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Trial of Management of Chronic Tinnitus by Sound Therapy and Cognitive Behavioral Therapy

2026年6月26日 更新者:Aya Ahmed Elsayed、Sohag University

Efficacy of Sound Therapy, Cognitive Behavioral Therapy and Their Combination in Management of Chronic Tinnitus

clinical trial: The main aim of this study is to compare the effectiveness of Cognitive Behavioral Therapy (CBT) and Sound Therapy, both individually and in combination, in the management of patients with chronic subjective tinnitus and to evaluate their impact on decreasing tinnitus severity, psychological wellbeing and quality of life.

Patients will be randomly divided into three groups:

  • Group A: patients will receive Sound Therapy.
  • Group B: patients will receive Cognitive Behavioral Therapy (CBT).
  • Group C: patients will receive Combined CBT + Sound Therapy.

研究概览

详细说明

Because of the multifactorial nature of tinnitus, its effective management requires a multidisciplinary approach. While there is no single pullet mechanism of cure, current treatment strategies primary focus on reducing tinnitus related perception and minimizing its associated distress through auditory and psychological interventions.

Among these approaches, is the Sound Therapy which aims to decrease the contrast between tinnitus and related neural activity by introducing external sounds, which facilitates habituation and reducing tinnitus perception .

In contrast, Cognitive Behavioral Therapy (CBT) targets the patient's cognitive and emotional reaction to tinnitus by modifying maladaptive thoughts and behaviors, there by improving coping strategies and reducing tinnitus-related distress (Andersson, 2011). Recent evidence suggests that combining both modalities may provide superior outcomes compared to either approach alone, highlighting the potential value for integrated treatment strategies in tinnitus management (Hall et

研究类型

介入性

注册 (估计的)

60

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

      • Sohag、埃及
        • Sohag faculty of medicine
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子

接受健康志愿者

不

描述

Inclusion Criteria:

  • o Age: 18-65 years.

    • Hearing level: Patients with normal hearing or mild to moderate sensorineural hearing loss (to ensure homogeneity of the sample) (National Institute for Health and Care Excellence, 2020)
    • Complaint: patients with chronic subjective tinnitus (> 3 months).
    • Psychological state: Patients with stable general and psychological condition.

Exclusion Criteria:

  • o Age: <18, >65 years

    • Hearing level: Patients with severe hearing loss not suitable for sound therapy
    • Complaint: Objective tinnitus (vascular or muscular origin)
    • Psychological state: Patients with active psychiatric disorders requiring immediate intervention.
    • Active middle or external ear disease

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
有源比较器:Group A: patients will receive Sound Therapy

Group A: Sound Therapy

  • Patients will receive individualized sound therapy using broadband noise or tinnitus maskers.
  • Daily use recommended for 2-4 hours/day.
  • Duration: 6 weeks.
  • Patient will be instructed on habituation-based listening techniques
有源比较器:Group B: patients will receive Cognitive Behavioral Therapy (CBT).

Group B: Cognitive Behavioral Therapy (CBT)

• Structured CBT program consisting of 6 sessions over 6 weeks.

Each session categorization:

  • Psychoeducation about tinnitus
  • Cognitive restructuring of negative thoughts
  • Relaxation techniques (breathing exercises, muscle relaxation)
  • Attention diversion strategies
  • Sleep hygiene education
有源比较器:Group C: patients will receive Combined CBT + Sound Therapy.

Group A: Sound Therapy

  • Patients will receive individualized sound therapy using broadband noise or tinnitus maskers.
  • Daily use recommended for 2-4 hours/day.
  • Duration: 6 weeks.
  • Patient will be instructed on habituation-based listening techniques

Group B: Cognitive Behavioral Therapy (CBT)

• Structured CBT program consisting of 6 sessions over 6 weeks.

Each session categorization:

  • Psychoeducation about tinnitus
  • Cognitive restructuring of negative thoughts
  • Relaxation techniques (breathing exercises, muscle relaxation)
  • Attention diversion strategies
  • Sleep hygiene education

Group C: Combined Therapy

• Patients will receive both sound therapy and CBT simultaneously following the same protocol as above.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Primary outcome: Changes in tinnitus severity
大体时间:Baseline, immediately after completion of treatment , and 3 months after completion of treatment
Assessment of tinnitus severity using the Tinnitus Functional Index (TFI) . Higher scores indicate greater tinnitus severity. the TFI total score ranges from 0 to 100, with higher score s indicating greater tinnitus severity and functional impact
Baseline, immediately after completion of treatment , and 3 months after completion of treatment

次要结果测量

结果测量
措施说明
大体时间
chang in Visual Analog Scale (VAS) score
大体时间:Baseline, immediately after completion of treatment , and 3 months after completion of treatment
Assessment of tinnitus severity using the Visual Analog Scale (VAS) . the VAS score ranges from 0 to 10, with 0 indicate no tinnitus and 10 indicates the worst imaginable tinnitus. higher scores indicating greater tinnitus severity
Baseline, immediately after completion of treatment , and 3 months after completion of treatment
change in Tinnitus Handicap Inventory (THI) score
大体时间:Baseline, immediately after completion of treatment , and 3 months after completion of treatment
Assessment of tinnitus-related handicap and quality of life using Tinnitus Handicap Inventory (THI). the THI total score ranges from 0 to 100, with higher scores indicating greater tinnitus-related handicap and poorer quality of life.
Baseline, immediately after completion of treatment , and 3 months after completion of treatment

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月10日

初级完成 (估计的)

2026年9月10日

研究完成 (估计的)

2026年12月10日

研究注册日期

首次提交

2026年6月11日

首先提交符合 QC 标准的

2026年6月17日

首次发布 (实际的)

2026年6月24日

研究记录更新

最后更新发布 (实际的)

2026年6月30日

上次提交的符合 QC 标准的更新

2026年6月26日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

No decision has been made regarding the sharing of individual participant data at this time

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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