Swallowing Disorders Clinical Trial
Official title:
Contribution of Respiratory Plethysmography by Inductance and of Informatic Tool for the Study of Swallowing Disorders in Geriatrics (PRIOD)
The purpose of this study is to evaluate the efficiency of a novel non-invasive method for swallowing disorders detection in geriatrics.
Interest: swallowing disorders exist at any age. More common among the elderly, their
prevalence is estimated at between 15 and 50% of more than 60 years. Recognized today as a
health problem of particular concern within this population, their pathological consequences
are multiple and severe: inhalation pneumonia, often a complication of "the wrong track",
was recognized in the USA in 1989, as 5th cause of death among patients aged 65, and the 3rd
leading cause of death of patients over 85 years. Malnutrition facilitates infections by
depression of the immune system and promotes the development of bedsores. The swallowing
disorders resulting in an increase in the prevalence of dehydration, social isolation, but
also an increase in mortality. Faced with such consequences, it is therefore necessary to
have a reliable, non-invasive approach adapted to the fragility of the elderly to detect
these disorders in order to promote preventive strategies and / or curative justified.
Originality: This work, which is part of a clinical approach uses a new method of swallowing
study, described in A. Moreau-Gaudry's Medicine thesis : "Assets of the respiratory
inductance plethysmography to the study of swallowing in geriatrics." The originality of
this lies in the combination of Respiratory Plethysmography by inductance (RPI) to the
informatic tool. The PRI allows continuous recording, thanks to a vest connected to a
laptop, the patient's breathing rate. Readily available at the patient's bedside, it is
non-invasive and perfectly suited to the fragility of the study population. The tool, by its
automatic guarantees objectivity and reproducibility of the analysis of deglutitions from
respiratory signal provided by the RPI.
;
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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