跳至主要内容
临床试验/NCT05589272
NCT05589272撤回不适用

TDCS-potentiated Generalization of Cognitive Training in the Rehabilitation of Long COVID Symptoms

University of Minnesota2 个研究点 分布在 1 个国家开始时间: 2023年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Cognitive improvement effects of WM training with active tDCS vs. sham

研究概览

简要总结

The overarching goals of this study are to employ cognitive testing to understand how transcranial direct current stimulation (tDCS), when used concurrently with cognitive training tasks, can affect cognitive impairment symptoms in individuals with long COVID, or post-acute sequelae SARS-CoV-2 infection (PASC), and to examine variability in response between active and sham tDCS treatment groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Ability to provide consent and comply with study procedures
  • Age 18 to 60 years old
  • Estimated IQ within the specified range (70 <= IQ E <= 115)
  • Current post-acute sequelae SARS-CoV-2 infection (PASC) as defined by the National Center for Health Statistics post-COVID-19 conditions survey ((Long COVID 2022), including impaired cognition symptoms, for at least 3 months post-infection
  • Ability to participate in four weekly 40' training sessions over four weeks and participate in two assessments
  • English speaking

排除标准

  • Any medical condition or treatment with neurological sequelae (e.g. stroke, tumor, loss of consciousness >30 min, concussion involving hospital admission, HIV)
  • Contraindications for tDCS (e.g. history of seizures)
  • Five or more sessions of neuromodulation (such as tDCS) or cognitive training in the past 6 months

结局指标

主要结局

Cognitive improvement effects of WM training with active tDCS vs. sham

时间窗: baseline and post-test assessment, 4 weeks

shown by WM task progression and performance on cognitive testing measures

Generalization of cognitive effects of active tDCS vs. sham

时间窗: baseline and post-test assessment, 4 weeks

includes effect on PASC-related cognitive impairment symptoms

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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