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The effect of Transcranial Direct Current Stimulation in addition to Tinnitus Retraining Therapy for treatment of chronic tinnitus patients: a study protocol for a double-blind controlled randomised trial

机译:经耳直流电刺激再加上耳鸣再训练疗法对慢性耳鸣患者的治疗效果:一项双盲对照随机试验的研究方案

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Background Currently, there still is no treatment that eliminates tinnitus in all patients. Recent studies have shown that Tinnitus Retraining Therapy (TRT) significantly improves quality of life for tinnitus patients. Also, several studies have reported that transcranial Direct Current Stimulation (tDCS) has a positive effect on attention, working memory, long-term memory and other cognitive processes. The aim of this randomised placebo-controlled double-blind study is to evaluate the added effect of tDCS to TRT in chronic tinnitus patients. To our knowledge, this is the first study to combine both methods. Methods Patients with chronic, non-pulsatile tinnitus will be randomised in two treatment groups: TRT and real tDCS versus TRT and sham tDCS. Evaluations will take place at baseline before therapy starts, at the end of the TRT and 3?months after therapy starts. The Tinnitus Functional Index will be used as the primary outcome measurement. Secondary outcome measurements will be the Visual Analogue Scale of Loudness, Hospital Anxiety and Depression Scale (HADS), Hyperacusis Questionnaire, psychoacoustic measurements and Event-related potential (ERP). Discussion To our knowledge this is the first study to combine TRT and tDCS. The objective is to evaluate whether tDCS can provide faster and/or more relief from the annoyance experienced in chronic tinnitus patients’ daily lives. The advantage of the study is that it is double-blind and placebo-controlled. Trial registration The present study protocol was registered on 31 October 2014 at Clinicaltrials.gov: NCT02285803 .
机译:背景技术目前,尚无消除所有患者耳鸣的治疗方法。最近的研究表明,耳鸣再训练疗法(TRT)可以大大改善耳鸣患者的生活质量。此外,一些研究报告说,经颅直流电刺激(tDCS)对注意力,工作记忆,长期记忆和其他认知过程具有积极作用。这项随机安慰剂对照双盲研究的目的是评估tDCS对慢性耳鸣患者TRT的附加作用。就我们所知,这是首次结合这两种方法的研究。方法将慢性非搏动性耳鸣患者随机分为两个治疗组:TRT和真实tDCS与TRT和假tDCS。评估将在治疗开始前的基线,TRT结束时和治疗开始后3个月进行。耳鸣功能指数将用作主要结局指标。次要结果测量将是响度的视觉模拟量表,医院焦虑和抑郁量表(HADS),听觉过敏问卷,心理声学测量和事件相关电位(ERP)。讨论据我们所知,这是结合TRT和tDCS进行的第一项研究。目的是评估tDCS是否可以更快和/或更大程度地缓解慢性耳鸣患者日常生活中的烦恼。该研究的优点是它是双盲的,并且是安慰剂对照的。试验注册本研究方案已于2014年10月31日在Clinicaltrials.gov上注册:NCT02285803。

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