Modelling of Pharyngeal Laryngeal Effectiveness

NARecruitingINTERVENTIONAL
Enrollment

520

Participants

Timeline

Start Date

April 14, 2023

Primary Completion Date

April 30, 2026

Study Completion Date

December 31, 2026

Conditions
Swallowing Disorders
Interventions
OTHER

Swallowing evaluation

"For patients with swallowing disorders: assessment of the swallowing performed according to the available reference examination (videofluoroscopy or nasofibroscopy). In parallel, they will carry the following sensors: microphone, accelerometer, surface electromyography, nasal cannula and pulse oximeter. The subjects will also perform a cough and phonation test and questionnaires. Each subject (or his caregiver) will be contacted by phone once a month for 6 months to monitor the occurrence of complications. The end of study visit at 6 months will be done either at the hospital with a new examination of the swallowing, by telephone, as medically indicated.~For healthy volunteers: Only one visit is planned for the evaluation of the swallowing with the examination of nasofibroscopy and the installation of the sensors. The procedures (tests, examinations and questionnaires) will be identical to the data collection of the initial visit of patients with swallowing disorders)"

Trial Locations (4)

31059

RECRUITING

University Hospital of Toulouse, Toulouse

33000

NOT_YET_RECRUITING

University hospital of Bordeaux, Bordeaux

37000

RECRUITING

University hospital of Tours, Tours

76038

NOT_YET_RECRUITING

University hospital of Rouen, Rouen

All Listed Sponsors
collaborator

National Research Agency, France

OTHER

collaborator

Institut de Recherche en Informatique de Toulouse (IRIT)

UNKNOWN

collaborator

Laboratoire parole et langage

UNKNOWN

collaborator

Swallis Medical

INDUSTRY

lead

University Hospital, Toulouse

OTHER