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Recruiting NCT07205354

Design of a Food Preference Assessment Tool for Older Patients in Geriatrics units_DYSPHAGING-PREFERENCES

Trial Parameters

Condition Hospitalisation in Geriatrics
Sponsor Hospices Civils de Lyon
Study Type OBSERVATIONAL
Phase N/A
Enrollment 209
Sex ALL
Min Age 70 Years
Max Age N/A
Start Date 2025-10-10
Completion 2026-01-10
Interventions
ADAPTATIONtest-retest reliabilityCross-sectional study

Brief Summary

Swallowing disorders - or oral dysphagia (OD) - are identified as a cause of malnutrition. They gradually lead patients to withdraw certain foods from their diet, leading to progressive dietary imbalances, or increased cardiovascular risks. Two European societies (the European Society for Swallowing Disorders and the European Union Geriatric Medicine Society) have defined recommendations that include raising awareness of OD, the use of screening scores, preventive measures, diagnostic standardization and interventions implemented (re-education, adaptation of textures). We recently reported the results of the DYSPHAGING Pilot Study that validated the feasibility of a standardized care path including a systematic screening of OD and the implementation of preventive measures in geriatric wards. DYSPHAGING Preferences is a three-step research program designed to develop (step 1) a specific device to evaluate food preferences in geriatric populations, adapted from the CFTPQ, evaluate its test-retest reliability (step 2), and perform a cross-sectional study to explore individual differences within the older population depending on their geriatric characteristics and, among them, on the presence or not of OD (step 3).

Eligibility Criteria

Inclusion Criteria: * Patient aged over 70 * Patient hospitalised in the healthcare sector (CSG, SMR) * Patient or patient under guardianship informed of the study and having expressed no objection to participating in the study * Patient under guardianship whose guardian has been informed of the study and has expressed no objection to the patient's participation in the study. Exclusion Criteria: * Patient unable to complete the questionnaire. * Patient unable to eat orally

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