Evaluation of the therapeutic effect of neurofeedback sessions on tinnitus

Study of the effect of neurofeedback sessions on reduction of tinnitus rate in patients with drug resistance Tinnitus

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20130311012782N30

Enrollment

Registered

2019-05-01

Start date

2019-03-21

Completion date

Unknown

Last updated

2019-05-21

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

Conditions

Tinnitus. Tinnitus

Interventions

Intervention group: Based on inclusion and exclusion criteria, 30 patients with Tinnitus are selected who are resistant to medical treatments. Neurofeedback sessions are designed by a psychiatrist and

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: The patient has subjective Tinnitus -Age over 18 years Have normal hearing threshold No neurological lesions such as epilepsy, Parkinson's and Alzheimer's

Exclusion criteria

Exclusion criteria: Any patient dissatisfaction to participate in the study

Design outcomes

Primary

Measure	Time frame
Tinnitus Handicap Inventory questionnaire scale. Timepoint: before starting the neurofeedback, After the end of neurofeedback sessions, one month, three months and six months afterwards. Method of measurement: Tinnitus Handicap Inventory questionnaire.;Visual Analogue Scale for Tinnitus in the ears of patients. Timepoint: before starting the neurofeedback, After the end of neurofeedback sessions, one month, three months and six months afterwards. Method of measurement: Visual Analogue Scale.	—

Measure

Time frame

Tinnitus Handicap Inventory questionnaire scale. Timepoint: before starting the neurofeedback, After the end of neurofeedback sessions, one month, three months and six months afterwards. Method of measurement: Tinnitus Handicap Inventory questionnaire.;Visual Analogue Scale for Tinnitus in the ears of patients. Timepoint: before starting the neurofeedback, After the end of neurofeedback sessions, one month, three months and six months afterwards. Method of measurement: Visual Analogue Scale.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Seyed Mojtaba Abtahi

Esfahan University of Medical Sciences

manyekdoost@yahoo.com+98 913 313 9294

Outcome results

None listed

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