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临床试验/NCT02220309
NCT02220309
已完成
不适用

Neural Dimensions of Threat Reactivity and Regulation for Understanding Anxiety

Stanford University3 个研究点 分布在 1 个国家目标入组 167 人2013年8月11日

概览

阶段
不适用
干预措施
Pramipexole Oral Tablet
疾病 / 适应症
Anxiety
发起方
Stanford University
入组人数
167
试验地点
3
主要终点
Assessments of symptoms and daily functioning
状态
已完成
最后更新
3个月前

概览

简要总结

This research study is aimed at understanding behaviors and brain circuits that relate to anxiety and depression. Our goal is to learn which circuits of the brain are involved in anxiety and how these circuits might affect daily functioning.

This study has recently added an additional treatment component: participants undergo a 12 week course of either Pramipexole medication or rTMS therapy (explained below). The ultimate goal of the study is to offer participants experiencing anxiety and depression a treatment that is alternative to ones that have failed them in the past, and to apply the knowledge we gain from investigating the brain circuits involved in anxiety and depression to help personalize treatments.

We invite anyone who has recently experienced any symptoms of anxiety and/or depression to participate (no diagnosis is required to participate).

详细描述

If you are eligible and choose to participate, we'll ask you to come in for 2 separate testing visits and 8 weeks of treatment in between. In both the pre-treatment and post-treatment testing visit, you would complete game-like tasks on the computer, undergo a non-invasive MRI brain scan, and answer some questions about your emotional health. The entire visit takes place during 1-2 days at Stanford and lasts about 4-5 hours. We'll also ask you to complete a follow-up 12 weeks later, from home, during which we'll again ask you some questions on your emotional health. The 8-week treatment phase will consist of your choice of either TMS (transcranial magnetic stimulation) or Pramipexole (a medication for depression). You will meet with study coordinators and MDs each week (Pramipexole) or each day (TMS) to receive treatment. You will also be asked to complete weekly online surveys to monitor your mood during the 2-month course of treatment. To inquire more about participation, you can either sign up online or contact us. Sign up online: http://med.stanford.edu/williamslab/research/current/rad.html Contact us: Call or text (650) 600-1609 or email rad-at-study@stanford.edu

注册库
clinicaltrials.gov
开始日期
2013年8月11日
结束日期
2025年4月2日
最后更新
3个月前
研究类型
Observational
性别
All

研究者

责任方
Principal Investigator
主要研究者

Leanne Williams

Professor

Stanford University

入排标准

入选标准

  • Recent experiences of anxiety and/or depression
  • Ages 18-65

排除标准

  • Specific psychiatric medications (case-by-case basis)
  • A diagnosis of Bipolar 1 Disorder, Schizophrenia, or Obsessive Compulsive Disorder
  • Any of the following medical conditions: Parkinson's disease; liver or kidney disease; history of epilepsy or seizures; history of cardiovascular disorders (specifically orthostatic hypotension)

研究组 & 干预措施

Anxiety and mood disorders

干预措施: Pramipexole Oral Tablet

结局指标

主要结局

Assessments of symptoms and daily functioning

时间窗: 12 weeks

General demographics questionnaires, alcohol use questionnaire, substance use questionnaires, Mood and Anxiety Symptom Questionnaire, Penn State Worry Questionnaire, Health at Work Performance Questionnaire, WHO Quality of Life questionnaire, Satisfaction with Life Survey, Emotion Regulation Questionnaire, Brief COPE questionnaire, Early Life Stress questionnaire, Quick Inventory of Depressive Symptomatology, Beck Depression Inventory, PTSD Checklist - Civilian Version, Beck Anxiety Inventory, Barratt Impulsiveness Scale, MINI Neuropsychiatric Interview

Brain imaging

时间窗: 12 weeks

Non-invasive MRI brain scan to see function and structure of brain.

Cognitive assessment

时间窗: 12 weeks

WebNeuro is an objective assessment of cognitive strengths and weaknesses. It provides an accurate and objective assessment of person's cognitive function and efficiency.

研究点 (3)

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