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Clinical Trial Summary

The purpose of the study is to evaluate the score of the Evaluation of the Impact of Deafness in Adults(ERSA)/150 questionnaire obtained at 3 months compared to the inclusion score.


Clinical Trial Description

This is a pilot, prospective, interventional, comparative, randomized, longitudinal, open, multicenter study comparing synchronous and delayed hearing aid and speech therapy. Patients will be randomly divided by drawing lots into 2 groups. Both groups will benefit from a hearing aid prescription and speech therapy for a series of 24 sessions at the rate of 1 per week, for an approximate duration of 6 months. Group A will benefit from speech therapy and synchronous equipment, and group B will begin speech therapy after 3 months after the installation of the equipment. Regarding the equipment, it will not be the same for all patients. Indeed, it is the one that will best suit the patient who will be chosen. The same will apply to the settings, in accordance with the usual support. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05946395
Study type Interventional
Source GCS Ramsay Santé pour l'Enseignement et la Recherche
Contact Arnaud DEVEZE, MD
Phone 683870819
Email dr.deveze@gmail.com
Status Not yet recruiting
Phase N/A
Start date April 2024
Completion date April 2026

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