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临床试验/NCT04294888
NCT04294888
终止
不适用

TMS in Preclinical and Prodromal AD: Modulation of Brain Networks and Memory

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 4 人2020年3月2日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Alzheimer Disease
发起方
Massachusetts General Hospital
入组人数
4
试验地点
1
主要终点
Paired Associative Face Name Memory Test
状态
终止
最后更新
上个月

概览

简要总结

The purpose of this study is to assess the effects of non-invasive brain stimulation on memory in cognitively unimpaired older adults and in patients amnestic mild cognitive impairment (aMCI) due to Alzheimer's disease (AD). This study will use repetitive Transcranial Magnetic Stimulation (rTMS) to stimulate nodes of the Default Mode Network (DMN)- which is thought to support episodic memory and to be affected by Alzheimer's pathology.

We will use functional connectivity MRI (fcMRI) to assess changes in functional network architecture following the stimulation. We will also assess putative cognitive improvements resulting from the stimulation by in-depth memory testing.

注册库
clinicaltrials.gov
开始日期
2020年3月2日
结束日期
2021年6月23日
最后更新
上个月
研究类型
Interventional
研究设计
Crossover
性别
All

研究者

责任方
Principal Investigator
主要研究者

Bradford Clark Dickerson, M.D.

Associate Neurologist

Massachusetts General Hospital

入排标准

入选标准

  • Between the ages of 60-85
  • All participants will be native English speakers
  • Willing and able to consent to the protocol and undergo imaging and neuropsychological testing at the specified time points
  • Participants with aMCI will be asked to bring a study partner to all visits
  • Only patients with very mild or mild cognitive impairment (CDR 0.5 or CDR 1) will be included in the prodromal AD cohort

排除标准

  • History of head trauma involving loss of consciousness or alteration in consciousness
  • Another major neurologic or psychiatric condition
  • Known presence of a structural brain lesion (e.g. tumor, cortical infarct)
  • Any contraindication to MRI, such as presence of pacemakers, aneurysm clips, artificial heart valves, ear implants, metal fragments, or foreign objects in the eyes, skin, or body
  • Longstanding premorbid history (i.e. longer than 10 years) of alcohol or substance abuse with continuous abuse up to and including the time that the symptoms leading to clinical presentation developed
  • Any significant systemic illness or unstable medical condition which could lead to difficulty complying with the study protocol.
  • Unwilling to return for follow-up, undergo neuropsychological testing, TMS, and MR imaging

结局指标

主要结局

Paired Associative Face Name Memory Test

时间窗: up to 5 weeks

A test of memory for face-name associations

次要结局

  • Changes in intrinsic functional connectivity(up to 5 weeks)

研究点 (1)

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