The 'Lombard Effect' in Patients Affected by Adductor Laryngeal Dystonia

NANot yet recruitingINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

May 1, 2024

Primary Completion Date

April 30, 2025

Study Completion Date

May 1, 2025

Conditions
Adductor Spasmodic Dysphonia
Interventions
OTHER

Lombard test

In this study a single-subject enrolment session will be set up, with the presence of a dedicated physician for informed consent, the performance of a tonal audiometric examination and a clinical practice phoniatric examination for all enrolled subjects, the collection of voice recordings both before and during the Lombard Test (LT) and the administration of the rating scales both before and after the LT performance. For each subject, voice recordings will be made of the vowel /a/ sustained for at least four seconds with a comfortable tone and volume and of the speech obtained from the reading aloud and volume of normal conversation of a phonetically balanced text (The Desert) lasting about 1 minute, first in a silent condition and then in the presence of noise. Specifically, for the LT, each subject will be exposed to a free-fieldwhite noise of speech(SWN) administered through headphones. The intensity of the noise will be 70 dB SPL. Voice recordings will be made in a quiet room.

Trial Locations (1)

00168

Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma

All Listed Sponsors
lead

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

OTHER

NCT06402214 - The 'Lombard Effect' in Patients Affected by Adductor Laryngeal Dystonia | Biotech Hunter | Biotech Hunter