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临床试验/NCT03944954
NCT03944954已完成早期 1 期

Neural Mechanisms of Cannabinoid-impaired Decision-Making in Emerging Adults

Michael J. Wesley, PhD1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2017年7月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
发起方
入组人数
66
试验地点
1
主要终点
Alpha Learning Rate

研究概览

简要总结

Emerging adults are a particularly vulnerable group for experiencing the immediate and potentially lifelong negative impacts of habitual cannabis use, and trends suggest that cannabis use disorder (CUD) will soon escalate in this population. The proposed research will combine clinical pharmacology, non-invasive brain stimulation, and neuroimaging techniques to establish the brain mechanisms of cannabinoid-impaired decision-making processes in emerging adults with CUD. Results from this project will inform CUD prevention/treatment efforts in this high-risk group and address a growing public health concern.

详细描述

This mentored career development award (K01) will enable Dr. Michael J. Wesley to achieve his long-term goal of becoming an independent investigator with a clinical research program examining cannabis use disorder (CUD) in emerging adults, which is a current NIDA funding priority. Dr. Wesley is a new Assistant Professor at the University of Kentucky (UK) College of Medicine. The activities proposed in this award build on Dr. Wesley's background in neuroimaging and drug abuse research and will allow him to accomplish these specific short-term objectives: Become an expert in (1) clinical pharmacology and (2) non-invasive brain stimulation research, and enhance/develop his (3) knowledge of the responsible conduct of research, (4) skills for scientific communication and grant writing, and (5) ability to manage an independent research program. UK has numerous faculty and projects focused on drug abuse research and is an ideal environment for Dr. Wesley to successfully complete this award. Dr. Wesley has assembled a stellar mentoring team consisting of Dr. Josh Lile (Mentor), who runs a successful NIH-funded clinical pharmacology research program at UK and Drs. Mark George (Co-Mentor) and Colleen A. Hanlon of the Brain Stimulation Laboratory at the Medical University of South Carolina, Together they will guide and oversee Dr. Wesley's training in clinical pharmacology, brain stimulation, and scientific communication and grant writing. Dr. Wesley has proposed to engage in a series of formal classes, lab exchanges, and research seminars/meetings that will assist him in accomplishing the objectives of this award.

The proposed research project is novel, innovative, and rigorous. It will combine the acute administration of Δ9-tetrahydrocannabinol (THC), the main psychoactive ingredient in cannabis, with brain stimulation and neuroimaging to examine the role of the dorsal lateral prefrontal cortex (DLPFC) and connected brain areas in drug-impaired decision-making processes. Specifically, transcranial magnetic stimulation (TMS) will be used to raise or lower DLPFC functionality following the administration THC in randomized, double-blind, placebo- and sham-controlled experiments.

Aim 1 will test the hypotheses that excitatory TMS (raising DLPFC functionality) will attenuate the impairing effects of THC on study outcomes.

Aim 2 will test the hypotheses that inhibitory TMS (lowering DLPFC functionality) will enhance the impairing effects of THC on study outcomes.

Results from this project will improve the investigator's understanding of the mechanisms involved in cannabis-impaired decision-making, which will inform CUD management and address a growing public health concern.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Investigator)

盲法说明

Functionality will be tested following combinations of THC and TMS will be tested in randomized, double-blind, placebo- and sham-controlled experiments.

入排标准

年龄范围
18 Years 至 34 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Habitual cannabis use problems
  • Body Mass Index ≤30

排除标准

  • Past or current serious physical or mental health
  • Sesame seed oil allergy
  • Irregular health issues identified by the Study Physician
  • Standard magnetic resonance imaging and transcranial magnetic stimulation exclusion criteria (e.g., metal implants, history of epilepsy, etc.)
  • Lack of affective form of birth control (females)
  • Pregnancy (females)

研究组 & 干预措施

Excitatory TMS

Experimental

Individuals assigned to this group will receive excitatory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Placebo TMS Real (Device)

Excitatory TMS

Experimental

Individuals assigned to this group will receive excitatory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Placebo TMS Sham (Device)

Excitatory TMS

Experimental

Individuals assigned to this group will receive excitatory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 10Mg Capsule TMS Sham (Drug)

Excitatory TMS

Experimental

Individuals assigned to this group will receive excitatory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 30Mg Capsule TMS Sham (Drug)

Excitatory TMS

Experimental

Individuals assigned to this group will receive excitatory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 10Mg Capsule TMS Real (Other)

Excitatory TMS

Experimental

Individuals assigned to this group will receive excitatory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 30Mg Capsule TMS Real (Other)

Inhibitory TMS

Experimental

Individuals assigned to this group will receive inhibitory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Placebo TMS Sham (Device)

Inhibitory TMS

Experimental

Individuals assigned to this group will receive inhibitory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 10Mg Capsule TMS Sham (Drug)

Inhibitory TMS

Experimental

Individuals assigned to this group will receive inhibitory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 30Mg Capsule TMS Sham (Drug)

Inhibitory TMS

Experimental

Individuals assigned to this group will receive inhibitory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Placebo TMS Real (Device)

Inhibitory TMS

Experimental

Individuals assigned to this group will receive inhibitory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 10Mg Capsule TMS Real (Other)

Inhibitory TMS

Experimental

Individuals assigned to this group will receive inhibitory (real and sham) TMS in combination with 0, 10, and 30mg THC.

干预措施: Marinol 30Mg Capsule TMS Real (Other)

结局指标

主要结局

Alpha Learning Rate

时间窗: Measure collected at 2 time points: Baseline (0HR) and Post TMS Administration (3HR)

In a Probabilistic Reinforcement Learning Choice (PRLC) task, two stimuli are presented and choosing either could result in a monetary reinforcer, but the reinforcement probabilities of the stimuli differ, and change throughout the task. Individuals attempt to optimize choices according to learned probabilities and track changing probabilities over time. PRLC performance allows mathematical modeling of trial-by-trial data under "real-world" uncertainty and yields computational parameters, such as the learning rate. Choice data were analyzed using a Rescorla-Wanger learning model with an alpha learning rate, beta inverse temperature, and perseveration global parameters. Model-derived learning rates are indicative of an individual's ability to learn from previous choice outcomes to update future decision-making. For this task, learning rates range from 0-1 with lower values indicative of more optimal learning.

Elasticity of Demand

时间窗: Measured 2 times: Baseline (0HR) and Post-TMS (3HR) after THC administration on each drug condition (0mg, 10mg, 30mg).

Elasticity of Demand was measured by the Cannabis Purchase Task (CPT) where participants are asked how many "hits" of cannabis they would consume at 16 different price points in ascending order ($0-$140). Higher elasticity values indicate a greater sensitivity to changing price points resulting in a reduced demand for "hits" of THC at increasing price points.

Working Memory Performance

时间窗: Measured 2 times: Baseline (0HR) and Post-TMS (3HR) after THC administration on each drug condition (0mg, 10mg, 30mg).

Working memory (WM), the ability to hold a finite amount of information for a set amount of time, is measured by the N-Back task. Here, participants were presented with a sequence of letters and must indicate when the letter currently being viewed matches the one from N steps earlier in the sequence. The load factor "N" is adjusted between 0, 1, and 2 to adjust the difficulty of the task (0-Back = no WM load, 1-Back = minimal WM load, 2-Back = greater WM load) where a higher score means better memory performance. Outcomes are reported as the Total Accuracy Percentage (Correct Choices/Total Choices) x 100%

Self-Report Subjective "High"

时间窗: Measured 2 times: Baseline (0HR) and 3 hours (3HR) after capsule administration on each drug condition (0mg, 10mg, 30mg)

A Visual Analogue Scale (VAS) was used to measure the acute subjective effects of THC at varying doses (0mg, 10mg, 30mg). Responses are made for VAS items along a 100-unit scale anchored on the extremes by "Not At All" (0) and "Extremely" (100) with a higher score meaning more of the effect. Participants were instructed to select "Not At All" (0) for all baseline (0HR) measures. Post-TMS administration (real or sham), participant self-reported their subjective "high" on the VAS with higher values indicating a more intense sensation of "high".

次要结局

未报告次要终点

研究者

发起方
Michael J. Wesley, PhD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Michael J. Wesley, PhD

Assistant Professor

University of Kentucky

研究点 (1)

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