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临床试验/NCT03579953
NCT03579953已完成早期 1 期

Theta-Burst Stimulation As A Tool To Change Smoking Behavior

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2018年5月22日最近更新:
适应症
干预措施

试验速览

阶段
早期 1 期
状态
已完成
入组人数
16
试验地点
2
主要终点
Changes in craving after a single session of cTBS

研究概览

简要总结

Prior and recent evidence suggests a role of medial prefrontal cortex (MPFC) in cigarette smoking. Episodic Future Thinking (EFT) has also been shown to be associated with increased delayed discounting and reduced cigarette self administration. In the present study, we will examine whether a single administration of theta-burst transcranial magnetic stimulation (tbTMS) can increase Episodic Future Thinking and delayed discounting while reducing craving for nicotine.

详细描述

The purpose of this study is to develop theta burst transcranial magnetic stimulation (tbTMS) as a potential treatment for nicotine addiction. Theta burst TMS is a non-invasive technique that uses magnetic pulses to temporarily stimulate specific brain areas in awake people (without the need for surgery, anesthetic, or other invasive procedures). This study will test whether tbTMS over the forehead can produce a reduction in things that may prompt individuals to want to smoke cigarettes. TMS has been approved by the Food and Drug Administration as an investigational tool as well as a therapy for depression. However, TMS is not approved by the Food and Drug Administration as a treatment for nicotine cravings and other addictions.

This study consists of one consent session and one TMS session. Participants will be asked to complete a series of questionnaires and computer assessments about nicotine both before and after a single tbTMS session.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • 18-65 years of age
  • Smoke at least 10 cigarettes a day (on average)
  • Not be pregnant
  • Meet all criteria on a standardized TMS safety screen (including to but not limited to implanted electronic devices, bullets or metallic fragments above the neck, hair clips that cannot be removed)
  • No barriers to making contact between the TMS coil and the skin (e.g. cornrows that cannot be removed, glasses that the participant is unwilling to remove)

排除标准

  • Report comorbid mental or physical illness (managed or unmanaged)
  • Currently using prescription medication that might affect smoking or nicotine metabolism
  • Using smokeless tobacco or alternative nicotine products
  • History of epilepsy or seizures (other than childhood febrile seizures)
  • History of chronic migraines

研究组 & 干预措施

Real cTBS to MPFC

Experimental

One session of real cTBS treatment delivered to the medial prefrontal cortex (MPFC) (2 trains of stimulation over the MPFC as defined by EEG coordinates (FP1); each train: 120 sec, 3 pulse bursts presented at 5Hz, 15 pulses/sec, 1800 pulses/train, 60 sec intertrain interval; 110% RMT, MagPro X100 Cool Coil; 3600 pulses total).

干预措施: Real cTBS (Device)

Sham cTBS to MPFC

Sham Comparator

One session of sham cTBS treatment delivered to the medial prefrontal cortex (MPFC) (2 trains of stimulation over the MPFC as defined by EEG coordinates (FP1); each train: 120 sec, 3 pulse bursts presented at 5Hz, 15 pulses/sec, 1800 pulses/train, 60 sec intertrain interval; 110% RMT, MagPro X100 Cool Coil; 3600 pulses total).

干预措施: Sham cTBS (Device)

结局指标

主要结局

Changes in craving after a single session of cTBS

时间窗: For the duration of the study, approximately 24 hours following real or sham cTBS

The effect of real versus sham cTBS on nicotine craving will be assessed by comparing pre-TMS and post-TMS changes in nicotine craving scores.

次要结局

  • Changes in delayed discounting after a single session of cTBS(For the duration of the study, approximately 24 hours following real or sham cTBS)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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