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Completed

NCT Number: NCT01624428

Varenicline on Reward Responses and Cognition 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.

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Key information

Age range

16 year–19 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Substance Abuse Center

New Haven, Connecticut, 06519, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Varenicline

Drug

1 mg bid varenicline titrated over a 2 week period

Other names: Chantix

Placebo

Drug

1 mg bid placebo titrated over a 2 week period

Primary outcomes

  1. neural responses to the MIDT

    Time frame: During MRI following14 days of varenicline treatment

    The Monetary Incentive Delay Task (MIDT) will be administered during the fMRI at the end of 14 days of varenicline treatment

  2. neural responses to the ROC

    Time frame: During MRI following14 days of varenicline treatment

    The Regulation of Craving (ROC)will be administered during the fMRI at the end of 14 days of varenicline treatment

  3. neural responses to the Stroop

    Time frame: During MRI following14 days of varenicline treatment

    The Stroop will be administered during the fMRI at the end of 14 days of varenicline treatment

Sponsors and collaborators

Lead sponsor

Yale University

Other

Registry information

Official study title

Examining the Effects of Varenicline on Reward Responses,Cognition, and Tobacco Cues in Adolescent Smokers

Acronym: GRAND

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jun 20, 2012
Registry last updated
Feb 3, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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