跳至主要内容
临床试验/NCT04061304
NCT04061304撤回不适用

A Clinical Trial Into the Efficacy of rTMS Treatment for Treating Anorexia Nervosa and Bulimia Nervosa

University of Manitoba0 个研究点开始时间: 2020年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Weekly Binge/Purge Frequency on Eating Disorder Examination

研究概览

简要总结

This is a pilot study to test the efficacy of repetitive transcranial magnetic stimulation (rTMS) in treating individuals with Anorexia Nervosa and Bulimia Nervosa. The main objective of this study is to determine the short and long-term efficacy of repetitive transcranial magnetic stimulation (rTMS) in reducing eating disorder symptoms (i.e. binging, purging, restricting, intense fear of gaining wait, etc;) in Anorexia Nervosa and Bulimia Nervosa.

The investigators will also be comparing the brain activity patterns of individuals with Anorexia Nervosa and Bulimia Nervosa to healthy controls using electroencephalography (EEG). Further, the investigators would like to examine if the activation patterns in these patients change after receiving rTMS.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Confirmed diagnosis of Anorexia Nervosa or Bulimia Nervosa, must pass rTMS screening questionnaire

排除标准

  • Diagnosis of another psychiatric disorder, except MDD.
  • Any rTMS counter-indications:
  • History of seizures
  • Metal in head
  • Currently pregnant
  • Having received rTMS for any reason in the past as this would interfere with participant blinding.

结局指标

主要结局

Weekly Binge/Purge Frequency on Eating Disorder Examination

时间窗: baseline, after week 1, week 2, and week 3 of treatment, 3 months post treatment, and 6 months post treatment.

Outcome measured by change of binge/purge episodes from baseline to the end of treatment. If the participant has a final score of 0 binges and 0 purges they will be considered in remission. A 50% improvement will be defined as a response to the rTMS.

次要结局

  • Change in Beck Anxiety Inventory (BAI)(baseline, after week 1, week 2, and week 3 of treatment, 3 months post treatment, and 6 months post treatment.)
  • Change in Beck Depression Inventory (BDI)(baseline, after week 1, week 2, and week 3 of treatment, 3 months post treatment, and 6 months post treatment.)

研究者

申办方类型
Other
责任方
Sponsor

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