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临床试验/NCT05445466
NCT05445466已完成不适用

Causal Lesion Network Guided Treatment of Bipolar Mania With Transcranial Electrical Stimulation

Beth Israel Deaconess Medical Center2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2022年12月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
2
主要终点
Young Mania Rating Scale (YMRS)

研究概览

简要总结

Mania is a core symptom of bipolar disorder involving periods of euphoria. Decreased inhibitory control, increased risk-taking behaviors, and aberrant reward processing are some of the more recognized symptoms of bipolar disorder and are included in the diagnostic criteria for mania. Current drug therapies for mania are frequently intolerable, ineffective, and carry significant risk for side effects. Presently there are no neurobiologically informed therapies that treat or prevent mania. However, using a newly validated technique termed lesion network mapping, researchers demonstrated that focal brain lesions having a causal role in the development of mania in people without a psychiatric history can occur in different brain locations, such as the right orbitofrontal cortex (OFC), right dorsolateral prefrontal cortex (DLPFC), and right inferior temporal gyrus (ITG). This lesion network evidence converges with existing cross-sectional and longitudinal observations in bipolar mania that have identified specific disruptions in network communication between the amygdala and ventro-lateral prefrontal cortex. The OFC is associated with inhibitory control, risk-taking behavior, and reward learning which are major components of bipolar mania. Thus, the association between OFC with mania symptoms, inhibitory control, risk-taking behavior, and reward processing suggests that this region could be targeted using non-invasive brain stimulation.

详细描述

Mania is a core symptom of bipolar disorder involving periods of euphoria, delusions, and overactivity. Mania occurs in multiple medical and psychiatric illnesses and can be refractory to existing treatments. Two recent studies using brain lesion mapping of psychiatrically healthy individuals presenting with mania identified causal locations in the brain, including the orbitofrontal cortex (OFC), dorsolateral prefrontal cortex (DLPFC), and inferior temporal gyrus (ITG), that were associated with new onset mania symptoms. Moreover, these identified brain regions have also been implicated in bipolar mania with specific disruption in network communication between the amygdala and ventro-lateral prefrontal cortex. The OFC is of particular interest because it is a brain structure that is associated with inhibitory control, risk-taking behavior and reward, which are major behavioral components of mania. Thus, the association between OFC with mania symptoms, inhibitory control, risk-taking behavior and reward suggests that this region could be targeted using noninvasive brain stimulation. While several studies have non-invasively targeted the DLPFC for mania, no study to date has non-invasively stimulated the OFC with either transcranial direct current stimulation (tDCS) or alternating current (tACS) in bipolar disorder and examined its effects on mania, inhibitory control, or risk-taking behavior. However, a study in healthy volunteers showed that cathodal stimulation to the OFC enhanced inhibitory control and decreased risk-taking behavior. Recently, researches have showed that targeting the OFC with tACS, personalized to the individual's intrinsic beta-gamma frequency of the reward network, that individuals showed rapid, reversible, frequency-specific modulation of reward-guided choice behavior and learning. Here we aim to answer the question of whether noninvasive brain stimulation when optimally targeted and personalized to an individual's beta-gamma frequency to the OFC can improve emotional cognitive processing and mania symptoms compared to tDCS or sham targeting. The knowledge gained from this study will provide a marker for clinical response and allow personalized treatment for patients with bipolar disorder.

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

  • Aged 18-65 years of age
  • Proficient in English
  • Able to give informed consent
  • Meet diagnostic criteria for bipolar disorder or schizoaffective disorder, bipolar type as verified by the SCID
  • History of mania ( >1 lifetime episode)
  • Experiencing mild to moderate symptoms of mania
  • No changes to mood stabilizing medications for a period of 2 weeks prior to participation
  • Has not recently participated in tES/TMS treatments

排除标准

  • Substance abuse or dependence (w/in past 6 months)
  • Those who are pregnant/breastfeeding
  • History of head injury with > 15 minutes of loss of consciousness/mal sequelae
  • DSM-V intellectual disability
  • Having a non-removable ferromagnetic metal within the body (particularly in the head)
  • History of seizures

结局指标

主要结局

Young Mania Rating Scale (YMRS)

时间窗: Change from baseline to 3-month follow-up

Measuring total Mania scores; 11 items used to access severity of mania (total score 0-60); higher scores represent higher severity of symptoms

Altman Self-Rating Mania Scale (ASRM)

时间窗: Change from baseline to 3-month follow-up

The ASRM is a 5-item self rating mania scale, assessing the presence and severity of manic symptoms. The scores for all five items are added together, resulting in a total score that can range from 0 to 20. A score of 6 or higher indicates a high probability of a manic or hypomanic condition.

Young Mania Rating Scale (YMRS)

时间窗: Change from baseline to 3-month follow-up

Measuring total Mania scores; 11 items used to access severity of mania (total score 0-60); higher scores represent higher severity of symptoms

Altman Self-Rating Mania Scale (ASRM)

时间窗: Change from baseline to 3-month follow-up

The ASRM is a 5-item self rating mania scale, assessing the presence and severity of manic symptoms. The scores for all five items are added together, resulting in a total score that can range from 0 to 20. A score of 6 or higher indicates a high probability of a manic or hypomanic condition.

Psychiatric Hospitalizations for Mania Post Study Entry

时间窗: Cumulative count of hospitalizations for mania from baseline to end of study

Psychiatric hospitalization for mania. Count of hospitalizations from baseline to end of study period assessed at Day 5, 1 Month \& 3 Month.

次要结局

  • Balloon Analogue Risk Task (BART)(Change from baseline to 3-month follow-up)
  • Electroencephalography (EEG) Resting State(Change from baseline to 3-month follow-up)
  • The Go/No Go Task(Change from baseline to 3-month follow-up)
  • Reinforcement Learning Task(Change from baseline to 3-month follow-up)
  • Social Functioning Scale (SFS)(Change from baseline to 3-month follow-up)
  • Global Assessment of Functioning (GAF)(Change from baseline to 3-month follow-up)
  • Positive and Negative Syndrome Scale (PANSS)(Change from baseline to 3-month follow-up)
  • Montgomery-Åsberg Depression Rating Scale (MADRS)(Change from baseline to 3-month follow-up)
  • Barratt Impulsiveness Scale-11 (BIS-11)(Change from baseline to 3-month follow-up)
  • Brief Assessment of Cognition (BACS)(Change from baseline to 3-month follow-up)
  • Balloon Analogue Risk Task (BART)(Change from baseline to 3-month follow-up)
  • The Go/No Go Task(Change from baseline to 3-month follow-up)
  • Electroencephalography (EEG) Resting State(Change from baseline to 3-month follow-up)
  • Reinforcement Learning Task(Change from baseline to 3-month follow-up)
  • Social Functioning Scale (SFS)(Change from baseline to 3-month follow-up)
  • Global Assessment of Functioning (GAF)(Change from baseline to 3-month follow-up)
  • Positive and Negative Syndrome Scale (PANSS)(Change from baseline to 3-month follow-up)
  • Montgomery-Åsberg Depression Rating Scale (MADRS)(Change from baseline to 3-month follow-up)
  • Barratt Impulsiveness Scale-11 (BIS-11)(Change from baseline to 3-month follow-up)
  • Brief Assessment of Cognition (BACS)(Change from baseline to 3-month follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paulo Lizano

Assistant Professor

Beth Israel Deaconess Medical Center

研究点 (2)

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