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sound therapy and auditory discrimination therapy effect on tinnitus

Comparison of the effect of sound therapy with and without active attention using personalized auditory discrimination training in tinnitus management

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260411069041N1
Enrollment
42
Registered
2026-05-25
Start date
2026-05-22
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

tinnitus. Tinnitus, unspecified ear

Interventions

Intervention 1: Control group: In this group, sound therapy is provided to the individual by means of white noise. The individual must listen to this sound three times a day for half an hour each time

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: People with tonal tinnitus (or tinnitus similar to narrowband noise whose frequency can be measured) with mild to moderate hearing loss at most (people with tinnitus similar to white noise and pulsatile tinnitus were not included in the study) People whose pitch matching to tinnitus is within the range of their hearing loss People with unilateral or bilateral tinnitus History of tinnitus for more than 6 months People with a maximum THI score of 56 Free from neurological and psychological diseases normal Otoscopy and immittance audiometry Not receiving any rehabilitation or at least 6 months have passed since receiving rehabilitation that has no effect on treating the person's tinnitus Have a minimum level of literacy so that they are able to read the questionnaire questions and make distinctions

Exclusion criteria

Exclusion criteria: Unwillingness and inability to cooperate in research Worsening tinnitus

Design outcomes

Primary

MeasureTime frame
TFI Questionnaire Scores: The Tinnitus Functional Index self-assessment questionnaire is a standard tool for assessing the various effects of tinnitus in causing disability and adverse conditions on the quality of life of these individuals. Timepoint: Before intervention, after intervention, 3 months after intervention. Method of measurement: Registration in the relevant forms.;THI Questionnaire Scores: The Tinnitus Disability Self-Assessment Questionnaire is a standardized tool used to assess the severity of tinnitus discomfort and assess the adverse impact of tinnitus on quality of life. Timepoint: Before intervention, after intervention, 3 months after intervention. Method of measurement: Registration in the relevant forms.;Tinnitus pitch matching: psychophysical frequency of tinnitus. Timepoint: Before intervention, after intervention, 3 months after intervention. Method of measurement: with audiometer.;Tinnitus loudness matching: Tinnitus loudness at the psychophysical frequency of tinnitus. Timepoint: Before intervention, after intervention, 3 months after intervention. Method of measurement: with audiometer.;Minimum Tinnitus Coverage Level: This refers to the minimum amount of noise decibels that causes tinnitus to be covered and not heard by the individual. Timepoint: Before intervention, after intervention, 3 months after intervention. Method of measurement: with audiometer.;Evaluation of the residual tinnitus interruption phenomenon: In this evaluation, noise is presented at an intensity level of 10 dB above the minimum tinnitus coverage level for 60 seconds and the cessation of the tinnitus sound is examined. Timepoint: Before intervention, after intervention, 3 months after intervention. Method of measurement: with a clock.;Quantitative Visual Analog Scale Score: A visual analog scale used to quantitatively determine the severity and annoyance of tinnitus in individuals. Timepoint: Before intervention, after intervention, 3 months after intervention. Met

Countries

Iran (Islamic Republic of)

Contacts

Public Contactshima sasanian

Tehran University of Medical Sciences

shimasasanian@mailfa.com+98 45 3327 4678

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026