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Efficacy Study for Development and Use of Neurofeedback-trainings for Patients Suffering From Chronic Tinnitus

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Tinnitus, Subjective

Treatments

Device: Non Tomographic Neurofeedback
Device: Tomographic Neurofeedback

Study type

Interventional

Funder types

Other

Identifiers

NCT02383147
USZ-ORL-KT-001

Details and patient eligibility

About

Chronic tinnitus affects about 10-15% of the population in industrialized countries. Investigations of the brain activity by using electroencephalography (EEG) showed that in localized regions of the hearing system brain activity was decreased. This reduction of activity is thought to be one of the reasons that keep the perception of the tinnitus going. Recent studies have shown that neurofeedback is a viable option for treatment of chronic tinnitus. By using neurofeedback it is possible to train brain functions by the simple principle of rewarding wanted changes and punishing unwanted ones. The purpose of the investigators study is to show the efficacy of specific localized neurofeedback training in comparison to global relaxing neurofeedback training. In order to achieve decreased tinnitus symptoms or even disappearance of the tinnitus, 15 neurofeedback trainings are planned. Before and up to 6 month after the training EEG-recordings are performed.

Enrollment

52 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-75
  • Chronic Tinnitus > 0.5 years
  • Informed Consent
  • Fluent in German language

Exclusion criteria

  • Psychological and neurological disorders other than tinnitus
  • Drug- or Alcohol abuse
  • Tranquilizer, antiepileptic drugs, antipsychotics or anesthetics intake
  • Impairing hearing loss or Cochlea Implant

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

52 participants in 2 patient groups

Tomographic Neurofeedback (TONF)
Experimental group
Description:
15x Neurofeedback Trainings, 1-2 times per week
Treatment:
Device: Tomographic Neurofeedback
Non Tomographic Neurofeedback (NTE)
Active Comparator group
Description:
15x Neurofeedback Trainings, 1-2 times per week
Treatment:
Device: Non Tomographic Neurofeedback

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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