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临床试验/NCT04155333
NCT04155333已完成不适用

Effects of Non-Invasive Brain Stimulation on Soldiers' Cognitive and Functional Performance

United States Army Aeromedical Research Laboratory2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2019年12月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
28
试验地点
2
主要终点
Cognitive function - Working Memory

研究概览

简要总结

Non-invasive brain stimulation has been shown to alter performance in both clinical and healthy populations on cognitive tasks. While the performance alterations have generally been shown to result in enhancement, mixed results remain in the literature. Much of the mixed results within the literature have been attributed to the use of different stimulation parameters, targeting of different brain areas, and using a variety of performance measures or assessing different constructs. However, non-invasive brain stimulation is a desirable method for enhancing Soldier performance given the ease of administration and minimal side effects as compared to other forms of performance enhancement (e.g., pharmaceuticals, caffeine). The objective of the current study is to evaluate the effects of non-invasive brain stimulation to the left dorsolateral prefrontal cortex in enhancing Soldier cognitive skills and performance on military tasks. A double blind within-subjects design will be used with healthy, rested Soldiers who will receive non-invasive brain stimulation and perform basic cognitive and operationally relevant tasks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Single (Investigator)

盲法说明

Subjects and the research team will both be blind to the stimulation condition delivered at each test session. Access will be limited to the study physicians, investigators, and device programmers.

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Must be 18 (if active duty), 19 (if non-active duty) up to 40 years old.
  • Must have normal hearing, vision or corrected to normal vision, and cognitive function as determined by self-report and screening by study physician
  • Must have obtained at minimum 6 hours of sleep prior to data collection, as assessed by actigraphy data and self-report.
  • Must have refrained from consumption of caffeine, 16 hours, nicotine, 2 hours, and alcohol, 24 hours, prior to the study, assessed by self-report.

排除标准

  • The following medically-related exclusionary criteria will be used, as assessed and verified by the study physician:
  • Haven taken any medications which induce drowsiness, such as over-the-counter antihistamines within 24 hours of participation in the study. Any self-medication will be assessed through self-report
  • No current medical conditions or medications affecting cognitive function or attention.
  • Any history of any attention deficit condition requiring medication.
  • Any history of psychological/psychiatric disorder.
  • Any history of seizures, migraines, or neurological disorders.
  • History of a head injury involving loss of consciousness.
  • Any metal implanted within the head (e.g., shrapnel, surgical clips) or any implanted devices (e.g., cardiac pacemaker, brain stimulator, hydrocephalic shunt).
  • Skin condition on the scalp, such as psoriasis or eczema, or wounds on the head.
  • Currently receiving hormonal therapy treatments, other than birth control or as determined by physicians.
  • Potential for caffeine withdrawal symptoms that will impede cognitive testing.
  • Females with a known pregnancy, who test positively for pregnancy, or refuse the test will be excluded, given the lack of available research regarding the effects of tDCS during pregnancy. Known pregnancy will be assessed during screening, females without a known pregnancy will be requested to provide a urine sample during the screening procedures to ensure the absence of pregnancy.

结局指标

主要结局

Cognitive function - Working Memory

时间窗: Approximately 2 minutes during stimulation

Digit span task

Cognitive function - Sustained attention

时间窗: Approximately 7 minutes during stimulation

Rapid Visual Information Processing Task

Military task performance

时间窗: Folllowing stimulation; task lasts approximately 40 min

Target acquisition

Cognitive function - Multitasking/Working Memory

时间窗: Approximately 5 minutes during stimulation

Dual n-back

Cognitive function - Selective Attention

时间窗: Approximately 3 minutes during stimulation

Stroop test

Cognitive function - Executive function

时间窗: Approximately 2 minutes during stimulation

Shifting Attention Task: Digit symbol substitution task

次要结局

  • Cognitive function - Cognitive Flexibility(Approximately 5 minutes after stimulation)
  • Cognitive function - Risk Taking/ Decision Making(Approximately 1 minute after stimulation)
  • Cognitive function - Impulsivity/Motor Control(Approximately 3 minutes after stimulation)

研究者

发起方
United States Army Aeromedical Research Laboratory
申办方类型
Fed
责任方
Sponsor

研究点 (2)

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