Evaluation Of Treatments Of Opioid And Cocaine Dependence
阿片类药物和可卡因依赖的治疗评估
基本信息
- 批准号:8736709
- 负责人:
- 金额:$ 113.28万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:AbstinenceAmazeBehavioralClinical TrialsCocaineCocaine DependenceCommitCommunitiesControlled StudyCuesDataDoseDouble-Blind MethodDrug usageEducationEffectivenessElectronicsEmotionalEnvironmental ExposureEvaluationEvidence based treatmentExposure toFailureFutureGoalsHIV riskHIV/STDHeroinIndividualInterventionKnowledgeMeasuresMethadoneMoodsOpiate AddictionOpioidParticipantPatientsPhysiologicalPlacebosPopulationPropranololRandomizedRisk ReductionSolutionsStressSubstance AddictionTechnologyTechnology TransferTestingaddictionbasecravingcue reactivitydesigndiariesdosageimprovedinsightmeetingsnon-compliancepsychosocialresponseself reported behaviorstressorsubstance abusertrend
项目摘要
The Treatment Section continues its long-term projects to improve treatment for substance dependence through behavioral, pharmacologic, and combined behavioral and pharmacologic interventions.
We completed a clinical trial examining the effectiveness of individualized methadone dosages of 100 to 190 mg/day, compared in a randomized, double-blind design with fixed dosages of 100 mg/day. Surprisingly, polydrug use (effect-size h = .30) and heroin craving (effect-size d = .87) were significantly greater in the individualized high-dose group than in the fixed-dose group, with no trend toward lower heroin use in the individualized high-dose group. This counterintuitive finding requires replication, but supports the need for additional controlled studies of high-dose methadone.
We also completed a double-blind interventional study of propranolol on cue-induced cocaine craving, in which a single administration of propranolol was intended to block reconsolidation of cocaine-associated emotional responses, thereby leading to an enduring reduction in cue-induced craving. Again, the results were unexpected. Cue reactivity, as assessed by craving scales and physiological responses, was unexpectedly greater in the propranolol group than in the placebo group. This counter-hypothesized group difference was present both acutely after propranolol administration and during the subsequent test sessions. Our results do not support the use of propranolol for cue-induced cocaine craving in opioid-maintained patients.
We also developed and deployed a video-based smartphone-delivered mobile HIV Risk Reduction (mHIVRR) intervention. We developed 3 video modules that consisted of a 10-minute HIVRR video, 11 acceptability questions, and 3 knowledge questions and deployed them as a secondary study within a larger study of ecological momentary and geographical momentary assessment. All 24 individuals who remained in the main study long enough completed the mHIVRR secondary study. All 3 videos met our a priori criteria for acceptability as is in the population: they achieved median scores of ≤2.5 on a 5-point Likert scale; ≤20% of individuals gave them the most negative rating on the scale; and a majority of individuals stated they would not prefer other formats over video-based smartphone-delivered (all p<0.05). Additionally, all of our video modules met our a priori criteria for feasibilty: ≤20% of data were missing due to participant noncompliance and ≤20% were missing due to technical failure. We concluded that video-based mHIVRR education delivered via smartphone is acceptable and feasible, and may increase HIV/STD risk reduction knowledge. Future studies, with pre-intervention assessments of knowledge and random assignment, are needed to confirm these findings.
Finally we continue to develop Geographical Momentary Assessment (GMA), a descriptive approach to better measure and understand the relationships among mood, drug use, and environmental exposure to psychosocial stressors. We remain committed to transforming description into intervention. For example, we have shown that electronic-diary studies can provide amazing insight into the daily lives of substance abusers during treatment and data that are sensitive to behavioral changes during even brief periods of abstinence. The technologies that enable us to collect data on drug use, craving, and stress in the field may also be used for delivery of treatment in the field, perhaps in response to the patients own self-reported behaviors or previously identified triggers.
治疗科继续其长期项目,通过行为、药理学以及行为和药理学相结合的干预措施改善对物质依赖的治疗。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Kenzie Preston其他文献
Kenzie Preston的其他文献
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{{ truncateString('Kenzie Preston', 18)}}的其他基金
Quantifying Exposure to Illicit Drugs & Psychosocial Stress in Real Time
量化非法药物的暴露程度
- 批准号:
8553260 - 财政年份:
- 资助金额:
$ 113.28万 - 项目类别:
Evaluation Of Treatments Of Opioid And Cocaine Dependence
阿片类药物和可卡因依赖的治疗评估
- 批准号:
8336419 - 财政年份:
- 资助金额:
$ 113.28万 - 项目类别:
Quantifying Exposure to Illicit Drugs & Psychosocial Stress in Real Time
量化非法药物的暴露程度
- 批准号:
8336460 - 财政年份:
- 资助金额:
$ 113.28万 - 项目类别:
Quantifying Exposure to Illicit Drugs & Psychosocial Stress in Real Time
量化非法药物的暴露程度
- 批准号:
10267529 - 财政年份:
- 资助金额:
$ 113.28万 - 项目类别:
Evaluation Of Treatments Of Drug Dependence In HIV Infected Patients
HIV 感染者药物依赖性治疗的评估
- 批准号:
7966764 - 财政年份:
- 资助金额:
$ 113.28万 - 项目类别:
Evaluation Of Treatments Of Opioid And Cocaine Dependence
阿片类药物和可卡因依赖的治疗评估
- 批准号:
8933802 - 财政年份:
- 资助金额:
$ 113.28万 - 项目类别:
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