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A Study on the Development of a Telemedicine System for Speech and Language Rehabilitation by Speech-Language Pathologists for Cochlear Implant and Hearing Aid Users

A Study on the Development of a Telemedicine System for Speech and Language Rehabilitation by Speech-Language Pathologists for Cochlear Implant and Hearing Aid Users - A Study on the Development of a Telemedicine System for Speech and Language Rehabilitation by Speech-Language Pathologists for Cochlear Implant and Hearing Aid Users

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000058567
Enrollment
210
Registered
2025-07-31
Start date
2025-06-12
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

hearing loss

Interventions

Combining telemedicine with face-to-face services (mapping and speech rehabilitation)

Sponsors

Sapporo Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: [Selection Criteria for Telemedicine in Cochlear Implant Users] Patients who have been using their cochlear implant(s) for 12 months or more (aged 6 years or older) Patients with either unilateral or bilateral cochlear implants Patients using cochlear implants compatible with telemedicine Patients whose mapping, created during face-to-face care within 6 months prior to the start of this study, is stable [Selection Criteria for Family Members or Caregivers of Cochlear Implant Users and Hearing Aid Users] Accompany the patient during telemedicine sessions Aged 18 years or older [Selection Criteria for Remote Speech Rehabilitation] Elementary school children who wish to receive articulation training Patients using either unilateral or bilateral cochlear implants or hearing aids Patients using cochlear implants or hearing aids compatible with telemedicine

Exclusion criteria

Exclusion criteria: Patients who decline to participate in this study Patients whom the investigators consider inappropriate as study subjects due to complications, treatment progress, or other reasons

Design outcomes

Primary

MeasureTime frame
Hearing performance of users under telemedicine and in-person care (monosyllabic word recognition test in quiet: 67S at 60 dBHL; aided threshold test; and, where available, word recognition test in quiet: CI2004 at 65 dBSPL and word recognition test in noise: CI2004 at 65 dBSPL with SNR +10 dB)

Countries

Japan

Contacts

Public ContactSumito Jitsukawa

Sapporo Medical University Department of Otolaryngology Head and Neck Surgery

sumitojjj@sapmed.ac.jp011-611-2111

Outcome results

None listed

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