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Bimodal Electrical-Sound Stimulation and Auditory Training for Chronic Tonal Tinnitus

Bimodal Electrical-Sound Stimulation and Auditory Training for Chronic Tonal Tinnitus

Recruiting
18-80 years
All
Phase N/A

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Overview

This study tests whether pairing non-invasive stimulation of the greater occipital nerve (NITESGON) with an attentionally demanding auditory frequency discrimination training task reduces tinnitus loudness and tinnitus-related distress. One hundred adults with chronic tonal tinnitus will be randomised to one of four groups in a 2×2 factorial design: real versus sham NITESGON and active versus passive listening during auditory stimulation. Participants complete eight sessions across four weeks, with outcomes assessed at baseline, end of treatment, 28 days post-treatment, and 6 months post-treatment.

Description

This is a single-centre, prospective, double-blind, placebo-controlled, 2×2 factorial randomised controlled trial conducted at Trinity College Dublin. The intervention combines transcutaneous electrical stimulation targeting the greater occipital nerve (NITESGON) with auditory stimulation delivered during a structured training paradigm. The two between-subjects factors are stimulation condition (real NITESGON vs sham NITESGON) and listening condition (active listening: auditory frequency discrimination training vs passive listening: visual distractor task while auditory stimuli are presented). One hundred adults with chronic tonal tinnitus will be randomised 1:1:1:1 to one of four arms. Participants complete eight sessions (two per week for four weeks). Primary outcomes-tinnitus loudness (VAS 0-100), tinnitus-related functional impact (TFI 0-100), and tinnitus handicap (THI 0-100)-and secondary outcomes are assessed at baseline (T0), end of treatment (T1), 28 days after treatment completion (T2), and 6 months after treatment completion (T3). Secondary outcomes include tinnitus psychoacoustics, extended high-frequency audiometry, speech-in-noise performance, EEG (resting-state and auditory oddball), autonomic/biomarker measures (pupillometry, heart rate, saliva), patient global impression of change, quality of life, and safety/blinding assessments.

Eligibility

Inclusion Criteria:

  • Adults aged 18-80 years
  • Continuous subjective tinnitus for \>3 months and ≤5 years
  • Predominantly tonal tinnitus (unilateral or bilateral)
  • Screening THI score 28-76
  • Minimum Masking Level (MML) 20-80 dB HL
  • No prior tinnitus neuromodulation treatment
  • Able to comply with eight sessions over four weeks and follow-up assessments

Exclusion Criteria:

  • Objective tinnitus or predominantly somatic tinnitus
  • Pulsatile tinnitus
  • Evidence of conductive hearing loss (abnormal otoscopy or tympanometry)
  • Pure-tone audiometry exclusions: \>40 dB HL at any frequency 250 Hz-1 kHz OR \>80 dB HL at any frequency 2-8 kHz in either ear
  • Hearing aid use initiated within the past 90 days
  • Active implantable medical device (e.g., pacemaker, DBS, cochlear implant)
  • LDL \<30 dB SL at 500 Hz in either ear
  • Diagnosis of temporomandibular joint disorder or occipital neuralgia
  • Severe anxiety (STAI \>120/160)
  • Cognitive impairment (MMSE \<25)
  • Severe depressive symptoms (BDI ≥30)
  • Diagnosis of Menière's disease
  • Current pregnancy
  • Involvement in medicolegal cases
  • History of auditory hallucinations
  • Current prescription of central nervous system drugs likely to alter neuromodulatory function (e.g., noradrenergic, dopaminergic, serotonergic, benzodiazepine, cholinergic, or other psychoactive medications)
  • Currently enrolled in another interventional study

Study details
    Tinnitus
    Subjective
    Tinnitus
    Chronic Tinnitus

NCT07393880

University of Dublin, Trinity College

26 February 2026

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