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临床试验/NCT03622749
NCT03622749已完成不适用

Pilot Study of Neuromodulation for Enhancement of Emotion Regulation in Bipolar Mood Disorders

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2019年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
19
试验地点
1
主要终点
Affective Multisource Interference Task - Reaction Time During Negative Interference Trials

研究概览

简要总结

The investigators are conducting this research study to better understand how individuals with bipolar disorder regulate their emotions, and if the study can use a technique called "transcranial magnetic stimulation" or TMS to help improve emotion regulation for individuals with bipolar disorder.

详细描述

Emotion dysregulation contributes to the development and maintenance of a wide range of psychopathology, but is especially relevant for individuals with bipolar mood disorders (BD). These individuals experience severe and episodic emotion dysregulation associated with maladaptive functioning, interpersonal problems, decreased work productivity, and suicidal ideation and behavior. To date, both pharmacological and psychosocial treatments fail to normalize emotion dysregulation for many bipolar patients. As a consequence, all too many experience poor outcomes. Thus, there is a significant need for new innovative approaches to target and improve emotion dysregulation in bipolar patients. Non-invasive neuromodulation using transcranial magnetic stimulation (TMS) may provide a viable strategy to help improve emotion dysregulation in bipolar mood disorders. As a first step to test this hypothesis, the current proposal seeks to experimentally identify specific neural target sites for improving emotion regulation using TMS. If the investigators can demonstrate target engagement of emotion regulation at the behavioral level using TMS, this will provide an important first step towards examining the potential utility of TMS as a viable strategy to help improve emotion dysregulation in bipolar mood disorders. While this is not a definitive clinical trial, the sham-controlled double-crossover design of this study will provide valuable information for target site selection for the development of TMS as an intervention strategy to improve emotion dysregulation in BD.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Crossover
主要目的
Health Services Research
盲法
None (Participant)

盲法说明

Participants are blinded to whether they received active versus sham (placebo) TMS.

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women
  • Ages 18-50 years
  • Patients diagnosed with bipolar I disorder (BD-I), current mood state euthymic.
  • On a stable psychiatric medication regimen for at least a month prior to and during study participation
  • Healthy Controls:
  • Men and women
  • Ages 18-50 years
  • Without major psychiatric illness

排除标准

  • Any change in psychiatric medications within a month prior to and during study participation
  • Legal or mental incompetency
  • Intellectual disability
  • Current manic (YMRS > 12) or severe depressive episode (HAM-D-17 > 5)
  • Substance use disorder (abuse or dependence) with active use within the last 3 months
  • Significant medical or neurological illness
  • Prior neurosurgical procedure
  • History of seizures
  • History of ECT treatment or clinical TMS within the past three months
  • Implanted cardiac pacemakers
  • Patients who have conductive, ferromagnetic or other magnetic-sensitive metals implanted in their head or neck, or are non-removable and within 30 cm of the treatment coil. These include:
  • Aneurysm clips or coils
  • Carotid or cerebral stents
  • Metallic devices implanted in the head (e.g. Implanted pacemaker, medication pump, vagal stimulator, deep brain stimulator, TENS unit, or ventriculo-peritoneal shunt)
  • Magnetically active dental implants
  • Cochlear/otologic implants
  • CSF shunts
  • Ferromagnetic ocular implants
  • Pellets, bullets, fragments less than 30 cm from the coil
  • Facial tattoos with metallic ink, permanent makeup less than 30 cm from the coil
  • Pregnant women
  • Healthy Controls:
  • History of major psychiatric illness, including psychosis
  • Has a first-degree relative with psychosis
  • Active use of neuropsychoactive medications
  • Legal or mental incompetency
  • Intellectual disability
  • Substance use disorder (abuse or dependence) with active use within the last 3 months
  • Significant medical or neurological illness
  • Prior neurosurgical procedure
  • History of seizures
  • History of ECT treatment or clinical TMS within the past three months
  • Implanted cardiac pacemakers
  • Individuals who have conductive, ferromagnetic or other magnetic-sensitive metals implanted in their head or neck, or are non-removable and within 30 cm of the treatment coil. These include:
  • Aneurysm clips or coils
  • Carotid or cerebral stents
  • Metallic devices implanted in the head (e.g. Implanted pacemaker, medication pump, vagal stimulator, deep brain stimulator, TENS unit, or ventriculo-peritoneal shunt)
  • Magnetically active dental implants
  • Cochlear/otologic implants
  • CSF shunts
  • Ferromagnetic ocular implants
  • Pellets, bullets, fragments less than 30 cm from the coil
  • Facial tattoos with metallic ink, permanent makeup less than 30 cm from the coil
  • Pregnant women

研究组 & 干预措施

Patients

Active Comparator

Individuals with Bipolar 1 Disorder

干预措施: Transcranial Magnetic Stimulation (TMS) (Device)

结局指标

主要结局

Affective Multisource Interference Task - Reaction Time During Negative Interference Trials

时间窗: Task administered 10 minutes pre TMS and 5 minutes post TMS

The Affective Multisource Interference Task is a behavioral task measuring the ability to identify an oddball number when overlayed on affective images as a proxy for emotion regulation. Outcome Measure 1: Slope of reaction time during trials with negative valenced stimuli where the oddball number is other than zero and in a location incongruent with the location on the button box

Affective Multisource Interference Task - Reaction Time During Positive Interference Trials

时间窗: Task administered 10 minutes pre TMS and 5 minutes post TMS

The Affective Multisource Interference Task is a behavioral task measuring the ability to identify an oddball number when overlayed on affective images as a proxy for emotion regulation. Outcome Measure 2: Slope of reaction time during trials with positive valenced stimuli where the oddball number is other than zero and in a location incongruent with the location on the button box

Emotion Conflict Resolution Task - Incongruent Fear Trials Reaction Time

时间窗: Task administered 10 minutes pre TMS and 5 minutes post TMS

The Emotion Conflict Resolution Task is a behavioral task requiring correct identification of an emotion word overlayed on photographs of facial expressions of emotion. Outcome measure 3: Slope of reaction time during trials when the image is of a fearful facial expression but the word is "Happy" (incongruent)

Emotion Conflict Resolution Task - Incongruent Happy Trials Reaction Time

时间窗: Task administered 10 minutes pre TMS and 5 minutes post TMS

The Emotion Conflict Resolution Task is a behavioral task requiring correct identification of an emotion word overlayed on photographs of facial expressions of emotion. Outcome measure 4: Slope of reaction time during trials when the image is of a happy facial expression but the word is "Fear" (incongruent)

次要结局

未报告次要终点

研究者

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

Kristen K. Ellard, Ph.D.

Instructor in Psychology

Massachusetts General Hospital

研究点 (1)

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