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VR/AR Auditory Training for New Hearing Aid Users

Short-term Efficacy and Safety of VR/AR-based Auditory Training During the Initial Phase of Hearing Aid Adaptation - Efficacy & Safety of VR/AR Auditory Training

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060560
Enrollment
12
Registered
2026-03-01
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Bilateral Mild-to-Moderate Sensorineural Hearing Loss

Interventions

This study implements a VR/AR-based auditory training program for individuals during the initial phase of hearing aid adaptation. The intervention consists of 12 weekly sessions over a 12-week period,

Sponsors

Gunma University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients aged 18 years or older with bilateral mild-to-moderate sensorineural hearing loss (30 dB to <70 dB) who have recently initiated bilateral hearing aid use at the time of enrollment. Participants must be capable of wearing a VR headset, performing the designated rehabilitation program, and providing consent for regular hospital visits and clinical evaluations throughout the study period.

Exclusion criteria

Exclusion criteria: Individuals who have difficulty using VR/AR devices due to severe dizziness, equilibrium disorders, or significant visual impairment. Other exclusion criteria include cognitive decline that impedes the understanding of instructions or performance of tasks, presence of structural ear diseases such as external auditory canal atresia or active cholesteatoma, and any other conditions deemed inappropriate for participation by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Hearing aid continuation rate at 3 months after the start of intervention

Secondary

MeasureTime frame
Speech perception in noise (J-Matrix) at 3 months after the start of intervention

Countries

Japan

Contacts

Public ContactMASAOMI MOTEGI

Gunma University Hospital Otolaryngology-Head and Neck Surgery

m_motegi@gunma-u.ac.jp0272207111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026