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临床试验/NCT04465136
NCT04465136终止不适用

The Effect of Cranial Electrotherapy Stimulation as Adjunctive Therapy on Anxiety Disorder in Elderly: an Open-label, Pilot Study

Kaohsiung Veterans General Hospital.2 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2021年2月19日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
27
试验地点
2
主要终点
The change of subjective anxiety symptom from baseline

研究概览

简要总结

The study aimed to investigate whether cranial electrotherapy stimulation(CES) could benefit anxiety symptoms, depressive symptoms, quality of sleep and quality of life in elderly patients with anxiety disorder.

详细描述

Several studies have shown cranial electrotherapy stimulation (CES) could decrease depression and anxiety symptoms in patients with mood disorder. However, none study so far focused on the elderly population to investigate the anti-depressant and anxiolytic effect in elderly patient with anxiety disorder. Hence, this pilot study aims to assess the safety and efficacy of CES on anxiety symptoms, depressive symptoms, sleep quality and life quality in elderly patient with anxiety disorder. The study was an open-label, one arm study. The study aimed to investigate whether cranial electrotherapy stimulation(CES) could benefit anxiety symptoms, depressive symptoms, quality of sleep and quality of life in elderly patients with anxiety disorder.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
60 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 60 to 85 years old
  • Anxiety disorder confirmed by Mini-international neuropsychiatric interview (MINI)
  • HAM-A score greater than 17 points
  • HAM-D score lower than 17 points
  • Mini-mental state examination score of 24 or more
  • No psychiatric medication adjustment within 3 months.

排除标准

  • Comorbid with another axis I psychiatric disorder, like schizophrenia, substance use disorder or other major mental illness screened by Mini-international neuropsychiatric interview (MINI)
  • Contraindications for CES
  • Implanted brain medical devices or mental in the head
  • History of seizures
  • History of intracranial neoplasm or surgery
  • Severe head injuries
  • Cerebrovascular diseases
  • Arrhythmia or with pacemaker implantation
  • Used to receive brain stimulation therapy.

结局指标

主要结局

The change of subjective anxiety symptom from baseline

时间窗: 1. Change from baseline BAI score after the 4 weeks and the 6 weeks. 2.Change from baseline BAI score after 4 weeks (week 10) after the full CES treatment course

evaluate the Beck anxiety inventory (BAI) for subjective anxiety The BAI contains 21 questions, each answer being scored on a scale value of 0 (not at all) to 3 (severely). Higher total scores indicate more severe anxiety symptoms. The standardized cutoffs are: 0-7: minimal anxiety; 8-15: mild anxiety; 16-25: moderate anxiety; 26-63: severe anxiety.

The change of objective anxiety symptom from baseline

时间窗: 1.Change from baseline HAM-A score after the 4 weeks and the 6 weeks. 2.Change from baseline HAM-A score after 4 weeks (week 10) after the full CES treatment course

evaluate the Hamilton Anxiety Rating Scale (HAM-A) for objective anxiety Each item is scored on a scale of 0 (not present) to 4(severe), with a total score range of 0-56, where \<17 indicates mild severity, 18-24 mild to moderate severity and 25-30 moderate to severe.

次要结局

  • The change of quality of sleep from baseline: Pittsburgh Sleep Quality Index (PSQI)(1. Change from baseline PSQI score after the 4 weeks and the 6 weeks. 2.Change from baseline PSQI score after 4 weeks (week 10) after the full CES treatment course)
  • The change of quality of life from baseline: Brief version of World Health Organization Quality of Life questionnaire (WHOQOL-BREF)(1. Change from baseline WHOQOL-BREF score after the 4 weeks and the 6 weeks. 2.Change from baseline WHOQOL-BREF score after 4 weeks (week 10) after the full CES treatment course)
  • The change of subjective depressive symptom from baseline(1. Change from baseline BDI-II score after the 4 weeks and the 6 weeks. 2.Change from baseline BDI-II score after 4 weeks (week 10) after the full CES treatment course)
  • The change of objective depressive symptom from baseline(1. Change from baseline HAM-D score after the 4 weeks and the 6 weeks. 2.Change from baseline HAM-D score after 4 weeks (week 10) after the full CES treatment course)

研究者

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

Che-Sheng Chu

Department of Psychiatry, MD, attending physician

Kaohsiung Veterans General Hospital.

研究点 (2)

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