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临床试验/NCT06695637
NCT06695637撤回1 期

Individualized Neuromodulation of Craving Control for Meth Use Disorders

University of Minnesota0 个研究点目标入组 40 人开始时间: 2025年9月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
撤回
入组人数
40
主要终点
Change in Connectivity between the Amygdala/Ventral Striatum and Frontopolar Cortex Measurement

研究概览

简要总结

Drug craving is one of the key aspects of substance use disorders (SUDs) and is associated with continued drug use and relapse. Approximately 70% of those entering treatment will relapse within one year. To improve treatment outcomes, new interventions targeting the underlying brain biomarkers of relapse vulnerability hold significant promise in reducing this critical public health problem.

This clinical trial is designed as a randomized, double-blind, sham-controlled study, aiming to investigate the effects of continuous theta burst stimulation (cTBS) on individuals diagnosed with Methamphetamine Use Disorders (MUDs). Only adults (22-65 years old) who are already living in an abstinence-based residential setting for substance use treatment will be recruited, and participants will be escorted to and from the MIDB center for their imaging and brain stimulation sessions. After a baseline assessment to determine eligibility, the study will include 40 participants, who will be randomly assigned to two groups: the active cTBS group and the sham cTBS group (a control group receiving a placebo treatment).

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
22 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Abstinent from any substance or alcohol use (excluding caffeine or nicotine) for a minimum of 1 week at study enrollment
  • •Has the intention to remain in their treatment program(s) until the end of the intervention portion of the study.
  • •Able to provide written consent and comply with study procedures.
  • •Meets the DSM-V MINI diagnostic criteria for methamphetamine use disorder (MUD).
  • •Subjects may have current comorbid drug use, but one of their major substance use disorder diagnosis needs to be methamphetamine use. Potential subjects will not be excluded for being on medication-assisted treatments (MATs), such as those used to treat substance use disorders.

排除标准

  • •Any contraindications for MRI scanning (up to the discretion of MIDB staff:
  • •metal implants, pacemakers or any other implanted electrical device, injury with metal, braces, dental implants, non-removable body piercings, pregnancy, breathing or moving disorder, moderate to severe heart disease).
  • •Any medical condition or treatment with neurological sequelae (i.e., stroke, tumor, HIV, intracranial lesions)
  • •Having epilepsy, a personal history of a seizure (beyond fever or withdrawal or medical induced seizure), or individuals with a family history of clinically proven epilepsy disorder in a first degree relative
  • •Over 9 months of abstinence from substance use
  • •A head injury resulting in a loss of consciousness exceeding 30 minutes (i.e., moderate or severe TBI)
  • •Presence of a condition that would render study measures difficult or impossible to administer or interpret
  • •Age outside the range of 22 to 65
  • •Entrance to the treatment program under a court mandate. (i.e., legally incarcerated)
  • •History of ECT or cortical energy exposure within the past 6 months, including participation in any other neuromodulation studies
  • •Being pregnant. For females of reproductive potential: negative pregnancy test or use of highly effective contraception for at least 1 month prior to baseline will be necessary for inclusion.
  • •Having current active suicidal ideations reported in baseline psychiatry interview
  • •Having active bipolar disorder (with a risk of mania)
  • •Using medications that significantly increase risk of seizure for this study based on the clinical judgement of the study's medical team such as immediate release bupropion (Wellbutrin IR), stimulants, and tramadol.

研究组 & 干预措施

Study group

Experimental

Individuals diagnosed with MUDs randomized for study intervention

干预措施: active cTBS (Radiation)

Sham control group

Sham Comparator

Individuals diagnosed with MUDs randomized for sham intervention

干预措施: sham cTBS (Radiation)

结局指标

主要结局

Change in Connectivity between the Amygdala/Ventral Striatum and Frontopolar Cortex Measurement

时间窗: baseline, 24 hours

Connectivity strength between the amygdala/ventral striatum and frontopolar cortex, measured by generalized psychophysiological interaction (gPPI) analysis. Measurement Tool: Connectivity strength measured using fMRI-based gPPI with Brainnetome atlas parcellation. Unit of Measure: Regression coefficient representing connectivity strength.

次要结局

  • Change in Self-Reported Craving in Methamphetamine Use Disorder (MUD)(baseline, 24 hours)
  • Baseline Connectivity Predicting Neural and Subjective Response to Individualized cTBS(baseline, 24hours)
  • Predictive Role of Individualized Current Density in Prefrontal Cortex for Subjective and Neural Response to cTBS density in the head models in the prefrontal cortex in both subjective and neural response to cTBS(baseline, 24 hours)

研究者

申办方类型
Other
责任方
Sponsor

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