A prospective, repeated-measures investigation to validate digital speech perception endpoints in adult cochlear implant recipients using the mobile research app: a master umbrella investigation
NCT ID NCT06098482
First seen Oct 22, 2026 · Last updated Oct 23, 2026 · Updated 1 time
Summary
The study is a feasibility, prospective, repeated-measures, multi-country, multi-centre, study of the Mobile Research App to measure and validate speech perception endpoints in adult cochlear implant recipients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 46 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Feb 2024
- Expected to finish
-
May 2027
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults 18 years of age or older. * Uses a hearing device or devices (hearing aid/s and/or cochlear implant/s). * Fluent speaker in the language used to assess clinical performance as judged by the investigator. * Willing and able to provide written informed consent. Exclusion Criteria: * Unable or unwilling to comply with the requirements of the clinical investigation as determined by the Investigator. * Investigator site personnel directly affiliated with this study and/or their immediate families; immediate family is defined as a spouse, parent, child, or sibling. * Cochlear employees or employees of Contract Research Organisations or contractors engaged by Cochlear for the purposes of this investigation. * Currently participating, or participated within the last 30 days, in another interventional clinical investigation/trial involving an investigational drug or device (unless the other investigation was/is a Cochlear sponsored investigation and determined by the investigator or Sponsor to not impact this investigation). * Women who are pregnant.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Hearing loss are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Denver Research and Technology Labs
Lone Tree, Colorado, 80124, United States
-
European Institute for Otorhinolaryngology (EIORL) ENT department Sint-Augustinus Antwerp
Antwerp, Antwerp, 2610, Belgium
-
HEARnet Clinical Studies
Melbourne, Victoria, 3053, Australia
-
Hoorzorg van Looveren
Wommelgem, Antwerp, 2160, Belgium
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- The nucleus hybrid L24 implant system: extended duration post approval study
- Can routine testing catch Cisplatin's toll on hearing and balance?
- Can a group program sharpen thinking in older adults with hearing loss?
- Can hearing aids reconnect people? scientists track First-Time users for 13 months
- Can using both ears boost speech understanding after a cochlear implant?
- Can a smartphone app replace the clinic for hearing aid tuning?