Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06646302
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-09
Brief Title:
The Effect of Different Sound Stimulation on The Residual Inhibition of Tinnitus
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Effect of Different Sound Stimulation on The Residual Inhibition of Tinnitus
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to compare the effect of different sound stimulation on the residual inhibition of tinnitus In this study tinnitus patients will be assigned to a cross-over intervention of tinnitus frequency-centered narrowband noise stimulation and low frequency burst sound stimulation
Detailed Description:
Residual inhibition RI is a common phenomenon of short-term suppression of tinnitus which refers to the suppression or reduction of tinnitus even after the end of the masking sound RI is instructive in selecting tinnitus patients suitable for sound therapy However the effect of different sound stimulation on the RI of tinnitus remains unclear
In this study we hypothesized that low frequency burst sound stimulation is superior to tinnitus frequency-centered narrowband noise stimulation for tinnitus relief as measured by subjective tinnitus loudness changes Meanwhile the neurophysiological mechanisms were further explored by EEG and fNIRS
In this study we hypothesized that low frequency burst sound stimulation is superior to tinnitus frequency-centered narrowband noise stimulation for tinnitus relief as measured by subjective tinnitus loudness changes Meanwhile the neurophysiological mechanisms were further explored by EEG and fNIRS
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None