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NRT & Bupropion Mechanisms of Efficacy in Smokers

NRT & Bupropion Mechanisms of Efficacy in Smokers
尼古丁替代疗法
批准号:
7218681
负责人:
DAVID G GILBERT
金额:
$56.12万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-09-30 至 2011-01-31
关键词:
AbstinenceAddressAffectAffectiveAnhedoniaAnteriorAntidepressive AgentsAreaArousalAttentionAttenuatedBrainBupropionCessation ResearchCigaretteCognitiveCollectionConditionControl GroupsCuesDesire for foodDopamineDropoutElectroencephalographyElectromagneticsEmotionalEndogenous depressionEventEvent-Related PotentialsExhibitsExperimental DesignsEyeFundingGenderGoalsImageIndividualIndividual DifferencesInterventionKnowledgeLeadLeftLocalizedMeasuresMediatingModelingMoodsNational Institute of Drug AbuseNatureNervous System PhysiologyNeuraxisNeurobiologyNicotineNicotine DependenceNicotine WithdrawalNorepinephrineParietalPatient Self-ReportPatternPerformancePersonalityPersonality TraitsPharmaceutical PreparationsPharmacotherapyPhasePhysiologicalPlacebo ControlPlacebosPrefrontal CortexPrincipal InvestigatorProceduresProcessPropertyQuestionnairesRandomizedRateRelapseRelative (related person)ResearchResearch PersonnelResolutionRestRewardsRoleSample SizeSiteSleep disturbancesSmokeSmokerSmokingSourceStimulusStressSupport of ResearchSymptomsTechniquesTestingTimeWaterWeekWithdrawal SymptomWorkapproach behaviorbasebiobehaviorcapsulecingulate gyruscravingdaydensitydepressive symptomsdesigndirected attentiondistractiondrug addiction therapyemotional stimulusexpectationexperiencegazehedonichuman PTCH2 proteinindexinginnovationinsightinterestneurobiological mechanismnicotine patchpillpleasureprogramspsychologicreinforcerresponsesmoking cessationtheoriestomographytraittreatment durationtreatment effectvigilancevisual information

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DESCRIPTION (provided by applicant): The first aim of this revised proposal is to accurately assess the duration and trajectories of smoking abstinence symptoms and associated biobehavioral indices across 66 days of quitting smoking in 3 different treatment groups: 1) bupropion SR (BIJP), 2) transdermal nicotine patch (TNP), and 3) a placebo. Study sensitivity and accuracy will be maximized by using procedures designed to maximize abstinence and minimize study dropout. The second aim is to characterize brain and psychological mechanisms by which BUP and TNP promote abstinence. While the efficacies of BUP and TNP in promoting smoking abstinence have been repeatedly demonstrated little is known about the mechanisms mediating this efficacy. The final primary goal of this competitive continuation proposal is to characterize individual differences in psychological and brain mechanisms mediating the beneficial effects of BUP and TNP on smoking abstinence and withdrawal symptoms. A secondary goal is to assess the ability of a battery of innovative brain and biobehavioral measures of attention and affect to predict relapse. To achieve these goals the effects of quitting smoking with or without the help of TNP and BUP will be assessed intensively across 66 days of abstinence, Dependent measures will be mood, vigilance, attentional bias to smoking and emotional stimuli, and related physiological measures (resting EEC activation and activation asymmetry indices of affective states and traits, and event-related potential activity elicited by emotional and smoking stimuli). Smokers will be randomly assigned to one of three immediate-quit groups (N = 80 per group): (1) bupropion + placebo patch (2) placebo pill ¿ nicotine patch, and (3) placebo pill + placebo patch or to a fourth (control) group (N = 60) that will quit after the final experimental session (after the other subjects have completed their 66-day abstinence period). Subjects in the 3 treatment groups and the control group will have the same set of biobehavioral measures assessed during the experimental sessions at the same points in time. It is hypothesized that BUF and TNP will have both common and unique mechanisms by which they reduce withdrawal symptoms and that gender and personality traits will moderate the effects of these treatments. (Note,* To avoid final-session mood and arousal effects subjects will actually quit for 67 days, but biobehavioral measures will be collected on the 66 day of abstinence
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