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临床试验/NCT01683019
NCT01683019已完成不适用

A MULTICENTER, RANDOMIZED, BLINDED, SHAM CONTROLLED, PARALLEL GROUP TRIAL TO TEST CLINICAL EFFICACY OF LOW FREQUENCY AC MAGNETIC FIELD INDUCED EEG SYNCHRONIZATION IN MAJOR DEPRESSION

Wave Neuroscience3 个研究点 分布在 2 个国家目标入组 52 人开始时间: 2008年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
52
试验地点
3
主要终点
Percent Change in Hamilton Depression Rating Scale (HAMD-17) at Baseline and the End of Week 4 of Treatment.

研究概览

简要总结

This feasibility study investigates effects of EEG-based low frequency, low emission magnetic cortical stimulation in comparison to a sham treatment in subjects with moderate to severe depressive disorder.

详细描述

Major Depressive Disorder (MDD) is associated with functional impairment and disability, and results in a significant burden on the affected individual, his or her family, and society in general. Psychopharmacological therapy has been shown to be effective, but may be accompanied by significant side effects. The investigators propose an alternative model, based on the relationship between symptoms, brain metabolism, and neural activity as recorded with electroencephalography (EEG). Subjects with MDD often have decreased brain metabolism, accompanied by increased EEG activity in the alpha band. The investigators hypothesis is that a gentle, non-significant risk, sinusoidal magnetic field above the subject's scalp, which oscillates at precisely his or her Intrinsic Alpha Frequency (IAF) can take advantage of this relationship to reduce symptoms without the significant side effects associated with pharmaceuticals. The investigators propose a 4-week, sham controlled, randomized, double-blind multi-center feasibility study to determine the efficacy of synchronized low energy magnetic fields delivered at the subject's IAF to treat MDD. Treatment will be given concomitant to the subject's existing medication, and will occur 5 days per week at the clinical site. Target enrollment is 45 adult subjects diagnosed with MDD.

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
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • 18 years of age or older
  • Diagnosis of MDD with HAMD-17 greater than or equal to 17
  • On a stable dose of existing medication or no medication for 1 month or longer prior to the study

排除标准

  • Diagnosed with another primary Axis I illness
  • Recent history of or current substance abuse
  • Clinically significant medical illness, including any thyroid disorders
  • Known pregnancy and/or lactation, or intent to become pregnant during the study

研究组 & 干预措施

Active Fixed Alpha Frequency Magnetic Stimulation

Active Comparator

Sinusoidal magnetic field set to the subject's intrinsic alpha frequency (IAF).

干预措施: NeoSync EEG Synchronization Therapy (Device)

Active Random Frequency Magnetic Stimulation

Active Comparator

Magnetic field hops to random frequencies in the alpha band (8-13Hz), once per second.

干预措施: NeoSync EEG Synchronization Therapy (Device)

Inactive Sham Treatment

Sham Comparator

Generate sound similar to active treatment, except that no magnetic field is generated.

干预措施: Sham NeoSync EEG Synchronization Therapy (Device)

结局指标

主要结局

Percent Change in Hamilton Depression Rating Scale (HAMD-17) at Baseline and the End of Week 4 of Treatment.

时间窗: Assessed at baseline and the end of Week 4 of treatment.

Outcome measured using the Hamilton Depression Rating Scale (HAMD-17) and calculated as percent change in severity score from baseline until the end of the 4th week of treatment. The HAMD-17 scale ranges between 0-54, with higher numbers indicating more severe symptoms. 0-7 is generally accepted to be within the normal range (or in clinical remission), while a score of 20 or higher indicates moderate to severe depression.

次要结局

未报告次要终点

研究者

发起方
Wave Neuroscience
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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