Skip to content

Comparison of auditory stimuli for Virtual Reality-based Sound localization test.

Comparison of auditory stimuli for Virtual Reality-based Sound localization test.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009368
Enrollment
100
Registered
2024-04-23
Start date
2024-02-15
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

None listed

Interventions

Behavioral, Others(Sound Localization test) : *4 Sound Directionality Tests - Test sound localization in a real soundproof booth - VR-based sound localization test using three stimuli 1) HRTF: Applin

Sponsors

Hallym University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - 40 normal hearing, 60 unilateral hearing loss - Age: 20-65 - [Normal hearing]: pure tone audiometry (PTA) on both side [(0.5k+1k+2k+4k)/4] = 20 dB HL - [Unilateral hearing loss]: normal hearing or mild to moderate hearing loss [PTA= 30 dB HL] in one side and profound to severe hearing loss [PTA quadrant =71 dB HL] in other side

Exclusion criteria

Exclusion criteria: - Usage of hearing device such as hearing aid. - Conductive hearing loss over 15dB. - Cognitive decline or a medical condition that counld make difficult to participate sound locazliation test. - Claustrophobia - Failure to provide informed consent - Any other person deemed unsuitable for this study by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Sound localization test (test in real soundproof booth,VR-HRTF stimuli, VR-individual recording stimuli, VR-KEMAR recording stimuli)

Secondary

MeasureTime frame
Spatial release from masking (K-DiN(digit in noise) test);Korean version - Speech, Spatial and Qualities of Hearing Scale, K-SSQ)

Countries

Korea, Republic of

Contacts

Public ContactSeung ik Jeon

Hallym University Medical Center

wjstmddlrrk9@naver.com+82-31-380-3840

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026