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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05055453
Other study ID # SRF-85, Sonova 2020_15
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 4, 2021
Est. completion date December 5, 2022

Study information

Verified date April 2022
Source Sonova AG
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

ESolutions functions for children and young people with the myPhonak app is a prospective study to investigate whether the myPhonak app can improve speech understanding in children with hearing aids. The study is linked to randomized patient and test allocation carried out.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date December 5, 2022
Est. primary completion date December 5, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 7 Years to 17 Years
Eligibility Inclusion Criteria: - Children and adolescents between the ages of 7 and 17 years old. - With normal middle ear characteristics - With a hearing impairment in the mild to severe range - With adequate speech development Exclusion Criteria: - Unreliability and lack of cooperation exists, - An effusion in the middle ear or local inflammation in the ear canal or middle ear with/without a running ear, - Mental limitations, - If the patient is unable to operate a smartphone, - Other objections to study participation in the opinion of the study director exist.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
MyPhonak Junior App
The primary objective is to evaluate the effects on speech intelligibility of resulting from the changes that children and adolescents (aged 7 to 17 years) make to the volume control, directionality and noise reduction of the hearing of the hearing aids using the myPhonak app. First, in a controlled laboratory environment under the guidance of the principal investigator is tested. Then, using sound scenarios, the child is allowed to try out two programs with the aid of using the app and the volume control, respectively. After this, the speech comprehension of sentences in noise is tested in the individual programs using the Oldenburg Sentence Test (OLSA).

Locations

Country Name City State
Germany Universitätsmedizin Mainz, HNO-Klinik Mainz Rheinland-Pfalz

Sponsors (1)

Lead Sponsor Collaborator
Sonova AG

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in OLSA score after subjects adjust hearing aid with MyPhonak Junior App At the first face-to-face the subject will be trained on the app, and complete the OLSA. After 2 week home trial, the OLSA will be re-administered to see if the adjustments the subjects made using the MyPhonak Junior app impacted speech intelligibility, which would be shown by the OLSA score at the second face-to-face visit. 4 weeks for each subject (2 face-to-face visits + 2 weeks home trial), 12 months in total for study to be completed
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