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临床试验/DRKS00030743
DRKS00030743尚未招募Unknown

Probing the efficacy of neurostimulation on reading and reading-related measures in adults with developmental dyslexia - ReDyslexia O4

Professur für Kognitive und Klinische Neurowissenschaften, Fakultät Psychologie, Technische Universität Dresden0 个研究点目标入组 85 人开始时间: 2023年3月2日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
85

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
All

入选标准

  • We plan to include 85 individuals (65 individuals diagnosed with DD and 20 controls) for this study.
  • The inclusion criteria for the participants with DD will be: (1) right-handed German speakers participants of both genders, diagnosed with DD according to participants’ self-report, lifelong symptoms from childhood; (2) reading accuracy and/or speed, as assessed by measures commonly used for diagnosis of DD in Germany (i.e., LGVT), of at least 1.5 standard deviations (SD) below the mean for typically-reading adults; (3) non-verbal Intelligence Quotient (nvIQ86) higher or equal to 85 (IQ = 85); (4) normal hearing and normal or corrected-to-normal vision.
  • For the control group, the inclusion criteria will be: (1) right-handed German speakers participants of both genders without any neurological disorders; (2) non-verbal Intelligence Quotient (nvIQ86) higher or equal to 85 (IQ = 85); (3) normal hearing and normal or corrected-to-normal vision.

排除标准

  • The exclusion criteria for the participants with DD involve the following: (1) the presence of other primary psychiatric/neurological diagnosis (e.g., depression, anxiety, autism, ADHD, but not dyscalculia); (2) a personal history of neurological/medical/genetic diseases; (3) ongoing drug treatment influencing brain function; (4) a personal history or first-degree relatives’ history of epilepsy; (5) incompatibility with tDCS; (6) incompatibility with MRI.
  • The exclusion criteria for the healthy participants involve the following: (1) the presence of any psychiatric/neurological diagnosis (e.g., depression, anxiety, autism, ADHD); (2) a personal history of neurological/medical/genetic diseases; (3) ongoing drug treatment influencing brain function; (4) a personal history or first-degree relatives’ history of epilepsy; (5) incompatibility with MRI.

研究者

发起方
Professur für Kognitive und Klinische Neurowissenschaften, Fakultät Psychologie, Technische Universität Dresden

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