跳至主要内容
临床试验/NCT01292382
NCT01292382Unknown不适用

Effects of rTMS on the Cognition of Elderly With Cognitive Impairment no Dementia ( CIND )

University of Sao Paulo General Hospital2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2010年11月最近更新:
适应症

试验速览

阶段
不适用
入组人数
34
试验地点
2
主要终点
Repetitive transcranial magnetic stimulation improves memory in elderly with memory complaints

研究概览

简要总结

Memory is constituted by a set of mental abilities of information processing that will be available at a later time. Flawless performance depends on several brain systems and other cognitive domains. Normal aging is characterized by cognitive deficits that may worsen the production capacity and quality of life. Such deficits represent variations of normal , and may stabilize,or even better progress. Include multiple cognitive domains, such as working and episodic memory, and attention. Despite the heterogeneity of the nature and severity of these deficits, common characteristics were observed in neuropsychological assessment of that population, for example, reduction in processing speed. There is an important gap in the therapeutic approach of these individuals.

Transcranial magnetic stimulation (TMS) is a noninvasive and promising intervention, with potential to improve memory and cognition activating networks that operate on memory or other networks that interfere with cognitive performance. The technique relies on generating a variable magnetic field originated from an alternating electric current applied to the human skull reaching focal cortical regions.

This study is a sham-controlled clinical trial, randomized, double-blind study. It will be evaluated the effects of repetitive transcranial magnetic stimulation (rTMS) on global cognition (memory, attention, language, executive functions, planning, logical reasoning, calculation and visual-spatial perception), especially memory, of elderly individuals with mild cognitive impairment, included in the domain of cognitive impairment no dementia (CIND).

详细描述

Subjects:

I. Eligibility criteria:

  1. Male and female participants
  2. Older adults aged 60-74 years
  3. Education ≥ 4 years
  4. Performance on neuropsychological tests below normal for age and education
  5. Availability to attend the sessions of the application of TMS and neuropsychological assessments
  6. Signing an informed consent by the participant or his guardian

II. No eligibility criteria:

  1. Prior diagnosis of dementia
  2. Any psychiatric disorder, except for mild depression in remission for at least 6 months. Shall be excluded those with scores > 12 on the Hamilton Depression Scale
  3. History of neurosurgery and implantation of metal clips, head trauma, implantation of cardiac pacemakers, stroke, transient ischemic attack, cardiac surgery
  4. Clinical or neurological diseases with impact on cognitive ability
  5. Neurodegenerative central nervous system disease(eg. Parkinson Disease)
  6. Alcohol and other drug abstinence for less than one year
  7. Use of psychotropic medications (anticholinergic, mood stabilizers, neuroleptics), except for antidepressants
  8. Chronic use of benzodiazepines with abstinence for less than 6 months
  9. Severe uncontrolled organic disease that might interfere with the conduct of the study, such as cancer, congestive heart disease, digestive disorders, diabetes mellitus type I or type II, dyslipidemia etc.
  10. Sensory impairments(to guarantee a adequate performance in the tests to evaluate cognitive functions)
  11. Magnetic resonance imaging of the brain with evidence of lacunar or large vessels infarctions, cerebral hemorrhage

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
60 Years 至 74 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participants of both sexes
  • Aged between 60 and 74 years
  • Schooling ≥ 4 years
  • Performance on neuropsychological tests of up to 1.5 standard deviations below normal for age and education
  • Signing an informed consent by the participant or his guardian.

排除标准

  • Prior diagnosis of dementia.
  • Any psychiatric disorder, except for mild depression for at least six months.
  • Shall be excluded those with scores> 12 on the Hamilton scale.
  • History of neurosurgery and implantation of metal clips, head trauma, implantation of cardiac pacemakers, stroke, transient ischemic attack, cardiac surgery
  • Clinical or neurological diseases with an impact on cognitive ability
  • Neurodegenerative central nervous system (eg Parkinson's disease)
  • Alcohol and other drug dependency with abstinence for less than a year
  • Use of psychotropic medications (anticholinergic, mood stabilizers, neuroleptics), except for antidepressants
  • Chronic use of benzodiazepines with abstinence for less than six months
  • Use of vitamin supplements (multivitamins, folic acid, vitamin B12), ginkgo biloba
  • Severe uncontrolled organic disease that could interfere in the conduct of the study, such as cancer, heart disease, digestive disorders, diabetes mellitus type I or type II, uncontrolled dyslipidemia etc.
  • Sensory disabilities, intellectual, preventing them from adequately perform the necessary tests to assess cognitive function
  • Cerebrovascular disease based on Hachinsky score.
  • History of head trauma.
  • Any other condition that in the opinion of the investigator makes problematic the inclusion of the patient in a trial of this nature, as well as patients who do not adhere or not to cooperate.
  • Worsening of the primary symptoms during the treatment.

结局指标

主要结局

Repetitive transcranial magnetic stimulation improves memory in elderly with memory complaints

时间窗: Neuropsychological tests: T1 - effects after rTMS, and T2: 4 weeks after rTMS

Neuropsychological tests - RBMT (Rivermead Behavioral and Memory Test)

次要结局

  • Repetitive transcranial magnetic stimulation improves global cognition of elderly with memory complaints(Neuropsychological tests: T1 - effects after rTMS, and T2: 4 weeks after rTMS)

研究者

申办方类型
Other

研究点 (2)

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