Actively Recruiting
Telemonitoring in Cochlear Implant Patient Care
Led by University Hospital, Montpellier · Updated on 2024-05-28
78
Participants Needed
1
Research Sites
130 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Montpellier
Lead Sponsor
U
University Hospital, Toulouse
Collaborating Sponsor
AI-Summary
What this Trial Is About
Following a sufficient delay after the cochlear implantation and initial implant activation, the patient will return to the hospital for follow-up visits for equipment maintenance and auditory performance evaluation only once per year. This frequency might appear either insufficient, in which case an additional patient check-up will be arranged, or excessive if patient performances and implant adjustments are stable. Using at-home testing tool for remote hearing performance monitoring can thus appear advantageous for both patients and clinicians, allowing to avoid an unnecessary journey to the implantation reference center for the first and to diminish a number of unscheduled medical appointments for the second.
CONDITIONS
Official Title
Telemonitoring in Cochlear Implant Patient Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Users of uni- or bilateral cochlear implants (Cl24RE series 400, 500, 600) and Cochlear Nucleus CP1000 or CP1150 processors for at least one year
- Have renewed their processor at least once
- Implanted for more than 5 years
- Age over 20 years
- Own Apple or Android smartphones compatible with Remote Check application
You will not qualify if you...
- Physical (visual, motor) or severe cognitive impairments preventing use of smartphone software and hearing tests
- Unable to give oral informed consent
- Living in areas with limited internet access
- Legally deprived of liberty by judicial or administrative decision
- Under legal protection measures (guardianship or curatorship)
- French is not the native language
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital Montpellier
Montpellier, France
Actively Recruiting
Research Team
F
Frédéric Venail, PhD, MD
CONTACT
O
Olivier Deguine, PhD, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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