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eurofeedback in treatment of chronic tinnitus

Not Applicable
Recruiting
Conditions
Chronic subjective tinnitus.
Tinnitus
Registration Number
IRCT20180609040024N1
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
72
Inclusion Criteria

All subjects over age 18 with necessary physical and mental ability enter to study(intervention group)
Subjects suffered from tinnitus who are over age 18 are matched to the intervention group in age and sex and are waited to be treated.

Exclusion Criteria

Subjects under age of 18
Unwillingness to enter or continue the participation
Subjects affected by Psychatric, neurologic, metabolic, pulsatile tinnitus ,meniere, otosclerosis, chronic headache, mental disorders
Subjects with conductive or mixed hearing loss
Using sedatives or medicines affecting the CNS, 3 months before treatment or during treatment

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
EEG results(amplitude of Waves),mean scores of ?Tinnitus Handicap Inventory. Timepoint: before and after 12 sessions of Neurofeedback therapy. Method of measurement: EEG(alpha,beta,delta,theta).
Secondary Outcome Measures
NameTimeMethod
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