A prospective study on the effectiveness of tinnitus retraining therapy based on mobile devices for tinnitus patients

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005845

Enrollment

Registered

2021-01-28

Start date

2020-12-22

Completion date

Unknown

Last updated

2021-02-23

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

Conditions

None listed

Interventions

Others(counseling of Tinnitus Retraining Therapy) : The control group are provided the counseling directly by using the &#39

Tinnitus Retraining Therapy&#39

PPT file by an otolaryngologist, and the experimental group uses mobile devices to the video contents of the &#39

recorded by an otolaryngologist. After counseling, sound therapy is performed using the white noise of mobile devices as is the same as the existing method.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with tinnitus for more than three months Over 20 years of age Mobile device (smartphone or tablet) users

Exclusion criteria

Exclusion criteria: Pulsatile tinnitus Patients with cognitive impairment and mental illness Who is cooperation is not possible

Design outcomes

Primary

Measure	Time frame
Tinnitus Handicap Inventory (THI)	—

Secondary

Measure	Time frame
Visual analog scale (VAS), State-Trait Anxiety Inventory-X1 & 2, Pittsburgh Sleep Quality Index, Score of TRT satisfaction questionnaire, Tinnitogram	—

Countries

Korea, Republic of

Contacts

Public ContactChae Dong Yim

Seoul National University Hospital

Outcome results