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临床试验/NCT05872750
NCT05872750招募中不适用

Rolling Deep With Gambling Disorder: From Building up of Scales, Biomarkers to Therapeutic Innovation

Taipei City Hospital2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2023年4月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
75
试验地点
2
主要终点
Change in gambling craving

研究概览

简要总结

The goal of this clinical trial is to investigate the efficacy of theta burst stimulation in individuals with gambling disorder. The main goal is to compare the severity of gambling problems following 2 weeks of intervention between active group and sham group. Participants will be randomized into active and sham group. The severity of gambling problems are assessed by self-reported questionaires.

详细描述

Gambling disorder, formerly known as pathological gambling, is a gambling behavior that causes significant function impairment in personal, social, occupational domains. Currently there is no pharmacological treatment for gambling disorder and it is urgent to develop innovative treatment modalities. Image studies have found a link between prefrontal circuit dysfunction and behavioral disinhibition, which supports the use of non-invasive brain stimulation as a potential treatment for gambling disorder. In this study, 75 patients with gambling disorder will be randomly assigned in a 2:1 ratio to the intervention group (50 patients) and the control group (25 patients) on double-blind basis. The study duration is 2 weeks, with 10 sessions of 20 minutes each. The intervention group will receive repetitive transcranial magnetic stimulation at the left dorsolateral prefrontal cortex and pre-supplementary motor area, while the control group will receive sham stimulation. The Chinese version of the Problem Gambling Severity Index (PGSI), the Gambling Symptom Assessment Scale (G-SAS), and the Visual Analogue Scale (VAS) for craving will be administered at week 0, 2, 4, 8, and the change in gambling severity between the two groups will be compared by repeated measures ANOVA.

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
Triple (Participant, Care Provider, 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

  • age between 18 and 65 years;
  • fulfilling at least 4 of the Diagnostic and Statistical Manual version 5 (DSM-5) criteria of gambling disorder for at least 12-month assessed by the Structured Clinical Interview

排除标准

  • Inability to provide informed consent or comprehend the study procedure;
  • A major psychiatric illness that required chronic psychotropic medication or inpatient treatment, including schizophrenia spectrum disorder, bipolar spectrum disorder, and major depressive disorder with psychotic features.
  • A current DSM-5 diagnosis of substance use disorder except nicotine use disorder or the use of one to two low-potency benzodiazepine tablets for sleep impairment;
  • Have known preexisting noise-induced hearing loss, concurrent treatment with ototoxic medications, or with cochlear implants.
  • Unstable medical illness, including malignancy, uncontrolled diabetes mellitus, unstable cardiac disease or recent myocardial infarction, or cerebrovascular or cardiovascular risk factors that require intensive medical management
  • On medications known to lower seizure threshold (e.g., TCA, bupropion, clozapine)
  • Implants controlled by physiological signals, including pacemaker, implantable cardioverter defibrillator, cochlear implant.
  • Metallic objects in the head, including stenting, suture.
  • Elevated risk of seizure due to traumatic brain history, seizure history, and head trauma, intracranial lesion, and alcohol or benzodiazepines withdrawal syndrome, stimulant intoxication.

结局指标

主要结局

Change in gambling craving

时间窗: Before intervention (week 0) and after intervention (week 2, 4)

Measured by visual analog scale, from 0-10

Change in gambling severity

时间窗: Before intervention (week 0) and after intervention (week 2, 4)

Measured by Gambling Symptom Assessment Scale, from 0-48

次要结局

  • Change in depression severity(Before intervention (week 0) and after intervention (week 2, 4))
  • Change in anxiety severity(Before intervention (week 0) and after intervention (week 2, 4))

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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