¸ñÀû: To assess the effectiveness of the 'TINI' laser device for tinnitus
symptom relief compared to a Sham device. ¹æ¹ý:The study included 36 chronic high-frequency tinnitus patients
with
hearing loss, divided into two test groups and a control group.
Group 1
received the ¡®TINI¡¯ laser for four weeks, Group 2 used the
¡®TINI¡¯
device for two weeks followed by a Sham device for another two
weeks,
and the Control Group used a Sham device for four weeks.
Evaluations
included the Tinnitus Handicap Inventory (THI), Tinnitus
Functional
Index (TFI), and Tinnitus Magnitude Index (TMI) at various
intervals. °á°ú:The study administered a 100-mW diode laser at 830-nm or sham laser to
36 participants. While overall THI scores didn't show significant
changes, Test Group 1 displayed a notable decrease in the emotional sub-
scale of THI after laser treatment. However, no significant changes were
observed in the TFI scores for Test Group 1, while Test Group 2 and the
Control Group exhibited a significant decrease in TFI scores after laser
treatment. TMI scores revealed significant changes in tinnitus loudness
and severity in Test Group 1 after laser treatment, indicating the
'TINI' device's effectiveness in reducing perceived tinnitus severity.
No adverse effects were reported. °á·Ð:The 'TINI' laser device showed potential in alleviating tinnitus
symptoms, particularly in emotional aspects and perceived
loudness and
severity. The absence of adverse effects underscores its safety.
However, further research is needed to optimize the treatment
protocol
for tinnitus management. |