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Investigating the effect of multi-site transcranial electrical stimulation in the treatment of chronic tinnitus

Comparison of the effect of multi-site transcranial electrical stimulation (tES) with different methods on psychophysical, psychological and electroencephalographic (EEG) indicators in people with chronic tinnitus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220901055849N1
Enrollment
40
Registered
2022-09-06
Start date
2023-01-21
Completion date
Unknown
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tinnitus. Tinnitus

Interventions

Intervention 1: First intervention group: In this group, the tDCS-tRNS method is used to provide multi-site electrical stimulation. In each session, first, tDCS stimulation with a current intensity of

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age range from 18 to 60 years At least six months of persistent non-pulsatile tinnitus perception Normal hearing thresholds (below 25 dB HL) at frequencies from 250 to 2000 Hz and hearing thresholds below 40 dB HL at frequencies above 2000 Hz The normal state of the outer and middle ear (normal otoscopy and obtaining a type A tympanogram with a static compliance between 0.3 and 1.6) Passing at least six months since receiving transcranial electrical or magnetic stimulation (regardless of the purpose of stimulation and the stimulation protocol used) Having the necessary abilities to perform the tests

Exclusion criteria

Exclusion criteria: Perceiving polyphonic tinnitus Observing a conductive component (Air-Bone Gap = 15 dB HL) in the audiogram Formal music training Having diseases of the ear, nose and throat The existence of obvious cognitive disorders and mental disability Suffering from chronic neurological diseases Suffering from chronic psychiatric disorders A history of alcohol and drug abuse or addiction Taking drugs that affect the function of the central nervous system A history of severe head trauma or surgery related to the central nervous system in the head and neck area Receiving other conventional treatment methods for tinnitus in at least the last six months Using a heart pacemaker or implantable electrodes in the head and neck area Pregnancy

Design outcomes

Primary

MeasureTime frame
Tinnitus psychophysical loudness. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Loudness matching.;Tinnitus loudness. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Visual Analogue Scale (VAS).;Tinnitus annoyance. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Visual Analogue Scale (VAS).;The degree of tinnitus handicap. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Tinnitus Handicap Inventory (THI).;The degree of negative effects of tinnitus. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Tinnitus Functional Index (TFI).;Satisfaction with quality of life. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: SF-36 Questionnaire.;Severity of depression. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Beck Depression Inventory-Second Edition (BDI-II).;Severity of anxiety. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Beck Anxiety Inventory (BAI).;Absolute power of EEG frequency bands. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: EEGLAB software.;Relative power of EEG frequency bands. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: EEGLAB software.;Current source density. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: sLORETA software.

Secondary

MeasureTime frame
Tinnitus pitch. Timepoint: Before, after and three months after the electrical stimulation sessions. Method of measurement: Pitch matching.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahand Nazeri

Tehran University of Medical Sciences

S_nazeri@razi.tums.ac.ir+98 21 7768 4889

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026