline.
- Color-blindness
- History of significant head trauma
- Metal in body
- Other medical conditions contra-indicated for MRI
- Past history of marked irritability or agitation when attempting to quit smoking, determined by the Minnesota Nicotine Withdrawal Questionnaire.
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:基础科学
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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安慰剂比较:安慰剂
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1 mg bid placebo titrated over a 2 week period
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有源比较器:伐尼克兰
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1 mg bid varenicline titrated over a 2 week period
其他名称:
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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 |
|---|---|---|
|
neural responses to the MIDT
大体时间:During MRI following14 days of varenicline treatment
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The Monetary Incentive Delay Task (MIDT) will be administered during the fMRI at the end of 14 days of varenicline treatment
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During MRI following14 days of varenicline treatment
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neural responses to the ROC
大体时间:During MRI following14 days of varenicline treatment
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The Regulation of Craving (ROC)will be administered during the fMRI at the end of 14 days of varenicline treatment
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During MRI following14 days of varenicline treatment
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neural responses to the Stroop
大体时间:During MRI following14 days of varenicline treatment
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The Stroop will be administered during the fMRI at the end of 14 days of varenicline treatment
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During MRI following14 days of varenicline treatment
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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。
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6月1日
初级完成 (实际的)
2013年11月1日
研究完成 (实际的)
2013年12月1日
研究注册日期
首次提交
2012年6月18日
首先提交符合 QC 标准的
2012年6月19日
首次发布 (估计)
2012年6月20日
研究记录更新
最后更新发布 (估计)
2014年2月3日
上次提交的符合 QC 标准的更新
2014年1月30日
最后验证
2014年1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.