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临床试验/NCT04760899
NCT04760899进行中(未招募)不适用

Bilateral Cerebellar Transcranial Direct Current Stimulation (tDCS) for the Treatment of Sports-Related Post-Concussion Syndrome (SRPCS)

University of Iowa2 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2021年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
31
试验地点
2
主要终点
Berg Balance Scale

研究概览

简要总结

This study is investigating the immediate and long-term effects of bilateral cerebellar transcranial direct current stimulation on cognition, balance, and symptom severity in people with sports-related post-concussion syndrome. The central hypothesis is that tDCS will provide improvements in cognitive deficits, balance, and overall symptom attenuation in people with SRPCS both acutely and at 2 and 4 week follow ups. The researchers further hypothesize that cerebellar tDCS will ameliorate the symptoms of people with SRPCS.

详细描述

The long term goal is to develop an effective and broadly applicable treatment modality for athletes who develop SPRCS. The objective of this study is to investigate the effects of multiple (5 consecutive daily) sessions of 2 milliampere (mA) right cerebellar tDCS on cognitive deficits, balance, and overall attenuation of symptoms on people with SRPCS. Cognitive deficits will be assessed with the N-back Working Memory test, list sorting test, and dimensional change card test. Balance deficits will be assessed with the Berg Balance Scale and Standing Balance Test (SBT), and symptoms will be assessed via the Rivermead Post-Concussion Symptom Questionnaire (RPQ). The cognitive and balance tasks are taken from the NIH motor toolbox and have been shown to be the most important for health and success in school and work, and the RPQ is one of the most widely used SRPCS evaluation tools. The central hypothesis is that tDCS will provide improvements in cognitive deficits, balance, and overall symptom attenuation in people with SRPCS both acutely and at 2 and 4 week follow ups. The researchers further hypothesize that cerebellar tDCS will ameliorate the symptoms of people with SRPCS. The rationale is that the results will improve the quality of life of these patients and may prevent impairment of cognitive function later in life.

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
Double (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Sign Informed Consent Document
  • Stated willingness to comply with all study procedures and availability for the duration of the study Male or female, aged 18-
  • Diagnosed with a concussion by a doctor greater than or equal to 1 month ago.
  • Concussion occurring during a sport/recreational activity
  • Meet the ICD-10 diagnostic criteria for Post Concussion Syndrome:
  • history of a traumatic brain injury at least a month in the past
  • 3 or more of the following symptoms: headaches, dizziness, fatigue, irritability, insomnia, concentration, memory difficulty
  • Rivermead Post Concussion Questionnaire score of at least 21 at baseline.
  • Comprehension of the protocol, as indicated by an ability to respond to questions about the study after reading the consent form.
  • Healthy enough to complete the protocol based, on information obtained from a clinical exam and past medical history.
  • Able to use and be contacted by telephone
  • Able to speak, read, and understand English, and complete questionnaires in English.
  • Healthy Controls
  • No history of mild traumatic brain injury or diagnosed concussion within the last year.
  • Not suffering from any PCS symptoms related to a brain injury
  • No History of a psychiatric condition (other than mild to moderate anxiety or depression)
  • Currently on no prescribed psychoactive medications
  • Comprehension of the protocol, as indicated by an ability to respond to questions about the study after reading the consent form.
  • Healthy enough to complete the protocol based, on information obtained from a clinical exam and past medical history.
  • Able to use and be contacted by telephone
  • Able to speak, read, and understand English, and complete questionnaires in English

排除标准

  • History/presence of secondary conditions such as seizure disorders (or on medications known to lower seizure threshold), hydrocephalus, diabetes mellitus, or claustrophobia
  • Currently diagnosed drug and/or alcohol addiction
  • Active Psychosis
  • History of a psychiatric condition (other than mild to moderate anxiety or depression)
  • Currently on no prescribed psychoactive medications
  • Not in any kind of memory improvement program or therapy during study participation.
  • No known fissures or holes in the skull
  • No metallic objects or implanted devices in the skull

结局指标

主要结局

Berg Balance Scale

时间窗: 2 weeks

Balance Assessment. This is a 14 item test with scores from 0 to 4, with 4 being no inhibition at all. The max score on this test is 56, higher scores indicating better balance.

List Sorting Working Memory Test

时间窗: 2 weeks

Assessment of Cognition

Flanker Inhibitory Control Test

时间窗: 2 weeks

Assessment of Cognition/

Dimensional Change Card Sorting Test

时间窗: 2 weeks

Assessment of Cognition

Standing Balance Test

时间窗: 2 weeks

Balance Assessment. Outcomes of this test are overall postural sway translated into a normalized t-score.

次要结局

  • Dimensional Change Card Sorting Test(2 and 4 week follow ups)
  • Standing Balance Scale(2 and 4 week follow ups)
  • Berg Balance Scale(2 and 4 week follow ups)
  • Flanker Inhibitory Control Test(2 and 4 week follow ups)
  • List Sorting Working Memory Test(2 and 4 week follow ups)

研究者

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

Justin Deters

Principal Investigator

University of Iowa

研究点 (2)

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