跳至主要内容
临床试验/NCT06401928
NCT06401928
已完成
不适用

Electrical Brain Stimulation for Improving Mental Health and Cognitive Functioning in Patients With Multiple Sclerosis

The National Brain Mapping Laboratory (NBML)1 个研究点 分布在 1 个国家目标入组 53 人2023年2月28日

概览

阶段
不适用
干预措施
transcranial direct current stimulation
疾病 / 适应症
Multiple Sclerosis
发起方
The National Brain Mapping Laboratory (NBML)
入组人数
53
试验地点
1
主要终点
Mini sleep questionnaire (MSQ)
状态
已完成
最后更新
上个月

概览

简要总结

Multiple Sclerosis (MS) is an autoimmune disease associated with physical disability, psychological impairment, and cognitive dysfunction. As a result, the disease burden is high, and treatment options are limited. In this randomized, double-blind study, the investigators planned to use repeated electrical stimulation and assess mental health-related variables (e.g., quality of life, sleep, psychological distress) and cognitive dysfunction in patients with MS.

注册库
clinicaltrials.gov
开始日期
2023年2月28日
结束日期
2024年1月31日
最后更新
上个月
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
The National Brain Mapping Laboratory (NBML)
责任方
Principal Investigator
主要研究者

Mohammad Ali Salehinejad

Principal Investigator

The National Brain Mapping Laboratory (NBML)

入排标准

入选标准

  • diagnosis of MS according to the diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria (Polman et al., 2011), certified by a professional neurologist
  • being 25-55 years old
  • providing written informed consent
  • If female, a negative urine pregnancy test
  • stable medication regime especially the classical neuroleptics and all CNS-activating medications, if taken, 4-6 weeks before the experiment and during the experiment
  • right handed

排除标准

  • alcohol or substance dependence
  • history of seizure
  • history of other neurological disorders than MS
  • history of head injury
  • presence of ferromagnetic objects in the body that are contraindicated for brain stimulation of the head (pacemakers or other implanted electrical devices, brain stimulators, some types of dental implants, aneurysm clips, metallic prostheses, permanent eyeliner, implanted delivery pump, or shrapnel fragments) or fear of enclosed spaces.

研究组 & 干预措施

active tDCS group

The patients in this group receive 10 daily sessions of 1.5-mA transcranial direct current stimulation (tDCS) targeting the left lateral prefrontal cortex and right orbitofrontal cortex with anodal and cathodal stimulation respectively.

干预措施: transcranial direct current stimulation

tDCS with cognitive rehabilitation group

The patients in this group receive 10 daily sessions of 1.5-mA transcranial direct current stimulation (tDCS) followed by a 30-minute cognitive training intervention.

干预措施: transcranial direct current stimulation combined with cognitive training

sham tDCS group

The patients in this group receive 10 daily sessions of 1.5-mA sham transcranial direct current stimulation (tDCS).

干预措施: transcranial direct current stimulation

结局指标

主要结局

Mini sleep questionnaire (MSQ)

时间窗: up to 1 day after the intervention

The Mini Sleep Questionnaire (MSQ) is used to screen for sleep disturbances in clinical populations. It consists of 10 items, each scored on a seven-point Likert scale ranging from "never" to "always". The questionnaire measures insomnia and oversleeping, with a high score indicating excessive sleepiness and a low score indicating insomnia.

Multiple Sclerosis Impact Scale (MSIS-29)

时间窗: up to 1 day after the intervention

The MSIS-29 is a questionnaire that comprises of 29 questions. The initial 20 questions are related to the physical impact, whereas the last 9 questions focus on the psychological impact. Each question is rated on a scale of 1 to 5, where 1 indicates "not at all" and 5 indicates "extremely". There are five response options available for the respondents to choose from.

and Depression Anxiety Stress Scale-21 (DASS-21)

时间窗: up to 1 day after the intervention

The DASS-21 is a tool used to assess the severity of symptoms related to depression, anxiety, and stress in individuals who have not been diagnosed before. The assessment has three scales, and responses to each are measured on a four-point Likert scale, ranging from 0 to 3.

次要结局

  • psychomotor speed task(up to 1 day after the intervention)
  • attention / vigilance task(up to 1 day after the intervention)

研究点 (1)

Loading locations...

相似试验