Evaluation of clinical efficacy of virtual reality-based tinnitus alleviating program on chronic subjective tinnitus

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006242

Enrollment

Registered

2021-06-10

Start date

2020-01-29

Completion date

Unknown

Last updated

2024-07-23

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

Conditions

None listed

Interventions

Others : Pre-program: Study consent, endoscopic eardrum examination, hearing examination, and tinnitus examination. Round 1: Tinnitus fusion, tinnitus exploration (city), questionnaire (*) trial, EEG

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Patients with chronic non-pulsatile tinnitus for more than 3 months 2) Patients who can communicate smoothly in Korean and agree to participate in the study

Exclusion criteria

Exclusion criteria: 1) Frequent noise exposure is expected professionally or as part of a hobby 2) When it is expected that a virtual reality program running with a headset cannot be manipulated

Design outcomes

Primary

Measure	Time frame
Change of significant tinnitus questionnaire before and after program implementation	—

Secondary

Measure	Time frame
Analysis of EEG test results and sLORETA program	—

Countries

Korea, Republic of

Contacts

Public ContactChoi June

Korea University Ansan Hospital

mednlaw@korea.ac.kr+82-31-412-5170

Outcome results