Classification of Substance Use Severity and Treatment Outcomes: NIDA CTN Studies
Classification of Substance Use Severity and Treatment Outcomes: NIDA CTN Studies
批准号:
8311820
负责人:
Li-Tzy Wu
金额:
$35.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-01 至 2015-08-31
关键词:
AddressAlcohol or Other Drugs useAlgorithmsAreaBeck depression inventoryBiologicalClassificationClinicalClinical Trials NetworkDataData AnalysesData FilesData SetDiagnosisDiagnosticDiagnostic and Statistical ManualDrug AddictionDrug usageEquipment and supply inventoriesEthnic OriginEthnic groupFoundationsFrequenciesFutureGenderHIVHybridsIndividualMeasurementMeasuresMediator of activation proteinMental DepressionMental HealthMethodsModelingNational Institute of Drug AbuseOutcomeParticipantPatient Self-ReportPatternPhaseProbabilityQuality of lifeRaceRandomizedRandomized Clinical TrialsResearchRiskRisk BehaviorsSF-36SeveritiesSex CharacteristicsSolidSymptomsTreatment outcomeWorkaddictiondata modelingdemographicsdesigndiagnosis qualityfollow-uphealth related quality of lifeimprovedindexinginsightinstrumentmeetingsprogramspsychological distressracial and ethnicracial and ethnic disparitiesracial/ethnic differenceresponsesexstatisticstheoriestreatment trial
中文摘要
点击翻译按钮获取中文摘要
英文摘要
ABSTRACT
This R21/R33 application is in response to RFA-DA-09-020. It seeks support to address one research
area recommended by this RFA ¿Secondary data analyses of multiple trials in the NIDA Clinical Trials
Network (CTN).¿ By capitalizing on the CTN¿s wealth of multisite treatment data from multiple trials,
we seek to, in the R21 phase (Year 1), 1) identify and create analyzable flat data files from the raw
trial data (stacked format), 2) generate study variables and codebooks by programming scoring
algorithms for multiple standardized clinical instruments, 3) evaluate the extent of missing data, and 4)
examine baseline clinical profiles (substance use and diagnoses, mental health, and quality of life) of
trial participants by gender and race/ethnicity in order to guide the R33 phase of work. In the R33
phase (Years 2-4), we plan to evaluate the construct, concurrent, and predictive validity of categorical
and dimensional models of substance use diagnoses. The multisite CTN trials present an
unparalleled, excellent opportunity to explore and evaluate these clinically and scientifically important
issues directly related to treatment outcomes and to the emerging Diagnostic and Statistical Manual
Version-IV (DSM-V). Study Aims for R33 are to 1) investigate measurement equivalence of DSM-IV
diagnostic questions by gender and race/ethnicity, 2) evaluate the construct and concurrent validity of
DSM-IV substance use diagnoses using categorical, dimensional, and integrated hybrid models of
diagnostic classification, 3) determine empirically defined drug dependence subtypes (an integrated
hybrid model) in predicting subsequent outcomes and to explore the mediator and moderators of the
associations, and 4) evaluate empirically-defined comorbid drug dependence subtypes in predicting
subsequent outcomes and to explore the mediator and moderators of the associations. Gender/sex
differences will be examined in all analyses either through stratified analyses or the inclusions of
interaction terms as appropriate.
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